7-Year-Old Died of Cardiac Arrest 13 Days After Pfizer Shot, VAERS Data Show

7-Year-Old Died of Cardiac Arrest 13 Days After Pfizer Shot, VAERS Data Show
VAERS data released Friday by the Centers for Disease Control and Prevention included a total of 1,168,894 reports of adverse events from all age groups following COVID vaccines, including 25,158 deaths and 203,888 serious injuries between Dec. 14, 2020, and March 4, 2022. 

by Megan Redshaw, The Defender
March 11, 2022

 

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,168,894 reports of adverse events following COVID vaccines were submitted between Dec. 14, 2020, and March 4, 2022, to the Vaccine Adverse Event Reporting System (VAERS). VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 25,158 reports of deaths — an increase of 331 over the previous week — and 203,888 reports of serious injuries, including deaths, during the same time period — up 3,557 compared with the previous week.

Excluding “foreign reports” to VAERS, 783,282 adverse events, including 11,505 deaths and 75,286 serious injuries, were reported in the U.S. between Dec. 14, 2020, and March 4, 2022.

Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.

Of the 11,505 U.S. deaths reported as of March 4, 17% occurred within 24 hours of vaccination, 22% occurred within 48 hours of vaccination and 60% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 554 million COVID vaccine doses had been administered as of March 4, including 327 million doses of Pfizer, 209 million doses of Moderna and 18 million doses of Johnson & Johnson (J&J).

Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed. Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

U.S. VAERS data from Dec. 14, 2020, to March 4, 2022, for 5- to 11-year-olds show:

The most recent death involves a 7-year-old boy (VAERS I.D. 2152560) from Washington who died 13 days after receiving his first dose of Pfizer’s COVID vaccine when he went into shock and suffered cardiac arrest. He was unable to be resuscitated and died in the emergency department.

  • 17 reports of myocarditis and pericarditis (heart inflammation).

The CDC uses a narrowed case definition of “myocarditis,” which excludes cases of cardiac arrest, ischemic strokes and deaths due to heart problems that occur before one has the chance to go to the emergency department.

U.S. VAERS data from Dec. 14, 2020, to March 4, 2022, for 12- to 17-year-olds show:

The most recent death involves a 14-year-old boy (VAERS I.D. 2148498) who experienced a cerebral aneurysm leading to death one day after receiving his first dose of Pfizer’s COVID vaccine.

  • 69 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 96% of cases attributed to Pfizer’s vaccine.
  • 650 reports of myocarditis and pericarditis with 631 cases attributed to Pfizer’s vaccine.
  • 161 reports of blood clotting disorders, with all cases attributed to Pfizer.
U.S. VAERS data from Dec. 14, 2020, to March 4, 2022, for all age groups combined, show:
CDC study concludes COVID vaccine adverse events ‘mild’

study funded by the CDC and published Monday in The Lancet concluded most COVID vaccine-related adverse events reported during the first six months of the rollout in the U.S were “mild and short in duration,” despite thousands of deaths reported to VAERS.

For the study, researchers analyzed data captured between Dec. 14, 2020, and June 14, 2021, by VAERS and v-safe, both of which are overseen by the CDC. Nearly 300 million doses of COVID vaccines were administered during the study period.

The authors found that of the 340,522 adverse events reported to VAERS, 27,023 (8%) were serious, 4,496 were deaths. The authors said the cause of the increased reporting of deaths during the first few days after vaccination might represent “reporting bias.”

The authors suggested that deaths occurring soon after vaccination were more likely to be reported than deaths that occurred later. This, they believe, is why the number of deaths asymptotically approaches zero as more time elapses since vaccination.

Jessica Rose, Ph.D., attempted to duplicate the Lancet authors’ findings through her independent analysis of the VAERS data. Despite filtering the database using three different date stamps, Rose was unable to duplicate the Lancet study’s results.

Florida surgeon general breaks with CDC, recommends against shots for healthy kids

Florida’s surgeon general on Monday said he will issue guidance formally recommending against COVID vaccines for healthy children. Florida is the first state to break with official guidance from the CDC, which recommends all children over age 5 get the vaccine.

Dr. Joseph Ladapo made the announcement at a roundtable, hosted by Gov. Ron DeSantis, featuring physicians and other medical experts who criticized CDC and government policies, including mask mandates and lockdowns, which they said were ineffective and harmful.

Ladapo and DeSantis said the new guidance had to do with lingering questions about the vaccines’ potential health risks for young people and the fact that children are in a low-risk category for severe COVID.

COVID vaccines may be enhancing disease 

COVID vaccines may be causing enhanced disease because they target an old version of the coronavirus, Dr. Robert Malone told the Epoch Times in a recent interview.

“The data are showing that vaccination can actually increase the risk of being infected with the Omicron version of this virus,” Malone said, referring to how in some areas, including Scotland and New Zealand, patients hospitalized with COVID are more likely to have received a COVID vaccine.

U.S. drug regulators identified vaccine-associated enhanced diseases (VAED) as an “important potential risk” of COVID vaccines, along with enhanced respiratory disease.

Some adverse events reported following COVID vaccination “could indicate” VAED, according to a CDC team.

VAED refers to disease “resulting from infection in individuals primed with non-protective immune responses against the respective wild-type viruses,” researchers said last year.

“Given that these enhanced responses are triggered by failed attempts to control the infecting virus, VAED typically presents with symptoms related to the target organ of the infection pathogen,” they added.

Vaccine researcher develops tinnitus after COVID shot, calls for further study

Dr. Gregory Poland, director of the Mayo Clinic’s Vaccine Research Group in Rochester, Minnesota, developed life-altering tinnitus, or ringing in the ear, after receiving his second dose of a COVID vaccine.

“It was like someone suddenly blew a dog whistle in my ear,” Poland told MedPage Today. “It has been pretty much unrelenting.”

Poland then received a booster, after which his tinnitus briefly disappeared but then returned at a slightly higher pitch. Poland realized his life may never be the same and says he has received emails from people across the world struggling with the same condition to the point they’re considering taking their own lives.

Poland, who said he supports COVID vaccines, believes there may be tens of thousands of people affected in the U.S. and is calling for more research to be done to provide help to people desperate for relief.

Michigan woman files claim over mom’s COVID vaccine-related death  

Tatum Strieter-Byron is asking the federal government to compensate her for the death in April of her mother Sandra Jacobs. An autopsy confirmed Jacobs died from a blood-clotting disorder caused by J&J’s COVID vaccine.

Strieter-Byron received confirmation Monday her claim to the Countermeasures Injury Compensation Program (CICP) had been received. The program was established to give pharmaceutical companies blanket liability protection from harm caused by their COVID vaccines.

In 2020, the U.S. Health and Human Services secretary invoked the Public Readiness and Emergency Preparedness (PREP) Act and declared COVID-19 a public health emergency, providing J&J other COVID vaccine makers immunity from lawsuits.

The only exception under the PREP Act is if a plaintiff can prove a vaccine-related death or serious physical injury was caused by “willful misconduct.” The protections, unless amended or rescinded, extend through Oct. 1, 2024.

Claims to the CICP must be made within one year of the date the vaccine was received.

Jacobs, 60, received the single-shot vaccine at a CVS pharmacy on April 8, 2021, just five days before federal health agencies temporarily paused the vaccine to examine numerous reports of a serious and potentially fatal blood-clotting disorder.

Jacobs died on April 21 of “complications of cerebral venous sinus thrombosis,” a type of stroke caused by the vaccine.

Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

 

©March 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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La Quinta Columna: Dr. Sevillano Discovers New Strange ‘Life Forms’ in Pfizer Vaccine Samples

Dr. Sevillano Discovers New Strange ‘Life Forms’ in Pfizer Vaccine Samples

by Orwellito, Orwell City
March 9, 2022

 

Dr. José Luis Sevillano is conducting research based on the observation and evolution of different possible unidentified life forms in the most detailed way possible.

He has spent several days identifying different structures: from filaments that are formed based on DNA crystalsMorgellons, and strange life forms.

In a recent program, he identified some structures that look like long leaves and others that are more vermiform and frightening.

Orwell City brings Dr. Sevillano’s observations and theories to English.



Transcript:

Dr. Sevillano: These are the ones I was telling you about. They’re all of this kind and look alike. And I don’t know if it’s contamination or something else. I don’t know if they’re plants or something else. That’s why I was saying that if there’s someone who’s an expert in these things, please tell me.

Ricardo Delgado: A botanical expert. A botanist.

Dr. Sevillano: Exactly. And there are many of them. I have observed this in the first sample that I took, and I have left it to dry. Let’s see if it dries completely. But these things have appeared so far. This doesn’t look like pollen or anything like that. So I wondered, is this contamination or what? I have my doubts about this, but there it is. Just in case, I’ll confirm it for you. Look at the shape of it. And look, this is what makes me suspect that the famous carbon deposits are releasing that sort of tube-like…

Ricardo Delgado: Filaments?

Dr. Sevillano: Filaments or I don’t know what is born from them. And that’s why I took the picture because I said I thought: “Couldn’t all this come out of the charcoals and then come to life? Or what’s that?”

There are more pictures, see? Another one again. That one looks like… These are… Anyway, I’ll confirm it when I see I look at tonight’s sample again. These are from the first sample. These things have been popping up over the last few of the last few days.

I have to confirm if this is contamination or something else that comes up after a few days in the sample.

Ricardo Delgado: My goodness.

Dr. Sevillano: It looks like a plant, right? Like it’s some kind of plant. You can see that when you leave it there on its side. And now, this is from the new sample that I have with the coverslip, on the drop. So, there’s no possibility of contamination there.

This is one of the famous microchips. This is a photo at 10X. And the previous one was at 40X. Look at this… 40X. So you can see that this previous structure isn’t crystal of any kind. Neither of sucrose. It’s not a crystal. It’s a plate of the kind we’ve already seen. A microchip or what has also been seen as a nanochip.

Ricardo Delgado: Look at that.

Dr. Sevillano: See? See the indentations that form there? That’s so you can see the self-assembly.

Ricardo Delgado: Unbelievable. All of this is seen in Pfizer’s vaccine.

Dr. Sevillano: Another one of the indentations. You can see that from a distance it looks like a crystal, maybe, but up close you realize that it’s nanotechnology. This is a strange structure that I have seen that was shaped like a pyramid with several… It’s very strange. And I took a picture of it. I don’t know exactly what that is.

Ricardo Delgado: Another one.

Dr. Sevillano: It’s another microchip. And this is something else. A ribbon that in the enlargement loops around. I took the screenshot of the two ends because then it kind of loops around, and it looks like it could make a… This isn’t a droplet, but it’s the ends extending.

Ricardo Delgado: Yes.

Dr. Sevillano: That’s where I took the starting photo because it was so big that I couldn’t capture it all in the same capture. And there is another one of the supposed plants. I’m sure it’s not contamination because I’ve made from this new sample that’s covered with a coverslip on the slide. Here is another one of these famous plants, like the ones I showed you the other days. That one. And now comes the most frightening one. This is a small one.

And then the next one and the one after that are the scariest ones I’ve ever seen. There you see it. This has appeared the day after I made the sample. I prepared it last night. And this afternoon, looking through the microscope, I spotted it. That hasn’t grown, but it was already in the drop. Here it is seen with less magnification. From far away. That’s seen at 10X. And then there’s another one. Let’s see if we can see another. That one is terrifying. That’s seen at 40X.

Ricardo Delgado: This one.

Dr. Sevillano:Yes. And now you’ll see it from far away. It’s too big too. There you can see the folds that make those… I don’t know if they’re leaves or what the heck is that. And now you’ll see it from far away. Horrible.

Ricardo Delgado: There.

Dr. Sevillano: That’s it.

Ricardo Delgado: Holy crap!

Dr. Sevillano: Those aren’t microchips, you know. That’s something else. So if people complain about things happening to them, how do they want nothing to happen? How do you want nothing to happen?

So far we’ve identified graphene, a microchip, they can go nanochips, this thing, what I showed you at the beginning, which is that sort of thing that looks like… I don’t even know what that is. We’re going to consider like that was contamination, but this thing that you just saw isn’t contamination for sure. I’m sure it’s not because I covered the sample as soon as I prepared it to avoid contamination. And that’s protected. The first thing you’ve seen looks to me like it’s no contamination. But until I see how this drop evolves now, I can’t guarantee it. I’ll be monitoring to see if the same shape appears, because those little ones that we saw at the beginning, I have the feeling that they’re also going to appear over time.

 Ricardo Delgado: Surely.

Dr. Sevillano: Anyway, I prefer to wait.

 

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CDC/FDA Smoking Gun of Smoking Guns

CDC/FDA Smoking Gun of Smoking Guns
They confess: they had no virus when they concocted the test for the virus; they “contrived” a model by pretending to find what they wanted to find; it’s called a self-fulfilling prophecy
This is the con and the crime that drove millions of lives, and economies, into ruin

 

by Jon Rappoport, No More Fake News
March 9, 2022

 

Quiz: If an agency of the federal government revealed they had no basis for constructing a diagnostic test that was used on millions of people; but the test was the cornerstone of a national lockdown; and the lockdown drove the economy off a cliff; and destroyed millions of lives; however, NOW, that agency says, they DO have a basis for the test; would you buy what they’re selling?

If your answer is yes, you’re in good company; the company I call Blind, Ignorant, Denialist, Hoaxing Journalists.

The CDC issued a document that bulges with devastating admissions.

The release is titled, “07/21/2021: Lab Alert: Changes to CDC RT-PCR for SARS-CoV-2 Testing.” It begins explosively:

“After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives.”

Many people believe this means the CDC is giving up on the PCR test as a means of “detecting the virus.” The CDC isn’t saying that at all.

They’re saying the PCR technology will continue to be used, but they’re replacing what the test is looking FOR with a better “reference sample.” A better marker. A better target. A better piece of RNA supposedly derived from SARS-CoV-2.

CDC/FDA are confessing there has been a PROBLEM with the PCR test which has been used to detect the virus, starting in February of 2020—right up to this minute.

In other words, the millions and millions of “COVID cases” based on the PCR test in use are all suspect. Actually, that statement is too generous. Every test result of every PCR test should be thrown out.

To confirm this, the CDC document links to an FDA release titled, “SARS-CoV-2 Reference Panel Comparative Data.” Here is a killer quote:

“During the early months of the Coronavirus Disease 2019 (COVID-19) pandemic, clinical specimens [of the virus] were not readily available to developers of IVDs [in vitro diagnostics] to detect SARS-CoV-2. Therefore, the FDA authorized IVDs based on available data from contrived samples generated from a range of SARS-CoV-2 material sources (for example, gene specific RNA, synthetic RNA, or whole genome viral RNA) for analytical and clinical performance evaluation. While validation using these contrived specimens provided a measure of confidence in test performance at the beginning of the pandemic, it is not feasible to precisely compare the performance of various tests that used contrived specimens because each test validated performance using samples derived from different gene specific, synthetic, or genomic nucleic acid sources.”

Translation: We, at the CDC, did not have a specimen of the SARS-CoV-2 virus when we concocted the PCR test for SARS-CoV-2. Yes, it’s unbelievable, right? And that’s the test we’ve been using all along. So we CONTRIVED samples of the virus. We fabricated. We lied. We made up (invented) synthetic gene sequences and we SAID these sequences HAD TO BE close to the sequence of SARS-CoV-2, without having the faintest idea of what we were doing, because, again, we didn’t have an actual specimen of the virus. We had no proof THERE WAS something called SARS-CoV-2.

This amazing FDA document goes to say the Agency has granted emergency approval to 59 different PCR tests since the beginning of the (fake) pandemic. 59. And, “…it is not feasible to precisely compare the performance of various tests that used contrived specimens because each test validated performance using samples derived from different gene specific, synthetic, or genomic nucleic acid sources.”

Translation: Each of the 59 different PCR tests for SARS-CoV-2 told different lies and concocted different fabrications about the genetic makeup of the virus—the virus we didn’t have. Obviously, then, these tests would give unreliable results. THE PCR TESTS USED CONTRIVED SPECIMENS OF THE VIRUS WE DIDN’T HAVE.

BUT, don’t worry, be happy, because NOW, the CDC and the FDA say, they really do have actual virus samples of SARS-CoV-2 from patients; they have better targets for the PCR test, and labs should start gearing up for the new and improved tests.

In other words, they were lying THEN, but they’re not lying NOW. They were “contriving,” but now they’re telling the truth.

If you believe that, I have Fountain of Youth water for sale, extracted from the lead-contaminated system of Flint, Michigan.

Here, once again, I report virology’s version of “we isolated the virus”:

They have a soup they make in their labs.

This soup contains human and monkey cells, toxic chemicals and drugs, and all sorts of other random genetic material. Because the cells start to die, the researchers ASSUME a bit of mucus from a patient they dropped in the soup is doing the killing, and THE VIRUS must be the killer agent in the mucus.

This assumption is entirely unwarranted. The drugs and chemicals could be doing the cell-killing, and the researchers are also starving the cells of vital nutrients, and that starvation could kill the cells.

There is no proof that SARS-CoV-2 is in the soup, or that it is doing the cell-killing, or that it exists.

Yet the researchers call cell-death “isolation of the virus.”

To say this is a non-sequitur is a vast understatement. In their universe, “We assume, without proof, we have the virus buried in a soup in a dish in the lab” equals, “We’ve separated the virus from all surrounding material.”

Virology equals “how to spread bullshit for a living and scare the world.” Other than that, it’s perfect.

 

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cover image credit: D1_TheOne / pixabay




Just Released Documents by Pfizer Show BioNTech Paid FDA $2,875,842.00 “Drug User Fee” for COVID-19 Vaccine Approval

Just Released Documents by Pfizer Show BioNTech Paid FDA $2,875,842.00 “Drug User Fee” for COVID-19 Vaccine Approval

by Brian Shilhavy, Health Impact News
March 2, 2022

 

As the news cycle continues to focus on the Ukraine situation, the FDA complied with a court order to begin releasing 55,000 pages of Pfizer data per month that was used to authorize their COVID-19 vaccine produced with BioNTech, with the first batch quietly released yesterday, March 1st.

There are 150 documents that the public can now download here.

One of the documents released was the “Prescription Drug User Fee Payment” that BioNTech paid to the FDA on 4/20/2021 for the “COMIRNATY COVID-19 mRNA Vaccine” which the FDA subsequently approved in August of 2021.

That “Prescription Drug User Fee Payment” was $2,875,842.00. (Source.)

Another interesting document I found was the “EXTERNAL DATA MONITORING COMMITTEE” found here.

Here is the stated purpose of this “External Data Monitoring Committee”:

This External Data Monitoring Committee (E-DMC) (hereafter referred to as “the committee”) is a single, external,  independent, expert advisory group established to oversee safety and efficacy data from the BNT162 Vaccine Program. The  primary rationale for establishing the committee is to make certain that appropriate external safeguards are in place to help ensure the safety of subjects and to maintain scientific rigor and study integrity while the trial is on-going.

The committee will review accumulating safety data across all studies, as well as efficacy data in the Phase 2/3 portion of the C4591001 study. The committee will advise Pfizer regarding the safety of current participants and those yet to be recruited, as well as the continuing scientific validity of the trial. In addition to safety review by the committee, qualified Pfizer personnel will review safety data as specified in the safety surveillance review plan and will inform the committee of  significant findings. Efficacy data from the C4591001 study will be available to the committee when there is a planned  interim analysis of efficacy or if this is considered necessary to conduct a risk-benefit assessment.

And to make sure that this Committee is doing their job properly to ensure “the safety of subjects and to maintain scientific rigor,” who at the FDA is responsible to make sure this happens?

Well, that would be no one. Pfizer is the one who was responsible, and BioNTech funded it.

“Pfizer is responsible for conducting this study. BioNTech is the regulatory sponsor of this study.”

The committee members are to be free from “conflicts of interest.”

The committee members will complete a CT22-GSOP-RF01 Independent Oversight Committee Member Conflict of Interest Form. Committee members should be free of apparent significant conflicts of interest. Any potential conflict of interest that develops during a member’s tenure on the committee must be disclosed by the committee member.

And who at the FDA is responsible for assuring that this committee who is overseeing “safety and efficacy data” is free from conflicts of interest?

Well, that would be no one. Again, Pfizer is responsible for that.

“Pfizer will determine if any potential conflict requires termination of committee membership.”

The question that then begs to be answered here is, what role did the FDA play, if any, in the “external” monitoring of the data to ensure integrity and safety of a new vaccine about to be injected into hundreds of millions people in the U.S.?

It would appear that all they did was rubber stamp the process that was completely managed by Pfizer, and funded by BioNTech.

Here are the members of the “External Data Monitoring Committee” that apparently were chosen by Pfizer, monitored by Pfizer, and investigated by Pfizer to make sure they were doing their job and that there were no “conflicts of interest.”

The other interesting thing this document reveals is that a significant number of people compiling the data for this committee to review were located in China.

Rong Zhang: Senior Statistical Programming Lead
4/F, Building 3, Lotus Business Park, Lane
60, Naxian Road,
Pudong ZhangJiang Hi-tech. Park, Shanghai,
China, 201203
Rong.Zhang@pfizer.com

Chen Xu*: Senior Statistical Programmer
4/F, Building 3, Lotus Business Park, Lane
60, Naxian Road,
Pudong ZhangJiang Hi-tech. Park, Shanghai,
China, 201203
Chen.Xu4@pfizer.com

Huan Liu* Senior Statistical Programmer
4/F, Building 3, Lotus Business Park, Lane
60, Naxian Road,
Pudong ZhangJiang Hi-tech. Park, Shanghai,
China, 201203
Huan.Liu@pfizer.com

Jiyang Chen*: Senior Statistical Programmer
4/F, Building 3, Lotus Business Park, Lane
60, Naxian Road,
Pudong ZhangJiang Hi-tech. Park, Shanghai,
China, 201203
Jiyang.Chen@pfizer.com

Bochen Zhu*: Senior Statistical Programmer
4/F, Building 3, Lotus Business Park, Lane
60, Naxian Road,
Pudong ZhangJiang Hi-tech. Park, Shanghai,
China, 201203
Bochen.Zhu@pfizer.com

Ran Xiong*: Senior Statistical Programmer
4/F, Building 3, Lotus Business Park, Lane
60, Naxian Road,
Pudong ZhangJiang Hi-tech. Park, Shanghai,
China, 201203
Ran.Xiong@pfizer.com

I wonder if the raw data is also located in China?

There is a lot more data I am still reviewing, and tens of thousands of more pages of data still to be released by the FDA.

But with everyone watching what is happening in the Ukraine right now, I wonder if anyone is even noticing this?

 

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cover image credit: Martino Glan  / Wikimedia Commons




The New York Times’ Disgraceful and Deceitful Attack on Robert F. Kennedy, Jr.

The New York Times’ Disgraceful and Deceitful Attack on Robert F. Kennedy, Jr.

by Edward Curtin, Behind the Curtain
March 2, 2022

 

The New York Times, floundering in the deep waters of truth and desperately trying to stay afloat in the shallows by continuing its history of lying for its CIA masters, has just published a front page of propaganda worthy of the finest house organs of totalitarian regimes.  Right below its February 26, 2022 headline denouncing Russia and Putin as evil dogs pursuant to the American empire’s dictates concerning Ukraine, it posts an unflattering photo of Robert F. Kennedy, Jr. sandwiched between American flags with the title of its hit piece, “A Kennedy’s Crusade Against Covid Vaccines Anguishes Family and Friends.”

It’s an exquisite juxtaposition: Putin as Hitler and Kennedy as a junior demon, suggestive of the relationship between C. S. Lewis’s Screwtape and his nephew Wormwood in The Screwtape Letters.  Evil personified.

The Times is big into anguish these days, not only for Nazis in Ukraine and upper class apartment hunters who can’t find a place for less than a few million, but for Robert Kennedy, Jr.’s family and friends.  It’s very touching.  That his sister, Kerry Kennedy, would harshly criticize him once again is genuinely pathetic, but of course she has to add how much she loves him, ostensibly to take the sting out of her inability to remain sisterly silent.

If he is so wrong about his work with Children’s Health Defense and his bookThe Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public Healthrather than ripping him to the press, why doesn’t she or her siblings, who agree with her, write a comprehensive article or book refuting his facts?

They don’t because they can’t; so the next best thing is to criticize their brother to media glad for any way to disparage the Kennedys.  One senses a very weird masochistic family dynamic at work.

Kennedy’s siblings do not seem to understand why the media have been attacking him for years.  His stance on vaccines and Anthony Fauci are the cover story they use to criticize him, and his siblings don’t get it.  That their brother has become a major thorn in the side of the CIA escapes them, the CIA that has caused so much devastation to their family and the world.  The CIA that has been deeply involved in the global vaccine push, working with medical technocrats like Anthony Fauci, billionaires such as Bill Gatesthe militarymediaBig Pharma, the World Economic Forum, etc.  Calling your brother brilliant while ignoring his book’s searing, evidence-based indictment of the intelligence-run Covid-19 operation is more than sad, especially when doing so to The New York Times, the CIA’s paper of record together with The Washington Post.

Character assassination of Robert F. Kennedy, Jr. is what the CIA and its media mouthpieces have been doing for years. This has become more and more necessary as they have realized the great growing danger he poses to their agenda. Calling him an anti-vaxxer, conspiracy theorist, and names far worse, is part of a concerted smear campaign to turn the public away from his message, which is multi-faceted and supported by deep research and impeccable logic. Like his father and uncle, he has become an irrepressibly eloquent opponent of the demonic forces intent on destroying the democratic dream.

The Times article by Adam Nagourney is a blatant hatchet job filled with sly jabs, innuendos, and ignorant lies.  As is par for the course, his hack piece completely avoids Kennedy’s arguments but relies on a form of social gossip that substitutes for logic and evidence.  He seems to have learned much from The National Enquirer and The New York Post’s “Page Six” whose styles the NY Times has emulated.

Nagourney tells the reader that RFK, Jr.’s work as the face of the vaccine resistance movement has “tested,” “rattled,” “anguished,” and “mystified” family, friends and his Hollywood crowd; that this man “of the often troubled life” …. “has effectively used his talent and one of the most prominent names in American political history as a platform for fueling resistance to vaccines that could save countless lives.”

Translation: Kennedy, a Hollywood hobnobber and former drug addict, is so mentally unbalanced that he will betray his family and friends and kill people with medical advice that runs counter to the truth.

No evidence is required to establish this “truth,” just Nagourney’s word and those of those he can get to say the same thing, in other words.  Such as:

His conduct ‘undercuts 50 years of public health vaccine practice, and he’s done it in a way I’ve never see [sic] anyone else do it,’ said Michael T. Osterholm, the director of the Center for Infectious Disease Research and Policy at the University of Minnesota. ‘He is among the most dangerous because of the credibility of who he is and what his family name has brought to this issue.’

Notice the implication:  that these experimental mRNA so-called vaccines have been around 50 years and Kennedy is against all vaccines, both of which are false.

Furthermore, Nagourney says RFK, Jr. not only “inveighs” against vaccines, especially Covid vaccinations, but has adopted other weird “unorthodox” views (implication: orthodox views are good) over the years.

One is his claim that Sirhan Sirhan did not kill his father Senator Robert F. Kennedy.  Nagourney might do a smidgen of research and discover that Kennedy is correct; but doing so would disrupt the flow of his ad hominem attack.  All serious writers on the case know that the senator was not shot by Sirhan; they know there are deep CIA connections to the assassination. The evidence conclusively proves, as the autopsy has shown, that Sirhan was in front of the senator when he fired his pistol but RFK was shot from the rear at very close range with all bullets entering his body from the rear.  Nagourney either knows nothing about the assassination or is dissembling the facts, which must be “unorthodox.”

Sounding like a U.S. government spokesmen telling the press something is true without an iota of evidence, he writes the following sentence as if it were true simply because he wrote it, while making sure not to mention the book’s title – The Real Fauci: Bill Gates, Big Pharma, and the Global War on Democracy – a brilliant, deeply researched and sourced book The Times will not review:

In a best-selling new book, he claimed that Dr. Anthony S. Fauci, who is President Biden’s top medical adviser for the coronavirus pandemic, and Bill Gates, the co-founder of Microsoft, were in cahoots with the pharmaceutical industry to profiteer off dangerous vaccines.

Notice Nagourney’s insidious method.  State RFK’s claim as if it’s false because Nagourney stated it, when in fact it is so abundantly true and backed up by massive evidence that if Nagourney dared to engage in actual journalism by checking Kennedy’s book he would discover it.  But his job is not to search for truth but to defile a man’s reputation. He accuses Kennedy of circulating false information on the coronavirus and the vaccines but of course doesn’t say what that is or why it is false.

His entire article is an ad hominem attack by statement with the author cunningly hidden behind deceitful objectivity.

He writes:

To the public distress of his wife, the actress Cheryl Hines, Mr. Kennedy invoked Anne Frank, the young German-Dutch diarist who died in a Nazi prison camp, as he compared government measures for containing the pandemic with the Holocaust at that rally in Washington.

However, that is not what he said.  He said that during the Holocaust Anne Frank could hide for a while and others could flee out of Germany, but with the new “turnkey totalitarianism” being introduced today, which is technological, it will be harder to escape, for every aspect of life will be monitored by the authorities in a digital dystopia. Such a perspective is in no way unusual, for it is shared by many scholars of technology and only the most naïve would consider it eccentric. His point and words were twisted to serve others’ purposes and to paint him as an insensitive Holocaust denier.  Here’s what he said:

What we’re seeing today is what I call turnkey totalitarianism. They are putting in place all of these technological mechanisms for control we’ve never seen before. It’s been the ambition of every totalitarian state since the beginning of mankind to control every aspect of behavior, of conduct, of thought and to obliterate dissent. None of them have been able to do it. They didn’t have the technological capacity.

Even in Hitler’s Germany, you could cross the Alps into Switzerland. You could hide in an attic like Anne Frank did. I visited in 1962 East Germany with my father and met people who had climbed the wall and escaped, so it was possible. Many died … but it was possible.

Yet his sister Kerry also ripped him for making a statement that was clearly true if you accept his argument about the technological lockdowns in progress.  You can disagree (I don’t) but to impugn his intentions and his words is really despicable, but Nagourney adds it to his ad hominem attacks, making sure to include his sister Kerry’s Tweet:

Bobby’s lies and fear-mongering yesterday were both sickening and repulsive. I strongly condemn him for his hateful rhetoric.

Nagourney: “ Even his most prominent critics say they do not doubt his sincerity, even as he has become one of the most prominent spreaders of misinformation on vaccines.”

Translation: RFK, Jr. means well but he’s deluded.

Big Daddy Fauci is introduced to tell the young whippersnapper the following after Kennedy delivered a briefing at The National Institutes of Health:

When it was over, Dr. Fauci walked Mr. Kennedy out of the conference room.

“I said, ‘Bobby, I’m sorry we didn’t come to any agreement here,’” he said. “‘Although I disagree factually with everything you are saying, I do understand and I respect that deep down you are really concerned about the safety of children.’ I said that in a very sincere way.”

Condescension and sincerity overflow as the “conspiracy theorist” patient is told by the good doctor that he means well but needs help.

Then, making sure to include The New York Times endlessly repeated CIA talking point, our no-nothing author writes:

The assassination of President John F. Kennedy, his uncle, in 1963, when Robert was 9, helped foster a modern culture of conspiracy theories. Now, many of the arguments that Mr. Kennedy has embraced — including that Dr. Fauci is part of a “historic coup d’état against Western democracy” — recall the theories of a secret assassin helping Lee Harvey Oswald from the grassy knoll in Dallas.

That it was the CIA that weaponized the use of the term “conspiracy theory” in a 1967 dispatch – #1035-960 – in order to disparage those questioning The Warren Commission and it’s cover-up of the CIA’s role in JFK’s assassination is another fact that our fair-minded scribe conveniently omits while insidiously implying that Lee Harvey Oswald killed JFK.  Yes, there are magic bullets and magical tricks used to make sure RFK, Jr. is seen as a “sincere” nutcase.

RFK, Jr. has been and is an astute critic of the CIA and all its machinations, including its involvement in the assassinations of his uncle JFK, his father Senator Robert F. Kennedy, its involvement in the COVID propaganda, and in its extensive deadly deeds and disinformation at home and abroad.  His critical siblings praise him for his great intelligence and political acumen but seem clueless themselves.  So they ally with the same media that have been stenographers for the CIA.  The Kennedy family may be very well known, but in these ways they are very typical of American families that are divided by those who know and those who don’t know who the real devils are.

But let me make two final points about this sickening piece of character assassination.

RFK, Jr. has spent decades as an environmental lawyer fighting the pollution of our air, earth, and water.  In other words, the pollution also of human beings who live in nature while nature lives in us. Some people know the outside and the inside are connected.  Yet Nagourney bemoans the tragic turn he took from such good work with the environment to such terrible work with Children’s Health Defense and vaccines. He writes:

The swerve in Mr. Kennedy’s career, from the environment to vaccines, is particularly startling because for many family members and other Kennedy associates, Robert Kennedy Jr. is the sibling who most recalls the level of charisma and political appeal of his late father.

Startling?  No, very consistent for one who can think.  There is an obvious link between the major corporate polluters of the outside environment and the major polluters of human bodies.  Big pharmaceutical, oil, chemical, agribusiness, military, etc. are an interrelated lot of criminal enterprises despoiling all life on earth.  Kennedy’s lifetime work has followed a natural trajectory and underlying it all is his critique of the CIA and its media accomplices, such as The New York Times.

Yes, those family and friends who say he’s brilliant are right, and he is following in his father’s footsteps in ways they do not grasp; for he is able to connect the dots, diagnose the patterns, and expose with facts the criminal syndicates that are destroying democracy and so many lives.

The reason The New York Times publishes hit pieces like this and does not review his recent books is because his critique of these nefarious forces has gained a large audience and as a result many people are awakening to the truths concealed by the likes of the paper of record” with its propaganda.

Hit pieces like Nagourney’s should cause anyone reading it intense “anguish.”  There is nothing “mystifying” about it.

It’s simply disgraceful and deceitful.

 

Connect with Edward Curtin

cover image credit: Adam63  / Wikimedia Commons




Woman Died of Blood Disorder After J&J Vaccine. CDC Says the Disorder Is Rare — But Is It?

Woman Died of Blood Disorder After J&J Vaccine. CDC Says the Disorder Is Rare — But Is It?
U.S. health officials continue to say blood-clotting disorders like the one that killed 52-year-old Monica Melkonianare two weeks after the J&J vaccine are rare — despite thousands of vaccine-induced blood-clotting events reported to the Centers for Disease Control and Prevention.

by Megan Redshaw, The Defender
March 2, 2022

 

The husband of an Oregon woman who died last year from a blood-clotting disorder — two weeks after receiving Johnson & Johnson’s (J&J) COVID vaccine — spoke out publicly this week about his wife’s death.

Stan Thomas told NBC News he’s fighting to ensure his wife’s sacrifice is not forgotten.

“When it’s 8 million doses and two people are going to die from it,” Thomas said, “who thinks it’s going to be you?”

NBC News characterized the risk of harm in general from COVID vaccines as “a 1-in-a-million risk.”

And U.S. health officials continue to say blood-clotting disorders like the one that killed Thomas’ wife are rare — despite thousands of vaccine-induced blood-clotting events reported to the Centers for Disease Control and Prevention (CDC).

Monica Melkonian, 52, received her J&J shot at a vaccination clinic on April 7, 2021 —  the same day the CDC and U.S. Food and Drug Administration (FDA) temporarily paused the vaccine while they investigated numerous reports of a rare blood-clotting disorder called vaccine-induced thrombotic thrombocytopenia (VITT).

VITT is a sometimes fatal condition characterized by simultaneous acute thrombosis and thrombocytopenia that presents after receiving a COVID vaccine.

Melkonian’s most notable symptoms included a persistent headache and pain behind her left eye. But Thomas said she and her husband continued to work around their home and carry out their daily activities.

Her headache was mostly gone by April 17, but at 4 a.m the next day, Thomas heard his wife call out as she hit the floor. She experienced a seizure and could not move her right arm. Thomas, who immediately suspected a stroke caused by the shot, called 9-1-1.

“The progression of this was just lightning-fast,” Thomas said, “which I am tragically grateful for.”

At the emergency room, Thomas asked his wife to squeeze his hand once for “yes” and twice for “no” in an effort to communicate with her.

“The last thing that I said to her was that I loved her and asked her to squeeze my hand twice,” Thomas said. “She did.”

CDC investigates Melkonian’s death

The CDC on April 22, 2021, launched an investigation into Milkonian’s death.

“This blood clot was seen in combination with very low platelets,” the Oregon Health Authority wrote in a statement. “Prior to the issuance of the pause, cases of this serious blood clot had been identified among six women around the country who received the vaccine.”

Both Melkonian and her husband were “experts in the field of occupational health and safety” and were directly involved in the COVID pandemic response, Thomas said.

Both were aware of risks associated with COVID vaccines, but they believed the risks paled in comparison to the risks associated with the virus.

Thomas said he is steadfastly “pro-vax,” but questions whether health authorities have done enough to help people understand their options.

U.S. acknowledges only nine deaths from blood clots following J&J shot

To date, the U.S. has confirmed only nine deaths due to VITT caused by the J&J shot, NBC reported.

During the CDC vaccine advisory panel’s most recent benefit and risk assessment meeting, on Dec. 16, 2021, the agency acknowledged only 54 cases of blood-clotting conditions among J&J recipients, including nine deaths.

Thirty-nine of the 54 reported cases occurred before the CDC and FDA paused the vaccine in April to investigate its link to blood clots.

The CDC’s COVID-19 Vaccine Task Force said it excluded “reports where [the] only thrombosis is ischemic stroke or myocardial infarction” — a move that significantly reduced the number of blood-clotting cases included in the task force’s analysis.

According to the CDC website, most strokes (87%) are ischemic strokes. An ischemic stroke occurs when blood flow through the artery that supplies oxygen-rich blood to the brain becomes blocked — a condition often caused by blood clots.

Myocardial infarction is a heart attack that occurs when the heart muscle doesn’t get enough blood due to a blockage — such as a blood clot — in the arteries that supply blood to the heart.

Because rates were still higher than previously estimated among both men and women, the panel voted 15 – 0 to “preferentially recommend” mRNA COVID vaccines Pfizer and Moderna over the J&J shot for adults 18 years and older.

However, both the Pfizer and Moderna vaccines also are associated with blood-clotting disorders.

According to data compiled by “Our World In Data,” between Dec. 14, 2021, and Feb. 18, 2022, 18.36 million doses of the J&J vaccine had been given.

During this same time period, 13,216 reports of blood clotting disorders following COVID vaccine disorders were reported to the Vaccine Adverse Event Reporting System (VAERS), with 2,568 attributed to J&J’s vaccine.

Data from VAERS show there were 2,275 reports of blood-clotting disorders following J&J’s COVID vaccine between Dec. 14, 2020, and Dec. 10, 2021 — a far greater number than the 54 cases acknowledged by the CDC during its December advisory meeting.

Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

Reports of clotting disorders following J&J shot

​​The Defender has reported on numerous cases of blood clots following COVID vaccination with the J&J shot:

  • Jessica Berg Wilson, a 37-year-old mother died from VITT after she received J&J’s COVID vaccine as a condition of volunteering at her child’s school.
  • Emma Burkey, an 18-year-old teen was put on a respirator and underwent three brain surgeries from blood clots after receiving J&J’s vaccine.
  • Anne VanGeest, a healthy 35-year-old, died of a brain hemorrhage 11 days after receiving J&J’s COVID vaccine.
  • Brad Malagarie, a healthy 43-year-old father of seven experienced a stroke from blood clots hours after receiving J&J’s COVID vaccine. The stroke left him unable to walk, talk and with paralysis on the right side of his body.
  • A 30-year-old man from California on April 8, 2021, was hospitalized and treated for a blood clotting disorder he developed after receiving J&J’s vaccine.
  • Barbara Buchanan developed blood clots in her lungs, stomach, brain and throat 6 to 8 days after receiving J&J’s COVID vaccine. She chose J&J because it was a one-dose shot, and because experts declared the vaccine was safe after they lifted a 10-day pause.
  • Kendra Lippy, a healthy 38-year old woman, was diagnosed with severe blood clots that subsequently sent most of her organs into failure after receiving J&J’s COVID vaccine. She also was left without most of her small intestine — and with crippling medical bills.
  • Sandra Jacobs, a 60-year-old woman died from blood clots after receiving the J&J shot, according to an autopsy report released Sept. 20, 2021, by a forensic pathologist for Michigan Medicine.

On April 13, 2021, federal agencies paused J&J’s COVID vaccine, marketed under its Janssen subsidiary, while they investigated the vaccine’s possible link to dangerous and potentially fatal blood clots.

During the April 23, 2021 meeting, the CDC’s vaccine advisory panel said it had identified 15 women diagnosed with rare blood clots, including three who died.

Only two of the women were older than 50, with the risk highest in women ages 30 to 39.

The CDC’s advisory panel said the link between blood clots and J&J’s COVID vaccine was “plausible,” but concluded the vaccine’s “benefits outweighed the risks” and recommended the vaccine for persons 18 and older in the U.S. under the FDA’s Emergency Use Authorization.

On April 26, 2021, the FDA amended its EUA for the J&J vaccine to reflect the risk of rare blood clots and said vaccinations could resume immediately.

 

©March 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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Shedding, Vaccines and Graphene Machines

Shedding, Vaccines and Graphene Machines

by Dr. Sam Bailey
video published February 22, 2022

 



Partial transcript provided by Truth Comes to Light:

Dr. Sam Bailey:

We should clarify that these injections are gene therapies, rather than vaccines.

Of course, as we have seen numerous times in recent years, definitions need to be changed to fit the new narratives. For example, not so long ago the Merriam Webster dictionary stated that a vaccine was a preparation of killed micro organisms, living attenuated organisms, or living fully virulent organisms that is administered to produce or artificially increase immunity to a particular disease.

Then, in January 2021, the definition suddenly changed. Now, what was happening around that time, the new definition in the dictionary look quite different and included: a preparation of genetic material (such as a strand of synthesized messenger RNA) that is used by the cells of the body to produce an antigenic substance (such as a fragment of virus spike protein).

Now, the fact checkers were quick to gaslight the public and say it was all taken out of context. Sit back and relax, they advised, because it was about the new technology of mRNA vaccines made publicly available in response to the Covid-19 pandemic.

Injecting genetic sequences into a human, in order for it to be taken out by the cells and then cause a change in cellular expression, is a gene therapy. Even wikipedia, at the moment at least, states under the gene therapy page that there are a variety of gene therapy modalities including RNA, DNA and gene editing tools such as CRISPR. And BioNTech, Moderna Therapeutics and CureVac focus on delivery of mRNA payloads.

This is not that important to those of us that know that vaccines are one of the greatest scams being run, as we are not interested in taking any of them.

However, it is important for the gene therapy recipients, as well as for the shedding question.

The sequences being injected are smuggled into the cells via the lipid nanoparticle technology. Without it the […] mRNA would be quickly broken down after injection.

These injections cause the body to produce the so-called spike protein. This is alleged to be a modified version of the SARS-COV-2 virus spike protein. However, the virus is a fictional construct, as the virus has never been shown to exist.

The spike protein comes from somewhere else.

And, even though Dr. Fauci was talking about spike protein vaccines back in 2005, after SARS 1, that virus was never shown to exist either.

The spike protein sequences can be found in lab experiments that stress and kill mammalian cells.

In any case, there is enough known about the spike proteins to see that they can be toxic if they are released inside the body. Anyone telling you otherwise is trying to sell a product or is making excuses for it. You may hear claims that, as it is only a tiny part of the virus, it’s safe. However, as there has been no virus shown to exist, they are simply parroting the virologist’s claims and big pharma marketing.

But can these spike proteins shed from the bodies of the injected and affect another person?

My supporter mentioned that shedding of particles seems to be a valid concept as it can occur with things like body odor. This is true and that the sweat glands secrete various compounds including proteins which can mix with skin organisms — and the resulting particle aerosols so that other people can smell them. The secretions themselves could also come into direct contact with another person.

However, I don’t believe this puts another person at significant risk from any potential spike proteins. Proteins coming into contact with intact skin are not going to be able to get in. And proteins are generally broken down rapidly if they are swallowed or inhaled.

Another question was whether Pfizer admitted that there was some risk of shedding from recipients, due to the way the original clinical trial protocol was written.

For example, under section 8.3.5, there are clauses stating environmental exposure may occur. ‘A male family member or healthcare provider who has been exposed to the study intervention by inhalation or skin contact, then exposes his female partner prior to or around the time of conception.’

It goes on to say this: ‘In the case of a life birth, the structural integrity of the neonate can be assessed at the time of birth. In the event of a termination…the structural integrity of the terminated faces should be assessed by gross visual inspection.’

One of the reasons I did not find it plausible that spike protein shedding could significantly affect other people is that we exposed the lack of evidence that proteins can be infectious in a chapter in ‘Virus Mania‘, which we titled BSE: The Epidemic That Never Was.

In 1997 Stanley Prusiner put forward his theory of infectious proteins, known as prions, being responsible for spongiform brain diseases, such as mad cow disease. Despite all the excitement and senseless slaughter of animals that it caused, the model was never demonstrated to be relevant in nature.

Experiments involving injecting protein mixtures directly into animals brains can hardly be said to be a representation of what happens in natural settings. Like the virus theory, the required evidence is conspicuously absent.

Of course, there are particular scenarios where transmission will occur and the most obvious is that of unborn babies whose mothers are producing spike protein. In fact, everything that has been injected into the mother is potentially going into the fetus or embryo — and that includes the spike protein, the mRNA coding sequence, the lipid nanoparticles and the undeclared constituents that we’ll get into soon.

