IN THE previous instalments I explored the extraordinary hold Bill Gates has over global health policy and the spread of its influence right into the heart of British public health policy via the funding by the Bill and Melinda Gates Foundation (GF) of science businesses, foundations and public bodies through a complex web of interconnection and crossover of personnel.
This, however, is not the sum total of the GF’s reach into the world of British science and public health. It has been funding British university science departments, projects, and individuals for more than two decades. The topics involved include research into and manufacturing of vaccines.
No government-appointed science committee has influenced public health policy as much as Sage. Many of its members, who cross over with Independent Sage and Nervtag and are already somewhat compromised by connections to the GF-funded GlaxoSmithKline and Wellcome Foundation, are also employees of universities and colleges which have received massive GF grants and, in some cases, work in partnership with them. Three of Sage’s members, Professors Graham Medley, Andrew Rambaut and Matt Keeling, are individual recipients of grants from the GF.
Readers may remember the three modelling papers produced by Imperial College London (ICL), Warwick University and the London School of Tropical Hygiene and Medicine (LSHTM) which received considerable press attention at the end of March, and their dramatic simultaneous warnings of a ‘third’ Covid-19 wave and new lethal variants; cautioning (yet again) how this will put the NHS under stress. All recommended stricter lockdowns, Test and Trace and, tellingly, booster vaccines.
SPI-M-O had assigned each university a specific task: ICL’s was ‘Evaluating England’s Roadmap out of Lockdown’, Warwick’s to produce ‘Road Map Scenarios and Sensitivity’ and LSHTM’s to make an ‘Interim roadmap assessment: prior to Step 2’.
Promoting the ICL paper was none other than the multi-tasking Sage member Professor Neil Ferguson, co-founder and Principal Investigator of the Centre for Global Infectious Disease Analysis (MRC GIDA) at Imperial College, a centre that works closely with the GF, the Global Fund and Gavi, Vice Dean of the Faculty of Medicine, School of Public Health at ICL, a Director and Adviser at the World Health Organisation (WHO) and a recipient of cloud computing time from Microsoft and Amazon for Covid-19 modelling.
Warwick’s paper emphasised the ‘danger’ of new variants to an even greater degree than the ICL paper. It warned that ‘stringent methods’ would be needed to counteract them and that the current vaccination programme might not adequately contain them.
The paper produced by the LSHTM group was the most pessimistic of all. It warned that a ‘third wave’ and new variants would bring a high death toll. It also stressed the need for Test and Trace which, together with that other Sage recommendation, vaccine passports, is the new formula for digital slavery and a surveillance state.
How Ferguson, whose modelling methodologies and predictions had been so comprehensively discredited, was getting away with this repeat performance seemed baffling, but for the fact that as a key member of the SPI-M-O subgroup he had been able to commission the new modelling research as well as that of supportive colleagues at Warwick University and the LSHTM.
Curiously, several SPI-M-O members turn out to be affiliated to one or another of these three universities too and are the very same academics who wrote these modelling papers. Given that they have commissioned themselves and sit on the subgroup, no independent assessment or scrutiny of their work has taken place. This is the epitome of jobs for the boys and girls.
Here are the SPI-M-O members connected to ICL:
Professors Neil Ferguson (Sage), Stephen Brett, Nicholas Grassly, Steven Riley, Wendy Barclay (Sage) and Drs Marc Baguelin, Samir Bhatt and Tim Lucas. Ferguson and Baguelin contributed to the ICL paper.
Here are the SPI-M-O members who work at Warwick University:
Professor Matt Keeling and Drs Louise Dyson, Edward Hill, Michael Tildesley and Joe Hilton. Keeling, Dyson, Tildesley and Hill are four out of five authors of the Warwick paper.
The following SPI-M-O members are connected to the LSHTM:
Professors John Edmunds (Sage), Mark Jit, Graham Medley (Sage), Drs Nick Davies, Rosalind Eggo, Sebastian Funk, Thibaut Jombart, Petra Klepac, Adam Kurcharski, Rohini Mathur, Sam Clifford, Elizabeth Fearon, Gwen Knight and Bill Quilty. Edmunds, Jit and Davies are three out of four of the authors of the LSHTM paper.
The Deputy Chief Medical Officer, Professor Jonathan Van-Tam, is a member of both Sage and SPI-M-O.
It will surprise few readers to learn that ICL, Warwick University and the LSHTM, are historically heavily funded by the GF.
The GF made its first grant to ICL of $31.9million in 2000. ICL received a further $46.7million from the GF in 2006 to research tropical diseases. The GF granted ICL a total of $446,205 in 2019 for research into enteric and diarrhoeal diseases, technology solutions, malaria, and ‘Discovery and Translational Sciences’. In 2020 it gave ICL a total of $91.5million for studies into polio, tuberculosis, global health, technology solutions, malaria, HIV, Discovery and Translational Sciences and family planning.
Last January, Sage member Professor Sir Mark Walport was appointed chair of the Imperial College Academic Health Science Centre (AHSC) Strategic Partnership. His ICL colleagues Professor Robin Grimes and Dr David Halpern sit on Sage too. Professor Ferguson and two ICL colleagues, Professors Wendy Barclay and Peter Openshaw, are members of Nervtag as well.
Warwick University’s GF funding goes back to 2015. An initial grant of $20,000 from the GF rapidly increased to a current total of $8.3million. In 2017, the GF awarded Warwick University $3million to research disease modelling, and in 2020 $2.2million to study neglected tropical diseases.
Sage member Professor Yvonne Doyle works at the LSHTM as does Nervtag member Professor John Edmunds and Independent Sage member Professor Martin McKee. Professor Edmunds was recently a recipient of a grant worth £5million from UKRI, which collaborates with the GF, to study disease modelling in Africa.
The late Professor Val Curtis, a member of Independent Sage, also worked at the LSHTM.
Predictably, none of the recent modelling by this closed shop takes into account the economic damage, social disintegration or consequences of lockdown, or the neglect of non-Covid-19 diseases as a result of lockdown and social distancing policies. Yet all this is now extensively catalogued. The conflicts of interest and cross over with these government advisers and highly directed research in universities heavily funded by GF, which has one narrow vision global vaccination agenda, is alarming.
Even more alarming is that it is on this basis that an unaccountable and unelected body has effectively dictated Government policy and our lives this past year. Its controversially modelled predictions of worst-case scenarios, none of which to date have been borne out, have been useful for two things: terrifying the populace into submission and priming the government, and us, into further lockdowns next autumn and winter – and establish them as the ‘new normal’.
Whether the men and women named here are useful idiots for Gates, or self-servers without moral compass, such scientific narrow vision reflects very poorly on them and their institutions.
The tentacles of the GF are everywhere. In the final part of this series I will be looking at its funding of the Oxford Recovery trials, Cambridge Science Park, its interconnections with the AstraZeneca project, its funding of several other universities, and finally at its investment in Serco, one of the outsourcing companies behind the Test and Trace programme.
After rollout under emergency authorisation, manufacturers of covid-19 vaccines now have their sights on regulatory approval. But what’s the rush, asks Peter Doshi, and is just six months of data from now unblinded trials acceptable?
In April 2021, Pfizer and Moderna announced efficacy results at the six month mark from the phase III trials of their respective covid-19 vaccines.1 2
Pfizer CEO Albert Bourla said the company’s data “confirm the favourable efficacy and safety profile of our vaccine and position us to submit a Biologics License Application to the US FDA [Food and Drug Administration].”1 And on 7 May it formally initiated that application which, if successful, will earn the Pfizer-BioNTech product, BNT162b2, the distinction of becoming the first covid-19 vaccine approved by the FDA.
Because lest we forget, all covid-19 vaccines currently in use in the US are available under emergency access only.
(The situation is similar in Europe, where four covid-19 vaccines have been granted “conditional marketing authorisations,” a fast track mechanism that can be used in emergencies. These can be converted into standard “marketing authorisations” pending positive data after authorisation, but this has not yet happened for any covid-19 vaccine being administered.)
As hundreds of millions of people around the world get vaccinated, it may seem like wordsmithing to highlight the fact that none of the covid-19 vaccines in use are actually “approved.” Through an emergency access mechanism known as Emergency Use Authorisation (EUA), the products being rolled out still technically remain “investigational.”3 Factsheets distributed to vaccinees are clear: “There is no FDA approved vaccine to prevent covid-19.”4
The approval-authorisation distinction is often misunderstood by the media,5 even in the scientific press. But it was the focus of much discussion back in September 2020. With large phase III trials by Pfizer and Moderna well under way, and the November US presidential election looming, many worried about political pressure resulting in the rollout of an unsafe or ineffective vaccine.6
The FDA had already come under fire, accused of bending to the White House in granting EUAs for two covid-19 treatments, hydroxychloroquine and convalescent plasma. But those fears largely dissipated when the FDA published a guidance document in early October outlining its expectations for the EUA. According to the document, at least half of a trial’s participants would need to be followed for at least two months.7 This alone made it all but certain no vaccine could cross the line before the election.
