Devastating COVID-19 Vaccine Side Effect Confirmed by New Data: Study

In one of the greatest violations of medical ethics in modern history, a new study from South Korea has uncovered devastating consequences from promoting and mandating the COVID-19 injections on the population.

These shots were pushed on babies and pregnant women, directly contradicting the ethical rule against introducing new medical interventions to such vulnerable groups before long-term effects are fully understood.

But they weren’t just aggressively promoted; they were enforced. Refusing the COVID-19 injection could cost you your job, bar you from concerts, businesses, and museums, and, in some cases, even deny you a life-saving surgery unless you complied with the mandate.

Now, as many doctors long warned, the consequences of such reckless health policy are surfacing, and one of the most alarming outcomes is a dramatic rise in cancer risk.

A large-scale population study out of South Korea has now found a 27% overall increase in cancer linked to the COVID-19 injections that were marketed as “safe and effective.”

Dr. John Campbell noted: “There’s a one in a thousand chance that this result arose by chance.” He illustrated the overall cancer rise with a stark graph, as seen in the short video below:

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Erasing Encephalitis — Why Vaccine Brain Injuries Became Autism

I’ve long believed that public relations (propaganda) is one of the most powerful but invisible forces in our society. Again and again, I’ve watched professional PR firms create narratives that most of the country believes, regardless of how much it goes against their self-interests.

What’s most remarkable is that despite the exact same tactics being used repeatedly on the public, most people simply can’t see it. When you try to point out exactly how they’re being bamboozled by yet another PR campaign, they often can’t recognize it — instead insisting you’re paranoid or delusional.

That’s why one of my major goals in this publication has been to expose this industry. Once you understand their playbook — having “independent” experts push sculpted language that media outlets then repeat — it becomes very easy to spot, and saves you from falling into the traps most people do. The COVID-19 vaccines, for instance, were facilitated by the largest PR campaign of our lifetime.

One of the least appreciated consequences of this industry is that many of our cultural beliefs ultimately originate from PR campaigns.1 This explains why so many widely believed things are “wrong” — if a belief were actually true, it wouldn’t require a massive PR investment to instill in society. Due to PR’s power, the viewpoints it instills tend to crowd out other cultural beliefs.

In this article, we’ll take a deeper look at what’s behind one of those implanted beliefs: “vaccines don’t cause autism.”

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Covid vaccines ‘might raise the risk of cancer’, contentious study claims – as it links jabs to six forms of disease, including breast and prostate

Covid vaccines may raise the risk of certain cancers, a highly contentious study has claimed. 

Korean researchers said they found proof the jabs raised the risk of six types of cancer including lung, breast and prostate.

The risk appeared greatest for over-65s, they wrote in a journal owned by a respected scientific publisher. 

But they did not explain exactly why the jabs may have increased this risk.  

Experts today dismissed the study labelling it ‘superficially alarming’ and warned its  conclusions were hugely overblown.  

The link between Covid jabs and cancer has previously been dismissed by academics and oncologists after claims it had led to ‘turbo cancers’. 

Scientists have long warned that there is no credible evidence that these vaccines disrupt tumour suppressors or drive any kind of process that results in cancer. 

It also comes as Reform UK last week distanced itself from Aseem Malholtra, an adviser to US health secretary Robert F Kennedy Jr, who suggested at its conference that Covid jabs were linked to the King and Princess of Wales’s cancers. 

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RFK Jr. Considering Adding Autism Symptoms To Vaccine Injury Program

Health Secretary Robert F. Kennedy Jr. is looking at updating symptoms after vaccination that are eligible for compensation under a federal program, an adviser said on Sept. 25.

We have a team looking at … a way to capture these kids,” Andrew Downing, senior policy adviser at the Department of Health and Human Services (HHS), told an autism roundtable in Washington.

“Do we broaden the definition of encephalopathic events? Do we broaden neurological injuries? How do we do that?

I was hoping that the changes to the program might have been rolled out before today, so that I could talk more in depth about them. As you can imagine, it’s not my place to do the rollout.

Downing is a lawyer who has represented individuals seeking compensation from the National Vaccine Injury Compensation Program.

The program was established by Congress to award damages to those who suffer vaccine-related injuries. He joined the HHS after Kennedy took office in February.

Kennedy said over the summer that the program would be revolutionized, including by addressing the lack of discovery.

The program has an enormous backlog of thousands of cases, just eight special masters who are able to adjudicate cases, and a table of eligible injuries that critics argue is too small.

Downing told the crowd on Thursday that when he first began filing cases with the program, encephalopathy cases could be approved for compensation if there was supportive medical literature. In rare cases, lawyers would have to bring in an expert.

The definition was changed in the 1990s, “making it almost impossible for a family to prevail,” he said.

