First Population-Wide Peer-Reviewed Study Finds COVID-19 “Vaccines” Increase Risk of Multiple Cancers — CONFIRMS Fears of “Turbo Cancer” Epidemic

A bombshell peer-reviewed study out of Italy has just shattered the narrative peddled by Big Pharma, corporate media, and government health bureaucrats.

For the first time, a population-wide cohort of nearly 300,000 people tracked over 30 months has revealed that the so-called “safe and effective” COVID-19 shots are linked to alarming spikes in multiple forms of cancer.

Researchers followed every resident aged 11 and older in Italy’s Pescara province from June 2021 through December 2023, examining hospital records and adjusting for age, sex, prior health conditions, and even prior COVID infection.

The researchers allegedly found that those who received at least one vaccine dose had a much lower risk of dying from any cause compared to the unvaccinated, and this protective effect was even stronger in people who had three or more doses.

When looking at cancer, the picture was less clear. People who had been vaccinated appeared somewhat more likely to be hospitalized with a new cancer diagnosis than those who were unvaccinated, particularly for cancers of the breast, bladder, and colon.

However, this increased risk was only evident in people who had never been infected with COVID-19, and it disappeared—or even reversed—when the analysis required at least twelve months to pass between vaccination and a hospital admission for cancer.

  • Hospitalizations for cancer were 35% higher in vaccinated individuals versus the unvaccinated (HR 1.23).
  • The link was strongest in men and in those with no prior COVID infection.
  • Overall Cancer Risk: +23% after just one dose
  • Breast Cancer: +54% risk after vaccination
  • Bladder Cancer: +62% increased risk
  • Colorectal Cancer: +35% increased risk

Even after multiple doses, the risks remained elevated across the board.

The authors noted that vaccinated individuals are usually healthier, wealthier, and more likely to get preventative care, a phenomenon called the “healthy vaccinee bias.”

If anything, the numbers should have shown lower cancer rates. Instead, cancers surged. That means the real danger could be far worse than what the data shows.

Doctors and whistleblowers have been warning for years about sudden, aggressive cancers appearing in otherwise healthy people after the jab.

This study, alongside more than 100 other peer-reviewed papers, confirms the link between mRNA injections and deadly cancer pathways. A new medical term has even been coined: COVID-19 Vaccine-Induced “Turbo Cancer.”

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RFK Jr. Tells Trump He’s Discovered What Is “Clearly” Causing Autism

During a cabinet meeting Tuesday, Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. informed President Trump that his department has discovered what is “almost certainly” causing autism in kids.

Kennedy vowed earlier in the year to investigate and get to the bottom of what is behind the massive increase in cases that once afflicted only one in every 10,000 children, but now account for one in every 31 nationwide.

In the state of California, a shocking one in every 12.5 boys is now diagnosed as autistic, while for kids overall, it’s one in 19.

Turning to Kennedy during the meeting, Trump stated “Bobby, autism is such a tremendous horror show, what’s happening in our country and some other countries, but mostly our country. How are you doing on that?”

“We are doing very well. We will have announcements as promised in September,” Kennedy replied, adding “We’re finding certain interventions now that are clearly, almost certainly, causing autism.”

“We’re going to be able to address those in September,” he further revealed, noting that a full public announcement will be made next month.

Referring to the numbers of cases, Trump declared, “It’s not even believable that that could be. And that was one in 10,000 not so long ago. I’ve been hearing these numbers, and they get worse and worse every year. There’s got to be something.”

He continued, “I think there’s nothing—including favored nations and everything else—there’s nothing that can be… If you can find out the reason that that’s happening, and I know we’re going to do some things.”

Strongly hinting that vaccinations are behind the huge increase in cases, Trump said “I think we maybe know the reason, and I look forward to that press conference—to be with you on that press conference. That’s going to be a great thing.”

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How The American Academy Of Pediatrics Betrayed Children Everywhere

The prime directive of Western medicine, its golden rule, is expressed by the Latin maxim primum non nocere – first, do no harm. Unfortunately, the Covid era taught us that from the patient’s point of view, a better motto for our times might be caveat emptor – let the buyer beware.

Every medical student is taught that, first and foremost, they should not cause harm to their patients, and every doctor is familiar with this maxim. It is echoed in the Hippocratic Oath, and it forms the basis for the four pillars of medical ethics: autonomy, beneficence, nonmaleficence, and justice.

This rule, and the core tenets of medical ethics that it underpins, were all abandoned during the Covid era. They were replaced with a brutal, inhumane, and unethical martial-law-as-public-health approach to medicine. The results were unconstitutional lockdowns, prolonged school closures, suppression of early treatment, mandated vaccinations, and silencing of dissenting views. These abuses were justified by constant propaganda and lies from public health authorities, the medical establishment, the mainstream media, and medical professional associations.

