EU state’s PM issues Covid vaccine warning
RT | April 23, 2025
Slovak Prime Minister Robert Fico has called for an immediate halt to government purchases of Covid-19 vaccines, citing a recent report that found mRNA jabs contain extremely high levels of DNA and substances that were not disclosed by the manufacturer.
Bratislava initially considered outright banning the vaccines when a commission led by Peter Kotlar, an orthopedic doctor and member of the ruling Slovak National Party, published a report in October claiming that the mRNA jabs alter human DNA, have been inadequately tested, and therefore should not be administered until they are proven safe.
Kotlar has also described the Covid-19 pandemic as an “act of bioterrorism” and a “fabricated operation,” and has accused vaccine manufacturers Moderna and Pfizer of turning vaccinated people into “genetically modified organisms.”
His report, however, was met with significant pushback from opposition parties, as well as former Slovak Health Minister Zuzana Dolinkova, who cast doubt on Kotlar’s qualifications with regard to the subject. She subsequently resigned from her position that same month, citing government backing for an anti-vaxxer and insufficient prioritization of health care.
In a post on X on Wednesday, Fico published a video in which he stated that ignoring the findings of the Kotlar-led commission on the quality of the Covid-19 vaccines would be “extremely irresponsible.”
Fico noted that in March, he instructed the Health Ministry to establish a working group to address the findings of the expert report submitted by Kotlar, but acknowledged that this may not produce results quickly enough.
The prime minister said he would try to resolve the issue in “a reasonable timeframe” and propose during an upcoming government meeting that apart from the working group, the Slovak Academy of Sciences (SAV) would also be asked to conduct a quantitative analysis of the presence of DNA and other substances in the vaccines.
Fico also suggested that the government should inform the population about the “serious findings” regarding the jabs. “Although Covid-19 vaccination rates are extremely low, people deserve such a warning,” he said.
The prime minister went on to propose that Slovakia suspend the purchase of additional vaccines from the unspecified manufacturer, which it is obligated to do under a contract signed by the former government in 2023.
Bratislava is still expected to procure nearly 300,000 doses of Covid-19 vaccines in 2025 and 2026, which is estimated to cost around $6.6 million, Fico said, stressing that “until the results of the additional quantitative analysis are delivered, the government should not procure further vaccines from this manufacturer or pay for them.”
How Your Family Doc Became a Vaccine & Drug Enforcement Agent
The rise of pharmaceutical compliance officers in primary care
By Dr. Roger McFillin | Radically Genuine | Apr 3, 2025
Remember when your family doctor was actually your doctor? That quaint historical period when physicians made independent medical judgments instead of reading from pharmaceutical scripts? When they looked at you as a unique human being rather than a collection of compliance metrics needing correction?
Those days are fucking gone.
Today’s primary care physician is something entirely different—a pharmaceutical compliance officer with a prescription pad, a corporate protocol to follow, and overlords tracking their every move. They’ve transitioned from healers to hustlers, from medical professionals to medication pushers, from trusted advisors to glorified drug dealers with better parking.
I recently had a conversation with a pediatrician that exposed the naked truth of modern medicine. He confessed to me—with a mixture of resignation and discomfort—that he was “mandated” to administer the PHQ-9A (depression screening) to every adolescent, and if they scored above a certain threshold, he MUST offer an SSRI antidepressant.
“What if the teen is just going through a breakup or having normal adolescent mood swings?” I asked.
He shrugged helplessly. “Doesn’t matter. If they hit the number on the screening, protocol says I have to offer medication.”
“But you know these drugs more than double the risk of suicidal events in teenagers,” I pressed. “The black box warning exists for a reason.”
His response chilled me: “If something happened to the teen and I didn’t follow protocol—if I didn’t offer the medication—I could be held liable. My hands are tied.”
And there it was—the perfect analogy hiding in plain sight. This highly educated physician with years of training wasn’t making independent medical decisions. He was a street-level drug dealer who feared what would happen if he didn’t move enough product for his overlords. The corner pusher fears his supplier’s enforcers; the modern physician fears “liability” and “protocol violations.” Different vocabulary, identical dynamic.
