New evidence FDA, CDC hid early data on myocarditis spurs questions of 'criminal coverup'
New evidence FDA, CDC hid early data on myocarditis spurs questions of 'criminal coverup'
Michael Nevradakis, Ph.D.
The Defender
Tue, 23 May 2023 06:39 UTC
New evidence suggests the Centers for Disease Control and Prevention and U.S. Food and Drug Administration may have violated the Public Readiness and Emergency Preparedness Act when they withheld knowledge about myocarditis safety signals from the public and from COVID-19 vaccine fact sheets.
New evidence suggesting public health officials knew early in 2021 that COVID-19 vaccines posed a heightened risk of myocarditis in young men — but withheld that information from the public — raises questions about whether federal health agencies violated any laws.
According to Dr. Meryl Nass, the U.S. Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC) knew about the myocarditis safety signal in February 2021, but "hid it until they got the vaccine authorized for 12-15-year-olds in May 2021," and then "kept pushing" the vaccine on the highest-risk groups."
Nass said the new evidence suggests the CDC and FDA may have violated the Public Readiness and Emergency Preparedness Act (PREP Act) when they withheld knowledge about myocarditis safety signals from the public and from fact sheets included with the COVID-19 vaccines.
The new evidence includes warnings the FDA received from multiple sources, including the Israeli Ministry of Health at least as early as February 2021.
Nass, an internist, biological warfare epidemiologist and member of the Children's Health Defense (CHD) scientific advisory committee, this week discussed the new revelations in two Substack posts and on CHD.TV.
In an interview with The Defender, Nass said the newly discovered revelations "provide clear evidence that the agencies knew of the connection and kept it under wraps, and did not inform their advisory committees till after the vaccine was approved for the teens."
Kim Mack Rosenberg, acting outside general counsel for CHD, told The Defender:
"As more and more information becomes publicly available, it becomes ever clearer that claims that EUA [Emergency Use Authorization] vaccines were safe and effective ring hollow, at best.
"While the PREP Act purposefully creates challenges to suing the parties responsible for this debacle, Children's Health Defense continues to pursue possible ways to seek justice for those injured and betrayed."
Brian Hooker, Ph.D., P.E., chief scientific officer for CHD and co-author of the October 2022 study that first revealed the CDC's and FDA's knowledge of the myocarditis safety signal in February 2021, said the new revelations suggest the actions of the two agencies were "criminal."
Hooker told The Defender:
"The paper I published with Dr. Karl Jablonowski makes it clear that the CDC knew about the myocarditis signal at least as early as Feb. 19, 2021 — when the signal became significant on VAERS [Vaccine Adverse Event Reporting System]. This is when the vaccination rate in the U.S. was about 8%.
"Despite mounting evidence from multiple sources that this was a huge problem, the CDC chose to hide this signal until they finally, quietly posted a new website suggesting there might be a myocarditis signal on May 27, 2021. At that point, the vaccination rate had risen to about 50%.
"CDC let 42% of the U.S. population get vaccinated, knowing full well that mRNA vaccines were causing myocarditis, which is criminal."
Cardiologist Dr. Peter McCullough, an outspoken critic of COVID-19 vaccines, characterized the delayed acknowledgment of myocarditis safety signals by the CDC and FDA as "astounding" and referenced the growing numbers of athletes affected by the condition after their vaccination.
McCullough told The Defender:
"What is even more astounding is that professional sports leagues — for example, the National Football League — mandated (starting August 2021) the heart-damaging COVID-19 vaccines after the CDC/FDA warning in June 2021.
"The cardiology position papers before COVID-19 clearly warned that exercise during active myocarditis is strictly prohibited because it can trigger a cardiac arrest. Once the vaccines were mandated, none of the teams took adequate safety measures for the players."
By April 23, 2021, VAERS data showed the discerned level of myocarditis in young men following COVID-19 vaccination had increased to an extreme statistical level, indicating a very low likelihood that the connection between the level of myocarditis cases in this population and COVID-19 vaccination was attributable to chance.
Despite this safety signal, the FDA on May 10, 2021, expanded the EUA of the Pfizer-BioNTech COVID-19 vaccine for use in people as young as 12 years old, and the CDC's Advisory Committee on Immunization Practices (ACIP) voted to recommend that all persons 12 or older get the vaccine.
According to researchers at the National Organization for Rare Disorders, myocarditis can result from infections or may result directly from a toxic effect such as a toxin or a virus. "More commonly the myocarditis is a result of the body's immune reaction to the initial heart damage."
