Fauci Likely to Birth His Own COVID Variant After Paxlovid
By Dr. Joseph Mercola | July 13, 2022
Pfizer’s Paxlovid was granted emergency use authorization to treat mild to moderate COVID-19 in December 2021.1 The drug consists of nirmatrelvir tablets — the antiviral component — and ritonavir tablets, which are intended to slow the breakdown of nirmatrelvir.2
What started out as a slow rollout — only 40,000 or fewer prescriptions were written for the drug in the U.S. each week through April 2022 — has gained steam, with more than 160,000 Paxlovid prescriptions now being issued each week.3 As of June 30, 2022, 1.6 million courses of Paxlovid have been prescribed in the U.S. since its emergency use approval in December.4
Yet, this increase in prescribing could be contributing to one of the significant downfalls of the drug — the creation of selective pressure on SARS-CoV-2, which promotes mutations that could make it resistant to the drug.5 The U.S. Centers for Disease Control and Prevention also issued a warning to health care providers and public health departments about the potential for COVID-19 rebound after Paxlovid treatment.6
This recently happened to Dr. Anthony Fauci, director of the U.S. National Institute of Allergy and Infectious Diseases (NIAID), who experienced a return of COVID-19 symptoms after taking Paxlovid. He then took a second course of the drug, which could trigger even more mutations in the virus.
Paxlovid Triggers Fauci’s COVID-19 Rebound
Fauci said he tested positive for COVID-19, with only minimal symptoms. As his symptoms increased, he took Paxlovid for five days, after which he tested negative for three consecutive days. On the fourth day of testing, he tested positive for COVID-19 again, with symptoms worse off than they were the first time.
“It was sort of what people are referring to as a Paxlovid rebound,” he said. “… Over the next day or so I started to feel really poorly, much worse than in the first go around.”7 He was then prescribed a second course of Paxlovid.
On June 30, he stated, “I went back on Paxlovid, and right now I am on my fourth day of a five-day course of my second course of Paxlovid. Fortunately, I feel reasonably good. I mean, I’m not completely without symptoms, but I certainly don’t feel acutely ill.”8 In the CDC’s health advisory regarding COVID-19 rebound after Paxlovid treatment it’s stated:9
“Recent case reports document that some patients with normal immune response who have completed a 5-day course of Paxlovid for laboratory-confirmed infection and have recovered can experience recurrent illness 2 to 8 days later, including patients who have been vaccinated and/or boosted …
These cases of COVID-19 rebound had negative test results after Paxlovid treatment and had subsequent positive viral antigen and/or reverse transcriptase polymerase chain reaction (RT-PCR) testing.”
COVID-19 Still Spreads During Paxlovid Rebound
People who take Paxlovid can still transmit COVID-19 to others, even if they’re asymptomatic, according to a preprint study.10 Study author Dr. Michael Charness of the Veterans Administration Medical Center in Boston told CNN, “People who experience rebound are at risk of transmitting to other people, even though they’re outside what people accept as the usual window for being able to transmit.”11
The CDC12 and Pfizer13 have suggested that sometimes COVID-19 naturally comes back after a person tests negative, implying that COVID-19 rebound is spontaneous and not necessarily linked to Paxlovid. However, Charness and colleagues didn’t find this to be the case. When they analyzed 1,000 cases of COVID-19 diagnosed among members of the National Basketball Association — none of whom took Paxlovid — no cases of COVID-19 rebound were found.14
Research published in Clinical Infectious Diseases 15 looked into why Paxlovid may be leading to rebound symptoms and suggests it could be the result of insufficient exposure to the drug.16 “Not enough of the drug was getting to infected cells to stop all viral replication,” UC San Diego Health reported. “They suggested this may be due to the drug being metabolized more quickly in some individuals or that the drug needs to be delivered over a longer treatment duration.”17
Pfizer Seeks FDA Approval for Paxlovid
Despite the many questions regarding Paxlovid’s association with rebound infections, Pfizer is moving ahead and seeking full approval of the drug from the FDA.18 The drug’s emergency use authorization restricts who the drug can be sold and marketed to. Once full FDA approval is granted, Pfizer can market the drug directly to consumers.
