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Biden regime & WHO finally realise nobody cares anymore, fold up last vestiges of the Covid circus

Polish health minister denounces Pfizer vax profiteering, amazingly asks if it is “only about money”

eugyppius: a plague chronicle | May 7, 2023

The Biden Administration have announced that their insane vaccine requirements for government employees and international travellers will finally end on 11 May, when the American pandemic state of emergency expires. The WHO have likewise declared that Covid-19 “no longer constitutes a public health emergency of international concern.” Three years and two months after it all started, the last remaining participants in the Covid circus are finally folding up their tables and going home.

It’s worth asking why now, because by any objective measure, there has been no virus activity worthy of the words ‘pandemic’ or ‘emergency’ for a very long time. The answer seems to be the failure of Corona to return in the winter, as long-absent influenza succeeded in suppressing Corona infections (in accordance with my prediction), and the increasing disinterest of the public in obtaining official test results has put all virus statistics in the toilet. They’re ending it now, in other words, not because anything on the ground has changed, but because they no longer have any hope of the scary headlines necessary to keep the machine up and running.

As in the beginning, so in the end: The pandemicists will give you always and forever the maximum virus suppression and the maximum vaccination that is politically possible. Not what is prudent, or what has any hope of achieving anything, or what has evidence in its favour, but simply the maximum that they can give you, for as long as they can give it to you. That is a reason in itself, never to let the pandemicists anywhere near the levers of power ever again.


The pandemic may be over, but there is no stopping the vaccines. Thanks to the incredibly stupid contracts that the EU concluded with Pfizer/BioNTech, we are drowning in them, and some of our less prosperous neighbours to the east have had enough:

With the Covid vaccination campaigns concluded, the European Union is sitting on an enormous vaccine surplus – and hundreds of millions more doses are expected to arrive this year and next… Because they are not needed, EU member states have been trying for months to retroactively adjust the contracts, without much success.

One country has now lost patience in the face of the tough negotiations, and is venting its anger. The Polish Health Minister Adam Niedzielski on Tuesday sent a letter to the “shareholders of Pfizer” [which] says that the delivery of hundreds of millions of doses planned by Pfizer despite a “stable epidemic situation” is “completely pointless.”

The excess doses can no longer even be given away; there is no government “interested” in Covid vaccines, said the minister …

Niedzielski also breaks prior agreements on the confidentiality of talks between governments, pharmaceutical companies and the mediating EU Commission … [and] reveals what Pfizer is offering the states: They’ll reduce the total quantity of the outstanding orders, in exchange for half the price of each dose that is not produced: “That’s a charge for literally non-existent doses that were never produced and will never be produced and that don’t cost Pfizer a penny.”

No wonder there has been such urgency to keep these negotiations secret.

Niedzielski writes that he is “extremely” sorry, but he is forced to conclude that the company is not prepared to show “a satisfactory level of flexibility and make any realistic proposals.” … The health minister called on Pfizer to “live up to its responsibility towards EU citizens and member states and work in good faith towards a solution that is fair for everyone.” Poland wants to continue to believe that the pharmaceutical industry is not only about money.

Hahhhahahahahahhhahahhhahahahahhahhahahhahhaha.

Video source

May 7, 2023 Posted by | Deception, Video | , , | Leave a comment

Unrepentant Corona arch-villain Christian Drosten re-emerges to give the vaccines credit for ending the pandemic

Insists that lockdowns and school closures remain policy options in the future

Virus-understander-in-chief Christian Drosten posing as a scrappy compassionate avatar of The Science, rather than the conniving and perpetually wrong loser that he is.
eugyppius: a plague chronicle | May 6, 2023

That eternal turd who will not flush, Christian Drosten, has resurfaced with an odious media interview, demanding that the vaccines receive credit for ending the pandemic and that oppressive non-pharmaceutical interventions like lockdowns and school closures remain on the table for future pandemics.

From Tagesspiegel :

The measures taken by the federal and state governments in the Corona pandemic proved highly controversial and triggered fierce debates. The Berlin Charité virologist Christian Drosten, among the advocates of harsh restrictions, has now warned against drawing the wrong conclusions. The “fundamental, ideological exclusion of lockdowns and school closures” is foolhardy, Drosten told the newspapers of the Funke Mediengruppe.

“Not all pathogens have the same characteristics. A virus could surface that is especially dangerous for children, for example, or that triggers insidious sequelae despite a harmless initial infection.”

“The school closures in 2020 and 2021 were a mistake, but please don’t take away our power to close schools again in the future! The next virus might really be dangerous to children! We don’t always cry wolf, except when we do!”

Infections such like mumps and measles have caused brain inflammation, diabetes or infertility, the director of the Institute of Virology added. “If such a virus developed into a highly transmissible pandemic pathogen, politicians would inevitably have to take measures. You can’t categorically rule out things like lockdowns and school closures, that’s neither realistic nor responsible.”

Yes, you can categorically rule out lockdowns and school closures. We literally never did any of this before at this scale or for this duration in response to any virus, nor were lockdowns or other invasive measures ever even contemplated until the Chinese gave you guys a bunch of evil ideas three years ago. What’s more, all of your interventions were utter, abject failures; they did nothing.

Drosten also criticised the public debate on Covid vaccinations, which “is often still destructive.” The fact that further Covid vaccinations for children and many adults are now no longer recommended “does not prove that vaccines have always been unnecessary,” the Charité professor emphasised.

“Rather, with the help of vaccinations, we have mitigated the impact of infections and developed a high level of immunity in the population. This is the only reason that the vaccine recommendations could now be changed.”

Had we vaccinated not a single soul, we’d have identical levels of immunity in the population right now from Omicron. We also wouldn’t have all those awkward vaccine injury headlines.

In case you’re not yet angry enough, though, it gets worse:

The director of the Institute for International Health at Charité, Beate Kampmann, warned against vaccine scepticism. “Vaccination is not only about the well-being of the individual, but also about the health of society as a whole, that is public health, and that also means solidarity,” she told the newspapers.

“Sometimes people forget that they contribute to the protection of everyone with their personal decision. That was true for Corona, but it’s also true for measles, for example.”

Why are these assholes always lying, I want to know. The vaccines were not intended to stop transmission, the trials weren’t designed to show whether they would stop transmission, and we’ve known beyond all doubt since the summer of 2021 that they don’t stop transmission. Nobody who was vaccinated against Corona contributed to anybody else’s health at all, this is all just a straight-up untruth.

The pandemicists aren’t going away. They have amassed a great toolkit of new powers, and they will be slinking around for decades waiting for the next opportunity to try them out all over again. Now that the virus hysteria has boiled off and some minimal standards of rationality have returned to the discussion, it should be a priority to discredit every last one of these virus pests, Corona astrologers, modellers, and panic mongerers, now and for all time. Otherwise we’re at great risk for getting the same thing all over again.

May 6, 2023 Posted by | Civil Liberties, Science and Pseudo-Science | , , | Leave a comment

How to fight for Covid truth

By Guy Hatchard | TCW Defending Freedom | May 6, 2023

The writer is in New Zealand.

Every day brings more news of extreme efforts to promote biotech vaccines and cancel those asking questions.

For example Dr Mark Tykocinski, an immunologist with a spotless academic record who is president of Thomas Jefferson University in Philadelphia may be about to lose his job. His sole mistake appears to be liking tweets by former New York Times journalist Alex Berenson who questions vaccine safety.

British MP Andrew Bridgen has been expelled from the Conservative Party. According to Bridgen, a senior UK politician has privately admitted to him that he may well be right about Covid vaccine harms, but said the government is expecting to suppress public information about Covid vaccine adverse effects for the next 20 years, citing ‘lack of political appetite’ for a public disclosure.

Statistician Professor Norman Fenton was locked out of his Twitter account following a complaint that he had broken German law by claiming Covid data manipulation was creating the appearance of vaccine efficacy, when in fact there was none. The German government is the main sponsor of BioNTech, the co-creator of the Pfizer mRNA Covid vaccine. Fortunately the complaint was not upheld and Fenton was reinstated.

Te Whatu Ora (Health New Zealand) has announced that from May 1, pregnant people (!) aged 16 to 29 years can now get an additional Covid-19 booster. They don’t seem to have noticed that stillbirths and miscarriages rose following the Covid vaccine rollout, or the absence of any data to confirm ‘safety’ assurances for pregnant women – quite the reverse, in fact.(See this article.) Is it possible that the NZ government have a lot of boosters left over after a poor response to their latest bivalent vaccine campaign and are now trying to offload them via deceptive advertising to mothers who naturally want to do the best for their child?

Highly vaccinated Portugal has seen a 73 per cent rise in emergency callouts for heart attacks. This mirrors the 83 per cent rise in heart attack hospitalisation in Wellington, NZ.

The continuing attacks from the media and vaccine advocates mean that some people must be seriously worried that the scientific data about vaccine harms is beginning to resonate with a wider audience. We are winning the argument.

Last week I reported correspondence from our Minister of Statistics Dr Deborah Russell MP in which she downplayed the significance of rising excess deaths in New Zealand. This appeared to be the result of misinformed policy rather than real statistics. Does the New Zealand government, in line with the UK, wish to hide Covid vaccine adverse effect statistics from the public until it becomes a matter of distant history? You tell me.

Should we be protesting on the streets?

