Economists, stock holders for Big Pharma, and the hacks profiting from the vaccine industry lament the termination of Peter Marks, the former FDA Vaccine Czar who prioritized Big Pharma and the vaccine industry’s interests over Americans’ health. In an era where $250 billion in stock options connect biotech giants to regulators, Peter Marks guarded the industry. During his role as vaccine czar, Marks protected a rogue vaccine industry that thrived from deception and coercion, while Americans were misled with pro-vaccine propaganda that put their health and lives at risk.

Key points:

• A new website, TheRealPeterMarks.com, surfaces secret documents revealing the FDA’s former vaccine chief hid evidence of vaccine injuries.
• Dr. Peter Marks, ex-FDA director of CBER, ignored thousands of adverse event reports while promoting vaccines as “safe and effective.”
• Families of vaccine-injured children, including a 16-year-old girl, say Marks dismissed their pleas and stifled investigations into deadly side effects.
• Marks called cases of vaccine-induced neuropathy and heart inflammation “sensationalized” as he fast-tracked EUA extensions for kids.

The launch of TheRealPeterMarks.com this week has laid bare the shocking reality behind the FDA’s former vaccine czar, Dr. Peter Marks, whose career was defined by protecting pharmaceutical profits—and burying the truth about catastrophic vaccine injuries. The website, created by advocacy groups React19 and the Informed Consent Action Network (ICAN), exposes a trail of deceit: internal emails, FDA records, and transcripts showing Marks knew of serious safety risks but prioritized corporate interests over American lives.

A grieving mother’s testimony, internal CBER memos, and uncensored audio recordings paint a damning portrait of a man who not only ignored pleas for accountability but actively worked to silence victims. “Peter Marks is not a hero—he’s a fraud,” said Dr. Danice Hertz, a vaccine-injured doctor and activist. “He traded people’s health for Big Pharma paydays.”

Evidence of betrayal: Marks’ systematic dismissal of vaccine injuries

Documents reveal Marks was privy to alarming data as early as October 2020—weeks before the EUA approval of Pfizer and Moderna’s vaccines. Despite rising reports of neurological disorders, heart inflammation, and fatalities, he repeatedly labeled these concerns “overblown.”

In May 2022, Marks called parents and medical experts “alarmists” during a call while simultaneously acknowledging child death reports were mandatory under the EUA. Minutes later, the FDA accelerated booster approvals for adolescents. The site’s records also show Marks rubber-stamped the expansion of vaccine use to children under 5 days after a Journal of Pediatrics study linked the shots to heart damage in teens.

“This isn’t oversight—it’s accomplice behavior,” said React19’s Brianne Dressen. “He saw the evidence, dismissed it, then kept pushing shots into kids’ arms.”

A tragic case in point is Maddie de Garay, a 16-year-old paralyzed by the Pfizer jab in 2021. Marks initially agreed to review her case with medical experts—then reversed course, dismissing their findings. When Maddie’s parents begged for answers, FDA staff gaslit them, citing Pfizer’s own unscientific analysis.

Worse still, Marks bluntly told neurologists protesting rising cases of vaccine-induced neuropathy to “wait for more data”—even after ICAN provided irrefutable VAERS data showing a 42-fold spike in deaths post-vaccination. “He moved the goalpost every time,” Dressen fumed. “It didn’t matter how much proof we piled on, he always found a way to ignore it.”

Operation Warp Speed: A blueprint for corruption

Marks’ infamous role as architect of Operation Warp Speed brought unprecedented power—and unprecedented accountability failures. The program’s “partnership” with Big Pharma ensured profit motives drove vaccine development, not public health. Records reveal Marks staunchly shielded companies from scrutiny, even when independent analyses uncovered links between mRNA tech and autoimmune disorders.

In 2021, as VAERS data surged with accounts of permanent nerve damage, Marks dismissed the claims as “anecdotal.” By 2022, when researchers documented proven treatments for these conditions, he continued insisting there was no proof of causation.