Paxlovid’s emergency use authorization allows it to be prescribed for adults and children ages 12 and older who are at high risk for progression to severe COVID-19.19 Pfizer estimates that up to 60% of the U.S. population meets these criteria and has at least one risk factor for severe illness, such as obesity or diabetes, making them eligible for the drug.20
However, concerns have risen over whether Paxlovid, which is said to cut the risk of hospitalization or death by 86% in high-risk patients, when taken within five days of symptoms starting,21 is effective in people who are not high-risk.
In fact, Pfizer stopped a large trial of Paxlovid in standard-risk patients because it didn’t show significant protection against hospitalization or death in this group.22 According to a news release from Pfizer:23
“In previously reported interim analyses, the company disclosed that the novel primary endpoint of self-reported, sustained alleviation of all symptoms for four consecutive days was not met, and a non-significant 70% relative risk reduction was observed in the key secondary endpoint of hospitalization or death (treatment arm: 3/428; placebo: 10/426).
An updated analysis from 1,153 patients enrolled through December 2021 showed a non-significant 51% relative risk reduction (treatment arm: 5/576; placebo: 10/569). A sub-group analysis of 721 vaccinated adults with at least one risk factor for progression to severe COVID-19 showed a non-significant 57% relative risk reduction in hospitalization or death (treatment arm: 3/361; placebo: 7/360).”
Is Paxlovid Triggering SARS-CoV-2 Mutations?
Initial reports have suggested that SARS-CoV-2 is not mutating and becoming resistant to Paxlovid, but some experts believe it’s only a matter of time before this occurs — and emerging research suggests it’s already happened.
David Ho, a virologist at the Aaron Diamond AIDS Research Center at Columbia University, was among the first to document resistance mutations in HIV 30 years ago and believes the same may be coming with SARS-CoV-2.24 He’s also experienced post-Paxlovid COVID-19 rebound firsthand. Bloomberg reported:25
“Ho said he came down with COVID on April 6 … His doctor prescribed Paxlovid, and within days of taking it, his symptoms dissipated and tests turned negative. But 10 days after first getting sick, the symptoms returned and his tests turned positive for another two days.
Ho said he sequenced his own virus and found that both infections were from the same strain, confirming that the virus had not mutated and become resistant to Paxlovid. A second family member who also got sick around the same time also had post-Paxlovid rebound in symptoms and virus, Ho says.
‘It surprised the heck out of me,’ he said. ‘Up until that point I had not heard of such cases elsewhere.’ While the reasons for the rebound are still unclear, Ho theorizes that it may occur when a small proportion of virus-infected cells may remain viable and resume pumping out viral progeny once treatment stops.”
Studies Show COVID-19 Virus Developing Paxlovid Resistance
Two separate studies cultured SARS-CoV-2 in a lab and exposed it to low levels of nirmatrelvir, which would kill some, but not all, of the virus. “Such tests are meant to simulate what might happen in an infected person who doesn’t take the whole regimen of the drug or an immunocompromised patient who has trouble clearing the virus,” Science reported.26
One of the studies revealed that SARS-CoV-2 developed three mutations after 12 rounds of nirmatrelvir treatment — “at positions 50, 166 and 167 in the string of amino acids that make up MPRO.”27 The mutations amounted to a 20-fold reduction in the virus’ susceptibility to nirmatrelvir.28 The other study29 also found mutations at positions 50 and 166, revealing that when they occurred together, SARS-CoV-2 became 80 times less susceptible to nirmatrelvir. According to the study:30
“Reverse genetic studies in a homologous infectious cell culture system revealed up to 80-fold resistance conferred by the combination of substitutions L50F and E166V. Resistant variants had high fitness increasing the likelihood of occurrence and spread of resistance.”
