We are pleased to republish the following article by our friend Meryl Nass, M.D., a member of Children’s Health Defense (CHD) Science Advisory Board. CHD is an official WCH coalition partner.
This is part one of an in-depth article by Meryl Nass. Stay tuned for part two! Tune in to Better Way Live on Monday to hear from Meryl on these important topics and more.
This report is designed to help readers think about some big topics: how to really prevent pandemics and biological warfare, how to assess proposals by the WHO and its members for preventing and responding to pandemics, and whether we can rely on our health officials to navigate these areas in ways that make sense and will help their populations. We start with a history of biological arms control and rapidly move to the COVID pandemic, eventually arriving at plans to protect the future.
Traditionally, the Weapons of Mass Destruction (WMD) have been labelled Chemical, Biological, Radiologic, and Nuclear (CBRN).
The people of the world don’t want them used on us—for they are cheap ways to kill and maim large numbers of people quickly. And so international treaties were created to try to prevent their development (only in the later treaties) and use (in all the biological arms control treaties). First was the Geneva Protocol of 1925, following the use of poison gases and limited biological weapons in World War I, banning the use of biological and chemical weapons in war. The US and many nations signed it, but it took 50 years for the US to ratify it, and during those 50 years the US asserted it was not bound by the treaty.
The US used both biological and chemical weapons during those 50 years. The US almost certainly used biological weapons in the Korean War (see this, this, this and this) and perhaps used both in Vietnam, which experienced an odd outbreak of plague during the war. The use of napalm, white phosphorus, agent orange (with its dioxin excipient causing massive numbers of birth defects and other tragedies) and probably other chemical weapons like BZ (a hallucinogen/incapacitant) led to much pushback, especially since we had signed the Geneva Protocol and we were supposed to be a civilized nation.
In 1968 and 1969, two important books were published that had a great influence on the American psyche regarding our massive stockpiling and use of these agents. The first book, written by a young Seymour Hersh about the US chemical and biological warfare program, was titled Chemical and Biological Warfare; America’s Hidden Arsenal. In 1969 Congressman Richard D. McCarthy, a former newspaperman from Buffalo, NY wrote the book The Ultimate Folly: War by Pestilence, Asphyxiation and Defoliation about the US production and use of chemical and biological weapons. Prof. Matthew Meselson’s review of the book noted,
Our operation, “Flying Ranch Hand,” has sprayed anti-plant chemicals over an area almost the size of the state of Massachusetts, over 10 per cent of its cropland. “Ranch Hand” no longer has much to do with the official justification of preventing ambush. Rather, it has become a kind of environmental warfare, devastating vast tracts of forest in order to facilitate our aerial reconnaissance. Our use of “super tear gas” (it is also a powerful lung irritant) has escalated from the originally announced purpose of saving lives in “riot control-like situations” to the full-scale combat use of gas artillery shells, gas rockets and gas bombs to enhance the killing power of conventional high explosive and flame weapons. Fourteen million pounds have been used thus far, enough to cover all of Vietnam with a field effective concentration. Many nations, including some of our own allies have expressed the opinion that this kind of gas warfare violates the Geneva Protocol, a view shared by McCarthy.
Amid great pushback over US conduct in Vietnam, and seeking to burnish his presidency, President Nixon announced to the world in November 1969 that the US was going to end its biowarfare program (but not the chemical program). Following pointed reminders that Nixon had not eschewed the use of toxins, in February 1970 Nixon announced we would also get rid of our toxin weapons also, which included snake, snail, frog, fish, bacterial, and fungal toxins that could be used for assassinations and other purposes.
It has been claimed that these declarations resulted from careful calculations that the US was far ahead technically of most other nations in its chemical and nuclear weapons. But biological weapons were considered the “poor man’s atomic bomb” and required much less sophistication to produce. Therefore, the US was not far ahead in the biological weapons arena. By banning this class of weapon, the US would gain strategically.
Nixon told the world that the US would initiate an international treaty to prevent the use of these weapons ever again. And we did so: the 1972 Convention on the Prohibition of the Development, Production and Stockpiling of Bacteriological (Biological) and Toxin Weapons and on their Destruction, or Biological Weapons Convention (BWC) for short, which entered into force in 1975.
But in 1973 genetic engineering (recombinant DNA) was discovered by Americans Herbert Boyer and Stanley Cohen, which changed the biological warfare calculus. Now the US had regained a technological advantage for this type of endeavor.