Enter the American Academy of Pediatrics.

The American Academy of Pediatrics (AAP) is the largest professional association for pediatricians in the United States. Nearly one hundred years old, the AAP’s motto is “Dedicated to the Health of All Children.” But as with so much of the medical establishment, the Covid era revealed that the AAP has abandoned its stated mission, and in the process, it has betrayed children everywhere.

During the Covid era, no group was harmed more – or more unnecessarily – than children, who lost multiple years of education, socialization, and normal growth and development. Many millions of kids also received the fraudulently tested, toxic, experimental mRNA-based injections that were coercively imposed upon the population at large. Countless children have been harmed or killed by these products, with myocarditis being only the most universally acknowledged of the many toxicities associated with the shots.

Adding insult to injury, it was known from the beginning of the pandemic that the gain-of-function-produced SARS-CoV-2 virus affected children very mildly, rarely causing severe illness, and almost never killing them. Even at the height of the pandemic, an article in the preeminent journal Nature described pediatric Covid deaths as “incredibly rare.” A very large population-based Korean study from 2023 found the case-fatality rate in children from Covid to be well under 1 death in every 100,000 cases. 

If no segment of the population was harmed more egregiously than children during the Covid era, few medical organizations betrayed their patient population more thoroughly than the American Academy of Pediatrics.

While the AAP has for many years taken questionable stances on a variety of issues, including the ever-enlarging pediatric vaccine schedule, “gender reassignment,” and others, at one early point during Covid, the AAP did attempt to advocate appropriately in the interest of children. It didn’t last long, however, and a review of this incident shows how the AAP, like so many other medical professional organizations, effectively sold its soul during Covid.

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FDA Revokes Emergency Authorization For COVID-19 Vaccines

The Department of Health and Human Services under Health Secretary Robert F. Kennedy Jr. revoked emergency authorization for COVID-19 vaccines.

“The emergency use authorizations for Covid vaccines, once used to justify broad mandates on the general public during the Biden administration, are now rescinded,” Kennedy posted to X on Wednesday.

The news comes as the FDA, which is part of HHS, announced the approval of the Pfizer-BioNTech COVID-19 vaccine for older adults and children as young as 5-years-old who have at least one condition that puts them at higher risk of severe COVID-19 outcomes, Pfizer said in a Wednesday statement.  

Regulators have issued similar approvals for COVID-19 jabs from Novavax and Moderna. 

HHS revoking emergency approval means that FDA clearance is no longer in place for some 240 million Americans, however “These vaccines are available for all patients who choose them after consulting with their doctors,” Kennedy sai. 

As the Epoch Times notes further, per federal law, the FDA approves products it determines are “safe, pure, and potent.” Emergency authorizations, in contrast, can only be offered under certain circumstances, such as during a public health emergency, and are for products that officials believe “may be effective” in treating or preventing a life-threatening disease or condition.

Updated Approvals

Dr. Marty Makary, the FDA’s commissioner, and Dr. Vinay Prasad, its top vaccine official at the time, signaled the change in May, when they said that the FDA would stop approving COVID-19 vaccines for many Americans absent clinical trial data.

The FDA can only approve products if it concludes, based on scientific evidence, that the benefit-to-harm balance is favorable. And we simply need more data to have that confidence for younger individuals at low-risk of severe disease,” Prasad said at the time.

In the United States, regulators in recent years have been authorizing updated COVID-19 vaccines annually in a bid to counter waning effectiveness and better match circulating variants. The model is based on the historical approach to influenza vaccines.

Regulators in 2024 cleared updated shots from Moderna, Pfizer, and Novavax without human data, citing animal tests and data from trials for previous versions.

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Surge in pilot deaths and incapacitation began in 2021, and the FAA has been trying to cover it up

  • A sudden, unprecedented surge in pilot deaths and incapacitations began in 2021, with a 40 percent increase in pilots dying before retirement age and a tripling of long-term disabilities, coinciding with COVID-19 vaccine mandates.
  • FAA regulations were violated en masse when airlines coerced pilots into taking experimental mRNA injections, despite federal laws prohibiting pilots from using unapproved medical products.
  • Pilots were trapped in an impossible choice: Violate their religious or medical convictions and risk their health, or refuse the jab and lose their livelihoods — all while the FAA abandoned its duty to track vaccine-related adverse events.
  • The spike protein produced by mRNA jabs is directly toxic, causing inflammation, blood clots, myocarditis, and neurological damage — conditions that are catastrophic in a cockpit.
  • The FAA dismantled its pilot incapacitation database in 2022, eliminating a critical tool for tracking trends in pilot health just as incidents began to skyrocket.
  • Near-misses and in-flight emergencies have reached crisis levels, with aviation officials attributing the chaos to everything but the elephant in the room: the COVID-19 vaccines.
  • Pilots describe a culture of fear and silence, where speaking out against the jabs means professional suicide, leaving passengers unknowingly at the mercy of impaired crews.

