Secret recordings with ousted FDA vaccines chief suggest disinterest in documenting vax injury

The Food and Drug Administration’s top vaccine official until late-March met online several times with a COVID-19 vaccine injury group’s leader, who, opposing the vaccines in part, begged him to no avail to take severe adverse events such as paresthesia as a precursor to neuropathy seriously and to urge doctors to treat them as such rather than write them off as “anxiety,” secret recordings suggest.

The Informed Consent Action Network (ICAN) released the videos, compiled on The Real Peter Marks website, with other documentary evidence from Marks’ leadership of the COVID response starting with Operation Warp Speed, at the National Press Club in Washington on Tuesday.

They also include a virtual meeting between San Francisco intensive care unit doctor Patricia Lee, Marks and other FDA officials, who asked no questions after Lee said a patient’s severe complications from vaccination at 22 weeks’ pregnancy and related death prompted a “nervous breakdown” among nurses on her shift, requiring a psychiatrist’s overnight visit.

ICAN CEO Del Bigtree shared pieces of Lee’s Oct. 22, 2021, conversation with FDA officials, who allegedly ignored her pleas for vaccine-injured patients until she brought “legal pressure,” on his show two weeks earlier with ICAN lawyer Aaron Siri and REACT19 founder Brianne Dressen, whose neurological injuries from the AstraZeneca vaccine trial were confirmed by the NIH

Organized as an animated vertical timeline that loads as it scrolls, the Marks website loaded slowly during Just the News’ review Wednesday. “They are receiving a ton of traffic and working on it,” a spokesperson said in the early afternoon.

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Neurodiversity Is A Strawman

A dear friend had a beautiful, healthy, engaged baby boy. After his first round of childhood vaccinations he went blind, non-verbal, started head banging, having seizures, lost all engagement, and fell into the abyss of autism. Today that child is 40. He is incontinent, cannot speak or feed himself, and is totally dependent upon his father to survive. 

Another friend had a son and a daughter. The daughter, following her first round of childhood shots, experienced almost exactly the same scenario described above, minus the blindness. At the time my friend did not connect the dots and when it came time for his son to be vaccinated, the child began to seize. In the room, my friend put it together and stopped the rest of the shots. Today, his son is only mildly autistic while his daughter, at 26, is non-verbal, incontinent, and often uncontrollable. Since the son is only mildly autistic, I suppose we shouldn’t look into the cause of his issues? It’s a gift, right? 

A mother (a client in one of the many tragic cases) had a teenage daughter who, after a round of the Gardasil vaccine, suffered a seizure and went into a coma. The young girl had been captain of her volleyball team, top of her class, poised for a full and happy life. Today, at nearly 20, she lives in total darkness because she has seizures every 30 seconds – cannot have any light. The neurodegeneration is unquantifiable. She cannot read or watch TV, let alone go on her first date, go to prom…experience the life she should have and would have. 

Another friend had a perfect, beautiful young daughter who was exceeding all of her milestones. After her second round of jabs, she locked in, stopped talking or making eye contact, developed a severe learning disability, and is still struggling today, at 6. 

She, too, will never experience the “normal” milestones we all would like to see for our children. 

Those stories, anecdotal though they may be, are the tip of the iceberg. 

I could share thousands, each one worse than the next, that would make most people sit in a room and cry forever.

The media machinery has conflated mild spectrum disorder with what I just described above specifically so that people will have the reaction they are having right now. This is normalization of extremes by conflating them with non-extremes so that it’s a step-by-step incremental (and coordinated) attack on those who would expose the root cause of the terrible suffering experienced by so many.

It’s executed so that people like RFK, Jr. are hobbled from doing their job. 

How does questioning the environmental harms and risk factors for autism and/or neurodegenerative disorders threaten or even conflict with the idea of autism as neurodiversity? Spoiler alert: it doesn’t. 

No other disease has people normalizing a spectrum (no pun intended) of symptoms ranging from terrible to non-debilitating in order to argue that it’s actually great. We don’t say there’s a spectrum of neurodegenerative disorder from paralysis to neuropathy and there are benefits to neuropathy therefore neurodegeneration is great. This is normalization at its best. 