The Biological Weapons Convention established conferences to be held every 5 years to strengthen the treaty. The expectation was that these would add a method to call for ‘challenge inspections’ to prevent nations from cheating and would add sanctions (punishments) if nations failed to comply with the treaty. However, since 1991 the US has consistently blocked the addition of protocols that would have an impact on cheating. By now, everyone accepts that cheating occurs and is likely widespread.
A leak in an anthrax production facility in Sverdlovsk, USSR in 1979 caused the deaths of about 60 people. While the USSR tried a sloppy cover-up, blaming contaminated black market meat, this was a clear BWC violation to all those knowledgeable about anthrax.
US experiments with anthrax production during the Clinton administration, detailed by Judith Miller et al. in the 2001 book Germs, were also thought by experts to have transgressed the BWC.
It has taken over 40 years, but in 2022 all declared stocks of chemical weapons had been destroyed by the USA, by Russia, and the other 193 member nation signatories. The chemical weapons convention does include provisions for surprise inspections and sanctions.
It is now 2023, and during the 48 years the Biological Weapons Convention has been in force the wall it was supposed to build against the development, production, and use of biological weapons has been steadily eroded. Meanwhile, especially since the 2001 anthrax letters, nations (with the US at the forefront) have been building up their “biodefense” and “pandemic preparedness” capacities.
Under the guise of preparing their defenses against biowarfare and pandemics, nations have conducted “dual-use” (both offensive and defensive) research and development, which has led to the creation of more deadly and more transmissible microorganisms. And employing new verbiage to shield this effort from scrutiny, biological warfare research was renamed as “gain-of-function” research.
Gain-of-function is a euphemism for biological warfare research aka germ warfare research. It is so risky that funding it was banned by the US government (but only for SARS coronaviruses and avian flu viruses) in 2014 after a public outcry from hundreds of scientists. Then in 2017 Drs. Tony Fauci and Francis Collins lifted the moratorium, with no real safeguards in place. Fauci and Collins even had the temerity to publish their opinion that the risk from this gain-of-function research was ‘worth it.’
What does gain-of-function actually mean? It means that scientists are able to use a variety of techniques to turn ordinary or pathogenic viruses and bacteria into biological weapons. The research is justified by the claim that scientists can get out ahead of nature and predict what might be a future pandemic threat, or what another nation might use as a bioweapon. The functions gained by the viruses or other microorganisms to turn them into biological warfare agents consist of two categories: enhanced transmission or enhanced pathogenicity (illness severity).
1) improved transmissibility may result from:
a) needing fewer viral or bacterial copies to cause infection,
b) causing the generation of higher viral or bacterial titers,
c) a new mode of spread, such as adding airborne transmission to a virus that previously only spread through bodily fluids,
d) expanded range of susceptible organs (aka tissue tropism); for example, not only respiratory secretions but also urine or stool might transmit the virus, which was found in SARS-CoV-2,
e) expanded host range; for example, instead of infecting bats, the virus is passaged through humanized mice and thus acclimated to the human ACE-2 receptor, which was found in SARS-CoV-2,
f) improved cellular entry; for example, by adding a furin cleavage site, which was found in SARS-CoV-2,
2) increased pathogenicity, so instead of causing a milder illness, the pathogen would be made to cause severe illness or death, using various methods. SARS-CoV-2 had unusual homologies (identical short segments) to human tissues and the HIV virus, which may have caused or contributed to the late autoimmune stage of illness, impaired immune response and ‘long COVID.’
Perhaps the comingling of funding was designed to make it harder for Congress and the public to understand what was being funded, and how much taxpayer funding was going to gain-of-function work, which might lead them to question why it was being done at all, given its prohibition in the Biological Weapons Convention, and additional questions about its value. Former CDC Director Robert Redfield, a physician and virologist, told Congress in March of 2023 that gain-of-function research had not resulted in a single beneficial drug, vaccine, or therapeutic to his knowledge.
Nonprofits and universities like EcoHealth Alliance and its affiliated University of California, Davis veterinary school were used as intermediaries to obscure the fact that US taxpayers were supporting scientists in dozens of foreign countries, including China, for research that included gain-of-function work on coronaviruses.