Primary care has been transformed from a healing profession into a pharmaceutical distribution network with doctors serving as glorified vending machines in white coats. They’re the street-level dealers in the medical-industrial complex, pushing products with the ruthless efficiency of a cartel but with better branding and tax benefits.
The parallels between how primary care physicians push psychiatric drugs and vaccines are so perfect they deserve admiration from a purely marketing perspective. It’s the same hustle with different packaging—one comes in pill form, the other in a needle, but the script is identical.
The SSRI Hustle
God forbid you or a family member is unfortunate enough to schedule a routine checkup during a particularly bad week. Walk into that sterile exam room while grieving a loss, stressing about work, or just experiencing one of life’s inevitable rough patches, and you’ll walk out with a ‘mild to moderate depression’ diagnosis faster than you can say ‘pharmaceutical kickback.
Within minutes, you’re handed a questionnaire with loaded questions like: “Feeling bad about yourself or that you have let yourself or your family down or that you are a failure?” (You just watched your ex’s vacation photos on Instagram while eating ice cream for dinner in your unwashed sweatpants, so… is this a trick question?)
Answer honestly, and congratulations! You’ve just self-diagnosed with “mild to moderate depression.”
You mean what we used to call sad?
Your doctor spends approximately 90 seconds validating this with probing questions like “And how long have you felt this way?” before reaching for the prescription pad.
“I think Lexapro would really help take the edge off,” they say with practiced compassion, already halfway through writing the prescription. “It will balance your brain chemicals.”
But it’s when you express hesitation that the real sales pitch begins—fear. This is where doctors transform into pharmaceutical fear merchants:
“You know, untreated depression can be very serious,” they warn ominously. “It can worsen over time. It can affect your relationships, your work, your entire life. Depression is a serious medical condition—in fact, it’s the leading cause of disability worldwide.”
The implication hangs in the air like a guillotine blade: refuse this medication, and you’re gambling with your life. They may even pull out the suicide card: “Depression can lead to suicidal thoughts if left untreated.” The cosmic irony of using suicide as a scare tactic to prescribe drugs with black box warnings about increasing suicidal ideation seems lost on them.
For teenagers, the fear tactics are directed at parents. “You don’t want to take chances with your child’s mental health, do you?” they ask, making parents feel like monsters for questioning whether their teen’s temporary sadness requires a medication that doubles their risk of suicidal events.
This isn’t medical counseling. It’s emotional manipulation through fear—the same tactic used by predatory salespeople in every industry. “Better safe than sorry” becomes the catch-all dismissal of legitimate concerns about medications with profound risks and modest benefits.
What they don’t mention:
The “chemical imbalance” theory of depression was thoroughly debunked years ago, joining phrenology and bloodletting in medicine’s hall of shame. SSRIs have never proven to be clinically meaningful beyond placebo.
Complying with their prescription pad evangelism could result in permanent sexual dysfunction—as in forever, as in the rest of your life.
Withdrawal can be so brutal and protracted that patients often mistake it for “proof they need the medication” rather than recognizing it as drug dependence.
And here’s the cosmic punchline: in the 4-6 weeks it takes for these medications to supposedly “work,” most situational “depression” would have naturally improved anyway.
When that happens?
The doctor smugly nods and thinks, “See, the drugs I prescribed fixed them!” Never mind that time, human resilience, and your own natural healing did all the heavy lifting while the medication was just along for the expensive, side-effect-laden ride.
The Vaccine Hustle
Now let’s watch the vaccine version of the same performance:
You visit for a completely unrelated issue—perhaps a sprained ankle or a skin rash. Before addressing your actual concern, your doctor casually mentions, “I see you haven’t had your COVID or flu shot this year.”
The framing is already perfect—you’re “behind” on something, implying non-compliance with an expected standard. Your medical record has been flagged for a deficiency that needs correcting, like a car overdue for an oil change.
Express hesitation, and witness the same script unfold: “These vaccines are very safe and effective. Side effects are usually just a sore arm or mild fatigue for a day.” (Myocarditis? Menstrual disruptions? Neurological issues, complete hijacking of my immune system? Those are so rare they’re not worth mentioning, apparently.)
