Tag Archive for: Vaccines

Ex-FDA Commissioners Against Higher Vaccine Standards Took $6 Million From COVID Vaccine Makers

Ten of the twelve former Food and Drug Administration (FDA) commissioners and acting commissioners opposed to the Trump administration’s stiffer standards for vaccines quietly disclosed ties to the pharmaceutical industry, a Daily Caller News Foundation review shows.

The FDA old guard criticized the new leadership in a Dec. 3 New England Journal of Medicine (NEJM) letter over a higher regulatory bar for vaccines, namely the expectation that most new vaccine approvals will require randomized clinical trials, arguing it could hamper the market.

“Insisting on long, expensive outcomes studies for every updated formulation would delay the arrival of better-matched vaccines when new outbreaks emerge or when additional groups of patients could benefit,” the former commissioners wrote. “Abandoning the existing methods won’t ‘elevate vaccine science’ … It will subject vaccines to a substantially higher and more subjective approval bar.”

But while the former commissioners disclosed their conflicts of interest to the medical journal — per standard practice in scientific publishing — reporters didn’t relay them to the broader public in reports in the Washington PostSTAT News and CNN.

The headlines about a bipartisan rebuke from former occupants of FDA’s highest office give the impression that the Trump administration is contravening established science, but closer inspection reveals a revolving door between pharmaceutical corporations and the agencies overseeing them.

Three of the signatories have received payments totaling $6 million from manufacturers or former manufacturers of COVID vaccines.

Scott Gottlieb has received $2.1 million in cash and stock from his position on the Pfizer board of directors, where he has advised on ethics and regulatory compliance since 2019, according to company filings to the Securities and Exchange Commission. Stephen Ostroff has received $752,310 from Pfizer in consulting fees since 2020, according to OpenPayments.

Mark McClellan has received $3.3 million from Johnson & Johnson as a member of the board of directors since 2013, SEC filings also show. McClellan also consults for the new pharmaceutical arm of the alternative investment management company Blackstone, which invested $750 million in Moderna in April 2025.

Gottlieb and McClellan did not respond to requests for comment. Ostroff could not be reached for comment.

FDA Center for Biologics Evaluation and Research Director Vinay Prasad outlined the higher standards and shared the results of an internal analysis validating 10 reports of children’s deaths following the COVID-19 vaccine in a Nov. 28 memo to staff. He called for introspection and reform at the agency.

The NEJM letter criticizes Prasad for cracking down on a practice called “immunobridging” that infers vaccine efficacy from laboratory tests rather than assessing it through real-world reductions in disease or death. The FDA under the Biden administration expanded COVID vaccines to children using this “immunobridging” technique, extrapolating vaccine efficacy from adults to children based on antibody levels.

Norman Sharpless — who in addition to previously serving as acting FDA commissioner also served as the head of the National Institutes of Health’s National Cancer Institute — consults for Tempus, a company that collaborates with COVID vaccine maker BioNTech. He has helped steer $70 million in investments in biotech through a venture capital firm he founded in November 2024. Sharpless also disclosed $26,180 in payments in 2024 from Chugai Pharmaceutical, a Japanese pharmaceutical company that markets mRNA technology among other drugs, on OpenPayments.

“I was grateful for the opportunity to serve as NCI Director and Acting FDA Commissioner in the first Trump Administration, and strongly support many of the things President Trump is trying to do in the current Administration,” Sharpless said in an email.

Margaret Hamburg, another former FDA commissioner and signatory of the NEJM letter, has since 2020 earned $2.8 million as a member of the board of Alnylam Pharmaceuticals, which markets RNA interference (RNAi) technology.

Hamburg did not respond to a message on LinkedIn.

Most signatories disclosed income from biotech companies testing experimental cancer treatments. These products could face tighter scrutiny under Prasad, a hematologist-oncologist long wary of rubberstamping pricey oncology drugs — which Prasad points out often cause some toxicity — without plausible evidence of an improvement in quality of life or survival.

