ICAN Sues CDC to Stop Hiding V-Safe Data from the Public
Informed Consent Action Network | December 29, 2021
The FDA and CDC have now made crystal clear that their promise of transparency with regard to COVID-19 vaccines was hogwash. As everyone now knows, the FDA has asked a federal judge to give it at least 75 years to produce the pre-authorization/licensure safety data. And we now know with certainty, federal health authorities similarly want to hide the post-authorization/licensure safety data.
The FDA and CDC have admitted their existing safety monitoring program, VAERS, was incapable of determining causation and therefore unreliable. The CDC has therefore deployed a new safety monitoring system for COVID-19 vaccines called v-safe, and now claims that these “vaccines are being administered under the most intensive vaccine safety monitoring effort in U.S. history.”
V-safe is a smartphone app that allows vaccine recipients to “tell CDC about any side effects after getting the COVID-19 vaccine.” The purpose of the app “is to rapidly characterize the safety profile of COVID-19 vaccines when given outside a clinical trial setting.” Data submitted to v-safe is “collected, managed, and housed on a secure server by Oracle,” a private computer technology company. Although the CDC has “access to the individualized survey data,” Oracle can only access “aggregate deidentified data for reporting.” Meaning, based on the CDC’s own documentation, the data submitted to v-safe is already available in deidentified form (with no personal health information) and could be immediately released to the public.
ICAN, through its attorneys, therefore asked in three FOIA requests that the CDC produce the deidentified data from the v-safe program in the same form in which Oracle can currently access it. The agency acknowledged that “v-safe data contains approximately 119 million medical entries” but denied producing that data because the “information in the app is not de-identified.” The CDC had apparently not read its own documentation regarding v-safe. But ICAN’s attorneys had and so they administratively appealed this decision and, at the same time, to leave no doubt what was being requested, submitted another request to the CDC that sought all data deidentified after it was submitted to the v-safe app (in other words, in the form that the agency made known that Oracle has the data). Incredibly, the CDC administratively closed this request stating it was duplicative of the original request.
Meaning, the first request was denied by the CDC because the CDC claimed it requested data that was deidentified when entered into the app, but then the CDC closed the second request (which was identical to the first request except for making clear it was seeking data deidentified at any point – before or after it was entered into the app) by claiming the second request was duplicative of the first request! The CDC is plainly playing games. It clearly does not want the v-safe data released.
The public should have immediate access to all v-safe data in deidentified form. Despite the fact that this deidentified data already exists, that it is already in the hands of a private company, and that the CDC has never objected to its production, the CDC has so far failed to produce it to ICAN or to the American public – the same people being mandated to take this liability-free product. But don’t worry, ICAN will not rest until this data is made public and so today has commenced a lawsuit against the CDC and HHS demanding that a court compel them to release this data.
You can read this lawsuit here.
Ivermectin and the Price of Life
By Justus R. Hope, MD | The Desert Review | December 13, 2021
What is your life worth? More to the point, what is your loved one’s life worth? What value would you place on your child, your mother, father, or spouse?
When the world experienced an average of nearly 15,000 COVID deaths per day, Dr. Andrew Hill decided on the price of a human life. Dr. Hill made that calculation during a conversation with Dr. Tess Lawrie, in January of 2021, during the peak of the Winter Surge.
In a zoom conversation between Dr. Tess Lawrie, nicknamed the “Conscience of Medicine,” and Dr. Andrew Hill, then the most influential Ivermectin advocate in the world, Dr. Hill chose dollars over human lives.
Hill’s parent institution, the University of Liverpool, had just received a 40 million dollar donation from UNITAID four days before Hill’s Ivermectin paper was published, and Dr. Hill’s conclusion was changed 180 degrees from his position just a few weeks earlier.
Andrew Hill admitted that his sponsors (UNITAID) pressured him to alter his conclusion. Hill explained, “I think I’m in a very sensitive position here.”
Dr. Lawrie called Hill out. She stated, “Lots of people are in sensitive positions; they’re in hospital, in ICUs dying, and they need this medicine.”
Lawrie criticized Hill, “This is what I don’t get, you know, because you’re not a clinician. You’re not seeing people dying every day. And this medicine prevents deaths by 80%. So 80 percent of those people who are dying today don’t need to die because there’s Ivermectin.”
Hill responded that the NIH would not agree to recommend IVM.
Dr. Tess Lawrie fired back, “Yeah, because the NIH is owned by the vaccine lobby…This is bad research. So at this point, I am really, really worried about you.”
Hill answered, “Okay. Yeah. I mean, it’s a difficult situation.”
Lawrie responded, “No, you might be in a difficult situation. I’m not because I have no paymaster. I can tell the truth… How can you deliberately try and mess up…you know? So, how long are you going to let people carry on dying unnecessarily – up to you? What is the timeline you’ve allowed for this, then?”
Andrew Hill reacted, “Well, I think… I think that it goes to WHO and the NIH, and the FDA, and the EMEA. And they’ve got to decide when they think enough is enough.”
Dr. Lawrie pointed out the obvious, “You’d rather… risk loads of people’s lives. Do you know if you and I stood together on this, we could present a united front and we could get this thing. We could make it happen. We could save lives; we could prevent people from getting infected. We could prevent the elderly from dying…
I’m a doctor, and I’m going to save as many lives as I can. And I’m going to do that through getting the message [out] on Ivermectin…Okay. Unfortunately, your work is going to impair that, and you seem to be able to bear the burden of many, many deaths, which I cannot do.”
Dr. Lawrie demanded to know the identity of the unknown UNITAID author who changed Dr. Hill’s conclusions, the person whose influence was to cause so many preventable deaths.
“So who is it in UNITAID, then? Who is giving you opinions on your evidence?”
Hill answered, “Well, it’s just the people there. I don’t…”
Dr. Lawrie pressed Hill, “Could you please give me a name of someone in UNITAID I could speak to, so that I can share my evidence and hope to try and persuade them to understand it?
Dr. Hill evaded, “Oh, I’ll have to think about who to, to offer you with a name… But I mean this is very difficult because I’m, you know, I’ve got this role where I’m supposed to produce this paper and we’re in a very difficult, delicate balance… Yeah, it’s a very strong lobby…”
The conversation concludes with Dr. Hill promising to do everything in his power to get Ivermectin approved if she could give him six more weeks.
Dr. Lawrie, “So, how long do you think the stalemate will go on for?”
Dr. Hill, “From my side. Okay… I think end of February, we will be there in six weeks.”
Dr. Tess Lawrie, “How many people die every day?”
Dr. Andrew Hill, “Oh, sure. I mean, you know, 15,000 people a day.”
Dr. Tess Lawrie, “Fifteen thousand people a day times six weeks… Because at this rate, all other countries are getting Ivermectin except the UK and the USA, because the UK and the USA and Europe are owned by the vaccine lobby.”
Dr. Andrew Hill, “My goal is to get the drug approved and to do everything I can to get it approved so that it reaches the maximum…”
Dr. Tess Lawrie, The Conscience of Medicine, concluded with this, “You’re not doing everything you can, because everything you can would involve saying to those people who are paying you, ‘I can see this prevents deaths. So I’m not going to support this conclusion anymore, and I’m going to tell the truth.’”
Finally, Dr. Lawrie added, “Well, you’re not going to get it approved the way you’ve written that conclusion. You’ve actually shot yourself in the foot, and you’ve shot us all in the foot. All of… everybody trying to do something good. You have actually completely destroyed it… I don’t know how you sleep at night, honestly.”
The fact that Dr. Andrew Hill allowed another person to change his paper’s conclusion has been known for more than six months and was published in the book, Ivermectin for the World.
“However, he [Dr. Andrew Hill] was reigned in before more damage [to the vaccine lobby] was done:
- He was invited to the NIH, along with Dr. Marik, probably to give the appearance of propriety.
- He was given a gag order and told not to speak to any more press until The WHO made an official decision on Ivermectin. It turned out that this decision would go against the drug despite Dr. Hill’s findings.
- Dr. Hill’s conclusion would be changed by someone else, and the rest is history.”
What was not known, until the transcript of the zoom conference between Dr. Hill and Dr. Lawrie was leaked, were the specifics of the quid pro quo. It turns out that the height of the COVID-19 Winter surge, when about 15,000 people per day were dying, was precisely the same time as the zoom conference, held on January 18, 2021. Moreover, it was days after Andrew Hill’s University of Liverpool took the $40 million payoff.
The transcript of this conference call appeared in Robert F. Kennedy Jr.s’ book, The Real Anthony Fauci, and in this article published by The Defender newsletter:
https://childrenshealthdefense.org/defender/ivermectin-big-pharma-rfk-jr-the-real-anthony-fauci/
World daily COVID deaths were averaging around 15,000 per day on January 18, 2021, and six weeks later were averaging some 9,700. Currently, the world is seeing about 7,500 per day die.
80% of these or more could have been prevented with Ivermectin, a statement with which Dr. Hill would likely agree.
Overall, since that fateful decision of Andy Hill to allow his sponsor to “change” his paper’s conclusion, 2.475 million people [11 months x 30 days per month x 7500 deaths per day] have died, 80% of them could have been saved had Ivermectin been approved. So precisely 1.98 million lives were lost as a result of the betrayal.
The price per life?
Forty million dollars was the value of the donation made to the University of Liverpool by UNITAID. This sum comes out to 20 dollars and 20 cents per life. That is what we are all worth in the calculus of the vaccine lobby.
UNITAID bills itself as a “global health agency” hosted by the World Health Organization and supported by the vaccine lobby.
The Bill and Melinda Gates Foundation contributed hundreds of millions to UNITAID. In October, they committed $120 million more to the new expensive Merck drug molnupiravir, a costly and genotoxic competitor of Ivermectin.