Severe myocarditis can permanently damage the heart muscle, possibly causing heart failure.
Contractor alerted FDA, CDC to safety signal in February 2021
In the first of her two Substack posts, Nass wrote, "I was told that the VAERS contractor for CDC and FDA (Oracle had the contract) told the agencies there was a myocarditis adverse event signal in February 2021. This was 2 months after the Pfizer and Moderna vaccines were authorized."
Nass referenced previous revelations by Dr. Robert Malone. Speaking at the Global COVID Summit on May 11, 2022, Malone said he had been "very actively engaged" with senior FDA personnel and William DuMouchel, Ph.D., chief statistical scientist for Oracle Health Sciences, when the COVID-19 vaccines were rolled out.
"We were talking by Zoom on a weekly or twice a week basis," Malone said. "This is the group that first discovered the signal of the cardiotoxicity" and "absolutely did know" of such adverse events — "and did not acknowledge it."
Nass also referred to a June 23, 2021, ACIP meeting, where during a presentation on myocarditis and pericarditis, the presenter acknowledged that in over 80% of instances, myocarditis appeared within four days of the second COVID-19 vaccine dose.
And she shared a letter that came into her possession, sent by the Israeli Ministry of Health to the European Medicines Agency on Feb. 28, 2021, "investigating a safety signal of myocarditis/peri-myocarditis in younger population (16-30 years old) following administration of Pfizer COVID-19 vaccine."
Data provided by the CDC in February following a Freedom of Information Act request by CHD showed that on Feb. 28, 2021, the Israeli Ministry of Health also contacted the CDC with a similar request.
"We are seeing a large number of myocarditis and pericarditis cases in young individuals soon after Pfizer COVID-19 vaccine," the letter stated. "We would like to discuss the issue with a relevant expert at CDC."
According to the letter, Israeli health officials had received reports of approximately 40 such cases of myocarditis and/or pericarditis.
"Israeli media were all over the story" by April 2021, Nass said, with estimates reported at the time that "young men had a 25 times elevated risk of myocarditis after the shots." But despite some coverage in international media, such as Reuters, "somehow the story never got legs" in the U.S.
But according to Nass, "The CDC and FDA ... managed to keep the story under wraps, denying any vaccine problems at an advisory committee meeting." This continued until the FDA's May 10, 2021, granting of EUA for the Pfizer-BioNTech COVID-19 vaccine for adolescents.
It took an additional six weeks for public health agencies to acknowledge the myocarditis safety signal.
"Having then pushed COVID vaccine clinics for kids in a major way, the agencies finally admitted there was a danger signal about 6 weeks later, on June 23, 2021, at the ACIP meeting," where "stunning" data were revealed, according to Nass.
CDC data full of discrepancies
In her analysis of the June 23, 2021 ACIP meeting, Nass referenced a presentation by the CDC's Dr. Tom Shimabukuro, showing that as of June 11, 2021, over two million males between the ages of 12 and 17 had received two doses of an mRNA COVID-19 vaccine, with 128 "observed" cases of myocarditis identified in this population.
According to Nass, the reason such a relatively low number of myocarditis cases was observed at this time in this population was that COVID-19 vaccines had been authorized for 12-15-year-olds for only 32 days before the data cutoff — and in those 32 days, adolescents would have had to receive both doses, develop myocarditis symptoms and have filed, or had someone file on their behalf, a VAERS report.
"It is curious that CDC did not separate the 12-15-year-olds from the 16-17-year-olds who were authorized to receive the vaccine six months earlier (on December 11, 2020 for the Pfizer shot)," Nass said.
She also referenced a separate June 10, 2021, talk by Shimabukuro to the FDA's vaccine advisory committee (VRBPAC), where preliminary safety data — including myocarditis cases recorded through May 31, 2021 — from VAERS, V-Safe and VSD (Vaccine Safety Datalink) were discussed.
Nass observed a discrepancy in the data, writing:
"The data were collected through May 31, 2021. There were only two [myocarditis] cases in 12-15-year-olds because there was not enough time for that age group to get their second shot: it was authorized for them on May 10, and they had to wait three weeks for the second dose. Three weeks later was May 31, the data cut-off.
"So, there should have been no myocarditis reports from the 12-15 year age group, because not enough time had elapsed for them to legally receive a second dose. Yet his chart claims 134,000 second doses had been administered by May 31."
