The Convoy That United the Country: Video Compilation by Canada’s Justice Centre for Constitutional Freedoms

The Convoy That United the Country: Video Compilation by Canada’s Justice Centre for Constitutional Freedoms

by Justice Centre for Constitutional Freedoms
August 15, 2022

 

The Justice Centre for Constitutional Freedoms presents: “The Convoy that United the Country”, which premiered at the 2022 George Jonas Freedom Award dinner honouring Tamara Lich.

 

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cover image is a screenshot from the video above




“Uninformed Consent”: Powerful Documentary by Matador Films — Exposing Massive Deception, Cruelty & Genocide Imposed Upon Humanity by Global Elites

“Uninformed Consent”: Powerful Documentary by Matador Films — Exposing Massive Deception, Cruelty & Genocide Imposed Upon Humanity by Global Elites

by Matador Films
July 31, 2022

 

Watch the official public release of Matador Films new “Uninformed Consent” documentary, presented by Librti.com and Vaccine Choice Canada.

An in-depth look into the Covid 19 narrative, who’s controlling it, and how it’s being used to inject an untested, new technology into almost every person on the planet.

The film explores how the narrative is being used to strip us of our human rights while weaving in the impact of mandates in a deeply powerful story of one man’s tragic loss.

Hear the truth from doctors and scientists not afraid to stand up against Big Pharma and the elite class who profit from mandates.

Written & Directed by Todd Harris, Matador Films.

https://uninformedconsent.ca/



“This film reveals that we have been massively deceived by our own governments, public health, and mainstream media.” – Ted Kuntz – President – Vaccine Choice Canada

“Can’t wait for this movie to come out. Crude propaganda ‘crisis of the uninjected’ followed by censorship, reprisal and totalitarian brute force on the people. I say bring it on!” – Dr. Peter McCullough – Internist & Cardiologist – Professor of Medicine

“Todd is a brilliant filmmaker who has a unique way of exposing the devastation to families from the mandates.” – Odessa Orlewicz – Partner – Librti.com

“Uninformed Consent is the most scientific and factual TRUTH to come out of Canada in the last 3 years. If you are a parent, this should be on the TOP of your viewing list. It is TRULY an eye-opener. Everyone needs to see this film!” – Amanda Forbes – Children’s Health Defense

“This is the most powerful documentary of the Covid era.” – Sherri Strong – Children’s Health Defense Canada

 

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CDC Drops Quarantine, Distancing Recommendations, as 1.3 Million COVID Vaccine Injuries Reported to VAERS

CDC Drops Quarantine, Distancing Recommendations, as 1.3 Million COVID Vaccine Injuries Reported to VAERS
VAERS data released Friday by the Centers for Disease Control and Prevention show 1,379,438 reports of adverse events from all age groups following COVID-19 vaccines, including 30,162 deaths and 251,075 serious injuries between Dec. 14, 2020, and Aug. 5, 2022.

by Megan Redshaw, The Defender
August 12, 2022

 

Editor’s note: In previous VAERS weekly updates, The Defender focused exclusively on U.S. reports in the sections where reports are broken out by age groups and types of adverse events. However, excluding foreign reports from these categories excludes thousands of vaccine injuries reported to the system, so those sections now include all — U.S. and foreign combined — reports submitted to VAERS in the categories indicated.

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,379,438 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and Aug. 5, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 7,964 adverse events over the previous week.

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 30,162 reports of deaths — an increase of 181 over the previous week — and 251,075 serious injuries, including deaths, during the same time period — up 1,959 compared with the previous week.

Of the 30,162 reported deaths, 19,462 cases are attributed to Pfizer’s COVID-19 vaccine, 8,038 cases to Moderna, 2,613 cases to Johnson & Johnson (J&J) and no cases yet reported for Novavax.

Excluding “foreign reports” to VAERS, 854,084 adverse events, including 13,972 deaths and 87,488 serious injuries, were reported in the U.S. between Dec. 14, 2020, and Aug. 5, 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 13,972 U.S. deaths reported as of Aug. 5, 7% occurred within 24 hours of vaccination, 15% occurred within 48 hours of vaccination and 54% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 604 million COVID-19 vaccine doses had been administered as of Aug. 3, including 357 million doses of Pfizer, 228 million doses of Moderna and 19 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.

VAERS data from Dec. 14, 2020, to Aug. 5, 2022, for 6-month-olds to 5-year-olds show:

VAERS data from Dec. 14, 2020, to Aug. 5, 2022, for 5- to 11-year-olds show:

VAERS data from Dec. 14, 2020, to Aug. 5, 2022, for 12- to 17-year-olds show:

  • 32,945 adverse events, including 4,189 rated as serious and 118 reported deaths.
    According to the CDC, “VAERS data available to the public include only the initial report data to VAERS. Updated data which contains data from medical records and corrections reported during follow up are used by the government for analysis. However, for numerous reasons including data consistency, these amended data are not available to the public.”
  • 268 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 94% of cases attributed to Pfizer’s vaccine.
  • 1,304 reports of myocarditis and pericarditis with 650 cases attributed to Pfizer’s vaccine.
  • 298 reports of blood clotting disorders with 275 cases attributed to Pfizer.
  • 26 cases of postural orthostatic tachycardia syndrome (POTS) with all cases attributed to Pfizer’s vaccine.

VAERS data from Dec. 14, 2020, to Aug. 5, 2022, for all age groups combined, show:

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

New CDC COVID guidance ditches distinctions between vaccinated and unvaccinated

The CDC on Thursday issued sweeping new recommendations as part of the agency’s efforts to overhaul its COVID-19 guidance.

“This guidance acknowledges that the pandemic is not over, but also helps us move to a point where COVID-19 no longer severely disrupts our daily lives,” the CDC’s Greta Massetti said in a press release.

Here are the biggest changes to the CDC’s guidance:

  • Unvaccinated people now have the same guidance as vaccinated people.
  • Those who are exposed to the virus are no longer required to quarantine regardless of vaccination status.
  • Students may stay in class even if they’ve been exposed to COVID-19.
  • Six-foot social distancing is no longer recommended.
  • Contact tracing and routine surveillance testing of symptomatic people are no longer recommended in most settings.

According to The New York Times, the CDC has been working for months on the new guidance which builds on previous guidance issued in February that reduced isolation times for those who get COVID-19.

The agency said it is making changes to its guidance now because “vaccination and prior infections have granted many Americans some degree of protection against the virus, and treatments, vaccines and boosters are available to reduce the risk of severe illness.”

According to The National Law Review:

“The CDC’s focus on individual responsibility, the removal of distinctions between vaccinated and unvaccinated, the removal of quarantine recommendations and the discussion of mask wearing as an individual responsibility are good news for employers who are considering relaxing COVID-19 workplace requirements.

“This likely will not be the last we hear from the CDC on this topic. Indeed, the CDC stated that it intends to issue more specific guidance for settings such as healthcare, congregate living, and travel.”

Pfizer vaccine efficacy in teens wanes 27 days after second dose

study published Aug. 8 in The Lancet showed the effectiveness of the Pfizer-BioNTech COVID-19 vaccine against symptomatic infection among adolescents “rapidly declined over time,” waning from just 27 days after the second dose.

Researchers analyzed data from 503,776 COVID-19 tests of 2,948,538 adolescents — ages 12-17 — in Brazil from Sept. 2, 2021, to April 19, 2022, and 127,168 tests of 404,673 adolescents in Scotland from Aug. 6, 2021, to April 19, 2022.

The study showed vaccine efficacy began to decline 27 days after the second dose for both countries, plummeting to 5.9% (95% CI 2.2–9.4) in Brazil and dropping to 50.6% (95% CI 42.7–57.4) in Scotland at 98 days after adolescents received the second dose.

While protection against symptomatic COVID-19 dropped dramatically in both countries less than one month after the second dose, protection against severe illness — defined as hospitalization or death within 28 days — remained above 80% in Brazil from 28 days to 98 days and beyond.

The authors sought to assess protection against severe illness in Scotland but were unable to do so because so few cases of severe COVID-19 in adolescents in Scotland were reported during the time of the study.

The authors concluded that “two doses are insufficient to sustain protection against symptomatic disease” in adolescents and recommended more research be done on the need for booster doses.

‘Stunning’ link between Pfizer vaccine and myocarditis in teens, study shows

preprint study conducted during Thailand’s national COVID-19 vaccination campaign showed what one physician described as a “stunning” association between myocarditis and the Pfizer-BioNTech vaccine.

The study analyzed 301 participants ages 13-18 who were healthy and without abnormal symptoms after receiving their first vaccine dose. Participants with a history of cardiomyopathy, tuberculous pericarditis or constrictive pericarditis and severe allergic reaction to the COVID-19 vaccine were excluded from the study.

Researchers found that 18% of the 301 teens analyzed had an abnormal electrocardiogram, or EKG after receiving their second dose of Pfizer, 3.5% of males developed myopericarditis or subclinical myocarditis, two were hospitalized and one was admitted to the ICU for heart problems.

Cardiovascular adverse events observed during the study included tachycardia (7.64%), shortness of breath (6.64%), palpitation (4.32%), chest pain (4.32%) and hypertension (3.99%).

Fifty-four adolescents had abnormal electrocardiograms after vaccination, three patients had minimal pericardial effusion with findings compatible with subacute myopericarditis and six patients experienced mitral valve prolapse.

All patients were male and had abnormal electrocardiograms, particularly sinus tachycardia. Researchers said the clinical course was mild in all cases.

Military using ‘Comirnaty’ vaccine produced at facility not approved by FDA

In an exclusive interview with The Defender, a U.S. Coast Guard (USCG) service member alleged the U.S. Department of Defense (DOD) is administering COVID-19 vaccines from vials of Pfizer’s Comirnaty-labeled vaccines that are not produced in a facility approved by the FDA.

Lt. Chad R. Coppin, in a July 30 declaration submitted to Sen. Ron Johnson (R-Wis.) under penalty of perjury, detailed his personal investigation into the availability and origin of Comirnaty-labeled COVID-19 vaccine vials at U.S. military facilities.

Coppin relayed his concerns in an interview with The Defender, as did Holly Freincle, the wife of a U.S. military service member stationed at Fort Detrick, Maryland, who corroborated Coppin’s claims that Comirnaty-labeled vaccine vials are appearing at military service facilities.

Until now, the DOD has claimed the Pfizer-BioNTech COVID-19 vaccine, administered under Emergency Use Authorization, is “interchangeable” with the fully licensed Pfizer Comirnaty vaccine — which until recently, was said to be unavailable at military facilities.

In his July 30 declaration, Coppin, who has served with the USCG since March 2002, reported that after a long period of unavailability, the “Comirnaty” vaccine began to appear at U.S. military facilities in June.

 

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©August 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.

cover image credit: geralt 




Former College Football Coach Fired for Refusing COVID Vaccine Files $25 Million Claim Against Washington State

Former College Football Coach Fired for Refusing COVID Vaccine Files $25 Million Claim Against Washington State
A former Washington State University football coach is seeking $25 million from the university for wrongful termination after he was fired last year for refusing to get vaccinated against COVID-19.

by Megan Redshaw, The Defender
August 11, 2022

 

A former Washington State University football coach is seeking $25 million from the university for wrongful termination after he was fired last year for refusing to get vaccinated against COVID-19, The Seattle Times reported Tuesday.

A tort claim was filed April 27 on behalf of Nick Rolovich with the state’s risk management office. Filing a claim is a prerequisite to filing a lawsuit against a state agency.

There’s a 60-day waiting period between when a claim is filed and when the claimant can file a lawsuit. As of Wednesday, a spokesperson for Attorney General Bob Ferguson said no suit had been filed, according to The Washington Post.

After denying Rolovich’s request for a religious exemption from Gov. Jay Inslee’s COVID-19 vaccine mandate for state employees, the university in October 2021 fired Rolovich.

At the time of his firing, Rolovich was subject to a five-year contract with three seasons remaining and was paid $3.2 million per year — the highest public salary in the state. He had coached 11 games with the Cougars over two seasons.

Rolovich’s attorney, Brian Fahling, said at the time his client would take legal action for religious discrimination. He filed a 34-page letter with the university appealing the university’s decision to fire Rolovich, but the appeal was denied.

Rolovich, a Catholic, is not the first person to file a claim for wrongful termination or religious discrimination over an employer’s failure to grant a religious exemption to a COVID-19 vaccine mandate.

Liberty Counsel on July 29 settled the nation’s first class action lawsuit on behalf of healthcare workers who were unlawfully discriminated against and denied religious exemptions to the COVID-19 vaccine mandate by their employer, Chicago-based NorthShore University HealthSystem.

The $10,337,500 settlement, filed in the federal Northern District Court of Illinois, compensates NorthShore employees who were “punished for their religious beliefs against taking an injection associated with aborted fetal cells.”

As part of the settlement agreement, NorthShore also will change its unlawful “no religious accommodations” policy to make it consistent with the law and must provide religious accommodations in every position across its numerous facilities.

In addition, employees who were terminated because they refused to receive a COVID-19 vaccine on religious grounds will be eligible for rehire if they apply within 90 days of the final settlement approved by the court, and they will retain their previous seniority level.

The amount of individual payments from the settlement fund will depend on how many valid and timely claim forms are submitted during the claims process.

If the settlement is approved by the court and nearly all of the affected employees file valid and timely claims, it is estimated employees who were terminated or resigned because of their religious refusal of a COVID-19 vaccine will receive approximately $25,000 each.

Also under the settlement, employees who were forced to get the shot against their religious beliefs to keep their jobs will receive approximately $3,000 each.

The 13 healthcare workers who are lead plaintiffs in the lawsuit will receive an additional approximate payment of $20,000 each for their role in bringing this lawsuit and representing the class of NorthShore healthcare workers.

Lawsuits over denied exemptions or insufficient accommodations to COVID-19 vaccine requirements began last September after the U.S. Food and Drug Administration granted full approval to the Pfizer-BioNTech Comirnaty vaccine, allowing more employers to enact vaccine mandates.

Workers as of May 19, 2022, had filed at least 66 lawsuits since September 2021 against private employers for refusing to grant exemptions to COVID-19 vaccine requirements, according to Bloomberg Law.

Judges rejected workers’ requests for immediate court orders blocking enforcement of mandates in 22 cases.

In one case involving United Airlines Inc., the airline changed its policy allowing accommodations rather than contest the lawsuit.

According to Bloomberg Law, 59% of lawsuits filed over COVID-19 vaccine mandates are related to an employer’s response to faith-based requests for accommodation.

About 22% of lawsuits involve contesting a company’s handling of both religious and disability requests and 5% involve health-related accommodations.

 

©August 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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Father Whose 7 Year Old Son’s Heart Was Destroyed by Myocarditis After Covid Shot Calls Up Pharmacist in Apoplectic Anger: “What Is Wrong With You?”

Father Whose 7 Year Old Son’s Heart Was Destroyed by Myocarditis After Covid Shot Calls Up Pharmacist in Apoplectic Anger: “What Is Wrong With You?”
“Are you braindead?..You know what the prognosis is? 20% of people with myocarditis die!”

by Celia Farber, The Truth Barrier
August 7, 2022

 

On these recordings, the raw, agonized truth if this epoch emerges. A father whose son was injected against his will rages at a pharmacist, for not having let the parent know about the documented risks.

“So you don’t want to scare the parents with something that is actually happening, that’s happened to my kid. Are you out of your mind?

 

[Video: Part 1]


[Video: Part 2]


[Video: Part 3]


[Video: Part 4]

 

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cover image credit: Geisteskerker / pixabay




The “Unvaccinated” Question (Revisited)

The “Unvaccinated” Question (Revisited)

by CJ Hopkins, Consent Factory, Inc.
August 6, 2022

 

 

 

On 1 September, 1941, Chief of Reich Security Reinhard Heydrich, one of the most fanatical, mass-murdering Nazis, issued a now notorious decree ordering Jews above the age of six to wear an identifying badge in public. The Jewish Badge, a yellow Star of David with the word “Jew” inscribed inside the star, was meant to stigmatize and humiliate the Jews and was also used to segregate them and monitor and control their movements.

Nothing like that is happening currently, especially not in New Normal Germany.

What is happening currently in New Normal Germany is the fascist fanatics in control of the government are rewriting the “Infection Protection Act,” again — as they have been doing repeatedly for the last two years — in order to allow themselves to continue to violate the German constitution (the “Grundgesetz) and rule the nation by arbitrary decree under the guise of “protecting the public health.”

This repeatedly revised “Infection Protection Act” — which has granted the government of New Normal Germany the authority to order lockdowns, curfews, the outlawing of protests against the New Normal, the mandatory wearing of medical-looking masks, the segregation and persecution of “the Unvaccinated,” etc. — is of course in no way remotely comparable to the “Enabling Act of 1933,” which granted the government of Nazi Germany the authority to issue whatever decrees it wanted under the guise of “remedying the distress of the people.”

There is absolutely no similarity whatsoever between these two pieces of legislation.

I mean, look at this “Autumn/Winter Plan” for the new revision of the “Infection Protection Act,” which will remain in effect from October until Easter, and which government officials and state propagandists (a/k/a the German media) are likening to “snow chain ordinances.”

There is absolutely nothing creepily fascistic or remotely Nazi about this plan.

 

 

Sorry, it’s in German. Allow me to translate.

On planes and trains and at the airports and train stations, everyone will be forced to wear doggy-snout masks — i.e., FFP2 “Filtering Face Pieces” as defined by the EN 149 standard — except for the staff of the airports and train stations, and the flight attendants, conductors, etc., who will only be forced to wear “medical-looking masks.” In hospitals, clinics, doctors’ offices, nursing homes and other healthcare facilities, everyone, including the staff, will not only be forced to wear the dog-snout masks but they will also be forced to submit to testing, unless they can provide proof of “vaccination” (or recovery, which also means being tested) within the previous three-month period. On the premises of private companies, i.e., offices, factories, warehouses, and so on, the previously rescinded Arbeitsschutzverordnung (“Corona Occupational Safety Ordinance”) — masks, tests, forced “vaccinations,” “social distancing,” plastic barriers, etc. — will go back into effect in October and will remain in effect until the Easter holidays.

The individual federal states will be empowered to impose other senseless “restrictions,” like general mask mandates in shops, restaurants, and every other type of “interior spaces,” limits on the number of people who can gather publicly or in their homes, and mandatory masks for kids in schools and testing in kindergartens and daycare facilities. In restaurants, bars, theaters, museums, sports facilities, and pretty much everywhere else in society, the federal states can demand that people show proof of recent “vaccination” or recovery to be exempted from having to wear a mask.

OK, allow me to translate again.

What that last part means is that anyone who refuses to submit to repeated “vaccination” or testing will be forced to wear a mask in public to identify themselves as “Unvaccinated” (i.e., the New Normal Reich’s official “Untermenschen”).

So, OK, maybe it’s a little creepily fascistic and not as non-Nazi as I suggested above. I put it this way in a recent tweet …

 

 

Needless to say, this could get confusing, as the New Normals are extremely attached to their masks, which they’ve been wearing — like Nazis wore swastika lapel pins — to publicly signal their “solidarity” (i.e., mindless conformity to the new official ideology) for going on the last two and half years. And now the masks will function like the “Jewish Badges” with the Star of David that the Nazis forced the Jews to wear, except on public transportation, and planes and trains, unless the federal states decide to force everyone to wear masks everywhere, in which case … well, you get the general idea.

Still, the fact that everyone will have to present their “vaccination papers” (or their “recovery papers”) to enter a restaurant, or a bar, or go to the cinema or the theater, and, basically, to do anything else in society, should make up for the mask confusion. I mean, what kind of a fascist society would it be if you didn’t have to show your “papers” to some beady-eyed goon to get a cup of coffee?

Now, before you report me to the BfV, i.e., Germany’s federal domestic intelligence agency, for “relativizing the Holocaust” and “delegitimizing the democratic state,” both of which are crimes here in Germany, I want to say, again, for the record, that I do not advocate using the yellow Star of David to protest the New Normal (as in the photo in the tweet above). I think it is foolish, and counterproductive. The New Normal has nothing to do with the Holocaust, or the Jews, or even Nazism per se.

But let’s be clear about what’s happening in Germany.

What is happening is, a new official ideology is being imposed on society. It is being imposed on society by force. And now, those of us who refuse to conform to it will be ordered to walk around in public wearing visible symbols of our non-conformity.

I’m sorry, but the parallels are undeniable.

 

 

This new official ideology has nothing to do with a respiratory virus or any other public health threat. At this point, I do not have to repeat this argument. The majority of countries around the world have finally rescinded their “emergency measures” and acknowledged the facts that we “conspiracy theorists” have been citing for the past two and a half years, and that we have been relentlessly demonized and censored for citing.

Not even Germany’s recent independent evaluation of its “Corona Measures” could produce any evidence supporting their effectiveness. Seriously, the New Normal German authorities are basing their claim for the efficacy of mask mandates on “the Golden Syrian Hamster Model.” (You probably think I’m joking, but I’m not.) And Karl Lauterbach, the fanatical Minister of Health, has openly stated that forcing “the Unvaccinated” to wear masks in public is a “motivation” tactic to harass them into following orders and submitting to a “vaccination” that even the German government now admits has killed or seriously injured tens of thousands of people, at minimum, in Germany.

No, this new official ideology, the New Normal — which is still very much in effect in places like Germany, China, Canada, Australia, New York, California, etc. — is nakedly, undeniably, purely ideological. It is based, not on facts, but belief. It is a belief system, as is every other ideology. It is essentially no different than an official religion … one which demonizes and persecutes all other religions, and non-religions, and all other belief systems.

According to this new official belief system, those of us who maintain different beliefs, and refuse to convert to the new official beliefs (or pretend to convert to the new official beliefs), are dangerous, foreign elements in society. And thus, from now on, in New Normal Germany, we will be forced to wear a visible symbol of our different beliefs (our “otherness”) in public, so that the authorities and the Good German masses will be able to identify us.

Is any of this sounding vaguely familiar?

I’m fairly certain that someone will read this (and see the tweets I included above) and report me for “relativizing the Holocaust.” For the record, I am not “relativizing the Holocaust.” I’m comparing one totalitarian system to another. Yes, Nazi Germany and New Normal Germany are two very different totalitarian systems, and I have outlined their essential differences and similarities, but, come on, this is not that fucking hard. In Nazi Germany, the Jews were the scapegoats. In New Normal Germany, it’s “the Unvaccinated.”

How much more blatant does it have to get before people stop pretending that this isn’t what it is? Do the authorities have to literally put us in camps? How many more people have to die or be seriously injured by “vaccinations” they did not need but were forced to submit to? I’m not talking to the New Normals now, nor to the people who have been fighting this all along. I’m talking to the people who see what is happening, and are horrified by what is happening, but, for whatever reasons, have refused to speak out … and, yes, I know there are very good reasons. Some of you have families to support, and careers to protect, and, seriously, I get it. But how far does it have to go? At what point do you feel you have to speak out regardless of the personal and professional consequences?

Maybe take some time and meditate on that.

Oh, and here’s a little visual aid that might help folks with their meditations. It’s some graffiti that someone painted on the wall of a courtyard here in New Normal Germany, in the Autumn of 2021, I think. I posted it back then, but it didn’t make much of an impression. Perhaps it will make one now.

I’ll translate. It reads “GAS THE UNVACCINATED.”

 

 

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Cancer Explosion: Pathologist Reports on Rise of Aggressive Cancers Since mRNA Shots

Cancer Explosion: Pathologist Reports on Rise of Aggressive Cancers Since mRNA Shots

sourced from Technocracy News
August 5, 2022

 

Doctors for Covid Ethics in Europe highlighted the professional observations of Dr. Ute Kruger, Chief of Pathology at Lunds University in Sweden: Cancer went haywire when the mRNA shots began. The health of the world population is being severely compromised by mRNA/DNA injections and yet they are not stopped, underscoring TN’s claim that Technocracy is at war with humanity. ⁃- Patrick Wood, Technocracy News Editor

 



[In this video (26 min, Swedish with English subtitles), MD/pathologist Ute Krueger describes her findings on breast cancer and other cancers in the era of gene-based COVID vaccines. She finds increased numbers of cancers, in younger patients, which are larger in size and growing more rapidly and aggressively already at the time of the initial diagnosis.]

 

Excerpt from article: Turbo Cancer by

Dr. Ute Kruger is a researcher and senior physician at Lunds University in Sweden. She’s the Chief of Pathology, a field that she’s worked in for the last 25 years, with a specialty in breast cancer diagnosis for the past 18 years. She’s studied thousands of autopsies and breast cancer samples. She’s extremely familiar with the industry and patient age, tumor size, and malignancy grade are all within her field of expertise and have had a natural rhythm throughout her career. That natural rhythm came to a halt in 2021 once the vaccine rollout began.

Doctors for Covid Ethics posted an interview with her where she shared her concerns about unusual features that have been showing up in samples from the past year.

    • Age – The average ages of the samples she received dropped, with a rise in the number of samples from people in their 30’s-50’s.
    • Size – It used to be unusual for Dr. Kruger to find a tumor 3 cm in size. In this new environment, she’s regularly seeing tumors of 4 cm, 8 cm, 10 cm, and the occasional 12 cm. In a shocking anecdote, 2 weeks ago she found a 16 cm tumor that took up an entire breast.
    • Multiple Tumors – Dr. Kruger has begun to see more cases of multiple tumors growing in the same patient, sometimes even in both breasts. She had 3 cases within 3 weeks of patients who had tumors growing in multiple organs. One had tumors in his/her breast, pancreas and lungs within months of getting vaccinated.
    • Recurrence – There has been an uptick in patients who have been in remission from their cancer for many years, suddenly getting an aggressive recurrence of their cancer shortly after vaccination.
Speaking Out

Dr. Kruger initially thought that these turbo cancers, as she calls them, were due to delayed doctor appointments from Covid lockdowns, but that period is long over, and the tumors are still growing aggressively, and in younger patients. She reported some of these cases to the FDA, and while some higher-ups initially agreed to meet with her, they canceled the meeting with no explanation the next day and sent a phone agent to take her report instead.

Six months ago Dr. Kruger appeared at a panel in Germany to present her theory that vaccination is causing aggressive tumors, and she asked for help from the doctors at that summit in collecting data. Unfortunately, few of them have been willing to collect that data and share it with her.

Autopsies

Part of Dr. Kruger’s time is spent on autopsies, and she drew attention to numerous concerning anomalies.

    1. A 60-year-old had multiple malignant diseases. He got 2 doses of the Covid vaccine during chemotherapy and then developed Guillain Barre Syndrome. She found inflammation in the spinal cord, brain, and blood vessels.
    2. An 80-yr-old woman became paralyzed one month after vaccination. Dr. Kruger found a hemorrhage in the spinal cord near the neck, which is something she’s never seen before. Under the microscope, she saw inflammation in the vessel that caused the rupture and caused bleeding. She also found inflammation in the heart muscles, which is myocarditis.
    3. Dr. Kruger was called to settle a dispute between a family of a deceased person, and the doctors who signed the autopsy. The family and their physician believed the death was a result of the Covid vaccine, yet the ones who performed the autopsy didn’t come up with any findings to support that and did not link the death to the vaccine. When Dr. Kruger performed her own autopsy, she found evidence of myocarditis and vasculitis- inflammation of blood vessels in the lungs. The original autopsy either missed those signals or didn’t look for them, and the family was correct. Dr. Kruger shared her opinion, supported by another senior-level pathologist from Germany, that the death was indeed due to the Covid vaccine.

Dr. Kruger outlined 3 major issues with the way autopsies are currently being run in practice:

    1. Patient information is sloppy. Dr. Kruger personally had several cases where clinicians had written that the patient was unvaccinated for the autopsy, when in fact in their medical files it was documented that they were vaccinated for Covid.
    2. The typical autopsy doesn’t run exams deep enough to diagnose the root cause of certain medical issues. They don’t do rigorous histopathological testing of the tissues where vaccine damage would likely show up, but which is necessary to detect markers of vaccine-induced injury, such as immunological infiltrates or spike proteins in myocardial tissues. Dr. Kruger ran more thorough exams and found myocarditis and inflammations that were missed by the original autopsy.
    3. There’s a lack of experience in evaluating these findings, and a lack of desire to properly contextualize cases. In addition, most autopsy clinicians don’t report cases to the FDA.

While Dr. Kruger’s testimony is by nature anecdotal, as a top-level pathologist of many years, her concerns should be taken very seriously and investigated further. Of course, that would require an honest regulation system which seems to be sorely lacking these days.

“I’m Watching People Being Killed”

Dr. Kruger stated that she sees vaccination as a trigger for fast-growing tumors and autoimmune diseases. She’s seeing a lot of inflammation alongside tumors, and of course, it’s not only breast cancer. Many other pathologists have reported to Dr. Kruger that they’re seeing an elevation in cancers, cancers in multiple organs, and rare cancers.

She ended off by saying “I studied medicine because I wanted to help people. But now it feels like I’m watching people being killed and there’s nothing I can do”.

The first step to solving any issue is acknowledging there’s a problem. We have a huge problem, and in order to begin to resolve it, it must be acknowledged. It’s time to start pressuring doctors to speak out. Any doctor who’s aware enough to understand that something is off must begin to address the issue. An additional motivation may be the pressure of knowing that it’s all about to blow up, and they don’t want to be standing on the wrong side of the line when it does.

 

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cover image credit: Justinite / pixabay




130 Coast Guard Members Sue Federal Government Over Vaccine Mandates

130 Coast Guard Members Sue Federal Government Over Vaccine Mandates
More than 130 U.S. Coast Guard members filed a class action lawsuit alleging the religious exemptions they filed in response to the Biden administration’s COVID-19 vaccine mandate for military service members were unlawfully denied. 

by Michael Nevradakis, The Defender
August 2, 2022

 

More than 130 U.S. Coast Guard members filed a class action lawsuit alleging the religious exemptions they filed in response to the Biden administration’s COVID-19 vaccine mandate for military service members were unlawfully denied.

The lawsuit, filed July 25 in the U.S. District Court for the Southern District of Texas —  Galveston Division, also challenges the constitutionality of the mandate.

The number of plaintiffs exceeds 130 and will likely end up surpassing 200, according to Dale Saran, one of the attorneys representing the service members.

The suit names four defendants: Alejandro Mayorkas, secretary of the U.S. Department of Homeland Security (DHS); Linda L. Fagan, commandant of the Coast Guard; Lloyd Austin, secretary of the U.S. Department of Defense (DOD) and Dr. Janet Woodcock, acting commissioner of the U.S. Food and Drug Administration (FDA).

Plaintiffs are either active-duty or reserve members of the Coast Guard, and all “have sincerely held religious beliefs that prohibit them from receiving the COVID-19 vaccine.”

According to the complaint, under the August 24, 2021, DOD vaccine mandate, the military theoretically offers “medical, administrative, and Religious Accommodation Requests (RARs) to the mandate,” while the Coast Guard’s vaccine mandate, issued two days later, “incorporates the provisions of the DOD mandate.”

The suit alleges:

“In practice, only servicemembers with medical or administrative reasons for an exemption from the mandate are accommodated, and even those sparingly, while RARs are universally denied unless the requester is eligible for administrative separation – i.e. imminently leaving the Service.”

This “conclusively demonstrates that the Armed Services have systematically and willfully violated service members’ free exercise rights under RFRA [Religious Freedom Restoration Act] and the First Amendment,” the lawsuit states.

In all, the lawsuit alleges:

  • Violation of the Religious Freedom Restoration Act.
  • Violation of the Free Exercise Clause of the First Amendment.
  • Violation of the Fifth Amendment’s Due Process clause, pertaining to substantive due process.
  • Violation of the Fifth Amendment’s Due Process clause, pertaining to procedural due process.
  • Violations of informed consent laws and the Public Health Service Act.
  • Violations of the Administrative Procedure Act.

The lawsuit also questions the DOD’s claim — which has come under judicial scrutiny — that the Pfizer-BioNTech COVID-19 vaccine, issued under an Emergency Use Authorization (EUA), is “interchangeable” with the FDA-licensed Pfizer Comirnaty vaccine.

Arguing that the plaintiffs “will suffer concrete and particularized harm” from these mandates, including potential involuntary separation, forced retirement, removal from senior or leadership positions, duty and promotion restrictions, PCS restrictions, letters of reprimand or counseling, loss of pay and benefits or other adverse actions, the service members are requesting from the court to:

  • Declare the DOD and Coast Guard mandates “unlawful and unconstitutional” and to vacate those orders.
  • Declare the defendants’ “no accommodation policy” is unconstitutional under the First and Fifth Amendments and violates the Religious Freedom Restoration Act.
  • Enjoin the implementation of the DOD and Coast Guard mandates with respect to the plaintiffs and all service members.
  • Enjoin any adverse or retaliatory action against the plaintiffs.
  • Award all legal, court and attorneys’ fees as well as other relief to the plaintiffs.

Remarking on the recent block placed on the vaccine mandate for the Air Force, Space Force and Air National Guard by a federal judge in Ohio, and the recent $10.3 million settlement awarded to over 500 Illinois healthcare workers over the denial of religious exemptions to a COVID-19 vaccine mandate, Travis Miller, one of the attorneys representing the plaintiffs in the Coast Guard lawsuit, told The Defender:

“The latest ruling against the Air Force COVID-19 vaccine mandate is further proof that the military has violated — and continues to violate — the rights of religious service members.

“Courts around the country have recognized this fact, and yet President Biden and Secretary Austin continue targeting the faithful for discipline and removal.  It’s an indictment of leadership.

“The $10.3 million class action settlement will hopefully lead the way for other successful challenges to employer COVID-19 vaccine mandates that  discriminate against those with sincerely held religious beliefs.”

Saran described the Coast Guard as “the forgotten branch of the Armed Services,” which has been largely overshadowed as mandate-related cases from other branches attained more public prominence.

Saran told The Defender:

“They are being treated at least as badly as any of the other Armed Services —  arguably worse — in part because they get little to no publicity about what they’re enduring, in part because they number less than 30% of the personnel of the Marine Corps, itself the smallest of the overseas warfighting forces [~45,000 active duty compared to ~175,000 active duty].

“These folks represent some of the most dedicated, selfless defenders of American lives here at home … They deserve better, they deserve advocates for their rights and that’s why we’re filing on their behalf.”

Service members forced to get vaccinated ‘under duress’

The lawsuit includes written testimony from several service members who shared their experiences in attempting to secure religious exemptions from the Coast Guard.

Sabrina Wilder is an operations specialist from Rosharon, Texas, serving at the Coast Guard Vessel Traffic Service in Houston/Galveston, Texas. She first joined the Coast Guard in 2016. In September 2021, she submitted a RAR, and received the following email in response:

“For both processes [medical or religious] we were told that you are still likely to be Administratively Separated if you receive either exemption.

“The exemption will just permit you to not receive the vaccine before you are … processed. Please do not think you will be allowed to continue to serve if you are exempted.

“This was the official communication in the brief today with the Sector Commander, Chaplin, and Medical present.”

Wilder proceeded with the RAR. According to Wilder, while the exemption requests of unvaccinated service members were pending, they were required to “walk around base with masks on, thus identifying them to the entire command,” while their travel was restricted to no more than 50 miles from base. Vaccinated members were under no such restrictions.

Wilder’s RAR was denied in January 2022, as was her appeal, on June 2, 2022. On June 15, she “was ordered to go to the nearest Walgreen’s to receive the vaccine.” When she refused, she received a counseling form and is now at risk of being discharged.

Timothy Jorden is a maritime enforcement specialist stationed in Houston. He has been on active duty in the Coast Guard since 2016, and previously served in the Marine Corps for four years.

His RAR was initially denied on Dec. 3, 2021. On Dec. 9, 2021, he submitted a request for all of the pertinent documentation relating to the denial and on Dec. 17, 2021, he submitted an appeal. He never received a response to his initial request, but received a “form denial” to his appeal five months later, despite a Coast Guard requirement that a response be granted within 30 days.

According to the lawsuit, the denial he received “was identical to those of other Coast Guard members he knows, despite being from different commands.”

In the meantime, like Wilder, Jorden was “restricted to within 50 miles of his base — in violation of military law,” and was required to wear a mask on base while those who were “vaccinated” were not. His previously approved leave to visit his family was revoked.

Despite these restrictions and initially being told “he was non-deployable because of his vaccination status,” he was almost immediately notified “he would have to be part of a Presidential security detail.” As the lawsuit states:

“Plaintiff Jorden has his leave and liberty restricted as a general matter, and was told he was non-deployable, but the very next day when his particular expertise was necessary to support missions around the country, including a Presidential protective detail, his ‘threat’ to others instantly evaporated.

“This is just one instance of many showing that the entire framework and claims about the unvaccinated are nothing more than facade.”

Michael Bazzrea is a senior chief party officer from Ardmore, Oklahoma, serving in Galveston, Texas. He has been enlisted in the Coast Guard since 1994. He remained on active duty until 1998, and remained part of the Reserve since then.