Ask about actual risk reduction—like how the flu vaccine isn’t efficacious and doesn’t prevent you from contracting the flu—and watch them shift uncomfortably.
Why would I even risk Guillain–Barré syndrome for this Doc? I am healthy and not that scared of the flu? Regardless of the low risk of complications… why even take that risk?
Dare to question whether a perfectly healthy 17-year-old who already recovered from COVID needs an experimental mRNA intervention that doesn’t prevent transmission—and has now been shown to actually INCREASE susceptibility to infection over time, not to mention the myocarditis risks, menstrual disruptions, and other “rare” side effects conveniently minimized in the sales pitch—and watch their face transform before your eyes.
First comes the reflexive smile-cramp, that frozen rictus of medical authority being questioned. Then the slightly widened eyes as they process your heretical departure from the script. Finally, that subtle hardening around the jaw as they shift from healthcare provider to pharmaceutical enforcement officer.
It’s like watching someone toggle between “friendly neighborhood doctor” and “COVID compliance commissar” in real-time, all because you had the audacity to weigh risks against benefits for your own child.
But regardless of whether they’re pushing pills or jabs, we see the identical sales pitch every time—a masterclass in pharmaceutical propaganda. They dramatically exaggerate even the most microscopic potential benefits while feverishly minimizing, dismissing, or flat-out denying any risks with the practiced ease of a seasoned con artist. Watch them transform a 1% absolute risk reduction into ‘90% effective!’ while simultaneously downgrading ‘known serious adverse events’ to ‘extremely rare side effects that aren’t worth discussing.’ It’s as if they’ve never read a single page of the actual scientific literature on the subject.
Spoiler alert: they haven’t.
Most haven’t ventured beyond industry-funded continuing education modules and pharmaceutical company press releases since medical school. The journal articles gathering dust in their mental libraries are pharmaceutical marketing materials disguised as science, cherry-picked datapoints that support the sales pitch while burying inconvenient truths beneath statistical sleight-of-hand. Their ‘expertise’ is just regurgitated talking points from the last drug rep who bought them lunch.
Your Doctor Now Reports to Corporate Masters
The corporate takeover of medicine didn’t happen overnight—it was systematically engineered, with the Affordable Care Act delivering the knockout blow to independent practice. While marketed as expanding “healthcare access,” Obamacare buried small practices under an avalanche of regulatory requirements, EHR mandates, and compliance costs that made independence financially impossible.
Before the ACA, over half of physicians owned their practices; today, that number has plummeted below 30%. The rest were forced to sell out to corporate healthcare systems where their compensation and job security now depend on following protocols—including pharmaceutical prescribing patterns and vaccination targets—established by administrators who’ve never touched a stethoscope.
Your family doctor didn’t willingly transform into a pharmaceutical enforcement agent; they were legislated into compliance, their medical autonomy sacrificed on the altar of corporatized healthcare while maintaining the illusion of independent judgment.
Primary care healthcare professionals are now following protocol with the unquestioning obedience of a first-grader desperate for a gold star sticker. It makes you wonder how many who flock to primary care medicine were those perfect little rule-followers their entire lives—the ones who color-coded their highlighters in medical school, memorized every algorithm without asking why, and spent their formative years as professional hoop-jumpers. The straight-A students who never risked a teacher’s disapproval, never colored outside the lines, never questioned authority figures even when those figures were demonstrably wrong. The ones whose entire identity became wrapped up in following instructions perfectly to achieve the next credential, the next white coat, the next professional validation.
Is it any surprise that these same personalities now cling to protocols like religious scripture, unable to exercise independent clinical judgment when a human being’s complex situation doesn’t fit neatly into their laminated flowchart? Critical thinking requires the courage to ask uncomfortable questions—a skill that was systematically extinguished in these pristine academic specimens long before they wrote their first prescription
Next time your primary care physician tries to prescribe you an SSRI for being human or jab you with the latest pharmaceutical subscription service, remember: you’re not a patient—you’re a customer they’re trying to upsell.
