Tag: human experimentation

Fauci: The Public Servant from Hell

If the allegations put forward by Tulsi Gabbard, former Director of National Intelligence, prove to be substantially true, Dr. Anthony Fauci’s legacy will be remembered as one of the greatest betrayals of the public trust in modern American history.

For four decades, Fauci occupied one of the most influential positions in the federal government. As Director of the National Institute of Allergy and Infectious Diseases (NIAID), he controlled billions of taxpayer dollars, directed research priorities, advised presidents of both parties, and enjoyed a level of public credibility rarely afforded to unelected bureaucrats. Americans were encouraged to trust him — not because he was elected, but because he was presented as the embodiment of objective science.

That trust is precisely what makes the controversies surrounding his tenure so consequential. Fauci’s history in this position of power is one that should not be overlooked. That is why Senator Rand Paul, as chairman of the Senate Homeland Security and Governmental Affairs Committee, issued a subpoena compelling Fauci to testify before Congress. Fauci had declined to appear voluntarily. 

Fauci is no stranger to controversy. As director of NIAID (1984–2022), he oversaw the institute that funded much of the nation’s HIV/AIDS research. For two decades, beginning in 1985, NIAID conducted research involving the treatment of society’s most vulnerable children during the AIDS epidemic. Investigative journalist Liam Scheff alleged that HIV-positive foster children and orphans were enrolled in experimental drug trials without adequate informed consent or independent advocacy. Official reviews raised legitimate ethical concerns about research involving vulnerable children.

Critics alleged that the treatment children received was brutal and unethical, with staff and doctors prioritizing trial compliance over the children’s well-being. Scheff reported that some children experienced significant side effects, and those who resisted the drugs were held down and force-fed. It is also on record that persistent refusers underwent surgical insertion of gastric (stomach) tubes for direct drug delivery. One reason this policy faced little resistance is that the foster children had no parents protecting their interests.

But this wasn’t the only experimentation under Fauci that exploited a vulnerable population.

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Former CIA Officer Drops Bombshell at MKULTRA Hearing: “I Don’t Believe the Research Stopped” — Luna Says Congress Was Lied to for 50 Years

Explosive testimony before the House Oversight Committee’s Task Force on the Declassification of Federal Secrets reveals decades of CIA crimes against unwitting Americans, evidence destruction, secret torture sites in Germany, and a continuing deep state effort to hide the truth from Congress and the American people.

Rep. Anna Paulina Luna (R-FL) chaired a powerful hearing Tuesday titled “Mind Control and Accountability: Uncovering the Truth of the CIA’s MKULTRA Experiments,” dropping bombshell after bombshell on one of the darkest chapters in American intelligence history.

The CIA’s infamous MKULTRA program, which ran from 1953 to 1973, subjected countless unwitting victims, including American citizens, hospital patients, prisoners, and veterans, to LSD, psychological torture, electroshock, hypnosis, and sensory deprivation in a quest for mind control techniques.

In her opening remarks, Luna called the program “crimes committed by the Central Intelligence Agency against American citizens” and “crimes against humanity.”

“This was a deliberate, systematic governmental operation… authorized by the very top of U.S. intelligence apparatus,” Luna said.

She detailed how CIA Director Richard Helms personally ordered the destruction of MKULTRA records in 1973 as he left office. Sidney Gottlieb and his team spent an entire day burning 152 files.

Gottlieb then had his personal papers destroyed. The head of the CIA’s own records center protested in writing and was overruled.

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Researchers Push AI DESIGNED ‘Super Vaccine’

Cambridge scientists are hailing an AI-crafted “super-antigen” as a breakthrough that could ‘get ahead of pandemics’, blanket-protect against every COVID variant, and spare the world future lockdowns while saving millions of lives.

Yet the same public that lived through the last round of experimental shots is not buying the hype. Responses to the announcements have been blunt, laced with references to documented harms, AI’s well-known limitations, and fresh warnings from cancer specialists who watched stable patients relapse after previous boosters.

University of Cambridge researchers, led by Professor Jonathan Heeney, say they have produced the first antigen designed entirely by artificial intelligence and tested in humans.

The team fed AI systems genetic sequences from multiple coronaviruses collected through ongoing surveillance programs. The algorithm then assembled a “super-antigen” intended to train the immune system to recognize whole virus families rather than single strains that keep mutating.

