By
- Veterans Today
July 19, 2023
This is the collage of four different articles on experiments which targeted African population and children too to discover dangerous lethal virus and test news vaccines.
The people were used as guinea-pigs by Pentagon and Metabiota (American company tied with Bidens), according to Russian experts on bacteriological research, but also by the notorious Bill gates.
Russian top brass: Pentagon wanted to test unregistered medicines on African population
The Pentagon planned to use its biolaboratories in Africa to test unregistered medicines on the local population, Chief of Russia’s Radiation, Chemical and Biological Protection Troops Lieutenant General Igor Kirillov said on Tuesday.
According to Kirillov, documents that were found in Ukraine indicate that the Pentagon planned to use the US army to test unregistered medical drugs on the local population and then submit them for approval by supervisory authorities “in the interests of the so-called big pharma.” For these ends, it was planned to use its biolaboratories and facilitating agencies, such as Metabiota.
“Take note of Metabiota’s commercial offer marked ‘confidential,’ which was found among documents at one of the biolaboratories in Ukraine. The offer is addressed to the United States Army Medical Research Institute of Infectious Diseases and concerns training of specialists in infectious diseases in Kenya and Uganda.
The document demonstrates that the Defense Threat Reduction Agency’s (DTRA) and the Department of Homeland Security were involved in the study of pathogens in African countries, while the US Agency for International Development and a number of European Union structures were engaged to make these activities look like ‘humanitarian cooperation,’” he said at a briefing on the analysis of documents concerning the United States’ military biological activities.
Apart from that, in his words, evidence was found showing that Metabiota had been involved in the study of the H7N9 bird flu virus and that it had played a leading role in the implementation of the Predict project for the study of new coronavirus types, under which their carriers – bats – had been caught.
“We have repeatedly pointed to the company’s ties with the son of the US incumbent president, Hunter Biden, and government organizations. Notably, Metabiota’s representatives admit that as a matter of fact they are establishing ties to ensure the Pentagon and other American agencies’ work abroad,” Kirillov added.
Originally published by TASS Russia News Agency
Russia has evidence of Metabiota’s work in Africa in US government’s interests
The documents obtained in the special military operation in Ukraine testify to the work of the US company Metabiota in Africa in the interests of US government agencies, including the Department of State, Chief of Russia’s Radiation, Chemical and Biological Protection Troops Lieutenant-General Igor Kirillov said on Monday.
“The documents obtained in the special military operation confirm the link between the Walter Reed Institute and the US Defense Threat Reduction Agency (DTRA) and its key contractor, the company Metabiota. The available financial and scientific documents testify to the company’s activity on the territory of Africa – in Kenya, Uganda and South Africa. In addition to the US Defense Threat Reduction Agency (DTRA), the documents list the US National Security Agency and Department of State among customers represented by the US government,” the general said.
The documents describe Metabiota’s ‘flexible’ methods of activity making it possible to cover up the US government’s participation in foreign projects and resolve bureaucratic issues through the hire of local officials. However, in the face of the international community’s growing concern, the Pentagon is forced to change its tactics in organizing ‘dual-purpose’ work, Kirillov said.
The chief of Russia’s Radiation, Chemical and Biological Protection Troops also pointed to the existence of a ramified network of branches of the US Walter Reed Army Institute of Research and the US Naval Medical Research Command. The Walter Reed Institute has four overseas branches furnished with laboratories featuring a high level of biological isolation and a network of regional units for sample selection and strain transportation, he said.
“The scale of ongoing work with dangerous pathogens can be evidenced by about 500 staff of the branch located in Thailand. The branch has units in Nepal, Cambodia and the Philippines, which, in turn, interact with 12 more Southeast Asian countries,” Kirillov said.
“Apart from the US Army Research Institute, the US Naval Medical Research Command also has a network of foreign branches. Its NAMRU subordinate laboratories carry out work with pathogenic microorganisms in North Africa, the Middle East and South America.
Such a ‘ramified’ approach implemented throughout the world allows the US defense agency to gain access to epidemically significant pathogen variants that are potential biological weapon agents. They include the Marburg and Ebola fevers, malaria and the Rift Valley fever,” the chief of Russia’s Radiation, Chemical and Biological Protection Troops said.
Originally published by TASS Russian News Agency
Trial of Gates-Funded Vaccine Patch for Infants in Gambia
An Atlanta-based biotech company last week said it successfully concluded the first-ever clinical trial testing of a microarray injection-free vaccine on children as young as 9 months old.