The spike proteins are not the only thing we have to worry about though. Numerous laboratories around the world have found graphene-based particles and what looks like nanotechnology, both in the vaccine vials and blood of recipients.

Pathologist Professor Arne Burckhardt in Germany, Dr. Pablo Campra of La Quinta Columna in Spain, Dr. Zandre Botha in South Africa, Dr. Marcelo Dignani in Argentina, and recently a physician here in New Zealand, are among those who have found these undeclared constituents.

There is much speculation about what the purpose of these particles are. But some appear to be nanorouters. It is also being reported that they are capable of receiving and transmitting signals, and even generating internet MAC addresses…

Whatever they can do, it is important to know about the nature of graphene and it’s useful to see what engineers had to say about the subject.

It is difficult to comprehend that graphene sheets can be a single layer of carbon atoms in thickness. And, as discussed in this 2013 publication, have extra ordinary electrical, mechanical and thermal properties. The paper points out that, because the particles are so minute, they can get into people quite readily through inhalation.

This is being studied previously and mice where researchers found that the particles cause harmful health effects in the lungs due to the inability of the host to clear them, and the failure of macrophages to clean them up. Their retention in the tissues then sets up an inflammatory response and through the tissue damage.

However, they did conclude that ‘our initial data also suggests that the graphene nanoplatelets are not fully bio-persistent, and clear slowly to the mediastinal lymph nodes. More research was required to see if the particles are subsequently cleared from the lymph nodes in body’.

Back to the engineers’ paper and they go on to say that, ‘in addition to occupational exposures, graphene family nanoparticles may be deliberately implanted or injected for biomedical applications that include biosensors, tissue scaffolds, carriers for drug delivery or gene therapy, antibacterial agents and bioimaging probes.’

They performed experiments to see how human cells responded to challenge with graphene microsheets. In these scanning electron micrographs, image A shows the graphene particles penetrating a human lung cell, while image C and D show the particles penetrating human skin cells.

The authors concluded — they ‘hypothesize that graphene microsheets that penetrate into hydrophobic lipid domains may be recognized as damage-associated molecular patterns by target cells that are the first line of defense against particles… The ability of graphene microsheets with large lateral dimension to penetrate and enter cells… may lead to cytoskeletal disruption, impaired cell motility, compromised epithelial barrier function, or other geometric and steric effects that deserve further study.’

In other words, the particles can slice through cells, disrupt the structure and normal function, and activate a generalized inflammatory response.

Combined with the fact that the body struggles to clear such particles, that could be a recipe for chronic inflammatory conditions and even cancer.

Despite the fact that graphene is bad news for humans, in 2021 these researchers associated with AstraZeneca produced Graphene Quantum Dot to deliver messenger RNA into cells.

…[image shown in video shows page 666 ChemistryOpen 2021, Wiley Online Library] on page 666 of the chemistry Europe publication. And they proceeded to describe the creation of the ‘Franken-molecule’ consisting of the graphene quantum dots linked to mRNA sequences.

They seem happy to announce that graphene quantum dots are able to respond to physical stimuli such as magnetic fields, ultrasound, and light. They also make the curious claim that the graphene quantum dots are not toxic, although cellular toxicity is a problem for these first-generation modified particles.

Cellular toxicity means they are toxic.

What is most disturbing to me about this work is that it demonstrates the integration between synthetic nanoparticles and biological molecules. While this might excite Dr. Evil and his acolytes, it is a desecration of our bodies and an example of how out of touch they are with the nature of life in the universe.

So, many of us will avoid intentional exposure to graphene nanoparticles, but can people injected with them shed these particles in and affect others in contact with them?

It would seem, from the published research discussed here, that the particles are difficult and slow to clear from the body. This would not be coming out of injected recipients very readily. However, if they were cleared, then potentially someone in close contact could be exposed.

I have received communication from a dark field microscopist who compared blood film from an injected and a non-injected subject. And a few nanoparticles were seen, albeit at a much lower concentration, in the non-injected subject.

This raises questions about how the small number of particles got into the non-injected subject. And exactly what we are seeing.

I can’t give you a definitive conclusion at this stage as we await more information. We know that the globalists have some set agendas they are attempting to roll out. And they want to disconnect us from spirituality in their perverted plan for humanity.

Dr. Harari and his devil buddies are so unconscious that they think they are gods. To them, you are livestock that is ripe for their transhumanist experiments and eventual enslavement. In other words, you need to be on your guard.

However, if you do not already know this, I can tell you that they don’t really have any power over you unless you give it to them. It is as easy as ignoring them and not walking into the cages that they are directing you towards.

A small number of us sounded the alarm in 2020 that the alleged Covid-19 pandemic was a ruse. It has been pushed with fraudulent science. But unfortunately, from my experience, even 99 percent of doctors cannot properly interpret the papers that claimed to show the existence of SARS-CoV-2.

It does not require a large number of people to be in on the scam. Most have been tricked and have gone along with it in ignorance.

The good news is that around the world more people are waking up. Many that have been injected are realizing that they had been deceived, and increasingly I’ve been contacted by people who have been jabbed but will never take another vaccine again.

I suspect plenty of individuals received the shot and didn’t produce spike proteins. There haven’t been damaged in that way.

With regards to the undeclared nanoparticles, there a lots of unknowns…

I have faith that people can heal from what has been done to them. But the first step is to stop listening to big pharma and the globalist sociopaths, to take back control of our own health.

 

Connect with Dr. Sam Bailey

cover image credit: Layers / pixabay




Legal Impact of mRNA Vaccines? Chile Enacts Law for Mutants

Legal Impact of mRNA Vaccines? Chile Enacts Law for Mutants

by Orwellito, Orwell City
February 27, 2022

 

Chile now has a law for mutants and genetically altered individuals. It’s a rather peculiar law, in addition to the neuro-rights law, which also exists in that country.

What could be the reason for the enactment of this new law?

Obviously, the reason for the origin of this law —which will probably soon be replicated in other countries— is because there’s already a considerable number of people in the population who are no longer human, but transgenic beings.

It’s a known fact that COVID vaccines are mutagenic and alter human DNA, not only because the RNA they contain, but also because of the DNA crystals that Dr. Pablo Campra has found in Pfizer vaccine vials.
Mik Andersen from Corona2Inspect has been investigating them too and, most recently, La Quinta Columna has observed how those crystals send signals to generate “life-forms.”

Every day there’s more evidence of this, especially with the birth of babies with black eyes and very curious physical characteristics, as described by Dr. Viviane Brunet.

In 2021, Dr. Chinda Brandolino warned the world that accepting an mRNA vaccine involves a change in the genome and that the person subjected to this experimental drug loses his human rights.

Orwell City brings into English a summary of this rare yet real law that Chile now has to prevent people from being discriminated in their jobs because they are mutants or have their genome altered in some way.



Narrator:

After becoming the first country to add neuro-rights to its Constitution, Chile now also becomes the first country in the world not to discriminate against mutants and genetically altered individuals after publishing Law 21.422 on February 16, 2022.

Specifically, this law forbids “employment discrimination in the face of mutations or alterations of genetic material.”

The question everyone is asking now is, what’s the reason for this law?

Since Chile is one of the most inoculated countries in the world, it’s not surprising that such a law has been enacted. As dissident doctors warned from the beginning, these inoculums contain secret materials and components that alter the human genome. Of course, this genetic modification is inheritable.

At the time, Dr. Chinda Brandolino warned that those who received injections of these inoculums would become transhumans and, therefore, property of the pharmaceutical companies and no longer enjoy human rights.

It should be recalled that in a 2013 court case, the U.S. Supreme Court ruled that human DNA cannot be patented because it was “a product of nature.” But at the end of the ruling, the Supreme Court ruled that if a human genome were modified by mRNA vaccines —which are currently being used—, then the genome can be patented.

And well, What does the new Chilean law establish?

1. No employer may condition the hiring of workers, their permanence or renewal of their contract, or promotion or mobility in their employment, to the absence of mutations or alterations in their genome.

2. The worker may give his free and informed consent to undergo a genetic test.

3. If these examinations are required by the employer, the employer shall bear the cost thereof.

4. The health establishments and laboratories that carry out this type of test, as well as the employers who have access to this information, shall adopt all security measures to protect the privacy of the worker and guarantee reserved handling of the data.

5. The worker will always have the right to access the information resulting from a genetic test.

With all these laws that are appearing, do you still believe that these inoculums are vaccines?

 

Read/Download “Law for Mutants” (Spanish)

 

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cover image credit: KELLEPICS / pixabay




Are the Pfizer-Injected Now GMOs?

Are the Pfizer-Injected Now GMOs?

by Dr. Mark Bailey
February 27, 2022

 

A study has just been published in Current Issues in Molecular Biology which may cause a few problems for the “fact-checkers” and government agencies who have emphatically claimed that the mRNA injections cannot alter or damage the recipient’s DNA.

The paper by Aldén, et al, titled “Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line,” published on 25 February 2022, reveals what some of us have been warning about since the experimental mRNA injections were released onto largely unsuspecting populations.  That is, the mechanisms do indeed exist for the genetic injections to change and/or damage the recipient’s genome.

In New Zealand, Medsafe approved the Pfizer injections for wholesale use in the country despite minimal safety data being available.  In 2021 they engaged their “experts,” Professor Peter McIntyre from the University of Otago and Dr Ian Town, Chief Science Advisor for the Ministry of Health to address any “concern that permanent alteration of DNA may occur.”  Bizarrely, they went way out on a limb in a few sentences in the following letter to NZDSOS:

Messenger RNA is unstable, which is why it must be stored at very low temperatures prior to use. As mRNA does not enter the nucleus and is rapidly broken down by the cell after protein transcription has occurred, it is unable to alter DNA (Ref 10) . This is shown in the graphic below (Ref 11).”

~ Report for Medsafe: Professor P McIntyre & Dr Ian Town, 14 June 2021

 

Nature is not directed by colourful man-made cartoons.

 

NZDSOS were concerned that this was an over-simplification of the state of the science and thus presented a paper to Medsafe the following week, specifically addressing the potential problems:

“The science on this is still unfolding and we are concerned that the authors claim a definitive statement on this topic. The first reference the authors provide is the Centers for Disease Control and Prevention website which is aimed at providing the public with a simple overview of the mRNA injection. The second reference (and diagram) only shows the ‘proposed sequence of events leading to the generation of adaptive immune responses upon mRNA vaccination’. From this the authors appear to conclude that it would be impossible for the injected mRNA to become integrated into our DNA because mRNA does not work that way.”

~ NZDSOS to Medsafe, 21 June 2021

The mechanism for the conversion of RNA to DNA is possible through reverse transcriptase enzymes.  Although some virologists have suggested that reverse transcriptase is specific to “retroviruses” it has long been known that the enzymes can be found in normal mammalian cells.  This has been well documented by The Perth Group and has gained more mainstream attention in recent years including in this SciTechDaily article in 2021:

“Thomas Jefferson University researchers provide the first evidence that RNA segments can be written back into DNA, which potentially challenges the central dogma in biology and could have wide implications affecting many fields of biology. ‘This work opens the door to many other studies that will help us understand the significance of having a mechanism for converting RNA messages into DNA in our own cells,’ says Richard Pomerantz, PhD, associate professor of biochemistry and molecular biology at Thomas Jefferson University.”

~ New Discovery Shows Human Cells Can Write RNA Sequences Into DNA – Challenges Central Principle in Biology. THOMAS JEFFERSON UNIVERSITY JUNE 12, 2021

I’m not sure why they think the central dogma of biology is only now being “potentially challenged” as it was never proven to be relevant from the day that Francis Crick first suggested it in 1958, but at least they are opening their eyes.

In any case, what did Aldén et al’s recent paper demonstrate?  I’ll outline some of the highlights:

“Our results indicate a fast up-take of BNT162b2 into human liver cell line Huh7, leading to changes in LINE-1 expression and distribution. We also show that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure.

“BNT162b2 DNA amplicons were detected in all three time points (6, 24, and 48 h). Sanger sequencing confirmed that the DNA amplicons were identical to the BNT162b2 sequence flanked by the primers.”

“In the BNT162b2 toxicity report, no genotoxicity nor carcinogenicity studies have been provided [26]. Our study shows that BNT162b2 can be reverse transcribed to DNA in liver cell line Huh7, and this may give rise to the concern if BNT162b2-derived DNA may be integrated into the host genome and affect the integrity of genomic DNA, which may potentially mediate genotoxic side effects.

~ Alden, M. et al. (2022.) Intracellular Reverse Transcription of Pfizer BioNTech COVID-19 mRNA Vaccine BNT162b2 In Vitro in Human Liver Cell Line. Curr. Issues Mol. Biol. 2022, 44(3), 1115-1126.

 

NZ Ministry of Health’s Infomercial for Pfizer: so many things wrong here, where should we start?

 

Now, to be clear this does not mean that those who have been injected with the Pfizer BioNTech product have had their DNA modified – but it raises very significant concerns. The study was carried out in vitro (in a test tube) with Huh-7 cells which are of human origin but derived from an abnormal (liver cancer) cell line.

Therefore, the next logical step would be to assess whether those that have been injected with the product have evidence that the sequence has been integrated into their DNA.

The authors didn’t proceed to test this themselves although suggested that genomic sequencing and integrity should be checked in “human subjects who received BNT162b2 vaccination.”  Who will (be allowed to) take up the challenge?

This paper comes hot on the heels of another major revelation related to these mRNA injections.  Dr Mikolaj Raszek has recently highlighted a potential problem that is apparent in the Australian Therapeutic Goods Administration’s (TGA) own “Nonclinical Evaluation Report” on Pfizer’s Comirnaty (BNT162b2).  Dr Raszek has previously discussed how the spike protein can circulate in the blood of the injected for months, which considering the recent Aldén et al paper, may be explained by the integration of the genetic sequence into the host’s DNA.  In effect, the jabbed may produce the spike protein indefinitely or at least have the potential to do so.  His latest revelation from the TGA’s report adds more weight to his theory that the spike proteins themselves are entering the nucleus of the cell and once it is inside it “could be a mutagen because it prevents the fixing of our DNA.”

All in all it makes the Australian TGA look like a complicit partner in this COVID-19 Fraud & War on Humanity as they gamble on their citizens lives under the influence of Pfizer:

“Neither the mRNA nor the lipid excipients of the LNP formulation are expected to have genotoxic potential. However, the potential of the LNP or the vaccine formulation for complement activation or stimulation of cytokine release was not adequately assessed in nonclinical studies. Further investigation (i.e., analysis of complement activation and cytokine stimulation) is recommended unless this particular concern is addressed by clinical data. The absence of a repeat dose toxicity study in a second species and genotoxicity studies with the novel excipients was adequately justified by the Sponsor…Short term protection studies, lack of pharmacokinetic data for the S antigen-encoding mRNA (BNT162b2 V9), suboptimal dosing interval in the repeat dose study, lack of repeat dose toxicity studies in a second species and genotoxicity studies with the novel excipients, and lack of studies investigating potential for autoimmune diseases were noted. However, these deficiencies are either adequately justified by the Sponsor or addressable by clinical data.”

~ Nonclinical Evaluation Report BNT162b2 [mRNA] COVID-19 vaccine (COMIRNATY™). Australian Government Therapeutic Goods Administration. January 2021.

Pfizer’s Comirnaty brought their corporation around US$36 billion in revenue in 2021, and they expect to top that in 2022.  Their product can’t possibly protect anyone from an undefined clinical entity and a “virus” that does not exist.  What we can see is that entire countries are being swindled out of billions of dollars while their hapless citizens are at risk of becoming genetically modified organisms in addition to the barrage of other toxic effects they are enduring from these injections.



 

Connect with Dr. Mark Bailey




Pfizer and Moderna Investors Are Running for the Exits

Pfizer & Moderna Investors Run for the Exits

by Justus R. Hope, MD, The Desert Review
sourced from 21st Century Wire

 

Wall Street investors are dumping their Moderna and Pfizer stock faster than the world can drop the mandates. Moderna is down 70 percent from its high, while Pfizer is off 19 percent. Former Blackrock Executive and investment adviser Edward Dowd calls for Moderna to go to zero and Pfizer to end under ten dollars per share.

How is this possible given that Pfizer now enjoys record earnings per share and a market capitalization of some $270 billion, making it the 29th largest corporation globally? With nothing but profits in sight for the Pharmaceutical giant, what could be the problem?

After all, in December, a Forbes’ headline read, “The Vaccine Maker Can Dominate The Covid Market For Years to Come, Wells Fargo Predicts.” In addition to the enormously profitable mRNA vaccines, Pfizer is rolling out potent antivirals like Paxlovid, which could earn $22 billion in 2022.

https://www.forbes.com/sites/sergeiklebnikov/2021/12/09/this-vaccine-maker-can-dominate-the-covid-market-for-years-to-come-wells-fargo-predicts/

Compared to the $81 billion in 2021 revenue, the earnings from the vaccines and the antivirals could top $102 billion for 2022, which is music to shareholders’ ears. However some are hearing shrieks, and these happen to be Wall Street’s finest, the smart money that beats the rest of the herd to the exits like clockwork.

These sophisticated investors make it their business to not go with the conventional wisdom but to do their own research, which often pays spectacular dividends.

Edward Dowd is one such investor. He saw the dot com bubble ready to burst and acted accordingly. But, unfortunately, other not-so-savvy investors later saw their dot com heavy portfolios collapse as the NASDAQ Composite Index lost 40% of its value in 2000.

Dowd, a graduate of Notre Dame University and former Portfolio Manager at Blackrock, grew his fund from $2 billion to $14 billion and commanded the respect of his investment community peers.

Today, after semi-retiring to the shores of South Maui, he remains a voice of stock market wisdom that many hedge funds continue to rely upon. LinkedIn lists him as a Consultant to Founder & Partner of Symphonic Capital, LLC.

But the dot com collapse is not the only one Dowd successfully navigated. While many other portfolio managers placed their client’s money in highly rated and lucrative mortgage-backed securities, Dowd hesitated and questioned. He considered that those might be grossly over-rated, and he was correct.

It turns out that the mortgage rating system was corrupted by the high profitability of predatory financial products tied to home mortgages. According to Edward Dowd, a large portion of the blame was shouldered by the rating agencies, those trusted organizations whose job it was to judge the risk of these subprime mortgage-backed securities – agencies like Moody’s, Standard & Poor’s and Fitch.

Dowd says they turned a blind eye to the true risk because it was profitable. So, in essence, these rating agencies were captured by the institutions backing these risky subprime securities.

https://www.theguardian.com/business/2017/jan/14/moodys-864m-penalty-for-ratings-in-run-up-to-2008-financial-crisis

Joseph Stiglitz, a Nobel Prize-winning economist, put it this way, “The incentive structure of the ratings agencies also proved perverse. Agencies such as Moody’s and Standard & Poor’s are paid by the very people they are supposed to grade. As a result, they’ve had every reason to give companies high ratings, in a financial version of what college professors know as grade inflation.”

https://www.vanityfair.com/news/2009/01/stiglitz200901-2

Dowd has sounded the alarm on Moderna and Pfizer as sinking ships that investors need to abandon. So what does the man who foresaw the dot com and the subprime mortgage crisis have to say about Moderna and Pfizer, and what trouble could exist in the paradise of COVID vaccine profits?

Here are Dowd’s words:

I want to liken here to what’s gone on in the Great Financial Crisis. We had rating agencies, third-party verification sources that were able to perpetuate the fraud because the money got too big, their institutions became corrupted with the institutional imperative, and they got triple-A ratings which we all know in hindsight were not triple-A ratings – let’s move forward to today. 

The FDA is the trusted third-party verification of pharmaceutical products. 50% of their budget comes from Pharma…due to the institutional imperative that was in place at the time and the speed with which they tried to approve these unproven products with this unproven technology, fraud did occur, and what’s my proof of that? The FDA, together with Pfizer, were trying to hide the clinical data. 

And it’s come out recently…that the all-cause mortality for the Pfizer product failed – that means there were more deaths in the vaccine group than the placebo group. Normally in such a case, you have NO drug approval for such drugs. It’s the gold standard. I’ve been told by all my people in the Biotech Industry they were horrified… See mark 25:10.

https://www.iheart.com/podcast/867-war-room-impeachment-52276954/episode/episode-1602-the-big-short-92212337/

And unfortunately, that is not all. Dowd feels that although he has successfully predicted three large frauds in his career, he now expects a global financial market collapse with the debt bubble getting ready to burst.

“So I’ve seen three frauds; the corporate fraud of the dot com boom, the bank fraud of the Great Financial Recession, and I believe the fraud has moved on to central banks and governments – because that’s the nature of our monetary system – you have to constantly create credit to keep this thing going.” See mark 2:22.

https://chute.rocks/qt7nvf3ccV2n

“The global debt bubble is at its peak…we are at the end…we are going to see lots of crazy things in the financial markets…we are going to see the credit markets become unhinged, the equity markets become unhinged. The Fed got a reprieve…under the cover of COVID, they were able to print 65% more money to keep this thing afloat, but we are at the end days here.” See mark 3:41.

https://chute.rocks/qt7nvf3ccV2n

He clarifies that the emergence of global totalitarianism is not purely about power and profit. Instead Dowd feels it is to control the masses when they realize the economy is collapsing – the ramifications of which may be the loss of pensions and social security income.

“A lot of what you are seeing in the response of global governments is setting up a system – under the guise of medical tyranny – to prevent the riots that are going to ensue once this thing all unwinds – that’s my personal belief…” See mark 4:04.

https://chute.rocks/qt7nvf3ccV2n

For the skeptics, consider that Pfizer stock lost $20 billion in market capitalization on February 8, 2022, when their record earnings fell short of more optimistic expectations.

https://www.forbes.com/sites/jonathanponciano/2022/02/08/pfizer-triggers-28-billion-stock-plunge-moderna-after-warning-covid-vaccine-sales-could-disappoint-this-year/

Also consider that Moderna’s stock is down some 70 percent from its high of $484 on August 9, 2021, wiping out almost $ 140 billion in investment.

https://www.forbes.com/sites/jonathanponciano/2022/02/14/moderna-stock-crash-losses-top-140-billion-as-insiders-sell-millions-of-dollars-in-shares/

Dowd predicts Moderna will drop to zero with bankruptcy as fraud related to concealing the COVID vaccine dangers surfaces, and he predicts Pfizer will become a sub-ten-dollar stock. Dowd explains that the smart money has already left Moderna and will soon be exiting Pfizer.

Dowd foresees an avalanche of lawsuits coming as the insurance industry continues to uncover the legions of mounting deaths coming from the complications of the mRNA COVID-19 vaccines.

Dowd teamed up with an insurance industry analyst and researched the life insurance claims. They found that since OneAmerica shocked the world by announcing a 40% rise in non-COVID deaths in younger working-class employees, multiple other insurance companies worldwide have seen the same thing – massive rises in non-COVID deaths. And the evidence inescapably points to the vaccines as the cause. See mark 13:16.

https://www.bitchute.com/video/hjMyF8epEEa3/

https://www.thedesertreview.com/opinion/columnists/life-insurance-deaths-up-40—dr-robert-malone-s-chilling-analysis/article_d24bccac-6f38-11ec-912f-1f6d8fc5fac4.html

Meanwhile, the funeral company stocks have outperformed the S&P. “Funeral Home companies are growth stocks. They had a great year in 2021 compared to 2020, and they outperformed the S&P 500. The peer group of Funeral Home stocks was up 40 plus percent while the S&P was up 26 percent – and they started accelerating price-wise in 2021 during the roll-out of the vaccines – You don’t need to be a rocket scientist to connect the dots here.” See mark 5:55.

https://www.bitchute.com/video/hjMyF8epEEa3/

Other insurance companies have reported the same or worse death numbers as OneAmerica. For example, “Unum Insurance is up 36%, Lincoln National plus 57%, Prudential plus 41%, Reinsurance Group of America plus 21%, Hartford plus 32%, Met Life plus 24%, and Aegon – which is a Dutch insurer – saw in their US arm plus 57% in the 4th quarter – in the 3rd quarter they saw a 258% increase in death claims.” See mark 07:55.

https://www.bitchute.com/video/hjMyF8epEEa3/

“They raised (mortality) expectations 300,000 for 2022 over 2021 due to COVID plus ‘indirect COVID,’ which I think we know what that’s code for… They (Aegon) did a

$1.4 billion reinsurance deal with Wilton Reinsurance…what they were reinsuring were high face amount individual policies from 1 million to 10 million… (So) I think there is an asymmetric information situation going on in the insurance industry where some people have figured out something’s going on. They are off-loading their risk – they are not going to say what it is as they don’t want that information to get out as they unload the risk.” See mark 08:49.

https://www.bitchute.com/video/hjMyF8epEEa3/

“Someone is going to be the bag holder here.” And Dowd is confident it won’t be the insurance industry. A court in France has already held that a life insurance company cannot be held liable for a death because of the mRNA vaccine.

https://freewestmedia.com/2022/01/14/life-insurer-refuses-to-cover-vaccine-death/

But that does not explain how mRNA manufacturers can be held responsible for an emergency product they were told was liability-free. Aren’t the vaccine manufacturers immunized from lawsuits?

After all, they were granted EUA, the specialized Emergency Use Authorization, which means they cannot be held legally accountable for deaths or adverse effects stemming from the experimental vaccines.

The idea is that no company – upon government request – should have to pay for unforeseen complications resulting from an emergency product that they released to the world out of their goodness of the hearts, with the best of intentions. Right?

Wrong – not when your company accomplishes this through deceit, also known as fraud.

Fraud undoes all these protections. If a company or person intentionally deceives another to profit, we have fraud. If Pfizer’s data showed increased all-cause mortality and hid this to motivate people to take the vaccine while claiming it was safe, then fraud exists.

Under common law, the required elements to prove fraud amount to:

#1. A materially false statement or purposeful failure to state or release material facts which non-disclosure makes other statements misleading.

#2. The false statement is made to induce Plaintiff to act.

#3. The Plaintiff relied upon the false statement, and the injury resulted from this reliance.

#4. Damages include a punitive award as a punishment that serves as a public example to discourage any future similar fraud. Punitive damages are generally proportional to the Defendant’s assets.

https://definitions.uslegal.com/f/fraud/

Dowd has been researching the COVID-19 vaccines and what he considers obvious evidence of knowing concealment of the actual risks of death – and he points to the Herculean efforts of Pfizer with FDA in withholding their data despite legal challenges to release it. He likens the FDA today to the rating agencies during the Mortgage Crisis.

“FDA is the trusted third party, just like the rating agencies were. And a lot of doctors in this country, a lot of local governments are placing their trust in the FDA which gets 50 percent of its budget from large cap pharma. It wasn’t any one person…I think they overlooked things…An all-cause mortality end-point should have stopped this thing in its tracks – and it didn’t.” See mark 1:51.

https://twitter.com/Sander_2021/status/1489746293002022912?s=20&t=nb7l5w4vfRvJsJ7TFfHyiQ

There were more deaths in the vaxxed group than in the unvaxxed. Dowd assumes fraud based upon the FDA backing Pfizer in not releasing their data. He believes this is a knowing attempt to conceal the deaths.

“When one party enters into a contract…and fraud was occurring when they entered into that contract, and the other party did not know that – the contract is void and null. There’s no indemnity if this can be proven, and I think it will be.” See mark 4:45.

https://www.bitchute.com/video/hjMyF8epEEa3/

“Pfizer got blanket immunity with EUA. If fraud occurred, to my mind and what I’m seeing from their refusal to release the data – if there is fraud and it comes out – and we need whistleblowers – and it’s looking more apparent that this product is deadly –

fraud eviscerates all contracts – that’s case law. So you go down the daisy chain, and that’s liability – that’s bankruptcy for Moderna, definitely Pfizer.” See mark 00:51.

https://twitter.com/Sander_2021/status/1489746293002022912?s=20&t=mNqs_wz572WqybdulzaK7A

Dowd remarks that no matter the effort, one cannot hide the bodies – and “the bodies are piling up.” See mark 12:56.

https://www.bitchute.com/video/hjMyF8epEEa3/

He notes that the deaths skyrocketed after the vaccine rollout when they should have dropped. And the deaths are what distinguished the 2021-2022 vaccine scandal as far worse than what happened with Enron.

“People are dying and being maimed. This is a fraud that goes beyond the pale…We have the VAERS data…We have the DoD leak…And now we have the insurance company results and the funeral home results…We don’t need to think too hard about this…Deaths should have gone down after the vaccines rolled out. This is the most egregious fraud in history of the nation – and it’s global…Pfizer’s involved, and they committed fraud,” Dowd explained. See mark 10:25.

https://www.bitchute.com/video/hjMyF8epEEa3/

“My job is to be ahead of the news and be a lead steer…when I use my stock picking skills outside the realm of stock picking, I am called a conspiracy theorist.” See mark 6:45.

https://www.bitchute.com/video/hjMyF8epEEa3/

Dowd emphasized that he is not short on Pfizer or Moderna stock. He explained that he does not profit from their share prices dropping. He also points out that his predictions are not the cause of the steep declines as these occurred before he came out with this analysis. See mark 13:45.

https://chute.rocks/qt7nvf3ccV2n

“Let me make a point here. The mainstream media may ignore this. Wall Street is not.” See mark 2:16.

https://www.bitchute.com/video/hjMyF8epEEa3/

“This is the most interesting hallucination I’ve ever seen in the financial markets.” See mark 12:06.

https://chute.rocks/qt7nvf3ccV2n

“So we don’t need the mainstream media…And I want you to know – Wall Street is rallying to this – I’m getting lots of inquiries from former colleagues. Nothing will convince a sleeping public more than red stocks or collapsing stocks. My goal is to awaken the country by seeing something is going on. And Wall Street is AWAKE!” See mark 2:33.

https://www.bitchute.com/video/hjMyF8epEEa3/

If money is any indicator, Edward Dowd is correct that insurance will win a fight between the insurance and the vaccine industries. The life insurance market in the US is worth some $900 billion, while the vaccine market pales in comparison.

https://www.pharmaceutical-technology.com/news/covid-19-vaccine-market-set-to-reach-19-5bn-by-2026-register-for-free-webinar/

https://www.ibisworld.com/industry-statistics/market-size/life-insurance-annuities-united-states/

If someone is left holding the bag, it will not be the insurance industry, but it just might be you and me, the average citizen.  However, there is one major caveat – if Edward Dowd succeeds in awakening the citizens, then they – the oligarchs – cannot get away with this – the Vaccine Fraud, the Great Reset, the Fourth Industrial Revolution and Global Totalitarianism.

https://www.thedesertreview.com/opinion/columnists/gates-fauci-and-daszak-charged-with-genocide-in-court-filing/article_76c6081c-61b8-11ec-ae59-7718e6d063ed.html

https://www.amazon.com/Ivermectin-Freedom-Justus-R-Hope-ebook/dp/B09M95F8NF

“There’s lots of people who got the jabs that didn’t understand what was going on. A lot of them are in the investment world. A lot of them are smart people – they were duped too. Some of these people that got the jab are doing the work on shorting these stocks because – you know, you can guess – because they are mad as hell – and you’ve awakened the sleeping giant known as Wall Street. And Wall Street is on the move. The smart money is moving first – as always there’s lead steers. Nothing gets going faster than a red momentum down-trending stock.” See mark 3:26.

https://www.bitchute.com/video/hjMyF8epEEa3/

Those of you who still think nothing’s going on, you don’t want to be – what I call – the bag holder. You don’t want to be the guy taking the fourth jab booster and holding these stocks (on their way) down – Moderna’s going to zero – I think Pfizer goes sub ten dollars once the lawsuits come out. ” See mark 4:06.

https://www.bitchute.com/video/hjMyF8epEEa3/

Dowd’s forecast can awaken not only Wall Street but the ordinary citizen. We are those sleeping giants of the world, those who can move mountains with the force of our stock sales and non-violent protests, the great silent majority who can remove dictators from power and elect new and fair leaders.

There is power in numbers, as the Canadian Truckers recently found. Courage is contagious as freedom convoys have sprung up everywhere. We hold the power if we choose to exercise it while we lose that power if we passively comply.

https://www.thedesertreview.com/opinion/columnists/trucker-convoy-drives-through-mandates/article_77693166-82cb-11ec-9642-dfbb0d0b2283.html

As this Freedom Trucker fireman said, “I don’t know what happened to our country. It’s disgusting. There’s nothing that’s going to be taken from us here today that they’re not going to take anyways – And people need to stand. With enough of us, they can’t do this.” See mark 1:58:10.

https://youtu.be/ZiIY5LpC890

If enough of us speak out NOW, collectively, we have the power to not only end the mandates, but to restore ALL freedoms in Canada, Australia, the UK, Europe and the United States, and we will win the day. We will never consent to authoritarian rule.

We will not leave a world of slavery to our children and grandchildren. We will protest every single day until the government realizes who truly is in charge. We believe in government of the people, by the people, and for the people. The cure for 1984 remains 1776.

Edward Dowd cautions those who continue to slumber, “If you are long these two stocks, you are long mandates, you are long government control, and you are long the selling of your freedoms.” Let us get everyone on board the freedom train. See mark 15:16.

https://www.bitchute.com/video/qt7nvf3ccV2n/7

With enough of us (awake), they can’t do this. Americans and Canadians are united in Freedom!

https://rumble.com/vvaw0n-urgent-message-to-canadians.html

Connect with 21st Century Wire

cover image credit: harpsandflowers / pixabay




Catherine Austin Fitts With Dr. Mark Skidmore: How Many People Died from the Covid-19 Inoculation? An Estimate Based on a Survey of the United States Population

Catherine Austin Fitts With Dr. Mark Skidmore: How Many People Died from the Covid-19 Inoculation? An Estimate Based on a Survey of the United States Population
The Covid-19 Survey With Dr. Mark Skidmore

by Catherine Austin Fitts, Solari Report
February 24, 2022

 



[Video available at Solari Report BitChute channel.]

 

[S]he lost her baby.”
[O]ur daughter, her whole body shut down after 2nd shot. If her brother were not there she would not have survived.”
She had a stroke within days of #2 Moderna vaccine. She has to use a walker and has speech issues. She was in her 40s. She is a registered nurse.”
Cousin 47-stroke  Cousin 28-blood clots  Aunt 63-death  Friend 41-death”

~ Covid-19 Survey, Appendix 3 (Respondents’ comments regarding the health condition of “the person they know best” who experienced an adverse event from a Covid-19 injection)

 

This week, Professor Mark Skidmore and I discuss the results of his important survey estimating injuries and deaths following Covid-19 injections in the U.S.

There is a wide range of opinion about the scale of injuries related to the Covid-19 injections. An unprecedented number of adverse events are being reported to official surveillance systems, but because these systems are known for their significant underreporting, it is difficult to know the true extent of injuries and fatalities. A well-designed survey of people’s beliefs and experiences can provide a useful estimate of what is actually happening on the ground.

The online survey, conducted in December 2021, included about 3,000 respondents representative of the general U.S. population, who described their own adverse-event-related experiences—and, equally importantly, the experiences of people in their social circles. Almost half of the respondents had received Covid shots themselves—with more than one in six experiencing health issues afterwards—and about one-fourth reported knowing others who had experienced significant post-injection health issues.

Dr. Skidmore notes that if one were to abide by the CDC’s count of “rare” injection-related fatalities (CDC acknowledges only nine Covid-vaccine-related deaths), then statistically, “in a survey of 3,000 people we should see ZERO (or close to zero) fatalities.” The survey provided a different picture, however. One in twelve respondents reported knowing someone who had died post-injection—a total of 55 fatalities—and the people described as likely vaccine-related deaths were, on average, 48 years old. Respondents also described numerous non-fatal but severe adverse events like heart-related issues, blood clotting, strokes, and paralysis.

Dr. Skidmore presented his survey results at the February 2022 Doctors for Covid Ethics Symposium III, and they are also available in his working paper titled “How Many People Died from the Covid-19 Inoculations? An Estimate Based on a Survey of the United States Population” posted at Dr. Skidmore’s Lighthouse Economics website. The working paper’s Appendix 3 includes respondents’ verbatim descriptions of the adverse events witnessed in their social circles.

The central question raised by Dr. Skidmore’s survey is this: What if the survey results, rather than CDC numbers, reflect the true ratio for fatalities and serious injuries following Covid injections? This would yield an estimated 260,000 to 300,00 fatalities and 1.1 million potentially life-threatening or life-shortening serious injuries—estimates that must be taken seriously by anyone still debating the injections’ safety.

 

Connect with Catherine Austin Fitts at Solari Report




Another Article Too Hot to Handle; Even Vaccine Critics Won’t Run With It

Another Article Too Hot to Handle; Even Vaccine Critics Won’t Run With It

by Jon Rappoport, No More Fake News
February 23, 2022

 

A few days ago — in my article The Test for Klaus Schwab and the World Economic Forum, I republished my proof that the medical cartel has been routinely killing millions of people, with its treatments, for at least the past 20 years.

And when I say proof, I’m talking about clear mainstream research.

Virtually no one has taken those research citations and run with them, despite the fact that I’ve highlighted them for years. I’ve highlighted them in articles and interviews.

What’s the problem?

Apparently, even many “alternative” journalists and doctors are keeping a piece of their souls in the official prison of fake medicine and fake science. On purpose.

They want to hedge their bets. They want to go halfway, but not all the way.

They want to admit some things, but not other things.

So today, I’m posting another one of my “too hot to handle” pieces. I’ve published this article at least four times. Even doctors who oppose the COVID vaccines won’t pick up on it.

Why?

It’s too REAL, because it proves the RNA injections were DESIGNED to fail, to be useless, from the get-go.

That’s right.

And if you expose THAT, you burn the whole house down.

The vaccine establishment collapses.

No one will believe anything the establishment says about vaccines. Nor should they.

And many journalists and doctors of all stripes want to “protect the public” from THE TRUTH.

I don’t want to bury the truth. I’m not settling for half.

Buckle up—

I wrote and posted this piece while the clinical trials of the COVID vaccine were in progress. It reveals how and why those trials were constructed and designed to fail. They did fail.

The vaccine makers DESIGNED a series of clinical trials that, even on their own terms (“the virus is real, fear the virus”) were destined to be a complete flop.

PART ONE

Peter Doshi, associate editor of the medical journal BMJ, and Eric Topol, Scripps Research professor of molecular medicine, have written a devastating NY Times opinion piece about the ongoing COVID vaccine clinical trials.

They expose the fatal flaw in the large Pfizer, AstraZeneca, and Moderna trials.

September 22, 2020, the Times: “These Coronavirus Trials Don’t Answer the One Question We Need to Know” (also, here):

“If you were to approve a coronavirus vaccine, would you approve one that you only knew protected people only from the most mild form of Covid-19, or one that would prevent its serious complications?”

“The answer is obvious. You would want to protect against the worst cases.”

“But that’s not how the companies testing three of the leading coronavirus vaccine candidates, Moderna, Pfizer and AstraZeneca, whose U.S. trial is on hold, are approaching the problem.”

“According to the protocols for their studies, which they released late last week, a vaccine could meet the companies’ benchmark for success if it lowered the risk of mild Covid-19, but was never shown to reduce moderate or severe forms of the disease, or the risk of hospitalization, admissions to the intensive care unit or death.”

BOOM. THE CLINICAL TRIALS WERE NOT DESIGNED TO SHOW THE VACCINE COULD PREVENT SERIOUS ILLNESS. OR HOSPITALIZATION. OR DEATH.

The Times: “To say a vaccine works should mean that most people no longer run the risk of getting seriously sick. That’s not what these trials will determine.”

BOOM.

This means these clinical trials are dead in the water.

And I could stop this article right here and walk away. Done. Finished. Nothing more need be said.

And you the reader could walk away. OK, done. The clinical trials of the vaccine were never intended to prevent serious illness of any kind. Never intended to prevent hospitalizations or deaths. End of story.

Goodbye. Forget the vaccine. Why would anyone want to take it?

But if you want to know WHY the clinical trials were designed this way, and HOW the con was played, and why it was actually necessary to design the clinical trials to be useless, read on.

The whole vaccine house is ALREADY burned down, but I’m going to say a lot more. I’m going to burn the ashes.

First of all, make sure you understand the clinical trials of the RNA vaccines were only designed to show effectiveness in preventing “mild cases of COVID,” which nobody should care about, because mild cases (cough, fever, chills) naturally run their course and cause no harm. THERE IS NO NEED FOR A VACCINE THAT PREVENTS MILD CASES.

Now let’s go deeper. Read the next section from the Times piece, and then I’ll make comments.

“The Moderna and AstraZeneca studies will involve about 30,000 participants each; Pfizer’s will have 44,000. Half the participants will receive two doses of vaccines separated by three or four weeks, and the other half will receive saltwater placebo shots. The final determination of efficacy will occur after 150 to 160 participants develop Covid-19…”

Now pay close attention. Here’s how it works. The vaccine companies are looking for a total of 150 mild COVID cases to occur, combined, in the two groups— those receiving the placebo and those receiving the vaccine. How would that happen? The researchers believe “the coronavirus is spreading everywhere” and it will pounce on some of the volunteers during the clinical trial.

Let’s say that, during the trial, 100 people receiving the placebo develop mild COVID-19 (cough, chills, fever), and only 50 people receiving the vaccine develop mild COVID.

The vaccine companies would say, “We just proved the vaccine is 50% effective in preventing COVID, and that’s all we need to do, in order to win emergency authorization from the FDA. Release the vaccine. Inject the world.”

The outcomes for ONLY 150 people equal “let’s shoot up seven billion people.”

That’s staggering.

But it gets even worse. The magic number of 150 COVID cases? How is a COVID case defined? The authors of the Times piece have the answer:

“In the Moderna and Pfizer trials, even a mild case of Covid-19 — for instance, a cough plus a positive lab test — would qualify and muddy the results. AstraZeneca is slightly more stringent but would still count mild symptoms like a cough plus fever as a case.”

But wait. The NY Times itself recently published an article stating that up to 90% of US COVID cases could very well be false positives—in other words, not cases at all. Why? Because the diagnostic PCR test, as it is performed by labs, is too sensitive. It registers “positive for COVID” when it shouldn’t.

So, in these vaccine clinical trials, the whole process of determining that “150 people developed COVID-19” is completely unreliable, useless, absurd, and nonsensical.

On the one hand, a positive PCR test is unreliable and means nothing. On the other hand, a cough and fever (“mild COVID”) are nothing to worry about, and don’t require a vaccine at all. We’re talking about 150 cases of “who cares.” That’s what the COVID vaccine is DESIGNED to prevent.

“So, Doctor, the magic number is 150 ‘who cares’ mild cases? That’s the number that will decide the immediate fate of the planet?”

“Of course.”

“And these 150 people, who you say develop mild COVID-19…no one should care, because those symptoms cure themselves, and no vaccine is needed.”

“Correct.”

“And come to think of it, the people receiving the vaccine in the clinical trials could develop symptoms indistinguishable from mild COVID-19, as a result of the effects of the vaccine.”

“Yes, that’s right.”

“But you’re very confident in the success of the vaccine.”

“Indeed.”

“Why?”

“I have to be confident. If we’re exposed as incompetent frauds, our bottom line will take a huge hit. And we’ll wind up in prison.”

PART TWO: THE DEVIOUS TRICK

Now I’m going to go over the vital information again, but this time I’m going to show you how…

The vaccine companies can use the fatal flaw in their protocol design to…

Actually win approval of their COVID vaccine.

Stick with me. This is big.

Only 150 people are needed to make the major clinical trials of a COVID vaccine look like a success.

Out of 30,000 volunteers in a trial, researchers are waiting for 150 people to “come down with COVID-19.” MILD cases. They assume this will happen because they believe the coronavirus is everywhere, and it’ll infect some of their volunteers.

Of course, their definition of a mild case of COVID-19 is meaningless. Cough plus fever, and a positive PCR test. The test spits out false positives like a rigged slot machine, and the visible mild symptoms could result from flu, polluted air, or too many candy bars.

Nevertheless, the researchers are waiting for a total of 150 people to “catch a mild case of COVID.” When that number is reached, everything stops.

Now comes the big moment. How many of those 150 COVID cases occurred in the group that received the vaccine, and how many in the group that received the placebo shot of salt water?

Let’s say only 50 COVID cases occurred in the vaccine group, and 100 in the placebo group. The researchers pop champagne corks. They say, “Look, the vaccine is 50% effective at preventing COVID, and that’s all we need to win emergency authorization from the FDA.”

BUT suppose 75 cases occurred in the vaccine group and 75 in the placebo group? No good. No good at all. No way to call the vaccine effective.

Now comes the “reshaping of the data.”

HERE WE GO.

The researchers say, “Wait. Thirty of the COVID cases in the vaccine group were REALLY just adverse reactions to the vaccine. They weren’t cases of COVID. You see, the vaccine can cause symptoms that are indistinguishable from mild COVID. Cough, fever, chills. ACTUALLY, there were only 30 cases of COVID in the vaccine group. There were 75 in the placebo group. That’s good enough. The vaccine IS effective. We’re golden. We can get emergency authorization from the FDA right now to shoot up everybody.”

Vaccine manufacturers HAVE KNOWN ALL ALONG that they could pull this trick.

Why leave things to chance?

Why risk a few hundred billion dollars of profit on a random distribution of mild COVID cases among the volunteers in their clinical trials?

The definition of a mild COVID case is EXACTLY what the vaccine manufacturers needed. It enabled them to hatch a plan, to make sure they didn’t fail.