In July 2021, Bazzrea tested positive for COVID-19 and subsequently submitted a RAR, which was denied, as was his appeal. He was told that once an “FDA-approved” vaccine was available, he would be ordered to take it “regardless of any civil rights complaints” he might have.

On July 6, 2022, Bazzrea was ordered to get vaccinated within 10 days. In his own words:

“I stated in my appeal that I did not want to take the vaccine and that being forced to do so would put me in duress. However, I was ordered to do so regardless.

“An email was sent out from [my] Chief of Staff stating anyone with a denied RA appeal that had not received the vaccination would NOT be eligible for advancement or promotion and that this email would serve as official policy.

“I was told I would be facing removal from the advancement eligibility list and the inability to take positions such as silver or gold badge positions as well as separation from the Coast Guard.”

The lawsuit states that “under great duress, moral conflict, and now with great remorse,” Bazzrea “took the first shot … against [his] religious and personal beliefs,” as “it was his last chance at advancement to Master Chief (E-9),” a promotion which entailed “a large financial difference in retirement to his family.”

Aaron Cheatum is a First Class Petty Officer in the Coast Guard Reserve, stationed in Galveston. He first enlisted in the Coast Guard in 2000, and was on active duty for 11 years before joining the Reserve.

Cheatum submitted his RAR on Nov. 29, 2021. It was denied on Jan. 31, 2022, despite stating that the Coast Guard did “not question the sincerity of [his] religious belief or whether vaccine requirements would substantially burden [his] religious practice.”

His appeal also was denied, even though in the meantime, Cheatum tested positive for COVID-19 on Jan. 28, 2022. In his own words:

“On July 8, 2022, facing a loss of earned retirement, loss of VA benefits, inability to advance in rank, loss of medical insurance, being processed for discharge with a less than Honorable discharge after 22 years, and under duress, I violated my own religious conviction by receiving the initial COVID-19 vaccine.”

Caleb Wadsworth is a lieutenant in the Coast Guard, assigned to the Coast Guard Sector/Air Station in Corpus Christi, Texas. He has been a member of the Coast Guard since 2013.

Wadsworth submitted his RAR on Sept. 28, 2021. It was denied on Dec. 2, 2021, despite affirming that his religious beliefs were “sincere.” Despite an appeal submitted on May 17, 2022, he was “officially counseled” on June 2 and ordered to receive a “fully FDA-approved COVID-19 vaccine” by June 8, under threat of disciplinary action.

In his own words:

“On this form I annotated that taking a COVID-19 vaccine was against my well-documented religious beliefs and that there was no FDA-approved vaccine available for administration, which would negate the legality of the order to vaccinate.

“On 03 JUN2022, I reported to the Air Station Corpus Christi Clinic, as ordered, and documented what vaccines were available for administration … I learned that Air Station Corpus Christi did not have any COVID-19 vaccines … [my flight doctor] was unable to locate an FDA Approved vaccine.

“On 06-07 June 2022, I visited four separate clinics in our area in an attempt to gain access to an FDA-approved/labeled vaccine. At each clinic I had health care professionals document NDC’s [National Drug Code] and lot numbers for the vaccines they had in stock, all of which were labeled as EUA vaccines.

“These details were captured in photos, documented in memo format, signed by health care professionals and a witness, and forwarded to my commanding officer.”

Wadsworth was told the EUA vaccines “could be administered interchangeably.” He subsequently received negative counseling on June 8, and has been told that “he is now no longer eligible to promote.”

As Wadsworth describes it, he was “treated poorly by my command and they flagrantly admitted to trying to coerce me into vaccinating, which was against my religious beliefs.”

Expert testimony questions myocarditis risks

The lawsuit also goes into extensive detail about the differences between EUA vaccines and fully approved vaccines, arguing that “publicly available information indicates that there are differences in the composition of the EUA and licensed products.”

According to the lawsuit, “there are significant differences between licensed vaccines and those subject to EUA that render them ‘legally distinct.’” This includes lower efficacy requirements and “minimal” safety requirements for EUA products.

According to the lawsuit, “EUA products are exempt from certain manufacturing and marketing standards, enjoy broader product liability protections, and cannot be mandated due to informed consent laws and regulations.”

And despite the DOD’s claim that the EUA and fully approved vaccines are “interchangeable,” the lawsuit argues, “the [U.S. Food and Drug Administration] FDA has never asserted that the EUA and licensed versions are legally interchangeable.” Instead, the FDA has “consistently acknowledged that the two vaccines are ‘legally distinct.’”

In two appendices containing expert testimony accompanying the lawsuit, cardiologist and immunologist Dr. Peter McCullough stated:

“The Pfizer, Moderna, and JNJ [Johnson & Johnson] vaccines are considered ‘genetic vaccines’, or vaccines produced from gene therapy molecular platforms, which according to U.S. FDA regulatory guidance are classified as gene delivery therapies and should be under a 15-year regulatory cycle with annual visits for safety evaluation by the research sponsors.”

“The current COVID-19 vaccines are not sufficiently protective against contracting COVID-19 to support their use beyond the current voluntary participation in the CDC-sponsored program.”

McCullough placed particular emphasis on the risk of vaccine-induced myocarditis, especially among young adults:

“COVID-19 vaccine-induced myocarditis has a predilection for young males below age 30 years.

“Multiple recent studies and news reports detail people aged 18-29 dying from myocarditis after receiving the COVID-19 vaccine.

“The FDA found that people 12-24 account for 8.8% of the vaccines administrated, but 52% of the cases of myocarditis and pericarditis were reported.”

Active-duty members of the Coast Guard are required to be between the ages of 17-35, and Reservists between the ages of 17-40, placing a significant number of service members within the age range at highest risk for vaccine-induced myocarditis.

McCullough referenced a July 29, 2021 report in the Journal of the American Medical Association (JAMA) by the Defense Health Agency, which found that “previously healthy service members have developed myocarditis, a severe and life-threatening inflammation of the heart, within an average of just four days of receiving their first shot of either the Pfizer-BioNTech or the Moderna vaccine.”

McCullough pointed out that in addition to the “superiority” of natural immunity conferred by COVID-19 infection, vaccination following infection is “dangerous,” according to recent research.

In reference to the military context, McCullough concluded:

“Vaccination is not the best way to minimize the risk posed by COVID-19 to military readiness. COVID-19 vaccination has led to record fatal and nonfatal organ injury syndromes according to over 1,000 publications in the preprint and PUBMED citation systems.

“Because U.S. military readiness depends on the health of our service men and women, and these data suggest the COVID-19 vaccines markedly decrease health and lead to disability and death, COVID-19 vaccination is not the best way to protect our military.”

 

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

 

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Sen. Johnson Points Out Conflicting CDC Statements on Surveillance of COVID-19 Vaccine Adverse Events

Sen. Johnson Points Out Conflicting CDC Statements on Surveillance of COVID-19 Vaccine Adverse Events

by Children’s Health Defense
July 29, 2022

 

WASHINGTON – On Monday, U.S. Sen. Ron Johnson sent a follow-up letter to Rochelle Walensky, Director of the Centers for Disease Control and Prevention (CDC), demanding clarity on whether the agency performed sufficient surveillance of COVID-19 vaccine adverse events. Recent conflicting statements by CDC officials about monitoring adverse events called into question CDC’s integrity and transparency.

In a June 2022 letter to the CDC, Sen. Johnson outlined the CDC’s Standard Operating Procedures (SOP) document dated January 29, 2021, in which the agency claimed it would “perform routine [Vaccine Adverse Event Reporting System (VAERS)] surveillance to identify potential new safety concerns for COVID-19 vaccines.”  The SOP also stated that the “CDC will perform Proportional Reporting Ratio (PRR) analysis . . . to identify [adverse events]” and “perform PRR data mining on a weekly basis or as needed.”

However, in response to a May 9, 2022 Freedom of Information Act (FOIA) request, the CDC wrote, “no PRRs were conducted.”

Dr. John Su, a CDC official on the agency’s Vaccine Safety Team, recently said the opposite to a media outlet claiming that the “CDC has been performing PRRs since Feb 2021, and continues to do so to date.”

The senator wrote, “CDC’s assertion and Dr. Su’s statement cannot both be true.”

“The American people deserve the truth and you have not been providing it. That is why I, together with millions of Americans, have completely lost faith in the CDC and other federal health agencies. It is time to start regaining their confidence and your agency’s integrity by coming clean, being transparent, and telling the truth,” the senator added.

Read more about the letter in the Washington Examiner.

 

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Children Are Being Sacrificed on the Altar of Covid Vaccines

Children Are Being Sacrificed on the Altar of Covid Vaccines

by Vera Sharav, Alliance for Human Research Protection (AHRP)
July 26, 2022

 

Children, who are at no risk from Covid-19, are being aggressively pursued and forcibly injected with an experimental injection whose ingredients are secret. The injection, which is marketed as a vaccine, has garnered more life-threatening adverse reactions within 18 months than all other FDA-licensed vaccines combined for the last 30 years.

Infants and young children are being injected within the framework of an experimental medical atrocity, an atrocity that is a chilling reminder of Nazi medical atrocities. FDA officials issued one after another Emergency Use Authorization for the use of the “vaccine” for ever younger age groups. The latest FDA authorization was issued on June 17th, authorizing the injections for very young children and infants as young as 6 months.

FDA officials ignored entirely the accumulating, unprecedented number of severe injury reports involving children aged 5 to 11. These reports were submitted to the FDA-CDC Vaccine Adverse Event Reporting System (VAERS).

An analysis of 58 VAERS case reports of severe adverse events suffered by babies and toddlers under 3 years of age following the mRNA Covid injection. The VAERS case reports reveal that the Covid-19 injections are attacking infants’ and toddlers’ brains, hearts, and other vital organs.

The analysis was submitted by Israeli journalists Ranit Feinberg & Yaffa Shir-Raz, to the FDA, prior to its advisory committee meeting on June 17th. The analysis was published by Rite Time an Israeli online magazine, on June 13, 2022.

The most common serious adverse events were life-threatening bleeding, anaphylactic shock, anticholinergic syndrome, encephalitis, hypoglycemia and neuroleptic syndrome. In most of the reported cases, these are multi-system injuries.

  • In some cases it is not clear what happened to the babies – did they survive? And if so, have they recovered?
  • Most reports do not specify under what circumstances the infants were vaccinated, and if they participated in the clinical trials.
  • Most reports do not record whether the babies died or survived.” (Emphasis in original)

(case number 1015467) Cardiac arrest, chest pain of a two-month-old baby boy, one Hour after Pfizer’s mRNA Experimental Vaccine

Torsade de Pointes/QT prolongation (broad), Anaphylactic reaction (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de Pointes) (narrow), Acute central respiratory depression (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Respiratory failure (broad), Hypoglycaemia (broad), Noninfectious myocarditis/pericarditis (broad)

(case number 1133837) is of a 43-day-old baby girl who reportedly received an “intramuscular” COVID-19 jab and immediately afterward suffered a variety of multi-system, life-threatening injuries.
These include: “‘Anaphylactic reaction (broad), Asthma/bronchospasm (narrow), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Hypersensitivity (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad).’”

While the section for noting whether or not the patient died was marked “No,” the recovery section was also marked “No.”

“What then happened to her? Is she alive, or did she die?” Does anyone employed by the FDA or CDC care about what happened to these babies?

FDA officials disregarded the evidence of harm entirely. It is unclear whether FDA shared the analysis of the 58 VAERS case reports with the advisory committee. The committee voted unanimously to recommend these clearly UNSAFE experimental injections for infants and young children – thereby lending their support to a morally perverse policy that subjects children to a medically unjustifiable experiment that exposes them to life-threatening hazards.

As of July 8th, VAERS received 278 case reports of adverse events following Covid-19 injections involving 5-month-old infants to less than 5-year-old young children. Of these, 137 cases were recorded since the FDA authorization. (MedAlerts.)

Case 2342486, a nine-month-old female infant who, submitted on June 27th — one day after the injection, her condition was life-threatening. ElectroencephalogramIntensive careSeizure
Her symptoms:  Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunization (narrow), Hypoglycemia

By July 15th, the number of case reports involving infants and young children under 5 who have suffered serious adverse reactions rose to 381.

Young children who have been forcibly injected in a massive, unethical vaccination experiment suffer from multiple life-threatening adverse reactions. The following are described in VAERS reports involving infants and young children::

“Inflammation and systemic symptoms syndrome, Anaphylactic reaction, Peripheral neuropathy, Guillain-Barre syndrome, Noninfectious encephalitis, delirium, Febrile convulsion, Generalised convulsive seizures following immunization, Decreased oxygen saturationSeizureUnresponsive to stimuliAbnormal sleep-related event, Acute pancreatitis, Hyperglycemia/new onset diabetes mellitus, Neuroleptic malignant syndrome, Anticholinergic syndrome, Systemic lupus erythematosus, Dementia, Convulsions, Acute central respiratory depression, Psychosis and psychotic disorders, Hostility/aggression, Hypotonic-hyporesponsive episode, Generalized convulsive seizures following immunization, Respiratory failure, Drug reaction and systemic symptoms syndrome, Hypoglycemia, Infective pneumonia Abnormal sleep-related event, Acute pancreatitis, meningitis…”

Most of these conditions have never before been diagnosed in young children, such as “Neuroleptic Malignant Syndrome,” which is induced by toxic psychotropic drugs.

Cleveland Clinic defines “Neuroleptic Malignant Syndrome” as:

“Neuroleptic malignant syndrome (NMS) is a rare and life-threatening reaction to the use of any neuroleptic medication. Neuroleptics, also known as antipsychotic medications.”

Since FDA officials authorized the toxic experimental shots for babies, 27 reported cases of Neuroloeptic Malignat Syndrome involved the youngest children. 

As the mother of an adult-aged son who died of Clozaril-induced Neuroleptic Malignant Syndrome, which led to organ failure, I am horrified that children, including infants and toddlers, are being exposed to multiple risks of death.

  • What are the undisclosed ingredients in these toxic injections?
  • Why did the manufacturers, distributors, as well as doctors, and public officials insist on getting total immunity from liability?

This extraordinary marketing scheme has resulted in hundreds of thousands of human casualties. Most were previously healthy men, women, and even younger children who have suffered profound, life-altering harm following the injections.

Are Children and Infants Targets of Deliberate Genocide?

The evidence that the medical establishment and the media ignore and disavow is documented in an unprecedented number of children who died following Covid injections:

Read the circumstances of their deaths at Health Impact News:

The evidence that children are dying in unprecedented numbers is also documented by the bulk orders for child-sized burial caskets since 2021, following the rollout of the Covid injections.

The tweet below was posted on  July 4, 2022, by Mick Haddock

Mick Haddock says that he has sold 5 years’ worth of child-sized caskets in 7 months. “Vaccines are killing children. If not, what is?”



Having escaped the Nazi genocidal agenda – i.e., the Final Solution– I am convinced that we are confronted with a genocidal war. This time, the genocide is on a Global scale. This time instead of Zyklon B gas, the weapons of mass destruction are genetically engineered injectable bioweapons.

This time, the Israeli Health Ministry follows in lockstep with FDA vaccine authorizations. Officials at the Health Ministry ignored the alarming VAERS data and ignored their own substantial data confirming that Pfizer’s Covid injections are causing severe harm and cutting short the lives of Israeli children in unprecedented numbers
[Read: Israel Was Caught Concealing Children’s Vaccine Injuries

Read the report below:

********* 

58 Babies Who Received mRNA COVID-19 Vaccines Suffered Life-threatening Adverse Events

Ranit Feinberg & Yaffa Shir-Raz June 13, 2022

An analysis of VAERS reports shows that contrary to the FDA’s briefing document claiming that the majority of adverse events in Pfizers’ clinical trial were non-serious – at least 58 cases of life-threatening side effects in infants under 3 years old who received mRNA vaccines were reported. For some, it is unclear if they survived. It is also unclear why the infants were vaccinated and whether they were part of the clinical trials. However, in the upcoming FDA meeting on Wednesday, the FDA will not be able to argue it did not know

    • While the FDA is preparing to approve the mRNA COVID-19 vaccine for infants and toddlers aged 6 months to four years and claims in its’ VRBPAC Briefing Document released today that the majority of adverse events found in Pfizers’ trial were non-serious – Real-Time magazine analysis reveals at least 58 life-threatening adverse events in infants and toddlers aged under 3 years old reported to VAERS.
    • The most common serious adverse events were life-threatening bleeding, anaphylactic shock, anticholinergic syndrome, encephalitis, hypoglycemia, and neuroleptic syndrome. In most of the reported cases, these are multi-system injuries.
    • In some cases, it is not clear what happened to the babies – did they survive? And if so, have they recovered?
    • Most reports do not specify under what circumstances the infants were vaccinated and if they participated in the clinical trials.
    • While the FDA claims in its’ briefing document that the vaccine efficacy in infants is 80.4%, the document reveals that the claim is based on a total of 10 symptomatic cases of COVID-19 identified in the trial among 1415 participants – 7 of them in the placebo group vs. 3 in the vaccine group.

Assisted in the preparation of the article Shani Cohen

 “Chest pain; cardiac arrest; Skin cold clammy”. This short description of a cardiac arrest, which occurred one hour after receiving a Pfizer-BioNTech COVID-19 vaccine, is taken from the VAERS system – the US Vaccine Adverse Eve Reporting System ( case number 1015467), and it does not refer to an elderly person, nor to a young adult, or even a teenager. It is hard to believe, but this report refers to a two-month-old baby. “A 2-month-old male patient received bnt162b2 (PFIZER-BioNTech COVID-19 VACCINE) lot number: EL 739, via an unspecified route of administration on 02 Feb 2021 at single dose for COVID-19 immunisation”, thus stated in the report.

“Patient administered vaccination, observed for 15 minutes left the clinic then returned one hour later on 02 Feb 2021, presenting as skin cold, clammy and with chest pain, cardiac arrest event then developed, patient stabilised and transferred for further medical treatment… The outcome of the events was unknown. This case was reported as serious with seriousness criteria-life threatening from HA. No follow-up attempts possible. No further information expected”.

How did a 2-month-old baby receive the mRNA vaccine? These vaccines have not yet received EUA (Emergency Use Authorization) for approved use in children ages five and under by the FDA, or any other regulatory authority, and even if it will, the EUA will only include babies 6 months and older.

Was this baby a participant in Pfizer-BioNTech’s clinical trials, testing efficacy, and safety among babies?

The answer is unclear. According to the person who wrote the report, “Unsure if the patient was enrolled in a clinical trial.” However, the author of the report also states that the report was ”received from a contactable Other Health Care Professional by Pfizer from the Regulatory Agency.” This note implies that the infant might have actually participated in Pfizer’s trial. The regulatory agency report Safety Report Unique Identifier GB-MHRA-ADR 24687611 – indicates that the report came from Great Britain (the first 2 letters in the report ID stand for the country of origin, GB- Great Britain, and MHRA indicate that the source of reporting was its’ drug authority).

Why did they not follow up on the 2-month-old baby’s condition after going into cardiac arrest an hour after receiving an experimental vaccine? Why is there no further information? Is it because he died? Or was the baby removed from an experiment? Why would the author of the report not mention this?

Shockingly, it turns out that this incident is not isolated but, in fact, one of many in the VAERS system describing babies and children under five exposed to mRNA Covid vaccines who suffered life-threatening adverse reactions.

Even though children under five were not considered eligible for these vaccines unless they were part of a clinical trial, astonishingly, it appears that there are many reports in the system describing babies and toddlers who were vaccinated. Some of the children suffered from life-threatening adverse events. In some cases, it is not clear what happened to them; did they survive and recover, do they still suffer from health problems, or did they die.

In a couple of days, on June 15, the FDA’s Vaccines and Related Biological Products Advisory Committee will discuss Moderna and Pfizer’s EUA requests for vaccines for infants and toddlers aged 6 months to 4 years – the only group not yet eligible for COVID-19 vaccination today. According to the FDA’s briefing document released today ahead of the VRBPA committees’ meeting, there were “245 US reports” to the VAERS system “in children 6 months through 4 years of age” who were injected (“product administered to the patient of inappropriate age” or “off-label use”) or exposed to the vaccine “via breastmilk.”

Nevertheless, both companies announced already in May that their findings indicate that their vaccines are safe and effective. The VRBPAC Briefing Document lists a variety of adverse events reported following the exposure to the vaccine in this age group, including “pyrexia…, body temperature…, cough, headache, rash, diarrhea”. According to the document, “Among US VAERS reports for individuals aged 6 months through 4 years, which may reflect unauthorized use of the vaccine or may reflect a reporting error, the majority (96.3%) were non-serious”. 

While the document specifies safety concerns identified from post-authorization safety surveillance data in VAERS, including anaphylaxis, myocarditis, and pericarditis, it does not relate to these safety concerns identified in the younger age group. Instead, it states: “No unusual frequency, clusters, or other trends for adverse events were identified that would suggest a new safety concern.”

But is that really the case? It seems that regardless of the results, and despite the disturbing and shocking findings that are being exposed from Pfizer’s documents, it is expected that both companies will receive the desired EUA very soon. In fact, the CDC website, already in April, had advertised a protocol regarding children’s vaccination, which included babies 6 months to 4 years as well.

In light of this expected approval, RT Magazine conducted an analysis of the cases reported in the VAERS system referring to babies up to 3 years old.

During the analysis, cases were removed in which it was stated that the exposure to the vaccine was through breastfeeding (these cases were analyzed separately and will soon be presented in a follow-up article), as well as cases that were identified as errors in the age registration.

The analysis shows there were at least 58 cases of severe and life-threatening adverse reactions among babies and toddlers 3 years old and younger. This finding is especially puzzling considering the fact that they weren’t supposed to be vaccinated at this age, to begin with. Sadly, similarly to the case reported above, most VAERS reports do not indicate how and under which circumstances they were exposed to the vaccine – were the participants in the companies’ trials? And if not, why and in which circumstances were they vaccinated?

Both companies have not yet released the safety data from their trials on this age group. However, one thing is clear from the VAERS reports: there were many babies who were injured after receiving the vaccine. Whether vaccinated in the trials or illegally in their communities, Pfizer and Moderna will definitely not be able to claim, when presenting their data to the FDA, that the vaccine is safe for babies and that there weren’t any severe adverse events in this age group. Moreover, the FDA’s committee experts who will discuss the EUA approval will not be able to ignore those cases and argue that they did not know. The data presented in this article demonstrate beyond any doubt the complete opposite, and this time – these data are presented to the public in advance before the EUA is granted and ahead of the VRBPAC discussion.

The outcome of the events: Did not recover

One of the most chilling reports refers to a 43-day-old female baby, who on January 30, 2021, received Pfizer’s Comirnaty vaccine. In the incident description (report no. 1133837), it is clearly stated that she was vaccinated and that the vaccine was injected into the muscle: “A 43-days-old female patient received bnt162b2 (COMIRNATY), intramuscular on 30Jan2021 (Lot Number: EK9788) as SINGLE DOSE for COVID-19 immunization”. Right after the vaccination, the baby suffered a variety of life-threatening multi-system injuries, such as:

“Anaphylactic reaction (broad), Asthma/bronchospasm (narrow), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Hypersensitivity (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad).” Although in the section reporting death, the statement states “No,” the section reporting recovery also states “No,” – meaning the baby has not recovered. What then happened to her? Is she alive, or did she die?

In addition, this report, like many others, raises some difficult questions. How did a 43-day-old baby receive a vaccine not yet approved for use in babies? Furthermore, the current clinical trials conducted are supposed to include babies and children over 6 months. Was this baby a participant in Pfizers’ trial? The report does not answer this question.

Just like this baby, it turns out that in most of the reported cases, several life-threatening side effects were recorded for the same baby. The most common severe adverse events were dangerous hemorrhaging; anaphylactic shock – a life-threatening allergy that can damage the respiratory system and cause dizziness, fainting, and even death; anticholinergic syndrome- a condition that occurs when the receptor sites for the neurotransmitter acetylcholine are blocked, which can lead to coordination problems, increased heart rate, and other symptoms; encephalitis – a brain infection, that can cause headaches, vomiting, loss of consciousness and death; hypoglycemia – very low blood sugar, a condition that can quickly escalate to death in infants; and neuroleptic syndrome – which is also life-threatening and can damage the heart muscles, other muscles, and the kidneys.

From the summary of the findings of the analysis according to age and gender groups, the following picture emerges:

In the age group of 0-6 months – there are 28 reports, of which 10 are males, 16 are females, and 2 whose gender was not specified.

9 of them (32%) suffered an anticholinergic syndrome, 9 (32%) had an anaphylactic shock, 8 (28.6%) suffered from Neuroleptic syndrome, 5 suffered from heart rhythm irregularities, and 5 had hypoglycemia.

In the age group of 6-12 months – in this group, 5 reports were found – 3 males, one female, and one whose gender was not specified. This group is small compared to the other groups. The list of adverse reactions included: anaphylactic shock, anticholinergic syndrome, and Neuroleptic syndrome.

In the age group of one-to-three year old – in this group, 25 cases were reported, of which 5 related to males, 19 related to females, and one to a baby whose gender was not specified.

6 of the babies (24%) had an anaphylactic shock, 6 (24%) suffered anticholinergic syndrome, 5 (20%) suffered from Neuroleptic syndrome, 4 (16%) suffered encephalitis, 3 (12%) had irregular heartbeats, one baby was hemorrhaging and one suffered from hypoglycemia.

It should be noted that the adverse events listed above are only some of the ones reported in VAERS with respect to babies. We have chosen to focus only on life-threatening and common adverse events.

Table No. 1: Analysis of reports by age and gender 

Table No. 2: Analysis of reports by adverse events

Are the babies alive?

Similarly to the previous case described, another baby, two months old, also went through anaphylactic shock after being exposed to a single dose of the Pfizer-BioNTech vaccine on January 6, 2021, and just like her, according to the report (no. 976433), she suffered from an array of multi-system symptoms. Regarding the method of administering the vaccine, it was stated ”via an unspecified route of administration”, meaning it is not clear in what circumstances the baby was exposed to the vaccine.

Was she part of Pfizers’ clinical trial? Again, it is unclear from the report.

However, the more important question that should be asked, just like in the previous case, is what happened to the baby? Did she survive? Is she alive?

And again, in the section reporting death, it states “No”, meaning the baby did not die. However, in the report description, it says, “The patient had not recovered from the event. No follow-up attempts possible. No further information expected”. Read the rest here

It is hard to believe, but this basic question – what happened to a baby after suffering such severe and life-threatening adverse reactions – also arises from other serious cases, such as the case of a 6-month-old baby (report # 2084418) who “received bnt162b2 (COMIRNATY), intramuscular” on December 29, 2021, and went through anaphylactic shock, anticholinergic syndrome, Neuroleptic syndrome, infectious pneumonia, other infections, and multi-system symptoms.

In this case, as well, the section reporting death states “No”, meaning supposedly the baby did not die, while in the event description it says “outcome ‘unknown’…  No follow-up attempts are possible. No further information is expected”.

In another case (report no. 1012508), a one-year-old baby who also received a Pfizer vaccine on January 19, 2021 (in this case, it is specified that the baby did not take part in a trial) developed pain in her left ear that escalated to full paralysis, which was diagnosed as Guillain Barre syndrome.  In the case described, it was stated that the baby suffered Guillain Barre Syndrome, face paralysis, non-infectious encephalitis, non-infectious meningitis, earaches, and hearing disorders. Nonetheless, in the summary of the report, it was again written that “No follow-up attempts are possible.”

And another shocking case (report number 1379484) emerges from the report of a baby who was only one month old, who suffered “Vaginal bleeding/ Constant heavy vaginal bleeding with chunks of clot” the following day after receiving the Pfizer-BioNTech vaccine on May 19, 2021.

Although the symptoms the baby suffered from were defined as “serious as medically significant,” in the incident description, it is stated that the result is “unknown” and that “No follow-up attempts are possible. No further information is expected”.

As mentioned, in some of the cases, it is stated the babies were not part of a clinical trial, while in others, it is not clear whether they participated in a clinical trial or were vaccinated in other unknown circumstances. But whether they were part of the trial or not, the report does not explain the absence of this critical information; what happened to these babies? Did they survive? And if so, did they recover? Why was there not a follow-up on the medical condition of babies who suffered from severe and life-threatening adverse events while it was clearly stated that they did not recover? Is it not required in such severe cases by the FDA that the company should make every effort to locate these babies, find out what their condition is and follow up on them?

“Redness in the injection area: the clinical trial protocol does not mention severe adverse reactions”

The press release issued in February 11, 2022, in which Pfizer-BioNTech announced that they intend to apply to the FDA for approval for infants from 6 months to 4 years of age, the safety findings from the company’s clinical trials in babies and toddlers at these ages are not mentioned, not even in a word. The information brochure regarding the clinical trials testing the safety and efficacy of the Pfizer vaccine in adults, children, and babies, on the FDA website clearly states, “No Study Results Posted on ClinicalTrials.gov for this Study.”  And as noted above, the newly released VRBPAC Briefing Document only lists a handful of non-serious adverse events reported in this age group, including, and concludes that there is nothing that would suggest a new safety concern. How could the FDA not know about so many serious adverse events that were reported to the CDC’s reporting systems? Alternatively, if they do know about them – why are they ignoring them?

How were adverse events in babies tested in the clinical trials? In an attempt to answer this critical question, intended to address the safety issues and to assure parents that the vaccine is safe for babies, we examined the study protocol found on the FDA clinical trial website.

It appears that no potential severe adverse events were listed. The list of potential adverse events that the study was supposed to evaluate according to the protocol (“outcome measure”) did include both local and systemic reactions. However, these are relatively non-serious adverse events.

The list of local adverse events that the trial was supposed to monitor includes: “Pain or tenderness at the injection site, redness, and swelling,” and the systematic reactions included ”Fever, fatigue, headache, chills, vomiting, diarrhea, new or worsened muscle pain, new or worsened joint pain, decreased appetite, drowsiness, and irritability”. Moreover, although the study is scheduled to end only on June 14, 2024, the time frame set for examining adverse events is limited to seven days after each of the doses – the first and the second dose.

The vaccine is ineffective in infants. The solution: lower the efficiency threshold and add a third dose

In addition to the substantial concerns regarding the vaccines’ safety for babies, their efficacy in this age group is questionable by and large. According to the available data, healthy children are at almost zero risk for severe illness, hospitalization, or death due to COVID-19.

Hospitalization due to COVID-19 is very rare among children, and death cases are even rarer. In Germany, for instance, a large study found that not even one child died of COVID-19 among 5-11 age group without pre-existing conditions. Under these circumstances, even one case of a serious adverse event, let alone death, is crucial and outweighs any possible benefit of the vaccine.

Not surprisingly, Pfizer clinical trials in babies under 4 proved that 2 vaccine doses do not increase their antibody count significantly. The FDA commissioner, Dr. Janet Woodcock, admitted in an interview in early April 2022 that “The antibodies that were developed were not as high, so they didn’t have the same antibody response to the two-shot series in the older kids.  It wasn’t as high as what we would have hoped for the younger as it was for the older kids.”  According to Woodcock, this is why Pfizer, which planned to apply for EUA approval for babies in February, postponed the submittal date and decided to add a third dose to the trial and wait for the findings after all babies got their third dose.

Furthermore, in a statement given on May 11, Dr. Peter Marks, director of the Center for Biologic Evaluation and Research at the FDA, announced that infant and toddler vaccines will not need to pass the 50% efficacy rate against Covid. A 50% efficacy rate is the threshold adult vaccines need to pass. However, Marks explains that despite the previous guidelines, the FDA will not deny companies now approval for babies and toddlers just because it did not reach the 50% efficacy in preventing symptomatic infections.

Pfizer issued a press release on May 23 announcing that “Vaccine efficacy of 80.3% was observed in the descriptive analysis of three doses during a time when Omicron was the predominant variant”. According to the press release, “The study suggests that a low 3-ug dose of our vaccine…, provides young children with a high level of protection against the recent COVID-19 strains”.

Yet, the FDA’s briefing document reveals that the claim for a “high level of protection” is based on a total of 10 symptomatic cases of COVID-19 identified in the trial, that occurred at least 7 days postDose 3. Three of them occurred among participants 6-23 months of age (which included 555 participants – 376 in the vaccine group and 179 in the placebo group) – with 1 case in the Pfizer-BioNTech vaccine group and two in the placebo group. Seven other cases occurred among participants 2-4 years of age (which included 860 participants – 589 in the vaccine group and 271 in the placebo group) – with 2 cases in the Pfizer-BioNTech vaccine group compared to 5 in the placebo group.

Nevertheless, the vaccine’s efficacy was framed by the FDA as 80,4%, and the document concludes that “Available data support the effectiveness of the Pfizer-BioNTech COVID-19 Vaccine 3-dose primary series (3 µg each dose) in preventing COVID-19 in the age group of 6 months through 4 years”. In addition, the document states that “Among infants and children 6 months through 4 years of age, rates of hospitalization and death due to COVID-19 are higher than among children and adolescents 5-17 years of age, and comparable to individuals 18-25 years of age, underscoring the benefit of an effective COVID19 vaccine in this age group”.

How ethical is it to give a baby a vaccine for a disease that the chances of getting severely ill or dying from are almost zero, while the benefits of the treatment are unclear and, and life-threatening adverse reactions are very significant?

This question was the topic of an article published in March this year in Bioethics. The researchers stated that not even one of the main claims argued to justify approval for babies is valid. According to them, the benefits of the vaccine for healthy children are minimal, and therefore, even though complications are rare, they outweigh the vaccine’s benefits, especially since it is highly unclear what the short and long-term risks are, and the experience with the vaccine is very short. The altruistic claim of protecting the environment is also very problematic, since as a vaccine exists, the groups at risk can defend themselves, and it was proven already that children are not the main transmitters of the virus.

Congress members demand answers

This ethical issue has been raised in recent days by 18 members of Congress in a letter issued to the FDA on June 7, demanding answers before the authority’s decision to grant an emergency permit for the infant vaccine. Members of Congress demanded to know why COVID-19 vaccines are necessary for this age group in light of the fact that the disease poses a very small risk to infants and young children, that vaccines have little efficacy, and that there are many unanswered questions regarding these vaccines’ safety and adverse events.

The letter presents 19 questions to the FDA, including, among others – why did the FDA delayed the publication of the hundreds of thousands of data pages from the manufacturers’ studies, the state of adverse events, and when can all FDA data be expected to be made public? The FDA was also asked to provide the public with more details regarding children who were severely injured or died from COVID-19 and how many children, in general, became seriously ill. Legislators also addressed the issue of cardiac risks in giving the mRNA COVID-19 vaccines to children, noting that following vaccinations given to large numbers of children aged 5-18, an increase in myocarditis and pericarditis was observed, with some cases ending in death, and the long-term effects of heart-related inflammation not yet quantified by health authorities. What’s more, lawmakers demanded to know why the FDA lowered the threshold of efficacy for the vaccines specifically for infants and youngest children, thus actually allowing companies to apply for EUA without any justification.

The FDA will not be able to argue it did not know

As stated, the data emerging from the analysis presented in this article demonstrate beyond any doubt that the vaccine is not safe for babies and toddlers. Whether these children were part of the study or not – these reports have been in the VAERS system for many months, so there is no chance that the FDA does not know them. Unfortunately, the fact that the FDA was aware of at least some of the serious adverse events, including increased risk of morbidity in the first days after vaccination, myocarditis, and increased risk of miscarriage and fetal malformations, and yet approved the vaccine for teens, children, and pregnant women, was later revealed too late – long after the EUA was granted to Pfizer and Moderna, when many have already been harmed. It only became clear thanks to FOIA (Freedom of Information) requests submitted to the FDA and other health authorities, and only after the FDA was forced by the court to disclose the documents. This time, the VAERS data presented here makes it possible to reveal this fact even before the approval. The FDA will not be able to claim that it did not know.

 

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cover image based on creative commons work of maggyona & ZIPNON  / pixabay




Ugly Covid Lies

Ugly Covid Lies

by Ron Paul, The Ron Paul Institute for Peace and Prosperity
July 25, 2022

 

After two years of unprecedented government tyranny in the name of fighting a virus, the prime instigators of this infamy are walking free, writing books, and openly pretending they never said the things they clearly said over and over.

Take Trump’s White House Covid response coordinator Deborah Birx, for example. She was, as the Brownstone Institute’s Jeffrey Tucker points out in a recent article, the principal architect of the disastrous “lockdown” policy that destroyed more lives than Covid itself. Birx knew that locking a country down in response to a virus was a radical move that would never be endorsed. So, as she admits in her new book, she lied about it.

She sold the White House on the out-of-thin-air “fifteen days to slow the spread” all the while knowing there was no evidence it would do any such thing. As she wrote in her new book, Silent Invasion, “I didn’t have the numbers in front of me yet to make the case for extending it longer, but I had two weeks to get them.”

She was playing for time with no evidence. As it turns out, she was also destroying the lives of millions of Americans. The hysteria she created led to countless businesses destroyed, countless suicides, major depressions, drug and alcohol addictions. It led to countless deaths due to delays in treatment for other diseases. It may turn out to be the most deadly mistake in medical history.