Some experts say it will stimulate the emergence of viral mutants and worsen the pandemic.
https://uk.news.yahoo.com/covid-pill-being-rolled-among-121237206.html
If that prospect is not concerning enough, consider this: One dose of Remdesivir, a drug that does not save lives, but one that is widely used on most United States ICU COVID cases, costs $3,100 per dose, or to put it bluntly, one dose of Remdesivir is worth roughly 153 lives. Yet, the worst drug earned the FDA’s approval while the best one, Ivermectin, was suppressed for money.
Ivermectin, a drug that has nearly eradicated River Blindness in much of the world, a safe drug already given to humans in over 4 billion doses, can be purchased mail-order from India at 1,000 12mg tablets for $163. That comes out to 16.3 cents per dose.
Dr. Alan Bain recently saved the life of 71-year-old Sun Ng thanks to a court order issued by Judge Paul Fullerton. Following the hospital’s initial refusal, Ng’s family sued Edward-Elmhurst Health and Sun Ng was administered the Ivermectin for five days. After the treatment, Ng “removed his breathing tube” and was taken out of ICU.
Sun Ng’s Recovery with Ivermectin
Dr. Bain, unable to get a local pharmacy to fill the prescription for Ivermectin, obtained the mail-order version and saved Ng’s life.
https://patch.com/illinois/naperville/covid-patient-given-ivermectin-edward-improving-report
Thus, five 12 mg doses cost about 82 cents but are worth more than the 20 dollar value placed by the vaccine lobby and Andrew Hill on a human life because pennies were all it took to purchase the Ivermectin that saved Sun Ng.
Ivermectin has 27 randomized controlled studies involving tens of thousands of patients showing reduced time to viral clearance, hastened recovery time, and reduced mortality. On the other hand, the vaccine lobby’s choice, Remdesivir, was rejected by the WHO as a drug that failed to improve survival and other outcomes.
https://covid19criticalcare.com/wp-content/uploads/2021/08/SUMMARY-OF-THE-EVIDENCE-BASE-FINAL.pdf
One thousand doses of Ivermectin can be purchased online for $163. Yet, UNITAID paid $40 million to change Dr. Hill’s conclusions to call for more studies [delaying Ivermectin approval], essentially condemning millions of human beings to death from COVID-19. So while 82 cents may be the price of life, it seems that twenty pieces of silver remains the price of death.
Dr. Justus R. Hope, writer’s pseudonym, graduated summa cum laude from Wabash College where he was named a Lilly Scholar. He attended Baylor College of Medicine where he was awarded the M.D. degree. He completed a residency in Physical Medicine & Rehabilitation at The University of California Irvine Medical Center. He is board-certified and has taught at The University of California Davis Medical Center in the departments of Family Practice and Physical Medicine & Rehabilitation. He has practiced medicine for over 35 years and maintains a private practice in Northern California.
FDA Should Need Only ‘12 Weeks’ to Release Pfizer Data, Not 75 Years, Plaintiff Calculates
By Seth Hancock | The Defender | December 17, 2021
U.S. Food and Drug Administration (FDA) officials skipped the start of oral arguments Tuesday as a federal district court weighed whether the agency can take 75 years to fully release documents on Pfizer’s Comirnaty COVID vaccine, according to a lawyer representing plaintiffs who sued the FDA for the documents.
A U.S. Department of Justice lawyer representing the FDA told the U.S. District Court for the Northern District of Texas the agency will produce more than 329,000 related documents as fast as it can, while safeguarding personally identifiable information and Pfizer trade secrets.
Public Health and Medical Professionals for Transparency (PHMPT), the group behind the Freedom of Information Act (FOIA) request and subsequent lawsuit, is seeking safety and effectiveness data, adverse reaction reports and a list of active and inactive vaccine ingredients.
PHMPT is a group of more than 30 scientists, medical professionals, international public health professionals and journalists. The group’s lawsuit argues the FDA is overestimating the time needed and understaffing the job.
“Assuming a low average of 50 pages per hour per person, even to review the hundreds of thousands of pages the FDA estimates, the agency would need just 19 reviewers to work full-time for 12 weeks to review and produce these documents — which is a tiny fraction of its approximately 18,000 employees,” said PHMPT in a legal brief filed Monday.
The day before oral arguments, the FDA released 14 document files, the largest file including 2,030 pages. PHMPT posted an updated list which shows documents released since Nov. 17.
FOIA does not mandate any particular processing schedule, only that the agency process requests “as soon as practicable,” the FDA said in a legal brief filed Monday.
“The bottom-line issue still remains what processing schedule is ‘practicable’ for the agency,” the FDA said.
At the agency’s proposed rate of 500 documents per month, the last documents would be released in 2096.
A quote from Business Intelligence Associates, an e-discovery company, estimated 400,000 pages could be produced within six to eight weeks at a cost of $132,000, according to PHMPT.
PHMPT wants the FDA documents released within 108 days. That’s the same amount of time the FDA spent reviewing the responsive documents for “the far more intricate task” of licensing Pfizer’s vaccine, the group said in its lawsuit.
Attorney Aaron Siri, who represents PHMPT, said:
“Americans must routinely produce documents, pay fines, and otherwise expend resources to comply with the law. Courts don’t inquire as to the ability or financial resources to comply with the law — they must comply.
“In fact, it would be laughable if a billionaire defendant came before a court and claimed poverty to escape making a document production, but that is the FDA’s position.”
The FDA budget for fiscal year 2019 was $6.1 billion.
In the FDA’s 64-page briefing, the agency argued it needed the full 75 years to redact and release the documents out of “fairness” to other FOIA requesters.
PHMPT defined fairness differently in its responding brief:
“Fairness would be giving millions of Americans who are mandated to receive this liability-free vaccine today assurance regarding the FDA’s review by allowing independent scientists access to the same data the FDA reviewed, without making them wait decades.
“Fairness would be allowing Americans injured by the vaccine today, who cannot sue Pfizer or anyone else for the harm, hope that independent scientists with access to that data can more readily develop treatments for their ailments.
“Fairness would be our federal health authorities allocating more than one person spending a few hours each month to review Pfizer’s documents for public disclosure after having given Pfizer over $17 billion of taxpayer money to develop and market the product.
“That would be fair to the American people.”
Siri noted that no decision has been made by the court and that a transcript of this week’s hearing should be released soon.
U.S. Rep. Ralph Norman (R-S.C.) earlier this month introduced a bill that would force the FDA to release them in 100 days.
© 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
The FDA approves boosters for minors – without testing boosters on minors
Age group testing? Zero.
Techno Fog | December 14, 2021
Late last week, on December 9, the FDA approved the Emergency Use Authorization (EUA) for the Pfizer COVID-19 vaccine, “authorizing the use of a single booster dose for administration to individuals 16 and 17 years of age.” The booster is to be given at least 6 months after vaccination.
Before we get to the data the FDA cited in the booster for kids aged 16-17, let’s go through the facts:
COVID-19 is not a threat to teenagers aged 16-17. On October 25, we warned that the FDA was about to approve an experimental COVID-19 vaccine for children. It seemed unnecessary to give the EUA Pfizer vaccine to minors, as CDC data showed that for children aged 5-11 years-old, there have been 1.8 million COVID-19 cases and only 138 deaths. For older kids, from our own calculations, there have been approximately 3 million COVID-19 infections for those aged 12-18 years, leading to approximately 400 COVID-19 deaths in those ages. Children who get COVID-19 (including the age range approved for the latest booster) generally have less severe symptoms. Even the CDC concedes that “children are less likely to develop severe illness or die from COVID-19.”
The Pfizer vaccine is particularly dangerous for young men aged 16-17. As we observed back in October, teenage boys are especially at risk for heart problems – like myocarditis – after getting the Pfizer vaccine:
“Boys between 16 and 19 years of age had the highest incidence of myocarditis after the second dose . . . The risk of heart problems in boys of that age was about nine times higher than in unvaccinated boys of the same age.” New York Times.
The risk of myocarditis for boys 16 – 19 years old is higher after the Pfizer second dose. What happens after the third dose??
That’s a good question.
One would rightly assume that the third dose might present more danger of heart problems than the second dose. But FDA doesn’t have the answer to this question. And why doesn’t it have the answer?
Because the FDA didn’t look.
Because the FDA decided against holding an advisory meeting to discuss the decision.
Because the FDA required ZERO tests in this age bracket before approving the latest Pfizer booster for this age bracket.
Instead, the FDA relied on prior (old) booster data from a study of “200 participants, 18 through 55 years of age.” Choosing to ignore the long-term data for the efficacy of the Pfizer booster shot, the FDA instead reviewed the old data showing “the antibody response against the SARS-CoV-2 virus one month after a booster dose of the vaccine.”
That’s it. That’s the rigorous studies that now meet FDA standards. Given the self-imposed and purposeful limitations the FDA has placed on its own own information, it has the audacity to conclude:
“The benefits of a single booster dose of the Pfizer-BioNTech COVID-19 Vaccine or Comirnaty outweigh the risks of myocarditis and pericarditis in individuals 16 and 17 years of age to provide continued protection against COVID-19 and the associated serious consequences that can occur including hospitalization and death.”
This is the FDA making a cost/benefit calculation without knowing the costs or benefits. It doesn’t know the real risks because it didn’t study the potential for adverse reactions in kids aged 16 – 17 years. It doesn’t know the real benefits because it chose a shitty study that was limited to one month efficacy data.
This robust FDA cost/benefit calculation might sound familiar to our loyal readers. That would be because the Government did the same thing when recommending the COVID-19 vaccines for “people who are pregnant.”