Lead study author Judith Margarete Gottwein with the University of Copenhagen told Science, “This tells us what mutations we should be looking for [in patients].”31 Ho, who was not involved in these studies, agreed that it appeared mutations were an inevitable outcome.
He told Science, “when you put pressure on the virus it escapes … Given the amount of infections out there, it’s going to come.”32 It’s also completely unknown what may happen when two courses of Paxlovid are taken in quick succession to treat COVID-19 rebound — as occurred with Fauci. It’s possible that ever-mutating COVID-19 variants could be created.
Other antivirals on the market to treat COVID-19 have also led to concerns over mutations. Molnupiravir (sold under the brand name Lagevrio) was developed by Merck and Ridgeback Therapeutics and approved by the FDA for emergency use December 23, 2021, for high-risk patients with mild to moderate COVID symptoms.
However, not only might it contribute to cancer and birth defects, it may also supercharge the rate at which the virus mutates inside the patient, resulting in newer and more resistant variants.33
Other Early COVID-19 Treatments Ignored
Using drugs that cause high rates of organ failure, like remdesivir, and drugs that cause the virus to rebound with a vengeance, like Paxlovid, and potentially trigger mutations don’t seem to be in the best interest of public health. The fact that U.S. health authorities have focused on these drugs to the exclusion of all others, including older drugs with high rates of effectiveness and superior safety profiles, sends a very disturbing message.
An investigation by Cornell University, posted on the University’s preprint server January 20, 2022, found ivermectin outperformed 10 other drugs against COVID-19, making it the most effective against the Omicron variant.34 It even outperformed Paxlovid, yet it’s been vilified by health officials and mainstream media.
Remdesivir costs between $2,340 and $3,120,35 and nirmatrelvir costs $529 per five-day treatment,36 while the average treatment cost for ivermectin is $58.37 Do you think this has anything to do with ivermectin’s vilification?
Paxlovid alone has cost U.S. taxpayers $5.29 billion,38 while safe and less expensive options exist. Dr. Pierre Kory, who is part of the group that formed the Front Line COVID-19 Critical Care Working Group (FLCCC) to advance early treatments for COVID-19, pleaded with the U.S. government early on in the pandemic to review the expansive data on ivermectin to prevent COVID-19, keep those with early symptoms from progressing and help critically ill patients recover — to no avail.39,40
However, if you’d like to learn more about its potential uses for SARS-CoV-2, FLCCC’s I-MASK+ protocol can be downloaded in full,41 giving you step-by-step instructions on how to prevent and treat the early symptoms of COVID-19.
Sources and References
- 1, 19 U.S. FDA December 22, 2021
- 2, 3, 5, 22, 24, 26, 28, 31, 32 Science June 29, 2022
- 4, 18, 20, 21 Forbes June 30, 2022
- 6 U.S. CDC May 24, 2022
- 7, 8 CNN June 30, 2022
- 9, 12 U.S. CDC, COVID-19 Rebound After Paxlovid Treatment May 24, 2022
- 10 Research Square May 23, 2022
- 11, 13, 14 CNN May 31, 2022
- 15 Clinical Infectious Diseases June 20, 2022
- 16, 17 UC San Diego Health June 21, 2022
- 23 Pfizer June 14, 2022
- 25 Bloomberg April 29, 2022 (Archived)
- 27, 29, 30 bioRxiv June 7, 2022
- 33 Revyuh May 1, 2022
- 34 Cornell University, January 20, 2022
- 35 AJMC June 29, 2020
- 36 Precision Vaccinations, November 19, 2021
- 37 JAMA 2022;327(6):584-587
- 38 Reuters November 18, 2021
- 39 FLCCC Alliance, Ivermectin & COVID-19
- 40 Mountain Home May 1, 2021
- 41 FLCCC Alliance, I-Mask+
UK Government considered tearing ‘Covid positive’ people from their homes
By Michael Curzon | Bournbrook | July 12, 2022
‘Boris’ Johnson loyalist Nadine Dorries appears to have admitted that the Government, which now prides itself on having imposed restrictions more lightly than others, considered tearing “mothers and fathers and families and children” from their homes if they ‘tested positive’ for Covid during lockdowns to be sent to isolation centres.