As she revealed in her book, she actually wanted to isolate every single person in the United States! Writing about how many people would be allowed to gather, she said: “If I pushed for zero (which was actually what I wanted and what was required), this would have been interpreted as a ‘lockdown’—the perception we were all working so hard to avoid.”

She wanted to prevent even two people from meeting. How is it possible that someone like this came to gain so much power over our lives? One virus and we suddenly become Communist China?

Last week in a Fox News interview she again revealed the extent of her treachery. After months of relentlessly demanding that all Americans get the Covid shots, she revealed that the “vaccines” were not vaccines at all!

“I knew these vaccines were not going to protect against infection,” she told Fox. “And I think we overplayed the vaccines. And it made people then worry that it’s not going to protect against severe disease and hospitalization.”

So when did she know this? Did she know it when she told ABC in late 2020 that “this is one of the most highly-effective vaccines we have in our infectious disease arsenal. And so that’s why I’m very enthusiastic about the vaccine”?

If she knew all along that the “vaccines” were not vaccines, why didn’t she tell us? Because, as she admits in her book, she believes it’s just fine to lie to people in order to get them to do what she wants.

She admits that she employed “subterfuge” against her boss – President Donald Trump – to implement Covid policies he opposed. So it should be no surprise that she lied to the American people about the efficacy of the Covid shots.

The big question now, after what appears to be a tsunami of vaccine-related injuries, is will anyone be forced to pay for the lies and subterfuge? Will anyone be held to account for the lives lost for the arrogance of the Birxes and Faucis of the world?

 

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cover image is in the public domain




DailyClout and Health Freedom Defense Fund File Citizen Petition With FDA to Halt COVID Injections for Young Children

DailyClout and Health Freedom Defense Fund File Citizen Petition With FDA to Halt COVID Injections for Young Children

by Health Freedom Defense Fund
July 26, 2022

 

Daily Clout and Health Freedom Defense Fund (HFDF) filed a Citizen Petition with the U.S. Food and Drug Administration (FDA) requesting that FDA revoke Emergency Use Authorization of COVID-19 vaccines for young children subsequent to FDA’s authorization of the COVID-19 injections for that age group on June 17, 2022.

Dr. Naomi Wolf, CEO of Daily Clout, asserted,

“With this decision, the FDA abandons its duty to protect the American people. COVID-19 poses statistically insignificant risk to babies and young children, and neither safety nor efficacy of the injections have been proven. But research from the WarRoom/DailyClout Pfizer Documents Research Volunteers, along with analyses of official databases, primary source documents, and peer-reviewed studies, shows that the mRNA vaccines damage many teens’ hearts, leave babies with GI problems, sleep problems, seizures, liver damage, and multiorgan system failure, and suppress leukocytes; the vaccines visibly damaged the hearts of animals in studies. Why on earth would we thus risk the health of small children and babies?”

In fact, ignoring this data is the definition of arbitrary and capricious, a clear legal dereliction of FDA’s duty.

While the COVID injections were promoted as the only way to end the COVID crisis, the real-world evidence has demonstrated the injections not only fail to prevent infection, they also do not stop transmission.

Moreover, clinical trial data from Pfizer and Moderna reveal that more children who received the vaccines were diagnosed with COVID and hospitalized, respectively, than those in the placebo group. In addition, recent research and data from around the world suggest the injections impair long-term immunity to the virus, rendering recipients more likely to be hospitalized or die from COVID.

Leslie Manookian, President of Health Freedom Defense Fund stated,

“Aside from not performing as purported, the injections pose serious known and unknown risks to young children. Leaked data from Japan revealed high levels of the lipid nanoparticles from the mRNA shots accumulate in the ovaries with unknown consequences. But menstrual irregularities and increased rates of miscarriage have been reported after the injections. A recent study identified reduced sperm concentrations and effects on sperm motility. With these safety concerns in mind, FDA authorizing the injections for young children defies reason and the precautionary principle.”

FDA is charged with protecting public health, not marketing the products of what is arguably the most powerful industry in the world.

Daily Clout and HFDF request that FDA reverse or at the very least pause its decision to issue an EUA for mRNA vaccines for six-month-olds to under-fives.  We ask instead that they further study the research available, including the research itemizing harms described above, and that they take into account over 130,000 comments submitted to the FDA regarding the dangerous step of authorizing these shots for young children, which they are legally required to consider.

Should FDA fail to reverse its authorization, Daily Clout and Health Freedom Defense Fund will take legal action to ensure that FDA abides by the law.

 

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cover image credit: Victoria_Art / pixabay




Dr. Birx Admits She and Fauci Made Up ‘The Science’ on Lockdowns, Social Distancing

Dr. Birx Admits She and Fauci Made Up ‘The Science’ on Lockdowns, Social Distancing

by Tyler Durden, ZeroHedge
July 21, 2022

 

President Trump’s former Covid-19 adviser Dr. Deborah Birx has made several stunning admissions of late – first telling the Daily Mail that Covid-19 “came out of the box ready to infect” when it hit Wuhan, China in 2019 – and that it may have been created by Chinese scientists who were “working on coronavirus vaccines.”

But it goes further than that.

As Fox News’ Jesse Waters lays out, Birx admitted in her new book that she and Dr. Anthony Fauci were essentially shooting from the hip when it came to national directives such as “two weeks to stop the spread,” and social distancing requirements.

According to Waters, Birx “admitted to making things up,” adding that she and Fauci “were lying to the president and to the American people about their COVID protocols.”

With the first lie; ’15 days to stop the spread’ – Birx writes “No sooner had we convinced the Trump administration to implement our version of the two-week shutdown than I was trying to figure out how to extend it.”

“So that 15 days to slow the spread was just a sneaky way to get their hooks into us, so they could lock us down for longer,” Waters opines. “And if you dared to leave your house, Birx told us, the only way to stay safe was to social distance.”

To that end, Birx writes that she “I had settled on 10 (feet) knowing that even that was too many, but I figured that ten would at least be palatable for most Americans – high enough to allow for most gatherings of immediate family but not enough for large dinner parties and, critically, large weddings, birthday parties, and other mass social events…”

Watch:

 

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Air Force Ordered to Stop Discharging Unvaccinated | Legal Victories in US & Uruguay Against Mandated Vaccination

Air Force Ordered to Stop Discharging Unvaccinated | Legal Victories in US & Uruguay Against Mandated Vaccination

by Del Bigtree with Jefferey Jackson, The HighWire
July 20, 2022

 



Despite reports otherwise, the Air Force has ceased discharges of unvaccinated airmen after a Federal Judge ordered a halt to the discharges of members who have religious exemptions to Covid vaccination, marking a huge win for thousands of members of the Air Force.

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The Pandemic Predictor Neil Ferguson: The Ghost in the Machine

The Pandemic Predictor Neil Ferguson: The Ghost in the Machine

by Jon Rappoport, Jon Rappoport’s Blog
July 20, 2022

 

Why do governments salute when he predicts a pandemic and tells them to lock down their countries?

Does anyone care about his past?

Why does he still have a prestigious job?

Who is he connected to?

Note: I’m republishing this piece, from 2020, so people don’t forget the criminal and the crime…

 

Neil Ferguson, through his institute at London’s Imperial College, can call the shots on a major percentage of the global population.

He’s Mr. Genius, when it comes to projecting computer models of epidemics.

Fellow experts puff up his reputation.

According to the Business Insider (4/25/2020), “Ferguson’s team warned Boris Johnson that the quest for ‘herd immunity’ [letting people live their lives out in the open in the UK] could cost 510,000 lives, prompting an abrupt U-turn [massive national lockdown in the UK]…His simulations have been influential in other countries as well, cited by authorities in the US, Germany, and France.”

Not only cited, not only influential, but swallowed whole.

Business insider continues: “On March 23, the UK scrapped ‘herd immunity’ in favor of a suppression strategy, and the country made preparations for weeks of lockdown. Ferguson’s study was responsible.”

There’s more. A lot more.

Same BI article: “Dr Deborah Birx, coronavirus response coordinator to the Trump administration, told journalists at a March 16 press briefing that the Imperial paper [Ferguson’s computer projection] prompted the CDC’s new advice to work from home and avoid gatherings of 10 or more.”

Ferguson, instigator of LOCKDOWN. Stripping away of basic liberties. Economic devastation.

So let’s look at Ferguson’s track record, spelled out in the BI piece:

“Ferguson co-founded the MRC Centre for Global Infectious Disease Analysis, based at Imperial, in 2008. It is the leading body advising national governments on pathogen outbreaks.”

“It gets tens of millions of dollars in annual funding from the Bill & Melinda Gates Foundation, and works with the UK National Health Service, the US Centres for Disease Prevention and Control (CDC), and is tasked with supplying the World Health Organization with ‘rapid analysis of urgent infectious disease problems’.”

Getting the picture?

Gates money goes to Ferguson.

Ferguson predicts dire threat from COVID, necessitating lockdowns—thus preparing people to accept a vaccine. The vaccine Gates wants.

Ferguson supplies a frightening computer projection of COVID deaths—to the CDC and WHO. Ferguson thus communicates a rationale for the Gates vaccine plan.

National governments surrender to WHO and CDC. LOCKDOWNS.

Business Insider: “Michael Thrusfield, a professor of veterinary epidemiology at Edinburgh University, told the paper he had ‘déjà vu’ after reading the [Ferguson] Imperial paper [on COVID], saying Ferguson was responsible for excessive animal culling during the 2001 Foot and Mouth [mad cow] outbreak.”

“Ferguson warned the government that 150,000 people could die. Six million animals were slaughtered as a precaution, costing the country billions in farming revenue. In the end, 200 people died.”

“Similarly, he [Ferguson] was accused of creating panic by overestimating the potential death toll during the 2005 Bird Flu outbreak. Ferguson estimated 200 million could die. The real number was in the low hundreds.” HELLO?

“In 2009, one of Ferguson’s models predicted 65,000 people could die from the Swine Flu outbreak in the UK — the final figure was below 500.”

So you have to ask yourself, why would anyone believe what Ferguson has been predicting in this COVID hustle?

Are his fellow experts that stupid?

Are presidents and prime ministers that stupid?

And the answer is: This is a monumental covert op; some people are that stupid; some are caught up in the op and are afraid to say the emperor has no clothes; some are aware of what is going on, and they want to destroy national economies and lead us into, yes, a new world order.

Gates knows he has his man: Ferguson. As the recipient of tens of millions of dollars a year from the Gates Foundation, Ferguson isn’t about to issue a model that states: COVID is nothing to worry about, let people live their lives and we’ll be all right. The chance of that happening is on a par with researchers admitting they never properly identified a new virus as the cause of illness in 2019, in Wuhan.

In order to justify injecting every man, woman, and child in the world with heavy metals, synthetic genes that alter genetic makeup, a host of germs, and who knows what else, Gates needs A STORY ABOUT A DEADLY VIRUS THAT NECESSITATES SHUTTING DOWN AND IMPRISONING THE PLANET, ACHIEVING A CAPTIVE AUDIENCE.

He’s got the story, all dressed up in a computer model, composed by a man with a past record of abject and devastating failures.

Neil Ferguson is the ghost in the machine. The machine is the World Health Organization and the CDC. The man behind the ghost is Bill Gates.

 

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cover image modified from creative commons work of Philafrenzy  / Wikimedia Commons




Informed Consent Action Network (ICAN): New Challenge to FDA on 12-15-Year-Old Covid Injections

Informed Consent Action Network (ICAN): New Challenge to FDA on 12-15-Year-Old Covid Injections

by Informed Consent Action Network (ICAN)
July 20, 2022

 

ICAN has filed a Citizen Petition with the FDA calling on the agency to reverse its reckless course on Covid-19 injections for teenagers. The Petition demands that the FDA revoke its emergency use authorization (EUA) for Pfizer’s product in children aged 12 through 15 and deny Moderna any future EUA for children aged 12 through 17.

The document, submitted through ICAN’s legal team, spans 20 pages, cites dozens of medical studies, and includes 94 footnotes and roughly 1,500 pages of sources, but it boils down to a few simple principles: There never was any emergency with this age group in the first place, rendering EUAs illegal under federal law; the clinical trials relied upon to authorize the vaccines were woefully deficient; almost all in the 12-15 age demographic currently have natural immunity to Covid-19; and the injury risks from injection are catastrophically higher than any purported benefit.

The Petition cites a Lancet article of March 2021 that found Covid’s death toll among children was a negligible 0.17 per 100,000 population. Since then, a large U.K. study posted in July 2021 found a Covid-19 fatality rate of just 0.005% among all those under 18. “Based on these facts, the current EUA for Pfizer’s vaccine for this population is without legal foundation or necessity,” the Petition observes, “because COVID-19 does not present a current emergency for children.”

Furthermore, the population has been developing robust natural immunity against the disease. As of February 2022, according to a study published on the CDC’s website, 75% of children aged 12-17 had developed infection-induced antibodies. NIH data showed an even higher percentage of natural protection, at 89.4%, for all children under 18. And that percentage could only have increased since.

But the gaps in FDA logic do not begin and end with its misappropriation of the word “emergency,” nor with its selective blindness on natural immunity.  As our Petition reminds the agency, quoting international scientists in an August 2008 PLOS Medicine paper, “inadequately powered studies should themselves be considered a breach of ethical standards.”

The FDA’s authorization for Pfizer’s injection rests on a trial in which only 1,131 children received the experimental product. Yet, even among that small and statistically insignificant group, at least seven recipients “had at least one serious adverse event.”  Among them was Maddie de Garay who, at 12 years old, was paralyzed from the waist down after receiving her second shot.  Among a multitude of horrific injuries, she became incontinent, and can now only receive nutrition through a feeding tube.

But Pfizer recorded her life-altering reaction as mere “functional abdominal pain” in the safety-evaluation data it turned over to the FDA and has since failed to ensure adequate medical care, including an appropriate diagnosis and treatment.

Nor has the safety profile for the mRNA shots improved since their problematic trials. As early as June 2021, the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) examined the growing issue of vaccine-induced myocarditis, where the heart muscle becomes inflamed and thereby weakened, especially in individuals under 30 years old. Moreover, as the Petition points out, “Moderna’s vaccine presents an even higher risk profile to this age group than Pfizer’s vaccine.”

Meanwhile, the Vaccine Adverse Events Reporting System (VAERS), though vastly understating the full extent of injection injuries, had accumulated 31,549 reports of adverse events among children under 18 as of May 6, 2022.  Of these, 1,812 were rated as serious and 44 were deaths.  This is to say nothing of the long-term effects.

And, if the glaring safety signals were not enough for the FDA to revoke its EUA for minors, the Petition also points out that several studies now show there is virtually no benefit from these shots since their efficacy wanes dramatically within just months or even weeks after inoculation.

The FDA has played very fast and extremely loose with its EUA powers when it comes to children’s health, invoking an emergency that never existed and accepting data that was never adequate.  Moreover, it has continued doubling down on its failed approach in spite of the overwhelming case against it.  Numerous additional VRBPAC meetings are scheduled to discuss authorizations for additional vaccines and age groups and ICAN plans to file as many petitions as are necessary to address the concerns of each.

The FDA’s increasingly reckless actions have prompted ICAN to file several Petitions with the FDA.  These include demands the agency adhere to federal law requiring promotional material for EUA vaccines to “clearly and conspicuously” state the product has not been approved or licensed by FDA, but only authorized for emergency use.  We have also called on the FDA to publicly clarify an individual’s statutory right to refuse medical products without coercion, penalty, or retaliation of any kind, and we have demanded that it obtain proper data before vaccine approvals.  On all counts, the FDA has failed miserably and ICAN will continue to hold its feet to the fire.

 

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Catastrophic Covid Experience in New Zealand. The Derogation of Human Rights and “The Basic Principles of Medicine”. The Protest Movement.

Catastrophic Covid Experience in New Zealand. The Derogation of Human Rights and “The Basic Principles of Medicine”. The Protest Movement.
We, as inherently free and autonomous individuals, are blessed with the responsibility of choice.

by Dr. Emanuel Garcia, Global Research
July 18, 2022

 

If there is a silver lining to the catastrophic Covid experience for us here in New Zealand it is the very clear and indisputable exposure of the political establishment.  The green clean smiling benevolent face of the New Zealand government is nothing more than a mask – yes, a mask – behind which is harsh dictatorial mien of a government that feels no need to answer to the needs of the people it purports to govern.

During the brief but compelling and compellingly beautiful gathering of the people at Parliament earlier this year, repeated calls for governmental officials simply to meet and simply to discuss issues of import, such as their imposed mandates and societal apartheid that resulted from them, went blithely and purposefully unheeded. Not one single politician from the Prime Minister’s office on down fulfilled their good-faith political obligations by engaging with those from whom they derive their political power.

Furthermore, on the eve of the brutal and unnecessary invasion of Parliament grounds to clear the protesters, it became clear that those in office never had a wish to engage. I was a member of a small task force who the afternoon before, at 1:30 PM to be precise, had gathered in Wellington to negotiate a settlement of the impasse. The police representative who was to join us cancelled at the last minute.

Later that same afternoon I sat as an observer at a meeting of the Human Rights Commission as a number of petitioners presented evidence of the harm against fundamental human rights, evidence of police abuses and other poignant testimony about the harsh consequences of the mandates. An honest Human Rights Commissioner would have taken up the mantle of protecting those whose rights had been violated and would be violated further by violence. He didn’t.

These past two and a half years have seen those who were, during that first harsh lockdown, lauded and thanked for being ‘essential workers’ terminated from their roles as physicians, nurses, midwives and other health-care practitioners for deciding personally and for their own reasons of health and conscience that a hastily concocted genetic inoculation masquerading as a vaccine was not for them.

As a psychiatrist who worked within the system in the general Wellington region and saw firsthand the tenuous nature of mental health services – services characterised by endemic staff shortages, variable levels of skill, and a form of management style emanating from the top which I can only describe as peculiarly vicious, corrupt and inept – the termination of much-needed and highly competent colleagues was a strange, sad and ironic testament to irrationality and a cold heedlessness of the public weal.

I remember working as a psychiatrist during the first lockdown, making home visits, volunteering time at a local primary care facility when I was on leave, and generally carrying on as one would expect a doctor to do: it was no big deal and I bristled at the division of society into ‘essential’ and ‘non-essential’.  This division, however, was a template for the later division of New Zealand into a veritable apartheid society comprised of the jabbed and the unjabbed or, psychologically speaking, the ‘good’ and the ‘bad’, the ‘clean’ and the ‘unclean’, remnants of which we may see among those who mask and those who don’t.

I note, in looking at the past, that no-one in government provided any actual evidence that could justify the extraordinary measures imposed upon the entire country: lockdowns, distancing or masks. Nor have they provided any evidence to justify their demand that all healthcare workers be inoculated to be able to work face to face with clients. Nor, of course have they been able to justify, nor can they justify or explain rationally, the imposition of an inoculation that circumvented the laborious and necessary trials over time, and that have already produced an astonishing legacy  of adverse events, including death. There is not nor can there ever be a substitute for time in the testing and approval of a medical intervention. Heaven knows what will transpire among the inoculated in the years to come.

Physicians who have from the beginning set about to explore the treatment of those who were afflicted by Covid found themselves in very lonely terrain, and worse. The New Zealand government, its Ministry of Health, and allied organisations such as the Medical Council, never once encouraged prevention or treatment. When I brought the issue of treatment up at my local hospital, I was referred to a specialist who told me, simply, that there was no evidence that any treatment worked. When I took the effort to send him quite a lot of substantive evidence, he was silent.

Over these past two and a half years the foundational principles of Medicine have been obliterated by our official organisations and our Ministry of Health: the principles of informed consent, individualised treatment and doing no harm. When physicians attempted to act in accordance with these principles they were hounded, derided and officially sanctioned, losing their licences and their jobs.  When physicians attempted to discuss natural immunity, the irrationality of attempting to eliminate a respiratory virus, the necessity of early treatment; when physicians attempted to engage with public officials to discuss pertinent matters of science and medicine – they were persecuted and rebuffed.

As of today there are nearly thirty thousand doctors in the Medical Council’s register. Of those thirty thousand a pittance have joined with New Zealand Doctors Speaking Out for Science (NZDSOS) to stand up for these foundational principles of our profession.  I am certain that if a mere ten percent of practicing physicians in New Zealand publicly affirmed the basic principles of Medicine we would not be living through the hell of the tyranny imposed by the government in the name of what they call ‘Medicine’ but which every physician understands is merely an Orwellian caricature.

Our government’s Medicine is a world where suffering patients go untreated, where a one-size-fits-all jab that neither prevents infection nor transmission of the pathogen for which it was engineered is safe as water, where informed consent is unnecessary and where masks, despite their inefficacy, should be worn to safeguard health despite the absurdity of how they have instructed people to use them, and despite the consquences of eliminating personal identity and depriving people of their quintessentially human features and means of emotional and expressive communication.

I am repeatedly asked how so many people can participate in cruelties and absurdities, how so many people can be persuaded to overlook what their eyes and ears and hearts tell them, how so many people can go along with what is so obviously destructive to us all.  The comprehensive answer might require a long essay or a book to elucidate. But here I will offer an abbreviated response.

Psychological operations like Covid work successfully by creating shock and awe, instilling fear, and inducing a response akin to something that is supernatural, that draws upon our emotionally regressive attitudes towards the miraculous, which transcends the laws of common sense or reason. The origins story of Covid and the incessant and inescapable drumbeat of deceptive case counts and death by the mainstream media worked wonders on a mainly gullible and trusting population. The inclusion of ‘supernatural’ elements, clearly seen by any analysis of the ridiculousness of the rituals of masking, are purposeful, for it is these supernatural elements that grip us unconsciously.  Masking is itself a propaganda tour de force; and propaganda is, at bottom, an act of violence.

I will conclude my ruminations with two quotations, which may help to frame my remarks.  The first is from Freud who, in his work on group psychology, wrote:

“ … in a group the individual is brought under conditions which allow him to throw off the repressions of his unconscious instinctual impulses. The apparently new characteristics which he then displays are in fact the manifestations of this unconscious, in which all that is evil in the human mind is contained as a predisposition.”

The second is from Goldhagen, who, referring to perpetrators of antisemitic cruelties in Hitler’s Willing Executioners, wrote:

“ … any explanation that fails to acknowledge the actors’ capacity to know and to judge, namely to understand and to have views about the significance and morality of their actions … cannot possibly succeed in telling us much about why the perpetrators acted as they did.”

The State, as all collections of Power tend, would like nothing better than absolute control over a faceless and masked citizenry of submissive digital peasants marching in lockstep to their pronouncements.

Many people, perhaps the great majority, relatively ignorant of history and politics, are primarily occupied with ekeing out an existence amidst the harsh realities of daily living. Trusting in government, they will accept the pronouncements of mainstream media and authorities as Gospel.

There is another group who see quite clearly through the captivating irrationalities and the Siren song of propaganda, and who willingly participate in falsehoods and cruelties not only to save their skins but also to derive pleasure and profit at the expense of others.

And then there are those who speak out.

We, as inherently free and autonomous individuals, are blessed with the responsibility of choice.

 

Dr. Garcia is a Philadelphia-born psychoanalyst and psychiatrist who emigrated to New Zealand in 2006. He has authored articles ranging from explorations of psychoanalytic technique, the psychology of creativity in music (Mahler, Rachmaninoff, Scriabin, Delius), and politics. He is also a poet, novelist and theatrical director. He retired from psychiatric practice in 2021 after working in the public sector in New Zealand.

 

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Death by Covid Vaccine

Death by Covid Vaccine

by Llewellyn H. Rockwell, Jr.
sourced from Global Research
July 18, 2022

 

When we’re dealing with a controversial topic, it’s a good item to start with something we know and go from there. What is something that we know for sure about Covid-19 vaccines? They kill people.

Jon Rappoport pointed this out a year ago: “A new May 4 report by independent researcher, Virginia Stoner, reveals US vaccine-death figures. The report is titled, ‘The Deadly Covid-19 Vaccine Coverup.’

Stoner uses the US government’s own numbers.

Here are key quotes from her report:

‘There has been a massive increase in deaths reported to the Vaccine Adverse Event Reporting System (VAERS) this year. That’s not a ‘conspiracy theory’, that’s an indisputable fact.’

‘We’re talking about a huge and unprecedented increase—so massive that in the last 4 months alone, VAERS has received over 40% of all death reports it has ever received in its entire 30+year history.”

‘The increase in VAERS death reports is not due to more vaccination.’

“Most recently, the death count went from 2794 on April 5, to 3005 on April 12, to 3848 on April 26….1054 deaths in 21 days.’

‘One hypothesis…is that the elderly and infirm, many in long-term care facilities, were the first to be targeted by the COVID-19 vaccine campaign, and they are much more likely to die coincidentally. These coincidental deaths then lead to an increase in suspected vaccine-induced deaths reported to VAERS.’

‘VAERS data just does not support that hypothesis. First, because all age groups—not just seniors—had a dramatic increase in VAERS death reports from COVID-19 vaccines…Across the board, all age groups experienced a dramatic increase in deaths reported to VAERS from the COVID-19 shots—even the under 18 group, which has had very few COVID-19 shots (so far).’

Stoner constructs a chart showing reported deaths from vaccinations in years prior to COVID, and deaths reported so far from COVID vaccines.

For prior years, we’re talking about roughly 100 deaths a year from somewhere between 250 million and 350 million vaccines administered. On the other hand, we’re talking about 3800 deaths from about 150 million COVID shots—not in a full year; in only four months.

The experts would say neither death figure (100 or 3800) is alarming, given the huge number of vaccines administered. But this is a deception.

Over the years, much has been written (even in the mainstream) about what sits behind REPORTED vaccine injuries and deaths. Estimates of TRUE injury numbers range from 10 to 100 times greater than the reported figures.

3800 reported deaths from COVID vaccines would skyrocket when you estimated the true figure.

As Stoner points out in her report, public health officials, in Orwellian fashion, keep repeating, ‘The vaccine is safe and effective.’ A straightforward analysis of their own numbers completely contradicts their stance.

Likewise, the mainstream press, politicians, corporations, and celebrities are on an all-out push to convince the public that the vaccine is a) necessary and b) a marvel, if only the ‘hesitant’ people would ‘follow the science’ and see the light.

Well, some cults are small; that one is huge.

Virginia Stoner’s report is a stark refutation of the conspiracy theory the cult is promoting.

When the entire population is being subjected to a vast experiment deploying a never-before-released RNA technology; when the shot in the arm is actually a genetic treatment; when the entire field of genetic research is riddled with pretense and lies and alarming miscalculations, leading to ripple effects in overall genetic structures; what else would you expect?

You would expect exactly what Stoner’s report shows and implies. The COVID vaccine is a building disaster.”

Vernon Coleman asks the appropriate question: exactly how many people has the Covid vaccine killed? “No one knows how many people the vaccines are killing – or how many they will kill.

But although I haven’t seen the mainstream media mention most of these deaths, people have already died or been injured after being given the vaccine:

SHOCKING – The latest covid jab deaths and injuries from VAERS (infants, teenagers and young adults are dying after the vaccine)

openvaers.com covid data (it is estimated that only 1% of vaccine adverse events is reported)

Note: The following paragraph has now been added to the UK’s Pfizer analysis data print, ‘A report of a suspected ADR to the Yellow Card scheme does not necessarily mean that it was caused by the vaccine…’ In my view, this is yet another attempt to draw attention away from the very real problems associated with the vaccines. We note that when patients die 60 days after a positive covid test, they are added to the covid death figures but if someone were to die 60 minutes after a covid vaccine, then it is just a coincidence.

PFIZER (UK data) – Some of the Injuries include: strokes, heart attacks, miscarriages, Bell’s Palsy, sepsis, paralysis, psychiatric disorders, blindness, deafness, shingles, alopecia and covid-19.

The following paragraph has now been added to the UK’s AstraZeneca analysis data print, ‘A report of a suspected ADR to the Yellow Card scheme does not necessarily mean that it was caused by the vaccine…’ In my view, this is yet another attempt to draw attention away from the very real problems associated with the vaccines. We note that when patients die 60 days after a positive covid test, they are added to the covid death figures but if someone were to die 60 minutes after a covid vaccine, then it is just a coincidence.

ASTRAZENECA (UK data) – Some of the many injuries include: blindness, strokes, heart attacks, miscarriages, sepsis, paralysis, Bell’s Palsy, deafness, shingles, alopecia and covid-19.

European database of suspected adverse drug reaction reports: ModernaPfizer-BiontechAstraZeneca and Janssen.

You might wonder, even if the Covid-19 vaccine kills people, doesn’t it also save lives? But in fact it is ineffective in warding off the so-called Covid “pandemic.” Vasko Kohlmayer says, “’Pfizer and BioNTech’s Covid-19 vaccine is just 39% effective in Israel where the delta variant is the dominant strain according to a new report from the country’s Health Ministry’ we read in a CNBC report.

Astonishment is one’s first reaction when coming across this piece of information, since it was not so long ago the vaccine manufacturers claimed their products were 92 to 98 percent effective.

The manufacturers’ initial claims, however, have been steadily revised down as real-world data has been coming in. In March of this year news came from South Africa that ‘AstraZeneca vaccine doesn’t prevent B1351 Covid.’ A couple of months later, the Hill ran a piece by a Baylor School of Medicine virologist who observed:

‘A new study published in the New England Journal of Medicine found that Pfizer-BioNTech vaccine provides only 51 percent protection against B.1.351 of South Africa.’

Just a couple of weeks ago, we learned that recipients of the Sinovac Biotech’s vaccine have no antibodies after six months. This effectually means that merely half a year after being injected into people’s bodies the vaccine has zero percent efficacy in protecting against Covid-19.

Even factoring for the variants, the hard data makes it quite clear that the initial claims of vaccine effectiveness were greatly exaggerated. This, of course, comes as no surprise to anyone familiar with the dynamic of the pharma industry. Drug manufacturers tend to wildly overstate the efficacy of their products, while doing their very best to understate their side effects. It is for this purpose they conduct trials that are manipulated to obtain the results they wish for. Sadly, they too often get away with it because of the corruption of the system by what is called regulatory capture. This is why the outcomes of manufacturers’ trials are almost never replicated by independent trials or real-world data.

This is what has apparently happened with the Covid vaccines. The manufacturers used the sense of emergency brought on by the Covid pandemic to conduct rushed and incomplete trials which were designed to yield the results they wanted to see. There is every reason to believe that the effectiveness of their injections was nowhere close to the 92-98% range they initially claimed even for the variants that were in circulation at that time.

Needless to say, one has a strong suspicion that even the meagre 39 percent figure is still overstated. This would only be natural, since everyone involved in the vaccination enterprise – the manufacturers, politicians, regulators, the medical establishment and corporate scientists – is trying their best to save face and reputation in the face of this fiasco. Bad though the data is, we can be quite sure that it has been massaged to soften the blow.

You can clearly observe this tendency at work in the CNBC piece which claims that even though Pfizer is only 39 percent effective, it still protects against serious disease. But this is simply not true, which you can easily see if you take the trouble to look into the data put out by the Israeli government. At roughly the same time that CNBC filed its report, the Israeli Ministry of Health published a bulletin which reported on Covid cases in the country. According to their data, there were 137 serious cases in Israel of which 95 were fully vaccinated and 42 unvaccinated or partially vaccinated (see here and here). In other words, the bulk of the serious cases was comprised of those who had received their shots. If the vaccine was as effective in protecting against heavy illness as the article claims, the numbers would look completely different. The figures published by the Israeli Ministry of Health shows that the claims of Pfizer’s efficacy of protecting against serious Covid are simply untrue.

This has been confirmed by the testimony of Dr Kobi Haviv, Director of Herzog Hospital in Jerusalem. In a recent TV interview, Dr Haviv stated that the fully vaccinated people account for about 90 percent of hospitalizations. Given that less than 90 percent of the Israeli population is fully vaccinated, it would appear that the vaccination not only does not prevent you from contracting the disease, but actually increases one’s chances of becoming a serious Covid case. Observes Dr Haviv: ‘yes, unfortunately, the vaccine… as they say, its effectiveness is waning.” And so it is, indeed. Dr Haviv’s interview is on YouTube so you can hear the truth straight from his mouth. It will be interesting to see how long it will take for the Establishment Censors to take it down.” See this.

But there is worse. Everybody knows how sensitive and delicate small children are. Now the monsters want to give them the killer jab too! Let’s listen to Kohlmayer again:” “’CDC recommends COVID-19 vaccine boosters down to age 12,’ says a recent CBC news headline.

The article opens as follows:

‘Millions of Americans between the ages of 12 and 15 can now get a booster shot of Pfizer’s COVID-19 vaccine, after the CDC formally adopted new recommendations backed by a majority of the agency’s outside vaccine advisers. The CDC now says that Americans as young as 12 who received Pfizer’s COVID-19 vaccine should receive a third dose as early as five months after their first two shots. The agency’s officials said that enough time has passed for around 5 million adolescents to be eligible’

‘Why in the world are they doing this?’ one asks in disbelief.

Three basic facts have been well established by data and studies:

  1. Healthy children are at virtually zero risk of serious Covid.
  2. The vaccines will not prevent children from contracting the virus.
  3. Covid injections carry risk of serious side effects.

According to a cost-benefit analysis conducted by Toby Rogers, Ph.D., in the 5 to 11 age range, 117 healthy kids will have to die of vaccine-related side effects in order to save one child from perishing of Covid 19.

study from Japan has shown that young people are seven hundred percent more likely to be killed by Pfizer jabs than by Covid.

We have been repeatedly told that we must follow facts and science when dealing with this pandemic.

The science on vaccinating children against Covid-19 is in, and it could not be any clearer: while healthy children are at negligible risk from the disease itself, they are at real risk from the shots.

Since the vaccines do not stop infection and transmission, they will protect neither children nor their communities from the spread of the virus.

It makes not scientific or medical sense to give them these shots. Vaccinating children for SARS-CoV-2 violates both the tenets of good medicine and evidence-based science.

According to Dr Robert Malone, who is one of the world’s preeminent vaccine scientists, the cost benefit analysis is not even close.

Those who want to vaccinate children follow neither the science nor logic. Subjecting children to Covid jabs needlessly exposes young lives to potentially grave risks.

The incidence of myocarditis and pericarditis may be as high as 1 in 317 in the young, especially boys, and increases further with each additional dose.

Then there is a danger of deadly blood clots as well as several other serious conditions such as Guillain-Barré syndrome.

Astonishingly, scores of children have already been injected with two doses that turned out to be ineffective, which is the reason a booster is now required.

The booster, however, already looks to be even more useless than the original offering. The booster, in fact, appears to have negative efficacy which means that those who receive it seem to be more likely to contract the virus.

Soon we will have a multitude of 12-year-olds who will have received three of these pointless and dangerous shots without any medical justification whatsoever.

Robert Kennedy, Jr. said that injecting children with the Covid vaccines is a crime. He is not incorrect.

A number of children have already been killed by the vaccines.

Some of the newly vaccinated children will develop serious conditions and some of them will die. The lives of these healthy children will be cut short for no good reason and their parents will be beside themselves with grief.”

We must do everything we can to stop them before they kill more. If we act on what we know, we can stop these demonic monsters.

 

Llewellyn H. Rockwell, Jr. [send him mail], former editorial assistant to Ludwig von Mises and congressional chief of staff to Ron Paul, is founder and chairman of the Mises Institute, executor for the estate of Murray N. Rothbard, and editor of LewRockwell.com. He is the author of Against the State and Against the Left. Follow him on Facebook and Twitter.

 

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From Covid to Global Control: Bait and Switch

From Covid to Global Control: Bait and Switch

by Jon Rappoport, Jon Rappoport’s Blog
July 19, 2022

 

“One new reality is global interconnectivity and the fact that all challenges must be addressed on the basis of ‘togetherness.’ Thus the most crucial factor in accepting the new reality and confronting its opportunities and risks is our willingness to develop shared norms on all levels.” (Klaus Schwab, founder of the World Economic Forum)

The above quote is a glimpse of the switch in the bait and switch.

First, in early 2020, there was a narrative, a story about a virus, and the selling of that story, and the selling of all the (ruinous) restrictions which would have to be put in place, in order to “curb the spread.”

Then came what you could call “transitional language”:

In order to be prepared for the next pandemic, we need early warning, on a global scale; and THIS means a much greater level of cooperation among nations.

You know, that sort of talk.

It included: We have to be able to identify human carriers of a virus before they develop symptoms, because they’re silently spreading a killer.

It included: These pandemics are never going to stop. With massive international travel, the transport of goods across national borders, with deadly viruses escaping from rain forests…we have to create a PERMANENT global society, with proper controls, which can withstand and survive the onslaught of these devastating germs.

Transitional language.

From the bait (a story about a virus), the con moves to the switch (a permanent global control grid).

Is there some sort of picture of what the control grid will look like? Just a sketch?

Why yes, there is.

We need to look to the nation which has garnered the most praise for its handling of the “pandemic crisis.” Praise from elite global players like the World Health Organization and the UN and Bill Gates.

Of course, I mean China.

China is the elite model. It locked down 50 million citizens overnight, at the beginning of 2020. And it’s doing it again.

