Tag: human experimentation

National Guard “Accidentally” Gives Service Members COVID-19 Vaccine Instead of Influenza Shot

This week it was revealed that the US National Guard wrongly administered the Covid vaccine to a group of service members who were expecting to receive an influenza vaccine, according to The Epoch Times. The incident occurred during a mobile vaccination clinic for the Maine National Guard and at least one member who refused the mRNA vaccine on religious grounds received the experimental injection without his knowledge.

That service member, Mathew Bouchard, is no longer a member of the National Guard. After the incident, he felt that the trust was completely broken. He was ordered to take a flu shot and feels like he was duped. Because the incident happened close to the end of his service contract, he chose not to renew.

Bouchard explained his decision to The Epoch Times:

“Bouchard said he was ordered to receive an annual flu vaccine and went to the clinic to get that vaccine. He verified his name, date of birth, and part of his social security number, and told officials at the clinic he was there for the flu vaccine. But he was injected with a dose of a messenger RNA COVID-19 vaccine, officials told him.

‘You know how you went in for the flu shot? Well, that wasn’t a flu shot. That was a COVID-19 vaccine,’” Bouchard told The Epoch Times, recounting the meeting with superiors.

“I think, in my mind, at that point, it was like, I completely didn’t know if I trusted any people in the military,” he added.”

In addition to Bouchard, two other service members “were accidentally given a Covid vaccine” instead of a flu injection that day, Maine National Guard spokesperson Maj. Carl Lamb explained in an email to The Epoch Times. The clinic was administering both types of vaccine, which likely led to the egregious error.

“Accident” or not, the incident is inexcusable. Especially considering the recent data that has been revealed about the dangerous and deadly adverse reactions caused by the experimental mRNA vaccines – particularly among otherwise healthy young adults. Just this week, the surgeon general of Florida announced new guidelines about the vaccine that show the jab causes a stunning 84% increase in cardiac-related death among 18-39-year-old men. The state of Florida now officially recommends that young males refrain from receiving the mRNA vaccine completely.

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Covid mRNA Vaccines Are Unregulated Military Countermeasures

mRNA Vaccines DID NOT UNDERGO a legally regulated drug approval or manufacturing process

It is important to recognize that an EUA is not part of the development pathway; it is an entirely separate entity that is used only during emergency situations and is not part of the drug approval process. (2009 Institute of Medicine of the National Academies publication, p. 28)

All mRNA products on the market and in development today became available as a result of the declared Covid pandemic, through legal pathways intended for CBRN (chemical, biological, radiological, nuclear) emergencies – in other words, war or terror incidents involving weapons of mass destruction (WMD).

These WMD-related laws include Emergency Use Authorization (EUA) and blanket legal indemnity granted through the PREP Act.

The manufacturing agreements for the Covid mRNA vaccines were military Other Transaction Agreements (OTA) signed by the Pentagon. This type of “other than contract” agreement is intended to supply the military with cutting-edge technology while bypassing pesky regulations and red tape. It is not intended for civilian use.

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The Case of the Damning FDA Memos

On July 21, 2025, the Informed Consent Action Network (ICAN) announced that it had secured the release of over 600,000 pages of Emergency Use Authorization (EUA) data used by the US Food and Drug Administration (FDA) to authorize and approve Pfizer-BioNTech’s COVID-19 vaccine (BNT162b2), following a successful lawsuit, culminating in a late 2024 court ruling.

These documents, now publicly available on ICAN’s website, are part of a broader release of over 1.6 million pages, including data from the vaccine’s licensure in August 2021 and the earlier EUA in December 2020.

This report builds on my prior investigative work analyzing thousands of FDA documents released following the Public Health and Medical Professionals for Transparency (PHMPT) lawsuit, which focused on the biological product file submitted by Pfizer for the full approval of its COVID-19 vaccine in August 2021.

I was one of the initial researchers to uncover and analyse the damning data hidden within Pfizer’s Pregnancy & Lactation Cumulative Review, Interim-Narrative-Sensitive document (3000+ pages), and Cumulative Analysis of Post-Authorization Adverse Event Reports document, among others.