A health minister at the time, Ms Dorries was approached by former Health Secretary Jeremy Hunt and told to adopt this ‘zero Covid’ approach, she told GB News.
The now-Culture Secretary told Dan Wootton, who decided not to dig deeper into the claims:
“[Jeremy] said ‘you’ve got to speak to Matt [Hancock]’. It was at the time Nightingale hospitals were being built. ‘You’ve got to tell him that you don’t put sick people in the hospitals, you follow a “zero Covid” policy… When someone tests positive, you take them from their home and you take them to an isolation centre and you leave them there… That’s the only way you can beat Covid.’”
Ms Dorries said she responded:
“‘The British public will not stand for mothers and fathers and families and children being removed from their family and their home and put in isolation.’ He said: ‘Who said they won’t?’ I said: ‘The behaviour and insights team who I’ve discussed this with. They won’t wear it.’” (My emphasis – video below)
This is quite revealing. Anyone with an ounce of humanity would have rejected this outright, whether they thought the public would accept it or not.
Remember, also, that those officials in SAGE believed the British people wouldn’t accept being ‘locked down’ at all until Italy made it clear that they would.
Professor Neil Ferguson told The Times in December 2020:
“[China] is a communist one party state, we said. We couldn’t get away with it in Europe, we thought… and then Italy did it. And we realised we could.”
So has Ms Dorries revealed that the only reason we weren’t pulled away from our families after seeing two red lines was because other Europeans weren’t first?
Judge says it’s legally okay to deny unvaccinated an organ transplant
By Thomas Lambert | The Counter Signal | July 13, 2022
Justice Paul Belzil just decided that it was legally okay for doctors to remove Canadians from organ transplant waitlists if they’re unvaccinated.
As reported by the Westphalian Times’s Marie Oakes, Belzil filed his decision on Tuesday in a case concerning Annette Lewis, who was essentially given the choice of ‘comply or die’ after doctors changed the rules surrounding organ transplant waitlists to require being fully vaccinated.
According to Lewis, a doctor “told me if I did not take the COVID-19 vaccine, I would not get the transplant, and if I did not get the transplant, I would die.”
She added, “I ought to have the choice about what goes into my body, and a life-saving treatment cannot be denied to me because I chose not to take an experimental treatment for a condition — COVID-19 — which I do not have and which I may never have.”
But judge Belzil disagreed, arguing that “her beliefs and desire to protect her bodily integrity [do not] entitle her to impact the rights of other patients or the integrity of the [transplant program] generally.”
He ultimately ruled that the charter doesn’t apply to clinical treatment decisions and that Lewis’s rights, therefore, had not been violated.
Lewis isn’t alone in her struggle either. As previously reported by The Counter Signal, hospitals and health networks across the country have chosen to deny the unvaccinated organ transplants even when prospective patients are healthy and have found a donor.
In October 2021, Toronto’s University Health Network (UHN) (the largest health research organization in Canada and Canada’s largest transplant centre) adopted a policy requiring all organ transplant patients to be fully vaccinated against COVID-19 before doctors operate on them.
The decision immediately affected roughly 4,300 Canadians awaiting life-saving care, some of whom have likely passed away by now.
Hong Kong unveils Covid quarantine bracelets
Samizdat | July 13, 2022
Hong Kong is set to introduce electronic tracking bracelets for citizens who decide to quarantine at home after testing positive for Covid-19, the health chief has announced. Violators of the isolation rules face hefty fines and possibly even jail time.
The territory’s secretary for health, Lo Chung-mau, announced the move during a Monday press briefing, saying the bracelets are meant to stop infected people from spreading the illness further and will operate on the ‘Leave Home Safe’ app rolled out last year.
