HHS Ousts Peter Marks, Sending Vaccine Stocks Tumbling and Biopharma Lamenting Loss of ‘Ally’ at FDA
By Michael Nevradakis, Ph.D. | The Defender | March 31, 2025
Pharma stocks tumbled today after Peter Marks, M.D., Ph.D., director of the agency within the U.S. Food and Drug Administration (FDA) responsible for authorizing vaccines, resigned under pressure from his new boss, Health and Human Services (HHS) Secretary Robert F. Kennedy Jr.
“If Peter Marks does not want to get behind restoring science to its golden standard and promoting radical transparency, then he has no place at FDA under the strong leadership of Secretary Kennedy,” an HHS official said in a statement.
Shares of Moderna, BioNTech, Novavax and Pfizer declined 11%, 7%, 6% and 2%, respectively, on the news, Fast Company reported. STAT News reported that Marks’ departure “is a worst-case scenario realized” for investors and “a biopharma industry that saw him as an ally.”
“Given Dr. Marks’ influence on the development of biologics and uncertainty as to who will replace him and how his legacy might continue, his departure will create a significant near-term overhang,” William Blair analyst Matt Phipps told Reuters.
The Biotechnology Innovation Organization, an industry lobbying group, said it was “deeply concerned” Marks’ resignation would “broadly impact the development of new, transformative therapies to fight diseases for the American people.”
Brian Hooker, Ph.D., chief scientific officer for Children’s Health Defense (CHD), said the reaction to Marks’ departure on the part of the markets and the pharmaceutical industry is indicative of the influence Big Pharma had over the FDA. He said:
“Marks gave an over $100 billion gift to Pfizer and Moderna via the woefully undertested and outright dangerous COVID-19 mRNA vaccine. So, yes, for the short term, I would imagine that some investors would not like his departure from the FDA.
“Marks’ departure also signals a shift from ‘sick care’ and ‘customers for life’ where, unfortunately, Pharma invests now, to ‘Make America Healthy Again’ where everyone benefits from ending chronic disease in the U.S.”
John Gilmore, executive director of the Autism Action Network, welcomed Marks’ departure. “The American people are well-served by Marks’ resignation.” Gilmore cited the “institutional failure” of the Center for Biologics Evaluation and Research (CBER) “to use the highest standards for evaluating the safety and efficacy of products that are injected in almost all American children.”
Marks has led the FDA’s CBER since 2012 and “played a key role,” The Wall Street Journal reported, in Operation Warp Speed in 2020, leading to the development of the COVID-19 vaccines.
In his resignation letter, Marks wrote: “It has become clear that truth and transparency are not desired by the Secretary, but rather he wishes subservient confirmation of his misinformation and lies.”
Marks’ ‘support of immunizations conflicted with Kennedy’s skepticism’
According to the Journal, an HHS official gave Marks a choice between resigning or being fired. His resignation is effective April 5. Marks wanted to remain in his position, but “his support of immunizations conflicted with Kennedy’s skepticism.”
“Undermining confidence in well-established vaccines that have met the high standards for quality, safety, and effectiveness that have been in place for decades at FDA is irresponsible, detrimental to public health, and a clear danger to our nation’s health, safety. and security,” Marks wrote in his resignation letter.
Marks said he was “willing to work to address” Kennedy’s concerns on vaccine safety, including through a series of public meetings, but that these proposals were rejected. He also accused Kennedy of spreading “misinformation and lies” during the “ongoing multistate measles outbreak.”
But in a post on X, Steve Kirsch, founder of the Vaccine Safety Research Foundation, said that while Marks “claimed he wanted to stop misinformation,” he “refused all offers to meet with the ‘misinformation spreaders’ to settle the question on just who is spreading the misinformation.”
While Marks claimed he was willing to address questions on vaccine safety, he also wrote, “Efforts currently being advanced by some on the adverse health effects of vaccination are concerning.”
One day before Marks’ resignation, Kennedy announced the creation of a new sub-agency under the Centers for Disease Control and Prevention (CDC) to focus on vaccine injuries — part of a broader restructuring of public health agencies, including the FDA.
In February, Kennedy promised that under his watch, HHS and CDC would develop a better system for tracking vaccine injuries.
Earlier this month, Reuters reported that unnamed sources within the CDC said the agency was planning to study the possible link between vaccines and autism. The story triggered negative mainstream news reports claiming the study isn’t needed.
Last week, The Washington Post, citing anonymous sources, reported that HHS had tapped researcher David Geier — a researcher and expert on the connections between toxic exposures and autism — to lead a study of possible links between vaccines and autism. The Post and other media outlets used the opportunity to attack Geier and the need for such a study.
Marks’ resignation also came as the FDA is considering a petition a group of scientists submitted earlier this year, calling upon the FDA to suspend or withdraw the mRNA COVID-19 vaccines.
Marks ‘became a cheerleader for the jab’
Writing on Substack, investigative journalist Maryanne Demasi, Ph.D., said it’s “evident there was a significant clash over vaccine safety” that led to Marks’ resignation. She said Marks’ departure “may be an opportunity for the FDA to refocus on its mission of protecting public health rather than rubber-stamping new vaccine approvals.”
Epidemiologist Nicolas Hulscher agreed. “Those who believe vaccine safety must not be questioned do not belong in our regulatory agencies. When it comes to injectable products, safety is more important than blind faith in vaccine ideology.”
According to The New York Times, while Marks “was viewed as a steady hand by many during the Covid pandemic,” he was criticized “for being overly generous to companies that sought approvals for therapies with mixed evidence of a benefit.”
The Times cited Marks’ role in pressuring two FDA scientists to approve full licensure of Pfizer’s mRNA COVID-19 vaccine in 2021, leading to the researchers’ resignation. Pfizer’s vaccine was fully licensed in August 2021 — one day later, the Biden administration mandated COVID-19 vaccination for military service members.
The rushed licensure of the Pfizer vaccine was the topic of a congressional hearing last year in which Marks testified. In a post on X Saturday, Rep. Thomas Massie (R-Ky.) wrote, “Instead of verifying safety and efficacy of the shots, Marks swept things under the rug and became a cheerleader for the jab.”
“In order to get the vaccines to people in need when thousands of people were dying, we actually allowed the safety to be authorized with just two months of median follow-up, rather than the normal six to 12. But we were confident that that would capture adverse events,” Marks testified at last year’s hearing.
‘It was clear that he did not want to know about our injuries’
While Marks was actively engaged in the licensure of the Pfizer COVID-19 vaccine, he “remained steadfast” in dismissing concerns about injuries related to the COVID-19 vaccines as “misinformation,” Demasi wrote.
In 2023, The BMJ wrote that “more than once” during FDA meetings, Marks “expressed confusion about why it would matter to doctors whether or not regulators acknowledged that a condition might be related to the vaccine.”
Documents CHD obtained last year through a Freedom of Information Act request showed that Marks was aware of COVID-19 vaccine injuries in early 2021 when several vaccine injury victims emailed him for help. Marks blew off scheduled meetings with them.
According to TrialSite News, even though Marks was aware of the growing number of COVID-19 vaccine injuries, “vaccine injury became a political hot potato under the Biden administration,” leading Marks to abandon the vaccine-injured.
Brianne Dressen, co-founder of React19, an advocacy group for the vaccine-injured, sustained serious injuries after participating in a clinical trial for the AstraZeneca COVID-19 vaccine in 2020 and later sought meetings with Marks but was rebuffed.
“Constant emails and calls with Marks … sent while I was in constant pain, literally begging for help, begging for them to help others, begging for a lifeline. A lifeline that never ever came,” Dressen said.
Dr. Danice Hertz, a retired gastroenterologist from California injured by the Pfizer COVID-19 vaccine, also communicated with Marks but said he “brushed off anyone who contacted him regarding vaccine side effects.”
“He systematically refused to hear our pleas for acknowledgment and help,” Hertz said. “This is why the medical community is unaware of these injuries and cannot help us. One would think that the FDA would want to know about serious adverse reactions to the novel COVID vaccines. I can say from first-hand experience that they don’t … It was clear that he did not want to know about our injuries.”