They could pawn off a MILD case of COVID as a reaction to the vaccine. They could fake that without causing ripples. The FDA would say, “The vaccine reactions aren’t serious. All right, no problem. We’ll approve this vaccine for emergency use.”

However…If the manufacturers designed their clinical trial protocol to prevent serious cases of COVID—-very serious pneumonia—then first of all, they would be waiting to see 150 cases of really sick people to occur among the volunteers.

That might never happen. In 100 years.

And second, if it did happen, and the manufacturers had to pull their devious switcheroo trick and blame the vaccine for some of these SERIOUS cases…

They would have to tell the FDA that their vaccine was causing life-threatening pneumonia; and the FDA, under a lot of scrutiny these days, would find it very difficult to overlook that.

FDA: “We can’t approve this vaccine. It could cause a few million cases of dire pneumonia…”

The vaccine companies didn’t make a titanic stupid mistake in their protocol design. In gearing the protocol to prevent MILD COVID cases, they did what they did on purpose. It allows them to “reshape their data” and win FDA emergency approval for their vaccine.

These companies have no intention of failing, starting over, and spending a year recruiting 30,000 new volunteers. They want success and money now. They want to win the race.

And they will win, if the truth isn’t known and shared widely.

The punchline:

Every “expert,” in August 2021, is instructed to say the vaccine is definitely protecting people against severe illness and hospitalization. This is their promotional message to the world.

“Yes, even if you’re vaccinated, you could become infected with the virus, you could develop COVID, and you could pass the virus to other people, BUT you must take the shot. It will protect you from becoming severely ill.”

As you can see from what I’ve written above, this is a straight-out lie.

It was always a fantastic lie, from the beginning of COVID vaccine development, because the design of the clinical trials had nothing to do with preventing serious illness.

—end of article—

OK, we’re back in the present now; 2022. Everything you’ve just read has been studiously ignored. Shoved to the side.

The vaccine was only designed, at best, to prevent mild cough, fever, chills. That’s it. A mild case of flu-like illness. Which cures itself.

That design was intentional. It allowed the vaccine makers to win approval for the injection.

If they had to wait around for 150 volunteers in the clinical trials to develop serious pneumonia, that could have taken years. Or forever.

The clinical trials proved nothing.

The vaccine, even in mainstream scientific terms, was worthless.

It was designed that way.

That’s a chunk of blockbuster news anybody with a half a brain should be shouting from the rooftops. Instead: SILENCE.

Why?

Again, because this blockbuster news burns the whole house down.

It takes down the whole vaccine establishment.

And there are lots of vaccine critics who DON’T WANT TO GO ALL THE WAY.

EVEN THOUGH THEY SHOULD.

They back away. They pretend they don’t know what they DO know.

They could shoot down, overnight, the whole basis for these COVID shots, and they would expose the vaccine that is maiming and killing of millions upon millions of people.

But they stay silent.

Show them this information.

Get them to tell you what their problem is.

 

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cover image credit: himmlisch / pixabay




The Test for Klaus Schwab and the World Economic Forum

The Test for Klaus Schwab and the World Economic Forum

by Jon Rappoport, No More Fake News
February 21, 2022

 

Knowing my regular readers can handle more than one major point in an article, I start with this: Justin Trudeau is not serving the interests of Canadians; he is loyal to the World Economic Forum (WEF) and the brand of Globalism it represents.

Meaning: global governance; the submerging of nations in a scheme of external top-down control; the expansion of poverty; wall to wall surveillance; a currency reset; and other totalitarian transformations.

If you watch these two brief videos (here and here), you’ll see Klaus Schwab confirm, in Trudeau’s presence, the prime minister’s loyalty to the WEF, as well as the penetration of Trudeau’s cabinet with WEF agents.

Schwab, the head of WEF, also mentions a new dawn of entrepreneurs who lead corporations dedicated to social responsibility.

And THAT is a test for Schwab. Because he certainly backs major pharmaceutical companies. Do those businesses display social responsibility?

I’m not talking about their pricing of drugs or their equitable distribution of drugs. I’m talking about killing and maiming people with the drugs. Many people.

And so I return to citations I’ve published a number of times. By the way, virtually no one takes these devastating references and runs with them.

I can only conclude journalists and doctors who otherwise criticize medical policies don’t want to admit the medical cartel has a very long track record of destroying populations.

These journalists and doctors only want to cherry pick their targets. In fact, they support the overall performance of the medical system. Why? You would have to ask them.

Here, I’m testing Klaus Schwab. Does he really think he can get away with his talk about “social responsibility” and his simultaneous support of Pharma?

Buckle up—

ONE: Journal of the American Medical Association, April 15, 1998: “Incidence of Adverse Drug Reactions in Hospitalized Patients.”

The authors, led by Jason Lazarou, culled 39 previous studies on patients in hospitals. These patients, who received drugs in hospitals, or were admitted to hospitals because they were suffering from the drugs doctors had given them, met the following fate:

Every year, in the US, between 76,000 and 137,000 hospitalized patients die as a direct result of the drugs.

Beyond that, every year 2.2 million hospitalized patients experience serious adverse reactions to the drugs.

The authors write: “…Our study on ADRs [Adverse Drug Reactions], which excludes medication errors, had a different objective: to show that there are a large number of ADRs even when the drugs are properly prescribed and administered.”

So this study had nothing to do with doctor errors, nurse errors, or improper combining of drugs. And it only counted people killed or maimed who were admitted to hospitals. It didn’t begin to tally all the people taking pharmaceuticals who died as consequence of the drugs, at home.

TWO: July 26, 2000, Journal of the American Medical Association; author, Dr. Barbara Starfield, revered public health expert at the Johns Hopkins School of Public Health; “Is US health really the best in the world?”

Starfield reported that the US medical system kills 225,000 Americans per year. 106,000 as a result of FDA-approved medical drugs, and 119,000 as a result of mistreatment and errors in hospitals. Extrapolate the numbers to a decade: that’s 2.25 million deaths. You might want to read that last number again.

I interviewed Starfield in 2009. I asked her whether she was aware of any overall effort by the US government to eliminate this holocaust. She answered a resounding NO. She also said her estimate of medically caused deaths in America was on the conservative side.

THREE: BMJ June 7, 2012 (BMJ 2012:344:e3989). Author, Jeanne Lenzer. Lenzer refers to a report by the Institute for Safe Medication Practices: “It [the Institute] calculated that in 2011 prescription drugs were associated with two to four million people in the US experiencing ‘serious, disabling, or fatal injuries, including 128,000 deaths.’”

The report called this “one of the most significant perils to humans resulting from human activity.”

The report was compiled by outside researchers who went into the FDA’s own database of “serious adverse [medical-drug] events.”

Therefore, to say the FDA isn’t aware of this finding would be absurd. The FDA knows. The FDA knows and it isn’t saying anything about it, because the FDA certifies, as safe and effective, all the medical drugs that are routinely maiming and killing Americans. Every public health agency knows the truth.

FOUR: “The Epidemic of Sickness and Death from Prescription Drugs.” The author is Donald Light, who teaches at Rowan University, and was the 2013 recipient of ASA’s [American Sociological Association’s] Distinguished Career Award for the Practice of Sociology. Light is a founding fellow of the Center for Bioethics at the University of Pennsylvania. In 2013, he was a fellow at the Edmond J. Safra Center for Ethics at Harvard. He is a Lokey Visiting Professor at Stanford University.

Donald Light: “Epidemiologically, appropriately prescribed, prescription drugs are the fourth leading cause of death, tied with stroke at about 2,460 deaths each week in the United States. About 330,000 patients die each year from prescription drugs in the United States and Europe. They [the drugs] cause an epidemic of about 20 times more hospitalizations [6.6 million annually], as well as falls, road accidents, and [annually] about 80 million medically minor problems such as pains, discomforts, and dysfunctions that hobble productivity or the ability to care for others. Deaths and adverse effects from overmedication, errors, and self-medication would increase these figures.” (ASA publication, “Footnotes,” November 2014)

FIVE: None of the above reports factor in death or injury by vaccine.

Medical crimes.

Medically caused deaths of friends, family members, loved ones, who are buried along with the truth.

No criminal investigations, no prosecutions, no guilty verdicts, no prison sentences.

But of course, you can believe everything leading lights of the US medical system tell you about COVID.

You can believe everything the press—who buries the truth about this medical holocaust—tells you about COVID.

Given the reports on medically caused death and maiming I’ve just cited and described in this article, it’s obvious that…

Leading medical journals around the world, which routinely publish glowing accounts of clinical trials of medical drugs…

Are spilling over with rank fraud, on page after page.

Indeed, here is a stunning quote from an editor who has quite probably read and analyzed more medical-drug studies than any doctor in the world:

“It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of The New England Journal of Medicine.” (Dr. Marcia Angell, NY Review of Books, January 15, 2009, “Drug Companies & Doctors: A Story of Corruption)

Compare that quote with one from “the father of COVID science,” Anthony Fauci. In an interview with the National Geographic, Fauci stated:

“Anybody can claim to be an expert even when they have no idea what they’re talking about…If something is published in places like New England Journal of Medicine, Science, Nature, Cell, or JAMA—you know, generally that is quite well peer-reviewed because the editors and the editorial staff of those journals really take things very seriously.”

They take things so seriously, they routinely publish glowing studies of medical drugs that are killing people in great numbers.

—So, Mr. Schwab, which is it? You support corporate social responsibility, and therefore you condemn, in the strongest possible way, the ongoing death-and-maiming count achieved by beloved pharmaceutical companies? Or you maintain your unwavering support for Pharma, and admit your pose of “social responsibility” is a complete fraud.

And to journalists and doctors who refuse to pick up the citations in this article and DO something with them, I ask: what’s holding you back? What’s been holding you back? I’ve been publishing and speaking about this information for more than 10 years.

What are you afraid of? Where do YOUR loyalties lie?

 

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cover image credit: Karenwolfewhitchurch / pixabay




TO KILL & CONTROL – A Brief History of Unlawful Human Experiments

TO KILL & CONTROL – A Brief History of Unlawful Human Experiments

by Greg Reese, Reese Report
February 19, 2022

 



 

Connect with Greg Reese at Reese Report




La Quinta Columna Continues Examination of Pfizer Vaccine: Filaments Attracting Crystals & Apparent Microcircuitry

La Quinta Columna Continues Examination of Pfizer Vaccine: Filaments Attracting Crystals & Apparent Microcircuitry

 

Morgellons-type structures that “feed” on crystals

by Orwellito, Orwell City
February 18, 2022

 

La Quinta Columna has shared with the world a very particular observation about the filament-like structures they have found when looking at vials of Pfizer vaccines under an optical microscope.

Dr. Sevillano noticed that within the particulate composition, there are some crystals that appear to be microcircuitry, but are actually some other material that would be a kind of food for the Morgellons-like filaments to grow. They don’t know what kind of crystals these are, but they continue in their research to try to unravel as many mysteries as possible.

Orwell City brings the key fragment.



Ricardo Delgado: So I’m going to move the microscope, and let’s go down. Here is the “hair.” See?

Dr. Sevillano: Here’s the hair. Yes.

Ricardo Delgado: Let’s see, I’m going to move it a little bit. There it is. See that you can even see… This sample is more dried out now. But look at the size of it.

Dr. Sevillano: And how it attracts the crystals. If you notice, you can see how it’s attracting them.

Ricardo Delgado: This one has been growing too. Here I’m going to focus it now to…

Dr. Sevillano: Let’s see if you find the generator pole. We have to look for the generator pole. Let’s see if we can see the deflection and the cubes generating around it. Let’s see if we can find the extreme.

Ricardo Delgado: This is incredible. Come on. Look at this. It’s still here. This is where I think it ends, right?

Dr. Sevillano: Yeah, it looks like this is where it ends.

Ricardo Delgado: This is where it ends. What happens is that in, here, there’s no longer any kind of aqueous suspension. I mean, it’s completely dried out.

Dr. Sevillano: It’s completely dried out. Maybe, for that reason, it has stopped… By not having… Maybe, it lacks something to… But look how it attracts all the material. How it’s full of crystals all over the place.

Ricardo Delgado: Surely, there must be more around here. Let’s see, I’m going to look around. Well, this is the content of the Pfizer vaccine. It’s crazy!

Dr. Sevillano: There…  I’m beginning to think, Ricardo, that most of the stuff we see there is circuitry. And probably, there’s also material that we’re talking about that’s used for the growth of that.

Ricardo Delgado: Yes.

Dr. Sevillano: The ones that don’t have “drawings” or that don’t have printed circuitry, those ones have to be the material that uses that to grow. That’s all.

Ricardo Delgado: This is the edge of the drop, which is already dry. This is where it ends.

Dr. Sevillano: Yes, more mysteries that we understand nothing about in all this.

Ricardo Delgado: Look what’s here.

Dr. Sevillano: There’s another one. Yes. It’s quite huge.

 

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Autopsies Show: Vaccinating Teens for COVID Is Literally ‘Heartbreaking’

Autopsies Show: Vaccinating Teens for COVID Is Literally ‘Heartbreaking’
Autopsies of two teenage boys who died days after receiving Pfizer’s COVID vaccine prove the vaccine caused their deaths. Pathological findings suggest there may be a way to distinguish SARS-COV-2 infection-induced myo/pericarditis from vaccine-induced cardiac injury. Vaccine-induced heart injury can be sub-clinical, but how often?

by Madhava Setty, M.D., The Defender
February 18, 2022

 

Pathologists who examined the autopsies of two teenage boys who died days after receiving Pfizer’s COVID-19 vaccine concluded the vaccine caused the teens’ deaths.

The three pathologists, two of whom are medical examiners, published their findings Feb. 14 in an early online release article, “Autopsy Histopathologic Cardiac Findings in Two Adolescents Following the Second COVID-19 Vaccine Dose,” in the Archives of Pathology and Laboratory Medicine.

The authors’ findings were conclusive. Two teenage boys were pronounced dead in their homes three and four days after receiving the second Pfizer-BioNTech COVID-19 dose.

There was no evidence of active or previous COVID-19 infection. The teens had negative toxicology screens (i.e. no drugs or poisons were present in their bodies).

These boys died from the vaccine.

Histopathological examination of their cardiac tissue revealed an important new finding: Neither heart demonstrated evidence of typical myocarditis.

Instead, the authors found evidence of microscopic changes consistent with a different form of heart injury called toxic cardiomyopathy. They wrote:

“The myocardial injury seen in these post-vaccine hearts is different from typical myocarditis and has an appearance most closely resembling a catecholamine-mediated stress (toxic) cardiomyopathy.”

The authors further explained what they observed under the microscope:

“Their histopathology does not demonstrate a typical myocarditis… In these two post-vaccination instances, there are areas of contraction bands and hypereosinophilic myocytes distinct from the inflammation.

“This injury pattern is instead similar to what is seen in the myocardium of patients who are clinically diagnosed with Takotsubo, toxic, or ‘stress’ cardiomyopathy, which is a temporary myocardial injury that can develop in patients with extreme physical, chemical, or sometimes emotional stressors.

“Stress cardiomyopathy is a catecholamine-mediated ischemic process seen in high catecholamine states in the absence of coronary artery disease or spasm. It has also been called ‘neurogenic myocardial injury’ and ‘broken heart syndrome.’”

The pathologists determined there was a different mechanism of heart injury at play in these two boys, distinct from a purely infectious process that would result directly from a viral infection like COVID-19.

This is an important finding. There may be a way to distinguish cardiac injury resulting from a SARS-COV-2 infection from cardiac injury where the vaccine predisposes the patient to stress cardiomyopathy before contracting COVID-19.

However, the authors are careful not to assume that cardiac injuries from COVID-19 and COVID-19 vaccines can always be sorted out under the microscope.

They explain that stress cardiomyopathy, or “broken heart syndrome,” may also occur in a rare hyperinflammatory state that is known to occur in COVID-19 infection as well:

“This post-vaccine reaction may represent an overly exuberant immune response and the myocardial injury is mediated by similar immune mechanisms as described with SARS-COV-2 and multisystem inflammatory syndrome (MIS-C) cytokine storms.”

The authors admit this pathological finding may also occur as a result of MIS-C, a known complication of SARS-COV2 infection.

Learning more about this condition requires a biopsy of heart tissue, or in this case an autopsy. We know very little about the nature of myocarditis in people who are clinically stable because heart biopsies are not conducted on them and autopsies are rarely done on patients who die from COVID-19.

There still is no practical way of screening for cardiac injury beyond assessing symptoms.

Unfortunately, the two boys did not have symptoms of myocarditis (fever, chest pain, palpitations, or dyspnea) prior to their cardiac arrest and death. One complained of a headache and gastric upset which resolved. The other had no complaints.

This is extremely concerning. These boys had smoldering, catastrophic heart injuries with no symptoms.

How many others have insidious cardiac involvement from vaccination that won’t manifest until they get a serious case of COVID-19 or the flu? Or perhaps when they subject themselves to the physical stress of competitive sports?

These findings suggest a significant subset of COVID-19 deaths in the vaccinated could be due to the vaccines themselves.

Furthermore, it raises this question: How often does this condition exist in a latent form in vaccinated individuals?

The CDC believes the risk of vaccine-induced myocarditis not significant

The Centers for Disease Control and Prevention (CDC) says the risk of myocarditis and pericarditis in adolescents who get the COVID-19 vaccine is “extremely rare” and “most cases are mild.”

But those assurances conflict with the agency’s own data.

The CDC’s Advisory Committee on Immunization Practices (ACIP) presented this disquieting information (see chart below) during its June 23, 2021 meeting convened specifically to address the risks of myo/pericarditis in 12- to 15-year-olds who received Pfizer’s COVID vaccine:

This slide is important for two reasons.

First, the incidence of this potentially lethal condition is significantly higher in the vaccinated (“Observed” column) compared to the background rate (“Expected” column), especially in males in the 18- to 24-year-old age range.

In the 12- to 17-year-old male cohort, the risk of myo/pericarditis is at least 11 times higher than the background rate.

With more than 2 million doses administered at the time when these cases of myo/pericarditis were identified, we can be confident these data represent an undeniable safety signal.

The second reason this slide is important is this: The CDC is drawing directly from the Vaccine Adverse Event Reporting System (VAERS), a system specifically designed to monitor for safety signals when vaccines are administered to the public.

As of Feb. 15, the CDC continues to assure the public that “Reports of adverse events to VAERS following vaccination, including deaths, do not necessarily mean that a vaccine caused a health problem.”

In essence, the CDC is acknowledging that reports of deaths and other adverse events following vaccination exist in VAERS but do not comprise any risk because causality has not been verified.

Then why did the ACIP choose to accept VAERS as a legitimate source of information on myo/pericarditis in their calculations?

The CDC released its conclusions immediately following the ACIP meeting:

“The facts are clear: this is an extremely rare side effect, and only an exceedingly small number of people will experience it after vaccination. Importantly, for the young people who do, most cases are mild, and individuals recover often on their own or with minimal treatment.”

But how do they know this?

One month after this comforting statement from the CDC, the U.S. Food and Drug Administration (FDA) admitted in this letter to Pfizer that the agency was not able to adequately assess the risk of myocarditis from Pfizer’s product:

“We have determined that an analysis of spontaneous postmarketing adverse events reported under section 505(k)(1) of the FDCA [Federal Food, Drug and Cosmetic Act] will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis.

“Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA is not sufficient to assess these serious risks.”

Commenting on the FDA’s letter, Dr. Meryl Nass said, “The FDA is saying that neither an analysis of the data in VAERS or of any of the other taxpayer-funded databases will provide sufficient assessment of the risk of this product.”

“This is a joke,” said Nass, adding:

“All this data, plus software, plus a team of analysts, and the FDA says it can’t assess the risk of myocarditis, despite identifying thousands of cases?

“Furthermore, unsaid, but implied by the FDA, is that if the FDA is incapable of assessing the risk of myocarditis despite thousands of reported cases, it cannot or will not be capable of assessing the other serious adverse events that have been reported in conjunction with COVID vaccines.”

If the FDA is not able to perform adequate surveillance of safety signals around vaccine-induced myocarditis, who will?

The FDA assigns this unenviable but essential task to Pfizer itself (again, from the FDA’S letter to Pfizer):

“Therefore, based on appropriate scientific data, we have determined that you are required to conduct the following studies…”

Is myocarditis ‘extremely rare’ after COVID-19 vaccination? 

As of Feb. 4, VAERS reported 495 cases of myo/pericarditis in 12- to 17-year-olds. VAERS data show that as of Feb. 10, there were 2,239 reported cases of myocarditis in people under the age of 30.

However, a widely cited CDC-sponsored study (Lazarus et al) concluded the incidence of adverse events is 10 to 100 times higher than are reported to VAERS.

More recent calculations estimate that adverse events are underreported by a factor of approximately 41.

From these estimates, we can conclude there may have been approximately 20,000 cases of myocarditis in 12- to 17-year-olds since Pfizer’s COVID-19 vaccine received Emergency Use Authorization and was rolled out to this age group..

The VAERS data from June 11, 2021 from the table above show 132 cases of myo/pericarditis were observed in 2,039,000 doses given to 12- to 17-year-old males. This is approximately 6.5 cases in 100,000 doses.

This study from Hong Kong found the incidence of myo/pericarditis after two doses with Pfizer’s Comirnaty vaccine was 37 in 100,000. This incidence matches nearly exactly with findings from this study that used the Vaccine Safety DataLink (VSD) system (37.7 12-17 year olds per 100,000 suffered myo/pericarditis after their second dose). This is more evidence that significant underreporting is in play in the VAERS system.

Will most of these teens “recover on their own”? How many other vaccinated people have varying degrees of “broken heart” syndrome that remain asymptomatic, undiagnosed and unreported?

These new findings indicate that no one can answer these questions right now — especially not the CDC and the FDA.

If the FDA has admitted it cannot assess the risk of myocarditis using the surveillance systems in place, how then is the CDC able to assure us that the risk is low enough to continue to proceed with a vaccination campaign that now includes 5- to 11-year-old children?

The FDA has abdicated its responsibility for monitoring the safety of these vaccines to the vaccine manufacturers.

The CDC is using VAERS data in its own analyses while urging the public to discount all adverse events, including deaths, that appear in the very same database.

There isn’t any regulation happening here. Our regulatory agencies have become mouthpieces for the very industry they are tasked to oversee.

 

Madhava Setty, M.D. is senior science editor for The Defender.

©February 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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Does HIV Exist? An Explosive Interview

Does HIV Exist? An Explosive Interview

by Jon Rappoport, No More Fake News
February 18, 2022

 

Before we get to Christine Johnson’s interview, a bit of background.

My first book, AIDS INC., was published in 1988. The research I engaged in then formed a foundation for my recent work in exposing the vast fraud called COVID-19.

In 1987-88, my main question eventually became: does HIV cause AIDS? For months, I had blithely assumed the obvious answer was yes. This created havoc in my investigation, because I was facing contradictions I couldn’t solve.

For example, in parts of Africa, people who were chronically ill and dying obviously needed no push from a new virus. All their “AIDS” conditions and symptoms could be explained by their environment: contaminated water supplies; sewage pumped directly into the drinking water; protein-calorie malnutrition; hunger, starvation; medical treatment with immunosuppressive vaccines and drugs; toxic pesticides; fertile farm land stolen by corporations and governments; wars; extreme poverty. The virus cover story actually obscured all these ongoing crimes.

Finally, in the summer of 1987, I found several researchers who were rejecting the notion that HIV caused AIDS. Their reports were persuasive.

I’m shortcutting a great deal of my 1987-8 investigation here, but once HIV was out of the picture for me, many pieces fell into place. I discovered that, in EVERY group supposedly at “high-risk” for AIDS, their conditions and symptoms could be entirely explained by factors that had nothing to do with a new virus.

AIDS was not one condition. It was an umbrella label, used to re-package a number of immunosuppressive symptoms and create the illusion of a new and unique and single “pandemic.”

Several years after the publication of AIDS INC, I became aware of a quite different emerging debate going on under the surface of research: DOES HIV EXIST?

Was the purported virus ever truly discovered?

And THAT question led to: what is the correct procedure for discovering a new virus?

The following 1997 interview, conducted by brilliant freelance journalist, Christine Johnson, delves into these questions:

How should researchers prove that a particular virus exists? How should they isolate it? What are the correct steps?

These questions, and their answers, reside at the heart of most disease research—and yet, overwhelmingly, doctors never explore them or even consider them.

Johnson interviews Dr. Eleni Papadopulos, “a biophysicist and leader of a group of HIV/AIDS scientists from Perth in Western Australia. Over the past decade and more she and her colleagues have published many scientific papers questioning the HIV/AIDS hypothesis…”

Here I’m publishing and highlighting excerpts from the interview. Technical issues are discussed. Grasping them is not the easiest exercise you’ve ever done, but I believe the serious reader can comprehend the vital essentials.

Christine Johnson: Does HIV cause AIDS?

Eleni Papadopulos: There is no proof that HIV causes AIDS.

CJ: Why not?

EP: For many reasons, but most importantly, because there is no proof that HIV exists.

… CJ: Didn’t Luc Montagnier and Robert Gallo [purportedly the co-discoverers of HIV] isolate HIV back in the early eighties?

EP: No. In the papers published in Science by those two research groups, there is no proof of the isolation of a retrovirus from AIDS patients. [HIV is said to be a retrovirus.]

CJ: They say they did isolate a virus.

EP: Our interpretation of the data differs. To prove the existence of a virus you need to do three things. First, culture cells and find a particle you think might be a virus. Obviously, at the very least, that particle should look like a virus. Second, you have to devise a method to get that particle on its own so you can take it to pieces and analyze precisely what makes it up. Then you need to prove the particle can make faithful copies of itself. In other words, that it can replicate.

CJ: Can’t you just look down a microscope and say there’s a virus in the cultures?

EP: No, you can’t. Not all particles that look like viruses are viruses.

… CJ: My understanding is that high-speed centrifugation is used to produce samples consisting exclusively of objects having the same density, a so-called “density-purified sample.” Electron microscopy is used to see if these density-purified samples consist of objects which all have the same appearance — in which case the sample is an isolate — and if this appearance matches that of a retrovirus, in terms of size, shape, and so forth. If all this is true, then you are three steps into the procedure for obtaining a retroviral isolate. (1) You have an isolate, and the isolate consists of objects with the same (2) density and (3) appearance of a retrovirus. Then you have to examine this isolate further, to see if the objects in it contain reverse transcriptase [an enzyme] and will replicate when placed in new cultures. Only then can you rightfully declare that you have obtained a retroviral isolate.

EP: Exactly. It was discovered that retroviral particles have a physical property which enables them to be separated from other material in cell cultures. That property is their buoyancy, or density, and this was utilized to purify the particles by a process called density gradient centrifugation.

The technology is complicated, but the concept is extremely simple. You prepare a test tube containing a solution of sucrose, ordinary table sugar, made so the solution is light at the top but gradually becomes heavier, or more dense, towards the bottom. Meanwhile, you grow whatever cells you think may contain your retrovirus. If you’re right, retroviral particles will be released from the cells and pass into the culture fluids. When you think everything is ready, you decant a specimen of culture fluids and gently place a drop on top of the sugar solution. Then you spin the test tube at extremely high speeds. This generates tremendous forces, and particles present in that drop of fluid are forced through the sugar solution until they reach a point where their buoyancy prevents them from penetrating any further. In other words, they drift down the density gradient until they reach a spot where their own density is the same as that region of the sugar solution. When they get there they stop, all together. To use virological jargon, that’s where they band. Retroviruses band at a characteristic point. In sucrose solutions they band at a point where the density is 1.16 gm/ml.

That band can then be selectively extracted and photographed with an electron microscope. The picture is called an electron micrograph, or EM. The electron microscope enables particles the size of retroviruses to be seen, and to be characterized by their appearance.

CJ: So, examination with the electron microscope tells you what fish you’ve caught?

EP: Not only that. It’s the only way to know if you’ve caught a fish. Or anything at all.

CJ: Did Montagnier and Gallo do this?

EP: This is one of the many problems. Montagnier and Gallo did use density gradient banding, but for some unknown reason they did not publish any Ems [photos] of the material at 1.16 gm/ml…this is quite puzzling because in 1973 the Pasteur Institute hosted a meeting attended by scientists, some of whom are now amongst the leading HIV experts. At that meeting the method of retroviral isolation was thoroughly discussed, and photographing the 1.16 band of the density gradient was considered absolutely essential.

CJ: But Montagnier and Gallo did publish photographs of virus particles.

EP: No. Montagnier and Gallo published electron micrographs of culture fluids that had not been centrifuged, or even separated from the culture cells, for that matter. These EMs contained, in addition to many other things, including the culture cells and other things that clearly are not retroviruses, a few particles which Montagnier and Gallo claimed are retroviruses, and which all belonged to the same retroviral species, now called HIV. But photographs of unpurified particles don’t prove that those particles are viruses. The existence of HIV was not established by Montagnier and Gallo — or anyone since — using the method presented at the 1973 meeting.

CJ: And what was that method?

EP: All the steps I have just told you. The only scientific method that exists. Culture cells, find a particle, isolate the particle, take it to pieces, find out what’s inside, and then prove those particles are able to make more of the same with the same constituents when they’re added to a culture of uninfected cells.

CJ: So before AIDS came along there was a well-tried method for proving the existence of a retrovirus, but Montagnier and Gallo did not follow this method?

EP: They used some of the techniques, but they did not undertake every step including proving what particles, if any, are in the 1.16 gm/ml band of the density gradient, the density that defines retroviral particles.

CJ: But what about their pictures?

EP: Montagnier’s and Gallo’s electron micrographs…are of entire cell cultures, or of unpurified fluids from cultures…

—end of interview excerpt—

If you grasp the essentials of this discussion, you’ll see there is every reason to doubt the existence of HIV, because the methods for proving its existence were not followed.

Worse yet, it appears that Robert Gallo and Luc Montagnier, the two scientists credited with the discovery of HIV—as well as other elite researchers—were aware they weren’t employing correct methods.

And so…as I’ve reported, there is every reason to doubt and reject the existence of the COVID virus, SARS-CoV-2, since correct large-scale electron microscope studies have never been done. And by large-scale, I mean: attempting to find and photograph the virus in a cohort of, say, 1000 people who are supposed to be “pandemic patients.” I’m NOT talking about one or two electron-microscope photos accompanying a study.

But even that isn’t the end of the story. There is one further potential limiting factor in virus research. I became aware of it about a year ago. Analysis of electron microscope findings is fraught with difficulty and doubt. Are scientists actually looking at what they think they’re looking at in these photos? I refer readers to the work of neurobiologist Harold Hillman, who concluded that researchers were, for the most part, looking at artifacts, not actual cells or entities within cells. Another suppressed controversy.

After more than 30 years of investigating medical research fraud, my general conclusion is, the deeper you go the stranger it gets. Or to put it another way, the worse it gets.

 

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cover image credit: madartzgraphics / pixabay




FDA Executive Officer Exposes Close Ties Between Agency and Pharmaceutical Companies

FDA Executive Officer Exposes Close Ties Between Agency and Pharmaceutical Companies

 



by James O’Keefe, Project Veritas
February 16, 2022

 

FDA Executive Officer Exposes Close Ties Between Agency and Pharmaceutical Companies: ‘Almost a Billion Dollars a Year Going into FDA’s Budget from the People we Regulate’

• FDA Executive Officer Chris Cole: “The drug companies, the food companies, the vaccine companies. So, they pay us hundreds of millions of dollars a year to hire and keep the reviewers to approve their products.”

• Cole on FDA fees: “Congress approved user fees for [the] FDA. Basically, we charge the industry millions of dollars in order to hire more drug reviewers and vaccine reviewers which will speed up the approval process. So, they [pharmaceutical companies] make more money.”

• Cole: “They [FDA] tone down the impact of the user fees on their operations because they know they’re dependent on the drug companies, and the vaccine companies, and these other companies for their agency to operate.”

• Cole on blowing the whistle: “There’s not an incentive to speak out in government, surprisingly. You would think there would be, but there’s not. It’s better just to just not say anything and just ignore it.”

• Cole on retaliation in government: “You’ll be marked from getting other jobs because another office is not going to want to hire you if you’ve spoken out about something, right or wrong. They don’t look at what you’ve spoken out about. They’re just not willing to- government’s about rocking the boat and they don’t want to- which is the problem I have with- one of the problems I have with government is, like, they don’t like people rocking the boat, for right or wrong, at all costs. They want to hire a safe person that can do the job but doesn’t necessarily- is a great hire.”

[WASHINGTON, D.C. – Feb. 16, 2022] Project Veritas published Part Two of its series on the FDA on Wednesday night which featured FDA Executive Officer, Christopher Cole, speaking about the inner workings of the agency including the FDA’s conflicts of interest, overspending, and why it’s hard for those within the agency to speak out on such abuses.

In the footage, Cole talks about the impact that pharmaceutical companies have on the agency including the process for approving drugs.

“A long time ago, Congress approved user fees for [the] FDA. Basically, we charge the industry millions of dollars in order to hire more drug reviewers and vaccine reviewers, which will speed up the approval process, so they make more money,” Cole says in the hidden camera footage.

He then reveals that the FDA tones down the impact that these user fees have on the agency’s operations because, “they’re dependent on the drug companies, and the vaccine companies and these other companies for their agency to operate.”

The incendiary footage, which features Cole talking about how the additional money the FDA brings in “gets banked” to be spent on “whatever you can, whether it’s right or wrong,’’ also features Cole discussing reasons why it’s difficult for anyone in government to speak out about practices he sees as “probably excessive.”

“I don’t think there’s enough people saying — they’re, like, ‘Look, that’s fine, but that’s not right. So, we’re not going to charge that.’ You don’t want to be that person. You’re not going to have a long shelf life in the agency if you’re always that person,” Cole said.

“There’s not an incentive to speak out in government, surprisingly. You would think there would be, but there’s not. It’s better just to just not say anything and just ignore it. The whistleblower, well, it’s high-profile whistleblower statutes and everything, that’s kind of ridiculous,” Cole said before adding “it’s better to just stay quiet and accept.”

Cole’s LinkedIn page lists him as an Executive Officer within the agency’s Countermeasures Initiatives, which plays a critical role in ensuring that drugs, vaccines, and other measures to counter infectious diseases and viruses are safe. He made these revelations on a hidden camera to an undercover Project Veritas reporter.

A spokesperson for FDA issued a statement yesterday saying, “The person purportedly in the video does not work on vaccine matters and does not represent the views of the FDA.”

This statement appears to contradict a phone call released Wednesday afternoon by Project Veritas wherein Cole reiterated, during the conversation with Project Veritas Founder and CEO, James O’Keefe, that he is “a manager in the office that helps oversee the approval of the COVID vaccines for emergency approval.”

 


See Part 1:



 

Project Veritas videos are available at Odysee and YouTube

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Corporate Vaccine Mandates and Vaccine Passports — Brought to You by BlackRock and Vanguard?

Corporate Vaccine Mandates and Vaccine Passports — Brought to You by BlackRock and Vanguard?
Investment giants BlackRock and The Vanguard Group stand to benefit from their ownership stakes in most of the corporations that imposed COVID vaccine mandates, and in some of the technology firms developing vaccine passports.

by Michael Nevradakis, Ph.D. , The Defender
February 16, 2022

 

After the U.S. Supreme Court last month froze the Biden administration’s COVID-19 vaccine mandate for large private employers, some companies — including BoeingGeneral Electric and Starbucks — dropped plans to implement the mandate.

Others, based on guidance issued in 2020 by the Equal Employment Opportunity Commission, left the mandates in place.

Most of the large employers that opted to mandate COVID vaccines for their employees, even though the Supreme Court ruled they didn’t have to, have something in common: BlackRock and The Vanguard Group have ownership stakes in them.

BlackRock and Vanguard, two of the world’s “Big Three” asset managers, also are among the top three shareholders of COVID vaccine makers PfizerModerna and Johnson & Johnson — which means the two investment giants stand to benefit from these companies’ soaring profits and the resulting rise in those companies’ stock prices.

BlackRock and Vanguard don’t just benefit from sales of COVID vaccines. As it turns out, they also have ownership stakes in technology companies developing vaccine passports and digital wallets.

BlackRock: the ‘fourth branch of government’?

Combined, BlackRock and Vanguard manage more than $15 trillion in global assets.

To put this figure into perspective, that amounts to more than three-fourths of the U.S. gross domestic product (GDP) and more than triple the GDP of the European Union’s economic powerhouse, Germany.

BlackRock is the world’s largest asset manager, with more than $9.5 trillion in assets as of July 2021, while Vanguard held more than $7 trillion in assets as of January 2021.

Notably, Vanguard is the largest stockholder in BlackRock (7.61%), while BlackRock is the biggest stockholder in Vanguard (13.06%) — though the actual ownership structure of these companies has been described as “dark.”

In an August 2021 article about the two firms, Dr. Joseph Mercola pointed out that, far from the appearance of competition promised by capitalism, BlackRock and Vanguard own significant shares in companies that ostensibly compete directly with each other, such as Google, Apple and Microsoft, or Coca-Cola and PepsiCo.

This influence extends to the media. BlackRock alone owns significant shares in supposed “competitors” such as Fox News, CBS, Comcast (NBC), CNN, Disney (ABC), Gannett (USA TODAY and 250 daily newspapers throughout the U.S.), Sinclair Media (whose television stations reach 72% of the American public), and the Graham Media Group (Slate, Foreign Policy).

BlackRock is also politically influential and well-connected, having been chosen by the Obama administration to buy up toxic assets following the 2007-2008 financial collapse.

In 2020, BlackRock received a no-bid contract from the U.S. Treasury Department to manage a $454 billion fund, under the Coronavirus Aid, Relief and Economic Security Act (CARES Act), for businesses adversely impacted by the COVID lockdowns early that year. It wasn’t the first time BlackRock had been granted a no-bid contract from the federal government.

BlackRock along with other firms also is engaged in a real estate purchasing spree, buying up entire neighborhoods of single-family homes and converting them to rentals, driving up home prices by reducing supply on the marketplace.

BlackRock’s real estate strategy echoes the words of the World Economic Forum: “You’ll own nothing, and you’ll be happy.”

This level of power and influence promoted none other than Bloomberg in 2020 to characterize BlackRock as the “fourth branch of government.”

BlackRock, Vanguard among top 10 stockholders in most companies mandating vaccines

It is unclear to what extent BlackRock and Vanguard are able to dictate the vaccination policies of the companies in which they hold a stake — but what is clear is that the two investment firms are among the top 10 stockholders in most of these companies.

Here’s a rundown of major U.S. employers that continue to mandate COVID vaccines for their employers, and these companies’ relationships with BlackRock and/or Vanguard (all ownership figures are accurate as of this writing):