Micron Biomedical tested microneedle-based delivery of the measles-rubella (MR) vaccine on children in Gambia with backing from the Bill & Melinda Gates Foundation and the Centers for Disease Control and Prevention (CDC).
Microarray injections are administered via a microneedle patch that looks like a Band-Aid and is applied by pressing it to the skin. Once applied, microneedles penetrate the upper layer of the skin to deliver the vaccine.
The study, which researchers presented last week at the Microneedles 2023 conference in Seattle, evaluated the safety, immunogenicity and acceptability of the leading commercially available MR vaccine from the Serum Institute of India delivered by Micron’s microarray technology in adults, toddlers and infants.
Proponents of this vaccination method, such as Gavi, the Vaccine Alliance — of which the Gates Foundation is a founding member — call the patches “the future of vaccination, where these lifesaving interventions are delivered painlessly, without the need for syringes or perhaps even trained medical professionals.”
“Supporting innovations in vaccine delivery is critical to addressing ongoing health inequities,” James Goodson, co-investigator for the study and senior scientist and epidemiologist at the CDC’s Global Immunization Division, said in the press release.
He added that the study also is a key step toward getting the patches licensed. Developers tout the technology as painless — it feels like Velcro, they claim — and more thermostable than traditional vaccines.
This would make widespread global distribution of the vaccines easier, they said, particularly in developing areas that may lack infrastructure, such as refrigeration, and trained professionals.
Extract by The Defender – read whole article here
Gates Commits $400 Million to Test New TB Vaccine on 26,000 People in Africa and Southeast Asia
The Bill & Melinda Gates Foundation and Wellcome Trust on Wednesday announced plans to fund a phase 3 clinical trial for a tuberculosis (TB) vaccine that will be tested on 26,000 people at 50 sites in Africa and Southeast Asia over the next four to six years.
Gates committed $400 million to the trial and Wellcome — the largest funder of medical research in the U.K. and one of the largest in the world — committed an additional $150 million. The trials will test the M72/AS01 vaccine, developed by pharmaceutical giant GSK (formerly GlaxoSmithKline) with partial funding from the Gates Foundation.
Experts told The Washington Post the news was “huge.” The Guardian heralded the announcement as “gamechanging,” while STAT called it “promising.”
But Brian Hooker, Ph.D., P.E., senior director of science and research for Children’s Health Defense told The Defenderthat the planned trials for the TB vaccine raised red flags.
“I’m concerned that they’re planning on conducting the trial in underdeveloped nations,” Hooker said. “It seems almost prototypical that the underserved have to be guinea pigs for the rest of the world.”
He added, “Fifty percent is incredibly low efficacy for such an ‘important’ intervention to go to essentially everyone in the developing world.”
TB more common among poor
GSK developed the vaccine and ran smaller, “proof-of-concept” phase 2b trials on it in 2018, reporting a 54% efficacy rate. But the vaccine maker didn’t move forward with the large-scale trials needed for a license.
Instead, it passed the license to the Gates Medical Research Institute, a nonprofit biotech spinoff of the Gates Foundation dedicated to developing “novel biomedical interventions” to treat global health problems.
The existing vaccine for TB, the BCG (bacille Calmette-Guérin) vaccine, was developed in 1921 and is effective at stopping TB infection among children but has limited efficacy in adults.
Recent estimates suggest up to 25% of the global population carries a latent (asymptomatic) TB infection, which may later become active among 5-15% of latent carriers. People with latent infection cannot spread the disease.
TB kills 1.6 million people per year, primarily in low and middle-income countries. It is treatable and curable with antibiotics. Drug-resistant strains have emerged, but those also are treatable and curable using second-line drugs.
TB is more common among poor people, who are more likely to work in poorly ventilated and overcrowded conditions, suffer from malnutrition and have more limited access to healthcare.
The funded trial will test whether the experimental vaccine can prevent adolescents and adults with latent tuberculosis from developing symptoms.
Extract by The Defender – read whole article here
LINKS MAIN SOURCES
GOSPA NEWS – WUHAN-GATES INQUIRY AND BIG-PHARMA
SOURCE: Gospa News
—————–
Puppies?! Fauci Tortured ORPHAN BABIES And CHILDREN In His AIDS Drug Experiments
HAFJanuary 7, 2022
Article via Silview.media
“In 2003, 04, 05, I was investigating this story. Children in an NYC orphanage (and the foster care system) used in clinical trials. The Associated Press took it national and found it going on in seven or more states.