Nevertheless, "people under age 25 comprised only 8.8% of the second doses received, but were 52.5% of the myocarditis cases reported," Nass said, adding that this age group was six times more likely to be diagnosed with myocarditis than the overall population.
Nass also observed that out of 12 million people who were enrolled in the VSD database, one-third of vaccinated 16-17-year-olds did not return to receive a second dose of the COVID-19 vaccine.
"Presumably most had a troublesome adverse reaction," Nass wrote.
Another potential discrepancy from the data presented at the June 10, 2021, meeting pertained to adverse events reported within 21 days of either dose of the Pfizer-BioNTech or Moderna mRNA COVID-19 vaccines.
According to Nass, the data presented indicated that all of the "prespecified outcome events" — as the adverse events were referred to — were "unassociated statistically with COVID vaccines."
"Not even one of the adverse events the CDC thought were most likely associated with COVID vaccines had generated a safety signal by May 29, 2021 in the VSD. Or so the CDC claimed," Nass said.
Nass suggested that such an outcome was not possible. According to Nass, the data presented at the meeting indicated that "people given other vaccines were more likely to get myocarditis than those who got a COVID vaccine."
However, Nass noted that "the only other vaccines that commonly cause myocarditis are smallpox and monkeypox, and neither was being given to civilians at the time."
Another possible discrepancy from the June 10, 2021, meeting pertained to statistics presented that showed "only 22 cases of diagnosed myocarditis in 16-39 year old enrollees in the VSD. Eighteen occurred after the second dose. Fourteen were in those who received Moderna."
According to Nass, this data was "strange," because "Even though 11 episodes of myocarditis occurred after the second Moderna dose, there is a claim that the adjusted rate ratio (ARR) is 'non-estimable.' Yet Dr. Shimabukuro estimated the ARR for Pfizer's first dose when there was only one myocarditis case."
"I think they did not want us to see the ARR for myocarditis associated with Moderna's second dose, because it would have been sky-high," Nass wrote, noting that studies have shown that "the Moderna vaccine is much more strongly associated with myocarditis than the Pfizer vaccine."
Nass also noted that the Department of Health and Human Services (HHS), the parent agency of both the CDC and the FDA, holds patents in Moderna's COVID-19 vaccine.
Even with such potential discrepancies in the data, Nass wrote that the information presented at the June 10, 2021, VRBPAC meeting made it "clear that even by May 29, the second dose caused over five times as many myocarditis cases as the first dose. For both brands," adding that "This cannot be a random event."
In Hooker and Jablonowski's October 2022 study, VAERS data was referenced, which showed 24,371 reports of myocarditis and pericarditis between Dec. 14, 2020, and Oct. 14, 2022. Of these, 1,333 reports occurred among 12- to 17-year-olds.
This was despite the fact that the CDC uses a narrowed case definition of "myocarditis" that excludes cases of cardiac arrest, ischemic strokes and deaths due to heart problems that occur before one has the chance to go to the emergency department.
VAERS has historically been shown to report only 1% of actual vaccine adverse events.
'I would call it a criminal coverup'
According to Nass, "the CDC worked to cover its derriere regarding the myocarditis 'signal' — I would call it a criminal coverup — regarding the data it was sitting on, and other data it was misrepresenting."
According to Nass, potential negligence on the part of federal public health agencies also extends to the fact sheets that are included with the COVID-19 vaccines.
"The fact sheets that substitute for informed consent, and are required to be given to all vaccine recipients, should have been updated with this warning immediately, according to the PREP Act. It requires that significant known risks be disclosed. I'd call heart damage and the risk of sudden death significant," Nass wrote.
This was despite what the FDA described in the June 10, 2021, presentation as "the most intensive vaccine safety monitoring in U.S. history."
For Nass, this delay in reporting the myocarditis safety signals may potentially be legally actionable, as "Willful misconduct is clearly demonstrated."
"I think an adolescent who received the Pfizer or Moderna COVID vaccine in May or before June 23, 2021, and developed myocarditis would have a very interesting lawsuit," Nass said, adding:
"The PREP Act requires that in lieu of informed consent, recipients must be given a fact sheet and it must disclose all significant risks. It did not, until months after myocarditis was known to be a risk. The risks were not told to the advisory committees either, in a timely way.
"The numbers appear to have been played with, or the method of assessing risk. With discovery, we will get even more information on how the statistics were fudged."
