Tag: human experimentation

Toddler Dies in Pfizer Gene Therapy Trial

Yesterday I republished a video and article entitled, “What Happened to Their Babies,” describing the lack of ethics and grossly inhumane experimentation that Pfizer conducted on babies and toddlers with their COVID-19 mRNA gene-editing injections.

Just a few hours ago, multiple industry outlets began breaking this official statement from Pfizer that a toddler died of a cardiac arrest in an investigational trial of boys, aged 2 to 4 year olds, to treat a rare form of muscular dystrophy with a recombinant adenovirus gene editing technology.

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DISTURBING FDA LOOPHOLE ALLOWS SCIENTISTS TO DO EXPERIMENTS ON HUMANS WITHOUT INFORMED CONSENT

An FDA rule change published on December 21, 2023 solidifies that scientists are allowed to conduct human experiments without informed consent, as long as the research poses “minimal risk” and includes “appropriate safeguards to protect the rights, safety, and welfare of human subjects.” Investigation by ICAN’s legal team revealed that efforts to undermine informed consent protections have long been in the works, going back to at least 1962. ICAN has filed a FOIA request to dig deeper into this violation of one of our most basic human rights.

Informed consent is one of the bedrocks of human rights. It requires that (1) you be fully informed of the risks and benefits of any intervention or procedure and (2) that you consent to participate without coercion of any kind. Unfortunately, it turns out that Congress and our federal health authorities have been working to weaken informed consent protections for over 60 years!

On the heels of FDA’s new draft guidance which further weakens the already paltry clinical trial requirements for vaccine approval, FDA is once again implementing rules that take aim at informed consent protections. On December 21, 2023, FDA issued a final rule that “allows an exception from the requirement to obtain informed consent when a clinical investigation poses no more than minimal risk to the human subject and includes appropriate safeguards to protect the rights, safety, and welfare of human subjects.”

An investigation by ICAN’s attorneys revealed that back in 1962, Congress passed an amendment to the Food, Drug, and Cosmetics Act which directed HHS to create regulations that required researchers to “obtain the consent of such human beings or their representatives, except where they deem it not feasible or, in their professional judgment, contrary to the best interests of such human beings.” (Emphasis added.)

In 1981, both the FDA and HHS issued updated federal regulations regarding “The Protection of Human Subjects.” HHS’s regulations for example “exempt[ed]  broad categories of research which normally present little or no risk of harm to subjects,” such as “study of data, documents, records and specimens.”

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Personalised medicine will make drug experimentation on populations the norm

In June 2023, the UK’s Medicines and Healthcare products Regulatory Agency (“MHRA”) announced it will be the first drug safety regulator in the world to pilot its own genetic “biobank,” to better understand how a patient’s genetic makeup can impact the safety of their medicines.

“The Yellow Card biobank, which will contain genetic data and patient samples … forms part of a long-term vision for more personalised medicine approaches … [to] enable doctors to target prescriptions using rapid screening tests, so patients … receive the safest medication for them, based on their genetic makeup,” a press release said.

In February 2024, as a personalised medicine project, the MHRA began recruiting patients who have experienced excessive bleeding after taking blood thinners to establish whether they have any special genetic traits which predispose them to excessive bleeding.

It may sound exciting however, personalised genetic medicine is a step towards an era where drug use and experimentation on populations become the norm.

As Dr. Guy Hatchard notes, whilst most pharmaceutical drugs entail adverse reactions and unanticipated side effects, drugs that are tailored to genetic characteristics may potentially have even more serious consequences and long-term adverse outcomes. This is because genetic systems are involved in all the functions of the physiology, its organs, bio-molecular messaging and overall immunity.

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CANADA: Non-Binary Diaper Fetishist Successfully Wins Case To Have The Government Fund Surgery That Will Construct Him A Penis And A Vagina

A trans-identified man and diaper fetishist in Canada who identifies as “non-binary” has won his legal case against the Ontario Health Insurance Plan (OHIP) to have them pay for an experimental surgery that would leave him with both his penis and a “neo-vagina.” Ontario taxpayers will now be forced to spend up to $70,000 flying him to Texas for the surgery due to its unavailability in Canada.

The man, 33, was simply identified as KS in the lawsuit, and made international headlines last week after Ontario’s Divisional Court began deliberating on whether he was entitled to have an “penis-preserving vaginoplasty” covered by the province’s public health scheme.