Perhaps to keep the lucrative funding going, fears about pandemics have been deliberately amplified over the past several decades. The federal government has been spending huge sums on pandemic preparedness over the past 20 years, routing it through many federal and state agencies. President Biden’s proposed 2024 budget requested “$20 billion in mandatory funding across DHHS for pandemic preparedness” while the DHS, DOD, and the State Department have additional budgets for pandemic preparedness for both domestic and international spending.
Although the 20th century experienced only 3 significant pandemics (the Spanish flu of 1918-19 and 2 influenza pandemics in 1957 and 1968) the mass media have presented us with almost non-stop pandemics during the 21st century: SARS-1 (2002-3), avian flu (2004-on), swine flu (2009-10), Ebola (2014, 2018-19), Zika (2016), COVID (2020-2023), and monkeypox (2022-23). And we are incessantly told that more are coming, and that they are likely to be worse.
We have been assaulted with warnings and threats for over 2 decades to induce a deep fear of infectious diseases. It seems to have worked.
The genomes of both SARS-CoV-2 and the 2022 monkeypox (MPOX) virus lead to suspicion that both were bioengineered pathogens originating in laboratories. The group of virologists assembled by Drs. Fauci and Farrar identified 6 unusual (probably lab-derived) parts of the SARS-CoV-2 genome as early as February 1, 2020 and more have been suggested subsequently.
I do not know if these viruses leaked accidentally or were deliberately released, but I am leaning toward the conclusion that both were deliberately released, based on the locations where they first appeared, the well-orchestrated but faked videos rolled out by the mass media for COVID, and the illogical and harmful official responses to each. In neither case was the public given accurate information about the infections’ severity or treatments, and the responses by Western governments never made scientific sense. Why wouldn’t you treat cases early, the way doctors treat everything else? It seemed that our governments were trading on the fact that few people knew enough about viruses and therapeutics to make independent assessments about the information they were being fed.
Yet by August 2021, there was no corresponding course correction. Instead, the federal government doubled down, imposing vaccine mandates on 100 million Americans in September 2021 in spite of ‘the science.’ There has been no accurate statement yet from any federal agency about the lack of utility of masking for an airborne virus (which is probably why the US government and WHO delayed acknowledging airborne spread by COVID for 18 months), the lack of efficacy of social distancing for an airborne virus, and the risks and poor efficacy of 2 dangerous oral drugs (paxlovid and molnupiravir) purchased by the US government for COVID treatment, even without a doctor’s prescription.
Never have any federal agencies acknowledged the truth about the COVID vaccines’ safety and efficacy. Instead, the CDC turns definitional and statistical cartwheels so it can continue to claim they are “safe and effective.” Even worse, with all that we know, a third generation COVID vaccine is to be rolled out for this fall and the FDA has announced that yearly boosters are planned.
All this goes on, even a year after we learned (with continuing corroborations) that children and working age adults are dying at rates 25 percent or more above the expected averages, and the vascular side effects of vaccination are the only reasonable explanation.
Both of the two US monkeypox/smallpox vaccines (Jynneos and ACAM2000) are known to cause myocarditis, as do all 3 COVID vaccines currently available in the US: the Pfizer and Moderna COVID-19 mRNA vaccines and the Novavax vaccine. The Novavax vaccine was first associated with myocarditis during its clinical trial, but this was downplayed and it was authorized and rolled out anyway, intended for those who refused the mRNA vaccines due to the use of fetal tissue in their manufacture.
Here is what the FDA’s reviewers wrote about the cardiac side effects noted in the Jynneos clinical trials:
Up to 18.4% of subjects in 2 studies developed post-vaccination elevation of troponin [a cardiac muscle enzyme signifying cardiac damage]. However, all of these troponin elevations were asymptomatic and without a clinically associated event or other sign of myopericarditis. p. 198
The applicant has committed to conduct an observational, post-marketing study as part of their routine PVP. The sponsor will collect data on cardiac events that occur and are assessed as a routine part of medical care. p. 200
In other words, while the only way to cause an elevated troponin level is to break down cardiac muscle cells, the FDA did not require a specific study to evaluate the extent of cardiac damage that might be caused by Jynneos when it issued its 2019 license. How frequently does myocarditis occur after these vaccines? If you use elevated cardiac enzymes as your marker, ACAM2000 caused this in one in thirty people receiving it for the first time. If you use other measures like abnormal cardiac MRI or echo, according to the CDC it occurs in one in 175 vaccinees. I have not seen a study with rates of myocarditis for Jynneos, but there was an unspecified elevation of cardiac enzymes in 10 percent and 18 percent of Jynneos recipients in two unpublished prelicensure studies available on the FDA website. My guess for the mRNA COVID vaccines is that they cause myocarditis in this general range, the vast majority of which remain undiagnosed and probably asymptomatic.
