by Brian Shilhavy
Editor, Health Impact News
We are talking about the most horrible scandal and scam ever perpetrated, not only in the name of “science,” but in humanity and all history.
The great lie of Hitler – it’s amazing, I think he would envy the job being done by members of the National Institutes of Health, and even the media, especially in this country.
And I will put the lie to the individuals of the NIH, particularly Gallo, Fauci, and Haseltine and Essex and the rest of these scoundrels of the worst order.
Criminals guilty of genocide, without a doubt.
I invite them to take me to court! I wish Burroughs Wellcome would take me to court!
Because they have been putting out a killer drug knowingly. Because in a court of law, I would have the opportunity to provide the absolute proof and evidence, as I have in my book, Deadly Deception.
Dr. Wilner is the author of the book, Deadly Deception: the Proof That Sex And HIV Absolutely Do Not Cause AIDS. To prove his point, Dr. Wilner injected himself on live camera with blood from an HIV infected person, to show that it was harmless.
This video clip from a presentation given on December 7, 1994, by Dr. Robert Wilner is circulating through the Internet today because of what he said over 25 years ago about Anthony Fauci, and others at the National Institute of Health at that time.
Dr. Wilner died less than a year after this presentation in April of 1995, supposedly from a heart attack (if you believe in Fairy Tales).
If what Dr. Wilner said was true of Anthony Fauci almost 30 years ago, of how many people he had killed back in 1994, what does that say about Anthony Fauci today in light of the number of bioweapons he helped create, including the AIDS virus that was purposely put into hepatitis vaccine to kill off drug addicts and homosexuals, several variants of swine and avian flu and finally the spike protein that was released in Wuhan China to cause the COVID-19 Plandemic?
The Plandemic was then fueled by lies perpetrated by Dr. Fauci, Bill Gates and the mainstream media, causing so much fear that tens of millions of people lined up like sheep to be injected with so-called COVID vaccines.
These injections do not stop the disease, but in fact create it. Moreover, they were designed to cause a slow and painful death. Some experts are predicting that these duped individuals will likely die within the first two years after being injected. In fact, thousands have already died within minutes hours and days after being injected.
We printed many articles on Anthony Fauci in 2020, and in case anyone wants to accuse me of exaggerating, let’s do a review of some of the crimes Anthony Fauci has been involved in for the past few decades.
Dr. Fauci and the NIH’s History in Experimenting on Foster Children and Using Aborted Fetal Tissue to Develop an HIV Vaccine
When we started MedicalKidnap.com in 2014, one of the shocking things we learned was that it was perfectly legal for medical researchers to use foster children as lab rats to develop drugs.
Once the state takes custody of a child away from the parents, and the child becomes a ward of the state, medical researchers no longer need parental approval to conduct medical research, and they can also bill the U.S. Government directly to fund this research, usually using Medicaid, even if the drugs being used are experimental and have not yet been approved by the FDA.
We published an article in May of 2015 highlighting this horrible practice that is legal in the U.S. See:
Some highlights from that article:
The U.S. federal government has mandated drug research with children. The need for children to participate in drug company research is high, and the temptation to overstep parental rights to force children to participate is great. Researchers publicly admit using money and other rewards to obtain participation of children in their drug trials.
Organizations that advocate for the rights of parents to make decisions regarding their children’s healthcare are finding that foster children in CPS custody are being enrolled in drug experiments without parental approval. State Child Protective Services are enrolling children in drug experiments without parental approval or court orders.
However, those who conduct these drug experiments for pharmaceutical companies, and those who are charged with monitoring such research, do not see a problem with their recruitment methods.
In a 2011 article in the Journal Pediatrics, researchers discussed the problem of recruiting children for participation in clinical trials for drug testing. Researchers from Ohio State University (Columbus) and Case Western Reserve University, confirm that the US federal government is mandating that children be included in clinical research studies.
Dr. Tishler, PhD, and Dr. Staats Reiss, PhD stated:
Since 1994, federal guidelines have called for the inclusion of children in clinical studies. Related federal incentives and laws such as the “pediatric rule” (the Pediatric Research Equity Act) and the pediatric exclusivity provision have also been passed to increase the number of pediatric clinical trials launched by pharmaceutical companies. Despite these mandates, the allocations to pediatric clinical trials in federal and private research and development budgets have remained limited. In addition, pediatric researchers continue to experience difficulty locating children and families who are willing to enroll in clinical trials.
Recruitment for pediatric studies is hampered by several factors including ethical concerns with using children as subjects, regulatory oversight that is significantly more restrictive for child trials than for adult trials, a lack of research infrastructure, the need to obtain consent from parents, and the challenge of determining appropriate payments for participation that are not coercive.
In 2005, a hearing with the title “Protections for Foster Children Enrolled in Clinical Trials” was held by the U.S. House of Representatives. The Subcommittee on Human Resources of the Committee on Ways and Means, investigated whether adequate safeguards were in place to protect foster children from being forced to participate in drug studies.
The allegation that they were investigating involved clinical drug trials on AIDS drugs that were conducted during the period from the late 1980s through 2001.
Since publishing this article back in 2015, much more information has come to surface, especially in light of the COVID Plandemic of 2020. The same group of people who have been involved in HIV/AIDS research to develop an HIV vaccine, a vaccine which has never come to market, are the same group of people now working with the U.S. Government to develop a COVID vaccine.
The public has a right to know more about the past research to develop an HIV vaccine, and how they experimented on children who were “legally” kidnapped from their families for research purposes, as well as the live aborted fetuses that were used to try and create “humanized mice” to produce this vaccine, since this is the same group that has been given hundreds of millions of dollars by the U.S. Government to now develop a COVID vaccine.
