A Young Child Died During Moderna Covid Vaccine Clinical Trial — Did FDA Know?

A preschool-aged child died of cardio-respiratory arrest after getting a COVID-19 booster in a Moderna clinical trial. However, Moderna didn’t reveal the death to the public and only recently reported it on a European regulatory agency database, Alex Berenson reported.

The death occurred in late 2022 or early 2023, Berenson said, when children under 5 who had already received Moderna’s original mRNA-1273 COVID-19 vaccine in the trial’s main phase were offered the “1273.214” booster against an early Omicron variant.

Berenson, a former New York Times reporter who now reports on his Unreported Truths Substack, today said the U.S. Food and Drug Administration (FDA) has declined to tell him whether the U.S. agency knew that a child died during Moderna’s clinical trial.

The failure of the FDA to provide a straightforward answer about whether it knew that a young child in a Moderna clinical trial died from cardiac-respiratory arrest is “vitally important,” Berenson told The Defender.

“Of all the mistakes public health authorities made around COVID, their insistence on pressing mRNA vaccines on children was probably the worst,” Berenson said.

By the time the COVID-19 vaccines were available for kids, it was clear that children were at almost no risk of serious illness or death from COVID-19, he said. “The shots had significant side effects, so the only rationale for giving them shots — even theoretically — was to reduce transmission.”

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Disturbing new details show how CIA drugged and tortured Americans in secret mind control program MKUltra

Newly declassified bombshell records of an infamous CIA mind control program, MKUltra, reveal how Americans were drugged and tortured more than 60 years ago.

The collection of more than 1,200 pages detail how the CIA used induced sleep, electroshocks and ‘psychic driving’ on drugged subjects who were psychologically tortured for weeks or months to reprogram their minds.

The subjects included criminals, mental patients and drug addicts, but also Army soldiers and average citizens who were given drugs without their knowledge.

A total of 144 projects were conducted from 1953 to 1964, aimed at developing procedures and drugs that could be used during interrogations, weakening individuals and forcing confessions through brainwashing and psychological torture.

The newly declassified pages detail how the CIA used methods such as induced sleep, electroshocks, and ‘psychic driving,’ under which drugged subjects were psychologically tortured for weeks or months to reprogram their minds.

While it has long been said that subjects only included prisoners, mental patients and drug addicts, one report showed that some CIA and Army officials and ‘subjects in normal life settings’ were ‘unwittingly’ given LSD over the decade-long experiment.

In a newly unsealed document from 1956, researchers were developing ‘an anti-interrogation drug’ by testing ‘materials capable of producing alterations in the human central nervous system which are reflected as alterations in human behavior.’

A memo about a classified meeting showed that the CIA contemplated the possibility of testing on foreign nationals,’ but decided that ‘unwitting testing on American citizens must be continued’ instead.

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COVID Vaxx Team Trialing Bubonic Plague Vaccine as Fears of Next Pandemic Grow

British scientists who worked on the Astrazeneca COVID-19 jab are calling for the UK to stockpile vaccines for the bubonic plague, as fears about the next global pandemic grow.

Britain’s Daily Telegraph reports that scientists with the Oxford Vaccine Group are worried the UK could be caught unprepared by a global pandemic of the disease which killed tens of millions of people the Middle Ages.

The Oxford Vaccine Group has been trialling a plague vaccine since 2021, on a group of 40 healthy adults. The group’s leader, Professor Sir Andrew Pollard, says the vaccine has proven a success, and results of the trial will be submitted to a scientific journal for peer review within weeks. Further clinical trials are expected.

Pollard said: “There are no licensed plague vaccines in the UK. Antibiotics are the only treatment. There are some licensed vaccines in Russia.

“The risk in the UK is currently very low. Previous historical pandemics that had high mortality were associated with initiation from fleas on rodents but were driven by person to person spread.”

Military scientists in the UK believe the plague, which still exists in isolated pockets around the world, has the “potential for pandemic spread.” Scientists from the UK government’s biological research facility at Porton Down recently wrote a paper claiming that vaccine production needs to be enhanced “to prevent future disastrous plague outbreaks.”

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They’re Trialing Self-Amplifying RNA-LNP-Based Products

On November 11, 2024, an article was published online in Business Wire pertaining to the launch of a clinical trial NCT06602531 intended to test “Safety and Immunogenicity Study of Self-Amplifying RNA Pandemic Influenza Vaccine in Adults.” 

Question: Why is the word “Pandemic” in the title? 

The article provides information on the ARCT-2304 product which is a “sa-mRNA vaccine candidate formulated within a lipid nanoparticle (LNP).”

So. Many. Questions. For example, beyond the use of the word pandemic in the study title, why is this product being called a vaccine? Why is a new version of a product riddled with unresolved compendial standard issues being trialed?