FDA Colludes with US Postal Service to Destroy Ivermectin Shipments
InfoWars | December 15, 2021
The US Food and Drug Administration is colluding with the US Postal Service to intercept inbound international shipments of Covid wonder drug ivermectin, reports circulating on social media claim.
According to letters from the FDA being shared online, the federal regulatory agency blocked shipments of ivermectin from reaching their intended recipients as they came through ports of entry.
“A shipment addressed to you from a foreign country is being held by the post office at the request of the US Food and Drug Administration,” reads one letter shared by attorney Aaron Siri.
According to the letter, the package containing 200 tablets of “Iverheal ivermectin tablets” was intercepted at the JFK Airport Port of Entry on November 9, 2021.
In another letter, the FDA intercepted 300 tablets of “Iverpac12” back in August, which they said were “subject to refusal of admission into the United States and are subject to administrative destruction.”
News of the FDA’s collusion with the US Postal Service comes as more people seek the effective drug and other preventative early treatments to remedy Covid-19 symptoms.
Meanwhile, the FDA has continued it’s fear-mongering campaign advising Americans not to consume the “horse dewormer” drug to treat Covid, as it has not been formally approved [for COVID use].
Comirnaty, liability, and how the HHS lies, cheats and steals
By Meryl Nass, MD | December 12, 2021
I checked the Federal Register and there has been no notice that Comirnaty has been added to the National Childhood Vaccine injury Program (NVICP). I confirmed this by checking whether Comirnaty had been added to the childhood schedule, and according to the HRSA, which manages both compensation programs, it has not.
So, if you receive the licensed Comirnaty vaccine, correctly labeled as the brand-name product and not the vaccine being fobbed off as licensed product, and you are injured, you are free to sue the manufacturer for your injury. Could this be why Pfizer wrote, “Pfizer does not plan to produce any product with these new [Comirnaty National Drug Codes] and labels over the next few months while EUA authorized product is still available and being made available for U.S. distribution.”
If, however, you receive the Pfizer-BioNTech vaccine under Emergency Use Authorization, or the Moderna or J and J vaccine, you can’t sue anyone. You have the right to beg HRSA for compensation of lost wages and unpaid medical bills, period. So far, HRSA and the Countermeasures Injury Compensation Program it administers have not paid out one dime for the approximately one million injuries and 20,000 deaths reported to VAERS for any COVID vaccine.
In other words, the federal government (DHHS) has not admitted a single injury was caused by a COVID vaccine. CDC says it has not linked a single death to a COVID vaccine–not even when the patient walked into the vaccination center but got carried out to the morgue. FDA doesn’t know much about myocarditis, Bell’s Palsy, thrombosis, thrombocytopenia, pulmonary emboli, etc. There are no black box warnings on any of the COVID vaccines.
HRSA, FDA, CDC and NIH are all agencies within the federal Department of Health and Human Services. They have all gotten their stories straight. They know nothing and they are just following orders. Heil HHS!
They can’t find a doggone problem in the 20 or so databases they are spending many $millions of your money to “study.”
Want to know the biggest conspiracy in the US right now? It is the HHS.
FDA has access to a bunch of electronic databases it has termed the “BEST” Initiative, and it published a plan to use them to study heart attacks, pulmonary embolism, thrombocytopenia, etc. back in July. Where are the results, FDA? What are you waiting for? (According to CDC, “More than 459 million doses of COVID-19 vaccines were administered in the United States from December 14, 2020, through November 29, 2021.”). It seems clear that we aren’t supposed to be informed of FDA’s findings until everyone possible has been vaccinated, at which point the results will be irrelevant.
In October 2020, FDA’s Steve Anderson told us there were even more databases that would be studied.
On August 23, 2021, FDA announced its databases were inadequate to assess myocarditis, so BioNTech would have to do it for them. Here is what FDA wrote about its inability to use VAERS and its many other databases:
- As noted above, the FDA acknowledges that “We have determined that an analysis of spontaneous postmarketing adverse events reported under section 505(k)(1) of the FDCA [in other words, VAERS–Nass] will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis.
- Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA [in other words, FDA’s many other databases that cost the taxpayer zillions–Nass] is not sufficient to assess these serious risks.”
NOT SUFFICIENT???
Unsaid, but implied, is that if FDA is incapable of studying thousands of reported cases of myocarditis, it probably cannot study the other serious adverse events that have been reported in conjunction with COVID vaccines.
VAERS has operated for 30 years, collecting reports of vaccine adverse events. It averaged under 100 cases of myocarditis reported yearly until this year. Through November, CDC reports it received 1949 reports of myocarditis and pericarditis, in those under 30. CDC didn’t say what the total number of reports for all ages was.
Somehow, these HHS don’t seem all that concerned that the admitted reporting rate of myocarditis is over 20 times the average during the past 30 years. Why?
CDC has been even more shady in its analyses of safety as FDA, if that is even possible. Below, Nancy Messonier, then head of Immunizations and Respiratory Diseases at CDC, presented this list of databases that CDC would be using in the evaluation of COVID vaccine safety, on December 10, 2020. Apart from the V-safe (which they stopped talking about last January), VSD (which somehow can’t find any problems, not even myocarditis) and VAERS, all these other databases have been MIA.
NIH, whose job has never been to issue treatment guidelines, but instead to do and fund research, suddenly took over the treatment guidelines for COVID early in 2020. It formed a committee of internal and eternal “experts” to make up the guidelines. How were they chosen? That is not clear, but what is clear is that 16 of these so-called experts had current or recent financial entanglements with Gilead, the maker of remdesivir. NIH and the US Army also owned pieces of remdesivir. A number of other had financial conflicts with Merck. While NIH is the biggest single funder of medical research in the world, I cannot recall seeing a single study it funded on the safety of COVID vaccines. But somehow vaccines are its number one recommendation.
But it is not even clear that the committee is functional. The NIH has been sued to learn whether a vote was even taken by the committee regarding its ivermectin guidelines, which fly in the face of the evidence on ivermectin. How was NIH somehow authorized to issue guidelines in the first place?
Here is what has obviously occurred. All these agencies were told they had to keep quiet on vaccine problems (and perhaps problems of other COVID treatments), and they had to fiddle with their data or their analytic methods, or both, to get the required results. And there was to be NO BAD NEWS, no matter what. And no good news regarding generic treatments.
As we have seen, the so-called scientists and physicians working as bureaucrats in these agencies all caved, sucked it up, did the dirty work, kept their jobs, and betrayed their oaths and the trust of the people of the USA and the world.
Disclosing Pfizer vaccine data ‘may take until 2096’
RT | December 9, 2021
The US Food and Drug Administration is cooperating with a Freedom of Information Act request for clinical data associated with Pfizer’s Covid-19 vaccine, but may require 75 years to do so – even longer than a prior estimate.
The FDA has insisted it cannot commit to a faster release of the medical data associated with the approval of the Pfizer-BioNTech coronavirus vaccine, according to a legal brief filed on Tuesday in response to the FOIA request. The agency reiterated that after processing 12,000 pages in about a two-month period, it will only be able to process 500 pages per month going forward. With tens of thousands of additional files up for review, plaintiffs fear the process may drag on two decades longer than the previous 55-year estimate.
Lawyer Aaron Siri sued the FDA on behalf of a group of doctors calling themselves Public Health and Medical Professionals for Transparency, who had previously complained the FDA wasn’t supplying the data they had requested in a timely fashion. Having pointed out last month that the FDA had looked through Pfizer’s documents in a mere 108 days in order to license the vaccine, Siri questioned why the agency now required a whopping 20,000 days to make the same documents public.
Approximately 451,000 pages regarding the clinical trials for a vaccine millions of Americans are being mandated to take will remain floating in legal limbo for up to 75 years if the agency has its way, Siri warned. He called it “dystopian” for the government to pay Pfizer billions of dollars, shield it from lawsuits and require citizens to be injected with its product, only to refuse access to the documents used to grant its licensure in the first place.
The FDA has justified the unusual timetable by pointing out its Center for Biologics Evaluation and Research – the body tasked with reviewing the records – only has 10 staffers, two of whom are “new.” The FDA also complained that stepping up the pace would divert “significant resources away from the processing of other FOIA requests that are also in litigation.”
Remember when the FDA’s top vaccine regulator said even a moderately effective Covid shot could produce herd immunity if 70 percent of people got it?
By Alex Berenson | December 7, 2021
In late July 2020, Dr. Peter Marks, who oversees vaccines for the Food and Drug Administration, spoke for an FDA-produced podcast about the Covid vaccines.
At the time, the big mRNA vaccine trials were just beginning, and the two-part interview was fairly straightforward. It opened with Marks explaining what a vaccine is.
Later, though, Marks explained how an effective vaccine might end the epidemic:
What we also know is that once one reaches a certain level of protection, roughly 70 percent, and if 70 percent of the population gets that vaccine, you start to get to a place where the infectious disease that you’re trying to prevent, in this case, let’s read COVID-19 into that, it doesn’t have anywhere to go and you start to be able to help wipe that infectious disease out…
70 percent protection by 70 percent of the population equals (basically) no more Covid. Got it, doc!
The next week, Marks again explained the importance of 70 percent protection – and this time, he used the magic h-word:
That’s the concept of herd immunity that you have enough people in the population that can’t get the disease, that the disease has nowhere to go if it shows up. That’s exactly what we’d like to ultimately see with a really effective vaccine, one that might have, I think, we estimate at least 70 percent efficacy…
This might be a good time to remind you that much of Western Europe hit Marks’s magic number months ago. In countries like Britain, 70 percent (okay, 69.3!) of people – not adults, the entire population – is fully vaccinated. And about 30 percent of Britons have now received a third dose.