The great airline vaccine heist: How pilots were strong-armed into a medical experiment

When the COVID-19 vaccines rolled out under Emergency Use Authorization, they came with a critical caveat: No one could be forced to take them. That legal protection was swiftly ignored. For airline pilots, the choice wasn’t really a choice at all. It was a gun to the head — comply or be erased. Major carriers like United Airlines didn’t just encourage the jab; they demanded it, offering cash bonuses to the compliant and pink slips to the resistant. Never mind that federal aviation law explicitly prohibits pilots from using experimental medications. Never mind that the FAA’s own Aeromedical Advice Manual warns against unapproved substances that could impair performance. The rules were rewritten in real time, not by scientists or safety experts, but by corporate executives and bureaucrats who had already decided the narrative: Get the shot, or get out.

Dr. Kevin Stillwagon, a retired airline pilot and immunology expert, doesn’t mince words. “They were illegal,” he says of the mandates. “You cannot put an experimental product into a pilot.” The law is clear: If a pilot takes an unapproved substance, flight surgeons must ground them until the FAA verifies its safety. But in 2021, that process was bypassed entirely. Airlines, backed by the federal government, bulldozed through legal and ethical barriers, turning pilots into lab rats in a real-world trial with no control group. The result? A wave of cardiac arrests, neurological disorders, and sudden deaths that has left the industry scrambling to explain away the carnage.

Stillwagon’s data is damning. Before 2021, pilot incapacitations were rare — about eight per year, according to a 2018 study in Aerospace Medicine and Human Performance. But in the wake of the vaccine rollout, the numbers exploded. At Washington National Airport alone, near-misses jumped from one in decades to 28 in a single year. The FAA’s own 2004 research found that pilot cardiac events were the leading cause of in-flight fatalities. Now, those events are happening at an unprecedented rate, and the agency’s response? Cricket sounds. Worse, they discontinued their centralized database for tracking pilot incapacitations in 2022, just as the crisis was unfolding. Coincidence? Stillwagon doesn’t think so. “The data silence that the FAA has created is preventing systemic trends from being detected,” he warns. In other words, they’re hiding the bodies.

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Sudden Deaths, Incapacitations Soar Among COVID-Jabbed Airline Pilots

“Something happened in 2021” that has jeopardized air travel safety, according to a disturbing report by Dr. Kevin Stillwagon, a retired airline pilot and immunology expert.

Mounting evidence points to the COVID-19 vaccinations that airlines, acting under pressure from the U.S. government, mandated or otherwise coerced their cockpit, cabin, and ground crews into taking.

Since 2021, there has been a marked increase in deaths of “younger” airline pilots while long-term disabilities for pilots have skyrocketed. All of this has been accompanied by an astronomical increase of near-miss incidents at the nation’s airports.

“Incapacitations of pilots are definitely increasing, especially in younger pilots,” Stillwagon said in a video discussion with Nicolas Hulscher, an epidemiologist and administrator at the McCullough Foundation.

“There was a 40% increase in pilots dying early – before mandatory retirement age of 65 – in 2021,” Stillwagon said.

“Starting in 2021, pilot long-term disabilities have tripled,” he noted. “Prior to 2021, there was only one near-miss at the Washington National Airport (DCA).  But after 2021, there were 28 near-misses per year.”

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FDA Suspends License For Chikungunya Vaccine After ‘Serious Adverse Events’

Federal regulators on Aug. 25 said they’ve suspended approval for a vaccine against chikungunya, a mosquito-borne virus.

Due to reports of serious adverse events following administration of the vaccine, the Food and Drug Administration’s Center for Biologics Evaluation and Research (CBER) “believes this vaccine is not safe and that continued administration to the public would pose a danger to health,” the FDA said in a statement.

France-based Valneva makes the vaccine, known as Ixchiq.

“As we determine potential next steps, and as the clear threat of chikungunya continues to escalate globally, Valneva remains fully committed to maintaining access to our vaccine as a global health tool for addressing and preventing outbreaks of this devastating illness,” Thomas Lingelbach, Valneva’s CEO, said in a statement.

Zachart Stieber reports for The Epoch Times that the FDA originally approved Ixchiq in 2023 to prevent disease caused by the chikungunya virus in adults deemed to have an increased risk of exposure. The Centers for Disease Control and Prevention in 2024 recommended the vaccine for people traveling to certain countries.

Health officials said in an alert in May that they were advising a pause in administering the vaccine to elderly adults due to reports that some of those vaccinated had been experiencing serious adverse events (SAEs), including neurologic and cardiac problems.