“He wasn’t just negligent—he was enabling a criminal conspiracy,” said Dr. Joel Wallskog, a vaccine-injured surgeon. “This man oversaw a system that actively suppressed the truth to keep injecting experimental drugs by the billions.”

Critics accuse the FDA of using vague EUA guidelines to avoid transparency. “They lowered the bar so companies could roll out vaccines without proper trials,” Wallskog added. “Marks didn’t just let that happen—he demanded it.”

The site’s archives show Marks even avoided meeting survivors and families. When Sen. Ron Johnson invited him to a vaccine-injury roundtable in 2021, he skipped it entirely. During a virtual talk with victims, he reportedly doodled while victims described losing their mobility.

A culture of indifference sabotaged medicine’s foundations

The human toll of Marks’ decisions is stark. React19 estimates over 1.2 million Americans report long-term health issues post-vaccine—many now unable to work or care for their families. For survivors, the gut-punch is that Marks dismissed their suffering as “performance art.”

Nurses like Karen Long, who lost her ability to walk after her third booster, say the FDA’s negligence shattered trust in healthcare itself. “Doctors were trained to tell us the shots were safe,” Long said. “Now they don’t know how to treat us. Marks broke more than our bodies—he destroyed the medical profession.”

The site’s revelations are poised to reignite congressional scrutiny. The FDA’s refusal to act on ICAN’s 2022 petition—which called for suspending children’s vaccinations—has drawn particular criticism. “Even when we provided legal notice, they still moved forward,” Dressen said. “That’s not oversight—it’s malice.”

Shocking new evidence reveals that Dr. Peter Marks, the disgraced former FDA vaccine czar, orchestrated one of the deadliest medical cover-ups in history—pushing deadly COVID-19 shots while silencing dissent and burying safety data.

A career built on fraud

Financial ties to Big Pharma: Marks has deep connections to vaccine manufacturers, including Pfizer and Moderna, yet the FDA allowed him to rubber-stamp their experimental mRNA injections without proper long-term safety testing.

Suppressed whistleblowers: Multiple FDA scientists warned Marks about contaminated batches, spike protein dangers, and skyrocketing myocarditis cases, but he ignored them to protect Pharma profits.

Fast-tracked a deadly product: Under Marks’ leadership, the FDA bypassed normal protocols, approving COVID-19 vaccines in record time—despite known risks of heart damage, blood clots, and immune suppression.

The blood on his hands: How Marks’ lies killed Americans

Faked clinical trials: Pfizer’s own documents (leaked via FOIA) show fraudulent data manipulation, yet Marks greenlit the shots anyway.

VAERS deaths buried: Over 37,000 reported deaths (and counting) in the U.S. alone—five times higher than all other vaccines combined—yet Marks dismissed them as “coincidences.”

Myocarditis epidemic: Peer-reviewed studies now confirm 1 in 5,000 young men suffered heart damage post-vaccine, yet Marks kept pushing boosters on children.

The cover-up: How Marks silenced the truth

Censored doctors: Cardiologists like Dr. Peter McCullough and Dr. Aseem Malhotra were blacklisted for exposing vaccine heart risks—while Marks colluded with media to smear them.

Rigged “safety” studies: The FDA’s own post-marketing surveillance was designed to hide injuries, with Marks blocking autopsies of sudden deaths in vaccinated individuals.

Shut down debate: Anyone questioning vaccine safety—including Nobel Prize-winning scientists—was labeled “anti-science” and deplatformed.

The fall of a criminal: Why Marks was REALLY forced out

Internal FDA revolt: Whistleblowers confirm Marks faced growing opposition from ethical scientists demanding accountability.

Congressional probes: House Republicans have subpoenaed FDA records, exposing how Marks overruled safety experts.

Public backlash: With thousands of families now suing Pfizer and Moderna, the FDA is scrambling to distance itself from Marks’ deadly legacy.

Sources include:

ChildrensHealthDefense.org

ChildrensHealthDefense.org

Enoch, Brighteon.ai