Why would our governments push 5 separate vaccines all known to cause myocarditis on young males who have been at extremely low risk from COVID, and who simply get a few pimples for 1-4 weeks from monkeypox unless they are immunocompromised? It’s an important question. It does not make medical sense. Especially when the vaccine probably does not work—Jynneos didn’t prevent infection in the monkeys in whom it was tested nor did it do well in people. And the CDC has failed to publish its trial of Jynneos vaccine in the ~1,600 Congolese healthcare workers on whom the CDC tested it for efficacy and safety in 2017. The CDC made the mistake of announcing the trial, and posting it to clinicaltrials.gov as required, but has not informed its advisory committee that reviewed the vaccine, nor the public, of the trial’s results.
There can be no question about it: our health agencies are guilty of malfeasance, misrepresentation, and deliberate infliction of harm on their own populations. The health agencies first incited terror with apocalyptic predictions, then demanded patients be medically neglected, and finally enforced vaccinations and treatments that were tantamount to malpractice.
The health authorities could have just been ignorant—that could possibly explain the first few months of the COVID vaccines’ rollout. But once they figured out, and even announced in August 2021 that the vaccines did not prevent catching COVID or transmitting it, why did our health authorities still push COVID vaccines on low-risk populations who were clearly at greater risk from a vaccine side effect than from COVID? Particularly as time went on and newer variants were less and less virulent?
Once you acknowledge these basic facts, you realize that maybe the vaccines were not made for the pandemic, and instead the pandemic was made to roll out the vaccines. While we cannot be certain, we should at least be suspicious. And the fact that the US contracted for 10 doses per person (review purchases here, here, here, here and here) and so did the European Union (here and here) and Canada should make us even more suspicious–there is no justification for agreeing to purchase so many doses for vaccines at a time when the vaccines’ ability to prevent infection and transmission was questionable, and its safety suspect or worrying.
Why would governments want ten doses per person? Three maybe. But ten? Even if yearly boosters were expected, there was no reason to sign contracts for enough vaccine for the next nine years for a rapidly mutating virus. Australia bought 8 doses per person. By December 20, 2020 New Zealand had secured triple the vaccines it needed, and offered to share some with nearby nations. No one has come forward to explain the reason for these excessive purchases.
Furthermore, you don’t need a vaccine passport (aka digital ID, aka a phone app that in Europe included a mechanism for an electronic payments system) unless you are giving out regular boosters.Were the vaccines conceived of as the means for putting our vaccinations, health records, official documents–and most importantly, shifting our financial transactions online, all managed on a phone app? This would be an attack on privacy as well as the enabling step to a social credit system in the West. Interestingly, vaccine passports were already being planned for the European Union by 2018.
The same US and other governments and the WHO that imposed draconian measures on citizens to force us to be vaccinated; take dangerous, expensive, experimental drugs; withheld effective treatments; and refused to tell us that most people who required ICU care for COVID were vitamin D-deficient; and never said that taking vitamin D would lessen COVID’s severity–decided in 2021 we suddenly needed an international pandemic treaty. Why? To prevent and ameliorate future pandemics or biological warfare events… so we would not suffer again as we did with the COVID pandemic, they insisted. The WHO would manage it.
To paraphrase Ronald Reagan, the words, “I’m from the WHO, and I’m here to help” should be the most terrifying words in the English language, after what we learned from the COVID fiasco.
How can anyone take seriously claims by the same officials who mishandled COVID that they want to spare us from another medical and economic disaster–by employing the same strategies they applied to COVID, after they masterminded the last disaster? And the fact that no governments or health officials have admitted their errors should convince us never to let them manage anything for us ever again. Why would we let them draw up an international treaty and new amendments to the existing International Health Regulations (IHR) that will bind our governments to obey the WHO’s dictates forever?
Fauci, Tedros, and their ilk at the WHO, and those managing biodefense and biomedical research for nation states are on one side, the side that gains access to ever more potential biological weapons, and the rest of us are on the other, at their mercy.
Amy Offutt
Edward B. Breitschwerdt
Madison Area Lyme Support Group 