In fact both the vaccinated and unvaccinated have been injured by government policy and experimental biotechnology. Even the pro-vaccine, pro-zoonotic origin NY Times has conceded that evidence is mounting that Covid came from a lab leak. We have a common cause.

It would certainly suit those who wish the pandemic gravy train and the biotech boom to continue, if the population were to remain polarised and the adverse effects hidden. At this time, it is my belief that launching ad hominem attacks, participating in lawful protests or expressing violent sentiments (never a good idea) will simply play into the hands of those from the media, corporates, medical professions and governments who are hoping that public concern can continue to be managed, marginalised and cancelled.

But this doesn’t mean remaining silent, we should be raising our voices and using our pens. I do believe we should always talk rationally and factually about issues that matter. This is an election year in New Zealand, when there is a higher chance of being heard. We can talk to candidates and demand answers, or even become candidates. In an election year, politicians know that all votes will matter. We can raise a voice of reasoned intelligence, express ourselves calmly, cite research, and send letters to our politicians. Politicians cannot find papers to back their views; published research is now firmly on our side of the debate. Our points cannot be dismissed.

Again and again I come back to ‘knowledge matters’. It might still be possible to nip dictatorial control in the bud before it gains more traction.

May 5, 2023 Posted by | Full Spectrum Dominance, Science and Pseudo-Science, Timeless or most popular, War Crimes | | Leave a comment

FDA Approves First RSV Vaccine, But Some Experts Say Weak Safety, Efficacy Data Suggest Benefits Don’t Outweigh Risks

By Michael Nevradakis, Ph.D. | The Defender | May 4, 2023

Describing it as a “long-sought scientific achievement,” the U.S. Food and Drug Administration (FDA) on Wednesday approved Arexvy, the first vaccine for respiratory syncytial virus (RSV).

GlaxoSmithKline Biologicals (GSK) developed Arexvy under the FDA’s Priority Review designation. The FDA approved it for people ages 60 and older.

According to CNBC, the U.S. “suffered an unusually severe RSV season” this past winter. The New York Times reported on a “tripledemic” involving RSV, flu and COVID-19, “that swamped children’s hospitals and some I.C.U. wards.”

One U.S. county — Orange County, California — declared a local health emergency and issued a proclamation of local emergency in November 2022, citing rising RSV cases among children in the region.

GSK described results from clinical trials for Arexvy as “positive,” and the company said the U.S. launch of the vaccine is planned before the 2023-24 RSV season.

Other RSV vaccines, including one produced by Pfizer, are in the pipeline and expectations are that the FDA will approve them.

During clinical trials for both the GSK and Pfizer vaccines, several participants were diagnosed with rare conditions such as Guillain-Barré syndrome (GBS) and acute disseminated encephalomyelitis (ADEM). One of the individuals who developed ADEM later died, according to the FDA.

Aside from concerns over potential serious adverse events related to RSV vaccines, some experts have questioned the need for such a vaccine in the first place.

According to the journal Science, “RSV is a common respiratory infection” with symptoms “similar to a cold,” adding that “The majority of individuals recover within a few days from an uncomplicated RSV infection, although occasionally the virus can cause lower respiratory infections requiring medical attention.”

Dr. Peter McCullough, a cardiologist, told The Defender:

“Respiratory syncytial virus is a negligible threat to even the most frail elderly adults. The effort of widespread vaccination is simply not worth it. Even rare side effects will outweigh any theoretical benefit.”

And in a November 2022 episode of “RFK Jr. The Defender” podcast, several medical and public health experts expressed concerns about RSV vaccines.

“We have to stop these shots,” said Dr. Meryl Nass, an internist and biological warfare epidemiologist. “It’s just extraordinary that we’re still vaccinating people … we have a lot of work to do.”

Robert F. Kennedy Jr., then-chairman and chief litigation counsel for Children’s Health Defense (now chairman on leave), described RSV as “a vehicle for re-implementing the COVID-19 playbook all over the country and responding with vaccines.”

And according to the National Vaccine Information Center (NVIC), “Cost analysis data presented to the ACIP [Advisory Committee on Immunization Practices] did not show the RSV vaccines to be cost-effective at reducing the burden of costs associated with RSV illness.”

Nevertheless, more RSV vaccines are expected to receive FDA approval this year — including a Pfizer RSV vaccine for pregnant women that led to a high incidence of adverse events for both the women and their infants during clinical trials, as well as several deaths and stillbirths.

Arexvy approval ushers in new ‘highly competitive and lucrative vaccine market’

The RSV vaccine market is estimated to be worth up to $10 billion by 2030.

According to Endpoints News, the FDA’s approval of Arexvy ends “half a century of failed efforts against the elusive, shape-shifting virus” and “officially start[s] what analysts expect will be a highly competitive and lucrative new vaccine market.”

In getting Arexvy approved, “GSK beat a crowded field of competitors to cross the finish line first.”

Arexvy “showed strong efficacy in stopping lower-respiratory tract infections as well as more severe disease” and will be administered as a single dose, according to Endpoints News.

STAT reported that a “vaccine that was developed by Pfizer and aimed at the same demographic [adults 60 and over] is expected to be approved by the end of the month,” while other RSV vaccines and therapeutics, including some intended for children and pregnant women, are in the pipeline and also are close to receiving FDA approval.

The FDA’s approval of Arexvy came after an FDA advisory panel reviewed data from GSK’s and Pfizer’s clinical trials on March 1. The panel unanimously agreed that GSK’s vaccine is effective and, in a 10-2 vote, deemed it “safe,” according to The Washington Post.

The same panel also approved Pfizer’s candidate vaccine, Abrysvo, but with a 7-4 vote.

On June 21 or 22, ACIP, which advises the Centers for Disease Control and Prevention (CDC), will convene to “make recommendations on the appropriate use of the vaccine in the U.S.,” according to GSK’s announcement. The ACIP must recommend the vaccines before they are marketed.

According to STAT, there is a likelihood that ACIP may not approve Arexvy for its intended age group, stating:

“Though Arexvy’s approval is for adults 60 and older, it remains to be seen if the CDC will recommend it for that entire group.

“At an advisory committee meeting in February, members of a work group studying the adult vaccines that will soon come before ACIP indicated that at present, they don’t believe the vaccine would be cost-effective in people aged 60 to 64 and they would not recommend to the wider committee that it include people 60 to 64 in its recommendation for the use of the vaccine. (The group held the same position for the Pfizer RSV vaccine.)”

In April, the European Medicines Agency (EMA) issued its own recommendation for Arexvy, for adults 60 and over, according to the Times. However, a final EMA regulatory decision is anticipated later this year. GSK is also awaiting licensure for Arexvy in Australia, China, Japan and other countries, STAT reported.

In an earnings presentation April 26, GSK said it has “millions of doses” of Arexvy “ready to be shipped.”

According to CNN:

“GSK’s RSV vaccine works by using a small piece of the virus: a protein that sticks out on its surface called the fusion, or F, protein, which helps the virus glom onto and infect cells in the body’s upper airways. The protein pieces in the vaccine are made in a lab, using cells specially programmed to manufacture them.”

CNN noted that the vaccine “builds on a pivotal discovery made a decade ago” by National Institutes of Health researchers, “including some of the same scientists who helped make the COVID-19 vaccines.” Specifically, the researchers figured out how to freeze the otherwise “wiggly” F protein, “in the shape it takes before it fuses onto a cell.”

STAT, quoting Phil Dormitzer, GSK senior vice president and global head of vaccines research and development, reported that although Arexvy “contains only one of the two RSV subtypes, RSV A,” studies showed that it is “virtually equally protective against both RSV A and RSV B” as the F protein on both subtypes is similar.

Dormitzer acknowledged natural immunity, telling STAT, “because older adults have all had RSV probably multiple times by the time they get [the vaccine], they’re primed against both A and B. So you’re able to get very solid boosting against both subtypes with a single adjuvanted F antigen.”

According to GSK, the Arexvy vaccine does not use mRNA technology, but “contains a recombinant subunit prefusion RSV F glycoprotein antigen (RSVPreF3) combined with GSK’s proprietary AS01E adjuvant.”

GSK, FDA claim Arexvy clinical trial data show vaccine is ‘safe and effective’ but annual shot may be needed

The FDA announcement stated:

“The safety and effectiveness of Arexvy is based on the FDA’s analysis of data from an ongoing, randomized, placebo-controlled clinical study conducted in the U.S. and internationally in individuals 60 years of age and older.”

According to the FDA, “approximately 12,500 participants … received Arexvy and 12,500 participants … received a placebo. Among the participants who have received Arexvy and the participants who have received a placebo, the vaccine significantly reduced the risk of developing RSV-associated LRTD [lower respiratory tract disease] by 82.6% and reduced the risk of developing severe RSV-associated LRTD by 94.1%.”

LRTD was “defined as two or more symptoms including shortness of breath, wheezing, cough, increased mucus production, crackles, low oxygen saturation, or need for oxygen supplementation,” according to CNBC, while according to CNN, “People were considered to have severe disease if they needed supplemental oxygen or needed mechanical help to breathe, like a ventilator.”

According to the FDA, half of the 25,000 participants received Arexvy, while the other half received a placebo.

The results of GSK’s clinical trials for Arexvy were published in the New England Journal of Medicine on Feb. 16.