However, challenging the PREP Act is a difficult proposition, said Nass:
"To bring a PREP Act lawsuit, you need to show willful misconduct and get the Secretary [of HHS] to okay a lawsuit. This is a bar to litigation higher than anything else in U.S. law.
"I was hopeful that with this level of evidence, the misconduct is blatant enough that the Secretary would be drawn in to say okay or refuse — and publicity could be obtained about that refusal."
Other legal experts who spoke to The Defender agreed and also noted that fact sheet requirements have frequently not been honored, with many COVID-19 vaccine recipients not having been provided the information at the time of vaccination.
As early as October 2021, Sweden's Public Health Agency paused Moderna's COVID-19 vaccine for people born 1991 and later, "as data pointed to an increase of myocarditis and pericarditis among youths and young adults that had been vaccinated," according to Reuters.
At around the same time, Finland's public health authorities also paused the vaccine in young people.
And in November 2022, Sweden paused the Novavax COVID-19 vaccine for those under 30, due to an increased risk of myocarditis and pericarditis.
Novavax received EUA from the FDA despite "Multiple events of myocarditis/pericarditis" recorded during clinical trials.
Michael Nevradakis, Ph.D.
Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV's "Good Morning CHD."
The WHO Will Have Authority to Mandate Vaccines Globally
Story at-a-glance
The 2005 International Health Regulations (IHR) is the instrument that empowers the World Health Organization to declare a Public Health Emergency of International Concern (PHEIC)
Hundreds of amendments to the IHR are being proposed, and these amendments will empower the WHO to become the de facto governing body of all member states, including the U.S.
As currently written, the IHR amendments will be legally binding and will supersede local and national laws. They even include enforcement tools to ensure that member nations comply with the WHO’s edicts
Areas of life that are being added in under the umbrella of “health” include climate, food production and even poverty, so the WHO will be able to claim sole global authority over anything to do with those issues as well
Importantly, the IHR amendments will abolish bodily autonomy and personal choice and replace these God-given rights and freedoms with one-size-fits-all medicine
In the video above, John Campbell, Ph.D., a retired nurse educator, reviews the proposed amendments to the 2005 International Health Regulations (IHR), which is the instrument that empowers the World Health Organization to declare a Public Health Emergency of International Concern (PHEIC).
If these amendments go through, however, the WHO will be empowered to do a whole lot more than that. It will become the de facto governing body of all member states, including the U.S.
Now, according to so-called “fact checkers,” the WHO will have no authority to dictate U.S. health policy under the amended IHR or the proposed pandemic treaty, nor will nations be stripped of their sovereignty.1 But they’re completely wrong. The only reason they’re denying these truths is because they don’t want the public to pressure government to reject these proposals, as they should.
As noted by Campbell and others, including bioweapons expert Francis Boyle, Ph.D., and researcher James Roguski,2 the pandemic treaty and the IHR amendments are obviously written by experts in both national and international law and appear “airtight.”
There’s simply no doubt that, as currently written, these instruments will be legally binding and will supersede local and national laws. They even include enforcement tools to ensure that member nations comply with the WHO’s edicts.
Another false propaganda angle is that these instruments only apply to infectious disease pandemics, but that isn’t true either. Areas of life that are being added in under the umbrella of “health” include climate, food production and even poverty, so the WHO will be able to claim sole global authority over anything to do with those issues as well.
In his video, Campbell goes through several of the proposed IHR amendments, and how they will impact national sovereignty and public health decisions. The article-by-article compilation of the proposed amendments3 can be found here.
Strikethroughs in the text indicate that the text is to be deleted, and the additions or revisions are underlined in bold. The following are some of the most disconcerting amendments, copied with the deletions and insertions of text showing.
New IHR Will Be Binding and Can Apply to Anything
Article 1 Definitions — “‘standing recommendation’ means
non-bindingadvice issued by WHO for specific ongoing public health risks pursuant to Article 16 regarding appropriate health measures for routine or periodic application needed to prevent or reduce the international spread of disease and minimize interference with international traffic;‘temporary recommendation’ means
non-bindingadvice issued by WHO pursuant to Article 15 for application on a time-limited, risk-specific basis, in response to a public health emergency of international concern, so as to prevent or reduce the international spread of disease and minimize interference with international traffic.”
Since the word “non-binding” is removed, this means that any recommendation from the WHO will be binding and member states will be required to follow the WHO’s recommendations.