Dr. Fauci and the National Institute of Allergy and Infectious Diseases Use of Foster Children in Developing an HIV Vaccine
Faith Dyson recently published an article on Facebook titled: What Was Fauci’s Role In Funding Tuskgegee-Like AIDS Experiments On Foster Children In Seven U.S. States?
In 2004 – investigative journalist, Liam Scheff, exposed the fact that hundreds of Foster children at Incarnation Children’s Center [ICC] in NYC were used and abused as lab rats for unsupervised and unrestricted AIDS research and Vaccine studies by Big Pharma and The National Institute of Allergy and Infectious Diseases [NIAID].
Years later in separate investigations – 13,878 children were discovered to have been made subject of the same fate during the 1980’s and 1990’s in six other states: Illinois, Louisiana, Maryland, North Carolina, Colorado and Texas.
As we found out in our own investigative report back in 2015, Congress knew about these medical experiments being conducted on foster children and conducted a hearing in 2005, with the title “Protections for Foster Children Enrolled in Clinical Trials.”
The transcript of these hearings used to be on the House.gov website, but since we published our article it has been removed. A copy can be found at Archives.org here.
Liam Scheff details what some of these foster children went through in his book.
In New York’s Washington Heights is a 4-story brick building called Incarnation Children’s Center (ICC). This former convent houses a revolving stable of children who’ve been removed from their own homes by the Agency for Child Services [ACS]. These children are black, Hispanic and poor.
Once taken into ICC, the children become subjects of drug trials sponsored by NIAID (National Institute of Allergies and Infectious Disease, a division of the NIH), NICHD (the National Institute of Child Health and Human Development) in conjunction with some of the world’s largest pharmaceutical companies – GlaxoSmithKline, Pfizer, Genentech, Chiron/Biocine and others.
The drugs being given to the children are toxic – they’re known to cause genetic mutation, organ failure, bone marrow death, bodily deformations, brain damage and fatal skin disorders.
If the children refuse the drugs, they’re held down and have them force fed. If the children continue to resist, they’re taken to Columbia Presbyterian hospital where a surgeon puts a plastic tube through their abdominal wall into their stomachs. From then on, the drugs are injected directly into their intestines.
In 2003, two children, ages 6 and 12, had debilitating strokes due to drug toxicities. The 6-year-old went blind. They both died shortly after. Another 14-year old died recently. An 8-year-old boy had two plastic surgeries to remove large, fatty, drug-induced lumps from his neck.
This isn’t science fiction. This is AIDS research. The children at ICC were born to mothers who tested HIV positive, or who themselves tested positive. However, neither parents nor children were told a crucial fact — HIV tests are extremely inaccurate. The HIV test cross-reacts with nearly seventy commonly-occurring conditions, giving false positive results. These conditions include common colds, herpes, hepatitis, tuberculosis, drug abuse, inoculations and most troublingly, current and prior pregnancy. This is a double inaccuracy, because the factors that cause false positives in pregnant mothers can be passed to their children – who are given the same false diagnosis.
Most of us have never heard this before. It’s undoubtedly the biggest secret in medicine. However, it’s well known among HIV researchers that HIV tests are extremely inaccurate – but the researchers don’t tell the doctors, and they certainly don’t tell the children at ICC, who serve as test animals for the next generation of AIDS drugs. ICC is run by Columbia University’s Presbyterian Hospital in affiliation with Catholic Home Charities through the Archdiocese of New York.
Does the issue of “inaccurate tests” sound familiar? It should, because we are seeing the exact same thing today with COVID tests.
Faith Dyson writes about her reaction after reading Liam Scheff’s reports:
When I read the report, I was much like the general public – totally ignorant of NIAID; its director, funding, etc. and I doubt at that time there were very many other people who would have known who was in charge of the Agency outside of government bureaucrats, scientists, researchers, activists and possibly those who were affected by ‘the AIDS/HIV virus’.
What’s interesting to note here is that the source and/or existence of that pandemic is another highly questionable subject, because it appears to mimic the same scenario that accompanies the latest super-bug to attack the world’s population, the Coronavirus.
In fact – they’re so much alike, one would think the exact same plan had been followed in the production of both epidemics; the older one, AIDS/HIV, using monkeys and the newer one, Corona, using bats. (See link #3 for a shocking revelation re: active viruses in childhood vaccines that cause AIDS, Cancer, and Leukemia plus a host of other diseases and disorders and see #4 for the traumatic details of how the effects are still plaguing our population decades later.)
Therefore – due to the results of the AIDS/HIV epidemic, those most affected by it had been demanding – from the same government Agency and pharmaceutical companies – some sort of treatment, vaccine, drug, etc. to stem the tide of the infection.
So the big question back then was:
“Where could Big Pharma and NIAID find lab rats to whom they could offer ‘free medical care’ in the guise of ‘helping to prevent and/or remedy their suffering’ all the while using them in AIDS/HIV drug and vaccine trails – without being bothered from outside interference, the same as was done in the infamous Tuskgegee Syphilis Experiment?” (See link #5.)
As Liam Scheff uncovered – the answer to their mad scientific prayers was the unsupervised and unprotected wards of the state, a.k.a. ‘Foster children’.
However – since the newest pandemic has arisen to overshadow all others, and we now have a much larger group of people demanding the same provisions from the same corporations and Government Agency, we all know who is the head of NIAID.
It’s Dr. Anthony Fauci, one of the lead members of the Trump Administration’s White House Coronavirus Task Force addressing the COVID-19 pandemic in the United States.
