China: Six-Year-Old Girl Subjected to Brain Gene-Editing Therapy Dies After Being Injected with Viruses

Neuroscientist Qiu Zilong of Shanghai Jiao Tong University is under investigation following the death of a six-year-old girl who was receiving gene-editing therapy during a human trial under his supervision. 

The child was administered an experimental treatment that involved injecting “trillions of viruses carrying the recipe for the base editor into her spinal fluid,” according to a report in Science magazine. 

Science told the heartbreaking story of how the girl bounced into Xinhua Hospital in Shanghai in March 2025, wearing “a pink jacket and blue pants decorated with cartoon bears.” She treated her visit to the hospital as if it were a vacation and her parents were confident she would receive the best of care at the hospital’s acclaimed pediatrics ward.

The child was suffering from a genetic mutation that was interfering with her cognitive development. The experimental cure involved using a gene editor — similar to the fabled CRISPR, but more advanced — to rewrite the mutated gene in her nervous system. The little girl became the first human being to undergo gene-editing therapy for her brain, an experimental procedure that cost over $860,000.

The details of what happened next have been kept secret until now by the arrogant Chinese Communist tyranny, which is very eager to displace the United States as the world’s leading biotech power. 

According to research by Science and Retraction Watch, a watchdog group that follows up on failed experiments and retracted scientific research, the hospital used a fast-track bureaucratic procedure that bypassed national regulations and Qiu and his team severely undersold the risks of the procedure to the girl’s parents. When the truth was finally revealed, international experts said the negative reactions observed during animal testing should have prevented the experimental treatment from advancing to human trials.

The process of gene editing involves using tailored viruses to deliver the altered genetic material to a patient’s cells — and the little girl had a fatal immune reaction to the bewildering cocktail of viruses injected into her spinal column. She died seven days after entering the hospital.

A hideous cover-up ensued, erasing all mention of the little girl and her fate from experimental literature. Most shockingly, Qiu and his team published an article about the animal studies in their gene-editing trial at Nature this year, but without telling the full story of the human child who died from the treatment or the enormous financial contributions her family made to the research.

Science noted that the hospital paid only a “modest fine to a local health authority” after the death of the child and Qiu was not publicly sanctioned until now. The girl’s parents said they came forward due to their anger at the lack of accountability although they still felt it was necessary to use pseudonyms.

“Learning the reality of these missing safeguards has fundamentally changed how we now view the entire project. We did not realize how unusual and dangerous many of the arrangements were,” said the girl’s father, a software engineer who asked to be called “Jason” in the story.

Dr. Qiu was another in a series of Chinese scientists who came to the United States for an education, then returned to Communist China in 2009, “as China was ramping up its efforts to lure its scientists back home.” 

Qiu was, somewhat ironically, an outspoken critic of “rogue geneticist” He Jiankui’s experiments using CRISPR to create genetically engineered human babies, but he still felt there was great potential in using gene editing techniques to address neurological disorders. His papers and video presentations caught the attention of “Jason” and his wife, who emailed the doctor in 2023 to say they were “willing and able to bear the costs” of getting his experimental treatment for their child. He responded to their inquiry in thirteen minutes flat.

Over the course of the next two years, Jason said he came under increasing pressure to pump money into the research, sometimes in dubious ways, such as paying members of his research team directly and informally.

The cost of the treatment increased dramatically and Jason was told that if he stopped providing the funds, everything he had already paid would be for nothing. Chinese law forbids charging patients or their families for unproven therapies, but this prohibition was circumvented by treating the huge sums provided by Jason’s family as “contributions” to advanced medical research.

Jason and his wife recorded all of their conversation with Qiu and other researchers, so they had a mountain of evidence to bring to the table when they decided to go public.

The general consensus from Science and its researchers is that serious medical work was conducted. The research was not a scam operation and Qiu does not appear to have taken any great portion of the money for himself, although he accepted some lavish gifts from the family. The researchers appeared to be reckless, disregarding evidence that their experimental treatment was dangerous and failing to take some precautions that might have been helpful, such as using more powerful preparatory drugs to suppress the little girl’s immune system.

Science and Retraction Watch referred to the case of “Baby KJ,” a Philadelphia boy named KJ Muldoon with a rare life-threatening metabolic condition that was saved by the world’s first personalized gene-editing treatment in 2025. Baby KJ’s landmark treatment and recovery were the kind of success Jason wanted for his child which Qiu evidently thought he could provide.

Jason referred to his child as “Mei,” a Chinese word that means “beauty.” The last week of her life was a terrible ordeal as her immune system fought to the death against the gene-editing viruses and lost. She began running a fever that Dr. Qiu confidently, and incorrectly, predicted would pass. Her kidneys failed, so she could not have any fluids. Qiu seemed baffled by her deteriorating condition.

In the aftermath of Mei’s death, her parents asked Qiu not to publish the paper he had been excitedly preparing for Nature, but he did it anyway — after removing the genetic data collected from Mei and her family and deleting a message of thanks to them.

Some of the international scientists who were excited by Qiu’s paper were later angry to discover he had already administered the experimental treatment to a young human patient who did not survive. Nature’s editors were annoyed to learn Qiu had not told them the full story before publication.

Qiu’s company had an insurance policy for the medical trial, but Mei’s parents received no settlement. Her shattered parents blamed themselves for not asking enough questions and apparently could not bear to speak with the friends who helped pay for Mei’s treatment.

The South China Morning Post (SCMP) reported on Sunday that Shanghai Jia Tong University has “established a special group to investigate” Qiu’s clinical study and the paper he published at Nature.

“The medicine school has always valued research integrity and standards, and resolutely opposes medical research that violates research ethics and regulations,” the university said.

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Moderna Injects First Participant With Experimental mRNA-4200 Cancer Shot That Forces the Body to Produce Seven Undisclosed Tumor Proteins

On Thursday, Moderna announced that it has injected the first participant in a Phase 1 clinical trial of mRNA-4200 (NCT06880549), an experimental mRNA product that causes the body to produce seven undisclosed tumor proteins following administration.

In other words, the product does not merely introduce tumor proteins into the body—it uses the body itself to manufacture them.

On purpose.

The study raises obvious safety and informed-consent questions about how long the body produces the purportedly encoded tumor proteins, what their long-term biological effects may be, and whether the product or its outputs could be shed from the original recipient onto others through exosomes or extracellular vesicles in excreted bodily fluids.

A 2021 Journal of Extracellular Vesicles study found that cells expressing a target protein can release extracellular vesicles that “carry” that protein, demonstrating that what is produced inside the body can be exported outside the cell in membrane-bound particles.

A separate 2023 Pharmaceutics review explains that exosomes are natural transport vesicles that carry proteins and nucleic acids throughout the body and are present in bodily fluids including blood, saliva, and other secretions—meaning they are not confined to the original cell or even the original location in the body.

You can contact Moderna here and the FDA here.

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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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