Dressen said it “didn’t matter what we said or how we said it, COVID vaccine injuries were not a priority at the FDA. Didn’t matter if it was safety signals for MIS-V, dysautonomia, neuropathy, tinnitus or reports of suicides. It was never enough. We begged, we pleaded, we pushed as hard as we could, and came up with nothing.”
According to Demasi, Marks instead “blurred the line between regulation and promotion” by participating in FDA videos promoting the COVID-19 vaccines and by authorizing COVID-19 mRNA vaccines for children without sufficient testing.
“Without randomized data regarding clinical outcomes, he repeatedly approved COVID boosters for kids as young as 6 months,” Dr. Vinay Prasad, professor of epidemiology and biostatistics at the University of California, San Francisco, wrote on Substack, calling these “some of the biggest regulatory errors in the 21st century.”
Demasi said Marks “repeatedly pointed to the Vaccine Adverse Event Reporting System (VAERS) as proof of rigorous safety monitoring, yet failed to improve its efficiency.”
During last year’s congressional hearing, Marks claimed that numerous false reports of vaccine injuries are submitted to VAERS, a government-run database. However, he acknowledged, “We probably have not done a good enough job of communicating sometimes the actual numbers of deaths versus what’s in VAERS.”
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
Canadian PM Mark Carney Downplays Role in Freedom Convoy Crackdown Despite Backing Emergency Measures
Carney called protest “sedition” and Urged financial chokehold
By Didi Rankovic | Reclaim The Net | April 1, 2025
Canada’s Prime Minister Mark Carney recently gave a masterclass in the art of political evasion and deflection – all the more “masterful” since one of the arguments he went for was that he is not really a politician.
This unfolded before TV cameras in the area of the 2022 Freedom Convoy blockade, which the authorities led by former PM Justin Trudeau and his Liberals clamped down on using unprecedented measures.
They included invoking the Emergencies Act to target the protesters against restrictive Covid-era policies with anything from extreme vilification to freezing their bank accounts.
“Sedition,” is what Carney decided to brand the civil protest in an op-ed published in the Globe and Mail on February 7, 2022, and, true to his previous roles in Big Finance, proposed to put an end to the protest (he called it “this occupation”) by “choking off the money” that funded it.
Now – given his current “affiliation” with the Liberal party, the new prime minister was asked to send a message to those Canadians who lost trust in the previous cabinet because of its handling of the protest.
Instead of doing that, Carney first sought to “distanced himself from himself” – saying that he has only been a politician for two months, and claiming that he took on his new role because he “knew this country needed big change.”
And he then proceeded to list all the allegedly significant changes achieved during his short time in office so far, thus deflecting from the Freedom Convoy question.
Despite his best efforts to paint himself as no more than a conscientious citizen determined to help his country through difficult times – three years ago this former governor of the Bank of Canada and the Bank of England was an informal advisor to Trudeau.
And he not only accused the Freedom of Convoy protestors of committing “sedition” and those donating to the cause of “funding sedition,” but was also mentioned in the Public Order Emergency Commission documents (which investigated the invocation of the Emergencies Act).
Spoiler: Carney supported that decision, along with the freezing of citizens’ bank accounts because they protested against the government.
But Carney’s failed upward now to become prime minister, and “re-earn trust” – not to mention, introduce “big change.”
“This Is Existential”: Billionaire Cancer Researcher Says Covid & Vaccine Likely Causing Surge In Aggressive Cancers
By Tyler Durden | Zero Hedge | March 28, 2025
Dr. Patrick Soon-Shiong – a transplant surgeon-turned-biotech billionaire renowned for inventing the cancer drug Abraxane – has issued a startling warning in a new in-depth interview with Tucker Carlson.
Soon-Shiong, founder of ImmunityBio ($IBRX) and owner of the Los Angeles Times, claims that the COVID-19 pandemic, and the very vaccines developed to fight it, may be contributing to a global surge in “terrifyingly aggressive” cancers. In the nearly two-hour conversation, the Los Angeles Times owner leveraged his decades of clinical and scientific experience to outline why he suspects an unprecedented cancer epidemic is unfolding. This report examines Dr. Soon-Shiong’s background and assertions, the scientific responses for and against his claims, new data on post-COVID health trends, and the far-reaching implications if his alarming hypothesis proves true.
Dr. Soon-Shiong’s Claims
Soon-Shiong is a veteran surgeon and immunologist who has spent a career studying the human immune system’s fight against cancer. He pioneered novel immunotherapies and even worked on a T-cell based COVID vaccine booster during the pandemic. In the interview, he draws on this background to voice deep concern over rising cancer cases, especially among younger people – something he describes as a “non-infectious pandemic” of cancer. He tells Carlson that in 50 years of medical practice, it was extraordinarily rare to see cancers like pancreatic tumors in children or young adults, yet recently such cases are appearing. For instance, Soon-Shiong was alarmed by seeing a 13-year-old with metastatic pancreatic cancer, a scenario virtually unheard of in his prior experience.
“I never saw pancreatic cancer in children… the greatest surprise to me was a 13-year-old with metastatic pancreatic cancer,” Soon-Shiong told Carlson, adding that he’s seen examples of very young patients (even children under 11 with colon cancer) and unusual surges in aggressive diseases like ovarian cancer in women in their 30s. These personal observations of more frequent, aggressive cancers in youth led him to probe what might have changed in recent years.
“We’re clearly seeing an increase in certain types of cancer, like pancreatic cancer, ovarian cancer… colon cancer… in younger people.”
— Dr. Patrick Soon-Shiong
According Soon-Shiong, the COVID era is the obvious change – and suggests that both the SARS-CoV-2 virus infection and the widespread vaccination campaigns could be key drivers behind this cancer spike. He emphasizes the massive scale of human exposure to the virus and its spike protein (via infection or vaccination).
“I don’t know how to say that without saying it. It scares the pants off me because I think what we may be, I don’ think it’s virus versus man now, this is existential. I think when I talk about the largest non-infectious pandemic that we’re afraid of, this is it.”
“Billions of people – literally billions – had the COVID virus. Over a billion got the spike protein vaccine,” said Carlson, adding “So that’s like, we’re talking like a huge percentage of the Earth’s population, unless I’m missing something.”
“Now you understand what keeps you awake at night and kept me awake at night for two years, two and a half years,” Soon-Shiong replied, suggesting that exposure to both is silently undermining the immune system’s natural defenses against cancer on a global scale.
Soon-Shiong frames COVID-era cancers as potentially virally triggered or exacerbated. In the interview, he described cases of “virally induced cancers” in clinics during the pandemic – patients whose cancers may have been kicked into overdrive by the cascade of inflammation and immune stress associated with COVID-19 (Dr. Patrick Soon-Shiong: You’re Being Lied to About Cancer, How It’s Caused, and How to Stop It). COVID infection causes a massive inflammatory response, and some cancers are known to exploit inflammation to grow.
TUCKER: “a lot people have pointed to both COVID, the virus, and to the mRNA COVID vaccines as potential causes. Do you think that they’re related?”
SOON-SHIONG: “The best way for me to answer that is to look at history. What we know about virally-induced cancers is well-established. We know that if you get hepatitis, you get liver cancer. Hepatitis is a virus infection. We know if you got human papillomavirus, HPV, you get cervical cancer.”
We know that certain viruses directly cause cancer (e.g. HPV, Epstein-Barr), so it’s not unprecedented for a virus to play a role in oncogenesis. While SARS-CoV-2 is not a known oncovirus, Soon-Shiong worries its indirect effects – chronic inflammation, immune exhaustion, or “suppressor cells” that emerge in the wake of infection/vaccination – could be accelerating tumor development. “The answer is to stop the inflammation… clear the virus from the body,” he argues, positing that until we eradicate lingering virus and restore immune balance, we may see mounting cancer cases.
In sum, Dr. Soon-Shiong’s claim is that the pandemic has set the stage for an explosion of aggressive cancers: the COVID virus itself (especially if it persists in survivors) might suppress immune surveillance, and the mRNA vaccines “that didn’t stop it” might inadvertently contribute to an immunosuppressive environment. These effects, in his theory, could be unleashing cancers that the immune system would ordinarily have kept in check.