  • Abbvie, a U.S.-based pharmaceutical company, mandated its employees either get vaccinated or undergo weekly tests and continue to follow anti-coronavirus measures. Vanguard and BlackRock are its top two stockholders, at 7.80% and 4.47%, respectively.
  • Albertsons, a grocery store chain, required its office employees to get vaccinated and offered its staff a $100 incentive to get the vaccine. BlackRock is its third-largest stockholder (0.85%), and Vanguard is the sixth largest (0.43%).
  • American Express imposed a vaccine requirement for employees in its U.S. offices. Vanguard is its top stockholder (5.78%), while BlackRock is the third largest (3.68%).
  • Anthem Inc., a health insurer, requires employees to be fully vaccinated to physically enter the company’s offices, offered financial incentives to its workforce to get vaccinated and requires new candidates to be vaccinated. Vanguard and BlackRock are its top two stockholders, at 7.38% and 4.68%, respectively.
  • AstraZeneca requires its U.S. employees and visiting clients to be vaccinated. Three of the top 10 mutual funds holding shares in AstraZeneca PLC are managed by Vanguard.
  • AT&T, in two separate policies, required company managers (by Oct. 11, 2021) and unionized employees (by Feb. 1), to be vaccinated. Vanguard and BlackRock are its top two stockholders, at 7.58% and 5.10%, respectively.
  • Blackstone, an investment management company, mandated employees be vaccinated and boosted in order to return to the office. Vanguard and BlackRock are its top two stockholders, at 5.57% and 3.14%, respectively.
  • CapitalOne required employees in office-based positions to be vaccinated. Vanguard is its second-largest stockholder (7.62%), and BlackRock is its fourth largest (4.79%).
  • Carhartt, a clothing and apparel company, issued a vaccine mandate for its employees. It is one of the few exceptions on this list, as it is privately owned.
  • Centene, a healthcare provider, required its workforce to be vaccinated, and gave employees up to 10 days’ paid leave and a $1,000 discount on health premiums as incentives. Vanguard is its largest stockholder (10.25%), while BlackRock is the fifth largest (4.34%).
  • Chevron issued a vaccination requirement for employees who travel internationally, expatriate employees, offshore workforce in the Gulf of Mexico and some onshore support personnel. Vanguard is its biggest stockholder (7.98%) while BlackRock is the third-largest (4.57%).
  • Cigna, a healthcare and insurance company, required employees working remotely who visit the physical worksite to be vaccinated as of Sept. 7, 2021, and employees whose roles can only be performed onsite to be vaccinated as of Oct. 18, 2021, with an alternate option for two weekly COVID tests. Employees also were offered a $200 incentive to get vaccinated. Vanguard is Cigna’s largest stockholder (7.62%) while BlackRock is its fourth-largest (4.52%).
  • Cisco allows only vaccinated “critical workers” to go to the office, and claims that 90% of its employees are vaccinated. Vanguard and BlackRock are its two biggest stockholders, at 7.54% and 4.87%, respectively.
  • Citigroup required employees be vaccinated before returning to its offices, claiming it has reached 99% compliance. Vanguard and BlackRock are its two biggest stockholders, at 8.00% and 4.75%, respectively.
  • Columbia Sportswear required employees in its corporate headquarters to get vaccinated as of Feb. 1, placing those who didn’t comply on unpaid leave and commencing a termination process against them. Vanguard is its largest stockholder (5.39%) and BlackRock is the fourth largest (4.15%).
    Columbia Sportswear CEO Tim Boyle previously said his company was “thrilled” with the Biden administration’s vaccine mandate.
  • CVS Health has a no jab, no job policy, requiring corporate staff and employees who interact with patients to have been fully vaccinated as of Oct. 31, 2021. Vanguard and BlackRock are its top two stockholders, at 7.79% and 4.41%, respectively.
  • Deloitte, one of the Big Four accounting firms, requires its staff to be vaccinated. It is another exception in that it is a partnership firm and not publicly traded.
  • Delta Air Lines indirectly imposed a vaccine mandate for its employees, charging those who are not vaccinated a $200 monthly health insurance surcharge. CEO Ed Bastian previously said the company is “not opposed” to mandates and claimed 90% of Delta’s employees were vaccinated as of October 2021. Vanguard and BlackRock are the top two stockholders, at 10.15% and 4.63%, respectively.
  • DoorDash permits only fully vaccinated employees to voluntarily return to the office, even as its office return is delayed indefinitely. Vanguard is its third-largest stockholder (3.26%), while BlackRock is the tenth largest (1.57%).
  • Eli Lilly, a pharmaceutical company, requires all employees be vaccinated. Vanguard is its biggest stockholder (6.86%), while BlackRock is the third biggest (4.04%).
  • Emergent BioSolutions, a pharmaceutical company that produced the Johnson & Johnson vaccine and which attained infamy for losing a $600 million federal contract after millions of vaccine doses were ruined, requires employees be vaccinated. The company’s federal contract allowed it to keep a “reasonable quantity” of COVID vaccine doses for its “employees and critical subcontractors, and their respective immediate families.” Vanguard and BlackRock are its two largest stockholders, at 10.07% and 9.81%, respectively.
  • The Equinox Group, which owns SoulCycle and a chain of gyms, required employees to provide one-time proof of vaccination. It is an exception in that it is privately owned.
  • Facebook, now known as Meta, requires employees coming to work at any of its U.S. locations to be vaccinated. Vanguard is its top stockholder at 7.30%, while BlackRock is the third largest, at 4.28%.
  • The Ford Motor Company imposed a vaccine mandate on its U.S. salaried employees. Vanguard and BlackRock are its two biggest stockholders, at 7.18% and 4.53%, respectively.
  • Frontier Airlines required employees be vaccinated or regularly take COVID tests, as of Oct. 1, 2021. Vanguard is its fourth-largest stockholder (1.29%).
  • Gap required employees in its New York, Bay Area and Albuquerque hubs be vaccinated as of Sept. 7, 2021, and conducts weekly $1,000 drawings for vaccinated employees as an incentive. Vanguard is its second-largest stockholder (7.20%), while BlackRock is fifth largest (2.51%).
  • Gilead Sciences Inc., a pharmaceutical company, requires all workers and contractors to be vaccinated. Vanguard and BlackRock are its second-largest and fifth-largest stockholders, at 7.96% and 6.30%, respectively.
  • Goldman Sachs requires anyone entering its offices be fully vaccinated, as of Sept. 7, 2021, while those who are not vaccinated are obliged to work remotely. Booster shots are mandated for employees physically working in its offices, as well as for visitors,  starting on Feb. 1. In January, the bank also required staff to receive twice-weekly COVID tests. Vanguard and BlackRock are its largest and third-largest stockholders, at 7.34% and 4.76%, respectively.
  • Google, also known as Alphabet, Inc., in a policy described as “compassionate,” gave most of its unvaccinated employees in the U.S. a Jan. 18 deadline to get vaccinated or be placed on paid administrative leave for 30 days. After 30 days, those who are still not vaccinated are placed on unpaid leave for up to six months, after which they will be dismissed. In November 2021, some employees at Google circulated a manifesto opposing the company’s widened vaccine mandate. Vanguard and BlackRock are its two biggest stockholders, at 7.21% and 4.32%, respectively.
  • Hasbro implemented a vaccine requirement for its employees. Vanguard is its largest stockholder, at 11.01%, while BlackRock is the fourth-largest, at 4.69%.
  • Hawaiian Airlines required its U.S. workers to be vaccinated as of Nov. 1, 2021. On Feb. 2, a judge denied a bid by seven Hawaiian Airlines employees to block the company’s vaccine mandate. BlackRock and Vanguard are their two biggest stockholders, at 14.41% and 9.71%, respectively.
  • Hershey implemented a vaccine mandate for its salaried employees that went into effect Oct. 4, 2021. Recently, the company announced a “small number” of employees who did not get vaccinated or receive an exemption were “separated from the company.” Frontline employees received four hours’ pay as an incentive to get vaccinated. Vanguard and BlackRock are the company’s two biggest stockholders, at 8.86% and 6.93%, respectively.
  • Hess, a petroleum company, mandated vaccination for its U.S. employees. Vanguard is its second-largest stockholder (9.39%), while BlackRock is fourth largest (4.45%).
  • Humana, a healthcare company, enacted a no-jab, no-job policy for its employees, requiring them to be vaccinated as of Oct. 22, 2021. The company offered employees rewards points as part of an existing employee incentive program to encourage them to get vaccinated. Vanguard is its second-largest stockholder at 7.39%, while BlackRock is the fourth-largest, at 4.32%.
  • IBM, the developer of New York State’s digital vaccine passport, the Excelsior Passallowed only fully vaccinated U.S. employees to physically return to the office, as of Sept. 7, 2021, and mandated employees be fully vaccinated by Dec. 8, 2021, or face an unpaid suspension. In December 2021, some IBM employees circulated an open letter questioning the company’s vaccine mandate. Vanguard and BlackRock are IBM’s biggest and third-biggest stockholders, at 7.94% and 4.87%, respectively.
  • Intel employees were given until Jan. 4 to get vaccinated or apply for an exemption, while employees who would not get vaccinated and who were not granted an exemption were to be placed on unpaid leave in April. This policy was, however, recently “paused.” Vanguard and BlackRock are Intel’s two largest stockholders, at 7.94% and 5.33%, respectively.
  • Jefferies, a financial services company, allows only vaccinated individuals into its physical offices and outside company events, while non-vaccinated employees can continue working remotely. The company recently claimed over 95% of its global workforce has been vaccinated and said boosters would soon be required as part of the company’s “JefVaxPass strategy.” Vanguard and BlackRock are its two biggest stockholders, at 8.84% and 6.46%, respectively.
  • Johnson & Johnson enacted a no-jab, no-job policy, and required all of its employees and contractors to be vaccinated, as of Oct. 4, 2021. Vanguard and BlackRock are its largest and third-largest stockholders, at 8.46% and 4.67%, respectively.
  • KraftHeinz enacted a no-jab, no-job policy for its U.S. employees and implemented a vaccine mandate as of January. Vanguard is its second-largest stockholder (4.21%), while BlackRock is the fourth largest (2.43%).
  • Lyft required corporate employees physically working in or entering its offices, but not its drivers, to furnish proof of vaccination to enter offices, as of Aug. 2, 2021. Vanguard is its biggest stockholder (7.18%), while BlackRock is the fourth biggest (3.47%).
  • McDonald’s required its corporate workforce, but not its restaurant-level workers, to get vaccinated. Vanguard is its largest stockholder (8.33%), while BlackRock is the third largest (4.56%).
  • MGM Resorts International requires salaried employees and all new-hires be fully vaccinated even if working remotely, while unvaccinated hourly employees can provide weekly negative COVID tests. Vanguard and BlackRock are its largest and third-largest stockholders, at 8.76% and 3.96%, respectively.
  • Microsoft required proof of vaccination for all employees, vendors and guests entering its physical locations in the U.S. as of September 2021. Vanguard and BlackRock are its two biggest stockholders, at 7.75% and 4.35%, respectively.
  • Moderna requires all U.S. employees be vaccinated. Vanguard and BlackRock are its second- and third-largest stockholders, at 6.34% and 4.61%, respectively.
  • Morgan Stanley required employees to get vaccinated before returning to its New York offices, and required staff to disclose their vaccination status by July 1, 2021. The policy was extended to contingent workers, clients, and visitors visiting its New York City and Westchester County, New York locations, as of July 12, 2021. As of August 2021, the company claimed 90% of its employees were vaccinated. Vanguard and BlackRock are its second- and third-biggest stockholders, at 6.27% and 3.81%, respectively.
  • NBCUniversal required U.S.-based workers returning to the office be fully vaccinated and provide details about their vaccination status, while a full return to the office has been indefinitely postponed. NBCUniversal is fully owned by Comcast, whose largest and third-largest stockholders are Vanguard (8.26%) and BlackRock (4.12%).
    Comcast, in turn, has required all of its employees to get vaccinated.
  • Netflix implemented a vaccine requirement for its U.S. offices and filming locations. Vanguard is its largest stockholder (7.14%), while BlackRock is the sixth largest (4.03%).
  • The New York Times Company requires proof of vaccination for employees who voluntarily wish to return to the office, and is eyeing a full return to the office in the first quarter of this year. Vanguard and BlackRock are its two biggest stockholders, at 9.25% and 7.32%, respectively.
  • Nike requires office-based employees be vaccinated, and in January made headlines for firing a vaccinated employee who refused to furnish proof of vaccination to a third-party verification service hired by the company. Vanguard and BlackRock are its two biggest stockholders, at 7.88% and 4.62%, respectively.
  • Novartis, a pharmaceutical company, requires U.S. staff to be vaccinated. Vanguard mutual funds are four of the top 10 mutual funds holding stock in Novartis AG.
  • Pfizer required all U.S. workforce and contractors to get vaccinated or participate in weekly COVID testing. Vanguard is its largest stockholder (7.77%), while BlackRock is its third largest (4.63%).
  • Pioneer Natural Resources mandated vaccination for its new-hires and offered a $1,000 incentive to employees who get vaccinated. Vanguard is its largest stockholder (9.53%), while BlackRock is the fifth largest (4.57%).
  • PwC (PriceWaterhouseCoopers) required staff visiting any physical office or client location to be fully vaccinated as of Nov. 1, 2021, and introduced a work-anywhere policy for its U.S. employees, allowing them to work remotely in perpetuity. PwC is an exception in that it is not publicly traded — it is the fourth biggest privately owned company in the U.S.
  • Roblox, a tech company, requires U.S. employees to be vaccinated. Vanguard is its seventh biggest stockholder (1.96%).
  • Roche, a pharmaceutical and medical equipment company, requires U.S. employees be vaccinated. The company is largely family-owned, but Vanguard mutual funds are two of the five largest mutual funds holding shares in Roche Holding AG.
  • Salesforce, a cloud software provider, requires office employees be vaccinated, but allows the majority of its global workforce to choose remote work. Vanguard is its largest stockholder (7.07%); BlackRock is the fourth largest (4.28%).
  • TJX, the parent company of retail chains such as HomeGoods, Marshalls and T.J. Maxx, required U.S. “home and regional office associates” be fully vaccinated as of Nov. 1, 2021, and mandated a booster shot by Feb. 1. Vanguard is its largest stockholder (7.17%), while BlackRock (4.13%) is the third largest.
  • T-Mobile US announced it will fire corporate employees who are not fully vaccinated by April 2. Vanguard and BlackRock are its two biggest stockholders, at 3.28% and 2.38%, respectively.
  • Twitter requires employees be vaccinated and demonstrate proof of vaccination prior to returning to the company’s offices in San Francisco and New York City. In May 2020, the company announced an indefinite work-from-home option for its workforce. Vanguard (8.35%) and BlackRock (4.49%) are its second- and third-largest stockholders, respectively.
  • Tyson Foods mandated vaccination for its employees, and in Nov. 2021, announced 96% of its workforce was vaccinated. Vanguard and BlackRock are its two largest stockholders, at 11.38% and 4.91%, respectively.
  • Uber requires U.S. office staff be vaccinated in order to return to the office, but did not extend this requirement to its drivers. Vanguard (4.07%) is its second-largest stockholder, while BlackRock (2.50%) is the fourth largest.
  • United Airlines implemented a no-jab, no-job policy and required employees be vaccinated five weeks after the U.S. Food and Drug Administration fully approved a COVID vaccine or five weeks after Sept. 20, 2021, whichever came first. In December 2021, a court declined a bid by some United employees to block the company’s vaccine mandate. Vanguard and BlackRock are the airline’s biggest and third-biggest stockholders, at 10.16% and 4.28%, respectively.
  • UPS required office workers in some of its U.S. locations get vaccinated. Vanguard and BlackRock are its two largest stockholders, at 8.39% and 4.60%, respectively.
  • Valero required new hires at its Louisiana and Texas refineries to be vaccinated, as of Oct. 1, 2021. Vanguard is its biggest stockholder (10.98%), while BlackRock (5.58%) is its third biggest.
  • Verizon required non-union employees — representing most of its workforce — provide proof of vaccination as of Dec. 8, 2021. Vanguard and BlackRock are its two largest stockholders, at 7.44% and 4.71%, respectively.
  • ViacomCBS requires all of U.S.-based employees working onsite during the company’s “Yellow Phase” be fully vaccinated, while the company is “still assessing” whether this mandate will be extended into its “Green Phase,” when most staff will physically return to the office. Vanguard (10.29%) is its largest stockholder, while BlackRock (5.03%) is third largest.
  • Walgreens required employees in the company’s U.S. support offices be fully vaccinated by Sept. 30, 2021, or enroll in a COVID testing program. Vanguard is the top stockholder of the Walgreens Boots Alliance (6.61%), while BlackRock is third largest (4.22%).
  • Walmart implemented a no-jab, no-job policy for corporate staff, but not for store or warehouse employees. It has, however, offered a $150 incentive to store and warehouse workers to get vaccinated. The company claimed the “overwhelming majority” of its employees who were mandated to get vaccinated, have done so. Notably, the company enforced a vaccine mandate for shoppers in Canada, generating criticism. Vanguard is its largest stockholder (4.31%), while BlackRock is the third largest (2.30%).
  • The Walt Disney Company required much of its U.S. workforce be vaccinated, though the company was obliged to pause this policy for its Florida employees after state lawmakers barred employers from requiring workers to get vaccinated. Vanguard and BlackRock are Disney’s two biggest stockholders, at 7.15% and 4.24%, respectively.
  • Warner Media, a subsidiary of AT&T, required salaried and non-union U.S. employees to get vaccinated before returning to the office in September 2021, while proof of vaccination is required to enter a WarnerMedia office building.
  • The Washington Post requires all employees, including new employees, to provide proof of vaccination, implementing a no jab, no job policy. The newspaper is owned by Nash Holdings LLC, which is fully owned by Jeff Bezos, founder and executive chairman of Amazon, whose two largest stockholders are Vanguard (6.19%) and BlackRock (3.51%).
What about the two asset management companies, BlackRock and Vanguard?

Of the two, only BlackRock has implemented a vaccine mandate, allowing vaccinated staff to return to the office in July 2021.Vanguard has not implemented a mandate, but offered a $1,000 incentive to its employees to encourage them to get vaccinated. Vaccine passport technology — another way BlackRock, Vanguard profit from vaccines BlackRock and Vanguard also are stakeholders in tech companies involved in the development of digital vaccine passports or “digital wallets” and technology that can track and allocate “personal carbon allowances.”

These companies include:

  • Apple, which is collaborating with several U.S. states to make official documents such as drivers’ licenses and medical records available digitally via Apple Wallet. Vanguard is its top shareholder (7.35%) and BlackRock is its third-biggest (4.12%).
  • Mastercard, which supports the Good Health Pass vaccine passport initiative that is also backed by the ID2020 alliance, and promoted technology that can be embedded into the DO Card, a credit/debit card that can keep track of one’s “personal carbon allowance.” Its top two stockholders are Vanguard (6.82%) and BlackRock (4.13%).

In turn, Mastercard is the fifth largest investor in Doconomy, a Swedish “FinTech” firm that is also heavily involved in the development of the DO Card.

Doconomy, in turn, collaborates with another Swedish “FinTech” firm, Klarna, in providing 90 million customers with “carbon footprint insights” based on their Doconomy transactions. While Klarna is privately held, its top investors include BlackRock and Visa.

  • Oracle is a backer of the SMART Health Card, which is gaining prominence in the U.S. as a de facto national digital vaccine ‘passport’, and also is a provider of cloud services to the U.S. Centers for Disease Control and Prevention. Its top two stockholders are Vanguard and BlackRock, with 5.16% and 2.99%, respectively.
  • Thales Group, is a founding member of the Security Identity Alliance, which is a stakeholder in the UN’s Legal Identity Agenda Task Force that has set the establishment of digital identification for all by 2030. Thales Group has also developed a “smart health card” and digital ID wallet technology.

While the government of France, which has imposed among the strictest COVID-19 restrictions in Europe and has used ‘vaccine passports’ to shut the unvaccinated out of many public spaces and activities, is Thales’ top shareholder (25.7%), Vanguard is the sixth largest, at 1.31%.

No moral core . . . no moral purpose

In podcaster Joe Rogan’s interview last month with Dr. Robert Malone — the interview that triggered the exodus of musicians and others from Spotify — Malone described companies like BlackRock and Vanguard as “large massive funds that are completely decoupled from nation states” and that “have no moral core … no moral purpose,” their only purpose being a “return on investment.”

As it turns out, BlackRock and Vanguard — and Moderna — also have ties to Spotify.

BlackRock is Spotify’s seventh-largest shareholder (1.37%), while Vanguard manages the top mutual fund holding Spotify Technology SA.

Baillie Gifford, a Scotland-based asset management firm in existence since 1909, is the top institutional stockholder (11.60%) in Spotify — and the top stockholder of Moderna (11.29%), the company that carries the largest overall weight in the firm’s portfolio, at $12 billion in holdings.

Other major Baillie Gifford holdings — including some companies listed above among those mandating COVID vaccines — include Tesla (second highest at 6.3% of its portfolio’s value), Amazon (fourth highest at 3.8%), Spotify (seventh highest at 2.8%), Netflix (ninth highest at 2.6%), Meta (12th, 1.4%), Microsoft (16th, 1.3%), Anthem (21st, 1.2%), Alphabet Inc. (22nd, 1.1%), BioNTech (29th, 0.9%), Mastercard (39th, 0.6%), DoorDash (45th, 0.6%), Salesforce (53rd, 0.5%), and Lyft (93rd, 0.2%).

Baillie Gifford, through its Scottish Mortgage Investment Trust, also maintains a significant stake in Palantir (0.2% of the firm’s net asset value, or NAV).

As reported by The Defender, Palantir developed the Tiberius vaccine allocation planning system operated by the U.S. Department of Health and Human Services.

Peter Thiel, co-founder of PayPal (which terminated the contracts of nonprofits opposed to vaccine mandates) and a Facebook board member, also is a co-founder of Palantir and serves on its board of directors.

Palantir’s top two stockholders are Vanguard (6.08%) and BlackRock (3.31%).

In turn, the top stockholders of BioNTech, Pfizer’s partner in the development of its COVID vaccine, include Baillie Gifford (biggest stockholder, 2.69%) and BlackRock (seventh highest, 0.59%), while Vanguard manages the top mutual fund with holdings in BioNTech (0.92%), and Baillie Gifford the ninth biggest (0.23%).

Tangled web of corporate connections raises host of questions

BlackRock and Vanguard are poised to continue expanding— as far back as 2017, Bloomberg predicted that by 2028, these two companies would be managing $20 trillion worth of investments.

The size and scope of the firms’ investments raise questions about how much influence BlackRock and Vanguard can wield over the formulation of corporate policies by the companies in which the two firms are heavily invested.

This ever-growing influence has led some analysts to describe the two firms as “kingmakers,” arguing their growing voting share in an increasing number of corporations would “hand them a de-facto veto on all major corporate decisions by 2040.

To what extent do companies mandating COVID vaccines have the best interest of their employees in mind? Or are these companies implementing policies under the guise of “protecting” employees, when in fact they are more concerned about appeasing major investors?

What else might these companies do, if “encouraged” in some way by major stockholders?

Moreover, do mandatory (or strongly encouraged) vaccination policies reflect the worldview of funds such as BlackRock and Vanguard, and their managers — in much the same way major corporations have embraced purportedly “green” policies which only barely cloak potentially totalitarian restrictions on civil liberties, such as “personal carbon allowances” and digital “vaccine passports”?

The answers may lie, in part, in the words of BlackRock CEO and chairman, Larry Fink.

In his 2022 annual letter to CEOs, Fink wrote that “employees are increasingly looking to their employer as the most trusted, competent and ethical source of information — more so than government, the media and NGOs.”

Fink said, “workers demanding more from their employers is an essential feature of effective capitalism” — an interesting viewpoint given that the BlackRock and Vanguard strategy to control as many corporations as possible, including competing ones, would seem to contradict the principles of capitalism, competition, and a free market.

Fink also warned that “companies not adjusting to this new reality and responding to their workers do so at their own peril.”

In other words, employees and workers of companies that have imposed vaccine mandates should take comfort in such policies, as their employer appears to know what’s best for them — at least according to Fink.

 


 

Michael Nevradakis, Ph.D., is an independent journalist and researcher based in Athens, Greece.

The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children’s Health Defense.

©February 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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New Diagnostic Manual With ADHD Listed Could Turn Childhood Into a Mental Disorder

New Diagnostic Manual With ADHD Listed Could Turn Childhood Into a Mental Disorder

 

Despite a 28% decrease in 0- to 5-year-old U.S. children taking psychostimulants since 2017, new changes to an international mental disorders manual could revert this and put them at risk. Watchdog relaunches PSAs for parents warning “Childhood is not a mental disorder.”

 

by CCHR International, The Mental Health Industry Watchdog
February 14, 2022

 

CCHR International warns there could be an increase in the number of children and adolescents prescribed powerful, addictive stimulants for Attention Deficit Hyperactivity Disorder (ADHD) with the new insurance billing codes released this month in the 11th edition of the International Classification of Diseases (ICD), Mental Disorders Section. For years, CCHR International, based in Los Angeles, has conducted a “Fight for Kids” public awareness campaign about the risks of childhood and teen behavior being mis-diagnosed as disorders and “medicated.”

However, changes to ICD-11 reinforce this and as such, it relaunched two Public Service Announcements (PSAs) reminding parents that “Childhood is not a Mental Disorder.”

CCHR welcomes a 28% decrease in U.S. children aged 0-5 years old being prescribed psychostimulants between 2017 and 2020. According to the IQVia Total Patient Tracker database that CCHR obtained for 2017 and 2020, there were 80,235 children in this age group in 2017 prescribed stimulants compared to 58,091 in 2020. Overall, for the 0-17 age group, there was a 14% decrease in the numbers taking psychostimulants.

The U.S. Diagnostic & Statistical Manual of Mental Disorders (DSM-5, being updated in March 2022) and ICD-11 have redefined and categorized ADHD as a “neurodevelopmental disorder,” making it appear to be a neurological or brain-based physical disease when scientific evidence does not substantiate this.

Dr. Fred Baughman, Jr., a retired pediatric neurologist and author of The ADHD Fraud: How Psychiatry Makes “Patients” of Normal Children, said that psychiatric associations representing ADHD as a biologic abnormality of the brain is “neurobiological propaganda” because “psychiatry has never validated ADHD as a biologic entity.”[1]

Prof. Allen Frances, the former Chairman of the DSM-IV Task Force said that the DSM-IV, published in 1994, already created “false epidemics” of ADHD.[2] He wrote that twenty years later, “The rate of ADHD in the U.S. has tripled to a ridiculously inflated 11%. Sales of ADHD medications are approaching an obscenely profitable $10 billion a year.” Frances was forthright about how diagnoses such as ADHD are determined: “There are no objective tests in psychiatry—no X-ray, laboratory or exam finding that says definitively that someone does or does not have a mental disorder….”[3] Inclusion of a disorder in the DSM is by consensus vote.

As such, the fact that ICD-11 and DSM-5 claim ADHD is neurobiological is misleading for parents who could erroneously believe that their child has a faulty brain requiring “medication” rather than an issue which can be handled with behavioral, dietary and educational solutions. Dr. Baughman adds that children have also been led to “believe they have something wrong with their brains that makes it impossible for them to control themselves without a pill.”[4] In saying that, he is not saying that children do not sometimes have trouble with their behavior, focusing, or their emotions; it just simply isn’t neurobiological.



CCHR produced several PSAs to help parents to see that childhood is not a mental disorder, and for children—represented by a young skateboarder—to show that their rambunctious zest for life or creative efforts do not make them dysfunctional or “ill.”



March 21 this year marks the 22nd anniversary of 14-year-old Matthew Smith’s death from a cardiac arrest while skateboarding. Oakland County (Michigan) Medical Examiner Ljubisa Dragovic determined that the skateboarding did not kill Matthew but rather the damage done to his heart from 10 years of taking prescribed methylphenidate, an ADHD psychostimulant that caused a “chronic change of the heart muscle and the small blood vessels in the heart.”[5] Michael’s tragic death was part of the impetus that started CCHR’s Fight for Kids campaign and PSAs.

In 2014, researchers from the University of Delaware and Drexel University College of Medicine reviewed research on the effects of psychostimulants like methylphenidate. They found the drug can impact the brain’s plasticity, interfering with a person’s ability to plan, switch between tasks, and be overall flexible in their behaviors. For a drug that’s supposed to offer better mental performance, they found that the long-term effects appear to do the opposite.[6]

“All proposed ADD and ADHD treatments” are “aimed at modifying observable behaviors rather than in treating their underlying causes,” say other researchers, including Dr. Howard Glasser, writing in Ethical Human Psychology and Psychiatry.[7]

In his last interview before his death in 2009, Dr. Leon Eisenberg, the “scientific father of ADHD” and a leader in child psychiatry for more than 40 years, admitted “ADHD is a prime example of a fictitious disease.”[8] The symptoms are so common that anyone could believe they have ADHD: fails to give close attention to details or may make careless mistakes; work is often messy or disorganized; has problems staying focused on tasks or activities; fails to complete schoolwork, chores or other duties; often fidgets with hands or feet or squirms in seat; often talks excessively and interrupts or intrudes on others (e.g., cuts into conversations).

The consequences of the drugs prescribed to quell such symptoms are telling: The U.S. Drug Enforcement Administration reports methylphenidate can lead to addiction and “psychotic episodes, violent behavior and bizarre mannerisms have been reported” with its use.[9] The manufacturer admits it is a drug of dependency.[10] Suicide is a major complication of withdrawal from it and similar amphetamine-like drugs.[11] FDA also warns of the risks of heart-related problems.

CCHR says the direction ICD-11 and DSM-5 have taken is not in sync with current thinking. Former United Nations Special Rapporteur Dainius Pūras, M.D., in a June 2021 interview with Psychiatric Times, said there is too much reliance upon “the biomedical model and biomedical interventions” for people with mental health or behavioral issues and this represents a “biased use of knowledge and evidence.” In 2017, he also called for a revolution in mental health care around the world, writing: “There is now unequivocal evidence of the failures of a system that relies too heavily on the biomedical model of mental health services, including the front-line and excessive use of psychotropic medicines, and yet these models persist.”[12]

CCHR brought their concerns about the worldwide mass diagnosing of ADHD and prescribing of stimulants to the attention of the UN Committee on the Rights of the Child, which responded with hearings and a recommendation for the establishment of a system for “monitoring of the excessive use of psychostimulants to children.” It also said that governments should “take the necessary measures to prevent any pressure on children and parents to accept treatment with psychostimulant drugs.”[13]

ICD-11 says it changed the category under which ADHD has been placed from “hyperkinetic” to “neurodevelopmental disorders” so that it is not equated as being “disruptive behavior,” but conveys the idea that a child has a deficiently developed brain disease, which experts say it is not. [14]

Child and adolescent video-gamers will also be a potential market under ICD-11 with “gaming disorder.”[15] This has been included in a newly added diagnostic grouping under ICD-11 called “disorders due to addictive behaviors,” again not in response to any scientific evidence but “to global concerns about the impact of problematic gaming, especially the online form.”

As for nebulous “conduct disorders,” such as oppositional defiant disorder and conduct‐dissocial disorder, these are grouped into a new label, “disruptive behavior and dissocial disorder.” ICD11 also expanded these from being limiting to children to include across the lifespan.[16] Disorders are no longer grouped by age but reflect a continuous lifespan approach[17]—anyone can be labeled and stigmatized.

Moreover, ICD10’s so-called gender identity disorders have been renamed as “gender incongruence” (the condition of not matching or being in agreement) in the ICD11 and moved from the mental disorders chapter to the new “sexual health chapter,” meaning that a transgender identity is no longer to be considered a mental disorder.[18] Under DSM, gender identity was called gender dysphoria (unwanted emotional state).[19]

Such arbitrary and capricious diagnosing has come under earlier criticism when in 1973, the American Psychiatric Association committee members voted—5,584 to 3,810—to delete homosexuality as a mental disorder from DSM after gay activists picketed the APA conferences.[20] As The Atlantic reported, “It’s not always that explicit, and the votes are not public. In the case of the DSM-5, committee members were forbidden to talk about it, so we’ll never really know what the deliberations were. They all signed non-disclosure agreements.”[21]

Lawrence Stevens, a former Assistant District Attorney in California, commented: “If mental illness were really an illness in the same sense that physical illnesses are illnesses, the idea of deleting homosexuality or anything else from the categories of illness by having a vote would be as absurd as a group of physicians voting to delete cancer or measles from the concept of disease.”[22]

The late Dr. Keith Conners, who “put ADHD on the medical map,” conducted the first formal trials on the use of methylphenidate. But in 2013, when he was asked to address the American Professional Society of ADHD and Related Disorders, he was so appalled at how many children had been saddled with ADHD, he called it “a national disaster of dangerous proportions.”[23]

The ICD-11 and DSM-5 update can only exacerbate the disaster. Parents, pediatricians, family doctors, and educators should be informed that ADHD is not a proven neurobiological disorder. The behavioral symptoms could be representative of any normal childhood behavior. In an article that has been widely quoted in literature, James T. Webb, Ph.D., reviewed the symptoms of ADHD and noted “almost all of these behaviors are found in bright, talented, creative, gifted children.”[24] Dr. Mary Ann Block, author of No More ADHD advises to look for and treat the underlying causes; don’t just cover symptoms with drugs but “find the cause and fix the problem.”[25]

All of which adds up to: Childhood, including ADHD, is not a mental disorder.

 

References:

[1] Samantha Gluck, “Does ADHD Exist?” Healthy Place, interview with Dr. Fed Baughman, https://aws.healthyplace.com/adhd/articles/does-adhd-exist

[2] “Watchdog Group Alerts Parents and Teachers About Gifted Children Being Mislabeled ‘ADHD’ and Given Stimulant Drugs,” CCHR International, 9 Aug. 2017, https://www.cchrint.org/2017/08/09/watchdog-group-alerts-parents-and-teachers-about-gifted-children-being-mislabeled-adhd-and-given-stimulant-drugs/, citing: Allen Frances, “DSM 5 Will Further Inflate The ADD Bubble,” Psychology Today, 2 Aug. 2011, https://www.psychologytoday.com/us/blog/dsm5-in-distress/201108/dsm-5-will-further-inflate-the-add-bubble

[3]  Allen Frances, “Most Active Kids Don’t Have ADHD,” Psychology Today, 11 Mar. 2014, https://www.psychologytoday.com/us/blog/saving-normal/201403/most-active-kids-don-t-have-adhd; Allen Frances, “Psychiatric Fads and Overdiagnosis,” Psychology Today, 2 June 2010, https://www.psychologytoday.com/us/blog/dsm5-in-distress/201006/psychiatric-fads-and-overdiagnosis

[4] Fred A. Baughman, Jr., MD, “Treatment of Attention-Deficit Hyperactivity Disorder,” Journal of the American Medical Association, Vol. 269, No. 18, 12 May 1993,  p. 2369

[5] Caroline Kern, “Death of 14-year-old Caused by Ritalin,” 14 Apr. 2000, http://www.drugfreechild.org/article/Death_of_14-year-old_Caused_by_Ritalin.html

[6] “Bad News For Ivy Leaguers: ADHD Drugs Hurt Your Memory,” TIME Health, 13 May 2014, http://time.com/97448/bad-news-for-ivy-leaguers-adhd-drugs-hurt-your-memory/

[7] Dr. Howard Glasser, et al., “The Online Nurtured Heart Approach to Parenting: A Randomized Study to Improve ADHD Behaviors in Children Ages 6–8,” Ethical Human Psychology and Psychiatry, Vol. 22, 1 Nov. 2020

[8] “New Federal Statistics Show Teen Overdose Deaths From ADHD & Anti-Anxiety Drugs On The Rise,” CCHR International, 22 Aug. 2017, https://www.cchrint.org/2017/08/23/teen-overdose-deaths-from-adhd-anti-anxiety-drugs-on-the-rise/, citing: “Father of ADHD calls himself a liar,” WND, 23 May, 2013 http://www.wnd.com/2013/05/father-of-adhd-calls-himself-a-liar/#SAe7LssguLIzLtry.99

[9] “Methylphenidate (A Background Paper),” U.S. Drug Enforcement Administration, Oct. 1995, p. 16

[10] https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/010187s077lbl.pdf

[11] DSM-III-R, (American Psychiatric Association, Washington, D.C., 1987), p. 136

[12] “UN Special Rapporteur Dainius Pūras Addresses Psychiatry’s Global Coercion & Crisis,” CCHR International, 7 June 2021, https://www.cchrint.org/2021/06/07/un-special-rapporteur-dainius-puras-addresses-psychiatrys-global-coercion-crisis/, citing: Awais Aftab, MD, “Global Psychiatry’s Crisis of Values: Dainius Pūras, MD,” Psychiatric Times, 3 June 2021, https://www.psychiatrictimes.com/view/global-psychiatry-crisis-values; “World needs ‘revolution’ in mental health care – UN rights expert,” United Nations Human Rights, Office of the High Commissioner, 6 June 2017, https://ohchr.org/EN/NewsEvents/Pages/DisplayNews.aspx?NewsID=21689

[13] UNCRC report to Sweden, 2015

[14] Michael B. First, Steven H. Hyman, Wolfgang Gaebel, “Innovations and changes in the ICD‐11 classification of mental, behavioural and neurodevelopmental disorders,” et al., World Psychiatry, 2 Jan. 2019, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6313247/

[15] Tolu Ajiboye, “3 Major Changes to Look for with ICD-11,” Pollen, 9 Oct. 2019, https://www.simplepractice.com/blog/3-major-changes-to-look-for-with-icd-11/

[16] Op. cit., World Psychiatry, 2 Jan. 2019

[17] “ICD 11 Takes Centre Stage,” Journal of Psychiatry Reform, 21 June 2019, https://journalofpsychiatryreform.com/2019/06/21/icd-11-takes-centre-stage/

[18] Op. cit., World Psychiatry, 2 Jan. 2019

[19] https://www.mayoclinic.org/diseases-conditions/gender-dysphoria/symptoms-causes/syc-20475255

[20] Lawrence Stevens, J.D., “Does Mental Illness Exist?” undated article, https://eqi.org/antipsy2.htm

[21] Hope Reese, “The Real Problems with Psychiatry,” The Atlantic, 2 May 2013, https://www.theatlantic.com/health/archive/2013/05/the-real-problems-with-psychiatry/275371/

[22] Op. cit., Lawrence Stevens

[23] “New Federal Statistics Show Teen Overdose Deaths From ADHD & Anti-Anxiety Drugs On The Rise,” CCHR International, 22 Aug. 2017, https://www.cchrint.org/2017/08/23/teen-overdose-deaths-from-adhd-anti-anxiety-drugs-on-the-rise/, citing: Gareth Cook, “Big Pharma’s Manufactured Epidemic: The Misdiagnosis of ADHD,” Scientific American, 11 Oct. 2016, https://www.scientificamerican.com/article/big-pharma-s-manufactured-epidemic-the-misdiagnosis-of-adhd; “ADHD: the statistics of a ‘national disaster’” Significance, Dec. 2016 https://rss.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1740-9713.2016.00979.x

[24] James T. Webb, Misdiagnosis And Dual Diagnoses Of Gifted Children And Adults: Adhd, Bipolar, Ocd, Asperger’s, Depression, And Other Disorders, (Great Potential Press Inc., Scottsdale, AZ, 2004), p. 195

[25] https://blockcenter.com/

 

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Informed Consent Action Network (ICAN) Obtains Email Showing Alliance Between White House, Facebook, and Pharma

Informed Consent Action Network (ICAN) Obtains Email Showing Alliance Between White House, Facebook, and Pharma

 

ICAN Legal Update

February 14, 2022

 

A White House email, obtained on behalf of ICAN, shows Facebook, Merck, and the CDC Foundation, whose corporate partners includes Pfizer, have formed an alliance “to use social media and digital platforms to build confidence in and drive uptake of vaccines.” No conflict there.

On August 12, 2021, ICAN, through its attorneys, submitted a Freedom of Information Act request for communications between White House staff and Facebook, Google, and YouTube.  In response to this request, ICAN received a June 15, 2021 email sent by Facebook’s then-Public Policy Manager, Nkechi “Payton” Iheme, to several White House employees.

In it, Iheme announces a new initiative, the “Alliance for Advancing Health Care,” between Facebook and several major companies and organizations, including Merck, the Vaccine Confidence Project, the Sabin Vaccine Institute, and the CDC Foundation.  Significantly, one of the CDC Foundation’s corporate partners is Pfizer.  In the email, Iheme explains that the Alliance is “focused on advancing public understanding of how social media and behavioral sciences can be leveraged to improve the health of communities around the world” and states that its first project is to “provide grants to researchers and organizations for projects that explore how to use social media and digital platforms to build confidence in and drive uptake of vaccines.”  Facebook announced this new initiative on June 9, 2021 here.

The conflict of interest is astonishing.  This email shows without a doubt that, through the CDC Foundation created “to support the [CDC’s] work,” the federal government, which is in charge of ensuring the safety of vaccines, has teamed up with Big Pharma and Big Tech to push a liability-free product on the world, while attempting to stomp out anyone who questions this arrangement.

Just as the pharmaceutical companies will never rest when it comes to promoting and selling their vaccine products, and the federal government will not rest in its efforts to assist them, we will never rest in exposing the truth regarding these products or in demanding full transparency and full informed consent for any and all vaccines.

 

Connect with ICAN (Informed Consent Action Network)

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Dr. Tom Cowan & Dr. Lee Merritt: Debunking Virus & mRNA Theory

Dr. Tom Cowan & Dr. Lee Merritt: Debunking Virus & mRNA Theory

 

Truth Comes to Light editor’s note: In the following video, Spacebusters uses images to artistically highlight & add clarity to an essential part of a conversation (Merritt Medical Hour — February 2, 2022) between Dr. Lee Merritt & Dr. Tom Cowan. See the entire interview at Merritt Medical Hour on BrighteonTV

 

by Dr. Lee Merritt with Dr. Tom Cowan
edited by Spacebusters
February 10, 2022



Spacebusters video available at Odysee and BitChute.

 

Connect with Dr. Tom Cowan

Connect with Dr. Lee Merritt

Connect with Spacebusters


 

Related document by Harold Hillman:

A Serious Indictment of Modern Cell Biology and Neurobiology by Harold Hillman (download PDF)

 

Related articles:

Dr. Stefan Lanka & Dr. Tom Cowan: How We Got Into This Mess — The History of Virology & Deep Medical Deceptions

Dare to Ask: Dr. Tom Cowan, Dr. Stefan Lanka & Dr. Andrew Kaufman on Freedom, Fear, and False Science About Viruses and the Nature of Reality Itself

Dr. Stefan Lanka 2020 Article Busts the Virus Misconception

Dr. Tom Cowan on the “Spiked Protein Toxin” & “Virus Created in a Lab” Stories

The Contagion Fairy Tale




Fact-Check: New Zealand Can’t Find the “SARS-CoV-2 Virus”

Fact-Check: New Zealand Can’t Find the “SARS-CoV-2 Virus”

 

by Dr. Mark Bailey
February 12, 2022

 

To those of us that know that virology’s “isolation” and genomic sequencing methodologies are anti-scientific, it is still interesting to see the proponents of the nonsense offer official explanations about what they are up to.

Here in New Zealand, the Institute of Environmental Science and Research (ESR) is responsible for some of the alleged isolation experiments and genomic sequencing of the imaginary “SARS-CoV-2” particle, that they claim is responsible for the clinically undefined illness “COVID-19”.  On the 9th of February 2022, they responded to questions surrounding the methodology of their cell culture and genomic sequencing experiments in relation to an Official Information Act request (which is analogous to a Freedom of Information request).

ESR couldn’t seem to find the “virus” but they featured this pretty picture.

So let’s have a look at the ESR’s “scientific” method with regards to their official records of a “SARS-CoV-2 virus”…

“Viral Culture/Experiment details –

Once the cells are 90 – 100% confluent, they are inoculated with 500 uL of diluted clinical sample (sample is diluted 1:10 in Infection media),10 mL of Infection Media is added to the flask.  Infection media is made up of DMEM with 1% pen/strep/gentamycin, 1% Nystatin, 1% Glutamax, 1.5% Hepes plus 4ug/mL TPCK added.”

~ Jill Vintiner, Joint General Manager Health and Environment Group, ESR, 9 Feb 2022.

The “clinical sample” will be something like a crude nasopharyngeal sample taken from a patient.  These specimens contain human tissue (from the host and other individuals in close contact with them), various bacterial and fungal elements, and whatever other material was in the patient’s mucosa.  Amongst all this biological soup is the alleged SARS-CoV-2 virus, which of course, has never been directly found in any person.  Apparently there can be 200 million copies of the virus in a sneeze but strangely they can’t find any in an “infected” individual.

Instead they resort to tissue culture experiments, as the ESR continues to explain…  

“The flasks are then placed into an incubator and monitored for cytopathic effect (CPE) A SARS-CoV-2 N gene PCR is performed on the diluted 1:10 clinical sample and on the supernatant of the flask after 1 week of incubation (or sooner if 100% CPE is evident). CT values for both specimens are used as well as the CPE observed in the flask to determine if viral culture has been successful.”

~ Jill Vintiner, Joint General Manager Health and Environment Group, ESR, 9 Feb 2022.

Cytopathic effects are non-specific and are simply the observation that cells being stressed in a test tube eventually break down and die, with some cells producing vesicles.  However, in the world of virology it is seen as evidence that a virus is at work and is somehow destroying the cells from within.  “SARS-CoV-2 N gene” is a misnomer because there has never been a demonstration of a viral particle that contains this genetic sequence.  Even more problematic is that there’s never been a demonstration of any viral particle.  However, here we see them claiming “successful” viral culture if they detect a single short genetic sequence by PCR amplification.  Note to virologists: detecting genetic sequences of unproven provenance does not equal virus.

Then we get to another interesting part…

“Viral culture/experiment details of the negative control – 

The method above is also used for the negative control and the flask undergoes the same conditions as the flasks used for viral culture, however we use Infection media only.

~ Jill Vintiner, Joint General Manager Health and Environment Group, ESR, 9 Feb 2022.

How on earth is this a comparable control experiment? – they added no control sample to their culture brew.  In their first experiment they added a veritable biological soup containing human tissue along with various microorganisms and other organic fragments (everything present in a respiratory tract sample), and their alleged virus of course.  Examples of valid control experiments would be:

  1. The same type of sample taken from a well person.
  2. The same type of sample taken from a person with a comparable clinical condition but said not to have “COVID-19” (without biased pre-selection in the form of a PCR result.)

Ironically, both of the above become meaningless in the case of “COVID-19” as it has no specific symptoms, signs, or investigations outside of the PCR result – a PCR result that has never been validated to a clinical condition.  In fact, a priori the PCR could never be validated in this application as it is simply a tool to amplify selected genetic fragments, not determine their origin or the significance of their presence in mixed biological samples.  So, in the case of (1) above, many well people are said to have “COVID-19” and in the case of (2), there is no way to distinguish a novel clinical condition.  Dr Sam Bailey explained these problems back in 2020 in “What is a COVID-19 Case?” – a video banned by Big Tech after several hundred thousand views but still available here.



The wheels really fall off the ESR’s response when they are asked to explain how they purify the alleged virus sample for genomic sequencing and compare this to a control:

“’Whole Genome’ Sequencing – Purity and Control Details: 

[• The degree of purity of the “virus” sample used in the sequencing experiment.]
The protocols used for amplification of the SARS-CoV-2 virus consists of primers that specifically and selectively amplify the viral material, any remaining host or bacterial material is filtered out programmatically prior to data analysis.”

~ Jill Vintiner, Joint General Manager Health and Environment Group, ESR, 9 Feb 2022.

Either they don’t understand the question or are being disingenuous here.  Their response doesn’t provide any evidence that they have a virus, let alone have attempted to purify it, in the analysis of its purported genome.  They are simply using a process that amplifies sequences they have artificially selected but as it is a mixed sample they cannot demonstrate the origin of them.  There is no way to claim this is “viral material” because no one has ever demonstrated that these sequences come from inside a virus, let alone belong to “SARS-CoV-2”.  They are simply building on the nonsense that has spun out of control on GISAID.org where not one of the millions of deposited “genomes” has been shown to come from inside a viral particle.  It’s turtles all the way down with these contrived “genomes”.

And with regards to the ESR’s “controls”?…

[• All details of the control group that was used when comparing the results of sequencing: 

o the total nucleic acid extracted from the “viral lysate” (from the experimental group), versus 

o the total nucleic acid extracted from the non-viral lysate (from the control group).] 

The protocols used to extract RNA from clinical samples do not yield a uniform quantity as this depends on the viral load within a sample. Details about the ranges obtained and used for further analysis are published in detail in several scientific peer-reviewed publications and can also be found on the publicly accessible protocols.io website, link provided below as requested.” 

~ Jill Vintiner, Joint General Manager Health and Environment Group, ESR, 9 Feb 2022.

They appear to have dodged the question and the protocols provide no evidence of valid control experiments.  The ESR have been asked to clarify this but we can already see they are not adhering to the scientific method.   I also looked at the four publications that they suggested but these simply confirmed the problem: there is no evidence of any virus and the world is being duped in this war on humanity.

In fact, by definition, there has never been a demonstration of any disease-causing virus ever, full stop.  Even if the ESR performed valid genomic control experiments there would still need to be further experiments to demonstrate the existence of a replication competent, obligate intracellular parasite that causes disease in a host.  In other words, the actual existence of a virus.  It makes me wonder whether the virologists are going to change the very definition of a virus soon in order to keep the whole façade afloat.  However, once people realise that virology has never fulfilled its own postulates, they can take a major step away from this health misconception and ignore any of the related damaging measures and “treatments” coming from the medical-pharmaceutical complex.

 

Connect with Dr. Mark Bailey & Dr. Sam Bailey

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Cocktails & Criminal Manslaughter

Cocktails & Criminal Manslaughter

by Rosanne Lindsay, Naturopath, Nature of Healing
February 11, 2022

 

In an October, 2021 Forbes article, AstraZeneca marketed an experimental “injectable antibody therapy cocktail” to a fearful public. Without valid research, or proof, it claimed its cocktail to be effective at preventing severe illness or death in people with mild or moderate Covid-19 infections. It claimed its therapy cut the risk of death or severe illness by two-thirds (67%) if given within five days of showing symptoms.

The cocktail was marked as experimental for a reason.

AstraZeneca, with its impressive corporate rap sheet, could make any claim it chose, since, by law, no pharmaceutical company is held accountable for side effects (or direct effects) from any “vaccine.”

Sound like fraud?

The Experiment Unravels

Neither AstraZeneca, nor any vaccine maker, has ever revealed the ingredients of its experimental antibody or mRNA cocktail to the public. Neither have they provided informed consent as part of the offer.

Everything is an offer to contract, whether it be a personal, medical, or a business relationship. Every vaccinated subject must sign that they take full responsibility. Because no one else will.

According to the AMA, Informed Consent is required in all medical contracts in order to provide the nature, purpose, burdens, and risks of the proposed medical intervention so the patient can formally consent. The informed consent process falls under 45 CFR 46, for human subjects in research, which sounds a lot like conducting human experimentation. Americans were warned by the Secretary of State in March of 2020 that COVID is a live exercise.

In the beginning, COVID injectables were deployed as Emergency Use Authorized, or EUA, meaning, Off-label, Experimental Research, Unapproved, and without Informed Consent. In other words, use at your own discretion. Until recently, if you wanted to know what was inside the injectable mRNA cocktails, you were handed a blank piece of paper. However, what was hidden is now being revealed.

Under the UK Corporate Manslaughter and Corporate Homicide Act of 2007, charges were recently filed against corporate entities for “Corporate Manslaughter and Gross Criminal Manslaughter.” These corporate defendants are the usual miscreants :

Corporate Defendants Identified:
  • AstraZeneca
  • Pfizer
  • Moderna
  • National Health Service (NHS)
  • Medicines & Healthcare products Regulatory Agency (MHRA)
  • Joint Committee on Vaccination and Immunisation (JCVI)
  • Her Majesty’s Government

According to the United Kingdom (UK) Case Briefing Document:

In November 2020 Dr Andreas Noack, a German chemist and one of the EU’s top graphene experts, released a video explaining that he had discovered graphene hydroxide contained in the COVID-19 experimental treatments. He described how the graphene hydroxide nano structures injected into the human body act as ‘razor blades’ inside the veins of recipients and how they would not show up on an autopsy or normal toxicology tests given their atomic size. On 26th November 2021, just hours after publishing his latest video about graphene hydroxide, he died in suspicious circumstances.

