POLITICO: How Bill Gates Took Over the Covid Pandemic
Bill Gates took over Covid just like he took over Operating Systems
By Igor Chudov | September 15, 2022
An amazing article from the least expected, mainstream source: Politico.
The title of the article was apparently edited in a hurry post-publication because Google News still lists it as “How Bill Gates and his partners took over the global Covid response”. Here’s the archive link to the original article with “Bill Gates” in the title — proving it was later edited in a hurry.
Even the article URL lists Bill Gates:
https://www.politico.com/news/2022/09/14/global-covid-pandemic-response-bill-gates-partners-00053969The article would be fascinating to read for people who were not previously aware of what most of us knew already — that the so-called “pandemic response” and global health are taken over by unaccountable private interest groups serving Bill Gates.
I highly recommend that you take a look!
The story given by the article is incomplete but very interesting.
It mentions that the pandemic response was taken over by the Bill and Melinda Gates Foundation, GAVI, CEPI, and the Wellcome Trust. All four organizations pretend to be independent, but all were financed by Bill Gates.
They participated in Event 201, planning out the pandemic, in October 2019.
“What makes Bill Gates qualified to be giving advice and advising the U.S. government on where they should be putting the tremendous resources?” asked Kate Elder, senior vaccines policy adviser for the Doctors Without Borders’ Access Campaign.
Several important items are glaringly missing from the article:
- Bill and Melinda Gates Foundation, along with the US government (Avril Haines representing the US intelligence community) and China CDC, planned out the pandemic in October of 2019 by means of an “exercise” called Event 201.
- Sars-Cov-2 is lab engineered and was designed intentionally
- As pointed out by our astute reader Mel, do not forget the 3.1 million shares of BioNTech that Gates bought in Sept 2019 for $18.10/share. That $55 million investment was worth $1.7 billion by Aug 2021.https://www.sec.gov/Archives/edgar/data/1776985/000119312519241112/d635330dex1036.htm
- Bill and Melinda Gates Foundation financed the organization that developed Sars-Cov-2 (EcoHealth Alliance) via grant INV-002838, and possibly more.
- Bill and Melinda Gates Foundation financed University of North Carolina, where Ralph Baric developed Sars-Cov-2 for EcoHealth Alliance, via 56 grants: INV-026327 INV-030330 INV-031704 INV-028991 INV-036494 INV-032887 INV-033909 INV-036560 OPP1192462 OPP1199232 OPP1201585 OPP1203327 OPP1195157 OPP1195363 OPP1191684 OPP1061107 OPP1090837 OPP1086528 OPP1108279 OPP1107923 OPP1235 OPP3436 OPP1142921 OPP38920 OPP38381 OPP23847 OPP17809 OPP1161858 OPP1158402 OPP1154943 OPP1172799 OPP1183027 OPP1181722 INV-006232 INV-001748 INV-005277 INV-016221 INV-019193 INV-016163 INV-003112 INV-001805 INV-003266 INV-002551 OPP1203712 OPP9404 OPP1014802 OPP1015539 OPP1024615 OPP1024664 OPP1015381 OPP1018000 OPP51976 OPP53107 OPP53450 OPP52037 OPP49260
- Bill Gates had close ties with Jeffrey Epstein and visited him numerous times
Nevertheless, the mere publication of this article has huge importance. The things that most of us know and talk about, are appearing in the so-called “mainstream press” — after the damage was all done, of course.
The virus was released; millions died; over a billion young people were force-vaccinated under false pretenses. When it is too late to change anything, Politico is finally stating the obvious. Still, it is better than nothing.
Almost everything in the Politico article was known a year ago. Where was Politico then? Busy taking government covid vaccine advertising money.
The pandemic was a crime, not an accident.
WHO’S DRIVING THE PANDEMIC EXPRESS?
By Dr David Bell and Emma McArthur | PANDA | September 4, 2022
Sceptics of the growing ‘pandemic prevention, preparedness and response’ (PPR) agenda celebrated recently, heralding a perceived ‘defeat’ of the World Health Organization’s (WHO) controversial amendments to the International Health Regulations (IHR). Although the proposed amendments would have undoubtedly expanded the WHO’s powers, this focus on the WHO reflects a narrow view of global health and the pandemic industry. The WHO is almost a bit-player in a much larger game of public-private partnerships and financial incentives that are driving the pandemic gravy train forward.
While the WHO works in the spotlight, the pandemic industry has been growing for over a decade and its expansion accelerates unabated. Other major players such as the World Bank, coalitions of wealthy nations at the G7 and G20 and their corporate partners work in a world less subject to transparency; a world where the rules are more relaxed, and a conflict of interest receives less scrutiny.
If the global health community is to preserve public health, it must urgently understand the wider process that is underway and take action to stop it. The pandemic express must be halted by the weight of evidence and basic principles of public health.
Funding a global pandemic bureaucracy
“The FIF could be a cornerstone in the construction of a truly global PPR system in the context of the International Treaty on Pandemic Prevention, Preparedness and Response, sponsored by the World Health Assembly.” (WHO, 19 April 2022)
The world is being told to fear pandemics. Ballooning socio-economic costs of the COVID-19 crisis are touted as justification for increased focus on PPR funding.
Calls for ‘urgent’ collective action to avert the ‘next’ pandemic are predicated on systemic ‘weaknesses’ supposedly exposed by COVID-19. As the WHO steamed ahead with its push for a new pandemic ‘treaty’ during 2021, G20 members agreed to establish a Joint Finance & Health Task Force (JFHTF) to ‘enhance the collaboration and global cooperation on issues relating to pandemic prevention, preparedness and response’.
A World Bank-WHO report prepared for the G20 joint task force estimates that US$ 31.1 billion will be required annually for future PPR, including US $ 10.5 billion per year in new international financing to support perceived funding gaps in low- and middle-income countries (LMICs). Surveillance-related activities comprise almost half of this, with US $4.1 billion in new funding required to address perceived gaps in the system.
In public health terms, the funding proposed to expand the global PPR infrastructure is enormous. By contrast, the WHO’s approved biennium programme budget for 2022-2023 averages US $3.4 billion per year. The Global Fund, the main international funder of malaria, tuberculosis and AIDS – which have a combined annual mortality of over 2.5 million – currently dispenses just US $ 4 billion annually for the three diseases combined. Unlike COVID-19, these diseases cause significant mortality in lower income countries and in younger age groups, year in, year out.
In April 2022, the G20 agreed to establish a new ‘financial intermediary fund’ (FIF) housed at the World Bank, to address the US $10.5 billion PPR financing gap. The FIF is intended to build upon existing pandemic funding to ‘strengthen health systems and PPR capacities in low-income and middle-income countries and regions’. The WHO is predicted to be the technical lead, landing them with an assured role irrespective of the outcome of current ‘treaty’ discussions.
The establishment of the fund has proceeded with breathtaking speed, and it was approved on June 30 by the World Bank Board of Executive Directors. A short period of consultation precedes an expected launch in September 2022. To date, donations totalling US $1.3 billion dollars have been pledged by governments, the European Commission and various private and non-government interests, including the Bill and Melinda Gates Foundation, Rockefeller Foundation, and the Wellcome Trust. The initial areas for the fund are somewhat all-encompassing, including country-level ‘disease surveillance; laboratory systems; emergency communication, coordination and management; critical health workforce capacities; and community engagement’.
In scope, the fund has the appearance of a new ‘World Health Organization’ for pandemics – to add to the existing (and ever-expanding) network of global health organisations such as the WHO; Gavi; the Coalition for Epidemic Preparedness Innovations (CEPI); and the Global Fund. But is this increased expenditure on PPR justified? Are the escalating socio-economic costs of COVID-19 due to a failure to act by the global health community, as is widely claimed; or are they due to negligent acts of failure by the WHO and global governments, when they discarded previous evidenced-based pandemic guidelines?
COVID-19: failure to act or acts of failure?
In the debate surrounding the growing pandemic industry, much attention is being directed towards the central role of the WHO. This attention is understandable given the WHO’s position as the agency responsible for global public health and its push for a new international pandemic agreement.
However, the WHO’s handling of the response to COVID-19 creates serious doubts about the competency of its leadership and raises questions about whose needs the organisation is serving.
The WHO’s failure to follow its own pre-existing pandemic guidelines by supporting lockdowns, mass-testing, border closures and the multi-billion-dollar COVAX mass-vaccination program, has generated vast revenue for vaccine manufacturers and the biotech industry, whose corporations and investors are major contributors to the WHO. This approach has crippled economies, damaged existing health programs and further entrenched poverty in low-income countries. Decades of progress in children’s health are likely to be undone, together with the destruction of the long-term prospects of tens of millions of children, through loss of education, forced child marriage and malnutrition. In abandoning its principles of equality and community-driven healthcare, the WHO appears to have become a mere pawn in the PPR game, beholden to those with the real power; the entities who are providing its income and who control the resources now being directed to this area.
Corporatizing global public health
Recently established health agencies devoted to vaccination and pandemics, such as Gavi and CEPI, appear to have been highly influential from the beginning. CEPI, is the brainchild of Bill Gates, Jeremy Farrar (director of the Wellcome Trust), and others at the pro-lockdown World Economic Forum. Launched at Davos in 2017, CEPI was created to help drive the market for epidemic vaccines. It is no secret that Bill Gates has major private financial ties to the pharmaceutical industry, in addition to those of his foundation. This clearly places a question mark over the philanthropic nature of his investments.
CEPI appears to be a forerunner of what the WHO is increasingly becoming – an instrument where individuals and corporations can exert influence and improve returns by hijacking key areas of public health. CEPI’s business model, which involves taxpayers taking most of the financial risk for vaccine research and development whilst big pharma gets all the profits, is notably replicated in the World Bank-WHO report.