Suddenly everyone’s kid is Rain Man. Suddenly everyone is “on the spectrum.” Ergo, it’s normal. Being a little bit weird is beautiful and normal and we are all a little bit weird so that’s not a disorder. This is a psyop and everyone is falling for it. No one is saying there is something wrong with neurodiversity or that we shouldn’t also be looking into that. But when it comes to discovering the contributing factors and co-factors, the environmental insults, and the increase itself in autism to date, we’re not talking about that. We are talking about, and have only ever been talking about, the above scenarios. 

The tactics to muzzle debate and halt real investigation are duplicated across all levels. (This should all sound eerily familiar when we recall the conflation, normalization, media machinations, and strawmen to emotionally activate opposition tactics used during Covid.)

It should be a red flag and alarm every American that pharmaceutical companies have no liability for vaccines and that they have managed to increase the pediatric schedule from 3 to 72 in one generation, and it should alarm every parent to learn that HHS itself draws a hard line in 1989 for autism – the year when vaccine formulation was changed to allow for combinations because in 1986 the vaccine space became a financial free-for-all. 

Unfortunately, the media is adept at keeping dots that should be connected in silos so that most people do not connect them, and there is no shortage of sock puppet “experts” willing to run around doubling down on the narrative. 

The Burbacher Study, if anyone were to know about it, let alone read it, SHOULD have at least sparked research into these potential harms. Instead, the spokesperson for the pharmaceutical industrial complex assigned to discredit parents and advocates, Paul Offit, dissects a strawman in public view…in this case the strawman is ethyl vs methyl mercury.

Allow me to explain how this tactic works and why it’s effective: Offit’s argument (and also the error in his argument) is that ethyl mercury (Thimerosal) clears from the brain faster than methyl mercury. First of all, that’s omitting the fact that there are organic and inorganic types, and for the organic type, Offit is right, but for the inorganic type, he’s dead wrong. Ethyl and methyl mercury are different, that’s true, but they both break down into organic and inorganic subtypes. The Burbacher study shows that the organic form of Ethyl mercury clears from the brain faster. 

The inorganic clearance rate couldn’t be determined because the slope of the rate of clearance is zero. So, according to this study, that form of mercury is in the brain forever. Compared to mercury derived from Thimerosal, both organic and inorganic forms of methyl mercury clear from the brain. Which goes against Offit’s claim that ethyl mercury is safer. At least the inorganic form clears from methyl mercury, but it never clears from ethyl mercury. 

But the real issue is…why are we comparing different kinds of lighter fluid around matches? No kind is desirable. (Strawman identified!) And no one is suggesting we are going to inject people with methyl mercury either…so he’s wrong to make the comparison in the first place. But once he’s made the comparison, he’s also wrong according to the data if you consider the inorganic form. Simply put, the Burbacher study proves that mercury does cross the Blood Brain Barrier. Did we put a hold on this? No. Instead, we did away with animal studies for mercury. 

This is just ONE example of ONE strawman designed and implemented to marginalize and sideline a set of risks and harms (even if that’s minority harm) and, yes, injury. There are too many others to list. For example, why aren’t we looking into the connection between autism and HHV-6? 

Between autism and chemicals like Glyphosate and PFAS and forever chemicals in our air, our water, our soil, and our food? Hint: it isn’t because I just thought of it now in my living room. It’s because bottom lines, and corporate and regulatory capture and corruption to maintain those bottom lines, are valued above human lives – above our children’s lives. 

Absence of evidence is not evidence of absence. Only ONE vaccine has ever been properly tested, and even then, never fully. If you shine a spotlight over one small area on a dark street and don’t find what you’re looking for, do you presume the entire street is free of whatever it is? Do we abandon first principles in order to pour concrete on our confirmation biases and further our narratives? Or do we ask the difficult, complex, and nuanced questions, do the hard work, and search for the truth? It appears that question has been asked and answered in the affirmative for the former. The latter is vehemently opposed. 

The assertion that these issues have been looked into is false. In fact it’s been DISALLOWED thus far, and look what’s happening when we try to look into it now. We have everyone outraged over a strawman that was never the point in the first place. It’s all a smoke screen. Once everyone is distracted and chaos ensues, any actual progress is effectively halted, which is precisely the point. It’s not organic. It’s the model, it’s coordinated, and it works. 