Professor Dr Pablo Campra, University of Almeria, Spain also examined Covid-19 experimental treatments in November 2021 using Micro-Raman Spectroscopy, the study of frequencies. He too confirmed the presence of graphene.

The charges center around the nano-ingredient, graphene hydroxide (GHO), discovered in EUA COVID injections. Considered to be a trade secret, GHO is not found on any label. Therefore, no one would be the wiser, except that GHO can be identified for its polymeric signature properties using Micro-Raman Spectroscopy. Other methods used to verify the serums morphologies and contents include: Optical Microscope, Dark-Field Microscope, UV absorbance and fluorescence spectroscope, Scanning Electron Microscopes, Transmission Electron Microscope, Energy Dispersive Spectroscope, X-ray Diffractometer, and Nuclear Magnetic Resonance instruments.

Damage Report

Trade secrets aside, Graphene hydroxide is well known in the world of science. A Pubmed database search generates over 18,000 published studies on ‘Graphene oxide’. Whether called graphene oxide (GO), or graphene hydroxide, (GOH), it is nanotechnology invisible to the human eye. Graphene has optical, thermal, mechanical, and electrical properties, with applications in silicon-based semi-conductor devices. Once inside the human body, graphene acquires magnetic properties and becomes a superconductor. The human superconductor.

In the body, Graphene hydroxide can generate the same symptoms as the supposed “SARS-CoV-2”, which includes blood clots, post inflammatory syndrome, cytokine storm, collapse of the immune system, inflammation of the mucus membranes, bilateral pneumonias, loss of smell and taste (anosmia) (see November 2021 Journal Circulation Abstract). Graphene’s applications in electrical conductivity also involve modulation of the neural network and the hypothalamus, for mind control. However, the majority of studies are focused in biomedical gene and drug delivery systems (See in Polymer Journal).

From the 2016 Journal of Particle and Fibre Technology:

Graphene is isolated from crystalline graphite. It is a flat monolayer composed of single-atom-thick, two-dimensional sheets of a hexagonally arranged honeycomb lattice. A summary of the findings detailed in the attached toxicology report reveals that Graphene nanomaterials (GFNs) can penetrate the body’s natural barriers and damage the central nervous system.

Summary of Graphene hydroxide (GOH) in biological systems:

  1. damages internal organs
  2. damages the reproduction and development system
  3. destroys blood health
  4. damages and destroys cells (harms sense of smell)
  5. triggers cancer and accelerates aging
  6. damages mitochondria and DNA
  7. triggers an inflammatory response and three different kinds of cell death
  8. causes changes in gene function
  9. triggers optical modulation of hypothalamus, neural activity, i.e. mind control.
Cocktail Contents

According to a Laboratory Report Summarya summary of the findings from RAMAN Spectroscopy discovered the following particles in the EUA treatments:

● Graphene
● SP3 Carbon
● Iron Oxide
● Carbon derivatives
● Glass shards

Epigenetic Toxicity

Epigenetic toxicity comes from toxic environmental exposures which exert undesirable genetic effects on living organisms. Epigenetic toxins are found in water, air, food, and medical drugs, including nanotech. The current focus of graphene nanotech utilizes its electromagnetic properties as a carrier and adjuvant in vaccines. For instance, UV Fluorescence test results from the Pfizer BioNanoTech vaccine, show nanomaterial present in the vial that corresponds perfectly to that of graphene oxide (340 nm).

Graphene was first detected in the aqueous suspension, COMIRNATY™, in a June 2021 report by a Spanish team titled “Graphene Oxide Detection in Aqueous Suspension, Observational study in Optical and Electron Microscopy,” followed by a report from Dr. Andreas Noack from Germany. In some cases, GO is grafted onto glass fibers (GFs) to improve its polymer properties of strength and toughness. What about its toxic properties?

The question you should ask Pfizer, is why are those razor blades in the vaccine?  – Dr. Andreas Noack

Toxicity is defined by dose and route of exposure. For instance, people are told that eating an emulsifier called Polysorbate 80, a food additive is not risky, since the liver can safely process and detoxify it before elimination. However, injecting Polysorbate 80 is harmful. The same is true of Thimerasol (mercury) and aluminum hydroxide when injected as adjuvants in vaccines. If ingesting graphene oxide, from eating barbequed foods, the smoke, or char, contains carcinogens called polycyclic aromatic hydrocarbons (PAHs) and heterocyclic amines (HCAs) from incomplete combustion. You can scrape them off your food to reduce your risk. Injecting graphene does not reduce any risks.

Magnetism, In All Its Forms

There are over 200 scientific papers on the magnetism of graphene in its various forms. Among the Graphene family materials, Graphene Oxide (GO)Graphene Oxide Nanoparticles (GONPs)Graphene Hydroxide (GOH) and Reduced Graphene Oxide (RDO) all have paramagnetic properties, a form of magnetism. Graphene-based nanomaterials utilize conductivity properties that act as nanosensors and biosensors for food quality analysis and smart food packaging. Graphene is “The New Plastic.” You can now find graphene oxide nanoparticles in cereals, PCR swabs (nasal vaccination), carssmartphones, and, of course, air pollution since graphene is now an international industry standard.

Due to its magnetic properties, Graphene oxide nanoparticles have the ability to absorb radiation from frequency 5G technology. Unfortunately, most MSDS sheets ignore contact by injection, and electromagnetic effects. If injected into the body, these nanoparticles have the ability to not only cause biological harm, but also to absorb radiation and convert gigahertz signals to terahertz signals, thousands of times higher than those created by silicon, alone. The European Union research group called EUCALL states:

What makes this feat possible is the highly efficient non-linear interaction between light and matter that occurs in graphene. The researchers used graphene containing a large number of free electrons that originated from the interaction between graphene and the substrate onto which it was deposited. When these electrons became excited by an oscillating electric field in room-temperature conditions, they rapidly shared their energy with bound electrons in the material.

Cell Tower Map (find towers near you)

An Intelligent Poison 

This is a “highly intelligent poison.” – Dr. Noack, German chemist and leading expert in activated carbon engineering and GRAPHENE, recently deceased.

This operation is not about killing people, it’s about controlling them. – Dr. José Luis Sevillano, Graphene researcher

It is best to lower expectations for justice to prevail in the UK case, or any case, of criminal corporations who geo-engineer humanity using experimental cocktails. After all, it is the individuals hidden behind the “corporate entity” who write history. For as long as humans have lived on earth, biology, along with history, has been altered. (See Arthur Firstenberg’s book, The Invisible Rainbow).  Nothing changes when criminal defendants are identified as “corporate entities,” without names and insurance bonds. It becomes impossible stop the interconnected crimes, let alone stop the madness.

History and biology continue to be rewritten and transformed. While fraud is allowed to continue under the guise of ineffective public shaming rituals that pass for justice, humanity is entering a new Transhuman Age. With so many corporate criminals protected by bubble indemnity, there is a question that must be asked. Is the Corporate Manslaughter and Corporate Homicide Act of 2007 and other Acts like it, a distraction, established to legalize the Act of Corporate Homicide, rather than deter it?

The way to rewrite history and biology is an individual process of knowing who you are and of rejecting The Transhuman Agenda.

 

Related articles:

Disclaimer: The author encourages you to consult your health care practitioner before making any health changes, especially any changes related to a specific diagnosis or condition. No information in this article should be relied upon to determine diet, make a medical diagnosis, or to determine or prescribe a treatment for a medical condition. This information is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended to build synapses for thinking.

 


Rosanne Lindsay is a Naturopath, writer, earth keeper, health freedom advocate and author of the books The Nature of Healing, Heal the Body, Heal the Planet and  Free Your Voice, Heal Your Thyroid, Reverse Thyroid Disease Naturally.

Rosanne Lindsay is available for consultation through Turtle Island Network.  Subscribe to her blog at natureofhealing.org.

 

Connect with Rosanne Lindsay, Naturopath

cover image based on creaetive commons work of josuenunes979 & Clker-Free-Vector-Images

 




National Institutes of Health Injected Puppies With Cocaine

National Institutes of Health Injected Puppies With Cocaine

by Simon Black, Sovereign Man
February 11, 2022

 

Through a Freedom of Information Request, a watchdog organization revealed that the National Institutes for Health spent $2.3 million of taxpayer money injecting puppies with cocaine.

The point of the experiment was to see how a certain prescription drug reacted with cocaine.

The dogs were then euthanized, or used in further experiments.

This is the second recent example of the NIH funding cruel experiments using puppies.

In October, we talked about an experiment from Anthony Fauci’s National Institute of Allergy and Infectious Diseases (a sub agency of the NIH) which forced beagle puppies into mesh cages to allow sand flies to attack their heads, and spread parasites.

Some of the dogs’ vocal cords were removed so that Fauci’s researchers did not have to hear them cry.

At the time, FDA officials clarified that none of these experiments require testing on dogs.

These are the totally ethical health experts we are supposed to trust.

Click here to read the full story.

 

Connect with Sovereign Man

cover image credit: PIX1861 / pixabay




FDA Ready to OK the Vaxx for Babies; Why Not Just Throw the Babies Off a Cliff Into a Volcano?

FDA Ready to OK the Vaxx for Babies; Why Not Just Throw the Babies Off a Cliff Into a Volcano?

by Jon Rappoport, No More Fake News
February 11, 2022

 

And the answer to that question is obvious. Throwing babies into a volcano makes no money for Pfizer.

On Feb. 15, the FDA will decide whether to approve the Pfizer COVID shot for children between the ages of six months and four years. The press and gov’t. spokespeople predict it’s a GO.

This is murder.

The FDA approval committee members will come in several categories: those who’ve been paid off; those who’ve been threatened; straight-out cold Nazi bureaucrats; those who’ve been blackmailed; and those who WANT TO murder babies.

You can’t get around this. Given the mainstream view of COVID, these FDA/CDC people KNOW the risk of the disease to babies is non-existent, and risks of the vaccine are absolutely devastating.

—Over a million vaccine injuries have already been reported to the US federal database; and this number represents vast UNDER-REPORTING.

Nevertheless, the FDA deciders are ready to say, unless exposed for what they are: inject the babies; kill the babies.

If you still think the government COVID response had anything to do with science or public health or human concern, if you’re still making excuses for Fauci and the whole rogue crew of predators and maniacs at the FDA and CDC, you’re an automatic robot; you just don’t know it.

Get a load of this. CNBC: “Pfizer amended its clinical trial in December to evaluate a third dose after two shots did not induce an adequate immune response in children 2- to 4-years-old. Pfizer and BioNTech said they will submit data on the third dose to the FDA in the coming months.”

I see. The vaccine didn’t work after 2 shots, but it’ll be approved anyway in few days, and Pfizer will let us know IN A FEW MONTHS how the third shot worked.

And that’s science. That’s the bullshit the educated class believes in. That’s the bullshit the deaf, dumb, and blind believe in.

And THE TRUCKERS are the terrorists. Sure. The government is righteous and just. Of course.

People “who spread misinformation about COVID” are terrorists. The government is righteous and just.

Love the government. Hate the terrorists.

Memo to parents: if you’ve been crazy enough to take the shots yourselves, are you ready to deliver your innocent babies into the hands of doctors and nurses who’ll spin the roulette wheel of death and inject their bodies? Is that what you’re going to do?

If so, why? Do you think it’ll make a nice talking point when you get together with friends? Do you think it’s a potent virtue signal? Do you think it proves you’re a loyal subject of the king?

Perhaps you can show up at a local school board meeting, with your infant in your arms; and you can look at the doughy morbid faces of the low-rent grifters sitting behind their long table, and you can say, “Look! I just had my baby shot with the vaccine! It’s wonderful!” And they’ll nod approvingly.

And some piece of dreck who picks up a paycheck as a city public health official will speak at the meeting. He might say vaccinated babies should wear masks. Ask him and find out. Look at his eyes. His brother-in-law, who knows the mayor, rescued him from a career as a gravedigger.

I want to know what the Pope thinks. He’s already stated taking the vaccine is a loving gift to God. What about the babies? Does Popius Maximus Jesuiticus believe The Lord wants infants injected? Let’s get this Pontiff on the record.

Would Mary, in her hut, have told the local doc to inject baby Jesus? Perhaps her husband Joseph, a minor character in the story up to that point, would have brandished a Glock and motioned the sawbones to the door.

Speaking of guns, I think four or five Secret Service agents, their weapons drawn, should usher Nurse Jill to the White House residence, where she will speak candidly and starkly to old Joe—spending as much time as necessary informing him about what the FDA is ready to do, until he UNDERSTANDS.

Then, the agents will force Joe in front of a camera—going live on major channels—where he will unambiguously declare his position on injecting babies.

If he supports the program, he will take full responsibility for the consequences.

After all, the FDA is an agency in the Executive Branch, under the President.

The buck stops with him. It should stop under harsh television spotlights, where no tap-dancing is permitted.

Of course, you parents will have the last word. Unless the guns of the State are pointed at you. If that comes to pass, are you ready to die fighting for your children?

Or will you sacrifice them on the altar of your own passivity and cowardice?

I STRONGLY suggest you make your position clear now.

Publically.

Leave no doubt.

Before it’s too late.

WE NEED AN UPROAR.

Are you standing up? Or are you grinning and virtue signaling—down on your knees?

 

Connect with Jon Rappoport

cover image credit:  vireshstudio / pixabay




As Covid Crumbles They’re Already Prepping the Next “Pandemic”

As Covid Crumbles They’re Already Prepping the Next “Pandemic”
The coronavirus may go but, from cancer to AIDS, the mRNA vaccines are here to stay. 

by Kit Knightly, OffGuardian
February 10, 2022

 

The Covid19 narrative is broken, that battle is over. Yes, there are still pockets of token resistance, little embattled squares who aren’t ready to give up the ghost just yet, but for the most part the establishment are letting it go.

Country after country after country are “relaxing” their Covid restrictions, abandoning vaccine passport plans and attempting to “get back to normal”.

It seems every week some new “expert” who spent the last two years predicting we’re all gonna die turns up on the news claiming we should “treat Covid like the flu”.

But just because they’re giving slack on Covid does not mean the agenda behind Covid is gone. Far from it.

In fact, even as they seek to dump this pandemic in a shallow grave, they are already prepping the public for the next health scare – AIDs.

In December Joe Biden claimed it was the aim of his administration to “end the HIV/AIDS epidemic by 2030”. A similar campaign, launched in the UK at the same, uses the same exact phrase, word for word.

Then, just last week it was suddenly reported there was a “new variant” of HIV circulating in Europe, this new strain is allegedly “more virulent”, “more transmissable”, and “progresses to AIDS faster”.

At the same time, papers are reporting that for the first time in years heterosexuals are more likely to contract HIV than homosexuals, and they are “more at risk of AIDS” because they’re “diagnosed late”.

On the back of this “news”, a Guardian opinion piece claims we need a “new strategy” for dealing with AIDS.

Following hot on the heels of this fresh wave of fear is a push for everyone to get AIDS tested as soon as possible, from politicians and celebrities and everyone in between.

Prince Harry is leading the charge, in a video that caused the press invoke the spirit of his mother Princess Diana, Harry insisted we all have a “duty” to get HIV tested “to keep other people safe”, comparing it to the COVID outbreak.

“Know your status“, the video says. Which will probably be a hashtag in the near future. (I just checked, and it actually is already.)

They’re really cranking through the gears on this one.

Even while the problem and reaction are still barely out of the research and development stage, they’re already talking about the solution.

Guess what it is?

If you said “another mRNA vaccine”, well done for paying attention

Yes, Moderna has apparently learned so much from making their rushed Covid vaccine which doesn’t work that they’re already making an HIV vaccine they hope will be just as “safe and effective”.

In a truly startling coincidence, Moderna’s HIV vaccine began clinical trials the exact same day the “new variant” of HIV hit the headlines, and the same week as the NHS’s annual “HIV Testing Week”. Funny old world, isn’t it?

Anyway, everyone get ready to line up for the AIDS shot.

Oh, and the cancer one as well.

The covid battle might be slowly winding down, but the mRNA “vaccine” war has potentially only just begun.

 

 

Connect with OffGuardian

cover image credit: geralt / pixabay




Dr. Andrew Kaufman Interviews Dr. William Trebing, Author of ‘Good-Bye Germ Theory’

Dr. Andrew Kaufman Interviews Dr. William Trebing, Author of ‘Good-Bye Germ Theory’

by Dr. Andrew Kaufman with Dr. William Trebing
February 5, 2022

 

 

Connect with Dr. Andrew Kaufman

Connect with Dr. William Treging




How the Age of AIDS Mirrors the Covidian Age, With a Twist

How the Age of AIDS Mirrors the Covidian Age, With a Twist

by Rosanne Lindsay, Naturopath,  Nature of Healing
February 7, 2022

 

The Coronavirus/COVID experience is a replay of the HIV/AIDS, with a twist.

As planned events, they show how history repeats itself when people are oblivious to the cyclical patterns of deception.

Note how NIAID’s Anthony Fauci is a common denominator between the antiretroviral drug treatment for HIV/AIDS and the antiretroviral drug treatment for Coronavirus/COVID19.

The AGE OF AIDS

Dr Robert Gallo made his famous announcement at a press conference on 23 April 1984 that “his” HIV virus was the probable cause of Acquired Immune Deficiency Syndrome (AIDS). From that moment on, the race was on to find a pharmaceutical weapon against it.

At the height of AIDS epidemic in 2005, the rhetoric about HIV danger and death penetrated every corner of the world. The rapid test for HIV was accepted as the test for AIDS, which divided people into positive and negative camps.

Flashback to June 2015, ten years after the height of the AIDS epidemic:

AIDS-related deaths have fallen by 35 percent since the peak of the epidemic in 2005 and the number of new infections continues to decline annually. That’s the good news. Nonetheless there are thought to be around 35 million people living with HIV globally; 19 million don’t currently know their HIV-positive status. Of those people who need antiretroviral drugs, only just over a third have access. That’s the bad news.

We have the scientific know-how to end AIDS and every month seems to bring news of another biomedical advance that could change the trajectory of the epidemic once and for all.

Last week the preliminary findings of the Strategic Timing of AntiRetroviral Treatment trial confirmed that early treatment is best for HIV.

No one thought that HIV might be lab-created.  No one knew that just before Gallo’s April 1984 announcement, someone had filed a United States Patent number: 9499480 for HIV/AIDS Virus invention, a designer bi-product of the U.S. Special Virus program.

No one knew that Gallo, himself, was ‘Project Officer’ for the federal Special Virus Program that ran from 1962-1978. See complete list of HIV patents. No one knows that engineered evidence is found from the ‘multiply-spliced’ nature of the HIV ‘tat’ sequence in Dr. Gallo’s 1971 Special Virus paper, “Reverse Transcriptase of Type-C virus Particles of Human Origin.”

Post HIV/AIDS Anomalies:

From 1985 to 1992 there were 12,000 deaths each year from AIDS. In 1992 the number increased suddenly to 15,000. Why? Because they added 5 new diseases to the AIDS definition! The actual number of cases of AIDS was on the decline until they added more diseases to the list, and still the number of new cases grew very slowly. – Dr. Robert Wilner, Deadly Deception, 1994.

HIV — it has never been found in sufficient numbers to cause disease.” –Peter Duesberg, 1991

The HIV/AIDS hypothesis is one hell of a mistake. – Kary Mullins, inventor of the PCR test.

Today, the official narrative still claims that no cure exists for AIDS, and that only toxic FDA antiretroviral drugs, including A.Z.T., D.D.I., and D.D.C., will slow down the progression of the disease.

“Why condemn a continent to death because of HIV, when you have other explanations for why people are falling sick?” – Dr John Papadimitriou, professor of pathology at the University of Western Australia in Perth and a co-author of the Journal of Nature Biotechnolgy study that found HIV tests to be inadequate.

Comparison of HIV and Coronavirus Tests. September 2020:

Sometimes testing can give you a false sense of security. That happened in the HIV epidemic, when people got a negative test and they presented it to their sex partners and spread disease, nonetheless. – Cue Mark Schlissel, M.D., Ph.D., President of University of Michigan, 

The U of M president knew of the flaws of the rapid HIV test. He knew the patterns of history. And for that he received pushback for equating the COVID-19 pandemic with the AIDS epidemic to justify the University’s decision not to widely test students. He was made to apologize for unrelated reasons, but added to his response:

My comments were intended only as a critique of the effectiveness of massive testing of asymptomatic students for the virus that causes COVID-19 in an effort to prevent its spread.  – Cue Mark Schlissel, M.D., Ph.D, President, U of M 2020 

The COVIDIAN Age

In the COVIDIAN Age, it is accepted that Coronavirus is a virus. However, Coronavirus is a family name that includes MERS-Cov, SARS-Cov, HCoV-229E, HCoV-NL63, HCoV-OC43, HCoV-HKU1, and many others. Coronavirus is not Corona virus. It is also accepted that people with underlying diseases are more susceptible to COVID19. This is likely due to a weakened innate immune system. Immunosuppressed people no longer have a functional defense system and are more likely to suffer from any infection, whether it be called a cold, a flu, toxic overload, or ‘COVID.’

The Twist:

Ironically, new research shows the opposite; that patients with advanced stages of AIDS show less severe COVID symptoms and recover faster than others.

A July 2021 study in the Journal Immun Inflamm Dis, titled “The clinical outcomes of COVID-19 in HIV-positive patients: A systematic review of current evidence” shows evidence that the majority of HIV patients show no severe symptoms and completely recovered from COVID19 infection.

Similar to The Age of AIDS, COVID patients will soon be offered antiretroviral drugs. On December 14, 2021, Merck and Pfizer pharmaceutical companies announced the development of COVID antiretroviral drugs. The companies claimed their drugs attack different parts of the virus. Ten days later, on December 24, 2021, the FDA authorized “emergency use” of Merck’s antiviral drug to treat COVID19.  FDA had previously “authorized” the first antiretroviral Molnupiravir in late November. Note: authorization does not equal approval.

When Pfizer introduced its antiretroviral red and blue pill for COVID19, it warned that the pills may be risky when taken with other medications. They did not mention vaccines.

Post Coronavirus/COVIDIAN Anomalies:

Just as the FDA authorized the first AIDS antiretroviral treatment, AZT, on March 19, 1987, in a record 20 months, the FDA authorizes the new COVID antiretrovirals.

Today, the FDA claims that the antiretroviral pill “should be initiated as soon as possible after diagnosis of Covid-19 and within five days of symptom onset,” – FDA Statement, December 22, 2021

In 1994, Dr. Robert Wilner wrote“Any antiviral therapy that is immune-suppressive and aimed at treating HIV is unnecessary, dangerous, unethical and bad medicine — you are already immune to HIV! 

Be FEAR Aware

Be aware that FEAR is a program. FEAR equals False Evidence Appearing Real. Each epidemic serves to elevate the same fear in a different year. Each time the CDC declares a pandemic, scientists also admit they have no record of any isolated infectious virus, including CoV – 2 and 19, MERSInfluenzaSARSPolioMeaslesHIV, XMRV, HTLV-1, HTLV-III/LAV, HPVEbola, Zika, just to name a few. Via FOIA requests, the CDC admits that there is no purification or isolation of any virus. The only way to isolate a virus is to isolate the human host in a hospital, or to culture/engineer it in a lab.

There is no test to find out a person’s “HPV status.” Also, there is no approved HPV test to find HPV in the mouth or throat. – CDC HPV Fact Sheet, 2022

We aimed to develop and deploy robust diagnostic methodology for use in public health laboratory settings without having virus material available. – Journal of Euro Surveillance, 2020

The current fallacious approach to therapy will only continue to result in millions of unnecessary and brutal deaths. – Dr. Robert Wilner, Deadly Deception, 1994

Buyer beware! The rhetoric about HIV/AIDS has returned. Then, as now, officials seek to distract and divide people to remove freedoms. In the process, officials make people fearful of touching each other. They will claim that COVID deaths have surpassed AIDS deaths. They will claim to find a more infectious HIV variant. They will claim that “HIV can be stopped by blocking cell to cell contact.

Will they also separate cells by 6 feet and mandate tiny masks?

Question Everything ….

If HIV does not cause AIDS, then does Coronavirus cause COVID19? 

If there is no isolated virus, are virologists legitimate? Is Anthony Fauci an actor? Why does he claim that wearing a mask after vaccination is “theatre?” Why does he hold 4 patents on an HIV component used to create COVID19?  

Why blame a pandemic on innocent animals? It sounds like this: “ANIMAL X” could be hiding a deadly virus that could trigger a pandemic worse than the Black Death and kill more than 75million people. They tried to blame Ebola on a bunny.

Did the Species Barrier disappear to allow for animal research to develop profitable drug models?

After mRNA injectables, why are AIDS patients successfully fending off the worst COVID symptoms and recovering faster without an immune system?

Do HIV patients somehow recognize the lab-created Coronavirus as similar? Does the mRNA nanotech somehow protect people without an immune system? Is that why antiretroviral will be required for COVID patients? 

Who to trust?

Trust your innate immune system.

Related articles:

Disclaimer: The author encourages you to consult a doctor before making any health changes, especially any changes related to a specific diagnosis or condition. No information in this article should be relied upon to determine diet, make a medical diagnosis, or to determine or prescribe a treatment for a medical condition. This information is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. It is intended to build synapses for thinking.

 


Rosanne Lindsay is a Naturopath, writer, earth keeper, health freedom advocate and author of the books The Nature of Healing, Heal the Body, Heal the Planet and  Free Your Voice, Heal Your Thyroid, Reverse Thyroid Disease Naturally.

Rosanne Lindsay is available for consultation through Turtle Island Network.  Subscribe to her blog at natureofhealing.org.

 

Connect with Rosanne Lindsay, Naturopath

cover image credit: CDD20 / pixabay




Deus Ex Machina and the Invention of “SARS-CoV-2”

Deus Ex Machina and the Invention of “SARS-CoV-2”

by Dr. Mark Bailey
February 6, 2022

 

A German mathematician working with Dr Stefan Lanka has just published a report titled “Structural analysis of sequence data in virology – An elementary approach using SARS-CoV-2 as an example.” It provides even more evidence that the virologists are caught up in a world of computer simulations – simulations that are unreliable even on their own terms, not to mention being disconnected from reality.  The analysis is an important contribution exposing another element of the anti-science being used to sustain this fake pandemic.  Further, it is a technical dismantling of how all “viruses” are being invented and then “found,” in an ongoing game of deception.



The paper is very technical and requires some understanding of how the virologists create a “genome,” starting with a crude sample from an alleged infected “COVID-19” patient.  To make it easier, I’ve produced a summary of the main findings as outlined below:

  • None of the genetic sequences used in producing the “SARS-CoV-2” genomes were shown to come from inside any viruses.  It is unclear where the genetic fragments originated from.
  • The original de novo “SARS-CoV-2” computer-constructed sequence published by Fan Wu, et al could not be reproduced by the methodology described in their paper, raising questions about how they produced it and announced the new “virus” to the world.
  • The PCR protocols are calibrated to sequences of unconfirmed origin that are clearly found in many humans and apparently other things as well.  The PCR process was not shown to detect a “virus,” let alone diagnose an invented illness called “COVID-19”.
  • The virologists are fooling themselves by running amplifications at 35 to 45 cycles, as it can result in “detecting” sequences that are not even present in the sample.  In effect, the methodology can result in “detecting” whatever sequences they are hoping to find.
  • Fan Wu, et al could have found better matches for “HIV” and “Hepatitis D virus” than “a new coronavirus” in their 41-year-old man from Wuhan, who presented with pneumonia as one of the first claimed “COVID-19” cases.  If they want to find a “virus”, it all depends on what they ask the computer to look for.

Of course, it makes much more sense when you get to the root of the problem: “SARS-CoV-2” is nothing more than a computer simulation and there was never a virus to start with – the entire thing is a global fraud.  Virology seems to be unaware that it is sinking further into an epistemological crisis and no more so than in the area of genomics, as outlined in this article by Mike Stone.   In Stone’s article, I noticed in the comments section that Dr Valendar Turner of The Perth Group pointed out that the late Sir John Maddox, former editor of Nature, had issued a pertinent warning in 1988.  It seems that those who become immersed in the world of indirect molecular detection techniques risk no longer seeing the wood for the trees as he presciently stated:

“Is there a danger, in molecular biology, that the accumulation of data will get so far ahead of its assimilation into a conceptual framework that the data will eventually prove an encumbrance? Part of the trouble is that excitement of the chase leaves little time for reflection. And there are grants for producing data, but hardly any for standing back in contemplation”. 

Maddox, J. Nature 335, 11 (1998)

We will endeavour to keep exposing these anti-scientific methodologies and encourage others to ask themselves if the multi-billion dollar virology industry and the associated bogus “treatments” coming from the behemoth pharmaceutical complex are actually helping anyone with their health.  For those of us that can see there is no sound basis to any of it, there is no way we would heed any advice from the doctors and scientists who promote these sick models.  And perhaps more importantly, we know not to take any of the fraudulent and increasingly perverse pharmaceuticals that are products of this pseudoscience, and used as vehicles to deliver nefarious and undeclared constituents.  Once again, you can avoid all of these problems by pointing out:

Where is the virus*?

*A tiny particle that is an obligate intracellular parasite (i.e. replication competent and transmissible) containing a genome surrounded by a protective, virus-coded protein coat.

 

Connect with Dr. Mark Bailey and Dr. Sam Bailey

cover image credit: PixxlTeufel / pixabay


 See related:

The Covid-19 Fraud & War on Humanity

Warning Signs You’ve Been Tricked by Virologists




Challenging the Foundations of Virology: Corona Investigative Committee With Dr. Stefan Lanka & Dr. Andrew Kaufman

Challenging the Foundations of Virology: Corona Investigative Committee With Dr. Stefan Lanka & Dr. Andrew Kaufman

 

Truth Comes to Light editor’s note:

This clip is from the Corona Investigative Committee’s  “The Virus of Power” series of interviews , Session 90, which took place on February 4, 2022.  See the entire Session 90 here (6+ hours long).

In this interview, Dr. Kaufman and Dr. Lanka challenge “germ theory”  and the “science” at the foundation of virology.  Of course, this is highly controversial because it shakes the foundation of modern medicine, questions the endless stream of vaccines and toxic medicines produced by big pharma — not to mention the generations of doctors, scientists and medical professionals who have dedicated careers to this “science”. 

Committee member Dr. Wolfgang Wodarg, who has been invaluable in exposing the pandemic fraud and is a key source of medical insight for the committee, challenges Dr. Kaufman and Dr. Lanka, and vehemently defends the prevailing view regarding viruses as cause of disease.  See Dr. Wolfgang Wodarg’s presentation during Session 90 here. His presentation occurred earlier in the session, prior to this conversation with Drs. Kaufman and Lanka.  

Below the Corona Investigative Committee video, we are providing documents, videos and articles for understanding the work of Dr. Lanka, Dr. Kaufman, Dr. Tom Cowan and others. 

Please do your own research and come to your own conclusions.



Video by Oval Media can be found at Corona Investigate Committee Odysee channel.

 

Documents by Dr. Stefan Lanka:

Dismantling the Virus Theory by Dr. Stefan Lanka (download PDF)

The Causes of Corona Crisis Are Clearly Identified — Virologists Who Claim Disease-Causing Viruses Are Science Fraudsters and Must Be Prosecuted by Dr. Stefan Lanka (download PDF)

How Dead Are Virus Anyway? All Claims of Virus Existence Refuted by Dr. Stefan Lanka (download PDF)

 

Related document by Harold Hillman:

A Serious Indictment of Modern Cell Biology and Neurobiology by Harold Hillman (download PDF)

 

Video on the work of Dr. Lanka:

The Final Refutation Of Virology by Dr. Stefan Lanka

 

Related articles:

Dr. Stefan Lanka & Dr. Tom Cowan: How We Got Into This Mess — The History of Virology & Deep Medical Deceptions

Dare to Ask: Dr. Tom Cowan, Dr. Stefan Lanka & Dr. Andrew Kaufman on Freedom, Fear, and False Science About Viruses and the Nature of Reality Itself

Dr. Stefan Lanka 2020 Article Busts the Virus Misconception

Dr. Tom Cowan on the “Spiked Protein Toxin” & “Virus Created in a Lab” Stories

The Contagion Fairy Tale

The Non-Existent Virus; an Explosive Interview With Christine Massey

The Contagion Myth: No Virus Has Ever Caused Disease

The Fraudulent Use of PCR / RT-PCR Techniques for the Manipulation, Harm and, Ultimately, the Destruction of Humanity

Warning Signs You’ve Been Tricked by Virologists

Jon Rappoport: My Bottom Line on the Existence of the Virus, Its Isolation and Sequencing

Exposing the Lie — Hippocratic Hypocrisy: A Tale of Two Snakes [A collaborative film by Spacebusters and Dr. Andrew Kaufman about how authentic medicine was hijacked by the power elite and turned into a deadly, sickness-for-profit industry.]

 

Connect with Dr. Stefan Lanka: http://wissenschafftplus.de/

Connect with Dr. Andrew Kaufman: https://andrewkaufmanmd.com/

Connect with Dr. Tom Cowan: http://drtomcowan.com/

 

Connect with Corona Investigative Committee




What Is a Disease Without a Cause?

What Is a Disease Without a Cause?

by Jon Rappoport, No More Fake News
February 4, 2022

 

A disease without a cause is a business model.

You make a list of symptoms. You say many people are experiencing this cluster of symptoms.

You give a label to this list of symptoms. A name. The name of a disease or a disorder or a syndrome.

Over time, through promotion, the name sticks.

You fund research to find the cause of the disease. This research can stretch out for a long time. Possibly forever.

Meanwhile, you develop and sell drugs to treat the disease. Money.

You keep reporting “progress” on finding the cause. “At first, we looked for environmental factors. But now we know the basis is almost certainly genetic. We’re homing in on the specific genetic dysfunction…”

Over time, what’s forgotten is this: is there really a single disease with a single cause?

And think it through; if you can’t verify a single cause, you don’t have a disease. You just have the original list of symptoms.

Alzheimer’s would be an example. Microcephaly (babies born with small heads and brain damage) would be another. The disease names seem to carry the day. “Well, if there’s a name, a label, there must be a unique disease.”

Wrong.

If there’s a name, a label, there is money.

Money for research, for drug development, money from drug and vaccine sales.

Researchers are tasked with making the list of symptoms seem compelling. “We’ve done brain studies. There are remarkable similarities among patients who have Disease X. As you can see from these scans, in Figure A…”

Still, no dice. No verified cause. Therefore, no justification for using the disease label or claiming you have found a unique disease.

But it doesn’t matter, because the business model is working well.

Here’s another example. ADHD. Has a single cause been found for this list of symptoms? No. Therefore, there is no laboratory test for ADHD. No test to confirm the diagnosis of ADHD. Because a test would detect the cause is present in the patient—and there is no cause to look for.

In fact, if you examine the complete catalog of all so-called mental disorders—about 300 of them—there is no defining lab test for ANY of them. Not a one. Each so-called disorder is simply a list of behaviors which have been clustered together by committees of psychiatrists and given a name. ADHD. Bipolar. Clinical depression. And so on.

But it doesn’t matter. Because the business model is working. Money is pouring in. Drugs are selling.

Let’s take this even further. A hundred years of Rockefeller medicine have “established” that there are thousands of separate and distinct and unique diseases, disorders, and syndromes. And each one has a cause. For many diseases, the cause “hasn’t been discovered yet.” Meaning: “We’re writing fiction. We have no justification for calling these diseases, diseases.”

For many other diseases, researchers claim, the causes have been found. The most popular type of cause? A virus.

A virus that had never been seen before. A virus that was “discovered” in a lab.

A lab—as I’ve discussed in depth—that lets in no outsiders, no truly independent observers, to see, in detail, what’s actually going on.

For that reason, and several others, there is no solid reason to believe these viruses, these causes are actually being discovered. Are actually real.

Which leaves us with thousands of lists of symptoms.

But there is always a business model. The full Rockefeller model is worth trillions of dollars. More dollars every day.

The drugs and the vaccines are the $$$ payoff.

I’ve spent decades demonstrating their toxicity.

Here’s a very interesting medical trick. A criminal trick. The researchers say a brain disorder called ABC exists but they haven’t found the cause yet. A parent has a child with severe problems and takes him to the doctor. The doctor pronounces a diagnosis: “Yes, your boy has ABC.”

The parent goes away and does some research. The list of symptoms for ABC could be the result of a vaccine. In fact, the boy developed his severe problems quite soon after vaccination.

She goes back to the doctor and says, “I think my son was damaged by the vaccine.”

The doctor says, “That’s impossible. Your boy is suffering from ABC. And you see, we’ve done studies of boys with ABC, and many of them were never vaccinated. So when you say the cause of your boy’s ABC was a vaccine, we’ve ruled that out.”

The parent doesn’t know what to do.

Of course, the trick is, ABC was never proved to be a unique disorder in the first place. It’s really the NAME of an unproven disorder. The studies the doctor is referring to are completely irrelevant.

ABC is a disorder without a proven cause. Therefore, it is no disorder at all. It’s just a list of symptoms.

The parent’s boy has many of those symptoms. He acquired them—and the damage he suffered—from a vaccine. If you wanted to put a name to what the boy has, call it what it is: vaccine damage.

Not ABC.

Part of the business model for ABC is: “We use that disease label so we can avoid having to pay out huge compensation-dollars for damage caused by a vaccine.”

If the impact of this trick isn’t getting through to you, let me give you a grossly exaggerated analogy.

Engineers claim there is a phenomenon called River Floundering. It is unique but the cause hasn’t yet been found. The basic symptom is: boats on rivers develop the propensity to sink.

Joe takes his boat out on a river. Overhead, a bridge collapses and destroys his boat. Joe barely escapes with his life. After six months, he emerges from the hospital and sues a number of parties.

But he loses his case. In court, experts testify that his boat was suffering from River Floundering. That’s why it sank. Many studies of Floundering show bridges-collapsing did not occur when “the sinking happened.” Therefore, the collapsing bridge was not the cause of Joe’s boat’s disorder, River Floundering.

What is a disease without a cause?

A business model.

 

Connect with Jon Rappoport

cover image credit: geralt / pixabay




Air Vaxxidents: The F-35/USS Vinson Incident

Air Vaxxidents: The F-35/USS Vinson Incident

by Joseph P. Farrell, Giza Death Star
February 3, 2022

 

Most readers here have probably heard of the F-35 crash that occurred recently in the South China Sea. The public narrative has it that a pilot was landing his F-35 on the carrier USS Vinson, but the glide path was too steep, and the plane did not catch the grappling wires, and tumbled over the side of the ship as the pilot ejected. The current coverage of the story has it that the US Navy and the Chinese navy are in a race to recover the airplane.

But according to this article shared by V.T., that may not be all there is to the story:

Navy Pilot Crashes Plane, Ejects, After Vax Reaction

According to this article, the pilot of the aircraft was experiencing chest pains as he approached the carrier, and actually blamed the vaccine for the pains (and the abortive landing) in communications with the carrier:

Aviators approaching within a mile of their carrier “call the ball,” a radio transmission indicating they have spotted the “meatball,” a nickname for the visual reference used by pilots to keep the proper glide slope during the approach to an aircraft carrier.

As the F-35C pilot neared the USS Vinson, he “called the ball,” but also said he was experiencing sudden and intense chest pain, as if “someone hit me with a baseball bat.” The Landing Signal Operator aboard the USS Vinson noticed at once that the F-35 was above glideslope and would miss the wires. He ordered the pilot to “wave off” just as the pilot’s crackled voice said on the radio, “Fucking vaccine.” The pilot had barely enough strength to eject safely, though several boatswain’s mates on the flight deck were injured when the plane struck the deck.

The pilot was recovered and taken to medical, where a physician determined he had suffered an acute case of myocarditis, or inflammation of the heart muscle, a common and potentially deadly side effect of Covid-19 vaccinations. The USS Carl Vinson, a Nimitz-Class carrier, has a fully functional medical ward on its 2nd deck, complete with diagnostic equipment, including CRT and MRI scanners, found in contemporary hospitals.

The pilot, current condition unknown, got his booster shot aboard the USS Vinson 72-hours prior to the accident. He had no comorbidities, and passed a medical examination on 9/5/2021.

Other aviators aboard the Vinson described him as “an accomplished and competent aviator with thousands of hours of flight time in a broad range of aircraft, and dozens of successful carrier landings.”

This information came to RRN via a senior Navy officer who said the U.S. Navy Judge Advocate General’s Corps received a briefing on the accident.

This story intrigued me, because one of the areas that I have received some articles about, is precisely the so-called  “vaxxidents”, accidents caused in whole or in part because of complications and adverse reactions from the covid injections. (Like Catherine Austin Fitts, I prefer not to refer to these injections as vaccines. They are not in any classical sense. They are experimental drugs at best, and hence my term “injections” and my preferred term “quackcines”.) I’ve had a veritable mountain of such stories, most of them unverifiable. This one, while anecdotal I strongly suspect has some fire behind the anecdotal smoke, because I’ve had other people share similar stories of pilots experiencing strange things after their injections.

This story disturbs for a far deeper reason, for if true, then it means that the whole issue of the injections and this administration’s attempts to force them on the military has become a national security issue because of the possibility of more such reactions. Let’s remember, US Army flight surgeon Lt. Col Teresa Long warned about precisely such sudden cardiac events in the case of pilots:  https://americanmilitarynews.com/2021/09/army-flight-surgeon-says-pilots-risk-sudden-cardiac-death-from-covid-vaccine-side-effect/

There has been much discussion on the idea of vaccine passports, but the reality is the opposite: if you’re flying a commercial airliner, would you, or would you not, like to know the vaccine status of your flight crew? Given Lt. Col. Long’s story, and now the allegations surrounding the USS Vinson F-35 crash, the answer to that question seems obvious. So now the real question is, how long before the military – as a matter of national security – refuses the injections? And how long before all this translates to the commercial airliners doing the same? And how long from there to the holding of the perpetrators and their media lackies accountable?

Time will tell…

See you on the flip side…

 

 

Connect with Joseph P. Farrell

cover image credit: 12019 / pixabay




Jon Rappoport: My Bottom Line on the Existence of the Virus, Its Isolation and Sequencing

My Bottom Line on the Existence of the Virus, Its Isolation and Sequencing

by Jon Rappoport, No More Fake News
February 3, 2022

 

What proof would I accept? What sort of proof would convince me that SARS-CoV-2 exists?

Suppose, for example, a study described how researchers actually DID separate a virus from all the material surrounding it in their cell-soup in the lab?

Would that be enough?

And the answer is no.

Why?

Because I don’t trust studies based on research conducted in elite labs where no independent outsiders are allowed. And that’s the situation, when it comes to purported virus isolation.

These labs are like the famous bunkers where key government officials are taken, in the event of a massive attack against the country.

Try getting in off the street.

And who are these researchers in the super-secret labs? To put it another way, what sort of establishment do they represent?

Is it a clean establishment with a track record of honesty? Or is it a cartel with a criminal history?

If it’s a cartel, why should I accept the “scientific methods” of these researchers or their honesty?

As my long-time readers know, I’ve spent decades exposing lies and crimes of the medical cartel. Chapter and verse. (For example this: Medical weapons of mass destruction)

When it comes to vital issues that mean the difference between life and death—drug/vaccine-fueled destruction of human life; mistreatment and errors in hospitals; faked disease case and death numbers; inaccurate, meaningless, and deceptive diagnostic tests; the fabricated existence of a whole range of phony diseases and disorders and syndromes; the true numbers of medically caused deaths—medical authorities have been lying and sliming their way out of accountability for MANY decades.

And all this doesn’t touch on the history of public health declarations of epidemics that have turned out to be duds.

Nor does it include the overall history of Rockefeller medicine, which is based on the fatuous notion that there are thousands of separate and distinct diseases, each one of which is caused by a germ that must be treated by a profit-making drug.

Nor does it include the history of vicious suppression of innovative treatments developed by individuals who’ve worked outside the mainstream.

Therefore, suspicion is warranted. Is absolutely necessary. And “suspicion” is a vast understatement.

I refuse to trust the researchers who simply claim they’re isolating viruses.

When it comes to the so-called basic building blocks of MANY so-called diseases—which ARE “the viruses”—all the discovery-research HAS BEEN conducted by insiders in their off-limit labs. Without independent witnesses. Without educated witnesses who can watch and question each and every step of “the accepted method” for isolation of new viruses.

Frankly, you would have to be crazy to accept anything coming out of these insider-club labs.

So NO. I don’t accept such findings.

Before I describe how outsiders SHOULD be allowed to witness and participate in secret lab work, let me give you two quotes to consider.

They come from decidedly mainstream and elite editors of elite medical journals. These editors have read and explored and probed and lifted the fake cover from published medical material for decades. Material they themselves have published. Therefore, these are CONFESSIONS.

ONE: “It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of The New England Journal of Medicine.” (Dr. Marcia Angell, NY Review of Books, January 15, 2009, “Drug Companies & Doctors: A Story of Corruption)

TWO: “The case against science is straightforward: much of the scientific literature, perhaps half, may simply be untrue. Afflicted by studies with small sample sizes, tiny effects, invalid exploratory analyses, and flagrant conflicts of interest, together with an obsession for pursuing fashionable trends of dubious importance, science has taken a turn towards darkness…”

“The apparent endemicity of bad research behaviour is alarming. In their quest for telling a compelling story, scientists too often sculpt data to fit their preferred theory of the world. Or they retrofit hypotheses to fit their data. Journal editors deserve their fair share of criticism too. We aid and abet the worst behaviours. Our acquiescence to the impact factor fuels an unhealthy competition to win a place in a select few journals. Our love of ‘significance’ pollutes the literature with many a statistical fairy-tale…Journals are not the only miscreants. Universities are in a perpetual struggle for money and talent…” (Dr. Richard Horton, editor-in-chief, The Lancet, in The Lancet, 11 April, 2015, Vol 385, “Offline: What is medicine’s 5 sigma?”)

