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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COVID-19 mRNA Shots Destroy Over 60% of Women’s Non-Renewable Egg Supply

The study titled, Impact of mRNA and Inactivated COVID-19 Vaccines on Ovarian Reservewas recently published in the journal Vaccines:

Objectives: This study aimed to elucidate the effects of messenger RNA (mRNA) and inactivated coronavirus disease 2019 (COVID-19) vaccines on ovarian histology and reserve in rats.

Methods: Thirty female Wistar albino rats, aged 16–24 weeks, were randomly divided into three groups (n = 10): control, mRNA vaccine, and inactivated vaccine groups. Each vaccine group received two doses (on day 0 and day 28) at human-equivalent doses. Four weeks post-second vaccination, ovarian tissues were harvested for analysis.

Results: Immunohistochemical analysis was performed to evaluate the expression of transforming growth factor beta-1 (TGF-β1), vascular endothelial growth factor (VEGF), caspase-3, and anti-Müllerian hormone (AMH) in ovarian follicles. Both vaccines induced significant increases in TGF-β1, VEGF, and caspase-3 expression, with more pronounced effects in the mRNA vaccine group. Conversely, AMH expression in the granulosa cells of primary, secondary, and antral follicles showed marked reductions (p < 0.001). The counts of primordial, primary, and secondary follicles decreased significantly in the inactivated vaccine group relative to controls and further in the mRNA vaccine group compared to the inactivated group (p < 0.001). Additionally, the mRNA vaccine group exhibited a decrease in antral and preovulatory follicles and an increase in atretic follicles compared to the other groups (p < 0.05). The serum AMH level was diminished with the mRNA vaccination in comparison with the control and inactivated groups.

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Secret recordings with ousted FDA vaccines chief suggest disinterest in documenting vax injury

The Food and Drug Administration’s top vaccine official until late-March met online several times with a COVID-19 vaccine injury group’s leader, who, opposing the vaccines in part, begged him to no avail to take severe adverse events such as paresthesia as a precursor to neuropathy seriously and to urge doctors to treat them as such rather than write them off as “anxiety,” secret recordings suggest.

The Informed Consent Action Network (ICAN) released the videos, compiled on The Real Peter Marks website, with other documentary evidence from Marks’ leadership of the COVID response starting with Operation Warp Speed, at the National Press Club in Washington on Tuesday.

They also include a virtual meeting between San Francisco intensive care unit doctor Patricia Lee, Marks and other FDA officials, who asked no questions after Lee said a patient’s severe complications from vaccination at 22 weeks’ pregnancy and related death prompted a “nervous breakdown” among nurses on her shift, requiring a psychiatrist’s overnight visit.

ICAN CEO Del Bigtree shared pieces of Lee’s Oct. 22, 2021, conversation with FDA officials, who allegedly ignored her pleas for vaccine-injured patients until she brought “legal pressure,” on his show two weeks earlier with ICAN lawyer Aaron Siri and REACT19 founder Brianne Dressen, whose neurological injuries from the AstraZeneca vaccine trial were confirmed by the NIH

Organized as an animated vertical timeline that loads as it scrolls, the Marks website loaded slowly during Just the News’ review Wednesday. “They are receiving a ton of traffic and working on it,” a spokesperson said in the early afternoon.

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Neurodiversity Is A Strawman

A dear friend had a beautiful, healthy, engaged baby boy. After his first round of childhood vaccinations he went blind, non-verbal, started head banging, having seizures, lost all engagement, and fell into the abyss of autism. Today that child is 40. He is incontinent, cannot speak or feed himself, and is totally dependent upon his father to survive. 

Another friend had a son and a daughter. The daughter, following her first round of childhood shots, experienced almost exactly the same scenario described above, minus the blindness. At the time my friend did not connect the dots and when it came time for his son to be vaccinated, the child began to seize. In the room, my friend put it together and stopped the rest of the shots. Today, his son is only mildly autistic while his daughter, at 26, is non-verbal, incontinent, and often uncontrollable. Since the son is only mildly autistic, I suppose we shouldn’t look into the cause of his issues? It’s a gift, right? 

A mother (a client in one of the many tragic cases) had a teenage daughter who, after a round of the Gardasil vaccine, suffered a seizure and went into a coma. The young girl had been captain of her volleyball team, top of her class, poised for a full and happy life. Today, at nearly 20, she lives in total darkness because she has seizures every 30 seconds – cannot have any light. The neurodegeneration is unquantifiable. She cannot read or watch TV, let alone go on her first date, go to prom…experience the life she should have and would have. 

Another friend had a perfect, beautiful young daughter who was exceeding all of her milestones. After her second round of jabs, she locked in, stopped talking or making eye contact, developed a severe learning disability, and is still struggling today, at 6. 

She, too, will never experience the “normal” milestones we all would like to see for our children. 

Those stories, anecdotal though they may be, are the tip of the iceberg. 

I could share thousands, each one worse than the next, that would make most people sit in a room and cry forever.