“We have to make sure that home isolation is more precise while being humane,” Lo said, adding that the trackers will be introduced on Friday.
Breaching Hong Kong’s quarantine order could result in fines up to $3,200 and a maximum of six months behind bars. Individuals who are able to isolate at home must do so for two weeks, though will be allowed to leave if they test negative for two days in a row and have their first pair of vaccine doses.
While the territory previously required overseas arrivals to use bracelets with unique QR codes to check in and account for their movements, the gadgets were later replaced with genuine tracking tech. The system is set to be expanded, though the government has not said what type of bracelet it will use for the latest initiative.
The health secretary also noted that Hong Kong will implement a color-coded system similar to the one in place in mainland China, which labels different levels of infection risk as yellow or red. Those with the red designation will face heavy restrictions on their movement, including outright bans on entering public venues, while yellow entails lesser limits.
However, the city’s recently inaugurated chief executive, John Lee, has since stressed that the traffic light system would only apply to “a specific and small number of people,” but nonetheless argued that Hong Kong needs “some identification method” to distinguish citizens with active infections from those quarantining as a precaution.
Local officials continue to warn that Hong Kong’s Covid-19 outbreak remains “very serious,” urging residents to minimize travel and observe social distancing rules, which were just extended for another two weeks on Tuesday.
The Department of Health said it recorded 2,558 new local coronavirus cases on Tuesday, as well as another 211 infections among travelers from abroad. It did not offer a daily update for fatalities, but noted the territory had tallied 9,420 deaths in total throughout the pandemic, most of them occurring this year.
Catastrophic Massacre – Outcomes of Injecting Babies – Dr. Jessica Rose
CHD.TV | July 8, 2022
References
SARS-CoV-2 Infection of Human Ovarian Cells: A Potential Negative Impact on Female Fertility
After extending the vaccine passport program, Canada threatens fines for those that don’t use it
By Ken Macon | Reclaim The Net | July 12, 2022
After extending the use of the controversial vaccine passport program, the Canadian government has threatened those who do not have a vaccine passport, which reveals someone’s vaccination status for travel, with fines.
Though the government suspended a Covid travel vaccine mandate last month, it has insisted on keeping the more controversial ArriveCAN in use.
International travelers and returning Canadians have to use the ArriveCAN app to submit their contact and travel information and their COVID vaccination status.
The ArriveCAN website states that all travelers will still be “required to submit their mandatory information in ArriveCAN (free mobile app or website) before their arrival in Canada.”
“If you don’t submit your travel information and proof of vaccination using ArriveCAN you could be fined $5,000.”
“All travelers still need a valid #ArriveCAN receipt within 72 hours before their arrival to Canada and/or before boarding a plane or cruise ship destined for Canada, regardless of vaccination status,” tweeted the Public Health Agency of Canada in the last week.
“Failure to complete your ArriveCAN submission can impact your eligibility exemptions, may result in fines, and creates longer wait times for all arriving at the border.”
The Conservative Party has called for the removal of the app, which has been blamed for delays at Canadian airports and airlines.
“Canadians have dealt with enough chaos at the airports. The Liberals need to listen to the science and end the ArriveCan app,” CPC’s interim leader Candice Bergen wrote on Twitter on Monday.
Despite the complaints from users and the delays, the Canadian government extended the use of ArriveCAN until at least September 30.
We’re “losing the fight against monkeypox”… apparently
By Kit Knightly | OffGuardian | July 11, 2022
According to the New York Times the US is currently “losing the fight with Monkeypox”. That’s probably news to you.
After all, given the fact the US has around 700 cases of Monkeypox (around 0.0002% of the population), that the entire world only 8000 “cases” (about 0.0001%), and that there have been just 3 reported deaths… well, you’d be forgiven for not realising there was a fight at all, let alone that we were losing.