So how come a vaccine that was supposedly 95 percent effective at preventing infection (and supposedly even better at stopping severe disease) in clinical trials has completely failed to stop the epidemic?
Or, put another way, if the vaccines work, what’s going on?
Oh well. We’ll figure it out next pandemic. Meantime, get yer free booster today!
SOURCE: https://www.fda.gov/news-events/fda-insight/fda-insight-vaccines-covid-19-part-1
https://www.fda.gov/news-events/fda-insight/fda-insight-vaccines-covid-19-part-2
2,809 Dead Babies in VAERS Following COVID Shots as New Documents Prove Pfizer, the FDA, and the CDC Knew the Shots Were Not Safe for Pregnant Women
By Brian Shilhavy | Health Impact News | December 4, 2021
The latest data dump into the U.S. Government’s Vaccine Adverse Events Reporting System (VAERS) happened yesterday (12/3/21) and covers data through 11/26/2021.
There are now 927,740 cases reported to VAERS following COVID-19 shots for the past 11 months, out of the total of 1,782,453 cases in the entire VAERS database filed for the past 30+ years.
Left image source, Right image source.
That means that 52% off ALL vaccine adverse reaction cases in VAERS for the past 30+ years have been reported in the last 11 months following the COVID-19 shots.
In addition, 68% of all deaths following vaccines reported in VAERS for the past 30+ years have been reported in the last 11 months following the COVID-19 shots.
We are on pace to see 21,307 deaths reported in the first year following the experimental COVID-19 shots, while the average yearly deaths reported after FDA-approved vaccines for the past 30+ years is 305 deaths.
That is an astounding 86% increase in reported deaths following the COVID-19 shots, a 70X increase over the average reported deaths following vaccinations for the past 30+ years!
- FDA-approved vaccines: 305 deaths per year
- COVID-19 EUA shots: 21,307 deaths per year
And as Dr. Jessica Rose has previously reported, the under-reporting factor in VAERS for the COVID-19 shots is 41X, as a conservative number, which means that at least 800,812 people have now died following COVID-19 shots based on the VAERS data.
Most, if not all, of those deaths are being reported in the pharma-owned corporate media as “COVID” deaths, as there are now more recorded “COVID deaths” for the first 11 months of 2021 than there were for the entire year in 2020, when there were no COVID vaccines until December. (Source.)
Record Number of Fetal Deaths Following COVID-19 Shots
As of this most recent update in VAERS, we have now found 2,809 fetal deaths following COVID-19 shots injected into pregnant and child-bearing women for the past 11 months. (Source.)
By way of contrast, using the exact same search parameters in VAERS, but excluding the COVID-19 shots, we found 2,168 fetal deaths following all FDA-approved vaccines for the past 30+ years. (Source.)
That’s an average of 72 fetal deaths per year following all FDA-approved vaccines for the past 30+ years, compared to what is on pace to be 3064 fetal deaths in 1 year following COVID-19 shots.
- FDA-approved vaccines: 72 fetal deaths per year
- COVID-19 EUA shots: 3064 fetal deaths per year
That is an 80% increase in fetal deaths recorded in VAERS following the COVID-19 shots. And yet, the CDC and FDA continue to recommend these EUA shots for pregnant women and nursing mothers.
Not only do they recommend these shots for pregnant women, we now have ample evidence that they have known since earlier this year that these shots are dangerous to pregnant women, and causing fetal deaths.
In a March 4, 2021 Advisory Commission on Childhood Vaccines (ACCV) meeting, the CDC submitted a report that contained a section titled: Maternal vaccination safety summary (starting on p. 39).
They stated (emphasis mine – my comments in red):
* Pregnant women were not specifically included in pre-authorization clinical trials of COVID-19 vaccines
– Post-authorization safety monitoring and research are the primary ways to obtain safety data on COVID-19 vaccination during pregnancy
* Larger than expected numbers of self-reported pregnant women have registered in v-safe
* The reactogenicity profile and adverse events observed among pregnant women in v-safe did not indicate any safety problems (based on what criteria???)
* Most reports to VAERS among pregnant women (73%) involved non-pregnancy specific adverse events (e.g., local and systemic reactions)
* Miscarriage was the most frequently reported pregnancy-specific adverse event to VAERS; numbers are within the known background rates based on presumed COVID-19 vaccine doses administered to pregnant women (no supporting evidence to backup these claims)
It is important to note through all of this reporting by the CDC that these are based on self-reporting data from pregnant women.
We know that it is politically incorrect to blame any health issue on a COVID-19 “vaccine,” and that doctors and nurses are pressured to NOT report these, so how many pregnant women had an adverse reaction, like a miscarriage, and never even thought to link it to their COVID-19 shot?
So back in March of this year (2021), there were already major concerns about the effects of the shots on pregnant women, as “larger than expected” pregnant women were reporting adverse reactions, and “the most frequently reported pregnancy-specific adverse event to VAERS” was “miscarriage.”
Then in August of this year (2021), the CDC presented a “new study” with “new data.”
Again, this “data” is dependent on pregnant women “self-reporting” adverse reactions, so we know these reports will be well below what was actually happening in the population, as it is politically incorrect to report any adverse reactions related to the experimental COVID-19 shots. To do so is to be branded an “anti-vaxxer” and shame you for life.
The August update admitted that 13% of the pregnant women who had received a COVID-19 shot reported a miscarriage. The CDC brushed this aside by stating “miscarriage typically occurs in about 11-16% of pregnancies.”
But of course ALL miscarriages are reported somewhere in the medical files, which is why they can even come up with a number range like this. So this figure is based on 100% of the reported data, while the COVID-19 related miscarriages are only based on what was self-reported, and we have no idea how many women never reported their miscarriages because they never related it to their COVID-19 shot.
One the main studies the CDC allegedly relied upon to declare that COVID-19 shots were safe for pregnant women, was a study published in the New England Journal of Medicine on June 17, 2021.
But on October 14, 2021, they issued a statement stating that some of their data was wrong in the June 17th study. (Source.) It dealt specifically with pregnancies in their 20th week or earlier.
“No denominator was available to calculate a risk estimate for spontaneous abortions, because at the time of this report, follow-up through 20 weeks was not yet available for 905 of the 1224 participants vaccinated within 30 days before the first day of the last menstrual period or in the first trimester. Furthermore, any risk estimate would need to account for gestational week–specific risk of spontaneous abortion.” (Source.)
It’s not surprising that the FDA wants to slow-walk the release of COVID jab reaction data
By Dr. Joseph Mercola | December 2, 2021
It took the U.S. Food and Drug Administration 108 days to review all the data Pfizer/BioNTech submitted in order to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021.
Considering the agency claims there are 329,000 pages of data, the fact that they were able to read, analyze and draw conclusions about its safety and effectiveness in just 108 days — about 80,000 pages a month — is no small miracle. They must employ some very efficient speed readers.
And that is why the FDA’s claim that it now needs half a century to review the documents before they can release them to the public doesn’t seem very credible. Even Reuters has expressed shock, and its former CEO is on the board of Pfizer.1
Expedited FOIA Request for Comirnaty Data
In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty.
This includes safety and effectiveness data, adverse reaction reports and lists of active and inactive ingredients. Approximately 400 additional FOIA requests by other individuals for all or part of this information have also been filed.2
In their FOIA application, the PHMPT asked the agency to expedite release of the documents — a reasonable request, considering we have no raw data and the shots are being pushed on children as young as 5.
FOIA guidelines include two conditions upon which a request may be expedited. One is “if the lack of expedited treatment could reasonably be expected to pose a threat to someone’s life or physical safety,” which one could easily argue is the case here.
The second condition is “if there is an urgency to inform the public about an actual or alleged federal government activity, if made by a person who is primarily engaged in disseminating information.” This too is clearly applicable.
“During a time when COVID-19 vaccine mandates are being implemented over the objection of those that have questions about the data and information supporting the safety and efficacy of the Pfizer Vaccine, and individuals with these questions are being expelled from employment, school, transportation, and the military, the public has an urgent and immediate need to have access to this data,” the PHMPT said in its request.3
FDA Now Wants 55 Years to Release COVID Jab Data
When, after a month, the FDA still had not responded to the FOIA request, the PHMPT sued.4 The FDA is now asking a federal judge to allow them to delay the full release of all documents until 2076 — 55 years from now.
According to the U.S. Department of Justice (DOJ) attorney who represents the FDA in this case, the agency will be able to “provide more pages to more requesters” if allowed to stick to a rolling schedule of 500 pages per month, “thus avoiding a system where a few large requests monopolize finite processing resources.”
They claim they only have 10 employees assigned to FOIA releases, and before material can be released, an FDA official has to go through them and redact any information that might reveal personal information about clinical trial participants and any confidential business or trade secret information.
The 1967 FOIA law requires federal agencies to respond to FOIAs within 20 days unless “unusual circumstances” exist that prevent a timely release. Circumstances that might warrant an extended release schedule include:
- Instances where response records must be searched for and collected from an entity other than the office processing the request
- Situations involving “voluminous” amounts of records that must be compiled, and
- Instances requiring consultation with another federal agency that has a substantial interest in the information
The DOJ attorney points out that the court has allowed for a 500-page maximum per month release schedule in other cases, and should allow the FDA the same leeway here.
Plaintiffs, on the other hand, argue the agency should be able to release everything by early March 2022, noting the FDA employs 18,000 people and has an annual budget of $6 billion. Between 2008 and 2017, the agency processed 114,938 FOIA requests, of which it granted 72.4%, either fully or partially.