The former FDA commissioners disclosed ties to Sermonix Pharmaceuticals Inc.; OncoNano Medicine; incyclix; Nucleus Radiopharma; and N-Power, a contractor that runs oncology clinical trials.

Andrew von Eschenbach, who like Sharpless formerly served both as FDA commissioner and the head of the National Cancer Institute, disclosed stock in HistoSonics, a company with investments from Bezos Expeditions and Thiel Bio seeking FDA approval for ultrasound technology targeted at tumors.

Some FDA commissioners who signed onto the letter opposing changes to vaccine approvals have ties to biotechnology investment firms, namely McClellan, who consults Arsenal Capital; Janet Woodcock, who consults RA Capital Management; and Robert Califf, who owns stock in Population Health Partners.

Califf did not respond to an email requesting comment. Woodcock did not respond to requests for comment sent to two medical research advocacy groups with Woodcock on the board. Eschenbach did not respond to a LinkedIn message.

The two signatories without pharmaceutical ties may find their judgement challenged by the FDA investigation into COVID-19 vaccine deaths, having either implemented or formally defended the Biden administration’s headlong expansion of vaccines and boosters to healthy adults and children.

David Kessler executed Biden’s vaccination policy as chief science officer at the Department of Health and Human Services, helping to secure deals for shots with Pfizer and Moderna.

Meanwhile Jane Henney chaired a National Academies of Sciences, Engineering, and Medicine report published in October 2025 that praised the performance of FDA and Centers for Disease Control and Prevention (CDC) vaccine surveillance during the pandemic — underwritten with CDC funding.

That assessment clashes with that of a Senate report, citing internal documents from FDA, finding that CDC never updated its vaccine surveillance tool “V-Safe” to include cardiac symptoms, despite naming myocarditis as a potential adverse event by October 2020, and that top officials in the Biden administration delayed warning pediatricians and other providers about the risk of myocarditis after their approval in some children in May 2021, months after Israeli health officials first detected it in February 2021. The Senate investigation named Woodcock, a signatory of the NEJM letter, as one of the FDA officials who slow-walked the warning.

AUTHOR

Emily Kopp

Investigative Reporter

RELATED ARTICLES:

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Biden Admin Spent Weeks ‘Downplaying’ COVID Vaccine Risks Before Issuing Formal Warning, Senate Report Alleges

EDITORS NOTE: This Daily Caller column is republished with permission. ©All rights reserved.


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Highly disturbing video from Dr. John Campbell on peer reviewed study on nano-structures in blood caused by mRNA injections

Welp. This is one. Has Campbell jumped the shark on this one? Or is the unbelievable true? or is it as he says, given that he links to peer reviewed papers from Japan and South Korea. Or was he set up to publish this to destroy his credibility for being over the target for so long now on so much government and phrama-fraud?

Watch and decide.

Also it is possible that this is a sort of crystallization phenomenon and may not be a deliberate effect of the vaxx, but some sort of Crystal structure that forms from some component in the vaxx.

No idea.

Link to peer reviewed study.

Several more related links.

RELATED ARTICLE: What’s Tim Walz’s Connection With the Wuhan Institute of Virology?

EDITORS NOTE: This Vlad Tepes Blog column with video posted by Eeyore is republished with permission. ©All rights reserved.

Largest organization of OB-GYNs in America accepted $11 million from HHS to promote COVID-19 vaccines to PREGNANT WOMEN

Demons.

Largest organization of OB-GYNs in America accepted $11 million from HHS to promote COVID-19 vaccines to PREGNANT WOMEN

Largest organization of OB-GYNs in America accepted $11 million from HHS to promote COVID-19 vaccines to PREGNANT WOMEN

By Arsenio Toledo, CDC News, August 23, 2023:

Documents obtained through Freedom of Information Act (FOIA) requests reveal that the main professional organization of obstetricians and gynecologists (OB-GYNs) in the United States accepted over $11 million in taxpayer money to promote the Wuhan coronavirus (COVID-19) vaccines and claim that they are safe for pregnant women and their unborn children.