Article 2 Scope and Purpose — “The purpose and scope of these Regulations are to prevent, protect against, prepare, control and provide a public health response to the international spread of diseases including through health systems readiness and resilience in ways that are commensurate with and restricted to
public health riskall risks with a potential to impact public health, and which avoid unnecessary interference with international traffic
andtrade, livelihoods, human rights, and equitable access to health products and health care technologies and know how.”
This really opens the door for the WHO to take over for just about any reason. It doesn’t even have to be a real public health threat. It could be a potential, unproven or suspected threat.
Human Dignity, Rights and Freedoms Will Not Be Factored In
Article 3 Principles — “The implementation of these Regulations shall be
with full respect for the dignity, human rights and fundamental freedoms of personsbased on the principles of equity, inclusivity, coherence and in accordance with their common but differentiated responsibilities of the States Parties, taking into consideration their social and economic development.”
In other words, bodily autonomy and personal choice are being replaced by one-size-fits-all medicine that has no regard for human dignity, human rights or fundamental freedoms. The right to so much as an opinion will also be removed on the national level.
Article 10 Verification — “If the State Party does not accept the offer of collaboration within 48 hours , WHO
mayshall , when justified by the magnitude of the public health risk, immediately share with other States Parties the information available to it, whilst encouraging the State Party to accept the offer of collaboration by WHO, taking into account the views of the State Party concerned.”
So, if the WHO suspects that an outbreak within a nation might pose an international threat, but the nation in question doesn’t want to collaborate with the WHO, the WHO will immediately tell the other members about the suspected threat, which will put pressure on the uncooperative nation, and the views of that nation will be deemed irrelevant.
Other amendments within this and other articles also specifically remove any involvement of the nation in the WHO’s decision-making. Article 13 below is but one example. As noted by Campbell, the director-general is repeatedly specified as the sole authority when it comes to making assessments and decisions. The director-general can also impose sanctions on nations that refuse to follow his dictates.4
How can a single person be given the authority to make decisions for the entire world? This kind of authoritarian top-down system can only damage public health, as public health is best served by local decision makers that have access to local data.
Director-General Can Act Unilaterally on Mere Suspicion
Article 12 Determination of a Public Health Emergency of International Concern, Public Health Emergency of Regional Concern, or Intermediate Health Alert — “If the Director-General considers, based on an assessment under these Regulations, that a potential or actual public health emergency of international concern is occurring, the Director-General shall notify all States Parties and seek to consult with the State Party in whose territory the event arises regarding this preliminary determination ...”
The key problem here is the addition of “potential or actual.” The WHO can take over if the director-general has a mere suspicion that a health emergency might be brewing. The threat doesn’t have to be real or evident.
Article 13 Public Health Response — “
At the request of a State Party,WHO shallcollaboratearticulate clearly defined assistance to a State Party offer assistance to a State Party in the response to public health risks and other events by providing technical guidance , health products, technologies, know-how, deployment of civil medical personals, and assistance and by assessing the effectiveness of the control measures in place, including the mobilization of international teams of experts for on-site assistance ...”
Again, input from the member state will not be accepted. It’s no longer about collaborating with the WHO on health emergencies. It’s about obeying it. The WHO will independently decide what’s to be done. The WHO may also send in its own medical personnel to address the situation.
Newly Added Articles
Several new articles have also been added to flesh out and describe the WHO’s authority, and what member states must do to comply with this new top-down order. Here are two telling ones.
NEW Article 13A WHO Led International Public Health Response — “States [sic] Parties recognize WHO as the guidance and coordinating authority of international public health response during public health Emergency of International Concern and undertake to follow WHO’s recommendations in their international public health response.”
In other words, member nations shall bow down to the WHO and do as they’re told. A newly added Article 53 goes on to detail how each member nation must implement a compliance committee to ensure the WHO’s directives are adhered to and executed.
New Article 13A Access to Health Products, Technologies and Know-How for Public Health Response — “1. Immediately after the determination of a public health emergency of international concern under Article 12, the Director General shall make an immediate assessment of availability and affordability of required health products and make recommendations, including an allocation mechanism, to avoid any potential shortages of health products and technologies ...
3. States Parties shall provide, in their intellectual property laws and related laws and regulations, exemptions and limitations to the exclusive rights of intellectual property holders to facilitate the manufacture, export and import of the required health products, including their materials and components.”