Watch:
A number of clinicians and researchers have reported similar worrying observations, though these remain largely anecdotal at this stage. One prominent voice echoing Soon-Shiong’s concern is Dr. Angus Dalgleish, a veteran oncologist and professor at St. George’s, University of London. In late 2022, Dalgleish wrote to the BMJ’s editor after noticing that some cancer patients who had been stable for years experienced “rapid progression of their disease after a COVID-19 booster.” He cited cases of individuals who were doing well until shortly after vaccination – new leukemias, sudden appearance of Stage IV lymphomas, and explosive metastases in patients who had post-vaccine bouts of feeling unwell.
“I am experienced enough to know that these are not coincidental,” Dalgleish wrote, noting that colleagues in Germany, Australia and the U.S. were independently seeing the same pattern. This frontline testimony aligns with Soon-Shiong’s fear: something about the immune system post-vaccination might be removing restraints on latent cancers. Dalgleish specifically pointed to short-term innate immune suppression after mRNA vaccination (lasting for several weeks) as a plausible mechanism. Many of the cancers he saw were ones normally held in check by immune surveillance (melanomas and B-cell cancers), so a temporary post-vaccine drop in immune vigilance could allow a tumor growth spurt. He also alluded to “suppressor gene suppression by mRNA in laboratory experiments” – a reference to preliminary studies that found the SARS-CoV-2 spike protein might interfere with key DNA repair or tumor-suppressor proteins in cells. These lab findings (while not yet confirmed in living organisms) lend some biological plausibility to the idea that spike exposure could affect cancer-related pathways.
Beyond individual doctors, some research is probing links between COVID and cancer behavior. For example, a 2022 study in Frontiers in Oncology explored how SARS-CoV-2 proteins interact with cancer cells. It found that the virus’s membrane (M) protein can “induce the mobility, proliferation and in vivo metastasis” of triple-negative breast cancer cells in the lab (Frontiers | SARS-CoV-2 M Protein Facilitates Malignant Transformation of Breast Cancer Cells). In co-culture experiments, breast cancer cells exposed to the viral protein essentially became more aggressive and invasive. The researchers concluded that COVID-19 infection “might promote… aggressive [cancer] phenotypes” and warned that cancer patients who get COVID could face worse outcomes.
While this is one specific context (breast cancer cells and one viral protein), it underpins Soon-Shiong’s general concern: the virus can directly alter the tumor microenvironment to the cancer’s advantage.
Another line of evidence involves latent viruses and inflammation. Doctors have documented unusual reactivations of viruses like Epstein-Barr (which is linked to lymphomas and other malignancies) during both COVID-19 and post-vaccine immune reactions. Such reactivations hint at a period of immune dysregulation that might also let nascent cancer cells slip past defenses.
Or course, fact-checkers and medical authorities argue that there is no credible evidence of vaccines causing meaningful immune suppression. “There isn’t evidence to date that COVID-19 vaccines cause cancer or lead to worsening cancer,” one infectious disease expert told FactCheck.org, though they do acknowledge rare side effects like myocarditis or blood clots were found, but not cancer.
Phinance Data Insights: Post-COVID Health Trends
While the scientific community debates mechanistic links between COVID and cancer, independent analysts have been parsing population-level data for unusual patterns. One notable effort is by Phinance Technologies, a research firm co-founded by former BlackRock portfolio manager Edward Dowd. Phinance has been analyzing excess mortality and disability data since the pandemic, looking for signals of broad health impacts in the aftermath of COVID and mass vaccination. Their findings reveal concerning trends, especially among younger, working-age populations, that lend some weight to Dr. Soon-Shiong’s general warning of a post-COVID health crisis (though not specific to cancer alone).
Phinance’s “Vaccine Damage Project” examined the U.S. population aged 16–64 (essentially the workforce) and stratified outcomes into four groups: no effect, mild injuries, severe injuries (disabilities), and death. Using official government databases (the CDC, Bureau of Labor Statistics, etc.), they estimated how each category changed starting in 2021 – when vaccines rolled out and COVID became widespread. The results are sobering. According to Phinance’s analysis, by the end of 2022 the U.S. had experienced approximately 310,000 excess deaths among adults aged 25-64 (a ~23% increase in mortality in that group over normal expectations). Notably, they argue that after mid-2021, with vaccines available and the virus itself becoming less deadly (due to immunity and milder variants), COVID-19 should not have been causing such high excess death rates. Therefore, those 310k “unexplained” deaths in 2021–2022 could represent an upper bound on vaccine-related fatalities or other pandemic collateral damage.
Even more striking is the data on new disabilities. Phinance found that from early 2021 through late 2022, about 1.36 million additional Americans (age 16–64) became disabled – a 24.6% rise in disability in that cohort, far above historical trend. This jump in disabilities among the workforce correlates in time with the vaccine rollout (and was disproportionately higher in the labor force than among those not working). The analysts note that the healthiest segment of the population (employed working-age adults) saw a greater relative increase in disabilities after Q1 2021 than the older or non-working groups. This is unusual, since typically health shocks hit the elderly hardest – but here something was impacting younger, healthy people to a significant degree. Phinance investigated further and found a tight relationship between the cumulative number of vaccine doses administered and the rise in disabilities in 2021-22. In fact, for the 16–64 population, they computed a ratio of about 4 new disabilities per excess death in that period, suggesting many survivors were left with lingering health issues even if they didn’t die.
NIH Pulls Plug on ‘Vaccine Hesitancy’ Research — Will mRNA Products Be Next?
By Michael Nevradakis, Ph.D. | The Defender | March 11, 2025
The National Institutes of Health (NIH) will no longer fund research on “vaccine hesitancy” and strategies for increasing vaccine uptake, The Washington Post reported Monday.
According to Science, the NIH sent notices canceling or reducing grants to the affected researchers, stating:
“It is the policy of NIH not to prioritize research activities that focus on gaining scientific knowledge on why individuals are hesitant to be vaccinated and/or explore ways to improve vaccine interest and commitment.”
NIH will terminate at least 33 vaccine hesitancy grants, Science reported. Nine other grants will be modified or reduced.
The terminations came after NIH, on behalf of interim director Matthew Memoli, asked each of its institutes to develop a list of ongoing and future vaccine hesitancy grants.
Science reported that the agency is considering taking similar action for research related to mRNA products.
Of the terminated grants, 14 were funded by the National Institute for Allergy and Infectious Diseases — the agency formerly led by Dr. Anthony Fauci — and focused on vaccines for COVID-19, chickenpox, mpox (formerly monkeypox), HPV and a hypothetical gonorrhea vaccine.
“The project appeared on the list because one of its aims ‘is to evaluate health care worker’s [sic] and potential patient’s attitudes towards acceptance of a gonorrhea vaccine if one is developed,’” Science reported.
Other canceled grants targeted modeling of disease outbreaks or “promoting vaccine uptake among racial minority groups or understanding why some parents are reluctant to accept childhood and adolescent vaccines.”
Memoli is temporarily leading the NIH pending the confirmation of Dr. Jay Bhattacharya, a Stanford University professor of health policy, co-author of the Great Barrington Declaration and President Donald Trump’s nominee to lead NIH.
NIH did not respond to a request for comment by press time.
Grants targeted ‘vaccine-hesitant’ minority and conservative communities
The Defender previously reported on multiple taxpayer-funded grants, including some awarded by the NIH, that funded research on decreasing vaccine hesitancy and increasing HPV vaccine uptake.
The Defender obtained the grant information through a series of Freedom of Information Act (FOIA) requests in 2023 and 2024
One set of documents, obtained in 2023, revealed that the U.S. Department of Health and Human Services (HHS) issued a $4.7 million grant to a scientist — and paid consultant for Merck — to conduct research on how to increase teen uptake of the HPV vaccine. Merck manufactures Gardasil, the only HPV vaccine available in the U.S.
In 2024, the grant’s principal investigator, Noel Brewer, Ph.D., a psychologist and professor in the Department of Health Behavior at the University of North Carolina Gillings School of Global Public Health, was appointed to the Advisory Committee on Immunization Practices, which advises the Centers for Disease Control and Prevention (CDC) on vaccine recommendations.
FOIA documents Children’s Health Defense (CHD) received in 2024 revealed that HHS issued $4 million to fund the development of an artificial intelligence (AI) tool designed to “inoculate” social media users against HPV vaccine “misinformation” posted on social media.