FDA and GSK officials provided glowing reviews of the new vaccine. Peter Marks, M.D., Ph.D., director of the FDA’s Center for Biologics Evaluation and Research, said in a statement:

“Older adults, in particular those with underlying health conditions, such as heart or lung disease or weakened immune systems, are at high risk for severe disease caused by RSV.

“Today’s approval of the first RSV vaccine is an important public health achievement to prevent a disease which can be life-threatening and reflects the FDA’s continued commitment to facilitating the development of safe and effective vaccines for use in the United States.”

Tony Wood, GSK’s chief scientific officer, described Arexvy’s approval as “a turning point in our effort to reduce the significant burden of RSV,” adding that “Our focus now is to ensure eligible older adults in the U.S. can access the vaccine as quickly as possible and to progress regulatory review in other countries.”

In turn, Dormitzer said, “There’s just the broad excitement of finally, after all these years, having good options emerging for RSV,” describing this as a “triumph of the basic science.”

While GSK is first out of the gate in the RSV vaccine race with Arexvy, Pfizer’s candidate vaccine has also completed clinical trials, which found it to be “nearly 67 percent effective in preventing R.S.V. – related illness,” according to the Times.

The FDA and GSK announcements did not mention the vaccines’ waning effectiveness. An analysis by the NVIC found that the effectiveness of the GSK vaccine peaked after two months and offered no protection after one year. This may result in recommendations for adults to receive annual doses of the vaccine.

Trial participant died from a rare inflammatory condition, others developed GBS

Despite positive comments from FDA and GSK officials, clinical trial data for Arexvy revealed instances of GBS and other rare conditions.

In its announcement Wednesday, GSK claimed:

“The vaccine was generally well tolerated with an acceptable safety profile. The most frequently observed solicited adverse events were injection site pain, fatigue, myalgia, headache, and arthralgia. These were generally mild to moderate and transient.”

The announcement did not mention GBS.

According to the FDA announcement Wednesday:

“The most commonly reported side effects by individuals who received Arexvy were injection site pain, fatigue, muscle pain, headache and joint stiffness/pain.

“Among all clinical trial participants, atrial fibrillation within 30 days of vaccination was reported in 10 participants who received Arexvy and 4 participants who received placebo.”

However, the FDA noted that in two other Arexvy studies involving approximately 2,500 participants 60 and over, “two participants developed acute disseminated encephalomyelitis (ADEM), a rare type of inflammation that affects the brain and spinal cord, seven and 22 days, respectively, after receiving Arexvy and the influenza vaccine.”

“One of the participants who developed ADEM died,” according to the FDA.

In another Arexvy study conducted by GSK, “one participant developed Guillain-Barré syndrome (a rare disorder in which the body’s immune system damages nerve cells, causing muscle weakness and sometimes paralysis) nine days after receiving Arexvy,” the FDA stated.

According to an FDA briefing document cited by CNBC:

“A 78-year-old woman in Japan was diagnosed with Guillain-Barré syndrome nine days after receiving GSK’s vaccine … She was hospitalized for six months before being released.”

CNBC reported that GSK claimed in February “There is insufficient evidence to confirm the woman got Guillain-Barre as a result of GSK’s shot.” However, the FDA “considers the case to be related to GSK’s vaccine.”

According to the FDA’s announcement:

“The FDA is requiring the company to conduct a postmarketing study to assess the signals of serious risks for Guillain-Barré syndrome and ADEM. In addition, although not an FDA requirement, the company has committed to assess atrial fibrillation in the postmarketing study.”

According to the Times, “Once the shots become available to the public, the agency said it would require GSK to monitor the incidence of Guillain-Barré and another rare condition that was possibly related to the shot.”

The FDA similarly flagged GSK “as a potential safety issue with Pfizer’s RSV vaccine for older adults,” CNBC reported after two clinical trial participants developed GBS. According to the Post, both participants — one man and one woman — were 66 years old.

CNBC in February reported that Pfizer “will conduct a safety study to further address Guillain-Barré syndrome if the FDA approves its vaccine.”

GSK’s chief commercial officer, Luke Miels, said the vaccine would cost upwards of $120 a dose, according to the Post, which also reported that private insurers may cover “many costs” associated with the vaccine, while Medicare patients with Part D coverage “won’t pay anything out of pocket” for the vaccine.

“Shares of GSK rose nearly 2% Wednesday following the approval,” CNBC reported.

GSK is also pressing forward with “A clinical trial that aims to expand the population who may benefit from RSV vaccination into adults aged 50-59, including participants with underlying comorbidities,” according to the company’s Wednesday announcement, with results “expected in 2023.”

Is there a need for an RSV vaccine?

According to the FDA:

“RSV is a highly contagious virus that causes infections of the lungs and breathing passages in individuals of all age groups. RSV circulation is seasonal, typically starting during the fall and peaking in the winter.

“In older adults, RSV is a common cause of lower respiratory tract disease (LRTD), which affects the lungs and can cause life-threatening pneumonia and bronchiolitis (swelling of the small airway passages in the lungs).”

The FDA cited CDC figures claiming each year in the U.S., RSV leads to approximately 60,000-120,000 hospitalizations and 6,000-10,000 deaths among adults 65 years of age and older.”

STAT reported that “RSV season has been unpredictable in the wake of the COVID-19 pandemic, though some experts believe RSV activity is moving back toward the seasonality seen in the pre-COVID days,” noting that “there was little transmission in 2020, when people were wearing masks and social distancing.”

But RSV “returned abnormally early in 2021,” STAT reported, but without an explanation for why this occurred, despite widespread masking and social distancing that year, too.

In the U.S., pediatric deaths from RSV are not common but the infection is the No. 1 cause of hospitalizations for children under the age of 1, STAT reported. Globally, however, it is the second leading cause of death in children under 1, after malaria.

According to STAT, “All but the youngest of children have had RSV multiple times, but few of us would know with any certainty that this bad cold was caused by that bad virus.”

Nevertheless, Pfizer is proceeding with the development of an RSV for infants as young as 6 months — “the age group at highest risk of being hospitalized with RSV,” STAT reported, noting that the vaccine for this age group is expected to gain FDA approval later this year and will be administered to pregnant women “to generate antibodies that protect both the pregnant person and their newborn.”

Data reported by Pfizer to the CDC indicated that 14% of pregnant women who participated in Pfizer’s trial sustained an adverse event, with 4.2% sustaining a “serious” adverse event, 1.7% experiencing a “severe” adverse event and 0.5% suffering a “life-threatening” adverse event.

Similarly, the same data showed that 37.1% of infants whose mothers received the experimental Pfizer vaccine experienced adverse events within one month of birth — with 15.5% classified as “serious,” 4.5% as “severe” and 1% as “life-threatening,” while efficacy waned within months of vaccination.

According to the NVIC, “The RSV clinical trial data also included the death of one pregnant woman, 18 still births (10 in vaccinated pregnant women and 8 in unvaccinated pregnant women), and 17 infant deaths (five from the vaccinated pregnancy group and 12 in unvaccinated pregnancy group).”

In its report to the CDC, Pfizer claimed the deaths were unrelated to the vaccine.

The FDA’s Vaccines and Related Biological Products Advisory Committee will meet virtually on May 18 to discuss approval of this vaccine. The meeting is open to the public, and a public comment period is open until May 17. A final FDA decision is expected in August.

According to the Times, “Moderna is also developing an RSV vaccine for adults 60 and over, with authorization expected in the first half of this year. The Times referenced clinical trial data released by Moderna claiming 82% efficacy, with “no safety concerns identified.”

Bavarian Nordic, known for its development of a vaccine in response to last year’s monkeypox outbreak, is also developing an RSV vaccine for adults 60 and over,” expecting to release Phase 3 clinical trial data by midyear, according to the Post and CNN.

AstraZeneca and Sanofi also are seeking FDA approval, but for nirsevimab, a monoclonal antibody treatment for RSV that would be administered to infants and toddlers up to age 2, according to the Times, which referenced clinical trial results claiming a reduction of illness of up to 75%.

According to the Post, nirsevimab “is already approved in Europe, the United Kingdom and Canada.”

However, the NVIC reported that the effectiveness of nirsevimab “is not known beyond 150 days” and it is unclear if the drug prevents ICU stays or deaths. It is being reviewed by ACIP, which according to the NVIC, is “a federal advisory committee charged with making vaccine use recommendations.”

“It is unclear why the ACIP … has chosen to go beyond its charge of making vaccine use recommendations,” NVIC states.

Safety concerns related to RSV vaccines nevertheless linger. According to CNN, an RSV vaccine developed in the 1960s for children initially delivered promising results during trials in children and animals.

However, once administered to children in the general population, “many of the children who were vaccinated required hospitalization and got more severe RSV disease than what would have normally occurred” — and two of the initial trial participants died.


Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

May 4, 2023 Posted by | Science and Pseudo-Science | , , , | Leave a comment

My MP and an exercise in vaccine damage denial

By Nicholas Britton | TCW Defending Freedom | May 4, 2023

A few weeks ago I wrote to my MP to ask if he attended Andrew Bridgen’s debate in the House of Commons about the safety and effectiveness of the Covid vaccines. Of course, I knew he wasn’t among the handful of people who stayed in the chamber for the debate, but I wanted to convey my deep disappointment at the lack of interest by those elected by us and paid by us to represent us on such important issues.