So, once a PHEIC is announced, the director-general will lay claim to all medical resources within the member states. Other additions also spell out that the WHO will control:5
The local production of health products
Intellectual property
Cell lines used in the production of biotherapeutics and vaccines
Allocation of medical resources
Biosurveillance
Development of regulatory guidelines for the fast-tracking of health products
Censorship of “false and unreliable information” about public health events, preventive strategies and pandemic countermeasures
A global health database (which is required for the implementation of vaccine passports)
IHR Amendment Greenlights Conflicts of Interest
The amendments also plainly allow for conflicts of interest that might harm public health. Under Article 9, the WHO can declare a public health emergency based on information from undisclosed sources. Those sources could include Big Pharma, WHO funders such as the Gates Foundation and the Gates-founded-and-funded GAVI Alliance, or any number of other players with conflicts of interest.
As reported by The Defender,6 “One of the biggest changes the WHO has seen in its 75-year history is a shift from funding from sovereign nations to funding from private parties.”
At present, the majority of the WHO’s funding comes from Bill Gates, through donations from the Bill & Melinda Gates Foundation, GAVI and the Coalition for Epidemic Preparedness Innovations (CEPI). Gates also funds the World Economic Forum, and his nonprofits are taking money from drug companies.
The IHR amendments open the door wide to mass medical experimentation on humanity without informed consent, and if the COVID pandemic is any indication, nothing good will come from that.
What this means is that Gates and drug companies wield enormous power over the WHO. It’s not even close to being independent. A majority of the WHO’s funding is also “specified,” meaning it’s earmarked for particular programs. So, the WHO cannot allocate those funds wherever they’re needed most, and this also massively influences what the WHO does and how it does it.
There’s no getting around this point: The WHO is an organization that does whatever its funders want it to do, and that does not bode well for global health, considering medical errors are already a leading cause of death, and have been for decades. The IHR amendments basically open the door wide to mass medical experimentation on humanity without informed consent, and if the COVID pandemic is any indication, nothing good will come from that.
PHEIC Definition Expanded to Include Just About Anything
The amendments also radically expand the situations that can constitute a PHEIC. A PHEIC is currently defined as an “extraordinary event” in one country that constitutes “a public health risk to other states through the international spread of disease and to potentially require a coordinated international response.”
Amendments seek to expand and broaden this definition to include things like clusters of infection with potential but unverified human-to-human transmission. The actual risks of such clusters don’t even need to be evaluated. What’s more, the proposed definition of a PHEIC does not specify that it must involve “severe” or “life-threatening” disease, so it could be invoked for just about anything.
One of the amendments also suggests giving the director-general the ability to declare an “intermediate public health alert” when the situation doesn’t fully meet the PHEIC criteria. In such an event, the director-general and/or a regional WHO director would be able to declare a public health emergency of regional concern (PHERC).7
As suggested by Campbell, to really understand what they’re trying to do here, browse through the Article by Article Compilation of Proposed Amendments8 for yourself. Most definitely, don’t believe the “fact checkers” who say there’s nothing to see here.
Treaty Will Expand WHO’s Power Beyond Pandemics
As mentioned earlier, when you add in the proposed pandemic treaty, the WHO’s powers expand even further, because in addition to expanding emergency powers during pandemics, the treaty also emphasizes the “One Health”9,10 agenda, and that covers just about everything you can think of.
As illustrated in the graphic11 below, the One Health agenda is based on the premise that a broad range of aspects of life and the environment can impact health and therefore fall under the “potential” to cause harm.
This graphic below isn’t comprehensive. The scope of One Health, according to a One Health Commission document,12 also includes communications, economics, civil society, global trade, commerce and security, public policy and regulation, research, noncommunicable diseases, agricultural land use (which involves forcing farmers off their land), disaster preparedness and response, disease surveillance, the “human-animal bond” (whatever that means) and much more.
Under the new treaty, the WHO will have unilateral power to make decisions about all of these areas, and its dictates will supersede and overrule any and all local, state and federal laws. For example, under One Health, the WHO will be able to declare climate change as a health emergency and implement climate lockdowns to address it.
One Health Is Part of The Great Reset Agenda
One Health basically mirrors The Great Reset agenda. It just uses a different name and justifies all these Great Reset changes as a means to “protect health.” Not surprisingly, One Health is financed and promoted by a long list of Great Reset backers, including the United Nations, the European Union and various U.S. federal agencies,13,14 the Bill & Melinda Gates Foundation, GAVI, the Wellcome Trust, UNICEF, CEPI, the World Economic Forum and the World Bank.
