CDC, FDA Prepare Mass Distribution of a Merck/Sanofi Six-in-One Vaccine for Kids, Turning Blind Eye to Safety Signals

Egregious oversteps endangering children’s lives.

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The FDA approved Vaxelis in late 2018, but only now is the shot being readied for widespread distribution — in Europe, where infants have been given six-in-one vaccines for years (including Vaxelis since 2016), the vaccines have been associated with reports of sudden infant death.

Since the mid-1980s, the number of childhood shots on the Centers for Disease Control and Prevention (CDC) vaccine schedule has more than quadrupled. When parents express reluctance about turning their little ones into perpetual pin cushions, drug makers and doctors have a ready answer — combination vaccines that “simplify” the schedule by decreasing the number of injections administered.

This month marks the U.S. launch of the Merck/Sanofi joint-venture vaccine, Vaxelis, a six-in-one (hexavalent) combination vaccine that contains diphtheria, tetanus and acellular pertussis (DTaP) components as well as components said to protect against polio, Haemophilus influenzae type b (Hib) and hepatitis B.

Public health officials optimistically believe that bundling all of these components into one shot will help close noncompliance loopholes and increase the likelihood that children will complete “all recommended vaccinations.”

Though Vaxelis is the nation’s first hexavalent injection, it joins other four- or five-in-one vaccines already on the CDC schedule. The U.S. Food and Drug Administration (FDA) approved Vaxelis in late 2018 — as a three-dose series for 2-, 4- and 6-month-old infants — but it is only now, two-and-a-half years later, that the shot is being readied for widespread distribution.

Warning signs were ignored

There are numerous warning signs that potent all-in-one vaccines are too much for immature immune systems to handle. Concerning safety signals have emerged not just for hexavalent but also pentavalent (five-in-one) vaccines.

In Europe, where infants have been given hexavalent vaccines for some years (including Vaxelis since 2016), the formulations have produced many troubling reports of sudden infant death.

Absurdly, none of the clinical studies assessing Vaxelis safety and efficacy conducted fair comparisons against an inert placebo. Instead, in the two U.S. clinical trials for Vaxelis, not only did investigators compare infants receiving Vaxelis to babies who received Sanofi’s five-in-one Pentacel — but babies in both groups also received rotavirus and pneumococcal vaccines at the same time!

In this context, the CDC’s sales pitch to the public — and its claims that side effects are “usually mild” — cannot be considered credible.

Here are some of the other facts missing from the CDC’s communications:

  • In the two U.S. trials six infants died (slide #27) in the Vaxelis group (some after receiving just one dose); one infant also died in the “control” group that received five-in-one vaccines.
  • All six Vaxelis recipients died within six weeks of vaccination. This timing matches other published accounts of infant deaths “clustering” following hexavalent vaccination.
  • The reported causes of death for the infants who received Vaxelis included asphyxia, sepsis, fluid in the brain and sudden infant death syndrome (SIDS). These outcomes correspond to the types of adverse events reported following hexavalent vaccination in Europe.
  • Package inserts for other vaccines on the CDC schedule list similar causes of death, suggesting these fatal Vaxelis outcomes are plausibly associated with vaccination.
  • In the clinical trials, the rate of fever was notably higher in Vaxelis recipients even when compared to children receiving five-in-one vaccines (47% vs. 34%).

Juicing vaccine sales

In the no-liability context enjoyed by vaccine makers in the U.S., combination vaccines are already quite popular. In fact, market watchers and health economists praise the jumbo shots as being a catalyst for positive industry trends and a “key to commercial success.”

 

Thus, financial analysts expect Vaxelis to “garner significant patient share following its [U.S.] launch” — predicting that it will account for almost a third of U.S. DTaP vaccinations by 2028 — or $841 million in annual sales.

These predictions represent good news for Merck and Sanofi, two of the “big four” pharma giants that dominate the childhood vaccine market in the United States. Merck is already doing a booming vaccine business, recently reporting annual sales growth of 14.8% for its pneumococcal vaccine (Pneumovax 23) and 5.4% for its human papillomavirus (HPV) vaccine Gardasil-9.

However, Merck also faces proliferating Gardasil-related lawsuits — including legal actions alleging that the company knew about and ignored life-changing adverse events from the get-go, many of which (when not fatal) have involved autoimmunity and chronic pain. In fact, before the advent of emergency use COVID vaccines (responsible for an alarming escalation of vaccine-related adverse events), Gardasil had had “more side effects reported than all other vaccines combined.”