Of those, 39.8% were designated as “complex,” and 81.5% of these complex FOIA requests were granted in 61 days or more. Considering these historical statistics, a backlog of 400 FOIA requests doesn’t appear excessively burdensome.
FDA’s Foot-Dragging Is Suspicious
Then there’s the sticky issue that it has already proven its capacity for rapid review. Aaron Siri of the law firm Siri & Glimstad wrote in the PHMPT’s court filing:5,6,7,8
“This 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer’s COVID-19 vaccine …
It took the FDA precisely 108 days from when Pfizer started producing the records for licensure to when the FDA licensed the Pfizer vaccine. Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure.
While it can conduct that intense review of Pfizer’s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public …
The entire purpose of the FOIA is to assure government transparency. It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.”
Shocking Revelations in First Batch of FOIA Docs
Two months after the lawsuit against it was filed, the FDA released a batch of 91 pages,9 and if this batch is any indication, it’s not surprising that the FDA wants to slow-walk the release of the rest. In a November 21, 2021, substack article, Kyle Becker cites directly from the released documents:10
“’It is estimated that approximately [REDACTED] doses of BNT162b2 were shipped worldwide from the receipt of the first temporary authorization for emergency supply on 01 December 2020 through 28 February 2021,’ the document states. ‘Cumulatively, through 28 February 2021, there was a total of 42,086 case reports (25,379 medically confirmed and 16,707 non-medically confirmed) containing 158,893 events …
Most cases (34,762) were received from United States (13,739), United Kingdom (13,404) Italy (2,578), Germany (1913), France (1506), Portugal (866).’ Below is a General Overview of the reported outcomes to the Adverse Events:
The chart lists 1,223 fatal outcomes in the Relevant Cases. Interestingly, the age range with the most relevant cases was 31-50 years old, which is not the age group considered to be at high risk from COVID-19.”
It’s worth noting that by redacting the specified number of doses shipped, it becomes more difficult to assess the potential ratio of injury. Still, even without that, 42,086 reports of injury, including 1,223 fatalities, are a significant signal in and of itself, especially when you consider that the 1976 swine flu vaccine was pulled after 25 deaths.
Glaring Disregard for Life
It’s even more disturbing when you consider that those 42,086 reports were received by Pfizer in just the first 2.5 months of the shot being rolled out. Pfizer even acknowledges the abnormal rate of injuries, but then sweeps it aside as being of no consequence. As noted by Siri, in a November 19, 2021 substack article, in which he discusses this first batch of documents:11
“Pfizer explains, on page 6, that ‘Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritized the processing of serious cases…’
Pfizer ‘has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports’ including ‘increasing the number of data entry and case processing colleagues’ and ‘has onboarded approximately [REDACTED] additional fulltime employees (FTEs).’
Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product …
But no cause for alarm since Pfizer explains to the FDA: ‘The findings of these signal detection analyses are consistent with the known safety profile of the vaccine.’ So, if they knew these issues were going to arise, then why didn’t they appear to have enough staff to process this expected volume of reports?
The grand conclusion by Pfizer to the FDA: ‘The data do not reveal any novel safety concerns or risks requiring label changes and support a favorable benefit risk profile of to the BNT162b2 vaccine.’ Nothing to see here.”
Clearly, there’s plenty to be seen in the hundreds of thousands of documents Pfizer/BioNTech submitted to the FDA. The fact that the FDA is stonewalling and wants 55 years to redact them before they’re fit for public view is telling in and of itself.
You don’t need a fanciful imagination to comprehend what they might be hiding. It almost seems they want to make sure the responsible parties are all dead by the time the full data set is out in the open and people can be held to account for their decisions. Let’s hope the judge is more interested in public health than protecting the FDA’s dirty secrets.
Sources and References
- 1 ZeroHedge November 23, 2021
- 2, 7 Daily Mail November 19, 2021, Updated November 20, 2021
- 3, 4 The Defender November 19, 2021
- 5 US District Court Northern District of Texas Case 4:21-cv-01058-P
- 6 US District Court Northern District of Texas Case 4:21-cv-01058-P Second Joint Report
- 8 The Vaccine Reaction November 21, 2021
- 9 PHMPT.org Pfizer documents
- 10 thekylebecker.substack.com November 21, 2021
- 11 aaronsiri.substack.com November 19, 2021
Fauci and the Great AIDS Swindle
A Partial Review of Robert F. Kennedy, Jr., THE REAL ANTHONY FAUCI
BY LAURENT GUYÉNOT • UNZ REVIEW • NOVEMBER 27, 2021
Robert F. Kennedy, Jr.’s new book, The Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public Health is not the book of a politician seeking attention. It is the book of a man determined to stake his own life in the resistance against the unfolding bio-terrorist assault on humankind by governments captive of the pharmaceutical industry. He is calling for mass insurrection, and his last word is: “I’ll see you on the barricades.” The book begins like this:
I wrote this book to help Americans—and citizens across the globe—understand the historical underpinnings of the bewildering cataclysm that began in 2020. In that single annus horribilis, liberal democracy effectively collapsed worldwide. The very governmental health regulators, social media eminences, and media companies that idealistic populations relied upon as champions of freedom, health, democracy, civil rights, and evidence-based public policy seemed to collectively pivot in a lockstep assault against free speech and personal freedoms. Suddenly, those trusted institutions seemed to be acting in concert to generate fear, promote obedience, discourage critical thinking, and herd seven billion people to march to a single tune, culminating in mass public health experiments with a novel, shoddily tested and improperly licensed technology so risky that manufacturers refused to produce it unless every government on Earth shielded them from liability. … Conscientious objectors who resisted these unwanted, experimental, zero-liability medical interventions faced orchestrated gaslighting, marginalization, and scapegoating. American lives and livelihoods were shattered by a bewildering array of draconian diktats imposed without legislative approval or judicial review, risk assessment, or scientific citation. So-called Emergency Orders closed our businesses, schools and churches, made unprecedented intrusions into privacy, and disrupted our most treasured social and family relationships.
Kennedy is not a newcomer to this frightening dystopia. “My 40-year career as an environmental and public health advocate,” he writes, “gave me a unique understanding of the corrupting mechanisms of ‘regulatory capture,’ the process by which the regulator becomes beholden to the industry it’s meant to regulate.” From the time he entered the vaccine debate in 2005, he realized that “the pervasive web of deep financial entanglements between Pharma and the government health agencies had put regulatory capture on steroids.” The Centers for Disease Control and Prevention (CDC), for example, owns 57 vaccine patents and spent $4.9 billion in 2019 buying and distributing vaccines. The Food and Drug Administration (FDA) receives 45 percent of its budget from the pharmaceutical industry. The National Institutes of Health (NIH), with its $42 billion budget, owns hundreds of vaccine patents and often profits from the sale of products it supposedly regulates. High-level officials receive yearly emoluments of up to $150,000 in royalty payments on products that they help develop and then usher through the approval process.
Dr. Anthony Fauci, “America’s reigning health commissar,” stands at the summit of that Leviathan. From 1968, he occupied various posts at the National Institute of Allergy and Infectious Diseases (NIAID), a sub-agency of NIH, of which he became director in 1984. With a $417,608 annual salary, he is the highest paid of all federal employees, including the President. “His experiences surviving 50 years as the panjandrum of a key federal bureaucracy, having advised six Presidents, the Pentagon, intelligence agencies, foreign governments, and the WHO, seasoned him exquisitely for a crisis that would allow him to wield power enjoyed by few rulers and no doctor in history.” He has nurtured a complex web of financial entanglements that has transformed the NIH into a subsidiary of Big Pharma. Reaching into the deep pockets of the Clinton and Gates Foundations, he has used his $6 billion annual budget to achieve dominance and control over many agencies, including the World Health Organization (WHO). He can make and break careers, enrich or punish university research centers, and dictate the outcome of scientific research across the globe, consistently prioritizing pharmaceutical industry profits over public health.
Kennedy’s book documents Fauci’s “two-decade strategy of promoting false pandemics as a scheme for promoting novel vaccines,” as well as “his actions to conceal widespread contamination in blood and vaccines, his destructive vendettas against scientists who challenge the Pharma paradigm, [and] his deliberate sabotaging of patent-expired remedies against infectious diseases.”
But of course, Kennedy’s book is not about a man: it is about an irremediably corrupt and predatory system created in the U.S. and exported worldwide. Ultimately, however, the system is built and run by humans, and focusing on its most emblematic representative shows its very soul.
Kennedy’s book puts the current crisis in historical perspective. But it doesn’t tell the story chronologically. It starts with a very long first chapter on the current Covid crisis—a book by itself—, then goes back, from chapter 3, to the 1980s and the search for the AIDS vaccine, the template for today’s pharmaceutical coup. In this review, I will focus on the AIDS episode, because it is the least familiar part of a history covering fifty years, and it helps make sense of what is happening today. It is an incredible story, that I would have had difficulty believing just three years ago, but that our current enslavement now makes utterly credible.
The thirty-year decampment of journalistic scrutiny means that there is still no coherent public narrative chronicling Dr. Fauci’s futile quest for his “inevitable” AIDS vaccine, much less accountability. Industry and government scientists have instead shrouded the scandalous saga in secrecy, subterfuge, and prevarication, obscuring a thousand calamities and a sea of tears deserving its own book. Every meager effort to research the debacle—on Google, PubMed, news sites, and published clinical trial data—yields only shocking new atrocities—a grim, repetitive parade of horribles: heartbreaking tragedies, entrenched institutional arrogance and racism, broken promises, vast expenditures of squandered treasure, and the recurring chicanery of Anthony Fauci, Bob Gallo, and Bill Gates.