But there’s more.

Much more.

I call your attention to a stunning article in The Atlantic. “The Panopticon Is Already Here” (September, 2020), by Ross Andersen.

Here are significant excerpts:

“Artificial intelligence has applications in nearly every human domain, from the instant translation of spoken language to early viral-outbreak detection. But Xi [Xi Jinping, president of China] also wants to use AI’s awesome analytical powers to push China to the cutting edge of surveillance. He wants to build an all-seeing digital system of social control, patrolled by precog algorithms that identify potential dissenters in real time.”

“China already has hundreds of millions of surveillance cameras in place. Xi’s government hopes to soon achieve full video coverage of key public areas. Much of the footage collected by China’s cameras is parsed by algorithms for security threats of one kind or another. In the near future, every person who enters a public space could be identified, instantly, by AI matching them to an ocean of personal data, including their every text communication, and their body’s one-of-a-kind protein-construction schema. In time, algorithms will be able to string together data points from a broad range of sources—travel records, friends and associates, reading habits, purchases—to predict political resistance before it happens. China’s government could soon achieve an unprecedented political stranglehold on more than 1 billion people.”

“China is already developing powerful new surveillance tools, and exporting them to dozens of the world’s actual and would-be autocracies. Over the next few years, those technologies will be refined and integrated into all-encompassing surveillance systems that dictators can plug and play.”

“China’s government could harvest footage from equivalent Chinese products. They could tap the cameras attached to ride-share cars, or the self-driving vehicles that may soon replace them: Automated vehicles will be covered in a whole host of sensors, including some that will take in information much richer than 2-D video. Data from a massive fleet of them could be stitched together, and supplemented by other [Alibaba] City Brain streams, to produce a 3-D model of the city that’s updated second by second. Each refresh could log every human’s location within the model. Such a system would make unidentified faces a priority, perhaps by sending drone swarms to secure a positive ID.”

“An authoritarian state with enough processing power could force the makers of such software to feed every blip of a citizen’s neural activity into a government database. China has recently been pushing citizens to download and use a propaganda app. The government could use emotion-tracking software to monitor reactions to a political stimulus within an app. A silent, suppressed response to a meme or a clip from a Xi speech would be a meaningful data point to a precog algorithm.”

“All of these time-synced feeds of on-the-ground data could be supplemented by footage from drones, whose gigapixel cameras can record whole cityscapes in the kind of crystalline detail that allows for license-plate reading and gait recognition. ‘Spy bird’ drones already swoop and circle above Chinese cities, disguised as doves. City Brain’s feeds could be synthesized with data from systems in other urban areas, to form a multidimensional, real-time account of nearly all human activity within China. Server farms across China will soon be able to hold multiple angles of high-definition footage of every moment of every Chinese person’s life.”

“The government might soon have a rich, auto-populating data profile for all of its 1 billion–plus citizens. Each profile would comprise millions of data points, including the person’s every appearance in surveilled space, as well as all of her communications and purchases. Her threat risk to the party’s power could constantly be updated in real time, with a more granular score than those used in China’s pilot ‘social credit’ schemes, which already aim to give every citizen a public social-reputation score based on things like social-media connections and buying habits. Algorithms could monitor her digital data score, along with everyone else’s, continuously, without ever feeling the fatigue that hit Stasi officers working the late shift. False positives—deeming someone a threat for innocuous behavior—would be encouraged, in order to boost the system’s built-in chilling effects, so that she’d turn her sharp eyes on her own behavior, to avoid the slightest appearance of dissent.”

“If her risk factor fluctuated upward—whether due to some suspicious pattern in her movements, her social associations, her insufficient attention to a propaganda-consumption app, or some correlation known only to the AI—a purely automated system could limit her movement. It could prevent her from purchasing plane or train tickets. It could disallow passage through checkpoints. It could remotely commandeer ‘smart locks’ in public or private spaces, to confine her until security forces arrived.”

“Each time a person’s face is recognized, or her voice recorded, or her text messages intercepted, this information could be attached, instantly, to her government-ID number, police records, tax returns, property filings, and employment history. It could be cross-referenced with her medical records and DNA, of which the Chinese police boast they have the world’s largest collection.”

Is China exporting this control-grid technology?

“The country [China] is now the world’s leading seller of AI-powered surveillance equipment. In Malaysia, the government is working with Yitu, a Chinese AI start-up, to bring facial-recognition technology to Kuala Lumpur’s police as a complement to Alibaba’s City Brain platform. Chinese companies also bid to outfit every one of Singapore’s 110,000 lampposts with facial-recognition cameras.”

“In South Asia, the Chinese government has supplied surveillance equipment to Sri Lanka. On the old Silk Road, the Chinese company Dahua is lining the streets of Mongolia’s capital with AI-assisted surveillance cameras. Farther west, in Serbia, Huawei is helping set up a ‘safe-city system,’ complete with facial-recognition cameras and joint patrols conducted by Serbian and Chinese police aimed at helping Chinese tourists to feel safe.”

“In the early aughts, the Chinese telecom titan ZTE sold Ethiopia a wireless network with built-in backdoor access for the government. In a later crackdown, dissidents were rounded up for brutal interrogations, during which they were played audio from recent phone calls they’d made. Today, Kenya, Uganda, and Mauritius are outfitting major cities with Chinese-made surveillance networks.”

“In Egypt, Chinese developers are looking to finance the construction of a new capital. It’s slated to run on a ‘smart city’ platform similar to City Brain, although a vendor has not yet been named. In southern Africa, Zambia has agreed to buy more than $1 billion in telecom equipment from China, including internet-monitoring technology. China’s Hikvision, the world’s largest manufacturer of AI-enabled surveillance cameras, has an office in Johannesburg.”

“In 2018, CloudWalk Technology, a Guangzhou-based start-up spun out of the Chinese Academy of Sciences, inked a deal with the Zimbabwean government to set up a surveillance network. Its terms require Harare to send images of its inhabitants—a rich data set, given that Zimbabwe has absorbed migration flows from all across sub-Saharan Africa—back to CloudWalk’s Chinese offices, allowing the company to fine-tune its software’s ability to recognize dark-skinned faces, which have previously proved tricky for its algorithms.”

“Having set up beachheads in Asia, Europe, and Africa, China’s AI companies are now pushing into Latin America, a region the Chinese government describes as a ‘core economic interest.’ China financed Ecuador’s $240 million purchase of a surveillance-camera system. Bolivia, too, has bought surveillance equipment with help from a loan from Beijing. Venezuela recently debuted a new national ID-card system that logs citizens’ political affiliations in a database built by ZTE…”

You could call all this Lockdown, Phase 2. But of course it’s much more. It’s designed to be permanent.

It’s a control grid, the switch in the bait and switch.

Ultimately, long term, we’re dealing with the switch, not the bait.

I’ll add a few more features to the “China plan.” Under the rubric of climate change, and “limiting CO2,” worldwide of production of energy would be significantly lowered. At the individual level, this would result in energy-use quotas. Strictly enforced.

“Mr. Jones, this is your phone helper. You’re nearing the limit of your energy use for the month. I don’t want to see you incur penalties. For example, your Guaranteed Universal Income allotment could be reduced. So for the next 10 days, I’ll be turning off some of your devices. Use your computer only between the hours of 2 and 4AM. Don’t drive. Don’t cook. The heat in your apartment will be shut down between midnight and 6AM. Remember, this is being done to curb the effect of climate change. We all have to do our part…”

Then there is 5G technology, which enables the Internet of Things (IoT). All sorts of products, from diapers to chocolate bars, will contain tags so these items can talk to each other and regulate your consumption and buying habits.

But the real kicker is more-control-grid. For instance, the top-down regulation of driverless cars on roads and highways; the moment to moment choice of routes and patterns of traffic for a whole city. The ability to stop all cars in a city, or clear them off roads in a “problem area.”

Because you’d be wearing a number of items tagged with their own tiny computers, law-enforcement could calculate and decide, at any given moment, that there are too many people in a park. The people “might constitute a threat.” So an order goes out to empty the park.

And in this article, I’m not getting into the far reaches of genetic modification of humans, or brain-computer interfaces, or the medical control of the body through inserted nano-sensors.

Let me give you that Klaus Schwab quote again. You read it at the top of this piece. Read it one more time and render it into its true meaning:

“One new reality is global interconnectivity and the fact that all challenges must be addressed on the basis of ‘togetherness.’ Thus the most crucial factor in accepting the new reality and confronting its opportunities and risks is our willingness to develop shared norms on all levels.”

This is a ten thousand year war called Freedom Versus Slavery.

Like it or not, we’re up to our necks in it.

 

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cover image credit: Sammy-Sander / pixabay




Historic Decision Against Mandatory Vaccination by Italian Court — Judge Declares in Her Decision That Covid Vaccines Are Producing Very Serious Adverse Effects & Thousands of Deaths

Historic Decision Against Mandatory Vaccination by Italian Court — Judge Declares in Her Decision That Covid Vaccines Are Producing Very Serious Adverse Effects & Thousands of Deaths

 



Video source: Corona Investigative Committee at Odysee


 

Historic Decision Against Mandatory Vaccination by Italian Court + Covid Vaccines Risk to Human Genome Now Legally Established (Italy)

by Children’s Health Defense Europe
July 18, 2022

 

On July 6th, 2022, the court of Florence has approved a sentence annulling the measure taken by the Order of Psychologists of Tuscany against one of its members, the reason being: ‘the suspension of the exercise of the profession risks compromising primary individual rights such as the right to a livelihood and the right to work’.

The judge ruled that the psychologist doesn’t need to be vaccinated in order to do his job by establishing that:

  • these substances don’t prevent infection and transmission. Therefore, in front of the Italian law, there can not be an obligation.
  • She also recognises that these substances provokes severe adverse events.
    Therefore, it even less legitimate to force anybody to be injected.
  • The judge put the dignity of the human being at the centre and referred twice to the period of Nazism and Fascism. Mandatory vaccination is possible if there is informed consent. For Covid injections, she explained that an informed consent is not possible as we don’t know the ingredients and the mechanisms of these substances because of industrial and alleged military secret.

This interim decision is grounded in serious conclusion: there is no right to suspend a citizen from the right to work based of this illegal request of vaccination with these experimental substances.

With this historic court decision, “the Risk to human genome is now legally established” Renate Holzeisen, attorney for the plaintiff, said in an interview for an Italian radio.

“This could be a milestone” said Reiner Fuellmich during the Corona Committee 113, interviewing Renate Holzeisen.

No Obligation as the official data show that these experimental substances don’t prevent infection and transmission amongst people treated with 3 or more Covid shots.

First of all, the judge declares that based on the datas published by the Ministry of HealthAIFA (Italian Medicines Agency) and the SSN (Italian Health Services), it is very clear that these substances (aka Covid vaccines), defined several times by the judge as “experimental”, don’t prevent infection from the virus. For a mandatory vaccination, the substances should be proven to work.

Therefore, as they don’t work, in front of the Italian law, there can not be an obligation.

Doctor leading the intensive care in Verona has declared in television that all Covid patients in intensive care are people treated with 3 Covid shots.

Nobody can be forced to be injected as these substances provoke severe adverse events and this is based on official public data regarding adverse events.

In the court decision, the judge also recognises that these substances cause very serious side effects that can even lead to death, and also refers to the risk of genetic mutation.

Therefore, it even less legitimate to force anybody to be injected.

The Dignity of the human being is at the centre. Mandatory vaccination is not possible because there is NO informed consent due to industrial and alleged military secret regarding the ingredients and the mechanism of these injections.

Even if these substances would work to prevent these infection, after the Nazi and fascism period, it can not be a mandatory without an informed consent.

The judge stated that there is no benefit for these substances BUT even if there was a benefit, we can not sacrifice the individual right in the name of the common interest, and put the dignity of the human being at the centre.

The judge referred twice to the Nazi and fascism period, to the Italian Constitution article 32 highlighting that there is a reason why Dignity is at the centre of the first article of the German constitution.

She explained that an informed consent is not possible as we don’t know the ingredients and the mechanisms of these substances (industrial and alleged military secret).

We should recall a group of Human Rights Italian activists who presented a Freedom of Information Act to the EMA and to the Italian Cares Authority asking for clear informations about the ingredients and the safety of these experimental substances aka Covid injections. As an answer, the EMA said that no information can be shared as there is a military secret in place.

In his decision, the judge stated it: no information are available about these substances and even if we ask for information publicly, we don’t receive it. There is no informed consent.

In this historic decision, the Tuscan judge concluded that based on all these, the discrimination of this psychologist and his suspension from work is totally illegal. Without hearing the other part (Chamber of Psychologist in Tuscany), she declared that there is no time to spend anymore for this psychologist who has been suspended last October 2021. Evidence is so clear.

This interim decision is grounded in serious conclusion: there is no right to suspend a citizen from the right to work based of this illegal mandatory vaccination with experimental substances. A future court hearing will take place on September 15th, 2022, when the judge will rule based on what the chamber of psychologists will present. But the judge shows as well that there is no need to go to the constitutional court as we know that these substances (aka Covid-19 vaccine) don’t prevent infection. In front of the Italian law regarding mandatory Covid vaccination, it is enough to say the suspension from labour of healthcare workers is illegitimate because these substances don’t do what the constitution request.

During the last 2 years, we saw incredible decisions where judges says that they can not take decisions going against governmental decisions. Mandatory vaccination for all workers and people over 50 are already in place in Italy, even if official data regarding severe adverse events show the danger of these substances. This happens in a country where ongoing advertising campaigns sell Covid vaccines as “safe and effective” – ie. Prime Minister Mario Draghi and President Sergio Mattarella, have declared several times that only people who get these treatments will survive and the others will dye and be responsible of the Covid deaths.

After two years of Covid pandemic – in which many have fought to defend their freedom and rights – ‘a great judge and a great sentence’ open a new glimmer of hope. This is the first decision with which an Italian judge declared the material truth and the imposition of the treatment is radically illegitimate.

———————

READ the Court Decision Here.

 

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

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cover image credit: GDJ 




Guitarist Who Lost 8 Fingers After J&J Vaccine Tells Rfk, Jr.: People Have to Be Held Accountable

Guitarist Who Lost 8 Fingers After J&J Vaccine Tells Rfk, Jr.: People Have to Be Held Accountable
On a recent episode of “RFK Jr. The Defender Podcast,” guitarist Jeff Diamond described having eight fingers amputated and losing his singing voice after developing blood clots about a week after getting the Johnson & Johnson COVID-19 vaccine.

by Rachel Militello, The Defender
July 12, 2022

 

On July 9, 2021, Jeff Diamond, a professional musician, vocal instructor and backup guitarist, got the Johnson & Johnson (J&J) COVID-19 vaccine.

About a week later, Diamond was found unconscious in his apartment and taken to a local hospital in Minnesota, where he remained in a coma for three weeks.

Pervasive blood clots — a known side effect of the J&J vaccine — had shut down his kidneys and other organs.

The condition caused doctors to amputate eight of his fingers, without his knowledge or consent, while he was still in a coma.

Diamond, a guest on the July 5 episode of “RFK Jr. The Defender Podcast,” told Robert F. Kennedy, Jr., he got the vaccine only because he’d been performing at an event in Atlanta, and didn’t want to risk infecting his mother.

“I was taking care of my mother, and that’s the only reason I got the shot in the first place,” Diamond said.

When Diamond awoke from the coma, he also found himself intubated, which impaired his singing voice.

With his kidneys barely functioning and his balance thrown off by all the medications he was prescribed, Diamond lay in the hospital for another three weeks until he was able to go into a nursing home.

While in the nursing home for six weeks, Diamond’s feeding tube burst open and he was rushed to an emergency room. “Blood was gushing out of my stomach,” he told Kennedy. It “almost killed me.”

A doctor in Minneapolis saved his life, but Diamond told Kennedy he’s been “in pain with these fingers ever since.” Diamond was fitted with prosthetic fingers, but while “they may look great,” he said, “they’re not working out for playing the guitar.”

Diamond’s singing voice has “bounced back a bit,” he said, but not all the way.

And it’s “all from, I believe, the Johnson & Johnson shot,” Diamond said.

Asked if doctors acknowledged a link between the vaccine and his injuries, Diamond said all but one were non-committal.

Now, a year after he was injured, Diamond said he’s taking things day by day, and hopes to someday play guitar again.

More importantly, though, he wants to get the word out about what happened to him.

“What happened to me … I don’t want to see this happen to anybody else,” Diamond said. “I think it’s a crime … People have got to be held accountable.”

Watch the podcast here:



Rachel Militello has worked extensively as a legal assistant at law firms and newspaper companies. She is also a self-published author of poetry that is geared toward mental health awareness.

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.

 

©July 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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FDA Colluded With Moderna to Bypass COVID Vaccine Safety Standards, Documents Reveal

FDA Colluded With Moderna to Bypass COVID Vaccine Safety Standards, Documents Reveal
According to Alexandra Latypova, an ex-pharmaceutical industry executive, documents obtained from the U.S. Department of Health and Human Services on Moderna’s COVID-19 vaccine suggest the U.S. Food and Drug Administration and Moderna colluded to bypass regulatory and scientific standards used to ensure products are safe.

 

by Megan Redshaw, The Defender
July 12, 2022

 

According to an ex-pharmaceutical industry and biotech executive, documents obtained from the U.S. Department of Health and Human Services (HHS) on Moderna’s COVID-19 vaccine suggest the U.S. Food and Drug Administration (FDA) and Moderna colluded to bypass regulatory and scientific standards used to ensure products are safe.

Alexandra Latypova has spent 25 years in pharmaceutical research and development working with more than 60 companies worldwide to submit data to the FDA on hundreds of clinical trials.

After analyzing 699 pages of studies and test results “supposedly used by the FDA to clear Moderna’s mRNA platform-based mRNA-1273, or Spikevax,” Latypova told The Defender she believes U.S. health agencies are lying to the public on behalf of vaccine manufacturers.

“It is evident that the FDA and NIH [National Institutes of Health] colluded with Moderna to subvert the regulatory and scientific standards of drug safety testing,” Latypova said.

“They accepted fraudulent test designs, substitutions of test articles, glaring omissions and whitewashing of serious signs of health damage by the product, then lied to the public on behalf of the manufacturers.”

In an op-ed on Trial Site News, Latypova disclosed the following findings:

  1. Moderna’s nonclinical summary contains mostly irrelevant materials.
  2. Moderna claims the active substance — mRNA in Spikevax — does not need to be studied for toxicity and can be replaced with any other mRNA without further testing.
  3. Moderna’s nonclinical program consisted of irrelevant studies of unapproved mRNAs and only one non-GLP [Good Laboratory Practice] toxicology study of mRNA-1273 — the active substance in Spikevax.
  4. There are two separate investigational new drug numbers for mRNA-1273. One is held by Moderna, the other by the Division of Microbiology and Infectious Diseases within the NIH, representing a “serious conflict of interest.”
  5. The FDA failed to question Moderna’s “scientifically dishonest studies” dismissing an “extremely significant risk” of vaccine-induced antibody-enhanced disease.
  6. The FDA and Moderna lied about reproductive toxicology studies in public disclosures and product labeling.

“Moderna’s documents are poorly and often incompetently written — with numerous hypothetical statements unsupported by any data, proposed theories, and admission of using unvalidated assays and repetitive paragraphs throughout,” Latypova wrote.

“Quite shockingly, this represents the entire safety toxicology assessment for an extremely novel product that has gotten injected into millions of arms worldwide.”

Finding 1: Moderna’s non-clinical summary contains mostly irrelevant materials.

According to Latypova, about 80% of the materials disclosed by HHS that FDA considered in approving Moderna’s Spikevax pertain to other mRNA products unrelated to SARS-CoV-2 or COVID-19.

“Approximately 400 pages of the materials belong to a single biodistribution study in rats conducted at the Charles River facility in Canada for an irrelevant test article, mRNA-1674,” Latypova said. “This product is a construct of 6 different mRNAs studied for cytomegalovirus in 2017 and never approved for market.”

Latypova said the study showed lipid nanoparticles (LNPs) distribute throughout the entire body to all major organ systems.

Latypova found it odd the study protocol, report and amendments related to the study were copied numerous times throughout the HHS documents, suggesting Moderna may have been trying to meet a minimum word count.

In between the repetitive copies of the “same irrelevant study,” Latypova found “ModernaTX, Inc. 2.4 Nonclinical Overview” for Moderna’s COVID-19 vaccine with the investigational new drug application reference IND #19745.

Module 2.4, she said, is a standard part of the new drug application and is supposed to contain summaries of nonclinical studies.

Latypova wrote:

“There are three separate versions of Module 2.4 included and many sections appear to be missing. It is not clear why multiple versions are included and there is no explanation provided as to which version specifically was used for the approval of Spikevax by the FDA.”

Latypova noted all three copies of Module 2.4 appear to have the same overview but reference a different set of statements and studies.

Latypova said the description of the finished supplied product differs between the two versions:

“Version 1 (p. 0001466) [says] mRNA-1273 is provided as a sterile liquid for injection at a concentration of 5 mg/mL in 20 mM trometamol (Tris) buffer containing 87 mg/mL sucrose and 10.7 mM sodium acetate, at pH 7.5.

“Version 2 (p. 0001499) [says] the mRNA-1273 Drug Product is provided as a sterile suspension for injection at a concentration of 20 mg/mL in 20 mM Tris buffer containing 87 g/L sucrose and 4.3 mM acetate, at pH 7.5.”

“It appears from reading section 2.4.1.2 Test Material (p.0001499) that Version 2 of the drug product had been used for manufacturing the Lot AMPDP-200005 which was used for nonclinical studies,” Latypova said. But “there is no explanation given for why the drug product in version 1 is different, and no comparability testing studies between the two product specifications are provided.”

Latypova pointed out that the package insert for FDA-approved Spikevax does not contain any information regarding the concentration of the product supplied in its vials.

Finding 2: Moderna said Spikevax mRNA does not need to be studied for toxicity and can be replaced with any other mRNA without further testing.

Latypova alleges Moderna, Pfizer and Janssen — manufacturer of the Johnson & Johnson shot — along with the FDA, have been deceptive in their assertions claiming the risks of COVID-19 vaccines are associated with the LNP delivery platform, and therefore, the mRNA “payload” does not need to undergo standard safety toxicological tests.

The documents state:

“The distribution, toxicity, and genotoxicity associated with mRNA vaccines formulated in LNPs are driven primarily by the composition of the LNPs and, to a lesser extent, by the biologic activity of the antigen(s) encoded by the mRNA. Therefore, the distribution study, Good Laboratory Practice (GLP)-compliant toxicology studies, and in vivo GLP-compliant genotoxicity study conducted with mRNA vaccines that encode various antigens developed with the Sponsor’s mRNA-based platform using SM 102-containing LNPs are considered supportive and BLA-enabling for mRNA-1273.”

Moderna is “claiming that the active drug substance of a novel medicine does not need to be tested for toxicity,” Latypova said. “This is analogous to claiming that a truck carrying food and a truck carrying explosives are the same thing. Ignore the cargo, focus on the vehicle.”

Latypova called the claim “preposterous,” as mRNAs and LNPs separately and together are “entirely novel chemical entities” that each require their own IND application and data dossier filed with regulators.

“Studies with one mRNA are no substitute for all others,” she added.

According to the European Medicines Agency, this chemical entity is entirely novel:

“The modified mRNA in the COVID-19 mRNA Vaccine is a chemical active substance that has not been previously authorized in medicinal products in the European Union. From a chemical structure point of view, the modified mRNA is not related to any other authorized substances. It is not structurally related as a salt, ester, ether, isomer, mixture of isomers, complex or derivative of an already approved active substance in the European Union.

“The modified mRNA is not an active metabolite of any active substance(s) approved in the European Union. The modified mRNA is not a pro-drug for any existing agent. The administration of the applied active substance does not expose patients to the same therapeutic moiety as already authorized active substance(s) in the European Union.

“A justification for these claims is provided in accordance with the ‘Reflection paper on the chemical structure and properties criteria to be considered for the evaluation of new active substance (NAS) status of chemical substances’ (EMA/CHMP/QWP/104223/2015), COVID-19 mRNA Vaccine is therefore classified as a New Active Substance and considered to be new in itself.”

“The reviewers specifically stated ‘modified RNA’ and not just the lipid envelope constitute the new chemical entity,” Latypova said. “All new chemical entities must undergo rigorous safety testing before they are approved as medicinal products in the United States, European Union and the rest of the world.”

Latypova said Moderna failed to cite any studies showing “all toxicity of the product resides with the lipid envelope and none with the payload” of the type and sequence of mRNA delivered to various tissues and organs.

“It is also not a matter of a mistake or rushing new technology to market under crisis conditions,” she added. “This scientifically fraudulent strategy was not only premeditated, it was also never really concealed.”

Latypova gave the example of a 2018 PowerPoint presentation by Moderna CEO Stéphane Bancel at a JP Morgan conference where he stated: “If mRNA works once, it will work many times.”

“This describes the deception practiced by the manufacturers, FDA, the Centers for Disease Control and Prevention (CDC), NIH and every government health authority or mainstream media talking head who participated in it,” Latypova said.

She continued:

“Imagine Ford Motor Company claiming that its crash testing program should be contained to the vehicle’s tires and that one test is sufficient for all vehicle models.

“After all both F150 and Taurus have tires, what’s in between the tires ‘worked once and will work again,’ and therefore it is inconsequential to safety, does not need to be separately tested and can be replaced at the manufacturer’s will with any new variation.

“This is the claim that Moderna, Pfizer, Janssen and other manufacturers of the gene therapy ‘platforms’ have utilized. Unlike Ford’s products, theirs have never worked as none of their mRNA-based gene therapy products have ever been approved for any indication. The fact that the regulators did not object to this argument raises an even greater alarm.”

“There is no question of incompetence or mistake,” Latypova said. “If this represents the current ‘gold standard’ of regulatory pharmaceutical science, I have very bad news regarding the safety of the entire supply or new medicines in the U.S. and the world.”

Finding 3: Moderna’s nonclinical program included only one non-GLP toxicology study of the active substance in Spikevax. 

According to Latypova, a non-clinical program for a novel product usually includes information on pharmacology, pharmacokinetics, safety pharmacology, toxicology and other studies to determine the carcinogenicity or genotoxicity of a drug and its effects on reproduction.

The more novel the product, the more extensive the safety and toxicity evaluations need to be, she said.

In Module 2.4 described above, Latypova was able to identify 29 unique studies but only 10 were done with the correct mRNA-1273 test particle. The other studies were conducted using a “variety of unapproved experimental mRNAs unrelated to Spikevax or COVID illness.”

For example, the in-vivo genotoxicity studies included an irrelevant mRNA-1706 and a luciferase mRNA that is not in Moderna’s COVID-19 vaccine.

“Of the 10 studies using mRNA-1273, nine were pharmacology (‘efficacy’) studies and only one was a toxicology (‘safety’) study,” Latypova said. “All of these were non-GLP studies, i.e., research experiments conducted without validation standards acceptable for regulatory approval.”

There was only one toxicology study included in Moderna’s package related to the correct test particle mRNA-1273, but the study was non-GLP compliant, was conducted in rats and was not completed at the time the documents were submitted to the FDA for approval.

The results of the study were indicative of possible tissue damage, systemic inflammation and potential severe safety issues — and they are also dose-dependent, Latypova said. Moderna noted its findings but “simply moved on, deciding to forgo any further evaluation of these effects.”

Regarding reproductive toxicology, the only assessment was conducted on rats.

Pharmacokinetics — or the biodistribution, absorption, metabolism and excretion of a compound — were not studied with Moderna’s Spikevax mRNA-1273.

“Instead, Moderna included a set of studies with another, unrelated mRNA-1647 — a construct of six different mRNAs which was in development for cytomegalovirus in 2017 in a non-GLP compliant study,” Latypova said. “This product has not been approved for market and its current development status is unknown.”

Moderna claimed the LNP formulation of mRNA-1647 was the same as in Spikevax, so the study using this particle was “supportive of” the development of Spikevax.

“This claim is dishonest,” Latypova said. “While the kinetics of the product may be studied this way, the toxicities may not!”

She explained:

“We do not know what happens with the organs and tissues when the delivered mRNA starts expressing spike proteins in those cells. This is a crucial safety-related issue, and both the manufacturer and the regulator were aware of it, yet chose to ignore it.

“The study demonstrated that the LNPs did not remain in the vaccination site exclusively, but were distributed in all organs analyzed, except the kidney. High concentrations were observed in lymph nodes and spleen and persisted in those organs at three days after the injection.

“The study was stopped before full clearance could be observed, therefore no knowledge exists on the full time-course of the biodistribution. Other organs where vaccine product was detected included bone marrow, brain, eye, heart, small intestine, liver, lung, stomach and testes.”

Given that LNPs of the mRNA-1647 were detected in these tissues, it’s reasonable to assume the same occurs with mRNA-1273 and “likewise would distribute in the same way,” Latypova said. “Therefore the spike protein would be expressed by the cells in those critical organ systems with unpredictable and possibly catastrophic effects.”

“Neither Moderna nor FDA wanted to evaluate this matter any further,” she added. “No metabolism, excretion, pharmacokinetic drug interactions or any other pharmacokinetic studies for mRNA-1273 were conducted,” nor were safety pharmacology assessments for any organ classes.

Finding 4: ‘Serious conflict of interest’ exists between Moderna and NIH.

According to Latypova, Moderna’s documents contain a letter from the Division of Microbiology and Infectious Diseases authorizing the FDA to refer to IND #19635 to support the review of Moderna’s own IND #19745 provided in “Module 1.4.”

Although Module 1.4 was not included in the documents provided by HHS, the FDA on Jan. 30 revealed the following timeline for Moderna’s Spikevax.

According to the FDA, Spikevax has two sponsors of its IND application package, including the NIH division that reports to Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases and chief medical advisor to President Biden.

The date of the pre-IND meeting for Spikevax was on Feb. 19, 2020. The IND submission for the NIH’s IND was on Feb. 20, 2020, while Moderna’s own IND was submitted on April 27, 2020.

According to the CDC, as of Jan. 11, 2020, Chinese health authorities had identified more than 40 human infections as part of the COVID-19 outbreak first reported on Dec. 31, 2020.

The World Health Organization on Jan. 9, 2020, announced the preliminary identification of the novel coronavirus. The record of Wuhan-Hu-1 includes sequence data, annotation and metadata from the virus isolated from a patient approximately two weeks prior.

Latypova said this raises several questions warranting further investigation:

  • Preparation for a pre-IND meeting is a process that typically takes several months, and is expensive and labor-consuming. How was it possible for the NIH and Moderna to have a pre-IND meeting for a Phase 1 human clinical trial scheduled with the FDA for a vaccine product a month before the COVID-19 pandemic was declared?
  • “How was it possible to have all materials prepared and the entire non-clinical testing process completed for this specific product related to a very specific virus which was only isolated and sequenced (so we were told) by Jan. 9, 2020?”
  • Ownership of the IND is both a legal and commercial matter, which in the case of a public-private partnership, must be transparently disclosed. “What is the precise commercial and legal arrangement between Moderna and NIH regarding Spikevax?”
  • “Does NIH financially benefit from sales of Moderna’s product? Who at NIH specifically?”
  • “Does forcing vaccination with the Moderna product via mandates, government-funded media campaigns and perverse government financial incentives to schools, healthcare system and employers represent a significant conflict of interest for the NIH as a financial beneficiary of these actions?”
  • “Does concealing important safety information by a financially interested party (NIH and Moderna) represent a conspiracy by the pharma-government cartel to defraud the public?”

Latypova further noted that immediately after the pre-IND meeting with the FDA, an “extremely heavy volume of orders for Moderna stock” began to be placed in the public markets.

This warrants an “additional investigation into the investors that were able to predict the spectacular future of the previously poorly performing stock with such timely precision,” she said.

Finding 5: FDA failed to question Moderna’s ‘scientifically dishonest studies’ dismissing an ‘extremely significant risk’ of vaccine-induced antibody-enhanced disease.

Moderna, prior to 2020, had never brought an approved drug to market.

“Its entire product development history was marked by numerous failures despite millions of dollars and lengthy time spent in development,” Latypova said. “Notably, its mRNA-based vaccines were associated with the antibody-dependent-enhancement phenomenon.”

For example, Moderna’s preclinical study of its mRNA-based Zika vaccine in mice showed all mice “uniformly [suffered from] lethal infection and severe disease due to antibody enhancement.”

The scientists were able to develop a type of vaccine that generated protection against Zika that “resulted in significantly less morbidity and mortality,” but all versions of the vaccine unequivocally led to some level of antibody-dependent-enhancement.

The Primary Pharmacology section for Spikevax includes nine studies evaluating immunogenicity, protection from viral replication and potential for vaccine-associated enhanced respiratory disease.

“These studies included the correct test article (mRNA-1273), however, all were non-GLP compliant,” Latypova said. The results of these studies are briefly summarized in the text of the document package, yet the study reports are not provided.

In the disclosed documents, Moderna claims “there were no established animal models” for SARS-CoV-2 virus due to its extreme novelty.

Yet, in the next sentence, “despite the extreme novelty of the virus,” Ralph Baric, Ph.D., at the University of North Carolina possessed an already mouse-adapted SARS-CoV-2 virus strain and provided it for some of Moderna’s studies, Latypova said.

According to Latypova’s assessment, there were other numerous contradictions in Moderna’s documents, and when enhanced disease risk was revealed in assays, the company waived off its own results with a statement regarding the invalidity of the assays and methods they used.

“As SARS-CoV-2 neutralization assays are, to this point, still highly variable and in the process of being further developed, optimized and validated, study measurements should not be considered a strong predictor of clinical outcomes, especially in the absence of results from a positive control that has demonstrated disease enhancement,” Moderna said.

“Clearly, both Moderna and FDA knew about disease enhancement and were aware of numerous examples of this dangerous phenomenon, including Moderna’s own Zika vaccine product of the same type,” Latypova said. “Yet, the FDA did not question Moderna’s scientifically dishonest ‘studies’ that dismissed this extremely significant risk without a proper study design.”

Finding 6: FDA and Moderna lied about reproductive toxicology studies in public disclosures and product labeling.

Although the FDA recommends Moderna’s COVID-19 vaccine for pregnant and lactating women, Moderna conducted only one reproductive toxicology study in pregnant and lactating rats using a human dose of 100 mcg of mRNA-1273.

Although the full study was excluded, a narrative summary of Moderna’s findings state, “high IgG antibodies to SARS-CoV-2 S-2P were also observed in GD 21 F1 fetuses and LD 21 F1 pups, indicating strong transfer of antibodies from dam to fetus and from dam to pup.”

Latypova said safety assessments in the study are very limited, but the following findings are described by Moderna:

“The mothers lost fur after vaccine administration, and it persisted for several days. No information on when it was fully resolved since the study was terminated before this could be assessed.”

In the rat pups, the following skeletal malformations were observed:

“In the F1 generation [rat pups], there were no mRNA-1273-related effects or changes in the following parameters: mortality, body weight, clinical observations, macroscopic observations, gross pathology, external or visceral malformations or variations, skeletal malformations, and mean number of ossification sites per fetus per litter.

“mRNA-1273-related variations in skeletal examination included statistically significant increases in the number of F1 rats with 1 or more wavy ribs and 1 or more rib nodules.

“Wavy ribs appeared in 6 fetuses and 4 litters with a fetal prevalence of 4.03% and a litter prevalence of 18.2%. Rib nodules appeared in 5 of those 6 fetuses.”

Moderna related the skeletal malformations to days when toxicity was observed in the mothers but waived away the finding as “unrelated to the vaccine,” Latypova said.

The FDA then “lied on Moderna’s behalf” in its Basis for Regulatory Action Summary document (p.14) stating “no skeletal malformations” occurred in the non-clinical study in rat pups despite the opposite reported by Moderna.

“No vaccine-related fetal malformations or variations and no adverse effect on postnatal development were observed in the study. Immunoglobulin G (IgG) responses to the pre-fusion stabilized spike protein antigen following immunization were observed in maternal samples and F1 generation rats indicating transfer of antibodies from mother to fetus and from mother to nursing pups.”

“In summary, the vaccine-derived antibodies transfer from mother to child,” Latypova said. “It was never assessed by Moderna whether the LNPs, mRNA and spike proteins transfer as well, but it is reasonable to assume that they do due to the mechanism of action of these products.”

Latypova said studies should have been done to assess the risks to the child by vaccinating pregnant or lactating women before recommending these groups receive a COVID-19 vaccine.

“We should ask the question why are they concealing the critical safety-related information from public, and making the product look better than the manufacturer has admitted,” Latypova said.

“The FDA did not have any objective scientific evidence excluding the skeletal malformations being related to the vaccine,” she added. “Thus, the information should have been disclosed fully in the label of this experimental and poorly tested product — not hidden from the public for over a year and then disclosed only under a court order.”

Latypova said FDA reviewers should have “easily seen through the blatant fraud, omissions, use of inadequate study designs and general lack of scientific rigor.”