I finally got a reply about a month later. He said he was in his constituency that day but was aware of Mr Bridgen’s speech. Below are some extracts from his letter. I have not identified him because this is not a name-and-shame exercise, but an illustration of how politicians are still in complete denial about this issue and are quite happy giving us misinformation in the form of the usual unsubstantiated slogans and tropes. I don’t know whether this MP believes any of what he wrote or whether he is just saying what he’s been told to say. I know he is a party loyalist who always falls in line with the leadership; he is not an independent thinker. Either way, I don’t like being lied to or hoodwinked.

It’s interesting that at no point does the MP refute anything Andrew Bridgen said, nor does he provide any evidence or argument to contradict his statements. That would be a tricky one, I guess, since Mr Bridgen was quoting from official figures. It’s also troubling to see such blatant denial of what is now being revealed around the world about the vaccines and which is even starting to creep into the MSM – I’ve recently noticed a few reports concerning vaccine injuries. Still, it remains an uphill struggle to convince some people that they are being lied to by the authorities. We are not trying to prove the existence of aliens or anything equally intangible, we are just trying to get those in authority to acknowledge what is screaming at them from their own official statistics. The result, as this letter shows, is for them to behave like recalcitrant children told to tidy their bedrooms, and to stick their fingers in their ears while loudly shouting ‘conspiracy theorist’, ‘misinformation’, or ‘anti-vaxxer’.

Here are the extracts (in bold) from the letter. I’ve added my thoughts below each.

‘I would point out that extensive independent research shows that COVID-19 vaccines are extremely successful at preventing deaths. They remain our best line of defence and the most effective way to enable us to live with the virus.’

‘Extremely successful’? Where is the independent evidence for that? I’d have thought he would be able to provide one or two examples of that ‘extensive independent research’ if he believes in it so fervently.

‘All vaccines must go through a rigorous testing and development process before authorisation to ensure that they meet the strict standards of safety, quality and effectiveness set by the independent medicines regulator, the Medicines and Healthcare products Regulatory Agency (MHRA).’

The Pfizer documents which the company wanted to keep under wraps for 75 years suggest more a rigorous cover-up than rigorous testing. As to quality, why have there been different rates of adverse events amongst different vaccine batches? In Japan, two men died after receiving shots from a batch contaminated with particles of stainless steel.

‘The independent Joint Committee on Vaccination and Immunisation (JCVI) provides the latest clinical and scientific evidence on vaccine safety and efficacy. Unfortunately, misinformation about Covid-19 vaccines has spread rapidly through social media and other platforms. It is crucial that we all rely on credible sources of information when it comes to vaccines. Misinformation causes harm and costs lives, and it does an incredible disservice to frontline workers who have been at the heart of the fight against coronavirus, working day and night to protect the NHS and save lives.’

He implies that the government and its ‘experts’ are the only credible sources of information and we should be trusting them alone. When were these people anointed the high priests of truth? Who in their right mind would trust Neil Ferguson and his dodgy computer models? There is indeed a vast amount of misinformation out there, most of it coming from those with connections to a certain wealthy sociopath with financial interests in the vaccine industry.

‘I reject baseless claims, including those which suggest vaccines are harming and killing many people, and that the damage is being covered up.’

As do many of us reject the government’s baseless, unevidenced, and politically-motivated claims that they are ‘safe and effective’ and that the damage is not being covered up.

‘The MHRA operates the Yellow Card reporting scheme, which allows individuals and health professionals to report any suspected reactions or side effects, even if the reporter is not sure they were caused by the vaccine. The nature of yellow card reporting means that reported events are not always proven side effects; some events may have happened anyway, regardless of vaccination.’

Ah yes, the Medical Homicide Racketeering Agency. That body which was once a gatekeeper ensuring the safety of medical products but which now calls itself an ‘enabler’. He is correct in saying that correlation is not proof of causation. However, the government deemed that a positive PCR test within 28 days of death was proof of death caused by Covid, even if you’d actually been flattened by a bus, so it seems that correlation can mean causation when it’s politically useful. The purpose of the Yellow Card system has historically been to flag up possible problems with medicines which need to be investigated. In the case of the Covid vaccines, there have been more red flags than at a Soviet Mayday parade, yet they have been ignored.

‘Where vaccine damage does tragically occur, it is right that individuals and their families can access payments via the Vaccine Damage Payment Scheme (VDPS). The VDPS is intended to support individuals and their families who have suffered severe disablement or bereavement as a result of having a vaccine. Covid-19 was added to this scheme in December 2020 and compensation payments under the scheme began last year.’

So why have the vaccine-injured been confronted with so many bureaucratic obstacles in their pursuit not just of the miserly £120,000 compensation but also recognition of their injuries, and of their need for practical help?

‘It is important to stress just how rare adverse reactions are. As with all vaccines and medicines, however, it is right that the safety of Covid-19 vaccines is continuously monitored.’

So why has the AstraZeneca vaccine, that triumph of British biotechnology, been quietly withdrawn in the UK and most other European countries? It has just been banned in Australia too. Switzerland has just removed recommendation for all Covid vaccinations for anybody, including the vulnerable. Surely it’s nothing to do with adverse reactions? The number of recorded adverse reactions for all Covid vaccines has vastly exceeded the total number for all other vaccine injuries over the past 30 years. Other vaccines and medicines have been withdrawn after far fewer recorded (suspected) adverse reactions.

***

I wonder how long politicians will keep up this pretence? I suspect they have dug themselves into such a deep hole they would have great trouble climbing out of it even if they eventually accept they have been complicit in the worst medical scam in history. My guess is they will keep digging because honesty and humility do not come easily to them.

May 4, 2023 Posted by | Deception, Science and Pseudo-Science | , , | Leave a comment

Ivermectin ban lifted: Australia

The ban on off-label prescribing of the anti-viral drug has been in place for over 18 months

By Rebekah Barnett |  Dystopian Down Under | May 3, 2023

Doctors will be free to prescribe ivermectin ‘off-label’ from 01 June 2023, the Therapeutic Goods Administration (TGA) announced today.

A regulatory U-turn

This is a reversal of a national ban on off-label prescribing of ivermectin, which the TGA enacted on 10 September 2021, in an attempt to prevent doctors from prescribing the drug to treat Covid.

At the time, the TGA stated that the restriction was necessary because:

  • People would be at risk if they took ivermectin instead of getting vaccinated
  • People who took ivermectin may choose not to get tested or to seek medical care if they had symptoms
  • Social media posts were promoting higher doses of ivermectin than what is normally recommended for approved uses
  • There had been a 3-4 fold uptake in ivermectin and the TGA was worried about a shortage disadvantaging vulnerable people who really needed the drug

So, instead of launching a nationwide education campaign and recommending that the Australian Government throw a few million dollars at bolstering the national stockpile of ivermectin, the TGA effectively banned the drug for all but a narrow set of uses.

The TGA has now relaxed the ban because, “there is sufficient evidence that the safety risks to individuals and public health is low when prescribed by a general practitioner in the current health climate.”

It would seem, though, that there was sufficient evidence of ivermectin’s safety all along. In July 2021, Rebecca Weisser wrote in Ivermectin. It’s as Aussie as Vegemite, for Spectator Australia:

As for safety, 3.7 billion doses of ivermectin have been used since 1987 and in 30 years, only 20 deaths following its use have been reported to the UN’s Vigi-Access database. Compare that to remdesivir, which has been given emergency use authorisation to treat Covid in Australian hospitals. In 12 months, there have been 551 deaths reported. Indeed, a study published in the prestigious Journal of the American Medical Association this week found remdesivir did not increase survival, just time spent in hospital.

The TGA’s stated concerns over ivermectin’s safety back in September 2021 seem incoherent when taken alongside its authorisation of remdesivir.

A doctor’s perspective

An Australian doctor, who prefers to remain anonymous, was suspended by industry regulator AHPRA for prescribing ivermectin off-label during the pandemic. He says,

“I think the restriction on prescribing ivermectin off-label was disingenuous from the start. It was always about coaching people toward the option of vaccination by removing a legitimate off-label therapeutic option. The decision effectively punished Australians for being self-educated and aware of the scientific evidence supporting ivermectin.

The reversal of the ban is a good step and it appears that doctors may be restored their full rights to off-label prescribing.

But, there remains the question of whether lives have in fact been lost due to the limitation of ivermectin through this policy.”

Did restrictions on off-label prescription of ivermectin cost lives?

This is the question posed by Kara Thomas, Secretary of the Australian Medical Professionals’ Society, and Andrew McIntyre, Gastroenterologist and Coordinator of the Doctors Against Mandates legal action, in an op-ed from March this year, also for Spectator Australia. The article raises more questions than answers, but serves to highlight the disparity between the safety profiles of ivermectin (better) and Covid vaccines (worse), as well as a summary of the scientific evidence for ivermectin’s effectiveness.

The effectiveness of ivermectin in treating Covid is hotly argued in all corners of the internet, but it is worth noting that internationally renowned ICU doctor Paul Marik wept when his hospital enforced a policy preventing him from using it in combination with other therapeutics. There are numerous other frontline doctors who similarly expressed dismay at being prevented from administering the drug, after seeing lives saved under their care.

Lifting of ban is not an endorsement

Though prescribing restrictions on ivermectin are to be lifted, the TGA does not endorse off-label prescribing of ivermectin for the treatment or prevention of Covid.

”A large number of clinical studies have demonstrated ivermectin does not improve outcomes in patients with COVID-19. The National Covid Evidence Taskforce (NCET) and many similar bodies around the world, including the World Health Organization, strongly advises against the use of ivermectin for the prevention or treatment of COVID-19.”

