RFK Jr. Reveals the COVID Vaccine Secret That Fauci Hid From Americans

For years, Dr. Anthony Fauci assured Americans that the COVID-19 vaccines were safe and effective. What he never mentioned, according to Health and Human Services Secretary Robert F. Kennedy Jr., is that he may have suffered one of those “rare” adverse events himself, and he hid it from the country while publicly insisting such injuries weren’t happening.

Kennedy appeared on Fox News’s The Ingraham Angle to discuss the newly released diary entries that Sen. Rand Paul (R-Ky.) made public, entries that document Fauci’s day-to-day life during the pandemic, on top of his disturbing obsession with himself and the power he wielded during the pandemic. When Laura Ingraham asked whether there would be any accountability for the trillions of dollars lost, the ruined education of America’s children, and the shattered reputation of the public health establishment, Kennedy didn’t hesitate.

“Yeah, and millions of people injured,” Kennedy said. “So he lied about masks, he lied about social distancing, he lied about the transmission, he lied about natural immunity, he lied about the capacity, as you just said, of the vaccine to prevent infection.”

Then came the bombshell.

“He got vaccinated at a very, very public press conference in January of 2021,” Kennedy said, noting that five months later, the diary reveals, Fauci “had a pulmonary infarction, which is one of the adverse events that NIH, CDC and FDA said are expected from the vaccine.”

“He never told anybody,” Kennedy said. “He got treated for it privately by the best doctors in America at the same time, he was telling everybody that was not an adverse event.”

Think about that for a second. The man who badgered every American into taking the shot, insisting it was perfectly safe, appears to have experienced one of the exact injuries his own agencies flagged, then quietly got elite private care while assuring the public that such reactions weren’t real. Ordinary Americans who reported similar problems got dismissed and mocked. Fauci got the best doctors in America.

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Czech data shows that those who got the Moderna vaccine died more

For the first time, I show the directly standardized survival curves for each 5 year age group in the Czech Republic using the publicly released record-level data.

This data consistently shows the people who got the Moderna vaccine were much more likely to die than those of the same age who got the Pfizer shot. The relative risk (RR) was >1.5 for those under age 60 which is a huge difference.

The comorbidity distribution for both groups of a given age range was very similar (SMD=.05)

This isn’t because Pfizer is more protective of a COVID death because the differences were not specific to COVID periods (and were too large to be explained by effectiveness differences).

There are two remaining explanations:

  1. The Moderna vaccine was more deadly
  2. There was a systematic distribution of vaccines in Czech Republic that no matter what age you were, if you were more likely to die, you were given the Moderna shots.

Explanation is 2 is much less likely because there was no systematic bias in vaccine distribution by brand, and even if there were, the fact that the DCCI distributions were similar and that the younger you were, the more pronounced the effect, would be unusual since 45 year old people are not concentrated in elderly homes and hospital beds.

So the most likely explanation is Moderna was more deadly.

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Top NIH Official Wanted to Shut Down Research Into COVID-19 Vaccine Injuries: Emails

Top officials with the National Institutes of Health (NIH) expressed misgivings about researchers with the agency studying people with neurological issues after they received COVID-19 vaccines, according to newly released emails.

Dr. Avindra Nath, a senior investigator with the NIH’s National Institute of Neurological Disorders and Stroke, was studying people with post-vaccination neurological problems in 2020 and 2021.

In an email on April 10, 2021, he sent a draft of a paper to the institute’s director, Dr. Walter Koroshetz, that outlined what he had found.

“Early recognition and treatment with corticosteroids can reverse the symptoms,” Nath wrote.

The following day, the institute’s director sent the manuscript to Dr. Anthony Fauci, who at the time was director of another NIH institute.

“There have been steady slow stream of reports to me of post vaccination neurologic conditions, seem to be mostly peripheral nerve disorders … maybe an occasional spinal cord issue,” Koroshetz told Fauci. “Avi has been collecting a bunch. He has a report sent out to publish. Hard to know not due to chance but are timed to the vaccination.”