Their script may be polished, but your bullshit detector doesn’t need a medical degree to function properly. Ask the uncomfortable questions they’re afraid to answer. Demand actual data, not rehearsed talking points. Walk out if necessary.
Find the rare physicians who still practice medicine instead of pharmaceutical compliance. And if your doctor looks horrified when you decline their latest pill or shot, smile sweetly and say, “Don’t worry, I’ll make sure my chart notes that YOU failed to convince ME—not the other way around.”
After all, the most rebellious act in modern healthcare isn’t refusing treatment—it’s insisting on informed consent in a system designed to eliminate it.
Your body, your mind, your choice. No prescription required.
RESIST
Pregnant women deserve better than “trust us” science
A major study has been used to reassure pregnant women that Covid-19 vaccines are safe. But the data behind the claim are fatally flawed.
By Maryanne Demasi, PhD | April 12, 2025
In medicine, few assurances carry more emotional weight—or greater responsibility—than the claim that something is “safe during pregnancy.”
Pregnant women are justifiably cautious about what they expose themselves to during this vulnerable time, and history has given them every reason to be.
The thalidomide disaster, diethylstilboestrol (DES), and other cautionary tales have shown what can happen when scientific rigour is sidelined in favour of commercial interests.
So, when a new study published in Pediatrics – the official journal of the American Academy of Pediatrics – claimed that Covid-19 vaccination in early pregnancy was safe, it came with an air of authority and reassurance.
News headlines followed suit, and public health recommendations continued to promote the vaccine’s safety in pregnancy.
But scratch the surface of this study, and something starts to unravel.
Not only are the data unverifiable and privately sourced, but the study contains a fatal flaw that renders its conclusions virtually meaningless.
The fatal flaw
The study analyzed 78,052 pregnancies that ended in a live birth—but left out 20,341 pregnancies that ended in miscarriage or other non-live outcomes.
That’s not a minor oversight.
The very purpose of studying vaccine safety in pregnancy is to assess whether exposure in utero leads to adverse outcomes—like miscarriage, birth defects, or foetal death. Yet one-fifth of the pregnancies were excluded from the analysis, removing exactly the kind of outcomes the study was supposed to detect.
This introduces what’s known as live-birth bias—a selection bias that arises when research includes only live births, disregarding the possibility that harmful effects may have caused some pregnancies to end prematurely.
Put plainly, if you only study babies who made it to birth, you’re ignoring the ones who didn’t—and any harm that may have played a role.
Even the study’s authors acknowledge this limitation, conceding that the exclusion “could lead to an underestimation of identified outcomes.” Still, they move forward to conclude there’s no association between the vaccine and birth defects.
Omitting over 20,000 pregnancies isn’t just a technicality – it’s a fatal flaw.
If even a small fraction of those pregnancies ended in miscarriage or birth defects linked to vaccination, the entire outcome could tip the other way.
Commercial data with no accountability
Then there’s the source of the data itself—a point entirely overlooked.
Rather than using clinical records from hospitals or national birth registries, the study relied entirely on a commercial database from Merative® MarketScan® Research Databases.
These databases are vast, aggregating de-identified insurance claims, prescriptions, lab results, and hospital records from more than 263 million Americans. But they are also privately owned, and their inner workings are entirely opaque.
Researchers using MarketScan data cannot verify whether the patients are real or theoretical, whether records have been altered, or how the data has been cleaned or processed before delivery.
In essence, they are working with a black box, one that comes with no guarantee of integrity.
Experts have already noted that the data from this unverified source shows signs of being unreliable.
The authors ran 93 separate statistical tests to look for differences in outcomes like birth defects. By chance alone, you’d expect a handful to be statistically significant. But none were.
The probability of that happening randomly is just 0.8%—a sign that the dataset may have been fabricated, or that its integrity is in question.
When two of the study authors – Dr Stacey Rowe and Dr Annette Regan – were asked if they had verified the authenticity of the MarketScan database—that is, if they could confirm these were ‘real’ patient data—they did not respond.