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Meet the Latest Vaccine Propagandist

On January 05, 2024, this Pharma Propaganda outlet published a video interview with Dr. Paul Offit, professional academic pediatrician and vaccine shill, in which he states a series of falsehoods in continuation of the gaslighting and falsehoods which both he and Dr. Peter Marks (FDA/CBER) are becoming known for.

Lets take a look at the transcript of this series of falsehoods.

First off, starting with the title, is Paul Offit actually a vaccine expert? What have his contributions actually been? Well, he self-identifies as the co-inventor of a licensed rotavirus vaccine (one of many, and not the first), and has received significant royalties from that. I should say currently licensed rotavirus vaccine, because there was a prior rotavirus vaccine (RotaShield – Wyeth) which was associated with an intolerable level of a clinical syndrome called “intussusception.”

If you know horses, you can think of intussusception as sort of like colic, but most often happening in children. More precisely, intussusception is a condition in which one segment of intestine “telescopes” inside of another, causing an intestinal obstruction (blockage). For some reason, rotavirus vaccines are associated with intussusception. It can be life threatening. The previously licensed rotavirus vaccine had a slightly higher rate of intussusception than the current one associated with Dr. Paul Offit (and Dr. H. Fred Clark, the senior of the two researchers).

This essay details the events surrounding the RotaShield withdrawal, including the role of Offit when participating in the Advisory Committee on Immunization Practices at the CDC. Basically, all US children are required to take either Offit’s vaccine or a competing similar live attenuated virus product. According to the CDC:

There is also a small risk of intussusception from rotavirus vaccination, usually within a week after the first or second dose. This additional risk is estimated to range from about 1 in 20,000 to 1 in 100,000 US infants who get rotavirus vaccine.

There are about 3.66 million births per year in the US, so that means between 36 to 180 cases of life-threatening intussusception in the US per year due to mandated administration of this product.

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What Is the PREP Act?

In conjunction with EUA (Emergency Use Authorization), the PREP Act is the legislation that enabled – and continues to perpetuate – the rollout and administration of mRNA “countermeasures” against Covid-19.

In this article I will discuss what the PREP Act says, how it was passed, what prominent politicians and legal experts said about it at the time, how it is related to COVID, and why I support efforts (1) calling for the HHS Secretary to immediately repeal the PREP Act emergency declaration for COVID, and (2) calling on legislators to repeal the law entirely.

WHAT THE PREP ACT SAYS

The PREP Act is a long and convoluted piece of legislation. You can read the entire thing here:

42 U.S. Code § 247d-6d – Targeted liability protections for pandemic and epidemic products and security countermeasures

This is a summary of the main sections of the law:

(a) Liability Protections

  • Anyone defined as a “covered person” is immune from legal liability related to the use or administration of anything defined as a “covered countermeasure.”

A “covered person” includes (A) “the United States” or (B) any person or “entity” that manufactures, distributes, plans a program for, prescribes, administers, or dispenses a covered countermeasure, or an official, agent or employee of any of the above.

A “covered countermeasure” includes any drug, biological product or device that is authorized under Emergency Use Authorization or approved through any other legal pathway.

  • Scope of claims for loss:
    • The immunity applies to any claim related to death, actual or fear of physical, mental or emotional injury, illness, disability, or condition; and loss of or damage to property, including business interruption loss.
    • The immunity applies to any causal relation to any of the above types of loss related to the design, development, clinical testing or investigation, manufacture, labeling, distribution, formulation, packaging, marketing, promotion, sale, purchase, donation, dispensing, prescribing, administration, licensing, or use of a covered countermeasure.
  • The immunity applies only if a countermeasure was applied or used during the effective period of the emergency declaration for that countermeasure, and was used for the disease, population and geographic area specified in the declaration.
  • For manufacturers or distributors, the immunity applies to any population in any geographic area, without regard to the population or area specified in the emergency declaration for the countermeasure.

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Recipients of Pfizer COVID-19 Vaccine Had Higher Mortality Than Those of Moderna: Study

Florida adults who received Pfizer’s COVID-19 vaccine were more likely to die following vaccination than Moderna COVID-19 recipients, according to a new preprint study that was co-authored by Florida’s top health official.

Dr. Joseph Ladapo, Florida’s surgeon general, and other researchers identified nearly 9.2 million Florida adults not living in institutions who received at least two doses of the Pfizer or Moderna vaccine less than six weeks apart between Dec. 18, 2020, and Aug. 31, 2021.