Another NIH employee sent the manuscript to then-NIH Director Dr. Francis Collins and Dr. Lawrence Tabak, a second top NIH official, and shared that the New England Journal of Medicine rejected the paper.

“What do you make of this?” Collins wrote in response. “The draft letter doesn’t explain how these 32 patients were referred—leaving one to wonder whether this is common or rare.”

Koroshetz told Collins that many reports had been lodged with the Vaccine Adverse Event Reporting System and that Nath had been attracting referrals because he had appeared on a podcast to discuss neurological problems following COVID-19 vaccination.

Koroshetz also said that Nath, and another employee at his institute, had suffered tinnitus after receiving COVID-19 vaccines, and that Nath had hearing loss.

Collins said the approach taken by Nath’s team was “very troubling,” adding, “collecting anecdotes and then trying to build a case isn’t scientifically compelling—and will have the main consequence of feeding vaccine hesitancy and social media overreaction.”

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‘Three-Way Collision’: How Genes, Mold and Vaccines Might Lead to Autism

Take a genetically susceptible child, expose that child to mold, and then add an immune trigger — like a vaccine — that “tips an already-strained system over the edge,” and you may create a “three-way collision” that can lead to autism, according to Dr. Christian Bogner.

Bogner, a physician and researcher, and other experts told The Defender that environmental triggers have become more prevalent in recent decades, with the expansion of the childhood immunization schedule and the widespread use of toxic pesticides, including glyphosate, to produce food.

Many blame toxic exposures for the drastic increase in autism diagnoses among U.S. children, which the Centers for Disease Control and Prevention measured at 1 in 31 children in 2022 — up from 1 in 10,000 in the 1970s.

Physician and author Dr. Neil Nathan believes there is “clearly a relationship” between one of those toxic exposures — mold toxicity — and autism, though studies attempting to identify a link have so far been few and inconclusive.

“It’s hard enough to get any studies done on toxic mold that get into the mainstream narrative — to say nothing of the vaccine issue,” said Dr. Margaret Christensen, a trained gynecologist, clinical educator and co-founder of the Carpathia Collaborative.

According to Christensen, exposure to toxic mold “affects everybody … as it is such a common environmental toxin.” She noted that at least half of homes and 60% of commercial buildings “have had sufficient water damage to have a toxic mold issue as a component to common environmental exposures, creating illnesses.”

Bogner said that each child has different levels of susceptibility when exposed to toxins. Even within the same household, two children exposed to the same toxins may have different outcomes — one may become very ill or develop autism while the other may remain healthy.

But there’s at least one common denominator among the sick children he’s treated: an imbalance in the gut.

“Triggers vary — some children were pushed by vaccines, some by mold, some by antibiotics, some by none of those — but every autistic child I have evaluated has dysbiosis,” Bogner said. These children “carry specific bacterial overgrowths” that lead to toxicity in the gut and the potential onset of neurological disorders.

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Multi-Year Study Involving 800+ Embalmers and Funeral Directors Across Five Countries Reveals 75.2% Noticed “Unusual White Fibrous Structures” in Corpses

On June 18, 2026, Sen. Ron Johnson (R-WI) wrote on X: “There has not been a bigger government scandal during my lifetime, and yet even now that we have documented proof of corruption, most of the legacy media refuses to report on it.”

The congressman was referring to his April 29 hearing, highlighting how Biden’s health officials intentionally ignored safety signals regarding COVID-19. Associated with the shot, there have been countless incidents of sudden cardiac death, pulmonary infarction, cerebral artery occlusion, basal ganglia stroke, and agonal rhythm, for example.

Earlier this month, a newly published peer-reviewed study in the International Journal of Innovative Research in Medical Science officially validated the phenomenon of postmortem blood clots that The Gateway Pundit has been reporting on for several years.