The FDA also said it would want a vaccine at least 50% effective (with a confidence interval reaching no lower than 30%) against a primary endpoint of preventing SARS-CoV-2 infection or covid-19 disease of any severity8—parameters it had previously defined as necessary for approval. Even for non-clinical parameters, like manufacturing quality, the FDA characterised its expectations for the EUA as “very similar” to those for approval.3
Six months: enough?
One key difference between EUA and approval (also called “licensure,” and which for vaccines is known as a BLA (Biologics License Application)) was the expected length of follow-up of trial participants. Unlike its clear articulation of two months for an EUA, the FDA has not committed to a clear minimum for approval.
Cody Meissner, a professor of paediatrics at Tufts University and member of the FDA’s advisory committee, was curious. “Is it possible to predict or estimate when conditions of safety and efficacy might be satisfied for BLA?” Meissner asked at the agency’s 10 December meeting which had been convened to consider the FDA’s first emergency authorisation for the Pfizer vaccine.
The FDA’s Doran Fink responded: “I couldn’t predict, but I will say that we typically ask for at least six months of follow-up in a substantial number of clinical trial participants to constitute a safety database that would support licensure.”
An approval based on six months of data would represent one of the fastest for a novel vaccine in FDA history. Among the six “first in disease” vaccines approved by the FDA since 2006, pre-licensure pivotal trials were a median of 23 months in duration, according to a recent analysis.9
Six months also seems substantially shorter than previously conceptualised expectations. A World Health Organization expert group on covid-19 vaccines (which included FDA regulators) in August 2020 called for follow-up “until at least month 12, or until an effective vaccine is deployed locally.”10 Another group, composed of industry and academic authors, similarly wrote in October 2020: “we recommend longer term follow-up of all participants … for at least a year after randomisation.”11
On paper, the phase III studies by Pfizer, Moderna, and Janssen are all of two years’ duration. But the FDA’s official position on minimum follow-up before licensure is unclear at best.
In its formal guidance last June, the agency said that for licensure applications, it wanted participants followed for covid-19 outcomes for “as long as feasible, ideally at least one to two years”12 after the first injection. But the same document states that safety assessments for “serious and other medically attended adverse events” should be studied “for at least six months after completion of all study vaccinations. Longer safety monitoring may be warranted for certain vaccine platforms.”
Asked to clarify whether its guidance is asking for follow-up of at least six months or one year, a spokesperson told The BMJ: “We do not have any further information beyond what is in the guidance document.”
Unblinded and without a control group—what about safety?
Duration of protection is not the only question that longer, placebo controlled trials can address. They also address vaccine safety.
“Very often, it’s the fact that we have that placebo controlled follow-up over time, that gives us the ability to say that the vaccine didn’t cause something at a longer period of time after vaccination,” the FDA’s Philip Krause explained last December.13
Yet there is a gap—currently of unknown size but growing—between any expectation of blinded placebo controlled data, and the reality that within weeks of the vaccines receiving an EUA the unblinding of trials commenced as placebo recipients were offered the chance to get vaccinated.
Steven Goodman, associate dean of clinical and translational research at Stanford University, told the FDA in an invited presentation last December, “Once a vaccine is made widely available and encouraged, maintaining a double blinded control group for more than a nominal period is no longer in the investigator’s (or regulator’s) control and undue pressure to do so may undermine the entire vaccine testing enterprise.”14
Goodman’s recommendation was to rapidly convert the trials into crossover studies, enabling those on placebo to get vaccinated (and vice versa), while maintaining the blind. The companies challenged the feasibility, calling it “onerous,” and a crossover never occurred.15
The BMJ asked Moderna, Pfizer, and Janssen (Johnson and Johnson) what proportion of trial participants were now formally unblinded, and how many originally allocated to placebo have now received a vaccine. Pfizer declined to say, but Moderna announced that “as of April 13, all placebo participants have been offered the Moderna covid-19 vaccine and 98% of those have received the vaccine.”2 In other words, the trial is unblinded, and the placebo group no longer exists.
Janssen told The BMJ: “We do not have specific figures on how many of our study participants have received a vaccine at this time.” But the company confirmed it was implementing an amended protocol across all countries to unblind all participants in its two phase III trials, the earlier of which passed the median of two month follow-up mark in January.
How the FDA will weigh the loss of blinding and placebo controlled follow-up is unclear, but just months ago the agency said these trial properties were vital.
“Continuation of placebo controlled follow-up after EUA will be important and may actually be critical to ensure that additional safety and effectiveness data are accrued to support submission of a licensure application as soon as possible following an EUA. … Once a decision is made to unblind an ongoing placebo controlled trial, that decision cannot be walked back. And that controlled follow-up is lost forever,” the FDA said last October.3
At its next advisory committee in December 2020, the FDA reiterated the importance of the placebo group: “Placebo controlled follow-up can be very important in showing that whatever happened in the vaccine group also happened in the placebo group. Because that’s our best way of knowing.”13
What’s the rush?
The US’s “Operation Warp Speed” delivered on its promise to get a novel vaccine into arms in record time (box). Millions of doses of vaccines are being administered daily across the US, making clear that lack of FDA approval is no barrier to access. So just what benefit is there in seeking, and granting, a BLA?
The BMJ asked the manufacturers why they were seeking a BLA. Moderna did not respond and Janssen only confirmed it intended to apply for a BLA “later in 2021.” Pfizer likewise did not answer but instead quoted an FDA webpage on medical devices, which stated: “Sponsors of EUA products are encouraged to follow up the EUA with a pre-market submission so that it can remain on the market once the EUA is no longer in effect.”16 But EUAs have no built-in expiry date—in fact, 14 EUAs for Zika diagnostic tests remain active despite the public health emergency expiring in 2017.17
Cody Meissner told The BMJ he saw some distinct advantages of a BLA over EUA. An approved vaccine, for one, would provide “an element of assurance,” increasing public trust in the vaccines, particularly for those currently sitting on the fence. It would also pave the way for claims of vaccine injury to be routed through a more established compensation programme, and for adding the vaccine to government funded schemes to reach children in financial need.18 Finally, it may affect the potential for vaccine mandates: “It is unlikely these vaccines will be mandated while an EUA is in place. Remember that currently these vaccines are still considered experimental.”
While still under EUA, an increasing number of educational and other institutions have already mandated vaccines, but debates over the legality of these actions has hinged on the distinction between authorisation and approval.19
But approving a vaccine in order to legally support mandates or convince people of its safety arguably puts the cart before the horse. Meissner responded that a BLA would not be issued until the FDA is convinced of the short and long term safety of these vaccines.
No new biodistribution studies for covid-19 vaccines
Officials have consistently emphasised that despite shaving years off traditional timelines for producing vaccines, no compromises in the process were taken.20 However one type of study, tracking the distribution of a vaccine once injected in the body, was not conducted using any of the three vaccines currently authorised in the US.
Such biodistribution studies are a standard element of drug safety testing but “are usually not required for vaccines,” according to European Medicines Agency policy,21 which adds, “However, such studies might be applicable when new delivery systems are employed or when the vaccine contains novel adjuvants or excipients.”
In the case of covid-19 vaccines, regulators accepted biodistribution data from past studies performed with related, mostly unapproved compounds that use the same platform technology.22232425
Janssen told The BMJ its covid-19 vaccine leverages the same technology as its Ebola vaccine, which received licensure last June. “Our confidence in our adenovirus vector Ad26 is based on our experience with this vector.”
Pfizer and Moderna did not respond to The BMJ’s questions regarding why no biodistribution studies were conducted on their novel mRNA products, and none of the companies, nor the FDA, would say whether new biodistribution studies will be required prior to licensure.
Footnotes
Competing interests PD gave a public statement at the October and December FDA advisory committee meetings mentioned in this article (transcripts here: https://faculty.rx.umaryland.edu/pdoshi/#publications), and may continue to engage in public input towards regulatory decision making around covid-19 vaccines. PD is also employed by a university that has mandated covid-19 vaccines for all faculty, staff, and students. The views and opinions expressed here are those of the author and do not necessarily reflect official policy or position of the University of Maryland.
US Food and Drug Administration. 161st Vaccines and Related Biological Products Advisory Committee (VRBPAC) meeting. 2020. https://www.fda.gov/media/143982/download
US Food and Drug Administration. Development, authorization and licensure of vaccines to prevent COVID-19. October 6, 2020. https://www.fda.gov/media/142723/download
. An overview of vaccine development, approval, and regulation, with implications for covid-19. Health Aff (Millwood)2021;40:25–32.doi:10.1377/hlthaff.2020.01620pmid:33211535
US Food and Drug Administration. 162nd Vaccines and Related Biological Products Advisory Committee (VRBPAC) meeting. 2020. https://www.fda.gov/media/144859/download
Goodman S. Considerations for placebo-controlled trial design if an unlicensed vaccine becomes available. Vaccines and related biological products advisory committee. 2020. https://www.fda.gov/media/144354/download
. Emergency use authorizations (EUAs) versus FDA approval: implications for covid-19 and public health. Am J Public Health2021;111:1065–9.doi:10.2105/AJPH.2021.306273pmid:33950730
“The pandemic represents a rare but narrow window of opportunity to reflect, reimagine, and reset our world to create a healthier, more equitable, and more prosperous future” — Klaus Schwab, WEF
Say it’s 2014 and you’ve had this idea for a technocratic Great Reset of the world economy for some time now, but it only works if the entire planet is rocked by a pandemic. How do you go about selling your idea?