The fact that more than half of the document package contains non-GLP studies for irrelevant, unapproved and previously failed chemical entities alone should have been sufficient reason to not approve this product, she added.

It would appear the FDA based its decision that the product is safe to administer to thousands of otherwise healthy humans on two studies in rats, Latypova said. The rest of the 700-page package was deemed to consist of “other supportive studies.”

The FDA noted studies were conducted in “five vaccines formulated in SM-102 lipid particles containing mRNAs encoding various viral glycoprotein antigens” but “failed to mention that these were five unapproved and previously failed products,” she said.

The regulators then concluded that using novel unapproved mRNAs in support of another unapproved novel mRNA was acceptable.

“The circular logic is astonishing,” Latypova said. Regulators allowed and personally promoted the use of failed experiments in support of a different and new experiment directly on the unsuspecting public.

Latypova called for the FDA, pharmaceutical manufacturers and “all other perpetrators of this fraud to be urgently stopped and investigated.”

 

©July 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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America’s New “Angels of Death”: Inject Humanity With a Gene-Altering Death-Dealing Technology. Medical Professionals Cannot Claim Ignorance.

America’s New “Angels of Death”: Inject Humanity With a Gene-Altering Death-Dealing Technology. Medical Professionals Cannot Claim Ignorance.

by  Prof. Bill Willers, Global Research
July 11, 2022

 

“The guilt for the mass murder is solely that of the political leaders….. I accuse the leaders of abusing my obedience. At that time obedience was demanded, just as in the future it will also be demanded of the subordinate. Obedience is commended as a virtue.”
Adolph Eichmann, Nazi, at his trial

Early in the declared Covid19 Pandemic, America’s medical community —  and this included America’s pharmacies    coalesced around a system of outlawing medicines known to be effective, safe and inexpensive, notably ivermectin and hydroxychloroquine  In time, it became obvious that withholding early treatment was crucial for the pharmaceutical industry’s project to vaccinate the world against a claimed Covid19 virus.

Had the effectiveness of inexpensive and available medicines been widely seen, the pretext for ‘Emergency Use Authorization’ of a warpspeed-produced experimental product would have vaporized. With a trillion dollar global vaccination project at stake, that couldn’t be allowed, so the lies of ivermectin and hydroxychloroquine being toxic were authoritatively enforced.  

The policy descended (and continues to descend) from administrative networks within the Department of Health and Human Services, (notably CDC and NIAID) to the states. These networks are part of, and fed by, an international complex involving the World Health Organization, itself under the control of international pharmaceutical interests focused primarily on vaccines, as well as on gene manipulations sold under the deceptive banner of “vaccine”.

This multi-pronged, vaccine-focused universe now includes research universities and medical schools, medical societies and fraudulent medical journals showcasing ghost-written “scientific” articles. A key player is the discipline of Public Health, a politicized field posing as objective science, enforcer of official narrative and hurler of the “misinformation” epithet at dissenters. And of course there is the compliant media. And money, endless rivers of it. 

At hospital level, commands from this complex flow through desk-bound administrators, with doctors and nurses induced to follow those commands for fear of losing needed hospital access. Failure to mind can even result in suspension of license to practice medicine. This control system extends to state medical boards under the umbrella of the Federation of State Medical Boards, the guidelines of which require practitioners to use treatments “… supported by the best available scientific evidence or prevailing scientific consensus”. But officially accepted “best available scientific evidence” is now so tightly controlled that one is literally forced toward the “prevailing scientific consensus”. 

The “consensus” referred to is a rigidly enforced story, and divergence from it is immediately attacked from all corners of officialdom as “misinformation”. A key branch of the army protecting the official, lie-riddled storyline has been the burgeoning fact-check industry, succinctly nailed by Dr. Bryan Ardis  “Fact checking is to divert you from the truth and take you back to the narrative you’re being sold worldwide.”

You doctors who have been obedient to an industry-inspired, governmentally-driven protocol have abdicated the doctor-patient relationship. And what is true for doctors in this respect applies to nurses as well. By withholding available treatments and sending sick people home; by injecting a trusting public with an experimental gene-altering technology that has potentially devastating long-range, even trans-generational impacts; by not seeing immediately the criminal idiocy of injecting children, for whom the claimed virus is known to be benign, you have made your patients de facto lab animals. 

FBI Director J. Edgar Hoover once wrote “The individual is handicapped by coming face to face with a conspiracy so monstrous he cannot believe it exists.” The Covid19 Pandemic, set up as justification for a global project to inject humanity with a gene-altering death-dealing technology, is certainly monstrous enough to handicap anyone, at least for a time. It is murderous on a scale so immense as to be unbelievable on first exposure. And that alone may have posed too great a barrier for most of the multitude to even want to take a closer look. 

But you medical professionals cannot claim ignorance at this late date, when mere minutes of online search can reveal that outstanding medical figures all over the world have been struggling against censorship and mainstream media vomitings to expose the lie-riddled Covid19/“vaccine” project ( 123…) For their troubles, of course, they continue to be attacked by the media network long known to be rotten to the core. Has your choosing to be obedient within this long nightmare been simply to hold on to a job? Or have you just been too lazy to search out censored information? Or too uncaring? Or are you just stupid? Only you would know for sure. 

Josef Mengele, like yourselves, was a medical doctor. At Auschwitz concentration camp, his grisly medical experiments won him a place in history as Todesengel, “The Angel of Death”. He is supposed to have said “The more we do to you, the less you seem to believe we are doing it.” Does that seem familiar, and do your patients still trust you? In any case, you medics who have been so obedient to the vaccine industry’s merciless global project might want to get to know Dr. Mengele. There are even books on the man. After all, he was a soul mate of yours, as you have, eyes wide open, made yourselves, whether by omission or commission, his medical heirs. 

*

Bill Willers is an emeritus professor of biology, University of Wisconsin at Oshkosh. He is founder of the Superior Wilderness Action Network and editor of Learning to Listen to the Land, and Unmanaged Landscapes, both from Island Press. He can be contacted at willers@uwosh.edu.

 

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‘Head-Spinning’: FDA Quietly Grants Full Approval of Pfizer Comirnaty Vaccine for Adolescents

‘Head-Spinning’: FDA Quietly Grants Full Approval of Pfizer Comirnaty Vaccine for Adolescents
In a move Children’s Health Defense President Mary Holland called “head-spinning,” the U.S. Food and Drug Administration on Friday granted full approval of Pfizer-BioNTech’s Comirnaty COVID-19 vaccine for adolescents 12 through 15 years old.

by Megan Redshaw, The Defender
July 11, 2022

 

The U.S. Food and Drug Administration (FDA) on Friday granted full approval of Pfizer-BioNTech’s Comirnaty COVID-19 vaccine for adolescents 12 through 15 years old.

In an FDA press release, the agency said full approval of Comirnaty follows a “rigorous analysis and evaluation of the safety and effectiveness data,” and the Pfizer-BioNTech vaccine “has been, and will continue to be authorized for emergency use in this age group since May 2021.”

Pfizer’s press release announcing the approval said the Comirnaty vaccine has been available under Emergency Use Authorization (EUA) since May 2021 for the adolescent age group.

Yet, Comirnaty is not available in the U.S for any age group and is not the same formula as the Pfizer-BioNTech vaccine currently authorized under EUA and being distributed as a “fully approved” vaccine.

“The approval of Comirnaty for adolescents 12 to 15 is head-spinning,” said Mary Holland, president and general counsel for Children’s Health Defense.

Holland added:

“The FDA failed to convene an expert committee and failed to appropriately weigh the risk-benefit profile of this vaccine for this age group. Even Vaccine cheerleader Dr. Paul Offit acknowledged FDA decisions are being made based on political pressure, not science when, in commenting on the agency’s vote last week to allow reformulated booster shots, he said it felt like ‘the fix was in.’”

Holland said that at base, “this is a move by pharma to ensure liability protection” under the National Childhood Vaccine Injury Act of 1986. Some states likely will attempt to put Comirnaty on the childhood vaccine schedule, despite the myriad known and unknown risks, Holland said.

“Pfizer‘s fraud and collusion with government is becoming more evident by the day,” Holland said. “CHD, already challenging the authorizations for those six months through age 11, will be at the forefront of challenging this approval for teenagers.”

Efficacy claims based on old analysis of 16- to 25-year-olds — before Delta, Omicron variants

Pfizer said Friday’s approval is based on data from a Phase 3 clinical trial of 2,260 participants ages 12 through 15.

About half of the participants, “elicited SARS-CoV-2–neutralizing antibody geometric mean titers (GMTs)” demonstrating “strong immunogenicity in a subset of adolescents one month after the second dose,” Pfizer said.

It is unknown what happened to antibody levels after one month, but peer-reviewed research suggests vaccine protection conferred by second and third doses of Pfizer’s COVID-19 vaccine wanes rapidly against the Omicron variant.

“Our study found a rapid decline in Omicron-specific serum neutralizing antibody titers only a few weeks after the second and third doses of [the Pfizer-BioNTech] BNT162b2,” said the authors of a May 13 study published in JAMA.

To further support its claim that Comirnaty is effective in the 12 to 15 age group, Pfizer used an old analysis of 16- to 25-year-olds conducted before the Delta and Omicron surges.

“The efficacy analysis was conducted between November 2020 and May 2021, which was before the Delta and Omicron surges,” and the “only SARS-CoV-2 variant of concern identified from the confirmed COVID-19 cases in this age group was Alpha,” Pfizer said in its press release.

FDA experts question neutralizing antibodies as standard for vaccine effectiveness

During a June 28 meeting of the FDA’s Vaccine and Related Biological Products Advisory Committee (VRBPAC), vaccine experts raised concerns that neutralizing antibodies did not correlate to clinical protection — noting Moderna’s COVID-19 vaccine had a two-fold increase in neutralizing antibody levels compared with Pfizer’s vaccine during clinical trials, but it did not translate into a clinically significant difference in terms of protection against severe disease.

Dr. Ofer Levy, VRBPAC member and infectious disease physician at Boston Children’s Hospital, said during the meeting there is still “no established correlate of protection,” referring to the level of antibodies needed to confer protection.

“You have a lot of data now,” Levy told Pfizer. “What is your relative protection?”

“I would say there is no established correlate of protection,” Kena Swanson, Ph.D., vice president of viral vaccines at Pfizer, told Levy.

Levy said:

“I would like to hear from FDA what their overall approach will be around improving our understanding of correlate protection. We spend a good amount of time reviewing antibody data. We have no doubt antibody data is important. We don’t have a level of antibody that anybody is comfortable stating is correlated [with] protection.

Levy, who said antibodies are important, but T cells are more important, called for federal leadership to establish a “standardization of the T-cell assay and encourage or in fact require the sponsors to gather that information.”

“So what is the effort to standardize the pre-clinical assays?” Levy asked. “This is an effort that’s critical not just now but for future cycles of vaccine revision. If we aren’t able to define a standard for correlate protection we are fighting with one arm behind our back.”

Dr. Peter Marks, head of the FDA’s Center for Biologics Evaluation and Research, acknowledged the importance of Levy’s question and said they are “having conversations” with colleagues at the National Institutes of Health and throughout government about how they might move forward, but it is something they “don’t have an answer to yet.”

Marks said as vaccines are developed in the future, it will “become even more important” to define a standard of correlate protection because “we won’t be able to have a large naive population to vaccinate with newer vaccines.”

“We will need to understand the T-cell response better,” Marks said. “I take your point, it’s just that we haven’t solved the problem yet.“

Comirnaty not available in the U.S. 

According to Pfizer’s press release, Comirnaty was previously made available to the 12 to 15 age group in the U.S. under EUA and 9 million U.S. adolescents in this age group have completed a primary series.

“The vaccine, sold under the brand name Comirnaty for adults, has been available under an emergency use authorization since May 2021 for the 12-15 age group,” Reuters reported. “It will now be sold under the same brand name for adolescents as well.”

Yet, Pfizer’s information hotline says it has no specific information on when Comirnaty will be available.

The FDA said Friday the Pfizer-BioNTech vaccine “has been, and will continue to be, authorized for emergency use in this age group since May 2021.”

The CDC’s website states that Comirnaty is “not orderable.”

A branch of the U.S. Department of Health and Human Services overseeing the Strategic National Stockpile indicated Comirnaty was not available because Pfizer did not have time to change the labels.

According to FDA documents, Comirnaty is not available in the U.S. and nobody has received a fully approved and licensed COVID-19 vaccine.

“Comirnaty has not been made available under EUA,” said Dr. Madhava Setty, physician and senior science editor for The Defender.

Setty added:

“The FDA and Pfizer have already stated very quietly, that they have no intent of manufacturing Comirnaty for distribution. Everyone is getting the non-licensed formulation that carries no liability for pharmaceutical companies.”

The CDC website confirms this, stating the Comirnaty formulation “will not be manufactured or made available in the near term even if authorized.”

The FDA on Aug. 23, 2021, approved Pfizer’s biological licensing application (BLA) for its COVID-19 vaccine named Comirnaty for people age 16 and older.

CHD challenged FDA on Comirnaty ‘approval’ for adults

As The Defender reported, there were “several bizarre aspects to the FDA approval” that proved confusing — which led to CHD suing the FDA over its approval of Comirnaty.

The FDA acknowledged that while Pfizer had “insufficient stocks” of the newly licensed Comirnaty vaccine, there was “a significant amount” of the Pfizer-BioNTech COVID vaccine — produced under EUA — still available for use.

The FDA said the Pfizer-BioNTech vaccine under EUA should remain unlicensed but could be used “interchangeably” with the newly licensed Comirnaty product.

The FDA also said the licensed Pfizer Comirnaty vaccine and the existing Pfizer-BioNTech vaccine were “legally distinct,” but proclaimed their differences did not “impact safety or effectiveness.”

Yet, there is a “huge real-world difference” between products approved under EUA compared with those the FDA has fully licensed.

EUA products are experimental under U.S. law and cannot be mandated. A licensed vaccine, such as Comirnaty, can be mandated by employers and schools.

Although Pfizer’s Comirnaty vaccine can be mandated, it has no liability shield. Vials of the branded product, which say “Comirnaty” on the label, are subject to the same product liability laws as other U.S. products.

Only COVID-19 vaccines distributed under EUA — which in the U.S. includes Pfizer-BioNTech, Moderna and Johnson & Johnson — have liability protection under the 2005 Public Readiness and Preparedness Act (PREP).

Under PREP, the only way an injured party can sue a pharmaceutical company for an injury caused by an EUA vaccine is if he or she can prove willful misconduct and if the U.S. government has also brought an enforcement action against the party for willful misconduct. No such lawsuit has ever succeeded.

Comirnaty cannot receive liability protection unless it is fully approved for children and added to the CDC’s immunization schedule bringing it under the auspices of the National Vaccine Injury Compensation Program.

Pfizer-BioNTech and Comirnaty vaccines aren’t interchangeable 

The FDA on Oct. 29, 2021, authorized a manufacturing change to allow an additional formulation of the Pfizer-BioNTech COVID-19 vaccine that uses tromethamine (Tris) buffer instead of phosphate-buffered saline (PBS) used in the originally authorized Pfizer-BioNTech COVID-19 vaccine.

The FDA on Dec. 16, 2021, approved a supplement to the Comirnaty BLA to include a new 30 mcg dose formulation that uses the Tris buffer instead of the PBS buffer used in the originally approved vaccine.

The Pfizer-BioNTech vaccine may contain either the PBS buffer or tris buffer, except for the 5 to 11 age group. The Comirnaty vaccine contains the Tris buffer.

The Pfizer-BioNTech vaccine used for the 5 to 11 age group uses a Tris buffer, despite clinical trials having been conducted using Pfizer’s vaccine containing the PBS buffer.

According to Pfizer’s July 8 press release, the FDA relied upon studies conducted prior to the formula change to justify the approval of Pfizer’s Comirnaty vaccine for adolescents ages 12 to 15.

The type of buffer used in a COVID-19 vaccine can affect the potency of the vaccine, how it is stored and the propensity to develop potential adverse events, TrialSite News reported.

​​According to Cleveland Clinic, Tris is commonly used for the prevention and treatment of metabolic acidosis associated with various clinical conditions such as heart bypass surgery or cardiac arrest. It is also used in other vaccines, including Moderna’s COVID-19 vaccine, dengue, smallpox and Ebola vaccines.

The FDA categorizes tromethamine as a category C drug and suggests using tromethamine only if clearly needed.

It is unknown if tromethamine will harm an unborn baby, but animal reproduction studies have shown an adverse effect on the fetus, and there are “no adequate and well-controlled studies in humans.”

“The FDA-evaluated manufacturing data [to] support the change in this inactive ingredient and concluded it did not impact the safety or effectiveness of the product,” Marks, said during an October 2021, press briefing.

According to the FDA’s Letter of Authorization, reissued on Oct. 29, “analytical comparability assessments” revealed the Pfizer-BioNTech COVID vaccine formulations containing Tris and PBS buffers were “analytically comparable.”

Yet, no human or animal trials were conducted to determine the safety or efficacy of the new formula.

 

©July 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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Uruguay Halts COVID-19 Vaccine for Kids Under 13, Judge Demands Government Officials Turn Over Pfizer Contracts

Uruguay Halts COVID-19 Vaccine for Kids Under 13, Judge Demands Government Officials Turn Over Pfizer Contracts
Uruguay suspended COVID-19 vaccines for children under 13 after a judge on Thursday issued an injunction halting vaccinations in that age group until government officials turn over its contracts with Pfizer.

by Megan Redshaw, The Defender
July 8, 2022

 

Uruguay suspended COVID-19 vaccines for children under 13 after a judge on Thursday issued an injunction halting vaccinations in that age group until government officials turn over its contracts with Pfizer.

Uruguayan government officials and Pfizer were ordered on Wednesday to appear in court after judge Alejandro Recarey gave them 48 hours to present detailed information on Pfizer’s COVID-19 vaccine while the court considered an injunction request to halt COVID-19 vaccinations for children 5 and older.

The government said a confidentiality clause in the contract prevents it from producing the documents, The Washington Post reported.

According to ABC News, the judge received answers to 18 questions about the safety and chemical composition of COVID-19 vaccines, signed by Health Minister Daniel Salinas, but did not turn over the contracts.

It is unknown whether the answers provided by government officials adequately addressed the questions posed by the judge, who ultimately ordered an injunction based on what was provided.

Salinas, after the court’s ruling, strongly defended the government’s vaccination plan and criticized the judge for questioning the safety of vaccines.

Alvaro Delgado, the secretary of the presidency, said the halt is a threat to public health.

“We’re convinced that it’s crazy to suspend voluntary vaccination because it has a strong scientific backing,” Delgado said at a news conference.

Vaccinations for those older than 13 will continue, the Health Ministry said in a statement.

The government plans to appeal the decision, according to ABC News.

As The Defender reported Wednesday, judge Recarey of the Administrative Litigation Tribunal used his inquisitorial powers to demand the Uruguayan Ministry of Public Health, State Health Services Administration and the President’s Office submit all information regarding the contracts for the purchase of COVID-19 vaccines, including contractual information related to any clauses of civil indemnity or criminal impunity of the suppliers in the event of adverse effects.

The judge is seeking, among other things, to know whether there are clauses in the contracts that promised pharmaceutical companies like Pfizer civil and criminal immunity for adverse effects caused by their vaccines.

Judge Recarey posed a series of questions to government officials and Pfizer regarding the chemical composition, efficacy and safety of COVID-19 vaccines, and required Pfizer to state whether it has “admitted, in any area, internal or external to it and its partners, the verification of adverse effects” of its COVID-19 vaccines in children.

 

©July 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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Biotech/Pharmaceutical Chemist Mike Donio on the Tyranny of Medical Dogma: Exposing the Corruption, Lies, and Medical Fraud in the Pharmaceutical Industry

Biotech/Pharmaceutical Chemist Mike Donio on the Tyranny of Medical Dogma: Exposing the Corruption, Lies, and Medical Fraud in the Pharmaceutical Industry

by Jeremy Nell, Jerm Warfare
sourced from July 8, 2022 “War Report” newsletter
video was uploaded July 4, 2022

 



Mike Donio is a pharmaceutical scientist who left the industry after pulling back the curtain on corruption, lies, and medical fraud.

His conversation with me was enlightening in that it confirms what other scientists have been saying,

America’s most cited cardiologist, Peter McCullough, said this week that he no longer trusts any Flu shot, due to the unbelievable corruption within the pharmaceutical industry.

I have never taken a Flu shot, and I will never take a Covid shot (because Covid doesn’t exist).

Also, I have never had a PCR test and, in fact, turned down a sponsored international trip because I refuse to legitimatise bogus PCR tests.

Take a listen to Sam Bailey’s story.

She is a medical doctor from New Zealand, who speaks out against pharmaceutical tyranny and poor medical science.

Sam was fired from her longstanding TV show after she stated that she would not get a Covid injection.

The tyranny of dogma indeed.

It’s a cult, as OffGuardian‘s Dustin Broadbery wrote in his great piece, The Anatomy Of A Cult.

But the fact that humanity is in an abusive relationship with its governments, is only one part of the problem. There’s a long history of cults infiltrating polite society. The cult of personality of Lenin and later Stalin once captured an entire nation. But never in history has the entire world fallen to a cult.

Yup.

Satirist CJ Hopkins refers to Covid cultists as Branch Covidians.

Don’t trust the science, as Mike Donio said.

Del Bigtree has revealed how the American government (including the CDC and FDA) collude with Big Pharma for monetary gain, particularly where safety trials are concerned. Or rather, the lack of safety trials.

Roman Bystrianyk co-authored a book called Dissolving Illusions, in which they use official data to show how, over the last century, no vaccine has worked in the way promised by the pharmaceutical industry and governments. Every vaccine was introduced way after its respective disease was on its way out. Measles, for example, was around 97% eradicated before its vaccine hit the market.

The point is that the pharmaceutical industry is untrustworthy, and few scientists are as close to the action as Mike Donio.

 

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Army Cuts 60,000 Unvaccinated Guard and Reserve Soldiers From Training and Pay as COVID Vaccine Mandate Deadline Passes

Army Cuts 60,000 Unvaccinated Guard and Reserve Soldiers From Training and Pay as COVID Vaccine Mandate Deadline Passes
The Army confirmed on July 1 that tens of thousands of military Guard and Reserve soldiers can no longer participate in training or receive benefits, as Army faces recruiting crisis.

by Megan Redshaw, The Defender
July 7, 2022

 

About 60,000 Army National Guard members and Army Reserve soldiers who refused to comply with a Department of Defense (DOD) COVID-19 vaccine mandate are no longer allowed to participate in their military duties and were cut off from some of their pay and benefits, Army officials announced July 1.

Of the more than 40,000 members of the Guard who remain unvaccinated, 14,000 have said they do not intend to ever receive a COVID-19 vaccine, Guard officials told CBS News.

Approximately 22,000 Reserve soldiers have refused to get vaccinated.

“Soldiers who refuse the vaccination order without an approved or pending exemption request are subject to adverse administrative actions, including flags, bars to service and official reprimands,” an Army spokesperson said in a statement.

If the soldiers continue to refuse to get vaccinated, the consequences could be even more severe.

“In the future, Soldiers who continue to refuse the vaccination order without an exemption may be subject to additional adverse administrative action, including separation,” the Army spokesperson said.

Despite the military’s deadline, the services said they wish to continue to work with the remaining holdouts as commanders face increased anger from critics concerned over a recruiting crisis that has left Defense Department officials struggling to fill the ranks.

According to Rep. Mike Johnson (R-LA), the Army is having “significant trouble filling its ranks” while simultaneously discharging soldiers who refuse to get vaccinated.

As of mid-April, the Army had “discharged 255 soldiers for refusing the COVID-19 vaccine and is on track to give another 2,500 to 3,000 the boot before the end of the year — a number roughly equivalent to two or three Army battalions,” Johnson wrote on his website.

Six Army officers, including two battalion commanders, have been relieved of command, while 3,330 active-duty soldiers have been issued written reprimands for refusing to get vaccinated.

“The Army priority remains vaccinating all soldiers to maintain readiness. In determining this policy, Army leaders considered the unique realities of each component,” Reserve spokesman John Bradley told U.S. News & World Report.

“Reserve component commanders are working through a deliberate process in as few as two days per month with geographically dispersed Soldiers to ensure they become fully vaccinated.”

Soldiers will be allowed to come on duty and earn their pay if it’s for the purpose of getting vaccinated or to take part in separation procedures. Part-time soldiers with a pending medical or religious exemption request may train with their units and collect pay and benefits, but exemptions are not being approved.

To date, only six Guard soldiers across all states and territories have received medical exemptions out of 53 who submitted requests, according to Army data. No Reserve soldiers have received a medical exemption.

No Guard or Reserve soldiers have been approved for a religious exemption despite nearly 3,000 requests.

The Army National Guard and Army Reserve deadline to receive the COVID-19 vaccine was June 30 — the final deadline among all the service branches subject to Secretary of Defense Lloyd Austin’s mandate issued last August.

As of July 1, 13% of the Army National Guard and 12% of the Army Reserve are unvaccinated.

According to internal documents shared with The Defender, 280,678 Army National Guard members are fully vaccinated (84.6%), and 7,735 have received one dose (2.3%) leaving 43,269 (13%), who have not yet received a single dose.

In some states, such as Oklahoma, the vaccination rate for Guard members is as low as 74.11%.

The document lists 15,698 members as “refusals” and 6,749 (2.0%) as going through an exemption process — with 6,257 (1.9%) requesting a religious exemption and 492 (0.1%) requesting a medical exemption.

The document also notes that 80% of unvaccinated Guard members are age 32 or younger, with an average age of 26.2 and median age of 24.

According to CBS News, vaccine compliance among Army National Guard members is the lowest in the U.S. military — the rate among active-duty Army, Navy, Air Force and Marine Corps is 97% or greater and the Air Guard uptake is about 94%.

 

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Pfizer Ordered by Uruguayan Judge to Report Composition of Covid-19 Vaccines Including Any Presence of “Graphene Oxide” or “Nanotechnological Elements”

Pfizer Ordered by Uruguayan Judge to Report Composition of Covid-19 Vaccines Including Any Presence of “Graphene Oxide” or “Nanotechnological Elements”

by Jim Hoft, Gateway Pundit
July 4, 2022

 

According to a recent ruling by an Uruguayan judge, the government and the pharmaceutical company Pfizer must provide all the information they have on the COVID vaccine’s biochemical composition, including any evidence of “graphene oxide” or “nanotechnological elements,” as well as proof of the vaccine’s efficacy and safety.

Administrative Litigation Court (TCA) Judge Alejandro Recarey made the order in response to a request to suspend the immunization of children from 5 years of age in Uruguay.

According to the court order released on Saturday, Judge Alejandro Recarey ordered the Presidency, the Ministry of Public Health, the State Health Services Administration (ASSE), and Pfizer to present all the information on Covid-19 vaccines within 48 hours, El Observador reported.

“A hearing will be held on Wednesday at 9:00 am where representatives of all the agencies and the company must appear,” the news outlet added.

TRENDING: BREAKING EXCLUSIVE: Information Uncovered Overnight Shows Highland Park Shooter, Bobby Crimo, Is Tied to Socialists, Progressives, Antifa and the Occult

More from France 24 (translated):

According to the decision, the Executive and the US laboratory must provide documentation on the composition of the vaccines, including the possible presence of “graphene oxide” or “nanotechnological elements”.

Data is also requested that demonstrates the “harmlessness” of “the substance called messenger RNA” and that proves with studies by the US agency of the United States, the FDA, “the experimental nature” of the vaccines.

The magistrate asks that the authorities “explain whether alternative anticovid-19 therapies have been studied” and “if not, clarify why these solutions were not explored,” according to the document.

The contracts signed between the government and Pfizer are also subject to scrutiny to see if they contain clauses “for civil indemnity or criminal impunity for suppliers regarding the occurrence of possible adverse effects,” among other details.

The court decision also requires explanations as to whether studies have been carried out “aiming to explain the notorious increase in deaths from covid-19 as of March 2021 in relation to the previous year.”

“Very especially, Pfizer will be instructed to state within 48 hours – with the provision of documentary data if applicable – if the company has admitted (…) the verification of adverse effects of vaccines against the so-called Covid-19. In general, and also in detail regarding the child population,” says the document.

 

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Court Again Blocks COVID Vaccine Mandate for Federal Workers

Court Again Blocks COVID Vaccine Mandate for Federal Workers
The Biden administration’s COVID-19 vaccine mandate for federal employees will remain blocked until at least September after a federal appeals court on Monday agreed to reconsider its previous decision to reinstate the mandate.

by Suzanne Burdick, Ph.D. , The Defender
June 28, 2022

 

The Biden administration’s COVID-19 vaccine mandate for federal employees will remain blocked until at least September after a federal appeals court on Monday agreed to reconsider its previous decision to reinstate the mandate.

The 5th U.S. Circuit Court of Appeals in New Orleans will revisit its April ruling by a three-judge panel that the administration has the legal authority to require federal employees to get vaccinated against COVID-19, The Associated Press reported.

The new injunction will remain until the case can be argued before the full court’s 17 judges. According to The Epoch Times, the court has tentatively scheduled the en banc oral arguments for the week of Sept. 12.

Back-and-forth rulings on federal worker vaccine mandate since January 

Biden introduced Executive Order 14043 in September 2021, requiring more than 3.5 million federal executive branch workers to undergo vaccination unless they secured approved medical or religious exemptions. The order did not allow workers to choose regular testing in place of getting the vaccine.

In December 2021, Feds for Medical Freedom — a grassroots organization with about 6,000 members throughout the federal civil service — sued the Biden administration and several federal agencies.

Other parties to the lawsuit included the American Federation of Government Employees (AFGE) Local 918, a union representing employees in the Federal Protective Service and the Cybersecurity and Infrastructure Security Agency, and several other individuals and federal contractors.

The groups sought to block two COVID-19 vaccine mandates: one covering federal employees and the other for federal contractors.

Lawyers representing the Biden administration argued the Constitution gives the president, as the head of the federal workforce, the same authority as the CEO of a private corporation, and that therefore mandating vaccination was under the president’s authority.

The plaintiffs disagreed, countering that such action oversteps a president’s powers.

“The main thrust of the argument [of the plaintiffs],” attorney Bruce Castor Jrtold The Epoch Times in February, “is that the president doesn’t have the authority to issue an order like this, pursuant to the powers granted him in Article Two of the United States Constitution, and that’s the same argument that won the day in the Supreme Court regarding the 100 or more employees; the president doesn’t have that authority.”

Castor, a lawyer with the law firm van der Veen, Hartshorn & Levin, which represented the AFGE union, added:

“Instead of going through the checks and balances of congressional approval, which includes feedback from the public, the executive order cuts all that out. It just says, ‘My way or the highway.’

“Certainly, the Constitution grants powers like that to the president in foreign affairs and protecting the nation from aggression from foreign powers. But he doesn’t have the authority, with a sweep of the pen, to affect the lives of millions of people, bypassing Congress.”

In January, U.S. District Judge Jeffrey Brown blocked the mandate, stating in his 20-page ruling that the president and his administration did not have the authority to impose such a mandate.

Brown questioned the president’s power to mandate federal employees undergo a medical procedure as a condition of their employment, writing in his decision:

“This case is not about whether folks should get vaccinated against COVID-19 — the court believes they should. It is not even about the federal government’s power, exercised properly, to mandate vaccination of its employees.

“It is instead about whether the president can, with the stroke of a pen and without the input of Congress, require millions of federal employees to undergo a medical procedure as a condition of their employment.

“That, under the current state of the law as just recently expressed by the Supreme Court, is a bridge too far.”

In February, a 5th Circuit panel of judges refused to block Brown’s ruling pending appeal.

But after hearing arguments in March, a different panel of judges ruled 2-1 in early April that Brown did not have jurisdiction in the case, overturning the lower court’s Jan. 21 injunction against the mandate and ordering the district court to dismiss the case.

Meanwhile, Biden’s vaccine mandate continues to draw fire from health freedom groups who alleged federal overreach. Four groups — including America’s Frontline Doctors and Airline Employees for Health Freedom — filed amicus briefs in June

 

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The “Lab-Leak Theory” Returns…as Yet Another Fake Binary

The “Lab-Leak Theory” Returns…as Yet Another Fake Binary

by Kit Knightly, OffGuardian
June 23, 2022

 

The theory that “Covid” originated in a bio-lab has been back in the headlines over the last few weeks, serving as a prime example of the type of fake binary OffG has been warning you about.

The “lab-leak theory” – which pushes the idea Sars-Cov-2 was bio-engineered in a lab as a “gain-of-function” program, and then either accidentally or deliberately released on an unsuspecting population – first came to the front pages as early as January 2020.

At the time it was deemed a “racist” “anti-china” conspiracy theory by the vast majority of the media, and it fell away from the narrative.

It had a resurgence in 2021, suddenly & inexplicably becoming not racist anymore.

In February 2021 the World Health Organization published a report finding the lab origin for Covid19 “extremely unlikely”. But WHO chief Tedro Adhanom was obviously keen not to let the idea die completely, publicly stating “more investigation was needed”.

Overall, around this time, it suddenly became much less taboo to suggest the “virus” originated in a lab.

The BBC had an explainer article titled “Covid origin: Why the Wuhan lab-leak theory is being taken seriously”, the New Yorker reported:

Scientists and political commentators are no longer dismissing the possibility that COVID-19 emerged from a Chinese laboratory.

As the Wikipedia page notes:

Since May 2021, some media organizations softened previous language that described the laboratory leak theory as “debunked” or a “conspiracy theory”

We did a brief coronavirus fact-check on “Covid is a bio-weapon” at the time.

Then, in December 2021, the Daily Mail reported that Dr Alina Chan had told the UK’s Science Select Committee that it is ‘reasonable to believe [the] virus was engineered in China’ and that “the lab origin is more likely than not”.

But after a brief furore over that, it again faded from the front pages.

Now it’s back. And gaining momentum.

In May, 18 scientists (including Chan) published an open letter in the Science journal demanding authorities properly “investigate the origins of Covid19”.

Two weeks ago the World Health Organisation released a report that they were still investigating the origins of Covid, and that no hypothesis had been completely ruled out.

On June 15th, the WHO chief told reporters at a press conference that ruling out the lab-leak theory had been “premature” and there had been a “push” to do so. He called on China to “be transparent, open and cooperate, especially on the information, raw data that we asked for at the early days of the pandemic.”

This time China responded, dismissing the lab leak theory as “lies” and “anti-China propaganda”, whilst suggesting that the real lab leak likely came from the US bioweapons lab in Fort Detrick.

Then, on June 18th, The Daily Mail reported that despite maintaining public neutrality Tedros Adhanom “privately believed” that Covid had originated in a lab.

In short, two apparently oppositional camps are springing up – the West is laying the groundwork to blame China for the pandemic, whilst China (and probably Russia, down the line) blame the USA.

This is a textbook fake binary.

What you need to notice is that both these allegedly opposing sides agree on the most important aspect of the pandemic lie – that Covid is a unique new and dangerous disease which needs be treated with masks, lockdowns and vaccines – and only disagree violently about where this “real and deadly new disease” might have come from.

You are supposed to take your cue from them.

They want you to forget  “covid” is just a meaningless new name for an old familiar cluster of “seasonal” symptoms. They want you to forget the whole thing was a scam – and to instead take a “side” in a scripted &  noisy & totally phony “origin” debate.

The minute you sign up for it they have you – because by agreeing to debate where “it” comes from you have accepted “it”  – ie a deadly new pathogen – exists & needs to be dealt with.

And that is all they want from you.

We think you should politely decline this staged “controversy”. Because however real the East-West divide actually is in other areas, when it comes to covid both sides are the same side & pushing the same story.

And it suits both East & West to encourage this fake binary  – and  “bioweapon” fear porn – at the expense of wider and more honest enquiry.

Just say no.

 

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Whistleblower Says With 120,000 Troops Still Unvaccinated, Army May Move June 30 Deadline Far Into Future

Whistleblower Says With 120,000 Troops Still Unvaccinated, Army May Move June 30 Deadline Far Into Future
An active-duty senior Army official told The Defender, on condition of anonymity, the U.S. Army is strongly considering pushing the June 30 deadline for compliance with the military’s COVID-19 vaccine mandate far into the future — but will not announce the date change until closer to, or even after, the upcoming deadline.

by Michael Nevradakis, Ph.D. , The Defender
June 22, 2022

 

As the June 30 deadline nears for compliance with the U.S. military’s COVID-19 vaccine mandate, U.S. Army officials publicly claim a very small percentage of its members are unvaccinated, reporting 96% or more of its members are fully vaccinated.

However, the Army’s vaccination rate is in fact significantly lower than 96%, an active-duty senior Army official with access to senior-level information told The Defender — so low, that if the Army were to enforce the deadline, the loss of up to 120,000 service members would render it “combat-ineffective.”

The official, who spoke on condition of anonymity, said the Army is strongly considering pushing the June 30 deadline much further into the future — but will not announce the date change until closer to, or even after, the upcoming deadline.

Concern about the number of unvaccinated service members was the topic of recent senior-level briefings, according to the official.