Both ICAN and PHMPT’s lawsuits sought to make public the FDA’s data on the Pfizer-BioNTech’s COVID-19 shot, asserting that transparency is critical for public trust and independent analysis, given the global administration of billions of doses of this experimental gene-based product that was mandated in several countries.

My preliminary review of ICAN’s EUA data reveals several irregularities, outlined below with references to key documents and downloadable sources. This report focuses on four critical issues: manufacturing oversight gaps, missing Bell’s palsy data, clinical trial site deficiencies, and the exclusion of unconfirmed COVID-19 cases.

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FDA Approves Therapy For Rare Disease Without Randomized Trial Data

The Food and Drug Administration on Aug. 14 approved a therapy for a rare disease called recurrent respiratory papillomatosis (RRP).

Regulators cleared Papzimeos, an immunotherapy made by Precigen, citing data from a single-arm, open-label trial that looked at how it performed in adults with RRP and who needed at least three surgeries a year.

Patients received four injections of the therapy over 12 weeks following surgical procedures.

About half of the participants needed no surgery in the year following treatment. The safety profile was also deemed favorable.

“Randomized trials are not always needed to approve medical products and this approval is proof of that philosophy,” Dr. Vinay Prasad, director of the FDA’s Center for Biologics Evaluation and Research, said in a statement.

“The FDA will always demand the correct clinical study for the specific medical product and disease. Our requirements for products given to tens of millions of healthy people will be different than products given to at most hundreds or thousands of patients with unique diseases.”

The approval is the first announcement from Prasad after he rejoined the FDA following his July resignation.

Prasad had received criticism for not approving enough new drugs and therapies, including from the editorial board of the Wall Street Journal, which said that Prasad “has long criticized such single-arm studies that have no placebo groups.”

Replimune’s treatment for advanced melanoma is among the drugs the FDA has rejected since Prasad became its top vaccine and biologics official.

Prasad said in May that he favors randomized clinical trials but that for some rare diseases, it would be difficult or even impossible to complete such trials. He said that the FDA would have a “flexible regulatory standard” that takes into account “the context of a disease.”

In June, in an article co-authored by FDA Commissioner Dr. Marty Makary, he said that for some products targeting rare diseases, “premarket randomized trials may not be feasible.”

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Eight Healthy Babies Born via IVF using DNA from Three People

In the United Kingdom, medical professionals have successfully delivered eight babies using a pioneering fertility procedure that incorporates DNA from three individuals.

This method aims to safeguard children from inheriting severe mitochondrial disorders. The births represent a cautious advancement in assisted reproduction, prioritizing family health and stability.

The mothers involved carried mutations in their mitochondria, risking life-threatening conditions for their offspring. Mitochondria serve as cellular energy sources, essential for bodily functions. Without intervention, these defects could devastate future generations.

The United Kingdom amended its laws in 2015 to permit this technique, reflecting deliberate ethical review. In 2017, regulators issued the initial license to Newcastle University’s fertility clinic. This institution led the development over two decades.

Among the newborns are four boys and four boys, including identical twins, from seven women. All show no evidence of the anticipated mitochondrial ailments. One additional pregnancy continues under medical care.

Professor Doug Turnbull, a key researcher, described the results as reassuring for families and scientists alike. He highlighted the relief in achieving positive outcomes for patients.

Professor Mary Herbert, a senior team member, expressed fulfillment in seeing eight healthy infants. She noted the achievement rewards the extensive collaborative work.

Human genes primarily reside in the cell’s nucleus, totaling around 20,000. However, mitochondria add 37 genes of their own. Faulty mutations here can lead to profound cellular energy deficits.