This included 38 SAE reports for 32 unique cases (7 U.S., 25 foreign), including 21 hospitalizations and three deaths.

After CBER Director Dr. Vinay Prasad resigned, the FDA, in early August, ended the recommended suspension, stating that an updated assessment of risks and benefits for Ixchiq showed the benefits still outweighed the risks for some people.

In the new announcement, regulators said that is no longer the case.

The latest risk-benefit assessment includes four new foreign reports that came to light since the FDA lifted the recommended pause, including a report of problems following vaccination in a 55-year-old male.

Prasad said in a memorandum dated Aug. 22 that of the 32 cases, five tested positive for the vaccine strain of the virus, making it nearly certain that the vaccine caused the problem.

“There are reasonable grounds to believe the risks of the vaccine outweigh its benefits, and that it poses a danger to health. Therefore, CBER is suspending approval,” Prasad said.

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Report: Trump Administration Planning to Phase Out COVID-19 Vaccine

The Trump administration is reportedly planning to phase out the COVID-19 vaccine, according to a report from the Daily Beast.

Dr. Aseem Malhotra, who is one of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr.’s “closest associates,” told the outlet that while a decision to remove the COVID-19 vaccine from the market could come “within months,” it could occur “in a number of stages.” Malhotra also added that “those closest” to Kennedy have reportedly expressed that they “cannot understand” why the COVID-19 vaccine “continues to be prescribed.”

“It could [happen] in a number of stages, including learning more about the data,” Malhotra, who is a British cardiologist, told the outlet. “But given the increased talk of vaccine injuries in the past few weeks among the administration, it could also come with one clean decision.”

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‘Right This Wrong’: GRACE Act Would Strip Federal Funding From Schools That Ban Religious Exemptions

A member of the U.S. Congress has drafted legislation that would strip federal funding from schools that don’t allow parents to apply for religious exemptions from vaccination requirements for their children.

The GRACE Act, or Guaranteeing Religious Accommodation in Childhood Education Act, drafted by Rep. Greg Steube (R-Fla.), would target elementary and secondary schools, as well as local and state educational agencies.

The legislation would not require state authorities or educational institutions to offer religious exemptions, but it would deny federal funds to those entities if they maintain vaccine mandates that don’t include provisions for religious exemptions.

“The denial of religious exemptions to families and children is un-American and unconstitutional,” said Michael Kane, CHD’s director of advocacy and founder of Teachers for Choice. “CHD and I thank Rep. Steube for putting forth this important legislation to right this wrong that is a clear violation of the First Amendment.”

The GRACE Act is a response to the “alarming erosion of civil rights” that occurred under the Biden administration, said Cait Corrigan, a former congressional candidate from New York and an advocate for medical freedom and religious liberty.

“This issue is one of religious freedom, individual liberty and parental rights, which I often describe as part of a broader response to years of increasing concern,” Corrigan said.

Steube’s office did not respond by deadline to The Defender’s request for comment on the legislation.

‘A matter of conscience, faith and the fundamental dignity of every family’

Corrigan said the proposed legislation is “not just an issue of policy” but “a matter of conscience, faith and the fundamental dignity of every family in this country.”

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ACIP Launches Sweeping Covid-19 Vaccine Review Under Retsef Levi

MIT professor Retsef Levi has been an outspoken voice on the CDC’s vaccine advisory committee (ACIP) since its dramatic overhaul in June.

He has pressed agency officials on uncomfortable questions, challenging the narrow surveillance windows used to track harms and insisting that delayed effects could not simply be ruled out.

He also raised concerns about the safety of RSV monoclonal antibodies after clinical trials showed a clear imbalance in infant deaths.

Now, Levi is no longer just a dissenter.

He has been appointed chair of the CDC’s new Covid-19 vaccine working group, and with today’s release of its Terms of Reference, the scale of his task has come into sharp focus.

Under the guidance of Levi and his colleagues, the ACIP working group now has a mandate unlike anything the committee has ever undertaken.

For the first time, federal advisers will investigate the unresolved issues that have dogged the vaccines since their rushed rollout in late 2020.

From DNA contamination in the manufacturing process to the persistence of spike protein and mRNA in the body, from immune class switching following repeated boosting to safety in pregnancy, cardiovascular risks, and long-term disability, the list of questions is as sweeping as it is sensitive. (full list below)

The Terms of Reference stretch far beyond the narrow remit that characterised ACIP’s early deliberations, when myocarditis was acknowledged as the only confirmed harm and most safety reviews stopped at 42 days.

Levi and his team are now tasked with probing long-term outcomes, mapping vaccine policies around the world, and assessing, to what extent, years of official reassurances about safety and efficacy hold up against emerging data.

It is a striking reversal for the CDC and the FDA.

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