Gavi, itself a significant WHO donor that exists solely to increase access to vaccination, is also under direct influence of Bill Gates, via the Bill and Melinda Gate Foundation. Gavi’s involvement (alongside CEPI) with the WHO’s COVAX program, which diverted vast resources into COVID-19 mass-vaccination in countries where COVID-19 is a relatively small disease burden, suggests the organisation is tied more strongly to vaccine sales than genuine public health outcomes.
Pandemic funding – ignoring the big picture?
At first glance, increased PPR funding to LMICs may seem a public good. The World Bank-WHO report claims that ‘the frequency and impact of pandemic-prone pathogens are increasing.’ However, this is belied by reality, as the WHO lists only 5 ‘pandemics’ in the past 120 years, with the highest mortality occurring in the 1918-19 H1N1 (‘Spanish’) influenza pandemic, before antibiotics and modern medicine. Apart from COVID-19, the ‘Swine Flu’ outbreak in 2009-10, which killed less people than a normal flu year, is the only ‘pandemic’ in the past 50 years.
Such a myopic focus on pandemic risk will do little to address the most serious causes of illness and death, and it can be expected to make matters worse for people experiencing the most extreme forms of socio-economic disadvantage.
Governments of low-income countries will be ‘incentivised’ to divert resources to PPR related programs, further increasing the growing debt crisis. A more centralised, top-down public health system will lack the flexibility to meet local and regional needs. Transferring support from higher burden diseases, and drivers of economic growth, has a direct impact on mortality in these countries, particularly for children.
The WHO-World Bank report states that the pillars of the global PPR architecture must be built on the ‘foundational principles of equity, inclusion and solidarity’. As severe pandemics occur less than once per generation, increased spending on PPR in LMICs clearly violates these basic principles as it diverts scarce resources away from areas of regional need, to address the perceived health priorities of wealthier populations. As demonstrated by the damage caused by the COVID-19 response, in both high and low-income countries, the overall harm of resource diversion from areas of greater need is likely to be universal. In failing to address such ‘opportunity costs’, recommendations by the WHO, the World Bank, and other PPR partners cannot be validly based in public health; nor are they a basis for overall societal benefit. .
One thing is certain. Those who will gain from this expanding pandemic gravy train will be those who gained from the response to COVID-19.
The pandemic gravy train – following the money
The new World Bank fund risks compounding existing problems in the global public health system and further compromising the WHO’s autonomy; although it is stated that the WHO will have a central ‘strategic role’, funds will be channelled through the World Bank. In essence, it financially side-steps the accountability measures at the WHO, where questions of relative worth can be raised more easily.
The proposed structure of the FIF will pave the way for organisations with strong ties to pharmaceutical and other biotech industries, such as CEPI and Gavi, to gain even greater influence over global PPR, particularly if they are appointed ‘implementing entities’ – the operational arms that will carry out the FIF’s work program at country, regional and global level.
Although the initial implementing entities for the FIF will be UN agencies, multilateral development banks and the IMF, plans are already underway to accredit these other international health entities. Investments are likely to be heavily skewed towards biotechnological solutions, such as disease surveillance and vaccine development, at the cost of other, more pressing, public health interventions.
Protecting public health rather than private wealth
If the world truly wants to address the systemic weakness exposed by COVID-19, it must first understand that this pandemic gravy train is not new; the foundations for the destruction of community- and country-based global public health began long before COVID-19.
It is unarguable that COVID-19 has proved to be a lucrative cash cow for vaccine manufacturers and the biotech industry. The public-private partnership model that now dominates global health enabled vast resources to be channelled into the pockets of corporate giants, through programs they directly influence, or even run. CEPI’s ‘100 days Mission’ to make ‘safe and effective’ vaccines against ‘viral threats’ within 100 days – to ‘give the world a fighting chance of containing a future outbreak before it spreads to become a global pandemic’ – is a permit for pharmaceutical companies to appropriate public money on an unprecedented scale, based on their own assessments of risk.
The self-fulfilment of the ‘increasing frequency of pandemic’ prophecy will be ensured by the push for increased disease surveillance – a priority area for the FIF. To quote the World Bank-WHO report:
“COVID-19 highlighted the need to connect surveillance and alert systems into a regional and global network to detect zoonotic transmission events, raise the alarm early to enable a swift public health response, and accelerate the development of medical countermeasures.”
Like many claims being made about COVID-19, this claim has no evidence base – the origins of COVID-19 remain highly controversial and the WHO’s data demonstrate that pandemics are uncommon, whatever their origin. None of the ‘countermeasures’ have been shown to significantly reduce the spread of COVID-19, which is now globally endemic.
Increased surveillance will naturally identify more ‘potentially dangerous pathogens’, as variants of viruses arise constantly in nature. Consequently, the world faces a never-ending game of seek and ye shall find, with never-ending profits for industry. Formerly once per generation, this industry will make ‘pandemics’ a routine part of life, where rapid fire vaccines are mandated for every new disease or variant that arrives.
Ultimately, this new pandemic fund will help to hook low- and middle-income countries into the growing global pandemic bureaucracy. Greater centralisation of public health will do little to address the genuine health needs of people in these countries. If the pandemic gravy train is allowed to keep growing, the poor will get poorer, and people will die in increasing numbers from more prevalent, preventable diseases. The rich will continue to profit, while fuelling the main driver of ill-health in lower income countries – poverty.
Dr. David Bell is a clinical and public health physician with a PhD in population health and background in internal medicine, modelling and epidemiology of infectious disease. Previously, he was Director of the Global Health Technologies at Intellectual Ventures Global Good Fund in the USA, Programme Head for Malaria and Acute Febrile Disease at FIND in Geneva, and coordinating malaria diagnostics strategy with the World Health Organisation. He is a member of the Executive Committee of PANDA.
AP ‘Fact’ Checks Slip-of-the-Tongue Video
By Dr. Joseph Mercola | August 28, 2022
A viral video showing Vassar College’s alumni president referring to a Bill and Melinda Gates foundation as “the Institute of Population Control” has The Associated Press trying to whitewash the slip of the tongue with a “fact” check.
The invited speaker at the event, Laurie Schwab Zabin, a founding director of the Bill & Melinda Gates Institute for Population and Reproductive Health, later corrected the name, the AP reports. However, that doesn’t mean that Zabin — who died in 2020 — and the foundation weren’t promoting population control.
In fact, the Institute for Population and Reproductive Health is a supporter of the International Conference on Family Planning, the Advance Family Planning advocacy group and the Population Reference Bureau, all of which advocate for population control in some way. Schwab also served on the national board of directors of Planned Parenthood, and helped shape its polices.
In tandem, she worked closely with obstetrician Dr. Alan Guttmacher, who was Planned Parenthood’s president and the American Eugenics Society’s vice president, in establishing the Guttmacher Institute, another agency promoting family planning.
SOURCES:
Bill & Melinda Gates institute for Population and Reproductive Health
The narrative managers have done their best to memory-hole the Nurenberg Codes
By Helen of desTroy | August 28, 2022
You would be forgiven for not knowing that last Friday was the 75th anniversary of the Doctors’ Trial, one of 13 Nazi war crimes trials conducted at Nuremberg after World War II and the event that birthed the Nuremberg Codes, the most important medical ethics document of the modern era. The Codes set ground rules for requiring informed consent from experimental test subjects; they anchor international agreements like the Helsinki Declaration, the Geneva Convention and the United Nations’ International Covenant on Civil and Political Rights and have been codified into law in the US and other countries.
Sixteen doctors were found guilty at Nuremberg of murder and torture for carrying out a euthanasia program on mentally and physically disabled German citizens deemed “unworthy of life” and experimenting on concentration camp inmates; nine were jailed and seven were executed. Yet the expected flood of commemoratory articles and events marking the anniversary of the Allies’ crowning (if illusory) moment of moral superiority over those Evil Nazis™ has not materialized. It’s downright unnatural for the US and Europe to miss a chance to give the dead Nazi horse a good beating, but any attempts to even discuss the Nuremberg Codes in the last two years have been squelched by militant fact-checkers. Meanwhile, a coterie of corrupt “public health professionals” and the international financial cartels who control them have pulled off perhaps the most shocking and deadly crime against humanity ever committed.
The Big Lie
Mentioning Nuremberg during Covid-19 was asking to be pilloried in the “respectable” press as an anti-science, horse-paste-guzzling right-wing extremist. Fact-checkers came out of the woodwork to reflexively deny that the Nuremberg Codes applied to any aspect of the Covid-19 response, from forced masking to vaccine mandates, sometimes issuing two denials in a single day in their compulsion to keep the claim from spreading. One particularly tenacious fact-check even took issue with the claim “It was the doctors on trial in Nuremberg,” arguing that because the other 12 trials put Nazi Party officials, lawyers, and corporate executives in the dock, the statement “lacked context.”
This display of ideological lockstep was supposed to intimidate anyone who wasn’t already 100% allied with society’s enlightened institutions in defense of The Science™ against the irrational, emotionally-driven forces of ignorance. Those still on the fence about getting their “Warp Speed” car-crash of a shot were shamed by peer pressure psyops like the UK’s “Clap for our carers,” while social media was seeded with controlled but approachable “experts” who carefully crafted the illusion of overwhelming consensus that the measures being taken in the name of “stopping the spread” were not only scientifically but morally beyond reproach.
But this wasn’t an organic moment of unity. These “fact-checkers” have all received big money from the Bill & Melinda Gates Foundation, the eugenics enthusiasts who have rapidly become the most powerful force in global health policymaking and who also control huge chunks of the education, agriculture, and “green” energy spheres. Most fact-checking organizations pay lip service to the rules set by the International Fact-Checking Network, which while it sounds like an upstanding professional association that’s been around a while was actually launched less than a decade ago. The IFCN, which admits it doesn’t follow its own code of principles, has been funded since its 2015 beginnings by the Gates Foundation, the Omidyar Network, George Soros’ Open Society Foundations, Google, Facebook, the US State Department, and CIA cutout the National Endowment for Democracy, among others. It’s hard to think of a worse group of stewards for a gaggle of helpless facts, aside from perhaps the Wikimedia Foundation, about which more later.