“Some states declined to participate in medical experiments. Tennessee said its foster care rules generally prohibit enlisting children in such trials. California requires a judge’s order. And Wisconsin “has absolutely never allowed, nor would we even consider, any clinical experiments with the children in our foster care system,” spokeswoman Stephanie Marquis said.
Officials estimated that 5 percent to 10 percent of the 13,878 children enrolled in pediatric AIDS studies funded by NIH since the late 1980s were in foster care. More than two dozen Illinois foster children remain in studies today.” No medical records were ever made available to official investigators. You make up your own mind.” – Liam Scheff
A National Scandal: AIDS Drug Experiments On Foster Care Children – Associated Press
The article has been deleted from the AP website, but the archive survived here.
On March 10, 2004, The Alliance for Human Research Protection filed a complaint with the FDA and the federal Office of Human Research Protection about a series of AIDS drug experiments conducted on New York City children in foster care. That complaint prompted two separate investigations by the FDA and OHRP which are still on-going.
Articles in The New York Post and a documentary by BBC raised the alarm among the African-American and Latino community in NY-some of who have been protesting weekly in front of Incarnation Children’s Center, the site of some of the drug experiments.
The Associated Press AP has just released its investigative report: the problem is a national scandal–the experiments were conducted in “at least seven states — Illinois, Louisiana, Maryland, New York, North Carolina, Colorado and Texas — and involved more than four dozen different studies.
AP’s investigation found that 13,878 children had been enrolled in pediatric AIDS studies funded by the government since the late 1980s. Of these, officials estimated that 5 percent to 10 percent were in foster care. Their age ranged from infants to late teens.
“More than two dozen Illinois foster children remain in studies today.”
Those who conducted the experiments in violation of federal regulations, are supported by taxpayers – thus they have a public responsibility which they violated. The children who were targeted to serve as human drug testing subjects – mostly poor children of color – were not afforded the protection of a personal advocate – as is mandated by federal regulations. (45 Code of Federal Regulations 46.409)
The institutional culture of arrogance is demonstrably in evidence at both medical research centers and government agencies: “Our position is that advocates weren’t needed,” said Marilyn Castaldi, spokeswoman for Columbia Presbyterian Medical Center in New York.
And officials of NYC Administration of Child Services “defend the decision to enlist foster children en masse, saying there was a crisis in the early 1990s and research provided the best treatment possibilities.”
The children are reported to have suffered painful side effects “such as rashes, vomiting and sharp drops in infection-fighting blood cells as they tested antiretroviral drugs to suppress AIDS or other medicines to treat secondary infections.”
In one study testing the drug dapsone, “at least 10 children died from a variety of causes, including four from blood poisoning, and researchers said they were unable to determine a safe, useful dosage. They said the deaths didn’t appear to be “directly attributable” to dapsone but nonetheless were “disturbing.”
“overall mortality while receiving the study drug was significantly higher in the daily dapsone group. This finding remains unexplained,” the researchers concluded.
“Another study involving foster children in the 1990s treated children with different combinations of adult antiretroviral drugs. Among 52 children, there were 26 moderate to severe reactions — nearly all in infants. The side effects included rash, fever and a major drop in infection-fighting white blood cells.
At least three states declined to use children in foster care in medical experiments: Tennessee said its foster care rules generally prohibit enlisting children in such trials. California requires a judge’s order. And Wisconsin “has absolutely never allowed, nor would we even consider, any clinical experiments with the children in our foster care system,” spokeswoman Stephanie Marquis said.
Not addressed in the AP report is the amount of money that these trials generated for the institutions involved in the experiments.
***The NYC Council, general welfare committee is holding a hearing about the unethical experiments conducted in NYC. The hearing will take place at City Hall at 11:15.
For information and to register to speak, call: Ms. Jackie Sherman at 212-788-7015
Contact: Vera Hassner Sharav
212-595-8974
Researchers Tested AIDS Drugs On Children – Associated Press
by JOHN SOLOMON
11:08 AM PDT, May 4, 2005
WASHINGTON – Government-funded researchers tested AIDS drugs on hundreds of foster children over the past two decades, often without providing them a basic protection afforded in federal law and required by some states, an Associated Press review has found.