It’s really more of a kerfuffle. At worst. Perhaps a fracas.
That is – of course – assuming there is any monkeypox “outbreak” at all, something we should never take on faith, especially in the post-Covid world.
Nevertheless, the NYT is sure…
There probably will be many more infections before the outbreak can be controlled, if at this point it can be controlled at all.
The US isn’t the only place getting a fresh batch of monkeypox fear porn this week.
Five days ago it was reported that Australia had recorded its first “case”, with the under-stated headline…
KILLER VIRUS SUDDENLY SPREADS IN AUSTRALIA
… clearly this went too far, even for the mainstream media, who quietly reworded the title a few hours later.
Not to be outdone, two days later New Zealand announced their first monkeypox case was isolating at home.
And just 15 minutes ago, at the time of writing, The Guardian published a news story headlined:
Efforts to curb UK monkeypox outbreak inadequate, warn experts
So, what is the cause of mankind’s imminent loss to the monkeypox peril? Well they really couldn’t be clearer about that – we’re not testing enough.
The NYT goes on about this at length:
the response in the United States has been sluggish and timid, reminiscent of the early days of the Covid pandemic, experts say, raising troubling questions about the nation’s preparedness for pandemic threats.
[…] The first cases of monkeypox were reported in May, but tests will not be readily available until sometime this month.
[…] The first missteps in the U.S. response to monkeypox were in testing. As in the early days of the coronavirus pandemic, samples from monkeypox patients are being funneled to the CDC for final diagnosis, a process that can take days.
Slate agrees, headlining “We Need to Keep Better Track of Monkeypox” and quoting on “expert”:
Testing is the key piece in getting answers to these questions, and currently we simply are not doing enough of it.”
We’ve seen this movie before, we know how it goes from here.
Since, as the NYT points out, Monkeypox tests will be “readily available sometime this month”, we can expect a BIG spike in cases coming up.
Far from being recognised for what it is – a huge number of false positives caused by PCR tests – this increase in cases will be sold as the “true size of the outbreak” after weeks of calling current “case” numbers “likely underestimates”.
The solution, we know, will be “increasing vaccine coverage” or “helping immunize the most vulnerable” or some buzz phrase like that.
But oh no! We don’t have enough vaccines!
At least, according the New York Times, and LA Times, and CBS, and Science and New York Magazine and NPR and NBC and the New York Post and…
… it’s the prevalent message, is what I’m trying to say.
Don’t worry though, a VERY familiar hero is about to ride over the horizon on a white horse:
Moderna is investigating potential monkeypox vaccines at a preclinical level, using its mRNA platform,”
Yes, Moderna started working on a new mRNA monkeypox vaccine back in May… so by Covid rules they’re probably nearly done by now.
Just inject in precisely one person, and if they don’t die instantly on the spot then it’s safe.
… and if they DO then they were already sick and the trial data is compromised and monkeypox is such an emergency we should grant it approval anyway. You can read the trial data in 2097.
We know how this works.
Tests to create the “problem”, vaccines to “solve” the “problem”. Both of them result in vast amounts of public money disappearing into bottomless private pockets.
There’s a lot of fog around monkeypox – we don’t know, in a lot of ways, where it’s going or what it’s even for. The narrative is only half-formed. First growing, then shrinking, then growing again.
It had a name change that never really materialised, and the decision to focus it on sexual transmission – especially among “men who have sex with men” (I don’t know why they ALL use that phrase and not “gay men”) – is one I just can’t puzzle out yet.
But while it’s yet to take definitively pick a size, direction or speed, it’s taking a very familiar shape: Tests and vaccines.
It’s always tests and vaccines.
Top climate scientists slam global warming “so-called evidence” as “misrepresentation, exaggeration & outright lying”
By Chris Morrison | The Daily Sceptic | July 11, 2022
Two top-level American atmospheric scientists have dismissed the peer review system of current climate science literature as “a joke”. According to Emeritus Professors William Happer and Richard Lindzen, “it is pal review, not peer review”. The two men have had long distinguished careers in physics and atmospheric science. “Climate science is awash with manipulated data, which provides no reliable scientific evidence,” they state.