It will now be at the discretion of Australian doctors to make their best clinical judgement on a case by case basis.

Research in progress

Monash University, Melbourne, is running a blinded and randomised clinical trial to test ivermectin’s efficacy for Covid prevention. The trial is led by Dr Kylie Wagstaff, whose preliminary in vitro study in collaboration with the Doherty Institute (April 2020) found that ivermectin stopped the replication of the SARS-CoV-2 virus in cell culture within 48 hours.

May 4, 2023 Posted by | Civil Liberties, Science and Pseudo-Science | , , | Leave a comment

Transplant surgery highlights evidence of vaccine deaths

By Guy Hatchard | TCW Defending Freedom | May 1, 2023

The writer is in New Zealand

More critical evidence of increased vaccine-induced strokes and deaths has come to light.

The Wellington Region health data leaked directly to me, on which I’ve reported here, shows that the incidence of strokes requiring hospitalisation in 2023 was up by 25 per cent on pre-pandemic levels. These rises in stroke incidence began in 2021, before the arrival of Covid in New Zealand, but after the vaccine rollout began. Despite this, published scientific papers continue to point to Covid-19 infection as the sole source of increased stroke incidence, in some cases, as in this paper, not even mentioning a possible role of Covid vaccination.

Accordingly, NZ Medsafe has been able to maintain that there have been only two vaccine-induced deaths, allowing politicians and health authorities to cling to the fiction that Covid vaccination is safe.

A pre-pandemic 2016 paper found that victims of fatal strokes are generally robust sources for organ transplant donation, especially if they are younger in age. The one exception was the need for caution with livers transplanted from those dying as a result of immune thrombocytopenia (ITP) whose recipients suffered poorer survival outcomes.

This paper published last month describes the case of an individual who in October 2021 died from a stroke caused by Covid vaccination, and whose organs were harvested for transplant. The paper notes in passing that: ‘Thrombosis combined with thrombocytopenia generally occurs in the first month following vaccination and can lead to fatal outcomes, even in young, previously healthy individuals. These young adults ultimately may become solid organ donors.’

In other words, young adults are dying following Covid vaccination in sufficient numbers to be appreciated by transplant surgeons as a new source of viable organs. In this single case, two harvested kidneys are still functioning well for the recipients. The authors leap from the one case study to a general conclusion: ‘Kidney allografts transplanted from vaccine-induced thrombosis and thrombocytopenia donors can have a good overall function with favourable outcomes.’

September 2022 paper reports on kidney transplants from 16 (yes, 16) victims in Britain of Covid vaccine-induced immune thrombocytopenia and thrombosis (VITT) to 30 recipients. Five of the recipients had concerning test results following surgery and two of them lost the graft. The authors conclude: ‘The involvement of VITT could not be completely excluded in one of these cases.’They go on to describe these outcomes as ‘favourable’ (?)

This paper published in August 2022 studying four successful transplants from a single deceased donor following VITT, notes: ‘There are increasing reports of thrombotic complications with various Covid-19 vaccines such as the Pfizer-BioNTech mRNA, Moderna mRNA, AstraZeneca Oxford (serum institute), and Johnson & Johnson/Janssen vaccines.’

This paper from Italy reports two cases of VITT and subsequent successful transplants, but this letter to the American Journal of Transplantation in July 2021 presents a far more concerning picture. Ten donors likely to have died from VITT donated 27 organs in total. Three of these organs subsequently failed, two had impaired function, and one patient died of a cardiac arrest. In total there were seven major thrombotic or hemorrhagic postoperative complications among six recipients (22 per cent) within nine days of transplant.

The authors concluded that the potential risks of transplanting organs from donors with VITT are twofold. First, early major thrombosis or clinically significant bleeding. Second, possible transmission of pathogenic lymphocytes (anti-PF4), characteristic of blood clotting associated with strokes. In other words, VITT deceased donors may somehow pass on aspects of their vaccine-induced fatal illness to transplant organ recipients.

You are probably beginning to get the picture. Transplant surgeons are very excited to have more available young donors. They announce that the use of organs from VITT is probably viable based on some case studies with very mixed results, but completely fail to comment on the significance of the increased number of cases of vaccine-induced death.

Transplant surgeons are narrowly focused on their discipline. Despite being aware of increases in Covid vaccine-induced death, they wrote papers which failed to sound the alarm. But it is worse than that: medical authorities, the people who collate statistics of hospitalisation and death, failed to communicate to medical personnel and specialists in disparate fields that there were many categories of vaccine-induced illness, including not only strokes, but also cardiac disease, kidney disease, reproductive disease, cancer and neurological disease.

Since releasing the leaked data last month, I have heard from a number of practising health professionals. Their reports include descriptions of unprecedented increases in the incidence of rare conditions that they would not normally see, including cancers. There are also reports of test result scores which are off the chart, for example D-dimer scores in the 20,000 to 30,000 range. D-dimer tests are designed to monitor the formation of blood clots associated with deep vein thrombosis, pulmonary embolism and stroke, and a normal score is considered less than 0.50. It is notable that the leaked Wellington Region health data reports around 4 per cent of D-dimer test results for both men and women are registering at elevated levels.

Most health professionals and the public are still being left in the dark as far as the overall data picture is concerned. When you hear politicians such as Ardern and Hancock calling for more censorship of discussion, it has to ring alarm bells.

The revelations of widespread ill health contained in the Wellington Region data leak demonstrate how the reverse is true. Government policies restricting access to health data and suppressing open debate are the real drivers of health misinformation and poor pandemic health outcomes.

May 1, 2023 Posted by | Science and Pseudo-Science | | Leave a comment

Texas Launch­es Inves­ti­ga­tion into Gain-of-Func­tion Research and Mis­rep­re­sen­ta­tions by Covid-19 Vac­cine Manufacturers

By Ken Paxton, Attorney General of Texas | May 1, 2023

Attorney General Paxton launched an investigation into the pharmaceutical companies Pfizer, Moderna, and Johnson & Johnson concerning whether they engaged in gain-of-function research and misled the public about doing so.

Paxton is also investigating whether the companies misrepresented the efficacy of their Covid-19 vaccines and the likelihood of transmitting Covid-19 after taking the vaccines in violation of the Texas Deceptive Trade Practices Act. The investigation will also look into the potential manipulation of vaccine trial data. This investigation concerns potentially fraudulent activity that falls outside the scope of legal immunity granted to manufacturers of the Covid-19 vaccine. It will also review the companies’ controversial practice of reporting the metric of “relative risk reduction” instead of “absolute risk reduction” when publicly discussing the efficacy of their vaccines.

In recent years, certain pharmaceutical companies have had record-breaking financial success, driven in part by sales made from products related to the Covid-19 pandemic. This vested interest in the success of these Covid-19 products, combined with reports about the alarming side effects of vaccines, demands aggressive investigation.

Texas’s investigation will force these companies to turn over documents the public otherwise could not access. Attorney General Paxton is committed to discovering the full scope of decision-making behind pandemic interventions forced on the public, especially when a profit motive or political pressure may have compromised Americans’ health and safety. Efforts by the federal government to coerce compliance with unjust and illegal pandemic interventions, even at the cost of citizens’ employment, means this investigation into the scientific and ethical basis on which public health decisions were made is of major significance.

Given the unprecedented political power and influence over public health policies that pharmaceutical companies now wield, it is more important than ever that they are held accountable if they take dangerous, illegal actions to boost their revenues.

“The development of the Covid-19 vaccine, and the representations made by and knowledge of Pfizer, Moderna, and Johnson & Johnson, are of profound interest to the public’s health and welfare. This investigation aims to discover the truth,” said Attorney General Paxton. “This pandemic was a deeply challenging time for Americans. If any company illegally took advantage of consumers during this period or compromised people’s safety to increase their profits, they will be held responsible. If public health policy was developed on the basis of flawed or misleading research, the public must know. The catastrophic effects of the pandemic and subsequent interventions forced on our country and citizens deserve intense scrutiny, and we are pursuing any hint of wrongdoing to the fullest.”

To read the CID for Pfizer, click here.

To read the CID for Moderna, click here.

To read the CID for Johnson & Johnson, click here.

May 1, 2023 Posted by | Civil Liberties, Corruption, Deception, Science and Pseudo-Science | , , , | Leave a comment

‘Tucker Twitter Files’ Reveal How WHO Helped Twitter Censor Tucker Carlson

By Michael Nevradakis, Ph.D. | The Defender | April 28, 2023

Tucker Carlson made headlines this week for being suddenly ousted by Fox News — but in the latest release of the “Twitter files” the former news commentator made headlines for a different reason.

The documents, titled the “Tucker Twitter files,” released Thursday by investigative journalist Paul D. Thacker, show that in June 2021, Twitter sought to censor Carlson after he published an op-ed for Fox News saying that the COVID-19 vaccines are dangerous for children.

Carlson’s op-ed cited information that was, up until that point, publicly viewable on the World Health Organization’s (WHO) website. However, after Carlson’s op-ed was published, that information disappeared from the site.

The files released Thursday also reveal that Twitter executives held internal debates over how best to censor the content in Carlson’s op-ed — an initiative that was led by a former press secretary for Sen. Chuck Schumer (D-N.Y.).

