Critics Must Be Silenced for Billionaires to Keep Profiting From Pandemic

Critics Must Be Silenced for Billionaires to Keep Profiting From Pandemic
By controlling the media, billionaires like Jeff Bezos and Bill Gates can prolong a crisis indefinitely while they accumulate unprecedented wealth and power over humanity. 

by Robert F. Kennedy, Jr., The Defender
February 16, 2021

 

On Feb. 15, the Jeff Bezos-owned Washington Post published a Feb. 11 Associated Press article applauding the censorship of those who criticize the government’s pandemic response policies.

The lockdown has netted Bezos $70 billion since its start. If you are Bezos, a permanent lockdown is a goldmine.

Bill Gates, meanwhile, has made $20 billion from the lockdown he previously war-gamed and then cheer-led. His strategy has included emasculating the independent media — the most likely sources of the sort of vigorous journalism that might otherwise scrutinize his self interest in the polices he helped successfully engineer for the rest of us.

Gates used millions in grants to transform the once proudly unbridled The Guardian into his personal newsletter. With $250 million, he purchased immunity from criticism by news operations like the BBC, NBC, Al Jazeera, ProPublica, National Journal, Univision, Medium, the Financial Times, The Atlantic, the Texas Tribune, Gannett, Washington Monthly, Le Monde and the Center for Investigative Reporting.

Gates also made large contributions to charitable organizations affiliated with news outlets, like BBC Media Action and the The New York Times, according to an August 2020 investigation by Columbia Journalism Review. He similarly disarmed NPR and Public Television by making them reliant on his support. In exchange, these outlets shield his sketchy projects from critical scrutiny.

Gates is arguably the world’s biggest vaccine maker. As its largest contributor, Gates controls the World Health Organization which, according to Foreign Affairs, makes no significant decision without consulting the Bill & Melinda Gates Foundation. He similarly exercises dictatorial authority over an army of quasi-governmental agencies that he largely created or funds: Path, GAVI CEPI, Unicef etc. These agencies have demonstrated their power to turn the globe into a captive market for Gates’ vaccine enterprise.

Meanwhile, Gates’ Big Pharma partners use their $9.6 billion in advertising expenditures to dictate round-the-clock pandemic panic and drum up blind support for highly subsidized, shoddily tested, zero-liability vaccines that prevent neither transmission nor death.

The mainstream network news shows, including CNN, ABC, NBC, CBS and Fox have put COVID Terror, Vaccines Salvation and the obligatory shaming of dissidents on a 24-hour loop with each segment (and I use this term in every sense of the word) with pharmaceutical advertisements.

These outlets have turned their weekly talk shows into fawning hagiographies for Gates’ regular satellite tours in which credulous, obsequious Sunday morning talk show hosts lob softball medical questions to a billionaire with no public health training.

Nobody ever asks Gates or his mini-me, Tony Fauci, why they chose to spend tens of billions in taxpayer dollars on speculative vaccines and zero dollars investigating the many off-the-shelf, off-patent medications that have demonstrated extraordinary success in the hands of private doctors — medications that might have ended the pandemic a year ago.

The media, which has enabled this global hostage crisis, is arguably the most consequential criminal enterprise in human history. As Rahm Emmanuel observed, “never let a good crisis go to waste.”

Gates and Fauci have demonstrated that by controlling the media, billionaires and their government cronies can prolong a crisis forever and accumulate unprecedented wealth and power over humanity.




653 Deaths + 12,044 Other Injuries Reported Following COVID Vaccine, Latest CDC Data Show

653 Deaths + 12,044 Other Injuries Reported Following COVID Vaccine, Latest CDC Data Show
The numbers reflect the latest data available as of Feb. 4 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 653 reported deaths, 602 were from the U.S. The average age of those who died was 77, the youngest was 23. 

by Children’s Health Defense Team, The Defender
February 12, 2021

 

As of Jan. Feb. 4, 653 deaths — a subset of 12,697 total adverse events — had been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. The numbers reflect reports filed between Dec. 14, 2020 and Feb. 4, 2021.

VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before confirmation can be made that the reported adverse event was caused by the vaccine.

As of Feb. 10, about 44.77 million people in the U.S. had received one or both doses of a COVID vaccine. So far, only the Pfizer and Moderna vaccines have been granted Emergency Use Authorization in the U.S. by the U.S. Food and Drug Administration (FDA). By the FDA’s own definition, the vaccines are still considered experimental until fully licensed.

According to the latest data, 602 of the 653 reported deaths were in the U.S, and 137 of the deaths were related to cardiac disorder. Fifty-three percent of those who died were male, 44% were female, the remaining death reports did not include the gender of the deceased. The average age of those who died was 77, the youngest reported death was of a 23-year-old. The Pfizer vaccine was taken by 58% of those who died, while the Moderna vaccine was taken by 41%.

As or Feb. 4, there had been 163 cases of Bell’s Palsy reported and 775 reports of anaphylaxis.

As The Defender reported today, the CDC is investigating the Feb. 8 death of a 36-year-old doctor in Tennessee who died about a month after receiving the second dose of a COVID vaccination. According to news reports, Dr. Barton Williams died from the adult form of multisystem inflammatory syndrome (MIS-A), a condition caused when the immune system attacks the body resulting in multi-system organ failure. New reports attributed the death to a reaction to an asymptomatic case of COVID, although Williams never tested positive for the virus.

On Feb. 8, Fox5 reported the death of a man in his 70s who collapsed and died Feb. 7 as he was leaving the Javits Center in Manhattan about 25 minutes after receiving a COVID vaccination.

On Feb. 7, a local Villa Hills, Kentucky news site reported on the deaths of two nuns following a “COVID-19 outbreak” that occurred two days after the nuns were vaccinated. Prior to beginning the vaccination program, there had been no cases of COVID at the monastery, which has been shut down to visitors during the pandemic. After vaccinations began, 28 of the women had tested positive for COVID as of Feb. 7.

The clinical trials suggested that almost all the benefits of COVID vaccination and the vast majority of injuries were associated with the second dose.

The Defender also reported this week that according to the New York Times, several doctors now link the Pfizer and Moderna COVID vaccines to immune thrombocytopenia (ITP), a condition that develops when the immune system attacks platelets (blood component essential for clotting) or the cells that create them. The Times article featured two women who are recovering from ITP after being vaccinated. Last month, Dr. Gregory Michaels died from ITP two weeks after he got the Pfizer vaccine.

While the VAERS database numbers may seem sobering, according to a U.S. Department of Health and Human Services study, the actual number of adverse events is likely significantly higher. VAERS is a passive surveillance system that relies on the willingness of individuals to submit reports voluntarily.

According to the VAERS website, healthcare providers are required by law to report to VAERS:

  • Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccination.
  • An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine.

The CDC says healthcare providers are strongly encouraged to report:

  • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event.
  • Vaccine administration errors.

However, “within the specified time” means that reactions occurring outside that timeframe may not be reported, in addition to reactions suffered hours or days later by people who don’t report those reactions to their healthcare provider.

Vaccine manufacturers are required to report to VAERS “all adverse events that come to their attention.”

Historically, fewer than fewer than 1% of adverse events have ever been reported to VAERS, a system that Children’s Health Defense has previously referred to as an “abject failure,” including in a December 2020 letter to Dr. David Kessler, former FDA director and now co-chair of the COVID-19 Advisory Board and President Biden’s version of Operation Warp Speed.

A critic familiar with VAERS’ shortcomings bluntly condemned VAERS in The BMJ as “nothing more than window dressing, and a part of U.S. authorities’ systematic effort to reassure/deceive us about vaccine safety.”

CHD is calling for complete transparency. The children’s health organization is asking Kessler and the federal government to release all of the data from the clinical trials and suspend COVID-19 vaccine use in any group not adequately represented in the clinical trials, including the elderly, frail and anyone with comorbidities.

CHD is also asking for full transparency in post-marketing data that reports all health outcomes, including new diagnoses of autoimmune disorders, adverse events and deaths from COVID vaccines.

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




David Icke: Murder by ‘Vaccine’ — The Evidence Mounts

Murder by ‘Vaccine’ — The Evidence Mounts

by David Icke
February 12, 2020

 



Video available at David Icke BitChute channel.




Red Alert Warning About Pfizer and Moderna COVID Inoculations

Red Alert Warning About Pfizer and Moderna COVID Inoculations

by Stephen Lendman, Global Research
February 11, 2021

 

Pfizer and Moderna mRNA inoculations aren’t what they’re promoted to be.

As medically defined by the CDC, vaccines are supposed to stimulate the “immune system to produce immunity to a specific disease.”

Immunization is a “process by which a person becomes protected against a disease through vaccination.”

The above is not what mRNA inoculations are designed to do. They’re something else entirely.

They’re gene modifying delivery systems that don’t produce immunity —what Moderna calls “gene therapy technology.”

Not designed to prevent seasonal flu-renamed covid illness, at most they may somewhat reduce symptoms short-term.

Promoting mRNA technology as vaccine protection from covid is part of a state-approved/media proliferated mass deception scam.

The above technology is unapproved by the FDA for human use because it’s experimental, inadequately tested, and high-risk — especially for the elderly with weakened immune systems.

The nanoparticle-based delivery system is unapproved.

mRNA inoculations contain hazardous polyethylene glycol (PEG) to deliver their DNA-altering technology to human cells.

The risk of adverse events increases greatly from follow-up inoculations, including to potentially life-threatening anaphylactic shock.

In 2017, Moderna abandoned mRNA technology and lipid nanoparticles because tests caused large numbers of adverse effects.

Yet the same gene therapy and nanoparticle delivery system are used by Moderna and Pfizer in their misnamed mRNA “vaccines” that aren’t what they’re called.

According to statnews.com, “mRNA is a tricky technology.”

“Several major pharmaceutical companies have tried and abandoned the idea, struggling to get mRNA into cells without triggering nasty side effects.”

“(N)anoparticles created a daunting challenge: Dose too little, and you don’t get enough enzyme to affect the disease.”

“(D)ose too much, and the drug is too toxic for patients.”

“Moderna could not make its therapy work, former employees and collaborators said.”

“The safe dose was too weak, and repeat injections of a dose strong enough to be effective had troubling effects on the liver in animal studies.”

Moderna earlier admitted that its lipid nanoparticles (LNP) risked “significant adverse events,” adding:

“No mRNA drug has been approved in this new potential category of medicines, and may never be approved as a result of efforts by others or us.”

“mRNA drug development has substantial clinical development and regulatory risks due to the novel and unprecedented nature of this new category of medicines.”

“(T)here can be no assurance that our LNPs will not have undesired effects.”

According to virologist Judy Mikovits, LNPs can enter the brain, risking pathologic neuro-inflammation that could cause multiple sclerosis, ALS, or other serious diseases.

Johns Hopkins explained that potentially serious adverse events may occur after receiving follow-up mRNA inoculations.

According to Children’s Health Defense, “doctors link Pfizer (and) Moderna ‘vaccines’ to (a) life-threatening blood disorder.”

Health Impact News reported the following:

“An entire school district in Ohio canceled classes on Monday this week after so many of the staff suffered side effects from one of the experimental COVID mRNA injections over the weekend.”

Fox News Cleveland reported that “(t)wo days after employees were given their first round of COVID-19 vaccinations, the Fairless Local School District canceled classes, attributing it to many developing side effects and becoming ill.”

Similar events to the above are happening in the US and European countries after Pfizer and Moderna inoculations.

The more people jabbed, the more adverse events that at times are fatal.

Going along with experimental mRNA inoculations is playing Russian roulette with human health.

There’s high risk of things turning out badly in the short or longer-term.

Deceased 39-year-old Dr. Keshav Raman Sharma is an mRNA statistic.

Inoculated on January 5, he was found dead at home five days later.

He’s not alone. Others suffered the same fate.

Protecting health and well-being requires avoidance of these experimental, inadequately tested high-risk, unapproved inoculations.

 

Connect with Stephen Lendman at Global Research




The PCR Test Can Kill You – and Can Be Used to Vaccinate You

The PCR Test Can Kill You – and Can Be Used to Vaccinate You

by Dr. Vernon Coleman
February 9, 2021

 



Original video available at Dr Vernon Coleman BrandNewTube channel.

[As a service to protect truth from censorship and to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

Transcript

We all know now that PCR tests are useless for finding cases of covid-19 but very good at helping governments keep us in our own homes under house arrest. In some parts of the world the PCR tests are banned as utterly useless. I explained precisely what’s wrong with these misused tests in a an article on this website subtly called `The PCR Test Is Useless for Covid-19 (But Useful for Crooked Governments).

The big problem, of course, is that the British Government, for example, deliberately ignores the WHO guidelines and does the test in a crooked way which would, in a just and sensible world, result in Johnson, Hancock and their advisors crowded into the dock.

You’d get as good a result if you just divided people into two groups: those with a vowel in their surname and those without a vowel, and then announced that the ones with the vowel all had covid-19 and the rest all needed to change their names within seven days or pay a huge fine.

So, everyone with functioning brain tissue knows that the PCR test is useless, except for political reasons, and that the whole testing programme is an outrageously expensive and disruptive shambles. Only government ministers, scientific advisors and pseudo-journalists at the wretched BBC think that PCR tests are valuable. Did you know, by the way, that the Government has allegedly hired 900 consultants to help with the test and trace scheme? The consultants are being paid £1,000 a day each though what they do for that I cannot imagine. That’s £900,000 a day. I suspect that 99.99% of the population would be happier if the £900,000 a day were spent on dentists.

But that’s not the half of it. Most people seem to have accepted the need for regular PCR testing. Indeed, people in the UK queue up to have it done as often as possible – as though they get some sort of thrill out of having a complete stranger stuff something into a bodily orifice – pushing it in as far as it will go, twizzling it about a bit, and then pulling it out and buggering off without so much as `a thank you very much I’ll give you a ring tomorrow and we’ll have dinner and then do it again’.

There is talk of children having daily tests though I haven’t been able to find any evidence that this would be a good idea for anyone other than the hugely profitable industry now involved in making and looking at the swabs .

What no one ever mentions is that the PCR tests are dangerous and can, if done improperly, cause excrutiating pain. This is probably why some countries don’t like them. There is indeed a great deal of confusion about how far the swab should go. (Or should that be the Klaus Schwab) In Australia the guidelines are that the swab should only go a few centimetres up the nostril but nasopharyngeal swabs can go much further. The United States Department of Health and Human services says that the swab should reach a depth equal to the distance from the nostril to the outer opening of the ear. That’s a huge distance. In Ottawa, Canada, the recommendation is half that distance.

In October last year I reported on at least one case where a healthy individual had noticed cerebrospinal fluid pouring out of her nose after an invasive PCR test. That really isn’t something you want happening. The woman concerned, who was in her 40s, had a PCR nasal swab test and later went to see a doctor complaining of vomiting, a runny nose, a headache and a stiff neck. The pseudo-journalists at the BBC can, if they are interested in facts, find the details in the JAMA Otolaryngology Head and Neck Surgery. Surgeons found that the fluid running down her nose was cerebrospinal fluid – the fluid that protects the brain.

Then there was the case which was accepted for The Medical Journal of Australia on the 4th December but which I don’t think has been published yet. This reported a healthy 67-year-old woman who had cerebrospinal fluid coming down her nose and the symptoms of meningitis. This followed a covid-19 swab test. How many are being killed – especially in care homes – by this useless and dangerous test?

The authors of the paper stated that the `techniques for deep nasal and nasopharyngeal swabs may be easily confused’. They offer instructions for those conducting the tests. Here’s one part of their instructions: `it involves swab insertion into the nasal cavity at a plane between the opening of the nose and the external ear canal on the patient, which can be considered as the horizontal plane for the purpose of relationship to surface anatomy. This will allow the swab to be inserted parallel to the nasal floor which would avoid injury to the middle turbinates. Swabs inserted in an upward orientation into the nasal cavity, (greater than 30 degrees) not only have a risk of failing to achieve an adequate diagnostic sample from the desired nasal mucosa and nasopharynx but also puts the patient at greater risk of injury to the thin and delicate areas of the skull base (attachment of middle turbinate and cribriform plate) which are superior and anterior to the sphenoid sinus ostium.’ There is then an illustration for swabbing and the authors conclude: `We urge that this angle is not exceeded when performing diagnostic tests as it places the patient at greatest risk of serious adverse events.’

I suggest that anyone having a PCR test should ensure that the person holding the swab has studied and understood these instructions – and will follow them.

In Tripura, a three-day-old boy bled to death after a nasal swab test. In Saudi Arabia an eighteen month old child died after a test swab broke inside his nasal cavity. These are not safe tests. Children are being traumatised by these incredibly invasive tests. These are not safe procedures and they’re often being done by people who know as much about medicine and human anatomy as I know about running a submarine – though I have seen Ice Station Zebra with Patrick McGoohan, and that film with Gene Hackman and Denzel Washington in it. And there was Red October with Sean Connery. Actually, come to think about it, I probably know far more about submarines than the average test and tracer tester knows about anatomy.

Quite a few things have puzzled me about the PCR test.

First, why the devil do they have to push the swab so far up your nose – and so close to your brain. Where is the indisputable scientific evidence that all the little covid-19 bugs are gathering up there for some reason? Do they like out of the way places? Normally, if you have a bug in your nose it will be in your nose. Where is the solid proof that the test only works if a sample is taken from a spot so far up your nose that the tissue up there probably speaks another language and only gets home once a year? Since these tests are now being performed by people who aren’t doctors or nurses or probably even boy scouts, we need some evidence that the test is essential. Actually, since the tests produce more false positives than real positives they are clearly a waste of time anyway and it would make as much sense if the testing swab were inserted into the umbilicus and given a good twizzle there.

Second, researchers at Johns Hopkins University in the US published a study describing a device which has been developed. It’s a tiny, star shaped micro-device capable of delivering a drug. The devices are no larger than a speck of dust but contain a metal core coated in heat sensitive paraffin wax. At the centre of the core there is the drug.

Now, we know that around half of Americans are reluctant to have the covid-19 vaccination.

I think that this hidden injection technology could be used to vaccinate people through nasal or anal PCR swabs. Is this why anal swabs are being introduced? The procedure works best on intestinal tissue.

This could be used to deliver a vaccine to people without their knowledge or consent.

People who think they are just being tested could be receiving the mRNA jab.

Is this going to happen? Is it going to happen?

How the hell would we know?

The authorities are already collecting the names and details of people who have declined the vaccine. Are they planning to use the PCR test to those who refuse the vaccination?

We cannot trust the government or its advisers. We cannot trust the mainstream media. We definitely cannot trust the BBC which has financial links to the Bill and Melinda Gates Foundation and which long ago betrayed us. We can only trust one another.

Giving vaccines nasally is nothing new. Children sometimes have the flu vaccine sprayed up their noses – that’s a live attenuated vaccine, by the way. Attenuated means it’s weaker. But it could still kill granny, of course. Personally, I might use the stuff to clear the drains but I wouldn’t squirt it up a child’s nose.

And you should perhaps know this: nasal vaccinations are already used on cattle.

 

Copyright Vernon Coleman February 9th 2021




Doctors Link Pfizer, Moderna Vaccines to Life-Threatening Blood Disorder

Doctors Link Pfizer, Moderna Vaccines to Life-Threatening Blood Disorder

A second New York Times article quotes doctors who say the mRNA technology used in COVID vaccines may cause immune thrombocytopenia, a blood disorder that last month led to the death of a Florida doctor after his first dose of the Pfizer vaccine.

by Children’s Health Defense Team, The Defender
February 9, 2021

 

For the second time in under a month, The New York Times has published an article about people who developed a rare autoimmune disease after receiving COVID vaccines.

Monday’s article featured two women, both of whom were described as healthy before they received the Moderna vaccine. The women, ages 72 and 48, are now being treated for immune thrombocytopenia (ITP), a condition that develops when the immune system attacks platelets (blood component essential for clotting) or the cells that create them, according to the Times.

On Jan. 13, the Times reported on the death of Dr. Gregory Michael, a Florida doctor who died 15 days after getting the Pfizer vaccine. Michael, who was 56 and described as “perfectly healthy” by his wife, developed ITP three days after being vaccinated. He died of a brain hemorrhage on Jan. 3. As The Defender reported on Jan. 13, Dr. Jerry L. Spivak, an expert on blood disorders at Johns Hopkins University, said it was a “medical certainty” the Pfizer vaccine led to Michael’s death.

Spivak, who was interviewed for Monday’s article in the Times, reiterated the link between the vaccine and ITP. Two other doctors, Dr. James Bussel, a hematologist and professor emeritus at Weill Cornell Medicine who has written more than 300 scientific articles on the platelet disorder, also said he thinks there is a “possible” association between the vaccines and ITP.

Bussel told the Times:

“I’m assuming there’s something that made the people who developed thrombocytopenia susceptible, given what a tiny percentage of recipients they are. Having it happen after a vaccine is well-known and has been seen with many other vaccines. Why it happens, we don’t know.”

Bussel and a colleague, Dr. Eun-Ju Lee, have identified 15 cases of ITP in COVID vaccine recipients by searching the government’s database — the Vaccine Adverse Event Reporting System (VAERS) — or by consulting with other physicians treating patients, and have submitted an article about their findings to a medical journal, according to the Times.

In a statement provided to the Times, Pfizer said it was aware of ITP cases in vaccine recipients and that the company is “collecting relevant information” to share with the U.S. Food and Drug Administration.

The vaccine maker added, however that “at this time, we have not been able to establish a causal association with our vaccine.” Moderna also provided a statement, but didn’t address cases of ITP, only saying that it “continuously monitors the safety of the Moderna Covid-19 vaccine using all sources of data” and routinely shares safety information with regulators.

Directly following Michael’s death, Pfizer said there was “no indication — either from large clinical trials or among people who have received the vaccine since the government authorized its use last month — that it could be connected to thrombocytopenia.”

But, as Lyn Redwood, RN, MSN, president emerita and director of Children’s Health Defense said at the time, Pfizer’s statement didn’t square with the facts — because ITP is a well-known adverse event associated with vaccinations.

The vaccine most often implicated in ITP is the measles-mumps-rubella (MMR) vaccine, where the disease occurs in approximately 1 in every 25,000 to 40,000 doses of the vaccine, Redwood said.

ITP has also been associated with hepatitis A and B virus (HBV), human papilloma virus (HPV)varicella-zoster, diphteria-tetanus-acellular pertussis (DTap)polio and pneumococcus vaccines.

According to the Times, ITP is “generally treatable” but can persist for months or become chronic and last for years. The American Hematology Society advises patients who already have ITP go ahead and get vaccinated, “but after consulting with their hematologists.”

Meanwhile, the two women featured in the Times yesterday are recovering. Luz Legaspi, 72, was hospitalized in New York City on Jan. 19 with a severe case of ITP, but is home now, being cared for by her daughter.

A 48-year-old Texas woman who asked that the Times not use her name spent four days in the hospital, receiving platelet transfusions, immune globulins and steroids to restore her platelet count — a situation she described as “terrifying.” She said her doctor told her to go ahead and get the second dose of the Moderna vaccine, but she has not yet decided if she will.

The Defender reached out to the Florida Department of Health for an update on the investigation into Michael’s death, but did not hear back by deadline. Florida health officials and the Centers for Disease Control and Prevention are investigating the death.

 

cover image credit parentingupstream / pixabay




The Evil Deception: Giving the Covid-19 Jab Without Informed Consent

The Evil Deception: Giving the Covid-19 Jab Without Informed Consent

by Dr. Vernon Coleman
February 7, 2021

 



Original video available at Dr Vernon Coleman BrandNewTube channel.

[As a service to protect truth from censorship and to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

Transcript:

I had to have a molar removed the other day. It wasn’t giving a lot of trouble but an X-ray showed it was rotten to the core and in too bad a state to try to fill and repair. So it had to come out before it caused serious pain. You have to deal with these things when you can, these days. You don’t want raging toothache if they decide to lock us all in our bedrooms like naughty children.

Before he got out the hammer and chisel, the dentist talked to me about the possible complications – the things that could go wrong.

Naturally, when removing a tooth things don’t always go smoothly.

The tooth can break, leaving part of it behind.

Removing the tooth involves a good deal of wiggling to start with. I don’t mean the dentist wiggles. He has to wiggle the tooth – move it from side to side to loosen it. And this can result in accidental damage to adjoining teeth.

My rotten molar was in my upper jaw and occasionally the removal of the tooth can create a fistula into the sinuses with the result that when you have a drink, the fluid comes down your nose instead of, or as well as, going down your throat. When this happens a bit of sewing up may be required.

And, of course, there’s the risk of a dry socket. You don’t want one of those.

So my dentist gave me lots of excellent advice. Don’t eat hard foods. Don’t eat on that side. Don’t brush the tooth and dislodge the clot. Then the next day rinse gently with salt in warm water. All that sort of stuff. He told me what to do if the bleeding started again. And suggested sleeping on an extra pillow.

And then he took the tooth out and made a great job of it.

The point is that that is what is meant by informed consent.

Before the treatment began I knew what to expect. I knew what problems there might be and what would need to be done about them if they happened.

Doctors are very careful to ensure that patients don’t start a new treatment without being properly informed.

They do this not just because they’re as kindly and thoughtful as my dentist.

They do it because it’s a legal protection.

If you take a drug which turns you blue or makes your ears fall off and you weren’t warned that it might do this then the prescribing doctor may well be sued.

Informed consent is a vital part of any medical procedure.

Except one.

And I bet you could sit there all day and not be able to work out what it is.

Vaccination.

When they give you a vaccination there isn’t a doctor in a million who will tell you exactly what could go wrong.

And that has never been truer than it is with the covid 19 vaccine.

They don’t tell you for three reasons.

First, they don’t know what will go wrong. Vaccines aren’t really properly tested. The nasty side effects don’t usually become obvious for a year or two – by which time the drug company making the stuff has made a fortune. If they know about problems they’ll probably cover them up, lie about them and make sure that any scientific papers exposing the dangers aren’t published. If you think I’m exaggerating you obviously haven’t watched my videos about some of the big vaccine companies and the bad, bad things they’ve got up to. They don’t know what will happen if you have the vaccine but are also taking some other medication – heart pills, cancer pills, arthritis pills, whatever. They haven’t tested to see what happens if you have the vaccine and then go home and take prescribed or non-prescribed medication. They have no idea. They can’t warn you about the potential problems because they don’t know what they are.

Second, the list of adverse events is so long that it would take too long to go through. And if they gave you a leaflet listing all the adverse effects – which include heart attack, stroke and death by the way – most people would roll their sleeves back down and hurry home to have a nice cup of tea and a biscuit instead.

Third, informed consent isn’t necessary with the covid-19 vaccine because Bill Gates insisted that the vaccine companies were given indemnity. You can’t sue them. If you have the vaccine and you die then that’s hard luck. If you are paralysed because of the vaccine then you won’t get a penny in compensation. The drug companies can’t be sued. And nor can anyone else associated with the vaccine. I bet the car companies and the tobacco companies wish they had that sort of deal.

So vaccines, particularly the covid-19 vaccine, are unique in that respect.

And not only do they not warn you about all the potential adverse events, but governments are hiring people to tell you that the vaccine is perfectly safe and that you should rush along and have one as soon as your name comes out of the hat.

My name came out the other day, by the way. Before declining I explained about the number of deaths and serious injuries that had been recorded.

`Did you know any of that?’ I asked.

The woman said she didn’t, then paused and added `I’ll put you down as `declined, then.’

And carried on filling the booking sheet with the names of deceived patients destined by ignorance to take part in the biggest experiment in medical history.

And if you don’t believe that this is an experiment, consider this:

The US government website clinicaltrials.gov contains details of the study to describe the safety, tolerability, etc. of mRNA vaccine candidates against covid-19 in healthy individuals.

And the trial, which was designed in April 2020, will continue for two years from the first vaccinations.

Note that: the trial will continue for two years.

No one knows how safe the vaccinations will be because the trials aren’t finished yet.

This is clear proof anyone having the covid-19 jab is taking part in an experiment.

So anyone who says that the vaccine is perfectly safe – even if it’s the Archbishop of Canterbury, who has said that the vaccine is safe – cannot possibly know what they are talking about.

It’s not just the Archbishop, of course.

Scores of celebrities have announced that the covid-19 vaccines are perfectly safe.

They can’t possibly know.

No one knows.

No doctor knows. No one in the Government knows if it’s safe or not.

It’s the world’s biggest experiment.

And for all anyone knows, the vaccine could kill or permanently damage the health of 50% of the people who have it.

So why are hundreds of celebrities and journalists lying about the vaccine?

Well, I can offer you one reason.

Maybe they’re being paid to say it’s safe.

How do I know?

Well the UK Government’s Cabinet Office is advertising for someone to persuade social media influencers to help promote the global warming lie in preparation for the conference being held in Glasgow in November 2021.

The persuader will be paid £65,000.

But here’s the thing: the Government has already paid £63,000 to 42 social media influences to promote the covid-19 test and trace service. TV celebrities and sports players have been paid.

So, how many of the witless morons promoting the lies about the vaccine have been paid?

I’m sure they didn’t put a few quid in the Archbishop’s back pocket.

They wouldn’t do that, would they?

But how many vaccine supporters have been paid with our money?

How many newspapers and journalists have been paid to promote the vaccine?

I would remind you, by the way, that so far at least 14 journalists around the world have been arrested for what the authorities called `unfair’ coverage of this fake pandemic. You can guess what they meant by `unfair’.

Finally, I leave you with a question: if the vaccine is so safe, why did Bill Gates insist the drug companies – including those with which he has financial links – be given legal indemnity to make sure that they couldn’t be sued?

And we should remember that Gates has financial links with many media companies – including the BBC and The Guardian.

Copyright Vernon Coleman February 7th 2021




Vaccine Hesitant Protected in Europe

Vaccine Hesitant Protected in Europe

by Del Bigtree w/ Jefferey Jaxen, The HighWire
February 8, 2021

 



Video available at The HighWire Brighteon and BitChute channels.

Europe’s leading rights organization, The Council of Europe, released a statement to ensure European citizens that the #COVID19 vaccine is not compulsory and calls for those who wish to not receive the vaccine not be discriminated against. While not legally binding, this is quite a shockwave since courts predominantly take the side of human rights organizations in trials.




Vaccine Airlines, Jewish Airlines, Islamic Airlines

Vaccine Airlines, Jewish Airlines, Islamic Airlines

by Jon Rappoport, No More Fake News
February 5, 2021

 

In this article, I present four brief conversations—-

ONE: “Hello, Vaccine Airlines. What is your destination?”

“I’m flying from Newark to Chicago.”

“Have you received the COVID-19 vaccine?”

“Of course.”

“Can you prove it?”

“How would I do that?”

“Do you have the Stasi App on your cell phone?”

“No.”

“I’m sorry. Until you do, and it indicates you’re vaccinated, you can’t fly with us.”

“I just want to buy your product.”

“Impossible. You must satisfy certain conditions before we allow you to buy it.”

TWO: Hello, Jewish Airlines. What is your destination?”

“I’m flying from Miami to New Orleans.”

“Are you Jewish?”

“Of course.”

“Can you prove it?”

“How would I do that?”

“You need the Moses App on your cell phone.”

“I don’t have a cell phone.”

“Then, as far as we’re concerned, you aren’t Jewish. You can’t fly with us.”

THREE: “Hello, Islamic Airlines. What is your destination?”

“I’m flying from New York to Cincinnati.”

“Do you practice the Islamic Faith?”

“Sure.”

“Can you prove it? We have a Central Registry. They do background checks.”

“You won’t take my word?”

“No.”

FOUR: “This is ridiculous. Vaccination isn’t in the same category as religious membership.”

“If I offered to show you evidence that the COVID-19 vaccine is ineffective and dangerous, would you examine that evidence?”

“Of course not.”

“Why not?”

“Because, first of all, social media are censoring that kind of ‘information,’ so I know it’s bogus. And second, all experts agree that vaccination is greatest medical discovery in history.”

“What if they’re wrong?”

“They can’t be wrong.”

“Why not?”

“Because if they were, Reality itself would be turned upside down, and we would all be living in some kind of fantasy.”

“That’s your bottom line?”

“Yes.”

There is another carrier called Trans Airlines. They only allow transgender persons to fly, but that is a much longer conversation, and I leave it to you to write it…

Keep this in mind. Months ago, the US Department of Health and Human Services issued a declaration stating that NO LIABILITY could be attached to any person who participates in medical counter-measures against SARS-CoV-2 [1] [2]. Therefore, it appears that, if a person takes the COVID vaccine, in order to fly (given airlines’ emerging demands), and suffers grave injury or dies from the shot, there will be no legal recourse.

The exception is a new “COVID vaccine court” set up by the federal government [3]. The complaining party pleads his case before a panel. However, I assume that convincing these judges a loved one died as a result of the vaccine, and not “another underlying condition,” will be a very tall mountain to climb.

Here is one more conversation that might interest you:

“Hello, Vaccine Airlines. What is your destination?”

“I want to book a flight, but I’m not taking the COVID vaccine. I’d like to speak with a person who’ll listen to my reasons for turning down the shot.”

“Certainly. Just a moment. I’ll transfer your call.”

“Hello, I’m Agent Martin, FBI Division of Domestic Terrorism. This call is being recorded. How can I help you?”


SOURCES:

[1] https://blog.nomorefakenews.com/2020/09/21/exposed-new-federal-court-to-handle-expected-covid-vaccine-injury-claims/

[2] https://www.federalregister.gov/documents/2020/03/17/2020-05484/declaration-under-the-public-readiness-and-emergency-preparedness-act-for-medical-countermeasures

[3] https://www.hrsa.gov/cicp/

 

cover image credit southtree / pixabay




501 Deaths + 10,748 Other Injuries Reported Following COVID Vaccine, Latest CDC Data Show

501 Deaths + 10,748 Other Injuries Reported Following COVID Vaccine, Latest CDC Data Show
The numbers reflect the latest data available as of Jan. 29 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 501 reported deaths, 453 were from the U.S. The average age of those who died was 77, the youngest was 23. 

 

by Children’s Health Defense Team, The Defender
February 5, 2021

 

As of Jan. 29, 501 deaths — a subset of 11,249 total adverse events — had been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. The numbers reflect reports filed between Dec. 14, 2020, and Jan. 29, 2021.

VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before confirmation can be made that an adverse event was linked to a vaccine.

As of Jan. 29, about 35 million people in the U.S. had received one or both doses of a COVID vaccine. So far, only the Pfizer and Moderna vaccines have been granted Emergency Use Authorization in the U.S. by the U.S. Food and Drug Administration (FDA). By the FDA’s own definition, the vaccines are still considered experimental until fully licensed.

According to the latest data, 453 of the 501 reported deaths were in the U.S. Fifty-three percent of those who died were male, 43% were female, the remaining death reports did not include the gender of the deceased. The average age of those who died was 77, the youngest reported death was of a 23-year-old. The Pfizer vaccine was taken by 59% of those who died, while the Moderna vaccine was taken by 41%.

The latest data also included 690 reports of anaphylactic reactions to either the Pfizer or Moderna vaccines. Of those, the Pfizer vaccine accounted for 76% of the reactions, and the Moderna vaccine for 24%.

As The Defender reported today, a 56-year-old woman in Virginia died Jan. 30, hours after receiving her first dose of the Pfizer vaccine. Doctors told Drene Keyes’ daughter that her mother died of flash pulmonary edema likely caused by anaphylaxis. The death is under investigation by Virginia’s Office of the Chief Medical Examiner and the CDC.

Last week, the CDC told USA TODAY that based on “early safety data from the first month” of COVID-19 vaccination the vaccines are “as safe as the studies suggested they’d be” and that “everyone who had experienced an allergic response has been treated successfully, and no other serious problems have turned up among the first 22 million people vaccinated.

Other vaccine injury reports updated this week on VAERS include 139 cases of facial asymmetry, or Bell’s palsy type symptoms, and 13 miscarriages.

States reporting the most deaths were: California (45), Florida (22), Ohio (25), New York (22) and KY (22).