So a recap of the facts we’ve learned from the corona outbreak – in conjunction with the AIDS/HIV funding that spawned the experiments at Incarnation Children’s Center and elsewhere – are as follows:
1) Dr. Fauci has been the director of NIAID, a division of The Executive Branch of The U.S. Government, since 1984, so he was also director during the Incarnation Children’s Center Experiments,
2) his NIAID profile states that he still currently “oversees an extensive research portfolio of basic and applied research to prevent, diagnose, and treat established infectious diseases such as HIV/AIDS, respiratory infections, diarrheal diseases, tuberculosis and malaria as well as emerging diseases such as Ebola and Zika.” (See link #6),
3) Fauci participates in Gate-sponsored Global Health Conferences and is listed on The Leadership Council for The Bill And Melinda Gates Foundation (See link #7 and #8.), which has a huge stake in the profits from a Vaccine, Contact Tracing, microchipping, and various other technologies,
4) NIAID illegally outsourced $3.7 Million in U.S. Tax-payer’s money to Chinese scientists in the Wuhan Lab at the center of the Coronavirus outbreak for researching its ‘gain of function’ – after a moratorium had called a halt to all U.S. involvement in such studies. (See link #9.)
5) Fauci famously predicted in a speech from 2017 at Georgetown University: “[…], but also there will be a surprise outbreak […], and the history of the last 32 years that I’ve been the director of NIAID will tell the next administration that there’s no doubt in anyone’s mind that they will be faced with the challenges that their predecessors were faced with” – in a battle with a pandemic of infectious disease. (See link #10)
Read the entire article by Faith Dyson here.
Judicial Watch Sues the FDA to Obtain Records on Purchases of “Fresh and Never Frozen” Fetus Parts for HIV/AIDS Research
Last year we published an interview between Robert F. Kennedy, Jr. and Dr. Theresa Deisher regarding the use of human fetal tissue to culture viruses for vaccines.
Most of the COVID vaccines being developed are using human fetal tissue to culture the coronavirus.
One of the more interesting questions Mr. Kennedy asked Dr. Deisher was why the manufacturers of vaccines switched from exclusively using animal tissue to culture viruses for vaccines, to start using aborted fetal tissue some years back.
Dr. Deisher’s reply was that the industry was getting a lot of pressure from the animal rights movement to stop using animals for experimentation.
Mr. Kennedy was shocked, and stated:
It’s kind of weird to think that the animal rights activists have more clout with the vaccine companies than do the anti-abortion activists.
Dr. Deisher replied:
They do. And you know what’s really alarming is the lack of outcry over human babies born alive at five to six months old so that their hearts can be obtained beating. And they have to be beating to be used in the research that’s being done.
If the heart has stopped beating, it’s not useful. You cannot use it.
And so these babies are delivered alive, and their hearts cut out without anesthesia.
I wouldn’t do that to a mouse….
Om June 23, 2020, Judicial Watch announced that they had obtained records showing that the FDA paid for “Fresh and Never Frozen” human fetal parts for use in “Humanized Mice” creation in the past for HIV/AIDS research.
Judicial Watch announced today it received 165 pages of records from the Food and Drug Administration (FDA) showing the FDA between 2012 and 2018 entered into 8 contracts worth $96,370 with Advanced Bioscience Resources (ABR) to acquire “fresh and never frozen” tissue from 1st and 2nd trimester aborted fetuses for use in creating “humanized mice” for ongoing research.
ABR is a non-profit firm which has been the subject of criminal referrals from House and Senate committees investigating whether Planned Parenthood or any other entity was illegally profiting from the handling of fetal tissue from aborted babies.
Judicial Watch filed the lawsuit in the United States District Court for the District of Columbia (Judicial Watch v. U.S. Department Health and Human Services (No. 1:19-cv-00876)) after HHS failed to respond adequately to a September 28, 2018, FOIA request seeking:
- All contracts and related documentation between FDA and Advanced Biosciences Resources (ABR) for the provision of human fetal tissue to be used in humanized mice research.
- All records reflecting the disbursement of funds to ABR for the provision of human fetal tissue to be used in humanized mice research.
- All guidelines and procedural documents provided to ABR by FDA relating to the acquisition and extraction of human fetal tissue for its provision to the FDA for humanized mice research.
- All communications between FDA officials and employees and representatives of ABR related to the provision by ABR to the FDA of human fetal tissue for the purpose of humanized mice research.
On February 13, 2020, Judicial Watch announced:
(Washington, DC) – Judicial Watch announced it received 676 pages of records from the National Institutes of Health (NIH) showing that the agency paid thousands of dollars to a California-based firm to purchase organs from aborted human fetuses to create “humanized mice” for HIV research.
The records show that NIH paid at least $18,100 between December 2016 and August 2018 to Advanced Bioscience Resources (ABR) for livers and thymuses from second trimester aborted fetuses. They include at least 26 such purchases from ABR by Dr. Kim Hasenkrug, senior investigator at the NIH lab in Hamilton, Montana.
Purchase orders associated with the transactions state: “These tissues, liver and thymus, are required [by] Ron Messer for ongoing studies of HIV in the Hasenkrug Lab. Our mice will be ready for reconstitution soon.”
The Trump Administration put a ban on using aborted human fetal tissue in federally funded research, but during the COVID Plandemic some members of Congress petitioned to get an exemption for COVID-19 research. (Source.)
Read the full article here.
Biden’s Border Crisis is Worse Than Most People Realize
Today under the Biden administration, tens of thousands of unaccompanied minors are crossing the border from Mexico into the United States with no documentation.
All of those children will enter into the Foster Care system, where many of them will be used for drug research, probably for future versions of the new mRNA bioweapons wrongly called “vaccines.”
Others will face a far worse fate, either being sexually trafficked or murdered outright for body parts, or to make the drug Adrenochrome.