Other documents CHD received in 2023 revealed that HHS granted $600,000 for research on how to increase HPV vaccine uptake among Black teens, and that NIH granted $519,399 for a four-year study on a smartphone tool to increase HPV vaccine uptake among adolescents whose parents are “vaccine-hesitant.”
The NIH also funded such studies overseas. FOIA documents CHD received in 2024 showed that NIH awarded $340,000 to test psychological tactics aimed at persuading South African fifth-graders and parents to accept the HPV vaccine.
In 2023, documents showed that the CDC had issued hundreds of millions of dollars in grants since 2021 for the development of “culturally tailored” pro-vaccine materials and for the training of “influential messengers” to promote COVID-19 and flu vaccines to communities of color in each U.S. state.
The CDC also funded “Chair Care,” a New Mexico program that trained and paid hairstylists as “trusted messengers” that would target the state’s Hispanic, Black, Native American and conservative populations, who were shown to have the lowest vaccine uptake and highest “vaccine hesitancy.”
‘Vaccine hesitancy’ research targeted personal choice not to vaccinate
Toby Rogers, Ph.D., a fellow at the Brownstone Institute for Social and Economic Research, welcomed the NIH decision to stop such studies. He questioned the premise of the “vaccine hesitancy” research — and the concept of “vaccine hesitancy” itself.
“There’s no such thing as ‘vaccine hesitancy,’” Rogers said. “The term itself is completely Orwellian. It was likely coined by an expensive Big Pharma PR firm. The purpose of the term is to cast aspersions on parents who do proper research on the risks of medical interventions,” Rogers said.
According to Rogers, studies like those being discontinued were likely backed by pharmaceutical companies to ascertain how to increase vaccine demand.
“Studies on so-called ‘vaccine hesitancy’ and ‘overcoming vaccine hesitancy’ are thinly disguised marketing studies on behalf of the pharmaceutical industry,” Rogers said. “Big Pharma makes plenty of money. American taxpayers should not be paying for marketing studies on behalf of one of the most vile industries on Earth.”
Epidemiologist Nicolas Hulscher said it is inappropriate for the NIH to allocate resources to study people’s personal health choices.
“The purpose of studying vaccine hesitancy is to find ways to increase vaccine uptake in individuals that have made the personal choice to not vaccinate with a particular product,” Hulscher said. “The federal government should simply respect their choice and not waste valuable resources and taxpayer money on trying to change their minds.”
Internal medicine physician Dr. Clayton J. Baker said that during the COVID-19 pandemic, efforts to address “vaccine hesitancy” resulted in gimmicks intended to increase uptake of the COVID-19 shots — and punish those who declined vaccination.
“During COVID, we had health officials combating ‘vaccine hesitancy’ with bribes of lottery tickets, donuts, even free beer, and meting out punishments such as being fired from one’s job. Medical practice surrounding vaccines descended to a disgracefully unethical state during COVID,” Baker said.
mRNA research grants next on NIH’s chopping block?
According to Science, the NIH may also curtail grants for mRNA vaccine research.
Citing an internal NIH memo sent March 6, Science reported that Memoli “has requested information on NIH’s investment in mRNA vaccines research,” including ongoing or planned grants and contracts, and collaborations with outside partners.
NIH institutes and programs were asked to respond by this week.
Hulscher drew parallels between mRNA research and “vaccine hesitancy” research.
“Vaccine hesitancy will remain high as a result of the federal government authorizing and mandating experimental modified mRNA injections that are suspected to have killed, injured or permanently disabled over a million Americans. The longer this disaster remains unacknowledged, the harder it will be to regain the trust of Americans,” Hulscher said.
According to the Post, it is “unclear” whether HHS Secretary Robert F. Kennedy Jr. “had a role, directly or indirectly, in the move to cancel these grants.”
HHS oversees federal health agencies, including NIH and the CDC.
‘Vaccine hesitancy’ grants funded ‘psychological manipulation programs’
Scientists and doctors quoted by the Post expressed concern over the NIH’s planned cuts of “vaccine hesitancy” research.
Manoj Sharma, Ph.D., a professor of social and behavioral health at the University of Nevada, Las Vegas, who received a previous CDC grant for vaccine hesitancy research, told the Post, “There is an urgent need to enhance vaccine acceptance behavior, especially due to the potential resurgence of measles and COVID-19 still looming.”
But for Baker, “This statement exemplifies the real goal of these studies, which is not to study behaviors, but to drive behaviors in a predetermined direction.” He added:
“‘Vaccine hesitancy’ grants do not fund scientific inquiry so much as psychological manipulation programs. They reject freedom of choice in favor of a predetermined behavior. It is a form of coercion. Coercion, be it subtle or obvious, is the opposite of informed consent.
“Informed consent is absolutely central to the ethical practice of medicine. NIH should not fund research that undermines the ethical practice of medicine.”
Hulscher suggested that NIH resources previously earmarked for “vaccine hesitancy” studies “should be allocated to proper safety testing of the entire childhood vaccine schedule, where there are currently no products licensed based on long-term placebo-controlled trials.”
Other experts suggested that these resources could be used to rectify harms related to the promotion — or mandate — of COVID-19 vaccines during the pandemic.
“The money saved from cancelling these studies should instead be paid to independent researchers who are documenting the experiences of the millions of Americans injured by vaccines,” Rogers said.
“The grant money would be better used to produce a historical document of the abuses of informed consent during COVID, than to continue these psychological manipulation programs disguised as scientific inquiry,” Baker said.
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
COVID-19 Vaccines Harms: What and When BC Public Health Knew
Review of FOI F23-1799 and BC Public Health’s Handling of COVID-19 Vaccines AEFI – Part 1
By Lex Acker | Truth, Investing, and Freedom | February 28, 2025
Background
In April 2023, Lee Turner, of Doak Shireff Lawyers LLP, took over conduct of the defence of Dr. Charles Hoffe vs. the College of Physicians and Surgeons of BC. Mr. Turner subsequently filed a Freedom of Information (FOI) request (F23-1799) with the Provincial Health Services Authority (PHSA) to obtain data on Adverse Events Following Immunization (AEFI). FOI F23-1799 can be accessed at this link.
FOI F23-1799 was released in June 2024 and comprised over 1,300 pages of internal emails between BC CDC staff, Bonnie Henry, Reka Gustafson, and Monika Naus (then head of BC CDC), along with dozens of AEFI reports.
Upon reviewing FOI F23-1799, I noted key elements: discussions of AEFIs in emails, screenshots of non-public AEFI reports available through an intranet, and public-facing AEFI reports presented in chronological order. This arrangement made it possible to determine what BC public health officials like Bonnie Henry, the BC CDC and all 50+ medical health officers scattered over BC health authorities knew and when they knew it.
I reached an unsettling conclusion: BC CDC had manipulated the definition of Serious Adverse Events Following Immunization to lower the reported rates of Serious AEFIs in public-facing reports, thereby concealing the true risks associated with COVID-19 vaccines. I publicly shared this finding on June 14, 2024, in a comment on Byram Bridle’s post titled Breaking News: BC Centre for Disease Control Caught Lying and Withholding Important Public Health Data.
While my expertise is not in medical science, I specialize in detecting and documenting corporate and institutional misconduct. My background is in financial statement analysis. I worked as a hedge fund research analyst and compliance officer for a boutique investment firm. I have about 15 years of independent financial research and analysis experience. My focus is uncovering white-collar fraud. I’m not a forensic accountant by any measure; I’m just someone with somewhat odd proclivities for large sets of unstructured data and enjoy immersing myself in new topics.
The Case Against Dr. Hoffe
The College of Physicians and Surgeons of BC cancelled its February 11, 2022 citation against Dr. Hoffe on February 5, 2025. According to one media outlet, this was done because of a “material change of circumstances.”
The College accused Dr. Hoffe of professional misconduct; specifically spreading misinformation about COVID-19 vaccines. Here’s an excerpt of the College’s accusations:
“… publicly expressing that the COVID-19 vaccinations cause microscopic blood clots that cause serious neurological harm, female infertility, and a high number of deaths that is not recognized by public health; …”
Many other doctors were publicly denouncing the COVID-19 vaccines and were persecuted by the College. However, the level of persecution against Dr. Charles Hoffe is particular. The College retained eight experts against Dr. Hoffe. Why is that?