Early human testing involved 39 volunteers and produced what researchers called modest immune responses but no major safety red flags in the initial readout. A larger study with roughly 200 participants is now running to measure stronger and more durable protection.

The same platform is being extended toward universal flu shots, H5N1 bird flu candidates, and vaccines against viral hemorrhagic fevers.

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Lyme Vaccine Clinical Trials: History Repeating?

Why is there so much controversy surrounding Lyme disease? Why does it seem you can’t get an accurate Lyme disease test?

The State of Lyme

The incidence of Lyme disease is approaching half a million cases per year in the United States, according to a 2021 Centers for Disease Control & Prevention (CDC) report based on data from commercial insurance claims. Yet fewer than 40,000 cases are reported to the CDC in any given year, exposing a massive discrepancy between the actual prevalence of the disease and the few cases that meet the CDC’s surveillance reporting definition.

Despite its alarming incidence rate and often catastrophic effects on human health, there has been little advancement in diagnostic and therapeutic technologies for Lyme in the last 40 years. The CDC and Infectious Diseases Society of America (IDSA) continually support only the use of outdated serological techniques that are known to be inadequate, while simultaneously acknowledging that better tests are needed. The reasons for such double-speak and neglect are inextricably intertwined with the sordid history of Lyme disease vaccines.

Lyme vaccine development has continued for the last three decades despite evidence that the causative organism—the spirochetal bacteria Borrelia burgdorferi—evades immunity in multiple ways that may make it impossible for a vaccine to prevent infection. The most recent effort, a candidate known as VLA-15 from Pfizer and French biotech Valneva, is now in phase III trials. Last February it was revealed that due to alleged violations of good clinical practice, Pfizer had shut down all trial sites run by contractor Care Access, eliminating roughly half of the enrolled participants.

Pfizer’s record of “engaging in illegal and corrupt marketing practices, bribing physicians and suppressing adverse trial results” may alone warrant suspicion about their recent actions. But in the context of a Lyme vaccine, suspicion should be heightened. The last Lyme vaccine on the market, SmithKline Beecham’s LYMErix, was withdrawn in 2002 amid numerous injury claims, federal agency hearings, and class action lawsuits. Which begs the question, is history repeating?

Stepping back three decades

In June 1994, the U.S. Food and Drug Administration’s (FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC) devoted a lengthy meeting to the three companies that had Lyme vaccines in development. According to the official meeting transcript, the primary order of business was to answer the question, “Is the CDC case definition for Lyme disease appropriate for a pivotal efficacy trial?”

Why would this even be a question? The standard diagnostics at the time—mainly the ELISA, a serologic assay that measures antibodies produced against the bacteria—were known to produce a large proportion of false negatives. When the CDC discontinued routine testing of samples in its labs in 1988, it stated in a letter to the Oregon Public Health Laboratory that the sensitivity of the ELISA ranged from 13% to 27% in clinically recognized cases. Obviously, this would hamper any trial operator’s ability to assess possible Lyme infection and the vaccine’s overall effectiveness. If you can’t diagnose cases, how can you determine whether your vaccine works?

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Secret Trial of Pfizer RSV Vaccine Killed Two Infants in the 1960s — Their Families Just Sued the U.S. Government

The families of two Black infants who died during a 1960s experimental RSV vaccine trial have filed a federal lawsuit against the U.S., alleging government researchers enrolled the babies in a dangerous medical experiment without their parents’ knowledge or consent, The New York Times reported.

The lawsuit, filed May 22 in the U.S. District Court for the District of Columbia, alleges the National Institutes of Health (NIH) and other researchers, in 1965 and 1966, subjected dozens of infants — most or all of them from low-income Black families — to testing of Pfizer’s Lot 100 experimental vaccine for respiratory syncytial virus, or RSV.

Two infants, Victor Marcellus King and Ross Otto Hambrick, later died after developing vaccine-associated enhanced respiratory disease (VAERD), a severe respiratory illness caused by the vaccine.

VAERD occurs when a vaccinated child who never had RSV is exposed to the virus and develops a more severe case of RSV than they would have if they hadn’t received the vaccine.