Sanofi, too, is embroiled in thousands of lawsuits worldwide — notably for its disastrous and sometimes fatal dengue vaccine. As with Merck, this has not dampened overall vaccine sales growth, which continues its strong upward trajectory, likely to be further strengthened by the U.S. Vaxelis rollout.

Although Sanofi has not been a front-runner in the COVID vaccine race, the company is currently running clinical trials for messenger RNA (mRNA) vaccines for both COVID and seasonal influenza.

Aluminum secrecy and grandfathered ingredients

Merck’s proprietary, “super-powered” aluminum adjuvant — amorphous aluminum hydroxyphosphate sulfate (AAHS) — which is believed to play a significant role in Gardasil’s risk profile, is also present in Vaxelis.

After Merck developed AAHS, it began to “preferentially” feature AAHS in its vaccines even though, as Danish scientists outlined last year, the company appears to have disregarded procedures ordinarily required for approval of new adjuvants.

According to the Danes, at the time AAHS appeared, it represented a “new type of aluminium adjuvant with excipients that [had] not been used earlier in [European Medicines Agency] authorised vaccines.” It should have been — but apparently was not — tested against an inert placebo. For this and other reasons, the Danish scientists question the ethical underpinnings of the Gardasil clinical trials.

In noting that Merck also “seems to have prevented independent studies of AAHS,” the Danes repeated a critique aired by world-famous aluminum expert Christopher Exley in 2018. In an extensive discussion of different aluminum-based adjuvants and their immunological mechanisms of action, Exley and co-authors emphasized the importance of studying aluminum adjuvants one by one, as each is “chemically and biologically dissimilar with concomitantly potentially distinct roles in vaccine-related adverse events.”

Concerningly, the Vaxelis liquid suspension is adjuvanted onto not just AAHS, but also another aluminum adjuvant — aluminum phosphate). The package insert disingenuously shorthands the combination of adjuvants as “aluminum salts.”

How this double whammy of aluminum (319 micrograms per vaccine dose) interacts with the vaccine’s six antigens, or Vaxelis’s numerous other ingredients, or the heavy aluminum load in other childhood vaccines is largely unknown.

According to the Vaxelis package insert, the vaccine also includes: polysorbate 80 (an ingredient flagged for its propensity to induce hypersensitivity reactions); glutaraldehyde and formaldehyde (problematic chemicals deemed necessary to inactivate pertussis toxin); bovine serum albumin (often harvested from bovine fetuses when female cows are found to be pregnant at slaughter); three different antibiotics (neomycin, streptomycin and polymyxin B); ammonium thiocyanate (also a rust inhibitor, weedkiller and defoliant); and yeast protein (associated, notably in hepatitis B vaccines, with autoimmune reactions).

Regulatory loopholes allow manufacturers to “grandfather” ingredients into new vaccines if the components are already present in other licensed vaccines — regardless of how inadequate the original safety testing may have been.

Thus, Merck and Sanofi perceived no need to test Vaxelis for DNA-damaging or cancer-causing effects, and conducted no studies of the ingredients’ pharmokinetics (i.e., how the substances move “into, through, and out of the body”).

The main cautionary note sounded in the meager Vaxelis patient information sheet is to not give Vaxelis to children if they are “allergic to any of the ingredients.”

For thee and thee … but not for me?

The CDC seems to be particularly interested in ensuring that poor and non-white children get Vaxelis. The agency began laying the groundwork to offer Vaxelis through the Vaccines for Children (VFC) Program — the agency’s vaccine program for the poor — over two years ago, in March 2019.

In September of that year, the CDC followed up with an affirmative vote. Public health departments have been promoting Vaxelis to participating VFC providers since early June 2021.

At its September 2019 meeting, CDC outlined another topic deemed important for discussion in the near future — raising the issue of whether Vaxelis should be “preferentially recommended” for the American Indian/Alaskan Native (AI/AN) pediatric population.

The tenuous rationale, according to the meeting notes, was because, “in the pre-vaccine era” (more than 35 years ago), “Hib disease occurred at a younger age among the AI/AN population compared to the general population.”

Wave of the future?