In early 2021, Dr. Hoffe submitted a temporally- and vaccine lot-associated cluster of 11 AEFI reports to Interior Health, 10 of which involved Moderna lot #300042698, administered between January 18 and February 5, 2021.
As Dr. Hoffe began filing AEFI reports in early 2021—most notably in April and May— and went on public tours in BC warning the public about the harms of COVID-19 vaccines his actions posed a direct threat to a state narrative that sought to suppress information about vaccine-related harm. His findings challenged the political and ideological foundation underpinning the mass vaccination program and the totalitarian controls over the population that came along with it.
The evidence in FOI F23-1799 suggests that Bonnie Henry, the BC CDC, all health authorities, and all 50+ Medical Health Officers in BC were fully aware of these issues. Dr. Hoffe’s real “offence” was exposing what the BC government concealed from the public since early 2021. Dr. Hoffe’s AEFI reports constituted a cluster of AEFI associated with unexpected harms which required public health authorities to investigate and disclose to the public.
This post, and a few more to come, will cover my findings and analysis of how BC public authorities handled the COVID-19 vaccine AEFIs. … continue
Covid vaccine injured – Silent no More
A book review
Health Advisory & Recovery Team | March 3, 2025
Was taking the Covid vaccine Worth a Shot? A new book by Caroline Pover, written on behalf of Brianne Dressen who lives in the USA, chronicles the horrific story of how she was severely injured by the Covid vaccine after enrolling on the AstraZeneca trial in November 2020. Caroline sensitively and professionally tells the heart wrenching, eye-opening account of how Brianne Dressen’s life was turned upside down and irreversibly changed forever the day she chose to volunteer to enroll on the UK-led AstraZeneca clinical trial. This book takes the reader along the rollercoaster ride of the devastating injuries caused by the vaccine and the blatant abuse of power by the healthcare system to denigrate, ignore, and cover up her injuries – along with many others labelled – as ‘misinformation’ spreaders by the medical-industrial-military complex. Every person on the planet was misled by governments, NGOs, regulatory agencies, corporations, Big Pharma, healthcare professionals, along with social and mainstream media. From how clinical trials are conducted to the lack of injury compensation, wide scale censorship, corruption and abuse of power, this book shows the myriad ways Brianne fought and continues to fight for truth and justice for the Covid-vaccine injured, who have been completely abandoned and often maligned by society.
The AstraZeneca Clinical Trial
In the introduction, Caroline Pover describes how she had been medically diagnosed with an adverse reaction to the Covid vaccine and was led to believe Brianne Dressen did not exist. It was only when she started posting on social media and heard about another woman who was dropped from a clinical trial because of an adverse reaction to the vaccine, that their paths crossed. Worth a Shot is a book based on real events that impacted on real people and is a narrative account of Brianne’s (Bri’s) story containing brutally honest struggles with how her life has changed irreversibly after the covid vaccine, including her plans to contemplate suicide. Bri had the perfect life: she was a fit, active lady who always pushed herself physically and mentally. She had a wonderful family life, married with two children with a dream house in the mountains. After having children, Bri set up her own preschool to help children who struggled in a typical educational environment. Then in 2020, Covid hit!
When the lockdowns happened and the talk of vaccine trials began, Bri wanted to help in any way possible with contributing to scientific advancements; once “Operation Warp Speed” was being regularly reported in the media, coupled with her husband’s scientific background, Bri felt excited to enrol in the new Covid vaccine trial set up by Oxford University in conjunction with AstraZeneca, which was recruiting in UK, Brazil, South Africa, and the USA. The opening in the USA was in Salt Lake City – just 40 minutes drive from Bri’s home. She had a phone interview with a trial representative for several hours to capture her medical history and was considered an excellent candidate for the trial. Things then went quiet, but out of the blue on 4th November 2020 – the day after the election – she was called into the trial. The consent form she signed was very thorough. It went through all the expectations and explained it was a double-blinded study and that so far 5,000 individuals had received at least one dose, and the side effects were mild to moderate but transient in nature. It also stated that if anyone did experience an adverse reaction they might be withdrawn from the study, but any medical treatment needed for reactions would be covered by AstraZeneca’s insurance policy. Bri took the vaccine, but tingling started within an hour of the injection.
Adverse Reaction
Bri’s reaction was severe. Tingling spread from below her right elbow all the way up her arm and shoulder, then to the other arm. The tingling got progressively worse and her eyes started to blur, and she saw double. Her hearing started to go muffled, but she assumed the symptoms would be gone by the next morning. However, her symptoms intensified, and now both legs were becoming weaker. She called the number on the consent form to report her reactions, but no one answered her call. Within days, she was confined to her bedroom, with drapes covering the window to shut out the light. Within weeks, her condition worsened so she saw a neurologist and visited an out-of-hours emergency clinic. Nausea, vision disturbances, tingling, extreme sensitivity to sound, limb weaknesses, as well as excruciating pain developed all over the body, including her teeth, stomach, bones, joints, legs and arms. She could not eat and lost 20 lbs within weeks. Her body seemed to vibrate and buzz from within constantly, and she could not bear anyone touching her, with extreme sensitivity to sound, light, and food. She spent weeks then months confined to her bed. She lost control of her bladder and her blood pressure was erratic. None of the pain medications helped.
Her husband and other family members and close friends helped with looking after the children and caring for her. Yet Bri and her husband did not want to broadcast these issues publicly when so many were struggling with Covid itself. Weekly and even sometimes daily visits to the hospitals baffled the doctors. Friends visited her but the visible transformation of her appearance shocked them, and she had to wear earplugs and sunglasses. Attempts at exercise were futile, as the pain was too unbearable. She visited multiple experts but to no avail. The principal investigator of the clinical trial suggested she might have multiple sclerosis (MS), but the trial clinic did not recommend any other specialists. Local neurologists recommended she visit the ER. The clinic staff told Bri that the ramifications were serious if she thought there was any possibility the vaccine had caused these symptoms. When she said her reactions were from the vaccine as she was a trial participant, most professionals were not interested and dismissed the symptoms as Covid. She had MRI scans but found nothing significant; there was nothing they could do. Bri was to report back to the trial clinic, which she did. They told her not to worry because AstraZeneca would reimburse all her medical costs – and they would be in touch soon. But no one contacted her.
No Diagnosis
She continued to go through the proper channels and medical experts to get answers. After a series of tests that ruled out MS and other neurological conditions, she was no closer to a diagnosis. By ploughing through scientific papers and doing their own research, Bri discovered post-vaccination transverse myelitis (TM), Guillain-Barre Syndrome (GBS) and acute disseminated encephalomyelitis (ADEM). Both TM and ADEM are conditions relating to inflammation of the spinal cord or central nervous system, which can lead to permanent damage. Despite Bri reporting this to the trial clinic, the trial was not put on hold. She was told to report everything back to AstraZeneca, which she did, but despite all the assurances, no one contacted her. Bri’s multiple trips to the hospital caused by the vaccine meant she was a burden to the healthcare system. Many physicians shrugged off her symptoms as psychiatric because none of the tests produced any explanation. She was put on antidepressants and gabapentin for neurological pain. Nothing had been put in place to deal with anyone who had an unexpected reaction to the vaccine.
On the next visit to her clinic, Bri hoped someone would be able to help her with her condition but was told no one could see her unless she signed a new consent form. She asked what was different about this form but they insisted they could not help her unless she signed it. Bri’s vision was so impaired that she could not read the form. She felt she had no choice but to sign it. Once she signed the form, two nasal swabs were taken and a blood test to confirm she did not have Covid, and she was discharged. Bri reached out to the CDC, and her husband filled out a VAERS report, but no one responded. Bri’s health deteriorated and the medical costs were mounting up, with assurances AstraZeneca would reimburse. After weeks of scouring the internet they discovered that IVIG (intravenous immunoglobulin) might be a possible treatment. When they showed this to the doctors and other experts, they were ignored and refused this treatment. The only interaction from AstraZeneca (via a third party) was that Bri was ‘unblinded’ from the trial at her request as she wanted to know if she had received the vaccine, which was later confirmed. The trial sponsor agreed she would not receive a second dose, but they offered no help or support about her continued deteriorating health.