Kennedy deserves praise and gratitude for his courage to bring this controversy out into the open, in a clear and well-documented exposé. His book is destined to become a landmark in the struggle for Life and Truth—and in the Kennedy heroic saga. This article reflects only a fraction of what can be learned from its 480 pages packed with data and references. Since page numbers in the kindle edition (recommended for its thousand hyperlinks) differ from those in the printing book, I have dispensed with them.
In the Beginning
In the first lines of his 2014 book Thimerosal: Let the Science Speak (documenting an astonishing 1,135 percent higher rate of autism among children who took hepatitis B vaccines), Kennedy prudently claimed to be “pro-vaccine” and to “believe that vaccines have saves the lives of hundreds of millions of humans over the past century.” Kennedy makes no such disclaimer in his new book. Rather, he sides with the critics of the popular dogma that vaccines played the key role in abolishing mortal contagious illnesses in North America and Europe, citing a 2000 study by CDC and Johns Hopkins scientists that concluded: “nearly 90 percent of the decline in infectious disease mortality among US children occurred before 1940, when few antibiotics or vaccines were available.” The main causes of the dramatic 74 percent decline in infectious disease mortality in the first half of the twentieth century were improved nutrition and sanitation.
From Kennedy, The Real Anthony Fauci, 2021
This revisionist but objective perspective explains why Fauci and Gates’s obsession with vaccine-preventable diseases has caused negative overall impacts on public health in Africa and Asia, by proportionally reducing assistance streams for nutrition, clean water, transportation, hygiene, and economic development. Gates and Fauci have actually hijacked WHO’s public health agenda away from the projects that are proven to curb infectious diseases, and diverted international aid to wedge open emerging markets for their multinational partners.
To understand their craze for vaccines, Kennedy reminds us of the pioneering influence of the Rockefeller Foundation. In 1911, after the Supreme Court ruled that Standard Oil constituted an “unreasonable monopoly” and splintered it into thirty-four companies, John D. Rockefeller inaugurated what Bill Gates would later call “philanthrocapitalism.” He provided large grants to scientists for synthesizing and patenting chemical versions of the molecules identified in traditional medicine. The Foundation provided almost half of the initial budget for the League of Nations’ Health Organization (LNHO) in 1922, and populated its ranks with its veterans and favorites. It imbued the League with its technocratic philosophy of health, inherited by its successor body, the WHO, in 1948.
The Rockefeller Foundation launched a “public-private partnership” with pharmaceutical companies called the International Health Commission, which first set about inoculating the hapless populations of the colonized tropics with a yellow fever jab. By the time John D. Rockefeller, Jr. disbanded it in 1951, the International Health Commission had spent billions of dollars on tropical disease campaigns in almost 100 countries and colonies. These projects had a hidden agenda, according to a 2017 report, U.S. Philanthrocapitalism and the Global Health Agenda: they allowed the Rockefeller family to open developing world markets for oil, mining, banking and other profitable trades, including pharmaceutical profits that grew tremendously when, in the 1970s:
a wave of new technologies, including PCR and super powerful electron microscopes, had opened windows on teeming new worlds containing millions of species of previously unknown viruses to scientists. … The lure of fame and fortune ignited a chaotic revolution in virology as ambitious young PhDs scrambled to inculpate newly discovered microbes as the cause of old malignancies. … Under this new rubric, every theoretical breakthrough, every find, became potentially the basis for a new generation of drugs.
By the mid-1970s, the CDC was seeking to justify its existence by tracking small outbreaks of rabies. “Drumming up public fear of periodic pandemics was a natural way for NIAID and CDC bureaucrats to keep their agencies relevant. Dr. Fauci’s immediate boss and predecessor as NIAID Director, Richard M. Krause, helped pioneer this new strategy in 1976.” That year the fake swine flu epidemic was concocted. The experimental vaccine was so fraught with problems that the Health and Human Services (HHS) discontinued the jab after vaccinating 49 million Americans. According to news accounts, the incidence of flu was seven times greater among the vaccinated than the unvaccinated. Furthermore, the vaccine caused some 500 cases of the degenerative nerve disease Guillain-Barré Syndrome, 32 deaths, more than 400 paralyzations, and as many as 4,000 other injuries. Injured plaintiffs filed 1,604 lawsuits. By April 1985, the government had paid out $83,233,714 and spent tens of millions of dollars adjudicating and processing those claims.
Another scandal broke in 1983, when a NIH-funded UCLA study found that the DTP vaccine developed by Wyeth—now Pfizer—was killing or causing severe brain injury, including seizures and death, in one in every 300 vaccinated children. While protecting children against diphtheria, tetanus, and pertussis, the DTP vaccine had ruined their immune systems, making them vulnerable to a wide range of other deadly infections.
The resultant lawsuits caused the collapse of insurance markets for vaccines and threatened to bankrupt the industry. Wyeth claimed to be losing $20 in downstream liability for every dollar it earned on vaccine sales, and induced Congress to pass in 1986 the National Childhood Vaccine Injury Act, which shielded vaccine makers from liability. (This incentive for unrestricted greed was strengthened in 2005 when George W. Bush signed into law the Public Readiness and Emergency Preparedness Act).
AIDS and AZT
In 1984, when Fauci became director of NIAID, the AIDS crisis was spiraling out of control. That proved “a redemptive juncture for NIAID and the launch pad for Dr. Fauci’s stellar rise.” In an April 1984 press conference, NIH scientist Robert Gallo linked AIDS to the virus that was soon to be named HIV. Dr. Fauci then moved aggressively to claim jurisdiction for his agency over the National Cancer Institute (NCI), another sub-agency of NIH. “As the nation’s newly appointed AIDS czar, Dr. Fauci was now a gatekeeper for almost all AIDS research … parroting NCI’s vows to cure cancer, Dr. Fauci promised Congress that he would quickly produce drugs and vaccines to banish AIDS.”
At the same time, he was deliberately spreading contagion terror, warning in a 1983 fear-mongering article that “the scope of the syndrome may be enormous”, since “routine close contact, as within a family household, can spread the disease”—despite the fact that AIDS was almost exclusive to intravenous drug users and male homosexuals. A year later, Fauci was forced to concede that health officials had never detected a case of the disease spread through “casual contact.” Nevertheless, Dr. Fauci’s systematic response was “to amplify the widespread panic of dreaded pestilence that would naturally magnify his power, elevate his profile, and expand his influence. Amplifying terror of infectious disease was already an ingrained knee-jerk institutional response at NIAID.”
Having seized control over AIDS research, Fauci captured the new flood of congressional AIDS appropriations flowing to NIH through the lobbying of a newly organized gay community. By 1990, NIAID’s annual AIDS budget reached $3 billion. In the ensuing decades, the federal government spent over half a trillion dollars in the quest for an elusive vaccine that never materialized. Dr. Fauci pumped up taxpayers’ money into nearly 100 vaccine candidates, with no other result than “massive transfers of public lucre to Dr. Fauci’s Pharma partners,” and a sea of tears for millions of unfortunate human guinea pigs.
NIAID’s lack of in-house drug development capacity meant that Fauci had to farm out drug research to a network of so-called “principal investigators” (PIs), academic physicians and researchers controlled by pharmaceutical companies and acting as liaisons, recruiters and spokespersons.
PIs are pharmaceutical industry surrogates who play key roles promoting the pharmaceutical paradigm and functioning as high priests of all its orthodoxies, which they proselytize with missionary zeal. They use their seats on medical boards and chairmanships of university departments to propagate dogma and root out heresy. … They are the credentialed and trusted medical experts who prognosticate on television networks—now helplessly reliant on pharmaceutical ad revenue—to push out Pharma content.
Dr. Fauci’s choice to transfer virtually all of NIAID’s budget to pharmaceutical PIs for drug development was an abdication of the agency’s duty to find the source and eliminate the explosive epidemics of allergic and autoimmune disease that began under his watch around 1989. … NIAID money effectively became a giant subsidy to the blossoming pharmaceutical industry to incubate a pipeline of profitable new drugs targeted to treat the symptoms of those very diseases.
In the late 80s and early 90s, PIs received every year between 4 and 5 billions of dollars from NIH’s budget. But “legalized bribes” from drug companies and royalty payments from drug products often dwarfed their government funding. Celia Farber’s 2006 Harper’s article, “Out of Control: AIDS and the Destruction of Medical Science,” laid bare the culture of squalor, corruption, and vendetta at Fauci’s AIDS Branch, the Division of Acquired Immunodeficiency Syndrome (DAIDS).
Despite his miserable track record at reducing illness over the previous decade, Fauci persuaded President Bill Clinton, in May 1997, to set a new national goal for science. In a speech delivered at Morgan State University, Clinton—perhaps not without cryptic irony— imitated Kennedy’s May 25, 1961 moonshot promise, saying, “Today let us commit ourselves to developing an AIDS vaccine within the next decade.”
A year later, Bill Gates, who had just founded his International Aids Vaccine Initiative (IAVI), sealed a deal with Fauci. “Over the next two decades, that partnership would metastasize to include pharmaceutical companies, military and intelligence planners, and international health agencies all collaborating to promote weaponized pandemics and vaccines and a new brand of corporate imperialism rooted in the ideology of biosecurity.” The story of Gates’ involvement in the vaccine business, of his murderous experiments in Africa and India, and of his rise as the unofficial top sponsor of the WHO (ordering in 2011: “All 193 member states, you must make vaccines a central focus of your health systems”), is told in chapters 9 and 10 of Kennedy’s book.