The published study was carried out by retired U.S. Air Force Major Thomas F. Haviland, who is a data analyst and mathematician, along with independent researchers Lauro Kasner and Dr. Daniel Santiago, a Doctor of Pharmacy. The researchers performed four annual cross-sectional surveys (2022–2025) targeting active embalmers in the United States, Canada, the United Kingdom, Australia, and New Zealand.

The aim of their study was to record, via anonymous surveys, the frequency of reported sightings of these strange white fibrous structures, the percentage of corpses impacted, and the timeline of their initial appearance.

Starting in 2020–2021, embalmers and funeral directors from various countries began to notice “large, tough, rubbery white or off-white fibrous structures in the veins and arteries of embalmed corpses,” which they identified as being different from traditional postmortem clots. These structures were described as “larger, more extensive, tougher, and different in color and handling from traditional chicken-fat or currant-jelly clots.” Some measured several inches to more than a foot long, occasionally reaching the length of a limb.

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COVID Vaccine in Early Pregnancy Led to Higher Rates of Two Birth Defects

A new study from Iran found that two rare birth defects — atrioventricular septal defects and cleft palate — occurred more often in infants whose mothers received an aluminum-containing COVID-19 vaccine during the first 12 weeks of pregnancy compared with mothers who received the vaccine later or not at all.

A new study from Iran found that two rare birth defects — atrioventricular septal defects (AVSD) and cleft palate — occurred more often in infants whose mothers received a COVID-19 vaccine during the first 12 weeks of pregnancy compared with mothers who received the vaccine later or not at all.

Unlike studies conducted in the U.S. and Europe, none of the women in the Iranian study received mRNA vaccines — however, all of the COVID-19 vaccines available in Iran contain 0.25-0.50 milligrams of aluminum adjuvant, Children’s Health Defense Senior Research Scientist Karl Jablonowski told The Defender.

Shots containing aluminum are not typically recommended for pregnant women in their first trimester, Jablonowski said.

Participants in the new study received either inactivated-virus or viral-vector COVID-19 vaccines. Researchers anonymized the specific vaccine brands “due to ethical and regulatory constraints.”

Other Iranian studies indicate that China’s Covilo, also known as Sinopharm, is the most commonly administered COVID-19 vaccine in Iran. That shot, Coviran Barkat, and the India-produced Covaxin were available in Iran at the time of the study.

The study, published last month in Sage Open Medicine, analyzed 1,352 pregnancies from two Iranian cities between 2022 and 2023.

Researchers compared three groups: 303 women who received no COVID-19 vaccine during pregnancy, 262 women who received at least one dose between conception and 11 weeks, 6 days of gestation — the window when fetal organs form — and 787 women vaccinated after the first trimester.

The authors said they were motivated by a gap in the research: COVID-19 vaccination is widely recommended for pregnant women worldwide, yet few studies have examined the link between early-pregnancy vaccination and birth defects.

“Research assessing whether these vaccines could influence embryonic development is crucial,” they wrote.

The authors cautioned that their findings are preliminary, based on small numbers of cases, and do not establish that vaccination caused the birth defects.

Jablonowski agreed that the study can’t establish causation but said it offers a starting point.

“It can generate hypotheses, and with this study, we’ve been handed a really good argument to start generating hypotheses,” particularly about vaccines that contain aluminum adjuvants.

Birth defects rare, but more common among women vaccinated in first trimester

Researchers evaluated birth defects detected during routine prenatal ultrasound examinations performed between 18 and 20 weeks of pregnancy between 2022 and 2023 among women in two major Iranian cities.

Demographic and pregnancy characteristics were relatively balanced across the groups, as were previous COVID-19 infection rates.

Although birth defects were uncommon overall, the researchers found that women vaccinated during the first trimester had babies who had them at higher rates.

