Tag: vaccines

Amyloidogenic Fibrin Microclotting Following Prenatal mRNA Vaccination Exposure

Scientific investigations involving emerging and potentially paradigm-shifting findings often walk a difficult line between the need for caution and the imperative to inform. While early publication of case studies carries inherent risks—such as overinterpretation of individual data points or lack of statistical power—it also provides critical, time-sensitive insight that can drive new lines of inquiry and inform ongoing clinical and public health decisions.

This report forms part of a rolling, real-time investigation into the proteopathic and vascular consequences of prenatal exposure to mRNA-based SARS-CoV-2 vaccines. The intention is not to draw definitive epidemiological conclusions at this stage, but to publicly document the emergence of novel findings as they occur. This transparent approach is particularly important in areas where existing safety literature has not yet integrated proteomic misfolding or amyloidogenic biomarker screening into its framework.

This investigative format mirrors the best practices seen in real-time pathogen tracking and pharmacovigilance. In such contexts, timeliness and transparency are essential for mitigating long-term risk and prompting refinement of public health frameworks.

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Former Japanese Minister of Internal Affairs proves he has developed cancer from the covid “vaccines”

Kazuhiro Haraguchi gained international attention a year ago when he gave a rousing speech at a protest against the World Health Organisation held in Tokyo, Japan. During his speech, he recounted his own battle with cancer shortly after receiving the mRNA injections. “Two out of the three supposed vaccines I received were lethal batches,” he stated. 

He then apologised for the Japanese government’s covid “vaccine” campaign and expressed his grief for those who succumbed to vaccine-related deaths.  “I apologise to all of you. So many have died, and they shouldn’t have,” he said.

“When I travel around to different areas, I see those who can’t stand, can’t walk, can’t go to school, can’t go to work. We could have prevented these injuries from happening, but we did not,” he added.

On Monday, he tweeted the following:

This is an analysis of my cancer cells. It was determined that the malignant lymphoma had metastasised to the tonsils, but the lesions were removed and sent to a research facility.

Even two years after receiving the covid-19 vaccine, spike proteins were found in the malignant lymphoma. Conversely, N proteins were not detected. This indicates that I had not been infected with covid-19.

We must put an end to the tragedies caused by the covid-19 vaccine as soon as possible.

This data is planned to undergo further detailed analysis and will be used for a research paper.

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Twin Babies Die a Week After Receiving 3 Vaccines, Police Interrogate Parents

When Andrea Shaw brought her 18-month-old twins in for their wellness visit on April 23, she told the pediatrician she had concerns about the twins receiving the flu shot because her husband’s family had a history of adverse reactions to the vaccine.

The pediatrician told her the babies would be OK and had nurses give the twins the shot. The twins also received the Hepatitis A vaccine and the DTaP (diphtheria, tetanus, pertussis) vaccine.

Roughly one week later, on May 1, Andrea found the babies — a girl named Dallas and a boy named Tyson — dead in their bed after apparently passing away in their sleep. Her husband, Nathaniel, the twins’ father, was at work at the time.

Police in Payette, Idaho, where the twins lived with their parents, launched a homicide investigation, which they said was standard procedure when a death from an unknown cause occurs.

On May 7, the local police chief told the media the deaths hadn’t been “definitively” ruled as homicides, and that the autopsy reports would provide more information. The investigation is still ongoing.

A spokesperson for the parents today said the lead detective is still waiting on toxicology reports and has not yet ruled out the parents as suspects. The parents, who are “beyond devastated,” the spokesperson said, have filed a report with the Vaccine Adverse Event Reporting System, or VAERS.

In an interview with Children’s Health Defense’s (CHD) Polly Tommey, Andrea and Nathaniel walked through the timeline of what happened in the days leading up to their children’s tragic deaths.

Before starting the interview, Tommey, CHD.TV program director, told viewers she was speaking with the twins’ parents only three days after the children passed.

“This is really, really raw,” Tommey said. “This has just happened.”

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Moderna Pulls Application for FDA Approval of Flu-COVID Shot After FDA Calls for New Clinical Trials

Moderna is withdrawing its application for U.S. Food and Drug Administration (FDA) approval of its mRNA-1083 combination flu and COVID-19 vaccine, the company announced today — just one day after the FDA said it would require new clinical trials to approve COVID-19 boosters for healthy people under 65.