In an exclusive interview with The Defender on Thursday, Thacker expounded on the significance of these findings — and hinted at what the next “Twitter files” dump might reveal.

Twitter ‘clipping Tucker Carlson’s wings’

Thacker, who wrote about his findings on his Substack, said that the “bird factory” — referring to Twitter — engaged in “clipping Tucker Carlson’s wings” via its attempted censorship of his op-ed.

Despite being “controversial and polarizing,” Thacker said, Carlson was “One of the few Americans to challenge the official framework of acceptable narratives” and, as such, was “hated by the mainstream reporters for daring to throw darts at liberal pieties.”

“Why did Twitter censor Tucker Carlson? Better yet, who helped Twitter do that?” Thacker asked.

Thacker noted that while he was “reading an endless sea of #TwitterFiles” pertaining to efforts to “censor alleged ‘COVID misinformation,’” he unexpectedly discovered documents detailing attempts to censor Carlson.

These efforts appear to have begun on June 24, 2021, when Elizabeth Busby, a policy communications specialist with “Twitter Comms,” sent an email to colleagues inquiring if an op-ed Carlson had written the previous day should be flagged for COVID-19 “misinformation.”

In her email, Busby inquired whether links to Carlson’s op-ed “violate our COVID-19 misleading information policy and qualify for enforcement under our URL policy.” She added, “We’ve seen some Tweets with the link … and some that contain counterspeech.”

In the same message, Busby noted that “in the past,” Twitter had applied a boilerplate warning “to sites containing COVID-19 misinfo” and “Given Tucker’s visibility, we anticipate there may be some press interest regardless of the enforcement outcome.”

Thacker discovered that Busby was not just an ordinary Twitter employee. She joined Twitter in 2020, after leaving the U.S. Senate, where she worked as the deputy national press secretary to then-Senate Majority Leader Schumer.

According to Thacker, “Busby’s work history includes a stint at SKDKnickerbocker, a PR and lobby shop closely aligned with the Democratic party. Busby now leads ‘trust and safety communications’ at Twitch.”

He also noted that Schumer was “a frequent critic of Tucker Carlson.”

WHO ‘stealth-edited’ its COVID vaccine guidance for children after Carlson’s op-ed

What was all the fuss about? Carlson’s June 23, 2021, op-ed for Fox News — “The COVID vaccine is dangerous for kids, Big Tech doesn’t want you to know that” — referred to language available on the WHO’s website that explicitly did not recommend the COVID-19 vaccines for children.

In that op-ed, which was adapted from Carlson’s opening commentary on that day’s broadcast of “Tucker Carlson Tonight,” he referred to then-new guidance from the WHO and also recommendations from medical experts.

Carlson said:

“Since the beginning of the pandemic, key pieces of medical guidance from the World Health Organization have proven to be disastrously false — false enough to cost lives. It was the WHO, you’ll remember, that told us COVID couldn’t be transmitted between people, even as the virus was spreading into the United States. It was the WHO that worked in stealth with the Chinese government to obscure the source of the outbreak at the beginning, and then hide its origins from the world. …

“… bureaucrats at the WHO published new vaccine guidance. Here’s what it says: Children should not take the coronavirus vaccine. Why? The drugs are too dangerous. There’s not nearly enough data to understand the long-term effects or to show that the benefits are worth the risk that they bring.

“This is terrible news, of course, for the pharmaceutical industry. Big Pharma has been planning to test the vaccine on 6-month-olds.”

According to Thacker, the WHO published an evaluation of vaccine safety and efficacy on April 8, 2021, for the Pfizer-BioNTech, Moderna, Johnson & Johnson (J&J) and AstraZeneca COVID-19 vaccines.

For children, the WHO issued the following recommendation:

“Children should not be vaccinated for the moment. There is not yet enough evidence on the use of vaccines against COVID-19 in children to make recommendations for children to be vaccinated against COVID-19.

“Children and adolescents tend to have milder disease compared to adults. However, children should continue to have the recommended childhood vaccines.”

The information that Carlson appears to have referenced was still on the WHO’s website as of June 22, 2021, according to Thacker. However, after Carlson’s op-ed was published, the WHO “stealth-edited their page,” according to Thacker, and replaced it with new guidance, which stated:

“Unless they are part of a group at higher risk of severe COVID-19, it is less urgent to vaccinate them than older people, those with chronic health conditions and health workers.

“More evidence is needed on the use of the different COVID-19 vaccines in children to be able to make general recommendations on vaccinating children against COVID-19.

“WHO’s Strategic Advisory Group of Experts (SAGE) has concluded that the Pfizer/BionTech vaccine is suitable for use by people aged 12 years and above.”

“In other instances where the WHO has updated their vaccine guidance, they note this change with a date at the top of the webpage,” Thacker wrote. “But no update exists for changes the WHO made the day of Tucker’s essay.”

Thacker added:

“While some of the language in Tucker’s piece could be viewed as inflammatory — the WHO did not say the vaccines were ‘dangerous’ — independent experts also were advising that children not receive the COVID vaccines, as rare but serious adverse events were not studied.”

The subtitle to Carlson’s op-ed read: “Even posting WHO guidance could get you censored.”

On April 10, 2021, WHO tweeted: “#COVID19 trials for children are under way. Following proven health measures is still the best way to keep everyone, including children, safe from COVID-19.” The tweet remains online to this day.

Twitter sought to censor Carlson while avoiding ‘political risks’

According to Thacker, the day after the WHO “stealth-edited” its vaccine guidance, Twitter officials began discussing Tucker’s essay — after Busby brought it to their attention.

Twitter employee Brian Clarke responded to Busby’s June 24, 2021, email that same day, writing, “We are going to proceed with labeling any Tweets linking to the article we detect that advance the claim that WHO has deemed the vaccine dangerous for children.”

However, Clarke said, “Given that this article’s narrative is related to ‘big tech censorship’, I want to be mindful that taking action on the URL level could lead to this particular article gaining more traction rather than mitigating the harm associated with it.”

“We’re going to keep an eye on any ongoing discussions related to the article and if it happens to gain traction we will review again under our URL guidelines,” Clarke added.

According to Thacker, “Twitter officials also discussed looping in top Twitter execs, such as the general counsel, due to the ‘political risks’ associated with such actions. Yoel Roth [then-head of Trust and Safety for Twitter] agreed with this approach to ‘escalate.’”

This included a recommendation that then-general counsel for Twitter Vijaya Gadde review any actions taken against Fox News, “given political risks,” while Roth stated that any action against Fox would be “escalated” internally within Twitter.

Joseph Guay, at the time Twitter’s senior policy specialist for “misinformation,” then shared an email with Busby, Clarke and other Twitter personnel, advising them on various options they had available to them to take action against tweets containing a link to Carlson’s op-ed, without directly censoring Fox News.

Thacker noted that Guay, who “seems to have made the [final] call on Tucker’s op-ed,” departed Twitter earlier this year for a position as TikTok’s “Global Policy Lead on Deceptive Actors & Behaviors.”

Upon departing Twitter, Guay, in a post on his LinkedIn page, referred to his work at Twitter policing “the bad guys”:

“Our teams worked tirelessly to ship bold new policies (such as the COVID-19 Misleading Information Policy, or the Crisis Misinformation Policy) to prevent virulent misinformation and cognitive manipulation from bringing harm to vulnerable people.

“I remain as committed as ever to building resiliency to weaponized information, and making it a little harder for the bad guys.”

Guay’s LinkedIn profile states he is engaged in “fighting information threats globally.”

Thacker also noted that Twitter’s apparent distaste for Carlson was evident in more than just this instance.

“Tucker Carlson would have never known this happened, but when Twitter held a meet and greet months, later, they wrote of Tucker’s producer, ‘[I]t was pretty apparent from the get-go we understood the very different goals we have at work,’” Thacker tweeted, referencing internal Twitter documents regarding a meeting between Twitter officials and Alex Pfeiffer, Carlson’s producer.

Thacker wrote:

“Months after Twitter took action against tweets advancing claims in Tucker’s essay, the company met with reporters in New York to strengthen ties with journalists covering social media.

“In their assessment of reporters, one Twitter official noted of Tucker’s producer, Alex Pfeiffer, ‘[I]t was pretty apparent from the get-go we understood the very different goals we have at work, this was mainly to relationship build.’”

In remarks he shared with The Defender, Thacker noted that Twitter was attempting to strike a balancing act between censoring Carlson’s narrative while not running afoul of Fox.

“They were trying to limit Tucker Carlson’s impact,” he said, “and they were doing it in a way that they would not be brought into direct conflict with Fox.”

According to Thacker, this balancing act nevertheless belied Twitter’s political bias.

“There’s this issue they had with conservative media, and they’re biased in one direction,” Thacker told The Defender. “The way you know this is that the person who brings it to their attention is the former deputy national press secretary of Sen. Chuck Schumer.”

Thacker said that while some of what Carlson had written in his op-ed was “inflammatory,” it nevertheless “wasn’t inaccurate.” He added:

“The WHO edited its website on the same day Tucker’s article came out, and the next day, Twitter starts to go after his story. What do you say about that? Who does Twitter work for?

“Apparently, you don’t question the WHO, or you don’t write what the WHO says. It shows you that you cannot trust these social media people. They are in the tank in one direction.”