When Dr. Fauci became head of NIAID, azidothymidine, known as AZT, was the only candidate as an AIDS remedy. AZT is a “DNA chain terminator,” randomly destroying DNA synthesis in reproducing cells. It had been developed in 1964 for cancer, but abandoned as too toxic even for short-term therapy. It was deemed so worthless that it was not even patented. In 1985, Samuel Broder, head of the National Cancer Institute (NCI), claimed having found that AZT killed HIV in test tubes. The British company Burroughs Wellcome then patented it as an AIDS remedy. “Recognizing financial opportunity in the desperate terror of young AIDS patients facing certain death, the drug company set the price at up to $10,000/year per patient—making AZT one of the most expensive drugs in pharmaceutical history. Since Burroughs Wellcome could manufacture AZT for pennies per dose, the company anticipated a bonanza.”
Fauci gave Burroughs Wellcome a monopoly control over the government’s HIV response. But all did not go smoothly. “AZT’s horrendous toxicity hobbled researchers struggling to design study protocols that would make it appear either safe or effective.” Another problem is that community-based doctors were achieving promising results with cheap, off-label therapeutic drugs. Dr. Fauci refused to test any of those repurposed drugs that had no Pharma patrons. When he did put on trial AL721, an antiviral that was far less toxic than AZT, he rigged the studies to fail, and abruptly cancelled Phase 2.
Meanwhile, he accelerated testing of AZT, skipping animal testing and allowing Burroughs Wellcome to proceed directly to human trials. In March 1987, Fauci’s team declared the human trials a success after only four months, and Fauci congratulated himself in front of the press. However, when in July 1987, the official report of Burroughs Wellcome’s Phase 2 trial was published, European scientists complained that raw data showed no benefit in reducing symptoms. FDA conducted its own investigation eighteen months later, but kept its results secret, until investigative journalist John Lauritsen obtained some of them by using the Freedom of Information Act; the documents showed that the Fauci/Burroughs Wellcome research teams had engaged in widespread data tampering. More than half of the AZT patients suffered adverse reactions so deadly that they needed multiple blood transfusions just to keep them alive. Nevertheless, Fauci kept on lying himself to the top of the world, with little scrutiny from mainstream media.
A key and enduring legacy of the AZT battle was Dr. Fauci’s emergence as the alpha wolf of HHS [Health and Human Services]. His enormous budget, and multiplying contacts on Capitol Hill, the White House, and the medical industry, thereafter allowed him to influence or ignore a succession of politically appointed HHS directors and to bully, manipulate, and dominate HHS’s other sister agencies, most notably FDA.
AZT was not the only subject of interest to Fauci. By June 2003, NIH was running 10,906 clinical trials on new antiviral concoctions in some four hundred clinical trials in ninety countries. Some of those trials seemed pulled out of Dickens’ worst nightmares. The Alliance for Human Research Protection (AHRP), a medical industry watchdog organization, has documented that between 1985 and 2005, NIAID conscripted at least 532 infants and children from foster care in New York City as subjects of clinical trials testing experimental AIDS drugs and vaccines. AHRP’s investigation revealed that many of those children were perfectly healthy and may not even have been HIV-infected. Yet 80 of them died. In 2004, journalist Liam Scheff chronicled Dr. Fauci’s secretive experiments on foster children at Incarnation Children’s Center (ICC) in New York City and numerous sister facilities between 1988 and 2002. These disclosures, comments Kennedy, beg many questions:
From what moral wilderness did the monsters who devised and condoned these experiments descend upon our idealistic country? How have they lately come to exercise such tyrannical power over our citizens? What sort of nation are we if we allow them to continue? Most trenchantly, does it not make sense that the malevolent minds, the elastic ethics, the appalling judgment, the arrogance, and savagery that sanctioned the barbaric brutalization of children at the Incarceration Convent House, and the torture of animals for industry profit, could also concoct a moral justification for suppressing lifesaving remedies and prolonging a deadly epidemic? Could these same dark alchemists justify a strategy of prioritizing their $48 billion vaccine project ahead of public health and human life? Did similar hubris—that deadly human impulse to play God—pave the lethal path to Wuhan and fuel the reckless decision to hack the codes of Creation and fabricate diabolical new forms of life—pandemic superbugs—in a ramshackle laboratory with scientists linked to the Chinese military?
Indeed, Kennedy shows in his final chapter, “Germ Games,” that Fauci’s investments in so-called “gain of function” experiments to engineer pandemic superbugs raise “the ironic possibility that Dr. Fauci may have played a role in triggering the global contagion that two US presidents entrusted him to manage.”
Africa is “the venue of choice for companies seeking cooperative government officials, compliant populations, the lowest per-patient enrollment costs, and lax oversight by media and regulatory officials.” In the early 1990s, African dictators rolled out the red carpet for Pharma, cashing in on the lucrative business of farming out their citizens for the booming clinical trial business. And on January 29, 2003, President George W. Bush announced at his State of the Union speech his Emergency Plan for AIDS Relief (PEPFAR), Fauci’s new swindle:
On the continent of Africa, nearly 30 million people have the AIDS virus. … Yet across that continent, only 50,000 AIDS victims—only 50,000—are receiving the medicine they need. … I ask the Congress to commit $15 billion over the next five years, including nearly $10 billion in new money, to turn the tide against AIDS in the most afflicted nations of Africa and the Caribbean.
Does HIV Cause AIDS?
Kennedy’s chapter 5, “The HIV Heresies,” opens up with the following note:
I hesitated to include this chapter because any questioning of the orthodoxy that HIV is the sole cause of AIDS remains an unforgivable—even dangerous—heresy among our reigning medical cartel and its media allies. But one cannot write a complete book about Tony Fauci without touching on the abiding—and fascinating—scientific controversy over what he characterizes as his “greatest accomplishment” and his “life’s work.”
The controversy illustrates how pharmaceutical industries and health agencies, acting in concert, engineer consensus on incomplete or fraudulent theories, and ruthlessly suppress dissent from even the most gifted recognized scientists. “From the outset,” Kennedy insists, “I want to make clear that I take no position on the relationship between HIV and AIDS.” However, there seems little doubt that his basic point is correct:
During the thirty-six years since Dr. Fauci and his colleague, Dr. Robert Gallo, first claimed that HIV is the sole cause of AIDS, no one has been able to point to a study that demonstrates their hypothesis using accepted scientific proofs. … Even today, incoherence, knowledge gaps, contradictions, and inconsistencies continue to bedevil the official dogma.
The success story of the HIV-AIDS dogma shows “many of the tactics Dr. Fauci has pioneered to dodge debate—bedazzling and bamboozling the press into ignoring legitimate inquiry of the credo, and undermining, gaslighting, punishing, bullying, intimidating, marginalizing, vilifying, and muzzling critics.” One of Fauci’s victims was Dr. Peter Duesberg, who in 1987 was still recognized as the world’s most accomplished retrovirologist. Duesberg argues that HIV does not cause AIDS but is essentially a “free rider” common to high-risk populations who suffer immune suppression due to environmental exposures. HIV, he says, is a harmless passenger virus that has almost certainly coexisted in humans for thousands of generations without causing diseases. While HIV may be sexually transmittable, Duesberg claims, AIDS is not.
Duesberg published his views in a groundbreaking 1987 article, then in a 724-page book, Inventing the AIDS Virus. Kennedy finds that “Duesberg’s rationales appear so clean, so elegantly crafted, and so compelling that, in reading them, it seems impossible that the entire [orthodox] hypothesis did not instantly collapse under the smothering weight of relentless logic.” But Fauci and Gallo never attempted to reply to Duesberg. Blaming AIDS on a virus was the gambit that had allowed NIAID to claim the jurisdiction—and cash flow—away from NCI, and Duesberg was severely punished for endangering this.
Dr. Fauci summoned the entire upper clergy of his HIV orthodoxy—and all of its lower acolytes and altar boys—to unleash a storm of fierce retribution on the Berkeley virologist and his followers. … the AIDS establishment, down to its lowliest doctor, publicly reviled Duesberg, NIH defunded him, and academia ostracized and exiled the brilliant Berkeley professor. The scientific press all but banished him. He became radioactive.
Surprisingly, however, Dr. Luc Montagnier, whose discovery of HIV Gallo had in fact stolen—as he admitted in 1991 after years of litigation—, became Duesberg’s most embarrassing convert, declaring at the San Francisco International AIDS Conference in June 1990, that “the HIV virus is harmless and passive, a benign virus.” He added that, according to his findings, HIV becomes dangerous only in the presence of a second organism, a bacteria-like bug called a mycoplasma. Montagnier, in fact, had never claimed that HIV was the only factor in AIDS, and grew increasingly skeptical of that theory. His repeated questioning of the establishment paradigm signaled the beginning of his vilification, for which his Nobel Prize hardly protected him.
Gallo’s “proof” that the cause of AIDS was a virus—as opposed to toxic exposures— provided the critical foundation stone of Dr. Fauci’s career. It allowed Fauci to capture the AIDS program and launch NIAID as the leading federal partner of the drug-production industry. This explains why Fauci never funded any study to explore whether HIV actually caused AIDS, and took vigorous preemptive action against any such study.
Kennedy cites other dissenting voices on AIDS epidemiology. Dr. Shyh-Ching Lo, the Chief Researcher in charge of AIDS programs for the Armed Forces Institute of Pathology, was shocked by Anthony Fauci’s unconventional claim that antibodies, normally the sign of a robust immune response, should, with HIV, be the signal for impending death. Since “HIV tests” do not in reality detect the elusive virus but only antibodies, there seems to be an Orwellian inversion at work. Kennedy also quotes Dr. David Rasnick, a PhD biochemist who has worked for thirty years in the pharmaceutical biotech field:
Fauci’s fundamental conundrum is that he has told everybody to diagnose AIDS based on the presence of HIV antibodies. With every other disease, the presence of antibodies is the signal that the patient has vanquished the disease. With AIDS, Fauci and Gallo, and now Gates, claim it’s a sign you’re about to die. Think about it; if the objective of an AIDS vaccine is to stimulate antibody production, then success would mean that every vaccinated person would also have an AIDS diagnosis. I mean, this is fodder for a comedy bit. It’s like someone gave the Three Stooges an annual billion-dollar budget!