The Moderna vaccine lot numbers associated with the highest number of deaths were: 025L20A (20 deaths), 037K20A (21 deaths) and 011J2A (16 deaths), 025J20A (16 deaths) . For Pfizer, the lot numbers associated with the most reports of deaths were: EK5730 (10 deaths), EJ1685 (23 deaths), EL0140 (19 deaths), EK 9231 (17 deaths) and EL1284 (13 deaths). For 135 of the reported deaths, the lot numbers were unknown.

The clinical trials suggested that almost all the benefits of COVID vaccination and the vast majority of injuries were associated with the second dose.

While the VAERS database numbers are sobering, according to a U.S. Department of Health and Human Services study, the actual number of adverse events is likely significantly higher. VAERS is a passive surveillance system that relies on the willingness of individuals to submit reports voluntarily.

According to the VAERS website, healthcare providers are required by law to report to VAERS:

  • Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccination
  • An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine

The CDC says healthcare providers are strongly encouraged to report:

  • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event
  • Vaccine administration errors

However, “within the specified time” means that reactions occurring outside that timeframe may not be reported, in addition to reactions suffered hours or days later by people who don’t report those reactions to their healthcare provider.

Vaccine manufacturers are required to report to VAERS “all adverse events that come to their attention.”

Historically, fewer than fewer than 1% of adverse events have ever been reported to VAERS, a system that Children’s Health Defense has previously referred to as an “abject failure,” including in a December 2020 letter to Dr. David Kessler, former FDA director and now co-chair of the COVID-19 Advisory Board and President Biden’s version of Operation Warp Speed.

A critic familiar with VAERS’ shortcomings bluntly condemned VAERS in The BMJ as “nothing more than window dressing, and a part of U.S. authorities’ systematic effort to reassure/deceive us about vaccine safety.”

CHD is calling for complete transparency. The children’s health organization is asking Kessler and the federal government to release all of the data from the clinical trials and suspend COVID-19 vaccine use in any group not adequately represented in the clinical trials, including the elderly, frail and anyone with comorbidities.

CHD is also asking for full transparency in post-marketing data that reports all health outcomes, including new diagnoses of autoimmune disorders, adverse events and deaths from COVID vaccines.

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




Children’s Health Defense – California Chapter Sends Letter to All California Superintendents Regarding Medical Ethics, Emergency Use Products, Voluntary Testing & Vaccine Safety

Children’s Health Defense – California Chapter Sends Letter to All California Superintendents Regarding Medical Ethics, Emergency Use Products, Voluntary Testing & Vaccine Safety

by Children’s Health Defense California Chapter
January 29, 2021

 

A Letter to CA Superintendents

Today, Children’s Health Defense – California Chapter sent a letter to 1,100 California Superintendents to let them know that Emergency Use Authorization products, like the RT-PCR test and COVID vaccines, cannot be mandated, as they are investigational and experimental. They must be voluntary. Further, according to both the CDC and WHO, if RT-PCR testing is offered voluntarily, it must only be offered to those with symptoms through their own doctor. This letter also contains science showing that children are not asymptomatic carriers of COVID, and that COVID vaccines have not been proven to prevent person-to-person transmission. Please share this letter, either using the article’s link or the PDF (CDE Superintendent Letter from Childrens Health Defense – California Chapter) with your own school district to educate them on medical ethics, the science, and the law.


Dear Superintendent,

Children’s Health Defense is a global leader in science, law, public policy and medical ethics. I am the President of the California Chapter of Children’s Health Defense, a 501(c)(3), and I write on behalf of our organization.

The purpose of this letter is to help you to understand the science, law and policy as summarized below and in the PDF enclosure. We welcome the opportunity to work with you to open safely, legally and ethically.

As the world learns to navigate COVID-19, opening schools safely is in everyone’s best interest. We have learned some California public school districts, such as LAUSD, and the California Department of Education (CDE) intend to mandate frequent Reverse-Transcriptase Polymerase Chain Reaction (RT-PCR) testing¹ on students and, when investigational COVID-19 vaccines are available to children, intend to mandate students and employees be vaccinated before they can return to campus. We are also monitoring CDE efforts to set up testing and vaccination centers on campuses.

Protracted school closures have created an educational and mental health emergency among students, due to learning loss from remote learning and isolation from their peers, sports, cultural activities, jobs and other support systems. Teen suicides are at an all-time high.² One of many tragic losses, teenager Dylan Buckner had “depression worsen significantly after COVID hit,” which led to his suicide. His father stated, “The family believes that had COVID not happened, or the country’s response to COVID had been more effective, Dylan would still be alive today.”³ In contrast, we invite you to learn more about how Alsea School Superintendent Marc Thielman opened schools in an Oregon county in Fall 2020 without incident.4

Mandating products approved for emergency use violates federal and state law since Emergency Use Authorization (EUA) means the products are investigational and experimental. Federal and state law is very clear that mandates are illegal for EUA products. Both the RT-PCR test and all COVID vaccines are not FDA-approved; they are available under an EUA.

The right to fully-informed consent has roots in the Nuremberg Code, which states the consent of the individual is “absolutely essential.”5 If an intervention causes greater harm, is ineffective for the stated aim, and illegal, as such you must re-evaluate implementing the proposed interventions as a condition for students to return to in-person learning.

Below we address the issues with your intended approach in four sections:

    1. The law surrounding Emergency Use Authorizations (EUA), under which both the RT-PCR and COVID investigational vaccines are being used on the public;
    2. Peer-reviewed science regarding
      1. (2a) The RT-PCR test, demonstrating that it is not a diagnostic tool and cannot determine if someone is sick or infectious, and;
      2. (2b) Emerging issues with the investigational COVID vaccine;
    3. Creation of on-campus COVID testing and vaccination centers; and
    4. Your institution’s real legal liability should you proceed with any plans to mandate investigational testing protocols or vaccines.

Note that while vaccine manufacturers may be shielded from liability by 42 USC 300aa-11 and 42 USC 300aa-22, your institution is not protected.6

You are hereby officially on notice that if you illegally or irresponsibly mandate products on students or public school employees, we may have no recourse but to take legal action. As an example, Children’s Health Defense has initiated a related suit in New York against the NYC Department of Education and Mayor de Blasio for arbitrary school closures and coerced PCR testing as a condition to in-person learning privileges.7 (Aviles, et al. V. de Blasio, et al. 20-CV-09829 (PGG)) 

(1) Emergency Use Authorizations (EUA): Illegal to Mandate Products Under EUA

PCR testing and COVID vaccines are not fully licensed products. They are EUA products,8 which by their very nature are legally considered investigational. As these are experimental medical products, it is unlawful and unethical for schools to mandate either the RT-PCR test or any currently available COVID vaccine. Federal law confirms explicitly that an EUA product must be voluntary because the federal statute requires “the option to accept or refuse administration of the product.”9

Mandating the RT-PCR and experimental COVID vaccines also violates California State law (CA Health & Safety Code § 24172).10 Federal and State law on this matter rest on the first principle of the Nuremberg Code requiring that the human subject be “so situated as to be able to exercise free power of choice without undue inducement or any element of force, fraud, deceit, duress or other forms of constraint or coercion.” This is a bright line that cannot be blurred.

Of note, specific laws such as the US Federal Regulations, notably the National Research Act [Title II, Public Law 93-348],11 Regulations for the Protection of Human Subjects of Biomedical and Behavioral Research [45 CFR 46]12 and revisions of various regulations, rules, and laws ([21 CFR 50]13, [21 CFR 56]14, [45 CFR 46 Subpart D]15, [10 CFR 745]16, [45 CFR 46 Subpart B]17, [45 CFR 46 Subpart D]18) specifically and permanently guarantee that all persons in the United States are entitled to exercise the right of informed consent to accept or to refuse to enroll in any medical experiment.

The CDC admits that it is illegal and unethical to mandate PCR testing in schools.19 Moreover, the States, and therefore public schools, cannot mandate the PCR test or COVID vaccines because the FDA and courts have found the federal preemption doctrine prevents States, and therefore public schools, from going outside the bounds of the Emergency Use Authorization law.20

This was also confirmed again last year at a CDC Advisory Committee on Immunization Practices (ACIP) meeting in August 2020, where ACIP Executive Secretary Amanda Cohn, MD stated:

“I just wanted to add that, just wanted to remind everybody, that under an Emergency Use Authorization, an EUA, vaccines are not allowed to be mandatory. So, early in this vaccination phase, individuals will have to be consented and they won’t be able to be mandated.”21

In conclusion, the law is clear that States, and therefore public schools, cannot mandate experimental products and are preempted from mandating an EUA product.22  The soonest the Moderna and Pfizer/BioNTech experimental vaccines could be considered by FDA for full licensure (in adults only) is when the trials are expected to conclude, on October 27, 2022 and January 31, 2023, respectively.

(2) The Faults with RT-PCR Testing and Emerging Dangers of the COVID Vaccines

The FDA may someday grant full licensure to the RT-PCR test and some COVID vaccines. For now, these products are approved for investigational emergency use only, as described above, so the problems with the reliability of the test and vaccine efficacy and safety are not technically relevant to the illegality of mandates.

Since the FDA may grant full licensure at some point, which may make it legal to consider mandating them, we must also advise you of the medical and scientific issues that make school mandates dangerous to the health and safety of the educational community under any circumstances.

Below we detail (a) documented issues with the reliability of the PCR test; and (b) COVID vaccine science showing no disruption of person-to-person transmission, concerning safety data, and other issues regarding COVID vaccines and children.

(a) Issues with PCR Testing as a Condition for In-person Learning or Teaching

We understand that California Public Schools intend to mandate regular RT-PCR testing on children, with the penalty of withholding access to in-person education if testing is not completed.  The CDC has declared mandatory PCR testing unethical and illegal.

The RT-PCR test does not confirm infectiousness. Food & Drug Administration (FDA) guidance states the RT-PCR test must only be used in the presence of symptoms. As such, the RT-PCR should never be used on healthy people, and should only be used in a clinical setting combined with an exam by a licensed medical professional.

On July 17, 2020 and updated on July 20, 2020, the CDC recommends a symptoms-based strategy for testing, meaning only those with symptoms should consider being tested.23

The EUA for the Roche PCR test states “positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status.”24

The Roche EUA also states “positive results do not rule out bacterial infection or co-infection with other viruses.” Any positive PCR test is unconfirmed if the patient is not also tested for flu, pertussis, tuberculosis, or many of the other 1400 human pathogens associated with symptoms similar to COVID-19. Skipping this standard differential diagnosis results in confirmation bias, attributing all symptoms like cough or a fever to COVID.

Since the RT-PCR test Cycle threshold (Ct) in the U.S. is set too high – at a Ct of 40 –  it can amplify a low viral load and be erroneously conflated with infectiousness.25   On January 21, 2021, the World Health Organization (WHO) further clarified that “careful interpretation of weak positive results is needed. The Ct needed to detect virus is inversely proportional to the patient’s viral load. Where test results do not correspond with the clinical presentation, a new specimen should be taken and retested using the same or different nucleic acid test (NAT) technology.”26

Dr. Anthony Fauci, Director of the National Institutes for Allergy and Infectious Diseases of the National Institutes of Health, acknowledged in July 2020 that a positive RT-PCR test above a 35 Ct is meaningless.

(“[I]f you get a cycle threshold of 35 or more, …the chance of it being replication-competent are [sic] miniscule. And we have patients – and it’s very frustrating for the patients as well as for the physicians – somebody comes in and they repeat their PCR, and it’s like 37 cycle threshold, but you almost never can culture virus for a 37 cycle threshold. So I think if someone does come in with 37-38, even 36, you got to say, ‘You know, it’s just dead nucleotides, period.”27

In fact, 97% of PCR positives are false positives if the cycle threshold is higher than 35. A critical review of the seminal Corman-Drosten study which established PCR testing standards concluded:

In case of virus detection, >35 cycles only detects signals which do not correlate with infectious virus as determined by isolation in cell culture; if someone is tested by PCR as positive when a threshold of 35 cycles or higher is used (as is the case in most laboratories in Europe & the US), the probability that said person is actually infected is less than 3%, the probability that said result is a false positive is 97%.”28

If you only read one reference in this entire letter, it should be the above to the Corman-Drosten Review: www.cormandrostenreview.com.  This paper describes in detail most of the shortcomings of the PCR test that is driving the fear of SARS CoV-2, the virus said to cause the symptoms called COVID-19.

Returning to the most egregious problem with the RT-PCR test, a scientific literature review study by Tom Jefferson MD found specific Ct values correlate with infectiousness or lack thereof, and suggests that a Ct of 35 is still too high: “The inability of PCR to distinguish between the shedding of live virus or of viral debris, means that it cannot measure a person’s viral load (or quantity of virus present in a person’s excreta.” In the review, all tests with Ct >30 resulted in non-infectious specimen. Jefferson also stated “weak positives (those with high Ct) are unlikely to be infectious, as a whole live virus is the prime requirement for transmission, not the fragments identified by PCR.”29

The RT-PCR test being set at a Ct of 40 in the United States is indeed far too high and creates what has been termed a “casedemic,” disrupting all of society but especially children’s education and mental health. We do not think California public schools should be furthering this problem by requiring a test that the scientific community has found to be utterly unreliable.

Even if RT-PCR tests do gain full licensure someday, California schools must certify to the students, staff and family the following, before our education system is further disrupted by a test that delivers a majority of false positives and doesn’t measure infectiousness:

      1. Provide all students and staff with fully informed consent and advise them of their right to decline taking a test, and the right for asymptomatic students and teachers to be in the classroom. In other words, testing must be voluntary.
      2. Refer symptomatic children and staff to their primary care physician for voluntary testing and treatment. Students and staff can return to in-person learning or work when they are symptom-free or have quarantined for the recommended 7 to 10 days.
      3. The primary care physician must rule out – via antibody or PCR testing – the other human pathogens that can cause symptoms similar to COVID-19.
      4. For any tests run on a student or staff member by the primary care physician, confirm the RT-PCR Cycle threshold is 28 or less, since that is the highest Ct with proof of replication-competent virus.
      5. Confirm with a DNA or RAT test that the presumptively ‘positive’ sample is positive and not just picking up dead RNA fragments or background noise by using Sanger sequencing on every potentially positive test, and then confirming any potential positives with a human cell culture to verify the existence of replication competent virus. If the sample is unable to be cultured, then the individual is not infectious.
      6. Demand that the test report includes viral load information, and not just a binary reading.
      7. Per the 1/21/21 WHO guidance, perform a second test if the first one is positive.
      8. Do not rely on antigen tests which are also fraught with issues of false positives and false negatives.

Current CDC guidance on testing in school settings states:

If a school is implementing a testing strategy [i.e. testing healthy and sick, not based on symptoms,] testing should be offered on a voluntary basis.  It is unethical and illegal to test someone who does not want to be tested, including students whose parents or guardians do not want them to be tested.30

Please also keep in mind that according to the CDC, schools should be the first to reopen and the last to close.31

Given the above, the best course of action for the CDE and Districts is to ensure that sick students stay home, as has been the policy for pre-COVID times. There are already many other evidence-based protocols in place to allow safe return to in-person schooling, such as: hand washing, temperature-taking, suggesting sick students stay home until symptoms have resolved, classroom disinfection, and improved HVAC systems. Students should not be the victims of an experimental test, which will lead to a furthering of the Educational Emergency and even more social isolation that leads to mental health issues and suicide.

(b) Children are Not Asymptomatic Vectors; Science Shows COVID Vaccines are Risky

It is well-accepted that children have a statistically zero chance of dying from COVID. The CDC shows the K-12 mortality rate from or with COVID is .00003.32 Any intervention, especially one that is prophylactic, must cause fewer harms to the recipients than the infection. Since children have the lowest death rate from COVID infection, the cost-benefit of administering to children an investigational vaccine with emerging safety issues is especially difficult to justify. Therefore, it is clearly irrational to vaccinate children with a COVID vaccine to protect them from death.

Given these facts, an unfounded theory has emerged to use students as pawns who, if vaccinated, could somehow stop transmission to teachers and school staff. However, the data show: students are not asymptomatic carriers, they and teachers have far lower rates of COVID diagnosis than the general population, and the vaccine does not prevent person-to-person transmission.

Contrary to popular opinion, asymptomatic transmission is unfounded. Students are not disease reservoirs and are clearly not COVID vectors. The School Response COVID Dashboard shows that students and staff are among the least likely to be diagnosed with COVID. Compared to the positivity rate of 8.1% in the general California population in the most recently available data period (12/13/20), only 0.56% of California students tested positive for COVID, and the staff positivity rate was only 1.46%, even though teachers are daily interacting with students. This proves it is a significant mistake to assume children are asymptomatic vectors.33 In fact, in Germany, students are valued as the “brakes” to COVID transmission.34

A recent CDC-funded study in Wisconsin concluded no staff members were infected by children, and transmission rates were very low:

In a setting of widespread community SARS-CoV-2 transmission, few instances of in-school transmission were identified among students and staff members, with limited spread among children within their cohorts and no documented transmission to or from staff members. Only seven of 191 cases (3.7%) were linked to in-school transmission, and all seven were among children.35 

You may be surprised to learn that Sweden – the country that famously did not lock down – had an excellent outcome among children. “Despite Sweden’s having kept schools and preschools open, we found a low incidence of severe Covid-19 among schoolchildren and children of preschool age during the SARS-CoV-2 pandemic. Among the 1.95 million children who were 1 to 16 years of age, 15 children had Covid-19, MIS-C, or both conditions and were admitted to an ICU, which is equal to 1 child in 130,000.”36

A meta-analysis of 54 studies on transmission amongst almost 78,000 participants found that only 0.7% of cases attributed to “household transmission” could have spread from pre-symptomatic or asymptomatic carriers in the household.37

Additionally, a study among 10 million residents of Wuhan China demonstrated that asymptomatic transmission was non-existent.38 Among 300 possible carriers, “virus cultures were negative for all asymptomatic positive and re-positive cases, indicating no “viable virus” in positive cases detected in this study. All asymptomatic positive cases, re-positive cases and their close contacts were isolated for at least 2 weeks until the results of nucleic acid testing were negative. None of detected positive cases or their close contacts became symptomatic or newly confirmed with COVID-19 during the isolation period.”

In contrast, a widely-quoted CDC-endorsed study claiming 59% of cases were due to asymptomatic transmission enrolled no subjects and is merely a mathematical model.39 To further clarify, here is a side-by-side comparison of the Wuhan study compared to the CDC study:

In a 2020 Health & Human Services press conference, Dr. Fauci stated “even if there is some asymptomatic transmission, in all the history of respiratory-borne viruses of any type, asymptomatic transmission has never been the driver of outbreaks.40 The driver of outbreaks is always a symptomatic person. Even if there’s a rare asymptomatic person that might transmit, an epidemic is not driven by asymptomatic carriers.”

Given the statistically zero COVID death rate in children, the low rate of COVID positivity in children, and the lack of asymptomatic spread, there is absolutely no case for the vaccination of children to protect them or others from COVID.

Should COVID vaccines become fully licensed in the future and still be (inexplicably) under consideration for schoolchildren and staff after reviewing the above, we explain below how the COVID investigational vaccines do not prevent person-to-person transmission and are fraught with mounting safety issues as reported in the media, in the V-Safe App (used post-vaccination by study participants,) and in the U.S. Vaccine Adverse Events Reporting System (VAERS.) Most significantly, the investigational vaccines have not been tested in children.

Since the COVID vaccines do not prevent person-to-person transmission, it is irresponsible to think this medical product could somehow protect adults by vaccinating children. Dr. Anthony Fauci admitted in October the goal of COVID vaccines is to provide personal protection only, not to prevent death, or person-to-person transmission. Fauci said he and his colleagues would “settle for … the primary endpoint to prevent clinically recognizable disease.”41 Moderna Chief Medical Officer Tal Zaks stated “our trial will not demonstrate prevention of transmission, because … you have to swab people twice a week for very long periods, and that becomes operationally untenable,” citing the need for a five-to-ten times longer trial length and even higher costs.42

Through January 15, 2021, 181 U.S. deaths43 have been reported after COVID vaccination to the Vaccine Adverse Event Reporting System (VAERS.)44 There are almost 8,000 total COVID vaccine reactions reported to VAERS so far, including 764 reports for serious adverse events.45 A CDC-funded study at Harvard Pilgrim concluded that “fewer than 1% of vaccine adverse events are reported” to VAERS, a passive reporting system.46 Therefore, it is reasonable to multiply any reported events by 100 to approximate the actual number of deaths and adverse events after any vaccination. In fact, the COVID vaccine serious injury rate, based on the December Advisory Committee on Immunization Practices meeting covering the first five days of COVID vaccination is 2.8%.47 Note that all approved COVID vaccines require two doses, so these data are mostly based on one dose. In the trials, the second dose was much more reactogenic, so we expect the serious injury rate to be much higher after the second dose.

In addition to these government-documented safety issues, hundreds of catastrophic injuries – like life-threatening anaphylaxis and a bizarre shaking syndrome – and deaths have been reported in the media and on social media.48 Most recently baseball great Hank Aaron died 18 days after receiving the first of two experimental COVID vaccines.49 These vaccines use brand new mRNA technology with known complications — and we can certainly anticipate many more unforeseen complications.50

In fact, today there are about two dozen vaccines in use in the United States and another 66 have been withdrawn, most for safety issues, such as LymeRix, RotaShield and DTP.51 These fully licensed vaccines were judged as safe with government approval. This shows a vaccine withdrawal rate of 73%. If three-quarters of fully licensed vaccines are withdrawn, the probability of a warp speed experimental vaccine being withdrawn is far higher.

We urge you not to put schoolchildren in harm’s way with an untested new technology in a quixotic attempt to prevent them from being asymptomatic vectors. COVID vaccines are more like a high-risk prophylactic drug that might only benefit the recipient, not anyone around them. There is no place for medical mandates, especially not for interventions that only provide personal protection. That is an individual choice. As mentioned above, manufacturers enjoy full liability protection when people are injured or killed by vaccines. The school district does not.

(3) On-Campus COVID Testing and Vaccination Sites

The CDE and some public school districts in California are contemplating or attempting to create COVID testing sites on school campuses. For all the reasons stated above, there should be no such sites established on any California public school campuses or school properties. While voluntary community or school testing might initially seem benign, these sites could easily be converted into vaccination centers for students, staff and the public. Again, because of the experimental nature of the vaccine, this too would be highly inappropriate.

(4) School District and California Department of Education Legal Liability 

In summary, mandating EUA products is illegal. Mandates do not allow for informed consent, which is spelled out clearly in California Health and Safety Code (CA Health & Saf Code § 24172).52 Relying on the RT-PCR or any other investigational testing product will lead to over-diagnosis and avoidable harms to many students and staff, including a discriminatory system where those who test negative can move freely while those who do not wish to be tested or those who test positive – even falsely positive – are denied their rights to an education and to work.

Those who are forced to learn remotely do not have equal access. Remote learning disadvantages the poor: some may not have a fast internet connection, and students may not have a quiet room with a computer to learn away from family distractions and household/neighborhood noise. Administering to students and staff a vaccine with known safety issues is reckless and will cause injury and death for which school districts and the CDE will be liable.

Being in the unenviable position of defending an illegal program in a Court of Law would certainly prove to be a distraction from your important work.

It is our sincere hope that your district would never seriously consider such mandates.

We respect your position and fully appreciate your duty to educate children safely. Children’s Health Defense – California Chapter will follow up with you to ensure you understand both the law and science. We aim to help you make the right decisions for the children of California. Please contact us at ca.team@childrenshealthdefense.org or 415-496-5301 should you need more information or if you would like scientific and legal help to operate lawfully and ethically.

Sincerely,

Alix Mayer, MBA
President & Board Director, Children’s Health Defense – California Chapter
Board Director, Children’s Health Defense

Cc: Ray L. Flores II, Attorney at Law


[1] Usually conducted via nasal swab.
[2] https://www.nytimes.com/2021/01/24/us/politics/student-suicides-nevada-coronavirus.html?referringSource=articleShare&fbclid=IwAR1SFUKTqmfiJB1F3_lEv_Xf3YAh9sUamm2_giT3cu6T9jARY6sbIlmP20M
[3] https://www.nbcchicago.com/news/local/suburban-football-star-dies-in-apparent-suicide-family-says-covid-worsened-depression/2411545/
[4] https://www.instagram.com/tv/CKUYGZGn4O8/?igshid=9xmjnp23bd8
[5] https://en.wikipedia.org/wiki/Nuremberg_Code
[6] https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title42-section300aa-22&num=0&edition=prelim
[7] https://childrenshealthdefense.org/defender/chd-sues-nyc-dept-of-education/?fbclid=IwAR3edlSvDa2QMqNAoCO5pSj4am0OPz9o-V9SMGkkTrdPoZJ-iFBD1lQmtOI
[8] (Decl. Varma ecf 19 P.43.)
[9] ” 21 USCS § 360bbb-3 (“Authorization for medical products for use in emergencies”).
[10] http://leginfo.legislature.cahttp://leginfo.legislature.ca.gov/faces/codes_displaySection.xhtml?sectionNum=24172.&lawCode=HSC.gov/faces/codes_displaySection.xhtml?sectionNum=24172.&lawCode=HSC
[11] https://www.govinfo.gov/content/pkg/STATUTE-88/pdf/STATUTE-88-Pg342.pdf#page=5
[12] https://www.ecfr.gov/cgi-bin/retrieveECFR?gp=&SID=83cd09e1c0f5c6937cd9d7513160fc3f&pitd=20180719&n=pt45.1.46&r=PART&ty=HTML
[13]https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=50&showFR=1&subpartNode=21:1.0.1.1.20.1
[14] https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCFR/CFRSearch.cfm?CFRPart=56
[15] https://www.hhs.gov/ohrp/regulations-and-policy/guidance/special-protections-for-children/index.html
[16] https://www.govinfo.gov/app/details/CFR-2011-title10-vol4/CFR-2011-title10-vol4-part745
[17] https://www.ecfr.gov/cgi-bin/retrieveECFR?gp=&SID=83cd09e1c0f5c6937cd9d7513160fc3f&pitd=20180719&n=pt45.1.46&r=PART&ty=HTML#sp45.1.46.b
[18] https://www.hhs.gov/ohrp/regulations-and-policy/guidance/special-protections-for-children/index.html
[19] https://www.cdc.gov/coronavirus/2019-ncov/community/schools-childcare/k-12-testing.html
[20] https://www.fda.gov/regulatory-information/search-fda-guidance-documents/emergency-use-authorization-medical-products-and-related-authorities
[21] US Centers for Disease Control (September 2020), August 2020 ACIP Meeting – COVID-19 vaccine supply & next steps.  https://www.cdc.gov/vaccines/videos/low-res/acipaug2020/Covid-19Supply-NextSteps_3_LowRes.mp4 (@1:14:40)
[22] See e.g., Lorillard Tobacco Co. v. Reilly, 533 U.S. 525, 570-71 (2001)
[23] https://www.cdc.gov/coronavirus/2019-ncov/hcp/disposition-in-home-patients.html and https://www.cdc.gov/coronavirus/2019-ncov/hcp/duration-isolation.html
[24] https://diagnostics.roche.com/us/en/products/params/cobas-sars-cov-2-test.html
[25] https://www.fda.gov/media/134922/download
[26] https://www.who.int/news/item/20-01-2021-who-information-notice-for-ivd-users-2020-05?fbclid=IwAR2FnuSklIn9qtxve9EEEK9ht5WVw-QzWyeRUJJ203q0II4YBJecbJRylrA
[27] TWiV 641: COVID-19, Video interview with Dr. Anthony Fauci, This Week in Virology, 4:22-5:10 (Jul. 16, 2020), at https://www.youtube.com/watch?v=a_Vy6fgaBPE
[28] www.cormandrostenreview.com
[29] https://www.medrxiv.org/content/10.1101/2020.08.04.20167932v4
[30] https://www.cdc.gov/coronavirus/2019-ncov/community/schools-childcare/k-12-testing.html
[31] https://www.cdc.gov/mmwr/volumes/70/wr/mm7003e1.htm?s_cid=mm7003e1_w
[32] https://www.cdc.gov/coronavirus/2019-ncov/community/schoolschildcare/k-12-testing.html
[33] https://statsiq.co1.qualtrics.com/public-dashboard/v0/dashboard/5f78e5d4de521a001036f78e#/dashboard/5f78e5d4de521a001036f78e?pageId=Page_c0595a5e-9e70-4df2-ab0c-14860e84d36a
[34] https://www.usnews.com/news/world/articles/2020-07-13/german-study-shows-low-coronavirus-infection-rate-in-schools and https://theweek.com/speedreads-amp/925304/german-researchers-argue-children-may-act-brake-coronavirus-infections
[35] https://www.cdc.gov/mmwr/volumes/70/wr/mm7004e3.htm?s_cid=mm7004e3_w#F2_down
[36] https://www.nejm.org/doi/full/10.1056/NEJMc2026670
[37] https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2774102
[38] https://www.nature.com/articles/s41467-020-19802-w
[39] https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2774707
[40] https://youtu.be/vrAvjU2LBkg
[41] https://finance.yahoo.com/news/fauci-vaccines-will-only-prevent-symptoms-not-block-the-virus-195051568.html
[42] https://www.bmj.com/content/371/bmj.m4037
[43] https://medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=NONE&EVENTS=ON&VAX=COVID19&VAXTYPES=COVID-19
[44] https://medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=AGE&EVENTS=ON&VAX=COVID19&VAXTYPES=COVID-19&DIED=Yes
[45] https://medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=AGE&EVENTS=ON&VAX=COVID19&VAXTYPES=COVID-19&SERIOUS=ON
[46] https://digital.ahrq.gov/sites/default/files/docs/publication/r18hs017045-lazarus-final-report-2011.pdf
[47] https://www.cdc.gov/vaccines/acip/meetings/downloads/slides-2020-12/slides-12-19/05-COVID-CLARK.pdf
[48] https://prezi.com/i/byzl22mqwfaa/experiences-following-cvv/
[49] https://childrenshealthdefense.org/defender/hank-aaron-dies-days-after-receiving-moderna-vaccine/?itm_term=home
[50] https://childrenshealthdefense.org/news/the-dengue-vaccine-a-cautionary-tale/
[51] https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/discontinued-vac.pdf
[52] http://leginfo.legislature.ca.gov/faces/codes_displaySection.xhtml?sectionNum=24172.&lawCode=HSC




Dr. Vernon Coleman: Doctors and Nurses Giving the Covid-19 Vaccine Will Be Tried as War Criminals

Doctors and Nurses Giving the Covid-19 Vaccine Will Be Tried as War Criminals

by Dr. Vernon Coleman
February 2, 2021

 

Truth Comes to Light editor’s note: This is a powerful, moving video presentation by Dr. Vernon Coleman.
You may find yourself sharing tears with him near the end as he speaks from his heart.



Original video available at Dr Vernon Coleman BrandNewTube channel.

[As a service to protect truth from censorship and to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

Dr. Vernon Coleman’s website: http://www.vernoncoleman.com/

Transcript:

I see that David Lammy, MP, a British politician, now says that the covid-19 vaccine is safe and it works. He is the latest in a long and growing list of celebrities who are enthusiastically endorsing the vaccine – though I rather fear that they have probably spent as much time looking into the facts of the vaccine as I have spent learning about flower arranging.

Just how Mr Lammy claims to know that the vaccine is safe and works is beyond me.

Let me tell you about Mr Lammy.

When he appeared on a television quiz show, he was asked to give the married name of scientists Marie and Pierre who won the Nobel Prize for physics in 1903 for their work on radium. Lammy’s reply was Antoinette. He got Marie Curie mixed up with Marie Antoinette.

When he was asked for the name of the building used as a prison by Cardinal Richelieu, he named Versailles instead of the Bastille. Versaille, for heaven’s sake! This is a man who served as a government minister.

He was asked who succeeded to the English throne after Henry VIII and offered Henry VII which showed a singular lack of mathematical skills.

And he once criticised the BBC for wondering whether the smoke from the Vatican would be black or white. He seemed to think there was an element of racism in this well-known way of announcing if a new Pope had been elected.

The thing about Lammy is that to me he doesn’t seem aware of the extent of his ignorance. He knows the covid-19 vaccine is safe and works because maybe he read it on a beer mat. Or maybe he has been conducting secret private clinical trials in his purpose built laboratory. Maybe he’s got a time machine which enables him to see into the future?

No, he says the covid-19 vaccine is safe and it works because someone in the Government says it’s safe and it works. Lammy is supposed to be a member of Her Majesty’s Opposition. His job is to question the Government and to protect his constituents. But he has rolled over and let Bill Gates, Prince Charles and Karl Schwab tickle his tummy.

Incidentally, I am well aware that a decent part of the medical and scientific community doesn’t believe that the stuff currently being promoted like a new brand of crisps is a vaccine at all. For the record I agree with them. It’s a form of gene therapy. I’d rather die than have that stuff in my body. But if I don’t call it a vaccine people who trust David Lammy, the Archbishop of Canterbury and the rest of the `roll over tickle my tummy and I’ll say whatever you want me to say’ celebrities won’t know what I’m talking about.

The fact is that even the WHO only expects these vaccines to help reduce the extent of the symptoms. They’re not promising that the vaccine will stop people getting covid-19 and they’re not expecting the vaccine to stop people spreading the infection if they do get it. If David Lammy and the Archbishop of Canterbury had done a little research they would know that.

They would also know that the vaccine is experimental.

The enthusiastic celebrities are promoting an experimental vaccine – or an experimental whatever it is.

The United States National Library of Medicine published details of the vaccine programme currently under way and they say that the trial will last two years.

Anyone having the vaccine is themselves taking part in an experiment. David Lammy and the Archbishop of Canterbury want your granny to take part in an experiment. And your granddad. And you too.

The medicines agency in the UK knows that it’s an experiment. They advertised for special software so that they could keep track of the high number of adverse events they were expecting.

For two years.

Of course, even after two years we still won’t know what’s going to happen to people who have the vaccine. Or what might happen to any children they might manage to have.

It’s all a mystery – though we do know that there are very real risks of changes to the immune system of those having the vaccine.

But it’s OK, David Lammy and the Archbishop of Canterbury say it’s OK.

They read it somewhere. Or someone told them. Or they saw a government advertisement. I bet you a pound to a peanut that they didn’t actually look through scores and scores of scientific papers before coming to that conclusion. I bet they didn’t make up their own minds before telling millions of people to take the bloody vaccine. They just repeated the garbage they were told. Garbage in, garbage out.

The fact is that no one – not even David Lammy – can possibly know if the vaccine is safe and effective because the trial is still under way. You can look at the paper yourself. It’s in the US National Library of Medicine. Look for clinicaltrials.gov. And you’ll see, on page 3 of 14, that the trial, or study, is expected to be completed on 31st January 2023.

Can you understand that, David? It’s an experiment. It’s not over yet. No one knows what is going to happen in two years. But vaccine loving Bill Gates – whose foundation is making a fortune – wants seven billion people to take part in the experiment.

We do know, however, that thousands of people who have had the vaccine have died or been seriously injured by it. That’s an undeniable fact.

Elderly people in care homes are dying in huge numbers. We’re told it’s the infection but it’s not, of course. It’s the damned vaccine they’re being given.

Now, let me tell you something else. And this should strike terror into every doctor, nurse or boy scout currently involved in giving or promoting these vaccines.

The Nuremberg Code on medical experimentation, written in 1947 for reasons which I hope I don’t have to explain even to David Lammy, stated that explicit voluntary consent from patients is required for human experimentation.

That means that patients must be told that they are taking part in a trial. And they must be warned of all the possible adverse events. That’s what informed consent means.

How many doctors and nurses jabbing people with this stuff are telling patients that it is a trial? How many are giving people the information they need to make a judgement?

I would guess somewhere close to none.

And so, legally, all those people giving vaccinations are war criminals.

War criminals never think they are war criminals, of course. At the end of World War II, the Nazis mostly claimed they were doing important work. Or just obeying orders. Doing what they were told.

None of that cuts the mustard, as they say.

Just doing what you’re told doesn’t stop you being a war criminal.

Let me be clear, everyone giving the covid-19 vaccines without explaining that it’s an experiment, and without listing all the possible adverse events, is a war criminal.

That’s not rhetoric. It’s not opinion. It’s fact.

If you don’t believe me, check it out for yourself.

War crimes are still taken fairly seriously, these days.