But while these entities are officially funding the pandemic industry, what’s really happening is they’re using taxes to fund wealthy people, who in turn exploit the poor. It’s as far from philanthropic as you can get.
Taxpayers are providing the money while private profiteers are deciding how that money is spent, and it’s being spent in ways that will benefit themselves. So, it’s a private-public “partnership” where the public is being robbed and all the benefits go to the private sector.
As reported by Paraschiva Florescu and Rob Verkerk Ph.D., with the Alliance for Natural Health International:15
“The One Health approach is aligned with WHO’s linear and reductionist thinking that seeks to distill all potential solutions to one view of the underlying science, one view on the necessary medicines, and only one truth.
This monolithic approach spells grave dangers for humanity given that it is bottom-up, decentralized, regionally specific approaches to complex health problems that have always been shown to work. Top-down, “one size fits all” approaches, especially ones twisted by conflicted interests, are doomed to failure.
Only those who fail to look at the wider scientific picture are prepared to convince themselves that the WHO’s first global attempt at managing a pandemic, involving masks, lockdowns and genetic vaccines, was a success.
At its core, the WHO’s extended powers will lead to even more censorship and will dismantle the notion of consensus science built on a transparent, scientific method ...
Without an international uprising by the grassroots, these amendments will go ahead. Our silence and passivity are our consent. It is, without question, part of the slow descent into totalitarianism, taking us further and further away from principles and values that have characterized many civilizations over recent millennia, namely the right to liberty, the rights of the individual, and the importance of national sovereignty.”
To learn more, check out the Stop Vax Passports Task Force webinar on One Health,16 available on NTD.com.
Global Threat Detection Network Launched
Already, the WHO has launched a global threat detection network, the International Pathogen Surveillance Network (IPSN), to “help protect people from infectious disease threats through the power of pathogen genomics.”17 Apparently, it fully expects to be granted all the powers that the IHR amendments and the pandemic treaty will impart.
This network will be used to collect and analyze pathogenic samples, which in turn will drive the WHO’s public health decisions. As described in a press release:18
“The IPSN, with a Secretariat hosted by the WHO Hub for Pandemic and Epidemic Intelligence, brings together experts worldwide at the cutting-edge of genomics and data analytics, from governments, philanthropic foundations, multilateral organizations, civil society, academia and the private sector.
All share a common goal: to detect and respond to disease threats before they become epidemics and pandemics, and to optimize routine disease surveillance ...
COVID-19 highlighted the critical role pathogen genomics plays in responding to pandemic threats. Without the rapid sequencing of the SARS-COV-2 genome, vaccines would not have been as effective, or have been made available so quickly.
New, more transmissible variants of the virus would not have been as quickly identified. Genomics lies at the heart of effective epidemic and pandemic preparedness and response, as well as part of the ongoing surveillance of a vast range of diseases, from foodborne diseases and influenza to tuberculosis and HIV.”
The problem, of course, is that the COVID “vaccines,” developed at warp speed using genomic sequencing, were neither effective nor safe. Many have died within two weeks of getting their jab, and after several months, the effectiveness become negative. This is the technology they now want to use for everything. The risks moving this agenda forward are near-incomprehensible.
So, to summarize and recap, the globalist takeover hinges on the successful creation of a feedback loop of surveillance for virus variants, declaration of potential risk followed by lockdowns and restrictions, followed by mass vaccinating populations to “end” the pandemic restrictions, followed by more surveillance and so on. The funding for this scheme comes primarily from taxpayers, while the profits go to corporations and their investors.
Current Timeline
Once the amendments are adopted by the World Health Assembly, nations will have only a limited time to reject them. Any nation that hasn’t officially rejected the amendments will then be legally bound by them, and any attempt to reject them after the six-month grace period will be null and void.
As it currently stands, the IHR amendments will be voted on in the World Health Assembly (WHA) in May 2024. They only need a majority vote to pass. If that vote happens as planned, then the 10-month deadline for member states to reject the amendments will expire in March 2025, and the amendments will come into force in May 2025. If a member state opts out, then the current 2005 IHR version will apply to that state.
The WHO pandemic treaty will also be voted on by the WHA in May 2024. It requires a two-thirds majority vote to pass, and 30 member countries to ratify it. Thirty days after ratification, the treaty will take force for the countries that signed it.
Bill Introduced to Require Senate Approval, but Is It Enough?