If you are World Economic Forum (WEF) Founder Klaus Schwab, you attempt to sell your vision of a global Utopia via a Great Reset of the world order in three simple steps:
Announce your intention to revamp every aspect of society with global governance, and keep repeating that message
When your message isn’t getting through, simulate fake pandemic scenarios that show why the world needs a great reset
If the fake pandemic scenarios aren’t persuasive enough, wait a couple months for a real global crisis to occur, and repeat step one
It took Schwab and the Davos elite about six years to watch their great reset ideology grow from a tiny Swiss seed in 2014 to a European super-flower pollinating the entire globe in 2020.
The so-called “Great Reset” promises to build “a more secure, more equal, and more stable world” if everyone on the planet agrees to “act jointly and swiftly to revamp all aspects of our societies and economies, from education to social contracts and working conditions.”
But it wouldn’t have been possible to contemplate materializing such an all-encompassing plan for a new world order without a global crisis, be it manufactured or of unfortunate happenstance, that shocked society to its core.
“In the end, the outcome was tragic: the most catastrophic pandemic in history with hundreds of millions of deaths, economic collapse and societal upheaval” — Clade X pandemic simulation (May, 2018)
So, in May, 2018, the WEF partnered with Johns Hopkins to simulate a fictitious pandemic — dubbed “Clade X” — to see how prepared the world be if ever faced with such a crisis.
A little over a year later, the WEF once again teamed-up with Johns Hopkins, along with the Bill and Melinda Gates Foundation, to stage another pandemic exercise called Event 201 in October, 2019.
Both simulations concluded that the world wasn’t prepared for a global pandemic.
And a few short months following the conclusion of Event 201, which specifically simulated a coronavirus outbreak, the World Health Organization (WHO) officially declared that the coronavirus had reached pandemic status on March 11, 2020.
“The next severe pandemic will not only cause great illness and loss of life but could also trigger major cascading economic and societal consequences that could contribute greatly to global impact and suffering” — Event 201 pandemic simulation (October, 2019)
Since then, just about every scenario covered in the Clade X and Event 201 simulations has come into play, including:
Governments implementing lockdowns worldwide
The collapse of many industries
Growing mistrust between governments and citizens
A greater adoption of biometric surveillance technologies
Social media censorship in the name of combating misinformation
The desire to flood communication channels with “authoritative” sources
A global lack of personal protective equipment
The breakdown of international supply chains
Mass unemployment
Rioting in the streets
And a whole lot more!
After the nightmare scenarios had fully materialized by mid-2020, the WEF founder declared “now is the time for a “Great Reset”.
Was it excellent forecasting, planning, and modeling on the part of the WEF and partners that Clade X and Event 201 turned out to be so prophetic, or was there something more to it?
Timeline
Below is a condensed timeline of events that tracks the Great Reset agenda that went from just a “hope” in 2014 to a globalist ideology touted by royalty, the media, and heads of state the world-over in 2020.
2014-2017: Klaus Schwab calls for Great Reset and WEF repeats message
Ahead of the 2014 WEF meeting in Davos, Switzerland, Schwab announced that he hoped the WEF would push the reset button on the global economy.
The WEF would go on to repeat that message for years.
Between 2014 and 2017, the WEF called to reshape, restart, reboot, and reset the global order every single year, each aimed at solving various “crises.”
2014: WEF publishes meeting agenda entitled “The Reshaping of the World: Consequences for Society, Politics and Business.”
2016: WEF holds panel called “How to reboot the global economy.”
2017: WEF publishes article saying “Our world needs a reset in how we operate.”
Then in 2018, the Davos elites turned their heads towards simulating fake pandemic scenarios to see how prepared the world would be in the face of a different crisis.
2018-2019: WEF, Johns Hopkins & Gates Foundation simulate fake pandemics
On May 15, 2018, Johns Hopkins Center for Health Security hosted the “Clade X” pandemic exercise in partnership with the WEF.
The Clade X exercise included mock video footage of actors giving scripted news reports about a fake pandemic scenario (video below).
The Clade X event also included discussion panels with real policymakers who assessed that governments and industry were not adequately prepared for the fictitious global pandemic.
“In the end, the outcome was tragic: the most catastrophic pandemic in history with hundreds of millions of deaths, economic collapse and societal upheaval,” according to a WEF report on Clade X.
“There are major unmet global vulnerabilities and international system challenges posed by pandemics that will require new robust forms of public-private cooperation to address” — Event 201 pandemic simulation (October, 2019)
Then on October 18, 2019, in partnership with Johns Hopkins and the Bill and Melinda Gates Foundation, the WEF ran Event 201.
During the scenario, the entire global economy was shaken, there were riots on the streets, and high-tech surveillance measures were needed to “stop the spread.”
Two fake pandemics were simulated in the two years leading up to the real coronavirus crisis.
“Governments will need to partner with traditional and social media companies to research and develop nimble approaches to countering misinformation” — Event 201 pandemic simulation (October, 2019)
The Johns Hopkins Center for Health Security issued a public statement on January 24, 2020, explicitly addressing that Event 201 wasn’t meant to predict the future.
“To be clear, the Center for Health Security and partners did not make a prediction during our tabletop exercise. For the scenario, we modeled a fictional coronavirus pandemic, but we explicitly stated that it was not a prediction. Instead, the exercise served to highlight preparedness and response challenges that would likely arise in a very severe pandemic.”
Intentional or not, Event 201 “highlighted” the “fictional” challenges of a pandemic, along with recommendations that go hand-in-hand with the great reset agenda that has set up camp in the nefarious “new normal.”
“The next severe pandemic will not only cause great illness and loss of life but could also trigger major cascading economic and societal consequences that could contribute greatly to global impact and suffering” — Event 201 pandemic simulation (October, 2019)
Together, the Johns Hopkins Center for Health Security, the World Economic Forum, and the Bill and Melinda Gates Foundation submitted seven recommendations for governments, international organizations, and global business to follow in the event of a pandemic.
The Event 201 recommendations call for greater collaboration between the public and private sectors while emphasizing the importance of establishing partnerships with un-elected, global institutions such as the WHO, the World Bank, the International Monetary Fund, and the International Air Transport Organization, to carry out a centralized response.
One of the recommendations calls for governments to partner with social media companies and news organization to censor content and control the flow of information.
“Media companies should commit to ensuring that authoritative messages are prioritized and that false messages are suppressed including though [sic] the use of technology” — Event 201 pandemic simulation (October, 2019)
According to the report, “Governments will need to partner with traditional and social media companies to research and develop nimble approaches to countering misinformation.
“National public health agencies should work in close collaboration with WHO to create the capability to rapidly develop and release consistent health messages.
“For their part, media companies should commit to ensuring that authoritative messages are prioritized and that false messages are suppressed including though [sic] the use of technology.”
Sound familiar?
Throughout 2020, Twitter, Facebook, and YouTube have been censoring, suppressing, and flagging any coronavirus-related information that goes against WHO recommendations as a matter of policy, just as Event 201 had recommended.
2020: WEF declares ‘Now is the time for a Great Reset’
After calling for a great reset in 2014, the Davos crowd repeated the same ideology for a few more years before pivoting towards simulating faux pandemic scenarios.
A few months after the WEF established that nobody was prepared to deal with a coronavirus pandemic, the WHO declared there was a coronavirus pandemic.
All of a sudden! the great reset narrative that the WEF had been nurturing for six years, found a place to pitch its tent in the “new normal” camp.
“The pandemic represents a rare but narrow window of opportunity to reflect, reimagine, and reset our world to create a healthier, more equitable, and more prosperous future,” Schwab declared on June 3, 2020.
And that’s where we’re at today.
The Davos elites said they wanted a global reset of the economy many years ago
They role-played what would happen if a pandemic were to occur
And now they’re saying that the great reset ideology is the solution to the pandemic, and it must be enacted quickly
The great reset is a means to an end.
Next on the agenda is a complete makeover of society under a technocratic regime of un-elected bureaucrats who want to dictate how the world is run from the top down, leveraging invasive technologies to track and trace your every move while censoring and silencing anyone who dares not comply.
Here is Politifact quoting me from the film Plandemic, which Politifact then disputed by citing a March 17, 2020 Nature Medicinearticle, which I had mentioned in the film as being bogus:
“I feel quite convinced that this was a laboratory designed organism.” — Dr. Meryl Nass, internal medicine specialist
POLITIFACT August 18, 2020: Research shows that the virus could not have been created in a lab. An article published March 17 says the genetic makeup of the coronavirus, documented by researchers from several public health organizations, does not indicate it was altered.
Now, it seems, many have awakened, after being spoon-fed an analysis of the facts by Nicholas Wade, and realized the Nature Medicinepaper makes absolutely no sense.