This is according to fetal-maternal medicine specialist Dr. James Thorp, who conducted an investigation into the massive damage the mRNA-based COVID-19 vaccines are doing to women, especially to those who are pregnant and their unborn children.

In an interview with COVID-19 vaccine expert and Big Pharma critic Dr. Naomi Wolf, Thorp laid out how the Centers for Disease Control and Prevention (CDC) and the Department of Health and Human Services (HHS) created what he called a “covenant of death” with the American College of Obstetricians and Gynecologists (ACOG) – the largest professional organization for OB-GYNs in the United States and the rest of the Americas – in exchange for $11 million.

“What’s in this covenant of death? … They took well over $11 million. They signed the covenant with death, and they’re not allowed to deviate one iota from the lethal narrative of HHS. If they do, they will be liable for paying back every single penny, which they’ve already pocketed,” said Thorp.

Thorp and Wolf noted that the contract uncovered by the FOIA requests provided for the return of the money to the HHS if ACOG did not adhere to the government’s “‘safe and effective’ for pregnant women and new moms script presented to them” by the federal government.

He added that ACOG is not the only professional medical association to have accepted money from the government. Other recipients of government funding in exchange for promoting the COVID-19 vaccines include the American Board of Obstetrics and Gynecology and the Society for Maternal-Fetal Medicine.

“[These organizations], to this day, are the evil organizations that perpetrated this crime on the world,” said Thorp.

“Doctors who treat the most vulnerable population in the world – pregnant women and their unborn babies – have been and are coerced to lie by organizations that oversee these doctors, that were paid to lie,” remarked Wolf. “At least one primary goal, of all this madness and evil of the past three years, whatever brand you chose, was to ruin women’s menses and to damage human reproduction at a global level. Team Pfizer or Team Moderna? A distinction without a difference.” (Related: If your doctor told you to get “vaccinated” for COVID, they were BRIBED, evidence shows.)

$13 billion in funding redirected to “influencers” to promote COVID-19 vaccines

In addition to the approximately $11 million provided by the government to ACOG, Thorp noted that his FOIA investigations – launched with the help of his wife, attorney Maggie Thorp – revealed that $13 billion in taxpayer money went to fund “influencers” to promote the mRNA vaccines.

Most of this $13 billion went to a variety of individuals and organizations. Notable are the organizations like ACOG that focus on medicine for pregnant women, such as the American Board of Obstetrics and Gynecology, the main medical certification board for practicing obstetricians and gynecologists in the U.S. and Canada, and the Society for Maternal-Fetal Medicine, an NGO.

According to Thorp, there are about 300 major organizations and influencers – including religious institutions like synagogues and churches – that accepted money from the HHS and the CDC in a “psyops campaign … to convince the United States and the entire world that this deadly shot was safe, effective and necessary in the most vulnerable population – pregnant women.”

Read full article.

AUTHOR

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HARD EVIDENCE Confirms Covid Shot Killed The Unborn and Massively Injured Babies

After using COVID-19 victims to promote medical tyranny, the mainstream media callously disregards the vaccine injured.

Dr. Bryan Ardis says SNAKE VENOM PROTEINS in COVID-19 shots behind MISCARRIAGES – Brighteon.TV.

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DATA ANALYSIS: Increase in miscarriages and stillbirths directly linked to COVID-19 vaccines.

EDITORS NOTE: This Geller Report is republished with permission. ©All rights reserved.

Not a Single U.S. State Is Requiring Kids to Get Vaccinated to Attend Public School. Why?

Economics may offer a clue as to why not one state is mandating vaccination to attend school in the 2022-2023 school year, even though many government officials support coercive vaccination policies.


September has arrived and many children are back in public schools (though fewer than previous years).

At a recent event, one parent joked to me we’re now officially in “vaccine season.” The comment made me laugh, but there’s at least a kernel of truth to it. It’s not unusual for states to require that children receive an array of vaccinations—from polio, diphtheria, and chickenpox to measles, mumps, and meningitis—to be enrolled in a public school system.