The IFCN is run by the Poynter Institute, a “journalism education” nonprofit funded by many of the same entities as its IFCN subsidiary. Loaded down with enough conflicts of interest to make that code of principles swoon, Poynter selects, sponsors, and trains journalists, prioritizing obedience to authority, ideological inflexibility and a total absence of shame. They are then turned loose to mow the internet’s epistemological lawn in military fashion, doxxing some popular opposition voice while merely tagging others for later deplatforming, arrest, or worse. The tactic’s resemblance to the work of Ukrainian vigilante website Mirotvorets, unofficially operated by the country’s Ministry of Information, is unlikely to be an accident, given that Omidyar and Soros both poured billions of dollars into 2014’s Maidan Square color revolution, which was itself choreographed by the State Department’s Victoria Nuland, who knows the value of a well-placed bullet or a warm cookie.
It’s easy to see why Gates just had to buy the industry for himself. If these fact-checkers could reinvent the most corrupt government in Europe, whose military was exposed by dozens of major western media outlets as a hive of neo-Nazi thugs, as a democratic paradise, surely they could spin the vaccine tycoon’s Final Solution as the solution to all humanity’s problems. The Covid-19 experiment saw the closest collaboration yet between the fact-checkers, Big Tech and governments around the world to construct an epistemological roach motel that users could enter easily but would face growing barriers – warning screens, computer failures, personal attacks, deplatforming, financial hardship and a lowered social credit score – if they tried to leave.
It’s no exaggeration to say Poynter’s army of fact-checkers set the narrative of Covid-19 for the public from Day One (or should we call it Year Zero?). The IFCN’s “Coronavirus Alliance” launched in January 2020, before most Americans even knew what a coronavirus was. While the first Twitter users in the western hemisphere were stumbling across bizarre videos of Chinese people dropping to the ground and convulsing, explained in the accompanying broken-English text to be the result of an unknown virus, the fact-checkers were implementing orders from their paymasters. One of the first narrative touchstones, the red and white 3D model of the coronavirus, soon became as ubiquitous as the footage of planes hitting towers on 9/11, triggering intense fear and doubt directed both at the outside world and at the self. After all, they might be an “asymptomatic carrier,” and the only way to be sure was to isolate from their loved ones. As with 9/11, this unfamiliar terror pushed the individual to seek solace in an increasingly totalitarian state that insisted its ‘tough love’ – locking us in our homes, forbidding us from earning money, and keeping us from our families – was for our own good. Frightened and confused, many turned on the TV and sucked down its narcotizing propaganda. Even CNN’s ratings went up that first pandemic year, as Chris Cuomo demanded Americans “sacrifice the me to the we” and compared binge-watching Netflix to landing on the beaches of Normandy while his brother mass-murdered elderly New Yorkers.
The complex choreography of the Covid-19 response could not have unfolded as it did without premeditation. The plot was lifted – not plagiarized, as the authors were the same – from Event 201, the tabletop coronavirus simulation sponsored by the Gates Foundation at Johns Hopkins University’s Center for Public Health Security. This took place just a month after the Global Preparedness Monitoring Board – the product of an unholy marriage between the WHO and the World Bank earlier that year – released a report demanding all UN member countries “conduct at least two system-wide training and simulation exercises” by the following September, “including one for covering the deliberate release of a lethal respiratory pathogen.” Video of Event 201 shows players uninterested in minimizing harm from the virus instead exploring how the “emergency” might be used to stifle undesirable narratives and ram through major changes in society. The “real” pandemic – simulation number two, by the GPMB’s counting – played out months later exactly along the exercise’s script. The WHO, Gates, the World Economic Forum and Big Business took the reins, filling the power vacuum left while individual governments, seemingly baffled by the outbreak despite having repeatedly run their own simulations, ran around in circles.
How to treat an Infodemic
The crisis was planned and then used to crack down on unauthorized views under the reasoning that humanity was in the midst of an infodemic – a surfeit of information encouraging irresponsible beliefs – and careless talk could cost lives. Spreading dissenting opinions could infect friends and loved ones with the virus of doubt, which while perhaps less deadly than the virus itself (with its 99.7% survival rate), could cause society to fracture at a time when all humanity had to unite or be destroyed by the invisible enemy. Reading or hearing “disinformation” about Covid could reduce one’s likelihood of getting vaccinated, putting one’s very life at risk.
Convincing test subjects to discard their self-preservation instincts and their critical capacity and embrace the most absurd statements as gospel truth was the main goal of the first part of the Covid-19 experiment, and given the single-mindedness with which the WHO zeroed in on the “infodemic” before it had even officially declared the real virus to be a pandemic, it’s hard to believe they were making it up as they went along, especially given that the term was allegedly invented during the original SARS outbreak in 2003 (by a Washington Post writer no less) and then apparently put on ice until almost two decades later. Seeking input on how to respond to this new threat, the WHO reached out to professionals of all stripes, with more than a quarter of advisory input coming from academics eager to test out their juiciest hypotheses on real people with no repercussions. Everyone who used social media in 2020 to discuss the Covid-19 pandemic and its aftermath thus became a test subject, “nudged” and prodded for the Public Good, and some of those experiments – particularly those aimed at developing an FBI-style psychological profile of believers in “conspiracy theories” so they can be locked up as domestic terrorists or institutionalized as incurable monsters are very much ongoing.
Those early academic papers describe a chaotic infosphere in which the WHO’s narrative failed to dominate on its merits alone. The academics rose to the challenge, burnishing their half-baked speculations with scientific-looking graphs and charts. Their solutions ranged from Orwellian – deploying “freedom of expression officers” to censor and label rogue content as much as European human rights law would allow; re-education programs for “influencers,” teachers, priests, and other likely “superspreaders,” who could then be suspended from social media entirely if they refused to get their minds right – to the lesser evils of sending in fact-checkers as the equivalent of UN peacekeeping troops to help “inoculate” social media users against the disinformation they were about to see. With distrust in public and private institutions hitting new highs, society didn’t just need a vaccine against the scary new virus, it needed one against “disinformation” as well! But like the Covid vaccines themselves, these digital inoculations didn’t come with an informed consent notice, and the clinical trial results aren’t looking good.
Experiment #1: Shock “therapy”
As the WEF’s Klaus Schwab himself admitted in his pandemic tome The Great Reset, Covid-19 is the least deadly ‘pandemic’ in the last two millennia. But he’s quite open about wanting to use the largely self-inflicted Covid-19 “crisis” to bring about the Fourth Industrial Revolution, a transhumanist “green” dystopia lovingly crafted for “stakeholder capitalists” and inspired by technocratic parasites like Yuval Noah Harari. This is no experiment for the “good of society,” nor are any efforts made to “avoid unnecessary mental and physical suffering,” as Nuremberg demands. If anything, the experiment’s designers deliberately ratcheted up the suffering, believing this was necessary to unfreeze the fixed ideas of western civilization – free will, individuality, rationality, democracy (not to be confused with Our Democracy™) in our minds and replace them with the WEF’s preferred picks: obedience, “equity” (a Newspeak term meaning equality of outcome rather than equality of opportunity), credulity, communitarianism. The group has admitted on its own website that the lockdowns and the rest of the “touchless torture” the Covid response has supposedly required constitute the “world’s biggest psychological experiment.”
The Great Reset is an especially noxious experiment in that it violates the minds and bodies of test subjects on multiple levels, burrowing down into the way we think in its megalomania. It’s the spiritual offspring of CIA-funded Canadian psychiatrist Ewen Cameron, who “de-patterned” his patients’ personalities with high-voltage electroshock, induced coma, and mega-doses of LSD, then attempted to’ ‘build them back better’ by playing their comatose forms 16 hours of tape-recorded messages at a time; and Milton Friedman, the University of Chicago economist and godfather of neoliberalism whose students, the so-called “Chicago Boys,” conducted campaigns of economic “shock therapy” on third-world nations the US worried were too left-wing, assisting far-right leaders in seizing power, further impoverishing the masses with austerity programs, terrorizing what political opposition remained with death squads and disappearances, and privatizing all state-run industries so as to attract foreign investors. Neither Cameron’s patients, most of whom came in with simple problems like anxiety or depression (and one of whom wasn’t even seeking treatment but just looking for a job) and left as husks no longer able to even use the bathroom themselves; nor the inhabitants of Chile, Brazil, Uruguay, Indonesia, Russia, or any of the long list of other countries subject to some variation on Chicago School shock treatment over the years, were ever told they were part of an experiment, let alone asked if they wanted to be.
The Great Reset has not only targeted the entire world with economic shock therapy, triggering a massive depression the current financial system is unlikely to ever shake off (spoiler alert: another experiment coming…) – it funneled unprecedented amounts of fear into populations already thrown off balance by the blinding speed of policy shifts. First scolded for “selfishly” wearing a mask, then attacked for “selfishly” not wearing one; informed their city would be “locking down” at 10pm, when a peek out the window yielded crowds of restive youths hanging out on the corner with nary a cop in sight; told vaccinations were mandatory for school, then told their child could have just “masked up” when little Polly drops dead of a heart attack not 24 hours after her first shot of Moderna; the average person soon lapsed into learned helplessness and became a shut-in, depatterning daily in the glow of the television as they degenerated into an obedient vegetable, capable of “masking up” and socially distancing but little else. Despite leaving a horrific trail of devastation in their wake, the experimental lockdowns were praised by the WEF for the slight dip in carbon emissions they caused, all but guaranteeing phase II of the nonconsensual clinical trials – climate lockdowns – will be rolled out within the year.