A lot of doctors and nurses are going to find themselves in the dock. And the people who endorsed the work they were doing may well find themselves there too. What’s the punishment, I wonder, for aiding and promoting the activities of a war criminal?

Meanwhile, those who believe David Lammy, the Archbishop of Canterbury and the other celebrities who have said that the covid-19 vaccine is safe and effective should know that the vaccine is turning out to be just as dangerous as I and other doctors warned it would be.

It was obvious before Christmas that these vaccines would kill and injure millions. For the proof, watch my previous videos or read the transcripts on my website www.vernoncoleman.com

Governments and government agencies are, of course, saying that the people who are dying and suffering awful neurological problems just happened to die or fall ill. They are claiming that the vaccine isn’t responsible.

Aint that odd?

They claim that if you die within 28 days of a fake test for covid-19 then you died of covid-19. The bus that ran you over had nothing to do with it. But they claim that if you die within 28 hours of having the jab then it’s a coincidence.

What bastards these people are. They lie, lie and lie again. This is genocide. When is the world going to wake up?

In America, courts have confirmed that deaths that occur 30 or even 50 years after an injury can be the result of the injury. To give but one example, in 1982, James Brady was shot by a man called Hinckley who tried to assassinate Ronald Reagan. Brady died in 2014 and his death was put down as a result of homicide.

It isn’t for government agencies to decide that deaths are coincidental. Coroners should be making the decision. There should be inquests on every patient who dies within 28 days or even longer of having a covid-19 vaccination.

But there won’t be.

Meanwhile, we have a horrifying avalanche of evidence showing that these damned vaccines are killing and maiming people – all for a disease which is proved to be no more dangerous than the annual flu.

I have read many, many reports of the deaths caused by the vaccines.

You can see details of the deaths on my website under the heading `How Many Are the Vaccines Killing’. The list also appears on Richie Allen’s website.

There is no doubt in my heart or in my mind.

This is global genocide.

How much longer are people going to be silent?

How many must die? How many must be crippled?

When will people like David Lammy admit that they’re wrong and stop promoting a deadly vaccine?




Manifesto: Stop Covid-19 Vaccination and Discrimination Against Unvaccinated Persons

Manifesto: Stop Covid-19 Vaccination and Discrimination Against Unvaccinated Persons

by Children’s Health Defense Europe
February 1, 2021

 

We must ensure that citizens are informed that the vaccination is NOT
mandatory and that no one is politically, socially, or otherwise pressured
to get themselves vaccinated, if they do not wish to do so themselves’

THE COUNCIL OF EUROPE IN STRASBURG,
JANUARY 27th 2021

 

FACT: COVID-19 VACCINATION IS NOT AN ACT OF SOLIDARITY, IT’S BLIND FAITH
The current Covid-19 ‘vaccines’ are not true vaccines but genetic engineering ‘injectables’

These products are injectables based on new experimental technologies that introduce genetic material into human cells.  In France, over 5000 citizens and doctors have filed a complaint against the use of the Pfizer and Moderna vaccines.     

mRNA Covid-19 injectables are a form of genetic hacking

This is a procedure in which foreign genetic material is inserted into our cells to give them new instructions.  Dr. Stephen Hoge, President of Moderna, has even compared this technology to the installation of new ‘software’.

Covid-19 ‘injectables’ are not legally required to undergo any type of GMO risk assessment

On July 15th, to accelerate the production of Covid-19 ‘vaccines’, the EU voted through a special waiver for these products, now not subject to EU GMO regulations.  The impact of these genetic engineering devices on our genome, or on the environment, will therefore not be assessed.  Manufacturers have ‘carte blanche’.  Children’s Health Defense Europe and several other NGOs have requested the annulment of this decision in the European Court of Justice.

Covid-19 ‘vaccines’ have not been shown to prevent transmission of the virus

In its press conference (at 18min) in early January 2021, on the vaccine roll out in Europe, the EMA confirmed that there is currently no data to show that the virus would block transmission.  The EMA ‘hopes’ that these injections will work but they just DO NOT KNOW.  This information was also repeated in a WHO press conference on January 28th.

Covid-19 ‘vaccines’ might slow down transmission OR might also accelerate spreading of the disease

In fact, countries such as the UK, Israel and South Africa, who have started mass vaccination campaigns, are now experiencing a surge of cases.  Reason asks to halt these campaigns and analyse the data before going on.

Taking a Covid-19 ‘vaccine’ is not an act of solidarity

You do not know what effect it will have on others.  Current Covid-19 vaccine clinical trials will not be completed until 2022 (EMA press conference). The only thing one can say is that you will be participating in a global experiment.

Some Covid-19 ‘vaccines’ have a very high rate of injury

22 severe side effects have been listed by the FDA, including anaphylactic shock, facial paralysis, permanent neurological damage, autoimmune reactions and cardiac arrest.  Significant numbers of deaths are tragically being reported such as in California, in Norway, in Gibraltar, in France and in the UK.

Many doctors refuse to take or administer these Covid-19 ‘vaccines’

Doctors have filed an official motion at the EMA to halt the Covid-19 vaccine clinical trials (and vaccination campaigns).  Doctors around the world are expressing their concerns about the safety of this vaccine and the requirement to respect free and informed consent: e.g. in California, in the USA, in France, in the UK.

There is a specific death risk associated with coronavirus vaccines

It is called Antibody-Dependent Enhancement (ADE) or immune facilitation or pathogenic priming and was observed in all previous attempts to develop a coronavirus vaccine.  ADE occurs when a vaccinated individual encounters the natural virus, which triggers an overreaction leading to organ failure and death.

The number of people who have died after a Covid ‘vaccine’ is alarming

In fact, several countries such as Germany and Norway are now hesitating to recommend the vaccine for the elderly or even reconsidering the use of these products at all.  The manufacturers contracted special deals to be exempt from liability so in the event of vaccine injury or damage, it is likely that nobody will be legally responsible and no one will pay any compensation.

PRINCIPLES: INFORMED CONSENT, NO PRESSURE, NO MANDATE
The Covid-19 vaccination campaign is a breach of the Nuremberg Code

Signed in 1947, after the horror of Nazi experimentation, this code has “identified informed consent as an absolute prerequisite for the conduct of research involving human subjects

The Covid-19 vaccination campaign is a breach of the Oviedo Convention

for the protection of human rights and the dignity of the human being with regard to biology and medicine”.

Coercion to take Covid-19 ‘vaccines’ would violate constitutional rights

In most countries, there are laws to enshrine each citizen’s free and informed consent to medical intervention.  For example, in France, the 2002 Kouchner law states that “no medical procedure or treatment may be performed without the free and informed consent of the individual, which consent may be withdrawn at any time”.

Coercion to take a Covid-19 ‘vaccine’ is a breach of the European Convention of Human Rights

On January 27th 2021 the Council of Europe, which advises the European Court of Human Rights in Strasburg, stated: ‘We must ensure that citizens are informed that the vaccination is NOT mandatory and that no one is politically, socially, or otherwise pressured to get themselves vaccinated, if they do not wish to do so themselves’.

Our decision-makers seem lost and confused

The “powers that be” are poorly informed, serving us with an incoherent discourse in constant contradiction with the epidemic reality.  We do not live in fear, guilt or contempt for alternative methods or the professionals who advocate them.

The Freedom We Demand Is a Lucid, Responsible and Evidence-Based Stance

The Manifesto is available in PDF. Click here. Download. Share.

 

© February 1, 2021 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 them in their efforts.




What’s in the COVID Tests? — Ongoing Deception & Horrific Crimes Against Humanity

What’s in the COVID Tests? — Ongoing Deception & Horrific Crimes Against Humanity

 

You’ll Never Guess What’s in the Tests (BitChute title)
Once Were the Living (Odysee title)
The Story of the 4th Industrial Modified Reset Man

by Spacebusters
February 1, 2021

 



What’s been put up your nose in nano dust “test swabs” and in your mRNA?

How the nano dust tech works.

4th Industrial Revolution & the Great Reset.

Transhumanist agenda.

Enslavement of humanity.

 

Connect with Spacebusters at Odysee and BitChute


See related by Spacebusters with Dr. Andrew Kaufman:
Hippocratic Hypocrisy: A Tale of Two Snakes 

See related by Dr. Tom Cowan:
Dr. Tom Cowan: Retrospective on 2020; How Science is Being Weaponized Against Us & Why We Must Understand Real Science




Community Bands Together to Rescue Elderly Woman Medically Kidnapped – The Life of a Senior Is Still Precious to Some

Community Bands Together to Rescue Elderly Woman Medically Kidnapped – The Life of a Senior Is Still Precious to Some

by Brian Shilhavy, Health Impact News
January 30, 2021

 

In a week where it was reported that the New York State Attorney General admitted that nursing home deaths in New York State for 2020, already recorded as numbering tens of thousands, were undercounted by as much as 50% with Governor Andrew Cuomo reportedly stating “Who cares?”, and where numerous reports all over the world have recorded hundreds of seniors dying in assisted care facilities this week after the roll out of the experimental COVID mRNA injections, something truly amazing happened in Vancouver, Washington last night.

The people of the community, many members of “People’s Rights Washington,” turned out in mass to rescue a 74-year-old woman at Legacy Salmon Creek Hospital where she had been medically kidnapped, and was being held against her will, and against the will of her daughter who has medical power of attorney for her mother.

This group of 40-50 citizens, 90% of whom were women (mothers) and their children, stared down an army dispatched from the Clark County Sheriff’s department in full riot gear, endured being grabbed by the throat and pepper sprayed, and refused to leave the hospital until 74-year-old Gayle Meyer was released back into the custody of her daughter, Satin.

Satin took her mother to the hospital the night before to get treatment for a urinary tract infection (UTI), and had been with her until 4 a.m. before returning home to get a few hours of sleep before heading back to the hospital the next day.

Their primary care physician had already written a prescription for an antibiotic, and Gayle was supposed to be released and sent home with her daughter, who is also her medical power of attorney.

But when Satin arrived at the hospital, she was told that not only could she not take her mother home, but that she could not even see her mother, because she refused to take a COVID test.

That’s when Satin called her friends, who responded by heading to the hospital to find out what was going on. The nursing staff allegedly changed their story a few times, first saying that Gayle had refused to take a COVID test and was therefore being quarantined, but then later allegedly changing their story and stating that Gayle did in fact take a COVID test, and had to remain in the hospital for at least 24 hours until the results of the test came back.

Her daughter Satin, who had been in the hospital with her mother the day before until 4 a.m., had made it clear that her mother did not need nor want a COVID test, since she only had a UTI and was only in the hospital to be put on fluids.

The nurses allegedly also stated to Satin that they had also put her mother on oxygen, which greatly surprised Satin and her friends who were now showing up at the hospital to support her and her mother. Her mother, Gayle, allegedly has never before had to be put on oxygen, and certainly a UTI does not warrant oxygen.

As we have documented many times since COVID started last year, many deaths blamed on COVID in fact are caused by improper treatment, especially when a patient is intubated and put on a ventilator, where the death rate is over 90%.

Obviously becoming very concerned at this point that her mother who had a simple UTI was now being medically kidnapped and forced to stay in the hospital against her will and receive treatments she did not want, Satin and her friends called the County Sheriff office to come and assist them get Gayle out of the hospital.

The woman who filmed the entire ordeal, Kelli Stewart, explained that she had spoken to the Sheriff dispatcher, and she was told that the Sheriff was not going to respond and get involved.

However, as they were talking, the dispatcher allegedly stated that now the hospital had also called, so they were sending officers to the scene.

As you will see in the video below, the Sheriff deputies and officers were there to protect the hospital and Big Pharma, and NOT to represent their constituents and fulfill their oath of office to protect their constituents, and in this case, to prevent a medical kidnapping.

In fact, at one point Satin attempts to enter the hospital behind another patient who was entering, and an officer grabs her by the throat, and pushes her back.

The officer then used pepper spray on the people who were standing outside, who were all unarmed and primarily women and children.

Everything was captured on video, and I have watched the entire 2 hours of film footage, and condensed it down to under 53 minutes. This is from our Rumble account, and it is also available on our Bitchute Channel.

Read the rest of the article at Health Impact News


 

Clark County Sheriff Page. Telephone: 564.397.2211 – Email: sheriff@clark.wa.gov

Legacy Salmon Creek Medical Center Page. Telephone: 360-487-1000 – Email.

Thanks to Cassandra Fairbanks at Gateway Pundit for breaking this story.


Truth Comes to Light editor’s note:

Full original video coverage of the event can be found at Ammon Bundy YouTube channel.  Part One. Part Two. An abbreviated version of the coverage can be found at Health Impact News rumble channel.

Additional coverage of the incident can be found at Gateway Pundit.


 

Connect with Brian Shilhavy at Health Impact News




How Many Millions Will Be Murdered by This Bio-Weapon Called the Covid-19 “Vaccine?”

How Many Millions Will Be Murdered by This Bio-Weapon Called the Covid-19 “Vaccine?”

by Gary D. Barnett, garydbarnett.com
January 30. 2021

 

People across this country and around the world are having horrible adverse effects or dying after taking this injection called an mRNA “vaccine.” It is not a vaccine at all, it is a bioweapon meant to cause any number of problems and death in order to satisfy the agendas of those few that claim to be the ruling class.

The elderly have been the hardest hit so far, because they are the first to be targeted with this weapon, and they already have in many cases, co-morbidities and compromised immune systems. The perpetrators of this “vaccine” policy fully understand this, and are attempting to claim that this injection has nothing to do with the very high percentage dying very quickly after taking the shot. This is the easiest group to target, because the state can manipulate the narrative much more effectively due to the age and weakened health condition of this targeted group. In addition, they are a captured control group that can be used for experimental purposes, and in the process, also be made much more vulnerable due to this captured state and close contact situation. This is by design. The evil Andrew Cuomo was able to take advantage of this tactic when he forced most all the people in nursing homes in New York to remain locked up together, even moving very many sick patients into these homes. That was simply a type of premeditated murder.

Mass injection at nursing homes is causing high percentages of deaths in a very short amount of time. The injection itself seems to be causing fatal sicknesses in these patients, causing stark changes in their health immediately, all leading to death.

These mRNA shots are not vaccines, but delivery systems meant to harm, control, and kill. No one knows the long-term and gene-altering effects of these poisons, so beginning with the elderly for this experiment was planned all along, and for obvious reasons. When the old and infirmed die, little attention is paid by this now indifferent and frightened population. Months or years from now when the long term effects begin to cause death in the younger and healthier crowd, it will all be blamed on some new or mutated virus strain, when in fact, it is likely that the fatal effects will have been due to vaccination of this bioweapon.

By using false PCR testing at high cycle rates, the old will be said to have Covid, when no such thing has ever been purified, isolated, or identified, and therefore does not exist. After testing positive, the deadly “vaccine” is given, and when the inevitable death occurs, it will be blamed on Covid. The narrative (propaganda) will then be that they had Covid so could not have died from the injection. How convenient for the state. They kill these poor people, and then use the deaths to further their agendas of fear in order to control all. These are evil psychopaths without any conscience or soul.

The highest percentage of deaths to date have been in nursing homes, but these deaths due to the state and its criminal partners in the pharmaceutical industry are being caused in most part by this toxic mRNA concoction that is more akin to a bioweapon than a vaccine.

Brian Shilhavy, editor at Health Impact News, has written about and described this situation thoroughly in his article titled:

24 Residents Dead in 3 Weeks as One Third of UK Nursing Home Residents Die After Experimental mRNA COVID Injections.

There is much research and information in this article, and what should be taken from all that is going on is to avoid this deadly bioweapon called a “vaccine” at all costs!

 

Copyright © 2020 GaryDBarnett.com

Connect with Gary D. Barnett




329 Deaths + 9,516 Other Injuries Reported Following COVID Vaccine, Latest CDC Data Show

329 Deaths + 9,516 Other Injuries Reported Following COVID Vaccine, Latest CDC Data Show
The numbers reflect the latest data available as of Jan. 22 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 329 reported deaths, 285 were from the U.S., and 44 were from other countries. The average age of those who died was 76.5.

by Children’s Health Defense Team, The Defender
January 29, 2021

 

As of Jan. 22, 329 deaths — a subset of 9,845 total adverse events — had been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before confirmation can be made that an adverse event was linked to a vaccine.

The reports, filed on the VAERS website between Dec. 14, 2020 and Jan. 22, describe outcomes ranging from “foaming at the mouth” to “massive heart attacks” to “did not recover.”

According to the Washington Post, as of Jan. 29, 22 million people in the U.S. had received one or both doses of a COVID vaccine. So far, only the Pfizer and Moderna vaccines have been granted Emergency Use Authorization in the U.S. by the U.S. Food and Drug Administration (FDA). By the FDA’s own definition, the vaccines are still considered experimental until fully licensed.

Even with the updated injury numbers released today, the CDC said Thursday that safety data shows “everything is going well.” According to USA TODAY:

“Early safety data from the first month of COVID-19 vaccination finds the shots are as safe as the studies suggested they’d be.

“Everyone who experienced an allergic response has been treated successfully, and no other serious problems have turned up among the first 22 million people vaccinated, according to the Centers for Disease Control and Prevention.”

According to the VAERS data, of the 329 reported deaths, 285 were from the U.S., and 44 were from other countries. The average age of those who died was 76.5.

States reporting the most deaths were: California (22), Florida (16), Ohio (18), New York (15) and KY (13). Most of the reports were from, or filed on behalf of people who had received only the first dose. About half of the people reporting had the Pfizer vaccine, the other half Moderna.

The Moderna vaccine lot numbers associated with the highest number of deaths were: 025L20A (13 deaths), 037K20A (11 deaths) and 011J2A (10 deaths). For Pfizer, the lot numbers were: EK5730 (10 deaths), EJ1685 (11 deaths), EL0140 (15 deaths), EK 9231 (12 deaths) and EL1284 (11 deaths).

Several deaths and multiple severe allergic reactions are under investigation in the U.S. and Europe.

Last week, California health officials temporarily paused a large batch of Moderna vaccines due to a high number of allergic reactions, but reversed that decision a few days later.

Anyone suffering from a serious injury will have little legal recourse because they will be directed to the Countermeasures Injury Compensation Program which has rejected 90% of vaccine-injury claims over the past decade.

On Jan. 3, Miami obstetrician Dr. Gregory Michael died after he suffered a hemorrhagic stroke. Michael died about two weeks after receiving Pfizer-BioNtech’s COVID vaccine. Although he became ill just three days after he got the shot, Pfizer said it didn’t think there was any direct connection to the vaccine. The New York Times quoted Dr. Jerry Spivak, a blood disorder expert at Johns Hopkins University, saying “I think it’s a medical certainty that the vaccine was related.”

Officials in Orange County, California, are investigating the death of a 60-year-old healthcare worker who died Jan. 9, four days after receiving his second injection of the Pfizer-BioNTech COVID vaccine. Tim Zook, an x-ray technologist at South Coast Global Medical Center in Santa Ana, was hospitalized on Jan. 5, several hours after being vaccinated. Zook’s wife, Rochelle Zook, told the Orange County Register that her husband’s health rapidly deteriorated over the next few days. She said she didn’t blame any pharmaceutical company and that people should still “take the vaccine — but the officials need to do more research. We need to know the cause.”

Data about deaths following receipt of the experimental Pfizer-BioNTech vaccine are also emerging from IsraelNorwayPortugalSweden and Switzerland. Norway launched an investigation into the vaccines after the Norwegian Medicines Agency received reports of 33 suspected adverse drug reactions with fatal outcomes following administration of the Pfizer-BioNTech vaccine. Pharma and federal agencies attributed the majority of these cases to “coincidence.”

Coincidence is turning out to be quite lethal to COVID vaccine recipients,” said Children’s Health Defense (CHD) Chairman Robert F. Kennedy, Jr. “If the clinical trials are good predictors, the rate of coincidence is likely to increase dramatically after the second shot.”

The clinical trials suggested that almost all the benefits of COVID vaccination and the vast majority of injuries were associated with the second dose.

While the VAERS database numbers are sobering, according to a U.S. Department of Health and Human Services study, the actual number of adverse events is likely significantly higher. VAERS is a passive surveillance system that relies on the willingness of individuals and professionals to submit reports voluntarily.

In December, CHD and Kennedy wrote to former FDA director, Dr. David  Kessler, co-chair of the COVID-19 Advisory Board and President Biden’s version of Operation Warp Speed. Kennedy told Kessler that VAERS has been an abject failure, with fewer than 1% of adverse events ever reported.

A critic familiar with VAERS’ shortcomings bluntly condemned VAERS in The BMJ as “nothing more than window dressing, and a part of U.S. authorities’ systematic effort to reassure/deceive us about vaccine safety.”

CHD is calling for complete transparency. The children’s health organization is asking Kessler and the federal government to release all of the data from the clinical trials and suspend COVID-19 vaccine use in any group not adequately represented in the clinical trials, including the elderly, frail and anyone with comorbidities.

CHD is also asking for full transparency in post-marketing data that reports all health outcomes, including new diagnoses of autoimmune disorders, adverse events and deaths from COVID vaccines.




German Medical Doctor Appeals to Her Colleagues Around the World

German Medical Doctor Appeals to Her Colleagues Around the World

by Children’s Health Defense Europe
January 21, 2021

 

“Physicians following their Hippocratic Oath must resolutely stand up for the well-being of their patients.”

Gerlinde Laeverenz-Foti, M.D., is a holistic physician and has been dealing with the issue around vaccination for many years. She turns to her colleagues on this occasion, stating that if physicians in particular are not attentive in this crisis, they will become complicit in a policy that makes a mockery of all human values and scientific standards.

Here is what she has to say:

I urge all physicians in this country and indeed around the world, without exception, to think outside the box of what we have been taught in medical school and beyond our further education.

Use your common sense, question and explore connections with a desire to know the truth. Trust in your gut feeling, something that every good doctor should be capable of. Do not be satisfied with what is written in your textbooks, but go one step further – on behalf of the human being, on behalf of your patients.

Being a doctor means being independent of any system, of opinions, of politics, of guidelines and directives, even of every (man-made) law. The only guideline that counts is to be found within yourself and your patient.

I would be very surprised if even one doctor could and would sign that vaccinations cannot pose a threat to a person’s health or life.

Why are vaccinations so trivialized and complications often neither recognized, let alone noted in the patient’s file?

And to those physicians who consider vaccinations to be useful – how many of you have studied them in depth, have delved deeper into immunology, studied the scientific and well-researched literature and listened to the testimonials of parents and patients?

To all of those who have seen or experienced as much suffering through vaccinations as I have, affecting children and their families, and to all of those who do not dismiss it from the outset with the sentence “this cannot come from the vaccine”. All of those that can no longer help but ask the questions and take a critical look at allopathic medicine.

Do not be complicit in this so-called “health policy” that neither respects the dignity and true development of man, let alone his soul and his being. Do not sell yourselves and the people entrusted to your care for fear of being defamed or because you believe that your professional existence will be threatened. This is an illusion anyway, because no one can take your vocation away from you except yourself. Rather work on rehabilitating the patients’ trust in the medical profession, which many people have now lost, and rightly so. Put your patients back in the centre of attention, listen to them with interest and a healthy curiosity. Take their concerns, doubts and fears seriously and take steps to educate yourselves independently. Especially in the context of vaccines and the current mask obligation!

Let us work together to ensure that we retain our sovereignty and independence. It is not up to politicians or a school principal to decide what is medically justifiable and how to assess a health risk to the individual! We as physicians should remain the decision makers here. Likewise, the patient entrusted to us must remain protected, and should not be made to discuss their personal health issues with a manager of a supermarket or their employer! This is degrading and shameful at the same time. This is a novel and absolutely unjustifiable disregard of human dignity, which we simply cannot accept!

And what about our children? We must protect them instead of handing them over to state measures! Right now, political fears and moves are being played out on the backs of our children – we physicians must not allow this under any circumstances, let alone accept it silently!

We must rise up, it is high time!

Dear colleagues, if you haven’t already done so, I urge you to come back to the ground of facts, to the real basis of medicine. Remember your Hippocratic Oath, the oath that you once took, and by which you committed yourselves to the well-being of the patient! Remember the reason for which you – hopefully – once became a doctor. Remember what is essential in life and what is really important in medicine. It is about the individual. And thus it is about the health of our society.

Remember what is essential when it comes to your medical responsibility.

You do have a great responsibility. Please be very serious about it. And, if you cannot do so because of fear or other reasons, then you should give up your license to practice medicine.

 

© [Article Date] 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 in their efforts.




Healthcare Worker Dies Four Days After Second Pfizer Vaccine, Death Under Investigation

Healthcare Worker Dies Four Days After Second Pfizer Vaccine, Death Under Investigation
The wife of Tim Zook, a 60-year-old x-ray technician who became seriously ill hours after getting his second Pfizer vaccine and died four days later, says “we need to know the cause.”

by Children’s Health Defense Team, The Defender
January 27, 2021

 

Officials in Orange County, California, are investigating the death of a 60-year-old healthcare worker who died four days after receiving his second injection of the Pfizer-BioNTech COVID vaccine.

Tim Zook, an x-ray technologist at South Coast Global Medical Center in Santa Ana, was hospitalized on Jan. 5, several hours after being vaccinated. Zook’s wife, Rochelle Zook, told the Orange County Register that her husband’s health rapidly deteriorated over the next few days. He died Jan. 9.

Rochelle Zook said her husband believed in vaccines, and that she didn’t blame “any pharmaceutical company” for his death. She also said:

“But when someone gets symptoms 2 1/2 hours after a vaccine, that’s a reaction. What else could have happened? We would like the public to know what happened to Tim, so he didn’t die in vain. Severe reactions are rare. In reality, COVID is a much more deadly force than reactions from the potential vaccine itself.

“The message is, be safe, take the vaccine — but the officials need to do more research. We need to know the cause. The vaccines need to be as safe as possible. Every life matters.”

Tim Zook was “quite healthy” his wife said, though he took medication for high blood pressure and was slightly overweight. “He had never been hospitalized. He’d get a cold and be over it two days later. The flu, and be over it three days later.”

According to news reports, Zook told his wife he wasn’t afraid to get the vaccine. He even photographed himself on Jan. 5 before he became ill, with a Band-Aid on his arm and holding a picture of his vaccination card.

In an email to the Orange County Register, Pfizer said it was aware of Zook’s death:

“We closely monitor all such events and collect relevant information to share with global regulatory authorities. Based on ongoing safety reviews performed by Pfizer, BioNTech and health authorities, (the vaccine) retains a positive benefit-risk profile for the prevention of COVID-19 infections. Serious adverse events, including deaths that are unrelated to the vaccine, are unfortunately likely to occur at a similar rate as they would in the general population.”

Zook’s death is the latest in a string of reports about deaths and/or allergic reactions to both Pfizer’s and Moderna’s vaccines.

As The Defender reported earlier this week, multiple state and federal officials are investigating the Jan. 21 death of a Placer County, California, man several hours after receiving a COVID vaccine. According to news reports, the man had tested positive for COVID in December. The cause of death and specific vaccine he received have not been released.

Last week, The Defender reported on the death of baseball legend Hank Aaron, 18 days after he received the first dose of the Moderna vaccine. Aaron’s death was initially reported as undisclosed, but according to USA Today, Aaron died of a massive stroke.

Earlier this month, a Johns Hopkins scientist told the New York Times it was a “medical certainty” that Pfizer’s vaccine caused the Jan. 3 death of a 56-year-old Florida doctor. Dr. Gregory Michael, whose wife described him as “perfectly healthy,” died of idiopathic thrombocytopenic purpura (ITP), a rare autoimmune disease, about two weeks after getting the first Pfizer vaccine. Florida health officials are investigating his death.

More than 40 deaths following vaccinations among elderly people in Norway and Germany prompted China health officials last week to call for a pause on the Pfizer and Moderna vaccines, especially among the frail elderly.

As of Jan. 15, 181 deaths have been reported to the U.S.government’s Vaccine Adverse Events Reporting System (VAERS) as possibly being related to COVID vaccines. A 2010 study by the U.S. Department of Health and Human Services concluded that “fewer than 1% of vaccine injuries” are reported to VAERS and experts say the government’s reporting system is “broken.”

Oddly, for the second day in a row, data from the Centers for Disease Control and Prevention’s VAERS WONDER System is “temporarily down.” Though you can’t see any of the data on adverse events that have been reported, you can still submit a report on any reactions to vaccines.




COVID: If They Haven’t Isolated the Virus, How Can They Make a Vaccine?

COVID: If They Haven’t Isolated the Virus, How Can They Make a Vaccine?

by Jon Rappoport, No More Fake News
January 27, 2021

 

Answer: They can’t.

“But…but, you see, we take a piece of RNA, and we inject it into the person, and the RNA forces the cells to manufacture a protein that’s very similar to a protein in SARS-CoV-2…and then the immune system swings into gear and produces antibodies to THAT protein, and THEN the person has achieved immunity from the virus…”

Sorry, no dice.

As I’ve been demonstrating for months now, there is no proof that SARS-CoV-2 exists [1] [2]. Therefore, “the piece of RNA” that’s injected can’t be assumed to be related to “the virus.”

Therefore, the protein which the cells produce in the body is merely CLAIMED to be similar to a protein in the unproven “SARS-CoV-2.”

There is no KNOWLEDGE here.

That piece of RNA which is injected into the body—why should we assume it has anything to do with a virus called SARS-CoV-2, when no one has an isolated specimen of this “SARS-CoV-2?”

We shouldn’t assume.

Therefore, everything that happens, inside the body, after the injection, is up for grabs. What is the immune system reacting to?

Why bother, in the first place, to make a vaccine against a virus when you don’t have the virus?

There are several ways to attack this absurdity, and they all come down to the same bottom line: no provable virus, forget the vaccine.

I keep coming up with analogies to explain the insanity of the COVID virologists—

“Three trains collided last night outside Chicago. Investigators who turned up at the scene this morning failed to find a shred of wreckage. But they insist the collision occurred, resulting in a vast explosion. The public is warned to stay away from the cordoned-off zone.”

That fanciful illustrations is LESS extreme than: “We’ve just released a vaccine for a virus that we never discovered.”

As I’ve explained in other articles and interviews, “discovering” the genetic sequence, the structure of the purported SARS-CoV-2, involves all sorts of conjecture [3] [4]. Researchers aren’t looking through some sort of cosmic microscope at rows of genes lined up like cars in a supermarket parking lot.

Researchers assume—on the basis of zero evidence—that certain older reference genetic sequences in libraries are contained in “the new virus.” They use a computer program to scavenge those sequences and build out the ASSUMED structure of “the new virus” and automatically smooth out any wrinkles or gaps.

This would be on the order of fabricating a hologram of a gun that the police will claim is the actual gun used in the commission of a crime.

“Yes, Your Honor, this image you see floating in mid-air IS the weapon Mr. Jones used when he held up the bank last month. It is not a ‘representation,’ as the defense counsel would have you believe. We’re talking about cutting-edge science. We have experts who will testify under oath…”

Judge: “In other words, sir, you’re telling this court that, if the bank teller had some sort of ‘anti-hologram’ program on his computer, he could have prevented the crime with a few clicks of his mouse. Very interesting. Let me ask you, which drugs are you on?”

Prosecutor: “None, Your Honor. Actually, such anti-hologram programs exist. In the area of COVID virology, they’re called vaccines, and they protect people against SARS-CoV-2…”

Above the entrances to virology institutes, they should inscribe: ALICE IN WONDERLAND.


SOURCES:

[1] https://blog.nomorefakenews.com/2021/01/26/sars-cov-2-has-not-been-proven-to-exist-shocking/

[2] https://blog.nomorefakenews.com/2020/12/01/the-sars-cov-2-virus-was-never-proved-to-exist/

[3] https://twitter.com/jonrappoport/status/1339769925402038273

[4] https://www.youtube.com/watch?v=R6-8VRGvNtQ




CNA Nursing Home Whistleblower: Seniors Are Dying Like Flies After COVID Injections

CNA Nursing Home Whistleblower: Seniors Are Dying Like Flies After COVID Injections

by Brian Shilhavy, Vaccine Impact
January 26, 2021

 

James (he gives his last name in the video) is a CNA (Certified Nursing Assistant), and he recorded this video as a whistleblower because he could not keep silent any longer.

James reports that in 2020 very few residents in the nursing home where he works got sick with COVID, and none of them died during the entire year of 2020.

However, shortly after administering the Pfizer experimental mRNA injections, 14 died within two weeks, and he reports that many others are near death.

The video is long (47 minutes), and it is clear that James is suffering from emotional stress, and he admits that he has nothing to gain from going public, and that he will probably lose his job for doing so.

But he makes it very clear that these were patients he knew and cared for (he is also a “lay pastor”), and that after being injected with the mRNA shot, residents who used to walk on their own can no longer walk. Residents who used to carry on an intelligent conversation with him could no longer talk.

And now they are dying. “They’re dropping like flies.”

His superiors are explaining the deaths as being caused by a COVID19 “super-spreader.”

However, the residents who refused to take the injections, are not sick, according to James.

James makes it very clear that as a Christian, he cannot live with his conscience anymore, and that he can no longer remain silent.

He is not anti-vaccine, but just sharing what he knows is true, regarding the people he has cared for in his profession for over 10 years now.

This is a very clear pattern now. Inject the elderly with the mRNA injections, then blame their illnesses and deaths on the COVID virus.

The only reason Big Pharma and their sponsored corporate media are getting away with this, is because more healthcare workers like James are not coming forward to speak up for the helpless.

Even many in the Alternative Media are guilty for not covering this genocide against our seniors, as James states, because people are more concerned with Donald Trump and Joe Biden political news, while people’s grandmother, grandfather, and others are being killed by these injections.

James calls upon other CNAs, nurses, and family members to go public and tell the world what is going on with these experimental mRNA COVID injections.

How many more lives need to be lost before we say something?

If you know what is happening, but are not speaking out, then you are part of the problem.

And shame on you in the Alternative Media who are more concerned about which tyrant should be president than you are about covering the greatest crime of genocide this country has ever seen.

Rescue those being led away to death; hold back those staggering toward slaughter.
If you say, “But we knew nothing about this,” does not he who weighs the heart perceive it? Does not he who guards your life know it? Will he not repay each person according to what he has done? (Proverbs 24:11-12)



Original video available at HealthImpactNews BitChute channel.

[As a service to protect truth from censorship and to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

Connect with Brian Shilhavy at Health Impact News 

cover image credit VaccineImpact.com

 




The CDC Just Solidified That Its Decisions Are Not Driven by Science

The CDC Just Solidified That Its Decisions Are Not Driven by Science

Sourced from ICAN NewsletterInformed Consent Action Nework
January 26, 2021

 

BREAKING NEWS:

The CDC, after removing the claim that “Vaccines do not cause autism” from its autism-vaccine webpage nearly six months ago, has just put back that claim in direct response to ICAN’s publicity about its removal! The science is clearly not there to support this claim. The CDC knows it. After capitulating to the removal of this claim for lack of science, in the end, the science did not matter.

This puts the nail in the coffin for any claim by the CDC that it follows the science. ICAN will be taking the CDC back to court to seek the removal of this unsupported claim.

This claim was first added to the CDC website in 2015. After relentless attacks pointing out that the science does not exist to support this claim, it was removed on August 27, 2020 without a whisper.

The removal followed ICAN’s lawsuit in which the CDC was forced to provide a list of the studies that the agency alleged support this claim. That list included twenty studies, not a single one of which involved any of the vaccines currently given to babies in the United States during the first six months of life.

Having been forced to face the fact that it cannot scientifically support its claim that vaccines do not cause autism, some individual or some group at the CDC did the right thing and removed this claim from the agency’s autism-vaccine webpage. That was six months ago.

A few days ago, ICAN broke the story of its removal, causing a public relations nightmare for the CDC. In response, the CDC, wasted no time putting its public image ahead of science by putting its unsupported claim that “vaccines do not cause autism” back on its website.

As long as the CDC makes this unsupported claim, the desperately needed research regarding vaccines and autism (and other neurological disorders) will never receive the serious funding it warrants. It may be only a few words on a webpage but those words have massive implications for the funding of vaccine-autism science.