The suit was filed by Sharlette Hambrick and Darius King, acting as representatives of the estates of their deceased brothers. They allege federal researchers failed to obtain informed consent from the children’s parents, withheld critical information about prior vaccine failures, and continued the study despite mounting evidence that the vaccine was causing severe reactions in participants.

The complaint also alleges that the tissue samples from the babies who died were later used to develop the RSV vaccines and monoclonal antibody shots that have been approved in the last several years — providing a financial boon for drugmakers.

“Medical research in the United States has a long, troubled racial history,” the complaint states, comparing the alleged conduct to other notorious examples of unethical experimentation involving Black Americans, including the Tuskegee Syphilis Study and the exploitation of Henrietta Lacks.

The infants’ families were unaware the babies had been subjected to the experiment until a reporter from Undark magazine contacted them while investigating the story in 2023.

The reporter found the babies’ names in a doctor’s government-issued laboratory notebook and other paperwork from the clinical trial, the Times reported.

Parents not told infants were being enrolled in trial for experimental vaccine

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The Bizarre Soviet Experiments That Attempted To Understand Psychic Powers

Could someone stop a heart with their mind? Could objects move through the use of mental imagery? Could someone communicate from the shore with a submarine through their thoughts? These were the premises of several strange experiments performed under direction of the Soviet Union. Citizens believed to possess unique parapsychological abilities were tested and studied by renowned scientists in an effort to illuminate the supposed physics that were thought to underlie supernatural abilities. Whether “bioplasma” or “psi particles,” brilliant minds were determined to reveal the science behind the paranormal.

The Cold War was a time rife with competition between the United States and the Soviet Union. The nations battled for control of territories left vulnerable in the aftermath of World War II and fought to claim ideological supremacy. Fear and paranoia were stoked in the American public by the declaration of an arms race, although it was later revealed that the Soviet Union did not have access to such destructive weapons as the U.S. had claimed.

Both governments also competed in the realm of scientific advancement, most famously characterized by the Space Race, in which the U.S. managed to land people on the moon. In a time of such fierce competition, it was all hands on deck, including some scientists with rather peculiar beliefs. The U.S. received intelligence that the Soviet Union was attempting to capture the paranormal using the tenets of the scientific method, gaining an upper hand through telekinesis, telepathy, and clairvoyance.

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Rep. Anna Paulina Luna Fires off Preservation Letter to CIA After Whistleblower Testifies that CIA Seized MKUltra and JFK Assassination Files from Tulsi Gabbard 

Rep. Anna Paulina Luna (R-FL) and the House Oversight Committee issued a warning and subpoena to the CIA and Director John Ratcliffe on Wednesday. The action came after a whistleblower accused the agency of seizing documents related to the JFK assassination and MKUltra — the CIA’s experimentation on human behavior and mind control through the use of drugs — from the Office of the Director of National Intelligence, Tulsi Gabbard.

CIA whistleblower James Erdman III testified during a Senate Homeland Security Committee hearing earlier that the CIA “took back 40 boxes of JFK files and MKUltra files being processed for declassification by DNI Gabbard” in what he described as “documented efforts to circumvent oversight.”

During an interview with News Nation’s Katie Pavlich following the bombshell testimony, Luna sounded the alarm on the CIA’s alleged refusal to follow President Trump’s executive orders and its aversion to transparency.

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CIA Went Rogue, Raided Tulsi’s Office to Seize Papers

A breaking news alert from Fox News, apparently confirmed by a Republican congresswoman, states that the Central Intelligence Agency went rogue, raiding the office of the Director of National Intelligence (DNI) to seize files.

It seems from the Fox News report that the CIA seized the files just now, though a whistleblower from the agency who testified to Congress today referred to the wrongful seizure of files in his testimony. It is therefore not clear if the raid occurred today or before the testimony, or if there was more than one seizure. In either case, Rep. Anna Paulina Luna is giving the CIA 24 hours to return the files in question or face consequences.

The CIA was allegedly after the files on the assassination of President John F. Kennedy and the MK-Ultra human experimentation scandal. The story on the raid is developing but seems to be legitimate, and illustrates the need for drastic cuts in our Deep State. Donald Trump cannot hope to prevent such egregious acts by merely replacing top leadership. The majority of employees at the CIA and FBI worked there during the Biden-era weaponization of justice and believe they are not accountable to Trump or We the People.