One vaccine that parents will not find on any state’s required list in 2022 are the Covid-19 shots, which have been a source of great debate in the US and other countries.

While a few US cities continue to push vaccine mandates to attend, Pew Charitable Trusts pointed out earlier this year that states have been surprisingly wary of mandating Covid shots for children.

“[Only] two states—California and Louisiana—have added COVID-19 vaccines to the list of immunizations mandated for schoolchildren,” Michael Ollove pointed out in January. “Both requirements would be enforced next school year, and then only if the vaccines receive full authorization by the U.S. Food and Drug Administration.”

Things have changed since then.

In May, Louisiana Gov. John Bel Edwards announced the Louisiana Department of Health would not require children attending the state’s daycares or K-12 schools to provide proof of vaccination. California, which in October 2021 became the first state to announce Covid vaccine requirements for school, announced in April that it would not require vaccination, noting the vaccines had not at that time been approved by the FDA for all school-age children. (They are now.)

The fact that not a single US state is requiring students to be vaccinated against Covid to attend K-12 school is probably a bit surprising to readers. (It was to this author.)

I’d like to think that policymakers and politicians finally woke up to the fact that vaccine mandates are immoral, inhumane, and a clear violation of bodily integrity. But that seems unlikely considering that many vaccine mandates remain in place, particularly at the federal and municipal levels.

It’s also possible that lawmakers have realized vaccinated individuals can still get sick and spread the virus, and therefore concluded vaccinations are a matter of personal health, not public health. Yet once again this theory is undermined by the presence of other vaccine mandates that remain in place. Some may contend that we’ve simply beaten the virus and mandates are no longer necessary, but official statistics show Covid deaths and cases remain stubbornly high.

So what’s the answer?

What’s most likely is that political considerations are at play. Yet this thesis too, at first blush, appears to be undermined by the reality that polls show Americans support Covid vaccine mandates in schools.

Some basic economics, however, can help us see that the politics are more complicated than that.

Public Choice Theory is a field of economics pioneered by the Nobel Prize-winning economist James M. Buchanan and economist Gordon Tullock. It rests on a simple assumption: politicians and bureaucrats make decisions primarily based on self-interest and incentives just like everyone else, not out of an altruistic goal of serving “the public good.” (This is why public choice economists have dubbed it “politics without romance.”)

I’ve previously pointed out that politicians were incentivized during the pandemic to embrace Covid restrictions even if they didn’t work because of the political climate in 2020. The absence of government regulations was viewed as actual violence by some public health experts, and those who didn’t embrace strict interventions were accused of genocide.

Moreover, the costs of these regulations tended to be dispersed, delayed, and hidden from view. Depression, drug overdoses, lost learning, and speech impediments were among the consequences of NPIs (Non-Pharmaceutical Interventions) imposed by governments. But the results of these policies were relatively “unseen” (to use a term from the 19th century economist Frederic Bastiat), at least compared to Covid deaths, which public health officials, the media, and even ordinary citizens tracked obsessively.

The costs of NPIs were quite serious, but they were quite low politically for the reasons stated above. The political costs of keeping a state open were much higher. No politician wants to explain why Mrs. Jackson, the 60-year-old math teacher, died from Covid while schools in your state remained open. (It would be just as tragic if Mrs. Jackson had died at home when schools were closed, but at least no politician would be blamed for her death in this case.)

In other words, the incentive structure early in the pandemic encouraged interventions, even if those interventions were ineffective and ultimately ended up doing more harm than good.

The incentive structure for vaccines is very different, particularly for young people.

Children can and do die from Covid, of course, but their risk is extremely low compared to other age groups. Even more important, perhaps, is that the costs of mandatory vaccination are not delayed, dispersed, or hidden from view. They are immediate, concentrated, and highly visible.

The sad reality is that vaccine injuries, though rare, do occur, as the CDC notes. And when they occur, they are the opposite of “unseen,” which means the political repercussions have the potential to be swift—and severe.