Some scientists have argued that the lab-leak hypothesis deserves to be taken much more seriously than it was earlier in the pandemic, and that dismissals of it as conspiracy theory were premature. Claims of complete certainty on either side remain unfounded.
No mention, of course, of Politifact’s previous smear of me and the movie. All the fact-checkers piled on me last August, as I described in a blog post, for saying the origin of Covid was a lab. Where are the rest of them now? Do the rest of the fact-checkers correct their facts?
Do the social media platforms that banned the movie resurrect it?
Verifying that it is in the Moderna COVID vaccine, I find a 12/30/20 CDC document titled: “COVID-19 Vaccines: Update on Allergic Reactions, Contraindications, and Precautions.” [1]
If you scroll down halfway through the document, you’ll see a chart titled, “Ingredients Included in mRNA COVID vaccines.” (pg 20)
The right-hand side of the chart shows ingredients in the Moderna vaccine. The fifth ingredient down is “SM-102: heptadecan-9-yl 8-((2-hydroxyethyl) (6-oxo-6-(undecyloxy) hexyl) amino) octanoate.”
Now we go to a document published by the Cayman Chemical Company of Ann Arbor, Michigan: “Safety Data Sheet acc. to OSHA HCS.” (04/11/2021) [2]
This data sheet lists the effects of SM-102. Here is the opening note: “For research use only, not for human or veterinary use.”
Far from comforting.
Then the safety data sheet lights up with adverse effects/warnings re SM-102. For example: “Suspected of causing cancer. Suspected of damaging fertility or the unborn child. Causes damage to the central nervous system, the kidneys, the liver and the respiratory system through prolonged or repeated exposure. Very toxic to aquatic life with long lasting effects.”
Several things to point out here. First, what dosage level of, and what duration of exposure to, SM-102 are we talking about? Details on these toxicity factors need to be known. HOWEVER, all that is overridden by the fact that SM-102 is being INJECTED into the body via the Moderna shot. We’re not just talking about inhalation or skin contact.
Obviously, the human body has layers of defense against attack. With injection, a number of those layers are bypassed.
And once deep within the body, where does SM-102 travel as it causes damage along the way?
I doubt that the Cayman safety data sheet even considered the possibility that SM-102 would be injected.
The experts and authorities will assure us SM-102 is safe. They’ll say only miniscule amounts are being injected. They’ll say the clinical trials of the vaccine revealed no problems. They’ll parrot, over and over again, as they always do: “safe and effective.”
You’re walking along a country path. You see a snake lying just ahead of you. He slowly raises his head and looks at you. On his hood, you read the words: “emergency use authorization granted.”
THE problem with the Covid-19 vaccines is that we simply do not have enough information about their side-effects, and no one should be shamed (especially not by the President of the United States) or have their lives restricted for having this reasonable, wholly unselfish concern.
Such information does not exist at all for under-18s. The small-scale trials were designed only to test the vaccine on adults. Yet, largely because of media hysteria which has been recently accompanied by outright incitement, local officials have taken it upon themselves to start vaccinating 17-year-olds, citing the bogeyman ‘Indian variant’ in our midst.
The vaccine nudgers in government and the media, aided this week by a multi-million-pound YouTube ad campaign to persuade young people to get vaccinated, deliberately miss the point about the supposedly ‘extremely rare’ side-effects of these experimental vaccines, which include fatal blood clots in some cases.
The trouble is that if our ‘brilliant’ scientists knew nothing about the blood clots when the vaccine was first administered to citizens in December, what else don’t they know about?
Last week, the British regulator MHRA reported 41 new cases and nine more deaths as a result of one of these side-effects, a particular kind of clot known as cerebral venous sinus thrombosis alongside low platelets or thrombocytopenia. To date, there have been 209 cases and 41 deaths reported in the UK for the AstraZeneca vaccine alone. The first were reported in January.
According to an analysis of published MHRA data by Dr Hamid Merchant, a total of 532 ‘blood system events’, including 20 deaths, came through the UK’s Yellow Card system relating to the AstraZeneca jab between January 4 and March 14. There were thousands of non-blood-related reports besides.
Let’s recap on the public guidance regarding the AstraZeneca vaccine. First we were told ‘this vaccine is safe, get vaccinated.’ Then they said, ‘the benefits of this vaccine outweigh the risks, get vaccinated.’ Then the goalposts were moved further: ‘The benefits of that vaccine outweigh the risks if you are over the age of 30, but get vaccinated.’ And now, ‘the benefits of this vaccine outweigh the risks if you are over 40, but get vaccinated, or else!’
If this is how much ‘the science’ has changed in a few months, what will ‘the science’ be a year or two from now? What will we know in the future that cannot be established now? Scientists have not begun to discuss other fatal adverse reactions to have emerged, most significantly the neurological ones for which the AstraZeneca trials were paused.
If countries such as Denmark and Slovakia can suspend the rollout of a vaccine as a precaution, why are individual citizens stupid or callous if they decline the vaccine as a precaution?
In the United States, the government has recorded more deaths after Covid vaccinations than from all other vaccines administered in the country between mid-1997 and the end of 2013, as was reported by Tucker Carlson on Fox News earlier this month. Nothing to see here, of course.
Any reasonable government would have at the very least stopped blackmailing people into getting vaccinated by now. Instead, they have the brass neck to demand that we put our lives in their hands as if we owe it to them. Coerced vaccination is not merely mandatory vaccination, it is mandatory trust, both in government and in ‘the science’, whatever that is.
It is worth reminding those with short memories that tobacco was ‘safe’ for decades. The scientific community promoted smoking not only as safe, but healthy. They were, of course, assisted by celebrities, some of whom would later become senior politicians. And for some 50 years, the overwhelming majority of people were dumb enough to believe it. Who could have guessed that inhaling tar into your lungs twenty times a day, every day, for years, might be bad for your health? We see grim warnings about heart disease, lung cancer and infertility on cigarette packaging today only because scientific outliers of yesterday eventually overwhelmed the consensus with evidence.
More recently and more relevant to the present fiasco, the swine flu vaccine, Pandemrix, was declared safe by regulators in 2009. It was safe, for most. But for some 1,000 people, most of whom were not at any significant risk from swine flu, the vaccine triggered narcolepsy, a crippling chronic sleep disorder that leaves sufferers unable to stay awake. It was only after it was too late for them that the authorities conceded there was a link between Pandemrix and narcolepsy.
One of the victims of Pandemrix, 23-year-old Katie Clack from Peterborough, committed suicide in 2014 because her narcolepsy left her with ‘no quality of life’.
In 2018, the progressive news website Buzzfeedpublished a powerful feature about NHS workers who had their lives and careers ruined by the side-effects of the swine flu vaccine. Nurse Meleney Gallagher, who now has narcolepsy, told Buzzfeed: ‘I was pressured into it.’
If history is anything to go by, the idiots out there who think it’s acceptable to bully their vaccine-hesitant friends, colleagues, strangers and even close family are going to look very silly ten years from now.
MIT did a study on Covid Skeptics and guess what? They found out we’re better at science, data analytics and communication than they are! Unfortunately this means we have to be stopped. I read from the study and give my commentary.
The US Center for Disease Control (CDC) is altering its practices of data logging and testing for “Covid19” in order to make it seem the experimental gene-therapy “vaccines” are effective at preventing the alleged disease.
They made no secret of this, announcing the policy changes on their website in late April/early May, (though naturally without admitting the fairly obvious motivation behind the change).
The trick is in their reporting of what they call “breakthrough infections” – that is people who are fully “vaccinated” against Sars-Cov-2 infection, but get infected anyway.
Essentially, Covid19 has long been shown – to those willing to pay attention – to be an entirely created pandemic narrative built on two key factors:
Inflated Case-count. The incredibly broad definition of “Covid case”, used all over the world, lists anyone who receives a positive test as a “Covid19 case”, even if they never experienced any symptoms.
Without these two policies, there would never have been an appreciable pandemic at all, and now the CDC has enacted two policy changes which means they no longer apply to vaccinated people.
Firstly, they are lowering their CT value when testing samples from suspected “breakthrough infections”.
From the CDC’s instructions for state health authorities on handling “possible breakthrough infections” (uploaded to their website in late April):
For cases with a known RT-PCR cycle threshold (Ct) value, submit only specimens with Ct value ≤28 to CDC for sequencing. (Sequencing is not feasible with higher Ct values.)
Throughout the pandemic, CT values in excess of 35 have been the norm, with labs around the world going into the 40s.
Essentially labs were running as many cycles as necessary to achieve a positive result, despite experts warning that this was pointless (even Fauci himself said anything over 35 cycles is meaningless).
But NOW, and only for fully vaccinated people, the CDC will only accept samples achieved from 28 cycles or fewer. That can only be a deliberate decision in order to decrease the number of “breakthrough infections” being officially recorded.
Secondly, asymptomatic or mild infections will no longer be recorded as “covid cases”.
That’s right. Even if a sample collected at the low CT value of 28 can be sequenced into the virus alleged to cause Covid19, the CDC will no longer be keeping records of breakthrough infections that don’t result in hospitalisation or death.