The CDC does not appear to have any serious concern that its most recent data shows that 1 in 36 children born this year in the United States will develop autism. This is a true epidemic. Instead of listening to the 40% to 70% of parents with an autistic child that continue to blame vaccines for their child’s autism, typically pointing to vaccines given during the first six months of life, the CDC and public health authorities insult and demean these families by continuing to claim, without adequate support, that vaccines do not cause autism.

The CDC should stop waging this false media campaign against these parents and, instead, fund independent scientists to do the needed science! But it is plain this will never happen because it is not what drives the CDC. It would rather avoid the issue in order to protect its holy vaccine program and its public image. Shame on the CDC.

ICAN plans to take the CDC back to court to demand it remove the claim “vaccines do not cause autism” from its website. It will certainly be interesting to see how the CDC explains its whipsaw changes in position regarding vaccines and autism. Stay tuned.

 

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The Murky Ethics of Paying People to Get the COVID Vaccine

The Murky Ethics of Paying People to Get the COVID Vaccine
Facing sluggish demand, especially among healthcare workers, for Pfizer’s and Moderna’s experimental COVID vaccines, employers float a variety of incentives that some say border on coercion.

by Children’s Health Defense Team, The Defender
January 26, 2021

 

Three weeks into January, following the December decision by the U.S. Food and Drug Administration (FDA) to grant emergency use authorization for Pfizer’s and Moderna’s experimental mRNA vaccines, roughly 14 million Americans have received one or more doses of coronavirus vaccine.

However, the 14 million adults vaccinated thus far fall significantly short of Operation Warp Speed’s goal of administering 20 million shots by the end of 2020. Officials are offering two primary reasons for the “sluggish” vaccine rollout: logistical (supply-side) problems and the demand-side hurdle of vaccine refusal.

Scott Gottlieb, the former FDA commissioner who passed through the revolving door to join Pfizer’s board of directors in 2019, predicts that demand for the shots will become “soft” after just a third of the U.S. population has accepted the jab.

The fact is, despite the omnipresent messaging in favor of the experimental vaccines, many Americans’ interest in COVID-19 vaccination is tepid at best. This is particularly the case among the healthcare and nursing home workers being asked to take the risk of rolling up their sleeves first. Many are refusing the shots, taking pains to explain that they are not “anti-vaxxers” but object to being “guinea pigs.”

From Los Angeles to Ohio to Maine, up to 60% of vaccine-eligible frontline health workers are declining the as-yet-unlicensed mRNA vaccines. Health systems — “intent on getting doses to as many people as possible, as quickly as possible” — report that in some locations, the vaccine is “‘literally sitting in freezers’ because healthcare workers [do] not want to take it.”

The situation is similar in the nation’s nursing homes, where “workers have been more reluctant than residents to be vaccinated.” According to a group that represents for-profit nursing homes, half of long-term care staff are unwilling to get the COVID shots. And over time, nursing home employees who witness elderly residents dying within hours or days of getting their injections may become even more reluctant to play vaccine roulette.

Discussing the issue of mandates, a Yale executive declared in early December that it is possible to “accomplish [vaccination] without forcing people,” citing as evidence an occasion when he received a piece of cake in exchange for getting a flu shotAcknowledging that acceptance of experimental COVID-19 vaccines might require “more than a sheet cake,” he nonetheless suggested that “small financial incentives” might be adequate to the task.

Apparently, America’s private sector has reached similar conclusions. A growing number of companies (including, but not limited to, the healthcare sector) are offering “wary staff members” financial and non-financial incentives aimed at shifting employees’ decisional balance in favor of COVID vaccination.

The carrot

What do these incentives look like?

In Nazareth, Pennsylvania, the Gracedale Nursing Home is offering employees who take the jab a one-time payment of $750, “using money received through the federal CARES Act for the pay-out.”

The county officials who approved the payments admit, “there may be some reticence on the part of some staff to be inoculated with the COVID-19 vaccination due in part to the rapidity of its development.”

In Texas, the 26,000-employee Houston Methodist hospital system is offering a $500 “hope bonus” to workers who accept the COVID vaccine. But the hospital expects to “eventually” make the injection mandatory for employees.

Other facilities are offering more modest compensation. For example, a Wisconsin nursing home is providing a $150 bonus for staff who complete both doses, amounting to about eight hours’ pay for most workers. Atlanta’s A.G. Rhodes, a long-term care company, is offering raffle prizes — TV sets, paid time off and paycheck bonuses worth up to $500 — to staff who get vaccinated.

Nursing homes in Maine are exploring strategies “such as bonuses or time off to get vaccinated,” but also view non-monetary tactics such as peer pressure as fruitful.

Eager to jump on the feel-good bandwagon and “promote the importance of vaccination,” the National Football League has offered free Super Bowl tickets and “game day experiences” to 7,500 health care workers — as long as they have received both doses of COVID vaccine.

In commerce, the global grocery chain Aldi plans to give hourly workers two hours of paid time off per dose of vaccine (a total of four hours), “ensuring that all hourly workers who wish to receive the vaccine are able to do so without concern about losing pay or taking time away from work.”

Trader Joe’s, owned by heirs of Aldi’s founders, is making the same offer, as is Dollar General, which will give employees “a one-time payment equivalent to four hours of pay after receiving a completed vaccination.”

Instacart, the online grocery platform, has announced a $25 COVID-19 “vaccine support stipend” for in-store team members and the company’s “shoppers” (individuals who get paid to shop and deliver groceries) “as they take time away from Instacart to get vaccinated.”

Think tanks and ethicists chime in

Discussions about financial incentives for vaccination have also been circulating at high-profile think tanks, and some of the proposals make Instacart’s $25 stipend pale in comparison.

For example, former presidential hopefuls John Delaney and Andrew Yang endorse the idea of paying $1500 to any American who provides proof of vaccination. Meanwhile, Brookings Institution fellow Robert Litan is advocating for a $1,000 (tax-free) payment — although the latter cleverly proposes delaying most (80%) of the payment to vaccinated individuals until the nation achieves its desired level of vaccine coverage (a moving target that front men like Dr. Peter Hotez and Dr. Anthony Fauci have been steadily “inching … upward”).

On Jan. 6, medical experts from Cornell and the University of Pennsylvania aired an opinion piece in the Journal of the American Medical Association (JAMA), criticizing “payment-for-vaccination proposals” as being “morally suspect,” but not for the reasons one might think. The two authors’ principal objection — based on the historical, Nuremberg-Code-denying and ethically dubious assumption that “people have a moral duty to be vaccinated” — is that payment would “rob the act [of being vaccinated] of moral significance.” At most, the two say that they could accept reimbursing the vaccinated for expenses, “analogous to the modest payment offered to citizens summoned for jury duty.”

While not their top objection, the two authors do acknowledge “genuine” ethical concerns “about the influence of such an incentive on decision-making” and the risk that incentives could appear to be “trading on financial insecurity.” They state:

“Offering payment as an incentive for COVID-19 vaccination may be seen as unfairly taking advantage of those U.S. residents who have lost jobs, experienced food and housing insecurity, or slipped into poverty during the pandemic.”

Bioethicist Julian Savulescu of the UK’s Oxford Centre for Practical Ethics has a solution for this concern, described at length in Britain’s Journal of Medical Ethics in November. In his treatise, Savulescu benignly proposes a “payment in kind” model rather than cash, arguing that “greater freedom to travel, opportunity to work or socialise,” and “the freedom to not wear a mask in public places … and not to socially distance” would represent “attractive benefits” for the vaccinated.

The stick

As Savulescu sees it, overt vaccine mandates come with hassles, expenses and attacks on liberty that rile the public. In the near term, therefore, and also because the Pfizer and Moderna vaccines are still investigational, most officials promoting COVID-19 vaccination deny the prospect of a government mandate.

Instead, they seem only too happy to let the private sector set the tone for vaccine coercion — with monetary incentives representing the first, less threatening step.

Several developments in December suggest that the situation will get worse. First, right after the FDA granted the Pfizer vaccine its emergency use authorization, a Dec. 15 poll conducted by Yale highlighted “a surprising amount of openness to the idea of mandates for vaccines” among current and recent CEOs of major U.S. companies, including Walmart, Goldman Sachs, eBay, American Airlines, MetLife,and Pizza Hut. Although most were not yet ready to make employment contingent upon COVID vaccination, almost three-fourths (72%) of the CEOs endorsed the idea of mandates sometime “down the road.”

Right on cue, the Equal Employment Opportunity Commission (EEOC) issued, on Dec. 16, pandemic guidance stating that employers “generally can mandate” that employees receive a COVID-19 vaccine if FDA-authorized or approved, subject to protections for employees who seek medical or religious exemptions.

Art Caplan, a pharmaceutical-industry-friendly celebrity bioethicist at New York University once accused by Salon of being as willing to dispense sound bites as “sound moral thinking,” recently bragged about his former role as instigator of “the whole idea of mandating flu vaccination for healthcare workers” upon pain of losing their jobs.

In response to health workers’ pushback against mandatory workplace flu shots, Caplan unsympathetically wrote in 2009, “Enough already with the whining, moaning, demonstrating and protesting by healthcare workers. Doctors, nurses, respiratory therapists, nurses’ aides and anyone else who has regular contact with patients ought to be required to get a flu shot or find another line of work.”

Caplan’s recent comments make it clear that he, and others, are gearing up to make the same case for COVID-19 vaccines. While he concedes the difficulty of mandating “something that’s out on an experimental use authorization,” he states that “once vaccines get licensed, we will see mandates [for healthcare workers and nursing home staff] within the next week.”

Caplan also predicts the adoption of similar measures from other types of employers, who “will be insisting on mandates or telling you to stay home.”

Caught off guard

Public health officials appear to have been caught off guard by the extent of COVID-19 vaccine refusal among healthcare workers, and they surely must be concerned that workers’ reported loss of faith “in big pharma and even the CDC [Centers for Disease Control and Prevention]” may make employees impervious to the relatively modest amounts being dangled as financial incentives.

Weighing the risks and benefits (an activity in which all healthcare workers — all people — should be allowed to engage), a pregnant nurse who declined the mRNA injection told the Los Angeles Times that she was “choosing the risk of COVID,” observed over many months of caring for COVID patients, over “the risk of the unknown of the vaccine.”

Dr. Peter Hotez — who initially expressed caution about coronavirus vaccines but now has become one of the injections’ most reliable cheerleaders — has inadvertently identified the real problem: the obsession with vaccines as sole solution. As Hotez recently admitted: “[W]e put all our eggs in the biotechnology basket. We’re now relying exclusively on vaccines to control this.”

An even more significant problem is the doublethink message that is now equating vaccination with “freedom.”




Injured by a Vaccine? Here’s How to Report It

Injured by a Vaccine? Here’s How to Report It
CHD is calling on anyone who has suffered a vaccine side effect to do three things: file a report on the U.S. government’s VAERS website, report the injury on VaxxTracker.com and also here, on the CHD website. 

by Children’s Health Defense Team, The Defender
January 25, 2021

 

Children’s Health Defense (CHD) has joined other organizations around the globe in an effort to encourage, and make it easy, for vaccine recipients to report injuries and adverse reactions to any vaccines, including the new COVID vaccines produced by PfizerModernaAstraZeneca and others.

CHD asks that anyone who suspects they have suffered any kind of adverse side effect, from any vaccine, do all three of the following:

  1. For U.S. residents, first file your report with the Vaccine Adverse Event Reporting System (VAERS), the official site of the U.S. Department of Health and Human Services (HHS).
  2. Go to VaxxTracker.com to file a report. This is an outside source vs. government.
  3. Using this page on the CHD website, share the information you reported to VaxxTracker and VAERS, including the reaction you suffered and the vaccine you received.

VaxxTracker users can click on the option to report anonymously.

“With vaccines so much in the spotlight now, we have a tremendous opportunity to draw attention to the issues of vaccine safety and vaccine choice,” said CHD President Lyn Redwood, RN, MSN. “But we need the public’s help. That’s why CHD has joined in this effort to ensure that vaccine injuries are reported, so they can be analyzed and appropriate actions can be taken.”

VaxxTracker gives people a safe place to report symptoms they believe resulted from a vaccine. Users can also view charts and graphs illustrating the types of symptoms being reported, the number of symptoms associated with specific vaccines, and other trends.

CHD and other organizations will closely monitor adverse event reports collected by VaxxTracker to follow trends and report signals to the responsible federal agencies, the vaccine manufacturers and the public, Redwood said.

“The pandemic has resulted in the largest-ever massive global effort to convince, and in some cases coerce and bully people into not only being vaccinated, but to accept without question unlicensed, experimental vaccines, rushed to market and approved for emergency use only,” Redwood said.

“Instead of focusing on prevention and effective therapeutics, mainstream media, aided by slick PR campaigns, continues to report that all COVID vaccines are safe and effective, and that they are the only way to end the pandemic.”

Still, news reports of injuries and deaths are surfacing, in the U.S. and other countries. As The Defender reported last week, as of Jan. 7, 66 deaths had been reported to VAERS as possibly being related to COVID vaccines.

By law, Redwood said, healthcare workers are required to report any adverse events they suspect may be related to a vaccine. “We know that historically, this hasn’t always happened,” she said. Sometimes, the side effect didn’t occur immediately, and neither the patient nor the doctor connected the dots.

With COVID, Redwood said, healthcare workers are even less likely to report side effects, “simply because they are overwhelmed with treating patients who have the virus.”

A 2010 federal study commissioned by HHS and performed by Harvard consultants on behalf of the Agency for Healthcare Research and Quality found that fewer than 1% of vaccine adverse events are ever reported to VAERS.

In his Dec. 18 letter to Dr. David Kessler, newly named co-chair of then-President Elect Biden’s COVID-19 Advisory Committee, Robert F. Kennedy, Jr., CHD chairman and chief legal counsel, said regulatory officials can’t count on post-marketing surveillance to reveal COVID-19 vaccine injuries because VAERS “is broken.”

Kennedy wrote:

“COVID vaccine advocates argue that post-licensing surveillance will remedy the deficiencies in the pre-licensing clinical trial data collection system. As you know, this is not true. The Vaccine Adverse Event Reporting System (VAERS), a voluntary reporting system co-administered by FDA and CDC since 1990, is a well-documented public failure.”

As The Defender reported earlier this week, a new peer-reviewed study focused primarily on the measles-mumps-rubella-varicella (MMRV) vaccine, called vaccine injury reporting systems worldwide “utterly inadequate.”

“VAERS clearly states that it is a ‘passive reporting system,’” Redwood said. “That means HHS isn’t going out of its way to track vaccine injuries — the system is totally dependent on people who are injured to do the reporting. It’s critical, as employers and health officials float the idea of mandating COVID vaccines, that all injuries get reported.”

Visit the VaxxTracker about us page to learn more about the system and how you can use it.

 

cover image credit KitzD66 / pixabay




Employers Retract COVID19 Vaccine Requirements!

Employers Retract COVID-19 Vaccine Requirements!

by Informed Consent Action Network
sourced from ICAN newsletter
January 25, 2021

 

Announcement via Informed Consent Action Network newsletter:

ICAN’s legal team, led by Aaron Siri, has taken legal action to challenge employers/schools that require their employees/students to receive a COVID-19 vaccine.  Employers and schools that previously required the COVID-19 vaccine have dropped those requirements!  This includes an employer that did so on the heels of ICAN’s legal team challenging the mandate in court.

If you or anyone you know is being required by an employer or school to receive a COVID-19 vaccine, ICAN is pleased to offer to support legal action on your behalf to challenge the requirement.  In order to obtain this potential assistance, please email us at freedom@icandecide.org and provide a copy of the written notice from your school or employer stating that the COVID-19 vaccine is required.

Without your support, our ability to fight these illegal COVID-19 vaccine requirements would not be happening.  Thank you for making our work possible!

Please note that while we hope to help everyone, and hope to have sufficient resources to do so, depending on the volume of individuals that contact us and the amount of support we receive, we cannot guarantee we will have the sources to assist everyone that contacts us.

 

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David Rasnick: New Strain of the Coronavirus, or a Giant Con? How Deep Do the Lies Go?

David Rasnick: New Strain of the Coronavirus, or a Giant Con? How Deep Do the Lies Go?

by Jon Rappoport, No More Fake News
January 25, 2021

 

David Rasnick [1], PhD chemist, with a long history working in the pharmaceutical industry (Abbott, Prototek, Arris), broke away from official science and served as the president of Rethinking AIDS: the group for the scientific reappraisal of the HIV hypothesis. He was a member of the Presidential AIDS Advisory Panel of South Africa.

Here is a recent explosive statement Rasnick made [2] about SARS-CoV-2 and HIV. Digesting it brings about a breakthrough revelation:

“Viruses are unstable, RNA [e.g, SARS-Cov-2] viruses especially. They are so unstable, there is no such thing as an un-mutated RNA virus. They are like snow flakes, no two are identical.”

“HIV is an RNA virus with 9,800 nucleotides. You can download the HIV Sequence Compendium here:” [3]

“In the Preface it says:”

“’The number of [genetic] sequences in the HIV database is still increasing. In total, at the end of 2017, there were 812,586 sequences in the HIV Sequence Database, an increase of 8.5% since the previous year.”

“None of the sequences of the world destroying [sarcasm], computer generated coronavirus with its 30,000 or so nucleotides, are identical.”

“The virus maniacs use computers to compare the menagerie of sequences to come up with ‘A Consensus Sequence’ for HIV, Coronavirus, and all the rest. The consensus sequence exists in two places: in computers and in strings of RNA synthesized in the lab.”

“Even consensus sequences are not stable. Different groups, using a variety of computer algorithms will invariably come up with different ‘consensus sequences’.”

The implications of Rasnick’s statement are enormous.

First of all, forget about the idea that SARS-Cov-2 has one genetic sequence.

And these multiple sequences aren’t assembled by looking through a magic microscope. They’re put together by computer programs which have pre-set algorithms.

In other words, the sequences are built by ASSUMPTIONS (not evidence) embedded in the algorithms.

ANY vaccine developed for SARS-Cov-2 (even if you believe in the theory of how vaccines are supposed to work) would face the task of producing immunity to an ever-mutating virus—not just one mutated strain, but endless numbers of mutations.

You would have an analog to seasonal flu, in which researchers make a guess about what the new version of the virus will look like every year and develop a new vaccine for that guess.

How well is this working out? Public health agencies report that, each and every year, there are a BILLION cases of seasonal flu, worldwide.

Going still deeper, if the genetic sequences of the ever-mutating viruses are not discovered, but concocted via computer programs, how likely is it that a vaccine utilizing that “data” would work?

And at the bottom of the whole pile of guesswork, is, of course, the realization that, if these genetic sequences are concocted—where is the ACTUAL isolated virus? WHERE IS THE PROOF THAT IT EXISTS?

Where is it, when, as I’ve been reporting for months now, researchers twist and torture the meaning of “isolated,” so that it indicates “the virus is somewhere in a soup in a dish in a lab”—definitely UN-isolated.

Such is the “science” of modern virology.

But don’t worry, be happy, the test “for the coronavirus” must be accurate, the case and death numbers must be accurate, and the consequent lockdowns which are destroying national economies and hundreds of millions of lives are necessary…right?

Sure. Why not? Let’s say it’s all, all right. Everybody can go back to sleep and let tyrants demolish Earth civilization.

OR, you can REBEL against the Police State built on a house-of-cards hoax called “science.”

As opposed to “the virus,” liberty and freedom are quite real. People can feel them in their bones, in their minds and souls. Even and especially if they are slaves, they can feel them.

Speaking of whether a virus actually exists, here is an article I’ve reposted several times:

DOES HIV EXIST? AN EXPLOSIVE INTERVIEW

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

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

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

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

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

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

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

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

Was the purported virus ever truly discovered?

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

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

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

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

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

Here I’m publishing and highlighting excerpts from the interview [4] [5]. Technical issues are discussed. Grasping them is not the easiest exercise you’ve ever done, but I believe the serious reader can comprehend the vital essentials.

CJ: Does HIV cause AIDS?

EP: There is no proof that HIV causes AIDS.

CJ: Why not?

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

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

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

CJ: They say they did isolate a virus.

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

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

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

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

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

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

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

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

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

CJ: Did Montagnier and Gallo do this?

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

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

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

CJ: And what was that method?

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

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

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

CJ: But what about their pictures?

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

—end of interview excerpt—

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

And so…as I’ve reported these past few months, there is every reason to doubt and reject the existence of the COVID virus, since correct large-scale electron microscope studies have never been done.

I kept the Christine Johnson interview, and other similar information, in mind when, for example, I explored the dud epidemics called SARS and 2009 Swine Flu.

How many viruses have been named as causes of disease, when in fact those viruses have never been isolated or proved to exist?

Of course, conventional-consensus researchers and doctors will scoff at any attempt to raise these issues. For them, “the science is settled.” Meaning: they don’t want to think. They don’t want to stir the waters.

A few years ago, chemist David Rasnick sent a request to the CDC, asking for evidence demonstrating that the Ebola virus had ever been isolated from a human. The answers he received did not begin to approach a level of certainty.

After 30 years working as a reporter in the area of deep medical-research fraud, I’ve seen that false science occurs in levels.

The deeper you go, the stranger it gets. To put it another way: the deeper you go, the worse it gets.


SOURCES:

[1] https://www.davidrasnick.com/

[2] personal communication

[3] https://permalink.lanl.gov/object/tr?what=info:lanl-repo/lareport/LA-UR-18-25673

[4] http://virusmyth.com/aids/hiv/cjinterviewep.htm

[5] https://www.immunity.org.uk/articles/christine-johnson/

 

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cover image credit squarefrog, pixabay 




181 Dead in the U.S. During 2 Week Period From Experimental COVID Injections – How Long Will We Continue to Allow Mass Murder by Lethal Injection?

181 Dead in the U.S. During 2 Week Period From Experimental COVID Injections – How Long Will We Continue to Allow Mass Murder by Lethal Injection?

by Brian Shilhavy, Health Impact News
January 24, 2021

 

The Vaccine Adverse Event Reporting System (VAERS) is a U.S. Government funded database that tracks injuries and deaths caused by vaccines.

A 2011 report by Harvard Pilgrim Health Care, Inc. for the U.S. Department of Health and Human Services (HHS) stated that fewer than one percent of all vaccine adverse events are reported to the government:

Although 25% of ambulatory patients experience an adverse drug event, less than 0.3% of all adverse drug events and 1-13% of serious events are reported to the Food and Drug Administration (FDA).

Likewise, fewer than 1% of vaccine adverse events are reported. Low reporting rates preclude or slow the identification of “problem” drugs and vaccines that endanger public health. New surveillance methods for drug and vaccine adverse effects are needed. (Source.)

Currently, data from the two experimental mRNA COVID injections that have been voluntarily reported is available for a two week period from the end of December through January 13, 2021.

The data covers 7,844 cases, including 181 deaths.

The largest amount of deaths occurred in people over the age of 75.

There was at least one death recorded of an unborn baby dying just after the mother received an experimental mRNA Pfizer shot while pregnant:

I was 28 weeks and 5 days pregnant when I received the first dose of the COVID19 vaccine. Two days later (12/25/2020 in the afternoon), I noticed decreased motion of the baby.

The baby was found to not have a heartbeat in the early am on 12/26/2020 and I delivered a 2lb 7oz nonviable female fetus at 29 weeks gestation. (Source.)

As we have previously reported here at Health Impact News, the guidelines for emergency use of the experimental mRNA Pfizer injection in the UK warned pregnant women, and women planning to soon become pregnant, to NOT get the experimental jab.

But the FDA guidelines issued in the U.S. for the same experimental Pfizer injection did not include such warnings. See:

Unlike UK, U.S. FDA Allows Pregnant and Nursing Women to Receive Experimental Pfizer COVID Vaccine

When reading the accompanying notes from these cases that were reported to VAERS, it is clear that many healthcare professionals are reluctant to report these cases, probably fearing repercussions for doing so.

In some cases, family members filed the report because the healthcare facility refused to do.

Some examples:

(VAERS ID # 913733) My grandmother died a few hours after receiving the moderna covid vaccine booster 1. While I don’t expect that the events are related, the treating hospital did not acknowledge this and I wanted to be sure a report was made.

(VAERS ID # 914621) Resident in our long term care facility who received first dose of Moderna COVID-19 Vaccine on 12/22/2020, only documented side effect was mild fatigue after receiving. She passed away on 12/27/2020 of natural causes per report. Has previously been in & out of hospice care, resided in nursing home for 9+ years, elderly with dementia. Due to proximity of vaccination we felt we should report the death, even though it is not believed to be related.

(VAERS ID # 914895) Injection given on 12/28/20 – no adverse events and no issues yesterday; Death today, 12/30/20, approx.. 2am today (unknown if related – Administrator marked as natural causes)

Since so few reports are actually recorded in the VAERS reporting system, what is the true number of people being killed by these lethal injections? For those who are not killed, how many will be crippled or suffer autoimmune diseases for the rest of their lives?

If during pre-COVID times less than 1% of all vaccine injuries and deaths were reported to VAERS, let’s make a conservative estimate and say that because it is widely known that the COVID injections were fast-tracked to market and have not yet been approved by the FDA, that a greater percentage are being reported, like 10% of the adverse reactions, including deaths.

We are looking at a pace of nearly 1000 deaths per week by injection due to non-FDA approved mRNA injections among nearly 40,000 cases a week of injuries due to these injections.

This is a public health crisis that is 100% avoidable and 100% caused by Big Pharma and the U.S. Government!

While Almost ALL Deaths in 2020 Were Recorded as COVID Deaths, Here’s Why NO Deaths in 2021 Will be Recorded as Vaccine Deaths

It is well known now that due to federal funding for COVID in 2020 that nearly all deaths were recorded as “COVID” deaths, even in cases where the death occurred by traffic accident, shooting, heart attack, etc.

Now we are seeing the exact opposite happen with the roll-out of the COVID experimental injections. NONE of them are being recorded as vaccine deaths. Why?

Because the CDC does not provide a category for “vaccine deaths” to be used on death certificates. To learn more about this, see an article we published in 2018 from a Death Certificate Clerk whistleblower who revealed the politics behind listing “cause of death” on death certificates.

Death Certificate Clerk Reveals How Cause of Death Reporting is Subjective and CDC Statistics are Not Reliable When Making Public Health Decisions

She wrote:

Our current system for capturing mortality rates can and does provide a mostly uninvestigated and inaccurate picture of what causes a death. The process for creating and registering causes of death for public records is a complicated, convoluted, politicized, completely open to both ignorance and the manipulations of personal, professional, and governmental interests.

I’m the one creating these statistics and I offer you this: If you take one thing away from this, take away a healthier skepticism about even the most accepted mainstream, nationally reported, CDC or other ‘scientific’ statistics.

What most people don’t know is that doctors are not allowed to attest to anything that is not a strictly NATURAL cause of death. (Full article.)

Criminal Charges for MURDER Need to be Filed IMMEDIATELY – Experimental Injections MUST BE HALTED!!

We are witnessing the mass murder of Americans right before our very eyes, and the genocide of our elderly population!

Complicit with these murders is the Pharma-controlled corporate media that not only fails to publish these statistics derived from a government reporting system, but actually publishes lies and fake news to encourage people to receive lethal injections.

As an investigative journalist, I have consistently presented the evidence that should be used to arrest and charge the criminals behind this atrocity which is nothing less than MASS MURDER, and crimes against humanity.

In the spirit and legal protection of the U.S. Constitution’s Bill of Rights, and the First Amendment which protects Freedom of Speech and Freedom of the Press to criticize public officials, here is the short list of government officials who need to be arrested immediately and have charges brought against them for intent to commit mass murder by lethal injections, among many other charges such as fraud.

There are literally thousands, if not tens of thousands that should be arrested and charged, but these are the top 3 most responsible and who should be brought to justice immediately.

MURDERERS ROW

Dr. Anthony Fauci – Director of the National Institute of Allergy and Infectious Diseases (NIAID)

The evidence against Anthony Fauci for mass murder is overwhelming. Not only does he profit from bringing an experimental mRNA vaccine to market, something he has worked on for decades together with Bill Gates, but he has publicly demonized safer, effective drugs already approved by the FDA, such as hydroxychloroquine, that many doctors have been using successfully to treat COVID patients.

He has used his public office at the NIH to bring great harm and death against the American people, by capitalizing on so-called “health crises” such as COVID, and HIV in the past.

For more of the evidence against Anthony Fauci, see:

Medical Doctors Across the U.S. Continue to Expose Murderous Anthony Fauci for Withholding Life-Saving HCQ for COVID

More Doctors Speak Out on Censorship and Mass Murderer Anthony Fauci’s False Information Regarding Hydroxychloroquine

SCANDAL! Anthony Fauci has been Mass Murdering People for Decades! Prevented AIDS Patients from Receiving Life-saving Cheaper Drug

Dr. Stephen Hahn – Director of the Food and Drug Administration (Former)

Stephen Hahn was appointed by President Trump to lead the FDA, and his actions prevented doctors across the country in emergency room and hospital settings from using safe, already approved by the FDA, drugs that doctors were saving lives with, such as hydroxychloroquine and ivermectin.

In addition, Hahn allowed fast-track approval of the experimental mRNA COVID injections illegally, because there were already other successful therapeutics in the market to treat COVID.

Hahn also ignored an ADMINISTRATIVE STAY OF ACTION that was filed with the Department of Health and Human Services and Food and Drug Administration (FDA) to stop emergency use authorization of the COVID injections, because the trials used the faulty PCR tests to determine the presence of COVID in evaluating the “effectiveness” of these new experimental injections. See:

“Stay of Action” Filed Against FDA to STOP Approval of COVID Vaccine for Using Faulty PCR Tests in Trials

His failure to act upon this “Stay of Action” makes him criminally liable for all of these deaths resulting from the COVID experimental mRNA injections. For more evidence against Stephen Hahn, see:

The FDA is Killing Tens of Thousands Americans by Refusing Physicians’ Request to Approve Outpatient use of HCQ

Donald J. Trump – President of the United States

I don’t know if Donald Trump is the current or only former President of the United States (depends who you ask), but one thing nobody can disagree about is that President Trump initiated “Operation Warp Speed” which resulted in the theft of America’s wealth and transfer over to Big Pharma, for several TRILLION dollars, to develop experimental mRNA COVID vaccines.

He ordered the military to participate in their distribution, and he pressured the FDA to issue emergency use authorization, threatening to fire the FDA director for not issuing the EUA quicker.

Up until his last day of this first term, he bragged about how these “vaccines” were brought to market in record time, whereas the normal FDA approval process takes 5-10 years.

These experimental COVID mRNA injections would not be in the market today killing people, if it were not for President Trump leading the way to their approval.

Donald J. Trump should be arrested and charged with mass-murder. For more evidence against President Trump, see:

Is President Trump’s “Illness” Really a Commercial for Regeneron’s New COVID Drug?

Trump to do Full 5-Day Course of Remdesivir – Betrayal of Hydroxychloroquine Doctors?

Is Trump the Most Pro-Pharma President in History? QAnons Continue to Lose Credibility

President Trump Threatens to Fire FDA Chief Unless He Approves Pfizer COVID Vaccine Immediately

If these three are indicted by a Grand Jury, brought to trial in front of a jury of their “peers”, and then convicted as “guilty,” they should be publicly hanged on a gallows for all to see, and Joe Biden and his administration and health officials should be warned that they are next, unless they stop these injections IMMEDIATELY.

To do this, of course, we will need the restoration or formation of militia groups as provided by the Constitution, and they will probably have to convene Grand Juries to bring charges against corrupt judges first, to remove them from the bench so honest judges can be appointed, or elected, so law and order can be restored to the Court Houses.

Constitutional Sheriffs [21] can also be utilized (many of their deputies serve as bailiffs in the court rooms,) as these crimes have been committed in probably every county in the U.S. where people have been injured or killed by these injections, and most every county is going to have dishonest, corrupt judges who need to be brought to justice and removed from the bench.

Because otherwise there is little hope for any political solution. We the People need to start exercising our Constitutional rights, and take our country back from the Globalist pedophiles who now run the show.

 

Comment on this article or connect with Brian Shilhavy at Health Impact News




Eagle Scout Sues Merck, Alleges Gardasil HPV Vaccine Destroyed His Life

Eagle Scout Sues Merck, Alleges Gardasil HPV Vaccine Destroyed His Life
This is the fifth Gardasil lawsuit Baum Hedlund and CHD Chairman Robert F. Kennedy, Jr. filed against Merck, challenging the company’s dangerous and defective HPV vaccine for causing severe and life-changing injuries.

by Robert F. Kennedy, Jr., The Defender, Children’s Health Defense
January 21, 2021

 

Before he got the Gardasil vaccine, our client Michael Colbath was a superlative athlete and scholar. A happy, healthy and active boy, he was an enthusiastic member of his school’s academic teams, soccer player, and long-distance runner who loved backpacking and skiing. At five years old, he could backpack five miles with ease. At six, he taught himself to speed read and handed in a book report on a 600-page novel.

Michael was a committed boy scout and member of his middle school’s cross-country team. He pursued his passions for robotics, played in his school band and practiced Tae Kwon Do, earning his second-degree black belt at age 14, just months before he received the Gardasil HPV vaccine.

He raised service dogs for the disabled and earned his certification in first aid with special training in emergency preparedness.

After the vaccine, that all went away.

Years of Merck’s relentless marketing persuaded Kathy Colbath to allow her child to receive Gardasil. Merck falsely claimed that Gardasil was safe and effective, and that it would protect children against certain cancers. Merck’s advertising said that good mothers must vaccinate their teenagers with Gardasil or face tragic consequences.

In the months following his first injection, exhaustion and extreme fatigue forced Michael away from the sports and hobbies that had been centerpieces of his life. He had trouble staying awake during the school day.

After his second Gardasil injection, Michael developed severe foot pain in both feet, so severe that he needed crutches to attend school. He had trouble waking up in the morning and getting out of bed.

As his symptoms worsened, multiple physicians and specialists treated him for migraine headaches; body pains and muscle aches; chronic fatigue; hypersomnolence (sleeping 15-22 hours in a 24-hour period), sleep drunkenness, unrefreshing sleep; excessive sweating, lightheadedness, and tachycardia; tunnel vision on standing; difficulty with concentration and memory; confusion and brain fog; intermittent or episodic paralysis, numbness; and stomach pains.

Michael’s post-Gardasil injuries and diagnoses, including postural orthostatic tachycardia syndrome (POTS)idiopathic hypersomnia (IH)myalgic encephalomyelitis / chronic fatigue syndrome (ME / CFS)complex regional pain syndrome (CRPS) and gastroparesis, kept him from his passions, sports and hobbies. He missed most of high school and only his formidable self-discipline allowed him to complete his school work at home — he could not walk or move unassisted, he earned his Eagle Scout award using a knee scooter.

Only this unusual talent and drive allowed him to earn admission into the University of California San Diego (UCSD), as a data science major. He can only take a class or two at a time.

Michael is currently taking a daily regimen of 10 strong medications. He can only walk about 500 steps per day.

If Mrs. Colbath had known that Gardasil could create these health issues, she never would have allowed him to receive it.

This is the fifth Gardasil lawsuit Baum Hedlund and I have filed against Merck challenging the company’s dangerous and defective HPV vaccine for causing severe and life changing injuries. In addition to Mike’s case filed this week, we have filed cases on behalf of Sahara Walker of WisconsinZach Otto of Colorado and Julia Balasco of Rhode Island. While each case is unique, they share common threads: All of our clients were happy, healthy, bright, active kids with unlimited potential until they received the Gardasil HPV vaccine. We look forward to getting these cases in front of a jury as soon as possible.




How Many People Are the Vaccines Killing?