Experiment #2: Hackable animals
Given the mountain of evidence against them, it’s perfectly logical that the ruling class would have tried to build up an impenetrable fort of bullshit using their captive fact-checking industry to deflect accusations of war crimes under the Codes. Several patterns pervade the apologist coverage, starting with the idea that these brand new mRNA Covid vaccines, tested on under 100,000 people by Pfizer and Moderna combined (and none who were pregnant or nursing) before receiving their coveted emergency authorization, are somehow not experimental procedures. They use the synonym investigational instead, as ‘experimental’ tends to trigger thoughts of, well, human experimentation, authoritarian regimes, the very Nuremberg Nazis the media establishment is trying its best to keep the average reader away from. But the effect is the same – mRNA vaccines of any kind weren’t tried on the general population until the end of 2020, and the torrent of side effects and death that has been unleashed in the meantime suggests neither Moderna nor Pfizer had informed consent from these gen-pop guinea pigs.
That’s a big deal, because Pfizer knew before it sought emergency authorization that more vaccinated test subjects had died than unvaccinated subjects – it even fudged the numbers for the FDA. Some 1,200 trial participants died in the 90 days following their injection, and Pfizer made sure to vaccinate the placebo group at the end of the trial in order to make sure further comparisons didn’t spoil its story. Indeed, it was so sure its vaccines were going to leave a pile of bodies behind that it refused to even sell them to countries whose governments wouldn’t shield them from liability for the damage caused. One should have expected this from a company with the dubious distinction of paying the largest fine in Justice Department history in 2009 for healthcare fraud, off-label prescribing, misleading marketing and miscellaneous criminality. Nevertheless, they won the “Warp Speed” lottery under Albert Bourla, a veterinarian with a doctorate in the biotechnology of reproduction who was for some reason promoted to CEO of the entire (human-focused) drug company a year before the Covid-19 outbreak. Given that his primary achievement prior to Operation Warp Speed was developing a “vaccine” that chemically castrated boars without ruining the meat, it becomes much more difficult to see the utter disaster the mRNA vaccines have created for both male and female fertility as an accident.
Still questioning authority? The fact-checkers then attempt to distance vaccine mandates – along with health passports, mask mandates, lockdowns and the other psychological aspects of the experiment conducted on the unwitting populace – from the Nuremberg zone by categorizing them as “public health interventions,” not research, or experiments. The Codes simply do not apply. Never mind that public health interventions are supposed to be evidence-based, and no western democracy has ever engaged in anything like the Covid lockdowns before, or that the CDC pulled the six-foot social distancing rule out of its ass, or even that the only “science” backing closing schools to “stop the spread” was a computer model from a 16 year old’s science project. Lockdowns arguably killed more people than Covid-19, and they have cut short many more lives by impoverishing, immiserating, and isolating millions. Arguing public health measures can’t be experimental because they’re public health measures is merely a last-ditch effort to wall the Codes off in a museum, inapplicable to anyone but those nasty Nazis who were – as the narrative managers never tire of reminding us – a unique and special case.
Discouraging cross-time contextualization is very important to the fact-checkers, who aren’t hesitant to shoot the messenger if all else fails. Anyone talking about the Nuremberg Codes in the context of Covid-19 is dismissed as an “alt-righter”, a “covid crazy,” dangerous “extremists,” “anti-vaxxers,” or even actual Nazis who apparently got confused about whose side their team was on back in WW2. In war, dehumanizing the enemy is key to beating him, and this is nothing if not a two-pronged war being fought in our brains and our bloodstreams. “Drawing a link between this final rollout of these vaccines and what the Nazi doctors were doing is morally grotesque,” the British Medical Association’s Dr Julian Sheather told FullFact ; he didn’t explain why, and it’s not apparent why one should not draw parallels between the two cases. According to the Vaccine Adverse Event Reporting System (VAERS), whose own creators admit it contains less than 1% of all adverse events associated with a given vaccine, the Covid shots have already caused nearly 30,000 deaths, over 170,000 hospitalizations, nearly 16,000 heart attacks (a common sight now on sports fields, where 60 times more athletes than normal are flatlining mid-game), and nearly 5,000 miscarriages in the US alone. Using tech entrepreneur Steven Kirsch’s calculations, the numbers are much higher: at least 478,000 Americans have been killed by Covid vaccines, to say nothing of millions permanently disabled, unable to work or function on a basic level. Worldwide, the number of deaths approaches 12 million.
While the number of victims the Nazi doctors left behind is not so meticulously recorded, especially given the high levels of typhus and malnutrition contributing to the mortality rate in the camps, one source has them consigning between 70,000 and 100,000 “unfit” Germans to death between 1939 and 1941 while sterilizing hundreds of thousands more – a detail that once again should send a chill down the spine of anyone who’s noticed the declining birthrates around the world. If the figures aren’t comparable, that’s only because the mRNA vaccine has been so much more efficient in its killing. There’s nothing “morally grotesque” about pointing that out. But since “everybody knows” the Nazis were the pinnacle of Evil™, the realization that Pfizer and Moderna’s death toll might have their doctors beat must be prevented at all costs. Thus even bringing up Nuremberg in relation to Covid-19 is deemed to be “trivializing” the crimes of the Nazis, even when the intention is to draw attention to the seriousness of their modern descendants’ crimes, and efforts are made to further poison the dialogue by suggesting there’s something antisemitic about the whole business.
In Part II: the war on “conspiracy theories,” why Nuremberg is to be memory-holed, infodemic terrorism, and more…
RNA for Moderna’s Omicron Booster Manufactured by CIA-Linked Company
BY WHITNEY WEBB |
UNLIMITED HANGOUT| AUGUST 17, 2022
Since late last year, messenger RNA for Moderna’s COVID-19 vaccines, including its recently reformulated Omicron booster, has been exclusively manufactured by a little known company with significant ties to US intelligence.
Earlier this week, the United Kingdom became the first country to approve Moderna’s reformulated version of its COVID-19 vaccine, which claims to provide protection against both the original form of the virus and the significantly less lethal but more transmissible Omicron variant. The product was approved by the UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) with the support of the UK government’s Commission on Human Medicines.
Described by UK officials as a “sharpened tool” in the nation’s continued vaccination campaign, the reformulated vaccine combines the previously approved COVID-19 vaccine with a “vaccine candidate” targeting the Omicron variant BA.1. That vaccine candidate has never been previously approved and has not been the subject of independent study. The MHRA approved the vaccine based on a single, incomplete human trial currently being conducted by Moderna. The company promoted incomplete data from that trial in company press releases in June and July. The study has yet to be published in a medical journal or peer reviewed. No concerns have been raised by any regulatory agency, including the MHRA, regarding Moderna’s past history of engaging in suspect and likely illegal activity in past product trials, including for its original COVID-19 vaccine.
The approval comes shortly before several Western countries, including the UK, plan to conduct a massive COVID-19 booster vaccination campaign this fall. Moderna has also noted that approval for its Omicron booster vaccine are pending in the US, EU, Australia and Canada – all of which are also planning fall vaccination campaigns focused on COVID-19. The company’s CEO, Stéphane Bancel, has called the reformulated vaccine “our lead candidate for a Fall 2022 booster.”
Moderna CEO Stéphane Bancel, Source: ClockworkOrange
However, unlike the company’s original COVID-19 vaccine, the genetic material, or messenger RNA (mRNA), for this new vaccine, including the newly formulated genetic material meant to provide protection against the Omicron variant, is being manufactured, not by Moderna, but by a relatively new company that has received hardly any media attention, despite its overt links to US intelligence. Last September, it was quietly announced that a company called National Resilience (often referred to simply as Resilience) would begin manufacturing the mRNA for Moderna COVID-19 vaccine products. Under the terms of the multi-year agreement, “Resilience will produce mRNA for the Moderna COVID-19 vaccine at its facility in Mississauga, Ontario, for distribution worldwide.”
“Reinventing Biomanufacturing”
National Resilience was founded relatively recently, in November 2020, and describes itself as “a manufacturing and technology company dedicated to broadening access to complex medicines and protecting biopharmaceutical supply chains against disruption.” It has since been building “a sustainable network of high-tech, end-to-end manufacturing solutions with the aim to ensure the medicines of today and tomorrow can be made quickly, safely, and at scale.” It further plans to “reinvent biomanufacturing” and “democratize access to medicines,” namely gene therapies, experimental vaccines and other “medicines of tomorrow.”
In pursuit of those goals, the company announced it would “actively invest in developing powerful new technologies to manufacture complex medicines that are defining the future of therapeutics, including cell and gene therapies, viral vectors, vaccines, and proteins.” It was founded with the reported intention “to build a better system for manufacturing complex medicines to fight deadly diseases” as a way to improve post-COVID “pandemic preparedness.”
The company initially marketed its manufacturing capabilities as “the Resilience platform”, and offers principally “RNA Modalities”, including RNA development for vaccines, gene editing and therapeutics; and “Virus Production”, including viral vectors, oncolytic viruses (i.e. a virus engineered to preferentially attack cancer cells), viruses for use in vaccine development and gene-edited viruses for unspecified purposes. It is worth noting that, to date, many controversial “gain-of-function” experiments have justified modifying viruses for the same purposes as described by National Resilience’s Virus Production capabilities. In addition, National Resilience offers product formulations and other modalities, such as biologics and cell therapies, to its clientele and the “Virus Production” of its website has since been removed.
Resilience CEO Rahul Singhvi, Source: Resilience
National Resilience, being such a young company, has very few clients and there is little publicly available information on its manufacturing capabilities aside from the company’s website. The firm only acquired its first commercial manufacturing plant in March 2021, located in Boston, MA and purchased from Sanofi, followed shortly thereafter by the acquisition of another separate plant located in Mississauga, Ontario, Canada. Makeovers were announced for the plants, but little is publicly known about their progress. Prior to the acquisitions, the company had been subleasing a Bay area facility in Fremont, California. Reporters were puzzled at the time as to why a company with roughly 700 employees at the time had acquired a total of 599,00 square feet of manufacturing space after having only emerged from stealth less than 6 months prior.
In April 2021, National Resilience acquired Ology Bioservices Inc., which had received a $37 million contract from the US military the previous November to develop an advanced anti-COVID-19 monoclonal antibody treatment. This acquisition also provided National Resilience with its first Biosafety Level 3 (BSL-3) laboratory and the ability to manufacture cell and gene therapies, live viral vaccines and vectors and oncolytic viruses.