No reliable scientific evidence can be provided either by the Intergovernmental Panel on Climate Change (IPCC), they say, which is “government-controlled and only issues government dictated findings”. The two academics draw attention to an IPCC rule that states all summaries for policymakers are approved by governments. In their opinion, these summaries are “merely government opinions”. They refer to the recent comments on climate models by the atmospheric science professor John Christy from the University of Alabama, who says that, in his view, recent climate model predictions “fail miserably to predict reality”, making them “inappropriate” to use in predicting future climate changes.
The ’miserable failure’ is graphically displayed below. Since the observations cut-off, global temperatures have again paused.

Particular scorn is poured on global surface temperature datasets. Happer and Lindzen draw attention to a 2017 paper by Dr. James Wallace and others that elaborated on how over the last several decades, “NASA and NOAA have been fabricating temperature data to argue that rising CO2 levels have led to the hottest year on record”. The false and manipulated data are said to be an “egregious violation of scientific method”. The Wallace authors also looked at the Met Office HadCRUT database and found all three surface datasets made large historical adjustments and removed cyclical temperature patterns. This was “totally inconsistent” with other temperature data, including satellites and meteorological balloons, they said. Readers will recall that the Daily Sceptic has reported extensively on these issues of late and has attracted a number of somewhat footling ‘fact checks’.
Happer and Lindzen summarise: “Misrepresentation, exaggeration, cherry picking or outright lying pretty much covers all the so-called evidence marshalled in support of the theory of imminent catastrophic global warming caused by fossil fuels and CO2.”
Professors Happer and Lindzen’s comments are included in a submission to the U.S. Securities and Exchange Commission, which is seeking to impose massive and onerous ‘climate change’ reporting requirements on public companies. But they form part of a wider scientific revolt by many scientists alarmed at the corruption of science to promote the command-and-control Net Zero agenda. Needless to say, these debates are largely ignored by mainstream media. Opponents of Net Zero politicised science are denounced as ‘cranks’ and ‘deniers’, labels at odds with their distinguished scientific achievements. Between them, Happer from Princeton and Lindzen from MIT have around 100 years of involvement in atmospheric science. Richard Lindzen was an early lead author for the IPCC, while William Happer was responsible for a groundbreaking invention that corrected the degrading effects of atmospheric turbulence on imaging resolution.
In their submission, Happer and Lindzen supply a basic lesson in science: “Reliable scientific theories come from validating theoretical predictions with observations, not consensus, peer review, government opinions or manipulated data”.
In the U.K., it will be interesting to see if Net Zero will feature as a major issue in the battle to find a new Prime Minister. At the moment, candidates seem to be steering a widish berth – something that can happen with virtuous green policies when actual votes are at stake. Happer and Lindzen state firmly that “science demonstrates there is no climate-related risk caused by fossil fuels and CO2, and therefore no reliable scientific evidence supporting the proposed rule”. The rule in this case refers to the SEC climate requirement, but it could equally apply to Net Zero. Many people now accept that a rigid Net Zero policy will lead to massive falls in living standards that will disproportionately affect the poorer in society, both in the U.K. and particularly in the developing world. Contrary to the incessant attack on fossil fuels, write Happer and Lindzen, “affordable, abundant fossil fuels have given ordinary people the sort of freedom, prosperity and health that were reserved for kings in ages past”.
Such prosperity, of course, has left the building in the case of Sri Lanka, where the prospect of famine and civil breakdown face 22 million people following (among other things) the decision of the Government to ban fertiliser in the interests of climate change and saving the planet. Such a collapse, with the President hastily fleeing the country, is likely to face any modern Net Zero society that seeks to tamper with reliable and affordable energy supply, restrict diet and try to grow enough food using ‘organic’ methods. Happer and Lindzen state that reducing CO2 and the use of fossil fuels would have “disastrous consequences” for the poor, people worldwide and future generations.