How Many People Are the Vaccines Killing?

by  Dr. Vernon Coleman
January 2021

 

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:

1) A 41-year-old Portuguese mother of two who worked in paediatrics died at a hospital in Porto just two days after being vaccinated against covid-19
Portuguese health worker 41 dies…

2) Norway is investigating the deaths of two nursing home residents who died after being vaccinated against covid-19
Norway investigating death of two people who…

3) Chinese health experts call to suspend the use of mRNA-based covid-19 vaccines following the deaths of 23 elderly people in Norway.
Chinese health experts call to suspend Pfizer’s mRNA vaccine…

4) In Florida, U.S., a doctor died after suffering a stroke after receiving a covid-19 vaccination.
Death of Florida Doctor

5) A 32-year-old medical doctor suffered seizures and was paralysed after receiving the covid-19 vaccine.
Doctor is paralyzed after…

6) Fifty-five people have died in the U.S. after receiving covid-19 vaccines.
55 people have died in US after receiving covid-19 vaccines

7) A 46-year-old healthcare worker dies 24 hours after receiving the covid-19 vaccine but government says death is not related to the jab
A 46-year-old healthcare worker…

8) German specialists are looking into the deaths of 10 people who died after being vaccinated against covid-19
German specialists probing 10 deaths of people vaccinated against covid-19

9) Norway warns frail patients over 80 of vaccine risks after deaths
Norway warns….

10) Norway investigates 23 deaths in frail elderly patients after vaccination
Norway investigates…

11) Doctors in California call for urgent halt of moderna vaccines after many fall sick
Doctors in California…

12) Two people in India die after receiving the covid jab
Two people die…

13) Coronavirus vaccine put on hold as volunteer suffers serious adverse reaction
Coronavirus vaccine put on hold…

14) California pause some covid vaccinations after reactions
California pause some…

15) Thousands of covid vaccine injuries and 13 U.S. deaths reported
Thousands of covid…

16) Nursing home had zero covid deaths then it vaccinates…
Nursing home had zero deaths…

17) Baseball legend dies of ‘undisclosed cause’ 18 days after receiving covid vaccine
Baseball legend dies…

18) Woman injured by vaccine (Warning: disturbing video)
Woman injured…

19) Mother seriously injured by covid vaccine (Warning disturbing video).
Mother seriously injured

Those are just some of the possible deaths and injuries that have followed vaccination.

I have no doubt that the authorities will claim that these deaths were coincidental.

And let us remember if a patient dies within 28 days of being tested positive for coronavirus (and the test doesn’t mean that the patient even has the disease since most tests are false positives) then the death will be listed as a covid-19 death and the patient will be said to have died ‘with’ covid-19. So by the same token, it is perfectly reasonable to say that if a patient dies or falls ill within 28 days of being vaccinated then the death or illness was related to the covid-19 vaccine.

Will the mainstream media ever start recording these deaths or illnesses? Or are journalists going to continue to promote the official government line – and to deny, distort or suppress the truth?

How many people have to die before the media wakes up?

NOTE: According to the National Vaccine Information Centre in the US, 13 people had died of the covid-19 vaccine by the 30th December 2020.

Other Important Covid Vaccine Information

1) Covid-19 vaccine side effects world map
vaccine side effects

2) Personal experiences relating to the new covid vaccines (Very important. Please read and share)

3) Pathogenic priming in older adults yet another concern with covid-19 vaccines
Pathogenic priming …

4) Top coronavirus official warns that second dose of covid vaccine tends to cause even worse side effects than first dose
Second dose of covid vaccine

5) CDC: Anaphylaxis rate with covid vax 10 times greater than for flu shots
Anaphylaxis rate…

6) Warning: mixing coronavirus vaccines
Warning: mixing…

7) UK draws up plans to mix coronavirus vaccines
UK draws up plans…

8) Helsinki Committee to declare Pfizer performing unauthorized human experiment in Israel
Helsinki Committee…

9) 12,400 people in Israel tested positive for coronavirus after being injected with the Pfizer vaccine
12,400 people in Israel…

10) Australian vaccine abandoned over false HIV positive results
Australian vaccine abandoned…

11) More vaccine adverse event reports
More vaccine…

Covid-19 Vaccine – Possible Vaccine Side Effects

The pro-vaxxers like to tell you that vaccines are perfectly safe and perfectly effective. Even when they wouldn’t be considered safe enough to use as oven cleaner, the fanatics enthuse about them. Young people and those who know little about medicine or science, talk about vaccines with reverence because they’ve been indoctrinated into believing the pro-vaccine lies.

And the pro-vaxxers are lying, of course.

Vaccines cause a lot of illness and quite a few deaths and they don’t always do what they’re supposed to do. Governments around the world have paid out many billions of dollars to patients who have been made ill by vaccines – or to the relatives of patients who were killed by a vaccine.

There are, for example, grave doubts about what the covid-19 vaccine actually does. Since the vaccine is a new type of vaccine and is being given before the usual tests and observations have been completed no one knows what will happen to the people who have the stuff injected into an arm.

What side effects will there be? How many will die?

Well, I don’t know and nor does anyone else.

What if a woman is pregnant when she has the vaccine or gets pregnant after being given the vaccine? The vaccine isn’t supposed to be given to pregnant women but not all pregnancies are planned.

Will the vaccine interfere with essential life-saving drugs? Many elderly patients already take a number of prescribed drugs. Will the vaccine interfere with them? No one knows. The covid-19 vaccine is the biggest experiment in history. And, unlike a proper clinical trial, it is largely unregulated. As with all vaccines most of the problems which develop will never be reported or recognised.

It is estimated that in the U.S., only 1 in 100 vaccine side effects is reported.

The best we have is a working list of possible adverse event outcomes which the FDA has published in the US. (Here is the link to the draft working list)

Since I believe everyone is entitled to know what side effects there could be with a heavily promoted vaccine, I’m going to read you the official list of possible side effects. This is, remember, not my list but a draft list compiled by the FDA – the Food and Drug Administration in the US.

Guillain-Barre syndrome
Acute disseminated encephalomyelitis
Transverse myelitis
Encephalitis
Myelitis
Encephalomyelitis
Meningoencephalitis
Meningitis
Encephalopathy
Convulsions
Seizures
Stroke
Narcolepsy
Cataplexy
Anaphylaxis
Acute myocardial infarction (heart attack)
Myocarditis
Pericarditis
Autoimmune disease
Death
Pregnancy, Birth outcomes
Other acute demyelinating diseases
Non anaphylactic allergy reactions
Thromocytopenia
Disseminated intravascular coagulation
Venous thromboembolism
Arthritis
Arthralgia
Joint pain
Kawasaki disease
Multisystem inflammatory syndrome in children
Vaccine enhanced disease

You aren’t necessarily going to get all of those or even any of them if you have the vaccine. But those are the possible side effects that the FDA has listed. They’re all unpleasant, most of them very serious and you can’t get more serious than death.

And if you are mad enough to have the vaccine then you and your doctor should keep a look out for the symptoms of all the diseases on the FDA’s list.

Your government won’t tell you about these dangers – they don’t believe in fully informed consent as far as vaccines are concerned.

Indeed, most governments are now doing everything they can to ensure that all criticisms of vaccines are banned. Depending on where you live it is, or soon will be, illegal even to mention that vaccines might not always work or might make you ill.

Finally, if your government really cared about you they would conduct a very simple, cheap trial.

They would keep a note of all the health problems affecting 20,000 patients who had the vaccine and compare that list with a list of all the health problems affecting 20,000 patients who didn’t have the vaccine in the same period. They make the comparisons every 3, 6 and 12 months.

Of course, they’d have to find some honest doctors to oversee the trial because it would be very easy to fiddle.

But it would give some very interesting results so I doubt if they’ll be doing it.




Healthcare Workers in India Fake COVID-19 Vaccine Jabs Concerned With Side Effects

Healthcare Workers in India Fake COVID-19 Vaccine Jabs Concerned With Side Effects

by GreatGameIndia
January 23, 2021

 

Numerous healthcare workers in India have been reported to fake taking the COVID-19 vaccine shots due to concerns of side-effects and pressure from the administration to take it.

Healthcare workers across Bengaluru are faking getting the Covid-19 vaccine, officials in Bengaluru admitted.

A senior BBMP health officer told the Times of India they have come across at least 20 instances where workers have not taken the vaccine, although they claimed to have.

This is because many healthcare workers have doubts about the safety and efficacy of the jab and are hesitant to take it.

“One medical officer said he did not trust the vaccine and did not want it, so he instructed the nurse to hold a small ball of cotton to his arm to make it look like he took the jab,” said the source.

Kamala (name changed), a nurse at a PHC in Shivajinagar, said a health worker who was afraid of getting the jab, faked the act by getting her colleague to simulate injecting the vaccine.

“Many are unhappy over being asked to take the vaccine as they do not trust it yet. The two deaths that were reported have added to fears,” Kamala said.




COVID Vaccine Reactions Rise Worldwide

COVID Vaccine Reactions Rise Worldwide

by Del Bigtree w/ Jefferey Jaxen, The HighWire
January 21, 2021

 



As mass vaccinations roll out across the globe, reports of deaths and dangerous reactions continue.

Hear the details on the allergic reaction cluster that shut down a vaccination super center in California and the new guidelines for vaccinating the elderly in Norway after 33 deaths following COVID vaccination.




Anthony Fauci Joins the Long List of People Incapacitated by Coronavirus Vaccine

Anthony Fauci Joins the Long List of People Incapacitated by Coronavirus Vaccine

by Adam Dick, Ron Paul Institute
January 23, 2021

 

Anthony Fauci, the director of the United States government’s National Institute of Allergy and Infectious Diseases, told reporters Thursday that he was “knocked out” for about 24 hours after, on Tuesday, taking the second dose of experimental coronavirus vaccine. Fauci has thus joined the large and growing list of people who have suffered serious harm from the injections that he and other government officials have been encouraging Americans to take.

Back on December 22, Fauci said just before publicly having his first shot of the two-shot regimen that he was being injected with the experimental vaccine “as a symbol to the rest of the country that I feel extreme confidence in the safety and the efficacy of this vaccine and I want to encourage everyone who has the opportunity to get vaccinated.”

It turns out Fauci also ended up a symbol of harm that can arise from taking the experimental vaccine.

In a Friday Daily Mail article, Natalie Rahhal provides more information about Fauci’s post-vaccination trouble, as well as the resistance by medical workers and other Americans against pressure to be injected with the experimental vaccine. You can read that article here.




Home Run King Hank Aaron Dies of ‘Undisclosed Cause’ 18 Days After Receiving Moderna Vaccine

Home Run King Hank Aaron Dies of ‘Undisclosed Cause’ 18 Days After Receiving Moderna Vaccine
The 86-year-old sports icon received the first of two doses of Moderna’s vaccine on Jan. 5, in an attempt to inspire other Black Americans to step up to the plate and get the vaccine.

by Children’s Health Defense Team, The Defender
January 22, 2021

 

Baseball legend Hank Aaron, who received the Moderna COVID vaccine on Jan. 5, has died. According to the New York Times, the Atlanta Braves confirmed the 86-year-old Hall of Famer’s death today, but did not provide further details.

CNN reported that Aaron died “peacefully in his sleep,” and that no cause of death was disclosed.

Aaron made headlines earlier this month when he was photographed getting the Moderna vaccine. He told the Associated Press at the time that getting vaccinated “makes me feel wonderful.” He added:

“I don’t have any qualms about it at all, you know. I feel quite proud of myself for doing something like this. … It’s just a small thing that can help zillions of people in this country.”

Aaron was vaccinated at the Morehouse School of Medicine health clinic in Atlanta, in what news reports said was an attempt to inspire other Black Americans to step up to the plate and get the vaccine. The AP reported at the time:

“Rolling up their sleeves to take the first of two doses, these octogenarians, their spouses and several other civil rights leaders who received the shots in a brand-new health clinic at the Morehouse School of Medicine acknowledged the legacy of mistrust that many African Americans have toward medical research, stemming from the infamous Tuskegee experiment in which U.S. health workers left syphilis untreated in Black men without their consent, making them suffer needlessly.”

In December, VOX reported on the launch of a global campaign using influencers and celebrities to help overcome “vaccine hesitancy,” stating that it “will be unprecedented” and many institutions will have a role, including government and public health authorities.

However, health officials continue to encounter pushback, including from healthcare workers.

Adverse events to the COVID vaccine have been reported worldwide. Germany and Norway have reported a combined 43 deaths among elderly people who received the Pfizer vaccine, prompting China health officials to call for the vaccines to be suspended, especially among the elderly.

On learning of Aaron’s death, Robert F. Kennedy, Jr., chairman and chief legal counsel for Children’s Health Defense, said: “Aaron’s tragic death is part of a wave of suspicious deaths among elderly closely following administration of COVID vaccines.”

“Studies show that self-interested pharmaceutical company researchers, physicians, nursing homes and health officials seldom report vaccine injuries. Instead, they dismiss injuries and deaths as ‘unrelated’ to vaccination,” Kennedy said. “Public health advocates worry that the vast majority of injuries and deaths will go unreported to the Vaccine Adverse Events Reporting System (VAERS), the notoriously broken voluntary surveillance system run by the U.S. Department of Health and Human Services (HHS).”

A 2001 HHS study concluded that “fewer than 1% of vaccine injuries” are reported to VAERS.

As The Defender reported last week, California was forced to recall a batch of 330,000 Moderna vaccines after a cascade of reported injuries, though now the company says it’s okay to resume administration of that batch.

The Defender also covered the story of a 56-year-old Florida doctor who died about two weeks after getting his first dose of Pfizer’s vaccine. His death is under investigation by Florida health officials. In addition, multiple severe allergic reactions have been directly linked to the Pfizer vaccine.




CDC Removes Claim ‘Vaccines Do Not Cause Autism’ From Its Website

CDC Removes Claim ‘Vaccines Do Not Cause Autism’ From Its Website

Sourced from ICAN Newsletter, Informed Consent Action Nework
January 21, 2021

 

ICAN, through its attorneys led by Aaron Siri, has been relentless in its legal demands and actions to compel the CDC to remove its blanket claim that “Vaccines Do Not Cause Autism” from its website.  We are excited to report that the CDC has finally capitulated to those demands!  It has removed this claim from its website!  

CDC’s Autism-Vaccine Page

The more than three-year journey for how ICAN, and its legal team, achieved this result is a story of determined persistence.  Here are the highlights.

ICAN’s Opening Salvo (Oct. 12, 2017 – Dec. 31, 2018)

The journey began with a letter sent to the Secretary of the U.S. Department of Health & Human Services (HHS) on October 12, 2017.  That letter explained why the CDC cannot scientifically claim that “Vaccines Do Not Cause Autism” on its website.  ICAN then ended with the following demand: “Please confirm that HHS shall forthwith remove the claim that ‘Vaccines Do Not Cause Autism’ from the CDC website, or alternatively, please identify the specific studies on which HHS bases its blanket claim that no vaccines cause autism?”

To put HHS and the CDC (an agency within HHS) on their heels, mere days after sending this letter, ICAN also sent a FOIA request on November 1, 2017, demanding:

All reports, scientific studies, and any other documents the CDC relied upon to support the assertion “Vaccines Do Not Cause Autism” located on its website at http://www.cdc.gov/‌vaccinesafety/concerns/autism.html.

The CDC quickly called ICAN’s counsel, Aaron Siri, regarding this request. After some negotiations, the CDC formally responded on November 7, 2017, stating that “A search of our records failed to reveal any documents beyond the records hyperlinked in the specific web site” to support the claim that vaccines do not cause autism.  The CDC had thus revealed a truth, one that HHS could not run from in its response to ICAN’s letter.

On January 18, 2018, HHS responded to ICAN’s October 12th letter.  In that letter, HHS provided a list of studies it said supported the conclusion on its website that “Vaccines Do Not Cause Autism.”  All of the studies cited related either to a single vaccine, MMR, or to a single vaccine ingredient, thimerosal.  None of these studies support the claim that vaccines given during the first six months of life do not cause autism.

Given that HHS failed to support its claim that “Vaccines Do Not Cause Autism,” ICAN responded by letter dated December 31, 2018 wherein ICAN asserted that “HHS cannot scientifically claim that ‘Vaccines Do Not Cause Autism’” and “must therefore remove this claim from the CDC website until it can produce the studies to support the claim.”

ICAN’s Pincer Maneuver (Jan. 1, 2019 to June 18, 2019)

In order to keep the pressure on to force the CDC to be honest with the public, during the first six months of 2019, ICAN submitted numerous requests for communications among key personnel within the CDC relating to autism.  Some of these requests sought emails going back decades.  The key players within the CDC with regard to vaccines and autism now knew we were watching, and that we would have their unvarnished, internal emails related to autism.

ICAN Drops the Gauntlet (June 19, 2019 to Dec. 30, 2019)

Now that ICAN had gathered the proof in the form of evidence and admissions it needed to hold the CDC’s feet to the fire, on June 19, 2019, ICAN demanded that the CDC produce copies of the studies it relies upon to claim that all the vaccines given during the first six months of life “Do Not Cause Autism.”  These vaccines include DTaP, HepB, Hib, PCV13, and IPV.  ICAN also demanded that the CDC produce studies to support that the cumulative exposure to these vaccines during the first six months of life “Do Not Cause Autism.”

ICAN, of course, already had the CDC’s admissions on these points from its prior FOIA request in November 2017, the HHS letter exchange, and the CDC’s internal emails.  The CDC had nowhere to hide and no way to dissemble.  As expected, it responded to ICAN’s request with the same list of studies involving MMR or thimerosal.  Not a single study supported that DTaP, HepB, Hib, PCV13, and IPV do not cause autism.

ICAN Battles the CDC in Court (Dec. 31, 2019 to March 5, 2020)

ICAN then put the pressure directly on the CDC.  Instead of walking away after the CDC effectively admitted it did not have the studies ICAN sought, ICAN sued the CDC in federal court.  The suit focused on the CDC’s claim that “Vaccines Do Not Cause Autism” on the basis that the CDC had not specifically listed the precise studies that it asserts support that claim.  This lawsuit also quoted from the deposition of Dr. Stanley Plotkin, the godfather of vaccinology, who admitted under oath that he was “okay with telling the parent that DTaP/Tdap does not cause autism even though the science isn’t there yet to support that claim.”

After a lot of wrangling between ICAN’s counsel Aaron Siri, and the Department of Justice, which was representing the CDC, the CDC finally capitulated and signed a stipulation that was entered as an order of the court on March 2, 2020 in which the CDC identified 20 studies as the universe of support it relies upon to claim that DTaP, HepB, Hib, PCV13, and IPV do not cause autism.  Here is a summary of the vaccines these studies cover:

1 relating to MMR (not a vaccine ICAN asked about);
13 relating to thimerosal (not an ingredient in any vaccine ICAN asked about);
4 relating to both MMR and thimerosal;
1 relating to antigen (not a vaccine) exposure; and
1 relating to MMR, thimerosal, and DTaP.

Incredibly, the one study relating to DTaP on the CDC’s list was a recent review by the Institute of Medicine (IOM), paid for by the CDC, which conducted a comprehensive review looking specifically for studies relating to whether DTaP does or does not cause autism.  The IOM concluded that it could not identify a single study to support that DTaP does not cause autism. Instead, the only relevant study the IOM could identify found an association between DTaP and autism.

In other words, the only study the CDC listed that actually looked at any of the vaccines given to babies during the first six months of life concluded that there are no studies to support that DTaP does not cause autism.  Yet, the CDC chose that study as one of the few that supports its claim that “Vaccines Do Not Cause Autism”!
This reality is truly incredible because, when it comes to autism, vaccines are the one suspected culprit that the CDC claims to have exhaustively investigated but, yet, the CDC could not provide a single study to support its conclusion that the vaccines given during the first six months of life do not cause autism.

The CDC regularly complains that those raising concerns about vaccine safety are unscientific and misinformed.  It is therefore truly stunning that when we asked the CDC for studies to support its claim that “Vaccines Do Not Cause Autism,” the March 2, 2020 stipulation and order made it abundantly clear that it was the CDC’s own claim that “Vaccines Do Not Cause Autism” that was unscientific.

 ICAN’s Coup de Grâce (Mar. 6, 2020 to Aug. 26, 2020)

And now for the coup de grâce.  ICAN’s demands at the end of 2019 and over which it took the CDC to court in early 2020 were for the studies the CDC “relied upon” to claim that Vaccines Do Not Cause Autism.  ICAN now had a court ordered stipulation that specifically listed the twenty studies the CDC “relied upon” to support this claim – none of which supported that the vaccines given during the first six months of life do not cause autism.

To assure that the CDC understood ICAN was never, ever, ever, letting this issue go, on March 6, 2020 (days after concluding the federal lawsuit) ICAN submitted the following FOIA demand to the CDC: “All studies supporting the claim that DTaP does not cause autism” and days later requested “Studies created or retained by CDC to support the claim that DTaP does not cause autism.”  The difference between this and ICAN’s prior requests is subtle but powerful.  Instead of asking for the studies the CDC “relied upon” to support that DTaP does not cause autism (as it did previously), ICAN was now seeking the studies that in fact support that DTaP does not cause autism.

In response to this request, the CDC could not list its MMR or thimerosal studies – its hands were tied.  It understood there was nowhere left to hide its unsupported claim that “Vaccines Do Not Cause Autism.”  And it knew that ICAN would again take it to court, and this time the outcome could be even harsher.

The CDC Capitulates

On the heels of the foregoing, and dozens of related demands regarding autism that ICAN continued to press, in the dead of the night, and without any fanfare or announcement, on August 27, 2020, the CDC website removed the claim that “Vaccines Do Not Cause Autism” from its website!  The CDC had finally capitulated to the truth!

Compare for yourself the CDC’s autism-vaccine webpage on August 26, 2020 versus August 27, 2020.

You may be wondering why we waited until now to announce this amazing news.  Well, ICAN and its legal team have been so busy fighting on dozens of vaccine related fronts (mandatory MMR vaccines, flu shot requirements, improper COVID vaccine trials, etc.) that we only realized the CDC’s vaccine-autism claim had been removed when we recently turned back to that front!  Like a Mayan temple hidden in plain sight for hundreds of years, ICAN only recently discovered the CDC’s silent capitulation.

 The Future

The most recent data from CDC shows that 1 in 36 children born this year in the United States will develop autism. This is a true epidemic. If the CDC had spent the same resources studying vaccines and autism as it did waging a media campaign against parents that claim vaccines caused their child’s autism, the world would be a better place for everyone.

To their credit, parents with autistic children have never backed down.  In the face of incessant brow beatings by public health authorities, studies have found between 40% and 70% of parents with an autistic child continue to blame vaccines for their child’s autism, typically pointing to vaccines given during the first six months of life.  These parents know what they experienced, what their parental instincts tell them, and no amount of shaming can change that truth.

With the removal of the claim that “Vaccines Do Not Cause Autism,” it is ICAN’s sincere hope that our public health authorities have turned or will soon be turning the corner on this issue.  That they will fund independent scientists to conduct the desperately needed studies of autism and the cumulative impact of the vaccines given during the first six months of life.

The cries of parents who know that vaccines caused their child’s autism should no longer be ignored.  The science must be done. And ICAN will continue to fight to make sure that that it is done.

Epilogue

The CDC’s website does continue to claim that “Vaccine ingredients do not cause autism” and so ICAN’s fight continues!  Our next step will be to force the CDC to admit whether or not they are also making this claim for aluminum adjuvants used in vaccines.  And if so, to produce the studies to support this claim.  (See ICAN’s white paper on aluminum adjuvants and autism here.)

Of course, whether one or more ingredients, like water used in vaccines, does not cause autism is not really the issue.  The question is whether the vaccine, the product itself as formulated, causes autism.  And we now know that the CDC finally understands that it can no longer claim that “Vaccines Do Not Cause Autism.”

This victory for truth and science could not have happened without the encouragement ICAN receives from its supporters like you.  Thank you for making our work possible!




13,000 NY Nursing Home Residents and Nearly Half of Staff Decline COVID-19 Vaccine

13,000 NY Nursing Home Residents and Nearly Half of Staff Decline COVID-19 Vaccine

by Tyler Durden, ZeroHedge
January 18, 2021

 

New York will be reallocating unused COVID-19 vaccines after more than ten thousand nursing home residents and nearly half of staffers declined the jab, according to Gareth Rhodes, a member of Governor Andrew Cuomo’s COVID-19 Response Task Force.

Rhodes said that out of 70,000 nursing home residents, 57,000 have been vaccinated, while 13,000 have declined. Meanwhile, out of 89,000 nursing home staff, 41,000 have declined.

Overall, 105,000 first-doses of the vaccine have been used so far in nursing homes, while 120,000 doses remain.

We’re gonna reallocate those that are used in the long-term facility program to the state program, but we’ll make sure that the residents who want to take it and the staff who want to take it, we will reserve their doses,” said Cuomo, who in July came under fire for ordering nursing homes to accept coronavirus patients from hospitals.

The reallocation comes more than a week after New York came under scrutiny over discarded vaccines – with officials changing regulations which required that extra doses to be tossed.

In a Monday letter to Health and Human Services Secretary Alex Azar, Cuomo called on the federal government to beef up vaccine supply, claiming that Azar falsely claimed that doses would be held in reserve, when they were in fact distributed to states.

New York has received approximately 1.2 million doses, of which around 860,000 have been administered. The figure doesn’t include shots allocated to nursing homes, while the CDC claims New York has received 1.8 million doses.

Cuomo last week extended the shots to anyone age 65 and over, but has repeatedly insisted the state has nowhere near enough doses to cover everyone who is now eligible.

The governor also sent a letter Monday to Pfizer chairman and CEO Albert Bourla asking him to let New York purchase COVID-19 vaccines directly from the company. –NY Post

“My job as governor of New York is to pursue every avenue,” said Cuomo, adding “The federal government increased eligibility dramatically but never increased the supply for the dosages.”

 

Read more by Tyler Durden at ZeroHedge




China Health Experts Call for Suspension of COVID Vaccines as Norway Investigates 33 Deaths, Germany Probes 10 Deaths

China Health Experts Call for Suspension of COVID Vaccines as Norway Investigates 33 Deaths, Germany Probes 10 Deaths
Norway upped the number of deaths under investigation, from 23 last week to 33, while in Germany, health officials said they are investigating 10 deaths that occurred among elderly patients who received the COVID vaccine.

by Children’s Health Defense Team
January 18, 2021

 

China health experts say Norway and other countries should suspend the use of mRNA vaccines like those produced by Pfizer and Moderna, especially among the elderly, according to Global Times.

Norway health officials said last week they were investigating the deaths of 23 elderly people who died shortly after receiving the vaccine, and had confirmed 13 of those were directly related to the vaccine.

Today, Bloomberg reported that the number of deaths under investigation in Norway had risen to 33 and that all had occurred in people ranging from age 75 to 80. According to Bloomberg, Camilla Stoltenberg, head of the Norwegian Institute of Public Health, said at a press conference today:

“It is important to remember that about 45 people die every day in nursing homes in Norway, so it is not a given that this represents any excess mortality or that there is a causal connection.”

The Norwegian Medicines Agency previously told Bloomberg that all of the deaths occurred in people who received the Pfizer-BioNTech vaccine, which until Friday was the only COVID vaccine approved for use in Norway.

The Norwegian Institute of Public Health, which had originally prioritized the elderly for the vaccine, has since revised its advice to urge more caution when vaccinating the elderly, especially those with underlying conditions.

The institute told Bloomberg that “for those with the most severe frailty, even relatively mild vaccine side effects can have serious consequences. For those who have a very short remaining life span anyway, the benefit of the vaccine may be marginal or irrelevant.”

The Institute also admitted to Global Times that the clinical trials that resulted in emergency approval of the vaccine included “very few people over the age of 85,” but added “we assume that the side effects will largely be the same in the elderly as in those over 65 years of age.”

According to the Global Times, a Beijing-based immunologist who requested anonymity said the mRNA vaccines had not proven safe for large-scale use or for preventing infectious diseases. Noting that people over 80 have weaker immune systems, he said they should not receive the vaccine, but instead should take medicines to improve their immune systems.

Meanwhile, The BMJ and other news outlets reported last week that in Germany, the Paul Ehrlich Institute is investigating 10 deaths in people ranging in age from 79 to 93 who died shortly after receiving the COVID vaccine.

U.S. health officials continue to push COVID vaccinations in nursing homes, despite growing resistance among nursing home employees to take the vaccine.

So far, there’s no word of any investigation into the deaths of 29 elderly people at a nursing home in New York. According to a Jan. 9 news report from Syracuse.com, a single nursing home in upstate New York vaccinated 193 residents beginning on Dec. 22 and subsequently reported 24 deaths within the span of a couple of weeks.

The facility attributed the deaths to a COVID-19 “outbreak,” even though there had been no COVID-19 deaths in any nursing homes in the entire county “until the first three deaths … were reported Dec. 29.”

Florida health officials and the U.S. Centers for Disease Control and Prevention are investigating the death of a 56-year-old doctor who died of a rare autoimmune disease 15 days after getting the Pfizer vaccine. A Johns Hopkins scientist told the New York Times it was a “medical certainty” that the death was related to Pfizer’s vaccine.

The U.S. Food and Drug Administration is investigating numerous severe allergic reactions, including anaphylaxis, in healthcare workers who received the vaccine.

Sunday night, California health officials called for a pause on the use of a huge batch of Moderna’s COVID vaccine due to its ”higher-than-usual number of possible allergic reactions.” As The Defender reported this morning, California’s top epidemiologist Dr. Erica S. Pan is recommending providers pause the administration of lot ‘041L20A’ of the Moderna COVID vaccine.

According to the latest figures, updated Jan. 7, from the Vaccine Adverse Event Reporting System (VAERS), 66 deaths have been reported in the U.S. as being possibly related to a COVID vaccine. It’s estimated that only 1% of vaccine injuries are reported to VAERS.

 

Anyone who suspects an injury or death related to the COVID vaccine, or any vaccine, can go to the VAERS website and file a report.




California Health Officials Stop Use of Moderna Vaccine Lot 041L20A After Severe Allergic Reactions

California Health Officials Stop Use of Moderna Vaccine Lot 041L20A After Severe Allergic Reactions

 

Moderna Stops COVID-19 Vaccination In California After Severe Allergic Reactions. Investigation Launched

by Great Game India
January 18, 2021

 

California health officials are recommending providers pause the administration of a specific batch of the Moderna COVID-19 vaccine due to possible allergic reactions that are under investigation.

California State Epidemiologist Dr. Erica S. Pan issued a statement on Sunday evening regarding batch ‘041L20A.’

“A higher-than-usual number of possible allergic reactions were reported with a specific lot of Moderna vaccine administered at one community vaccination clinic. Fewer than 10 individuals required medical attention over the span of 24 hours,” Dr. Pan said.

According to the statement,

“Out of an extreme abundance of caution and also recognizing the extremely limited supply of vaccine, we are recommending that providers use other available vaccine inventory and pause the administration of vaccines from Moderna Lot 041L20A until the investigation by the CDC, FDA, Moderna and the state is complete. We will provide an update as we learn more.”

Earlier, a woman from Oakland City, Indiana in the United States warned others to not get the experimental Moderna COVID-19 vaccine after she suffered tongue spasms and whole body convulsions. She posted her videos on Facebook where her entire body is seen shaking uncontrollably. The CDC said such side-effects are “mild” and “normal”.

According to pharma giant Moderna, the COVID-19 mRNA based experimental vaccines are Operating System designed to program human DNA. These vaccines are being approved for emergency use for the first time in history.




Coffey County, Kansas, Health Department Nurses Refuse to Give COVID-19 Vaccines

[1/17/2021 CORRECTION — Truth Comes to Light editor’s note: The NY Post article below mentions “Coffee” County. The county’s name is spelled “Coffey“. See another article from WIBW, Kansas — “Coffey County Health Department nurses decline to give the COVID vaccine”.]

Kansas nurses refuse to give COVID-19 vaccines

 

Department chief Lindsay Payer and her staffers have opted out of giving the injections because they have doubts about the safety of the Moderna vaccine, which the county is offering, local TV station WIBW reported.

Payer told WIBW that her employees made up their own minds and “not without considerable thought.” The county will hire at least one outside nurse, who will be paid with COVID-19 funds.

“I will tell you we will have to contract staff…because my staff is not comfortable with that. It’s a new technology. We’ve never seen it before. It was only studied in 45 people before it was approved…,” Payer said.

“It’s somewhat discomforting to a nurse who has to put that in people’s bodies.”

Read more at New York Post

 

cover image credit: New York Post

 




Tip of the Iceberg? Thousands of COVID Vaccine Injuries and 13 U.S. Deaths Reported in December Alone

Tip of the Iceberg? Thousands of COVID Vaccine Injuries and 13 U.S. Deaths Reported in December Alone
In December, 3,916 COVID vaccine-related adverse events, including 13 deaths, were reported to VAERS. As more adverse events — ranging from life-threatening anaphylaxis to death — occur, it will be tougher to “sell” the experimental injections.

by Children’s Health Defense Team, The Defender
January 14, 2021

 

When the U.S. Food and Drug Administration gave Pfizer/BioNTech and Moderna permission to distribute their experimental mRNA coronavirus vaccines to Americans on an “emergency use” basis in December, it opened the floodgates for other countries to quickly follow suit.

By Jan. 11, counting China and Russia, 43 countries had administered at least 26 million doses of vaccine — especially Pfizer’s — with far more ambitious plans for the coming year. The companies’ global delivery targets for 2021 include two billion Pfizer/BioNTech doses and at least 600 million Moderna shots.

Drawing on the tried-and-true marketing technique of drumming up the “illusion of scarcity” to “accelerate demand,” U.S. officials have been attempting to direct the public’s attention to the concocted drama of vaccine supply shortages and a slower-than-expected rollout.

However, as the early warning signs already apparent during clinical trials begin to translate into serious adverse reactions on a wider scale, officials now face a new public relations challenge — that of “managing expectations” to ensure population willingness to take the vaccine.

As more people hear about adverse events, and more adverse events occur — ranging from life-threatening anaphylaxis and emergency room visits to brain inflammation and death — “selling” the experimental injections may become an increasingly uphill battle.

Deaths … so far

In the U.S., the primary mechanism for reporting adverse reactions is the Vaccine Adverse Event Reporting System (VAERS), a flawed passive surveillance system that relies on the willingness and ability of parents and professionals to submit reports voluntarily.

As Children’s Health Defense Chairman Robert F. Kennedy, Jr. wrote on Dec. 18, 2020 to the co-chair of the new COVID-19 Advisory Board, VAERS has been an abject failure, with fewer than 1% of adverse events ever reported, according to a 2010 federal study.

Given the abysmal track record of VAERS in capturing serious adverse events, it is noteworthy that 13 deaths — a subset of 3,916 total adverse events reported following COVID-19 vaccination — had already been recorded by the system by the end of December (as per the MedAlerts search engine).

Nine of the deaths followed the Pfizer vaccine and four followed the Moderna shot (see table below). Nearly all of the deceased were institutionalized (primarily in nursing homes), although one 63-year-old male received the injection at work.

Five (and possibly six) of the deaths occurred on the same day as vaccination, all in women and sometimes within 60 to 90 minutes of the injection — and without any “immediate adverse reaction” having been observed.

The reports describe outcomes ranging from “foaming at the mouth” to “massive heart attacks.” Three of the deceased were in their early to mid-60s.

The write-ups that accompany VAERS reports furnish details about these sad fatalities, including the astonishing fact that some of the deceased had actually experienced and recovered from COVID-19 (raising questions about why they were vaccinated).

The write-ups also illustrate the subtle pressure to attribute the cause of death to something other than COVID-19 vaccination. For example, a grandchild who submitted a report wrote, “My grandmother [age 85] died a few hours after receiving the moderna covid vaccine booster 1. While I don’t expect that the events are related, the treating hospital did not acknowledge this and I wanted to be sure a report was made.”

A nursing home submitting a report on behalf of an 89-year-old who died five days after receiving the Moderna injection likewise wrote, “Due to proximity of vaccination we felt we should report the death, even though it is not believed to be related.”

And when a 78-year-old died two days after the Pfizer shot, the report simply stated, “no adverse events and no issues yesterday; Death today … (unknown if related – Administrator marked as natural causes).”

The 13 deaths communicated to VAERS do not include any deaths in the state of New York. However, a disturbing news report from Syracuse.com suggests that COVID-19 vaccines could be linked to a shocking number of additional deaths in the elderly in that state.

According to the news account, a single nursing home in upstate New York vaccinated 193 residents beginning on Dec. 22 and subsequently reported 24 deaths within the span of a couple of weeks. Although the facility has attributed the deaths to a COVID-19 “outbreak,” there had been no COVID-19 deaths in any nursing homes in the entire county “until the first three deaths … were reported Dec. 29.”