Suspicion is warranted. It’s absolutely necessary. And again, “suspicion” is a vast understatement.

More than a year ago, I mentioned how virus-isolation research—if the word “research” applies at all—should be done.

And I issue this now, as a challenge, to the entire insider-club of virologists, all of whom claim their established method of finding and sequencing new viruses is scientific and rigorous:

Let’s have a film crew on site. As you work. In your lab. Looking over your shoulders and recording every move you make.

And with the film crew, let’s have several knowledgeable, outside, independent researchers. People whom you would ordinarily refuse to give the time of day. People who are insightful. Possibly, people like Dr. Stefan Lanka, Dr. Andrew Kaufman, Dr. Tom Cowan.

As the film crew works, and as you conduct and describe your step-by-step “isolation” of a new virus, these outsiders can stop you at any moment and question you. In depth.

“Why did you just do that?” “Why didn’t you record that step?” “Explain that answer you just gave me. It makes no sense.” “Exactly what did you just withdraw from the solution in the dish, and how do you know what it was?”

This is not a public relations exercise or an educational documentary for medical students. This is REAL. This is research about your research. No holds barred.

You give a slippery answer to a question; you evade with a vague generality; you try to pull rank; you get nailed to the wall. On film.

THIS is the procedure I want.

All the way from start to finish. Including the so-called sequencing of the “new virus.”

And then we would know a great deal more about what you’re actually doing and not doing in your labs. In the absence of what I’m proposing and demanding, THERE IS NO REASON TO ASSUME THE PROCESS OF VIRUS-ISOLATION IS LEGITIMATE.

Virologists, your work affects every human on Earth. Profoundly. To see this, all a person has to do is look around him these days, at what is called “COVID.” It proceeds from your so-called discovery of SARS-CoV-2.

I view you virologists as I would view the court magicians and soothsayers and high priests who surrounded and advised the leaders of tribes and nations in ancient times.

Those “experts” huddled with the leaders in their very private rooms and spun stories and predictions, and recommended strategies to deal with supposed ongoing and looming crises.

And then the leaders took actions that affected the lives of all the people.

So it is now. With you virologists.

So my demands are entirely within bounds. If you have a shred of honesty, and if you stop and think about it, what I’m demanding is prosaically simple:

You account for every step you take. In real time. Where you work. Right there, you submit yourselves to the detailed scrutiny of independent outsiders.

That’s my bottom line.

And I challenge any scientist, analyst, investigator, doctor, researcher, reporter, alt. reporter who says what I’m demanding is not necessary. You’re wrong. You’re dead wrong.

You either haven’t thought things through, or you’re lying.

Someone is going to tell me what I’m demanding, as proof, is impossible. It would never happen. “They” would never let it happen. They would never let independent outsiders into their holy labs.

You think I don’t know that?

If outsiders can’t get into their labs, what does that tell you?

And someone will say, “We just have to rely on the best evidence we have.”

No we don’t. Because the best available evidence is no evidence.

In a vast sea of death-dealing medical lies, a sea that has existed for more than a hundred years (actually much longer), if experts tell you they’re discovering viruses in labs you can’t enter, and they say you must believe them, and you buy that…

I have condos for sale on the far side of the moon. Full cash only, no payments.

Here it is: Virologists are saying and writing they’ve found a purple man with pink hair and green lips and four arms living a thousand miles under the surface of a planet in the next solar system over. And he causes disease.

Then they’re saying, “Prove us wrong.”

On top of that, they’re saying, “You can’t watch us work while we discover such creatures.”

Conclusion: the purple man doesn’t exist.

Virologists, text me when you’ll let my people into your lab.

Until then, get lost.

Dear reader, the elephant in the room is trust, not data.

When it comes to the “discovery of viruses,” there are no reliable data. We, on the outside, are told that what happens behind locked doors is irrefutable. Period.

We’re told we just can’t understand what the pros are doing. The problem is our lack of knowledge, our lack of training.

We’re the peasants toiling in the valley. Our better, the baron, is up in his castle on top of the mountain. He’s planning our lives, he’s taking care of us.

Sure. Of course. Uh-huh.

Sounds familiar. It’s pretty much the history of the world.

Or it was, until people who came before us finally staked out a territory called freedom, which involved opening locked doors and finding out what lay behind them.

Consider a parochial example: the mafia. They, too, plan behind closed doors. They concoct methods of carrying out crimes. They record their profits. Then, finally, a prosecutor announces, “We were able to get into their books. We saw the details. We made arrests.”

I want my independent accountants to get into the virologists’ books. But not after the fact. I want my people to BE there while the virologists are creating the books, entry by entry, in the lab.

“Why did you just make that entry? Where did your conclusion come from? Who are you trying to kid? You’re just fabricating this stuff? You know, that’s called RICO. That’s a RICO case. Continuing criminal enterprise. They’ll send you away for a long time…”

And all of a sudden, the high and mighty virologist, who’s been able to con the world with his hustle, who knows how to come off sounding superior in every way, feels a dent in his armor. A big dent. He smells his own blood.

And he starts talking.

He wants to make a deal. He’ll roll over on his colleagues. He’ll expose the whole sham.

“…You don’t understand. It’s the money. It’s all about the money. Where it comes from. We have to do this kind of work. Otherwise, we starve. They cut us off. I know the people on the funding committees. I’ll give you their names. They take orders, too. The whole thing is a system. I can draw you a map. I can’t go to jail. I have a family. I’m paying eighty grand a year just to send my kids to college. There’s the mortgage, and the cottage on the Cape…”

The whole bluff POPS and deflates, and we begin to hear words we understand, at last. The words of confession. The down-to-earth sordid truth.

There was never a towering mystery in the castle on the hill.

There was just the passing of the buck. The soiled buck. From hand to hand.

The “science” was the front.

“…You see, it works this way. The pharmaceutical companies have to have new viruses. For every fake virus, they develop a real drug and a real vaccine. It’s marketing. That’s what they’re doing. That’s what they’ve always been doing. This is much bigger than anyone realizes. I’m just a little fish. The big boys run the whole show. They pay the Congress and the FDA. They pay everybody…”

He keeps talking. He can’t stop. He’s way past “isolation, purification and sequencing.” They’re in his rear-view mirror. Now he’s fighting for his freedom from prison. Now he’s telling the truth.

And the ever-present storm clouds over the valley where we peasants toil are blowing away. The air is fresher.

We’re breathing easier.

The big-cheese baron is really a shrunken little man—when he takes his perp walk in chains.

 

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cover image credit: Tumisu / pixabay




Landmark Book on AIDS That Exposes the Criminality of Anthony Fauci and Government Technocrats: Free Download

Landmark Book on AIDS That Exposes the Criminality of Anthony Fauci and Government Technocrats: Free Download

by Edward Hendrie, Great Mountain Publishing
January 29, 2022

 

Peter Duesberg is a molecular biologist and a molecular and cell biology professor at the University of California, Berkeley. At one time, he was an acclaimed scientist who was the world’s foremost expert on AIDS. That all changed when he was blackballed by Anthony Fauci and the scientific establishment for the temerity of revealing the truth that HIV does not cause AIDS. Duesberg was slandered as a homophobe for revealing the scientific evidence that AIDS was caused by the use of certain dangerous recreational/pharmaceutical aphrodisiacs by the sodomite community that over time broke down the immune systems of the users who then developed AIDS. He revealed that the prevalence of AIDS in Africa is simply explained by recategorizing as HIV the endemic immune deficiencies that were always understood to be caused by malnutrition, tainted drinking water, and various infections.

Dr. Duesberg reveals how Fauci pushed the toxic drug called AZT (Zidovudine) to people who were found to have antibodies to HIV.  Those patients were poisoned by the drug (AZT) that was supposed to treat them. AZT, in actuality, caused AIDS, which eventually killed the patients. That is much like the present regime of treating COVID-19 with unsafe and ineffective mRNA vaccines and toxic therapeutics like Veklury® (remdesivir) while suppressing safe and effective therapeutics like hydroxychloroquine and Ivermectin.

Duesberg’s book exposes the incompetence, megalomania, and in some cases criminality of Anthony Fauci, and other NIH, FDA, and CDC officials. It reveals the genesis of the establishment of what has become a cabal of ruling technocrats in government which has now brought Orwellian oppression across the United States and indeed the world through the COVID-19 scare and mandatory experimental vaccinations.

There were very powerful interests who tried to kill Duesberg’s book before it ever saw the light of day. The publisher, Regnery, in its preface to the book explains how Peter Duesberg went through two publishers who backed out of publishing the book at late stages, apparently due to some hidden pressure from an unseen hand.

This book is now out of publication. But there is still robust demand for the book which has driven the price up. While Amazon offers the audible version of the book at a reasonable price, as of January 28, 2022, the hardcover version was priced at $1,260.00 and the paperback was priced at $536.00.

It is now a free PDF download.

Excerpt From the Publisher’s Preface:

Regnery is the third publisher to have contracted to publish Inventing the AIDS Virus. Addison Wesley initially announced the book in 1993. St. Martin’s signed it in January 1994 and subsequently assigned its contract to us in January 1995. We announced it, initially, in the fall of 1995 and finally published it in February 1996. Bryan Ellison, Duesberg’s former research assistant and original co-author, became disenchanted with Duesberg’s and his publisher’s insistence on careful documentation and self-published his own version under the title Why We Will Never Win the War on AIDS in 1994. We sued Ellison for breach of contract and copyright violation and, after a two-week federal court jury trial, were awarded a six-figure verdict and an injunction against Ellison’s edition. Inventing the AIDS Virus has been edited by at least five editors, has been agonized over by the publishers of three major publishing firms, and concurrently praised and damned by countless critics.

Excerpt from the foreword by Nobel Laureate Kerry Mullis, creator of the PCR test:

We have not been able to discover any good reasons why most of the people on earth believe that AIDS is a disease caused by a virus called HIV. There is simply no scientific evidence demonstrating that this is true.

We have also not been able to discover why doctors prescribe a toxic drug called AZT (Zidovudine) to people who have no other complaint than the presence of antibodies to HIV in their blood. In fact, we cannot understand why humans would take that drug for any reason.

We cannot understand how all this madness came about, and having both lived in Berkeley, we’ve seen some strange things indeed. We know that to err is human, but the HIV/AIDS hypothesis is one hell of a mistake.

I say this rather strongly as a warning. Duesberg has been saying it for a long time. Read this book.

Kary B. Mullis
Nobel Prize in Chemistry, 1993


Prior to his untimely death on August 7, 2019, Kerry Mullis had this to say about Anthony Fauci and his ilk:

“Guys like Fauci get up there and start talking, you know, he doesn’t know anything really about anything and I’d say that to his face. Nothing. The man thinks you can take a blood sample and stick it in an electron microscope and if it’s got a virus in there you’ll know it. He doesn’t understand electron microscopy and he doesn’t understand medicine and he should not be in a position like he’s in. Most of those guys up there on the top are just total administrative people and they don’t know anything about what’s going on in the body. You know, those guys have got an agenda, which is not what we would like them to have being that we pay for them to take care of our health in some way. They’ve got a personal kind of agenda. They make up their own rules as they go. They change them when they want to. And they smugly, like Tony Fauci does not mind going on television in front of the people who pay his salary and lie directly into the camera.”

Notice the book, Inventing the AIDS Virus, on the table in front of Mullis during the interview.



 

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The Pharmaceutical Companies Have a Financial Incentive to Make Their Vaccines Injurious

The Pharmaceutical Companies Have a Financial Incentive to Make Their Vaccines Injurious

by Edward Hendrie, Great Mountain Publishing
January 6, 2022

 

Congress passed the National Vaccine Injury Act (NVIA) of 1986, which granted immunity to the pharmaceutical companies for injuries caused by the vaccines they manufactured. As explained by the U.S. Supreme Court in Bruesewitz v. Wyeth 1, the reason for that protection is that Congress deemed vaccines to be unavoidably unsafe, 2 thus no manufacturer would make a vaccine if they had to suffer the liability for injuries they would unavoidably cause. 3

Mary S. Holland explains the issue: “The success of the national vaccine program has come at a cost. Some children are permanently disabled or die from their vaccine exposures. … Between 1980 and 1986, people who claimed vaccine injury brought over three billion dollars of damages claims to U.S. civil courts against vaccine manufacturers.” 4

In response to the litigation that held them accountable for the injuries caused by their vaccines, the vaccine manufacturers lobbied Congress, and in 1986 they were able to get the NVIA law passed. That law had the effect of protecting them from civil liability for injuries caused by vaccines that they manufactured.

The underlying legal reasoning of Congress for the 1986 NVIA law was a concept borrowed from the Restatement of Torts law that vaccines were “unavoidably unsafe.” Holland explains that “[t]he Restatement describes all vaccines as ‘unavoidably unsafe’ products and implicitly recommended that manufacturers not be liable for injuries if doctors administered them properly.” 5

The NVIA set up a system of government compensation for vaccine injuries that has in practice served more to prevent compensation than anything else. Robert F. Kennedy explains:

Parents, legal guardians and legal representatives can file on behalf of children, disabled adults, and individuals who are deceased. According to the vaccine-injured and their loved ones, the program has failed miserably as a litigious, broken system where the injured are up against a government vaccine program, government owned vaccine patents, government health officials who administer the program and government paid attorneys from the Department of Justice. There is no judge, no jury of your peers and no discovery. Claimants feel the system is set up for their claims to fail. 6

The U.S. Supreme Court in Bruesewitz, supra, ruled that language in the statute categorically preempts even design defect claims against vaccine manufacturers. Holland explains that U.S. Supreme Court ruling “removed incentives for pharmaceutical corporations to conduct the extensive research and development necessary to ensure that FDA-approved vaccines remain as safe and effective as possible after licensure. FDA approval alone has not been a sufficient guarantee of drug safety, owing in part to the FDA’s limited authority to compel further safety research after final approval.” 7

Holland reveals the real-world consequences of the NIVA for vaccine recipients:

[Gayle] DeLong showed that the proportion of people that reported a serious complication from a vaccine after [enactment of the NVIA in] 1986 is more than double the proportion of people who experienced a serious complication from a disease before a vaccine for it was available. The difference is statistically significant and is likely greater because of underreporting.

DeLong’s analysis suggests that the Vaccine Act “gave firms greater incentives to capture the regulator: If consumers cannot sue firms for product liability, the only barrier to sales is regulatory approval.” 8

The NVIA protects vaccine makers from liability for “unavoidable” injuries caused by vaccines. The NVIA states in pertinent part:

No vaccine manufacturer shall be liable in a civil action for damages arising from a vaccine-related injury or death associated with the administration of a vaccine after October 1, 1988, if the injury or death resulted from side effects that were unavoidable even though the vaccine was properly prepared and was accompanied by proper directions and warnings. 9

In order to make sure the immunity from liability pill goes down easier for the public, the NVIA mandated that the Secretary of HHS “promote the development of childhood vaccines that result in fewer and less serious adverse reactions than those vaccines [presently] on the market.” 10

That requirement was supposed to be performed by a task force made up of the “Director of the National Institutes of Health [NIH], the Commissioner of the Food and Drug Administration [FDA], and the Director of the Centers for Disease Control [CDC].” 11

The NVIA statute required that “within 2 years after December 22, 1987, and periodically thereafter, the Secretary [of HHS] shall prepare and transmit to the Committee on Energy and Commerce of the House of Representatives and the Committee on Labor and Human Resources of the Senate a report describing the actions taken pursuant to subsection (a) during the preceding 2-year period.” 12

The NIH, FDA, and CDC scoundrels thumbed their noses at Congress. They violated the law by not filing the required reports with the U.S. Congress. Why did they not file the required reports? The only logical reason is that they did not meet as required, and they did not “promote the development of childhood vaccines that result in fewer and less serious adverse reactions than those vaccines [presently] on the market” 13 as required by the statute.

That is clear evidence that the component agencies of HHS (CDC, NIH, and FDA) have no interest in the development of safe vaccines for children.

Robert F. Kennedy Jr. discovered the scofflaws at HHS when he filed a Freedom of Information Act request with HHS requesting the reports prepared and transmitted to Congress as required by the NVIA. HHS refused to comply with the request. He sued HHS. 14 After being served with the lawsuit, HHS admitted that they never filed any required reports with Congress. 15 That means that the component agencies of HHS (CDC, NIH, and FDA) never formed the required task force and made no effort to see that vaccines were made safer.

The CDC, NIH, and FDA never met to develop a plan for safe vaccines for children. Why? Because CDC, NIH, and FDA know that the pharmaceutical companies have no interest making vaccines safe for children! Vaccines are unavoidably unsafe and the vaccine makers like it that way. Pharmaceutical companies get rich when people are made sick. It is a racket where they cause injury via their vaccines and then make the patent medicines to address the symptoms of the injuries they have caused. There was a fly in their ointment, and that was civil liability for the injuries they caused. The immunity granted by the NVIA solved that problem. Since the NVIA, the pharmaceutical companies have been off to the races creating one ineffective and unsafe vaccine after another.

As explained by Texans for Vaccine Choice, “[t]he [NVIA] removed all liability from vaccine manufacturers when their products injure or kill. Realizing that removing consumer accountability would eliminate any motivation for manufacturers to ensure their products are as safe and effective as they can possibly be, the Mandate for Safer Childhood Vaccines clause was added to the the Act as a check-and-balance.” But we now know that there is no check-and-balance. Robert F. Kennedy Jr. explains:

This speaks volumes to the lack of seriousness by which vaccine safety is treated at HHS and heightens the concern that HHS doesn’t have a clue as to the actual safety profile of the now 29 doses, and growing, of vaccines given by one year of age. 16

The CDC, when asked, was unable to provide any evidence that any childhood vaccine has ever been tested for safety using a placebo control. Indeed, Robert F. Kennedy Jr. points out that “not one of the 72 vaccines on the schedule mandated for our children, have been tested with a placebo.” There is a reason. No vaccine could ever survive being tested for safety and effectiveness against a placebo. The pharmaceutical companies know that their vaccines are not only ineffective, they are injurious. Research has shown that childhood vaccines cause injuries. 17 And that is by design. A design for which the U.S. Supreme Court has ruled the drug companies have immunity from civil liability.

The CDC, NIH, and FDA know it is a fool’s errand to try to convince the drug companies to manufacture something safe when to do so would undermine the drug companies’ pecuniary interests. The surreptitious goal of the drug companies is to make people sick through vaccines. That is why the CDC, NIH, and FDA had nothing to report to Congress regarding their efforts to develop vaccines with “fewer and less serious adverse reactions.” The goal of the vaccine makers is to cause injury. The pharmaceutical companies, CDC, NIH, and FDA all know that vaccines will unavoidably cause injuries. They have no interest in mitigating the damage caused by vaccines because those injuries make the pharmaceutical companies rich through the patent medicines they sell to address the injuries caused by the vaccines.

For example, on December 13, 2021, Pfizer announced:

Pfizer will acquire Arena, a clinical stage company developing innovative potential therapies for the treatment of several immuno-inflammatory diseases. Under the terms of the agreement, Pfizer will acquire all the outstanding shares of Arena for $100 per share in an all-cash transaction for a total equity value of approximately $6.7 billion. The boards of directors of both companies have unanimously approved the transaction. 18

Pfizer is acquiring a company that makes drugs that treat the very immuno-inflammatory injuries caused by Pfizer’s COVID-19 vaccine. Arena has drugs in the pipeline to treat cardio inflammatory diseases like myocarditis; the Pfizer COVID-19 vaccine has become notorious for causing myocarditis. 19 Also notable is Arena’s development of a drug (Termanogrel) to address microvascular obstructions, which several doctors have identified as the root cause of many illnesses resulting from Pfizer’s COVID-19 vaccine. 20 For example, Dr. Charles Hoffe, MD — who practices in British Columbia, Canada — explained in very simple terms how the mRNA COVID vaccines create the spike proteins which cause widespread microscopic blood clotting that will eventually kill many people within three years of taking the shots. 21 Pfizer now wants to get in on the action of offering overpriced patent medicines to give to desperate patients suffering from the deadly side-effects of their vaccine. How much more Machiavelian can you get?

Please be mindful that the COIVD-19 vaccine manufacturers are also protected from civil liability. The COVID-19 vaccines will be subjected to the even more exacting standards and limited compensation of the Public Readiness and Emergency Preparedness Act (PREP Act), which authorizes the Countermeasures Injury Compensation Program (CICP) to provide benefits to injured parties. A notable limitation under the CICP is that an injured party will be subjected to the statute of limitations that forecloses all legal actions not filed within one year of vaccination. 22 That is compared with the statute of limitations for an approved vaccine under the National Vaccine Injury Act (NVIA) of 3 years from the occurrence of the first symptom of injury from the vaccine. 23

Experts specializing in vaccine injury cases say that the bar for obtaining compensation is very high under the PREP Act. 24 Over the last ten years, 94% of injured patients who filed claims under the PREP Act received no compensation. 25 In reference to the virtually insurmountable hurdles erected under the CICP, Renée Gentry, director of the Vaccine Injury Litigation Clinic at the George Washington University Law School, said COVID-19 vaccine claimants have two rights: “You have the right to file,” she said. “And you have the right to lose.” 26 Altom Maglio, whose 22 lawyer law firm, Maglio Christopher & Toale, specializes in vaccine injury cases, says that you’re out of luck if you’ve suffered an injury related to any of the COVID-19 vaccines in receiving any compensation for your injury. 27 That all is not intended to suggest that the NVIA is fair. The NVIA has its own problems. Two out of three claims filed under the NVIA are denied. 28

A “declared public health emergency” as described in the PREP Act is the legal landscape under which the COVID-19 vaccine is being developed. Under the PREP Act, there is a moral hazard where manufactures of the COVID-19 vaccines will be protected from any liability for injuries caused by their COVID-19 vaccines. They have no financial incentive to make a vaccine that is safe or effective. They can sit back and count their billions in profits as they injure the public with impunity. The demand for the product is guaranteed by a marketplace that is rigged by the U.S. and state governments, which will pay for the vaccine and then mandate that the public consume that vaccine. The attitude of the vaccine manufacturers toward the consumer who is injured is “oh well, too bad, so sad, it sucks to be you.”

“For the love of money is the root of all evil: which while some coveted after, they have erred from the faith, and pierced themselves through with many sorrows.” 1 Timothy 6:10.

 

Endnotes

3 National Vaccine Injury Compensation Program, Children’s Health Defense, https://childrenshealthdefense.org/national-vaccine-injury-compensation-program/ (last visited on January 6, 2021).

4 Mary S. Holland, Liability for Vaccine Injury: The United States, the European Union, and the Developing World, Emory Law Journal, Vol 67, 2018, https://scholarlycommons.law.emory.edu/elj/vol67/iss3/3/.

5 Mary S. Holland, Liability for Vaccine Injury: The United States, the European Union, and the Developing World, Emory Law Journal, Vol 67, 2018, https://scholarlycommons.law.emory.edu/elj/vol67/iss3/3/.

6 National Vaccine Injury Compensation Program, Children’s Health Defense, https://childrenshealthdefense.org/national-vaccine-injury-compensation-program/ (last visited on January 6, 2021).

7 Mary S. Holland, Liability for Vaccine Injury: The United States, the European Union, and the Developing World, Emory Law Journal, Vol 67, 2018, https://scholarlycommons.law.emory.edu/elj/vol67/iss3/3/.

8 Mary S. Holland, Liability for Vaccine Injury: The United States, the European Union, and the Developing World, Emory Law Journal, Vol 67, 2018, https://scholarlycommons.law.emory.edu/elj/vol67/iss3/3/. Quoting Gayle DeLong, Is “Delitigation” Associated with a Change in Product Safety? The Case of Vaccines, Rev. Ind. Org. (June 14, 2017).

11 42 U.S.C. § 300aa–27.

12 42 U.S.C. § 300aa–27.

13 42 U.S.C. § 300aa–27.

14 RFK, Jr. Proves HHS is in Violation of the “Mandate for Safer Childhood Vaccines” as Stipulated in the Vaccine Injury Compensation Act, Children’s Health Defense, September 13, 2018, https://childrenshealthdefense.org/child-health-topics/federal-failures/rfk-jr-proves-hhs-is-in-violation-of-the-mandate-for-safer-childhood-vaccines-as-stipulated-in-the-vaccine-injury-compensation-act/. ICAN v. HHS, Complaint for Declaratory and Injunctive Relief, April 12, 2018, https://childrenshealthdefense.org/wp-content/uploads/rfk-complaint-against-united-states-department-of-health-and-human-services.pdf. See also ICAN & RFK, Jr. Call Out DHHS for Vaccine Safety Violations, Texans for Vaccine Choice, July 18, 2018, https://texansforvaccinechoice.com/ican-rfk-jr-call-out-dhhs-for-vaccine-safety-violations/.

15 ICAN v. HHS, Stipulation, July 9, 2018, https://childrenshealthdefense.org/wp-content/uploads/rfk-hhs-stipulated-order-july-2018.pdf.

16 RFK, Jr. Proves HHS is in Violation of the “Mandate for Safer Childhood Vaccines” as Stipulated in the Vaccine Injury Compensation Act, Children’s Health Defense, September 13, 2018, https://childrenshealthdefense.org/child-health-topics/federal-failures/rfk-jr-proves-hhs-is-in-violation-of-the-mandate-for-safer-childhood-vaccines-as-stipulated-in-the-vaccine-injury-compensation-act/.

17 Edward Hendrie, Study Shows That Vaccinated Children Are Significantly Less Healthy Than Unvaccinated Children, December 20, 2020, https://greatmountainpublishing.com/2020/12/20/study-shows-that-vaccinated-children-are-significantly-less-healthy-than-unvaccinated-children/. Edward Hendrie, Vaccines Increase Mortality of Infants, August 17, 2020, https://greatmountainpublishing.com/2020/08/17/vaccines-increase-mortality-of-children/. Edward Hendrie, Vaccines Cause Autism and Allergies, August 5, 2020, https://greatmountainpublishing.com/2020/08/05/vaccines-cause-autism-and-allergies/.

18 Pfizer to Acquire Arena Pharmaceuticals, December 13, 2021, https://www.pfizer.com/news/press-release/press-release-detail/pfizer-acquire-arena-pharmaceuticals.

19 Edward Hendrie, Follow the SILENCE: Paper Proving That COVID-19 Vaccines Cause Myocarditis Is Removed From Publication Without Explanation, October 31, 2021, https://greatmountainpublishing.com/2021/10/31/follow-the-silence-paper-proving-that-covid-19-vaccines-cause-myocarditis-is-removed-from-publication-without-explanation/. See also Edward Hendrie, The FDA and Pfizer Concealed Evidence That COVID-19 Vaccines Will Cause Myocarditis in Children, November 7, 2021, https://greatmountainpublishing.com/2021/11/07/the-fda-and-pfizer-concealed-evidence-that-covid-19-vaccines-will-cause-myocarditis-in-children/.

20 Pfizer buys immuno-inflammatory firm Arena Pharmaceuticals for $6.7b, December 13, 2021, Outsourcing-Pharma, https://www.outsourcing-pharma.com/Article/2021/12/13/Pfizer-buys-immuno-inflammatory-firm-Arena-for-6.7b.

21 Edward Hendrie, Doctor Finds That His Patients Have Permanent Organ Damage from Blood Clots Caused by COVID-19 Vaccines, Great Mountain Publishing, October 23, 2021, https://greatmountainpublishing.com/2021/10/23/doctor-finds-that-his-patients-have-permanent-organ-damage-from-blood-clots-caused-by-covid-19-vaccines/, quoting CFT Team, Doctor Warns How COVID mRNA ‘Vaccines’ Will Cause Delayed Strokes & Heart Attacks — ‘The Worst Is Yet To Come’, July 14, 2021, https://christiansfortruth.com/doctor-warns-how-covid-mrna-vaccines-will-soon-cause-strokes-heart-attacks-the-worst-is-yet-to-come/.

22 Countermeasures Injury Compensation Program, Request for Benefits Form Instructions, OMB Control No. 0915-0334, Expiration Date: 3/31/2023, https://www.hrsa.gov/sites/default/files/hrsa/cicp/cicp-request-form-instructions.pdf.

23 42 U.S. C. § 300aa–16.

24 McKenzie Sigalos, You Can’t Sue Pfizer or Moderna If You Have Severe Covid Vaccine Side Effects. The Government Likely Won’t Compensate You for Damages Either, CNBC, December 17, 2020, https://www.cnbc.com/2020/12/16/covid-vaccine-side-effects-compensation-lawsuit.html.

25 McKenzie Sigalos, You Can’t Sue Pfizer or Moderna If You Have Severe Covid Vaccine Side Effects. The Government Likely Won’t Compensate You for Damages Either, CNBC, December 17, 2020, https://www.cnbc.com/2020/12/16/covid-vaccine-side-effects-compensation-lawsuit.html.

26 Megan Redshaw, Injured by a COVID Vaccine? Want Financial Compensation? Too Bad, Says Injury Compensation Law Firm, The Defender, July 1, 2021, https://childrenshealthdefense.org/defender/covid-vaccine-injury-no-compensation-program/.

27 Megan Redshaw, Injured by a COVID Vaccine? Want Financial Compensation? Too Bad, Says Injury Compensation Law Firm, The Defender, July 1, 2021, https://childrenshealthdefense.org/defender/covid-vaccine-injury-no-compensation-program/.

28 Vaccine Injury Fund: Lessons From a Vaccine Lawyer-“Covered” Vaccines in the Court (and the DtaP), Widman Law Firm, https://www.widmanlawfirm.com/vaccine-injury-fund-lessons-from-a-vaccine-lawyer-covered-vaccin.html (last visited on August 28, 2021).

 

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Medical Sleezballs

Medical Sleezballs

by Dr. Mark Sircus
January 28, 2022

 

Sleezballs is too mild a term for the scum of the Earth who have taken over the field of medicine and public health. Just for starters, Fauci and Gates are running neck and neck for the most disgusting examples of what humans can become, and the CEO of Pfizer seems to take the cake for the number one medical monster of history. This list goes on and down into the rank and file of medical doctors who have thrown their brains away so they can ignore all the suffering and dying that COVID vaccines are bringing to the public.

A complaint with the International Criminal Court (ICC) accused 16 individuals of genocide, crimes against humanity, war crimes, and crimes of aggression. The 16 defendants include Dr. Anthony Fauci, Dr. Peter Daszak, Bill and Melinda Gates, the CEOs of Pfizer, Moderna, AstraZeneca and Johnson & Johnson, U.K. Prime Minister Boris Johnson along with several other British authorities, as well as the presidents of the Rockefeller Foundation and the World Economic Forum.

Hitler’s medical monsters were hung after the Nuremberg Trials, and it’s anyone’s guess how far this and other legal processes will go against our present crop of medical monsters. However, in terms of the gain of function research that medical devils who invested billions in creating COVID, we could line up the nasty deeds of all the evil men in history and still not balance the scales. So it is now or never for medicine, humanity, truth, justice, and the prevalence of good over evil.

The whole game of detracting the reality of this pandemic resulting from lab-created gain of function research is so the principal people involved would not be shot on sight. Die from taking one of these experimental COVID shots, and the chances are excellent your life insurance company will rule death by suicide and not pay your family the benefits.

Its insane actions now are killing people while seeking to punish those who refuse to walk sheepishly into America’s version of the gas chamber, the Anthony Fauci “vaccines.” ~ James Howard Kunstler

No writer can vomit enough bad words to address the glee of Fauci as he predicts vaccinating babies with COVID shots. No one can cry enough tears for the mothers who trusted their doctors only to lose their babies in the womb. There must be three thousand of them. Is anyone in the world of medicine crying for them? Have we gotten so stone cold?

U.S. health officials claim no one has died due to the COVID jabs proving to the world how deliberately blind influential medical and health leaders can be. They are standing at the edge of a precipice because official vaccine adverse event reporting systems in Europe, England, and America easily together report 50,000 deaths and millions of severe vaccine reactions.

But yes, anyone can remain a complete idiot and pretend COVID vaccines are safe and effective. Did anyone ever guess how many complete idiots there were in modern medicine and public health two years ago?

If anyone thinks I am exaggerating things a bit, read: On January 1, 2022, video announcement Dr. Reiner Fuellmich— a U.S.-German consumer protection trial lawyer and co-founder of the German Corona Extra-Parliamentary Inquiry Committee announced they now have in their possession damaging data, “enough to dismantle the entire vaccine industry.”

How Bad Can the Bad Be?

Fuellmich even has evidence that the vaccine makers were using different lot numbers to carry out an experiment within an experiment, unbeknownst to the public. According to Fuellmich, it looks like an experiment to determine the dosage needed to kill and maim people. In other words, people have not been getting identical products. Different lots or batches contain different dosages and even different ingredients. It looks like five percent of the batches caused 100 % of the deaths.

Intracranial infection cases up 60-fold since vaccines rolled out.

A 10-year-old girl from São Paolo, Brazil, has suffered a cardiac arrest and was in critical condition 12 hours after taking a dose of the Pfizer vaccine. Following the incident, the municipality of Lençóis Paulista suspended the vaccination of children aged between 5 and 11 years old for seven days. However, the Government of São Paulo and the Ministry of Health claimed that the cardiac arrest was not caused by the COVID vaccine but by a mysterious Martian ray gun. After all, Pfizer vaccines are safe, so it is impossible they could be the cause of such problems.

Conclusion

James Howard Kunstler writes, “The American people have been played backward and forwards, inside and out, through and through, and up and down; driven to the very edge of national suicide by a combine of enemies within and without. If China’s CCP wanted to take maximum advantage of a weakened, confused USA, they couldn’t have found more zealous help-mates than the seditious Democratic Party, along with Dr. Anthony Fauci’s treasonous public health empire, the murderous pharmaceutical companies, the recklessly dishonest news media, and a demonic host of federal agencies, especially the three-stooge “Intel Community” — the CIA (Moe), DOJ (Larry), FBI (Curley) — plus the many secret horror chambers in the Pentagon. Throw in the Big Tech tyrants, the Marxist mandarins on campus, and the satanic narcissists of Hollywood. Oh, and let’s not forget the evil principality of grift and swindling that is Wall Street.”

Time to pray to your Fauci candle, the saint of modern medicine, or is he the ultimate sleaze bag?

 

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Pfizer’s Poison Covid Pill

Pfizer’s Poison Covid Pill
Pfizer’s Paxlovid is being rolled out around the world. But in some ways it’s even more experimental than the pharma company’s Covid shot. For example, Health Canada — which, like the US FDA, is a decades-long ally of the pharma industry — admits that, “Not many people have taken Paxlovid. Serious and unexpected side effects may happen.” 

by Rosemary Frei, MSc
January 26, 2022

 

The gigantic truck convoys are rolling toward Ottawa, accompanied by wall-to-wall supporters and media coverage.

At the same time though, Pfizer’s Paxlovid is starting to be rolled out relatively quietly across North America, Europe, the U.K. and beyond.

It’s a set of pills for Covid – and it’s the second part of a one-two punch that started with the company’s  mRNA Covid shot.

Together, they’re powering Pfizer to dizzying levels of profit and market capitalization.

But there’s little if any ‘pax’ (the Latin word for peace) likely to come from these pills.

Paxlovid has been tested on very few people so far. It’s not being studied at all on vaccinated people or those who’ve had Covid. The pills negatively interact with many very widely used medications. Plus of course the studies are being manipulated to produce seemingly good results.

I’ve heard that behind the scenes some regulatory-agency employees are sick and tired of yielding to intense pressure from politicians, public-health officials and Big Pharma. They don’t want members of the public to take this extremely poorly studied and potentially very dangerous set of pills.

 

Each dose of Paxlovid consists of one pill of ritonavir — a repurposed old HIV drug — and two pills of a new drug named nirmatrelvir. Both of these drugs are protease inhibitors.

This nirmatrelvir/ritonavir combo was authorized for use in the U.S. by the Food and Drug Administration under an Emergency Use Authorization (EUA) on Dec. 22, 2021, and for use in Canada by Health Canada on Jan. 17, 2022.

And it’s rapidly being okayed elsewhere: for example, it got the nod in Israel on Dec. 26, 2021, South Korea on Dec. 27, 2021, the U.K. on Dec. 31, 2021, and France on Jan. 21, 2022.

It’s allowed in youth — 12 years of age and older — and adults in the U.S., Israel and South Korea. In other countries including the U.K. and Canada it’s authorized for people 18 years old and above.

(Note that authorization isn’t approval; it’s very rapid evaluation followed by the nod to let tens of millions of people take it, because supposedly we’re in an unprecedented public-health crisis akin to a war.)

Also, a test in a petri dish by Pfizer scientists showed it may have some effect on Omicron — see the first paragraph on page 36 of the Canadian Jan. 22 spec sheet (AKA product monograph) on it. Based on this very thin evidence, mainstream media are widely reporting that “the pills are expected to be effective against Omicron.”

 

The nirmatrelvir/ritonavir pills are being authorized for use by people who test positive for Covid, have mild or moderate symptoms and are deemed to be ‘at high risk for progression to severe COVID-19.’

But how does Pfizer define high risk?

Being 60 years of age or older. Or overweight. Or having high blood pressure. Or a number of other things – including having “other conditions or factors (i.e., race or ethnicity) that may place patients at high risk for progression.” (See page 8 of the Canadian Jan. 22 spec sheet.)

That’s an extremely broad definition.

 

Another alarming fact is that the U.S. and Canadian decisions to authorize nirmatrelvir/ritonavir were based only on interim analyses of an ongoing study. This trial started on Aug. 25, 2021, and is scheduled to finish on about April 24, 2022.

In total only approximately 1,000 people had been randomized to receive nirmatrelvir/ritonavir at the time U.S. and Canadian authorities gave it the thumbs up. 

(It’s very hard to decipher what the specific numbers are – both the Nov. 5, 2021, Pfizer news release describing the interim analysis examined by the FDA and the Jan. 17, 2022, Canadian product monograph — which has an interim analysis from a slightly later date — have a range of numbers, as well as several types of data analyses.)

Furthermore, only 13% of those small number were people 65 years of age or over, and just 3% were 75 and older. (See section 1.2, titled ‘Geriatrics,’ on page 4 of the Jan. 17, 2022, Canadian product monograph for Paxlovid.)

Plus, even those interim results were manipulated to the max in the study write-up (more on this below) – which in the case of the US was simply a Nov. 5, 2021, Pfizer news release.

 

 

 

And Pfizer didn’t even make public the original data it supplied to Health Canada, as far as I can determine. Furthermore, the company’s Jan. 17, 2022, news release announcing the authorization in Canada had very few details.

It was all very predictable.

That’s obvious from the fact that more than a month before the FDA authorization — on Nov. 18, 2021 — the US government signed a $5.3-billion deal for 10 million courses of nirmatrelvir/ritonavir (i.e., $530 US per course), pending FDA authorization.

Ditto in Canada: on Dec. 3, 2021, the Canadian government announced its pledge to buy an initial one million courses of nirmatrelvir/ritonavir from Pfizer, pending Health Canada authorization. That is worth about $690 million (Canadian dollars) when you do the math based on $530 US per course.  (A ‘course’ means the total number of doses needed to complete a treatment regimen.)

(The same announcement said the Canadian government also had signed an agreement with Merck to buy 500,000 courses of Merck’s Covid pill molnupiravir — with options for buying 500,000 more courses — also pending Health Canada authorization.)(Molnupiravir was authorized by the US FDA a short time later, on Dec. 23, 2021, despite significant concerns. Those include its low effectiveness, high toxicity and potential for women who take it during pregnancy to give birth to children with birth defects. The FDA authorized Merck to sell it for people aged 18 or over with mild to moderate Covid who test positive and are at ‘high risk’ of developing severe Covid. Health Canada has not yet given it the nod. And media report that other countries also are getting cold feet about it.)

 

There’s more. For example, nirmatrelvir/ritonavir hasn’t been tested at all in people who have been vaccinated and/or have had Covid. [corrected Jan. 28 – in the original I’d inadvertently incorrectly written ‘haven’t been vaccinated and/or haven’t had Covid.’]. Despite this, they are among the people that officials want first in line for it.

It also isn’t being tested at all in pregnant or breastfeeding women.

Pfizer states on page 12 of the product monograph that Paxlovid “should not be used in pregnant women unless the potential benefits outweigh the potential risks to the fetus.”

But there’s no such warning for the use of nirmatrelvir/ritonavir by breastfeeding women.

 

As I noted earlier in this article, each dose of Paxlovid consists of two tablets of nirmaltrelvir and one tablet of ritonavir. Each set of three pills is to be taken twice a day for five days, starting within five days of symptom onset.

Ritonavir has been used since 1996 in people who test positive for HIV. It is widely known to cause serious, life-threatening conditions such as pancreatitis, heart-rhythm problems, liver problems, severe skin rash and allergic reactions.

Yet nirmatrelvir/ritonavir hasn’t been studied in people with liver-function impairment. And neither Pfizer nor government officials are warning that nirmatrelvir/ritonavir should not be taken by, for example, people at risk of developing abnormal liver function (including those who have had hepatitis B, hepatitis C or elevated results on liver-function tests).

 

Instead, they’re putting on the front lines the frail, the elderly, and/or those who live in poverty or are otherwise disadvantaged.

For example, a Jan. 25 CBC News article reports that Canada’s deputy chief public health officer, Howard Njoo, recommends the first to receive the pills should be “people who are immunocompromised, 80 years of age and over, or [those] who may not have access to health care because of geographical or socioeconomic concerns[,] are first in line — regardless of vaccination status.” [Bolding added by me.]

Quebec is one of the first places poised to start using it in these vulnerable people. By March they’re expecting to receive enough of the pills to treat more than 25,000 people. That includes those with “serious conditions who cannot be vaccinated.” After that, they’ll open up the queue to others.

 

Therefore, it appears politicians, government officials and Pfizer are stoking demand using the same playbook as they did with vaccines.

They’re only making a relatively small number of pills available initially.

And the mainstream media are helping to hype it. For example one CBC report alone — by Montreal journalist Verity Stevenson on Jan. 18 — called it a “sought-after” drug that has been “lauded for its potential to reduce hospitalizations from the virus” via Pfizer’s reporting “that Paxlovid reduced the risk of hospitalization or death by an impressive 89 per cent compared with a placebo.”

And here’s another example of the overall very positive coverage; it’s in the Toronto Star today.

 

 

Jan. 25, 2022National Post article is somewhat of an exception: the author, Tom Blackwell, flags the problem of Paxlovid interfering with the effects of other medications (more on this below). However, he doesn’t mention most of the other major drawbacks of the pills.

 

Yet even the Canadian federal government admits, on its web page for the general public on the pill, that “Not many people have taken Paxlovid. Serious and unexpected side effects may happen. Paxlovid is still being studied, so it is possible that all the side effects are not known at this time.” [Bolding added by me.]

 

 

Further down on that same page, it says people should report any suspected side effects directly to Health Canada.

Unfortunately, however, we know from the vast under-reporting of serious effects and deaths from, for example, the Covid jabs, that it’s highly unlikely the feds will faithfully tally and publicly display all such reports.

For its part, the FDA asked Pfizer to report to it the “serious adverse events and all medication errors associated with the use of Paxlovid,” as part of the EUA. It also stipulated that healthcare facilities and healthcare providers receiving Paxlovid will track and report serious adverse events and medication errors. However, this also is very unlikely to result in a full and honest public reporting.

(The FDA also asked the company to provide the FDA with further trial results relating to safety and effectiveness until the study concludes in April.)

 

So they’re not even trying to pretend that it’s been shown to be safe and effective.

After all, this is the pharmacocene epoch of our planet’s history.

 

Here are three more red flags among the many surrounding Paxlovid:

  1. The US FDA omitted the important step of getting input from an advisory panel before giving an Emergency Use Authorization to Paxlovid.

That panel is called the Antimicrobial Drugs Advisory Committee. Members of the panel scrutinize pharma companies’ data on drugs the firms are seeking approval of. The panel’s meetings are public and are attended by media and others.

(In contrast, in the case of molnupiravir it was convened, at the end of November, 2021 [the members voted for it, 13 to 10; then on Dec. 23, 2021, the FDA authorized it].)

I found this out when I stumbled on a Jan. 6, 2022, SonsOfLibertyMedia.com article on Paxlovid. The article describes, among many other insightful information, a Dec. 22, 2021Bloomberg Law article on the controversy caused by the FDA skipping this important step.

The panel meeting usually is just a rubber stamp, but nonetheless skipping it is very unusual.

  1. In addition to being a protease inhibitor, ritonavir reduces the activity of a highly important enzyme called CYP3A4. CYP3A4 is produced in the liver. There, it’s central to metabolizing (i.e., breaking down) a large number of drugs and toxins; this is a necessary before the drugs and toxins can be cleared from the body.

Since ritonavir (and by extension Paxlovid) reduces CYP3A4’s activity, that means those large number of drugs and toxins will stay in the body longer.

The Canadian federal-government website on Paxlovid admits that “many medicines interact with Paxlovid. Taking Paxlovid with these medicines may cause serious or life-threatening side effects.” [Bolding added by me.]

In total, there are more than 100 medications that Pfizer says shouldn’t be taken with Paxlovid. They include very widely used ones like lidocaine, warfarin, phenobarbital, erythromycin, St. John’s wort, fentanyl, methadone, midazolam and prednisone.