Both Happer and Lindzen have long held out against the current demonisation of atmospheric CO2, pointing out that the current 415 parts per million (ppm) is near a record low and not dangerously high. They note that 600 million years of CO2 and temperature data “contradict the theory that high levels of CO2 will cause catastrophic global warming”. Omitting unfavourable data is an egregious violation of scientific method. Facts omitted by those who argue there is a climate emergency include that CO2 levels were over 1,000 ppm for hundreds of millions of years and have been as high as over 7,000 ppm; CO2 has been declining for 180 million years from about 2,800 ppm to today’s low; and today’s low is not far above the minimum level when plants die of CO2 starvation, leading to all other life forms perishing for lack of food.
Finally, the authors note that the logarithmic influence of CO2 means its contribution to global warming is “heavily saturated”. The scientists calculate that a doubling of current CO2 levels would only reduce the heat escaping to space by about 1.1%. This suggests warming of around 1°C or less. The saturation hypothesis explains, they say, the disconnect between CO2 and temperature observed over 600 million years.
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
Joe Biden and Other Politicians, not Coronavirus, Caused Children’s Educations to Suffer

By Adam Dick | Ron Paul Institute | July 7, 2022
President Joe Biden declared Tuesday at Twitter: “Due to the pandemic, kids are behind in math and reading.” This is yet another example of politicians’ blame shifting we have seen throughout the coronavirus scare. Kids in America have fallen behind in their educations during the coronavirus scare, but not because of coronavirus. They have fallen behind because of coronavirus crackdown actions supported by Biden and many other politicians in the name of protecting students, teachers, and staff at schools from coronavirus that did not improve safety but did interfere with students’ ability to learn.
Since early on in the coronavirus scare it was known that children tended to be in miniscule danger from serious sickness or death from coronavirus. It was also known that, at schools, teachers and other adults tended not to get coronavirus from students. Yet, most American politicians with control over education policy did not say that “for the children” schools would be kept open and continue operating normally, something that was done in other countries and a few places in America without problems. Instead, as politicians are apt to do, they used the “for the children” plea as an excuse to wreak havoc. They shut down schools, then replaced them to some extent with dysfunctional attempts at virtual education, and ultimately reopened the schools in an absurd and menacing manner.
Many schools, when they finally reopened, had all kinds of mandates that made the schools insufferable. The mandates, while failing to protect people from coronavirus, did carry health dangers of their own. Mask mandates, obsessive disinfecting of surfaces at schools and even of children’s hands, enforcement of “social distancing,” the presence of ubiquitous plastic barriers separating people, coronavirus testing, and pressure or even mandates for students to take experimental coronavirus “vaccine” shots were among the nasty changes confronting students at their “new normal” schools. Students found themselves trudging through a real life version of a dystopian novel.
No wonder students’ learning suffered through the coronavirus scare. Learning was not high on the priority list of many politicians rushing to exercise their new powers. And, due to government pressure and bad choices by people in charge, the situation was similarly awful at many private schools as at government schools.
Fortunately, this dark cloud of politicians harming student’s educations in the name of countering coronavirus does have a silver lining, though only for a small subset of students. “Enough is enough,” decided some parents along the way of witnessing the school closures, the dysfunctional virtual learning efforts implemented to replace regular school, and the dystopian “new normal” schools that ultimately came into being. These parents took their children’s educations into their own hands, moving their children to homeschooling. The result is that many more children now than before the coronavirus scare are free from the politicians’ harmful meddling, whether undertaken in the name of protecting children from phantom coronavirus danger or accomplishing other objectives at variance with advancing the math and reading skills Biden mentioned at Twitter. It is a safe bet that most of these new homeschooling parents will do a much better job than the schools they left behind at making sure their children’s educations serve their children’s needs and interests.