Despite being in the earliest stages of developing its “revolutionary” manufacturing capabilities, National Resilience entered into a partnership with the Government of Canada in July of last year. Per that agreement, the Canadian government plans to invest CAD 199.2 million (about $154.9 million) into National Resilience’s Ontario-based subsidiary, Resilience Biotechnologies Inc. Most of those funds are destined for use in expanding the Ontario facility that Resilience acquired last March and which is now manufacturing the mRNA for Moderna’s COVID-19 products. Canada’s Minister of Innovation, Science and Industry, François-Philippe Champagne, asserted at the time that the investment would “build future pandemic preparedness” and help “to grow Canada’s life science ecosystem as an engine for our economic recovery.” More recently, in 2022, the company has announced a few new clients – Takeda, Opus Genetics and the US Department of Defense.
According to National Resilience’s executives, the company’s ambitions apparently go far beyond manufacturing RNA and viruses. For instance, Resilience CEO Rahul Singhvi has claimed that the company is seeking to build “the world’s most advanced biopharmaceutical manufacturing ecosystem.” Yet, Singhvi has declined to offer much in the way of specifics when it comes to exactly how the company plans to become the planet’s most elite biomanufacturing company.
In an interview with The San Francisco Business Times, Singhvi states that Resilience is looking to fill its massive manufacturing plants with “technologies and people that can set and apply new standards for manufacturing cell therapies and gene therapies as well as RNA-based treatments.” Prior to Resilience, Singhvi was CEO of NovaVax and an operating partner at Flagship Pioneering, which played a major role in the creation and rise of Moderna.
Singhvi has further insisted that National Resilience is “not a therapeutics company, not a contractor and not a tools company” and instead aims “to boost production using the new therapeutic modalities” such as RNA-based treatments, which have become normalized in the COVID-19 era. Whereas contract manufacturers “are like kitchens, with pots and pans ready for any recipe,” “what we’re trying to do is fix the recipes,” Singhvi has explained. One member of Resilience’s board of directors, former FDA Commissioner and Pfizer Board member Scott Gottlieb, has described the company as seeking to act as the equivalent of Amazon Web Services for the biotechnology industry.
Essentially, Resilience bills itself as offering solutions that will allow “futuristic” medicines, including mRNA vaccines, to be produced more quickly and more efficiently, with the apparent goal of monopolizing certain parts of the biomanufacturing process. It also appears poised to become the manufacturer of choice for mRNA vaccines and experimental therapeutics in the event of a future pandemic, which some public health “philanthropists” like Bill Gates have said is imminent.
Perhaps the company’s most noteworthy ambition relates to their claims that they support clients through the government regulatory process. Given the company’s emphasis on speedy mass production of experimental gene therapies, its stated intention of getting the “futuristic” medical products it manufactures to market as quickly as possible seems at odds with the slower, traditional regulatory processes. Indeed, one could easily argue that the approvals of mRNA vaccines for the first time in human history during the COVID-19 crisis were only possible because of the major relaxing of regulatory procedurse and safety testing due to the perceived urgency of the situation.
Resilience seems intent on seeing that phenomenon repeat itself. As previously mentioned, the company claims to allow for the setting and application of “new standards for manufacturing cell therapies and gene therapies” and also says it plans to become a “technology-aggregating standards bearer that helps therapies come to market more efficiently.” It previously offered on its website “regulatory support” and “strategy consulting” to clients, suggesting that it would seek to mediate between clients and government regulators in order to fulfill its goal of having the products it manufactures taken to market more quickly. In addition, upon launch, the company claimed it planned to obtain unspecified “regulatory capabilities.” If so, it is certainly notable that former top Food and Drug Administration (FDA) officials are either on the company’s board or, as will be noted shortly, played a major role in the company’s creation.
The People Behind Resilience
Resilience was co-founded by Biotech venture capitalist Robert Nelsen, who is known for listening “to science’s earliest whispers, even when data are too early for just about anyone else.” Nelsen was one of the earliest investors in Illumina, a California-based gene-sequencing hardware and software giant that is believed to currently dominate the field of genomics. As mentioned in a previous Unlimited Hangout investigation, Illumina is closely tied to the DARPA-equivalent of the Wellcome Trust known as Wellcome Leap, which is also focused on “futuristic” and transhumanist “medicines.” Nelsen is now chairman of National Resilience’s board, which is a “Who’s Who” of big players from the US National Security State, Big Pharma and Pharma-related “philanthropy.”
Bob Nelsen of ARCH Venture Partners, Source: ARCH Venture Partners
However, while Nelsen has been given much of the credit for creating Resilience, he revealed in one interview that the idea for the company had actually come from someone else – Luciana Borio. In July of last year, Nelsen revealed that it was while talking to Borio about “her work running pandemic preparedness on the NSC [National Security Council]” that had “helped lead to the launch of Nelsen’s $800 million biologics manufacturing startup Resilience.”
At the time of their conversation, Borio was the vice president of In-Q-tel, the venture capital arm of the CIA that has been used since its creation in the early 2000s to found a number of companies, many of which act as Agency fronts. Prior to In-Q-Tel, she served as director for medical and biodefense preparedness at the National Security Council during the Trump administration and had previously been the acting chief scientist at the FDA from 2015 to 2017.
Borio is currently a senior fellow for global health at the Council on Foreign Relations, a consultant to Goldman Sachs, a member of the Bill Gates-funded vaccine alliance CEPI, and a partner at Nelsen’s venture capital firm ARCH Venture Partners, which funds Resilience. Nelsen’s ARCH previously funded Nanosys, the company of the controversial scientist Charles Lieber. Around the time of her conversation with Nelsen that led to Resilience’s creation, Borio was co-writing a policy paper for the Johns Hopkins Center for Health Security that recommended linking COVID-19 vaccination status with food stamp programs and rent assistance as a possible means of coercing certain populations to take the experimental vaccine.
Borio is hardly Resilience’s only In-Q-Tel connection, as the CEO of In-Q-Tel, Chris Darby, sits on the company’s board of directors. Darby is also on the board of directors of the CIA Officers Memorial Foundation. Darby was also recently a member of the National Security Commission on Artificial Intelligence (NSCAI), where members of the military, intelligence community and Silicon Valley’s top firms argued for the need to reduce the use of “legacy systems” in favor of AI-focused alternatives as a national security imperative. Among those “legacy systems” identified by the NSCAI were in-person doctor visits and even receiving medical care from a human doctor, as opposed to an AI “doctor.” The NSCAI also argued for the removal of “regulatory barriers” that prevent these new technologies from replacing “legacy systems.”
Resilience Board Member Drew Oetting, Source: 8VC
Another notable board member, in discussing Resilience’s intelligence ties, is Drew Oetting. Oetting works for Cerberus Capital Management, the firm headed by Steve Feinberg who previously led the President’s Intelligence Advisory Board under the Trump administration. Cerberus is notably the parent company of DynCorp, a controversial US national security contractor tied to numerous scandals, including scandals related to sex trafficking in conflict zones. Oetting is also part of the CIA-linked Thorn NGO ostensibly focused on tackling child trafficking that was the subject of a previous Unlimited Hangout investigation.
Oetting is also the co-founder of 8VC, a venture capital firm that is one of the main investors in Resilience. 8VC’s other co-founder is Joe Lonsdale and Oetting “started his career” as Lonsdale’s chief of staff. Lonsdale is the co-founder, alongside Peter Thiel and Alex Karp, of Palantir, a CIA front company and intelligence contractor that is the successor to DARPA’s controversial Total Information Awareness (TIA) mass surveillance and data-mining program. In addition, Oetting previously worked for Bill Gates’ investment fund.
Also worth noting is the presence of Joseph Robert Kerrey, former US Senator for Nebraska and a former member of the conflict-of-interest-ridden 9/11 Commission, on Resilience’s board. Kerrey is currently managing director of Allen & Co., a New York investment banking firm which has hosted an annual “summer camp for billionaires” since 1983. Allen & Co. has long been a major player in networks where organized crime and intelligence intersect, and is mentioned repeatedly throughout my upcoming book One Nation Under Blackmail. For instance, Charles and Herbert Allen, who ran the firm for decades, had considerable business dealings with organized crime kingpins and frontmen for notorious gangsters like Meyer Lansky, particularly in the Bahamas. They were also business partners of Leslie Wexner’s mentors A. Alfred Taubman and Max Fisher as well as associates of Earl Brian, one of the architects of the PROMIS software scandal – which saw organized crime and intelligence networks cooperate to steal and then compromise the PROMIS software for blackmail and clandestine intelligence-gathering purposes. Allen & Co. was a major investor in Brian’s business interests in the technology industry that Brian used in attempts to bankrupt the developers of PROMIS, Inslaw Inc. and to market versions of PROMIS that had been compromised first by Israeli intelligence and, later, the CIA.
In addition to these intelligence-linked individuals, the rest of Resilience’s board includes the former CEO of the Bill & Melinda Gates Foundation, Susan Desmond-Hellmann; former FDA Commissioner and Pfizer board member, Scott Gottlieb; two former executives at Johnson & Johnson; former president and CEO of Teva Pharmaceuticals North American branch, George Barrett; CalTech professor and board member of Alphabet (i.e. Google) and Illumina, Frances Arnold; former executive at Genentech and Merck, Patrick Yang; and Resilience CEO Rahul Singhvi.
To Boost or Not to Boost
It is certainly telling that the normally publicity hungry Moderna has said so little about its partnership with Resilience and that Resilience, despite its ambitious plans, has also avoided the media limelight. Considering Moderna’s history and Resilience’s connections, there may be more to this partnership that meets the eye and concerned members of the public would do well to keep a very close eye on Resilience, its partnerships, and the products it is manufacturing.