  1. The study results in the Pfizer US Nov. 5, 2021, press release relied on ‘intent-to-treat’ statistical analyses. These are not at all rigorous.

If you look up what ‘intent-to-treat’ means, you’ll see it’s based on assuming that study subjects received the treatment, whether they in fact did or not. Many articles on this approach profess it to be solid. But objectively it is not at all. (I started to notice intent-to-treat analyses in medical research studies at least 20 years ago. It was — and still is, to my knowledge — a popular way to avoid honest reporting of the effects and efficacy of drugs being tested.)

And just to be clear, the Pfizer news-release study didn’t stop there – its intent-to-treat analyses use a ‘modified’ approach. Specifically they include, for example, people “who at baseline did not receive nor were expected to received COVID-19 therapeutic mAb [monoclonal antibody] treatment.”’

 

You can’t make this stuff up.

I sincerely hope that the employees who, behind the scenes, are pushing back against the pressure to let Paxlovid be given to many people will win the day.

 

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COVID Vaccines Causing Miscarriages, Cancer and Neurological Disorders Among Military, DOD Data Show

COVID Vaccines Causing Miscarriages, Cancer and Neurological Disorders Among Military, DOD Data Show
Attorney Thomas Renz on Monday told a panel of experts that data provided to him by three whistleblowers show COVID-19 vaccines are causing catastrophic harm to members of the U.S. military.

by Pam Long, The Defender
January 26, 2022

 

Attorney Thomas Renz on Monday told a panel of experts that data provided to him by three whistleblowers show COVID-19 vaccines are causing catastrophic harm to members of the U.S. military while not preventing them from getting the virus.

Following Monday’s panel discussion on COVID vaccines and treatment protocols, led by Sen. Ron Johnson (R-Wis.), Renz summarized data obtained from the Defense Medical Epidemiology Database (DMED), the military’s longstanding epidemiological database of service members.

The data show:

  • Miscarriages increased 300% in 2021 over the previous five-year average.
  • Cancer increased 300% in 2021 over the previous five-year average.
  • Neurological disorders increased 1000% in 2021 over the past five-year average, increasing from 82,000 to 863,000 in one year.

The whistleblowers provided the data knowing they would face perjury charges if they submitted false statements to the court in legal cases pending against the U.S. Department of Defense (DOD).

Renz told the panel a “trifecta of data” from the DMED, the DOD’s military-civilian integrated health database, Project SALUS, along with human intelligence in the form of doctor-whistleblowers suggest the DOD and the Centers for Disease Control (CDC) and Prevention have withheld COVID vaccine surveillance data since September 2021.

“Our soldiers are being experimented on, injured and sometimes possibly killed,” Renz said.

Following Renz’s presentation, attorney Leigh Dundas reported evidence of the DOD doctoring data in DMED to conceal cases of myocarditis in service members vaccinated for COVID.

The military whistleblowers reported a DMED search of “acute myocarditis” resulted in 1,239 cases in August 2021, but the same search in January 2022 resulted in only 307 cases.

Cardiologist Dr. Peter McCollough, commenting on Renz’s presentation, told the panel myocarditis is being falsely described as mild and transient when in reality it causes permanent heart damage and is life-limiting in most cases.

The military did not take any safeguards for the most at-risk age group for vaccine-induced myocarditis — 18- to 24-year-olds.

Renz also highlighted a broader data set from Project SALUS, run by the DOD in cooperation with the Joint Artificial Intelligence Center (JAIC), which sends weekly reports to the CDC.

Project SALUS analyzed data on 5.6 million Medicare beneficiaries aged 65 or older. Data were aggregated from Humetrix, a real-time data and analytics platform that tracks healthcare outcomes.

According to Renz, the Project SALUS data as of late last year show:

“71% of new cases are in the fully vaccinated, and 60% of hospitalizations are in the fully vaccinated. This is corruption at the highest level. We need investigations. The Secretary of Defense needs investigated. The CDC needs investigated.”

The Humetrix presentation summarizing the data in Project SALUS, “Effectiveness of mRNA COVID-19 vaccines against the Delta variant among 5.6M Medicare beneficiaries 65 years and older” (Sep. 28, 2021) has not been made public.

The Project SALUS report also included data on natural immunity, stating the vaccines have waning protection. The data also showed an upward trend of breakthrough cases suggesting booster shots could contribute to prolonging the pandemic.

“Breakthrough infection rates 5 to 6 months post-vaccination are twice as high as 3-4 months post-vaccination,” the report said.

According to the Humetrix overview of the Project SALUS data, Congress must investigate vaccine failure, along with increased risk reported for breakthrough cases (or vaccine failure) in North American Natives, Hispanics, Blacks, and males.

People with kidney disease, liver disease, heart disease and cancer treatment, along with people over age 75 are the most likely to experience breakthrough cases, while medical authorities advocate vaccines to these same populations to allegedly “protect the vulnerable.”

Project Salus reported the vaccines were only 41% effective. This low level of infection prevention needs to be analyzed against the counterweight of a threefold to tenfold increase in chronic disease signaled in DMED.

The U.S. Food and Drug Administration (FDA) requires only two adequate and controlled studies to approve a biologic, even if those studies are industry-sponsored.

The FDA now has data from the entirety of 3 million people employed by the DOD and 5 million people in Medicare. This data serves as independent substantiation that scientific fraud has occurred.

Based on this data, the FDA must revoke the Emergency Use Authorization for the ModernaPfizer and Johnson & Johnson COVID vaccines, and the Biologics License Application for Pfizer’s Comirnaty vaccine.

It would be wrong for the FDA to extrapolate the industry’s clinical trial data to pediatrics without halting the use of the vaccines and conducting an investigation based on this real-world data.

Watch Renz’s testimony here:



 

Pam Long is graduate of USMA at West Point and is an Army Veteran of the Medical Service Corps.

The views and opinions expressed in this article are those of the authors and do not necessarily reflect the views of Children’s Health Defense.

 

©January 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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Doctors, What Are They Good For?

Doctors, What Are They Good For?

by Dr. Sam Bailey
January 25, 2022

 

People keep asking me where they can find a good doctor.

The real question they need to ask is whether they even need a doctor, because the medical system has become detached from health. But has this happened recently or did medicine go off the rails long ago?



References:

“Terrain” the film – register here

  1. A long shadow: Nazi doctors, moral vulnerability and contemporary medical culture, 2012
  2. One in 20 East German doctors spied on patients or colleagues, 2007
  3. The burden of the past: problems of a modern historiography of physicians and medicine in Nazi Germany, 1987
  4. Medical and Dental Councils statements
  5. Deadly Medicines and Organised Crime
  6. Failing the Public Health — Rofecoxib, Merck, and the FDA, 2004
  7. Expression of Concern: Bombardier et al., “Comparison of Upper Gastrointestinal Toxicity of Rofecoxib and Naproxen in Patients with Rheumatoid Arthritis,” 2005
  8. Vioxx Killed Half a Million? The Facts Are Grim, 2012
  9. Doctors’ strikes and mortality: A review, 2008
  10. Why Do Patients Stop Dying When Doctors Go on Strike?, 2015

 

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‘We Got the World Behind Us’: Massive Support for Truckers Travelling Through Alberta

‘We Got the World Behind Us’: Massive Support for Truckers Travelling Through Alberta
Thousands came out in towns and cities across Alberta to show their support for the convoy.

by Mocha Bezirgan, Rebel News
January 25, 2022

 



With the Truckers Freedom Convoy having arrived in Calgary, Alberta the night before, the second day embedded with the group started around 9 a.m. at a Flying J gas station surrounded by 2000–3000 freedom-loving Canadians showing their support for this movement.

Pastor Artur Pawlowski, who Rebel News viewers should be very familiar with, delivered a powerful speech (as per usual), fanning the flames of freedom before the convoy departed, which left the crowd in a frenzy of energy.

After that, we joined the convoy, and hit the road.

Continuing onwards, it suddenly became very clear that potentially everyone had underestimated the amount of traction and momentum the truckers rebellion carried with them.

The driving force behind this convoy, no pun intended, is not only a sight to be hold, but a pleasure to bare witness too.

The commitment and determination of those aligned with the Truckers Freedom Convoy was truly something to behold.

See more of our coverage at ConvoyReports.com, as we travel across the country bringing you the other side of this truly inspiring story.

 

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The Jab-5G Knock Out Punch

The Jab-5G Knock Out Punch

by Rosanne Lindsay, Naturopath
January 24, 2022

 

When the media reports that illegal mandates are ending, it is necessary to read between the lines. Because there is always more to the story.

On January 19, 2022, UK Prime Minister Boris Johnson was reported to say that so-called Plan B measures would lapse on Jan. 26, as face masks would not be legally enforced anywhere and COVID passes would not be mandatory.

Our scientists believe it is likely that the Omicron wave has now peaked nationally… because of the extraordinary booster campaign, together with the way the public have responded to the Plan B measures, we can return to Plan A.

While this may sound positive on its surface, the idea of legally enforcing illegal mandates is an oxymoron. By reading between the lines, we see that OMICRON is an anagram for moronic and oncomir (i.e., tumor forming). And the wave represents 5G mm wave frequencies.

If mandates are on the outs, then they have served a purpose, by design. What’s next? In the world of sports metaphors, it is the jab followed by the right-hook punch, which translates to a strategy of injections plus added wave frequencies.

5G Upgrade

U.S. Telecom services have expanded to C-Band or Midband 5G.

The new, faster level of 5G connectivity will significantly augment Verizon’s “5G Ultra Wideband” network, which, until now, has relied solely on extremely-fast-but-very-hard-to-find millimeter wave spectrum.

On Jan 18th, the American media reported that AT&T (T.N) and Verizon Communications (VZ.N) temporarily deferred turning on some wireless towers near key airports (or 10% of network) “to avert a significant disruption to U.S. flights as they roll out 5G service that will bring faster wireless service to tens of millions of people.” British Airways cancelled US flights over similar concerns.

Did the Federal Aviation Administration fail to plan for this oversight?

The Jab-5G Right Hook Punch

The new mRNA injections are known to contain graphene oxide (nanometals) which is part of a self assembly process of nanobots (i.e., nanotechnology). Graphene oxide acquires magnetic properties and is extremely toxic. It’s toxicity is dependent on the electromagnetic radiation it absorbs. Once injected, it has an affinity for the central nervous system and electrical organs, such as the heart. Consequences include fainting, arrhythmias, or syncope, and sudden death. To understand why boosters will be recommended every 3 months to keep the graphene oxide in the body, watch this explanation. This is the jab.

The Jab-5G Strategy could be a very effective knock-out punch for a global government to exert more control over large populations, including the depletion of the human species. This is a crime against humanity, a strategy first tested in China and South Korea in 2019.

On June 29, 2019, China’s new law, The Vaccines Administration Law was promulgated. Soon after, 2 billion doses of COVID vaccine were deployed in China, enough for 1 billion people, or 76 percent of China’s 1.4 billion population.

Later, in November 2019, China launched the largest 5G network, under the concept of “connectivity and faster downloads.” Reports followed of people suddenly “dropping dead in the street,” whether true or not. By March 31, 2020, China’s national vaccine tracking system was launched.

Nine months later, by mid-December 2020, 2 billion doses of COVID vaccine were deployed in the U.S. The CDC claims 210 million of 310 million people are “fully vaccinated.” Two years later, on January 19, 2022, the 5G network was switched on.

By now, it is widely known that 5G towers utilize frequencies that affect all life at the level of DNA. These are microwave, radio wave frequencies that range from 3 kilohertz (kHz) up to 300 gigahertz (GHz). Within this range is the range is the absorption spectrum of oxygen molecules, at 60 GHz.

Since 2008, 5G research scientists have shown that the coiled portion of the sweat duct in the upper skin layer is regarded as a helical antenna in the sub-THz band. In their December 2019 article in Bio Heat Transfer, they warn:

One must consider the implications of human immersion in the electromagnetic noise, caused by devices working at the very same frequencies as those, to which the sweat duct (as a helical antenna) is most attuned. We are raising a warning flag against the unrestricted use of sub-THz technologies for communication, before the possible consequences for public health are explored.

DNA, Water & Your Health

Helical is also a word used to describe DNA, in skin cells or any cell. DNA is more than a series of four base pairs (CGAT). DNA is a transmitter, a receiver, and a translator of information. There is a deep relationship between DNA, water, and your health. Water molecules surround the structure of your DNA, through hydrogen bonds, making it highly responsive to stimuli, such as light frequencies. [Read more in The Nature of Healing].

Now, add cell towers that emit 5G frequencies strategically placed atop water towers all over the U.S. What happens when the structure of water is altered by incoherent frequencies before entering your body? What happens to your DNA? Do you need to consider a safer water source? Do you wonder why your government has not vetted 5G technology for safety and health as it relates to water or air travel?

The use of the 60 GHz RF (Radio Frequency) band along with EIRP (Effective Isotropic Radiated Power) include the following world locations: US, Canada, Europe, Japan, Australia, China, South Korea. Note, Switzerland halted the rollout of 5G over health concerns to further test the potential impact of radiation exposure.

The symptoms of sub-THz band frequencies appears similar to “COVID” symptoms and includes: lack of oxygen, seizures, and a phlegm-less cough. While the 5G frequency network has been launched in every continent without verifying safety, millions of people have consented to experimental mRNA vaccines that utilize “gene therapy” technology.

Knock-Out Punch

An Editorial published in the July 2020 J Biol Regul Homeost Agents, suggests that 5G waves are a critical factor to sudden deaths attributed to an influenza-like condition dubbed COVID. Read that article in full (that has been retracted), here: 5G Technology and Induction of Coronavirus in Skin Cells:

In this research, we show that 5G millimeter waves could be absorbed by dermatologic cells acting like antennas, transferred to other cells and play the main role in producing Coronaviruses in biological cells. DNA is built from charged electrons and atoms and has an inductor-like structure. This structure could be divided into linear, toroid and round inductors. Inductors interact with external electromagnetic waves, move and produce some extra waves within the cells.

The shapes of these waves are similar to shapes of hexagonal and pentagonal bases of their DNA source. These waves produce some holes in liquids within the nucleus. To fill these holes, some extra hexagonal and pentagonal bases are produced. These bases could join to each other and form virus-like structures such as Coronavirus. To produce these viruses within a cell, it is necessary that the wavelength of external waves be shorter than the size of the cell. Thus 5G millimeter waves could be good candidates for applying in constructing virus-like structures such as Coronaviruses (COVID-19) within cells.

The authors write:

When an electromagnetic wave passes the cell membrane and the nuclear membrane, it induces an extra magnetic field within the DNA inductor and interacts with its fields.

A DNA is built from charged particles and according to laws of physics, by any motion of these particles, some electromagnetic waves emerge. Also, the structure of a DNA is similar to the structure of an inductor in a receiver and can produce some waves. Thus, a DNA could emit some waves and interact with external waves. However, most waves have a length more than the size of cells and pass them without any effect. Only limited waves with lengths smaller than millimeter could penetrate into cell membrane and interact with DNA inductors. These wavelengths could be observed in 5 G technology.

After the jab was rolled out in the U.S. in December 2021, doctors presented strong evidence of the destructive effects of the immune system, at the Doctors for COVID Ethics Symposium.  Introducing a synthetic spike protein into the body, via injection, directs the DNA to express proteins it was never meant to express. The Doctors for COVID Ethics (DCE) write:

A natural infection with coronavirus will, in most individuals, remain localized to the respiratory tract. In contrast, the vaccines cause cells deep inside our body to express the viral spike protein, which they were never meant to do by nature. Any cell which expresses this foreign antigen will come under attack by the immune system, which will involve both IgG antibodies and cytotoxic T-lymphocytes.

These results support a November 2021 study in Abstract 10712: Mrna COVID Vaccines Dramatically Increase Endothelial Inflammatory Markers and ACS Risk as Measured by the PULS Cardiac Test: a Warning.

Note: Millimeter waves are currently used by the U.S. Army as a crowd control dispersal weaponry called Active Denial Systems.

Solutions

With contradictory media messages that serve to confuse, know who you are. Under your skin suit, you are first and foremost a part of Nature, a being of light frequency. Every thought, emotion, and action, is a frequency you emit through your DNA, your biological internet. Understand that artificial frequencies introduced into the environment are scrambling and altering your natural frequency. How do you negotiate life in a boxing ring

Return to Nature. Eliminate all WI-fi devices, or hard wire them. If you have a Smart meter on your house or apartment, you can block those waves using a Smart Meter Guard or Block. Eat clean, organic foods to keep your immune system at peak performance. Drink clean, filtered water. Use herbs that promote a strong immune system. Research the use of the mineraloid, Shungite, as protection carried on your body. Make sure you cleanse Shungite regularly. All of these tools work to help to maintain a strong natural frequency.

Stop watching and listening to media talking heads. Shut off the Tel-A-Vision, which emits a low frequency for TV programming. Scrutinize leaders who offer no real solutions, but only fear based sound bites. Raise your own frequency by spending time in Nature, and by meditating to keep you from beLIEving the propaganda.

Understand that you are your own healer and this life is the self-healing journey.  Part of the journey is to see through fear-based illusions. Once you find your center, you can ground yourself, like a martial artist or kick boxer. Then you can duck the jabs and right hooks. You can avoid the knock-out punches altogether.

 

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Rosanne Lindsay is a Naturopath, writer, earth keeper, health freedom advocate and author of the books The Nature of Healing, Heal the Body, Heal the Planet and  Free Your Voice, Heal Your Thyroid, Reverse Thyroid Disease Naturally.

Rosanne Lindsay is available for consultation through Turtle Island Network.  Subscribe to her blog at natureofhealing.org.

 

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cover image based on creative commons work of kalhh & BedexpStock




Nano-Man

Nano-Man

by Spacebusters
January 25, 2022

 



A deep dive expose’ into radioactive lithium hydrogel nasal test swabs, injectible quantum dots, nanorouters, UPC bluetooth and the UN Agenda 21 Great Reset Nano-man.

Plus a look at why the Government might hate Ivermectin.

 

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cover image credit: julientromeur / pixabay


See related by Spacebusters:



The story of the 4th Industrial Modified Reset Man.

What’s been put up your nose in nano dust “test swabs” and in your mRNA, 4th Industrial Revolution, Great Reset, how the nano dust tech works, it’s all in there.

 


 See related work by La Quinta Columna

See related work by Mik Andersen




Thailand Government Will Pay Compensation for Vaccine “Side Effects” and Deaths: One Billion Baht

Thailand Government Will Pay Compensation for Vaccine “Side Effects” and Deaths: One Billion Baht

by Bangkok Post [December 28, 2021]
commentary by Michel Chossudovsky, Global Research
January 25, 2022

 

What is important in this report by the Bangkok Post is that the Royal Thai Government (member state of the UN and the WHO) firmly acknowledges the deaths and adverse events affecting Thais who have taken the vaccine jab. 

“Out of the 11,707 people who filed a claim with authorities, 8,470 people, or 72.3% of all claimants, have been compensated”. 

1,962 individuals, namely 23% of the claimants “were left permanently paralysed or died after receiving their Covid-19 shot”. 

The implications are far-reaching. 

People in Thailand and around the World will be informed of the decision of the Thai government and will refuse to take the jab.

And this decision establishes a legal precedent. Class action law suits as well criminal charges against Big Pharma and corrupt governments are forthcoming.  

National governments will no longer be able to deny the devastating impacts of what is widely recognized as a killer vaccine. 

Nor will they be able to impose a vaccine passport. 

Also, if you have any doubts read  the report on the“Confidential Report” by Pfizer released under Freedom of Information which confirms unequivocally the criminal nature of the mRNA vaccine which has resulted in a Worldwide wave of deaths and injuries:

“What is contained in  Pfizer’s “confidential” report is detailed evidence on the impacts of the “vaccine” on mortality and morbidity. This data which emanates from the “Horse’s Mouth” can now be used to confront as well formulate legal procedures against Big Pharma, the governments, the WHO and the media.”

~ Michel Chossudovsky, Global Research, January 25, 2022

Our thanks to the Bangkok Post for bringing this article to our attention.

 


Almost one billion baht in compensation has been paid out to Thais who suffered adverse side effects from the Covid-19 vaccine over the past eight months, says the National Health Security Office (NHSO).

About 927 million baht [28 million dollars] in compensation was approved between April 5 and Dec 26, it said.

Out of the 11,707 people who filed a claim with authorities, 8,470 people, or 72.3% of all claimants, have been compensated, said Atthaporn Limpanyalert, spokesman and deputy secretary-general of the NHSO.

The claims were grouped into three categories, the first being claims filed by vaccine recipients who reported mild to moderate side effects after receiving their Covid-19 jab.

In total, there are 6,298 people in this category, Dr Atthaporn said, noting they are eligible to receive no more than 100,000 baht in compensation from the government.

The second category, Dr Atthaporn said, comprises claims filed by those who experienced temporary paralysis and/or loss of other bodily functions after they were vaccinated, noting the 210 people in this category will receive up to 240,000 baht in compensation.

The final category is made up of individuals who were left permanently paralysed or died after receiving their Covid-19 shot. The 1,962 people in this category are eligible to claim up to 400,000 baht in compensation.

Out of the 11,707 claims filed, 1,752 were rejected because the claimants failed to meet the criteria set out — 615 of whom have lodged an appeal.

Claimants are entitled to seek the compensation for themselves and/or relatives without having to prove without doubt that their health condition was indeed caused by receiving the Covid vaccine.

Dr Atthaporn said the NHSO has set up 13 committees throughout the country to process the compensation claims, adding compensation will be paid within five days of the petition being approved.

Meanwhile, the NHSO transferred an additional 31.3 billion baht to 1,942 medical facilities and hospitals nationwide in October and November to help the fight against Covid-19, said NHSO secretary-general Jadet Thammathat-aree.

 

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cover image credit: AdenArdenrich / pixabay




How Billions in COVID Stimulus Funds Led Hospitals to Prioritize ‘Treatments’ That Killed, Rather Than Cured, Patients

How Billions in COVID Stimulus Funds Led Hospitals to Prioritize ‘Treatments’ That Killed, Rather Than Cured, Patients
In the second half of an interview this month on Del Bigtree’s “The Highwire” — “COVID-19: Following the Money” — policy analyst A.J. DePriest reported on the impact of billions in COVID stimulus funds, which, according to some doctors and lawyers, turned hospitals and medical staff into “bounty hunters,” and COVID patients into “virtual prisoners.”

by Children’s Health Defense Team, The Defender
January 24, 2022

 

As reported last week by The Defender, federal monies from the 2020 and 2021 COVID stimulus bills dramatically reshaped K-12 educational priorities, turning American school officials into lackeys for federal agencies more intent on masking and vaccinating every last child than on supporting meaningful education.

So, too, with the stimulus-induced reshaping of hospital priorities.

In the second half of a January interview on Del Bigtree’s “The Highwire” — “COVID-19: Following the Money” — policy analyst A.J. DePriest reported on the untoward consequences set into motion as a result of COVID funds provided to hospitals.

Managed by the U.S. Department of Health and Human Services (HHS), the federal government allocated a total of $186.5 billion to the Provider Relief Fund (PRF), with two-thirds ($121.3 billion) disbursed as of January 2022.

The first tranche of $50 billion for hospitals and other Medicare providers — “for healthcare-related expenses or lost revenues … attributable to COVID-19” — began flying out the door in April 2020.

Almost immediately, alert doctors and astute journalists warned the Medicare add-on payments built into the relief package created perverse incentives unfriendly to patients’ interests.

As summarized by Dr. Scott Jensen — former Minnesota state senator and current gubernatorial candidate — “anytime healthcare intersects with dollars it gets awkward.”

Nearly two years down the road, the “awkwardness” is increasingly difficult to hide.

In the view of DePriest and many others, HHS’s stimulus slush fund has been every bit as dangerous for hospital patients as the U.S. Department of Education’s handouts have been for the nation’s schoolchildren.

Making out like bandits

Dr. Elizabeth Lee Vliet and Ali Shultz, J.D., who wrote a widely distributed op-ed in late 2021 for the Association of American Physicians and Surgeons (AAPS), summed up the disturbing situation prevailing in hospitals. The AAPS’s professional calling card is its “dedication to the highest ethical standards of the Oath of Hippocrates.”

Not mincing their words, the two argued that Centers for Medicare and Medicaid Services (CMS) payment directives turned hospitals and medical staff into “bounty hunters,” and COVID patients into “virtual prisoners.”

Highlighting the slew of CMS add-ons and other incentives established with the Coronavirus Aid, Relief and Economic Security (CARES) Act — and also the Paycheck Protection Program and Health Care Enhancement Act (PPPHCEA) — they emphasized the payments hinge on hospitals’ willingness to slavishly follow the National Institutes of Health’s (NIH’s) guidelines “for all things related to COVID-19.”

As itemized by Vliet and Shultz, compliant hospitals garner CMS payments for:

  • Each completed diagnostic test (required in the emergency room or upon admission).
  • Each COVID-19 diagnosis.
  • Each COVID admission.
  • Use of the intravenously administered Gilead drug remdesivir (brand name Veklury), which yields a 20% bonus payment on the entire hospital bill.
  • Mechanical ventilation.
  • COVID-19 listed as cause of death.

Citing a Becker’s Hospital Review breakdown, published in April 2020, of CARES Act payments to different states, DePriest told Bigtree payments ranged from $166,000 per COVID patient in Tennessee hospitals, for example, to far higher payments in states such as North Dakota ($339,000), Nebraska ($379,000) and West Virginia ($471,000).

In addition, for hospitals ascertained to be in COVID “hotspots,” HHS distributed special “high-impact” funds — $77,000 per admission initially, later downsized to $50,000 per admission.

HHS explained it used COVID admissions “as a proxy for the extent to which each facility experienced lost revenue and increased expenses associated with directly treating a substantial number of COVID-19 inpatient admission [sic].

The remdesivir ruse

The National Institute of Allergy and Infectious Diseases (NIAID) and the Centers for Disease Control and Prevention (CDC) spent $79 million developing remdesivir for Gilead, which itself dished out $2.45 million during the first quarter of 2020, to lobby for the drug’s use with COVID patients.

On May 1, 2020, the U.S. Food and Drug Administration (FDA) authorized remdesivir for emergency use in individuals hospitalized with severe COVID illness, and members of an NIH expert panel (many with financial ties to Gilead) added the drug to the agency’s treatment guidelines.

A scant five months later, FDA granted full approval to remdesivir for hospitalized COVID patients over age 12.

The World Health Organization (WHO), in contrast, advised against remdesivir, stating the drug has “no meaningful effect on mortality or on other important outcomes for patients.”

Remdesivir sailed through regulatory hoops in the U.S. despite an abysmal track record of “adverse effects serious enough to kill” any individual hapless enough to take it.

Children’s Health Defense Chairman Robert F. Kennedy, Jr. discusses remdesivir’s toxicity in his best-selling book, The Real Anthony Fauci, outlining the lethal problems — multiple organ failure, acute kidney failure, septic shock, hypotension and death — experienced by participants in NIAID’s clinical trial of remdesivir as an Ebola therapy.

When the trial, which compared remdesivir against three other drugs, killed more than half (54%) of the remdesivir recipients within 28 days — the highest mortality rate among the four groups — an oversight board forced the NIAID to end the prong of the study focused on remdesivir.

As if remdesivir alone weren’t bad enough, Vliet and Shultz estimate mechanical ventilation kills anywhere from 45% to 85% of COVID patients. Moreover, NIH’s skimpy treatment guidelines prescribe dexamethasone concurrently with ventilators.

Dexamethasone, often described as a “double-edged sword,” is a highly potent corticosteroid that suppresses the innate immune system.

Like remdesivir, dexamethasone’s potentially significant adverse impacts include kidney damage. Additional side effects include interference with the normal function of other organ systems such as the cardiovascular, digestive, endocrine, musculoskeletal and nervous systems.

Ironically, dexamethasone can also increase the need for mechanical ventilation as well as for blood pressure intervention.

Therapies like these are a large part of why, as Vliet and Shultz note, the U.S. COVID mortality rate is so “shockingly high” compared to the rest of the world.

Remdesivir’s trail of destruction could get worse — on Jan. 21, FDA expanded use of remdesivir to “high-risk” adult and pediatric outpatients (age 12 and older) “for the treatment of mid-to-moderate COVID-19 disease,” permitting administration of the intravenous drug in various outpatient facilities.

FDA’s side effects warnings include possible liver injury and allergic reactions such as “changes in blood pressure and heart rate, low blood oxygen level, fever, shortness of breath, wheezing, swelling …, rash, nausea, sweating or shivering.”

Getting involved and bringing transparency

Referring to the 20% add-on payment that hospitals receive for administering remdesivir to COVID patients, DePriest commented that a “bonus” is a “weird thing to call something when you’re murdering people.”

Journalist Jon Rappoport agreed, preferring to characterize hospitals’ behavior toward COVID patients as “a federally incentivized protocol for murder” — or “cash for death.”

All of the above parties concur that the best-case scenario is to treat COVID early at home and avoid hospitals — “because we know from experience what happens there.”

In cases where hospitalization is unavoidable, DePriest encourages communities to get more involved:

“[W]hen you know these hospitals are doing that, the people of that community need to show up at that hospital en masse and start telling them that you, as a community, are going to be advocating for every single COVID patient that walks through those doors, and you are going to hold that hospital accountable — to their patient bill of rights, to their stated visitation policies — and if your state is not in a state of emergency anymore, there shouldn’t be any reason why patients are medically kidnapped and separated from their families and isolated.

“There’s absolutely no reason for it, but the communities have to get involved and they have to confront these hospitals and tell them, ‘We’re done, you’re not killing any more of us.’”

 

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©January 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.




30,000+ Demand End to Vaccine Mandates, Government Overreach at DC Rally

30,000+ Demand End to Vaccine Mandates, Government Overreach at DC Rally

More than 30,000 people attended the “Defeat the Mandates” rally Sunday in DC, calling for an end to vaccine mandates and government overreach.

by Children’s Health Defense Team, The Defender
January 24, 2022

 

More than 30,000 people attended the “Defeat the Mandates” rally Sunday in Washington, DC, calling for an end to vaccine mandates and government overreach.



Children’s Health Defense organized and sponsored the event along with the Vaccine Safety Research FoundationFront Line Covid-19 Critical Care AllianceGlobal Covid SummitWorld Council for Health and JP Sears.

Americans of every race, creed, political affiliation, sexual orientation and vaccination status attended the event, including groups of police officers, firefighters and teachers.

Watch the latest video at foxnews.com

Robert F. Kennedy, Jr., Children’s Health Defense chairman and chief legal counsel, gave a powerful speech encouraging everyone to stand up for democracy and freedom.



Other speakers included: Del Bigtree, Lara Logan, Dr. Paul MarikDr. Pierre Kory, Chris Martenson, Steve Kirsch, Dr. Robert MaloneDr. Peter McCullough, Dr. Christina Parks, Dr. Paul Alexander, Attorney Tricia Lindsay, Kevin Jenkins, Rev. Aaron Lewis, Rabbi Epstein, Tramell Johnson, Jo Rose (Jo Speaks Truth), Angela Stanton King, Kwame Brown, Trahern Crews and others.

Watch the entire event here:

Rally starts @ 23:00

JP Sears @ 52:40

Kevin Jenkins @1:05

Peter McCullough @1:15

Richard Urso @ 1:22

Pierre Kory @1:29

Talley Bowden @ 1:33

Paul Merik @ 1:36

Paul Alexander @ 1:41

Kat Lindley @ 1:43

Ryan Cole @ 1:44

Aaron Kheriaty @ 1:48

Robert Malone @ 1:53

Joel Wallskog @ 2:16

Steve Kirsch @ 2:36

Robert F. Kennedy, Jr. @ 2:46

Tess Lawrie @ 3:15

Rizza Islam @ 3:18

Zev Epstein @ 3:29

Aaron Lewis @ 3:35

Christina Parks @ 3:41

Will Witt @ 3:46

Trahern Crews @ 3:50

Tyler Fischer @ 3:52

Del Bigtree @ 4:00

 

©January 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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A Nano-Transistor That Enters Cells

A Nano-Transistor That Enters Cells

by Orwellito, Orwell City
January 23, 2022

 

In its most recent program, La Quinta Columna discussed a 2010 article on a nano-transistor capable of entering cells as if it were a virus.

This is one of the many articles that has attracted the attention of Spanish researchers since perfectly fits with what was found in vaccination vials analyzed by Dr. Campra.

All this would be part of the whole nano- and micro-technological system that’s formed in the human body, creating nano-networks.

More details about this are on the fragment selected by Orwell City.

Note: Remember that you can find all the information related to the research of La Quinta Columna and other independent researchers in the archive.



Video available at Orwellito Rumble channel.

 

Ricardo Delgado:

Let’s take a look at the following article published by El País in 2010.

A transistor that enters cells like viruses. The Harvard-made nanosensor can record biological activity without disrupting it. Coming out of Harvard University’s laboratories and shaped like a V, a new nano-transistor smaller than many viruses can be inserted inside a cell and record its activity without disrupting it. The new device is 100 times smaller in diameter than those used until now, which were also flat, while this one is flexible and three-dimensional.”

This flexible property is somehow familiar to us. Sorry.

“These field-effect nano-transistors…”

Like the famous graphene transistors.

“…known as nanoFETs, represent the first measurement of the inside of a cell with a semiconductor device, says Charles M. Lieber, director of the project, whose results are published in Science.”

This Lieber guy was the one we saw yesterday, I think, right?

“Scientists claim…”

Dr. Sevillano:

Yes. If I’m not mistaken.

Ricardo Delgado: 

Yes.

“Scientists claim that these transistors can be used to measure the flow of ions or electrical signals in cells, especially neurons.” Aimed at the neurons, huh. “They can also be associated with receptors or other biological elements” “to detect the presence of biochemical compounds inside a cell. The diameter of human cells ranges from 10 microns (such as neurons) to 50 microns (such as cardiac cells). The new sensors are in the nanometer range (which is three orders of magnitude less)…” That’s 1,000 times less. “…and scientists have found that they’re accepted by the cell membrane in a similar way to what happens with viruses and bacteria when they coat them with a phospholipid double layer, similar to the structure of the membrane. We have found that the nanosensors can be inserted and removed from the cell many times without detectable damage to the cell, Lieber explains.”

“The transistor is integrated into a V-shaped nanowire that connects to electrical wires to function.” “This work can be a breakthrough in the understanding of intracellular structures, said Zhong Lin Wang,” a nanotechnology expert.”

Of course, he’s Chinese. And it’s this. We’ve seen quite a bit of these “tweezers” in vaccines too, you know?

Let’s see. Well. Here they put the scale representation of a nanosensor inserted in a cell to record the internal activity. Like neurons, as well. Well, this was already published, as I said, by El País in 2010.

Dr. Sevillano:

Yes, right. Since then, the time has passed, and things have been done. They have done everything we have seen there. Everything. You know, nanotubes, self-assembling structures… Everything.

But they haven’t asked anybody’s permission. Nor said, “We’re just going to…” They haven’t asked anybody’s permission. Have they asked anybody’s permission? Have they said, “We’re going to do this and…?” And have they told anybody anything? “No, no…” “That’s a lie, that’s a lie.”

Is the thief going to tell you that he’s robbing you or the murderer that he’s killing you?

Ricardo Delgado: 

Exactly.

 

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Healthy Athletes Are Still Inexplicably Collapsing

Healthy Athletes Are Still Inexplicably Collapsing

by Jefferey Jaxen & Del Bigtree, The HighWire
January 21, 2021

 



Video available at The HighWire Rumble & Brighteon channels.

Healthy athletes and youth are still facing mounting health issues, many cardiac related.

The public is starting to notice this phenomenon, as more top athletes suffer sudden, catastrophic health issues.

 

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Dr. Tom Cowan & Dr. Andrew Kaufman: A Challenging Response to Dr. Mercola’s Article “Yes, SARS-CoV-2 Is a Real Virus”

Dr. Tom Cowan & Dr. Andrew Kaufman: A Challenging Response to Dr. Mercola’s Article “Yes, SARS-CoV-2 Is a Real Virus”

 

A Response to Dr. Mercola’s Recent Statement on if SARS-Cov-2 Is a Real Virus With Dr. Andrew Kaufma

by Dr. Tom Cowan with Dr. Andrew Kaufman
January 21, 2022

 

“…I think there has been, you know, a total wave right of criticism of the the truth that viruses don’t exist and cause disease. And we see that, seemingly at the same time, that the pandemic seems to be drawing near an end. Right?

We see suddenly lifting restrictions all over the world.

And even Bill Gates predicted in 2022 that would be the end of the pandemic.

The Wall Street journal printed an editorial saying that…essentially last three weeks a major drop in cases, and it signifies, you know, what do they call it — the herd immunity. Right? Which is another thing we can debunk.

So, as they’re kind of ending out of this — and, you know, I’m sure that there’s more planned in the future. And I don’t know if it’s going to be a health crisis or not. But if this does peter out, they want to make sure that as we, you know, get this relief and come out of it — and probably they want us to look at them in a favorable light.

But they want to make sure that we still believe in deadly and dangerous viruses.

And they want to make sure that we still believe that there are safe vaccines, even if we question the safety of these particular genetic injections.

That we retain those important beliefs, so that they can still continue to profit and manipulate and, you know, run operations in the future.”

~ Dr. Andrew Kaufman

 



Video available at Dr. Tom Cowan BitChute channel.

 

See Dr. Mercola’s article “Yes, SARS-CoV-2 Is a Real Virus” here.

Here are the additional links referenced during the discussion:
– Virus Isolation – Is It Real? – https://www.bitchute.com/video/UnpfmjmXNH0O/
– An Open Letter to Dr. Mercola – https://www.fluoridefreepeel.ca/open-letter-to-dr-mercola-january-17-2022/
– What is a Virus? – https://www.youtube.com/watch?v=thsDCmtkcOA

 

Connect with Dr. Tom Cowan

Connect with Dr. Andrew Kaufman


See related:

Virus Isolation…Is It Real? Andrew Kaufman, MD Responds to Jeremy Hammond

Christine Massey: An Open Letter to Dr. Mercola in Response to His Claim That SARS-CoV-2 Has Been Isolated

Questioning ‘The Science’: What Is a ‘Virus’? How Is a ‘Virus’ Seen & Isolated?




Swiss Olympic Sprinter Gets Pericarditis After Pfizer Booster, 22,193 Deaths After COVID Shots Reported to CDC

Swiss Olympic Sprinter Gets Pericarditis After Pfizer Booster, 22,193 Deaths After COVID Shots Reported to CDC
VAERS data released Friday by the Centers for Disease Control and Prevention included a total of 1,053,830 reports of adverse events from all age groups following COVID vaccines, including 22,193 deaths and 174,864 serious injuries between Dec. 14, 2020, and Jan. 14, 2022. 

by Megan Redshaw, The Defender
January 21, 2022

 

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,053,830 reports of adverse events following COVID vaccines were submitted between Dec. 14, 2020, and Jan. 14, 2022, to the Vaccine Adverse Event Reporting System (VAERS). VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 22,193 reports of deaths — an increase of 448 over the previous week — and 174,864 reports of serious injuries, including deaths, during the same time period — up 4,418 compared with the previous week.

Excluding “foreign reports” to VAERS, 732,883 adverse events, including 10,162 deaths and 66,059 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Jan. 14, 2022.

Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.

Of the 10,162 U.S. deaths reported as of Jan. 14, 19% occurred within 24 hours of vaccination, 24% occurred within 48 hours of vaccination and 61% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 525.2 million COVID vaccine doses had been administered as of Jan. 14, including 307 million doses of Pfizer, 200 million doses of Moderna and 18 million doses of Johnson & Johnson (J&J).

Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed. Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

U.S. VAERS data from Dec. 14, 2020, to Jan. 14, 2022, for 5- to 11-year-olds show:

The most recent death involves a 7-year-old girl (VAERS I.D. 1975356) from Minnesota who died 11 days after receiving her first dose of Pfizer’s COVID vaccine when she was found unresponsive by her mother. An autopsy is pending.

  • 14 reports of myocarditis and pericarditis (heart inflammation).
  • 22 reports of blood clotting disorders.
U.S. VAERS data from Dec. 14, 2020, to Jan. 14, 2022, for 12- to 17-year-olds show:
  • 27,205 adverse events, including 1,559 rated as serious and 35 reported deaths.The most recent death involves a 15-year-old girl from Minnesota (VAERS I.D. 1974744), who died 177 days after receiving her second dose of Pfizer from a pulmonary embolus. An autopsy is pending.
  • 65 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 96% of casesattributed to Pfizer’s vaccine.
  • 594 reports of myocarditis and pericarditis with 583 cases attributed to Pfizer’s vaccine.
  • 152 reports of blood clotting disorders, with all cases attributed to Pfizer.
U.S. VAERS data from Dec. 14, 2020, to Jan. 14, 2022, for all age groups combined, show:
40% rise nationwide in excess deaths among 18- to 49-year-olds, CDC Data Show

Death certificate data from the CDC show excess deaths increased by more than 40% among Americans 18 to 49 years old during a 12-month period ending in October 2021, compared to the same time period in 2018-2019 before the pandemic. COVID caused only about 42% of those deaths.

Excess deaths are defined as the difference between the observed number of deaths during a specific time frame and the expected number of deaths during that same period.

State-level data for the same 12-month period also show increases. For example, in Nevada, excess deaths were as high as 65%, with COVID accounting for only 36%. The District of Columbia saw an increase of 72% — with COVID not being a factor in any of the deaths.

Increases in excess deaths were most noticeable in the Midwest and western and southern states, while states seeing the lowest increases were primarily from the Northeast.

Swiss Olympic sprinter gets pericarditis after Pfizer’s COVID booster

In a Jan. 17 social media post, swiss Olympic sprinter Sarah Atcho said she is experiencing pericarditis after receiving a Pfizer booster shot.

On Dec. 22, Atcho received a booster because she “didn’t want to struggle with this when the season started” and was told it was safer to get Pfizer — even though she had Moderna the first time — to avoid cardiac side effects.

On Dec. 27, Atcho said she started experiencing tightness in her chest and felt dizzy while walking. A cardiologist diagnosed Atcho with pericarditis — inflammation of the thin membrane that surrounds the heart.

Atcho is not allowed to get her heart rate up for several weeks to allow her heart to rest and heal from the inflammation. Said she is upset nobody talks about the “heavy side-effects” young and healthy people are experiencing after receiving COVID vaccines.

Experts call on UK regulators to reassess COVID vaccines for 12- to 15-year-olds

In a letter to the UK’s Joint Committee on Vaccines and Immunisation, more than 30 politicians, doctors and medical experts in immunology asked UK regulators to overhaul the country’s COVID vaccine rollout for 12- to 15-year-olds based on new data showing a high risk of myocarditis in that age group.

The experts said data proved “for males under 40, risk of myocarditis was up to 14 times higher after vaccination than after infection” and the risk of myocarditis in young men and boys increased “significantly after a second dose of the vaccine.

They also argued vaccines are less effective “at stemming the transmission of Omicron compared to Delta” and therefore there may be few advantages to exposing young people to the potential increased risks and long-term harm.

Prior COVID infection more protective than vaccination during Delta wave

People with a history of previous COVID infection were better protected against infection and related hospitalization during periods of predominantly Alpha and Delta variant transmission, suggesting natural immunity was more protective against the variants than vaccines, according to the CDC.

New data released Wednesday by the CDC showed people who survived a previous infection had lower rates of COVID than people who were vaccinated alone.

Hospitalization rates were also lower among people who had recovered from COVID than among those who had been vaccinated.

For the study, health officials in California and New York gathered data from May through November 2021, which included the period when the Delta variant was dominant. The agency said there were limitations to the study and results were not applicable to the new Omicron variant.

However, the agency concluded vaccination “remains the safest and primary strategy to prevent SARS-CoV-2 infections, associated complications and onward transmission,” due to the risks associated with COVID infection.

The agency did not compare the risks of infection in those with and without underlying medical conditions and did not analyze the risks associated with vaccinating those with a history of previous COVID infection.

Major businesses, attorneys general, respond to Supreme Court ruling

The U.S. Supreme Court’s ruling last week striking down the Biden administration’s vaccine-or-test mandate for private businesses has left many companies scrambling to decide whether they should abandon the mandate or force their employees to be vaccinated anyway while the case plays out in the lower courts.

As The Defender reported today, Starbucks was the first major business to announce it would not enforce its COVID vaccine mandate against employees in light of the Supreme Court’s ruling, while Carhartt CEO Mark Valade announced in an email to staff the company’s vaccine mandate for its 3,000 U.S. employees would remain in place.

Both decisions sparked backlash on social media with calls to boycott both companies.

Meanwhile, a coalition of attorneys general from 27 states is calling on the Occupational Safety and Health Administration to rescind its Emergency Temporary Standard for private businesses with more than 100 employees because it lacks the authority to issue a broad vaccine mandate.

Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

 

©January 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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Bill Gates, Indian Government Targeted in Lawsuit Alleging AstraZeneca Vaccine Killed 23-Year-Old

Bill Gates, Indian Government Targeted in Lawsuit Alleging AstraZeneca Vaccine Killed 23-Year-Old
A lawsuit against Bill Gates, the Indian government and others, citing extensive case law, is attracting renewed scrutiny of Gates and his long-term, controversial involvement in India’s vaccine program.

by Michael Nevradakis, Ph.D., The Defender
January 20, 2022

 

In what may be the first legal case of its kind globally, a petitioner in India is seeking to prosecute Bill Gates, Indian vaccine czar Adar Poonawalla, and Indian government and public health officials over the death of a 23-year-old man who died after receiving AstraZeneca’s Covishield vaccine.