After all, when a young person dies after taking a vaccine designed to protect him, it’s a tragedy. When a young person dies of myocarditis after taking a vaccine he was forced to take to attend school, it’s a tragic event and a political disaster with a wide radius, even if some studies show the risk of myocarditis is greater after Covid infection than after Covid vaccination.

All of this analysis is dark and a bit troubling, of course. Now you see why they call public choice theory “politics without romance.”

But it might help explain why even state leaders comfortable with mandatory vaccination and vaccine passports have been reluctant to compel children to get the shot, even if they truly believe it could save lives.

Whether mandatory vaccination would have done more harm than good is a question we’ll never know, though it’s a debate that will likely continue for years to come. But because vaccines have the power to both save lives and claim lives, the decision to accept or refuse them can only morally be made by one person: the individual (or parents, if the decision concerns a child).

So at least state leaders are getting it right this time, even if they are doing so for the wrong reasons.

AUTHOR

Jon Miltimore

Jonathan Miltimore is the Managing Editor of FEE.org. His writing/reporting has been the subject of articles in TIME magazine, The Wall Street Journal, CNN, Forbes, Fox News, and the Star Tribune. Bylines: Newsweek, The Washington Times, MSN.com, The Washington Examiner, The Daily Caller, The Federalist, the Epoch Times.

EDITORS NOTE: This FEE column is republished with permission. ©All rights reserved.

VIDEO: Dr. Naomi Wolf on Pfizer Documents from April 5th, ‘They hid, they concealed, they redacted.’ Its bad

Still waiting for an authoritative analysis of the most recent massive data dump from Pfizer. But lets have a look at what the last batch of 55,000 pages had. Naomi breaks some of it down.

And yes, we have posted this before. But to get a sense of scale of how much and easily these agencies tell massive lies, its good to be reminded. Especially when you hear people say, “They never said the vaccines would stop the spread or stop you from getting sick! They always said it would reduce the number of hospitalizations!”

UPDATE: There IS some analysis on the newest data dump. Please check this link. A small fraction is below.

Happy Cinco de Mayo kids! You might wanna grab a margarita or a Corona with a lime before you read this one.

This drop had 80,000 pages of data.  So I had to prioritize what needed to be read first.  Interesting findings.

OK first.  Remember how we discussed the vaccine likes to congregate in the liver?  Like, within HOURS of getting vaccinated?  I thought those poor Wistar Rats probably met their fate at the 48 hour mark.  But here we find a crumb of data that says nope, they now produced 300 hour post vaccine data comparing the lipid nano particles from the vaccine in the blood plasma versus in the liver.  THIS IS HORRID. Plasma levels peaked and dropped.  The liver?  Not so much.  It is still SEVERELY ELEVATED with mass nano particles at the 300 hour mark hanging out in the liver.  What does the liver do?  Metabolizes and excretes body waste.  Metabolizes medications.  Wonder if THIS is why we are seeing autoimmune hepatitis happening in kids right now?  You don’t suppose breastfeeding babies with moms full of lipid nano particles and spike proteins could possibly cause baby to have issues with THIER liver now, do you?

EDITORS NOTE: This Vlad Tepes Blog column by Eeyore is republished with permission. ©All rights reserved.

England Ends Mask and Vaccine Mandate, Czech Republic Does Too, But US Democrats WANT MORE HARSH MANDATES

England ends mask mandates, working from home and vaccine passports. But in many countries, draconian restrictions still apply. So we must continue to campaign to end the mandates, restrictions and vaccine passports in other countries.

 

Prime Minister Boris Johnson ends mask and vaccine requirements in England

By Karen Curtis | WFTL January 19, 2022

Prime Minister Boris Johnson has scrapped his Covid-19 Plan B in England, no longer requiring face masks in school or working from home, signaling the beginning of the end of coronavirus.

Johnson also ended the use of Covid-19 passports.

Boris Johnson’s announcement followed a “welcome decrease” in the number of coronavirus infections throughout the UK.