Given that we now live in a world where government regulatory decisions on the approval of medicines are increasingly influenced by corporate press releases and normal regulatory procedures have fallen by the wayside for being too “slow,” there is likely to be little scrutiny of the genetic material that Resilience produces for the “medicines of tomorrow.” This seems to be already true for Moderna’s recently retooled COVID-19 vaccine, as there has been no independent examination of the new genetic sequence of mRNA used in the Omicron-specific vaccine candidate or its effects on the human body in the short, medium or long term. For those who are skeptical of the outsized role that intelligence-linked companies are playing in the attempted technological “revolution” in the medical field, it is best to consider Resilience’s role in the upcoming fall vaccination campaign and in future pandemic and public health scenarios before trying its “futuristic” products.
Whitney Webb has been a professional writer, researcher and journalist since 2016. She has written for several websites and, from 2017 to 2020, was a staff writer and senior investigative reporter for Mint Press News. She currently writes for The Last American Vagabond.
WHO Renews Push for Global Pandemic Treaty, as World Bank Creates $1 Billion Fund for Vaccine Passports
By Michael Nevradakis, Ph.D. | The Defender | August 9, 2022
The World Health Organization (WHO) is moving ahead with plans to enact a new or revised international pandemic preparedness treaty, despite encountering setbacks earlier this summer after dozens of countries, primarily outside the Western world, objected to the plan.
A majority of WHO member states on July 21, during a meeting of WHO’s Intergovernmental Negotiating Body (INB), agreed to pursue a legally binding pandemic instrument that will contain “both legally binding as well as non-legally binding elements.”
STAT News described the agreement, which would create a new global framework for responding to pandemics, as “the most transformative global health call to action since [the] WHO itself was formed as the first specialized United Nations agency in 1948.”
Meanwhile, the World Economic Forum, African Union and World Bank — which created a $1 billion fund for “disease surveillance” and “support against the current as well as future pandemics” — are developing their own pandemic response mechanisms, including new cross-country vaccine passport frameworks.
WHO’s ‘pandemic treaty’: what’s been proposed and what would it mean?
Ongoing talks to formulate a new or revised “pandemic treaty” are building on the existing international framework for global pandemic response, the WHO’s International Health Regulations (IHR), considered a binding instrument of international law.
On Dec. 1, 2021, in response to calls from various governments for a “strengthened global pandemic strategy” and signaling the urgency with which these entities are acting, the WHO formally launched the process of creating a new treaty or amending the IHR, during Special Session — only the second in the organization’s history.
During the meeting, held May 10-11, WHO’s 194 member countries unanimously agreed to launch the process, which previously had been discussed only informally.
The member countries agreed to:
“Kickstart a global process to draft and negotiate a convention, agreement or other international instrument under the Constitution of the World Health Organization to strengthen pandemic prevention, preparedness and response.”
The IHR, a relatively recent development, were first enacted in 2005, in the aftermath of SARS-CoV-1.
The IHR legal framework is one of only two binding treaties the WHO has achieved since its inception, the other being the Framework Convention on Tobacco Control.
The IHR framework already allows the WHO director-general to declare a public health emergency in any country, without the consent of that country’s government, though the framework requires the two sides to first attempt to reach an agreement.
The proposals for a new or revised pandemic treaty, put forth at the special ministerial session of the WHO in May, would “somewhat” strengthen the WHO’s pandemic-related powers, including establishing a “Compliance Committee” that would issue advisory recommendations for states.
However, according to the Daily Sceptic, while the IHR is already legally binding, the amendments proposed in May would not strengthen existing legal obligations or requirements:
“The existing treaty regulations, like all (or most) international law, do not actually compel states to do anything other than talk to the WHO and listen to it, and neither do they specify sanctions for non-compliance; almost all their output is advice.
“The proposed amendments don’t alter that. They don’t allow the WHO unilaterally to impose legally binding measures on or within countries.”
The Daily Sceptic noted one of the risks stemming from the negotiations for a new or updated treaty include the potential codification of “the new lockdown orthodoxy for future pandemics,” which would “replace the sound, science-based, pre-COVID recommendations” previously in place.
According to Dr. Joseph Mercola, such a treaty would grant the WHO “absolute power over global biosecurity, such as the power to implement digital identities/vaccine passports, mandatory vaccinations, travel restrictions, standardized medical care and more.”
Mercola also questioned a “one-size-fits-all approach to pandemic response,” pointing out that “pandemic threats are not identical in all parts of the world. In his view, he said, “the WHO is not qualified to make global health decisions.”
Similar concerns contributed at least in part to opposition against the proposals presented at the special ministerial session, during which a bloc of mostly non-Western countries, including China, India, Russia and 47 African nations, prevented an agreement from being finalized.
Will opposition fade away?
Although no final agreement was achieved at the May meeting, consensus was reached to organize a new special ministerial session of the WHO later this year, possibly after the WHO’s World Health Assembly, scheduled for Nov. 29 through Dec. 1, Reuters reported.
Mxolisi Nkosi, South Africa’s ambassador to the UN, told the WHO’s annual ministerial assembly the new special session would “consider the benefits for such a convention, agreement or other international instrument.”
Nkosi added:
“Probably the most important lesson COVID-19 has taught us is the need for stronger and more agile collective defences against health threats as well as for building resilience to address future potential pandemics.
“A new pandemic treaty is central to this.”
At the time, the U.K.’s ambassador to the UN, Simon Manley, addressing the lack of an immediate agreement and the consensus to hold a new meeting, tweeted “negotiations may take time, but this is a historic step towards global health security.”
The INB, at its meeting held in Geneva July 18-21, also agreed with this view, reaching a consensus that its members will work on finalizing a new legally binding international pandemic agreement by May 2024.
As part of this process, the INB will meet again in December and will deliver a progress report to the 76th World Health Assembly of the WHO in 2023.
According to the WHO, “Any new agreement, if any when agreed by Member States, is drafted and negotiated by governments themselves, [which] will take any action in line with their sovereignty.”
The WHO further claims that “governments themselves will determine actions under the accord while considering their own national laws and regulations.”
The Biden administration expressed broad support for a new or updated pandemic treaty, with the U.S. heading previous negotiations on this issue, along with the European Commission, via its president Ursula von der Leyen, who, as previously reported by The Defender, is also a strong proponent of vaccine passports and mandatory COVID-19 vaccination.
An analysis by the Alliance for Natural Health International speculated that any final agreement may simply strengthen the existing IHR or, alternatively, may involve an amendment to the WHO’s constitution — or both.
Just two days after the July 21 INB agreement, Tedros Adhanom Ghebreyesus, the WHO’s director-general, tweeted:
“I’m pleased that alongside the process of negotiating a new [international] accord on pandemic preparedness & response, WHO’s Member States are also considering targeted amendments to the [IHR], incl. ways to improve the process for declaring a [public health emergency of international concern, or PHEIC].”
In the same Twitter thread, he also declared the ongoing monkeypox outbreak “a public health emergency of international concern,” one “that is concentrated among men who have sex with men, especially those with multiple sexual partners.”
Notably, the WHO director-general overruled an expert panel that was divided over whether to classify the outbreak as a global public health emergency.
With this declaration, three “global health emergencies” are now in place, as determined by the WHO: COVID-19, monkeypox and polio.
Busy summer for vaccine passport proposals
While the WHO and global governments weigh plans for an updated or new pandemic treaty, other organizations are moving forward on vaccine passport technologies and partnerships.
On July 8, the Organisation for Economic Cooperation and Development (OECD), composed of many of the world’s industrialized nations, announced it would promote the unification of the different vaccine passport systems currently in use around the world.
Thirty-six countries and international organizations participated in a July meeting with the goal of “creating a multilateral framework for establishing a global vaccine passport regime,” according to Nick Corbishley of Naked Capitalism.
The development is a continuation of efforts involving the WHO to harmonize global vaccine passport regimes.
In February, the WHO selected Germany’s T-Systems as an “industry partner to develop the vaccination validation service,” which would enable “vaccination certificates to be checked across national borders.”
T-Systems, an arm of Deutsche Telekom, was previously instrumental in developing the interoperability of vaccine passport systems in Europe.
Also in July, 21 African governments “quietly embraced” a vaccine passport system, which in turn would also be interlinked with other such systems globally.
On July 8, which is also Africa Integration Day, the African Union and the Africa Centers for Disease Control launched a digital vaccine passport valid throughout the African Union, describing it as “the e-health backbone” of Africa’s “new health order.”
This follows the development in 2021, of the Trusted Travel platform, now required by several African countries, including Ethiopia, Kenya, Togo and Zimbabwe, and air carriers such as EgyptAir, Ethiopian Airlines and Kenya Airways, for both inbound and outbound travel.
Beyond Africa, Indonesia, which currently holds the rotating presidency of the G20, is conducting “pilot projects” that would bring about the interoperability of the various digital vaccine passport systems currently in use globally. The project is expected to be completed by November, in time for the G20 Leaders’ Summit.
Naked Capitalism highlighted the role of South African company Cassava Fintech in the efforts to develop an interoperable vaccine passport for all of Africa.
A subsidiary of African telecommunication company Econet, Cassava initially developed the “Sasail” app, which the company described as Africa’s first “global super app” that combines “social payments” with the ability to send and receive money and pay bills, chat with others and play games.
Cassava and Econet entered into a strategic partnership with Mastercard, “to advance digital inclusion across Africa and collaborate on a range of initiatives, including expansion of the Africa CDC TravelPass.”
As previously reported by The Defender, Mastercard supports the Good Health Pass vaccine passport initiative that is also backed by the ID2020 alliance and endorsed by embattled former U.K. prime minister Tony Blair.
Mastercard has also promoted technology that can be embedded into the DO Card, a credit/debit card that keeps track of one’s “personal carbon allowance.”
ID2020, founded in 2016, claims to support “ethical, privacy-protecting approaches to digital ID.” Its founding partners include Microsoft, the Rockefeller Foundation, Accenture, GAVI-The Vaccine Alliance (itself a core partner of the WHO), UNICEF, the Bill & Melinda Gates Foundation and the World Bank.