When you look at Anthony Fauci on TV, does he look more like a 60-year-old man, or an 80-year-old man?
He is 80 years old. Does he consume Adrenochrome to stay looking young?
This article was written by Torsten Engelbrecht and Konstantin Demeter and published on Off-Guardian.org last year.
Saying the untruth and not answering is a characteristic behaviour that runs through Fauci’s entire 36 years in which the now 79-year-old has been director of the National Institute of Allergy and Infectious Diseases (NIAID). And this has very serious consequences.
Because with a current annual budget of almost six billion dollars, Fauci’s institute is a giant in AIDS, tuberculosis, malaria and autoimmune research — while he himself is perhaps the most powerful man in the global virus circus.
The abundance of lies Fauci puts into the world is so great that you don’t even know where to start to enumerate them all. One of the many topic fields he is sending out factually untenable statements to the whole world is without question COVID-19. In order to become aware of this, one has to realize that:
- a) the RT-PCR tests are scientifically meaningless in detecting so-called SARS-CoV-2 infections,
- b) even according to orthodox researchers so-called SARS-CoV-2 is not excessively dangerous
- c) people, referred to as COVID-19 victims, probably did not die of so-called SARS-CoV-2 but of non-viral factors such as cancer and other serious underlying diseases, the experimental administration of highly toxic drugs and/or invasive ventilation.
Thus, Fauci‘s narratives about the alleged novel coronavirus become downright a fairy tale. And a fairy tale teller, a modern-day Munchausen “Baron of Lies”, Fauci has been since he became the director of the NIAID in 1984 — the year Ronald Reagan was US president and AIDS was put on the world stage.
This was a turning point in modern world history. Since then the virus hunters enjoy god-like status, and this was accomplished by lies and deceit. Fauci played a decisive role in its creation, and the parallels to the “installation” of COVID-19 are striking.
How Fauci’s Falsehoods turned AZT into a “magic bullet”
How could this happen? Not least due to the swine flu disaster in 1976 in which 50 million US citizens were persuaded to get vaccinated, resulting in side effects in 20 percent to 40 percent of recipients, including paralysis and even death, the US National Institutes of Health (NIH) and the Centers for Disease Control and Prevention (CDC) came into unsettled political waters at the end of the 1970s.
As a result, the great contemplation began at these two most powerful organizations related to health politics and biomedical science.
In fact, Red Cross officer Paul Cumming told the San Francisco Chronicle in 1994 that “the CDC increasingly needed a major epidemic” at the beginning of the 1980s “to justify its existence.” And the HIV/AIDS theory was a salvation for American epidemic authorities.
As a result, “All the old virus hunters from the National Cancer Institute put new signs on their doors and became AIDS researchers. [US President Ronald] Reagan sent up about a billion dollars just for starters,” noted Kary Mullis who received the Nobel Prize for his invention of the Polymerase Chain Reaction (PCR) which plays a central role in the context of COVID-19. “And suddenly everybody who could claim to be any kind of medical scientist and who hadn’t had anything much to do lately was fully employed.“
Among those who jumped over from cancer research to AIDS research, the best known is Robert Gallo. “HIV didn’t suddenly pop out of the rain forest or Haiti. It just popped into Bob Gallo’s hands at a time when he needed a new career,” as Mullis, who unfortunately died last year, noted with a wink.
And it started with big lies. The most important one was announced in April 1984 by Gallo, working under Fauci, when he claimed in a press conference that gained worldwide attention that „the probable cause of AIDS has been found.“
NB. Gallo’s papers were printed in the journal Science over one week after his press conference and also after he had filed a patent application for an antibody test later misleadingly named “HIV test”. Thus, nobody was able to review his work prior to his spectacular TV appearance, and for some days afterwards.
This presented a severe breach of professional scientific etiquette. And as review later showed Gallo’s studies did not deliver any proof for the virus thesis.
Mullis confirmed it as well:
People keep asking me, ‘You mean you don’t believe that HIV causes AIDS?’ And I say, ‘Whether I believe it or not is irrelevant! I have no scientific evidence for it!’ I might believe in God, and He could have told me in a dream that HIV causes AIDS. But I wouldn’t stand up in front of scientists and say, ‘I believe HIV causes AIDS because God told me.’ I’d say, ‘I have papers here in hand and experiments that have been done that can be demonstrated to others.’ It’s not what somebody believes, it’s experimental proof that counts. And neither Montagnier, Gallo, nor anyone else had published papers describing experiments which led to the conclusion that HIV probably caused AIDS.”
Mullis even had the opportunity do ask Montagnier personally about a reference proving that HIV causes AIDS. But he couldn’t name one. “It was damned irritating,“ as Mullis reported. “If Montagnier didn’t know the answer, who the hell did?“
Of course, whoever is in possession of a solid peer-reviewed study that proves that HIV causes AIDS may please present it to me or my co-author!
I have searched for such a study by myself, but haven’t found it, either. I have also approached Anthony Fauci and his NIAID several times asking them, among other things, to send me such a study showing that HIV is a retrovirus that causes a deadly infection. Finally, I was told by Hillary Hoffman from the NIAID’s News and Science Writing Branch that:
Dr. Fauci respectfully declines to respond to the questions that you emailed.”
About this practice of refusing to answer questions Horace F. Judson, historian of molecular biology, wrote in his book The Great Betrayal: Fraud in Science:
Central to the problem of misconduct is the response of institutions when charges erupt. Again and again the actions of senior scientists and administrators have been the very model of how not to respond. They have tried to smother the fire. Such flawed responses are altogether typical of misconduct cases.”