“The numbers in intensive care not only remain low but are actually also falling.”

England will go to “Plan A”, on January 26th and the PM told the House of Commons that soon, self-isolation rules for people who test positive will be scrapped as well.

Will President Biden follow suit in the US? The president will speak today and take questions from the press about the COVID surge on this one year anniversary of his presidency.

England’s Covid Plan B restrictions including work-from-home guidance will be scrapped, the Prime Minister has announced.

Boris Johnson told MPs that people are no longer being asked to work from home and, from Thursday next week when Plan B measures lapse, mandatory Covid certification will end.

The Government will also no longer mandate the wearing of face masks anywhere from next Thursday and they will be scrapped in classrooms from tomorrow.

The Prime Minister also confirmed the intention to end the legal requirement to self-isolate when the regulations expire on March 24 and said the Government may move that date forward. (The Independent)

And in the Czech Republic:

Meanwhile, in barking mad left-wing America:

England ends mask mandates, working from home and vaccine passports. But Democrat America wants harsher measures still, including taking away your children…

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EDITORS NOTE: This Geller Report column is republished with permission. ©All rights reserved.

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Subscribe to Geller Report newsletter here — it’s free and it’s critical NOW when informed decision making and opinion is essential to America’s survival. Share our posts on your social channels and with your email contacts. Fight the great fight.

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Studies Proving Generic Drugs Can Fight COVID Are Being Suppressed

Treatment is never discussed but these failed vaccines with Gd knows what in them are mandated.

Studies Proving Generic Drugs Can Fight COVID Are Being Suppressed

Why do repurposed drugs require numerous trials prior to an agency recommendation, while high-profit, novel, patented drugs get routinely approved after only a single trial?

By Pierre Kory, The Federalist, December 16, 2021:

Omicron emerging in the United States and news of the first reported death in the United Kingdom remind us how little we understand the novel coronavirus, and with vaccines less effective against the new variant, how much we are in need of additional ways to fight it. To broaden our knowledge of COVID-19 and identify the best ways to treat and prevent it, doctors should be able to use every possible safe means at their disposal to help patients. Unfortunately, that is impossible in our current political climate.

Since the summer of 2020, U.S. public health agencies have continually shut down the use or even discussion of generic treatments that are minimally profitable. The National Institutes of Health (NIH) funded 20 large research studies of patented pharmaceutical industry drugs before only recently (and slowly) agreeing to study repurposed generic medicines.

The Food and Drug Administration and the Centers for Disease Control have recommended next to none. Instead, the Biden administration has thrown its political weight almost solely behind mass vaccinations, and hospitals and pharmacies have dogmatically followed suit. But this approach is proving insufficient to arrest COVID-19.

Repurposed Generic Medicines That Help Fight COVID

Just look at the evidence on, a widely used generic antidepressant. A randomized controlled trial (RCT) published in November 2020 showed that the drug led to far less clinical deterioration in treated patients. Another, larger, double-blind RCT, published in The Lancet in October of this year, found fluvoxamine reduced COVID-19 mortality rates by up to 91 percent and hospitalizations by two-thirds. This is an FDA-approved drug. Dosed correctly and for such short periods, it is safe. And it costs about a dollar a pill.

These findings have since been further reinforced by another study published by the Journal of the American Medical Association in November, which showed a strong “class effect” of benefits from anti-depressants very similar to fluvoxamine against COVID-19. Yet, despite the large double-blind, placebo-controlled trial, neither the NIH nor the Infectious Diseases Society of America (IDSA) has arrived at a recommendation for routine use of these drugs to treat COVID-19.

The NIH to date has ignored the study. Its last update on fluvoxamine dates back to April, more than seven months ago. More disturbing is the fact that the IDSA recently reviewed this high-quality trial, yet still held fast to its recommendation of “do not use outside of a clinical trial.” Why do repurposed drugs require numerous trials prior to an agency recommendation, while high-profit, novel, patented drugs get routinely approved after only a single trial?