He said he’s blowing the whistle now because many service members who remain unvaccinated and/or who are “on the fence” about getting the vaccine may feel compelled to do so to meet the June 30 deadline — unaware the deadline may soon change.

He said by going public with this information now, service members who have not yet been vaccinated but who are feeling increasing pressure to get the COVID-19 vaccine may reconsider.

Real numbers of unvaccinated Army members ‘higher than anybody thought’

As far back as December 2021, an article on the U.S. Army website stated 96% of the Army’s 461,209 members were fully vaccinated.

In March 2022, as the Army began to announce the initiation of separation procedures for unvaccinated soldiers, officials again claimed 96% of its service members were fully vaccinated.

Later that month, an article on the U.S. Department of Defense (DOD) website claimed “the entire force may be vaccinated for COVID-19 by early summer.”

According to the whistleblower though, the “real numbers of unvaccinated service members are way higher than anybody thought,” adding that while “everyone thought” the number of unvaccinated in the Army was approximately 8,000-10,000 members, it is actually around 120,000.

To confirm that number, the official confidentially shared an internal U.S. Army document, dated June 2022.

According to the document, in the Army National Guard (ARNG), there are 280,678 members who are fully vaccinated (84.6%), and 7,735 who are partially vaccinated (1 dose) (2.3%) — leaving 43,269, or 13%, who have not yet received a single dose.

In some states, such as Oklahoma, the document shows the vaccination rate for members of the ARNG is as low as 74.11%. Of those, the document lists 15,698 members as “refusals” and 6,749 (2.0%) as going through an exemption process — with 6,257 (1.9%) requesting a religious exemption and 492 (0.1%) requesting a medical exemption.

The document also notes that 80% of unvaccinated soldiers in the ARNG are age 32 or younger, with an average age of 26.2 and median age of 24.

The document adds that “unvaccinated soldiers in their first 1-3 years of service and 4-7 years of service represent the greatest risk to readiness” for the ARNG, and that “Infantry, Maintenance, Engineer and Transportation career fields represent the greatest areas [of] concern for the ARNG.”

The document also states “projected losses could drive [the ARNG] below 70% available strength.”

According to the document, “Current forecasts project unprogrammed, vaccination mandate-related losses to range from … 3-6% of assigned strength,” which would require an anticipated “seven-year effort at 1,500-2,000 ramp per year to restore [the] End Strength necessary to meet required Force Structure.”

The same document also provides figures for the U.S. Army Reserve (USAR), stating that 157,390 members are fully vaccinated (87.9%), with an additional 1,411 members partially vaccinated with one dose (0.8%), leaving 19,872 members (11.3%) fully unvaccinated.

Among the unvaccinated, 7,623 members (4.3%) are listed as “refusals” and 4,100 (2.3%) are listed as undergoing an exemption process, with 3,982 members (2.2%) having requested a religious accommodation, and 118 (0.1%) having requested a medical exemption.

In some states, such as Wyoming, the vaccination rate in the USAR is as low as 80.9%, according to the document.

The document also notes 65% of unvaccinated soldiers in the USAR are age 30 or younger, with an average age of 28 and a median age of 26.

“Supply and Services, Mechanical Maintenance, Engineer and Transportation career fields represent the greatest areas [of] concern for the USAR,” the document states.

The document recommends commanders counsel “every unvaccinated Soldier,” “explore [the] impact of Bars to Reenlistment” and “publicize [the] Novavax option as [U.S. Food and Drug Administration (FDA)] approves” as it “may appeal to some seeking religious exemptions.”

The number of unvaccinated service members in the ARNG and USAR is confirmed in a second document — an internal “information” document — that the whistleblower shared with The Defender.

According to the whistleblower, this leaves approximately 56,000 unvaccinated service members in the U.S. Army itself.

These figures refer only to the Army, the whistleblower said. He does not know the figures for other branches of the armed forces, such as the Navy, Marines and Air Force.

The reason most members of the Army thought the number of unvaccinated was much smaller, aside from the information provided via the Army’s official channels, is that the Army has been “very tight-lipped” about these figures, “not leaking [them] to anybody, even internally,” according to the whistleblower.

“Those who are not vaccinated are segregated, so it is hard to find out who isn’t vaccinated,” he said. “The Army has done a very good job of not letting that information be leaked across the service.”

As a result, according to the whistleblower, “sometimes you feel you’re the only one, that there’s only a few people left” who have not received the COVID-19 vaccine.

However, those who are unvaccinated and who are privy to the real figures are, as the whistleblower described it, “re-energized and encouraged” by these numbers.

Army will be ‘combat-ineffective’ unless it moves June 30 deadline

The whistleblower told The Defender the DOD still plans to separate the unvaccinated soldiers, but instead of enforcing the June 30 deadline, “what they are going to do is hold off on separating soldiers on July 1,” and “will most likely push that into 2023 at the earliest.”

The June 2022 Army document confirms this, as it proposes that a “phased approach to involuntary separation” for unvaccinated service members would begin on October 1, 2022, with a “mandatory bar to reenlistment,” while “mandatory involuntary separations for COVID vaccine refusal” would begin January 1, 2023, and “last up to approximately 2 years.”

The document also recommends “separations for Soldiers start in FY23 [fiscal year 2023] with a phased approach.”

The whistleblower said the later date and “phased approach” are necessary because the Army is having a difficult time recruiting new troops, as “recruiting numbers have tanked over the past six months.”

The June 2022 document confirms this, describing an “extremely challenging recruiting environment.”

Moreover, the whistleblower claims that “the Army knows they cannot separate 120,000 soldiers,” as the Army would become “combat-ineffective,” which the whistleblower states is another reason why the real figures have been tightly guarded.

“Strength is in numbers,” he said.

Instead of getting the high numbers of vaccinated soldiers the DOD was hoping for, it appears the military now has to manage a larger-than-expected number of service members who have refused the COVID vaccine.

“The Pentagon knows that too many [service members] have said no and that there is not much they can do about it,” said the whistleblower.

Service members, unaware of an impending change to June 30 deadline, face a ‘very hard’ decision

While the DOD may be ready to move the June 30 COVID-19 vaccination deadline to a later date, the whistleblower said officials are keeping this information under wraps for the time being.

“Between now and July 1, nothing will change with the guidance,” he said, adding the new deadline will be announced at a later date.

However, in the period between now and June 30, unvaccinated service members who remain unaware of this possible change will “have to make a very difficult decision: Get the vaccine or be separated,” the whistleblower said.

Separately, Rep. Matt Gaetz (R-Fla.) last week called for the DOD to reinstate all troops discharged from any branch of the U.S. military, with their same rank, benefits and back pay.

And Sen. Ron Johnson (R-Wis.) last week once again demanded the DOD turn over all documents related to management of the military’s medical database between 2016 and 2020, following accusations by other DOD whistleblowers that the database was altered in order to obscure evidence of injuries related to the COVID-19 vaccines.

 

©June 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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French Attorney Diane Protat Warns of Side Effects of COVID Injections During Air Travel

French Attorney Diane Protat Warns of Side Effects of COVID Injections During Air Travel 

by Children’s Health Defense Europe
June 20, 2022

 



In this interview, French lawyer Diane Protat representing the group Navigants Libres, explains their fight in court defending pilots, flight attendants and all flight personnel who have experienced the severe and deadly effects of the Covid -19 vaccine shots and mandates.

Due to the life-threatening consequences of not just those commandeering flights but the entire population of airline passengers, it is crucial to evaluate these cases and stop the government regulations that continue to pose un-safe and grave consequences.

Serious health incidents and factual medical data coming from flight personnel is also being questioned worldwide through other international aviation organizations. The Global Aviators Coaliton, is partnering with Navigants Libresand others who areworking to reveal that theses health risks and dangerous outcomes of the mandatory vaccines are being experienced globally within the airline industry.

Protat sites several cases where flights were forced to perform emergency landings due to pilot and co-pilot death or illness after the vaccine and the accounts of many pilots who have been grounded due to new health issues not allowing them to pass routine health examinations.

Flight crew members such as flight attendants have suffered female reproductive issues that pose serious problems and prevent them from returning to work in this sector. Because of this specific phenomenon with women, Protat has also been heard in the Senate representing the woman’s groups “Where is My Cycle” and a collective of Midwives called, “Key Woman”, where thousands of women members are reporting reproductive health issues after the Covid vaccine.

Protat argues that these mandatory vaccines present too high a risk and evidenced hazard for aviation employees and citizens around the world who embark on airplane travel, and that measures must be taken immediately to prevent any further risk.

 

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Sen. Johnson Demands DOD Contractor Turn Over Military’s Medical Database Records

Sen. Johnson Demands DOD Contractor Turn Over Military’s Medical Database Records
U.S. Sen. Ron Johnson (R-Wis.) is asking the company that manages the U.S. Department of Defense’s Defense Medical Epidemiology Database to turn over records after the company failed to fully comply with a previous request seeking information about its “awareness of potential data problems” with the military’s database.

by Megan Redshaw, The Defender
June 21, 2022

 

Sen. Ron Johnson (R-Wis.) is asking the company that manages the U.S. Department of Defense’s (DOD) Defense Medical Epidemiology Database (DMED) to turn over records after the company failed to fully comply with a previous request seeking information about its “awareness of potential data problems” with the military’s database.

This is the second time Johnson has requested the records from Unissant Inc.

Johnson’s office previously sent three letters to the DOD following allegations by DOD whistleblowers that the DMED showed significant increases in registered medical diagnoses in 2021 following the authorization of COVID-19 vaccines and implementation of the DOD’s vaccine mandate.

The DMED is the military’s longstanding epidemiological database of service members.

Claiming the DMED data for 2016-2020 was incorrect, the DOD temporarily disabled the database — after whistleblowers came forward — then updated it with accurate figures, which resulted in less of an increase in medical conditions that potentially could be related to the vaccines.

The DOD said the DMED system was taken offline to “identify and correct the root cause of the data corruption.”

Given what Johnson said was the DOD’s lack of transparency, the senator asked his staff to contact Unissant to discuss its “awareness of potential data problems in DMED.”

Johnson, a ranking member of the Permanent Subcommittee on Investigations, first sent a formal letter to Unissant on March 7, requesting records related to its management of the DMED.

Unissant responded by stating it was prohibited from answering Johnson’s questions or “providing any details about the work it performs for the Defense Health Agency.”

Johnson’s staff provided Unissant with information from the DOD stating the company did not need the DOD’s consent to answer questions from Congress. A DOD contracting officer informed Unissant that “when it comes to Congressional or Senatorial inquiries, you don’t need my permission” to respond.

Despite approval to release information to Johnson’s office, Unissant requested written approval from its DOD contracting officer to release the information.

“Our letter explains why we are making this request even though you’ve stated we do not need your permission,” the email stated.

The DOD on May 2 gave Unissant permission to provide responsive documents to Johnson’s initial March 7 request, but Unissant’s letter detailing why it needed the DOD’s written permission was omitted from the records provided to his office.

“The records Unissant has provided to date as well as the company’s unclear explanation for requesting DOD’s approval to respond to Congressional inquiries raise additional questions,” Johnson said in a June 14 letter to Kenneth Bonner, president and chief growth officer of Unissant.

Johnson asked Unissant to provide the following additional information no later than June 28.

Johnson wrote:

1. Does Unissant agree with DOD’s claim that “the data in DMED was corrupt for the years 2016-2020 when accessed after September 2021?” If so, please explain why the DMED data for registered diagnoses of certain medical conditions from 2016-2020 was incorrect.

2. Please explain why registered diagnoses of myocarditis in 2021 decreased from 1,239 registered cases as of August 29, 2021, to 273 registered cases as of January 10, 2022. Please explain why the average annual registered diagnosis of myocarditis from 2016-2020 increased from 216 as of August 29, 2021, to 559 as of January 10, 2022.

3. Unissant claimed that on February 10, 2022, DOD discovered the need to “fix DMED monthly data for 2021.” However, emails produced by Unissant show that on Jan. 31, 2022, Unissant’s Vice President Stephen Gehring wrote that, “the team worked over the weekend to identify and resolve the issues” with DMED. Later that day, a DOD employee confirmed that “DMED access was restored after the data was corrected.”

Did Unissant identify the issues discussed on January 31, 2022, in its list of issues relating to DMED (see enclosure)? Were the issues discussed on January 31, 2022, different from the issue identified on February 10, 2022? Did DOD or Unissant discover the issues discussed on January 31, 2022? Please provide all communications showing this.

It does not appear that Unissant provided communications referring or relating to the DMED issue discovered on February 10, 2022 (as requested in the March 7, 2022 letter). Please provide those documents.

4. Provide a list of communications and documents discussing the “need to fix DMED monthly data for 2021” and the communications relating to the DMED issues discovered on Feb. 10, 2022, that Unissant failed to disclose with the previous request.

5. On January 31, 2022, Unissant Vice President Stephen Gehring noted that his team had “worked over the weekend to identify and resolve the issues” with DMED. He added that “the team uncovered other findings in testing that need to be addressed.” What were those “other findings”? Did those finding [sic] relate to issues with DMED? If so, were those findings identified in Unissant’s chart regarding issues relating to DMED (pursuant to the March 7, 2022 letter)?

If these findings were not identified, please provide a description of those findings, when Unissant communicated those findings to DOD, and the status of any corrective action(s).

6. In a March 3, 2022 email provided by Unissant, a Unissant representative informed Unissant officials Kenneth Bonner and Stephen Gehring that as recently as August 2021, DOD and Unissant were aware of problems with DMED but still let it “go live” with those problems. What were the problems? Why did Unissant allow DMED to “go live” if it knew it had problems?

7. On April 22, 2022, Unissant’s President Kenneth Bonner attached a letter to an email to DOD Contracting Officer Kevin Hodge regarding DOD’s permission to release information to Sen. Johnson. This attachment was not included in Unissant’s May 4, 2022 production. Please provide this letter.

8. Unissant’s May 4, 2022 production included several emails between the company’s representatives and DOD officials regarding DMED issues in August 2021. It does not appear those issues were identified in Unissant’s production Exhibit 3 or Exhibit 4 (enclosed). What were those issues, who discovered those issues and when, how long did those issues exist in DMED and when were those issues corrected?

9. Unissant’s May 4, 2022 response noted that because its employees use DOD email addresses to communicate with DOD employees referring or relating to DMED, “Unissant does not have access to these documents and communications.” Does Unissant not maintain records of its employees’ communications between and among Unissant and DOD employees regarding their contracted work?

When performing work on behalf of the federal government, how does Unissant ensure that its employees are following federal record preservation requirements if Unissant cannot access its employees’ documents and communications?

DOD changes DMED data on myocarditis after whistleblowers come forward

The first COVID-19 vaccine was authorized by the U.S. Food and Drug Administration on December 14, 2020. Secretary of Defense Lloyd Austin on Aug. 24, 2021, issued a memorandum mandating service members receive COVID-19 vaccinations.

According to downloaded data from DMED provided on Aug. 29, 2021, to Johnson’s office, there were 216 cases of myocarditis reported from 2016 to 2021 — an average of 43.2 diagnoses per year.

There were 1,239 cases of myocarditis in 2021 alone — a 2,868% increase over the 2016-2020 average.

According to a spreadsheet based on a complete DMED data set provided by whistleblowers to Johnson’s office in January 2022, figures for myocarditis had changed dramatically since the August 2021 download.

“Total myocarditis diagnoses 2016-2020 increased to 559 from 216 causing the annual average to increase to 111.8 from 43.2 diagnoses per year,” Johnson’s June letter to Unissant stated.

“For the year 2021, myocarditis diagnoses decreased from 1,239 to 263 causing the annual percentage increase to decline from 2,868% to 235% over the 2016-2020 average.”

In other words, after the DOD enforced its vaccine mandate, the database was altered to reduce the increase in myocarditis cases in 2021, compared to the previous four years.

Attorney exposes DMED data at January panel discussion led by Johnson

Attorney Thomas Renz in January told experts during a panel discussion on COVID-19 vaccines and treatment protocols that was led by Johnson, that data provided to him by three whistleblowers showed COVID-19 vaccines were causing catastrophic harm to members of the U.S. military while not preventing them from getting the virus.

Data from DMED provided by whistleblowers — who knew they would face perjury charges if they submitted false statements to the court in legal cases pending against the DOD — showed miscarriages increased 300% in 2021 over the previous five-year average, cancer increased by 300% and neurological disorders increased 1,000% in 2021 over the past five-year average — increasing from 82,000 to 863,000 in one year.

Other conditions that spiked over the same five-year period included:

  • Hypertension: 2,181% increase.
  • Diseases of the nervous system: 1,048% increase.
  • Malignant neoplasms of the esophagus: 894% increase.
  • Multiple sclerosis: 680% increase.
  • Malignant neoplasms of digestive organs: 624% increase.
  • Guillain–Barré syndrome: 551% increase.
  • Breast cancer: 487% increase.
  • Demyelinating: 487% increase.
  • Malignant neoplasms of thyroid and other endocrine glands: 474% increase.
  • Female infertility: 472% increase.
  • Pulmonary embolism: 468% increase.
  • Migraines: 452% increase.
  • Ovarian dysfunction: 437% increase.
  • Testicular cancer: 369% increase.
  • Tachycardia: 302% increase.

Renz also said DMED data showing registered diagnoses of myocarditis had been removed from the database.

Renz told the panel a “trifecta of data” from the DMED and Project SALUS, the DOD’s military-civilian integrated health database, along with human intelligence in the form of doctor-whistleblowers, suggest the DOD and the Centers for Disease Control and Prevention withheld COVID-19 vaccine surveillance data since September 2021.

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-19.

Johnson demands DOD respond to whistleblower claims

Johnson asked the DOD in February what it was doing to investigate whistleblower reports of big spikes in miscarriages, neurological disorders, cancer and other illnesses among members of the U.S. military since its rollout of COVID-19 vaccines.

Johnson also asked if the DOD had removed reports of vaccine-induced myocarditis from the DMED.

The Defense Health Agency on Jan. 26 created and preserved “a full backup of the DMED,” at Johnson’s request.

On Jan. 28, a DOD spokesman told PolitiFact there was a glitch in the DMED database that “gave the false impression that there was a huge spike in miscarriages, cancer and other medical issues among military members in 2021.”

The spokesman said the database had “been taken down to identify and correct the problem.”

 

©June 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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The Federal Republic of New Normal Germany

The Federal Republic of New Normal Germany

by CJ Hopkins, Consent Factory
June 20, 2022

 

So, the government of New Normal Germany is contemplating forcing everyone to wear medical-looking masks in public from October to Easter on a permanent basis. Seriously, the fanatical New Normal fascists currently in charge of Germany’s government — mostly the SPD and the Greens — are discussing revising the “Infection Protection Act” in order to grant themselves the authority to continue to rule the country by decree, as they have been doing since the Autumn of 2020, thus instituting a “permanent state of emergency” that overrides the German constitution, indefinitely.

Go ahead, read that paragraph again. Take a break from the carnage in non-Nazi Ukrainethe show trials in the US congressmonkeypoxmaniaSudden Adult Death SyndromeSudden Bovine Death Syndromefamily-oriented drag queensnon-“vaccine”-related facial paralysis, and Biden falling off his bike, and reflect on what this possibly portends, the dominant country of the European Union dispensing with any semblance of democracy and transforming into a fascist biosecurity police state.

OK, let me try to be more precise, as I don’t want to be arrested for “spreading disinformation” or “delegitimizing the state.” Germany is not dispensing with the semblance of democracy. No, the German constitution will remain in effect. It’s just that the revised Infection Protection Act — like the “Enabling Act of 1933,” which granted the Nazi government the authority to issue any edicts it wanted under the guise of “remedying the distress of the people” — will grant the New Normal German government the authority to continue to supersede the constitution and issue whatever edicts it wants under the guise of “protecting the public health” … for example, forcing the German masses to display their conformity to the new official ideology by wearing medical-looking masks on their faces for six or seven months of every year.

In addition to a ritualized mass-demonstration of mindlessly fascist ideological conformity (a standard feature of all totalitarian systems), this annual October-to-Easter mask-mandate, by simulating the new paranoid “reality” in which humanity is under constant attack by deadly viruses and other “public health threats,” will cement the New Normal ideology into place. If not opposed and stopped here in Germany, it will spread to other European countries, and to Canada, and Australia, and the New Normal US states. If you think what happens in Germany doesn’t matter because you live in Florida, or in Sweden, or the UK, you haven’t been paying attention recently. The roll-out of the New Normal is a global project … a multi-phase, multi-faceted project. Germany is just the current “tip of the spear.”

Sadly, the majority of the German masses will mindlessly click heels and follow orders, as they have since the Spring of 2020. They’re all enjoying a “summer break” at the moment, but come October they will don their masks, start segregating and persecuting “the Unvaccinated,” and otherwise behaving like fascists again. I hesitate to blame it on the German character, because we’ve witnessed the same mindlessly fascistic behavior all around the world over the past two years, but, I have to admit, there is something particularly scary about how the Germans do it.

 

Meanwhile, Germany’s FBI (der Bundesverfassungsschutz, or BfV) is hard at work enforcing the new Gleichschaltung. According to a report in Die Welt, the BfV is not just surveilling people who use terms like “Corona dictatorship” (and presumably a long list of other “wrongspeak” words), but it is also “surveilling people and groups that disseminate conspiracy theories, or call the democratic nature of the state into question.” Politicians are insisting that the BfV “toughen up the classification of political crime, especially regarding the Corona deniers.”

 

Yes, that’s right, publicly challenging the official Covid-19 narrative, or protesting official New Normal ideology, is a political crime here in New Normal Germany. It has been since May 2021, when the Bundesverfassungsschutz established a new official category of domestic extremism … “Anti-democratic or Security-threatening Delegitimization of the State.” I covered this in one of my columns at the time (“The Criminalization of Dissent” ) as did some corporate press, like The New York Times (“German Intelligence Puts Coronavirus Deniers Under Surveillance”), but, for some reason, the story didn’t get much traction.

“Delegitimization of the State” … let that language sink in for a moment. What it means is that anyone the New Normal authorities deem to be “delegitimizing the state” can be arrested and charged as a “political criminal.” I wasn’t entirely clear on what is meant by “delegitimizing,” so I looked the word up, and the definition I found was “to diminish or destroy the legitimacy, prestige, or authority” of something, or someone, which … I don’t know, sounds a little overly broad and subject to arbitrary interpretation.

For example, if I, right here in this column, were to propose that the German government had no legitimate reasons whatsoever for locking down the entire population, forcing everyone to wear medical-looking masks, and demonizing and segregating “the Unvaccinated,” that might make me a “political criminal.” Likewise, if I were to describe Karl Lauterbach, the Minister of Health of New Normal Germany, as a fanatical fascist, and a sociopathic liar, that might make me a “political criminal.” Or, if I were to point out how the German state media have deceived and gaslighted the German public for over two years like the proverbial Goebbelsian keyboard instrument, that might make me a “political criminal.” Or, if I were crazy enough to publish a book of essays written over the past two years documenting The Rise of the New Normal Reich, including essays about New Normal Germany, that might also make me a “political criminal.”

Naturally, I am a little uneasy, living in a former-Nazi country where I could be classified as a “political criminal” for my activities as an author and a political satirist … which, of course, is the point of the new classification. It is meant to scare dissidents like me into silence. Or … OK, it isn’t meant for me. It is meant for German dissidents like me. I’m an American, not a German citizen. So the chances of a heavily-armed “Special Commando” team storming my apartment in the wee hours of the morning and arresting me on trumped-up weapons charges — as they recently did to Dr. Paul Brandenburg, an outspoken opponent of the New Normal Reich — are probably (hopefully) fairly remote.

In any event, I would never do that, i.e., attempt to diminish the prestige or authority of the Federal Republic of New Normal Germany, or in any way compare it to Nazi Germany, or any other totalitarian system, or describe it as a nascent biosecurity police state wherein the rule of law has been supplanted by the arbitrary edicts of fascist fanatics, because that would just be asking for trouble. After all, if we’ve learned anything from history, the smart thing to do during times like these is to keep one’s mouth shut and follow orders, and if you hear a train coming … well, just look the other way.

 

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cover image credit: nina108 / pixabay




More Vaccine-Injured Pilots Speak Out as Groups Pressure Airlines, Regulators to End Mandates

More Vaccine-Injured Pilots Speak Out as Groups Pressure Airlines, Regulators to End Mandates
In exclusive interviews with The Defender, more commercial airline pilots discuss COVID-19 vaccine injuries and the “hostile” industry environment injured and unvaxxed pilots must navigate.

by Michael Nevradakis, Ph.D. , The Defender
June 17, 2022

 

Sharp chest pains. Myocarditis and pericarditis. Heart attacks. Strokes and subsequent blindness.

These are just some of the many COVID-19 vaccine-related adverse events reported by commercial airline pilots and by a growing number of advocacy groups representing aviation industry workers.

According to these individuals and groups, the number of pilots speaking out about their vaccine injuries is dwarfed by the number of pilots who are still flying despite experiencing concerning symptoms — but not speaking out because of what they describe as a culture of intimidation within the aviation industry.

These individuals fear they will lose their jobs and livelihoods in retaliation if they reveal their symptoms or go public with their stories, sources told The Defender.

Still, a growing number of pilots are coming forward.

Last month, The Defender published the accounts of several pilots — and of the widow of a pilot who died from a vaccine-related adverse event.

Since then, more pilots have shared their stories, including one who is currently flying for a commercial airline.

A growing number of advocacy organizations, representing workers across the aviation industry and in several countries, are joining these pilots in speaking out.

The Defender previously reported on actions by the U.S. Freedom Flyers (USFF) and other legal advocates in the U.S.

Since then, representatives from the Global Aviation Advocacy Coalition (GAA) and the Canada-based Free To Fly also spoke with The Defender about their initiatives.

Meanwhile, pilots in Canada and the Netherlands recently reported significant legal victories in separate vaccine-related cases.

More pilots come forward, speak to The Defender

Steven Hornsby, a 52-year-old pilot with a legacy passenger airline company, was once an active weightlifter and cyclist, biking 10-26 miles every other day.

He is also a veteran of the U.S. Marine Corps and Operation Enduring Freedom. Per FAA requirements, he passed 24 medical exams in the past 12 years, including 12 electrocardiograms (ECGs).

Hornsby told The Defender, “I’ve never had any cardiovascular issues in my life, nor have I ever had any major health issues … I eat healthy and live what I believe to be a balanced lifestyle.”

Hornsby, however, is not flying today because, he said, he was “coerced … to get the COVID-19 vaccine,” and his employer “made it very clear that all employees would be required to get it and that medical/religious exemptions would be very difficult to get.”

Hornsby’s difficulties began after receiving the second dose of the Pfizer COVID-19 vaccine.

“After my second shot, I initially had zero issues, with little more than light fatigue on day two, Hornsby said. “The 12th day, however, was the culmination of the vaccine and the continuous stress I was adding to my heart from rigorous exercise.”

As he was driving with family, Hornsby said he felt sharp chest pains, “pain radiating through my left arm, and my heart rate spiked as if beating in my neck.”

Hornsby said it took several different diagnoses from doctors and medical practitioners to make a connection between his health issues and the vaccine.

A nurse at an urgent care facility first told him his symptoms did not correlate to a heart attack and were most likely unrelated to the vaccine. Later, at a hospital emergency room, he was again told his symptoms were not likely to be related to the vaccine.

“At that point,” Hornsby said, “I was indignant. Why would a healthcare provider dismiss that perspective? This was my eye-opening reality that a major cover-up was in play.”

Hornsby was ultimately diagnosed with elevated blood pressure but was told he had not suffered a heart attack. Doctors advised him to follow up with a cardiologist, and told him they would not report his case to the Vaccine Adverse Event Reporting System (VAERS).

Hornsby said his cardiologist, after performing blood work, told him his heart was healthy, and though the doctor didn’t dismiss the possibility that his heart issues were connected to the vaccine, he told him the symptoms were “most likely from stress or a musculoskeletal problem.”

“I had to stop trying to force my perceived diagnosis — bias against the vaccine — and listen to the professionals,” Hornsby said, adding “I needed to be patient,” even after a union doctor also dismissed Hornsby’s concerns that his symptoms were related to the vaccine.

Hornsby continued experiencing “intermittent pains,” despite taking home remedies such as tea and supplements to calm his heart rate, which he said were helpful.

It was only in December 2021, when his medical certification was due for renewal, that his aeromedical examiner (AME) advised him to wear a Holter monitor (a type of portable ECG) for one week to monitor his heart.

“That is when I discovered that I had arrhythmia issues, heart palpitations and [an] irregular heart rate, which was occurring almost exclusively at night,” said Hornsby. “I reported back to my AME, who then told me I was grounded and that I should go find a good cardiologist and get healthy.”

The following month, another cardiologist diagnosed Hornsby with vaccine-induced myocarditis.

“My heart was inflamed,” said Hornsby. “After an echocardiogram, it showed my heart mildly dilated with fluid behind my heart.”

Hornsby said he’s “doing much better,” but he’s still not flying. He’s disappointed with the dismissive manner in which several doctors addressed his concerns.

“Had doctors been willing to view my case — and I suspect others — with an open mind, this could have been diagnosed much, much earlier,” he said. “Looking back, had my heart not been healthy, I would have surely died from cardiac arrest like you’re seeing in young athletes.”

Hornsby said he believes other pilots with similar symptoms are still flying.

“I suspect there are many pilots flying around with minor and perhaps major issues,” Hornsby said. “The vaccine is/was experimental and for good cause. No one knows the long-term effects.”

He added:

“How many years have been shaved from my life? Will I develop scar tissue in my heart? Will I get cancer as a result? Has this trash degraded my immune system? Only God knows.”

Pilot injured by Moderna shot: ‘I have a family to feed’

In fact, The Defender interviewed another pilot — currently flying for a commercial airline in the U.S. — who is experiencing such health difficulties.

The pilot, who spoke to The Defender on condition of anonymity, said:

“I was experiencing chest pain, usually at night, almost like somebody had their hand around my heart and was squeezing.

“Generally, [the pain] would subside during the day, but … would appear occasionally out of nowhere and I would need to lie down.

“It would manifest as pain, but also like something was lodged deep in my esophagus, like I had a piece of food or air that was pressing upon my chest area.”

According to the pilot, his symptoms “began about a week after the second Moderna vaccination.

He said the airline he works for threatened to terminate anyone who didn’t get the vaccine. “I have a family to feed, so I was left with little choice.”

He said he is “on reserve” and not flying often. While his symptoms have recently subsided, he felt that “looking into further treatment would result in an answer that would be unfavorable to my medical [certification].”

He added:

“In the back of my mind though, the thought of what it could mean for my future health is there.

“The current situation I am faced with is that supporting a family is what is most important to me. Fear of loss of my pilot medical [certification] after being mandated to get this vaccine is the path I am currently on.”

Terminated after 19 years for refusing COVID shot, former Australian pilot advocates for others

Australia, like Canada, has a government-level vaccine mandate for airline crew and airport workers. In Australia, this mandate went into effect on Nov. 15, 2021.

Glen Waters is a former captain with Virgin Australia who is now a spokesman for a group of employees from the same airline.

Waters, who had held the rank of captain for 19 years before being terminated by Virgin Australia for refusing the vaccine, spoke to The Defender on behalf of several pilots who are suffering from vaccine injuries.

According to Waters, “none of the pilots suffering from injuries are prepared to talk” because “the company is actively trying to terminate anyone reporting vaccine injury.”

Waters said employees whose health issues are characterized as “unrelated” to the vaccine are being treated by Virgin Australia “as you would expect a company to care for its employees.”

Waters stated “there are several reasons injured pilots will not come forward,” including:

  • “There is a stigma attached to anti-vaccine sentiment in any form.
  • There is a reluctance on the part of the medical community to get involved with possible vaccine injuries.
  • Vaccine makers will actively fight against injury claims.
  • Insurance companies have distanced themselves from claims involving the vaccine.
  • Pilots don’t want to lose their medical certifications, jobs or careers.

Waters said of approximately 900 pilots flying with Virgin Australia, he is aware of nine who are no longer flying because of medical complications that could be linked to the vaccine.

“No doubt there are many more who are continuing to fly with troubling symptoms,” he said.

These symptoms, according to Waters, most commonly include myocarditis and pericarditis. Some symptoms, however, are even more serious.

Waters told The Defender:

“We have one captain [who had] a stroke and went blind, and another had a heart attack and fell down the boarding stairs after landing.

“There have been complaints of constant headaches and numerous reports of chest pains and shortness of breath.

“A number of cabin crew have reported pins and needles in their limbs, almost like electric shocks that persist for hours at a time.

“I have heard [about cases of] tinnitus, vertigo and brain fog, including temporary blindness, in several crew. Disrupted menstrual cycles are reported frequently, perhaps affecting dozens [of employees].”

However, according to Waters, perhaps due to the work environment, not all pilots are comfortable in stating openly that there may be a connection between their health difficulties and the vaccines.

“I’m only aware of three who say the symptoms started within an hour of the vaccine, one within seven days,” he said.

“The stroke and heart attack victims are not attributing their medical event to the vaccine as far as I am aware. Neither [did] the captain who died of a sudden onset of cancer early this year.”

Some employees may not understand their symptoms might be related to the vaccine, Waters said. “Many of the early warning signs — persistent headaches, chest pains, breathlessness — are not recognized by aircrew as possible adverse reactions,” Waters said.

“The heart attacks and strokes are occurring in otherwise fit and healthy individuals. They are sudden and are a real risk to flight safety.”

Waters explained that Australia’s Civil Aviation Safety Authority, similar to other such bodies globally, has “a 1% rule” for pilots: If they have a medical condition “that presents a greater than 1% chance of resulting in an incapacitation event within the next 12 months, then they are considered medically unfit to fly.”

In light of this, according to Waters, “numerous aviation doctors, including Lt. Col.Theresa Long and Lt. Col. Peter Chambers, have recommended tests that will help determine the real risk to pilots.”

These include the D-dimer test for blood-clotting conditions, a complete blood count, post-vaccination ECG analysis, a cardiac MRI and others.

As pilots speak out, there are some legal victories

Despite what numerous pilots call a hostile environment in the aviation industry toward claims of vaccine injury, a recent series of legal decisions were in pilots’ favor and more legal actions are in progress.

A judge at the Amsterdam Court of Appeals in the Netherlands on June 2 ruled in favor of the Dutch Airline Pilots Association, in a case that challenged vaccine mandates introduced by Dutch airline KLM for new pilots.

According to the ruling:

“It is considered that requesting and demanding a vaccination against corona constitutes an unjustified infringement of the fundamental rights of the candidate pilots.

“In particular, it infringes the privacy (Article 8 ECHR) [the European Convention on Human Rights] of the candidate pilots.

“After all, the decision whether or not to have yourself vaccinated is something that belongs pre-eminently to this private sphere.

“Requiring the candidate pilot to be vaccinated and to give a positive answer to that question about vaccination status, therefore, violates this. KLM thus leaves no choice to candidate pilots who want to join KLM.”

Per the June 2 ruling, KLM is prohibited from requesting or collecting such information from candidate pilots, or rejecting candidates on the basis of their vaccination status, under penalty of €100,000 (approximately $105,000) per violation.

Following the ruling, the Dutch Pilots Association issued a statement, remarking:

“The [association] endorses the government’s position that vaccination is important, but that compulsory vaccination by the employer is not permitted.

“We were of the opinion that KLM did not comply with this and, moreover, violated our agreements about this, without there being any operational necessity.”

In Canada, the federal government on June 14 announced most travel-related vaccine mandates would be lifted as of June 20.

Responding to this announcement, in a statement sent to The Defender, Free to Fly credited those who opposed the mandates, stating:

“This dark season helps reinforce an important maxim; true change only comes about through tenacity, courage, and the relentless pursuit of truth by principled men and women.

“Across our nation, many Canadians refused to give up on freedom and fought for our fragile democracy. We feel no ‘gratitude’ towards an emboldened state for ceasing to violate God-given freedoms.

“We must never forget our recent travails, and cannot be lulled into complacency, certainly with Trudeau’s government openly threatening reinstatement of mandates with any ‘new variant’.”

“We will continue to pursue them, insisting on uncompromising standards in our industry and the assurance we never again go down this road of medical segregation.”

In another recent development, Canadian pilot Ross Wightman became just one of a small number of people who have received compensation from Canada’s Vaccine Injury Support Program.

Wightman was diagnosed with Guillain-Barré Syndrome, a rare condition that affects the nervous system and may cause muscle weakness, paralysis or even death.

He developed the condition within days of receiving his first and only dose of the COVID-19 vaccine. For the past year, Wightman has been unable to work, as he has substantially limited mobility in his arms and legs.

Global Aviation Advocacy Coalition pens open letter to aviation industry

In an open letter to the aviation industry, the GAA raised serious allegations regarding industry vaccine mandates, which the GAA said resulted in a growing number of vaccine-injured pilots who are unable to fly and who may never do so again — and an increasing number of pilots who continue to fly while experiencing potentially serious symptoms.