The Department of Justice, which represents the HHS in cases filed with the program, later made it even harder to win some cases, according to Downing.

One change that should happen is that in borderline cases, compensation should be awarded to injured people, Downing said.

That is how the vaccine program was originally designed, and it’s been hijacked, for lack of a better word. Hopefully not for much longer,” he added.

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RFK Jr’s hand-picked CDC advisory panel recommends against combo vaccine for kids 

Health Secretary Robert F. Kennedy Jr.’s overhauled vaccine panel voted on Thursday to no longer recommend a combination shot protecting against chickenpox, measles, mumps and rubella for young children. 

In an 8-3 vote, with one member abstaining, the Advisory Committee on Immunization Practices (ACIP) decided against recommending the MMRV vaccine for children under the age of 4. 

The panel, which advises the Centers for Disease Control and Prevention (CDC) on which vaccines to recommend to the American public, said children younger than 4 should instead be immunized for varicella (the virus that causes chickenpox) separately from a combined shot for measles, mumps and rubella (MMR). 

Concerns over the rare risk of fever-induced seizures related to MMRV vaccines were brought up by some members of the panel. 

Committee member Dr. Cody Meissner, who voted to continue recommending the MMRV vaccine for young children, described so-called “febrile seizures” as “a very frightening experience” for parents during the ACIP meeting. 

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Moderna’s COVID Shot Plasmid Contains Human Blood Gene Fragment Capable of Integrating Into DNA—Same System Dominating Post-Vaccine Injuries

Moderna’s COVID-19 vaccine plasmid contains a human α-globin DNA fragment regulating blood and cardiovascular biology, and because plasmids are integration-competent DNA molecules, this fragment is capable of inserting into the human genome—precisely as blood and cardiovascular injuries like myocarditis and pericarditis emerge as the dominant serious adverse events following Moderna vaccination.

In plain terms, Moderna’s shot carries a piece of human blood gene code that can lodge itself into patient DNA, raising the possibility that the very blueprint of the vaccine is fueling the same heart and blood injuries now seen at the top of its safety reports.

While most public discussion blames the spike protein or lipid nanoparticles for Moderna’s adverse events, the evidence here points to something no one is talking about—the plasmid blueprint itself may be driving the blood and heart injuries dominating the safety signal.

A September 2025 peer-reviewed paper in Molecular Therapy: Nucleic Acids confirms that Moderna’s mRNA-1273 (Spikevax) vaccine plasmid carries a 3’ untranslated region (UTR) from the human α-globin (HBA1) gene.

  • α-globin encodes part of hemoglobin, central to red blood cell stability and oxygen transport.
  • Its regulation is directly tied to blood and cardiovascular function—mutations cause α-thalassemia, anemia, and cardiac stress.
  • By design, Moderna’s blueprint hard-codes this human blood gene regulator into the plasmid template.

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The Strange Disappearance of the Word “Retarded” in the Vaccine Era

For decades, vaccines were recognized to cause brain injury and mental retardation.

So “retarded” was banned, the injuries were relabeled as autism, and autism’s ambiguity was used to hide it all.

Lived experiences were turned into word games. But the paper trail shows it was never an accident.

In this report, 

A Midwestern Doctor exposes the games that have been played to hide vaccine injuries for generations.

This information comes from the work of medical researcher A Midwestern Doctor. For all the sources and details, read the full report below.

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‘Worrying’: RSV Shot Linked to Drug-Resistant Strains in Infants

A “substantial proportion” of infants immunized against the RSV virus with the monoclonal antibody shot nirsevimab — marketed by Sanofi and AstraZeneca as Beyfortus — developed a nirsevimab-resistant strain of the illness, according to a French study.

Over 12.5% of infants with breakthrough cases of RSV following immunization had variants of the illness with “intermediate to high-level resistance” to nirsevimab, including new strains of the virus not seen previously.

“The emergence of RSV-resistance described by this paper is simply incredible,” Children’s Health Defense Senior Scientist Karl Jablonowski said. He added:

“Most studies that shed light on the emergence of pathogens resistant to prophylaxis are population-wide and after many years of their use. Examples include the pertussis vaccine, the pneumococcal vaccine and the meningitis vaccine.

“This paper appears to show, with a high degree of certainty, the genesis of resistance.”

The study, designed to monitor escape variants of the virus and published on The Lancet’s preprint server, was conducted by a team of researchers from hospitals and research institutions across France.

The preprint follows a peer-reviewed paper published in The Lancet earlier this year by some of the same authors showing escape variants among a smaller number of infants. However, that study concluded the emergence of mutated variants was rarer.

The RSV monoclonal antibody shots were approved by the European Union and the U.K. in November 2022 and by the U.S. Food and Drug Administration in July 2023.