DNI Tulsi Gabbard was reportedly in the process of declassifying the JFK and MK-ULTRA files, and it seems the CIA gave us indirect confirmation that there is something in those files that they desperately do not want anyone to know. The problem is that we don’t know if they will be able to destroy the files or not before the Trump administration can get them back. If the raid just occurred and did not happen previously in the last couple of days, it is interesting to note that President Trump was out of the country in China, and therefore unable to be present personally to deal with the situation. Hopefully, Vice President Vance is on the job.

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CIA Ran MK-ULTRA Experiments on Prisoners of War in U.S. Custody, Declassified Docs Confirm

Korean prisoners of war in the 1950s were subjected to early MK-ULTRA experiments while in American custody, according to recently declassified CIA documents which confirm these experiments for the first time.

The only reporting that previously referenced Koreans being used as guinea pigs for these experiments was journalist John Marks’s landmark 1979 book, The Search for the “Manchurian Candidate.” Using CIA documents, Marks traced the now-infamous MK-ULTRA project to its start, when it was known as Project Bluebird. In the book, Marks describes how, in October 1950, 25 unnamed North Korean POWs were chosen as the first test subjects to receive “advanced” interrogation techniques, with the overt goal of “controlling an individual to the point where he will do our bidding against his will and even against such fundamental laws of nature as self-preservation.”

While MK-ULTRA is best known for its invasive experimentation — like LSD dosing and torture — the documents confirm Korean POWs were the unwitting subjects of less splashy attempts at mind control, like being subjected to polygraph tests, with plans for other invasive testing.

The declassified documents, which the National Security Archive released between December 2024 and April 2025, are available through a special collection titled “CIA and the Behavioral Sciences: Mind Control, Drug Experiments and MK-ULTRA.” The National Security Archive website states that the collection “brings together more than 1,200 essential records on one of the most infamous and abusive programs in CIA history.”

The first reference to “Project Bluebird” in the NSA’s collection is an office memorandum from April 5, 1950. Addressed to CIA Director Roscoe H. Hillenkoetter, the document lays out the project’s goals, required training, and budget, all while emphasizing that knowledge of Project Bluebird “should be restricted to the absolute minimum number of persons.”

The memo includes detailed plans for interrogation teams trained to utilize the polygraph, various drugs, and hypnotism “for personality control purposes.” These teams were to be made up of three people: a doctor (ideally a psychiatrist), a hypnotist, and a polygraph technician. The memo clarifies that while the doctor and technician would need to undergo approximately five months of training, the Inspection and Security Staff’s own department hypnotist could be made available immediately. In a later memo from February 2, 1951, there are inquiries into acquiring six “hypospray” devices: experimental instruments designed to covertly inject sedatives through the skin via “jet injection.” There’s a request to investigate modification of a “tear gas pencil” and other “devices of unestablished action,” such as the “German ‘Scheintot’ [sic] (appearance of death) pistol.”

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Big Pharma Giants Pfizer and BioNTech Forced to Shut Down COVID-19 Booster Shot Trials After Americans Refuse to Be Guinea Pigs

Major Big Pharma companies have abruptly halted their latest COVID-19 mRNA “booster” trial because they literally couldn’t find enough willing participants.

After years of gaslighting the American public, raking in hundreds of billions in profits from experimental shots that were shoved down our throats under the guise of “public health,” the same corporations that partnered with the Biden regime, Anthony Fauci, and the lying mainstream media are now facing the cold, hard reality: Americans are done being lab rats.

According to internal letters sent to trial investigators and obtained by Reuters, Pfizer is ending its study of “updated” shots in healthy adults aged 50 to 64.

The company admitted it was “unable to generate relevant data” because recruitment had effectively hit a brick wall.

Reports indicate that more than 80% of potential recruits didn’t even make it past pre-screening, or simply refused to participate.

The trial, which aimed to enroll a massive 25,000 to 30,000 participants, folded after failing to meet even the most basic enrollment targets.

This comes at a time when the “science” is being scrutinized like never before. Under the current administration, the FDA has been pressured to actually require randomized placebo-controlled trials, the very thing skeptics have been demanding for years.

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