Calling AZT trials “scientifically controlled” is like referring to garbage as “haute cuisine”
Such behavior, which smells of misconduct, runs like a golden thread through Fauci‘s 36-year history as director of the NIAID.
A particularly blatant example is the approval of azidothymidine – commonly known as AZT – that became the first authorized AIDS medication. The basis for this was the so-called Fischl study which was published in July 1987 in the New England Journal of Medicine (NEJM) — and already then Fauci was in charge of federal AIDS funding.
John Lauritsen, journalist, Harvard analyst and active in the Gay Rights Movement since the 1970s, had viewed the FDA documents on the Fischl study and came to the conclusion that the study was “fraud”; the Swiss newspaper Weltwoche termed the experiment a “gigantic botch-up” and NBC News in New York branded the experiments, conducted across the US, as “seriously flawed.“
Even the FDA toxicology analyst Harvey I. Chernov concluded — months before publication of the mentioned pivotal AZT study – in an FDA document obtained under the Freedom Of Information Act by John Lauritsten that:
The available data are insufficient to support FDA approval [of AZT].”
The Fischl experiments were, in fact, stopped after only four months, after 19 trial subjects in the placebo group (those who did not receive AZT, but rather an inactive placebo) and only one participant from the so-called verum group (those who were officially taking AZT) had died. Through this, according to the AIDS establishment, the efficacy of AZT appeared to be proven.
But the Fischl study was not even worth the paper it was printed on. Not only was it financed by AZT manufacturer Wellcome (today GlaxoSmithKline), which is clearly a conflict of interest, but it was “clear that Fauci‘s NIH and the FDA had far too ‘cozy’ a relationship with Burroughs-Wellcome,”as Lauritsen writes.
Apart from that, the study was stopped after only four months. A clinical trial observation period of only four months is much too short to be informative, considering the usual practice of administering AIDS medications over years, or even a lifetime.
Moreover, the Fischl study had been conducted in a downright fraudulent manner. “It is almost beyond the bounds of probability that the mortality data could be correct,” as Lauritsen states. “There are many ways that errors can occur in research. But in this particular study the most parsimonious explanation would be deliberate fraud.”
For example, the double-blind conditions of the study (according to which neither the researchers nor patients should have known who was taking AZT and who was taking placebos) were no longer existent after a short time. NBC lead reporter Perri Peltz stated in 1988, that almost immediately everyone knew who was getting what. Patients told how they can distinguish AZT from placebo by the taste.
Furthermore, the FDA documents show that the study results were distorted. For example, sicker patients were placed in the placebo group or because the group that swallowed AZT (and therefore had to cope with the severe side effects) received more supportive medical services than the placebo subjects.
NBC reported that there was widespread tampering with the rules of the Fischl trial. The rules had been violated coast to coast, and if all patients with protocol violations were dropped, there wouldn’t be enough to be able to continue the study.
Same Old Scam: From AZT to “swine flu” vaccines, PrEP & remdesivir
The list of Fauci‘s assertions, which he must know he cannot substantiate scientifically, is almost endless. This cannot be stressed often enough.
In the context of so-called “bird flu” (H5N1) which was exaggerated to a world threat by the WHO, politicians, scientists and the mainstream media between 2003 and 2005, Fauci predicted that “even in the best-case scenarios” it would “cause 2 to 7 million deaths” worldwide. As the journalist Michael Fumento writes in his article:
Dr. Fauci’s recurring disease ‘nightmares’ don’t materialize.”
In fact, even the World Health Organization (WHO) estimated that by May 16, 2006, H5N1 had killed “only” 100 people.
Equally unsubstantiated was Fauci’s aggressive promotion of H1N1 influenza (“swine flu”) vaccine in 2009. Back then he was reassuring that serious adverse events were “very, very, very rare”. Unfortunately, this statement was also irresponsibly unfounded, because the underlying studies were fast-tracked ones and lacked solid double-blind placebo-controls. There were also heavy conflicts of interests.
To make matters worse, only one year later, in 2010, the Swedish Agency for the Regulation of Prescription Drugs reported cases of children and adolescents suffering from narcolepsy after a swine flu vaccination — a neurological disorder that leads to a disturbance of the circadian rhythm (the biological clock that regulates the sleep-wake cycle).
Further analysis confirmed that the Pandemrix vaccine also caused the disease in vaccinated people in other countries. That the swine flu vaccine causes narcolepsy has been confirmed by the courts.
Nevertheless, Fauci did not let himself be put off.
In December 2015, for instance, the NEJM published his article Ending the HIV–AIDS Pandemic: Follow the Science. In this piece he made a case for “dramatically scale up HIV testing and treatment around the world” — including preexposure prophylaxis (PrEP), i.e. “using ART [antiretroviral therapy] for HIV prevention in HIV negative persons.”
That is to say, healthy people should take highly toxic drugs. But here again: As self-assured as he presents his statements, he was not prepared to substantiate them factually.
In my mentioned request to the NIAID, in relation to his 2015 article about PrEP I asked:
- In your NEJM article you write that the IPERGAY study showed that ‘persons who took PrEP… were 86% less likely to acquire HIV infection than those taking placebo.’ But in which study it has been shown that HIV is a very special retrovirus that causes a deadly infection?
- Or in other words: If even Luc Montagnier admits, that on the images done by electron microscopy of the cell culture that he used he “saw some particles but they did not have the morphology typical of retroviruses”xxxii — in which study it has been proven that HIV, which is said to be a retrovirus, is a deadly retrovirus?
- In your article you are making a case for “dramatically scale up HIV testing”—but in which study it has been proven that so-called HIV tests are in fact HIV tests?