This week, the court ruled 3-0 that KS was entitled to have the surgery funded by the taxpayer after finding that the province had incorporated standards written by the World Professional Association for Transgender Health (WPATH) into its health insurance law. These international standards endorse radical “gender affirming” surgeries far beyond the scope of Canadian surgical guidance, including castration.

Reduxx has now learned that KS celebrated the result on a Reddit board dedicated to “bigenital” people, revealing his social media handles and providing insight into the man behind the lawsuit.

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Texas gender clinic performs experimental surgeries like ‘Barbie-dolling,’ nullification, giving patients both male and female genitals

A gender clinic in Texas has come under scrutiny for performing hundreds of unconventional and experimental genital surgeries. 

According to the Daily Mail, the Crane Center for Transgender Surgery, located in Austin, offers a range of surgeries catering to individuals who identify as transgender or non-binary. The clinic, nicknamed “Frankenstein’s Lab,” offers procedures that include the creation of both a penis and vagina in patients as well as the complete removal of sex organs, something critics are referring to as “barbie-dolling.” 

Dr. Curtis Crane, who heads the clinic, touts himself as one of the few practitioners skilled in both plastic surgery and urology, specializing in transgender surgery and reconstructive urology. 

“I can’t think of a time that a patient has come up with a surgical request that I haven’t been able to fulfill,” Crane said in a Facebook Live video in 2020. 

However, Crane and his clinic have faced at least eight lawsuits from former patients, who allege incorrect and unnecessary surgeries, negligence in addressing infections and complications, and misleading claims about success rates. 

The Crane Center reportedly performs over 200 top surgeries and 150 vaginoplasties annually, along with various other procedures involving the removal of healthy sex organs for transgender individuals. These practices have raised concerns among medical experts, as the long-term effects and complications of such surgeries remain inadequately researched. 

Nearly all procedures carried out by the Crane Center are covered by insurance, per the Daily Mail. However, Crane complained that this includes a mandatory mental health referral and specific diagnoses that may not align with what the patient is experiencing. 

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Scientists Put Tardigrade Proteins Into Human Cells. Here’s What Happened.

Freeze ’em, heat ’em, blast them into empty space; with survival skills unlike any other organism on the planet, those hardy critters known as tardigrades will only come back for more.

While it’s clear their ability to withstand stress is in part due to their ability to turn their insides into gel, the mechanisms behind this act of metabolic preservation haven’t yet been made clear.

A new study led by researchers from the University of Wyoming found that expressing key tardigrade proteins in human cells slowed metabolism, providing critical insights into how these virtually indestructible invertebrates can survive under the most extreme conditions.

The team focused on a particular protein called CAHS D, already known to protect against extreme drying (desiccation). Through a variety of methods, the researchers showed how CAHS D transformed into a gel-like state when under stress, keeping molecules protected and protecting against drying.

“This study provides insight into how tardigrades, and potentially other desiccation-tolerant organisms, survive drying by making use of biomolecular condensation,” write the researchers in their published paper.

“Beyond stress tolerance, our findings provide an avenue for pursuing technologies centered around the induction of biostasis in cells and even whole organisms to slow aging and enhance storage and stability.”

Tardigrades have already shown they can survive hot and cold temperatures and high levels of radiation that would be fatal to human beings, and long periods without any water – normally so essential to life. They can even survive in space.

Previous research has revealed an impressive number of tricks that tardigrades use to stay alive, built up over hundreds of millions of years. Essentially, they’re very good at slowing the processes of life right down with the help of CAHS D, and that could be useful in human cells too.

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Duke University researchers help transgender woman, 50, breastfeed her GRANDCHILD using experimental hormone drugs so she could feel what it’s like to be a real mom – but critics call it ‘frankly disturbing’

A trans woman has been helped to breastfeed her grandchild, in what is thought to be a world first.

The unidentified 50-year-old was helped to express up to 30ml of milk at a time, after a four week course of hormone treatment.

Researchers from Duke University reported the woman ‘lactated for a total of two weeks’ and was able to feed the four-month-old baby.

The motivation for inducing lactation was to create a ‘bond from breastfeeding that she had not been able to experience with her own five children’.

She was moved to tears by the experience, which she said had the added benefit of affirming her female gender and making her breasts larger.

The patient later stopped the course of treatment ‘due to logistical barriers’.

According to the researchers, who published their study in the journal Breastfeeding Medicine, the patient had said they had ‘a last-minute idea’ about breastfeeding their grandchild.