Furthering this point, Thacker highlighted a potential conflict of interest between Twitter and one of the COVID-19 vaccine manufacturers, J&J. In Thacker’s previous “Twitter files” revelations, he found that Twitter partnered with J&J on a COVID-19 vaccine “marketing strategy.”

Such efforts were not limited to COVID-19 vaccines. “By the summer of 2021,” Thacker wrote as part of his previous “Twitter files” release, “Johnson & Johnson began a full court press to market a ton of their products on Twitter, including a controversial antidepressant.”

“I don’t know what else is influencing Twitter,” Thacker told The Defender. “Johnson & Johnson was one of the vaccines mentioned on the WHO site, and that was a client of Twitter’s.”

Remarking on the revelations made in the “Tucker Twitter files,” Michael Rectenwald, Ph.D., author of “Google Archipelago: The Digital Gulag and the Simulation of Freedom” and a former New York University liberal studies professor, told The Defender :

“This installment of the Twitter files proves that not only the government but also international governance bodies like the WHO established direct censorship channels within Twitter — to censor information that contradicted the narrative of vaccine safety, even when ‘the science’ contradicted the narrative.

“No doubt we will learn that international NGOs like the World Economic Forum also had such channels.”

Rectenwald was a guest on the final “Tucker Carlson Originals” broadcast on Fox News before Carlson was let go by the network.

WHO partnered with social media platforms to combat ‘misinformation’

Indeed, in several instances, the WHO has partnered with social media platforms such as Twitter to police alleged “misinformation” and “disinformation” pertaining to COVID-19 vaccines and countermeasures — and has also previously expressed misgivings about Elon Musk’s plans to allow more “free speech” on the platform.

Dr. Mike Ryan, executive of WHO’s Health Emergencies Programme, stated on April 26, 2022 — when Musk was contemplating purchasing Twitter — that Musk will have a “huge influence” over the curbing and potential spreading of vaccine misinformation on Twitter, and that Twitter and all social media platforms must address “misinformation.”

Thacker: Twitter attempted to ‘manufacture consent’

Thacker compared Twitter’s actions to what Noam Chomsky once described as “manufacturing consent.” Chomsky described manufacturing consent in a 2018 interview, during which he said:

“The myth is that the media are independent, adversarial, courageous, struggling against power.

“That’s actually true of some. There are often very fine reporters, correspondents. In fact, the media does a fine job, but within a framework that determines what to discuss, not to discuss.”

However, in an Oct. 24, 2021, interview, Chomsky suggested that unvaccinated individuals should be isolated, claiming they were placing the public at risk.

Chomsky said at the time:

“If people decide ‘I am willing to be a danger to the community by refusing the vaccine’ they should then say, ‘well, I also have the decency to isolate myself. I don’t want a vaccine but I don’t have the right to run around harming people.’

“That should be a convention. Enforcing is a different question. It should be understood, and we should try to get it to be understood. If it really reaches the point where they are severely endangering people, then of course you have to do something about it.”

In a follow-up interview, Chomsky doubled down on his previous remarks. “How can we get food to them? Well, that’s actually their problem.”

On his Substack, Thacker noted that the media’s response to the recent news that Carlson was ousted from Fox News is characteristic of what Chomsky had once warned about. He wrote:

“The majority of reporters have shrugged aside their colleagues’ reporting fiascoes and the damage done to their own reputations, and continue to blame most failures in journalism on one person: Tucker Carlson.

“So it was not surprising that reporters began a week-long celebration this Monday when Fox fired Tucker.”

Referring to the latest Twitter files revelations about Carlson, Thacker told The Defender, “I can’t believe this is not everywhere, that everyone is not reading this right now.”

He said he will soon release more documents as part of the “Twitter files”:

“There are more stories. I had another story that I was working on, and I pushed that aside to work on this one.

“There’s probably another 10 stories, with more examples of the way they were working with the media, especially the media they favored.”


Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

April 30, 2023 Posted by | Deception, Full Spectrum Dominance, Science and Pseudo-Science, Timeless or most popular, War Crimes | , , | Leave a comment

Red Line Crossed: DNA Contamination of mRNA “Vaccines” Poses Risk to Everyone on the Planet

Why the disturbing discovery of DNA contamination with plasmids poses a severe risk to the mRNA  “vaccinated” and the people around them

Written by the WCH Health and Science Committee | April 27, 2023

The following article is the World Council for Health’s summary and interpretation of the conclusions of the outstanding paper by McKernan et al (2023): Sequencing of bivalent Moderna and Pfizer mRNA vaccines reveals nanogram to microgram quantities of expression vector dsDNA per dose

Another red line has been crossed…

In a recent publication by a group of experienced geneticists, more contamination in mRNA “vaccines” (Pfizer and Moderna), excluding metal residues, which had been identified in the past, was found. Multiple methods highlighted high levels of DNA contamination.

Of special concern was that they found replicable DNA, so-called plasmids, in both the monovalent and bivalent vaccines, which should not be there at all. This time the researchers found DNA contamination that far exceeded the European Medicines Agency (EMA) requirement and the U.S. FDA’s dose requirements.

But why is this find so alarming?

The Threat of DNA Integration

As we knew from the beginning, Covid-19 (C19) injections have been a gene therapy, and the definition of a vaccine had to be altered to call them a vaccine. While we are still told of the safety and the effectiveness of the injections, Swedish researchers have shown that the mRNA of the Pfizer vaccine was integrated into liver cells.

This raised many eyebrows about whether the interference with our genome could pose the risk of integration of the mRNA coding into our genome. Usually, the body needs an enzyme called reverse transcriptase to do so. But now, findings of this new paper suggest a different scenario in which DNA integration may occur.

The Role of So-Called Plasmids

Plasmids are circular DNA that enable bacteria to exchange information. When scientists became aware of this, they soon started using these plasmids to produce custom-made proteins by genetically modifying their information. This is, for example, how insulin is currently produced. Plasmids are also the “production site” of the novel mRNA used in the Covid-19 injections. Once the DNA templates or plasmids are transcribed into strands of mRNA the injection vials should be filtered out to prevent continuous production of the information. Yet these plasmids are precisely what the scientists found. Why it is there gives rise to many explanations ranging from carelessness, the impossibility of ensuring complete separation, or even potential intent, which, knowing what we know, can no longer be excluded.

Plasmid Integration into Bacteria

So what could be so concerning about the integration of this information? The human body contains far more bacteria than cells, known as the human microbiome. The origin of the used plasmid stem from E. coli bacteria, which also happens to be a part of our intestinal microbiome, suggesting that there is the possibility for plasmid integration into our microbiome.

Plasmid Integration into Human Cells

While it was believed that plasmid integration was restricted to bacteria, other researchers observed that integration could occur in the telophase of cell division. Whether this can now occur with the mRNA injections should be a top priority for all regulatory bodies like EMA and FDA to address. Residual injected DNA can result in so-called type I interferon responses and increase the potential for DNA integration. A so-called SV 40 promotor also enables the plasmid integration into human cells.

An urgent evaluation into these mechanisms in the context of the covid mRNA-producing plasmids is needed to determine the extent to which this foreign genetic information is able to become a part of us.

Implication of Integration

The highly concerning consequence of genomic integration into microbiome cells is that this would ensure the ongoing production of mRNA and, thus, the production of pathogenic viral particles, the spike proteins. Typically, mRNA begins to degrade in the body after 10 minutes. Genetic modification, however, has made the C19 ‘vaccines’ mRNA more stable and it has now been observed to last up to 60 days. In autopsies in Germany, it was even found that mRNA was produced in endothelial cells after 12 months. mRNA has also been found in breast milk.

Could the persistence of plasmids and, thus, the integration into our genome be the reason for this?

Potential of Shedding

In a recent publication: “Persistent Nonviral Plasmid Vector in Nasal Tissues Causes False-Positive SARS-CoV-2 Diagnostic Nucleic Acid Tests” by Beck at al., asymptomatic laboratory workers who tested positive for SARS-CoV-2 were found to harbor a laboratory plasmid vector containing SARS-CoV-2 DNA, which they had worked with in the past, in their nasal secretions. While prior studies had documented contamination of research personnel with PCR amplicons (bits of DNA sequences artificially produced), their observation was novel, as these individuals shed the laboratory plasmid over days to months, including during isolation in their homes.

This suggests that the plasmid was in their nasal tissues or that bacteria containing the plasmid had colonized their noses. Thus we urgently ask the global health care systems to screen for plasmids in vaccinated and unvaccinated individuals.

As we breathe out, we usually exhale multiple elements from our gut microbiome. If we now can assume that cells from it have been instructed to produce mRNA, what will be the consequence for people in proximity to the individual spreading them? We need to find out as soon as possible.

Plasmid Contamination

The paper also alerts us to plasmid contamination from E. coli as preparations are often co-contaminated with lipopolysaccharides (LPS). E. coli endotoxin contamination can lead to anaphylaxis upon injection and thus should certainly not be present.

Antibiotic Resistance

For plasmids to remain stable, they are usually antibiotic-resistant to two antibiotics (Neomycin, Kanamycin). This information could also be integrated into the microbiome or body cells.

What WCH Health and Science Committee Conclude

First, it demonstrates again the apparent neglect of scientific and regulatory board standards.

The Nuremberg Code (August 19, 1947) Article 10 clearly states that:

“During the experiment, the scientist in charge must be prepared to interrupt the experiment at any moment when he begins to believe that the continuation of the experiment may involve injury, disability, or death to the subject.”