Among the findings:

  • Six cases of AVSD, a congenital heart defect, occurred in the first trimester, compared with none in the unvaccinated group and one in the group of women who received the vaccine after the first trimester.
  • Two cases of cleft palate occurred among women vaccinated before 12 weeks, compared with no cases in either comparison group.

The study did not capture spontaneous abortions occurring before routine ultrasound screening, or pregnancies terminated before anomaly scans, the authors said.

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Another MAHA Betrayal: Trump’s Nominee for CDC Director Calls mRNA Technology ‘Safe and Effective’

When asked at a U.S. Senate hearing whether she thinks mRNA vaccines are safe and effective, Centers for Disease Control and Prevention (CDC) director nominee Dr. Erica Schwartz replied, “I do believe that mRNA technology is safe and effective.”

Both the question and the answer show a serious lack of scientific understanding.

Here’s the scientifically accurate answer to the question: We don’t know the full safety profile of either of the two types of approved mRNA vaccines or the technology. First, It’s all too new. Second, we’re not even collecting the full data.

Read on for details.

According to U.S. Food and Drug Administration (FDA) scientists and other experts in the field, comprehensive safety data isn’t known until a new drug (including vaccines) has been on the market and in widespread use for 7-12 years.

Even now, we aren’t getting full information on safety profiles because the data isn’t even being collected in the comprehensive manner required for accurate analysis.

The established scientific process requires that all illnesses after vaccination be meticulously recorded regardless of whether a patient or doctor thinks the illness is actually connected to the vaccine.

Most doctors are not following the process. Some misunderstand. Others are willfully ignoring. And no authority is ensuring they do their job.

Doctors typically aren’t even asking their ill patients whether they had an mRNA vaccine (for COVID-19 or RSV), which one(s), and when. So they aren’t collecting that crucial data.

Most people, including physicians, don’t understand that patients being treated for any illness are supposed to be queried.

This means, for example, someone who comes to the ER with a retinal detachment should be asked if he had a COVID-19 vaccine, which one, how many, and when, and then the data should be reported to the Vaccine Adverse Event Reporting System (VAERS).

Same with someone who becomes sick with a rash, headaches, tendon rupture, stiff neck, depression or chest congestion. Everything.

Even when patients do tell a physician they think an illness might be vaccine-related, the physician frequently, improperly, determines on the front end that he doesn’t need to report the possible adverse event to the established database unless he thinks it’s connected to the vaccine. That’s not how the system works.

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The Official Louisiana State Data Has No Other Explanation: US Childhood Vaccines Are Increasing Infant Mortality

Executive summary

This is it. This is the big one. Finally.

This is the story of the most damaging childhood vaccine study ever done.

I asked all four major AI engines to predict the outcome before showing them the results. All four said the same thing: the OR will be <1 and there will be minimal sex differences.

The actual result: OR >1 in 54/55 subgroup analyses and massive sex differences.

You would simply never see these results if the childhood vaccines were safe.

Nobody can explain the relatively higher deaths in the vaccinated cohorts if they were not caused by the vaccines. They all try to deceive you into believing the study methodology is subject to confounders and should be considered unreliable.

There are 3 biases that impact this study:

  1. Selection bias: The healthy vaccinee effect moves OR < 1 so that doesn’t explain the signal.
  2. Immortal time bias: This was caused by requiring everyone to be vaccinated before they die. Thus, if all kids are never vaccinated <60 days, then the unvaxxed group cannot die until they’ve been vaccinated. This was a big oversight in the paper. It might move OR > 1 depending on the data. If most all kids had their first vaccine < day 60 like their HepB vaccinate at birth, then this bias makes no difference. I’ve made the study authors aware of this. The limitation can be corrected by requiring a vaccination record match found prior to the landmark date (day 90).
  3. Right truncation bias: This affects only the Vaxelis group because Vaxelis was only available starting in 2021 so these recipients had less time to die than the unvaccinated group. This inflates the OR for the vaccinated group, but even after correction, it’s still a problem. I’ve made the study authors aware of this.

