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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US officials delayed warning public about heart inflammation risk from COVID shot: report

U.S. health officials knew about the risks of myocarditis from COVID-19 vaccines but downplayed the concern and delayed informing the public about the risks of taking the jab — that is according to a new Senate report released by Sen. Ron Johnson Wednesday.  

Johnson, R-Wis., chairman of the Senate Permanent Subcommittee on Investigations, has been investigating the safety and efficacy of the COVID-19 vaccines. Earlier this year, he subpoenaed the Department of Health and Human Services (HHS) for records relating to COVID-19 vaccine safety data and communications about the pandemic. 

The interim report, spanning 55 pages, obtained and reviewed by Fox News Digital, revealed that Biden administration officials “withheld crucial health information from the Subcommittee and the public.” 

Since 2021, Johnson has sent more than 70 oversight letters, which he says were “either completely ignored or inadequately addressed.” 

The report highlights the records Johnson has obtained pursuant to the subpoena from the new, Trump administration-led health agency. Specifically, the report focuses on HHS’ awareness of and response to cases of myocarditis—a type of heart inflammation—following COVID-19 vaccination.

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Texas House OKs Bill To Sue Vaccine Makers for False Ads

In a major victory for accountability and informed consent, the Texas House of Representatives passed HB 3441 yesterday, a bill that would allow Texans to sue vaccine manufacturers whose advertising leads to injury or harm.

The unprecedented move comes as CDC data show there have been an alarming 2,665,796 adverse events linked to vaccines since 1990, the vast majority related to COVID-19 jabs.

But if fewer than 1% of adverse events are reported – as a 2010 HHS-funded Harvard analysis confirms – the real number could exceed 266 million, or roughly 7.6 million per year, or 20,800 per day.

First filed in February, the new bill passed yesterday by a vote of 88–31, moving the legislation one step closer to becoming law.

The pioneering legislation boasts a whopping 79 brave sponsors, 74 Republicans and 5 Democrats.

The bill is spearheaded by Representatives Shelley Luther (R-62), Jeff Leach (R-67), Marc LaHood (R-121), Oscar Longoria (D-35), and Mike Schofield (R-132).

If you want this kind of bill passed in your state or at the federal level, you can find your local, state, and U.S. representatives here and let them know.

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Jim Jordan probes politics of Pfizer COVID vax trial as research suggests jabs hurt fertility

The political pressures around clinical trials for COVID-19 vaccines in the 2020 presidential campaign first drew scrutiny from Democrats, with then-nominees Joe Biden and Kamala Harris spreading mistrust of Operation Warp Speed and suggesting they would avoid jabs developed in the Trump administration.

The parties largely switched sides in the Biden administration, with then-Vice President Harris claiming it was “starting from scratch” on a vaccine strategy and even mandating vaccinations for her own campaign employees once she replaced Biden at the top of the 2024 ticket.

Yet Republicans have continued claiming Operation Warp Speed saved millions of lives based on modeling studies, amid five years of global research on severe adverse events in certain groups following COVID vaccination, from heart inflammation to neurological disorders, and the jabs’ mediocre-to-negative performance against infection.

House Judiciary Committee GOP leaders seized on new evidence Thursday that Pfizer withheld what it considered positive trial results until after the 2020 election, with the result that President Trump couldn’t take credit for a finished vaccine, giving Republicans something to unite around amid internal divisions over the pace of reversing Biden’s COVID vaccine policies.

The Department of Health and Human Services is reportedly planning to stop recommending routine COVID vaccines for pregnant women, teens and children, more than 100 days into the Trump administration and after new peer-reviewed research suggests COVID vaccines worsen fertility and mRNA jabs specifically can produce spike protein for up to eight months.

Yet another peer-reviewed study this year, published in the Endocrine Society’s Journal of Clinical Endocrinology and Metabolismfound the risk of underactive thyroid “significantly increased from 6 to 12 months” after vaccination, and that both under- and overactive thyroid was “significantly elevated at 12 months” for mRNA vaccine recipients specifically.

The Taiwanese researchers “used a huge database, carefully matched vaccinated and unvaccinated patients, and followed outcomes for a full year,” former New York Times drug industry reporter Alex Berenson wrote. “That combination gave the study very strong statistical power, meaning that its findings are probably not the result of chance.”

“25,000 children a day are getting the latest version of the mRNA shot,” Texas doctor Mary Talley Bowden, an early victim of COVID treatment policing whose litigation prompted the FDA to stop demonizing ivermectin on social media, wrote on X Friday.

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Defense Health Agency Must Not be Allowed to Thwart an Honest Investigation Into COVID-19 Shot Injuries, Say Those Who Witnessed the Devasting Effects Firsthand

Secretary of Defense Pete Hegseth’s efforts to restore the military are appreciated, but those injured by the COVID-19 shot are feeling abandoned.

After being forced to take two doses of the Moderna COVID-19 shot to remain in the Army in 2021, Karolina Stancik, now 25 years old, has suffered three heart attacks, a stroke, an emergency pacemaker surgery, neurological maladies, the contemplation of suicide, and other adverse events. In October 2023, it was determined that her debilitating heart injury did, in fact, occur “In Line of Duty” and was linked to the shot.