L: Dr Stacey Rowe, R: Dr Annette Regan
This isn’t a hypothetical problem.
The medical literature has already been rocked by the Surgisphere scandal, where fraudulent hospital datasets were used to produce papers in The Lancet and The New England Journal of Medicine.
Those papers were eventually retracted, but only after independent researchers demanded to see the raw data and were denied – the data were likely fabricated.
Reassurance without evidence
Despite these glaring problems, the study’s conclusions are being used to reassure pregnant women.
In Australia, for example, the government’s official guidance recommends Covid-19 vaccination in pregnancy, stating that the “recommendations for pregnant women are the same as the general population.”
This, despite the fact that pregnant women were excluded from the pivotal clinical trials and no randomised studies have ever been completed to assess the vaccine’s safety in early-pregnancy.
The result is a landscape where pregnant women are asked to make a “shared decision” with their doctors—based on scientific literature that’s increasingly built on unverifiable data, flawed assumptions, and little to no independent scrutiny.
We are drifting into a new era where conclusions are based on data that sit behind corporate firewalls. An era where trust is expected, but no longer earned.
The Pediatrics study is a case in point.
It carries the imprimatur of authority, published in the flagship journal of the American Academy of Pediatrics. But, in reality, the analysis was based on commercial datasets that cannot be independently verified, and a methodology that systematically excludes the very outcomes it was supposed to assess.
This isn’t just bad science—it’s misleading by design.
And when it comes to pregnancy, where the stakes are literally life and death, that kind of scientific chicanery is a betrayal.
Pregnant women deserve better than a “trust us” approach to medicine.
They need full access to the data, honest communication about uncertainties, and above all, respect for their right to make informed decisions based on real evidence, not selective reporting.
Until that happens, we should remain sceptical of any study that asks us to believe in the evidence without seeing it.
Did Head of CDC Vaccine Safety Office Delete COVID Vaccine Injury Records?
By Michael Nevradakis, Ph.D. | The Defender | April 11, 2025
A key official at the Centers for Disease Control and Prevention (CDC) responsible for monitoring vaccine safety and reports of vaccine injuries may have mishandled or deleted official records subpoenaed by Congress, Sen. Ron Johnson (R-Wis.) alleged earlier this week. The New York Post first reported the story on Thursday.
Dr. Tom Shimabukuro, director of the CDC Immunization Safety Office, maintained the records in question. Shimabukuro previously authored a key paper and participated in public messaging claiming the COVID-19 vaccines were safe and effective for pregnant women.
Johnson, chairman of the U.S. Senate Permanent Subcommittee on Investigations, requested the records in a subpoena sent in January to the U.S. Department of Health and Human Services (HHS). The subpoena pertained to an investigation into internal COVID-19 vaccine safety communications.
According to the New York Post, the subpoena led HHS to discover “potential discrepancies” in the emails maintained by Shimabukuro.
“HHS officials recently informed me that Dr. Shimabukuro’s records remain lost and, potentially, removed from HHS’s email system altogether,” Johnson wrote in a letter he sent earlier this week to U.S. Attorney General Pam Bondi, FBI Director Kash Patel and HHS Principal Deputy Inspector General Juliet Hodgkins.
Johnson called Shimabukuro’s possible mishandling of his official records “highly concerning.”
Journalist Paul D. Thacker, a former U.S. Senate investigator, said, “Every American should be concerned about government scientists deleting or hiding federal information to shape a political agenda. That information belongs to the taxpayers.”
Nebraska chiropractor Ben Tapper, whose questioning of the COVID-19 vaccines led the Center for Countering Digital Hate to add him in 2021 to its “Disinformation Dozen” list of the “leading online anti-vaxxers,” said he was “not surprised” by Johnson’s allegations.
“For years, I’ve seen patterns like this before regarding vaccine safety data. The public health establishment often prioritizes profits over people and continuously seems to protect the lies over the truth. The idea that critical records might vanish — whether through negligence or intent — fits a familiar playbook,” Tapper said.
California attorney Rick Jaffe said Johnson’s allegations are “troubling, but not surprising, given longstanding concerns about transparency at the CDC.”