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Meet The Dystopian Startups Making ‘Biological Computers’ From Human Cells

Picture a dystopian future where computers don’t just mimic human thinking – they’re powered by actual human brain cells. That future is taking shape in a Cambridge, England, lab, where a groundbreaking device called CL1 is blending biology and technology in ways that could transform how we compute. Developed by Australian startup Cortical Labs and U.K.-based bit.bio, this shoebox-sized machine houses 200,000 lab-grown brain cells wired to silicon circuits, creating a “biological computer” that’s already turning heads.

Unlike traditional computers, which guzzle energy, CL1 operates with the efficiency of a human brain. “Our brains process information using a fraction of the power that modern electronics need,” Hon Weng Chong, CEO of Cortical Labs, told FT. “This could open doors to smarter robots, stronger cybersecurity, and immersive virtual worlds.”

Oh, joy.

Low-energy computing has fueled a race to develop biological systems, with Cortical Labs leading alongside competitors like FinalSpark in Switzerland and Biological Black Box in the U.S.CL1’s brain cells, grown from human skin-derived stem cells, are carefully arranged in layers: one type sparks electrical activity, while another keeps it in check. “It’s like balancing a gas pedal and brakes,” Chong explains. This precision, says bit.bio’s Tony Oosterveen, gives CL1 an edge over rival approaches using less uniform “mini-brains.” The result is a platform for testing how brain cells handle information, with early experiments already yielding insights for neuroscience and drug development.

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Trump Closes Notorious EPA Lab that Conducted Illegal Human Experiments

President Trump is trying to save money by terminating leases on facilities used by federal agencies. One of these is EPA’s Human Studies Facility located at the University of North Carolina-Chapel Hill. “Scientists are trying to save it,” reports Nature magazine. But being a waste of money is the least interesting aspect of the infamous lab.

In 2011, through the Freedom of Information Act (FOIA), I exposed the lab’s illegal experimentation on humans with air pollutants that EPA considers to be deadly. The lab’s central feature is an actual gas chamber into which EPA pumped exhaust from a diesel truck idling outside in a parking lot. You can see a photo of the twisted arrangement here.

After filtering out the carbon monoxide, EPA concentrated the exhaust’s fine particulate matter (soot, called “PM2.5” by EPA) to unrealistically high levels and pumped it into the chamber in which human guinea pigs inhaled it for periods of two hours. The purpose of the experiments was to observe the effects, if any, of inhaling PM2.5. For these experiments, EPA had recruited: asthmatics; people with heart disease and diabetes; and elderly persons up to 80 years of age. EPA paid its human guinea pigs as much as a couple thousand dollars for their participation in the experiments.

All this may seem harmless enough. But was it? EPA had previously concluded that PM2.5 was, essentially, the most toxic substance known to man. Any inhalation could cause death within hours, the agency had determined.  It had also stated that the people most at risk from inhaling PM2.5 were: asthmatics; people with heart disease and diabetes; and the elderly. Those at risk from PM2.5 were the very sort of people upon whom it had been experimenting.

But EPA had not disclosed any of this to, and so did not obtain legally required “informed consent” from its human guinea pigs. Instead of informing its human guinea pigs in writing that the agency believed the experiments could kill them, as was required by federal regulations, state law and the Nuremberg Code on human experimentation, the agency’s consent forms only disclosed that some temporary coughing or wheezing may result from the experiments.

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The U.S. government secretly dosed millions with radioactive iodine—and what they’re hiding now

The invisible poison: How I-131 infiltrated America

Unlike natural background radiation, I-131 is a man-made isotope with a sinister affinity for the thyroid gland. Once released, it clung to grass, seeped into cows’ milk, and found its way into the bodies of unsuspecting children—the most vulnerable to its effects. The National Cancer Institute admits that nearly every American alive during the testing era ingested this radioactive poison. Yet, at the time, officials dismissed concerns, assuring the public that fallout was “harmless.”

Historical records reveal a darker truth: the government knew. Internal documents from the Atomic Energy Commission (AEC) acknowledged the risks but prioritized Cold War dominance over public safety. As Princeton’s research shows, fallout maps paint a damning picture—radioactive particles didn’t stop at state lines. They blanketed the nation, carried by rain into soil, water, and food supplies.