As of May 1, 2021, CDC transitioned from monitoring all reported vaccine breakthrough cases to focus on identifying and investigating only hospitalized or fatal cases due to any cause. This shift will help maximize the quality of the data collected on cases of greatest clinical and public health importance. Previous case counts, which were last updated on April 26, 2021, are available for reference only and will not be updated moving forward.
Just like that, being asymptomatic – or having only minor symptoms – will no longer count as a “Covid case” but only if you’ve been vaccinated.
The CDC has put new policies in place which effectively created a tiered system of diagnosis. Meaning, from now on, unvaccinated people will find it much easier to be diagnosed with Covid19 than vaccinated people.
Consider…
Person A has not been vaccinated. They test positive for Covid using a PCR test at 40 cycles and, despite having no symptoms, they are officially a “covid case”.
Person Bhas been vaccinated. They test positive at 28 cycles, and spend six weeks bedridden with a high fever. Because they never went into a hospital and didn’t die they are NOT a Covid case.
Person C, who was also vaccinated, did die. After weeks in hospital with a high fever and respiratory problems. Only their positive PCR test was 29 cycles, so they’re not officially a Covid case either.
The CDC is demonstrating the beauty of having a “disease” that can appear or disappear depending on how you measure it.
To be clear: If these new policies had been the global approach to “Covid” since December 2019, there would never have been a pandemic at all.
If you apply them only to the vaccinated, but keep the old rules for the unvaccinated, the only possible result can be that the official records show “Covid” is much more prevalent among the latter than the former.
This is a policy designed to continuously inflate one number, and systematically minimise the other.
What is that if not an obvious and deliberate act of deception?
An interesting recent article by international lawyer John Whitbeck suggests that the billions of dollars that the United States gives to Israel annually is not technically “foreign aid” as the Jewish state is as measured by per capita GDP the 19th wealthiest in the world, ahead of countries like Germany. It is, instead “tribute,” which is defined as the “payment made periodically by one state or ruler to another, especially as a sign of dependence.”
That the United States has surrendered key aspects of its national sovereignty to Israeli control has been observed by many. Whitbeck dates the submission to the events surrounding the Israeli attack on the USS Liberty in June 1967, in which 34 crewmen died and 172 were injured in an attempt to sink the ship and kill all the crew. To protect Israel, President Lyndon B. Johnson and his Secretary of Defense Robert McNamara initiated a cover-up that has persisted until this day. The unavenged killing of large numbers of US servicemen has signaled to a series of Israeli governments since that time that they could do anything to Washington without any consequences, including spying on its benefactor, involving Washington in its own wars, and exploiting the US Treasury as its own resource.
The United States has favored Israel above all other nations while a series of Republican and Democratic administrations have accepted that the US is the junior partner in the relationship virtually without demur, culminating in the unprecedented Barack Obama arrangement whereby Israel would receive $38 billion over the course of ten years, automatically and with no conditions placed on the Jewish state’s actions vis-à-vis American regional interests. And now, with the bloodletting continuing unabated in Gaza, Honest Joe Biden has agreed to “sell” the Israelis $735 million worth of new weapons to replenish their arsenal.
Whitbeck’s analysis is convincing, but one might also see a more personal element in how Israel has achieved dominance. Any American politician who seeks to object to the “most favored nation” status of Israel is likely to get unelected the next time he or she has to run for office. The list of the fallen includes Senators Chuck Percy and William Fulbright as well as congressmen Paul Findley, Pete McCloskey, Cynthia McKinney and James Traficant. The key to defeating incumbents in electoral office was and is money and the power and access that it buys. Israel and its supporting cast of 600 pro-Zionist Jewish organizations have billions of dollars to play with and they also include in their ranks co-religionists and other bought sympathizers who control the editorial and news content of America’s printed, television and radio media. Those congressmen who make a show of strongly supporting Israel are rewarded with campaign donations, a friendly media and a virtual lock on reelection. Those who do not are “disappeared.”
The last president who successfully made Israel back down was Dwight D. Eisenhower, who compelled Israel, France and Britain to cease their attempt to seize the Suez Canal from Egypt in 1956. George H. W. Bush was the most recent president to try to pressure Israel, when he refused to guarantee loans that Israel intended to use to expand its illegal settlements, a move which Bush correctly perceived as being bad for US relations through the region. The media subsequently piled on Bush when he ran for a second term, discovering that there was something “wrong” with the economy, which was not true. That and other contrived stories led to Bush’s loss to safely Zionist Bill Clinton. Bush’s son George W. learned the lesson from his father’s loss, even failing to investigate the possible Israeli role in 9/11 so as not to irritate his masters in Tel Aviv. W also acquired along the way a throng of neocon Jewish advisers at the Pentagon and National Security Council who were the architects of the disastrous Iraq War and the Global War on Terror (GWOT) which still plagues us to this day.
Israel’s power to control developments in the United States has recently been manifest in its ability to influence government decision making even down to the state and local level. An increasing number of public schools now have mandatory holocaust education, which, in Wisconsin for example, includes both grade school and high school levels and also applies to private schools. Also, thirty-three states now have laws punishing citizens who promote or participate in boycotts of Israeli products, the non-violent so-called Boycott Divestment and Sanction (BDS) option. Many states have special trade agreements with Israel that are designed to benefit the import of products and services from the Jewish state without mandating any reciprocity while the federal government likewise allows Israel to bid on contracts, including those relating to defense, intelligence and national security.
The Israelis take advantage of their easy access to US infrastructure by spying on both the American government and on private organizations that it considers to be unfriendly. Last year a number of electronic intrusion devices were discovered near federal buildings in Washington. They were planted by the Israelis but nothing was ever done about it. One also recalls how Israeli snoopers were recording White House phone calls under Bill Clinton, some of which were conversations with Monica Lewinsky, at the time potential blackmail material.
Another part of the Zionist game plan is the aggressive use of the anti-Semitism label to silence critics as well as the exploitation of the so-called holocaust with its assertion of perpetual victimhood of the Jewish people to create eternal sympathy for Israel. Of course, it helps to have a media willing to support such nonsense rather than expose it for what it is, but that is what having gross overrepresentation of Zionists as media owners and editors is all about.
All of which brings us to the present, in which an Israeli terror campaign against the Palestinians which has included removing families from their homes and marches through the remaining Arab parts of Jerusalem by angry mobs of armed settlers chanting “death to Arabs” while also calling for “burning” and “hanging” the local residents. The Palestinians have finally had enough and are fighting back and the Israeli armed forces have characteristically responded by attacking targets including apartment buildings in Gaza, killing numerous children.
And a bit of context is necessary. Israel has for many years denied the Palestinians basic human rights while also stealing their homes, land and water. Houses and even villages have been demolished and an estimated millions of productive olive trees burned or destroyed. Palestinians are not free to travel in the West Bank, are arrested and held in prison for no reason, including children, and are shot with no consequences for the Israeli army or police shooter.
US media attempts to portray the violence taking place currently as some kind of even-handed struggle, which it is not. Israel has had control of the historic Palestine for more than fifty years. It has the most powerful military in the Middle East and the Palestinians are basically unarmed, hitting Israel with “rockets” that are largely home-made and ineffective as demonstrated by the disparity in the casualty count. Human Rights Watch, which has been timid about how it treats Israel, has finally reported with stacks of evidence how Israel is an apartheid state that commits numerous human rights violations and occasional war crimes, just as it is doing right now. The intention of all this is to make the life of Palestinians so miserable that they all leave. Israel would prefer not to have to do the job by killing all of them, a route nevertheless endorsed by a number of leading Israeli politicians, but would much prefer that they go voluntarily.
The fact is that the United States enables Israeli behavior by cravenly heeding Netanyahu’s warning not to interfere. It has already blocked several resolutions in the United Nations Security Council to stop the fighting because they are too critical of Israel. The fact that Washington, like a broken record, continues to voice support of Israel the perpetual victim even when it is clearly the aggressor is shameful. If you want to know just what kind of country we Americans now live in, Jen Psaki, White House press spokesperson has provided the answer. She has announced that our government’s position on the ongoing violence in the Middle East is that “The president’s support for Israel’s security, for its legitimate right to defend itself and its people, is fundamental and will never waiver. We condemn ongoing rocket attacks by Hamas and other terrorist groups against Jerusalem.”
Excuse me, but even some minimal compassion for dead Arab children seems to be missing in Biden’s statement, though its ruthlessness inevitably is exceeded by Donald Trump’s bleat “When I was in office we were known as the Peace Presidency, because Israel’s adversaries knew that the United States stood strongly with Israel and there would be swift retribution if Israel was attacked. Under Biden, the world is getting more violent and more unstable because Biden’s weakness and lack of support for Israel is leading to new attacks on our allies. America must always stand with Israel and make clear that the Palestinians must end the violence, terror, and rocket attacks, and make clear that the U.S. will always strongly support Israel’s right to defend itself.”
