Tag: vaccines

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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FDA Directs COVID-19 Vaccine Makers to Expand Heart Inflammation Warning

The Food and Drug Administration (FDA) has directed COVID-19 vaccine manufacturers to expand the warning for two forms of inflammation, according to letters made public on May 21.

The FDA told BioNTech, which produces a vaccine with Pfizer, and Moderna to update warnings regarding myocarditis—or heart inflammation—and the related condition pericarditis.

Richard Forshee, acting director of the FDA’s Office of Biostatistics and Pharmacovigilance, said that new information has emerged, including a 2024 FDA study that found that some myocarditis patients had signs of heart scarring months after vaccination.

The companies must update labels to state that following administration of the 2023–2024 versions of the vaccines, “the highest estimated incidence of myocarditis and/or pericarditis was in males 16 through 25 years of age,” Forshee said. The highest estimated incidence of the post-vaccination inflammation is about 38 cases per million doses for both vaccines, according to the proposed update.

The current warnings say that the highest observed risk after Moderna vaccination is in males aged 18 to 24 and that the highest risk after Pfizer-BioNTech vaccination is in males aged 12 to 17.

The companies were also directed to add new information summarizing the FDA study, including that “at a median follow-up of approximately 5 months post-vaccination, persistence of abnormal cardiac magnetic resonance imaging (CMR) findings that are a marker for myocardial injury was common.” The updates should also state that “it is not known if these heart MRI findings might predict long-term heart effects of myocarditis,” according to the letters.

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Another “Conspiracy Theory” PROVEN TRUE about mRNA CLOT SHOTS reveals tricked human cells keep producing DEADLY SPIKE PRIONS indefinitely

We called it at the beginning, when Big Pharma and the CDC were lying through their teeth, claiming that the mRNA “technology” would only have your cells create spike proteins for a short amount of time, just long enough for your immune system to create antibodies, and then end the production of the virus-mimicking prions. Big fat lie.

First off, the prions don’t just remain at the site of injection. That was a lie. The spike protein prions spread throughout the vascular system, invade the cleansing organs, the brain and the ovaries, and use light to join together to form white, rubbery clots that drive all-cause mortality rates to skyrocket.

Clot shots altered the injected humanoids to be walking prion factories who are dying of all-cause mortality that all boils back to the mRNA Trojan Horse “technology”

Millions of nanoparticles are created by tricked cells for indefinite periods of time, possibly forever, and the injected humanoids around the globe are suffering mass health detriment. That’s right, Moderna and Pfizer clot shots hijack the immune cells, rewrite your DNA and RNA, and prolong spike protein prion production POSSIBLY FOREVER, in the shortened life of the billions of gene-altered humans who succumbed to the plandemic scam. What a shame.

A groundbreaking study published in Nature has upended long-standing assurances from health authorities that mRNA COVID-19 vaccines quickly degrade in the body. Instead, the research reveals that Pfizer and Moderna shots reprogram immune cells to extend their genetic instructions, forcing prolonged spike protein production — contrary to official claims that effects would last only “a few weeks.” The findings, led by Polish researchers (Krawczyk et al., 2025), expose a hidden mechanism that could have serious long-term health implications, raising urgent questions about safety, transparency, and regulatory oversight.

The study found that immune cells, particularly macrophages, activate an enzyme called TENT5A in response to mRNA vaccines. This enzyme rewrites the vaccine’s genetic code, doubling the length of its poly(A) tail — a molecular timer that determines how long mRNA survives. In some cases, Moderna’s mRNA tail extended from 100 to 200 nucleotides, drastically prolonging spike protein production.

“This wasn’t just persistence—it was amplification,” said Dr. Peter McCullough, a cardiologist and vaccine safety advocate. “The body is essentially tricked into editing the shot’s instructions to make it last longer. This was never part of the clinical trials.”

Public health officials, including CDC advisor Dr. Paul Offit, previously asserted that spike protein production would last only “a couple of weeks.” Yet studies have since detected spike protein in blood samples for up to 709 days post-injection. Moderna’s own 2024 internal documents acknowledged “unacceptable toxicity” risks, yet regulators fast-tracked the shots without addressing these concerns.

Molecular biologist Dr. Jessica Rose likened the process to “giving someone a self-replicating memo. The memo was supposed to be read once and discarded. Instead, the recipient photocopies it endlessly.”

Unlike mRNA vaccines, Novavax’s protein-based shot — which delivers pre-made spike protein — does not trigger TENT5A activity. Immunologist Dr. Byram Bridle explained, “The lipid nanoparticles in Pfizer and Moderna’s shots are the Trojan horse. They smuggle synthetic mRNA into cells, but the payload doesn’t just fade away — it gets enhanced by the immune system.”

The Nature study challenges the foundational safety claims of mRNA vaccines, revealing a mechanism that could lead to prolonged spike protein exposure and unknown health risks. With mounting evidence of regulatory oversights and undisclosed dangers, the findings demand urgent scrutiny. As the scientific community grapples with these revelations, millions who received the shots now face unanswered questions about their long-term well-being. The era of blind trust in rushed medical interventions may be over—but for many, the consequences are just beginning.

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