They narrowed the group to nearly 1.5 million, half who received Pfizer’s vaccine and half who received Moderna’s vaccine, by matching them based on criteria such as age and sex. They then analyzed the records to see which group had the higher risk for all-cause mortality, or death from any cause, in the 12 months following vaccination.

That analysis found that more Pfizer recipients died, with 847 deaths per 100,000 recipients, compared to 618 deaths per 100,000 for Moderna recipients. Pfizer recipients were also more likely to suffer heart-related deaths and COVID-19 deaths.

Pfizer and Moderna did not respond to requests for comment.

The study was published as a preprint, which means it has not been peer reviewed, on the medRxiv server on April 29.

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RFK Jr: “Pediatricians who vaccinate 80-85% of the kids in their office, get these GIANT bonuses!”

This is perhaps the most important — and most dangerous — article I have ever posted.

But I have to print the truth wherever I find it.

Let’s start with this clip from RFK Jr. explaining how pediatricians are given an incentive to vaccine your children with ALL the vaccines produced by Big Pharma…

So to summarize what he just said, he claims that pediatricians are given a monetary payout — a BONUS — if they vaccinate a high rate of children in their clinic.

He claims it can be as high as $400/child….

But ONLY IF they maintain high levels of vaccination overall at the clinic.

Which is why they freak out on you if you refuse to get the vaccines or don’t want to follow the CDC schedule.

It’s not hard to imagine in this scenario where they start to see each little kid with a dollar sign over their heads instead of a patient!

RFK Jr. explains how the business model is to increase traffic into the clinic.

Unlike when we were kids, and you only went to the doctor if you got hurt, now you go all the time!

Why?

“BUSINESS MODEL”.

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RFK Jr. Says New Parents Should ‘Do Your Own Research’ Into Vaccines

Health Secretary Robert F. Kennedy Jr. has advised new parents to research vaccines recommended for their children, as he also disclosed that health officials are looking into how some children start experiencing symptoms of autism shortly after vaccination.

During an April 28 town hall with Phil McGraw, also known as Dr. Phil, a mother asked Kennedy what his advice would be to new mothers with regard to vaccines.

“I would say that we live in a democracy, and part of the responsibility of being a parent is to do your own research,” Kennedy said. “You research the baby stroller, you research the foods that they’re getting, and you need to research the medicines that they’re taking as well.”

Kennedy, who heads the Department of Health and Human Services (HHS), said before becoming health secretary that no vaccines are safe. During his confirmation hearings, he described himself as “pro-safety” and not “anti-vaccine.” “I believe vaccines have saved millions of lives and play a critical role in healthcare,” he said at one point.

About a third of respondents to a Gallup survey in 2021 said that they do their own research when their doctor gives them important medical advice.

The Centers for Disease Control and Prevention, which is part of HHS, currently recommends children receive 12 vaccine doses in their first four months of life, and dozens more before they become adults. Many of the vaccines are required to attend school.

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RFK Jr. Leaves NewsNation Panel Speechless With One Brilliant Point on Measles

RFK Jr. is perhaps the most impactful HHS Secretary we’ve ever seen—but if you read the mainstream news, you’d think his first 100 days were a disaster.

While chronic disease drains trillions from Americans every year, the press can’t stop obsessing over measles.

Just look at these headlines:

It makes you think measles is a really big problem, but in reality, it’s not.

RFK Jr. expertly flipped this media narrative on its head in real time during his Wednesday night appearance on NewsNation—and it was so brilliant the audience gave him a round of applause.

NewsNation’s Chris Cuomo asked Kennedy:

“You weren’t saying that [get vaccinated] during COVID. That’s why people aren’t getting vaccinated. And now it’s a problem. How do you deal with that issue, and what responsibility do you have in terms of how people feel about getting vaccinated?”

Kennedy delivered a sharp, measured response. First, he pointed out that measles is a far smaller problem in the U.S. than it is globally.

He explained, “Right now we have about 842 cases, Chris. And Canada, they have about the same number. They have one-eighth of our population. Europe has ten times that number. Our numbers have plateaued.”

He noted that for years, the CDC has insisted the only way to manage measles is through universal vaccination. But Kennedy challenged that approach.

He argued that people who have concerns about the MMR vaccine—whether it’s due to aborted fetal debris or DNA particles—deserve access to treatment options.