ARCT-2304 is a gene-therapy-based prodrug that uses self-amplifying RNA technology (specifically, the RNA-dependent RNA polymerase (RdRP) gene, which allows it to replicate autonomously) that originates from an Alphavirus. Just so you know, this makes these products genetically-modified organisms (GMOs) and this is because of the fact that the coding template is a modified Alphavirus genome with the virus sub-genomic bits spiked out and the foreign flu genes ‘spiked in.’ The genetic material is capable of reproduction. The following slide shows how they did this for the Covid-19 version (KOSTAIVE® (ARCT-154) Monovalent: JN.1). 

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Experiments on Your Kids

Just this week, the Boston Globe published an article by Newton South High School math and physics teacher Ryan Normandin admitting that an allegedly progressive education experiment had been a failure.

Mind you, it was obvious to every single person on this planet that this experiment would fail.

But in the minds of these people, your kids exist to be experimented on, and to help usher in the progressive future.

Here was the experiment:

Let’s put all students in the same math class, regardless of skill.

Let’s put all students in the same foreign-language class, regardless of skill.

You already know a major motivation behind the policy: why, separating students by academic skill level yields insufficient “diversity” in the classroom.

Not keeping up with the latest in modern educational theory, you might have asked a coarse question like, “Will this new arrangement mean a better education for my kids?”

Oh, dear reader. The thought never even crosses their minds.

Precisely what you’re assuming would happen, happened.

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Psychiatric Drug Cocktails – Risky Experiments on Human Minds

Despite zero understanding of how even one psychiatric drug “works” as “treatment” for alleged mental disorders, the rate of cocktail (polypharmacy) drugging among children is increasing. One doctor called for informed consent about the benefits and risks associated with the “contraindicated” drugging.

A recent study from Lawrence Kleinman, professor of pediatrics at Rutgers Robert Wood Johnson Medical School, reviewed Medicaid data for more than 141,000 patients (under 21) receiving any psychiatric medication and found that nearly 400 of those patients received at least one “potentially dangerous combination” of psychiatric drugs.

Dr. Kleinman warned that “good practice demands that patients and caregivers be informed of and assent to risks and benefits, including informing them that the intended pair of medications is typically contraindicated.” What Kleinman is warning is that there are serious risks to prescribing cocktails of psychiatric drugs and it is not recommended.

According to Kleinman’s research, polypharmacy (more than one drug prescribed together) is a common practice, with nearly 38 percent of patients in the study filling two or more medications with at least one month overlap, generating more than 11,000 distinct drug combinations.

Kleinman found that the most contraindicated combination involved the antipsychotic Ziprasidone, approved by the Food and Drug Administration (FDA) for the “treatment” of schizophrenia and bipolar. And the research further revealed that “other risky combinations involved antidepressants such as Fluoxetine (Prozac) and Trazodone paired with various antipsychotic medications…”

This isn’t the first of its kind research as a report in February of this year showed that kids in the state of Maryland also are receiving cocktails of psychiatric drugs at ever increasing rates. Yes. It’s a veritable behavioral chemical lobotomy for America’s children at the whim of the prescribing doctor, despite the serious risks associated with such prescribing.

According to the Maryland research conducted by University of Maryland School of Pharmacy graduate student Yueh Yi Chiang, between 2015 and 2020, those children under the age of 17 were receiving “multiple psychiatric drugs during that time that rose from 4.2% in 2015 to 4.6% five years later.” And sadly, those kids who were disabled or in foster care “were significantly more likely than individuals with low income to receive three or more psychotropic classes overlapping for 90 days or more.”

Three or more psychiatric drugs at one time? How is this prescribing not criminal? Physicians are abundantly aware of the serious risks associated with cocktail drugging, especially in light of the fact that not one doctor has even a clue about how these drugs “work” in the brain as “treatment.”

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1970 Hearing Reveals ADHD as Government-Funded Drug Experiment on Children

In 1970 a lawmaker wanted to know if the federal government had a hand in drugging school-age children that largely has today remained an unspoken, well-funded, uncontrolled clinical drug trial.

September 29, 1970, New Jersey Congressman Cornelis E. Gallagher held a hearing into the federal government’s role in promoting the use of amphetamines and Ritalin as behavior modification of grammar school children.

Fifty-four years later, AbleChild applauds Representative Gallagher for presiding over the House Special Studies Subcommittee of the Committee on Government Operations investigation as it was one of the first hearings to draw attention to the government’s funding of experimental drug research using school-age children.

Gallagher wanted to know from the experts how it was okay to drug children with amphetamines and Ritalin to modify behavior in school, while at the same time pushing an active national campaign against drug abuse stating that “speed kills.”

The Congressman was concerned about whether the drug therapy being used by the child would become a permanent part of the child’s school record, thus years later negatively impacting the child’s life.

And, finally, the Congressman raised concerns “about the mislabeling of the child and packaging an ill-conceived program as an answer to our ills in the education of our children.”