The research funded by the National Institutes of Health spanned the country. It was most widespread in the 1990s as foster care agencies sought treatments for their HIV-infected children that weren’t yet available in the marketplace.
The practice ensured that foster children — mostly poor or minority — received care from world-class researchers at government expense, slowing their rate of death and extending their lives. But it also exposed a vulnerable population to the risks of medical research and drugs that were known to have serious side effects in adults and for which the safety for children was unknown.
The research was conducted in at least seven states — Illinois, Louisiana, Maryland, New York, North Carolina, Colorado and Texas — and involved more than four dozen different studies. The foster children ranged from infants to late teens, according to interviews and government records.
Several studies that enlisted foster children reported patients suffered side effects such as rashes, vomiting and sharp drops in infection-fighting blood cells as they tested antiretroviral drugs to suppress AIDS or other medicines to treat secondary infections.
In one study, researchers reported a “disturbing” higher death rate among children who took higher doses of a drug. That study was unable to determine a safe and effective dosage.
The government provided special protections for child wards in 1983. They required researchers and their oversight boards to appoint independent advocates for any foster child enrolled in a narrow class of studies that involved greater than minimal risk and lacked the promise of direct benefit. Some foster agencies required the protection regardless of risks and benefits.
Advocates must be independent of the foster care and research agencies, have some understanding of medical issues and “act in the best interests of the child” for the entirety of the research, the law states.
However, researchers and foster agencies told AP that foster children in AIDS drug trials often weren’t given such advocates even though research institutions many times promised to do so to gain access to the children.
Illinois officials believe none of their nearly 200 foster children in AIDS studies got independent monitors even though researchers signed a document guaranteeing “the appointment of an advocate for each individual ward participating in the respective medical research.”
New York City could find records showing 142 — less than a third — of the 465 foster children in AIDS drug trials got such monitors even though city policy required them. The city has asked an outside firm to investigate.
Likewise, research facilities including Chicago’s Children’s Memorial Hospital and Johns Hopkins University in Baltimore said they concluded they didn’t provide advocates for foster kids.
Some states declined to participate in medical experiments. Tennessee said its foster care rules generally prohibit enlisting children in such trials. California requires a judge’s order. And Wisconsin “has absolutely never allowed, nor would we even consider, any clinical experiments with the children in our foster care system,” spokeswoman Stephanie Marquis said.
Officials estimated that 5 percent to 10 percent of the 13,878 children enrolled in pediatric AIDS studies funded by NIH since the late 1980s were in foster care. More than two dozen Illinois foster children remain in studies today.
Some foster children died during studies, but state or city agencies said they could find no records that any deaths were directly caused by experimental treatments.
Researchers typically secured permission to enroll foster children through city or state agencies. And they frequently exempted themselves from appointing advocates by concluding the research carried minimal risk and the child would directly benefit because the drugs had already been tried in adults.
“Our position is that advocates weren’t needed,” said Marilyn Castaldi, spokeswoman for Columbia Presbyterian Medical Center in New York.
If they decline to appoint advocates under the federal law, researchers and their oversight boards must conclude that the experimental treatment affords the same or better risk-benefit possibilities than alternate treatments already in the marketplace. They also must abide by any additional protections required by state and local authorities.
Many of the studies that enrolled foster children occurred after 1990 when the government approved using the drug AZT — an effective AIDS treatment — for children.
Arthur Caplan, head of medical ethics at the University of Pennsylvania, said advocates should have been appointed for all foster children because researchers felt the pressure of a medical crisis and knew there was great uncertainty as to how children would react to AIDS medications that were often toxic for adults.
“It is exactly that set of circumstances that made it absolutely mandatory to get those kids those advocates,” Caplan said. “It is inexcusable that they wouldn’t have an advocate for each one of those children.
“When you have the most vulnerable subjects imaginable — kids without parents — you really do have to come in with someone independent, who doesn’t have a dog in this fight,” he said.
Those who made the decisions say the research gave foster kids access to drugs they otherwise couldn’t get. And they say they protected the children’s interest by carefully explaining risks and benefits to state guardians, foster parents and the children themselves.
“I understand the ethical dilemma surrounding the introduction of foster children into trials,” said Dr. Mark Kline, a pediatric AIDS expert at Baylor College of Medicine. He enrolled some Texas foster kids in his studies, and doesn’t recall appointing advocates for them.