Judging from its website, the CDC perceives combination vaccines to be the wave of the future, and has signaled its strong endorsement of Vaxelis by incorporating the new vaccine into its 2021 vaccine schedule.

As if exposure to six antigens were not enough, FDA and CDC also say it is okay for healthcare providers to administer the six-in-one shot at the same time as other vaccines.

These agencies’ characterization of the Vaxelis safety profile as “acceptable” indicates they have either not done their due diligence, or are willing to accept a high level of collateral damage in exchange for the “convenience” of six-in-one shots.

However, as the “overwhelmed by guilt” parents of COVID-vaccine-injured teens are increasingly finding out, convenience is poor consolation for life-changing or life-threatening adverse outcomes.

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Israel News: “The almost vast majority of the deceased are vaccinated people” due to “immuno-erosion” - Compilation of Israel news clips shows they are questioning the "vaccine" efficacy.
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FLASHBACK | COVER-UP: ‘Scientific Reductivism’, The Talented Mr. Fauci

A look into Anthony Fauci’s involvement into medical/health corruption.

In light of recent revelations, with the now admission from Fauci himself, that the coronavirus may have originated (been created) in the Wuhan lab instead of occurring naturally, and that it would be worth it to take a closer look –

(although last year every mainstream news media and “fact-checker” on the planet was insisting that this assertion was “debunked” and a “baseless conspiracy theory”)

– not to mention the gain of function controversy and the $600,000 funding (at least) that Fauci sent to the Wuhan Institute specifically for bat-to-human transmission viruses – and Fauci’s OWN admission in May 2020 that “The best evidence shows the virus behind the pandemic was not made in a lab in China”,

I felt it would be prudent to bring up the following article as a flashback to the corruption that Fauci and his cohorts have been engaged in with other viruses that have haunted humankind.

Before I get into that, I also want to highlight this particular section as another opportunity to present how many times the lead talking head of directing the coronavirus response has flip-flopped on his OPINION (NOT FACT) – on what should be founded on scientific basis and actual research, not just based on assumptions, “leanings”, and “indications”:

“If you look at the evolution of the virus in bats, and what’s out there now it’s very, very strongly leaning toward this [virus] could not have been artificially or deliberately manipulated—the way the mutations have naturally evolved,” he responded.

“A number of very qualified evolutionary biologists have said that everything about the stepwise evolution over time strongly indicates that it evolved in nature and then jumped species,” Fauci added.

In May 2021, PolitiFact’s Kate Sanders asked Fauci if he was “still confident” that COVID-19 developed in nature.

“No, actually … I am not convinced about that,” Dr. Fauci said. “I think we should continue to investigate what went on in China until we continue to find out to the best of our ability what happened.”

“Certainly, the people who investigated it say it likely was the emergence from an animal reservoir that then infected individuals,” he continued, “but it could have been something else, and we need to find that out. So, you know, that’s the reason why I said I’m perfectly in favor of any investigation that looks into the origin of the virus.”

– Source: Dr. Fauci Keeps Changing His Wuhan Lab Funding Story, Jay Battacharya Tells Laura Ingraham

Uh huh… And why has his sudden inclination to actually investigate the origins of the coronavirus instead of dismissing it as most likely from a natural biological transmission now such a huge agenda for Mr. Fauci? After A WHOLE YEAR of repeated insinuations that it was naturally occurring?

It couldn’t possibly have anything to do with Rand Paul’s testimony that he has proof that the gain-of-function research for this SPECIFIC virus came under the direction of Fauci and his institution, right? Exposing the relationship that Dr. Shi Zhengli (who perhaps unwittingly made mention of her collaboration) has with the NIH institution, thanking Fauci personally for funding the research at the end of her paper?

VIDEO: Rand Paul Says Fauci ‘Absolutely’ Committed Perjury When Denying Wuhan Gain-of-Function Research

Methinks the WHO is obviously complicit in this whole ordeal as well…

“A joint report into the origins of COVID by the World Health Organization (WHO) and China has found it is “extremely unlikely” that the virus escaped from a lab, according to a draft version seen by AP News.”
‘Extremely Unlikely’ COVID Came From Lab Draft WHO Report Says, As Ex-CDC Head Touts Claim

I don’t know if I have to mention it, but Mr. Fauci is not the only one who should be under the radar… We already know about Bill and Melinda Gates’ involvement in all of this as well, but what about Mrs. Fauci? What does she do, again?