Pointing out that 24 deaths among 193 vaccinated residents equates to a 12.4% mortality rate, one observer notes that this reflects a “124-fold increase in mortality over and above the COVID-19 death rate for the population at large.”

Another compelling source of data about deaths following receipt of the experimental Pfizer/BioNTech shot comes from a growing number of incidents being reported from Israel and Europe:

  • Israel: Four individuals die “shortly after receiving the vaccination,” including two elderly men, aged 75 and 88, who experience apparent heart attacks two to three hours post-Pfizer-vaccine.
  • Norway: Two nursing home residents die within “a few days” of Pfizer COVID-19 vaccination.
  • Portugal: Health worker Sonia Acevedo, 41-year-old mother of two, dies suddenly two days after receiving the Pfizer injection.
  • Sweden: An elderly man, age 85, dies of a heart attack one day after receiving the Pfizer vaccine.
  • Switzerland: An elderly man, age 91, dies not long after getting the Pfizer shot.

Finally, in early January, news outlets, including The Defender, also described the tragic U.S. case involving Miami obstetrician-gynecologist Gregory Michael, who at age 56 died within two weeks of receiving the Pfizer vaccine — with the cause of death attributed to a “highly unusual clinical case of severe [immune] thrombocytopenia” (ITP).

ITP is considered a Type II “hypersensitivity reaction” (“immune responses that are exaggerated or inappropriate against an antigen or allergen”). Because Michael did not start experiencing symptoms until three days post-vaccination, his case was not captured in a Jan. 6 Centers for Disease and Control (CDC) report on serious allergic reactions following COVID-19 vaccination that limited the analysis to reactions occurring within the first 24 hours.

Serious allergic reactions

Critics familiar with VAERS’ shortcomings — and the ways in which officials can manipulate its data — bluntly condemn VAERS as “nothing more than window dressing, and a part of U.S. authorities’ systematic effort to reassure/deceive us about vaccine safety.”

As an example of the “effort to reassure,” one need look no further than the Jan. 6 CDC news release about post-vaccination anaphylaxis and non-anaphylaxis allergic reactions. In this report, the CDC’s tally of the hundreds of VAERS reports received per day during the first 10 days of the Pfizer vaccine rollout totaled 4,393 adverse events from December 14 to 23 — including 175 incidents flagged by CDC “for further review as possible cases of severe allergic reactions, including anaphylaxis, based on descriptions of signs and symptoms.”

Following its review, the CDC chose to include only 21 cases, excluding 154 cases either because they did not meet narrow criteria defined by the Brighton Collaboration (a global group that publishes “standardized case definitions” for countable adverse events); or because symptom onset occurred “later than the day after vaccination”; or because CDC judged the events to be “nonallergic” despite signs and symptoms to the contrary.

Based on the 21 cases, the public health agency then produced an estimate of 11.1 cases of anaphylaxis per million vaccine doses, whereas including all 175 events reported as severe allergic reactions would have yielded a rate of 92.4 cases per million doses.

Even so, the CDC’s conservative estimate of the anaphylaxis rate for experimental COVID-19 mRNA vaccines is roughly 10 times greater than for flu shots, including in individuals with no prior history of allergic reactions.

News reports have added to the frightening picture of post-COVID-19 allergic reactions that is emerging. These include the “hundreds” of Israelis describing “severe anaphylactic shock,” other allergic symptoms such as tongue and throat swelling, tingling sensations, dizziness and weakness; the two health workers in the UK who suffered “anaphylactoid reactions” on the first day of the Pfizer vaccine rollout; the two hospital workers in Alaska who experienced allergic symptoms — a serious anaphylactic reaction in one case and “eye puffiness, light headedness and scratchy throat” in the second case — within 10 minutes of getting the Pfizer jab; and the “mild to moderate” side effects from the Pfizer injection, including pain and dizziness, reported by four Bulgarians.

Reactions have not been confined to allergic symptoms, however. Additional descriptions of adverse events include:

  • A “rare, multisystem inflammatory syndrome,” including heart damage, developed by a 23-year-old male social worker in Israel 24 hours after receiving the Pfizer injection.
  • The seizures and encephalomyelitis (brain and spinal cord inflammation) experienced by 32-year-old Mexican internist Karla Cecilia Perez hours after getting the Pfizer shot.
  • The Bell’s palsy developed by a U.S. nurse within three days of her injection. On YouTube, she warns Americans, “Do not take this vaccination,” saying “I would not wish this on my worst enemy.”
Adverse mRNA vaccine reactions — no picnic

Setting the stage to “manage expectations,” The Atlantic told readers in mid-December that while COVID-19 injections have “a kick” and involve “more than the usual unpleasantness of getting a shot,” they are still “nowhere near as bad as COVID-19 itself.”

Some of the individuals described above and others submitting reports to VAERS might beg to differ.

For example, in a write-up accompanying one VAERS report (available through MedAlerts), a 36-year-old female who received the Pfizer vaccine on Dec. 17 was described as experiencing “disabling” light-headedness and dizziness 15 to 20 minutes post-vaccination, followed by an elevated heart rate and “really high” blood pressure.

After several hours in a monitoring station, where health workers gave her Benadryl and “lots of water” along with measuring her blood pressure “every five minutes,” she spent another four hours undergoing “continual monitoring” in the emergency room, followed by “a few more hours” in the ER the following day and a recommendation to start taking blood pressure medication. By Dec. 20, her blood pressure still had not normalized, and she had developed a bad headache. The health provider who submitted the report to VAERS on the woman’s behalf concluded that a causal association between Pfizer’s vaccine and the event could not be ruled out “based on a compatible temporal relation.”

Among Pfizer vaccine recipients with reactions categorized in VAERS as “life-threatening,” there are many other disquieting write-ups, often concerning young women in their 30s:

  • Female, age 31: “40 min after injection my throat and tongue started to feel weird and tight, pharmacy…gave me [Benadryl and Tylenol]. At about 1 hr 45 min after injection my throat got to the point of so swollen and itchy I couldn’t swallow. I went to nearest emergency room….”
  • Female, age 35: “5 minutes after getting the vaccine began itching that quickly developed into rash/hives to face, neck, chest, abdomen. At 20 minutes post vaccine developed severe leg weakness with lightheadedness, chest tightness, and [shortness of breath]. 22 minutes out collapsed to the floor unable to bear weight…and had severe cramping and tingling in legs, still unable to move them. Was rushed to the ER….”
  • Female, age 30: “Approximately 2 minutes after injection, felt flushed and tingly. This subsided, but developed a cough. Felt fine enough to leave the vaccination area after being monitored for 15 minutes. Cough continued, and developed a scratchy throat that eventually led to swelling of the throat at approximately 30-35 mins post administration. Sought care in the ED, where I was tachycardic and hypertensive…. Discharged home, but symptoms returned around 2pm. Sought care in a different ED, where I remained hypertensive and tachycardic.”
What’s next?

An objective analysis of the COVID-19 vaccine rollout necessarily raises serious questions about product safety and the assessment of risks versus benefits.

The VAERS reports submitted through December indicate that over half (53%) of those affected by mRNA vaccine reactions are 17-44 year-olds in the prime of life.

More than one in five (n=877) adverse events resulted in an emergency visit, 140 were rated “serious,” 100 led to hospitalization, 41 were “life-threatening” and 5 produced permanent disability.

Supplementing VAERS, the CDC has been encouraging COVID-19 vaccine recipients to use a smartphone app called v-safe to “quickly tell CDC” about mRNA vaccine side effects. On Dec. 19, v-safe tallies for the first five days of COVID-19 vaccination showed that among 215,362 vaccine recipients registered with v-safe, 5,052 individuals self-reported serious “health impact events” following their first dose of vaccine — events requiring care from a fellow health professional and rendering the person unable to work or perform normal daily activities. This, too, is concerning, translating into a one-in-43 injury rate (2.3%) for the v-safe group.

In the new year, many states are planning to aggressively scale up distribution of both the Pfizer vaccine and the even more reactogenic Moderna vaccine, including at drugstoressupermarketsbig-box storesdental offices and temporary sites like stadiums and even Disneyland.

This has prompted concerns among allergists, in particular, who question whether drive-thru sites and under-trained personnel will be able to recognize and handle the sudden adverse reactions that the two mRNA vaccines seem capable of eliciting — especially since both contain the notorious allergenic ingredient polyethylene glycol (PEG).

In the U.S., some allergists are recommending that consumers with known allergies be “proactive” and ask prospective vaccination venues “pointed questions” about their emergency training, equipment and ability “to respond swiftly if something goes wrong.”

A growing number of healthcare experts are going even further, with one Wyoming public health official describing the injections as “biological weapons of mass destruction,” and many others urging the public to “just say no” to experimental injections that health officials and the vaccine makers admit aren’t proven to prevent COVID or stop transmissibility, but could do long-lasting harm.




Massachusetts Department of Public Health Has Withdrawn the Mandate for All Students to Receive an Influenza Vaccine

Massachusetts Department of Public Health Has Withdrawn the Mandate for All Students to Receive an Influenza Vaccine

by ICAN (Informed Consent Action Network)
sourced from ICAN newsletter
January 15, 2021

 

As of today, January 15, 2021, the Massachusetts Department of Public Health has withdrawn the mandate for all students to receive an influenza vaccine.  An ICAN-funded lawsuit brought about this amazing development for all in the Commonwealth of Massachusetts.
 
Last week, we reported to you about a lawsuit funded by ICAN, brought against the Massachusetts Department of Public Health (DPH), to challenge the legality of a flu shot vaccine mandate for all children in childcare and all students in school, ages 6 months through 29 years old.  Episode 197’s Legal Update segment explained the legal bases for the lawsuit.
Today we bring you even better news: on the same day that the DPH was to file its response to the lawsuit with the Court — including responding to a request for a preliminary injunction striking the flu shot mandate — the DPH capitulated and withdrew the mandate in its entirety!  This means that NO STUDENT will be MANDATED to receive the flu vaccine in order to attend school!
The DPH’s updated list of required vaccines does not contain influenza vaccine.  This is an enormous and significant victory and a huge relief for thousands of individuals and families across Massachusetts who had been backed into a corner by the DPH’s fiat.
The DPH first showed signs of weakness when, within days of being sued and the Court ordering an expedited hearing, it pushed back the original December 31, 2020 deadline for receipt of the vaccine to February 28, 2021.
Then, yesterday, the day before the DPH was due to submit its opposition to the Plaintiffs’ motion for a preliminary injunction, its attorneys contacted ICAN’s legal team, led by Aaron Siri, to inform them that the mandate would be withdrawn.  Today, the DPH has done just that.
ICAN is beyond proud that its funding and its legal work continues to make real life changes for real people every day. Victories like this will continue to motivate us to never rest and to always stand up for informed consent and people’s right to choose!
Affidavit from the Massachusetts Department of Health
confirming that the flu shot mandate has been formally withdrawn. 



COVID Vaccine Secret, a Stunner

COVID Vaccine Secret, a Stunner

by Jon Rappoport, No More Fake News
January 15, 2021

 

From the off-guardian, January 3, 2021, “What Vaccine Trials?” by Iain Davis:

“…the WHO protocols Pfizer used to produce the mRNA [for the vaccine] do not appear to identify any nucleotide sequences that are unique to the SARS-CoV-2 virus. When investigator Fran Leader questioned Pfizer they confirmed: ‘The DNA template does not come directly from an isolated virus from an infected person’.”

And there we are, right back where I started, some time ago. If you don’t have the isolated virus, how can you claim you’ve sequenced it?

And if you’ve sequenced it by ASSUMPTION and GUESS, how can you claim the sequence—or the virus—is real?

Answer: You SAY the sequence and the virus are real, but you have zero proof. Because you’re a “scientific authority,” people automatically believe what you SAY.

A man visits a vast auto junkyard looking for parts. Over the office door, he sees a sign: “1972 Ferrari 365 GTB/4 Daytona Spider. Inquire within.”

The owner of the junkyard tells him, “We’re offering shares in the Ferrari. Three thousand a share. When we eventually sell it, you’ll make at least double your investment.”

The man says, “Where is the car? I’d like to see it.”

“Well,” the junkyard owner says, “look around you. We’ve got several square miles of cars and parts. The Ferrari is out there somewhere. We recently ran a test on exhaust fumes with a special instrument. It concluded that the ’72 Ferrari had recently been driven through the yard here…”

This is the sort of thing that happens in virology.

Of course, no mainstream virologist would admit it. He would talk about analogues and gene banks and PCR and representative samples and in silico (computer modeling).

But the stark reality is clear.

Assumption and guess and slippery inference do not carry the day.

You either have the isolated virus or you don’t. If you don’t, anything you say about “it” is useless. You can’t validly claim it exists.

As I’ve written and said dozens of times now, the virological meaning of the word “isolate” is quite different from the ordinary meaning.

In the technical world of the con and the hustle, “isolated virus” means: “We have the virus in a soup in a dish in the lab. The soup contains human and monkey cells, toxic drugs and chemicals, and other genetic material. Some of the cells are dying. This means the virus is killing them.”

That assertion is false. The drugs and chemicals can be killing the cells. And the cells are being starved of vital nutrients. That alone could explain the cell-death.

Furthermore, a supposed virus mixed in a soup in a dish in a lab is definitely not “isolated.”

Bottom line: there is no persuasive evidence that a virus is in the soup.

What’s in the COVID vaccine? Among other material, a supposed fragment from a supposed virus that hasn’t been proven to exist.

Consider the PCR test. Several levels of valid criticism have been aimed at the test.

First, different labs will come up with different contradictory test results. This is true.

Drilling down a little deeper, the test, when it amplifies the tissue sample taken from a patient, is useless and dangerous when more than 34 cycles or steps of amplification are deployed. Why? Because then, huge numbers of false-positives occur.

Down yet another level, we discover that the PCR doesn’t detect a virus at all. It identifies a piece of RNA presumed to come from a virus.

And finally, the test identifies a piece of RNA from a virus that hasn’t been proven to exist.

This is the root of the poisonous tree.




Death by Coincidence?

Death by Coincidence?
Declarations by health officials and vaccine makers that deaths and injuries following COVID vaccinations are unrelated coincidences are becoming a pattern. They’re also depriving people of the information they need to make informed decisions.

by Robert F. Kennedy, Jr., Children’s Health Defense
January 14, 2021

 

The official handling last week of the deaths of two Danes and a Miami doctor following their COVID jabs highlights the gaping holes in the government’s surveillance system for detecting post-marketing vaccine reactions.

These incidents suggest that health officials will be unlikely to give the public authentic risk profiles for the emergency use COVID vaccines.

Accurate risk profiles allow regulators to determine if a medical intervention is causing more harm than good and consumers to make rational choices about their own use of a product.

Regulators usually develop risk assessments during preclinical trials by comparing health outcomes in individuals receiving the intervention against a placebo group. Such studies must be large enough to detect rare injuries and of sufficient duration to reveal ailments with long diagnosis horizons.

The existence of the placebo group makes it difficult to conceal or misattribute injuries. Conversely, the absence of a placebo group in post-vaccination surveillance systems makes it easy for self-interested pharmaceutical and regulatory officials to undercount injuries by attributing them to coincidence.

Coincidence is turning out to be quite lethal to COVID vaccine recipients.

Death by coincidence

Shortly after reporting the Danish deaths and prior to any autopsies, Tanja Eriksen, acting head of Denmark’s Pharmacovigilance Unit, told the Danish newspaper, EkstaBladet, that the Danish Medicines Agency had determined that coincidence probably killed the two Danish citizens whose deaths followed their vaccinations.

One of the deaths was a citizen who had “severe lung disease.” The existence of the comorbidity suggested that the death was therefore coincidental. The second citizen received the vaccine at a “very old age,” and therefore also expired from coincidence.

“When vaccinated in fragile groups, one would expect there to be deaths,” explained Eriksen, using logic seldom applied by health officials to deaths from the COVID-19 virus. “This will happen regardless of whether they are vaccinated or not.”

These simple declarations — that deaths and injuries following vaccination are unrelated coincidences — are becoming a pattern.

On Dec. 20, 2020, World Today News reported the death of an 85-year-old man in Kalmar, Sweden, one day after he received the vaccine. Dr. Mattias Alvunger of the Kalmar Hospital dismissed concerns about the death being related to the vaccine, calling the fact that it was reported to the Swedish Medical Products Agency as “routine.”

On January 1, Sonia Acevedo, a 41-year-old Portugese nurse and mother of two, died two days after receiving the Pfizer/BioNtech vaccine. Her father told the Daily Mail that she never drank alcohol and was in perfect health. Nevertheless, Portugal’s Health Authority dismissed her death as a sad coincidence.

Israel also reported two deaths from the coincidence pandemic: one in a 75-year-old man in Beit She’an, and the other an 88-year-old man. Both died two hours after vaccination. Israeli health officials warned the public not to attribute the deaths to the vaccine.

In Lucerne, Switzerland, a 91-year-old man died five days after getting Pfizer/BioNtech’s vaccine. Swiss authorities called any connection “highly unlikely.”

On January 3, Dr. Gregory Michael, a beloved Miami obstetrician and enthusiastic COVID-19 vaccine booster, died of a hemorrhagic stroke after receiving Pfizer/BioNtech’s vaccine. Dr. Michael developed acute idiopathic thrombocytopenia purpura (ITP) — a known vaccine side effect — immediately after receiving the jab. His platelet count dropped from 150,000 to zero and never rebounded.

An army of experts from around the world, involved in the vaccine program, consulted in doomed efforts to restore Dr. Michael’s platelet count. The inevitable brain hemorrhage killed him two weeks later. Michael’s wife said that her husband’s death was “100% linked to the vaccine. She added that he was physically healthy, exercised often, rarely drank alcohol, never smoked cigarettes and had no known comorbidities.

Nevertheless, Pfizer dismissed Michael’s injuries as another sad coincidence: “We do not believe at this time that there is any direct connection to the vaccine.” Pfizer pointed out that ITP is also caused by excess drinking and reasoned that “there have been no recorded safety signals identified in trials from vaccinations so far.”

On Tuesday, the New York Times quoted Dr. Jerry Spivak, a blood disorder expert at Johns Hopkins University, saying “I think it’s a medical certainty that the vaccine was related.”

But Pfizer/BioNtech would not have been likely to see the thrombocytopenia signals in its brief, under-enrolled clinical trials. Thrombocytopenia occurs in 1 in approximately every 25,000-40,000 doses of the MMR vaccine. It is also a similarly rare, but persistently reported side effect of hepatitis A, TB, HPV, chickenpox, DTaP, polio and HiB vaccines.

An injury that occurs at that frequency would not likely be seen in Pfizer/BioNtech’s Phase II clinical trial because only 22,000 people received the vaccine. However, an injury of this severity occurring once in every 25,000 shots could debilitate or kill 12,000 of the 300 million Americans to whom the company hopes to give the jab.

The public can expect to see more of this strategic chicanery: When a healthy 32-year-old Mexican doctor was hospitalized with encephalitis — inflammation of his brain and spinal cord —  after receiving the Pfizer/BioNtech vaccine, Mexican doctors dismissed the injury as unrelated to the vaccination, reasoning that the condition had not been detected in Pfizer/ BioNtech’s clinical trials.

This week an Auburn, New York nursing home reported, without any apparent irony, that 32 of 193 residents have died since the facility began administering the Pfizer vaccine on Dec. 21. The company claims that its clients are dying of COVID-19 infections, not the vaccine.

Equally disturbing, additional deaths may have gone altogether unreported.

Among Dr. Michael’s many grateful patients was Tessa Levy, who had a scheduled appointment with him for the Tuesday after his death on Jan. 3. Michaels delivered all four of Tessa’s children, saving one of them with an ingenious split-second diagnosis of a rare heart condition that would have otherwise killed the boy.

Tessa is the daughter of my close friend, the famous Beverly Hills surgeon, Dr. George Boris. “He was a healthy, strong, vigorous guy,” Tessa told me about Michaels. “He never showed any health problems.”

On New Year’s Eve, Dr. Boris’s brother-in-law, Murray Brazner, also died suddenly, one week after receiving the Pfizer vaccine. Neither the vaccine company nor any health agency took notice of his sudden unexpected death. “No autopsy was performed, and his death isn’t recorded as a vaccine injury. It makes you wonder,” Dr. Boris told me.

Mr. Brazner’s death illustrates an even graver problem: Many injuries may be escaping notice by the surveillance system and the media. Unreported stories similar to Dr. Brazner’s tragedy are already common complaints on social media.

On Jan. 2, Janice Hisle lamented on Facebook that her friend’s mom, an Ohio woman, died after receiving the vaccine. According to Hisle, the woman developed a high fever hours after the jab and died a “couple days” later. “I am so angry for my friend,” she commented, “who is crying because relatives were not allowed to see her before she was vaccinated. They thought the vaccine would ‘open the door.’”

We could find no mention of the Ohio woman’s death in media records or official COVID-vaccine death tallies.

One might assume that if deaths following COVID-19 vaccine can be so easily dismissed or ignored, lesser injuries will also escape notice.

The all-too-familiar vaccine propaganda playbook

The routine of reflexively dismissing suspicious deaths and injuries as unrelated to vaccination not only calls into doubt the official data tallies on vaccine injuries, it also contrasts markedly with the habit among public health officials of authoritatively attributing every death to COVID-19 so long as the deceased tested positive for COVID within 60 days of death using a PCR test notorious for producing false positives.

In fact, the $48 billion COVID vaccine enterprise shares three defining features with every new vaccine introduced since 1986:

1. Systematic exaggeration of risk from the target disease. (Pharma calls this project “Disease Branding.”)

2. Systematic exaggeration of vaccine efficacy.

3. Systematically downplaying vaccine risks.

1. Exaggerating disease risk:

Regulatory agencies count every death as a COVID death, so long as the deceased tested positive for COVID within 60 days of death — no matter that he may have died in a motorcycle crash.

In September, the Centers for Disease Control and Prevention (CDC) admitted that 94% of individuals whose deaths the CDC officially attributed to COVID had other illnesses that may have actually killed them. The average deceased had 2.8 comorbidities. Yet in CDC’s official tabulations, CDC always presumes that COVID-19 did the killing.

But as we see from the examples above, when it comes to COVID vaccine injuries, the opposite presumption governs: the comorbidity is always the cause of death — even when, as with Dr. Michaels, there are no known comorbidities.

2. Systematic exaggeration of vaccine efficacy:

Pfizer touts a 95% efficacy rate in its clinical trials, but this is a meaningless measure of “relative efficacy” based on a tiny cohort of 94 people in the placebo group who got mild cases of COVID during the clinical trials.

The “absolute,” or “actual,” efficacy of the vaccine during clinical trials was 0.88%. According to the British Medical Journal, this means that health authorities must administer 155 vaccines to avert a single case of mild COVID.

3. Downplaying vaccine risks:

The true risk of vaccine injury will continue to be obscured by the habit among public health officials of routinely dismissing reported injuries as unrelated to vaccination.

The practices of systematically overestimating vaccine safety, underestimating vaccine deaths, and exaggerating risks of COVID-19 effectively deprive the public of their right to informed consent.

And so what do we really know about the true risk of COVID-19 vaccines?

Public health officials and industry spokespeople like to say that the risks of serious injury from vaccination are “one in one million.. However, in the first week of distribution, Americans took 200,000COVID vaccines and reported 5,000 serious” (meaning missed workdays or medical intervention required) injuries.

This is an injury rate of 1 in every 40 jabs. This means that the 150 shots necessary to avert one mild case of COVID will cause serious injury to at least three people.

If the clinical trials are good predictors, that rate is likely to increase dramatically after the second shot (the clinical trials suggested that almost all the benefits of COVID vaccination and vast majority of injuries were associated with the second dose).

We don’t know the true risk of death from the vaccine since regulators have rendered virtually every death invisible by attributing them all to coincidence.

The 1-in-40 risk of “serious injury” from Pfizer’s COVID vaccine is consistent with what we know about other vaccines.

For many years, the U.S. Department of Health and Human Services (HHS) has maintained a post-licensing surveillance system known as the Vaccine Adverse Event Reporting System (VAERS). Even government insiders like Surgeon General Dr. David Kessler acknowledged that VAERS is an abysmal failure.

Nevertheless, it is only by clinging to this “designed to fail” system that regulators and industry have maintained their pretense that current vaccine risk profiles are acceptable.

A 2010 study funded by HHS concluded that VAERS captured “fewer than 1% of injuries.” In other words, the actual injury rates from mandated vaccines are more than 100x what HHS has been telling the public!

The 2010 HHS study found that the true risk for serious adverse events was 26/1,000, or one in 37.

Similarly, Merck’s clinical trials for Gardasil found that an astonishing half of all vaccine recipients suffered from adverse events, which Merck euphemistically called “new medical conditions,” and that 2.3% of vaccine recipients (1 in 43) suffered from autoimmune disease within six months of vaccination.

Similarly, a recent Italian study found that 41% of vaccine recipients (412 adverse events per 1,000 doses) suffered adverse events, with 11% of these rated “serious,” meaning 38 serious adverse events per 1,000 vaccinated individuals. These include grave gastrointestinal and “serious neurological disorders.” This amounts to a “serious” injury rate of 1/26.

Holocaust survivor Vera Sharav of the Alliance for Human Research Protection has observed that, “Everyone who gets any of these vaccines is participating in a vast medical experiment.”

Health officials generally concur that the granting of “emergency use authorization” to the rollout of experimental vaccine technologies with only a few weeks of safety testing, two years before the scheduled completion of Phase 2 testing, is a great human experiment, involving millions of subjects.

But researchers are unlikely to see all of the safety signals if a badly designed surveillance system allows local health officials and company employees the discretion to dismiss any serious injury as unrelated.

This is an injury rate of 1 in every 40 jabs. This means that the 150 shots necessary to avert one mild case of COVID will cause serious injury to at least three people.

If the clinical trials are good predictors, that rate is likely to increase dramatically after the second shot (the clinical trials suggested that almost all the benefits of COVID vaccination and vast majority of injuries were associated with the second dose).

We don’t know the true risk of death from the vaccine since regulators have rendered virtually every death invisible by attributing them all to coincidence.

The 1-in-40 risk of “serious injury” from Pfizer’s COVID vaccine is consistent with what we know about other vaccines.

For many years, the U.S. Department of Health and Human Services (HHS) has maintained a post-licensing surveillance system known as the Vaccine Adverse Event Reporting System (VAERS). Even government insiders like Surgeon General Dr. David Kessler acknowledged that VAERS is an abysmal failure.

Nevertheless, it is only by clinging to this “designed to fail” system that regulators and industry have maintained their pretense that current vaccine risk profiles are acceptable.

A 2010 study funded by HHS concluded that VAERS captured “fewer than 1% of injuries.” In other words, the actual injury rates from mandated vaccines are more than 100x what HHS has been telling the public!

The 2010 HHS study found that the true risk for serious adverse events was 26/1,000, or one in 37.

Similarly, Merck’s clinical trials for Gardasil found that an astonishing half of all vaccine recipients suffered from adverse events, which Merck euphemistically called “new medical conditions,” and that 2.3% of vaccine recipients (1 in 43) suffered from autoimmune disease within six months of vaccination.

Similarly, a recent Italian study found that 41% of vaccine recipients (412 adverse events per 1,000 doses) suffered adverse events, with 11% of these rated “serious,” meaning 38 serious adverse events per 1,000 vaccinated individuals. These include grave gastrointestinal and “serious neurological disorders.” This amounts to a “serious” injury rate of 1/26.

Holocaust survivor Vera Sharav of the Alliance for Human Research Protection has observed that, “Everyone who gets any of these vaccines is participating in a vast medical experiment.”

Health officials generally concur that the granting of “emergency use authorization” to the rollout of experimental vaccine technologies with only a few weeks of safety testing, two years before the scheduled completion of Phase 2 testing, is a great human experiment, involving millions of subjects.

But researchers are unlikely to see all of the safety signals if a badly designed surveillance system allows local health officials and company employees the discretion to dismiss any serious injury as unrelated.




Robert F. Kennedy, Jr. Explains His Positions on Vaccines to His Family

Robert F. Kennedy, Jr. Explains His Positions on Vaccines to His Family

by Robert F. Kennedy, Jr., Children’s Health Defense Europe
January 14, 2020

 

Three of my Kennedy relatives published an article criticizing my advocacy for safe vaccines. Our contentious family dispute highlights the fierce national donnybrook over vaccinations that has divided communities and raised doubts about the Democratic Party’s commitment to some of its defining values: abhorrence of censorship, wariness toward excessive corporate power, support for free speech, religious freedom, and personal sovereignty over our bodies, and the rights of citizens (codified in the Nuremberg Code and other treaties to which we are signatories) to decline unwanted government-mandated medical interventions. The debate has also raised questions about the independence of our press and its role as a champion of free speech, and First Amendment rights as a bulwark against overreaching by government and corporations.

I love my family and sympathize with their anxieties when I call out government officials for corruption. The Kennedys have a long, close, and continuing relationship with public health agencies so it is understandably difficult for us to believe that powerful regulators would lie about vaccines. “All issues are simple,” the saw goes, “until you study them.”

My skepticism

I’ve arrived at my skepticism after 15 years spent researching and litigating this issue. I have watched financial conflicts and institutional self-interest transform key sectors of our public health bureaucracies into appendages of the very pharmaceutical companies that Congress charged them to regulate.

Multiple investigations by Congress and the HHS Inspector General have consistently found that an overwhelming majority of the FDA officials directly charged with licensing vaccines, and the CDC officials who effectively mandate them for children, have personal financial entanglements with vaccine manufacturers. These public servants are often shareholders in, grant recipients from, and paid consultants to vaccine manufacturers, and, occasionally, patent holders of the very vaccines they vote to approve. Those conflicts motivate them to recommend ever more vaccines with minimal support from evidence-based science.

The pharmaceutical industry also enforces policy discipline through agency budgets. FDA receives 45% of its annual budget from industry. The World Health Organization (WHO) gets roughly half its budget from private sources, including Pharma and its allied foundations.  And CDC, frankly, is a vaccine company; it owns 56 vaccine patents  and buys and distributes $4.6 billion in vaccines annually through the Vaccines for Children program, which is over 40% of its total budget. Further, Pharma directly funds, populates and controls dozens of CDC programs through the CDC foundation.  A British Medical Journal editorial excoriates CDC’s sweetheart relationship with pharma quotes UCLA Professor of Medicine Jerome R. Hoffman “most of us were shocked to learn the CDC takes funding from industry… It is outrageous that industry is apparently allowed to punish the CDC if the agency conducts research that has potential to cut into profits.”

HHS partners with vaccine makers to develop, approve, recommend, and pass mandates for new products and then shares profits from vaccine sales. HHS employees can personally collect up to $150,000 annually in royalties for products they work on. For example, key HHS officials collect money on every sale of Merck’s controversial HPV vaccine Gardasil, which also yields tens of millions annually for the agency in patent royalties. Furthermore, under the 1986 Act that created the National Vaccine Injury Compensation Program, HHS is the defendant in Vaccine Court and is legally obligated to defend against any claim that a vaccine causes injury. Despite high hurdles for recovery, HHS pays out hundreds of millions of dollars annually (over $4 billion total) to Americans injured by vaccines. Hence, if HHS publishes any study acknowledging that a vaccine causes a harm, claimants can use that study against HHS in Vaccine Court. In June 2009, a high-level HHS official, Tom Insel, killed a $16 million-dollar budget item to study the relationship between vaccines and autism by the Interagency Autism Coordinating Committee. Insel argued that petitioners would use these studies against HHS in vaccine court.

Such conflicts are a formula for “agency capture” on steroids. “Instead of a regulator and a regulated industry, we now have a partnership,” says Dr. Michael Carome, a former HHS employee who is now the director of the advocacy group Public Citizen. Carome says that these financial entanglements have tilted HHS “away from a public health perspective to an industry-friendly perspective.”

In 1986, Congress—awash in Pharma money (the pharmaceutical industry is number one for both political contributions and lobbying spending over the past 20 years) enacted a law granting vaccine makers blanket immunity from liability for injuries caused by vaccines. If vaccines were as safe as my family members claim, would we need to give pharmaceutical companies immunity for the injuries they cause? The subsequent gold rush by pharmaceutical companies boosted the number of recommended inoculations from twelve shots of five vaccines in 1986 to 54 shots of 13 vaccines today. A billion-dollar sideline grew into the $50 billion vaccine industry behemoth.

Since vaccines are liability-free—and effectively compulsory to a captive market of 76 million children—there is meager market incentive for companies to make them safe. The public must rely on the moral scruples of Merck, GlaxoSmithKline, Sanofi, and Pfizer. But these companies have a long history of operating recklessly and dishonestly, even with products that they must market to the public and for which they can be sued for injuries. The four companies that make virtually all of the recommended vaccines are all convicted felons.  Collectively they have paid over $35 billion since 2009 for defrauding regulators, lying to and bribing government officials and physicians, falsifying science, and leaving a trail of injuries and deaths from products they knew to be dangerous and sold under pretense of safety and efficacy.

Doesn’t it require a kind of cognitive dissonance to believe that vaccines are untainted by the greed, negligence, and corruption that bedevil every other pharmaceutical product?

No safety testing

Such concerns only deepen when one considers that, besides freedom from liability, vaccine makers enjoy another little-known lucrative loophole; vaccines are the only pharmaceutical or medical products that do not need to be rigorously safety tested. To win an FDA license, companies must safety test virtually every other drug for years in randomized comparisons against an inert placebo. Yet, not a single vaccine currently on the CDC’s childhood schedule was tested against an inert placebo before licensing. Without placebo testing, regulators have no capacity to assess a medicine’s risks. During a January 2018 deposition, Dr. Stanley Plotkin, the world’s most influential vaccinologist, acknowledged that researches who try to ascertain vaccine safety without a placebo are in “La La land”. According to Dr. Drummond Rennie, Deputy Editor of the Journal of the American Medical Association, “It is the marketing department, not the science, that is driving the research.”  It seems plain wrong to me that Democratic-controlled legislatures across the country are frantically passing coercive mandates for pharmaceutical products for which no one knows the risks.

Furthermore, safety testing, which typically requires five or more years for other medical products, often lasts only a few days with vaccines—not nearly long enough to spot cancers or chronic conditions like autoimmune disease (e.g., juvenile diabetes, rheumatoid arthritis, multiple sclerosis), allergic illnesses (e.g., food allergies, allergic rhinitis, eczema, asthma), or neurological and neurodevelopmental injuries (e.g., ADD, ADHD, narcolepsy, epilepsy, seizure disorders, and autism). Manufacturers’ inserts accompanying every vial of mandated vaccines include warnings about these and over 400 other injuries including many serious immune, neurological, and chronic illnesses for which FDA suspects that vaccines may be the cause. Federal law requires that the package insert for each vaccine include “only those adverse events for which there is some basis to believe that there is a causal relationship between the drug and the occurrence of the adverse event.”

Many of these illnesses became epidemic in American children after 1986, coterminous with the exploding vaccine schedule. For American kids born in 1986, only 12.8% had chronic diseases. That number has grown to 54% among the vaccine generation (those born after 1986) in lockstep with the expanding schedule.  Evidence including HHS’s own surveillance reports, manufacturers’ inserts, and peer-reviewed studies link all of these injuries to vaccines. However, the associations are not definitive because CDC has failed to conduct the necessary randomized studies to prove or disprove causation.

HHS has directed the Institute of Medicine (IOM, now the National Academy of Medicine) to oversee the CDC’s vaccine safety science. IOM has repeatedly rebuked the agency for failing to study whether vaccines are causing these epidemics. In my experience, vaccine proponents rarely cite specific peer-reviewed studies to support their assertions that all vaccines are safe, relying instead on appeals to authority; CDC, FDA, WHO, or the AAP. My relatives, for example, argue that vaccines are safe because WHO, HHS, CDC, and FDA say so. But HHS designated the IOM as the ultimate arbiter of vaccine safety. And IOM says that the existing scientific literature does not support these claims.  Despite requests by the IOM, CDC has steadfastly refused to perform safety studies.