A recent and most brazen example is Merck’s expensive new anti-viral COVID-19 drug, molnupiravir. The FDA rapidly approved it based on a single study of modest benefits in mildly ill outpatients, and the Biden administration swiftly agreed to pay $700 per course of treatment. That was all despite the fact the medicine costs about $20 per course to manufacture, according to a World Health Organization consultant, and may prove less effective or even harmful in practice.

With our national debt registering at $2.77 trillion and inflation rampant, building the capacity in our federal government to study cheap, generic medicines would be a smart economic move. But there appears to be no appetite for fiscal prudence or scientific inquiry beyond the expensive, newly minted solutions churned out by our nation’s pharmaceutical industry.

Hospital Bans Proven Treatment

Doctors who don’t toe the line are subjected to censorship and threatened with the loss of their livelihood, regardless of their clinical experience. My colleague Dr. Paul Marik, a scientist-physician practicing in Norfolk, Virginia, is among them. He has treated patients throughout the COVID outbreak and was an early advocate for the use of steroids to treat COVID patients — a practice initially discouraged by federal health officials that has since proven effective.

When evidence first emerged about fluvoxamine, we began studying the medicine and sharing clinical data with physicians in the Frontline COVID-19 Critical Care Alliance (FLCCC), a non-profit physician group we run together. We added it to our FLCCC protocol seven months ago. Marik began treating his patients with the medicine in addition to steroids and a number of repurposed generic medicines, which contributed to halving deaths in his hospital.

That progress is now in jeopardy: Marik’s employer, Sentara Norfolk General Hospital, has forbidden the use of fluvoxamine as well as several other FDA-approved generic drugs to treat COVID-19 — and mortality rates are already rising.

What is the hospital’s justification for denying patients a treatment that’s proving effective in clinical trials? It sounds a lot like the NIH’s website, and rings equally hollow: “Many [of these medicines] do not have published peer-reviewed, RCT [randomized controlled trial] available to assess both efficacy and safety in COVID-19.”

Over the last two years, our political and public health authorities have talked often of trusting science to guide an effective response to this terrible virus, but their actions have more often been dictated by tribalism and greed.

We will surely face new COVID-19 variants after Omicron, and other infectious disease outbreaks in the future. We can prepare by building the capacity in our government to study cost-effective treatments quickly and efficiently, and by empowering doctors to pursue every possible treatment that can help patients.

RELATED ARTICLE: Biden to Introduce New COVID Measures, Issue ‘Stark Warning’ to Unvaccinated

EDITORS NOTE: This Geller Report column is republished with permission. ©All rights reserved.

Quick note: Tech giants are shutting us down. You know this. Twitter, LinkedIn, Google Adsense, Pinterest permanently banned us. Facebook, Google search et al have shadow-banned, suspended and deleted us from your news feeds. They are disappearing us. But we are here. We will not waver. We will not tire. We will not falter, and we will not fail. Freedom will prevail.

Subscribe to Geller Report newsletter here — it’s free and it’s critical NOW when informed decision making and opinion is essential to America’s survival. Share our posts on your social channels and with your email contacts. Fight the great fight.

Follow me on Gettr. I am there, click here. It’s open and free.

Remember, YOU make the work possible. If you can, please contribute to Geller Report.

Stanford Epidemiologist Says COVID Vaccination Is Primarily a Matter of Personal Health, Not Public Health

An abundance of scientific data undermine justifications for COVID vaccination mandates, which violate long-standing principles of bodily autonomy and individual rights.


As one-size-fits-all COVID vaccine mandates sweep government, academia, and corporate America, new data are emerging that undermine the public health justifications for these policies. Studies from multiple countries now indicate that vaccination alone is less effective than the acquired immunity many already possess and unable to prevent transmission in the medium-to-long term.

Since the pandemic began, more than 100 million Americans have recovered from the virus. Many are workers deemed “essential” just last year. While the government paid others to sit at home, essential workers were required to continue working, exposing themselves to the coronavirus in a pre-vaccine world.