Kiran Yadav late last year filed a criminal writ petition for murder, Smt. Kiran Yadav v. The State of Maharashtra & Ors. (herein referred to as Yadav v. Maharashtra), with the Bombay High Court of Judicature, on behalf of her deceased son, Shri Hitesh Kadve.

Her son was vaccinated on Sept. 29, 2021. According to the complaint, he died that same day due to side effects brought on by the vaccine.

The complaint alleges Kadve died “due to [an] act of willful commission and omission attributable to some public servants who are misusing their position to bring policies to help the pharma mafia and thereby [are] responsible [for] mass murders.”

The complaint further states Yadav’s son was “unwillingly” compelled to get vaccinated based on the “false narrative” that the vaccine was entirely safe, and because the State of Maharashtra prohibited the non-vaccinated from riding on railroads or entering retail spaces such as shopping malls.

The complaint alleges Maharashtra’s restrictions “are against the Central Government’s policy that, there cannot be any discrimination between vaccinated and unvaccinated people.”

Other defendants in the case include the commissioner and director-general of the Maharashtra State Police, the Indian Central Bureau of Investigation and the principal secretary of the Indian Ministry of Health and Family Welfare.

The complaint also brings charges against Bill Gates and Adar Poonawalla, CEO of the Serum Institute of India, the world’s largest vaccine manufacturer by number of doses produced and sold.

The Serum Institute produces the Covishield vaccine, as well as over half of the world’s vaccines that are administered to babies.

In all, Yadav is requesting 1,000 crores (10 billion rupees, or $134 million USD) in compensation, including 100 crores ($13.4 million USD) in interim compensation.

She is seeking lie detector and narcoanalysis tests from Gates, Poonawalla and others.

According to the complaint, the Indian government admitted the Covishield vaccine may have harmful, and potentially fatal, side effects, but the vaccine was administered despite this knowledge.

The complaint in Yadav v. Maharashtra was filed by attorneys Shivam Mehra and Siddhi Dhamnaskar of Mumbai, and appears to have first been publicized in English by the Indian Bar Association, an informal group of Indian lawyers (the Bar Council of India is the country’s official bar association).

Judges of the Supreme Court of India have generally adopted a pro-vaccine stance. Nevertheless, Yadav’s 265-page complaint stands out for the extensive legal precedent it draws upon, from Indian and common law, calling into question the legality of mandatory vaccination and other compelled medical acts.

The complaint also stands out for the specific allegations made against figures such as Poonawala and Gates, a figure of extensive controversy in India.

Extensive legal precedent casts doubt on legality of India’s mandatory vaccination policy

One of the main court rulings referenced in the Yadav v. Maharashtra complaint is that of Registrar General, High Court of Meghalaya v. State of Meghalaya (herein referred to as Meghalaya). The central finding of the ruling, issued June 23, 2021, held that vaccination by force or deception, or through the introduction of restrictions on the non-vaccinated, is a violation of fundamental human rights and a civil and criminal wrong.

This judgment overturned an order in the state of Meghalaya that required vendors, taxi drivers, shopkeepers and other individuals to get vaccinated before resuming or reopening their businesses.

In reference to this, the court held that while vaccination was “the need of the hour,” the vaccination policy of a welfare state “can never affect a major fundamental right, i.e. the right to life, personal liberty and livelihood.”

Referring to Article 21 of the Indian Constitution, the court in Meghalaya addressed the right to health, arguing that when such healthcare is provided through coercive means, it encroaches upon the fundamental right to privacy.

The court also drew from another Indian court ruling, Justice K.S. Puttaswamy (Retd.) v. Union of India (2018), which held the fundamental right to health is violated when individuals are deprived of their right to personal choice, bodily autonomy and integrity, and the overarching right to privacy.

The court in Meghalaya added:

“[V]accination by force or being made mandatory by adopting coercive methods, vitiates the very fundamental purpose of the welfare attached to it. It impinges on the fundamental right(s) as such, especially when it affects the right to means of livelihood which makes it possible for a person to live.

“Compulsory administration of a vaccine without hampering one’s right to life and liberty based on informed choice and informed consent is one thing. However, if any compulsory vaccination drive is coercive by its very nature and spirit, it assumes a different proportion and character.”

The court in Meghalaya also referenced English common law, specifically, the case of Airedale NHS Trust v. Bland (1993), a decision which held that if an unwilling adult is compelled to receive a flu vaccination through force, this action would amount to a crime and to a civil wrong.

Remarking on this, the Indian court found:

“[T]hus, coercive element of vaccination has, since the early phases of the initiation of vaccination as a preventive measure against several diseases, have been time and again not only discouraged but also consistently ruled against by the Courts for over more than a century.”

The court in Meghalaya also referred to Article 19 of the Indian Constitution regarding the “freedom to practice any profession or carry on any occupation, trade or business,” and that vaccine-related restrictions were “palpably excessive.”

The court added:

“In this case, there is a clear lack of legitimacy in prohibiting freedom of carrying on any occupation, trade or business amongst a certain category or class of citizens who are otherwise entitled to do so, making the notification/order ill-conceived, arbitrary and/or a colourable exercise of power.”

From an administrative point of view, the court in Meghalaya also found not only had the central Indian government not mandated vaccinations, instead holding that vaccination must remain voluntary, but there was no regulation or directive that allowed state governments to impose vaccination requirements within their own territory.

Yadav case draws upon extensive Indian legal precedent, scientific studies

The criminal complaint in Yadav v. Maharashtra also drew upon several other Indian court rulings, including recent COVID vaccines-related decisions such as Dinthar Incident v. State of Mizoram and Others (2021) and Madan Mili v. Union of India (2021).

These rulings found vaccinated individuals can also get infected with COVID and can spread infection, just as those who are unvaccinated, and accordingly, there cannot be any discrimination between those who are vaccinated or unvaccinated. Such discrimination would contravene Articles 14, 19, and 21 of the Indian Constitution.

Yadav v. Maharashtra also references the following cases and English common law:

“[A]ll adults with capacity to consent have the right of self-determination and autonomy. The said rights pave the way for the right to refuse medical treatment … [a] competent person who has come of age has the right to refuse specific treatment or all treatment or opt for an alternative treatment …

“The best interest of the patient shall override the State interest.”

“Restraining people who are yet to get vaccinated from opening institutions, organizations, factories, shops, etc., or denying them their livelihood by linking their employment … to their getting vaccinated would be illegal on the part of the State, if not unconstitutional.

“Such a measure would also trample upon the freedom of the individual to get vaccinated or choose not to do so.”

“An adult person of sound mind is entitled to decide which, if any, of the available forms of treatment to undergo, and her consent must be obtained before treatment interfering with her bodily integrity is undertaken.”

Yadav v. Maharashtra also references an Oct. 8, 2021, directive from Satyendra Singh, the undersecretary of the Indian Health Ministry, reaffirming that vaccination remains voluntary, that the Indian government “has not formulated or suggested any policies for discrimination between citizens of India on the basis of their vaccination status,” and that no citizen can be forced to be vaccinated.

The complaint also draws upon Indian legislation, specifically the Disaster Management Act of 2005, which holds that state governments cannot formulate any rules that contravene the guidelines of the national government. Nor can such prohibitions be circumvented indirectly, according to the Yadav v. Maharashtra complaint, referring to another Indian court case, Noida Entrepreneurs Association v. Noida (2011).

The complaint also refers to several clauses from UNESCO’s Universal Declaration on Bioethics & Human Rights (2005), including:

  • Article 3 on human dignity and human rights, which holds that “[t]he interests and welfare of the individual should have priority over the sole interest of science or society.”
  • Article 6, which holds that “any preventive, diagnostic and therapeutic medical intervention is only to be carried out with… prior, free and informed consent.”
  • Article 8 on respect for human vulnerability and personal integrity.
  • Article 11, which states that “[n]o individual or group should be discriminated against or stigmatized on any grounds, in violation of human dignity, human rights and fundamental freedoms.”

The complaint then goes on to name specific individuals, such as Venugopal G. Somani, the Drug Controller General of India, and Randeep Guleria of the All India Institute of Medical Science (AIIMS), as individuals who participated in a “dishonesty and cheating campaign” and the “furtherance of [a] conspiracy,” by making the “false and misleading statement” that the COVID vaccines were completely safe.

The complaint accuses Somani and Guleria of following a “one-line agenda to give wrongful profit to the vaccine companies” and goes on to cite Indian case law holding that because “conspiracies are hatched on secrecy … no direct evidence is required to prove it. The offense can be proved from circumstantial evidences.”

A total of 81 research papers were also referenced in the complaint, addressing, among other issues, the higher protection those with natural immunity have against COVID, as opposed to those who are vaccinated, as well as the lower efficacy of the vaccines against variants such as Delta.

The vaccine-related death of Dr. Snehal Lunawat

The Yadav v. Maharashtra complaint references the case of Dr. Snehal Lunawat, an Indian doctor from Maharashtra who died March 1, 2021, from complications stemming from the Covishield vaccine he received on Jan. 28, 2021.

This incident gained visibility in India due to the efforts of Lunawat’s family to get an investigation launched regarding her death.

Lunawat, who was 33 years old, experienced a “rare blood-clotting event” after taking the Covishield vaccine.

Subsequently, her family wrote to the Indian government and the Serum Institute, requesting that Lunawat’s death be investigated, as it had not been registered as an adverse event in the country’s “Adverse Event Following Immunisation” (AEFI) database.

However, a satisfactory response was not provided, prompting the family to reach out to the World Health Organization (WHO), which then investigated the incident.

Ultimately, due to the family’s pressure and the intervention of the WHO and the All India Drugs Network, the AEFI committee accepted on Sept. 25, 2021, after nearly seven months, that Lunawat’s death was vaccine-related.

Specifically, the rare blood clotting complication resulted in her blood platelet count decreasing because of increased bleeding in her brain.

This was only the third vaccine-induced death recognized by AEFI. The process of reporting vaccine-related deaths to the AEFI database is reportedly “not easy.”

The Yadav v. Maharashtra complaint refers to Lunawat’s death, and its subsequent classification as vaccine-related, as “ex facie” evidence of the “falsity of claims by the … accused officials and doctors” regarding the safety of the COVID vaccines

#ArrestBillGates: Controversy, legal battles in India surrounding Gates and his foundation

The Yadav v. Maharashtra complaint makes extensive references to Bill Gates, who is described as a “habitual offender of mass murder by vaccination in conspiracy with Government officials.”

Gates is also referred to as a “mastermind … who is manufacturing ‘Covishield’ in partnership with [the] Serum Institute.”

The complaint seeks lie detector, brain mapping and narcoanalysis tests of Gates, Poonawalla and others to “unearth the complete conspiracy,” and demands the registration of a “first information report” (FIR) against individuals who marketed the vaccines as completely safe.

The request for Gates and others to undergo narcoanalysis tests is considered perplexing by some analysts, as such tests are not legally admissible in Indian courts, as the person being interrogated is in a state of semi-consciousness.

The complaint argues Gates and Poonawalla should be considered “co-conspirators to mass murder” who were “working for the welfare of the vaccine companies only,” charges which would result in them facing the death penalty and confiscation of their assets in India.

The complaint notes that under Indian law, one can be found guilty for false marketing of a product via “commission and omission.”

The complaint also references the activity of the Bill & Melinda Gates Foundation (BMGF) in India, including its alleged encouragement of a partnership between AstraZeneca and Oxford University to develop the Covishield vaccine, which was then delivered to countries such as India.

The BMGF is also noted to have previously committed, in June 2020, $750 million towards the development of the AstraZeneca vaccine at Oxford University, and conditional funding of $150 million to the Serum Institute.

In a posting on his official blog in December 2020, Gates wrote that his foundation “took on some of the financial risk” for the vaccine, so that if the Oxford-AstraZeneca vaccine was not approved, the Serum Institute “won’t have to take a full loss.”

The Yadav v. Maharashtra complaint references prior court rulings against Gates and the BMGF in India. One such example is an Indian Supreme Court ruling in Kalpana Mehta v. Union of India (2018) regarding the death of eight female children who took part in an unauthorized trial of two Human Papillomavirus (HPV) vaccines: Gardasil, manufactured by Merck, and Cervarix, produced by GlaxoSmithKine (GSK).

The trial, which began in 2009, took place in two Indian states, Andhra Pradesh and Gujarat. It was carried out by an American NGO, the Seattle-based Program for Appropriate Technology in Health (PATH), which is connected to the BMGF’s Children’s Vaccine Program.

In reference to these deaths, the Yadav v. Maharashtra complaint refers to a report by an Indian parliamentary committee that found government officials were “involved in the conspiracy,” along with a recommendation that the BMGF and other NGOs associated with Gates be investigated.

According to the complaint, “the evidentiary value” of the report was upheld in the Kalpana Mehta v. Union of India case.

The controversy over the deaths that resulted from the HPV vaccine trial led to a grassroots campaign in India in May 2021, calling for Gates and his foundation to be charged for these deaths, as they had funded the vaccination program.

The #ArrestBillGates hashtag trended on Indian Twitter that month as a result of this campaign, accusing Gates and his organization of using the girls as “guinea pigs.”

Parental consent was in many cases not obtained for the participation of the girls in the trial, which involved 14,000 tribal girls between the ages of 10 and 14, many of whom lived not with their parents but in government-run hostels.

In some instances, parental ‘consent’ consisted of a thumbprint impression from the girls’ poor and illiterate parents, while for many girls, no consent forms whatsoever could be located.

Symptoms the girls experienced included epileptic seizures, early onset of menstruation, heavy bleeding, severe menstrual cramps, severe stomach aches, headaches and mood swings.

An Indian government investigation concluded the girls’ deaths were unconnected to the vaccination, but ethical and regulatory failings in the vaccine trial were discovered, which resulted in the BMGF being restricted from the country’s vaccination program in 2013.

Despite this, the foundation continued to work with the Indian Health Ministry via the latter’s Immunization Technical Support Unit (ITSU).

Nevertheless, the investigative committee’s conclusion that the deaths were not vaccine-related, but instead due to such causes as suicide, accidental drowning, malaria, viral infections and subarachnoid hemorrhage, did not go unquestioned.

Representatives of the Sama Women’s Health NGO visited one of the affected regions, Khammam, in March 2010, on a fact-finding mission. As reported by India’s Economic Times, the Sama report found “HPV vaccine as a possible, if not probable, cause of suicidal ideation cannot be ruled out” for the girls’ deaths.

The Yadav v. Maharashtra complaint also calls out the activities of Gates and the BMGF with regard to the administration of polio vaccines in India, funded by the BMGF to the tune of $450 million.

The program foresaw the administration of 50 doses of the vaccine to children below the age of five, via overlapping vaccination programs.

This campaign was blamed for “a devastating non-polio acute flaccid paralysis (NPAFP) epidemic that paralyzed 490,000 children [in India] beyond expected rates between 2000 and 2017.”

In 2017, Gates’ involvement in the polio vaccine campaign was “dialed back.” Following this, “NPAFP rates dropped precipitously.”

As detailed in a scientific study published in 2012:

“Nationally, the non-polio AFP rate is now 12 times higher than expected. In the states of Uttar Pradesh (UP) and Bihar, which have pulse polio rounds nearly every month, the non-polio AFP rate is 25- and 35-fold higher than the international norms … children who were identified with non-polio AFP were at more than twice the risk of dying than those with wild polio infection.

“The international incidence of non-polio AFP is said to be 1 to 2/100,000 in the populations under 15 … In 2011, an additional 47,500 children were newly paralyzed in the year, over and above the standard 2/100,000 non-polio AFP that is generally accepted as the norm … [t]his large excess in the incidence of paralysis was not investigated as a possible signal, nor was any effort made to try and study the mechanism for this spurt in non-polio AFP.

“From India’s perspective the exercise has been extremely costly both in terms of human suffering and in monetary terms. It is tempting to speculate what could have been achieved if the $2.5 billion spent on attempting to eradicate polio were spent on water and sanitation and routine immunization.”

The specific vaccine administered to Indian children was the oral polio vaccine. As of Jan. 1, 2000, the CDC withdrew this vaccine from immunization schedules except in “special circumstances,” as the oral vaccine was itself found to be causing polio.

Nevertheless, Gates had reportedly hired a well-known Indian actor, Amitabh Bachchan, to promote the oral polio vaccine via a series of television advertisements.

Gates, Poonawalla at the center of vaccine controversy in India

India has stood out among most of the world’s countries by not offering blanket immunity to manufacturers of COVID-19 vaccines.

In 2021, the Indian government’s negotiations with Pfizer fell through when Indian regulators refused to provide it legal protection via indemnity.

Such protection was not provided to the three COVID-19 vaccines that received an emergency use authorization in India: Covishield, Covaxin and Sputnik V.

This did not occur without dissent, however. Poonawalla, as head of the India-based Serum Institute, had called for protection from lawsuits for COVID vaccine injuries.

The Yadav v. Maharashtra complaint describes Poonawalla and other personnel of the Serum Institute, which manufactures the Covishield vaccine, as “complicit” in Kadve’s death, and as “habitual offenders of earning profits by selling vaccines with death-causing side effects,” placing them “in the category of mass murderers.”

However, the controversy over Gates’ and Poonawalla’s vaccine-related work in India spans beyond the Yadav v. Maharashtra case.

In April 2021, for instance, Gates and the BMGF received criticism for their refusal to share COVID-19 vaccine technologies with India and other developing countries.

This criticism prompted the CEO of the BMGF, Mark Suzman, to reverse course and support a temporary waiver on vaccine-related intellectual property.

In 2006, the BMGF co-founded, with the Indian government, the Public Health Foundation of India (PHFI) as a public-private partnership. The PHFI is funded, in part, by pharmaceutical companies, including Pfizer and Merck.

The PHFI has also been active in producing research related to COVID-19, with at least one such study, titled “Impact of Crop Diversity on Dietary Diversity among Farmers in India during the COVID-19,” also crossing over into the agricultural realm.

In Gates’ aforementioned Nov. 2019 visit to India, he heaped praise on three Indian vaccine manufacturers, including the Serum Institute.

But Gates’ connection to the Serum Institute goes beyond verbal praise. Since November 2012, the Serum Institute has been the recipient of BMGF grants — in that initial instance for the development of an HPV vaccine. Gates toured the Serum Institute earlier that year.

The Serum Institute received a $4 million grant from the BMGF in October 2020 to support research and development as part of the COVID-19 response, while in August 2020, the Serum Institute, in partnership with the BMGF and GAVI-The Vaccine Alliance, agreed to produce up to 100 million doses of COVID-19 vaccines for low- and middle-income countries.

Also known as the “Vaccine Alliance,” GAVI proclaims a mission to “save lives and protect people’s health,” and states it “helps vaccinate almost half the world’s children against deadly and debilitating infectious diseases.”

GAVI was established in 1999, with the BMGF as one of its co-founders and one of its four permanent board members.

GAVI then goes on to describe its core partnership with various international organizations, including the WHO, UNICEF, the World Bank and the BMGF.

As previously reported by The Defender, GAVI, through its INFUSE initiative, has called for “innovations that leverage new technologies to modernize the process of identifying and registering the children who are most in need of life-saving vaccines.”

GAVI also closely collaborates with the ID2020 Alliance, founded in 2016, which claims to advocate in favor of “ethical, privacy-protecting approaches to digital ID,” adding that “doing digital ID right means protecting civil liberties.

Microsoft is a founding member of the ID2020 alliance (in 2018) and appears to partner with it, while Kim Gagné, ID2020’s board chairman, is a former Microsoft executive.

Controversy has surrounded GAVI’s activity in India. GAVI, along with the PHFI and the BMGF, have promoted the Pentavalent vaccine, which combines five vaccines – diphtheria, hepatitis B, tetanus, whooping cough, and haemophilus influenza type B (which causes pneumonia and meningitis) – into one.

The Indian Health Ministry found the deaths of three infants in the Indian state of Tamil Nadu to have had “a consistent causal association to immunization” — that is, to the Pentavalent vaccine, while in total, 54 infant deaths were classified with the AEFI as adverse reaction deaths.

GAVI provided a $165 million grant in August 2009 for the phased introduction of Pentavalent in India, in addition to subsidizing each injection for five years thereafter.

Regulatory capture and a “revolving door” between the Indian government and GAVI also appears to exist, as in the example of Anuradha Gupta, formerly an official with the Indian Health Ministry and director of the National Health Mission. Gupta in 2014 was named deputy CEO of GAVI, and remains in the position to this day.

Gates involved in controversial digital ID schemes in India

In 2009, the Indian government launched a national digital identification card system known as Aadhaar, now the world’s largest biometric identification system.

The Aadhaar Card contains biometric and demographic data and provides individuals with a unique 12-digit identity number, though it is in and of itself not considered proof of Indian citizenship, just of Indian residence.

The Aadhaar identification number was linked with numerous public and private services, including the opening of bank accounts, verification of electoral identity, filing income tax returns, making digital payments, receiving government pensions, subsidies and welfare payments and registration of mobile SIM cards.

Aadhaar has generated controversy in India, such as over the government’s plans to link it to the national voter database.

And in 2017, it was reported that HIV patients in India were being coerced into submitting their Aadhaar number, leading them to drop out of treatment programs due to privacy concerns.

Chinese hackers also reportedly targeted the Aadhaar database.

Aadhaar also was at the center of legal controversy. A 2013 ruling by the Indian Supreme Court found no person should be denied government services, benefits or subsidies for not possessing the Aadhaar card.

A subsequent Supreme Court ruling in 2018 upheld the constitutionality of the Aadhaar system, but found it cannot be made mandatory for use by private organizations, such as banks or mobile providers.

Civil society groups in India, such as the Citizens Forum for Civil Liberties, expressed opposition to Aadhaar on the basis of privacy concerns. The National Advisory Council and the Central Employment Guarantee Council of India opposed Aadhaar “on the grounds of civil liberties.”

Nevertheless, Gates, on his personal blog, praised Aadhaar — describing it as “a valuable platform for delivering social welfare programs and other government services” — and Nandan Nilekani, who developed the Aadhaar system and who now works with the World Bank Group to help other countries develop similar schemes.

Gates also dismissed privacy concerns surrounding Aadhaar, stating that “Aadhaar in itself doesn’t pose any privacy issue because it’s just a bio ID verification scheme,” adding that “We [the BMGF] have funded the World Bank to take this Aadhaar approach to other countries.”

In 2020, the Indian government announced the launch of the Ayushman Bharat Digital Mission, a system that would complement Aadhaar by providing a unique digital health ID to all citizens and that would be linked to their personal health records.

The program was initially trialed in six Indian regions and was launched nationally on Sept. 27, 2021. As of Nov. 2021, 96% of Ayushman Bharat Digital Mission users were linked with Aadhaar.

The launch earned Gates’ praise. He tweeted congratulations to Indian President Modi, stating the program “will help ensure equitable, accessible healthcare delivery and accelerate progress on India’s health goals.”

Notably, in October 2021, the Ayushman Bharat Digital Mission received a $350,690 grant from the BMGF to support its “rollout and strengthening,” raising concerns have been raised regarding privacy, informed consent and data leakage.

Freedom of information requests revealed that Indian authorities generated health IDs for individuals who provided their Aadhaar number when receiving a COVID-19 vaccine, enrolling them in the Ayushman Bharat Digital Mission without informed consent.

 

Michael Nevradakis, Ph.D., is an independent journalist and researcher based in Athens, Greece.

 

©January 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

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See related:

Yohan Tengra Exposes the Public Health Mafia in India




British Medical Journal: ‘Pharma Must Release of All Vaccine and Treatment Data Immediately’

British Medical Journal: ‘Pharma Must Release of All Vaccine and Treatment Data Immediately’

by 21st Century News
January 20, 2022

 

The British Medical Journal (BMJ), one of the world’s oldest and most prestigious medical journals, has now called for the full and immediate release of all data relating to the COVID-19 experimental vaccines and treatments. According to the BMJ, ‘Data should be fully and immediately available for public scrutiny.’

Will the pharmaceutical cartel members Pfizer, AstraZeneca, Moderna and others, along with their allies in government regulatory bodies like the FDA comply with this crucial request? 

BMJ reports…

In the pages of The BMJ a decade ago, in the middle of a different pandemic, it came to light that governments around the world had spent billions stockpiling antivirals for influenza that had not been shown to reduce the risk of complications, hospital admissions, or death. The majority of trials that underpinned regulatory approval and government stockpiling of oseltamivir (Tamiflu) were sponsored by the manufacturer; most were unpublished, those that were published were ghostwritten by writers paid by the manufacturer, the people listed as principal authors lacked access to the raw data, and academics who requested access to the data for independent analysis were denied.1234

The Tamiflu saga heralded a decade of unprecedented attention to the importance of sharing clinical trial data.56 Public battles for drug company data,78 transparency campaigns with thousands of signatures,910 strengthened journal data sharing requirements,1112 explicit commitments from companies to share data,13 new data access website portals,8 and landmark transparency policies from medicines regulators1415 all promised a new era in data transparency.

Progress was made, but clearly not enough. The errors of the last pandemic are being repeated. Memories are short. Today, despite the global rollout of covid-19 vaccines and treatments, the anonymised participant level data underlying the trials for these new products remain inaccessible to doctors, researchers, and the public—and are likely to remain that way for years to come.16 This is morally indefensible for all trials, but especially for those involving major public health interventions.

Unacceptable delay

Pfizer’s pivotal covid vaccine trial was funded by the company and designed, run, analysed, and authored by Pfizer employees. The company and the contract research organisations that carried out the trial hold all the data.17 And Pfizer has indicated that it will not begin entertaining requests for trial data until May 2025, 24 months after the primary study completion date, which is listed on ClinicalTrials.gov as 15 May 2023 (NCT04368728).

The lack of access to data is consistent across vaccine manufacturers.16 Moderna says data “may be available … with publication of the final study results in 2022.”18 Datasets will be available “upon request and subject to review once the trial is complete,” which has an estimated primary completion date of 27 October 2022 (NCT04470427).

As of 31 December 2021, AstraZeneca may be ready to entertain requests for data from several of its large phase III trials.19 But actually obtaining data could be slow going. As its website explains, “timelines vary per request and can take up to a year upon full submission of the request.”20

Underlying data for covid-19 therapeutics are similarly hard to find. Published reports of Regeneron’s phase III trial of its monoclonal antibody therapy REGEN-COV flatly state that participant level data will not be made available to others.21 Should the drug be approved (and not just emergency authorised), sharing “will be considered.” For remdesivir, the US National Institutes of Health, which funded the trial, created a new portal to share data (https://accessclinicaldata.niaid.nih.gov/), but the dataset on offer is limited. An accompanying document explains: “The longitudinal data set only contains a small subset of the protocol and statistical analysis plan objectives.”

We are left with publications but no access to the underlying data on reasonable request. This is worrying for trial participants, researchers, clinicians, journal editors, policy makers, and the public. The journals that have published these primary studies may argue that they faced an awkward dilemma, caught between making the summary findings available quickly and upholding the best ethical values that support timely access to underlying data. In our view, there is no dilemma; the anonymised individual participant data from clinical trials must be made available for independent scrutiny.

Journal editors, systematic reviewers, and the writers of clinical practice guideline generally obtain little beyond a journal publication, but regulatory agencies receive far more granular data as part of the regulatory review process. In the words of the European Medicine Agency’s former executive director and senior medical officer, “relying solely on the publications of clinical trials in scientific journals as the basis of healthcare decisions is not a good idea … Drug regulators have been aware of this limitation for a long time and routinely obtain and assess the full documentation (rather than just publications).”22

Among regulators, the US Food and Drug Administration is believed to receive the most raw data but does not proactively release them. After a freedom of information request to the agency for Pfizer’s vaccine data, the FDA offered to release 500 pages a month, a process that would take decades to complete, arguing in court that publicly releasing data was slow owing to the need to first redact sensitive information.23 This month, however, a judge rejected the FDA’s offer and ordered the data be released at a rate of 55 000 pages a month. The data are to be made available on the requesting organisation’s website (phmpt.org).

In releasing thousands of pages of clinical trial documents, Health Canada and the EMA have also provided a degree of transparency that deserves acknowledgment.2425 Until recently, however, the data remained of limited utility, with copious redactions aimed at protecting trial blinding. But study reports with fewer redactions have been available since September 2021,2425 and missing appendices may be accessible through freedom of information requests.

Even so, anyone looking for participant level datasets may be disappointed because Health Canada and the EMA do not receive or analyse these data, and it remains to be seen how the FDA responds to the court order. Moreover, the FDA is producing data only for Pfizer’s vaccine; other manufacturers’ data cannot be requested until the vaccines are approved, which the Moderna and Johnson & Johnson vaccines are not. Industry, which holds the raw data, is not legally required to honour requests for access from independent researchers.

Like the FDA, and unlike its Canadian and European counterparts, the UK’s regulator—the Medicines and Healthcare Products Regulatory Agency—does not proactively release clinical trial documents, and it has also stopped posting information released in response to freedom of information requests on its website.26

Transparency and trust

As well as access to the underlying data, transparent decision making is essential. Regulators and public health bodies could release details 27 such as why vaccine trials were not designed to test efficacy against infection and spread of SARS-CoV-2.28  Had regulators insisted on this outcome, countries would have learnt sooner about the effect of vaccines on transmission and been able to plan accordingly.29

Big pharma is the least trusted industry.30 At least three of the many companies making covid-19 vaccines have past criminal and civil settlements costing them billions of dollars.31 One pleaded guilty to fraud.31 Other companies have no pre-covid track record. Now the covid pandemic has minted many new pharma billionaires 32, and vaccine manufacturers have reported tens of billions in revenue…

Continue this article at the BMJ

 

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Christine Massey: An Open Letter to Dr. Mercola in Response to His Claim That SARS-CoV-2 Has Been Isolated

Christine Massey: An Open Letter to Dr. Mercola in Response to His Claim That SARS-CoV-2 Has Been Isolated

 

[Truth Comes to Light editor’s note: On January 17 when this article was first published, a live link to Dr. Mercola’s article could still be found at his site. Due to attacks from mainstream media, his articles only remain open for public view for 48 hours. It is now available behind a paywall at his archived site. However, you can find a copy here or at many other websites and blogs that reposted the original. ]

 

This image is a screenshot from Dr. Mercola’s article which is now found in his archives and at many other websites and blogs.

 

Open Letter to Dr. Mercola January 17, 2022

by Christine Massey, M.Sc., Flouride Free Peel
January 17, 2022

 

Hi Dr. Mercola,

You’ve published an blog titled “Yes, SARS-CoV-2 Is a Real Virus“.

One of the sources you relied most heavily on for this claim is a recent blog by Steve Kirsch, which is really interesting because in that blog Steve admitted right off the top that he actually has no idea whether or not the alleged virus has even been isolated and that he relies on other people’s opinions.

I wrote an educational Open Letter to Steve Kirsch in response to that blog and strongly suggest you and your readers review it.

Now in your blog you state that: “SARS-CoV-2 has been isolated, photographed, genetically sequenced, and exists as a pathogenic entity.

I hope we can agree that a specific thing must be known to exist in order to know that “it” is pathogenic. Not believed, imagined, assumed, or wanted to exist, but known. Because otherwise it’s impossible to establish even a correlation, let alone prove causation of anything.

Yet nowhere in your blog did you present or cite any proof that that the alleged RNA genome of 30,000 base pairs surrounded by a spikey protein shell actually exists.

I’ll briefly review some of the sources you’ve cited to explain why I say this.

You start out with a video that features Jeremy Hammond insisting that “the virus” is real, has been isolated, and is a necessary factor in “COVID-19”.

(For the record, I had an extensive email exchange with Jeremy on this topic, between October 25 and November 14, 2020. I encourage you and your readers to review it.)

In this video, Jeremy made bold claims indeed. But despite stating that the “virus” existence issue is “probably” his “biggest pet peeve“, he came to this interview armed with zero sources showing that the alleged virus does exist. In fact Jeremy cited no studies of any kind. Just unsubstantiated claims, and reliance on the beliefs of others. They could do this, they could do that. They can’t do this, they can’t do that. So-and-so says this, so-and-so says that.

Instead, Jeremy insisted that the following is the “gold standard” for “isolation” of a disease spreading “virus”: irrational and unscientific interpretation of cytopathic effects in a cell culture – typically malnourished monkey kidney cells to which toxic drugs have been added, and further contamination in the form of fetal bovine serum is added as food for the cells, along with a patient sample (not a purified sample of anything).

This, in Jeremy’s mind, establishes the existence and presence of a virus. Which is why he’d make a great virologist. Jeremy doesn’t think like a scientist, and as I always point out, “virology is not a science“.

And Jeremy lied through his teeth when he went along with the naïve (I’m giving her the benefit of the doubt) comment from his interviewer that virologists then pull “the virus” from the cell culture. “It really is that simple.” (I challenge Jeremy or you, Dr. Mercola, to cite any study where a specific thing was “pulled”, even from a monkey/cow/human mixture aka cell culture, and shown scientifically to be a disease-spreading “virus”.)

And according to Jeremy, we just “know” what “coronaviruses” look like, despite the fact that no specific thing alleged to be a “coronavirus” has ever been purified from any patient sample (or even from a cell culture) so that it could be studied logically and scientifically. Who needs science? We just know these things.

Jeremy insists that the CDC has isolated “SARS-COV-2”. Well, yes they have according to the meaningless, antiscientific approach to “isolation” used by Jeremy and virologists.

But did the CDC researchers apply even a modicum of logic or scientific method and actually establish the existence of the alleged virus? That’s an entirely different matter and the answer is a resounding “No”.

The CDC’s “SARS-COV-2 isolation” study is just another example of the typical fraudulent monkey business (literally) that plagues our world. I have addressed the CDC’s study previously, and will address this same issue of virology’s blatantly bogus “isolation” methods below.

Jeremy carried on with more bizarre claims: that scientists never isolate/purify anything, and don’t have the technology to purify things like alleged viruses.

Jeremy also strangely implied that people (such as myself) who say that proof of a disease-spreading “virus” requires purification actually demand that the alleged virus be floating in a vacuum.

Dr. Mercola, I’ve been involved in this issue for almost 2 years now and don’t know a single man or woman who defines isolation/purification as “floating in a vacuum“.

And I make explicitly clear in my Freedom of Information requests that this is not how I define isolation/purification. Below is a screenshot from a recent FOIA request to the CDC. They have no records, like all 164 other institutions in roughly 30 countries, that have been asked by people around the world. No one on the planet has purified a sample of the alleged “virus” from a disease human, or knows of anyone who has, even though supposedly millions and millions of people are infected and spewing this “virus” every time they breath.

And no, contrary to Jeremy’s claim, it is not people such as Dr. Andrew Kaufman, or Jon Rappoport, or Drs. Sam and Mark Bailey, who bizarrely redefined the word “isolation”. It’s virologists who redefined it, to mean mixing various complicated substances together and drawing wild conclusions – quite the opposite of its historical meaning.

It’s funny how everyone knows that “isolate” means “separate” when it comes to isolating humans and the “confusion” only arises when it comes to theoretical “viruses”. And how a virologist’s use of the word “isolate” gives the impression of legitimate science when nothing could be further from the truth.

Dr. Mercola, I couldn’t help but notice the unicorn in the background over the shoulder of Jeremy’s interviewer. Was this video inserted into your blog as someone’s idea of a joke? I mean, these people proved a virus no more than a unicorn, and unicorns are a popular analogy for imaginary viruses these days, thanks to Dr. Tom Cowan, and I can’t for the life of me imagine why you would have purposely included this video when it’s completely useless to anyone looking for proof of a virus.

 

And no Dr. Mercola, we are not confused. We’re quite familiar with what virologists have been getting away with.

As distressing as it is to do so, since you have chosen to rehash Steve Kirsch’s summary of the curious “science” of Sabine Hazan, I will briefly address it once again, here, as I did in my educational Open Letter to Steve.

To put it bluntly, Sabine Hazan’s study is 100% useless and fraudulent. The RNA used in her “sequencing” was a genetic soup from various sources, including patients, and not shown to involve any alleged “virus”.

She fabricated meaningless codes on a computer that have never been shown to correspond to anything in the physical realm and falsely passed these off a “viral genomes”.

Sabine compared her meaningless “sequencing” results to the results of her utterly meaningless and fraudulent PCR tests (that she is quite secretive about, at least with me) that also have never been shown to have anything to do with a “virus”.

Sabine comes unhinged when directly challenged on the validity of her so-called “science”. I encourage your readers to try this themselves and see what happens (and send me the results at cmssyc@gmail.com).

Dr. Mercola, I also already addressed ATCC’s very expensive and fraudulent “virus” product that you are now promoting as well, in my educational Open Letter to Steve Kirsch. Please be sure to review that section. It includes a  Buyer Beware! from Dr. Saeed A. Qureshi, PhD, who spent 30+ years as a scientist (as opposed to a virologist) with Health Canada.

Dr. Mercola, I challenge you to track down the origin and contents of any ATCC “SARS-COV-2” product, as I did last year for the so-called “SARS-COV-2 isolate” that is referred to as “MUC-IMB1” aka “BavPat1” and sold by companies like EVA for 2 000,00 € per vial, and report back to your readers what you learn. Report the detailed methods that were used to allegedly verify that the product contains any disease-causing “virus” whatsoever.

Regarding your claim that “Germ Theory and Terrain Theory Both Have Merit”, can you prove with science that virology has any merit whatsoever?

Please prove the existence of a specific physical thing alleged to be a disease-spreading “COVID-19 virus/variant” aka “SARS-COV-2” and prove that that specific thing spreads disease from host to host via natural modes of exposure in animals or humans.

I challenge you to publish a study proving that such a thing exists. Show with science that only subjects that are exposed to that specific thing get “COVID-19” respiratory disease, as claimed by Jeremy, whose wild unsubstantiated claims you are now disseminating.

Dr. Mercola, as evidence that “the virus” has been isolated and sequenced, you are citing studies that rely in part on PCR “tests”. Without bothering to go into all the well documented fatal flaws with these so-called tests, a little logic is in order.

  1. It is impossible to validate any “test” without a gold standard.
  2. It is impossible to validate any “test” claimed to “confirm” the presence of a “virus” (or a “viral infection”) before the alleged “virus” has been proven to exist.
  3. It is impossible to validate any “test” claimed to “confirm” a “viral disease” before the alleged “virus” has been a) proven to exist and b) proven to cause the disease.

Obviously an indirect test for a “virus” cannot logically be used to prove the existence of the alleged “virus”. The test is what it is. In the case of PCR, in the very best case scenario, it is evidence of the presence of the very tiny target genetic sequence. Nothing more. Not a virus, not a genome, just a tiny little sequence.

And cytopathic effects on a cell culture, any cell culture, are just that – effectsAn effect is not the cause of the effect. And wild assumptions about the cause of the effect are just that – wild assumptions, not science. This is especially true when the cells in question have been malnourished by lowering the level of food for the cells (typically fetal bovine serum) and poisoning the cells with toxic drugs.

Dr. Mercola, I am shocked that you actually published this quote from the sketchy, brief Letter from Italy that you cited, as evidence that a “virus” has been sequenced:

“[Vero E6 aka monkey kidney] Cell culture supernatants from passage 1 (P1) of four isolates were collected, and RNA was extracted…”

First of all, as you seem to understand and as should be clear by now, “isolates” do not mean purified, isolated specimens in virology. Quite the opposite. In the case of “SARS-COV-2” studies, they are monkey/cow/human mixtures. And the authors are telling you in plain language that they extracted the RNA from the cell culture supernatants. Not from a purified specimen of an alleged virus.

These authors are telling the world that they have a soup of genetic material, and are going to concoct on their computer a so-called “viral genome” out of the zillions of sequences that they (kinda, maybe, sorta) detect therein. Because this is virology, not science.

Do we really need to discuss this any further?

Dr. Mercola, fabricated “genomes”, meaningless, impossible-to-validate PCR “tests”, wild assumptions about the cause of effects on a malnourished/poisoned cell line, and arrows added to EM images and pointing at particles that were never purified, never sequenced, never characterized, never studied with controlled experiments does not add up to science.

Virology is not a science.

Dr. Mercola, it is very distressing to see you promoting blatant pseudoscience that has been used for decades to fool and coerce people around the world in myriad ways, not limited to the utterly useless and harmful injections that have fraudulently been passed off as “immunizations”.

Every time you (or someone like Peter McCullough) do this, people such as myself have to spend hours clearing up all the confusion you have caused with the public.

You need to do your due diligence, find and share the “missing” scientific proof of viruses, or retract your blog, apologize to your readers, and get on the right side of history. You’ve had 2 years already to figure this out.

Hopefully the public will soon tire of relying on “experts” and simply read the ridiculous “virus isolation” studies for themselves. When that happens, this pseudoscience (which is really too generous a word) is finished forever.

 

Best wishes,
Christine Massey, M.Sc.
Peterborough, Ontario, Canada

Pdf of my Jan. 18, 2022 email to Dr. Mercola:
https://www.fluoridefreepeel.ca/wp-content/uploads/2022/01/Open-Letter-to-Dr.-Mercola-January-17-2022.pdf

 

Connect with Christine Massey, M.Sc.


See related:

156 Responses From 25 Countries: FOI Requests Affirm That No Record of SARS-Cov-2 Isolation Exists Anywhere

Virus Isolation…Is It Real? Andrew Kaufman, MD Responds to Jeremy Hammond

The Non-Existent Virus; an Explosive Interview With Christine Massey

Christine Massey Interviewed by Prof. Michel Chossudovsky: On FOIA Requests & Responses to the Question — Has SARS-CoV-2 Ever Been Isolated? Does the “Virus” Exist?




Pfizer Trials: All Injected Mothers Lost Their Unborn Babies

Pfizer Trials: All Injected Mothers Lost Their Unborn Babies
Pfizer trial documents reveal attempts to cover up the death of 100% of unborn babies in outcomes actually reported

by Dr. Mark Trozzi
sourced from Global Research
January 19, 2022

 

Please recall our November 23, 2021 post titled “The FDA and Pfizer are a Match Made in Hell”.

There we described how the FDA took only 108 days to approve Pfizer’s injection, but wanted 55 years to produce the documents!

Thankfully Public Health and Medical Professionals for Transparency filed a lawsuit after the FDA denied their request to expedite the release of the records, and the records are being released, albeit still too slowly.

Among the first reports handed over by Pfizer was a ‘Cumulative Analysis of Post-authorization Adverse Event Reports’ describing events reported to Pfizer up until February 2021. You can download this entire report here.

Look at table 6 from this Pfizer report. It is titled “Missing Information”. Its first heading under the topic “Missing Information” is “Use in pregnancy and lactation”. It includes this paragraph:

“Pregnancy outcomes for the 270 pregnancies were reported as spontaneous abortion (23),outcome pending (5), premature birth with neonatal death, spontaneous abortion with intrauterine death (2 each), spontaneous abortion with neonatal death, and normal outcome (1 each). No outcome was provided for 238 pregnancies (note that 2 different outcomes were reported for each twin, and both were counted).”

On the surface this states that of 270 pregnancies, there were 23 spontaneous abortions, 5 “outcomes pending”, 2 premature birth with neonatal death, 2 spontaneous abortions with intrauterine death, 1 spontaneous abortion with neonatal death, and 1 normal outcome. But note also “no outcome was provided for 238 pregnancies”.

So really we have no idea what happened with 243 (5 + 238) of the pregnancies of these injected women; they have just not been included in the report. What we do know is that of 27 reported pregnancies (270 subtract 243), there are 28 dead babies! This appears to mean that someone was pregnant with twins and that 100% of the unborn babies died.

Here is an excellent article by LifeSite News which goes into greater depth about these shocking revelations. LifeSite News cuts Pfizer some slack on the 5 “outcomes pending” which creates  the possible impression that 87.5% of the babies of the injected women died. With all respect to LifeSite, I feel correct in not counting the 5 “outcomes pending” and hence arrive at the conclusion that 100% of the unborn babies died in the injected women for whom results are presented.

The LifeSite News article also reveals deceptive number games in another article titled “Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine”, which was published in the New England Journal of Medicine on December 31, 2020. These deceptive practices attempted to cover up the fact that in first trimester pregnancies, the Pfizer injection produced 82% miscarriages.

On January 12th we shared the excellent analysis by the Canadian Covid Care Alliance of this same “Safety and Efficacy” article from the New England Journal of Medicine. This Pfizer-friendly study is a complete sham; it is replete with misrepresentation and deceptive methods. The deception and truth is revealed in detail in this video and article by the CCCA.

Dr Trozzi’s brief and Dr Nagase’s excellent interview discussing this sham article is here.

They’re killing babies; what can we do?

These injections are criminal; period. Help us serve the Cease and Desist Declaration of the World Council for Health, to any and all governments, clinics, hospitals, medical regulatory bodies, doctors, nurses, politicians, or anyone participating in any way in the manufacture, shipping, distribution, promotion, or administration of these injections. The message to anyone involved in these injection campaigns is “Stop now. This is a crime. You will be criminally and civilly responsible. The cat is out of the bag. Justice is coming.”

The Declaration can also be found here along with information and instructions for serving it.

Please keep photos and notes of to whom, when and where the declaration and notice is served. We are finalizing more resources on the World Council for Health web site to upload these photos and details. These resources will be fine tuned and found here very soon.

There are at least five million Canadians, and billions of global citizens who have resisted the injections. We, as well as many coerced injection victims who are waking up with buyer’s remorse, must be the army that stops this, and return human rights and real health care to our society.

Do not submit; unite!

 

Connect with Dr. Mark Trozzi

cover image credit: marjorie_schochow / pixabay