In total, three IOM reports (19911994, and 2011/2012) investigated 231 adverse events associated with vaccines. For 34 conditions, IOM found that the evidence supported a causal connection between the vaccine and the adverse event. But for 184 adverse events, fully 80% of the conditions reviewed, the IOM found that HHS’s evidence was inadequate to accept or reject vaccine causation. How can our public health officials claim safety when there is no follow-up research on reported adverse events?

Autism and vaccines

Let’s drill down on bedrock dogma that science has thoroughly debunked any links between autism and vaccines. That assumption is so engrained that media ridicules anyone who questions this orthodoxy as a dangerous heretic. But, look for a moment, at the facts. In 1986, Congress specifically ordered CDC to determine if pertussis-containing vaccines (DTP, later DTaP) were causing autism.  Then, as today, many parents with autistic children were claiming that vaccines were a cause of their child’s autism and DTP/DTaP vaccines were/are a popular suspect.

On its website, CDC declares that, “Vaccines don’t cause autism,” citing IOM’s comprehensive 2011/2012 literature review of vaccination safety science. However, the IOM study and the follow-up HHS study in 2014 both say that CDC has never performed a study to support CDC’s claim that DTaP does not cause autism.  The same is true for Hep B, Hib, PCV 13, and IPV. The only vaccine actually studied with regard to autism is MMR, and a senior CDC scientist claims the CDC did find an increased rate of autism after MMR in the only MMR/autism study ever conducted by the CDC with American children. Moreover, HHS’s primary autism expert recently provided an affidavit to the DOJ explaining that vaccines can cause autism in some children.

Autism has grown from about 1 in 2,500 prior to 1986 to one in 36 among vaccine generation children today. Why are we content with the CDC’s claim that the exponential explosion of autism is a mystery? CDC spares no expense systematically tracking the source of 800 measles cases. But when asked about the cataclysmic epidemic of upwards of 68,000 new autism cases annually, CDC shrugs. Why are we not demanding answers? “CDC is paralyzed right now when it comes to anything to do with autism,” explains former senior vaccine safety scientist Dr. William Thompson, who is still a CDC employee. Thompson told Congressman Bill Posey under oath that CDC bigwigs ordered him to destroy data that showed a link between autism and vaccines and to publish a fraudulent study dismissing the link. Today, he is remorseful, “When I see a family with a child with autism, I feel great shame because I have been part of the problem.”

We are killing children

HHS has also ignored its statutory obligations to study vaccine injuries and improve vaccine safety. In 1986, Congress—recognizing that drug companies no longer had any incentive to make vaccines safe—ordered HHS to study vaccine injuries, work to improve vaccine safety, and report to Congress on its progress every two years. A year ago, I brought a lawsuit that forced HHS to admit that in 36 years it had never performed any of those critical studies.

Post-licensure vaccine safety surveillance is also in shambles. The CDC’s Vaccine Adverse Event Reporting System (VAERS), to which doctors and patients may voluntarily report adverse vaccine events, received 58,381 reports in 2018, including 412 deaths, 1,237 permanent disabilities, and 4,217 hospitalizations. An HHS-funded review of VAERS concluded that “fewer than 1% of vaccine adverse events are reported” to VAERS. This suggests that there are a hundredfold more adverse vaccine events than are reported. The CDC has nonetheless refused to mandate or automate VAERS reporting.

On March 9, 2019, Dr. Peter Aaby issued a scathing rebuke to the world’s public health agencies for continuing to allow pharmaceutical companies to sell vaccines without proper safety testing.  Dr. Aaby, who has authored over 300 peer-reviewed studies, is one of world’s foremost authorities on WHO’s African vaccine program and the winner of Denmark’s highest honor for health care research. Dr. Aaby was one of five co-authors of a 2017 study of the diphtheria tetanus, and pertussis (DTP) vaccine, the most widely used vaccine on earth, which found that children who received DTP had ten times the risk of dying compared to DTP-unvaccinated children. For thirty years, doctors, including Aaby, never noticed the danger because vaccinated children were succumbing to illnesses and infections apparently unrelated to the vaccine. It turns out that while the vaccine protected children from diphtheria, tetanus, and pertussis, it so badly weakened their immune systems that they were dying in droves from unrelated infections. The researchers concluded: “The DTP vaccine may kill more children from other causes than it saves from diphtheria, tetanus and pertussis.”  In March, an alarmed Aaby plead for a policy change, “Most of you think we know what our vaccines are doing. But we don’t…. We are killing children.”

The world’s most aggressive vaccine schedule has not given our country the world’s healthiest children. We now rank 35th in overall health outcomes—just behind Costa Rica, making the U.S., by most measures, including infant mortality, the sickest in the developed world. In addition to those 400 chronic diseases and injuries that FDA suspects may be vaccine related, the vaccine generation suffers unprecedented levels of anxiety and depression and behavioral disorders running the gamut from aggression to anorexia. Peer-reviewed animal and humanstudies have linked all these symptoms to vaccines. The present generation is the first in a century to lose I.Q., having suffered an extraordinary drop of seven points.  Researchers concluded that some environmental cause is the trigger. In the U.S., SAT and, more recently, bar exam scores are plummeting. Could these declines be the outcome of injecting virtually every child with multiple doses of two of the world’s most potent neurotoxins—mercury and aluminum—in bolus doses beginning on the day of birth? Shouldn’t we be doing the research to reject this hypothesis? The logical approach to doing so would be to compare health outcomes between vaccinated and unvaccinated children. For years, public health officials, including the IOM, have urged CDC to conduct such studies.

In 2013, the IOM found that, “No studies have compared the differences in health outcomes… between entirely unimmunized populations of children and fully immunized children…. Furthermore, studies designed to examine the long-term effects of the cumulative number of vaccines or other aspects of the immunization schedule have not been conducted.” In a 2008 interview, former NIH Director Bernadette Healy explained that HHS refuses to perform safety studies out of fear that they will expose dangers, “that would scare the public away” from vaccines.  Healy continued, “First of all, I think the public is smarter than that… I don’t think you should ever turn your back on any scientific hypothesis because you’re afraid of what it might show.”

Media malpractice

The suppression of critical safety science documented by the IOM would not be possible without a mass epidemic of media malpractice. Mainstream and social media outlets which collectively received $9.6 billion in revenues from pharmaceutical companies in 2016 have convinced themselves they are protecting public health by aggressively censoring criticism of these coercively mandated, zero liability, and untested pharmaceutical products.  But, the absence of press scrutiny leaves industry no incentive to improve vaccine safety.  Muzzling discussions of government corruption and deficient safety science and abolishing vaccine injuries by fiat is not a strategy that will solve the growing chronic disease epidemic.

The children who comprise this badly injured generation are now aging out of schools that needed to build quiet rooms and autism wings, install wobble chairs, hire security guards and hike special ed spending to 25% to accommodate them. They are landing on the social safety net which they threaten to sink. As Democratic lawmakers vote to mandate more vaccines and call for censorship of safety concerns, Democratic Presidential candidates argue about how to fix America’s straining health care system. If we don’t address the chronic disease epidemic, such proposals are like rearranging the deck chairs on the Titanic. The good news for Pharma is that many of these children have lifelong dependencies on blockbuster products like Adderall, Epi-Pens, asthma inhalers, and diabetes, arthritis, and anti-seizure meds made by the same companies that made the vaccines.

My belief that all or some of these injuries might be vaccine related has been the catalyst that wrenched so much of my focus away from the environmental and energy work that I love, and prompted me to become an advocate for vaccine safety. I have sacrificed friendships, income, credibility, and family relationships in an often-lonely campaign to force these companies to perform the tests that will definitively answer these questions.

People will vaccinate when they have confidence in regulators and industry.  When public confidence fails, coercion and censorship became the final options.  Silencing critics and deploying police powers to force untested medicines upon an unwilling public is not an optimal strategy in a democracy.

My uncle and my father argued that in a free and open society, the response to difficult questions should never be to shut down debate. What we need is science, not censorship. I am not anti-vax. I am pro-safety and pro-science. I want robust, transparent safety studies and independent regulators. These do not seem like the kind of radical demands that should divide our party or our families. As Americans and Kennedys, we ought to be able to have a civil, science-based debate about these legitimate concerns.




Johns Hopkins Scientist: ‘A Medical Certainty’ Pfizer Vaccine Caused Death of Florida Doctor

Johns Hopkins Scientist: ‘A Medical Certainty’ Pfizer Vaccine Caused Death of Florida Doctor
Dr. Jerry L. Spivak, an expert on blood disorders at Johns Hopkins University, told the New York Times Tuesday that he believes “it is a medical certainty” that Pfizer’s COVID vaccine caused the death of Dr. Gregory Michael.

by Children’s Health Defense Team
January 13, 2020

 

The Florida Health Department and the Centers for Disease Control and Prevention are investigating the death of a Florida doctor who died Jan. 3 from a rare autoimmune disorder he developed on Dec. 21, three days after receiving Pfizer’s COVID vaccine.

As The Defender reported last week, Heidi Neckelmann, the wife of Dr. Gregory Michael, said that in her mind, her 56-year-old husband’s death was “100% linked” to the vaccine.

Now, at least one doctor has come forward publicly to say he also believes the vaccine caused Michael to develop acute idiopathic thrombocytopenic purpura (ITP), the disorder that killed him.

According to the New York Times:

“Dr. Jerry L. Spivak, an expert on blood disorders at Johns Hopkins University, who was not involved in Dr. Michael’s care, said that based on Ms. Neckelmann’s description, ‘I think it is a medical certainty that the vaccine was related.’

“‘This is going to be very rare,’ said Dr. Spivak, an emeritus professor of medicine. But he added, ‘It happened and it could happen again.’”

Spivak told the Times he based his reasoning on the fact that Michael’s disorder came on quickly after the shot, and “was so severe that it made his platelet count ‘rocket’ down.”

Spivak also offered two other reasons to back up his theory. One, the fact that Michael was healthier and younger than most people who develop chronic forms of ITP. And two, the fact that about 70% of people who develop ITP are women.

As Spivak told the Times: “A sudden case in a man, especially a relatively young, healthy one, suggests a recent trigger.”

Pfizer said it is also investigating Michael’s death, though the drugmaker told multiple news outlets it doesn’t “believe at this time that there is any direct connection to the vaccine.”

Shortly after the first reports surfaced of Michael’s death, Pfizer told USA Today:

“There is no indication — either from large clinical trials or among people who have received the vaccine since the government authorized its use last month — that it could be connected to thrombocytopenia.”

But, as Lyn Redwood, RN, MSN, president of Children’s Health Defense (CHD), said last week, Pfizer’s statement doesn’t square with the facts — because ITP is a well-known adverse event associated with vaccinations.

The vaccine most often implicated in ITP is the measles-mumps-rubella (MMR) vaccine, where the disease occurs in approximately 1 in every 25,000 to 40,000 doses of the vaccine, Redwood said.

ITP has also been associated with hepatitis A and B virus (HBV), human papilloma virus (HPV)varicella-zoster, diphteria-tetanus-acellular pertussis (DTap)polio and pneumococcus vaccines.

According to Redwood, a study comparing adverse effects following influenza vaccination found that ITP was the third most common autoimmune condition (after Guillain Barre and rheumatoid arthritis).

Redwood also pointed out that ITP has been reported to occur following exposure to drugs containing polyethylene glycol (PEG), a compound used in both the Pfizer and Moderna vaccines.

“Considering that according to the U.S. Court of Federal Claims, cases of ITP have been compensated in the National Vaccine Injury Compensation Program (NVICP), it is completely disingenuous for vaccine manufacturers to deny this risk,” Redwood said.

An official with the Miami Dade medical examiner’s office on Jan. 11 told the media that the cause of Michael’s death is “pending the completion of studies” by the medical examiner and the Centers for Disease Control and Prevention.




Dr. Tom Cowan: Overview of the Real Science Related to the COVID Narrative; How Science is Being Weaponized Against Us

Dr. Tom Cowan: Retrospective on 2020; How Science is Being Weaponized Against Us & Why We Must Understand Real Science
Year End Review and Thoughts on the Future

by  Dr. Tom Cowan

 



Original video is available at Dr. Tom Cowan YouTube channel.

[As a service to protect truth from censorship and to share widely, mirrored copies of this video are available at Truth Comes to Light BitChute, Brighteon, Lbry/Odysee channels. All credit, along with our sincere thanks, goes to the original source of this video. Please follow links provided to support their work.]

Topics covered:

  • How science is being weaponized against us and why we must understand real science.
  • What do virologists actually do?
  • Where do they get the genome?
  • The creation of an imaginary genome of a make-believe virus.
  • Looking into the science of the so-called COVID vaccine — an injectable product that is nothing like any vaccine ever made.
  • Genetic engineering.
  • The theory of vaccines.
  • mRNA drug development meant to act as an operating system in our bodies.
  • Dr. Tom Cowen’s strategies for keeping himself and his family well.

 

Excerpts — Unofficial Partial Transcript

…There’s nothing unique about this. They’re simply testing for pieces of genetic material, having no idea the origin of this genetic material. 

So, as far as I know, and I know this, I think, as well as anybody could know it. There is not one study out there — there has never been with this virus or many other viruses  — that has properly isolated the virus, properly sequenced the virus. And if you can’t properly isolate it, you cannot say that a sequence of it comes only from that virus.

And, if you’ve never isolated it… you could never prove that the virus is the cause of this disease.

Isolation is the key. And no matter how many people say they’ve isolated, no matter how many people criticize me and us for saying it, I still contend that there is simply no evidence that this kind of isolation has ever happened with this or many other of the viruses that we are told cause disease.”

___

“Let’s move on a little bit to talk about… the so-called COVID vaccine… We need to understand thoroughly that this injectable product is nothing like any vaccine that has ever been made, and actually, in no way should be called a vaccine…

The first thing we have to know is that in genetics… there is something called a central dogma. 

The central dogma of genetics — meaning the foundational principle of genetics — is that the genetic material in all animals, including humans, is found in the nucleus it’s found in this substance called DNA, which we’re told is the house of the genes. In other words, each strand of DNA contains many different genes which are composed of so-called nucleotides, which are composed of base pairs, which are either A, T, C or G. 

So a gene is a long string, like word, made of say AATTCGAT, etc. So it’s got a certain number of length. And the sequence of those nucleotides is what constitutes a gene. And there’s many genes in sequence, not necessarily one after the other, laying on this piece of DNA.

Now, the central dogma is, this DNA, which is formed sort of like a zipper, right? So there’s a strand here and this is A. And every A matches up with T. And then the next one is C and every C matches up with G, and then so on down the line. 

[Dr. Cowan is demonstrating with his hands during this explanation — near the 21 minute mark in the video.]

So they’re like this and then you separate them. And then two strands will form if it’s mitosis, so that A always matches up again with T and the C always matches up again with G. And so then you make two exact copies of it. And that’s how a cell reproduces itself.

Now, sometimes the DNA — let’s just use the word “wants” — to make protein. So the way that works is, you get this separation, And so, here’s the A — and it makes T, C…whatever the complimentary nucleotide. And that new structure is called m (or messenger) RNA. And that process of turning the DNA into a homologous copy of RNA, messenger RNA, is called transcription.

Now, that process, we think, happens in the nucleus. Then the mRNA goes out of the nucleus into the cytoplasm.  And now we have a homologous copy. And then through a process called translation, this RNA is converted into a protein, which obviously has the same sequence as the DNA did in the first place…

And that sequence of nucleotides creates the amino acids, which is essentially the backbone or the material out of which a protein is made. And then the protein does all the functions that are happening in a living organism.

So, again, the central dogma is, quite simply — this is a one-directional process. DNA makes messenger RNA, called transcription. Messenger RNA makes protein, which is called translation.

The central dogma tells us that protein never makes RNA, RNA never makes DNA, and DNA never makes protein directly.

It’s always in that very specific sequence: DNA, messenger RNA, protein. Transcription, translation, action. The action molecule is the protein. The blueprint is the DNA.

Now, here’s the interesting thing, all those facts that I just said — and, I’m sure some of you this won’t come as a surprise to — are actually incorrect. One of the things I’m going to do in this next year is dissect that whole process and show very clearly how many of the things that I just said, which are reported as fact, are actually not fact at all. 

And one of the things that’s not fact is, starting with the discovery of what are called retroviruses (or in other words RNA viruses)…

So again, a virus is a piece of genetic material, either DNA or RNA, in a protein coating. So that’s what a virus is. 

Then a bunch of people — Gallo, Montagnier and others — came up with the theory that this disease called AIDS is caused by a virus called HIV. Human Immunodeficiency Virus. But the trouble was, this virus, which also was never isolated or proven to cause anything (but that’s another story) was an RNA virus. And the question then for them was, how does this RNA virus insert itself into the DNA of the tissues and the cells to make copies of itself.

Since there is no — or at that time, there was no idea that RNA could reverse this central dogma and make DNA. So, they discovered in researching this that there’s something called reverse transcriptase (which is abbreviated RT — which is what the RT-PCR test means) that can convert RNA, messenger RNA, into DNA , that can then get itself inserted into the animal or human DNA. And this process is basically based on an enzyme called reverse transcriptase. And, at the time, the theory was this reverse transcriptase, this enzyme that could do this process of reversing the central dogma, was only found in so-called retroviruses. There was no normally, naturally-occurring reverse transcriptase in any animal or any human…

___

What we didn’t know is that this process of converting RNA into DNA is actually a normal repair process, and any tissue in any system, any mammalian living system, actually has it’s own reverse transcriptase. And that there is a continual interplay between RNA and DNA…

So, you may be asking why is this something I need to know about? The reason is, for the first time humans are injecting other humans with messenger RNA

…The expectation of the injection of messenger RNA into an animal is to make that messenger RNA insert itself into the human DNA, the human genome, which is basically the definition of genetic engineering…”

 


 See related: Dr. Tom Cowan w/ Jon Rappoport: SARS-CoV-2 Has Never Been Isolated, Is Only an Imaginary or Theoretical Virus, and, Therefore, No Test Can Detect It



Frontline Workers Refuse COVID Vaccine

Frontline Workers Refuse COVID Vaccine

by Del Bigtree w/ Jefferey Jaxen, The HighWire
January 8, 2021

 



Medical workers have first access to new #COVID19 vaccines. However, many of them are not receiving the shot. Find out why.




A Nursing Home Had Zero Coronavirus Deaths. Then, It Vaccinates Residents for Coronavirus and the Deaths Begin.

A Nursing Home Had Zero Coronavirus Deaths. Then, It Vaccinates Residents for Coronavirus and the Deaths Begin.

by Adam Dick, Ron Paul Institute
January 10, 2021

 

Things seem to be working backwards at The Commons on St. Anthony nursing home in Auburn, New York. Vaccinating people is supposed to reduce or end coronavirus deaths. Right? But, at The Commons, such deaths are reported to have occurred only after residents began receiving coronavirus vaccinations.

James T. Mulder wrote Saturday at syracuse.com that until December 29 there had been no coronavirus deaths at The Commons. December 29, when deaths of residents with coronavirus began occurring at The Commons, is also, Mulder’s article discloses, seven days days after the nursing home began giving coronavirus vaccinations to residents, with 80 percent of residents so far having been vaccinated.

Over a period of less than two weeks since December 29, Mulder relates that 24 coronavirus-infected residents at the 300-bed nursing home have died.

Is the timing just a strange coincidence?

Read Mulder’s article here.

This is the penultimate paragraph of Mulder’s article, where vaccinations at The Commons is mentioned:

The nursing home began vaccinating residents Dec. 22. So far 193 residents, or 80%, and 113 employees, or less than half the staff, have been vaccinated. The nursing home plans to do more vaccinations Jan. 12.




10 Facts From the UK Government Pfizer Vaccine Guidance That Promote “Vaccine Hesitancy”

10 Facts From the UK Government Pfizer Vaccine Guidance That Promote “Vaccine Hesitancy”

Official government guidance has been released in the United Kingdom to assist healthcare professionals in administering the Pfizer/BioNTech vaccine BNT162b2. While the UK government goes to war against supposed misinformation, the official narrative is clearly based on very little to no supporting data from incomplete clinical trials. This article examines the document “Reg 174 Information for UK Healthcare Professionals” and narratives being pushed in the mainstream media that directly contradict that document.

by Johnny Vedmore, Unlimited Hangout
December 30, 2020

 

Healthcare professionals globally have begun the controversial campaign to vaccinate large swathes of their respective populations with various experimental medical products. The vanguard of the mainstream pro-vax extremists have been busy enacting mass censorship tactics and committing blatant acts of digital book burning on a scale never before seen in the internet era. So-called “trusted sources” have become indistinguishable from the state-run media apparatus of your bog-standard dictatorship with the usual MSM outlets working non-stop to skew any information that threatens their hyper-aggressive official narrative. Throughout 2020, our basic civil liberties have been quickly stripped away by countless unelected officials from a wide array of unaccountable global power structures, all of them connected to a small group of elites who are sitting aloft the COVID-19 money train and using the heavily exaggerated epidemic to achieve their own long term goals.

Any useful data, scientific paper, or other credible research contradicting the official narrative is being purposely hidden from view. Too many uncomfortable, yet ultimately necessary, questions for vaccine companies such as Moderna, AstraZeneca, Pfizer, and their many collaborators, are being heavily censored by those pushing their own various COVID-related agendas. The promised “war on truth” is in full swing throughout all nations globally and their respective state media machines are nearly all towing their official government lines. Mainstream talk shows and podcasts worldwide are also in lockstep, and have often been caught publicly guilt-tripping their easily swayed audiences to help push them deeper into queues for mass medical trials for vaccines and other products that lack research studies on their long term effects. This inconvenient lack of completed research will not stop the money men from pumping this milky white liquid into the arms of hundreds of millions of people worldwide.

At this point in the process, the medical professionals who are administering these heavily rushed vaccines are being given the opportunity to defer responsibility and accountability for their actions to the government’s vaccine-related guidance. As the Stanley Milgram experiments have proven, when the option to defer responsibility is present, then roughly 65% of participants will follow the orders they have received regardless of the risk to their subjects. In 1974, Stanley Milgram detailed the behaviour of his participants in his famous study and suggested that people have two basic states of behaviour when they are in a social situation: “The autonomous state”, where people direct their own actions and ultimately take responsibility for the results of those actions and “the agentic state”, where people allow others to direct their actions and then pass off the responsibility for the consequences to the person giving orders, in essence acting as agents of another person’s will.

The majority of the people who are injecting these experimental drugs into their trusting patients are not likely to question the official guidance, as the overwhelming majority will often simply be in an agentic state. Thus, it should be in the best interest of anyone thinking of receiving a mRNA vaccine to first study the guidance offered by the various government sources. And, when one does study the official guidance given to healthcare professionals, one will find many different glaring contradictions and shocking admissions.

While all official bodies are attacking any inconvenient fact as misinformation, they are all busy defrauding the global population with their own misinformation campaigns that surely would have inspired awe in the likes of Joseph Stalin. So, let’s study their own words and examine the NHS guidance given to the medical professionals in the UK for the administration of the recently approved Pfizer-BioNTech vaccine.

An Introduction to Reg 174 Information for UK Healthcare Professional(#1-4)

The short ten page official guidance being given to UK healthcare professionals contains many interesting admissions. In fact, the document, released in early December 2020 to accompany the vaccine rollout, appears to advise healthcare practitioners not to risk giving the experimental injection to the majority of the people who are due to receive the vaccine, particularly “prioritized” populations. Those in charge are pushing to vaccinate as much of the population as possible, before any critical public questions can be asked and answered, a situation that has left the safety and ethics of the vaccination campaign questionable at best and inhumane at worst.

In going through the Reg 174 document, it becomes very clear that there are many issues and recommendations that are being hidden from the general public. Here are ten of the most notable causes for concern contained within the official UK guidance document.

1. This medicinal product does not have UK marketing authorisation but has been given authorisation only for temporary supply

The authorisation to produce and supply this experimental vaccine in the UK was given by the UK Department of Health and Social Care, led by Matt Hancock – the UK Secretary of Health, and also by the Medicines & Healthcare products Regulatory Agency (MHRA). While the MHRA is part funded by the Department of Health and Social Care for the regulation of medical devices, the costs of medicine regulations are met through fees paid by the pharmaceutical industry. The agency’s financial reliance on Big Pharma has led to suggestions by some Members of the UK Parliament that the MHRA is not actually independent. Being in associated roles at the MHRA since 1985, June Raine was officially appointed as CEO in September 2019 and had previously been the Director of Vigilance and Risk Management in the Medicines Division.

2. The official Phase III safety trials will not be completed until 2023

Section 1 of the medical guidance clearly states that this vaccine guidance refers specifically to the “Pfizer/BioNTech COVID-19 mRNA Vaccine BNT162b2 concentrate for solution for injection.” On 2 December 2020, the MHRA became the first medicines regulator in history to approve an mRNA vaccine for human use, granting emergency authorisation for BioNTech and Pfizer’s BNT162b2 COVID-19 vaccine for widespread use only a week after its first Phase III eight-week trial had finished. However, the Phase III trials for BNT162b2 will not actually be fully completed until January 2023 meaning that, if you’re ready to take the vaccine now, then you should be informed that the safety trials for these experimental vaccines have at least two more years before the results are in. Regardless of that fact, Raine told reporters “no corners have been cut in approving it” and that “the benefits outweigh any risk”.

3. Will you be truly “protected” from COVID-19?

The official guidance clearly states that individuals may not be protected until at least 7 days after their second dose of the vaccine. This fact has again been ignored by various reckless pro-vax media campaigns where powerful elites such as Tony Blair have contradicted this specific recommendation, suggesting recently in an interview that people should only be given a single dose of any vaccine. Mr Blair told BBC Radio 4’s Today programme that “Does the first dose give you substantial immunity, and by that I mean over 50 percent effectiveness? If it does, there is a very strong case for not, as it were, holding back doses of the vaccine.” Blair, writing in the Independent, stated that the current vaccination strategy needed to be “altered and radically accelerated”. In responding to Blair’s call for radical acceleration, Professor Wendy Barclay, chair of virology at Imperial College London and member of the UK government’s NERVTAG, said: “I think that the issue with [Mr Blair’s suggestion] is that the vaccine is on the basis of being given in two doses, and the efficacy is on that basis.” Barclay went on to point out that “To change at that point, one would have to see a lot more analysis coming out from perhaps the clinical trial data.”

It is very important to pay attention to the wording of Reg 174 because the Pfizer vaccine purportedly boosts the immune system, rather than stopping the transmission of the virus. This would suggest that you will not be fully “protected” from COVID-19 and that you will still be able to catch the virus and could still suffer complications. The official guidance also states that “Immunocompromised persons, including individuals receiving immunosuppressant therapy, may have a diminished immune response to the vaccine,” with the guidance admitting “No data are available about concomitant use of Immunosuppressants.”

Reg 174 goes on to make this most pertinent of points when it states:  “As with any vaccine, vaccination with COVID-19 mRNA Vaccine BNT162b2 may not protect all vaccine recipients.” The guidance also states clearly that “administration of COVID-19 mRNA Vaccine BNT162b2 should be postponed in individuals suffering from acute severe febrile illness and that individuals receiving anticoagulant therapy or those with a bleeding disorder that would contraindicate intramuscular injection, should not be given the vaccine unless the potential benefit clearly outweighs the risk.”

4. The complicated multistage dilution and thawing process of the vaccine vials opens the major possibility of human error

In investigating the official instructions for the vaccine’s administration, we can clearly see that there are plenty of opportunities for potential human error. Section 2 of this document describes the distributed vaccine as coming in “a multidose vial and must be diluted before use.” Confirming that each vial contains 0.45 ml (which equates to 5 doses of 30 micrograms) of BNT162b2 RNA embedded in lipid nanoparticles. The delicate preparation process will be repeated 100s of millions of times globally and the multidose vial will be stored frozen and must be thawed prior to dilution. The guidance describes the process for preparing the frozen vials stating that they should be transferred to temperatures of between 2 °C to 8 °C to thaw or, alternatively, the frozen vials may also be thawed for 30 minutes at temperatures up to 25 °C for immediate use. Once thawed, the undiluted vaccine can be stored for up to 5 days at 2 °C to 8 °C, and up to 2 hours at temperatures up to 25 °C. The thawed vial must then come to room temperature and be gently inverted 10 times prior to dilution.

Some of the featured diagrams and instructions found in Reg 174

The complicated thawing and dilution process will obviously leave room for individual error. Healthcare practitioners are also warned not to shake the vials and instead to gently turn them 10 times. Prior to dilution, the vaccine should present as an off-white solution with no particulates visible. The guidance states that you must discard the vaccine if particulates or discolouration are present. The thawed vaccine must be diluted in its original vial with 1.8 mL sodium chloride 9 mg/mL (0.9%) solution for injection, using a 21 gauge or narrower needle and aseptic techniques and this complex, multistage process isn’t completed there.

The healthcare professional should then equalise vial pressure before removing the needle from the vial by withdrawing 1.8 mL of air into the empty diluent syringe. Then they should gently invert the diluted solution 10 times, again being careful not to shake the solution. The official guidance continues: “The diluted vials should be marked with the dilution date and time and stored between 2 °C to 25 °C. After dilution, the vial contains 5 doses of 0.3 mL.” The healthcare professionals are then told to “withdraw the required 0.3 mL dose of diluted vaccine using a sterile needle and syringe and discard any unused vaccine within 6 hours after dilution.”

The instructions must be followed precisely to safely administer the mRNA vaccine; there are no data available on potential consequences for the vaccine recipient if anything goes wrong during this tedious and complex multistage process. On 19 December 2020, video emerged of an official drive-thru vaccination hub which had begun operating out of a car park of Hyde Leisure Centre in Greater Manchester. The video in question, shared by No Comment TV on YouTube, shows people being vaccinated outdoors at Hyde Leisure Centre by gloveless staff and in less than sterile conditions. In an article in the Manchester Evening News four days prior to the videos release the local news site stated that “The first batch of the Pfizer/BioNTech vaccine arrives in the borough on Tuesday, with vaccinations starting at Hyde Leisure Centre on Wednesday, December 15.”

No Data Available (#5-10)

When reading Reg 174, you will soon notice a recurring theme throughout the document. The guidance clearly states on multiple occasions that there are no data available concerning some of the most important questions surrounding the mRNA vaccine. As previously noted, the actual Phase III section of the safety trials will not be completed until January 2023, meaning that two years of trials are still to be run before the vaccine can be confirmed as safe, effective and ethical.

5. The safety and efficacy of COVID-19 mRNA Vaccine BNT162b2 in children under 16 years of age have not yet been established

Although the guidance states that the safety and efficacy of the COVID-19 vaccine has not been established in children, it doesn’t mean that children have not been included within the studies. In fact, in the official Pfizer study entitled “Protocol C4591001”, one of the two main study groups included children as young as 12 years old. The inclusion of children in trials but not the guidance raises the important question, why were children included in the trial? If the vaccine is not to be given to those under the age of 16 years old, then why include children as young as 12 in the trials for an experimental vaccine technology never before authorised for use in humans?

The mainstream media, instead of raising concerns about the involvement of children in the Pfizer clinical trials, have been fully supportive of the move to test experimental pharmaceuticals on minors. CNN reported on children as young as 12 being involved in trials in an October 2020 article entitled “This 12-year-old is happy to be testing a Covid-19 vaccine” while Microsoft News recently announced that “China begins Covid test trials on children as young as age three.”

6. No data are available on the use of COVID-19 mRNA Vaccine BNT162b2 in persons that have previously received a full or partial vaccine series with another COVID-19 vaccine

We are currently witnessing the very first of many tailor-made vaccines being rolled out for general use, so don’t expect the COVID-19 jabs to be the only vaccines coming our way. With a 20 to 1 return on investment on many of these new technologies, most pharmaceutical giants will surely be lobbying governments across the globe for the next “necessary” vaccination program. The idea of multiple COVID-19 vaccinations throughout the year is already being presented as a very possible outcome for the future of humanity. Yet, no studies have been completed showing the risk of taking different types of vaccines. There have also been suggestions that people will have to have the same vaccine that they had previously taken every six months or so. This will leave Astrazeneca, Pfizer and Moderna picking up repeat vaccine contracts worth billions in secured future revenue before there are any real data on the results of the vaccines.

7. No interaction studies have been performed and there are no, or a limited amount of, data from the use of COVID-19 mRNA Vaccine BNT162b2

Admissions like these should be a cause for concern for anybody reading the official guidance. While officials and carefully chosen “trusted sources” are telling you that “no corners have been cut” in the race to approve these vaccines, it is also true that no full length studies have been completed either. These two facts are juxtaposed and obviously contradict the official narrative that is being thrust upon the general public by all of those involved.

It is clear that the officials have no real data on what will happen next and that there is a tsunami of ethical questions that are not being answered. In the absence of data, there will be speculation.

8. It is unknown whether COVID-19 mRNA Vaccine BNT162b2 is excreted in human milk and It is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility

It is vital to note the potential dangers posed by the BNT162b2 to unborn and newborn babies as well as the reproductive organs in general. There are so many parts of the Pfizer/BioNTech clinical trials that have not yet been completed. Dr. Peter Klatsky, the Director of Fertility Preservation at the Bay Area’s Spring Fertility, talking about the coming animal trials which are to be performed over the coming months was quoted in SFGate as saying, “It will reassure me an awful lot if the protein expression is not seen on the placenta. That the mRNA isn’t making it to the placenta in animals,” he said. “I don’t expect to see any.” The article goes on to explain that it will be about another 9 months until the data has been collected and analyzed.

Section 4.6 of the official guidance recommends pregnant women should not recieve the BNT162b2 vaccine

Big names in mainstream media have also been caught recklessly promoting the vaccine to pregnant women, such as Karen Weintraub writing for USA Today, whose recent article quickly states, “Although there are very little data on how pregnant and nursing mothers will respond to a COVID-19 vaccine, professional organizations and individual doctors say the benefits are very likely to outweigh the risks.” Even though the clinical trials intentionally excluded pregnant women, Weintraub went on to state that “23 women in the Pfizer-BioNTech trial and 13 in Moderna’s became pregnant during the trial.”

While the UK’s official guidance is left sounding ambiguous, on the European continent, the European Medicines Agency (EMA) states that “the Pfizer vaccine should be considered on a case by case basis for pregnant women”, but they also reserve the right to alter the guidance if more data becomes available. It seems there is no longer any erring on the side of caution with some regulators when it comes to the COVID-19 vaccinations.

9. Non-clinical data reveal no special hazard for humans based on a conventional study of repeat dose toxicity but animal studies into potential toxicity to reproduction and development have not been completed

Animal studies have not been completed and, as referred to in the previous section, the data on those animal trials will not be available for another 9 months.  It is, of course, a very rare decision to approve an experimental medical technology before any animal studies have been completed. This should be a great cause for concern for any free thinking man or woman. The fact that they have had to use what they refer to as “non-clinical” data in these studies is also in conflict with the idea that the trials were conducted to the highest professional standard. The document also fails to clearly define what non-clinical data actually means.

10. In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products

Possibly the most fascinating admission in the entire document is the absence of any compatibility studies when somebody is given the vaccine while on any other medication or medical treatment. The guidance clearly states “this medicinal product should not be mixed with other medical products.” This completely jaw dropping sentence will lead many to assume that if you are on any medication at all, then you shouldn’t be given the vaccine. Whether this refers to the mixing of other medical properties directly together with the vaccine, or simultaneous dosing of any other medical product is unclear from the official guidance.

The Mail Online and The Guardian reported in 2019 that a staggering 1 in 4 people in England – nearly 12 million people – were taking what was described as “addictive” prescription medicines such as antidepressants, sleeping pills and opioid painkillers, saying that “the NHS must take action”. Those statistics throw into question the mass rollout of a vaccination with no compatability studies. This makes the fact that elderly care home residents, followed by those aged over 80, will be the first to recieve the experimental Pfizer vaccine an extremely risky strategy. Also in 2019, Age UK reported that nearly 2 million older people were on more that 7 prescription medicines and were at “risk of side effects that are severe in some cases, and occasionally even life threatening.” This worrying issue has been barely reported by the “trusted news sources”.