One of these individuals is my friend, Adam, an occupational therapist and rehabilitation director treating patients at a small nursing home in Aroostook County, Maine. He never worked from home. His patients needed him there in person. Like many healthcare workers on the frontlines, Adam was infected by the coronavirus while on the job, stayed home until he tested negative, and then went back to work.

As far as COVID is concerned, Adam is among the safest people in America to be around. Multiple studies (including one out of Israel that has received global attention) now indicate that those who have recovered from infection possess a natural immunity more robust than what current vaccines provide. Further, three epidemiologists at Harvard, Oxford, and Stanford have specifically recommended in the Great Barrington Declaration (now co-signed by nearly 15,000 medical and public health scientists, as well as 44,000 medical practitioners) that “nursing homes should use staff with acquired immunity” to protect patients.

So why have both President Joe Biden and Governor Janet Mills (D-ME) issued mandates threatening Medicare and Medicaid reimbursements to all healthcare providers unless they fire people like Adam? Mandates that make no exception for those with demonstrated acquired immunity make little sense for public health.

Additionally, in light of recent studies and documented “breakthrough infections,” the public health basis for mandatory vaccination is increasingly shaky for even those without any degree of natural immunity.

During my four years as Senate Chairman for Maine’s Health and Human Services Committee, mandatory vaccination policies in schools were a regular source of heated debate. The arguments for robust enforcement often rested on the need for “herd immunity”—the point at which one person transmits a virus to one or fewer people due to pre-existing immunity within a population.

Before the advent of vaccination, herd immunity relied on the development of natural immunity through widespread exposure to a virus. Since vaccination became common, many viruses once plaguing society are now virtually eradicated. To maintain herd immunity for subsequent generations and prevent the return of our old viral enemies, widespread vaccination is widely regarded as essential. For COVID vaccination, however, this does not appear to be the case.

According to Dr. Jay Bhattacharya, a professor of medicine who studies epidemiology at Stanford University, recent studies indicate that the mRNA vaccines produced by Moderna and Pfizer do not contribute to herd immunity.

During a September 2021 interview with New York Times best-selling author Tom Woods, Bhattacharya, one of the authors of the Great Barrington Declaration, cited a study from Qatar with important findings on vaccine effectiveness. While vaccinated individuals were up to 95 percent safer from severe disease six months after vaccination, protection against infection and transmission was fleeting. Immunity began to diminish after five weeks. At 20 weeks, the vaccinated were as likely to become infected and transmit the virus as those unvaccinated.

This failure to confer a lasting immunity that protects the public does not negate the demonstrated positive effects for the individual. Battacharya hails the vaccine as “a wonderful achievement” that has “protected so many people from severe outcomes of the disease.” He credits the vaccine with aiding his own recovery from a COVID infection and strongly recommends it to others, especially the “older and vulnerable.”

“It’s better to have the vaccines first and then get the disease than the other way around,” he says.

At the same time, Bhattacharya concludes that, without contributing to herd immunity, COVID vaccination is a matter of personal health, not public health. As the benefits rest primarily with the individual, not society, government officials have no greater moral authority to prescribe vaccination than they do to prescribe chemotherapy. These are decisions for the individual to decide in consultation with their own physician.

Unlike pre-existing requirements in schools for traditional vaccinations, existing data undermines herd immunity justifications for universal COVID vaccination mandates. Further, these mandates push many with robust acquired immunity out of the workplace and society to the detriment of public health, increasing the likelihood of transmission to the vulnerable.

Mandatory COVID vaccination oversteps the bounds of public health, violating long-standing Western principles of bodily autonomy and individual rights. Lacking even the clear positive externalities often used to justify past vaccination requirements, these mandates should be opposed at all levels of policymaking.

COLUMN BY

Eric Brakey

Eric Brakey is the senior spokesperson for Young Americans for Liberty. As a state senator from 2014 to 2018, Brakey served as senate chairman for the Maine Health and Human Services Committee.

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