Donald Trump’s “peace presidency?” Does he include his attacks on Syria and his assassination of a senior Iranian official? Another wannabe with GOP presidential aspirations Florida’s Ron DeSantis, self-designated as “Israel’s governor,” puts it another way, “Hamas is a terrorist organization and Israel has the right to defend itself against terrorist attacks.” Is this a Monty Python sketch? Israel was attacked and is defending itself? Time to wake up America. Israel the victim is preparing a genocide and the fact that no one is Washington is willing to say “no” gives it a green light to go ahead. The blood will be on our hands this time around as Joe Biden and company could have made the decision to stop the developing madness over the past month by putting pressure on Israel to stop the home expulsions and riots by settlers, but clearly that did not and will not happen. And when it all blows up and maybe tens of thousands will die, we will likely hear the same noise coming out of Washington: “Israel has a right to defend itself.”
To conclude with another comment by John Whitbeck relating to his desire to see the United States reclaim its sovereignty would be appropriate. He writes “For many years, I have had a recurring but thus far unrequited dream: Someday, during a Senate confirmation hearing, a nominee will respond to demands to… pledge allegiance to [Israel] with a simple affirmation of pure and genuine patriotism: ‘Senator, with all due respect, I owe my allegiance to the United States of America and to no other country. If you have a problem with that, don’t vote to confirm me.’”
Philip M. Giraldi, Ph.D., is Executive Director of the Council for the National Interest, a 501(c)3 tax deductible educational foundation (Federal ID Number #52-1739023) that seeks a more interests-based U.S. foreign policy in the Middle East. Website is https://councilforthenationalinterest.orgaddress is P.O. Box 2157, Purcellville VA 20134 and its email is inform@cnionline.org
Comedian Steven Crowder has announced that last Thursday (May 14, 2021), his company, Louder with Crowder LLC, gave a legal notice to YouTube announcing its intent to file a lawsuit and seek an injunction to stop YouTube deplatforming his channel.
“Once we hit the new year and a new president ascended, the landscape of social media shifted in favor of the left,” Louder with Crowder’s editor at large, Courtney Kirchoff, noted in a blog post announcing the legal action against YouTube. “Democrats took control of the presidency and now have control of both houses of Congress. As such, YouTube and other Big Tech platforms feel emboldened, with very few lawmakers standing in their way.”
In a video about the legal action they plan to take against YouTube, Crowder and his lawyer Bill Richmond discussed how the channel is now just one strike away from being deleted after receiving a warning strike and two hard strikes this year.
The warning strike was issued on a coronavirus lockdown anniversary video where someone in the studio said “young children are more likely to die of the flu than COVID.”
“It is tantamount to saying that no conservatives or people who cite the CDC and believe that relevant information like young children have a different immune response to COVID than the standard flu, and it is significantly less lethal to young people but more lethal to old people, which we’ve always talked about, YouTube is saying anyone with that point of view is not welcome on this channel, on this platform, I guess,” Crowder said when discussing this warning strike.
Crowder said he didn’t make any such claims and described this first strike as “investigative journalism being a violation of the policy if someone doesn’t like it.”
The second hard strike was issued on a May 10 video where Crowder described the Columbus police shooting of Ma’Khia Bryant as “an example of a justified police shooting” that was “necessary to save the life of someone who is in the process of being stabbed.”
According to YouTube, this video violated its rules around “content reveling in or mocking the death or serious injury of an identifiable individual.”
Crowder noted that Big Tech platforms allowed posts that were favorable to Bryant and critical of the police officer to remain up. But when he challenged the criticism of the police officer and argued that the shooting was justified because she had a knife in her hand and was about to swing at another girl, his video was removed and he was suspended.
“That means that the lie is allowed and the truth is not because the truth is simply from a point of view which is impermissible,” Crowder said.
“It’s an incredible indictment of how YouTube enforces its policies and, and really the reason why we’ve had to give the notice, serve the notice of moving for an injunction, to prevent the deplatforming,” Richmond added.
Richmond continued by discussing how he and Crowder’s team are concerned about YouTube actively looking for violations that aren’t actually violations and explained that this is why they’ve moved forward with this injunctive notice which will request immediate relief to protect the existence of Crowder’s YouTube channel.
“This is something that concerns every person who values any type of democracy,” Richmond added. “What they’re saying is ‘these ideas are so dangerous that we can’t address them and rebut them, we can’t criticize them, we just have to extinguish the opinions entirely, we have to eradicate these opinions from the planet because we can’t deal with them.’ But the reality when everyone looks at this is, this is a comedy show that takes on important issues. Commentary, politics, issues that are facing everyone in every part of the nation in the world. And we have to be able to talk about them.”
While the world’s media can’t get enough of India today, in its rush to support a narrative of terror about Covid-19, twelve years ago when there was a real story going on there, the world’s media was nowhere to be seen.
SOME BACKGROUND
In 2009, a Bill and Melinda Gates Foundation (BMGF) funded NGO carried out unauthorised clinical trials of a vaccine on some of the poorest, most vulnerable children in the world. It did so without providing information about the risks involved, without the informed consent of the children or their parents and without even declaring that it was conducting a clinical trial.
After vaccination, many of the participating children became ill and seven of them died. Such were the findings of a parliamentary committee charged with investigating this wretched affair. The committee accused the NGO of “child abuse” and produced a raft of evidence to back up its claim. This entire incident barely registered on the radar of Western media.
PATH (formerly the Program for Appropriate Technology in Health) is a Seattle based NGO, heavily funded by BMGF but which also receives significant grants from the US government. Between 1995 and the time of writing (May 2021), PATH had received more than $2.5bn from BMGF.
In 2009, PATH carried out a project to administer the Human Papillomavirus (HPV) vaccine. The project’s aim was, in PATH’s own words, “to generate and disseminate evidence for informed public sector introduction of HPV vaccines”. It was conducted in four countries: India, Uganda, Peru and Vietnam. Another Gates-funded organization, Gavi, had originally been considered to run the project, but responsibility was ultimately delegated to PATH. The project was directly funded by BMGF.
Significantly, each of the countries selected for the project had a different ethnic population and each had a state-funded national immunisation program. The use of different ethnic groups in the trial allowed for comparison of the effects of the vaccine across diverse population groups (ethnicity being a factor in the safety and efficacy of certain drugs).
The immunisation programs of the countries involved provided a potentially lucrative market for the companies whose drugs were to be studied: should the drugs prove successful and be included on these countries’ state-funded national immunisation schedules, this would represent an annual windfall of profits for the companies involved.
Two types of HPV vaccine were used in the trial: Gardasil by Merck and Cervarix by GlaxoSmithKline(GSK). In this article, we are going to examine PATH’s trial of Gardasil in India.
It’s worth noting here the relationship between BMGF and one of the companies whose drugs were being tested. In 2002, BMGF had, controversially, bought $205m worth of stocks in the pharmaceutical sector, a purchase which included shares in Merck & Co. The move had raised eyebrows because of the obvious conflict of interest between the foundation’s role as a medical charity and its role as an owner of businesses in the same sector.
The Wall Street Journalreported, in August 2009, that the foundation had sold its shares in Merck between 31st March and 30th June of that year, which would have been around the same time that the field trials of the HPV vaccine were starting in India. So for the entirety of this project (which was already in operation by October 2006), right up to its final field trials, BMGF had a dual role: as both a charity with a responsibility for care, and as a business owner with a responsibility for profit.
Such conflicts of interest have been a hallmark of BMGF since 2002. When Gates was makingregularTVappearances last year to promote Covid-19 vaccination, giving especially ringing endorsements of the Pfizer-BioNTech effort, his objectivity was never brought into question. Yet his foundation is the part-owner of several vaccine manufacturers, includingPfizer, BioNTech and CureVac.
HPV VACCINE
HPV vaccine aims to prevent cervical cancer. Gardasil had been launched successfully by Merck in the US in 2006, but its sales suffered after a series of articles in American medical journals had judged that its risks outweighed its benefits. Especially damaging was an analysis of reports made to the CDC’s Vaccine Adverse Event Reporting System (VAERS) about adverse reactions to Gardasil.
This analysis was published in the Journal of the American Medical Association (JAMA) on August 19th 2009. The 12,424 adverse reactions which had been reported included 772 which were considered serious, 32 of which were deaths. Other reported serious side effects included autoimmune disorders, venous thromboembolic events (blood clots) and Guillain-Barré syndrome.
In the same edition of JAMA, Dr. Charlotte Haug, then editor-in-chief of the Journal of the Norwegian Medical Association, wrote,
Whether a risk is worth taking depends not only on the absolute risk, but on the relationship between the potential risk and the potential benefit. If the potential benefits are substantial, most individuals would be willing to accept the risks. But the net benefit of the HPV vaccine to a woman is uncertain. Even if persistently infected with HPV, a woman most likely will not develop cancer if she is regularly screened. So rationally she should be willing to accept only a small risk from the vaccine.”
Dr. Haug also noted, “When weighing evidence about risks and benefits, it is also appropriate to ask who takes the risk, and who gets the benefit”, in a clear dig at Gardasil manufacturer Merck.
Merck’s attempts to promote Gardasil had been controversial. Dr. Angela Raffle, one the UK’s leading experts on cervical cancer screening, described Merck’s marketing strategy as “a battering ram at the Department of Health and carpet bombing on the peripheries.”