“And that’s what we’re developing at CDC right now,” Kennedy said, “protocols for treating measles.”

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Pharma-Friendly Public Health Officials Launch New Project to ‘Shore Up U.S. Vaccination Policy’

A group of public health figures has launched a new project they hope will “shore up U.S. vaccination policy,” which they believe is under threat from U.S. Health and Human Services (HHS) Secretary Robert F. Kennedy Jr.

The “Vaccine Integrity Project,” launched Thursday, is funded by iAlumbra, a nonprofit founded by Walmart heiress and philanthropist Christy Walton. It will be based at the University of Minnesota’s Center for Infectious Disease Research and Policy (CIDRAP).

Michael Osterholm, Ph.D., CIDRAP director and a member of the COVID-19 Advisory Board under the Biden administration, said the project “acknowledges the unfortunate reality that the system that we’ve relied on to make vaccine recommendations and to review safety and effectiveness data faces threats.”

Former U.S. Food and Drug Administration (FDA) Commissioner Margaret Hamburg and Dr. Harvey Fineberg, former president of the Institute of Medicine and current president of the Gordon and Betty Moore Foundation, will co-chair an eight-member steering committee leading the initiative.

The group behind the project cited “a growing chorus of voices” in the U.S. questioning the safety and efficacy of vaccines as one of the inspirations for launching the project, Fierce Biotech reported.

In an op-ed published in STAT News, Hamburg and Fineberg said the project will use “the best available evidence” to “safeguard vaccine policy, information and utilization.”

The project will hold information-gathering sessions with public health stakeholders and share its recommendations with “nongovernment entities … that are free of outside influence and focus on protecting Americans from vaccine-preventable diseases.”

According to a press release, the project’s recommendations will be “grounded in the best available science.”

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A new study finds that flu vaccines have negative efficacy, meaning the risk of getting flu is higher after vaccination

Based in Ohio, USA, Cleveland Clinic is considered a leader in clinical research, education and care. With tens of thousands of employees, they are uniquely placed to investigate outcomes of staff vaccination policy including covid and influenza vaccine mandates.

In 2022, Cleveland Clinic researchers led by Dr. Nabin Shrestha and Dr. Steven Gordon at the Department of Infectious Diseases followed over 51,000 employees. They found that the proportional risk for covid infection increased with the number of covid vaccine doses an individual received.

This is known as negative efficacy and can be due to a multitude of factors, including but not limited to:

  • the fact that RNA viruses (including coronaviruses and influenza) mutate rapidly, rendering vaccines targeting prior strains useless. This is known as immune imprinting, or “original antigenic sin”;
  • immune suppression caused by persistence of circulating covid vaccine-induced spike protein can increase the risk of infection as well as other immune-related disorders;
  • repeated exposure to vaccine-induced spike protein can result in antibodies switching from protective IgG1, IgG2 and IgG3, to the less protective and immune-suppressing IgG4 class, which is also associated with other risks.

Influenza is also an RNA virus, but with haemagglutinin (“HA”) and neuraminidase (“NA”) proteins on its surface, rather than the spike proteins present on coronaviruses. As with the spike protein, HA and NA proteins mutate rapidly. This forms the theory behind annual updates to influenza vaccines as manufacturers attempt to predict evolutionary changes to the HA and NA proteins.

In a recent study, the same Cleveland Clinic researchers followed over 53,000 employees through the 2024-2025 US influenza season, which lasted for 25 weeks from 1 October 2024. The preprint of their study was published at ‘Effectiveness of the Influenza Vaccine During the 2024-2025 Respiratory Viral Season’.

Cleveland Clinic employees are mandated either to receive an annual influenza vaccine or to seek an exemption on medical or religious grounds. By the end of the study, 82.1% of the study cohort had received an influenza vaccine, and 98.7% of these received an inactivated 3-valent influenza vaccine.

A proportional hazards model was used to calculate the relative risk between vaccinated and unvaccinated people, adjusting for age, sex, clinical nursing job and location to minimise potential bias. Participants were only counted as vaccinated seven days after receiving a single dose of influenza vaccine.

The outcome for influenza-vaccinated employees by the end of the study was a statistically significant 26.9% increased risk of testing positive for influenza compared with employees who did not receive the seasonal vaccine.

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