In response to a Freedom of Information Act (FOIA) request last year, the CDC told Children’s Health Defense the agency has no records of certain internal email communications relating to the agency’s follow-up investigation of safety signals associated with COVID-19 vaccines.
HHS, CDC and Johnson’s office did not respond to requests for comment.
Missing records ‘could contain unfiltered insights’ into vaccine adverse events
Citing an unnamed aide from Johnson’s office, the New York Post said it is unclear which specific records are missing. But according to Johnson’s letter, Shimabukuro’s role included “monitoring adverse events relating to the COVID-19 vaccines.”
Tapper said Shimabukuro may have been “handling sensitive data on adverse events linked to the COVID-19 vaccines,” including data from the U.S. government-run Vaccine Adverse Event Reporting System (VAERS) and the V-safe database, as well as studies, raw data and internal communications on vaccine-related safety signals.
Tapper said:
“These records could contain unfiltered insights into side effects that were downplayed or unresolved during the pandemic. For example, I’ve seen cases in my practice where patients developed symptoms like persistent fatigue or heart palpitations post-vaccination, yet struggled to get clear answers from authorities.
“Missing records could hide similar signals, undermining efforts to validate patient experiences or refine vaccine protocols.”
Internal medicine physician Dr. Clayton J. Baker said, “Such records would likely be very damning to all CDC officials who perpetuated the false ‘safe and effective’ narrative about the COVID-19 vaccines from 2021 until the present.”
“Given how damning any evidence of ignored or falsified safety signals would be, I think it is highly likely that Biden-era officials might try to destroy such records if they could. Better to be accused of destruction of federal records than to be charged as an accessory to mass negligent homicide,” Baker said.
In an April 2023 presentation to the CDC Advisory Committee on Immunization Practices, Shimabukuro claimed that surveillance conducted by international regulatory and public health partners “has not detected a safety concern for ischemic stroke following bivalent COVID-19 mRNA booster vaccination.”
Yet, a peer-reviewed study published in November 2024 found that mRNA COVID-19 vaccines pose a 112,000% greater risk of brain clots and strokes than flu vaccines, and a 20,700% greater risk of those symptoms than all other vaccines combined. The study called for a global moratorium on mRNA vaccines.
In 2021, Shimabukuro was the lead author of a study in The New England Journal of Medicine (NEJM) on the safety of COVID-19 vaccines for pregnant women. The study concluded that “preliminary findings did not show obvious safety signals among pregnant persons who received mRNA Covid-19 vaccines.”
However, a peer-reviewed study published in 2022 showed that the authors of the NEJM study performed a “statistical sleight-of-hand” that substantially lowered the miscarriage rate in pregnant women, presenting it as 12.6% instead of 82%.
In a Substack post, epidemiologist Nicolas Hulscher said Shimabukuro’s “potential involvement in the deliberate manipulation of critical safety data on COVID-19 mRNA injections during pregnancy carries grave implications — resulting in immeasurable harm to mothers and their unborn children worldwide.”
Shimabukuro ‘may have violated multiple federal laws’
According to a press release from Johnson’s office, Shimabukuro’s actions, if proven to have occurred, “may have violated multiple federal laws.”
Those laws include the Federal Records Act, which requires federal employees to preserve materials “made or received by a Federal agency under Federal law or in connection with the transaction of public business,” the New York Post reported.
Johnson wrote that the destruction of records subpoenaed by Congress may also be “grounds for contempt of Congress,” which, according to the New York Post, is punishable by up to a six-figure fine and 12 months in prison.
Jaffe said Shimabukuro may also face other penalties. He said:
“Under federal law, he could be charged with obstruction of justice or destruction of official records — risking fines, restitution and up to 20 years in prison. His federal pension could also be garnished to satisfy any judgment against him.
“Beyond criminal penalties, he faces permanent disqualification from federal service and career-ending reputational harm.”
In addition, if records relating to vaccine-injured people are missing or destroyed, impairing their legal cases, “courts could impose evidentiary sanctions or presume the destroyed records were unfavorable to the government,” Jaffe said.