Dr. Raffle was concerned that the push to mass vaccination would harm the successful screening programme which had operated in the UK since the 1960s.
“My worry is that the commercially motivated rush to make us panic into introducing HPV vaccine quickly will put us back and worsen our cervical cancer control programme.”
Professor Diane Harper
Professor Diane Harper, then of Dartmouth Medical School in New Hampshire, had led 2 trials of the vaccine and was adamant that Gardasil could not protect against all strains of HPV.
When Merck launched a huge public relations campaign in 2007 to persuade European governments to use the product to vaccinate all the continent’s young girls against cervical cancer, she said:
Mass vaccination programmes (would be) a great big public health experiment…. We don’t know a lot of things. We don’t know the vaccine will continue to be effective. To be honest, we don’t have efficacy data in these young girls right now. We’re vaccinating against a virus that attacks women throughout their whole life and continues to cause cancer. If we vaccinate girls at 10 or 11 we won’t know for 20 to 25 years whether it is going to work or not. This is a big thing to take on.”
So at the time that PATH was carrying out its trials in India, Uganda, Peru and Vietnam, Gardasil was a controversial vaccine: its safety, efficacy and Merck’s attempts to promote it were being questioned, not by “anti-vaxxers” and “conspiracy theorists”, but by the international medical establishment and the respected mainstream media.
THE GIRLS OF KHAMMAM
Children of the Koya tribe, Khammam
Khammam district, in 2009, was a part of the eastern Indian state of Andhra Pradesh (boundary changes made in 2014 mean that today Khammam district belongs to the state of Telangana). The region is predominantly rural and is considered to be one of the poorest and least developed parts of India.
Khammam is home to several ethnic tribal groups,with some estimates putting its tribal population at about 21.5% (approximately 600,000 people). As is common for indiginous people throughout the world, the tribal groups of Khammam suffer from a lack of access to education. Consequently, their level of literacy is of a standard considerably lower than that of the region as a whole.
Some 14,000 girls were injected with Gardasil in Khammam district during 2009. The girls recruited for PATH’s project were between 10 and 14 years of age and all came from low-income, predominantly tribal backgrounds. Many of the girls did not reside with their families; instead they lived in ashram pathshalas (government-run hostels), which were situated close to the schools the children attended.
Professor Linsey McGoey, of the University of Essex, later stated she believed girls at ashram pathshalas had been targeted for the project as this was a way of:
“side-stepping the need to seek parental consent for the shots.”
Although we have seen a lot of India in the news recently, coverage of this country and its affairs is usually low-key. Despite being home to almost one fifth of the world’s population, reporting on India is sparse.
Such failings have been taken advantage of by unscrupulous profit-seekers for decades. Western media only reports on the consequences of these actions when their magnitude is too great to ignore.
We learned that up to 7,000 people were killed and more than half a million were injured after being exposed to deadly methyl isocyanate gas, following a gas leak at the Union Carbide pesticide plant in Bhopal. But we learned nothing in the years leading up to it of the culture of poor standards and disregard for regulation which was ultimately responsible for the disaster.
So it was typical that PATH’s project to administer and study the effects of the HPV vaccine went unheralded in the West. Typical, too, that the same was true in India itself: the Indian media is no more renowned for its reporting on tribal groups than the Western media is for its coverage of Indians.
Despite concerns expressed about the project in October 2009 by Sama, a Delhi-based NGO that advocates for women’s health, the matter remained absent from India’s news.
Members of the advocacy group Sama
This project, then, couldn’t have been more off-the-map had it taken place on the moon, and it remained so for several months until, early in 2010, stories began to filter out from Khammam that something had gone terribly wrong: many of the girls who had been involved in the trials had subsequently fallen ill and four of them had died.
In March 2010, members of Sama visited Khammam to find out more about the emerging stories. They were told that up to 120 girls had experienced adverse reactions, including epileptic seizures, severe stomach ache, headaches and mood swings. The Sama representatives remained in Khammam to investigate the situation further.
The involvement of Sama finally brought the matter to the attention of the Indian media and, amid a barrage of negative publicity, the Indian Council of Medical Research (IMCR) suspended the PATH project.
At this point theIndian Parliament’s Standing Committee on Healthbegan an investigation into the affair.
On May 17th, Sama produced a damning report highlighting, among other things: that the trials had been promoted as a government immunisation programme and not a research project, that the girls had not been made aware that they could choose not to participate in the trials, and that parental consent had neither been asked for nor given in many cases.
The report stated that:
“Many of the vaccinated girls continue to suffer from stomach aches, headaches, giddiness and exhaustion. There have been reports of early onset of menstruation, heavy bleeding and severe menstrual cramps, extreme mood swings, irritability, and uneasiness following the vaccination. No systematic follow up or monitoring has been carried out by the vaccine providers.”
Sama also disputed the Andhra Pradesh State Government’s claim that the deaths of four of the girls who had participated in the trials had nothing to do with vaccination.
THE PARLIAMENTARY COMMITTEE
Parliament House, seat of the Parliament of India, New Delhi
The wheels of bureaucracy are slow to turn. It was more than three years later, on 30th August 2013, when the report of the Indian Parliament’s Standing Committee on Health was finally published. Although many had expected the report to be a whitewash, it was anything but: it made for shocking reading.
The report excoriated both PATH and the IMCR, concluding that the “safety and rights of children were highly compromised and violated.” The committee found that PATH, despite operating in India since 1999, had no legal permission to do so. It noted that although the organisation had finally received a certificate from India’s Registrar of Companies in September 2009, this certificate itself was in breach of the law.
“PATH… has violated all laws and regulations laid down for clinical trials…. its sole aim has been to promote the commercial interests of HPV vaccine manufacturers…. This is a serious breach of trust… as the project involved the life and safety of girl children and adolescents who were mostly unaware of the implications of vaccination. The violation is also a serious breach of medical ethics.This act of PATH is a clear cut violation of the human rights of these girl children and adolescents. It is also an established case of child abuse.”
The committee charged thatPATH had lied to it and had attempted to mislead it during the course of its investigation and recommended that the Indian Government report PATH’s violations of human rights to the WHO, UNICEF and the US Government.
The report declared that PATH’s whole scheme was a cynical attempt to ensure ongoing profits for Merck and GSK.
“The choice of countries and population groups; the monopolistic nature, at that point of time, of the product being pushed; the unlimited market potential and opportunities in the universal immunisation programmes of the respective countries are all pointers to a well-planned scheme to commercially exploit a situation. Had PATH been successful… this would have generated a windfall profit for the manufacturers by way of automatic sale, year after year, without any promotional or marketing expenses. It is well known that once introduced to the immunisation programme it becomes politically impossible to stop any vaccination.”
It went on:
“To achieve this end effortlessly, without going through the arduous and strictly regulated route of clinical trials, PATH resorted to an element of subterfuge by calling the clinical trials ‘Observational Studies’ or ‘a Demonstration Project’ and various such expressions. Thus the interest, safety and well being of subjects were completely jeopardized by PATH by using self-determined and self-servicing nomenclature which is not only highly deplorable but also a serious breach of the law of the land.”
Samiran Nundy, editor emeritus National Medical Journal of India
These charges were echoed by leading voices in India’s medical community. “It is shocking to see how an American organization used surreptitious methods to establish itself in India,” said Chandra M.Gulhati, editor of India’s influential Monthly Index of Medical Specialities, “(this) was not philanthropy”.
Samiran Nundy, editor emeritus of the National Medical Journal of India and a long-standing critic of corrupt practices in health, did not mince his words:
“This is an obvious case where Indians were being used as guinea pigs.”
The standing committee’s report was also highly critical of the relationship between PATH and members of several of India’s health agencies, highlighting multiple conflicts of interest.
On the issue of informed consent, the committee confirmed the allegations made by Sama to be true, finding that the majority of consent forms weren’t signed by either the children or their parents, that many consent forms were postdated or not dated at all, that multiple forms had been signed by the same people (often the caretakers of the hostels the girls lived in) and that many signatures didn’t match the name on the form. It found that parents had not been given information on the necessity of vaccination, its pros and cons or its potential side effects.
No insurance was provided for any of the children in the event of injury and “PATH did not provide for urgent expert medical attention in case of serious adverse events.”
Further, PATH seriously contravened Indian health regulations by carrying out a clinical trial of a drug on children before first conducting a trial of the drug with adults as subjects.
Regarding the girls who had died, the committee criticized PATH, Indian medical authorities and the Andhra Pradesh State Government for summarily dismissing the link between their deaths and vaccination without conducting thorough investigations. By 2016, some 1,200 of the girls who had been subjects in the two HPV vaccine trials in India were reporting serious long-term side effects, more than 5% of the total cohort of 23,500. By then, the total number of deaths had risen to seven.
A DEATHLY SILENCE
This appalling breach of medical ethics and human rights went almost completely unmentioned outside India. The Indian Parliament’s Standing Committee on Health had literally accused an American NGO of child abuse, providing extensive evidence to support their charge, yet practically no mention of this was to be found anywhere in the Western media.