According to Fierce Biotech, the company will resubmit its application when data from a Phase 3 trial of its mRNA-1010 flu vaccine, which is a component of the combined shot, are available later this year. The company expects to have interim data from the trial available this summer.

Markets reacted negatively to the news, with Moderna’s shares falling 1.4% in premarket trading on Wednesday, The Guardian reported.

According to Reuters, Moderna’s decision to withdraw its application at this time “is the latest sign of increased regulatory scrutiny of the vaccine approval process since Robert F. Kennedy Jr. took the top U.S. health job earlier this year.”

Last week, for instance, the FDA approved Novavax’s new COVID-19 vaccine, but limited its approval to groups that are considered high-risk.

Sayer Ji, co-founder of Stand for Health Freedom and founder and director of GreenMedInfo, said Moderna’s decision to withdraw its application is “telling” and “appears to reflect not only concerns over efficacy but also a growing public skepticism toward hastily developed, multi-antigen formulations that lack sufficient long-term safety data.”

Ji said:

“The withdrawal may be a preemptive move to avoid public scrutiny or regulatory resistance tied to unresolved questions in their clinical data. Combination shots, especially those involving mRNA platforms, introduce compounded risks due to the simultaneous delivery of multiple immunogenic agents.

“These risks are poorly understood and grossly under-evaluated, particularly in vulnerable populations. The immunological complexity of such a vaccine also raises questions about long-term impacts on immune regulation, potential autoimmunity and unintended synergistic effects that could compromise health rather than protect it.”

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FDA Forces Moderna and Pfizer to Admit Covid “Vaccines” Cause Lasting Heart Damage in Young Males

For years, parents and medical professionals have sounded the alarm about the dangerous link between mRNA COVID-19 vaccines and heart inflammation in young males—only to be dismissed as “anti-vaxxers” or conspiracy theorists. Now, in a stunning reversal, the U.S. Food and Drug Administration (FDA) has ordered Pfizer and Moderna to strengthen their warning labels, finally admitting that these shots can cause long-lasting heart damage, particularly in adolescent boys and young men.

But this admission comes far too late—after millions of doses were administered under false pretenses, after countless young lives were altered by myocarditis, and after public health agencies actively suppressed the truth. The FDA’s belated action raises a critical question: How many more injuries could have been prevented if the government had prioritized transparency over blind vaccine promotion?

Key points:

  • The FDA has mandated that Pfizer and Moderna update their COVID-19 vaccine labels to include stronger warnings about myocarditis and pericarditis, particularly in males aged 16 to 25.
  • New data reveals that myocardial injury is often long-lasting, contradicting earlier CDC claims that heart inflammation “tends to resolve quickly.”
  • The highest incidence of myocarditis occurs in young males, with 38 cases per million doses—far higher than previously acknowledged.
  • Internal government emails show that health officials deliberately avoided warning the public about these risks, even after detecting safety signals in 2021.
  • The FDA’s action follows a Senate investigation exposing how federal agencies downplayed and hid vaccine injuries.

A long-overdue admission of harm

For years, independent researchers and medical professionals warned that mRNA vaccines posed a disproportionate risk to young, healthy individuals—especially males. Yet, public health agencies dismissed these concerns, insisting that the benefits outweighed the risks. Now, the FDA has been forced to acknowledge what health freedom fighters have said all along: These vaccines can cause serious, sometimes permanent, heart damage.

The updated labels must now state that myocardial injury is common among those who develop post-vaccination myocarditis, with data showing persistent damage five months after vaccination. This directly contradicts the CDC’s previous assurances that cases were “mild” and “resolved quickly.”

Why did it take so long? Internal documents obtained through FOIA requests reveal that as early as May 2021, the CDC and FDA considered issuing a public warning but ultimately chose silence over transparency.

The suppression of truth and the cost of deception

The Senate’s Permanent Subcommittee on Investigations recently released a damning report exposing how federal health agencies systematically concealed the myocarditis risk linked to COVID-19 vaccines. Internal emails reveal that officials engaged in a coordinated cover-up by refusing to update the V-safe reporting system to include cardiac symptoms, ensuring countless cases were never documented. Additionally, they blocked a planned Health Alert Network warning that would have alerted doctors and the public to the dangers, prioritizing public perception over transparency.