Johnson’s letter also referred to Dr. David Morens, an employee of the National Institute of Allergy and Infectious Diseases who was a close aide of the agency’s former director, Dr. Anthony Fauci. Morens allegedly deleted emails and instructed colleagues to contact him at a personal email account to sidestep FOIA rules.
In his letter, Johnson accused HHS of a “lack of transparency” and failure to investigate the allegations against Morens.
“I had always suspected that Dr. Morens was not the sole evader of federal record-keeping requirements at HHS,” Johnson wrote. “The extent to which HHS officials systemically mishandled, deleted, or destroyed their communications, data, and other information relating to the COVID-19 pandemic and the vaccines must be thoroughly investigated.”
Johnson’s letter asks the FBI, the U.S. Department of Justice and the HHS Inspector General’s Office to investigate the matter, including whether records were intentionally destroyed to “avoid or subvert Congressional oversight or the Freedom of Information Act.”
The letter builds on Johnson’s efforts to investigate COVID-19 vaccine safety.
Earlier this week, Johnson sent letters to the heads of four COVID-19 vaccine manufacturers, requesting they turn over records related to the development and safety of the COVID-19 vaccines and their communications with Big Tech platforms about vaccine-related adverse events.
In November 2024, Johnson wrote a letter to HHS, CDC and FDA, asking the agencies to “preserve all records referring or relating to the development, safety, and efficacy of the COVID-19 vaccines.”
In an October 2023 letter to the then-heads of CDC and FDA, Johnson accused the agencies of an “appalling” lack of transparency regarding COVID-19 vaccine safety signals, depriving Americans of “the benefit of informed consent.”
During the Biden administration, Johnson wrote over 70 letters to HHS officials and its health agencies requesting information on COVID-19 vaccine adverse events and related communications, according to a Jan. 29 press release.
Last year, Johnson hosted a congressional roundtable to discuss the risks of COVID-19 vaccines. Medical experts, political figures, journalists and whistleblowers were among the participants.
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.
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
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China and India have ‘low intellectual potential’ – top Zelensky aide
RT | September 13, 2023
The people leading India and China lack the ability to predict the long-term consequences of their policies, a senior aide to Ukrainian President Vladimir Zelensky has claimed.
Mikhail Podoliak pointed to what he called “the problem of the modern world,” singling out India and China, in an interview with Ukrainian media on Tuesday.
“The problem with these countries is that they do not analyze the consequences of their own moves. These countries, unfortunately, have low intellectual potential,” he said.
Podoliak suggested that even though India has a lunar exploration program, it “does not mean that this nation understands what the modern world precisely is.”
The dismissive remarks were in the context of Beijing and New Delhi’s refusal to support Kiev in its conflict with Moscow. Podoliak complained that India, China and Türkiye were “profiting” from the war by maintaining trade with Russia.
“Technically, it is in their national interests,” he acknowledged, before presenting his view of what would benefit China in the long-run.
“China should be interested in Russia disappearing, because it is an archaic nation that drags China into unnecessary conflicts,” he claimed. … continue
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- Rights Group Warns Israel’s Genocide Isn’t Over in Gaza
- No Tricks Zone
- New Study Finds A Higher Rate Of Global Warming From 1899-1940 Than From 1983-2024
- Meteorologist Dr. Ryan Maue Warns “Germany Won’t Make It” If Winter Turns Severe
- Merry Christmas Everybody!
- Two More New Studies Show The Southern Ocean And Antarctica Were Warmer In The 1970s
- Der Spiegel Caught Making Up Reports About Conservative America (Again)
- New Study: 8000 Years Ago Relative Sea Level Was 30 Meters Higher Than Today Across East Antarctica
- The Wind Energy Paradox: “Why More Wind Turbines Don’t Always Mean More Power”
- New Study Reopens Questions About Our Ability To Meaningfully Assess Global Mean Temperature
- Dialing Back The Panic: German Physics Prof Sees No Evidence Of Climate Tipping Points!
- Astrophysicist Dr. Willie Soon Challenges The Climate Consensus … It’s The Sun, Not CO2
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