All Bradford Hill causality criteria are satisfied. So this isn’t just correlation. This is CAUSATION. The sex signal is not subject to any of the biases identified above.

This means that the recommended vaccines for 2 month old kids are unsafe.

There is no credible way to attack this study.

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Moderna Injects First Participant With Experimental mRNA-4200 Cancer Shot That Forces the Body to Produce Seven Undisclosed Tumor Proteins

On Thursday, Moderna announced that it has injected the first participant in a Phase 1 clinical trial of mRNA-4200 (NCT06880549), an experimental mRNA product that causes the body to produce seven undisclosed tumor proteins following administration.

In other words, the product does not merely introduce tumor proteins into the body—it uses the body itself to manufacture them.

On purpose.

The study raises obvious safety and informed-consent questions about how long the body produces the purportedly encoded tumor proteins, what their long-term biological effects may be, and whether the product or its outputs could be shed from the original recipient onto others through exosomes or extracellular vesicles in excreted bodily fluids.

A 2021 Journal of Extracellular Vesicles study found that cells expressing a target protein can release extracellular vesicles that “carry” that protein, demonstrating that what is produced inside the body can be exported outside the cell in membrane-bound particles.

A separate 2023 Pharmaceutics review explains that exosomes are natural transport vesicles that carry proteins and nucleic acids throughout the body and are present in bodily fluids including blood, saliva, and other secretions—meaning they are not confined to the original cell or even the original location in the body.

You can contact Moderna here and the FDA here.

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Bipartisan Bill Would Move COVID Vaccine Injury Claims Into VICP in Biggest Reform Push in Decades

U.S. House of Representatives lawmakers on Tuesday introduced bipartisan legislation to overhaul the National Vaccine Injury Compensation Program (VICP), proposing to move pending COVID-19 vaccine injury claims into the program.

The Vaccine Injury Compensation Modernization Act would transfer covered COVID-19 vaccine injury claims from the Countermeasures Injury Compensation Program (CICP) into the VICP.

The bill would also update compensation limits, expand vaccine coverage and increase the number of officials who decide claims.

React19, a nonprofit that advocates for people injured by COVID-19 vaccines, called the proposal the “most significant effort in decades to restore fairness to America’s vaccine injury compensation system.”

“For React19’s community, the bill represents far more than a policy proposal,” the organization said. “It represents hope.”

React19 co-founder Brianne Dressen said the legislation reflects years of advocacy by people who felt they had been forgotten.

“Today is the culmination of years of relentless advocacy by people who refused to let their injuries be ignored,” Dressen said. “This legislation sends an important message: every American deserves to be heard.”

House Ways and Means Committee members Lloyd Doggett (D-Texas) and Lloyd Smucker (R-Penn.) introduced the bill.

‘Everybody knows someone who has been injured now’

Wayne Rohde, a longtime vaccine injury compensation advocate and author who has written extensively about the VICP, said the bill addresses an issue lawmakers can no longer ignore.

“We need to address the injuries caused by the COVID vaccine,” Rohde told The Defender. “If we’re going to have a viable vaccine policy in the U.S., if we do not compensate those who have been injured, [then in] the next pandemic, you will see a complete withdrawal from the public to accept any countermeasures because everybody knows someone who has been injured now.”

At the same time, Rohde said he has reservations about moving COVID-19 vaccines into the VICP because the legislation could bring additional vaccines developed with similar mRNA technology into the program.

“I have concerns about the technology used to develop it, and that it will allow traditional vaccine manufacturers to use that same technology for other vaccines covered in the program,” he said.

He also noted that the bill would expand VICP coverage to additional adult vaccines.

“If they add RSV, shingles and dengue, what that tells me is that the next vaccine down the pike will be swept into program, too,” Rohde said.

The VICP currently covers only those vaccines the Centers for Disease Control and Prevention recommends for routine administration to children and pregnant women.

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