“To say as a group that foster children should be excluded from clinical trials would have meant excluding these children from the best available therapies at the time,” he said. “From an ethical perspective, I never thought that was a stand I could take.”
Illinois officials directly credit the decision to enroll HIV-positive foster kids with bringing about a decline in deaths — from 40 between 1989 and 1995 to only 19 since.
NIH, the government health research agency that funded the studies, did not track researchers to determine if they appointed advocates. Instead, the decision was left to medical review boards made up of volunteers at each study site.
A recent Institute of Medicine study concluded those Institutional Review Boards (IRBs) were often overwhelmed, dominated by scientists and not focused enough on patient protections. An ethicist who served 22 years on such boards said they lack the resources to ensure the safety of foster children.
“Over the last half century, IRBs have basically broken under the strain of some of the structural changes in research,” said Gregory E. Pence, a University of Alabama-Birmingham bioethicist.
The U.S. Office for Human Research Protections, created to protect research participants after the infamous Tuskegee syphilis studies on black men, is investigating the use of foster children in AIDS research. The office declined to discuss the probe.
NIH said it considers patient safety its top priority and awaits the outcome of the investigation. “If we find that patient protections need further strengthening, we will take action to do so,” spokesman John Burklow said.
AP’s review found that if children were old enough — usually between 5 and 10 — they also were educated about the risks and asked to consent. Sometimes, foster parents or biological parents were consulted; other times not.
“Our policy was to try and contact the (biological) parents because it was fairly common when we got done the foster kid would go back to the parents,” said Dr. Ross McKinney, a pediatrics AIDS expert at Duke University.
Research and foster agencies declined to make foster parents or children in the drug trials available for interviews, or to provide information about individual drug dosages, side effects or deaths, citing medical privacy laws.
Other families who participated in the same drug trials told AP their children mostly benefited but parents needed to carefully monitor potential side effects. Foster children, they said, need the added protection of an independent advocate.
“I don’t believe a foster care parent can do it,” said Vinnie DiPoalo, a New Jersey woman whose 10-year-old adopted son has participated in three AIDS drug trials. “There are informed consents that have to be signed. There are follow-up blood appointments.
“I think that’s the role the advocate should take, because a foster parent may only have this child for three months and then the child moves on and someone needs to be watching all the time,” she said.
Many studies that enlisted foster children involved early Phase I and Phase II research — the riskiest — to determine side effects and safe dosages so children could begin taking adult “cocktails,” the powerful drug combinations that suppress AIDS but can cause bad reactions like rashes and organ damage.
Some of those drugs were approved ultimately for children, such as stavudine and zidovudine. Other medicines were not.
Illinois officials confirmed two or three foster children were approved to participate in a mid-1990s study of dapsone. Researchers hoped the drug would prevent a pneumonia that afflicts AIDS patients.
Researchers reported some children had to be taken off the drug because of “serious toxicity,” others developed rashes, and the rates of death and blood toxicity were significantly higher in children who took the medicine daily, rather than weekly.
At least 10 children died from a variety of causes, including four from blood poisoning, and researchers said they were unable to determine a safe, useful dosage. They said the deaths didn’t appear to be “directly attributable” to dapsone but nonetheless were “disturbing.”
“An unexpected finding in our study was that overall mortality while receiving the study drug was significantly higher in the daily dapsone group. This finding remains unexplained,” the researchers concluded.
Another study involving foster children in the 1990s treated children with different combinations of adult antiretroviral drugs. Among 52 children, there were 26 moderate to severe reactions — nearly all in infants. The side effects included rash, fever and a major drop in infection-fighting white blood cells.
New York City officials defend the decision to enlist foster children en masse, saying there was a crisis in the early 1990s and research provided the best treatment possibilities. Nonetheless, they are changing their policy so they no longer give blanket permission to enroll children in preapproved studies.
“We learned some things from our experience,” said Elizabeth Roberts, assistant commissioner for child and family health at the Administration for Children’s Services. “It is a more individualized review we will be conducting.”
Researchers likewise defend their work, saying they often sat with foster families to explain the risks and benefits, and provided them literature and 24-hour phone numbers.
“We talk about it. Then they come the next time. There is no rush,” explained Dr. Ram Yogev, the chief pediatric AIDS researcher in Chicago whose patients include a large number of foster children.
Kline, the Texas researcher, added: “I never wanted a parent or guardian to ever say ‘yes’ simply because they thought that it was what I wanted them to do. I wanted it to be the right choice for them. I think there is not any single right answer for any family.”