Mastercard’s top two stockholders are Vanguard and BlackRock, which hold significant stakes in dozens of companies that supported the development of vaccine passports or implemented vaccine mandates for their employees. The two investment firms also hold large stakes in vaccine manufacturers, including Pfizer, Moderna and Johnson & Johnson.
Mastercard provides funding for the World Bank’s Identity for Development (ID4D) Program, which “focuses on promoting digital identification systems to improve development outcomes while maintaining trust and privacy.”
The Center for Human Rights and Global Justice at the New York School of Law recently described the ID4D program, which touts its alignment with the UN’s Sustainable Development Goals (SDGs) , as one which could pave the way to a “digital road to hell.”
According to the center, this would occur through the prioritization of “economic identity” and the use of an infrastructure that has “been linked to severe and large-scale human rights violations” in several countries.
Mastercard is also active in Africa through its joint initiative with another fintech (financial technology) company, Paycode, to “increase access to financial services and government assistance for remote communities across Africa” via a biometric identity system containing the data of 30 million individuals.
World Bank, WHO promote ‘pandemic preparedness’ and vaccine passports
The World Bank in late June announced the creation of a fund that will “finance investments in strengthening the fight against pandemics” and “support prevention, preparedness and response … with a focus on low- and middle-income countries.”
The fund was developed under the lead of the U.S., Italy and current G20 president Indonesia, “with broad support from the G20,” and will be active later this year.
It will provide more than $1 billion in funding for areas such as “disease surveillance” and “support against the current as well as future pandemics.”
The WHO is also a “stakeholder” in the project and will provide “technical expertise,” according to WHO’s director-general.
The agreement follows a 2019 strategic partnership between the UN and the World Economic Forum, to “accelerate” the implementation of the UN’s 2030 Agenda for Sustainable Development and its SDGs.
Although the agreement has recently circulated on social media, it was announced in June 2019, prior to the COVID-19 pandemic. It encompasses six areas of focus, including “health” and “digital cooperation.”
In terms of health, the agreement purports that it will “support countries [sic] achieve good health and well-being for all, within the context of the 2030 Agenda, focusing on key emerging global health threats that require stronger multistakeholder partnership and action.”
In turn, the “digital cooperation” promoted by the agreement will purportedly “meet the needs of the Fourth Industrial Revolution while seeking to advance global analysis, dialogue and standards for digital governance and digital inclusiveness.”
However, despite rhetoric preaching “inclusiveness,” individuals and entities that have refused to go along with applications such as vaccine passports have faced repercussions in their personal and professional lives.
Such was the example of a Canadian doctor who was fined $6,255 in June over her refusal to use the country’s ArriveCAN health information app — which is being investigated over privacy concerns — to enter the country.
Dr. Ann Gillies said she was fined when re-entering Canada after attending a conference in the U.S.
Andrew Bud, the CEO of biometric ID company iProove, a U.S. Department of Homeland Security contractor, described vaccine certificates as driving “the whole field of digital ID in the future,” adding they are “not just about COVID [but] about something even bigger” and that “once adopted for COVID [they] will be rapidly used for everything else.”
Michael Nevradakis, Ph.D., is an independent journalist and researcher based in Athens, Greece.
© 2022 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.
U.S. Declares Monkeypox Health Emergency, FDA Offers Vaccine to Some Kids Despite No Clinical Trials
By Megan Redshaw | The Defender | August 5, 2022
The U.S. declared monkeypox a public health emergency to raise awareness and allow for additional funding to fight the disease’s spread, U.S. Department of Health and Human Services Secretary Xavier Becerra said on Thursday.
“We’re prepared to take our response to the next level in addressing this virus, and we urge every American to take monkeypox seriously and to take responsibility to help us tackle this virus,” Becerra said.
Becerra said he also is considering a second declaration that would allow federal officials to expedite medical countermeasures — such as potential treatments and vaccines — designed to ensure drugs are safe and effective.
President Biden said in a tweet he remained “committed to our monkeypox response: ramping-up vaccine distribution, expanding testing, and educating at-risk communities.”
“That’s why today’s public health emergency declaration on the virus is critical to confronting this outbreak with the urgency it warrants,” Biden said.
The last time the U.S. declared a public health emergency was in January 2020, for COVID-19.
According to the Centers for Disease Control and Prevention (CDC), more than 7,100 cases of monkeypox have been reported in the U.S., including five cases in children.
Symptoms of monkeypox infection are usually mild and include fever, rash and swollen lymph nodes, and occasionally intense headache, back pain, muscle aches, lack of energy and skin eruptions that can cause painful lesions, scabs or crusts.
The virus is rarely fatal and no deaths have been reported in the U.S.
Monkeypox primarily is spread through skin-to-skin contact during sex and affects mostly gay and bisexual men, public health officials say, although the virus can affect anyone.
According to the CDC, about 98% of monkeypox patients who provided demographic information to clinics identified as men who have sex with men.
Public health emergency paves way for vaccine for kids
Now that the Biden administration has declared the monkeypox outbreak a public health emergency, the U.S. Food and Drug Administration (FDA) can move to issue an Emergency Use Authorization for the JYNNEOS vaccine for children under 18.
There are two vaccines that may be used “for the prevention” of monkeypox virus infection: JYNNEOS — also known as Imvamune or Imvanex — and ACAM2000, which is licensed by the FDA for use against smallpox and “made available for use against monkeypox under an Expanded Access Investigational New Drug application.”
The FDA told ABC News on Thursday that while the current monkeypox vaccine, JYNNEOS, is approved only for adults ages 18 and older, it will be available for kids on a case-by-case basis.
The JYNNEOS vaccine, delivered in a two-dose series, was not tested through clinical trials in children.
However, the FDA confirmed to ABC News that “numerous” children have been granted access to the vaccine through a special permission process, but declined to state exactly how many children have received the vaccine to date through this process.
“If a doctor decides a person under 18 was exposed to monkeypox and the benefit of the vaccine is greater than any potential risk, they can submit a request to the FDA,” ABC News reported.
According to the CDC, the “immune response” takes “14 days after the second dose of JYNNEOS and 4 weeks after the ACAM2000 dose for maximal development.”
The CDC website also states: “No data are available yet on the effectiveness of these vaccines in the current outbreak.”
According to the latest data from the Vaccine Adverse Event Reporting System (VAERS), between June 14 and July 21, 2022, 31 adverse events were reported following vaccination with JYNNEOS — manufactured by Bavarian Nordic.
The World Health Organization (WHO) declared monkeypox a global health emergency after more than 26,000 cases were reported across 87 countries.
A global emergency is the WHO’s highest level of alert, but the designation does not necessarily mean a disease is particularly transmissible or lethal.
The U.S. makes up 25% of confirmed cases globally although the U.K. was the first to alert the world to the outbreak in May after confirming several cases.
A monkeypox fictional simulation was held in March 2021
As The Defender reported in May, the Nuclear Threat Initiative, in conjunction with the Munich Security Conference, in March 2021 held a “tabletop exercise on reducing high-consequence biological threats,” involving an “unusual strain of monkeypox virus that first emerged in the fictional nation of Brinia and spread globally over 18 months.”
This is similar to “Event 201,” a “high-level pandemic exercise” organized by the Johns Hopkins Center for Health Security, along with the World Economic Forum and the Bill & Melinda Gates Foundation — just weeks before the COVID-19 outbreak — that mirrored what later followed with COVID-19 pandemic.
According to the Nuclear Threat Initiative, the monkeypox exercise, which was “developed in consultation with technical and policy experts,” brought together “19 senior leaders and experts from across Africa, the Americas, Asia, and Europe with decades of combined experience in public health, biotechnology industry, international security, and philanthropy.”
The fictional start date of the monkeypox pandemic in this exercise was May 15, 2022. The first European case of monkeypox was identified on May 7, 2022.
Key participants in the simulation included Johnson & Johnson and Janssen, the Bill & Melinda Gates Foundation, the Chinese Centers for Disease Control and Prevention, the Nuclear Threat Initiative, GAVI — the Vaccine Alliance, Merck and the WHO.
Several of the participants listed above also “participated” in Event 201.
Megan Redshaw is a staff attorney for Children’s Health Defense and a reporter for The Defender.
© 2022 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.
WHO Wants To Run the World?
By Paul Frijters, Gigi Foster, Michael Baker | Brownstone Institute | July 11, 2022
In Geneva in late May at the 75th meeting of the WHO’s decision-making body, the World Health Assembly (WHA), amendments to its International Health Regulations (IHRs) were debated and voted upon. If passed, they would grant the WHO the right to exert unconscionable pressure on countries to accept the WHO’s authority and health policy actions if the WHO decides that there is a public health threat that might spread beyond a country’s borders.
As Ramesh Thakur, the second man at the UN for years, noted, the amendments would mean “the rise of an international bureaucracy whose defining purpose, existence, powers and budgets will depend on outbreaks of pandemics, the more the better.”
This is the first clear instance of a globalist coup attempt. It would subvert national sovereignty worldwide by putting real power into the hands of an international group of bureaucrats. It has long been suspected that the authoritarian elites arisen during covid times would try to strengthen their positions by undermining nation states, and the this 75th jamboree is the first solid evidence of this being true.
What an opportunity then to see who is in the conspiring club. Who drafted the amendments? What was in them? Which individuals supported them or spoke out against them?
WHO were the conspirators?
The amendments on the table at the May WHA meeting had been transmitted to the WHO by the US Department of Health and Human Services on January 18, circulated by WHO to its member states (‘States Parties’) on January 20 and formally introduced to the WHA on April 12.
The proposals, according to an announcement on January 26, were co-sponsored by 19 countries plus the European Union. Even if some co-sponsors had little direct involvement in drafting them, they all would have approved in principle the overarching goal of tightening up the WHO’s authority over member states in the face of a public health event.
Loyce Pace, the HHS’s Assistant Secretary for Global Affairs – the leading US official nominally responsible for the proposed amendments – arrived at the Biden administration fresh from a stint as executive director of an advocacy organization called the Global Health Council.