‘The patient first expressed the unique desire to breastfeed her expected grandchild at an appointment with her endocrinologist in the spring of 2022,’ they wrote.

‘She disclosed that this was a last-minute idea that came to her very close to her daughter’s due date.

‘At five weeks after initiating treatment changes for lactation induction, she reverted to her previous medication regimen.

‘She states that she stopped pursuing her personal goal to breastfeed due to logistical barriers, such as the need to take care of her grandchild while her daughter was pumping.’

‘Her primary motivation for inducing lactation was to experience the bond from breastfeeding that she had not been able to experience with her own five children.

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Chinese Scientists Implant First Pig Liver Into Brain-Dead Human

Who says nothing interesting ever happens in the world anymore? This week, in a “first of its kind” operation, a brain-dead human subject was implanted with the world’s first gene-edited pig liver transplant, according to SCMP. 

In what could be a pioneering move, Chinese scientists have transplanted a gene-edited pig liver into a human, aiming to potentially mark a solution to organ shortages, the report says.

The liver was modified to reduce rejection risks and was implanted into a brain-dead recipient, showing no rejection signs four days post-operation, as per the Air Force Medical University. SCMP writes that this procedure could significantly aid those with end-stage liver disease, possibly revolutionizing liver transplants. 

Gene editing advancements in China also promise to enhance efficiency and accessibility in plant modification, reflecting broader strides in medical innovation, the report continues.

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WHO “pandemic treaty” normalizes bioweapon development and vaccine experiments, incentivizes nations to share data on “gain-of-function” research

In an effort to normalize bioweapon development and predatory vaccine experiments, the World Health Organization (WHO) is pushing every nation to sign a “Pandemic Treaty” that would require each nation to participate in bioweapons development, gain-of-function data sharing and DNA surveillance.

Critics of the treaty warn that this global pact is nothing but a power grab that incentivizes the creation of a biomedical police state. Critics also warn, that by centralizing gain-of-function data, it would be impossible to trace the source of future biolab leaks. The treaty would enable perpetual experimentation on human populations, through pandemic propaganda campaigns or through new vaccine and testing programs that are mandated into existence.

The WHO’s pandemic treaty would continue to disguise bioweapon and vaccine profiteering as “pandemics” that require fearful obedience

With WHO and its financiers calling the shots, all future biolab leaks could be hidden and disguised. Any investigation into misconduct at these biolabs would be forbidden. WHO would immediately call lab leaks “conspiracy theory” or “misinformation.” This is currently how WHO and its body of experts handle any inquiry that comes their way about COVID-19, and it is exactly how the WHO helped quash investigation into the very real possibility of a laboratory leak for SARS-CoV-2.

Director-General of the WHO, Tedros Adhanom Ghebreyesus, has struggled to garner global support for the globalist’s “pandemic treaty.” The treaty would help normalize predatory testing and vaccine development, which requires gain-of-function research to understand how pathogens will infect and harm human populations.

The WHO claims the treaty will help “prevent future pandemics.” However, as seen during the covid-19 scandal, there are several multinational business interests that seek to capitalize on pandemic messaging, fear-based propaganda and the ensuing hysteria. COVID-19 testing programs, which failed from the start, are just one of the lucrative business plans built into the “pandemic treaty.” Further mRNA experiments will continue to bring in billions of dollars for pharmaceutical companies, as governments are leveraged to enforce unlawful mandates onto populations.

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Alzheimer’s transmitted from person to person

Alzheimer’s can be transmitted from person to person, discovered after patients who received human hormones decades ago went on to develop the disease.

Five cases of Alzheimer’s are believed to have been caused by medical treatment given as children.

The new study provides the first examples of Alzheimer’s disease in living people to have been ‘caught’ during a medical procedure.

In these cases, it appears to have been due to doctors administering children with a human growth hormone taken from dead donors.

According to the University College London (UCL) and University College London Hospitals (UCLH) researchers, the findings may have important implications for understanding and treating Alzheimer’s disease.

And although the procedure that led to this transmission was stopped in the 1980s, experts recommend medical procedures should be reviewed to ensure rare cases of Alzheimer’s transmission do not happen in the future.

Alzheimer’s, the most common form of Alzheimer’s, is caused by the build-up of the proteins in the brain, and usually occurs later in adult life with no specific family link. More rarely, it can be an inherited condition that occurs due to a faulty gene.

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