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Trump DOJ stings conservatives with positions on abortion pill regulation, vaccine trial integrity

The Trump Justice Department is continuing its predecessor’s legal arguments against lawsuits by red states against abortion pills by mail and a whistleblower’s case against the drugmaker Pfizer, creating two unexpected setbacks for causes championed by conservatives.

The Food and Drug Administration is at the center of both disputes.

Idaho, Missouri and Kansas argue the FDA’s deregulation of the abortion pill mifepristone violated those states’ abortion restrictions. Meanwhile, the clinical trial whistleblower Brook Jackson’s lawsuit alleges fraudulent data was used to grant emergency use authorization to Pfizer’s COVID-19 vaccine.

The government first stayed out of the False Claims Act case filed four years ago by Jackson, who oversaw Pfizer’s outsourced Phase 3 trials in Texas, even though it had the power to dismiss because Jackson is a “relator” suing on the federal government’s behalf.

It then supported Pfizer’s motion to dismiss, arguing the FDA would have approved the vaccine even if 3% of data were fraudulent, as Jackson claims from her test sites.

The FDA unsuccessfully asked a court for 55 years to fully release its Pfizer vaccine approval documents. The Centers for Disease Control and Prevention admitted three years ago hiding the vast majority of its COVID data in part to protect the reputation of vaccines.

“We’re simply asking DOJ to step aside and let us handle Pfizer,” Jackson wrote on X in explaining the Trump DOJ’s continuation of its predecessor’s posture. “We don’t need their help—we just need them out of the way.”

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Dr. McCullough Drops the Hammer in the Senate — FDA Concedes with Expanded Myocarditis Warning

“When a product causes death, that demands a black box warning — immediately.”

That was the clear and urgent message from Dr. Peter McCullough, testifying before the Senate Homeland Security and Governmental Affairs Committee this week at a hearing titled: “The Corruption of Science and Federal Health Agencies: How Health Officials Downplayed and Hid Myocarditis and Other Adverse Events Associated with the COVID-19 Vaccines.”

Dr. McCullough presented data from both his clinical experience and the peer-reviewed literature, exposing the widespread risks of COVID-19 mRNA injections — particularly myocarditis in young men and fatal vaccine outcomes confirmed by autopsy.

“I’ve examined thousands of patients with this problem,” he told the Senate. “Before the pandemic, I had seen just two cases in my entire career.”

Just one day before the hearing, likely for preemptive damage control purposes, the FDA quietly updated its myocarditis warning on Pfizer and Moderna’s COVID-19 vaccines, expanding the risk category to males aged 16 to 25 and citing an incidence of 8 cases per million doses for the 2023–2024 formulations. Unfortunately, no mention of death was added — despite robust, peer-reviewed autopsy evidence confirming fatal vaccine-induced myocarditis.

Dr. McCullough referenced multiple such cases, including the tragic findings of Gill et al, who documented two teenage boys (ages 16 and 17) found dead at home just days after receiving the Pfizer vaccine. Autopsies confirmed unequivocal myocarditis as the cause of death.

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The Century of Evidence Vaccines Cause Sudden Infant Death Syndrome

•Since at least 1933, the medical community has known that vaccines cause infant deaths. To conceal this, those deaths were renamed “crib death” and then “Sudden Infant Death Syndrome” (SIDS), eventually being attributed to infants not sleeping on their backs.

•This revisionism is not supported by the existing evidence nor the historical changes in the frequency of SIDS. Most recently, SIDS rates have had an unprecedented decrease in tandem with the COVID-19 lockdowns reducing vaccination rates.

•The vaccine most strongly associated with SIDS, DPT, was protected for decades by the government despite knowing a large body of evidence around the world showed it killed infants—particularly when an inevitable hot lot was released. Eventually, so many injury lawsuits were filed that in 1986, the government had to give blanket immunity to the vaccine manufacturers.

•This article will concisely review the vast body of evidence showing vaccines cause SIDS and reveal the mechanism modern research has now repeatedly proven causes vaccines to trigger infant death.

We’re always told that vaccines were a medical marvel that safely ended the dark age of infectious disease. However, when the actual records are examined, they often abjectly failed to prevent those diseases, and worse still, frequently caused outbreaks and severely injured many of the recipients.