“Christine Grady is an American nurse, bioethicist, and a senior investigator. She currently serves as the Chief of the Department of Bioethics at the National Institutes of Health Clinical Center. She also serves as Head of the Department’s Section on Human Subjects Research.”
Christine Grady Wiki Bio

“Head of the Department’s Section on Human Subjects Research

…Hmm… make of that what you will.

FLASHBACK: The original article was first published on April 05, 2020.

The following information has been reblogged from rielpolitick.com
(original post can be found at journal-neo.org | The Remarkable Doctor A. Fauci)

COVER-UP: ‘Scientific Reductivism’, The Talented Mr. Fauci

Source – journal-neo.org

“…Fauci, Birx and Redfield, all incestuously complicit in the HIV/AIDS frauds and malpractice, today hold the future of not only American public health, but also of the entire world economy in their hands. Not a good situation. As their work on the proved HIV=IDS fraud shows, the coronavirus tests do not at all prove presence of a deadly virus in any patient. If this is so, it is perhaps the greatest criminal fraud in medical history”

The Remarkable Doctor A. Fauci – By F. William Engdahl

Dramatic political and social decisions are being made across the United States and around the world on what emergency quarantine measures and other steps must be taken. In many cases the radical and severe measures, such as shutting down the world economy, are being justified by COVID-19 case projections of morbidity into the future. If there is one person who is the face of the current strategy of dealing with the coronavirus in Washington it is the Director of the US National Institute for Allergy and Infectious Diseases (NIAID) of the NIH, Dr. Tony Fauci. What major media conveniently leave out in discussing Fauci’s role is his highly controversial and conflicted history since he first joined NIAID in 1984 during the beginnings of the AIDS panic. His role then sheds valuable light on his remarkable and highly controversial actions today.

Tony Fauci, a leading member of the White House Coronavirus Task Force, is being promoted by major US media such as CNN, MSNBC or the New York Times as the great expert on all related to the Covid19 outbreak. He had dismissed the President’s efforts to promote a known malaria medication as treatment for severe corona patients as “anecdotal,” even though seven years before he backed the same drug. He has publicly taken projections from an institute created in Washington State by the Gates Foundation, the same foundation that virtually owns the WHO and owns major stakes in the leading vaccine makers, to claim that up to 200,000 Americans could die from COVID19. Fauci stated that COVID19 is “probably about 10 times more lethal than the seasonal flu,” which would mean 300-600,000 coronavirus deaths this year, at the same time in a respected medical journal he compared Covid-19 as similar to seasonal flu in morbidity. When questioned how long the shutdown of much of the US economy must last, Fauci replied only when there is zero new covid19 positive tested cases, something impossible given the defective testing. He has also backed direct human tests of novel vaccines with no prior animal tests, including with radical non-tested mRNA gene-edited vaccines.

Fauci has more influence over US national policy on the unprecedented Covid-19 pandemic than anyone, including the President.

Much of media treats him with awe as an unimpeachable scientist, one of the world’s finest. A closer look at Anthony Fauci’s career gives a starkly different picture, a very alarming one in fact.

America’s AIDS Czar

Tony Fauci has held the top post at the NIAID in Washington for an astonishing 36 years. Today he is well past retirement age at 79, and holds the funds to determine which drug companies or university researchers will get precious government funds or not from NIAID’s annual $5 billion budget.

Let’s go back to 1984 when Fauci was named head of NIAID during the Reagan era. That year an AIDS researcher, Robert Gallo, working under Fauci, held a press conference to announce that he had “discovered” the AIDS virus. He said it was HIV– human immunodeficiency virus. The shocking announcement which went around the world, was in complete disregard of scientific procedures of prior peer-reviewed published scientific evidence, including the required electron microscope analyses. It was a case of “science by press conference” as a critical scientist, Prof. Peter H. Duesberg described it. Duesberg was an award-winning researcher at Berkeley who isolated the first cancer gene through his work on retroviruses in 1970, and mapped the genetic structure of these viruses.