Fortunately, the U.S. Senate is not entirely clueless about the ramifications of this treaty, and 17 Republican senators, led by Sen. Ron Johnson, R-Wis., have introduced a bill to thwart the WHO’s power grab.19
The “No WHO Pandemic Preparedness Treaty Without Senate Approval Act,”20 introduced February 15, 2023, would require a Senate supermajority (two-thirds or 67 senators) to pass the pandemic treaty.
However, according to Boyle,21 an expert on international laws and treaties, even this bill might not be enough to protect us were President Biden to sign the treaty. The reason for this is because the treaty is written “specifically to circumvent the Senate-approval process.”
A far more effective strategy, he says, would be for Congress to withhold its annual contributions to the WHO — and then withdraw the U.S. from the WHO altogether.
I believe it may be worth supporting all of these strategies. So, please, contact your representatives and urge them to support the “No WHO Pandemic Preparedness Treaty Without Senate Approval Act,” to withhold funding for the WHO and, ultimately, support U.S. withdrawal from the WHO.
Think Globally, Act Locally
National vaccine policy recommendations in the U.S. are made at the federal level but vaccine laws are made at the state level. It is at the state level where your action to protect your vaccine choice rights can have the greatest impact.
It is critical for EVERYONE to get involved now in standing up for the legal right to make voluntary vaccine choices in America because those choices are being seriously threatened.
Not only are lobbyists representing drug companies, medical trade associations and public health officials trying to persuade legislators to strip all vaccine exemptions from public health laws, but global political operatives lobbying the United Nations and World Health Organization are determined to take away the human right to autonomy and protection of bodily integrity.
We must take action to defend our constitutional republic and civil liberties, including the right to autonomy, in America. That includes reforming oppressive mandatory vaccination laws and stopping the digital health ID that will make vaccine passports a reality for us, our children and grandchildren if we don’t take action today.
Signing up to use the free online Advocacy Portal sponsored by the National Vaccine Information Center (NVIC) at www.NVICAdvocacy.org gives you immediate, easy access to your own state and federal legislators on your smartphone or computer so you can make your voice heard.
NVIC will keep you up to date on the latest bills threatening to eliminate — or expand — your legal right to make vaccine choices and give you guidance about what you can do to support or oppose those bills. So, please, as your first step, sign up for the NVIC Advocacy Portal.
Internet Resources Where You Can Learn More
I encourage you to visit the four websites of the National Vaccine Information Center, at www.NVIC.org, a nonprofit charity that has been educating the public about the need to prevent vaccine injuries and deaths since 1982. The information you get on their websites is fully referenced and will help you become an effective vaccine choice advocate in your community:
NVIC.org — This website was established in 1995 and is the oldest and largest consumer operated website publishing information on diseases and vaccines on the internet. Learn about vaccine reactions, injuries and deaths and the history and current status of vaccine science, policy, law and ethics in the U.S. on more than 2,000 web pages.
NVICAdvocacy.org — This communications and advocacy network, established in 2010, is your gateway to taking action to protect your right to make vaccine choices where you live.
TheVaccineReaction.org — This weekly journal newspaper published by NVIC since 2015 is dedicated to encouraging an “enlightened conversation about vaccination, health and autonomy.”
MedAlerts.org — This is a user-friendly search engine for the federal Vaccine Adverse Event Reporting System (VAERS) established under the 1986 National Childhood Vaccine Injury Act and sponsored by NVIC since 2006. Search for descriptions of vaccine injuries and deaths reported to VAERS on this popular website.
Find a Doctor Who Will Listen and Care
If your doctor or pediatrician refuses to provide medical care to you or your child unless you agree to get vaccines you don't want, I strongly encourage you to have the courage to find another doctor. Harassment, coercion and refusal to provide medical care to someone declining one or more doses of government recommended vaccines is a violation of the informed consent ethic.
Unfortunately, it is becoming routine among members of the medical establishment to be reluctant to share vaccine decision-making power with patients and parents of minor children, especially during the aggressive push for all Americans to get COVID shots.
There are doctors out there who respect the precautionary and informed consent principles, so take the time to locate a doctor who treats you with compassion and is willing to listen and respect the health care choices you make for yourself or your child.
- Sources and References
3, 8 WHO Article by Article Compilation of Proposed Amendments to the 2005 IHR
10, 14 CDC One Health
12 Stop Vax Passports Task Force webinar on One Health, 52:20
17, 18 WHO May 20, 2023
20 No WHO Pandemic Preparedness Treaty Without Senate Approval Act