The letter was signed by organizations including the USFF, Free To Fly Canada, the Aussie Freedom Flyers, the UK Freedom Flyers, the Southwest Freedom Flyers, the International Medical Alliance, the Global Covid Summit, the Canadian Covid Care Alliance, the UK Medical Freedom Alliance, the Association of American Physicians and Surgeons, and several other groups in the U.S., France, the Netherlands, Switzerland and the U.K., as well as more than 17,000 physicians and medical scientists from around the world and “thousands of pilots at over 30 global airlines.

The GAA said it is in communication with pilots at the following U.S.-based airlines: Alaska, American, Delta, Frontier, JetBlue, Southwest, Spirit and United, and 12 major air carriers in Australia, Canada, France, Germany and the Netherlands.

According to the GAA’s open letter, the organization and the scientists and doctors it works with “are hearing daily from vaccine-injured airline pilots” about conditions including “cardiovascular issues, blood clots [and] neurological and auditory issues.”

The injured pilots are experiencing a broad spectrum of symptoms, “ranging up to death,” the GAA wrote, adding the symptoms “at least correlate to receiving COVID-19 vaccinations.”

The GAA wrote that in many instances, these conditions are serious enough that “pilots have lost medical certification and may not recover the same,” while others “are continuing to pilot aircraft while carrying symptoms that should be declared and investigated, creating a human factors hazard of unprecedented breadth,” and “a landscape which should greatly concern airlines and the traveling public.”

Pilots continue to fly despite experiencing such symptoms, said the GAA, because those “who report their injury face possible loss of licensing, income, and career while receiving little to no support from their unions, and a prosecutorial invective from employing airlines.”

The GAA said many pilots were reluctant to receive the COVID-19 vaccine and opposed mandates:

“Pilots are trained to be careful analysts of their environment, recognizing risks and actively mitigating. For many, their training and differential risk analysis led to concerns and negative conclusions regarding the compatibility of COVID-19 vaccination with health and flight safety.

“Not only did many pilots disagree with arbitrary requirements embodied in vaccination mandates, but they also saw risks in the unanswered questions and unjustified speed and pressure behind the vaccine rollouts. They lobbied their airlines and politicians, recommending caution and opposing mandates.”

However, stated the GAA, for many pilots, it was a choice between vaccination and job loss:

“Once airlines mandated vaccination, many pilots steadfastly refused based on risk and were subsequently put on unpaid leave or outright terminated.

“Principled professionals were forced out of aviation and the industry lost hundreds of thousands of hours of experience. Now, the global airline industry is heading into a dire staffing crisis.

“Thousands of other pilots were coerced into vaccination to provide for their families. This has taken a toll on their mental health.”

For the GAA, blame lies with the mandates — and more broadly, with the airlines, regulators and unions:

“ … there appears to be no evidence of aviation regulators, airlines or unions having performed any of their own due diligence into COVID-19 vaccines and the impact on pilot health or performance.

“This is at complete odds with existing aviation medical standards. Questions exist around competence and possible negligence.

“Failure to address this potential medical watershed will make the airlines and unions complicit in a culture shift that has rocked the aviation mantra of ‘safety first, always.’”

The GAA called on civil aviation authorities such as the Federal Aviation Administration, Transport Canada, UK Civil Aviation Authority, the European Union Aviation Safety Agency and Australia’s Civil Aviation Safety Authority to begin fulfilling their regulatory obligations.

“The crisis in pilot health must be publicly addressed by airlines and representing unions to restore flight safety to what we once knew,” their letter stated.

GAA called for:

  • “Where it exists, mandated COVID-19 vaccination for aviation workers must be discontinued.
  • A permissive environment for self-reporting needs to be reemphasized by regulators and airlines.
  • Thorough and objective aviation medical screenings of pilots and cabin crew need to be a high priority. These must be backed by the regulator and should focus on high prevalence harms which are now showing up in the general public and in our flight crews.
  • Airlines and regulators hold data about sickness and medical certificate suspension, including symptoms and causal reasons. This data should be analysed by independent third parties to establish or rule out COVID-19 vaccination as a possible cause.”
Free to Fly pursues legal action against Canadian authorities, airline

Canada-based Free to Fly represents close to 3,000 aviation professionals, according to its director, Greg Hill, who spoke to The Defender.

These professionals include pilots, flight attendants, air traffic controllers, maintenance workers and customer service representatives.

According to Hill, industry workers have reported a wide range of health issues, including “generalized chest pains, myocarditis, enlarged heart, blood clots, hearing loss, partial paralysis, lymph issues [and] broad autoimmune dysfunction.”

Some of the injured pilots are “high-end athletes” who experienced a “major decrease in their performance capacity.”

“We’ve had some inexplicable deaths at unreasonably young ages,” Hill said, and “an increase in in-flight diversions with one of our airlines in particular.”

While Hill left open the possibility that at least some of these incidents weren’t vaccine-related, he said that Canadian authorities show “an unwillingness to do a proper investigation.”

“Transport Canada, the airline industry, the airlines and the unions have been uniformly silent on the matter,” Hill said.

Indeed, Hill said the aviation industry, regulators and unions in Canada have not been responsive to outreach from Free to Fly.

Referring to a document, prepared in conjunction with the Canadian COVID Care Alliance, that said flight crew pilots were most at risk of vaccine-related adverse effects due to their work environment, Hill said:

“We gave this to the two largest pilot unions in the country, the Air Canada Pilots Association and ALPA, the Airline Pilots Association … they have refused to respond to it.

“We also sent it to management at two of our largest airlines … they also have refused to even respond to it. And this was raising very explicitly the risks that these medical professionals felt needed, at the very least, to be investigated.

“And as yet, we’ve had nothing but silence formally as far as a response from these groups, as far as adverse events, vaccine injuries.”

The document provides: information on a union’s obligation to its members; a differential risk analysis of COVID-19 versus the vaccines; an analysis of natural versus vaccine-induced immunity; an analysis of adverse reactions to the vaccines and particular risks faced by flight crews; a list of alternate treatment options for COVID-19; and a discussion of informed consent and coercion.

According to Hill, the policy is “no jab, no job” for pilots and aviation professionals in Canada, unless they are granted religious or medical exemptions.

But, said Hill, even in the rare instance when an exemption is granted, those employees nevertheless have found themselves out of work, due to airline practices that Hill described as extortionate.

Hill told The Defender:

“If you’re not willing to take the jab and you can’t be accommodated with a religious or medical exemption, then you are either on unpaid leave or outright terminated. Some of our pilots have already been terminated.

“The vast, vast majority of these accommodations were outright denied … some of the stories of people that were denied medical accommodations are truly shocking, the same on the religious aspect.

“The handful that were approved … are simply another round of extortion. Some of them were denied, then they were approved retroactively … essentially they were approved, but then it didn’t change anything … you continue your unpaid leave, but you’re allowed your benefits.”

Similar to claims made in an open letter hand-delivered to the U.S. Federal Aviation Administration (FAA) and major U.S. air carriers in December 2021, Free to Fly also alleged a violation of existing aviation regulations, this time in Canada.

According to Hill:

“There was, at one point, on the Transport Canada website, this was July 2021, a line that specifically said it remains a general position of Transport Canada … that participation in medical trials is not considered compatible with aviation medical certification.

“A number of us were asking questions … and saying, ‘Well, what’s up with this?’ And the answer was these [vaccines] are approved. And we said, ‘No, they’re not fully approved, they’re approved under interim order.’

Hill said if you read that interim order, it was quite laughable. It basically said, ‘We’ll roll these vaccines out and we’ll gather data. Right now we feel that they’re okay and we’ll continue to assess as we continue to jab people,’ which just seems insane.

“So we asked these explicit questions, got no suitable answers,” Hill said. “And the week following … they simply memory-holed it, they removed that line and it’s no longer on the website. That was their response.”

Hill also described a culture of intimidation in Canada among pilots and flight crews, resulting in a reluctance to come forward with vaccine injury claims:

“Unless the individuals involved are willing to speak to it, I can’t say … every pilot that’s currently still employed … is living in fear of speaking explicitly, certainly in any public forum … for fear of the retribution that has been rolled out against those of us who no longer have work because we refuse to go down this road and insisted upon medical freedom and in doing a proper analysis of what we’re up against here.”

This has not stopped Free To Fly from pursuing legal action in Canada. According to Hill, in Canada, “ … you can’t seek private representation against your company. You have to do it through your union. And when the unions decide to not engage, you’re left between a rock and a hard place.

Hill added:

“ … if you read through the case law precedent over the past year or two in Canada, the courts have very, very much chosen a side. And the concern is within an English common law system, if we continue to litigate, litigate and lose and lose and lose, you create precedent that makes it harder and harder to dig your way out.

“Unfortunately, in this country, the law is downstream of politics. It’s heavily influenced by it, certainly in my opinion. And politics, of course, is downstream of culture. So unless you impact culture and impact the broader narrative, it’s very difficult to see legal solutions.”

Free to Fly on June 6 sent a letter to Canada’s minister of transport, co-signed by the GAA, containing “important, detailed questions regarding COVID-19 vaccines and flight safety,” according to Hill.

As of this writing, the minister has not responded.

Hill said:

“It’s just mind-boggling … we’ve literally stood the [aviation industry’s] safety culture on its head, and that’s the greatest concern to us.

“It’s not an interest in a desire for conflict. I long for the world before this became an all-consuming role, where we’re pushing to try and get ourselves back to a sense of normalcy and proper risk assessment and risk mitigation, which is what pilots are really dedicated to.

“So that’s all we want: that ability to look at this properly and analyze it properly … aviation medical screenings focusing on some of the high prevalence harms that we’ve seen, that we’re hearing about … these screenings need to be backed by the [Canadian] regulator who, in our opinion, has not done their job properly over the past couple of years.”

As far as suspensions, Hill said, pilot who are off and on have not been able to get their medical [certification] back. And these need to be analyzed by independent third parties.

Some pilots and aviation professionals, in addition to speaking out, are joining advocacy groups.

For instance, Hornsby and the pilot quoted in this story who opted to remain anonymous, have joined USFF, according to its co-founder, Josh Yoder, as are the pilots and air traffic controllers who previously shared their stories with The Defender.

USFF has recently begun filing a series of lawsuits against airlines and federal agencies in response to the vaccine mandates and their aftermath.

Ultimately, though, the public — not just pilots and aviation professionals — must also speak out, according to Hill.

“Whether it’s Canada, the United States, Australia, the United Kingdom, etc., we’d like to see the public as a whole rising up and speaking out publicly about these issues, asking why the regulators haven’t done proper risk assessments in regards to where we’re at with these jabs.”

 

©June 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 Normal: Plane Makes Emergency Landing as Captain Remains ‘Ill’ in Bathroom

New Normal: Plane Makes Emergency Landing as Captain Remains ‘Ill’ in Bathroom

by Amy Mek, RAIR Foundation
June 17, 2022

 

Last month an international coalition of aviation and medical professionals sounded the alarm about vaccine damage among pilots.

A British EasyJet plane made an emergency landing last Sunday at the Edinburgh airport in Scotland after the pilot suddenly ‘got unwell.’ The aircraft had taken off from the Greek Island of Crete at around 1 am local time and was landed by the co-pilot while the captain was in the bathroom ill.

The plane flew from Heraklion – the largest city on the Greek island of Crete – to the Scottish capital. Passengers reported seeing the captain entering the toilet and not reappearing, which was not confirmed by the airline when asked by The Sun.

One passenger, who asked to remain anonymous, told the Scottish newspaper that five fire engines and two ambulances were waiting on the runway when they made the emergency landing.

“A very young-looking co-pilot announced through the intercom that the pilot had become unwell. It is unknown if the pilot returned to the cockpit for landing. No one saw him come out of the toilet,” said the passenger.

An EasyJet spokesperson confirmed that flight EZY6938 from Heraklion to Edinburgh had to make an emergency landing on June 12 because the pilot had become unwell. The spokesman added that ambulance personnel took care of the pilot after landing as a precaution. “The safety and well-being of our passengers is always our top priority.”

‘Vaccine’ Advocates and Damage

EasyJet encourages its flight crews to have jabs, but the budget carrier has not ordered them to do so. However, in January 2021, the pro-covid “vaccine” British discount airline trained cabin crew members and pilots to administer the controversial mRNA injections. “As cabin crew, we are in a great position to support the “vaccination” effort because of the first aid and safety-focused training we receive for our job, cabin crew member Katy Bryant said. Ironically the crew did not seem to be able to help the ill captain locked in the bathroom.

RAIR Foundation USA has previously reported medical complications to pilots post mRNA injections. “Stories of medical problems pilots describe are chilling, particularly after several recent near-catastrophes with incapacitated pilots.”

Pilot Greg Pearson shared his shocking story of rapid onset atrial fibrillation after being injected with the experimental Covid “vaccine.” Pearson reveals that his story is more common than leaders are telling us. As a result, many people have questioned whether vaccinated pilots are a flight risk.

Last month an international coalition of aviation and medical professionals sounded the alarm about vaccine damage among pilots. The coalition receives daily messages from pilots with vaccination damage. EasyJet, among others, employs pilots who have suffered vaccination damage. The coalition calls on aviation authorities to intervene to tackle this health crisis.

 

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The Murdered Infant Comes to the Virology Lab; the Ivory Tower Is Befouled

The Murdered Infant Comes to the Virology Lab; the Ivory Tower Is Befouled

by Jon Rappoport, No More Fake News
June 17, 2022

 

In a groundbreaking article for Children of God For Life, titled “Forsaking God For the Sake of Science,” [1] [1b] Debra Vinnedge outlines how the Rockefeller-Harriman eugenics movement gave rise to the practice of medical abortions for research purposes, including live births during which the infant was murdered and its organs harvested:

“…Abortion wasn’t legal yet; this was 1936. But abortion was most certainly legal and acceptable [to eugenicists] if it meant ending the life of a child who would be born to a ‘feeble-minded’ woman, one who might end up less than perfect or who might have to rely on society to pay for their care.”

And therefore, why not perform abortions for medical research? Behind closed doors, out of view, this was happening in several countries, including the US.

Consider this research report: “Human embryos of two and one-half to five months gestation were obtained from the gynaecological department of the Toronto General Hospital…No macerated specimens were used and in many of the embryos the heart was still beating at the time of receipt in the virus laboratory.”

Here is the citation [2]: Joan C. Thicke, Darline Duncan, William Wood, A. E. Franklin and A. J. Rhodes; Cultivation of Poliomyelitis Virus in Tissue Culture; Growth of the Lansing Strain in Human Embryonic Tissue, Canadian Journal of Medical Science, Vol. 30, pg 231-245. [June 1952]

The authors are certainly describing an infant who was taken from the womb alive, and after cells were harvested, was killed. For research on “growing virus in cell culture.”

Here is another research report that indicates the infant was born alive, its tissues taken, and then killed:

“Embryos of between 12-18 weeks gestation have been utilized. Rarely tissues were obtained from stillborn fetuses, or from premature infants at autopsy…In the experiments 3 sorts of embryonic materials were used: elements of skin, connective tissue, muscle; intestinal tissue; brain tissue…Whenever possible the embryo was removed from the amniotic sac.., transferred to a sterile towel and kept at 5 C until dissected.”

The citation [3]: Thomas H. Weller, John F. Enders, Studies on the Cultivation of Poliomyelitis Viruses in Tissue Culture : I. The Propagation of Poliomyelitis Viruses in Suspended Cell Cultures of Various Human Tissue; Journal of Immunology 1952;69;645-671. [June 1952]

Again, the infant’s tissue was used, in the lab, to “grow virus in cell culture.” The cells were from the infant.

My readers know that, for the past year, I’ve been exposing virologists’ absurd claims that they’re isolating viruses in their labs. [4] [4b] [4c]

In fact, they create soups in dishes, containing toxic drugs and chemicals, monkey cells and human cells, and a mucus sample from a patient. When the cells start dying, they claim this is proof the virus is in the mucus, in the soup, and is deadly.

Of course, this is nonsense, because the toxic drugs and chemicals are perfectly capable of killing the cells; and the cells in the soup are being starved of nutrients, which would also lead to cell-death.

The isolation of viruses is no isolation at all. It’s a fraud.

But it never occurred to me, until now, that some of these human cells in the soup in the lab came from infants, taken from the mother’s womb alive, for harvesting, who were then killed.

This completes a circle of evil.

Of course, out of the virological research fraud and infant murder come THE VACCINES, including the COVID vaccines, which are causing huge numbers of injuries and deaths across the world.

People of faith everywhere must see that declaring a religious exemption from the shots is a DUTY, whether or not the authorities allow the exemption.

The last time I looked, appealing to Pontius Pilate for an exemption didn’t work, and the status of Anthony Fauci is not higher than the Authority to whom, at minimum, four billion people of faith pray.


SOURCES:

[1] https://cogforlife.org/2012/06/13/forsaking-god-for-science/

[1b] https://cogforlife.org/wp-content/uploads/AbortedFetalCellLines.pdf

[2] https://cdnsciencepub.com/doi/10.1139/cjms52-031

[3] https://cogforlife.org/wp-content/uploads/poliovax1952.pdf

[4] https://blog.nomorefakenews.com/2021/02/26/covid-the-virus-was-never-proven-to-exist-a-statement/

[4b] https://blog.nomorefakenews.com/2021/04/21/isolation-of-sars-cov-2-refuted-in-step-by-step-analysis-of-claim/

[4c] https://blog.nomorefakenews.com/2021/09/20/the-failure-to-prove-the-virus-exists/

 

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Florida Stands Alone in Defiance of the mRNA Drug Cartel

Florida Stands Alone in Defiance of the mRNA Drug Cartel
49 States Order COVID Injections for Kids Under 5

by Jordan Schachtel, The Dossier
June 17, 2022

 

49 states have decided to follow the federal government’s lead in ordering COVID injections for children under 5, despite glaring evidence of a failed pharmaceutical product that doesn’t serve any benefit to them whatsoever, and has the potential to cause serious side effects.

[direct link to video of Ron DeSantis announcement]

On Friday, the FDA authorized mRNA COVID shots (both Pfizer and Moderna) under emergency use for children under 5 down to 6 months of age. The approval made its way through the halls of the federal bureaucracy, regardless of any studies showing a positive benefit for injecting young children with mRNA shots, which, even in adults, do not effectively prevent coronavirus infection.

 

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Children’s Health Defense Reports That a Third Judge Was Asked to Step Down in COVID Vaccine Mandate Case

Children’s Health Defense Reports That a Third Judge Was Asked to Step Down in COVID Vaccine Mandate Case

by Children’s Health Defense

Press Release dated June 15, 2022

 

New York, NY – U.S. District Judge Valerie E. Caproni of the Southern District of New York issued an order Monday recusing herself from further involvement in two consolidated federal lawsuits challenging New York City Department of Education (DOE) COVID vaccine mandates. Plaintiffs moved to disqualify Judge Caproni last Thursday after discovering she held up to $100,000 in Pfizer stock in 2020.

“Federal law prohibits federal judges from taking part in a case in which they have any financial interest, no matter how small,” Sujata Gibson, an attorney for the plaintiffs, told The Defender. “Pfizer stocks have been impacted by court injunctions against COVID vaccine mandates, and ownership of this stock constitutes a conflict of interest.”

The Court then appointed Judge Edgardo Ramos to the case. However, Plaintiffs quickly filed a  joint motion to disqualify Judge Ramos as well, due to his financial investments in COVID vaccine manufacturers. Last night, Judge Ramos recused himself and was replaced by Judge Naomi Reice Buchwald. Plaintiffs filed yet another motion to disqualify Judge Buchwald after finding that she holds up to $250,000 in Pfizer stock and $100,000 in Johnson & Johnson as of 2020.

“The fact that we are on our third motion in twenty-four hours to disqualify a judge because of financial conflicts of interest emphasizes the enormity of our Plaintiffs’ battle,” Gibson said.

Judicial financial conflicts of interests are under increasing scrutiny in response to a Wall Street Journal investigation that found 152 federal judges around the nation have violated US law and judicial ethics by overseeing 1,076 court cases involving companies in which they or their family owned stock. Plaintiffs were able to access the financial disclosures of the three conflicted judges after President Biden signed the bipartisan Courthouse Ethics and Transparency Act on May 13, 2022, creating stricter reporting requirements for federal judges.

“Thousands of beloved teachers and educators have been suspended and terminated in violation of their sincerely held religious beliefs,” said Barry Black, co-counsel for plaintiffs. “It is crucial that no financial conflict compromise the decision-making process.”

Kane v. de Blasio plaintiffs are represented by Sujata S. Gibson of the Gibson Law Firm PLLC, Mary Holland of Children’s Health Defense, and Michael Sussman of Sussman & WatkinsKeil v. City of New York plaintiffs are represented by Jonathan R. Nelson, Barry Black and Sarah E. Child of Nelson Madden Black LLP.

Defendants, including the city of New York, are jointly represented in both cases by Lora Minicucci of the New York City Law Department.

###

Children’s Health Defense is a 501(c)(3) non-profit organization. Our mission is to end childhood health epidemics by working aggressively to eliminate harmful exposures, hold those responsible accountable, and establish safeguards to prevent future harm. For more information, visit ChildrensHealthDefense.org.

 

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The Babies and The Vaccine

The Babies and The Vaccine
Protecting your baby from a virus that doesn’t exist, with a killshot

by Jon Rappoport, Jon Rappoport’s Blog
June 16, 2022

 

So you’ve had your eight-month-old baby injected with the COVID vaccine.

Of course.

And the SARS-CoV-2 virus doesn’t exist.

I’ve heard that. But it’s not the issue for us.

What is the issue for you?

Making a fashion statement.

How so?

We need to stay in the forefront of trends.

Why?

Why wouldn’t we?

Have you seen the federal database that records vaccine injury and death reports?

Of course.

So you know your baby could die from the shot.

Yes.

And that doesn’t matter to you.

Not as much as being able to tell our friends we had our baby vaccinated.

You, as parents—

That’s a misunderstood term. We don’t consider ourselves parents. The State is the parent. We’re the monitors.

Monitors?

We observe, and carry out limited functions.

Even if you assume the virus exists, the chances of your baby catching it and becoming ill are incredibly tiny.

That’s right. But this isn’t what we’re about. As I said, we’re keeping pace with fashion.

Are you human?

It depends on how you define the term. Humans are biological machines. Most people believe in something beyond that, but the content of belief is predetermined by a person’s upbringing, genes, conditioning, and so on.

Have you ever questioned vaccine science?

There’s nothing to question. We understand science. I have a PhD in psychology, and my husband is a software engineer. My IQ is 141. My husband’s is 136. We’re equipped to deal with vaccine issues.

If your baby died from the shot, would you mourn?

Yes. We would post photos and statements on our Facebook page.

—No doubt, some people would take offense at this “interview.” How could I? Here’s how. I wrote it. I wrote it because the government and Pfizer and Moderna—no matter how they interpret COVID and “the virus”—are moving ahead to inject as many babies as possible—which is a crime of mass assault and mass murder. Many parents will go along with it.

 

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Hands Off Our Children: The Vaccine Injured Speak Out

Hands Off Our Children: The Vaccine Injured Speak Out

 

From Children’s Health Defense newsletter, June 14, 2022:

The U.S. Food and Drug Administration (FDA) is likely to grant Emergency Use Authorization (EUA) for Pfizer’s BioNTech SARS-CoV-2 vaccine for children ages 6 months through 4 years and Moderna’s COVID-19 mRNA vaccine for infants and children ages 6 months through 5 years and 6 years through 17 years in their upcoming meetings today and tomorrow (June 14-15).

CHD is poised to take legal action against the FDA should they grant these emergency use authorizations. We seek to hold FDA accountable for recklessly endangering our children with products that have little, no or even negative net efficacy. These products may put them, without warning, at risk of many adverse health consequences, including heart damage, stroke, other thrombotic events and future reproductive harm.

URGENT! Send Your Lawmakers RFK, Jr.’s Letter to FDA VRBPAC Committee Members

by Children’s Health Defense
June 12, 2022

Our children need your help! On Tuesday and Wednesday, June 14 and 15, the FDA VRBPAC committee is likely to make a catastrophic decision by voting to grant Emergency Use Authorizations (EUA) to allow for infants and young children to receive Pfizer’s and Moderna’s COVID shots.

Please take 30 seconds to tell your lawmakers to STOP the FDA from granting EUAs for COVID vaccines in babies and children by sending Robert F. Kennedy, Jr.’s letter to FDA VRBPAC committee members. His letter lays out all of the available science and data that proves vaccinating children for COVID is not only unnecessary, but will recklessly endanger their lives. There is no emergency whatsoever for children from COVID, therefore there is no justification for issuing an Emergency Use Authorization.

Time and mounting evidence have continued to prove that children have essentially zero risk of dying from COVID (99.995% recovery rate), and the vast majority of kids have little to no symptoms. There is no statistically valid evidence that shows the Pfizer and Moderna COVID injections are able to prevent severe disease or deaths in children at all. These shots have a worse safety record than all previous vaccines combined, and have been found to cause serious injuries including myocarditis, encephalopathy, blood clots, diabetes, neurological issues and death.

Link here to the form provided by Children’s Health Defense to tell your lawmakers to STOP THE FDA from harming our children with these disastrous shots.

 

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cover image credit (creative commons images of children): abeermutebRaphealny, & Bessi




Injecting 6-Month-Old to 5-Year-Old Children? NO! — Murder Has No Statute of Limitations

Injecting 6-Month-Old to 5-Year-Old Children? NO! — Murder Has No Statute of Limitations

 

Injecting 6 mo. olds to 5yo’s? – NO!
Murder has no statute of limitations

by Coquin de Chien
June 14, 2022

 

The United States Government, at the behest of Pharma oligarchs and government employees who own stock in the Pharma companies, hopes to approve an amendment to the EUA (Emergency Use Authorization) to inject babies 6-months-old to toddlers 4-years-old with the C19 faux-vaccine.

Before the committee meets to recommend the amendment, the FDA allows people to comment on the FDA government web site. One such comment was provided to this author and is offered to you below. The United States of America is indeed facing a government #ClotShot plot.


This comment is NOTICE of possible criminal liability to Lauren K. Roth and members of the Vaccines and Related Biological Products Advisory Committee who owe duties of care, diligence, good faith, and loyalty in recommending “for” or “against” the EUA amendment for COVID-19 mRNA vaccine in children 6 months through 4 years of age.

Only two deaths are listed herein to establish knowledge.  If the amendment is approved, it will have been done by committee members “knowing” of felony crimes in context.

Your investigation of these deaths should include death certificates, autopsy records, witness interviews, and immunization records.

Massachusetts Death Certificate 2022 SFN 5980 is a 7yo girl died January 18, 2022 listed as died from U071 “COVID-19”, B49 “unspecified mycosis”, J450 “predominantly allergic asthma”, and R091 “pleurisy”.

VAERS_ID 2038120 is a 7yo girl in Massachusetts, who received her 2nd dose 1/13/2022 and was reported to VAERS 1/15/2022.  PRIOR_VAX states, “Severe nausea and vomiting from 5min post vaccination and for the next 8-10 hours.”  SYMPTOM_TEXT states, “Spiked a 103 fever, severe stomachache, has not had a bowel movement since the day before vaccination, which makes today 3 days without one.  First vaccine caused severe nausea and vomiting from 5minutes post injection and for the next 8-10 hours.”

This little girl suffered immeasurably 4 to 5 days as her intestines shut down due likely to impeded blood vessels servicing intestines.

Massachusetts Death Certificate 2021 SFN 56611 is a 48yo man died 11/16/2021 listed as died from U071 “COVID-19” and E669 “OBESITY”.

SFN 56611 is known to have died less than 24 hours after inoculation.

In both cases, the Medical Examiners listed the cause of death as “COVID-19”, when it was clearly not COVID-19.  And in both cases, the Medical Examiners omitted listing causes Y590 “Viral vaccines“ and T881 “Other complications following immunization, not elsewhere classified”, when these clearly were proximate and actual causes.

Death certificates from the state of Massachusetts are sent to the CDC, a federal entity.  Thus, fraud on a state death certificate is a federal crime as it affects federal death records.  Several federal felony crimes apply in this instance and are listed below.

If you dismiss this NOTICE and recommend the EUA amendment without first investigating these two deaths, you become liable for inchoate crimes and the felony crime of “misprision of felony.”  If a single person subsequently dies as a result of the amendment, all the elements will have been satisfied for you to face felony murder charges or involuntary manslaughter.  Qualified immunity is not a valid defense.

18 USC § 4 – Misprision of felony

“Whoever, having knowledge of the actual commission of a felony …, conceals and does not as soon as possible make known the same to some … civil or military authority …, shall be fined under this title or imprisoned not more than three years, or both.”

Felony murder is a homicide that occurs during the commission of an inherently dangerous felony, showing a conscious disregard for human life.  A jury decides whether recommending an injection, that you “know” caused death, and that you refused to investigate while “knowing” it caused death, is inherently dangerous.

Here are a few federal statutes likely violated by Medical Examiners in Massachusetts.  You are duty-bound to call for investigation of:

  • 18 USC § 4 Misprision of felony
  • 18 USC § 286 Conspiracy to defraud the government with respect to claims
  • 18 USC § 287 False fictitious or fraudulent claims
  • 18 USC § 371 Conspiracy to commit offense or to defraud United States
  • 18 USC § 1035 False statements relating to health care matters
  • 18 USC § 1040 Fraud in connection with major disaster or emergency benefits

There were found sixty likely C19 vaccine deaths in a 25-minute perusal of the 2021 and 2022 death certificates, which extrapolates to hundreds, probably thousands of C19 vaccine deaths in Massachusetts.

Refusal to investigate these fraudulent records is a crime that, because of the felony murder aspect, has no statute of limitations.  Five, ten, or twenty years from now, if a federal prosecutor were to learn of this NOTICE, he or she would have significant evidence to bring charges for felony murder.

In summary, this NOTICE places you in a position requiring you to investigate these deaths prior to recommending the amendment.  If you dismiss this NOTICE, you may be criminally liable for involuntary manslaughter, felony murder, and a list of federal crimes and inchoate crimes.

Please make the appropriate decision for yourselves and for the children of the United States of America.

Comment Tracking Number

l4d-m52d-ge4m

 

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cover image credit: binggnu93 / pixabay

 


See related:

Hands Off Our Children: The Vaccine Injured Speak Out




Why Are So Many Young People Dying?

Why Are So Many Young People Dying?

by Jefferey Jaxen & Del Bigtree, The HighWire
June 10, 2022

 


A growing number of young healthy adults are mysteriously dying. Watch Jefferey Jaxen and Del try to make sense of, what is now being called, “Sudden Adult Death Syndrome” (SADS).

#SADS #HealthyAdultsDroppingDead #SIDS

 

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New England Journal of Medicine Study Reveals 80% Miscarriage Rate in Early Pfizer Recipients

New England Journal of Medicine Study Reveals 80% Miscarriage Rate in Early Pfizer Recipients

by Children’s Health Defense
June 11, 2022

 



First New England Journal of Medicine Pfizer Study Reveals 80% Miscarriage Rate in Recipients in their First or Second Trimester — Dr. Christiane Northrup also reports rising number of stillbirths on ‘Friday Roundtable’ Infertility: A Diabolical Agenda Q+A

WATCH THE FULL Q+A:
https://live.childrenshealthdefense.org/shows/chd-friday-roundtable

 

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See related:

Infertility: A Diabolical Agenda




Health Freedom Defense Fund Guide to Contest COVID-19 Employer Discrimination

Health Freedom Defense Fund Guide to Contest COVID-19 Employer Discrimination

by Health Freedom Defense Fund
June 10, 2022

 

Americans across the country have been faced with discrimination. We have received many questions as to the correct process to rectify this. Our legal team has put together a step-by-step guide to help you through the process. If you have been discriminated against please see the instructions below. Everyone can start taking action now if they have faced discrimination in the workplace.

Our legal team has broken it down into 3 steps:

STEP 1: FILE A COMPLAINT WITH THE EEOC.

STEP 2: FILE A COMPLAINT WITH YOUR STATE GOVERNMENT.

STEP 3: FILE A CIVIL LAWSUIT.

For full detailed information on the steps for each state, please see the guide below.

Read and Download PDF
Steps to Contest COVID-19 Employer Discrimination

 

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Tell the FDA to Get Their #HandsOffOurChildren

Tell the FDA to Get Their #HandsOffOurChildren

by Children’s Health Defense Team, The Defender
June 6, 2022

 



The U.S. Food and Drug Administration (FDA) is declaring war on our children and it’s on each of us to be unrelenting as we defend the next generation from Big Pharma and its allies. We must stop the FDA’s attack, beginning with a campaign to end unethical and unsubstantiated Emergency Use Authorizations (EUA) that will subject our younger and most vulnerable children to the unnecessary risks of COVID shots.

The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) is scheduled to meet on four separate occasions in June to discuss additional EUAs that would provide cradle-to-grave COVID shots and consider a “Future Framework” that will permanently lower the bar for safety and efficacy going forward.

Their itinerary is as follows:

  • June 7 — Emergency Use Authorization for Novavax’s COVID shot for adults.
  • June 14 — Amendment to Moderna EUA to include primary series to children and adolescents 6 through 17 years of age.
  • June 15 — Amendment to Moderna’s EUA to include primary series for children 6 months to 5 years and amendment to Pfizer’s EUA to include the primary series to children 6 months through 4 years of age.
  • June 28 — Proposed “Future Framework” for COVID shots.

Dr. Toby Rogers aptly calls the June meetings a “blitzkrieg” because it is an overwhelming all-out attack (on informed consent) designed to create psychological shock and demoralizing chaos. But we can change the outcome by arming up with real data and creating a blitzkrieg of our own.

We need Defenders like YOU to hold the line and stop the approval of EUA amendments that profoundly impact the health and safety of our kids. Tell VRBPAC members that:

There is no COVID emergency for children.

Children under 18 with no comorbidities have virtually no risk of death from COVID. They have a 99.995% recovery rate and the vast majority of children have minimal symptoms. A study published in Nature described how children between 3 and 11 years of age mount effective, robust and sustained immune responses to COVID. The CDC’s own data show that at least 75.2% of children ages 0 to 11 years and 74.2% of adolescents ages 12 to 17 years already have superior natural immunity.

mRNA shots offer little in the way of protection.

There is no clinically significant health benefit from the mRNA vaccines. Moderna’s own press release acknowledges that “the absence of any severe disease, hospitalization or death in the study precludes the assessment of vaccine efficacy against these endpoints.” Preliminary data showed the shots were only about 44% effective at preventing symptomatic infection in children 6 months to 2 years old, and 37% effective in children ages 2 to 5 years old — both below the 50% level that regulators had generally called the minimum level for EUA approval in 2020. In New York, officials observed that Pfizer’s efficacy against Omicron plummeted from 68% to 12% after 7 weeks in children ages 5 to 11.

Injuries from COVID shots in children are catastrophic.

Vaccinated children face a substantial risk of myocarditis. Moderna’s EUA application, originally filed in June 2021, has already been held up because of a clear safety signal for myocarditis, which has prompted a number of European countries to prohibit its use in young people. Additionally, the Vaccine Adverse Events Reporting System (VAERS) has over 48,500 reports of adverse events in children, including 112 deaths (as of May 20, 2022) and a growing number of reports of encephalopathies, clotting issues, diabetes and neurological issues in children following COVID shots.

The FDA is poised to make decisions regarding our children and the future of this country that may have a devastating impact on children’s health.

Please send a message to FDA and CDC officials, VRBPAC members and elected representatives demanding that they reject the Pfizer and Moderna EUA applications for children and ensure our government agencies are following the science.

Take Action: Tell the FDA No EUA of COVID Shots for Babies and Children

 

©June 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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1,287,595 Injuries Reported After COVID Shots, Vaccine Injury Compensation Programs ‘Overwhelmed’

1,287,595 Injuries Reported After COVID Shots, Vaccine Injury Compensation Programs ‘Overwhelmed’
VAERS data released Friday by the Centers for Disease Control and Prevention show 1,287,595 reports of adverse events from all age groups following COVID-19 vaccines, including 28,532 deaths and 235,041 serious injuries between Dec. 14, 2020, and May 27, 2022.

by Megan Redshaw, The Defender
June 3, 2022

 

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,287,595 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and May 27, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 9,615 adverse events over the previous week.

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 28,532 reports of deaths — an increase of 220 over the previous week — and 235,041 serious injuries, including deaths, during the same time period — up 2,347compared with the previous week.