For Gallo and Fauci, that was unimportant as millions in research funds flowed into NIAID to research the new virus, HIV. Fauci and Gallo claimed that AIDS was highly contagious, also by sexual transmission, especially among homosexual men. Notably, before the Gallo claim to have found the HIV AIDS virus, NIAID had been doing research on the role of drugs, poppers or nitrites, proven immune-suppressants, in the deaths of the earliest AIDS patients. That was quickly dropped in favor of researching a “cure” for AIDS. Media was told that AIDS was the “public health threat of the Century.” Gallo went on to make millions on his patented blood test for HIV, despite the fact that the test was often giving false positives and did not test directly for the alleged virus but for active antibodies, something immunology practice said was not valid, as antibodies merely suggested a past infection response and not necessarily presence of AHIV. At this time in the 1980’S Fauci was responsible for AIDS research at NIAID, a post he still holds.

False Tests?

The issue of HIV/AIDS tests is central. While a frightened world was clamoring for a test, Gallo and Fauci promoted their deeply flawed tests of antibodies. In 2006 Gallo claimed, “HIV tests were highly accurate from the time they were developed in 1984 and have become much more accurate over time…” Highly accurate in 1984 but more accurate than highly over time? Gallo added in response to criticism, “A PCR test for the presence of the virus itself can accurately determine a child’s HIV status.”

In a sharp rebuttal of the Gallo claims, claims endorsed by Fauci and the NIAID as well as CDC, Roberto A. Giraldo, MD and Etienne de Harven, MD, the scientist who produced the first electron micrograph of a retrovirus, pointed out that both the ELISA and Western blot, and a genetic test, the PCR or ‘Viral Load’ test,” the two major tests used to determine if one has AIDS, are invalid. “None of these tests detect the HIV virus itself, nor do they detect HIV particles.” They add that there are “more than 70 different documented conditions that can cause the antibody tests to react positive without an HIV infection.” Among the false positive cases are influenza, the common cold, leprosy or the existence of pregnancy. The same tests are used today to determine SARS-CoV-2-positive.

They concluded, “The fact that after 25 years of intense research HIV has been neither isolated nor purified in terms of classical virology indicates to us that the infectious view of AIDS as a contagious viral disease is based on an apparently non-existent microbe!”

Giraldo and de Harven declared, “The alleged existence of HIV was asserted from the study of proteins, reverse transcriptase activity (RT), and RNA fragments that were found in culture supernatants, not from the direct analysis of purified viral particles.” The CDC requires a positive antibody test for HIV to determine AIDS in the USA. Yet in Africa since 1985 the WHO requires no HIV test or any other laboratory test. Merely the patient’s symptoms that can include weight loss, chronic diarrhea, prolonged fever, persistent cough and such, symptoms endemic to chronic poverty, malnutrition and lack of sanitation.

Yet this fraud has shaped the career of Tony Fauci for more than 35 years. Fauci as head of NIAID has taken millions from the Bill & Melinda Gates Foundation as well as the Clinton Foundation along with tens of billions from US taxpayers for this bogus research. Suspiciously, the 2006 article by Giraldo and de Harven was suddenly retracted by the journal in 2019 just before the coronavirus Wuhan outbreak.

Despite the fact that he knew the established rules of virology, Fauci, as head of NIAID, recommended the Burroughs Wellcome chemotherapy drug, AZT as a “preventive drug” for HIV diagnosed patients even without symptoms! Burroughs Wellcome gave NIAID the study that was deliberately biased for AZT. Fauci even backed AZT for pregnant women despite the grave risk to the fetus.

One mark of pregnancy in all women is a higher level of antigens as the natural immune system fights any infection to protect the fetus. AZT or Retrovir, a failed leukemia drug, has been proven to be a highly toxic drug. It was approved for AIDS testing in a record 5 days by Fauci and the US Government in 1987. Today despite more than thirty years funded research and billions of dollars, no effective vaccine for HIV/AIDS exists.

Fauci and Gilead

According to people who have studied the role of Tony Fauci as head of NIAID, his focus has been what is called scientific reductivism, described as “a 19 Century-style, single-germ theory for a complex web of factors that collapsed the immune systems of a subset of gay men in the early 1980s.” He has refused to explore the documentation that a variety of lethal drugs and other toxins such as nitrites could play a role. As a result he has wasted tens of billions of taxpayer dollars since 1984 on dead end experiments.

One of his most nefarious was his collaboration with Gilead Sciences.

Not satisfied with having developed a false positive test for AIDS and having gained FDA fast-track approval for AZT to treat HIV-positive patients with serious illness symptoms, Fauci decided to collaborate with Gilead (as in the Biblical “balm of Gilead”) on what came to be called PrEP experiments.