- Do you agree that:
- so-called HIV tests respond “positive” to a wide range of physiological conditions
- HIV test kits were approved only for blood screening
- these tests do not claim to diagnose infection
- proteins such as p18 or p24 are not specific for HIV, and that
- there is no gold standard for an HIV test?
- You say in your article that “the early promise of durable effects from combination therapy has been realized for many patients.” But how can we conclude that ART being introduced in 1995/1996 is life-prolonging and responsible for having decreased the number of AIDS deaths in industrialized countries if:
- in 1995/1996 only a fraction of patients received ART
- statistics from the CDC and the RKI clearly show that the number of AIDS deaths actually reached the peak (mortality summit) as early as 1991,
- no reliable statements can be made as to whether a single drug and ART are life-prolonging, since the basic prerequisite for this is lacking: a solid placebo-controlled study that has demonstrated the superiority of the drug/ART?
Unfortunately, as mentioned, Hillary Hoffman from NIAID just let me know that:
Dr. Fauci respectfully declines to respond to the questions that you emailed.”
Another example of a Fauci farce is Gilead Sciences’ rapid-release drug remdesivir, which was approved on May 2, 2020 in the context of COVID-19 for emergency use only. A few days before, the NIAID director claimed that a study found remdesivir would reduce recovery time and reduce mortality.
This can only be described as another scandal in which Fauci plays a central role—especially when you look at the fraudulent way in which the drug was approved and which is very similar to the way AZT was authorized in 1987.
An article from the Alliance for Human Research and Protection (AHRP) — Fauci’s Promotional Hype Catapults Gilead’s remdesivir — brought up the following painful subject:
Fauci has a vested interest in remdesivir. He sponsored the clinical trial whose detailed results have not been peer-reviewed. Furthermore, he declared the tenuous results to be ‘highly significant,’ and pronounced remdesivir to be the new ‘standard of care.’ Fauci made the promotional pronouncement while sitting on a couch in the White House, without providing a detailed news release; without a briefing at a medical meeting or in a scientific journal — as is the norm and practice, to allow scientists and researchers to review the data.
When he was asked about a recently published Chinese study on remdesivir, in The Lancet (April 29th , 2020); a trial that was stopped because of serious adverse events in 16 (12%) of the patients compared to four (5%) of patients in the placebo group, Dr. Fauci dismissed the study as ‘not adequate.’
But while the Chinese study that Fauci denigrated, was a randomized, double-blind, placebo-controlled, multi-center peer-reviewed, published study in a premier journal, The Lancet, with all data available, the NIAID-Gilead study results the remdesivir approval is based on have not been published in peer-reviewed literature — nor have details of the findings been disclosed.
“However, they were publicly promoted by the head of the federal agency that conducted the study, from the White House,” as the AHRP underlined. “What better free advertisement?”
By the way, regarding Fauci’s financial relations with Gilead, there is a petition that requests that he discloses them, since he hasn’t done it yet.
What the virus tsar also failed to disclose to the public in his promotional pronouncement of remdesivir was that the primary outcomes of the study that led to its emergency use approval were changed on April 16, 2020. Changes in the primary outcome are posted on clinicaltrials.gov.
Where previously there was an 8-point scale, which also included the deceased patients, from then on there has been only a 3-point scale, which leaves the deceased patient out of the equation and which at the same time only measures the time until recovery or being released from the hospital.
“Changing primary outcomes after a study has commenced is considered dubious and suspicious,” as the AHRP pointed out. And Reuters News reported that respected prominent leaders in the medical community — such as Steven Nissen MD, the chief academic officer at the Cleveland Clinic and Eric Topol MD, director and founder of the Scripps Research Translational Institute in California — were unimpressed by remdesivir’s tentative, modest benefit at best.
Referring to the Lancet report, Topol stated:
That’s the only thing I’ll hang my hat on, and that was negative.”
As for the NIAID modest results, Dr Topol was unimpressed:
It was expected to be a whopping effect. It clearly does not have that.”
The change in primary outcome measures raised serious red flags for scientists; but was largely ignored by the mainstream media which mostly repeated Fauci’s promotional script.
Steve Nissen told The Washington Post:
I think that they thought they weren’t going to win, and they wanted to change it to something they could win on. I prefer the original outcome. It’s harder. It’s a more meaningful endpoint. Getting out of the hospital early is useful, but it’s not a game-changer.”
As you can guess, all the questions I have asked the NIAID regarding remdesivir have remained unanswered as well…
How toxic remdesivir is, is also shown by the fact that just recently, on October 2, the European Medicines Agency (EMA), the regulator of medicinal products of the European Union, started a safety review of remdesivir. Reason: Some patients taking the drug reported serious kidney problems.
About two weeks later, on October 15, the WHO reported that in its own trial named “Solidarity” which started in March this year remdesivir not only failed to produce any measurable benefit in terms of mortality reduction, but that it also didn’t reduce the need for ventilators, or the length of hospital stays.
Robert F. Kennedy Jr’s organization Children’s Health Defense pointed this out on October 23 on its website. Fauci, by contrast, again remained silent about this study.
But Gilead shot ahead and commented in all seriousness “it is unclear if any conclusive findings can be drawn from the [Solidarity] study results,” because the trial hadn’t been peer reviewed or published in a scholarly journal.
But this comment is downright ridiculous.
On the one hand, it was no less a figure than Tedros Adhanom Ghebreyesus, Director-General of the WHO, who initiated this multi-center, global Solidarity trial (more than 11,300 adults with Covid-19 in 405 hospitals in 30 countries) for the very reason that:
Multiple small trials with different methodologies may not give us the clear, strong evidence we need about which treatments help to save lives. This large, international study is designed to generate the robust data we need, to show which treatments are the most effective.”