At the time of the 1970 hearing, researchers were then labeling hyperactive children with Minimal Brain Dysfunction (MDA), then renaming it as Hyperkinetic disorder (HKD) or Hyperkinesis and finally settling on attention deficit hyperactivity disorder (ADHD).

At the time of the hearing, none of the experts testifying could provide any scientific data proving the alleged brain abnormality existed.

Still, fifty-four years later, there is no science to prove the alleged brain abnormality ADHD exists.

Ironically, one of the experts that testified at 1970 hearing warned that the drug therapy would “zoom” from its then usage in approximately 200 to 300 thousand American children.

The prophecy was fulfilled. In 2020 alone, 9,585,203 Americans were taking some form of psychiatric mind-altering drug as “treatment” for the alleged ADHD.

Almost four and a half million Americans between the ages of 0 and 24 alone were prescribed ADHD drugs in 2020.

The “experts” testifying before Gallagher’s subcommittee were as clueless then as the “experts” are today when it comes to any understanding of how the drugs worked as “treatment.”

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American Pharmaceutical Companies Accused of Carrying Out Clinical Trials With Chinese Military

A bipartisan House committee has revealed that American pharmaceutical companies carried out drug trials in conjunction with the Chinese military for more than 10 years.

The revelation came in a letter penned by Republican and Democratic leaders on the House Select Committee on the Chinese Communist Party (CCP) to the commissioner of the Food and Drug Administration (FDA), Robert Califf. In the letter, they pressed him to supply information about these clinical trials for new medications.

In their letter, they explained: “These collaborative research activities raise serious concerns that critical Intellectual Property is at risk of being transferred to the [Chinese military] or being co-opted under the People’s Republic of China’s National Security Law.”

They also expressed reservations about how much the results of clinical trials produced by China can be trusted.

The letter states that hundreds of clinical trials for drugs have been carried out at medical centers and hospitals in China that are affiliated with the People’s Liberation Army (PLA) at sites such as the PLA’s Air Force Medical University and the PLA’s General Hospital and Medical School.

One of the institutions is operated by the PLA’s Academy of Military Medical Sciences, an institution which the Department of Commerce has banned businesses in the United States from sharing technology with due to national security concerns.

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Under The Skin: The Internet Of Bio-NanoThings

The Internet of Things (IoT) has become an important research topic in the last decade, where things refer to interconnected machines and objects with embedded computing capabilities employed to extend the Internet to many application domains. While research and development continue for general IoT devices, there are many application domains where very tiny, concealable, and non-intrusive Things are needed.

The properties of recently studied nanomaterials, such as graphene, have inspired the concept of Internet of NanoThings (IoNT), based on the interconnection of nanoscale devices. Despite being an enabler for many applications, the artificial nature of IoNT devices can be detrimental where the deployment of NanoThings could result in unwanted effects on health or pollution. The novel paradigm of the Internet of Bio-Nano Things (IoBNT) is introduced in this paper by stemming from synthetic biology and nanotechnology tools that allow the engineering of biological embedded computing devices.

Based on biological cells, and their functionalities in the biochemical domain, Bio-NanoThings promise to enable applications such as intra-body sensing and actuation networks, and environmental control of toxic agents and pollution. The IoBNT stands as a paradigm-shifting concept for communication and network engineering, where novel challenges are faced to develop efficient and safe techniques for the exchange of information, interaction, and networking within the biochemical domain, while enabling an interface to the electrical domain of the Internet.

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AI Industry Growing Human Brains in a Lab: Wetware

Recently, there’s been a great deal of hoopla about brains, specifically presidential and presidential-candidate brains. Perhaps because of this, my own brain has been thinking about the broader issue of brains. 

And I happened to run across something about that and wanted to share it with you. I recently learned of a Swiss startup that is creating human brains — and planning to link them together into superbrains. 

Why do this?  

Because you can apparently get artificial intelligence more effectively, more cheaply, and with less environmental consequence — by using actual brain cells. 

Not yours, and not mine. No, they’re growing brains to order in the lab. 

I know there was a time when this sounded like science fiction. But this… is real. 

Once they whip up some mini human brains, they interconnect a bunch of them, and voila!  A pretty effective network for AI. (Brain cells communicate with each other and the rest of the body through electrical signals — which makes them compatible with silicon chips.)

Only it’s not called AI. It’s called “:ware” — as opposed to “hardware” (and not to be confused with “wetwork”) — defined as thinking human brain cells without any inconvenient bodies attached.  

My first reaction was to wonder where they got the brain cells, and if they’re fussy about the source. Did they prefer the brains of brainy professors — dead ones, of course.  

Answer: From stem cells — derived from human skin. But they don’t say whose stem cells. Stem cells are fascinating. They can be coaxed into becoming other kinds of tissue, from bone to brain. A paralyzed man can now walk again, thanks to stem cell therapy

Maybe someday these magical cells will be sold over the counter in jars at a drugstore near you. 

Well, I scarcely know what to do with this.   

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