That council receives funding from the Bill & Melinda Gates Foundation and its members include Eli Lilly, Merck, Pfizer, Abbott Labs, and Johnson & Johnson. You get the idea. Via one of the foxes-turned-chicken-guard, it appears the HHS ‘worked closely’ on these amendments with large pharmaceutical companies, who will be chomping at the bit for a more proactive (read: profitable) response to any public health emergency, real or imagined.
So the conspiring club consists primarily of the US government and its Western allies in lockstep with Big Pharma, and they are looking to undermine both the sovereignty of their own governments and that of other countries, presumably with the idea that the Western elites would do the running.
What was in them? A blizzard of acronyms and euphemisms
To understand what the US proposed at the WHA, we need first to understand how things have worked in the WHO to this point.
The IHRs in their current form have been in force as international law since June 2007. Among other things, they impose requirements on countries to detect, report and respond to ‘public health events of international concern,’ or PHEICs. The WHO Director-General consults with the state where a possible public health event has occurred, and within 48 hours they are meant to come to a mutual agreement on whether or not it actually is a PHEIC, whether or not it needs to be announced to the world as such, and what counter-measures, if any, should be taken. It’s essentially an early-warning system on major health crises. This is a good thing if it’s run by people you can trust and if it has checks and balances to rein in expansionary tendencies.
The proposed amendments would greatly strengthen the power of the WHO relative to this baseline, in a number of ways.
First, they lower the threshold for the WHO to declare a public health emergency by empowering its Regional Directors to declare a ‘public health event of regional concern’ (PHERC, italics ours) and for the WHO to put out a new thing called an ‘intermediate public health alert.’
Second, they permit the WHO to consider allegations about a public health event from non-official sources, meaning sources other than the government of the state concerned, and allow that government only 24 hours to confirm the allegations and a further 24 hours to accept the WHO’s offer of ‘collaboration.’
Collaboration is essentially a euphemism for on-site assessment by teams of WHO investigators, and concomitant pressure at the whim of WHO personnel to enact potentially far-reaching measures such as lockdowns, movement restrictions, school closures, consumption of medicines, administration of vaccines and any or all of the other social, economic, and health paraphernalia that we have come to associate with the covid circus.
Should the state’s government acceptance of the WHO’s ‘offer’ not be forthcoming, the WHO is empowered to disclose the information it has to the other 194 WHO countries, while continuing to pressure the state to yield to the WHO’s invitation to ‘collaborate.’ A non-collaborating country would risk becoming a pariah.
Third, the proposal includes a new Chapter IV, which would establish a ‘Compliance Committee’ consisting of six government-appointed experts from each WHO region tasked with permanently nosing around to ensure the member states are complying with IHR regulations.
There are more crossings-out of the existing IHR language and new language added in, but the flavour of what the US-led alliance is shooting for is a WHO that can unilaterally decide whether there is a problem and what to do about it, and can isolate countries that disagree.
Compliant WHO member states could act as a supporting cast in the isolation effort, through the distribution of their own health budgets and their ‘health-related’ policies, which would include travel and trade restrictions. The WHO would become a kind of command-and-control center for globalist agendas, pushing the produce of (Western) Big Pharma.
Why and how would this work?
We learned during covid times why it would make sense that the US and its allies are insisting on these amendments.
Lowering the bar for declaring a global (or regional) public health threat triggers a huge opportunity for Western pharmaceutical companies. As legal experts have observed: “WHO emergency declarations can trigger the fast-track development and subsequent global distribution and administration of unlicensed investigational diagnostics, therapeutics and vaccines.
This is done via the WHO’s Emergency Use Listing Procedure (EULP). The introduction of an ‘intermediate public health alert’ in particular will also further incentivise the pharmaceutical industry’s move to activate domestic fast-track emergency trial protocols as well as for advance purchase, production and stockpile agreements with governments before the existence of a concrete health threat to the world’s population has been detected, as is already the case under WHO’s EULP via the procedures developed for a ‘pre-public health emergency phase’.”
You can bet that the WHO ‘expert teams’ sent in to make on-the-ground assessments, under the banner of ‘collaboration’ with the host country experiencing the health event, will be chock-a-block with operatives from the CDC and who knows what other Western agencies, all poking around potentially sensitive facilities that a host government might justifiably claim a sovereign right to keep to itself. Likewise with the ‘Compliance Committee’ proposed by the US under the new Chapter IV of the IHRs: its government-appointed members have an open-ended brief, enshrined in international law, to be busybodies.
In layman’s terms, the WHO would be turned into an international thug, with its member states offered the role of backyard gang members.
As a bonus for Western elites, the proposals are a sneaky form of rewriting history. By cementing authority within an international organisation to determine the existence of public health crises and direct potentially draconian emergency responses, Western governments would get to enshrine and legitimise their own extreme responses to the covid outbreak, as we have pointed out previously. Their backsides would thereby be given some protection from legal challenges.
The refusniks: Developing countries
The proposals were pushed primarily by Western countries: the US was joined by Australia, the UK and the EU in arguing for passage. The resistance was led by developing countries who saw it as a colonialist ambush in which their ability to set policy and respond to health threats in a manner commensurate with their domestic situations would be overridden.
Brazil reportedly went so far as to threaten to withdraw from the WHO, and the African group of almost 50 countries, along with India, argued that the amendments were being rushed through without adequate consultation. Russia, China and Iran also objected.
Failure on the first try, but the US and its allies in the West will get more shots to push it through.
How do we expect them to do this? Well, when a proposal gets bogged down inside a giant bureaucratic machine like the WHO, the inevitable response is to set up committees to work in the background and circle back with a new set of proposals to be presented at a future meeting. True to form, a ‘working group’ and ‘expert committee’ are being assembled to accept member state proposals on IHR reform by the end of September this year. These will be ‘sifted through’ and reports will be prepared for review by the WHO’s executive board in January next year. The objective is to have a fresh set of proposals on the table when the WHA convenes for the 77th time in 2024.
Not all was lost
Salvaging something from the fact that the WHA failed to get a consensus around its biggest agenda item, the US and its allies got a small victory on the point of when they can try again – though in their desperation they needed to violate the IHRs’ own rules to accomplish it. Article 55 of the IHRs states unambiguously that a four-month notice period is required for any amendments.
In this instance, revised amendments were presented on May 24, the same day that the first lot were rejected. These were discussed, further amended on May 27 and then adopted on the same day. The approved amendments halve the two-year period for any (further) approved amendments to the IHRs to take effect. (The IHRs that came into force in 2007 were agreed to in 2005 – but under the new resolution, anything agreed to in 2024 would come into effect in 2025 rather than 2026.)
Yet, what was achieved in terms of fast-tracking the force of new amendments was lost in slow-tracking their implementation. Nations would have up to 12 months – double the previous suggestion of six months – to implement any IHR amendments that newly enter into force of law.
State of play
Where is all this going?
If the WHO takes the reins on decisions about what constitutes a health crisis, and can pressure every country into a one-size-fits-all set of responses that it, the WHO, also determines, that’s bad enough. But what about if its invitation to ‘collaborate’ with countries is backed up with teeth, such as sanctions against those who demur? And what about if it then broadens the definition of ‘public health’ by, for example, declaring that climate change falls under that definition? Or racism? Or discrimination against LBTQIA+ people? The possibilities thereby opened up for running the world are endless.
A global ‘health’ empire would bring huge harms to humanity, but a lot of power and money is pushing for it. Don’t think it can’t happen.
Paul Frijters is a Professor of Wellbeing Economics at the London School of Economics: from 2016 through November 2019 at the Center for Economic Performance, thereafter at the Department of Social Policy
NEJM: Global Warming Causes Stillbirths, Birth Defects, Infant Heart problems
Finally you can laugh a bit
By Igor Chudov | June 28, 2022
Okay, enough birth rate sadness, let’s lighten up a bit. We have a long road ahead of us, we cannot be sad all the time, so it is time to smile.
We have some climate change news.
Remember that a couple of days ago, I asked, why is the birth rate in Germany dropping? What is going on with a 23% drop in live births in Taiwan? Why are births dropping 10% in Switzerland this year? Why is the UKHSA vaccine surveillance report not reporting live births since February, for which it showed a 10% year-to-year drop in live births, and nothing since?
Fortunately, science has an answer for us. These baby problems have a known cause. It is climate change. Here’s an amazing article. It came out just in time for the birth rate scandal, which is obviously just a coincidence.
This article refers to a study, published in New England Journal of Medicine, a prestigious bellwether of medical science and a guide to all doctors worldwide.
The article explains that global warming may cause many problems in developing and unborn children. “All children are at risk”, says the study. Some of these problems are very familiar to us, and I am glad that scientists finally could attribute them to global warming.
Let me list them, coming verbatim from the NEJM article:
The article, further, admonishes physicians to be aware of the new medical consensus:
Protection of children’s health requires that health professionals understand the multiple harms to children from climate change
So if parents ask a doctor, why are their children having heart problems, neurological issues, etc, the doctor would be able to cite the NEJM article and explain how those problems are caused by climate change.
One of the two coauthors of this global warming article, Kari Nadeau, is a well-published scientist who also published an interesting study explaining why vaccine-induced immunity is better than natural immunity. That study was, purely coincidentally, financed by the Bill and Melinda Gates Foundation. It also contradicts everything that we know from practical experience, of course. What else did you expect?
Financing of such authors by the Bill and Melinda Gates Foundation, obviously, is nothing to worry about. I also wonder, how can Kari Nadeau be equally good at writing on matters of immune imprinting and immunology, as well as on totally unrelated matters of climate change? I am not sure.
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The Lancet Accused Of Sacrificing The Poor On Pollution
By Paul Homewood | Not A Lot Of People Know That | January 18, 2018
I have highlighted much of the mendacious nonsense coming out of the Lancet concerning climate change and pollution issues.
Now a hard hitting report by Mikko Paunio, a specialist in public health matters has destroyed both the credibility and integrity of two of the Lancet’s recent papers on pollution. … continue
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