Losing Hope
Exhausted and losing hope, Bri and her husband reached out to the NIH. They were surprised when a specialist neuroimmunologist, Dr Avinthra Nath, Director of the National Institute of Neurological Disorders and Stroke at the NIH, and a researcher at the National Institute of Allergy and Infectious Diseases (NIAID) who worked directly under Dr Anthony Fauci, responded with interest to learn more about Bri’s condition. An appointment was arranged and he seemed very sympathetic and gave the impression he was keen to help. Bri then learned the shocking news that the AstraZeneca vaccine was authorized for use throughout the UK. Publicly the trials were being celebrated as hugely successful, but Bri knew otherwise. She felt suicidal – she was a climber, skier, and dancer who was now a completely non-functioning member of the family barely able to leave her bedroom. Bri’s circle of friends started to diminish. Their savings were also being rapidly depleted because of the skyrocketing medical costs. What about all the assurances on the consent form? What happened to all the promises of the costs being reimbursed? Bri began to lose hope. A trip into nature with her sister that aimed to be a temporary distraction for her resulted in a candid but dark exchange. Her sister asked her to promise her not to kill herself. Bri replied “I cannot promise you that”. The chapter describes how she planned to take her own life, so she was less of a burden to her family. Mercifully, she changed her mind and instead directed her focus on finding and helping others who might be injured and experiencing the same nightmare she was going through.
The Many Injured
It didn’t take long before Bri joined support groups online. After some time she saw a posting from another lady who was also injured in the AstraZeneca trial. Finally, she could talk to someone who knew exactly what she was going through! Within a few days she found another clinical trial participant (Moderna trial) who also experienced similar debilitating reactions. In this patient’s case, she had her left lymph nodes removed as they were so swollen but she became bedridden owing to complications of the surgery. Bri befriended Dr Danice Hertz, a retired gastroenterologist who had developed Mast Cell Activation Syndrome (MCAS) following the Pfizer jab and was suffering ongoing allergic-type reactions including tinnitus, chest pains, and severe nerve damage to her face. Danice increased the number of patients referred to the NIH and Dr Nath for his study. Soon she was inundated with emails from others who had experienced adverse effects from covid vaccines. Sheryl Reutters was harmed by the Moderna jab, experiencing a severe neurological reaction, and soon became a close friend of Bri. Mary Johnson a front-line ER and critical care physician who was injured by the vaccine, and was driven out of her job and confined to her home. Kristi Dobbs and Candace Hayden were also damaged by the vaccine. Bri trusted the NIH to take care of all these injured and would talk to them each week to learn about their stories.
The number of people with vaccine injuries kept mounting and they were all being ignored by doctors and the drug companies. So, the group decided to create a Covid vaccine injury support group on Facebook. However, anyone publicly criticising the vaccines soon became labelled as ‘conspiracy theorists’ and more prominent healthcare workers with dissenting voices became known as the “Disinformation Dozen”. After taking a default position of always giving the benefit of the doubt, Bri was now beginning to realise they had been strung along for months. Her own children were starting to struggle at school, and were developing anxiety, and her son was afraid of leaving the house. Then Bri discovered Maddie, a 12-year-old girl who was completely healthy before receiving the Pfizer vaccine, who was left unable to walk or eat, incontinent, and with seizures and fainting episodes. Bri and the core group of vaccine injured decided enough was enough – they had to go public!
Going Public
They started to post their testimonies and videos about their experiences on the website; some of the stories were harrowing. The videos found their way onto TikTok and were receiving millions of views, as traffic to their website exploded, with over 300,000 views per week. More and more stories poured in from around the world. Facebook seemed to be where many of the support group interactions were residing. By early 2021, although Bri had yet to find anyone else injured by the AstraZeneca jab, in the UK reports of blood clots were flooding in. Slowly news reporters began contacting them and they promised to cover the stories of the vaccine injured along with statements from governments and drug companies. The group reached out to the CDC, FDA, and VAERS but no one received a significant response. How many others were out there with the same relentless pain, alone and with overpowering thoughts? Petitions were submitted to the FDA, CDC, VAERS, and the White House, after one lady who was part of the injured group took her own life. They went to the top, and contacted Dr Peter Marks, Director of the Centre for Biologics Evaluation and Research at the FDA. Word was now spreading among the vaccine-injured community that the NIH had been contacted about hundreds of people with adverse reactions.
Bri and her newfound friends detected a distinct unease among most doctors and nurses whom they engaged with during their multiple visits to the hospital. Bri spent a week at the NIH having multiple tests, which confirmed she had nerve damage in her legs and autonomic nervous system issues. She was diagnosed with “post-vaccine neuropathy”, and recommended IVIG therapy – the very treatment Bri had pleaded with the doctors to try but were ignored. One of Bri’s friend’s, Casey, was an NIH employee who had suffered severe neurological complications as a result of the vaccine. Casey met with Dr Nath, who had previously reassured them that they were documenting and researching all the injuries. When Casey then confronted Dr Nath about his research he flatly denied any such research was underway even though Bri had spent a week at the NIH having tests and being placed on the IVIG protocol. They had no choice but to get political, so they arranged a call with Wisconsin’s Senator Johnson who had been outspoken about the harms caused by the covid vaccines and the censorship, and had been critical of the lockdown policies. Bri was cautious of accepting Senator Johnson’s help because of how he had been portrayed, but on meeting him found he was full of kindness and willing to expose himself to attack on their behalf.
Senator Johnson agreed to hold a press conference. The vaccine injured community felt the politicisation of their health and ‘vaccine stance’ was very draining. One of the support groups that came together with Bri’s group was named “A Wee Sprinkle of Hope” to reflect the culture of compassion. The real objective of the vaccine injured movement was to help people who were suffering. No headline news from the press conference was on the mainstream media, it was mentioned as an aside before going to the next item. Every vaccine injury was not misinformation and their abandonment by the manufacturers was not misinformation. Instead, the news reporters centred the stories not around the vaccine injuries, but around the fact it was led by what they claimed was a crazy, right-wing ‘conspiracy theorist’: Senator Johnston.
Censorship
Then the censorship started. Within 24 hours of the press conference, Facebook began shutting down the support groups. The injured gathered together and then joined with A Wee Sprinkle of Hope. Thousands had joined, and the group was getting larger by the day. Then 5 days after the press conference, and without warning, Facebook shut down the largest Covid vaccine injury support group in the world. Now the injured could not even talk to each other! The social media platform was actively restricting people suffering from extreme physical and emotional pain from communicating with each other. Soon the group decided to develop code words so they could still communicate under new names. Then a mainstream news article exposed one of the code words, and a new group of 30,000 members was shut down too! Warnings appeared beneath people’s posts on their own pages urging viewers to go to Facebook’s Community Guidelines on ‘accurate’ information about vaccines. The warnings also deterred other Facebook users, suggesting they should not interact with ‘repeat offenders’ posting misinformation about vaccines. People’s posts were also being ‘shadowbanned’ or hidden by Facebook algorithms.
Bri was eventually paid a measly $590.20 from AstraZeneca, which coincided with her learning of other injured people in the UK in early 2021. The injured were getting mixed messages from the NIH. On the one hand, they were paying for people’s tests and diagnosis, but then they denied any research was being done. Eventually Dr Nath stopped responding to emails and the FDA stopped communicating with Danice. The NIH then shut down the entire study of the covid vaccine injured and cancelled Bri’s upcoming trip to the NIH. Some of the “Disinformation Dozen” also had their social media accounts shut down or restricted. By now, authors, doctors, patients, activists and even celebrities were being censored. Bri’s husband studied all the clinical trial study reports that had come out, matching the injured participants they knew of to the recorded reactions and found most had been downplayed or even omitted.
It was becoming clear that the institutions they had previously trusted, such as the media, science, pharmaceutical companies, and the government were hiding the truth or outright lying about Covid vaccine adverse reactions. They were being silenced. Free speech was officially over. But another threat was looming: vaccine mandates! The idea of mandating Covid vaccines was terribly distressing to many of the injured. They knew first hand that no one would be there for anyone if they developed a severe reaction. Being fully vaccinated meant you could go to work, visit restaurants or travel without restriction. Those same ‘privileges’ would not be open to the unvaccinated. The coercion, propaganda, bribes and incentives to get the vaccines was extraordinary. Next they were going to jab children.