A Conclusive Lack of Real Data

After examining the official guidance, one fact becomes glaringly obvious — there is little to no data on the official Pfizer vaccine in key areas. In the clinical trials, children as young as 12 years old were used as unnecessary guinea pigs. There also wasn’t enough care taken to avoid pregnant women being involved in the initial clinical trials and under the cover of unyielding and uneducated mainstream propaganda, the safety of some of the most vulnerable people involved in the vaccine trials have been ignored by Pfizer and the politicians who have successfully pushed for the public vaccination campaign to essentially replace mass clinical trials. The stage has been set for a potential disaster on an unimaginable scale. It isn’t only the participants of the trials who are risking their health for the sake of big pharmaceutical companies’ hyperinflated profit margin, but it is also the medical professionals who could be risking their futures by collaborating in these risky experimental trials, which will certainly see many people dead and irreversibly injured.

In one section of Reg 174, the Big Pharma giant lays out the risk to people’s health from the Pfizer/BioNTech vaccine. The most common adverse reaction in participants 16 years of age and older was pain at the injection site, which affected a massive 80% of those taking part in the Pfizer trials. Fatigue came a close second with 60% of trial participants becoming sluggish and tired. Half of those involved in the studies suffered from a headache as the experimental vaccine went to work while myalgia was experienced by 30% of vaccine recipients, though the results do not indicate whether the myalgia was acute (short-term) or chronic (long-term). Almost a third of participants came down with chills, while just under 1 in 5 people suffered from arthralgia (joint pain) and 1 in 10 from pyrexia (increased body temperature).

Adverse reactions reported in clinical trials are listed in the study in decreasing order of frequency and seriousness. Just under 1 in 10 people who take the vaccine will suffer from the very common and common adverse reactions referred to in the latter paragraph, such as headaches, myalgia and chills, but the more serious issues are classified as uncommon – including Lymphadenopathy (which causes swollen or enlarged lymph nodes) and nervous system disorders – which may affect up to 1 in 100 people. Rare adverse reactions that could affect up to 1 in 1000 people and very rare adverse reactions that would affect less than 1 in 10,000 of the vaccine recipients were not included in Pfizer’s self-reported safety information. It has obviously been decided that this information should be kept out of the public domain as much as possible to avoid any further vaccine hesitancy.

Not only does the official guidance actively hide the types of rare and very rare adverse effects, but they have also been leaving out some of the adverse reactions reported during the clinical trials. As I write this, the Reg 174 guidance for healthcare professionals is on version 10.1 of the document and, since its release, they have yet to admit to the potential of a certain uncommon adverse reaction to the vaccine being a specific nervous system disorder. Structural nervous system disorders include brain or spinal cord injury, Bell’s palsy, cervical spondylosis, carpal tunnel syndrome, brain or spinal cord tumors, peripheral neuropathy, and Guillain-Barré syndrome. However, previous versions of the guidance gives no clue as to what type of nervous system disorders they were referring to. However, recent articles in the USA Today, heavily promoted by the Microsoft Network, suggested that the Bell’s palsy some people came down with in the vaccine trials wasn’t related to the Pfizer jab. The article states that on Dec. 10, the FDA’s Center for Biologics Evaluation and Research held the 162nd meeting of the Vaccines and Related Biological Products Advisory Committee to discuss the emergency use authorization of the Pfizer-BioNTech COVID-19 vaccine. The USA Today piece even goes on to admit that , “a 53-page briefing noted that there had been four cases of Bell’s palsy among the vaccinated group and none among the placebo group.”

Bell’s palsy causes drooping facial muscles similar to the effects of a stroke, image source PTHealth.com

Even though Miriam Fauzia, who wrote the USA Today piece, claims that the Bell’s palsy was not related to the experimental Pfizer vaccine, the 53-page briefing she sources clearly states, “Among non-serious unsolicited adverse events, there was a numerical imbalance of four cases of Bell’s palsy in the vaccine group compared with no cases in the placebo group, though the four cases in the vaccine group do not represent a frequency above that expected in the general population.” While it is true that 1 to 4 people in 10,000 will develop Bell’s palsy within the general population, it should be noted that the 4 cases in the vaccine trials and none in the placebo group makes for a statistical anomoly that must be examined more thoroughly. Instead, the mainstream media moved quickly to discredit the Bell’s palsy links to the Pfizer vaccine using various mislead tactics to achieve their aims.

Many mainstream outlets were caught spouting the same misleading information with articles entitled “Why you shouldn’t worry about a connection between Bell’s palsy and COVID-19 vaccines,” from Business Insider and a Reuters article from 14 December 2020 entitled, “Fact check: Photo does not show three recipients of Pfizer’s COVID-19 vaccine that developed Bell’s palsy.”

In the case of the Reuters article, which is described as written by “Reuters Staff” rather than a specific journalist, the focus was not on the four Pfizer clinical trial participants who developed Bell’s palsy but instead the article discredits a random post on social media of three people with Bell’s palsy unconnected to the Pfizer vaccine. These type of misinforming mainstream media articles are commonly found to be using obvious fallacies to mislead their readership and with no individual taking responsibility for writing the misinforming piece, a trick repeated by many other media companies complicit with the official narrative. The Reuters article even goes on to admit that: “According to the FDA’s briefing document dated December 10, Bell’s palsy was reported in four vaccine participants and none in the placebo group, out of the 44,000 total participants of the late-stage vaccine trial.” However, the title of the Reuters article would mislead even some of the most keen eyed observers.

The mainstream media has been creating a flood of misleading stories, but it appears as though they have been given carte blanche to continue to do so, probably because they are sticking so tightly to the official narrative. It’s a narrative that is thick with irony, for it is the “trusted sources” who are being caught systematically misleading the general population again and again while also declaring a propaganda war against “fake news”.

The official guidance noted in Reg 174 doesn’t only highlight the serious lack of real data gained from Pfizer’s clinical trials for its Covid-19 vaccine so far, but it also exposes the wealthy medical professionals involved in these experimental vaccine development programs as complacent, reckless and very naive. It’s no secret that children are, more often than not, incapable of giving informed legal consent for such a risky and unethical enterprise. But the pro-vax extremists are using every tactic to coerce and manipulate children and their guardians into becoming human guinea pigs for Big Pharma. Pregnant women are also treated as acceptable collateral damage to advance the new science of gene, mRNA and DNA manipulation, a science and technology that pushes a sinister transhumanist agenda.

Don’t be fooled by the carefully worded vacuous celebrities, self-serving politicians, Big Pharma, and the mainstream medias authoritarian style misinformation campaigns. Keep your humanity intact and read their own words. The government guidance to healthcare professionals clearly states on multiple occasions that there are “no data available”.

 





Robert F. Kennedy, Jr.: New York Times Declines My Rebuttal to Defamatory Op-Ed on COVID Vaccines

New York Times Declines My Rebuttal to Defamatory Op-Ed on COVID Vaccines
On Dec. 30, 2020, the New York Times published an opinion piece by my niece, Dr. Kerry Meltzer. Although the piece contained factual errors and defamatory accusations, the Times declined to publish my letter to the editor correcting those false claims.

by Robert F. Kennedy, Jr., Children’s Health Defense
January 5, 2021

 

The “right of reply” — the opportunity to defend oneself against public criticism in the same venue where that criticism was published — is a constitutional right in some European countries and in Brazil. The BBC’s editorial guidelines state:

“When our output makes allegations of wrongdoing, iniquity or incompetence or lays out a strong and damaging critique of an individual or institution the presumption is that those criticized should be given a “right of reply,” that is, given a fair opportunity to respond to the allegations.”

Even where there is no legal right, respectable journalistic outlets, including the New York Times, have traditionally regarded it as their moral, ethical and professional obligation to publish the replies by people who have been criticized in their pages.

The Times, which claims to encourage the expression of “a diversity of views” on its letters page, formerly extended this courtesy automatically to public figures who suffered criticism in its pages. But the paper draws the line at anyone who questions orthodoxies promoted by the ascending Medical Cartel. The practice of reporting only facts and opinions that comply with  official narratives has long been de rigueur in electronic media outlets dependent on Pharma advertising revenues.

On Saturday, my niece published an error-filled and defamatory article about me on the Times editorial page. I immediately submitted the thoroughly sourced letter below.

Yesterday, the Times let me know that they would decline to print my reply.

Orwellian censorship and the gaslighting of dissent in service to the interests of Big Pharma has more recently become universal in the liberal print and online news sites once presumed to be the antidote to corporate subversion of democracy.

In May 2019, three of my other family members similarly defamed me in a long article in Politico. Politico likewise declined to print my thoroughly sourced reply.

Neither of these long critiques by my family members cite a single example of a factual error by me. Their complaint is that I question official pronouncements about vaccine safety.

It’s a bad omen for democracy when citizens can no longer conduct civil, informed debates about critical policies that impact the vitality of our economy, public health, personal freedoms and constitutional rights. Censorship is violence and this systematic muzzling of debate which proponents justify as a measure to curtail dangerous polarization is actually fueling those divisions.

It is most ironic to me that it is self-identified liberals and liberal journals — once the most energetic first amendment champions — who are most fiercely calling for censorship. It is self-identified human rights advocates who are supporting government policies that trample our constitutional rights. We might recall, at this strange time in our history, my father’s friend, Edward R. Murrow’s warning that: “The right to dissent … is surely fundamental to the existence of a democratic society. That’s the right that went first in every nation that stumbled down the trail to totalitarianism.”

As Murrow predicted, the imposition censorship has masked the systematic demolition of our constitution including attacks on freedom of worship (including abolishing religious exemptions and closing churches), freedom of assembly, private property (the right to operate a business), due process (including the imposition of far reaching restrictions against freedom of movement, education, association with notice and comment rule making) and the 7th amendment right to jury trials (in cases of vaccine injuries caused by corporate negligence).

Those policies are obliterating the middle class, shifting trillions of dollars to billionaires, dismantling all the social programs created by Democrats since the New Deal and sweeping away the obstacles against our country’s dark slide into authoritarian plutocracy anathema to every value of democracy, liberalism and humanity.

Here’s my letter — which the New York Times refused to publish — in response to the op-ed by my niece, Dr. Kerry Meltzer:

Without offering any examples of factual errors, my niece, Dr. Kerry Meltzer, accuses me of spreading “vaccine misinformation,” a term currently applied to any statement that departs from official pronouncements, regardless of its truth.

The term’s traditional definition might encompass Kerry’s claim that the Pfizer-BioNTech vaccine is safe because it caused life threatening anaphylaxis in only 11 of 2.1 million recipients (1/200,000). Rate of adverse events, according to the Centers for Disease Control and Prevention, is 1 in 42 — based on the first week’s distribution of more than 200,000 vaccines, with more than 5,000 reports of individuals incapacitated to the point that they missed work or had to seek medical attention. This outcome is likely to increase, as clinical trials for both Pfizer’s and Moderna’s vaccines suggest that the second shot of the vaccine series leads to far higher injury rates.

Pfizer’s mRNA vaccines use a novel vaccine technology never before used on human subjects. On Sept. 25, I wrote a letter to Dr. Fauci — who Kerry cites as her reliable authority for vaccine safety — warning that the polyethylene glycol (PEG) -coated nanoparticles in the mRNA vaccines were likely to cause anaphylaxis in vulnerable recipients. Dr. Fauci ignored that warning.

FDA now acknowledges that PEG is the probable culprit in the anaphylactic reactions. The COVID pandemic is the third time since Dr. Fauci arrived at National Institutes of Health that the federal government rushed out vaccines for a potential pandemic.

In 1976, 45 million Americans received a vaccine for a disease that didn’t exist, before hundreds of cases of paralyzing Guillain Barre’ syndrome resulted, ending the program.

In 2009, rushed vaccines for swine flu caused seizures in 1/100 Australian children and 1,300 cases of debilitating narcolepsy in European children before the program was discontinued. A month earlier, Dr. Fauci appeared on TV to assure the world that the vaccines were safe.

The mRNA vaccines are experimental drugs with potential for long-term harm. It’s only prudent to demand — as I have — proper testing and to treat the claims of interested government and industry officials with appropriate skepticism.




A Pandemic of Insanity

A Pandemic of Insanity

by Arthur Firstenberg, Global Research
January 7, 2021

 

You see them everywhere. Men and women walking down the street, all of them with masks on their faces and cell phones in their hands. People jogging, with masks covering their faces and cell phones in their hands. Mothers wheeling their babies with one hand, holding a cell phone in the other hand, with a mask covering their face.

The world has gone insane.

Back in May, the President of Tanzania announced that a goat, a quail, and a papaya had tested positive for COVID-19. People did not stop eating papayas. But when farmed minks began testing positive, the response has been to kill them all.

After a few minks in the Netherlands tested positive in April, 570,000 minks were slaughtered. Minks started testing positive and being killed in Denmark in June, and on November 4, Denmark announced it would destroy the rest of its 17 million minks. Sanity finally broke out in that country, and the eradication campaign stopped after only 2.5 million minks were slaughtered. But minks have also been killed in Spain, Sweden, Greece, France, and the United States.

Lions, tigers and leopards in zoos have tested positive.

People have been testing their dogs and cats, and lo and behold, some of them have tested positive, and on May 6, the Centers for Disease Control created a webpage titled “What to Do if Your Pet Tests Positive for the Virus that Causes COVID-19.”

This is what you are supposed to do: “Isolate the pet from everyone else, including other pets.” “Keep your pet at least 6 feet away from other pets and people.”

“If you have a private backyard where your dog can go to the bathroom, do not take them for walks.” But, the CDC warns, “Do not wipe or bathe your pet with… hand sanitizer,” and “Do not try to put a mask on your pet.”

It is becoming obvious that no matter what you test — minks, lions, dogs, papayas, people, or anything else — you will get positive results, and that the results mean nothing. Just wait until someone tests a cow. Kill all the cows, and no more meat or dairy products! Vaccinate every pet and farm animal in the world! Do contact tracing for every pet that comes in contact with an infected pet!

We have a pandemic, all right, but it is a pandemic of insanity, not COVID-19. The world — the entire world, not just a few people or a few countries or a few cultures — has forgotten what life is. Life is community. It is social contact, touching, breathing, sharing. It is oxygen. People are dying because their masks are making them hypoxic. Cancer cells thrive in the absence of oxygen.

If you have cancer, and you wear a mask, you are making your cancer grow. And life is bacteria and viruses. Ninety-nine percent of all bacteria and viruses are beneficial and necessary — necessary for life, and necessary for evolution. If you disinfect the surface of the earth, you will put an end to life. We did not disinfect the world for smallpox, influenza, measles, or tuberculosis. But we are doing it for “COVID-19.”

And we are blaming every symptom known to man on “COVID-19.” COVID-19 is a respiratory virus, closely related to the common cold. But we have made a caricature of it. Suddenly a coronavirus is a magical piece of RNA, created by Dracula, that will damage your kidneys or your heart or give you a stroke.

There is another, very real pandemic that is out of control: a pandemic of radiation. A pandemic that does cause kidney and heart damage and strokes, in addition to pneumonia. The radiation is produced by cell phones. The cell phones with which mothers are irradiating their babies, and joggers are irradiating their hearts. The cell phones with which 7 billion people are irradiating the birds, insects and flowers around them. The radiation that will kill all 7 billion of us, unless we put an end to it.

Take Back Your Health Conference, January 23-24, 2021

I will be speaking about these issues at the 2021 Take Back Your Health (TBYH) Conference. This year’s conference, featuring doctors, immunologists, environmental experts, and others, is titled Our Global Microbiome: Understanding Our Relationship with the Viruses, Bacteria and Molds Around Us.

The conference will be held online January 23 and 24. Details and registration information are here: https://conference.tbyhguide.com/.

___

Arthur is founder of ECHOEarth (End Cellphones Here On Earth) and the author of The Invisible Rainbow: A History of Electricity and Life.

 

cover image credit itssinaali / pixabay




Their ‘Vaccines’ Are Genetic-Engineered Drugs

Their ‘Vaccines’ Are Genetic-Engineered Drugs

by Dr. Tom Cowan
January 7, 2021

 

Two Amazing Admissions from Pfizer and Moderna

I want to wish everyone a Happy New Year. Those words seem almost absurd to say right now, given all that is happening in the world, but hopefully we all continue to experience wonders and joy. We are living in the midst of world-shaking, cosmic events, the likes of which most people never get to experience. We are finding new friends, finding our courage, and many of us are finding our voices as we speak out against the treachery we see all around us. Many of us are finding our way back to divine inspiration and new meaning in our lives. We all have to admit and accept that we simply can’t and don’t know where this all will lead, but that has always been the case. Now, more than ever, it’s time to enjoy the ride.

Today I want to address two things that are commonly referred to as “conspiracy theories” in the mainstream narrative. The first is that some of us are saying researchers have never isolated the “corona virus” nor proven that it exists. Proving the existence of the virus is, obviously, the first step in showing that it could cause a disease called COVID-19. The corollary to this claim is that any so-called COVID vaccine can’t possibly be based on something that is actually from a virus, as the virus has never been found.

An email correspondence was sent to me this morning from a woman who asked Pfizer to describe what the company is using as the template for its new vaccine. Here is what the customer-service person said to her in writing:

When asked where the DNA template for the virus came from, she replied:

“The DNA template used does not come directly from an isolated virus from an infected person.”

The statement begs the question, “so where does the genetic material being put in the vaccine actually come from?” Here is the same person’s response to this question:

“The DNA template (SARS-Cov2, Gen Bank:MN9089473) was generated via a combination of gene synthesis and recombinant DNA technology.”

In other words, as I and others have said, they are injecting people with GMO products for who knows what reason. Or, as I jokingly like to say, at least you won’t have to worry about eating GMO food after the “vaccine” as you, yourself, have been GMO’d.

One of the main points here is this drug is NOT a vaccine in any conventional use of that word. It is a genetic-engineered drug designed to have its effect through some sort of modification of your DNA. If that isn’t a scary proposition, I don’t know what is.

The second “conspiracy theory” that the mainstream media has “debunked” is that the Moderna “vaccine” is actually an operating system designed to allow an interface between the human being and some computer network. As always, I trust that no one would believe me for such an outlandish claim, but what does Moderna, the Gates-funded maker of one of the major “vaccines” now being used, actually say? Here are words from their own website:

“Recognizing the broad potential of mRNA science, we set out to create an mRNA technology platform that functions very much like an operating system on a computer. It is designed so that it can plug and play interchangeably with different programs. In our case, the “program” or “app” is our mRNA drug — the unique mRNA sequence that codes for a protein.”

Two things stand out in this statement. First, if the idea that mRNA “vaccines” are meant to be operating systems is a hoax, then apparently Moderna is in on the hoax. How could the company make it clearer that this is the point of their mRNA drugs?

Second, this mRNA “vaccine” is no vaccine at all. Not that any vaccine is any good, but this product is an mRNA drug. So why call it a vaccine? Simple. Most people think vaccines are “good,” so that helps with marketing. More important, though, is that calling this drug a vaccine allows the company to escape any liability if people are harmed. If it were classified as a drug and the company were sued, it would have to produce science showing it actually works and is safe. It would also have to pay damages if found liable. With vaccines, none of this applies.

I have wrestled during these Holy Nights with the question of whether human beings who willingly agree to have an mRNA operating system downloaded into their bodies can claim to be free, spiritual beings again. Frankly, I don’t accept that sending your child to a Waldorf school, or meditating daily, or eating the perfect food will somehow mitigate the damage to the human being that will result from the choice of getting these drugs. I believe we are at a crossroads, and this is the free human being’s chance to say “not me.” All it takes is courage.

In the words of Alexander Solzhenitsyn:

“You can resolve to live your life with integrity. Let your credo be this: Let the lie come into the world, let it even triumph. But not through me.”




Norwegian Nursing Home Patients Dead After Receiving First Dose of Pfizer COVID Vaccine

Norwegian Nursing Home Patients Dead After Receiving First Dose of Pfizer COVID Vaccine

by Tyler Durden, ZeroHedge
January 7, 2021

 

More suspicious deaths have surfaced in Europe involving patients who recently received their first dose of the coronavirus vaccine. Following reports about a Portuguese nurse dying shortly after receiving her first dose of the vaccine, our attention turns to Norway, where two nursing home residents have passed away under similar circumstances.

According to RT, the departed were among the first in the country to receive the Pfizer-BioNTech vaccine. Medical authorities said they will investigate the circumstances of these deaths to try and figure out if the vaccines had anything to do with it. Norway’s National Institute of Public Health will be leading the charge.

“We have to assess whether the vaccine is the cause of death, or if it is a coincidence that it happened soon after vaccination,” Medical Director Steiner Madsen said in a statement to the press.

To be sure, due to the advanced age of the residents, it’s possible their deaths were unrelated to the vaccine.

Around 400 people die every week in Norwegian nursing homes (on a tangential note, we can’t help but wonder how many deaths in these facilities have been mislabeled as “COVID-19 deaths”).

But a smattering reports about adverse reactions and potentially related deaths have raised eyebrows around the world. In Israel, 100s of people were infected with the virus after receiving their first dose of the vaccine.

As we reported the other day, the rate of “adverse” reactions to the COVID-19 vaccine might already be as much as 50x higher than the flu vaccine.

Vaccinations with the drug began in Norway on Dec. 27. Scientists in the US and elsewhere have criticized European leaders for the slow rollout of vaccinations (with France coming in for particularly intense criticism). The pace is set to quicken, however, now that the EMA has approved Moderna’s mRNA vaccine for emergency use in the EU on Wednesday.




Dear Police, Healthcare Workers, and First Responders: Regarding COVID-19 Vaccine Concerns

Dear Police, Healthcare Workers, and First Responders: Regarding COVID-19 Vaccine Concerns

by Vaccine Choice Canada
January 5, 2021

 

Dear Police, First Responders and Healthcare Workers

Re: COVID-19 Vaccine Concerns

I am writing on behalf of Vaccine Choice Canada to express our deep concern for you and your colleagues.

We understand that first responders and frontline healthcare workers are being targeted to receive the initial deployment of the COVID-19 vaccine. After a thorough review of the available scientific literature, it is our contention that the Pfizer and Moderna products authorized for use in Canada carry substantial risks.

We recognize the importance of first responders and frontline workers and feel a sense of urgency to share this information with those we rely on most during times of emergency. The attached document addresses the following concerns:

  • Human experimentation: The Pfizer and Moderna vaccines granted ‘interim approval’ by Health Canada have not been adequately tested for either safety or efficacy. This means that the use of the COVID-19 vaccine is human experimentation.
  • The Vaccine May Not Prevent Infection or Transmission: COVID-19 vaccine makers are not required to demonstrate that their product prevents either infection or transmission of the virus.
  • COVID-19 – A Low Lethality Illness: The coronavirus is statistically shown to be far less deadly than portrayed by mainstream media and health officials.
  • Health Canada Oversight Insufficient: The safety testing of the COVID-19 vaccine products is incomplete and less rigorous than that for other vaccines.
  • No Individualized Risk-Benefit Analysis: A proper risk-benefit analysis has not been conducted. Implementing a “one-size-fits-all” policy fails to recognize that the risk of infection varies greatly depending upon several variables including age and pre-existing conditions.
  • Informed Consent: Those advocating for mandates and coercive measures that remove the right to consent are undermining essential individual rights and freedoms. This is a clear violation of the Canadian Charter and also medical ethics.

Our intention in writing this letter is to bring to your awareness the experimental nature of this vaccine. It is our hope that this information will help to protect your right to voluntary informed consent, free of any coercion or constraint. Thank you for your service to Canadians.

Sincerely,

Vaccine Choice Canada

1. The COVID Vaccine Is Human Experimentation

The Pfizer and Moderna vaccines were granted ‘interim approval’ by Health Canada but have not been adequately tested for either safety or efficacy. This means that the use of the COVID-19 vaccine is technically considered to be human experimentation[i]

The normal development timeline of a vaccine product is 5 – 10 years. It is impossible to identify the effects of a vaccine in the few months the product has existed. The most significant concern with the Pfizer and Moderna vaccines is the introduction of ‘messenger RNA/DNA technology’. This technology has never before been injected into humans on such a mass scale. The consequences of injecting genetic altering technology into a human body is unknown.

The potential exists for catastrophic consequences, not only for the person receiving the vaccine, but for all future generations as it is highly likely that the mRNA/DNA in the vaccine will combine with the recipient’s own DNA and be transmitted to their offspring.

The use of this novel technology is especially disconcerting given COVID-19 vaccine manufacturers have been granted total immunity from liability for any harm or injury caused by their products. Federal procurement minister Anita Anand justified the indemnity in the following statement – “All countries, generally speaking, are faced with the issue of indemnification of companies, especially in cases of novel technologies like this.” [ii] Ordinarily, a ‘novel technology’ would demand a higher level of oversight and accountability, not less.

Normal protocols to test the safety of vaccines include testing in animals prior to testing in human subjects. This protocol is even more essential for a coronavirus vaccine. All previous efforts to develop a coronavirus vaccine over the last 60 years have failed because the vaccine caused an exaggerated immune response upon re-exposure to the virus. [iii] This ‘pathological priming’ resulted in severe injury and death to the test animals. An earlier attempt to create a similar RSV vaccine resulted in an 80% hospitalization rate and the death of two of the 35 children in the trial. In the rush to develop a COVID vaccine, Health Canada has permitted vaccine makers to bypass animal testing and move directly to testing on humans.

Health Canada has also granted Pfizer and Moderna permission to deploy their vaccines in the general population without completing Phase III trials. This is unprecedented in vaccine development. Health authorities admit that long-term safety data does not exist for the vaccine. [iv] There is no data that defines the vaccine’s interaction with other vaccines or prescription medications. [v] COVID-19 vaccines have not been tested for their ability to cause cancer, induce organ damage, change genetic information, impact the fetus of a pregnant woman or to impair fertility. William Haseltine, a former Harvard Medical School professor states that, “These protocols seem designed to get a drug on the market on a timeline arguably based more on politics than public health.” [vi]

2. The Vaccine May Not Prevent Infection or Transmission

Many individuals eager to receive a COVID-19 vaccine are under the notion that the vaccine will protect them from the SARS-CoV-2 virus. The reality is that COVID-19 vaccine makers are not required to demonstrate that their product prevents either infection or transmission of the virus. Vaccine manufacturers are also not required to demonstrate that the vaccine will result in a reduction in severe illness, hospitalization, or death. [vii] [viii] [ix]

According to a report in the British Medical Journal, “Hospital admissions and deaths from COVID-19 are simply too uncommon in the population being studied for an effective vaccine to demonstrate statistically significant differences in a trial of 30,000 people. The same is true of its ability to save lives or prevent transmission: the trials are not designed to find out.” [x]

This begs the question – what benefit will the COVID-19 vaccine actually confer?

Public health authorities have stated that vaccine recipients will still be required to wear a face covering, maintain physical distance, and avoid crowds. CDC’s own data confirms that over 80% of individuals who test positive for COVID-19 are asymptomatic. For these individuals a risk-benefit analysis could only conclude that a COVID-19 vaccine will result in substantially more risk than benefit.

3. COVID-19 Is A Low Lethality Illness

Many individuals who intend to be at the front of the line for a COVID-19 vaccine will do so because they believe COVID-19 is an illness with a high rate of mortality. This fear creates a sense of panic that compels people to accept a medical product with an unknown safety profile.

Our federal and provincial governments and the mainstream media persist in describing COVID-19 as a “deadly” condition. This is simply not true for the vast majority of the population. The risk of mortality is primarily to those over 80 years of age in poor health, residing in extended care facilities. [xi] The median age of death attributed to COVID-19 is 82 years. Almost all were frail with several co-morbidities. According to the CDC, the case survival rate of COVID-19 in patients ages 0 – 19 is 99.997%, 99.98% in patients 20 – 49 years, and 99.5% in patients 50 – 69 years. [xii] [xiii]

What is also rarely acknowledged by our government, public health officers, and the corporate media is that safe and effective drugs for the prevention and treatment of COVID-19 have been identified.[xiv] [xv] [xvi] Such treatments negate the need for an ‘emergency use’ vaccine. Unfortunately, these treatments are rarely discussed, much less encouraged.

4. Health Canada Oversight Insufficient

Many Canadians assume Health Canada provides rigorous oversight and would never permit a vaccine to be introduced to the Canadian public without robust testing to ensure both safety and effectiveness. The fact is that Health Canada does not conduct its own clinical trials to determine the safety and efficacy of a vaccine. Instead, Health Canada relies on the data provided by the vaccine manufacturers. Health Canada also holds the perspective that it is not necessary for vaccine makers to test their products against a neutral placebo, the gold standard for safety testing.

Canadians may not be aware that vaccine producers such as Pfizer, Merck and GlaxoSmithKline have paid billions in criminal penalties and settlements for research fraud, faking drug safety studies, failing to report safety problems, bribery, kickbacks, and false advertising. [xvii] [xviii] In 2009, Pfizer paid $2.3 billion to resolve criminal and civil allegations in what was then the largest health care fraud settlement in history. [xix] Canadians may also not be aware that the Vaccine Injury Compensation Program in the United States has paid out more than $4.4 B in compensation for vaccine injury and death since 1989, and that Canada is one of only two G20 Nations without a national vaccine injury compensation program. While a vaccine injury compensation program has been promised, the details have yet to be announced.

Vaccines are not benign medical products. Vaccination is an invasive medical procedure that delivers by injection complex biochemical drugs and now genetic modifying technology. Because of this complexity and uncertainty, the level of safety testing ought to be even more rigorous. But this is not the case. The safety testing of the COVID-19 vaccine is less rigorous and more incomplete as compared with other pharmaceutical drugs.

The consequences of rushing a novel and inadequately tested product can be serious, permanent, and even deadly. Data following the administration of the Pfizer vaccine reveals that 3.6% of test subjects experienced a ‘health impact’ significant enough such that they were “unable to perform normal daily activities, unable to work, and required care from a health professional.” [xx]

5. No Individualized Risk-Benefit Analysis

The arguments used to legitimize, legalize and implement COVID-19 vaccination are political and  ideological rather than evidence-based. In the rush to approve a COVID-19 vaccine an analysis of the risks vs benefits has not been conducted. Indeed, how does one conduct a risk-benefit analysis when both the risks and the benefits are unknown? Some researchers have described the use of a COVID-19 vaccine in the general population as the most reckless and brazen experiment in the history of humanity.

Further, implementing a “one-size-fits-all” policy assumes the risk-benefit is the same for everyone. This fails to take into consideration the established fact that the risk of COVID-19 infection varies greatly depending upon several known variables, most especially age and pre-existing conditions. These variables must be considered when assessing the risk and benefit of this medical device.

6. Informed Consent Is Essential

The mandate of Vaccine Choice Canada has been and continues to be protecting the health sovereignty of Canadians, which inherently includes the right to informed consent. Informed consent is the most fundamental aspect of health sovereignty, an ethical medical system, and a free and democratic society.

It is imperative that any individual contemplating getting a COVID-19 vaccine be fully aware that the vaccine has not undergone the most basic testing to demonstrate either safety or efficacy and that they are participating in human experimentation. In a letter dated October 3, 2020, Dr. Michael Yeadon, a former Vice President of Pfizer stated – “All vaccines against the SARS-CoV-2 virus are by definition novel. If any such vaccine is approved for use under any circumstances that are not EXPLICITLY experimental, I believe that recipients are being misled to a criminal extent.”

Secondly, we hold that any medical intervention requires voluntary consent. Canada is a signatory to The Universal Declaration of Bioethics and Human Rights which describes consent as follows: “Any preventive, diagnostic and therapeutic medical intervention is only to be carried out with the prior, free and informed consent of the person concerned, based on adequate information. The consent should, where appropriate, be expressed and may be withdrawn by the person concerned at any time and for any reason without disadvantage or prejudice.”

According to the Nuremberg Code, developed in response to the medical abuses of the Nazi regime, informed voluntary consent means that “the person involved… should be able to exercise free power of choice, without the intervention of any element of force, fraud, deceit, duress, over-reaching, or other ulterior form of constraint or coercion.”

Those advocating for mandates and other coercive measures that remove the right to voluntary consent are undermining essential individual rights and freedoms. This is a clear violation of the Canadian Charter and also medical ethics. It is important to understand that we have the legal right to refuse any unwanted medical intervention.

We would be glad to provide you with further documentation should you wish.

For more information, visit: www.vaccinechoicecanada.com

References:

[i] https://off-guardian.org/2021/01/03/what-vaccine-trials/

[ii] https://q107.com/news/7521148/coronavirus-vaccine-safety-liability-government-anand-pfizer/

[iii] childrenshealthdefense.org/defender/pfizer-COVID-vaccine-trial-pathogenic-priming/

[iv] https://www.fda.gov/media/144416/download

[v] COVID-vaccine.canada.ca/info/pdf/pfizer-biontech-COVID-19-vaccine-authorisation.pdf?fbclid=IwAR0vCv09_332PjR41OUBJOy1k1ESQg–_CbAqcGpk1ZWY71xBztuLDE05oE

[vi] https://www.washingtonpost.com/opinions/2020/09/22/beware-covid-19-vaccine-trials-designed-succeed-start/

[vii] https://blogs.bmj.com/bmj/2020/11/26/peter-doshi-pfizer-and-modernas-95-effective-vaccines-lets-be-cautious-and-first-see-the-full-data/

[viii] https://www.nytimes.com/2020/09/22/opinion/covid-vaccine-coronavirus.html

[ix] https://stopmedicaldiscrimination.org/home#af86c044-aed2-496d-92bb-e1d76dca284e

[x] www.bmj.com/content/371/bmj.m4037

[xi] https://www.cihi.ca/sites/default/files/document/covid-19-rapid-response-long-term-care-snapshot-en.pdf?emktg_lang=en&emktg_order=1

[xii] https://www.cdc.gov/coronavirus/2019-ncov/hcp/planning-scenarios.html

[xiii] https://www.breitbart.com/politics/2020/09/25/cdc-data-shows-high-virus-survival-rate-99-plus-for-ages-69-and-younger-94-6-for-older/

[xiv] www.americasfrontlinedoctors.com/hcq-protocols/

[xv] www.youtube.com/watch?v=BLWQtT7dHGE

[xvi] https://anthraxvaccine.blogspot.com/2021/01/first-country-bans-ivermectin-lifesaver.html

[xvii] www.corp-research.org/merck

[xviii] https://www.theguardian.com/business/2012/jul/03/glaxosmithkline-fined-bribing-doctors-pharmaceuticals?CMP=share_btn_fb

[xix] https://abcnews.go.com/Business/pfizer-fined-23-billion-illegal-marketing-off-label/story?id=8477617

[xx] https://www.cdc.gov/vaccines/acip/meetings/downloads/slides-2020-12/slides-12-19/05-COVID-CLARK.pdf


Printable PDF

Click here for a similar letter to share with your family, friends and colleagues.

 

Further reading:

Questioning the Covid Narrative and Measures – List of Resources

1st Responders Covid-19 Vaccine Flyer (pdf)

Covid-19 Resources




The Politicization of Medicine & the Dangerous Vaccine Agenda Created

The Politicization Of Medicine & the Dangerous Vaccine Agenda Created

by Ryan Cristian, The Last American Vagabond
January 6, 2021

 



Joining me today is Dr. James Lyons-Weiler, here to discuss the very real dangers of taking the experimental COVID-19 vaccines, the politicization of the medical & scientific fields, and how that has led to pharma-controlled industries which consider your health and safety a secondary concern – if considered at all.

All of this has not only been allowed, but actively participated in, by the very politicians and agencies charged with your safety.

Now, in a time of shockingly absent transparency and government accountability, COVID-19 is being used as the final catch-all justification to put the finishing touches on the complete pharma take over of the US medical industry.

All Video Source Links Can Be Found Here At The Last American Vagabond:

https://www.thelastamericanvagabond.com/illusion-safety-trials-covid-isolation-dangerous-obfuscation-vaccine-side-effects/

Video available at Last American Vagabond channels:

https://odysee.com/@TLAVagabond:5
https://www.bitchute.com/channel/24yVcta8zEjY/


See related:

Spiro Skouras w/ Dr. James Lyons-Weiler: Vaccinated vs Unvaccinated — The Study the CDC Refused to Do
Created in a Lab: James Lyons-Weiler, PhD & Del Bigtree on Corona Virus Genome Sequence