This in part resulted from the inherent toxicity of vaccines and in part because manufacturing challenges regularly resulted in hot lots being released. Rather than address this, the vaccine industry chose to create a variety of strategies to conceal those issues, such as enshrining the dogma “all vaccines are safe” and giving blanket legal immunity to all the “safe” vaccines.

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Vaccine Side-Effects: Democrats Lied, Thousands Died

So now we learn not only that Joe Biden has Stage Five prostate cancer, but that starting in February 2021, the POC/LGBTQ committee that was operating Biden like a Muppet concealed, then downplayed the risk of heart disease from the COVID vaccines.

It’s funny how we find out all this dirt, within 48 hours after the committee’s announcement about Joe’s cancer.  Because he’s got a few months to live, he’s now officially the “Fall Guy.”

Everything bad can be blamed on him, if it can’t be blamed on Trump.  All the Muppeteer committee members can pretend they’re innocent and resume their White House and Cabinet posts on January 20, 2029 if the Democrat party Deep State (DPDS) steals another presidential election.

From Daily Wire:

According to the report from the Senate Permanent Subcommittee on Investigations, officials knew as early as February 2021 that the vaccines were associated with myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the thin sac surrounding the heart). Still, they waited to warn the public until June as they pushed the vaccine on Americans.

The report concludes that U.S. health officials “knew about the risks of myocarditis,” “downplayed the health concern,” and deliberately “delayed informing the public about the risk.”

Sen. Ron Johnson (R-WI), who chairs the committee and will lead a hearing on it later this afternoon, told The Daily Wire that Biden officials delayed reporting the side effects because they were concerned about “vaccine hesitancy.” 

“But in being concerned about that, they violated the inviolable principle of informed consent,” Johnson said.

Here is the full subcommittee report.  This report never would have been prepared if Democrats had kept control of the Senate last fall.  The Subcommittee on Investigations would have been launching new bogus investigations into Team Trump instead.

Spearheaded by Dr. Anthony Fauci, the official diktat of the DPDS was that the vaccines were “safe and effective.”  They knew better.  The Israelis had started distributing Pfizer vaccines several weeks before we did.  So they knew that vaccinated patients were getting myocarditis with alarming frequency, months before we did.
They were warning Joe’s Muppeteer committee, but that committee wasn’t passing on this warning to the American people.

This is another one of Fauci’s many crimes against humanity, the most evil being his funding of gain-of-function research at the Wuhan Institute of Virology, using our tax dollars.  That’s how COVID was unleashed upon the world, causing the deaths of 2 million people worldwide, including a million Americans.

Very few government figures in recent history — Hitler, Stalin, Chairman Mao and Pol Pot, for example — have killed more of their own countries’ people.

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COVID Vaccine “Safe and Effective” Narrative Collapses on Camera

The “safe and effective” narrative collapsed on camera during Senator Ron Johnson’s explosive Senate hearing on COVID-19 vaccine injuries Wednesday afternoon.

Senator Ron Johnson brought the receipts, exposing how the Biden administration DELIBERATELY hid vaccine harms from the public.

Then Dr. James Thorp (OB-GYN) revealed miscarriage data so disturbing, it left the room silent.

This is the Senate hearing they never wanted you to see. I turned three hours of footage into a five-minute read.

Senator Ron Johnson opened the hearing with a bombshell: the Biden administration knew about deadly heart risks tied to the COVID shots, and deliberately kept it from the public.

Johnson released newly subpoenaed records exposing a detailed timeline of what officials knew and when. While Pfizer and Moderna received insider updates, doctors and citizens who raised concerns were silenced.

In February 2021, Israeli health officials warned the CDC of “large reports of myocarditis, particularly in young people” following Pfizer injections, just two and a half months after the vaccine received emergency use authorization.

By April, the CDC was already reviewing myocarditis data from Israel and the Department of Defense. But instead of alerting the public, they stayed quiet.

By the end of that month, VAERS had recorded 2,926 deaths, nearly half of which occurred within three days of injection. “Somebody ought to be looking at it,” Johnson said.

In May, the CDC considered issuing a formal health alert—but scrapped it. They replaced it with watered-down guidance that removed a key warning for doctors to restrict physical activity in myocarditis patients.

Francis Collins, then director of the NIH, brushed it all off. “Senator, people die,” he told Johnson.

In just six months, the toll was staggering: 384,270 reports of adverse events, 4,812 deaths, and 1,736 of those occurred within just 48 hours of injection.

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