Eventually, Bri discovered Dr Doshi, an Associate Professor at the University of Maryland with an interest in the drug approval process and an expert in clinical trials, who was also a Senior Editor at the British Medical Journal. Bri and others set up a call with him, and he suggested organising a roundtable discussion in Washington, with senators, health officials and all media. Other pharmaceutical policy experts were brought in, and Bri and her friends started to gather the vaccine injury testimonials. Fundraising was needed to pay for the injured to travel to the event. Some organizations donated together with crowdfunding efforts that raised £37,000 to pay for everyone’s travel and accommodation. The roundtable event at the Senate lasted over 4 hours, which sparked some media interest. The clinical trial company offered a single ‘full and final settlement’ payment to Bri of £1,243.30. This amount did not even cover one-half of the cost of a single IVIG infusion. It seemed the second consent form that Bri had signed (under duress) had significant changes that included all the symptoms she had suffered since the jab, effectively invalidating the previous consent form. After meeting another vaccine victim, Dr Joel Wallskog, Bri and others formed a new group: React19.
Going Global
A Pfizer Whistleblower, Brook Jackson, had been a regional director at one of the clinical trial sites and expressed serious concerns about how the Pfizer Covid vaccine trial was conducted. Despite the stories some mainstream channels promoted about vaccine misinformation and “anti-vaccine propaganda”, clips of the roundtable event were going viral. Many of the vaccine injured, including healthcare professionals and doctors were risking their careers by speaking out against the vaccines. While React19 was originally set up to support the American’s who were injured, it ultimately became a hub for the vaccine injured all over the world. What became clear was that vaccine injury support groups before the covid vaccines faced similar medical gaslighting. The difference this time was never had a vaccine been administered to so many people at the same time – an estimated 5 billion globally – so the global repercussions would be huge. A chat group was initiated for React19, which grew with international leaders, creating a unified effort. Charlet Crichton set up the UK-based UKCVFamily around the same time as React19, as the healthcare system in the UK is different to the USA and more people in the UK had been given the AstraZeneca vaccine. Both groups now collaborated.
It was also becoming clear that as the vaccine injured community grew, the adverse reactions in all the trials had been hidden or misrepresented. Throughout her journey, Bri had started out searching to find the support she needed, but since taking on a leadership role in React19 she was now the support. The end of the book chronicles how finding allies was not as easy as some might assume. There was still no research paper from Dr Nath from the NIH, and when it finally did materialize on a preprint publication, it only published data from 24 patients (despite having over a hundred cases). Furthermore, any links to the adverse events of the vaccine were completely downplayed. When the injured were invited to speak at events by ‘advocates’ on behalf of the injured, often it was more for appearances. Some people in the freedom movement wanted to raise their profile through association with the vaccine injured, but were not directly offering help. Gradually the environment changed so that it was more ‘acceptable’ to discuss vaccine injuries. The film produced by Mark Sharman (former ITV and BSkyB News Executive) “Safe and Effective: A Second Opinion” released on YouTube in October 2022, was removed from the platform within hours following its mention in a Parliamentary debate, despite amassing over a million views!
Find the Science, Find the Money
The immunization surveillance systems such as VAERS, Yellow Card report scheme and others were not working. It is estimated fewer than 1% of adverse reactions are even logged on these sites and so the true nature and scale of such reactions are far greater than captured on these systems. A staggering statistic of the VAERS system is that in the 30 years of vaccine injury, 50,000 reports had been logged. In 2021, there were 750,000 reports of adverse reactions. In other words, the covid vaccine reports in 1 year outnumbered all adverse event reports from the prior 30 years combined. Many of the VAERS reports were not being followed up or being processed properly. Studies submitted to journals that had any data that questioned the vaccines, were often rejected from multiple journals.
Compounding the issue, the 1986 US National Childhood Vaccine Injury Act (NCVIA) removed any financial liability from the manufacturers if any deaths or injuries were caused by vaccines. Moreover, vaccine damage payment schemes, such as the VICP in the USA, were wholly inadequate as proving vaccine was the cause meant hardly any claims were successful and any moderate payments often took years. The PREP (Public Readiness and Emergency Preparedness) Act established in 2005, also granted pharmaceutical companies immunity from federal or state litigation, in circumstances such as a pandemic. So, the companies making the vaccines have no responsibility for damage and little if any incentives to carry out scientific research into any injuries caused. The vaccine injured had to find the “science to follow” rather than “follow the science”. A combination of the “fact-checkers” who demolished any “anti-vaccine” testimonials and that medical reimbursement was non-existent, the out-of-pocket medical expenses the vaccine injured faced often exhausted personal savings to the point that many were refinancing or selling their homes.
Conclusion
The fear-mongering that had contributed to many of those injured by the vaccine to choose to get vaccinated in the first place was now continuing for this marginalized section of society. Those injured by the Covid-vaccine also learned from people who had been injured by past vaccines. The censorship tale was all too familiar, but the React19 community started doing their own research and discovered alternative therapies – be it pharmaceutical, natural, physical, spiritual – and lifestyle adjustments could help with their symptoms. The Covid vaccine rollout left a trail of devastation and damage in its wake. Social cohesion and disconnection also set in with the vaccine-injured ostracised from society. Whether vaccinated or unvaccinated, most people have been affected by the loss of relatives, friendships, relationships, and often life-long careers and financial autonomy. For many, finding support in such dark times has literally been the difference between life and death. We all need healing from the collective trauma of the Covid era, which is still ongoing. By sharing this poignant story of the many Covid-vaccine injured, we hope this will inspire more kindness, connection, compassion, and courage to be open about the truth. That is Worth a Shot!
Worth a Shot?: Secrets of the Clinical Trial Participant Who Inspired a Global Movement―Brianne Dressen’s Story, told by Caroline Pover, was published in November 2024 by Skyhorse Publishing, ISBN: 9781510783461.
All proceeds from the book go to UKCVFamily and React-19, support vaccine -injured in UK and worldwide.
The questions they didn’t ask Marty Makary at his confirmation hearing
By Maryanne Demasi, PhD | March 9, 2025
By all accounts, Marty Makary’s confirmation hearing to lead the FDA went smoothly. As an experienced surgeon at Johns Hopkins with impeccable credentials, he handled questions with ease.
But the real issue was not what the senators asked Makary—it was what they didn’t ask him that was most concerning. They sidestepped the FDA’s recent, glaring failures, leaving critical issues unaddressed.
Much of the hearing consisted of senators pressing Makary for commitments on data he had not yet reviewed, such as mifepristone, vaping, and food additives. They also questioned him about recent FDA job cuts—decisions in which he had no involvement. As a result, there were no substantive revelations.
Makary promised greater transparency at the FDA and vowed to restore public trust. But why did no one press him on the agency’s most egregious missteps?
Speedy drug approvals
One of the most troubling trends at the FDA is its increasing reliance on expedited drug approval pathways.
Today, 65% of new drugs are pushed through these faster routes, despite clear evidence linking them to greater safety risks and a higher likelihood of requiring black box warnings.
The case of Aducanumab, the controversial Alzheimer’s drug, exemplifies this problem. It was approved in 2021 based on surrogate markers rather than meaningful clinical outcomes.
Despite an almost unanimous vote against its approval by the FDA’s advisory committee, the agency proceeded regardless, leading three committee members to resign in protest.
Harvard professor of medicine Aaron Kesselheim called it “probably the worst drug approval decision in recent US history.” Yet not a single senator questioned Makary on how he planned to reform this broken system.
When drugs are rushed through accelerated pathways, companies are required to conduct confirmatory trials to confirm efficacy and safety. But these confirmatory trials are frequently delayed, never completed, or ignored when results are unfavourable.
The FDA rarely penalises companies for non-compliance, allowing unsafe or ineffective drugs to remain on the market. Yet, the senators failed to ask Makary whether he would commit to stricter enforcement of these requirements.
A culture of secrecy
The FDA is the only major drug regulator in the world that receives individual participant data from clinical trials—yet it refuses to routinely release these data for independent scrutiny. If the agency stands by its approvals, why not allow external verification?
During the Covid-19 pandemic, the FDA granted Emergency Use Authorisation (EUA) for Pfizer’s mRNA vaccine trial in just 22 days—an unrealistic timeframe for proper analysis.