In September 2023, France was one of the first countries to launch a national immunization campaign with nirsevimab for newborns.

Many countries, including the U.S., followed France’s lead. The Centers for Disease Control and Prevention (CDC) added the shots to the childhood immunization schedule, recommending that either pregnant mothers get vaccinated or newborns get the monoclonal antibody shot.

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New Look at Old Data Shows COVID Vaccine Dangers Hiding in Plain Sight

Soon after the rollout of COVID-19 vaccines in 2020, top scientific journals published studies declaring the vaccines to be safe and effective — even amid mounting evidence of serious health concerns that eventually led vaccine manufacturers to add warning labels and pull products off the market.

In a new preprint study, scientists from Children’s Health Defense (CHD) and the Brownstone Institute reanalyzed data from those studies. Their analysis found clear health risks linked to the Pfizer and AstraZeneca shots, suggesting the studies “appear biased by design.”

CHD Senior Research Scientist Karl Jablonowski, an author of the preprint, criticized the highly credentialed researchers involved in one of the earlier studies.

“The bedrock, the foundation, the cornerstones, and the pinnacle of the scientific establishment” published an analysis of 46 million adults in England only “to proclaim ‘cardiovascular safety’ where, in fact, there is a veritable cardiovascular catastrophe,” he said.

For their preprint, Jablonowski and his co-researchers performed a safety analysis of the Pfizer and AstraZeneca COVID-19 vaccines using information from several large datasets from the U.K. — the same datasets used as the basis for numerous earlier studies, published in major journals, that concluded the vaccines were safe.

The new analysis confirmed that a significant risk for myocarditis and pericarditis associated with the Pfizer vaccines was evident in those earlier studies. Yet the studies’ results explicitly promoted the “cardiovascular safety” of the shots. The Moderna vaccines were also linked to heart risks.

CHD and Brownstone researchers also found that the risks for cardiovascular disease and death from the AstraZeneca vaccine were significantly higher than those of the Pfizer vaccine.

The AstraZeneca vaccine was a non-mRNA vaccine. It was never authorized or approved in the U.S., but was widely distributed in the U.K. during the early phase of the vaccine rollout. Like other vaccines, the AstraZeneca shot was advertised as safe and effective.

In 2024, AstraZeneca admitted in court documents that its shot could cause deadly blood clotting known as thrombosis with thrombocytopenia syndrome — also referred to as vaccine-induced thrombotic thrombocytopenia. The Johnson & Johnson shot was also linked to the condition.

Months later, AstraZeneca withdrew its vaccine from the market, though it denied the move was linked to the drug’s serious health risks.

At this time, major studies were published — including a highly cited 2024 study in Nature Communications — that promoted the safety of the AstraZeneca vaccine and other COVID-19 shots.

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Vaccine Safety Myth Crumbles at Senate Hearing

The September 9 hearing on vaccine safety led by Sen. Ron Johnson (R-Wis.) exposed what many Americans are now beginning to realize: the medical community has arguably been duped into believing that vaccines are unequivocally safe.  The hearing, titled “How the Corruption of Science has Impacted Public Perception and Policies Regarding Vaccines,” was led by Johnson’s Permanent Subcommittee on Investigations.  It followed other hearings conducted by Johnson on the subject of COVID-19 pandemic and the COVID-19 mRNA shots.

Three witnesses —  physician Dr. Jake Scottattorney Aaron Siri, and Stanford infectious diseases researcher Dr. Toby Rogers, with Scott defending vaccine research and trials and Siri and Rogers questioning them — offered sharply divergent pictures on the reliability of vaccine research and, by extension, vaccine safety.  Both camps cited data, but Siri and Rogers proved to be the more nimble and better-informed interpreters of the evidence.  Taken together, their testimony reinforced the growing impression that vaccines have never been subjected to the kind of rigorous study the public assumes.

Importantly, the committee put into the public record two irreconcilable records about how vaccine safety should be demonstrated.  Siri submitted to the committee an unpublished study conducted inside Henry Ford Health in Detroit.  The Ford study contends that real-world comparison is the most meaningful.  It studied two cohorts over time, vaccinated vs. unvaccinated children, showing large, repeated signals of vaccine harm in the Ford health system.

The study tracked 18,468 children from birth within the Henry Ford system (1,957 unvaccinated, 16,511 who received at least one vaccine).  Using Cox proportional hazard models, the analysis found that vaccination exposure was independently associated with elevated risks across several outcomes: any chronic condition (HR 2.53, 95% CI 2.16–2.96), asthma (HR 4.25, 3.23–5.59), autoimmune disease (HR 4.79, 1.36–16.94), atopic disease (HR 3.03, 2.01–4.57), eczema (HR 1.31, 1.13–1.52), and neurodevelopmental disorder (HR 5.53, 2.91–10.51).

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