Moreover, Gilead forgot to mention in its statement that the pivotal trial of remdesivir leading to its emergency use approval, as outlined, had not been peer reviewed and published in a solid journal on the day of its approval (May 2nd), either, and that it was seriously flawed.
Nevertheless, the study funded by Fauci’s NIAID has been finally published on October 8 in the New England Journal of Medicine (ie in the same journals as the fraudulent pivotal trial of AZT). The only alleged benefit reported was a shorter recovery time for patients receiving remdesivir compared to those in the placebo group.
But this result has no validity, not only because of the seriously flawed underlying data. The way in which this drug got its approval is very reminiscent of the outlined fraudulent way in which AZT received its approval in 1987 in an alleged placebo trial. But in reality, almost from the beginning, everyone knew who was getting what (AZT or placebo) and patients even had their pills analyzed in the craving for the alleged miracle drug.
Who wants to rule out that this did not happen with remdesivir as well?
Especially since the placebo subjects in the remdesivir study did not receive a real placebo. Instead, the bulk of the patients got a “placebo” containing the same ingredients as remdesivir except the agent, for example sulfobutylether-beta-cyclodextrin, which can cause serious damage.
Hydroxychloroquine illustrates Fauci’s mendacity
The story of the drug hydroxychloroquine also illustrates Fauci’s phoniness. At the end of March, US president Trump called this agent “a gift from God”, while Fauci warned against jumping on conclusions.
On May 27, Fauci even stated on CNN about hydroxychloroquine, “The scientific data is really quite evident now about the lack of efficacy.”
And his comments came days after the Lancet published a 96,000-patient observational study that concluded that hydroxychloroquine had no effect on Covid-19 and may have even caused some harm.
Too bad that shortly after, this Lancet study was retracted, because:
several concerns were raised with respect to the veracity of the data and analyses conducted by Surgisphere Corporation and its founder and our co-author, Sapan Desai.”
Hence, Fauci’s assertion on May 27, “The scientific data [about hydroxychloroquine] is really quite evident now about the lack of efficacy,” was definitely a voluntary false statement, simply because at that date Fauci must have known that scientific data backing his claim did not exist.
Or as Politico put it on May 27:
There is no data yet from randomized, controlled clinical trials of hydroxychloroquine—the gold standard for evaluating potential treatments.”
In fact, in 2005 the Virology Journal published an article concluding that chloroquine (of which hydroxychloroquine is a slightly milder derivative) is a “potent inhibitor of SARS coronavirus” dubbed SARS-CoV-1, as health care expert Kevin Corbett points out in a Twitter post on October 26. And so-called SARS-CoV-2 is claimed to be genetically related to so-called SARS-CoV-1.
Of course, the Virology Journal study lacks validity because the science behind SARS-CoV-1 and SARS-CoV-2 is totally unfounded, and not least also because the study was just a cell culture and not a patient trial.
But Fauci is the world’s number one herald of the official corona narrative, and the study has been conducted by CDC scientists. So he should actually be totally convinced that chloroquine (and thus also hydroxychloroquine) is helpful in the context of corona.
Nevertheless, Fauci was unequivocal on Wednesday May 27, saying that “the data are clear right now” that hydroxychloroquine is not effective against the coronavirus.
This is why I asked Fauci’s NIAID, “How did Anthony Fauci come to his conclusion on May 27?”. But I have not received an answer to this question, either.
Conversely, this does not mean that the effectiveness of the drug has been properly proven. Let’s not forget that hydroxychloroquine is far from a candy, it can have many serious side effects and even be fatal by causing cardiac arrhythmias, for example. Especially if it is given in higher doses, which is what happened in the treatment of so-called COVID-19 patients.
As mentioned, the experimental administration of high doses of potentially lethal drugs such as hydroxychloroquine is the major factor for the excess mortality observed in some (but not all!) countries. “I agree about hydroxychloroquine overdosing, both from a reduced function point of view and toxicity,” writes me Yale epidemiologist Harvey Risch by e-mail.
Risch belongs to the best-known researchers who see a potential curative effect in the drug. The relevant studies with COVID-19 patients “all showed significant benefit for high-risk outpatients,” says Risch.
A view that is also expressed, for example, in the almost 40-page inquiry of Paul V. Sheridan to Fauci with copies sent to President Trump and others.
But even if we assume that administering hydroxychloroquine in lower doses alone, or in combination with an antibiotic and possibly zinc, to so-called COVID-19 patients may help decreasing the hospitalization and mortality risk, for instance, there is definitely no solid proof that this is due to an antiviral/anti-SARS-CoV-2 effect, as claimed. So the only conclusion would be that the positive effect is due to hydroxychloroquine having an anti-inflammatory effect, antibiotics clearing pathogenic bacteria and zinc boosting the immune system and metabolism function.
Furthermore, it must be considered in this context that administering hydroxychloroquine alone or in combination with an antibiotic and maybe zinc cannot be at all a sustainable long-term therapy nor does it represent a real causal therapy.
This approach also just follows “modern biomedicine’s basic formula with its monocausal-microbial starting-point and its search for magic bullets: one disease, one cause, one cure,“ as American sociology professor, Steven Epstein, writes in his book Impure Science — AIDS, Activism and the Politics of Knowledge. An approach that finally is just escapist.
This was expressed by Allan Brandt, a medical historian at Harvard Medical School, stating in his book No Magic Bullet: The promise of the magic bullet has never been fulfilled.
Apart from that, there is only one way to prove that a drug or a combination of agents help reducing mortality or hospitalization or is effective in relation to any other clinical endpoint, that is if you do compare it with a real placebo.