Worse still, it failed to conduct trial site inspections, despite knowing billions of doses would be administered, with experts calling the FDA’s oversight “grossly inadequate.”
When whistleblower Brook Jackson provided documented evidence of scientific misconduct in Pfizer’s pivotal clinical trial, the FDA ignored her.
The agency’s own Office of Criminal Investigations, whose job it is to conduct criminal investigations into illegal activities involving FDA-regulated products, turned a blind eye.
How can the agency expect public trust when it turns ignores such evidence?
Adding to its opacity, the FDA attempted to withhold Pfizer’s vaccine trial data for 75 years, only relenting after a legal battle. The Judge in this case said the court order would “pierce the veil of administrative secrecy.”
This should have been a major topic at the hearing. I personally have had an FOIA request pending with the FDA for over three years, and the last time I checked, the agency claimed it was still “in triage.”
Concealing data
The FDA knew early on that the immunity conferred by Pfizer’s mRNA vaccine waned rapidly, yet it withheld these findings for months, during which time millions of people queued to get vaccinated under the assumption they offered lasting protection.
The agency, despite promising transparency early in the pandemic, consistently delayed releasing safety data, preventing doctors and the public from making informed decisions. None of this was brought up by Senators at the hearing.
FDA’s drug promotion
The FDA is a regulatory body, not a marketing agency—yet it actively promoted Covid-19 vaccines, claiming they prevented long Covid despite no supporting evidence.
Former FDA Commissioner Robert Califf falsely stated that the Pfizer’s antiviral Paxlovid could prevent long Covid and even admitted to deliberately “cheerleading” the drug.
Meanwhile, the agency mocked alternative treatments like ivermectin, infamously tweeting: “You are not a horse, you are not a cow, seriously, y’all. Stop it.” It later removed the tweet after being sued. The FDA has no business dictating treatment choices or engaging in pharmaceutical advertising.
The agency also capitulated to political pressure.
The Biden administration pushed for universal Covid-19 booster approval despite weak data, prompting the resignation of two top vaccine officials, Marion Gruber and Phillip Krause. Senators should have demanded to know exactly how Makary would prevent future political interference.
False advertising
Pfizer CEO Albert Bourla publicly claimed that the company’s Covid-19 vaccine prevented transmission, even though the FDA’s own EUA documents stated this was never assessed.
The agency did nothing to correct this false advertising, yet no senator questioned Makary about how he would address misleading pharmaceutical advertising going forward.
Nor did they raise the issue of banning direct-to-consumer advertising—a policy Robert F. Kennedy Jr. has pledged to end.
Unanswered safety questions
Despite the pandemic ending, Moderna and Pfizer vaccines for young children remain under EUA. Why? There is no emergency justifying this continued authorisation.
Moreover, independent researchers have repeatedly raised concerns about excessive residual DNA in Covid-19 mRNA vaccines. The FDA has refused to investigate these findings, even as scientists continue to warn of potential risks.
Now, legal and medical experts have petitioned the FDA, citing regulatory violations and concluding the vaccines were “unlawfully approved.” Why was this not discussed at the hearing?
Beyond vaccines, the FDA has persistently ignored citizen petitions on other drug safety issues.
One example is its failure to update SSRI labelling to include warnings about post-SSRI sexual dysfunction (PSSD), despite overwhelming evidence. This inaction has led to legal action against the agency. Why did no senator demand accountability?
The task ahead
Makary was not responsible for the FDA’s past transgressions, but when confirmed, he inherits an agency in crisis.
To his credit, he was one of the few who publicly challenged flawed Covid policies during the pandemic.
Many hope he will now use his surgical precision to excise the rot within the FDA.
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From the Archives
The Occupied Mentality Syndrome
Saudi Arabia on the American chessboard – Part 2
By B. J. Sabri | American Herald Tribune | April 19, 2016
Since the Korean War, but particularly since the Iranian Revolution of 1979 until today, the United States has been steadily escalating its military presence in the Persian Gulf. Taking advantage of many colossal events of the past 36 years, [1] the hyper-empire has institutionalized its massive presence on land and sea, and expanded its objectives to include the unambiguous physical control of the area, as well as the clear understanding that local Arab governments should abide by them. The pretext is always the same: in “defense” of the national interests and security of the United States. From observing how the United States has been interacting with the governments of the region, and by judging from the size of its expeditionary force, we could reach a basic conclusion. The United States is occupying, de facto, the entire Arabian Peninsula. (Yemen, devastated by Saudi and American jets is yet to be conquered. Oman? Britain returned not as colonial ruler but as a soft occupying power.)
Under this articulation, Saudi Arabia, Qatar, Kuwait, and the United Arab Emirates are virtually occupied countries. If we compare this type of occupation to the mandate and protectorate regimes of the past, the results might be identical—the nations affected by it lose sovereignty. When Arab governments comply with the objectives of a foreign power that station military forces on their national milieu, then that power controls them in multiple ways including how they react to policy deliberations and what decisions they intend to take on specific issues. A good method to verify the concept of effective occupation is this: take notice of what the United States says and wants, and then compare it to what the gulf rulers do in response. (I shall discuss this detail at some point in the upcoming parts.)
If the presence of US forces or other means of political pressure are a factor in Saudi Arabia’s interventionist Arab wars, then we need to debate this issue. However, from the history of resistance to colonialism, we learnt: if a powerful state imposes its order on a nation by military means or other forms of coercion, and if this nation does not resist that imposition, then a mental subordination to the powerful state will ensue. This is especially true in the case of Saudi Arabia. One single event, 9/11, has transformed it from a US “ally” into an instant political hostage of the American Empire. … continue
Blog Roll
Aletho News- Britain’s Lebanon surveillance network: A digital map for war
- Bahrain faces scrutiny for opposition crackdown after detainee killed
- Hegseth’s Pentagon Purge Designed to Prevent a Mutiny: Karen Kwiatkowski
- Greek shipping firms secretly transporting oil, weapons to Israel
- UN vote on Hormuz force delayed as Iran issues warning
- Trump and the debris of Iran war
- IRGC hits US tech giant Oracle’s data center, computing site in UAE over new assassinations
- Bombing Iran Back Into the Stone Age /Lt Col Daniel Davis & Jim Jatras
- UAE rejects report claiming it is ready to join war on Iran to reopen Hormuz
- A New Resistance Front: How Does Syria Factor into the Regional War?
- If Americans Knew
- Israel-US kill negotiators, destroy civilian structures, but Iran’s military capabilities still largely intact – Daily Update
- ‘War crime’: Global condemnation as Israeli ministers celebrate death penalty law targeting Palestinian prisoners
- 7 Ways Israel Is Turning Lebanon Into Gaza
- World’s Leading Football Bodies Under Fire Over Israel Policies
- Experts warn of possible use of nukes against Iran
- Israeli invasion of Lebanon could be worse than 1982, warn European officials
- Passover: Liberation and collective punishment
- Trump says the quiet part out loud: (Israel’s) war on Iran > Americans’ health – Daily Update
- Gaza families reunite years after babies evacuated amid Israel’s war
- International Rescue Committee warns Gaza’s children face grave protection risks
- No Tricks Zone
- Low Intensity Tornado Wrecks Major Solar Farm, Creating A Potential Toxic Dump
- New Study Finds Warming Saves Lives…Cold Temperatures 12 Times More Deadly Than Excess Heat
- German Science Blog Accuses PIK Climate Institute Of Hallucinating Climate Tipping Points
- Devastating Assessment Of Comirnaty Vaccine By Former Senior Pfizer Europe Toxicologist
- New Study: CO2 Is ‘Effectively Negligible’ As An Explanatory Climate Change Factor Since 2000
- Former Pfizer Toxicologist Dr. Helmut Sterz Tells Bundestag Hearing Pfizer Vaccine Should Have Never Been Approved
- Energy Expert: Germany’s Nuclear Phaseout Was A “500 Billion Euro Mistake”
- New Research: South Australia’s Mid-Holocene Sea Surface Temperatures Were 4°C Warmer Than Today
- Storing Green Energy To Last Germany 10 Days Would Require A 60-Million Tonne Battery
- New Studies: UK Sea Levels Were 4 Meters Higher Than Today During The Mid-Holocene
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