_____
Researcher Rachel Landau in Washington and reporter Carla K. Johnson in Chicago contributed to this story. On the Net:
Documents associated with this story are available at: http://wid.ap.org/inv/foster.html
Liam Scheff’S BOMBSHELL Interview:
Includes nurses who participated in the experiments!
An excerpt below from Kennedy’s explosive book describing Fauci’s medical experiments on children:
Robert Kennedy sat for an interview this past month to journalist James Corbett where he laid out some key arguments from the book and specifically explained the facts on Fauci’s illegal testing on orphan children:
- Fauci tested harsh chemotherapy drugs on orphan children in order to determine its use for AIDS treatments in the 1980s
- Fauci got control of foster homes in 7 states
- Children were tortured to death
- Children were denied guardians and any kind of legal protector
- Children who refused to take Fauci’s drugs had feeding tubes installed so drug companies could administer the drugs even when the kids fought back
- Most of the children did not have HIV/AIDS, they were just used as guinea pigs to see if they could survive the harsh drug regimen
- At least 85 kids died as part of these experiments
The graveyard where these children were thrown into a pit, filled with hundreds of coffins sometimes stuffed with multiple children, is buried under an astroturf pit in New York. These are the victims of Fauci’s crimes, says Kennedy.
The Gateway Pundit was able to locate this memorial to the orphan children killed by Dr. Fauci and the NIH in New York State.
The orphans are not forgotten. There are toys and flowers left at the memorial.
The names of the orphans are listed on the memorial wall.
And an angel holds a stuffed Teddy Bear.
These photos were taken from Google.
RFK Jr.: Reporter Found Monument To Dead Orphans Tortured And Killed By Monster Fauci (VIDEO)
by Jim Hoft, Gateway Pundit
Robert F. Kennedy, Jr. joined The High Wire recently to discuss his best-selling book on monster Dr. Tony Fauci.
During the discussion, RFK Jr. revealed that reporter Cecelia Farber went to the cemetery in New York state where the tortured orphan children were buried. These victims were Fauci’s experimental patients.
The Gateway Pundit reported earlier on this monument and cemetery in New York State.
Fauci has a long history of mass death, barbarism and lies.
In 2004 Dr. Fauci’s NIH was also caught funding experiments on AIDS orphans at a New York City hospital. The Gateway Pundit reported on this dark Fauci chapter in October.
The Fauci NIH approved experiments on hundreds of New York City orphans. Government agencies and pharmaceutical companies used the orphans in deadly AIDS drug trials.
In 2005, the city of New York hired the VERA Institute to form a final report on the drug trials. VERA was given no access to medical records for any of the children used in trials. Their report was published in 2008.
They reported that twenty-five children died during the drug studies, that an additional fifty-five children died following the studies (in foster care), and, according to Tim Ross, Director of the Child Welfare program at VERA (as of 2009), 29% of the remaining 417 children who were used in drug studies had died (out of a total 532 children that are admitted to have been used). [LINK]
The WIKIPEDIA writers cover up all details, as is expected.
No payment or compensation has been paid to any of the children used in the trials, or to their families.
A hospital nurse later spoke out to reporters about the testing. She reported that children would immediately get sick, break out or throw up during the testing.
They were orphans at the Incarnation Children’s Center in New York City.
Also mirrored on BitChute.com:
https://www.bitchute.com/embed/WGMDPce0Wuk7/
On Tuesday The Gateway Pundit reported on Dr. Fauci’s torture and medical murder of at least 85 orphan minority children in New York, children who were vulnerable, could not consent, and who would not be missed.
Ann Rosen at LifeSiteNews wrote a good recap of Fauci’s crimes against children earlier this month.
These children were buried in mass graves at the Gate of Heaven Cemetery in Hawthorne, NY in Westchester County and otherwise forgotten.
Robert F. Kennedy Jr. says that Anthony Fauci is America’s Joseph Mengele for what he did to poor orphan minority kids in the 1980’s.
These extreme claims are the subject of a new book by Robert F. Kennedy, Jr., called “The Real Anthony Fauci.” In Chapter 7, the Kennedy heir lays out “NIAID’s Barbaric and Illegal Experiments on Children”
Kennedy refers to Fauci as ‘America’s homegrown Mengele.’
BIG BROTHER in the 21. Century 