The nature of AIDS—a syndrome, not a disease—is itself subject to questions, since it was made to encompass a galaxy of some thirty separate well-known diseases, all of which occur in individuals who have no HIV infection. “In the hands of Dr. Fauci’s opportunistic PIs, AIDS became an amorphous malady subject to ever-changing definitions, encompassing a multitude of old diseases in hosts who test positive for HIV.” Nobel Laureate Kary Mullis, the inventor of the PCR tests, pointed out that the PCR was capable of finding HIV signals in large segments of the population who suffered no AIDS symptoms. On the other hand, AIDS commonly occurs in people who test HIV negative, as Geoffrey Cowley documented in a 1992 Newsweek article, followed by Steve Heimoff in the Los Angeles Times.
These very inconsistencies were not a problem for Fauci and his standing army of pharmaceutical mercenaries. Quite the opposite: they opened up Africa’s AIDS bonanza. Researchers funded by Fauci, using PCR tests and murky statistical models, declared that up to 30 million Africans were suffering from AIDS, nearly half the adult population in some nations. While in Western nations, AIDS continued to be a disease of drug addicts and homosexual “poppers” (consumers of the amyl nitrite vasodilator providing relaxation of the anal musculature, packaged into the “popper” container patented by Burroughs Wellcome and advertised in the gay press throughout the AIDS epidemic), mysteriously, in Africa, 59 percent of AIDS cases were women, and 85 percent were heterosexuals.
But in the early 1990s, the character of AIDS changed dramatically with the proliferation of AZT. As they started to give AZT to people who were in fact not even sick but simply positive on the HIV test, AIDS started to look increasingly like AZT poisoning. And the death rate climbed precipitously. According to the Duesbergians, the vast majority of “AIDS deaths” after 1987 were actually caused by AZT. The medication that Dr. Fauci was prescribing to treat AIDS patients actually did what the virus could not: it caused AIDS itself. In 1988, the average survival time for patients taking AZT was four months. In 1997, recognizing the lethal effect of AZT, health officials lowered the dose; the average lifespan of AZT patients then rose to twenty-four months. According to Dr. Claus Köhnlein, a German oncologist, “We virtually killed a whole generation of AIDS patients without even noticing it because the symptoms of the AZT intoxication were almost indistinguishable from AIDS.”
Conclusion
In July 2019, Dr. Fauci made a surprise announcement: he finally had a working HIV vaccine, the potential “nail in the coffin” for the epidemic. He conceded that his new vaccine didn’t prevent transmission of AIDS, but predicted that those who took the jab would find that when they did get AIDS, the symptoms would be much reduced. Kennedy comments:
So confident was Dr. Fauci of the media’s slavish credulity that he assumed, correctly, that he’d never need to answer the many questions raised by this feverish gibberish. That entire odd proposition received zero critical press commentary. His success at slapping lipstick on this donkey and selling it to the world as a Thoroughbred may have emboldened his ruse—a year later—of placing similar cosmetics on the COVID vaccines that, likewise, neither prevent disease nor preclude transmission.
By 2019, the AIDS rope started to wear out. Who still cared about AIDS anyway? The “Covid-19 Pandemic” came as the perfect opportunity for a reset and an update in the pharmaceutical racket. As Winston Churchill reportedly said, “Never let a good crisis go to waste”. With complicit corporate media blacking out the scandalous track record of his white-coat mafia, Fauci emerged, again, as the good doctor, the savior.
“Is it fair to blame Dr. Fauci for a crisis that, of course, has many authors?” asks Kennedy. To some extent, it is.
Under Dr. Fauci’s leadership, the allergic, autoimmune, and chronic illnesses which Congress specifically charged NIAID to investigate and prevent, have mushroomed to afflict 54 percent of children, up from 12.8 percent when he took over NIAID in 1984. Dr. Fauci has offered no explanation as to why allergic diseases like asthma, eczema, food allergies, allergic rhinitis, and anaphylaxis suddenly exploded beginning in 1989, five years after he came to power. On its website, NIAID boasts that autoimmune disease is one of the agency’s top priorities. Some 80 autoimmune diseases, including juvenile diabetes and rheumatoid arthritis, Graves’ disease, and Crohn’s disease, which were practically unknown prior to 1984, suddenly became epidemic under his watch. Autism, which many scientists now consider an autoimmune disease, exploded from between 2/10,000 and 4/10,000 Americans when Tony Fauci joined NIAID, to one in thirty-four today. Neurological diseases like ADD/ADHD, speech and sleep disorders, narcolepsy, facial tics, and Tourette’s syndrome have become commonplace in American children. The human, health, and economic costs of chronic disease dwarf the costs of all infectious diseases in the United States. By this decade’s end, obesity, diabetes, and pre-diabetes are on track to debilitate 85 percent of America’s citizens. America is among the ten most over-weight countries on Earth. The health impacts of these epidemics—which fall mainly on the young—eclipse even the most exaggerated health impacts of COVID-19.
Dr. Fauci has done nothing to advance NIAID’s core obligation of researching the causes of chronic allergic and autoimmune diseases that have mushroomed under his tenure. Instead, Fauci has “reshaped NIAID into the leading incubator for new pharmaceutical products, many of which, ironically, profit from the cascading chronic disease pandemic.” Instead of researching the causes of Americans’ failing health, Dr. Fauci funnels the bulk of his $6 billion budget to the research and development of new drugs and vaccines that are largely responsible for weakening our natural immunity. “Of late, he has played a central role in undermining public health and subverting democracy and constitutional governance around the globe and in transitioning our civil governance toward medical totalitarianism.”
I was reminded of Dr. Knock, the central character of Jules Romains’s famous novel Knock or the Triumph of Medicine, written in 1923. Dr. Knock is a shady medical doctor of dubious competence who professes that “health” is an obsolete and unscientific concept, and that all men are sick and need to be informed about it by their doctor. To advance his plan of converting a whole town into permanent patients, he enlists the help of the school teacher and of the pharmacist, who suddenly sees his clientele booming (watch unforgettable moments of Guy Lefranc’s 1951 film adaptation with Louis Jouvet here and here).
Louis Jouvet as Dr. Knock in 1951
To some extent, however, Fauci is himself the product of a civilizational orientation that could only, in the long run, lead to the tyrannical medical technocracy that is now trying to enslave us. Rather than a new Dr. Frankenstein, Fauci is our own monster coming back after us. Kennedy hints at this vast aspect of the question, pointing to the need for deep questioning. The way Americans and Westerners in general have come to view health care has been shaped by the philosophy of the Rockefeller Foundation: “a pill for an ill.” In the debate between the “miasma theory”—that emphasizes preventing disease by fortifying the immune system through nutrition and by reducing exposures to environmental toxins and stresses—versus the “germ theory”—which blames disease on microscopic pathogens—we have unambiguously opted for the latter. We have signed up for an approach to disease that requires to identify the culpable germ and tailor a poison to kill it. The choice was not forced upon us. We have surrendered responsibility for our health to medical experts and insurance brokers.
As Dr. Claus Köhnlein and Torsten Engelbrecht observe in their book Virus Mania (2007) quoted by Kennedy: “The idea that certain microbes—above all fungi, bacteria, and viruses—are our great opponents in battle, causing certain diseases that must be fought with special chemical bombs, has buried itself deep into the collective conscience.” It is a warlike paradigm, perfectly suited for manufacturing consent on the way to dictatorship. As Kennedy wrote in his preface to Dr. Joseph Mercola and Ronni Cummins, The Truth About Covid-19 (2021), “demagogues must weaponize fear to justify their demands for blind obedience.”
Government technocrats, billionaire oligarchs, Big Pharma, Big Data, Big Media, the high-finance robber barons, and the military industrial intelligence apparatus love pandemics for the same reasons they love wars and terrorist attacks. Catastrophic crises create opportunities of convenience to increase both power and wealth.
Laurent Guyénot, PhD, is the author of The Unspoken Kennedy Truth and of a film on the same subject.
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Is America behind the massive surge in Kiev regime’s child trafficking?
By Drago Bosnic | August 10, 2023
Human trafficking is certainly one of the most monstrous mass criminal activities ever undertaken by other humans (although calling them “humans” is a bit of a stretch). And yet, there’s a special kind of this deeply repulsive crime that pushes it to diabolical proportions – child trafficking. Underage kids, particularly those who were abandoned, sold or have very poor/abusive family backgrounds, are by far the most vulnerable group. The depraved criminals who engage in such illicit activities specifically target unfortunate children and given there are millions of them all around the globe, particularly in war-torn areas, the “recruitment pool” is effectively endless. Unfortunately, the demand on the black market also seems to be constant and growing, making it a very lucrative and appealing prospect for criminals.
Children are usually forced into literal slavery that includes forced labor, sexual exploitation or prostitution, drug smuggling, forced begging, organ harvesting, etc. Many terrorist groups and narco-traffickers even use them as child soldiers, forcing them into dangerous firefights with rival groups or even official security forces such as the police and/or military. Although estimates vary significantly, as the exact data is incomplete at best, expectedly, the world’s most populous countries have the highest number of child trafficking victims. And yet, it seems the United States is the most profitable market for such criminal activities. Back in 2018, Tim Swarens of USA Today calculated that adults purchase children for sex at least 2.5 million times a year in the US alone. Worse yet, this is only based on available data. … continue
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