Excluding “foreign reports” to VAERS, 825,454 adverse events, including 13,150 deaths and 83,454 serious injuries, were reported in the U.S. between Dec. 14, 2020, and May 27, 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 13,150 U.S. deaths reported as of May 27, 16% occurred within 24 hours of vaccination, 20% occurred within 48 hours of vaccination and 59% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 586 million COVID-19 vaccine doses had been administered as of May 27, including 346 million doses of Pfizer, 221 million doses of Moderna and 19 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 May 27, 2022, for 5- to 11-year-olds show:
U.S. VAERS data from Dec. 14, 2020, to May 27, 2022, for 12- to 17-year-olds show:
  • 31,858 adverse events, including 1,833 rated as serious and 44 reported deaths. VAERS reported 44 deaths in the 12- to 17-year-old age group last week.
  • 62 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. VAERS reported 63 reports in the 12- to 17-year-old age group last week.
  • 654 reports of myocarditis and pericarditis with 642 cases attributed to Pfizer’s vaccine.
  • 167 reports of blood clotting disorders with all cases attributed to Pfizer. VAERS reported 168 cases of blood clotting disorders in the 12- to 17-year-old age group last week.
U.S. VAERS data from Dec. 14, 2020, to May 27, 2022, for all age groups combined, show:
COVID-19 shots for kids under 5 could begin by June 21, White House says

COVID-19 vaccines could be available for children younger than 5 as early as June 21 if U.S. health regulators clear the shots, White House coronavirus response coordinator Ashish Jha said Thursday.

According to The Washington Post, states can start ordering vaccines today, with 10 million initially available. The FDA vaccine advisors are scheduled to meet June 14 and 15 to discuss pediatric vaccines. The CDC will meet shortly after to sign off on the decision.

Pfizer and BioNTech on Wednesday submitted their request for emergency authorization of a three-shot regimen for children 6 months to 4 years old. Moderna submitted its request in April for a two-shot regimen for children 6 months to under 6 years old.

There are about 19 million children under 5 in the U.S.

Young males have highest risk of heart damage from COVID vaccines

Young males are more likely to report heart damage following vaccination with an mRNA COVID-19 vaccine, and the damage is more likely to be reported after the second dose, according to researchers who reviewed the scientific literature and vaccine injury databases in the U.K., EU and U.S.

Research published May 25 in The BMJ showed 18,204 reports of myocarditis and pericarditis were submitted to U.K., U.S. and EU regulators during the study period, beginning when the mRNA vaccines first rolled out until mid-March 2022.

In the U.S., 2,986 events following Pfizer’s vaccine and 1,640 events following Moderna’s vaccine were reported to VAERS.

According to the CDC, 124.12 million people were fully vaccinated with Pfizer and 75.57 million people fully vaccinated with Moderna during the study period.

For Pfizer, the reporting rate was 14.70 cases of myocarditis and 9.36 cases of pericarditis per 1 million fully vaccinated individuals. The combined rate of myocarditis and pericarditis is 12.03 cases reported per 1 million fully vaccinated individuals.

For Moderna, there were 12.35 cases of myocarditis and 9.36 cases of pericarditis reported per 1 million fully vaccinated recipients. The combined reporting rate of both myocarditis and pericarditis is 10.86 per 1 million.

There were 13,573 events of myocarditis and/or pericarditis reported in observational studies included in the systematic review of the literature, but these cannot help to calculate the overall rate of these adverse events.

Vaccine injury compensation programs overwhelmed by thousands of reports

Federal programs compensating people who suffered injuries from vaccines or COVID-19 pandemic treatment are facing so many claims that thousands of people may not receive payment for their injuries for a long time, Politico reported.

The first program, the Vaccine Injury Compensation Program (VICP), has too little staff to handle the number of reported injuries resulting from pediatric vaccines such as polio and MMR, leaving thousands of patients waiting years for their cases to be heard.

The second program, the Countermeasure Injuries Compensation Program (CICP), designed to compensate people for injuries caused by COVID-19 vaccines and countermeasures, has seen unsustainable growth.

Between 2010 and 2020, the CICP received only 500 complaints. Since the start of the pandemic, it has received more than 8,000 complaints — 5,000 of which are related to COVID-19 vaccines.

To date, the CICP has paid zero claims, although it did approve one in December 2021.

Should COVID-19 vaccines become routine, any injuries would be handled by the already overwhelmed VICP. There are fears the public will mistake the situation for “too many injuries flooding the program,” which will lead to vaccine hesitancy.

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

 

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.

©June 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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44,821 Dead 4,351,483 Injured Following COVID-19 Vaccines in European Database of Adverse Reactions

44,821 Dead 4,351,483 Injured Following COVID-19 Vaccines in European Database of Adverse Reactions

by Brian Shilhavy, Health Impact News
May 27, 2022

 

The European (EEA and non-EEA countries) database of suspected drug reaction reports is EudraVigilance, verified by the European Medicines Agency (EMA), and they are now reporting 44,821 fatalities, and 4,351,483 injuries following injections of five experimental COVID-19 shots:

From the total of injuries recorded, almost half of them (1,972,105) are serious injuries.

Seriousness provides information on the suspected undesirable effect; it can be classified as ‘serious’ if it corresponds to a medical occurrence that results in death, is life-threatening, requires inpatient hospitalisation, results in another medically important condition, or prolongation of existing hospitalisation, results in persistent or significant disability or incapacity, or is a congenital anomaly/birth defect.”

Health Impact News subscriber in Europe ran the reports for each of the four COVID-19 shots we are including here. It is a lot of work to tabulate each reaction with injuries and fatalities, since there is no place on the EudraVigilance system we have found that tabulates all the results.

Since we have started publishing this, others from Europe have also calculated the numbers and confirmed the totals.*

Here is the summary data through May 21, 2022.

Total reactions for the mRNA vaccine Tozinameran (code BNT162b2Comirnaty) from BioNTech/ Pfizer: 21,070 deathand 2,207,919 injuries to 21/05/2022

  • 67,512   Blood and lymphatic system disorders incl. 303 deaths
  • 78,229   Cardiac disorders incl. 3,061 deaths
  • 694        Congenital, familial and genetic disorders incl. 63 deaths
  • 29,164   Ear and labyrinth disorders incl. 16 deaths
  • 2,801     Endocrine disorders incl. 10 deaths
  • 32,801   Eye disorders incl. 54 deaths
  • 161,894 Gastrointestinal disorders incl. 837 deaths
  • 550,894 General disorders and administration site conditions incl. 5,821 deaths
  • 2,542     Hepatobiliary disorders incl. 121 deaths
  • 24,583   Immune system disorders incl. 134 deaths
  • 123,754 Infections and infestations incl. 2,182 deaths
  • 41,268   Injury, poisoning and procedural complications incl. 441 deaths
  • 53,565   Investigations incl. 582 deaths
  • 14,151   Metabolism and nutrition disorders incl. 368 deaths
  • 253,409 Musculoskeletal and connective tissue disorders incl. 287 deaths
  • 2,466     Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 241 deaths
  • 348,167 Nervous system disorders incl. 2,266 deaths
  • 3,188     Pregnancy, puerperium and perinatal conditions incl. 85 deaths
  • 301        Product issues incl. 4 deaths
  • 39,004   Psychiatric disorders incl. 242 deaths
  • 8,112     Renal and urinary disorders incl. 312 deaths
  • 95,775   Reproductive system and breast disorders incl. 8 deaths
  • 92,246   Respiratory, thoracic and mediastinal disorders incl. 2,233 deaths
  • 98,876   Skin and subcutaneous tissue disorders incl. 185 deaths
  • 5,415     Social circumstances incl. 27 deaths
  • 25,013   Surgical and medical procedures incl. 251 deaths
  • 52,095   Vascular disorders incl. 936 deaths

Total reactions for the mRNA vaccine SPIKEVAX/mRNA-1273 (CX-024414) from Moderna: 11,916 deathand 720,662 injuries to 21/05/2022

  • 19,456   Blood and lymphatic system disorders incl. 134 deaths
  • 24,903   Cardiac disorders incl. 1,315 deaths
  • 224        Congenital, familial and genetic disorders incl. 15 deaths
  • 8,515     Ear and labyrinth disorders incl. 8 deaths
  • 741        Endocrine disorders incl. 6 deaths
  • 9,632     Eye disorders incl. 36 deaths
  • 57,258   Gastrointestinal disorders incl. 451 deaths
  • 190,630 General disorders and administration site conditions incl. 3,850 deaths
  • 968        Hepatobiliary disorders incl. 64 deaths
  • 8,062     Immune system disorders incl. 39 deaths
  • 31,759   Infections and infestations incl. 1089 deaths
  • 10,916   Injury, poisoning and procedural complications incl. 215 deaths
  • 15,827   Investigations incl. 405 deaths
  • 5,813     Metabolism and nutrition disorders incl. 282 deaths
  • 89,472   Musculoskeletal and connective tissue disorders incl. 238 deaths
  • 860        Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 92 deaths
  • 118,849 Nervous system disorders incl. 1,146 deaths
  • 1,032     Pregnancy, puerperium and perinatal conditions incl. 13 deaths
  • 120        Product issues incl. 3 deaths
  • 11,834   Psychiatric disorders incl. 193 deaths
  • 3,818     Renal and urinary disorders incl. 230 deaths
  • 19,671   Reproductive system and breast disorders incl. 9 deaths
  • 29,456   Respiratory, thoracic and mediastinal disorders incl. 1,264 deaths
  • 37,258   Skin and subcutaneous tissue disorders incl. 107 deaths
  • 2,747     Social circumstances incl. 45 deaths
  • 5,716     Surgical and medical procedures incl. 218 deaths
  • 15,125   Vascular disorders incl. 449 deaths

Total reactions for the vaccine AZD1222/VAXZEVRIA (CHADOX1 NCOV-19) from Oxford/ AstraZeneca8,958 deathand 1,267,883 injuries to 21/05/2022

  • 14,856   Blood and lymphatic system disorders incl. 320 deaths
  • 23,037   Cardiac disorders incl. 946 deaths
  • 269        Congenital familial and genetic disorders incl. 10 deaths
  • 14,620   Ear and labyrinth disorders incl. 7 deaths
  • 784        Endocrine disorders incl. 6 deaths
  • 21,601   Eye disorders incl. 33 deaths
  • 114,466 Gastrointestinal disorders incl. 474 deaths
  • 337,830 General disorders and administration site conditions incl. 2,084 deaths
  • 1,154     Hepatobiliary disorders incl. 80 deaths
  • 6,407     Immune system disorders incl. 44 deaths
  • 54,461   Infections and infestations incl. 745 deaths
  • 14,617   Injury poisoning and procedural complications incl. 219 deaths
  • 30,652   Investigations incl. 223 deaths
  • 14,191   Metabolism and nutrition disorders incl. 142 deaths
  • 182,458 Musculoskeletal and connective tissue disorders incl. 188 deaths
  • 854        Neoplasms benign malignant and unspecified (incl cysts and polyps) incl. 50 deaths
  • 252,545 Nervous system disorders incl. 1,298 deaths
  • 698        Pregnancy puerperium and perinatal conditions incl. 22 deaths
  • 205        Product issues incl. 1 death
  • 22,791   Psychiatric disorders incl. 78 deaths
  • 4,703     Renal and urinary disorders incl. 91 deaths
  • 18,099   Reproductive system and breast disorders incl. 3 deaths
  • 44,746   Respiratory thoracic and mediastinal disorders incl. 1,200 deaths
  • 56,079   Skin and subcutaneous tissue disorders incl. 77 deaths
  • 2,221     Social circumstances incl. 10 deaths
  • 2,869     Surgical and medical procedures incl. 39 deaths
  • 30,670   Vascular disorders incl. 568 deaths            

Total reactions for the COVID-19 vaccine JANSSEN (AD26.COV2.S) from Johnson & Johnson2,877 deaths and 152,918 injuries to 21/05/2022

  • 1,529     Blood and lymphatic system disorders incl. 65 deaths
  • 3,353     Cardiac disorders incl. 244 deaths
  • 55           Congenital, familial and genetic disorders incl. 2 deaths
  • 1,688     Ear and labyrinth disorders incl. 3 deaths
  • 135        Endocrine disorders incl. 2 deaths
  • 2,012     Eye disorders incl. 12 deaths
  • 10,769   Gastrointestinal disorders incl. 106 deaths
  • 41,462   General disorders and administration site conditions incl. 816 deaths
  • 191        Hepatobiliary disorders incl. 17 deaths
  • 713        Immune system disorders incl. 11 deaths
  • 12,281   Infections and infestations incl. 246 deaths
  • 1,425     Injury, poisoning and procedural complications incl. 31 deaths
  • 7,093     Investigations incl. 154 deaths
  • 950        Metabolism and nutrition disorders incl. 77 deaths
  • 19,497   Musculoskeletal and connective tissue disorders incl. 63 deaths
  • 123        Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 11 deaths
  • 26,795   Nervous system disorders incl. 274 deaths
  • 110        Pregnancy, puerperium and perinatal conditions incl. 1 death
  • 34           Product issues
  • 2,205     Psychiatric disorders incl. 31 deaths
  • 666        Renal and urinary disorders incl. 43 deaths
  • 3,864     Reproductive system and breast disorders incl. 6 deaths
  • 5,401     Respiratory, thoracic and mediastinal disorders incl. 358 deaths
  • 4,636     Skin and subcutaneous tissue disorders incl. 13 deaths
  • 546        Social circumstances incl. 7 deaths
  • 1,119     Surgical and medical procedures incl. 96 deaths
  • 4,266     Vascular disorders incl. 188 deaths  

Total reactions for the COVID-19 vaccine NUVAXOVID (NVX-COV2373) from Novavax0 deaths and 2,101 injuries to 21/05/2022

  • 44           Blood and lymphatic system disorders
  • 116        Cardiac disorders
  • 26           Ear and labyrinth disorders
  • 1             Endocrine disorders
  • 46           Eye disorders
  • 154        Gastrointestinal disorders
  • 463        General disorders and administration site conditions
  • 3             Hepatobiliary disorders
  • 8             Immune system disorders
  • 102        Infections and infestations
  • 19           Injury, poisoning and procedural complications
  • 57           Investigations
  • 13           Metabolism and nutrition disorders
  • 275        Musculoskeletal and connective tissue disorders
  • 2             Neoplasms benign, malignant and unspecified (incl cysts and polyps)
  • 373        Nervous system disorders
  • 1             Pregnancy, puerperium and perinatal conditions
  • 1             Product issues
  • 36           Psychiatric disorders
  • 11           Renal and urinary disorders
  • 39           Reproductive system and breast disorders
  • 105        Respiratory, thoracic and mediastinal disorders
  • 142        Skin and subcutaneous tissue disorders
  • 3             Social circumstances
  • 9             Surgical and medical procedures
  • 52           Vascular disorders

These totals are estimates based on reports submitted to EudraVigilance. Totals may be much higher based on percentage of adverse reactions that are reported. Some of these reports may also be reported to the individual country’s adverse reaction databases, such as the U.S. VAERS database and the UK Yellow Card system. The fatalities are grouped by symptoms, and some fatalities may have resulted from multiple symptoms.

Here are some faces and names to put on these cold, hard statistics.

Horrible: A Mom Films Her Daughter Receiving The Jab – The Young Girl Ends Up Puking, Then Dying ?? (Brazil) ??

Listening to her mom cry over the phone is one of the saddest things I’ve ever heard.

These are unspeakable atrocities against children and it needs to stop now. I don’t like sharing these types of videos but as a truth seeker it’s my duty to warn others.

From Covid BC Telegram channel.

This is from our Odysee channel, and it is also on our Bitchute and Telegram channels.



Read the full article at Health Impact News

 

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Jefferey Jaxen Breaks Down the Latest Meeting in Davos

Jefferey Jaxen Breaks Down the Latest Meeting in Davos

by Jefferey Jaxen with Del Bigtree, The HighWire
May 27, 2022

 

Switzerland was the location for both the World Economic Forum and the WHO’s World Health Assembly.

Watch as the worlds ‘elite’ brag and boast about their perceived control.

Not everyone was flying high as Modera’s CEO whined about having to toss 300M Covid shots in the trash.

 



 

Link to Health Freedom Defense Fund’s World Freedom Declaration

 

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18 Major Airlines, FAA, and DOT to Be Sued Over COVID Vaccine Mandates

18 Major Airlines, FAA, and DOT to Be Sued Over COVID Vaccine Mandates
First Lawsuit Against Atlas Air Has Been Filed 

by Enrico Trigoso, The Epoch Times
May 25, 2022

 

John Pierce Law has filed a lawsuit against Atlas Air, on behalf of US Freedom Flyers (USFF) and Atlas employees, and plans to sue all major airlines, 18 altogether, plus the Federal Aviation Administration (FAA) and the Department of Transportation (DOT), contending that the vaccine mandates imposed by these agencies on the airlines’ employees infringed on their constitutional, religious, and medical liberties.

The lawsuit against Atlas Air was filed in federal court in the Southern District of Florida, with over 100 plaintiffs pursuing litigation.

“Fundamentally, this case is about whether Americans should be required to choose between their livelihoods and being coerced into taking an experimental, dangerous medical treatment,” reads the lawsuit (pdf).

Plaintiffs are mostly unvaccinated pilots, flight attendants, as well as other Atlas staff.

“It is also about the safety of America’s airline industry. Should pilots—under federal regulation required to be among the healthiest workers in the United States—who have taken an experimental ‘vaccine’ that is now shown to have potentially deadly, long-term side effects, be allowed to fly massive aircraft in our skies? While those who have (smartly) refrained from such a course be forced out of their jobs?” it states.

Atlas Air is one of the industry’s largest cargo carrier companies and the world’s largest operator of the Boeing 747 aircraft.

The law firm was founded by Att. John Pierce, who founded the National Constitutional Law Union. He previously represented George Papadopoulos in connection with the 2016 “Russia Hoax,” reaching a dismissal of the DNC’s case and helping secure a presidential pardon. He is also currently representing defendants being charged in connection to the Jan. 6 Capitol breach.

“So the complaint has been filed. We’re in the process of serving everyone. And then, we’ll likely be looking for some kind of injunctive relief here soon to make sure that all the COVID-related mandates stop immediately. And then we’ll proceed [with] litigation, motion, practice, and discovery and then onward to trial eventually,” Pierce told The Epoch Times.

This week, John Pierce Law plans to file another lawsuit against United Airlines.

“We’ll be hitting basically all of them in sequence, and then we’ll be going after the FAA as well. We’re gonna get these vaccine mandate type of rules and COVID restrictions ruled unconstitutional. And we’re gonna get findings that there was discrimination under Title Seven. We’re gonna get punitive damages for intentional infliction of emotional distress and things like that,” Pierce said.

“It’s going to require a big fix, ultimately. And that’s probably going to require legislation and kind of getting all the stakeholders at the table, but the first step is civil litigation.”

Airlines, which are government contractors, are affected by President Joe Biden’s order from September of last year that states all employees of those companies have to be vaccinated against the Chinese Communist Party virus.

Pierce said that as soon as he heard about the airline mandates he predicted that it would be the next big wave of litigations.

“[These lawsuits are] absolutely crucial. It’s a very, very red line—If you get to the point where you have to choose between getting an experimental drug shot in your arm and your paycheck, that’s just unAmerican, it’s unconstitutional, it’s outrageous, it’s sickening.”

“If that’s not the hill to die on when it comes to liberty, that’s about as close as I can imagine it,” Pierce said.

Josh Yoder, a major airline pilot and a spokesperson for Freedom Flyers who recently supported the trucker-led “The People’s Convoy,” says that there has been harassment, threats, intimidation, vaccine injuries, and even “suicides that have come out of these mandates.”

“We’re not doing class action. We’re doing individual litigants. And the reason we’re doing it that way is because so many people have been harmed and people have experienced different levels of harm. We have the unvaccinated who have been harassed, threatened, and intimidated into getting vaccinated. Then we have many people as well who got vaccinated against their will, who were coerced and forced into doing it under threat of losing their employment,” Yoder said.

“And then, in addition, we have the vaccine-injured, and the numbers of vaccine-injured are growing by the day,” Yoder went on, “It’s just incredible what’s happening with pilots.”

Pilots have to maintain a flight physical in order to maintain their licenses.

The Epoch Times recently reported that a pilot for American Airlines, one of the top 3 largest airlines in the country, suffered a cardiac arrest between two flights, about 6 minutes after landing.

“And so what we’re seeing is many pilots are experiencing health conditions. Specifically, cardiac issues [are] what we’re seeing a lot of. And many of these pilots are afraid to come forward because if they come forward they lose their flight physical, they lose their flight medical. So they’re continuing to fly. We have a lot of pilots that are flying with chest pain and neurological conditions, because if they come forward they lose their careers,” Yoder said.

Freedom Flyers is now acting as an advocacy group between the pilots, the FAA, and the companies in order to assist them in coming forward and speaking out on their conditions.

“We have a massive team of medical professionals who are helping these people, but we’re asking everyone to come forward. While it’s absolutely devastating to their careers, we need them to come forward because this is the safety of the American public that we’re talking about,” Yoder said.

According to a group of attorneys, doctors, and other experts—and a pilot who says his career ended due to adverse reactions from a vaccine—the FAA has been breaking its own rule that states pilots should not fly after having taken medications that have been approved for less than a year, The Epoch Times reported in December.

 

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Moderna CEO Laments ‘Throwing 30 Million Doses in the Garbage Because Nobody Wants Them’

Moderna CEO Laments ‘Throwing 30 Million Doses in the Garbage Because Nobody Wants Them’

by Tyler Durden, ZeroHedge
May 24, 2022

 

Moderna CEO Stéphane Bancel is complaining about having to ‘throw away’ 30 million doses of Covid-19 vaccine because nobody wants them.’

“It’s sad to say, I’m in the process of throwing 30 million doses in the garbage because nobody wants them. We have a big demand problem,” Bancel told an audience at the World Economic Forum, adding that attempts to contact various governments to see if anyone wants to pick up the slack was a total fail.

“We right now have governments – we tried to contact … through the embassies in Washington. Every country, and nobody wants to take them.

“The issue in many countries is that people don’t want vaccines.”

Watch:

Bancel’s comments come days after Bloomberg reported that EU health officials want to amend contracts with Pfizer and other vaccine makers in order to reduce supplies.

During a virtual meeting organized by Polish Health Minister Adam Niedzielski, governments shared a joint letter to the EU Commission which reads: “We hope that the discussion with the commission and among member states will allow flexibility in the vaccine agreements,” adding “We are also counting on vaccine producers to show understanding to the exceptional challenges that Poland is facing supporting Ukraine and giving shelter to millions of Ukrainian citizens fleeing the war.”

Some countries are seeking to amend so-called advanced purchase agreements signed with producers, as demand for shots wanes and budgets come under strain from the fallout of the war in Ukraine and the costs of accommodating refugees.

Adjusting deals with suppliers could grant member states the right to “re-phase, suspend or cancel altogether vaccine deliveries with short shelf life,” Estonia, Latvia and Lithuania’s prime ministers wrote in a joint letter to Commission President Ursula Von Der Leyen late last month.

Meanwhile, in a separate letter the health ministry of Bulgaria called for an “open dialog” with the commission and pharmaceutical companies, arguing that the current arrangement forces member states to “purchase quantities of vaccines they don’t need.”

 

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The Viral Delusion (2022) Docu-Series: The Tragic Pseudoscience of SARS-CoV2 & the Madness of Modern Virology

The Viral Delusion (2022) Docu-Series: The Tragic Pseudoscience of SARS-CoV2 & the Madness of Modern Virology

by Paradigm Shift
April 2022

 

The doctors, scientists and journalists featured in THE VIRAL DELUSION examine in detail the scientific papers that were used to justify the pandemic, and what they find is shattering. In this shocking, five-part, seven hour documentary series, they explode every single major claim, from the “isolation” of the virus to its so-called genetic sequencing, from the discovery of how to “test” for SARS-CoV2 to the emergence of “variants” that in reality, they explain, exist only on a computer. Their point: that the so-called SARS-CoV2 virus exists only as a mental construct whose existence in the real world has been disproven by the science itself.

They then go back through history to reveal how the birth and growth of virology has led to massive misunderstanding and misdiagnosis of disease: from Smallpox to the Spanish Flu, Polio to AIDS, to COVID itself – putting the pandemic in a whole new context better understood not as settled science, but the tragic culmination of misunderstood biology by the growing cult of virology, built on pseudo-science, to which much of the rest of the medical profession defers without understanding or examination, and the tragic consequences that have been wrought in its name.

In 2019, the virologists took center stage, and for the first time on film, their methods, miscues and tragedy they have wrought are put under the spotlight, revealing the extraordinary leaps of fantasy buried in their methodology, the contradictions quietly acknowledged in their papers, their desperate effort to change language to justify their findings, the obvious incongruence of their conclusions and the extraordinary stakes for our entire society in whether we continue to blindly follow their lead into a full-scale war against nature itself.

Featuring: Andrew Kaufman, MD; Tom Cowan, MD; Stefan Lanka, Virologist; Torsten Engelbrecht, journalist; Claus Kohnlein, MD; Kevin Corbett, PhD RN; David Rasnick, Biochemist PhD; Mark Bailey, MD; Dawn Lester and David Parker, Authors; Stefano Scoglio, Biochemist PhD; Saeed Qureeshi, Chemist PhD; Celia Farber, Journalist; Harold Wallach, PhD; Pam Popper, PhD, ND; Charles Geshekter, PhD; Amandha Vollmer ND, Jim West, Author; Larry Palevsky MD; and more.

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Videos (Episodes 1 – 5) and summaries found below are courtesy of QR Archive Odysee channel.

 

The Viral Delusion (2022) Episode 1:The Tragic Pseudoscience of SARS-CoV-2

When doctor Andrew Kaufman began reading the first virology papers out of Wuhan in December 2019, he was shocked to discover that the scientists had come nowhere close to proving that a new virus had emerged… yet saw the media and authorities already claiming a viral pandemic was on it’s way.

In this extraordinarily revealing opening episode, a group of biologists, chemists, doctors and journalists take apart the SARS-COV-2 narrative piece by piece — from the non-isolation of the virus, to the hidden problems with purported photographs of the virus, to the claims that it has been genetically sequenced, to the invalidity of the PCR “covid-test.”

From the treatment protocols for COVID to the assumption of its transmission, Episode One unpacks the science of the claims that changed the world – in which these doctors and scientists make the case that every single claim the authorities made about the so-called SARS-COV2 virus has been based not on evidence, but pseudoscience.




The Viral Delusion (2022) Episode 2: Monkey Business: Polio, Measles And How It All Began

How did it all begin?

How could the scientific establishment have possibly gotten so big a story so wrong?

Everyone knows the story of Polio…or do they?

What from that story is actual history and what is medical marketing?

How did a small branch of the scientific establishment come to convince the world polio was the result of a virus and not from environmental toxins?

Learn what the actual experiments were upon which this theory was based — and how shockingly unconvincing they are.

Discover too how the medical establishment’s efforts to squeeze the symptoms of polio into a virus model formed the very foundation of modern virology, and how that commercially successful model has steered modern science ever since, evidence be damned.




The Viral Delusion (2022) Episode 3: The Mask of Death – The Plague, Smallpox and The Spanish Flu

What about Smallpox?

The Spanish Flu?

The Black Plague?

Go back, back, back in time to examine the claims and counter-claims as to what truly caused these deadly epidemics.

Are the rats of Europe innocent? Turns out they have to be…

And in that discovery we see how the superstitions of our time have clouded the eyes of “science” to avoid the most obvious of insights about disease.




The Viral Delusion (2022) Episode 4: AIDS, The Deadly Deception

AIDS. It was the defining epidemic of a generation.

But it was also the coming of age for many leading scientists and doctors who came to realize that blaming the illnesses known as AIDS on a virus was not only unsupported by science, it was downright nonsensical.

What were the true causes of the many illnesses labelled AIDS around the world?

How many suffered from their misdiagnosis?

How the scientific establishment fell into the deadly AIDS delusion is crucial to understanding the pandemic, and health, today.




The Viral Delusion (2022) Episode 5: Sequencing The Virus, Without The Virus

With the rise of computing and genetic research in the 90’s the virologists go high-tech.

They move away from experiments altogether and into genetic modeling — but do the models have any connection to reality?

The wonders of genetic sequencing have been pointed to as the proof of virology’s explanatory power — but when the claimed sequencing of SARS-COV2 is put under the microscope, has the game changed from the realm of science, to science fiction?

What’s really going on the claim of genetically identifying the SARS-CoV-2 virus is made?



 

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Inclusion, Wokeness, and Davos 2022

Inclusion, Wokeness, and Davos 2022

by Richard Hugus
May 23, 2022

 

 

The picture above is of a sign outside a performing arts theater in Santa Barbara, California. Looks like everyone is welcome. Well, not really. It turns out that if you’re  not “vaccinated” you’re not welcome. If you haven’t arrived at the ticket booth with ID and proof of being injected with two doses of an emergency use experimental gene treatment for “covid 19” — a treatment which has no efficacy and is associated with millions of serious injuries and deaths — this #LoveForAll message doesn’t actually apply to you. If you’re not “vaccinated” the only way you can get into the theater now is if you have taken a test proving you don’t have the plague. Don’t want a PCR swab up your nose? Too late for an antigen test? Tough luck. This rainbow venue welcomes EVERYONE, except for carriers of the plague.

“Who doesn’t love LOVE?” Apparently, the state of North Carolina doesn’t. The founder of Insist On Love For All which makes and sells the $60 sign displayed above, took a trip to Asheville, North Carolina a few years ago and was impressed by signs “embracing diversity.” Says Insist On Love’s founder,

shop owners started displaying these signs over two years ago [2018] to encourage tourism following the passage of the controversial House Bill 2 in North Carolina, which requires certain public bathrooms to be designated for use by males or females based on their biological sex. “The signs in Asheville moved me. Love is the only weapon we can use to fight hate . . . “

In this case, “hate” was displayed by 1) the idea that men and women should have separate bathrooms, 2) the idea that men (or men who think they’re women) don’t have a right to walk into women’s bathrooms, and vice versa,  3) the fact that other sexes besides male and female have not been acknowledged, and 4) the fact that the state of North Carolina thus discriminated against all those who don’t have male/female privilege. There is also the ‘hate’  involved in the unwillingness of North Carolina to provide separate bathrooms for a theoretically unlimited number of other genders. Unless #LoveForAll is somehow a front for a consortium of plumbing supply companies (this would actually be comforting news), there is nothing left for us to conclude but that ‘love’, as the term is being used here, is indeed a weapon, not to fight hate, but to fight reason. ‘Love’ is now a buzzword in a well-established “diversity and inclusion” narrative sent down from academic critical theory to the progressive left to the mainstream media to the culture at large. Has there ever been a time when good things have been so twisted into their opposite? This is not about love or inclusion. This is shallow virtue signaling by people who have been swallowed up by a political machine designed to turn cultural norms upside down, not for the purpose of bringing needed change, but for the purpose of creating chaos and a loss of rationality, after which new supposed norms can just be lifted into place.

“All sexual orientations”, cited in the sign, is also a topic at the current May 22-28 Davos forum, where “resilience through equity” and “inclusivity” for the “LGBTQI+ community” is on the formal agenda. Do the corporate bosses, social engineers, and preening politicians at this forum really care about equality, or are they just using the brand to create the upheaval necessary to bring in fantastic profits and power? The answer is obvious. The agenda is exclusion, not inclusion; fascism, not liberalism. Their plan is for the majority of humanity, gay or straight, to be excluded from their rights, autonomy, and independence, while the bosses enjoy their wealth and slave labor. Like #LoveForAll,  everyone is welcome in the Great Reset except those who believe there are only two sexes — that is, just about everybody since the beginning of human history. Everyone is welcome in virtue-signaling countries, corporations, and institutions except those who choose not to accept a medical intervention also never heard of before in human history — that of altering the human genome on the pretext of defeating a virus. In other words, everyone is welcome except those who have chosen not to go insane. The insanity is called wokeness. Wokeness is nothing but a tool being used to effect a very ugly and very ambitious power grab. When the job is done, everyone duped into thinking they were fighting for the victims of oppression and equality for all will be swatted away like flies.

The would-be gods at Davos brought us their own version of the Apocalypse — plague, war, famine, and death became covid, Ukraine, food shortages, and vaccines. Do such people even remotely care about racial prejudice and gender dysphoria? No. They either massively exploited or completely made up these issues to create disorder. Indeed, their eugenicist predecessors had certain, ahem,  opinions about people with disabilities, sexual deviants, and racial groups which they know can’t be mentioned in polite society today. So they went the other way. Not believing in God, the Davos elite see themselves as gods. The further this delusion takes them, the harder they will fall. There will also come a time of reckoning for the collaborators in this program — those who, wittingly or not, aided this monstrosity. Galling self-righteousness, ignorance, and hypocrisy were the least of the crimes in this class. The ones higher up — those who made the plans, gave the orders, and knew what they were doing — face a reckoning that perhaps we do not have words for. It may be a regular new round of guillotining such as we have seen before in history. Or it may be that this time wickedness has gone so far it will have to be ended forever. Prospects for the Davos crew do not look good.

 


Richard Hugus is the founder of Cape Cod Against Medical Mandates “We are residents of Cape Cod, Massachusetts who support freedom of choice in all matters having to do with our own and our childrens’ health.”  Connect with them here.

Read more of Richard’s writings: http://www.richardhugus.com/

Richard Hugus is a contributing writer at Truth Comes to Light.

 

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CHD Seeks Help From Texas Parents in Lawsuit Challenging FDA’s Authorization of COVID Vaccines for Kids 5-11

CHD Seeks Help From Texas Parents in Lawsuit Challenging FDA’s Authorization of COVID Vaccines for Kids 5-11
Children’s Health Defense seeks help from parents in 13 Texas counties, after a U.S. District Court on Tuesday granted CHD 45 days to amend its lawsuit against the U.S. Food and Drug Administration’s Emergency Use Authorization of COVID-19 vaccines for children ages 5 to 11.

by Children’s Health Defense Team, The Defender
May 20, 2022

 

A U.S. District Court on Tuesday gave Children’s Health Defense (CHD) 45 days to amend its lawsuit against the U.S. Food and Drug Administration’s (FDA) Emergency Use Authorization (EUA) of COVID-19 vaccines for children ages 5 to 11.

CHD’s lawsuit, filed Jan. 24 in the U.S. District Court for the Western District of Texas, alleges, among other things, that the FDA — under pretext of EUA powers — “authorized a dangerous drug for minor children as young as 5 years old to address COVID-19, which poses less risk to a 5-year-old than the ordinary flu.”

CHD last month filed a motion to stay asking the court to suspend the FDA’s authorization of the vaccine for young children pending judicial review of the lawsuit.

During Tuesday’s hearing Judge Alan Albright heard arguments on CHD’s motion to stay and also on the FDA’s motion to dismiss CHD’s lawsuit.

Judge Alan Albright denied CHD’s request to suspend authorization of the vaccines until the lawsuit is resolved, stating he was skeptical of CHD’s organizational standing and the standing of the two parents named in the suit, given the lack of any children’s COVID-19 vaccine mandate in the district at this time.

Judge Albright said for CHD to have standing, it must show “diversion of resources.”

For the parents named in the complaint — Deborah L. Else and Sacha Dietrich — to have standing, they must show their children are at demonstrable risk of vaccination against the parents’ wishes.

Attorney Robert Barnes, arguing for CHD, said if the FDA’s interpretation of standing were correct, then no one could sue the FDA because it would mean the FDA is completely insulated from judicial scrutiny.

Barnes also argued the harm to plaintiffs is not simply the threat of vaccination, but includes the FDA’s false assertions that the vaccines are safe, effective and actually vaccines, i.e. products that prevent infection and transmission.

U.S. Department of Justice attorney James Harlow, arguing on behalf of the FDA, said the agency cannot mandate products and that products authorized for emergency use clearly permit patients to accept or reject them.

Harlow also argued that Texas Gov. Greg Abbott issued an executive order prohibiting COVID-19 mandates at schools, thus undermining an argument for any threat.

After hearing arguments from both sides, Judge Albright said given the importance of the case, he wanted to give CHD and plaintiffs Else and Dietrich the opportunity to assert standing, and would give them 45 days to amend their lawsuit.

The judge also provided a roadmap for how to amend the case.

CHD is seeking help from the public in order to provide the court the necessary evidence to prove standing in its case against the FDA.

Parents in 13 counties in the Western District of Texas who have information about coercive COVID-19 vaccine policies for children or adolescents are asked to submit that information to chd@childrenshealthdefense.org with subject line “CHD v. FDA.”

The 13 counties are: Bell, Bosque, Coryell, Falls, Freestone, Hamilton, Hill, Leon, Limestone, McLennan, Milam, Robertson and Somervell.

CHD is especially interested in these types of situations occurring in the counties listed above:

  • Hospitals or medical facilities that require COVID-19 vaccination for treatment
  • Children in foster care, correctional settings or other institutional settings who are required to receive COVID-19 vaccinations
  • Vaccination clinics or vaccination stations in schools or youth facilities promoting COVID-19 vaccines for kids
  • Evidence of school pressure to vaccinate children even without an explicit mandate
  • After-school programs or extra-curricular activities requiring COVID-19 vaccines.

CHD in May 2021 filed a citizen petition with the FDA and the U.S. Department of Health and Human Services outlining the arguments against EUA and/or licensing of COVID-19 vaccines.

The FDA on Tuesday granted Pfizer’s request for EUA of a third COVID-19 shot for children ages 5 to 11, and the Centers for Disease Control and Prevention on Thursday signed off on the shots.

 

©May 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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