Fauci in 2007 began to finance clinical trials of the AZT drugs in HIV “negatives,” on the theory the chemotherapy would “protect” them from becoming “positive.” That is, testing toxic HIV drugs on otherwise healthy persons to “insure” they never got AIDS. If it sounds mad, it was. Gilead supplied the drug, Truvada, to NIAID between 2007-2012 for Phase III human tests on HIV negative subjects. Four tests of at least 2,000 and up to 5,000 test subjects each, were done. The project was called “pre-exposure prophylaxis” or “PrEP.” Healthy subjects were given doses of chemotherapy drug Truvada on the thesis it could prevent them from one day getting HIV-positive. CDC, in its May 2014 recommendation urged physicians to prescribe Truvada for negatives in the so-called “risk groups,” an official government imprimatur for an extremely profitable drug.

The FDA ignored two of the four Truvada tests that had failed and been halted. Despite that and owing to data manipulation by Fauci’s NIAID and Gilead, the FDA approved the dangerous Truvada for PrEP. Today Gilead lists the side effects of Truvada: Kidney problems, including kidney failure; worsening Hepatitis B; too much lactic acid in your blood (lactic acidosis), which can lead to death; severe liver problems, which can lead to death; bone problems. They state that Truvada “can help reduce the risk of getting HIV-1 through sex, when taken every day and used together with safer sex practices.”

The Fauci-Gilead scam of promoting Truvada for healthy people to “reduce risk” of HIV is a marker for the level of medical malpractice and in some cases evident criminal abuse of human health that the current White House coronavirus guru, A. Fauci, represents.

Fauci and COVID-19

In October, 2019 Fauci and his NIAID got $100 million from the Gates Foundation to develop “gene-based” therapies for HIV and sickle cell disease. That means Fauci still to the time of the first claims of novel coronavirus in Wuhan China, Fauci was still promoting a 35-year fraud around HIV. Fauci is also part of the Gates Foundation cabal. In 2012 Fauci was named one of the five Leadership Council of the Gates Foundation-created Global Vaccine Action Plan.

This is highly relevant to his role today as the Trump Administration coronavirus “pope.” Has his NIAID or any other laboratory in the world rigorously, with electron microscopy, isolated and purified samples of patients tested SARS-CoV-2 positive for Covid-19? Or are the virus proofs as faulty as Fauci and the AIDS clique have made for HIV?

In addition NIAID is working with Gilead to conduct Phase II human trials on Gilead’s drug, remdesivir, as a potential treatment for hospitalized adult patients diagnosed with COVID-19.

A coincidence?

Relevant also is the fact that all top scientific advisers to the US President’s Task Force on COVID-19 are tied since decades to the bogus and destructive HIV/AIDS research and propagation of false theories. Alongside Tony Fauci of NIAID stands Deborah L. Birx, M.D., Obama appointee as US Global AIDS Coordinator who worked under Tony Fauci at NIAID from 1983-1986.

Robert Redfield is the current Director of the Centers for Disease Control and Prevention, center of the recent coronavirus testing scandal. Redfield cofounded with the discredited Robert Gallo, former Fauci colleague in the AIDS scandals of the early 1980’s at NIH, the Institute of Human Virology based at University of Maryland. Redfield and Birx also coauthored numerous scientific articles on purported HIV vaccines, none of which have been effective.

Fauci, Birx and Redfield, all incestuously complicit in the HIV/AIDS frauds and malpractice, today hold the future of not only American public health, but also of the entire world economy in their hands. Not a good situation. As their work on the proved HIV=IDS fraud shows, the coronavirus tests do not at all prove presence of a deadly virus in any patient. If this is so, it is perhaps the greatest criminal fraud in medical history.

_____________________

F. William Engdahl is strategic risk consultant and lecturer, he holds a degree in politics from Princeton University and is a best-selling author on oil and geopolitics, exclusively for the online magazine “New Eastern Outlook.”

https://journal-neo.org/2020/04/15/the-remarkable-doctor-a-fauci/

ONE LAST NOTE FROM E.A.R. (excerpt below taken from the post “Anthony Fauci Caught ‘Lying’ – Several Times”)

An interesting piece from 1994 on Kary Mullis and his views on a couple of questionable individuals:

In the end, “Nightline” ran a two-part series, the first on Kary Mullis, the second on the HIV debate. Mullis was hired by ABC for a two-week period, to act as their scientific consultant and direct them to sources.