The media machinery has conflated mild spectrum disorder with what I just described above specifically so that people will have the reaction they are having right now. This is normalization of extremes by conflating them with non-extremes so that it’s a step-by-step incremental (and coordinated) attack on those who would expose the root cause of the terrible suffering experienced by so many.

It’s executed so that people like RFK, Jr. are hobbled from doing their job. 

How does questioning the environmental harms and risk factors for autism and/or neurodegenerative disorders threaten or even conflict with the idea of autism as neurodiversity? Spoiler alert: it doesn’t. 

No other disease has people normalizing a spectrum (no pun intended) of symptoms ranging from terrible to non-debilitating in order to argue that it’s actually great. We don’t say there’s a spectrum of neurodegenerative disorder from paralysis to neuropathy and there are benefits to neuropathy therefore neurodegeneration is great. This is normalization at its best. 

Suddenly everyone’s kid is Rain Man. Suddenly everyone is “on the spectrum.” Ergo, it’s normal. Being a little bit weird is beautiful and normal and we are all a little bit weird so that’s not a disorder. This is a psyop and everyone is falling for it. No one is saying there is something wrong with neurodiversity or that we shouldn’t also be looking into that. But when it comes to discovering the contributing factors and co-factors, the environmental insults, and the increase itself in autism to date, we’re not talking about that. We are talking about, and have only ever been talking about, the above scenarios. 

The tactics to muzzle debate and halt real investigation are duplicated across all levels. (This should all sound eerily familiar when we recall the conflation, normalization, media machinations, and strawmen to emotionally activate opposition tactics used during Covid.)

It should be a red flag and alarm every American that pharmaceutical companies have no liability for vaccines and that they have managed to increase the pediatric schedule from 3 to 72 in one generation, and it should alarm every parent to learn that HHS itself draws a hard line in 1989 for autism – the year when vaccine formulation was changed to allow for combinations because in 1986 the vaccine space became a financial free-for-all. 

Unfortunately, the media is adept at keeping dots that should be connected in silos so that most people do not connect them, and there is no shortage of sock puppet “experts” willing to run around doubling down on the narrative. 

The Burbacher Study, if anyone were to know about it, let alone read it, SHOULD have at least sparked research into these potential harms. Instead, the spokesperson for the pharmaceutical industrial complex assigned to discredit parents and advocates, Paul Offit, dissects a strawman in public view…in this case the strawman is ethyl vs methyl mercury.

Allow me to explain how this tactic works and why it’s effective: Offit’s argument (and also the error in his argument) is that ethyl mercury (Thimerosal) clears from the brain faster than methyl mercury. First of all, that’s omitting the fact that there are organic and inorganic types, and for the organic type, Offit is right, but for the inorganic type, he’s dead wrong. Ethyl and methyl mercury are different, that’s true, but they both break down into organic and inorganic subtypes. The Burbacher study shows that the organic form of Ethyl mercury clears from the brain faster. 

The inorganic clearance rate couldn’t be determined because the slope of the rate of clearance is zero. So, according to this study, that form of mercury is in the brain forever. Compared to mercury derived from Thimerosal, both organic and inorganic forms of methyl mercury clear from the brain. Which goes against Offit’s claim that ethyl mercury is safer. At least the inorganic form clears from methyl mercury, but it never clears from ethyl mercury. 

But the real issue is…why are we comparing different kinds of lighter fluid around matches? No kind is desirable. (Strawman identified!) And no one is suggesting we are going to inject people with methyl mercury either…so he’s wrong to make the comparison in the first place. But once he’s made the comparison, he’s also wrong according to the data if you consider the inorganic form. Simply put, the Burbacher study proves that mercury does cross the Blood Brain Barrier. Did we put a hold on this? No. Instead, we did away with animal studies for mercury. 

This is just ONE example of ONE strawman designed and implemented to marginalize and sideline a set of risks and harms (even if that’s minority harm) and, yes, injury. There are too many others to list. For example, why aren’t we looking into the connection between autism and HHV-6? 

Between autism and chemicals like Glyphosate and PFAS and forever chemicals in our air, our water, our soil, and our food? Hint: it isn’t because I just thought of it now in my living room. It’s because bottom lines, and corporate and regulatory capture and corruption to maintain those bottom lines, are valued above human lives – above our children’s lives. 

Absence of evidence is not evidence of absence. Only ONE vaccine has ever been properly tested, and even then, never fully. If you shine a spotlight over one small area on a dark street and don’t find what you’re looking for, do you presume the entire street is free of whatever it is? Do we abandon first principles in order to pour concrete on our confirmation biases and further our narratives? Or do we ask the difficult, complex, and nuanced questions, do the hard work, and search for the truth? It appears that question has been asked and answered in the affirmative for the former. The latter is vehemently opposed. 

The assertion that these issues have been looked into is false. In fact it’s been DISALLOWED thus far, and look what’s happening when we try to look into it now. We have everyone outraged over a strawman that was never the point in the first place. It’s all a smoke screen. Once everyone is distracted and chaos ensues, any actual progress is effectively halted, which is precisely the point. It’s not organic. It’s the model, it’s coordinated, and it works. 

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