As Marcia Angell, former Editor in Chief of the New England Journal of Medicine, states quite rightly in her book The Truth About the Drug Companies:
If there is really doubt about whether a standard treatment is effective, the FDA should require that clinical trials of new treatments have three comparison groups—new drug, old drug, and placebo.”
Unfortunately, there is no such placebo-study for hydroxychloroquine and COVID-19 showing that this drug is superior compared to doing nothing.
In this context, Robert F. Kennedy Jr. wrote on August 2 on Instagram, Fauci “insists he will not approve HCQ [hydroxychloroquine] for COVID until its efficacy is proven in ‘randomized, double blind placebo studies.’”
On this point one can indeed only agree with the virus tsar. And at the beginning of June, researchers reported the results of the first gold-standard clinical trial of hydroxychloroquine in Covid-19, concluding that it did not perform any better than placebo.
But here as well Fauci’s hypocrisy shows up in the end. Not only did the results of the said “first gold-standard” placebo study become known only at the beginning of June — thus a couple of days after Fauci made his unfounded claim that “The scientific data [about hydroxychloroquine] is really quite evident now about the lack of efficacy.”
Also, “to date, Dr Fauci has never advocated such [placebo] studies for any of the 72 vaccine doses added to the mandatory childhood schedule since he took over NIAID in 1984,” as Robert F. Kennedy Jr. also notes in his Instagram post. “Nor is he requiring them for the COVID vaccines currently racing for approval. Why should chloroquine be the only remedy required to cross this high hurdle?”
Read the full article (there’s more!) at Off-Guardian.org.
And regarding Kary Mullis, mentioned in the Off-Guardian article, who received the Nobel Prize for his invention of the Polymerase Chain Reaction (PCR) test, this is what he had to say about Fauci before he died:
Trump’s Operation Warp Speed Dream Team: Fauci, Birx, Redfield, Slaoui who together with Bill Gates were all one big happy club developing drugs and vaccines for AIDS – But then Judy Mikovits Crashed the Party
President Trump’s “Operation Warp Speed” which has basically given a blank check for government funds to be spent on vaccine development for COVID, now is funding HIV/AIDS vaccine research as well, according to the pharmaceutical trade publication, FierceBiotech.
The National Institute of Allergy and Infectious Diseases (NIAID) is launching a new clinical trial network to seek out and add thousands of volunteers to major clinical tests for vaccines and monoclonal antibodies against the pandemic.
The so-called COVID-19 Prevention Trials Network (COVPN) was borne from the merger of four existing NIAID-funded clinical trial networks: the HIV Vaccine Trials Network, based in Seattle; the HIV Prevention Trials Network, based in Durham, North Carolina; the Infectious Diseases Clinical Research Consortium, based in Atlanta; and the AIDS Clinical Trials Group, based in Los Angeles.
While continuing to push for that long-sought vaccine for HIV prevention, as well as for other infectious diseases, they will now also focus on their new COVID-19 roles.
“Establishing a unified clinical trial network is a key element of President Trump’s Operation Warp Speed, which aims to deliver substantial quantities of a safe, effective vaccine by January 2021,” said Department of Health and Human Services Secretary Alex Azar. (Emphasis added.)
How clever! After years of spending hundreds of millions of dollars of U.S. government funding to develop an HIV/AIDS vaccine with no success, now they can utilize the fast-tracking emergency authorized funds for the COVID vaccine through Operation Warp Speed to continue their quest for an HIV RNA vaccine.
The funding will be used to start more than 100 clinical trials in the U.S. and around the world.
In a statement, the NIAID said: “The network will use a harmonized vaccine protocol developed by the Accelerating COVID-19 Therapeutic Interventions and Vaccines (ACTIV) public-private partnership. This will enable analyses of correlates of protection across multiple vaccine trials. The network is expected to operate more than 100 clinical trial sites across the United States and internationally.” (Full article.)
One has to wonder where they are going to find all these “volunteers” to participate in so many vaccine trials? We know from the history of past HIV drug trials, that many children who were the ward of the State were enrolled to these trials, because they had been removed from their parents and put into Foster Care, where the state has total control over their lives, including enrolling them in experimental drug trials.
So of all the scientists who worked at the NIH to develop AIDS drugs, were they all corrupt?
No. One of them became a whistleblower, Dr. Judy Mikovits.
I met Judy in 2015, just shortly after the gag order against her was lifted. I was so shocked by what she was telling me, that I assigned my top investigative reporter at that time, John Thomas, to interview her and publish a series of articles. See:
In May of 2020, filmmaker Mikki Willis released a trailer on a film he was producing on the Coronavirus fraud: PlanDemic.
In the trailer he interviewed Dr. Judy Mikovits.
I don’t think even Mr. Willis could have predicted how popular that trailer would become. It was quickly yanked from YouTube, Facebook, and all social media sites, but we had a copy, as did many others, and that interview went viral in a big way. By some estimates, almost 1 billion people around the world watched it.
In this interview, she clearly exposes Anthony Fauci for who he really is.
If you have never seen it, this is MUST viewing:
Conclusion: It is Time for Anthony Fauci to be Removed from Government and be Tried for his Crimes Against Humanity
EVERYTHING published in this article is OLD information. Yet for some reason, Fauci is now on the hot seat for his involvement in the Wuhan lab and the creation of a COVID-19 bioweapon.
Senator Rand Paul and others are finally starting to ask questions and raise some concerns, but none have gone far enough yet, as nobody has dealt with the abundance of evidence contained in this article.
Is Fauci too untouchable to face justice?
Maybe here on earth, but justice will most certainly catch up to him at some point, hopefully sooner than later, to stop the carnage of human lives this man has caused, all funded by the American taxpayers.
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