The great betrayal: Lies, lawsuits, and a legacy of suffering

The government’s silence wasn’t just negligence—it was a criminal conspiracy. By the time the Radiation Exposure Compensation Act (RECA) was passed in 1990, generations had already suffered. Thyroid cancer rates spiked in high-fallout zones, yet victims were met with bureaucratic hurdles. “Prove it was our nukes,” officials demanded, knowing full well that decades-old exposures were nearly impossible to trace.

Dr. Helen Caldicott, a renowned anti-nuclear advocate, put it bluntly: “This was a mass poisoning, sanctioned by the state.” Even today, RECA’s payouts are a pittance compared to the suffering inflicted. And what of the unstudied fallout from Soviet tests, Pacific detonations, or Hiroshima’s radioactive blow back? Researchers suspect California and the Pacific Northwest bore the brunt—but without comprehensive studies, the full toll remains hidden.

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Mutant Rice and Lab Rats: Bill Gates Sparks Outrage After Referring to India as ‘Testing Ground’ for Experiments

In late 2024, Bill Gates sparked outrage in India after describing the country as “a kind of laboratory to try things.” The controversy resurfaced with the May 5 announcement that India became the first country to officially release two genome-edited rice varieties that critics warn may come with serious unintended consequences and risks.

In late 2024, Bill Gates sparked outrage in India after describing the country as “a kind of laboratory to try things” during a podcast with Reid Hoffman. Gates emphasized the nation’s stability as a “testing ground” for global initiatives.

His remarks were widely condemned. Social media erupted, with many Indians accusing Gates of reducing their nation to a mere experimental ground for Western interests.

Social media users labelled Indians as “guinea pigs” in Gates’ laboratory and questioned the ethics and motives behind such experimentation.

A widely reported response on X captured the sentiment:

“India is a laboratory, and we Indians are Guinea Pigs for Bill Gates. This person has managed everyone from the Government to opposition parties to the media. His office operates here without FCRA, and our education system has made him a hero! I don’t know when we will wake up!”

(FCRA refers to the Foreign Contribution (Regulation) Act, which regulates foreign contributions to ensure they are not detrimental to the national interest.)

The controversy resurfaced with the May 5 announcement that India became the first country to officially release two genome-edited rice varieties: Kamala (DRR Dhan 100 Kamala) and Pusa DST Rice 1.

These are not classified as genetically modified (GM) crops. Unlike traditional GM crops, which deliberately introduce foreign DNA, these gene-edited varieties use CRISPR-Cas SDN-1 and SDN-2 technologies, which are often claimed not to introduce foreign DNA but only to alter existing genes.

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Joe Rogan Guest Reveals Facebook’s Secret Experiment That Manipulated 700,000 Users Without Warning

Joe Rogan sat down with Harvard professor and mind control expert Rebecca Lemov, and it didn’t take long for the conversation to dive into one of his favorite topics: government interference in our digital lives.

Rogan opened the conversation by saying, “There are so many different kinds of mind control.”

“One of the things we’ve talked about a lot on this podcast is, that an enormous percentage of what you’re seeing on social media in terms of interactions and debate is not real. It’s not organic,” he explained.

“It’s state-run and state-funded, and it’s whether it’s foreign governments or our government or even corporations, you’re getting inorganic discourse that’s designed to form a narrative and which is a form of mind control,” he added.

Lemov picked up on that point and took it further. Even when people know something is fake, she explained, our brains still react as if it were real.

“Yeah. I mean, I think even on a basic level, people, it’s known and studies have shown that we respond as if it were organic and real,” she said.

“Even when somebody likes a post of yours, the response is the same as, like, in-person interaction,” she added.

It’s not just governments pulling the strings, she warned. The platforms themselves are designed to influence how we feel.

“I think at the root, there is a kind of way that, on an emotional level, it’s not just manipulation of ideas,” she said, “but there’s a kind of emotional engineering that’s built into the platforms and doesn’t even demand, you know, at first, government involvement.”

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