Retired Navy Medical Service Corps officer Lt. Ted Macie told The Gateway Pundit he is not surprised.

As the whistleblower who exposed a significant rise in incidents of myocarditis, pulmonary embolism, ovarian dysfunction, and more across the Department of Defense (DoD) following former Defense Secretary Lloyd Austin’s now-rescinded 2021 COVID-19 shot mandate, he said, “I know others who were injured from the shot, and I know people who died from it—and the latter can’t even claim to be vax injured because they’re no longer here to do so.”

On the heels of Defense Secretary Hegseth determining that the shot was “unlawful as implemented,” TGP spoke to Stancik. She wants Hegseth to acknowledge “someone’s unlawful actions caused injury … severe injury … and even death.”

The former member of the Army National Guard questions “what will be done about the unlawful actions that caused grave injury, destroyed lives, and even led to death in some cases?”

What support is there for people like her? And what consequences will there be for those who unlawfully implemented the shot?

She admitted that not every person who supported the shot mandate knew it was unlawful, but after the advice of countless service members facing separation informed them, many willfully violated the law.

The author of this article has reviewed dozens of Religious Accommodation Requests that also spelled out the illegalities of the COVID-19 shot mandate to their chain of command.

For example, service members, including Stancik, expected but did not receive informed consent, nor were they ever offered a “vaccine” approved by the Federal Drug Administration.

Rather, they were subjected to an experimental shot approved for emergency use only and were told they “might have some cold symptoms” as a result.

So, as one example, what about the military leaders that knowingly violated the law after being fully informed about 10 U.S.C. § 1107a at the start of the mandate? “We have to start with proper investigations to find out who they were,” Stancik pleaded. “My patient rights, my human rights, were violated at minimum.”

And if SecDef Hegseth genuinely believes the mandate was “unlawful as implemented,” she said, “a crime has been committed and there must be Uniform Code of Military Justice (UCMJ) action taken against those who broke the law.”

There must be a penalty for their actions, even some that might lead to courts-martial.

“Despite the fact they broke the law,” Stancik said, “we cannot violate their rights and deny due process in return. We must act lawfully to correct this.”

For her, it is imperative for people to understand “a lot of our lives have been completely destroyed by what people claimed for a few years to be lawful.”

If this is truly no longer the case, injured service members are waiting in the background for SecDef Hegseth to publicly address the issue of the physical harms the mandate caused.

“At the end of the day, there’s so many people who lost their jobs, kicked out of the military,” Stancik shared. “But it’s not just the people who lost their jobs; there are injured service members who are being ignored,” she lamented.

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Thirty-Five People Died the Same Day as Their Covid Shot – But Authorities Did Not Investigate

Australians are routinely assured that deaths arising from Covid vaccination are vanishingly rare, based on the drug safety regulator’s claim that it has identified only 14 deaths linked to vaccination out of more than 70 million doses given.

The other thousand plus deaths reported to the Therapeutic Goods Administration’s (TGA) safety surveillance database, the DAEN, are widely assumed to be merely coincidental, and the TGA has encouraged this perception, frequently asserting that “most deaths that occur after vaccination are not caused by the vaccine”.

Moreover, the TGA gives the impression that all reported deaths are thoroughly investigated, stating that “the TGA closely reviews all deaths reported in the days and weeks after COVID-19 vaccination”.

However, new documents released under Freedom of Information (FOI) laws and obtained by Canberra Daily suggest that the public has been misled.

Contrary to widespread belief, the documents show that the TGA does not thoroughly investigate every death reported to the DAEN. This is even the case where people died on the same day that they received their Covid shot.

Canberra Daily can reveal that out of 35 reports of Australians whose deaths occurred on the same day as their Covid vaccination, the TGA completed a causality assessment for only 24. The remaining 11 deaths had no causality assessment report available.

Further, not a single one of these 35 ‘day zero’ deaths was referred to the Vaccine Safety Investigation Group (VSIG), an expert panel which is supposed to be convened for the most serious adverse events following immunisation (AEFI), especially ones that have the potential to change the benefit-risk balance of a vaccine or to threaten public confidence in vaccine safety.

In correspondence with the TGA, Canberra Daily was additionally able to confirm that the drug safety watchdog has never ruled out a causal link between the vast majority of deaths reported and Covid vaccination.

In fact, all reported deaths are considered by the regulator to be possibly linked to vaccination, despite regular public statements implying the opposite.

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FDA warns seniors to avoid this vaccine after deadly complications

Older adults are being warned against receiving the chikungunya vaccine before traveling.

The Ixchiq vaccination, developed by Valneva to prevent the mosquito-borne chikungunya virus, was approved by the Food and Drug Administration (FDA) in November 2023 as the first of its kind.

The approval applies to anyone aged 18 and older who has a risk of being exposed to the virus.

But the FDA and the Centers for Disease Control and Prevention (CDC) released a safety notice on May 9 recommending that adults over 60 years old pause use of the vaccine due to fatal complications.

“FDA and CDC will continue the evaluation of post-marketing safety reports for Ixchiq,” the release reads.

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