The show was superb, and represented a historic turning point, possibly even the end of the seven-year media blackout on the HIV debate. But it still didn’t fulfill Mullis’ ultimate fantasy. “What ABC needs to do,” says Mullis, “is talk to [Chairman of the National Institutes of Allergy and Infectious Diseases (NIAID) Dr. Anthony] Fauci and [Dr. Robert] Gallo [one of the discoverers of HIV] and show that they’re assholes, which I could do in ten minutes.

But I point out, Gallo will refuse to discuss the HIV debate, just as he’s always done.

“I know he will,” Mullis shoots back, anger rising in his voice. “But you know what? I would be willing to chase the little bastard from his car to his office and say, ‘This is Kary Mullis trying to ask you a goddamn simple question,’ and let the cameras follow. If people think I’m a crazy person, that’s okay. But here’s a Nobel Prize-winner trying to ask a simple question from those who spent $22 billion and killed 100,000 people. It has to be on TV. It’s a visual thing. I’m not unwilling to do something like that.”

He pauses, then continues. “And I don’t care about making an ass of myself because most people realize I am one.”

(Kary Mullis)
The Corona Simulation Machine: Why the Inventor of The “Corona Test” Would Have Warned Us Not To Use It To Detect A Virus

It seems as if this self-described “ass” actually has a heart of gold and was trying to expose possible corruption as early as the 1990’s.

As Celia Farber, the interviewer, mentions: “One time, in 1994, when I called to talk to him about how PCR was being weaponized to “prove,” almost a decade after it was asserted, that HIV caused AIDS, he actually came to tears.

Sadly Kary Mullis passed away on August 17, 2019, allegedly from pneumonia. Just weeks away from when Event 201 took place in October 2019, and a few more weeks from when an actual “surprise outbreak” erupted, allegedly as early as November 2019. And just a couple of months after that, we have the PCR tests that Mr. Kary Mullis himself invented and was against using for viral detection, being used (and abused) for viral detection en masse – at the behest of the “expert scientists”.

Fact checking is extremely important. I want to reiterate not to take everything at face value; no matter what you read, where you read it from, or who you hear it from. And to be clear, do not rely on “fact checking” websites to give you accurate information either. These are just as likely, (if not even more likely…), to feed false information and false debunking accounts to manipulate the reader. Please take everything into consideration before adhering to a certain narrative – and always keep your mind open to other possibilities.

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Get an Earful

Is Mankind Able to Prevent Abuse of New Technologies Against Democracy and Human Rights? - An investigative look into the government's attempts to assault (control) our mind.
Vaccines to Genetically Modify/Change Our DNA – Mind Control and Weaponization – Anthony Patch Prediction From 2014 - What is the REAL reason for the vaccines? Some say depopulation. Some say mind control. Maybe it's both.
Vaccination Status Is Temporary, Boosters For Life Required - Constant changing of definitions and moving of goalposts... "Fully vaccinated" and "vaccines" are an endless misnomer.
Don’t Vaccinate Kids: Urgent Message from Doctors’ Summit - Speakers at the Summit included Doctors: Peter McCullough, Robert Malone, Paul Alexander, Tara Gesling, Pierre Kory, Ryan Cole and more.
Walensky and Fauci Fumble in Their Responses to the Senate Committee, with Rand Paul’s Call for Fauci to Resign – But is the Senate Culpable as Well? - Rand to Fauci: "You won't admit that it's dangerous, and for that lack of judgement, I think it's time that you resign."
Israel News: “The almost vast majority of the deceased are vaccinated people” due to “immuno-erosion” - Compilation of Israel news clips shows they are questioning the "vaccine" efficacy.
Government’s Own Data Proves COVID-19 Shots Are Causing Blood Clots, Heart Disease, and Death - 17,619 COVID vaccine deaths reported into VAERS as of October 2021 (keep in mind that only a small percentage of events are even reported)
As More People “Wake Up”, We Have Been Given Warning Signs of What’s to Come – They All Point to One Thing - Whether we're in the "end days" or not, we need to prepare ourselves and strengthen our faith in God/Jesus Christ.