Popular science publications Nature and Science each contained a brief article about the debacle, but neither goes into any detail about PATH’s legal and ethical breaches. While the Science article is at least slightly critical, the Nature piece gives more space to a rebuttal of the charges by PATH director Vivien Tsu.
The Guardian, for all its claims to give a voice to the most vulnerable in the world, stayed curiously silent about the young girls of Khammam. That is, except for one article, published in October 2013, about six weeks after the release of the standing committee’s report.
The article was written not by one of the girls or one of their parents, not by one of the women from Sama who had advocated on the girls’ behalf, not even by one of the Indian parliamentarians who had been charged with investigating the affair.
No. It was written by an American man called Seth Berkely. Berkely is the CEO of Gavi, another BMGF funded health behemoth.
Seth Berkley, CEO GAVI
Berkely used his forum in The Guardian to claim that the girls who had died after being vaccinated in Khammam had committed suicide. Speaking about the 14,000 subjects involved in the trials, he said, “it would have been unusual if none of them went on to kill themselves.”
Compassion wasn’t the only element missing from his article. Not once did Berkley address the multiple breaches of law and ethics which had occurred or the role of PATH and that of his employers, the Gates Foundation, in his dismissal of this iniquity.
The Guardianbegan receiving funding from BMGF in August 2010. Prior to that arrangement, in 2007, the newspaper had published two separate articles which were critical of the lobbying tactics used by Merck to promote Gardasil and which questioned the efficacy of its use in mass vaccination programs.
Subsequent to their arrangement with Gates, all coverage by the Guardian of this drug (and of HPV vaccination in general) has been positive.
HOW THINGS TURNED OUT
BMGF headquarters, Seattle
The Indian government was reluctant to take any of the measures recommended by the committee. After all, there were huge amounts of money being made available to the state, institutions and individuals from organisations likePATH.
So no official reports of human rights violations were ever made by the Indian government to the WHO, to Unicef or to the US government, as had been recommended by the standing committee.
However, in 2017, it announced it would no longer accept grants from BMGF for its Immunisation Technical Support Unit, an organisation which provides “vaccination strategy advice” in relation to an estimated 27 million infants. Nevertheless, the Indian government continues to accept the foundation’s grants in other areas.
Merck, and their HPV vaccine Gardasil, have done very well since the dismal events recounted in this article. The Khammam scandal never really affected the company, due to a lack of awareness about it outside India. In 2018 alone, Gardasil sales amounted to more than $3bn, thanks to its inclusion on immunisation schedules around the world, and its launch that year in China.
PATH has never been better. Just like Merck, the lack of reporting about what happened in Khammam meant the organisation didn’t suffer. Since 2010, it has continued to receive huge funding from BMGF and, to a lesser extent, the US Government. During this period, BMGF has provided PATH with more than $1.2bn in funding.
The Bill and Melinda Gates Foundation has continued expanding its web of influence. Describing the organisation’s practices around the time of the events outlined here, Jacob Levich said:
“In essence, BMGF would buy up stockpiled drugs that had failed to create sufficient demand in the West, press them on the periphery at a discount, and lock in long-term purchase agreements with Third World governments.”
The foundation has since moved on to even more lucrative pastures. The Covid-19 pandemic has really pushed BMGF to centre stage. Gates himself has seen his public profile and political influence grow to an extent that would have been unimaginable even in 2019.
Well, those poor children and their plight wasn’t even widely known outside of India back in 2010. To say they had been forgotten would be to imply that anybody knew about them or cared about them in the first place.
Bernard Marx is the pseudonym used by a writer and teacher based in Ireland. Bernard’s areas of interest include history, politics and popular music. You can read more of his work at Notes from the New Normal
BILL Gates’s company Microsoft has changed our lives. It turned him into one of the richest men in the world and allowed him to turn philanthropist. His endeavour began in 1994 when he established the William H. Gates Foundation, soon to be followed by the Gates Learning Foundation in 1997. He merged the organisations in 2000 creating the Bill & Melinda Gates Foundation (GF). After the couple transferred $20billion of their Microsoft stock to the GF it became the largest charitable foundation in the world and over the next twenty years the most powerful charity in the world. Its endowment as of 2019 was $50billion.
The GF made its first donation to the World Health Organisation (WHO) in 1998. Soon after Gates pledged a further $750million to set up the Global Alliance for Vaccines and Immunization (Gavi), the stated aim of which is to increase immunisation rates in low-income countries, with the WHO and the UK amongst its original founders and donors. Last year Boris Johnson pledged Gavi £1.65billion over five years at the June 2020 Global Vaccine Summit replenishment conference, which the UK hosted. Six months later Johnson met Gates and pharmaceutical bosses to discuss Britain’s vaccine rollout and future pandemic plans.
The GF holds a permanent seat on Gavi’s board. Gavi’s core partners today are the GF, the WHO, Unicef and the World Bank, with the GF giving Gavi $4.1billion since its inception. Gavi is also the fifth largest funder of the WHO, giving $355.4million last year. With the WHO, Gavi dominates global vaccination campaigns including the Covid-19 vaccine rollout.
The WHO’s list of top 20 donors for the two-year budget cycle of 2018 and 2019 shows the GF coming second only to the US (their $893million donation accounting for 20 per cent of the WHO’s budget) with a $531 million donation (equal to 12 per cent of WHO’s budget). The GF and Gavi together outstrip all single country donations, except that of the US.
Since its inception the GF has given $54.8billion to a multitude of organisations. It has expanded globally, opening offices in Beijing in 2007 and London in 2010, and funding works in 135 countries. A letter from President Xi Jinping to Bill Gates, which you can read here, suggests Gates’s closeness to the Chinese Communist Party.
Donations from billionaires over the past 25 years have extensively bolstered the GF’s finances. Between 1994 and 2018 Mr and Mrs Gates donated $36billion of their own money, and in 2006 Warren Buffet pledged $30billion.
Eight years after establishing Gavi, Gates stepped down in 2008 as Microsoft CEO to commit more of his time to his foundation. By that time the GF was the largest charitable foundation in the US, and questions were being raised even then about its long reach in shaping US government health policies. After going into financial partnership with the GF, the publicly funded US National Institutes of Health (NIH) shifted their focus from the health and welfare of American citizens to global health. Concerns about the power, complexity and lack of accountability of GF, and Gates’s potential – effectively now realised – to become WHO’s largest donor continue to be articulated.
In 2010, with Warren Buffett, the Gateses launched Giving Pledge, a vehicle through which the very wealthy could donate to charity. To date there are no public details of who donates what through Giving Pledge, though this endeavour has turned into a tax haven for billionaires.
The GF is also a co-founder and funder of CEPI (Coalition for Epidemic Preparedness Innovations), as influential as Gavi but less known. CEPI is a Norwegian venture which invests in vaccines and is also funded by the Indian and Norwegian governments, the British-based Wellcome Trust and the World Economic Forum. Jeremy Farrar, director of the Wellcome Trust and member of Sage, sits on the CEPI board. In 2017 Gates said that the world was unprepared for pandemics and that CEPI’s investments in ‘DNA/RNA vaccines’ would mitigate that. Both the GF and Wellcome Trust have pledged to fund CEPI with $100million annually from 2017 to 2022.
The initial endeavours of the William H. Gates Foundation to support scientific research and local charities have morphed into a global juggernaut with unaccountable power. Vast amounts of money are being channelled according to the thoughts, passions and prejudices of one man with questionable judgment.
In 1998, Gates was hauled before the US Senate to answer questions about Microsoft’s anti-trust practices. His demeanour while giving testimony was dishonest and arrogant. His performance is disturbing to watch, captured in this clip (from 1 minute 29 seconds) where he rocked repeatedly in his chair and insisted he didn’t understand the word ‘concern’.
When the WHO was formed as an intergovernmental organisation, it would have been unimaginable that a private foundation could have such influence or set the global health agenda. Though awareness of the GF’s influence over the WHO and Gavi is growing, what is less well documented is its extensive reach closer to home and its control over British science, medicine and public health. This I will be reporting on in the coming days.
Seventy senior Israeli-centric neoconservatives have written an open letter to Congress imploring them to do more to ensure Iran complies with the conditions of any agreement finally reached with the P5+1 over Iran’s nuclear program.
While the neocons are ostensibly asking Congress to ensure compliance, it is clear that their real aim is to convince members of Congress to support the bill currently passing through the Senate which calls for tighter sanctions against Iran in the event of any waywardness on Iran’s part.
The neocons are eager to see the bill currently passing through the Senate with enough support to make it veto-proof, not so much because they are concerned about Iran’s so-called nuclear weapons program – there’s still not a skerrick of hard evidence that Iran has a nuclear weapons program – but, rather, because embedded within the bill is this clause:
… if the Government of Israel is compelled to take military action in legitimate self-defense against Iran’s nuclear weapon program, the United States Government should stand with Israel and provide, in accordance with the law of the United States and the constitutional responsibility of Congress to authorize the use of military force, diplomatic, military, and economic support to the Government of Israel in its defense of its territory, people, and existence…
Essentially, the clause is an automatic trigger for the US to attack Iran at any time the Israelis choose to launch a first strike – regardless of whether President Obama is in favour or not.
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