This has happened multiple times, and the crossing of several safety signals questioning safety and efficiency has filled countless pages.

Apart from the manufacturers’ fraudulent approach, the more concerning aspect is the regulatory bodies’ failure to react to these apparent problems. This is not surprising as they are mainly financed by the industry itself (EMA around 90%). Ensuring the ongoing distribution of these harmful and dangerous injections lacks any moral and ethical backbone.

This also highlights the EMA limits for DNA contamination, which doesn’t consider the nature of the DNA contaminants. Replication-competent DNA should arguably have a more stringent limit. DNA with mammalian promoters or antibiotic resistance genes may also be of more concern than just background E. coli genomic DNA from a plasmid preparation. More mRNA means more production of the pathogenic part of SARS-CoV-2 that was chosen to be produced by our own cells, namely the spike protein.

The potential of shedding even to the unvaccinated poses a serious question for the entire population of this planet.

We can only speculate how it will end, but what needs to happen today after the publication of this paper is an immediate stop of the “Covid-19 vaccine” program.

Meanwhile, we should boost our oral and nasal microbiome by walking in the woods and inhaling beneficial microbes. And improve our gut microbiome through the consumption of fermented foods such as freshly unpasteurized Sauerkraut or Kimchi  and prebiotic foods such as colorful root vegetables.

In a recent interview with The New American, Dr Mark Trozzi explains the role of bacterial plasmids and E. coli bacteria in the manufacturing process of mRNA injections. Watch the full interview here.

April 30, 2023 Posted by | Science and Pseudo-Science, Timeless or most popular, War Crimes | | Leave a comment

Let a Hundred Schools of Thought Contend

By Michael Tomlinson | Brownstone Institute | April 28, 2023

The thrust of Let a hundred flowers bloom was that the world’s response to COVID-19 should not have been exempted from the normal processes of policy formation and development, which in a democracy have informed debate at their core. By exempting pandemic policy from critique, governments were attempting to ensure that the correct response was undertaken, but in fact increased the likelihood of falling into serious error.

Governments felt that in a public health emergency there was no time to explore policy alternatives, and it was essential to take a disciplined approach to defeat the enemy (i.e. the virus). It was necessary for governments to control information given out to the population from the centre and to suppress ‘unreliable’ sources of information that might promulgate ‘incorrect’ information, and thereby cause the deaths of people who were led astray from the true path.

Jacinda Ardern, the former Prime Minister of New Zealand, notoriously declared ‘we will continue to be your single source of truth.’ She advised the New Zealand people to listen to the Director General of Health and the Ministry of Health and ‘dismiss anything else.’

There should be no scenarios in which governments and government agencies are the single source of truth. No organisation, no individual and no groups of individuals can be infallible. She is now headed to Harvard University to expound on disinformation with and to the best and brightest.

Therefore, we need to go through a divergent phase of policy development in the first instance, in which all the relevant diverse sources of knowledge and diverse voices are consulted. This is sometimes referred to as ‘the wisdom of crowds,’ but ‘the wisdom of crowds’ must be distinguished from ‘the groupthink of herds.’

The prices of companies on the stock market are thought to reflect the combined knowledge of all traders and therefore the true market price. But stock prices go through cycles of boom and bust, in which true underlying prices are distorted for a time by the famous ‘animal spirits,’ and rise exponentially before falling, much like the pandemic curve indeed.

The need to bring diverse perspectives to bear on common problems is why we have parliaments and congresses instead of dictatorships. There is widespread disillusionment with parliaments, but they exemplify Winston Churchill’s famous dictum: ‘Democracy is the worst form of government – except for all the others that have been tried.’ Deliberative decision-making in which all voices are heard is an essential safeguard which can lead to sound policy formation if deployed carefully, avoiding the pitfalls of groupthink, and it is superior to all other forms of decision-making that have been tried.

Governments must choose a path forward, they must make strategic choices, but they should do so with full knowledge of the policy options, and they should never attempt to prevent other options from being discussed. But this is what happened in the COVID-19 pandemic.

It was driven by a simplistic view of science in which the scientific community supposedly formed a ‘scientific consensus’ about the best ways to handle the pandemic, based on universal measures aimed at the entire population. But the Great Barrington Declaration advocated an alternative strategy of ‘focused protection’ instead, and was originally signed by 46 distinguished experts, including a Nobel Prize winner. It has subsequently been signed by over 16,000 medical and public health scientists, and nearly 50,000 medical practitioners. Whatever you may think about the Great Barrington Declaration, these simple facts demonstrate that there was no consensus.

When activists refer to ‘the scientific consensus,’ what they mean is ‘the establishment consensus’ – the consensus of sages and worthies of the type referred to by Jacinda Ardern and referred to in ‘Let a hundred flowers bloom.’ These agency heads, advisory panels, and ministries of health are naturally predisposed to accept their own advice and ignore contrarian voices. Yet contrarian voices remind us of ‘inconvenient facts,’ data that conflicts with the establishment view. It is through the dialogue between diverse voices that we work closer to the truth. ‘The authorities’ must be held accountable, even in a pandemic.

The key point about the establishment consensus is that it is always entirely devoid of individual insight. In order to qualify to be a sage or a worthy and to sit on government advisory panels or be an agency head, you have to show your capacity to toe the line at all times and never say anything remotely controversial. This was expressed so well by George Bernard Shaw: ‘The reasonable man adapts himself to the world; the unreasonable man persists in trying to adapt the world to himself. Therefore all progress depends on the unreasonable man.’

The pandemic response has been dominated by the reasonable ones who trim to the wind and accept the current framework whatever it is.

In early 2020, an establishment consensus formed within weeks around the grand strategy (which, remember, was neither grand nor strategic) of suppressing the spread of the pandemic through lockdowns until vaccination could end it. At that stage, there were no vaccines in existence and there was literally zero evidence that lockdowns could ‘stop the spread,’ but alternative strategies were never considered. Since then, the establishment has had greater success in suppressing debate than in suppressing spread of the virus.

Maryanne Demasi, who has a fatal tendency to think for herself that has got her into trouble in the past, has written about this ‘consensus by censorship’ in a Substack article: ‘It is not difficult to reach a scientific consensus when you squelch dissenting voices.’ Scientists such as Norman Fenton and Martin Neill, with hundreds of publications to their name, have been unable to get papers published if they raise any questions about papers with favourable findings on COVID-19 vaccines. They have written about their experiences with the Lancet here. Eyal Shahar has given three examples here.

This is unacceptable. COVID-19 vaccines, like any other therapeutic product, should be subject to rigorous ongoing analysis for safety, and strategies must be adapted where necessary in the light of emerging knowledge. Again, there can be no exemptions from this.

Even with these impediments, some papers slip through the net, such as the rigorous analysis of the primary clinical trial evidence by Joseph Fraiman, Peter Doshi et al: Serious adverse events of special interest following mRNA COVID-19 vaccination in randomized trials in adults.’ But many papers with adverse findings about the vaccine are blocked at the pre-print stage, such as the paper on COVID vaccination and age-stratified all-cause mortality risk by Pantazatos and Seligmann, which concluded that the data suggests ‘the risks of COVID vaccines and boosters outweigh the benefits in children, young adults and older adults with low occupational risk or previous coronavirus exposure.’

Pantazatos described his experience with the medical journals here. This demonstrates that the most effective tactic to dispose of contrarian research is not to refute it, but to suppress it and then ignore it. Indeed, establishment researchers have ignored the whole issue and have not addressed the effect of COVID-19 vaccines on all-cause mortality at all. This is extraordinary, as the entire goal of the pandemic response is supposed to be to reduce mortality. But two years after the commencement of mass vaccination, researchers have not conducted controlled studies of its effect on overall mortality, even retrospectively. This is incomprehensible. Are they afraid of what they might find?

Demasi’s blog came under attack from the ultra-orthodox David Gorski, who wrote in response: ‘Antivaxxers attack scientific consensus as a “manufactured construct.”’ The title is a big giveaway – since when was ‘antivaxxer’ a scientific term? His blog merely throws mud at Demasi, without engaging with her arguments about pandemic policy, let alone engaging with the analysis in the pre-print she wrote with Peter Gøtzsche: ‘Serious harms of the COVID-19 vaccines: a systematic review.’

Gorski has nothing to contribute on the subject. The nearest thing he has to an argument is that individual studies do not necessarily invalidate a scientific consensus. But Gøtzsche and Demasi’s paper is based on a meta review of 18 systematic reviews, 14 randomised trials and 34 other studies with a control group. It has been open for review on the pre-print site and I am not aware of any substantive objections to the information and analysis therein.

Words like ‘anti-vaxxer,’ ‘anti-science,’ and ‘cranks’ are thought-stoppers – rhetorical devices designed to signal to the orthodox that their cherished convictions are safe, and they don’t need to understand the arguments and evidence put forward by dissidents because they think they are by definition disreputable people out to mislead. Resorting to these methods and ad hominem attacks is in fact anti-intellectual,

The fake consensus has indeed been ‘manufactured.’ The scientific debate on COVID-19 was closed from the outset, particularly at the level of opinion, whereas a hallmark of true scientific consensus is openness.

Consider, as a case study, the great debate between the advocates of the ‘big bang’ theory of the origins of the universe and the ‘steady state’ theory, the history of which is related in this account by the American Institute of Physics. The steady state theory (in which the universe is expanding at a steady rate with matter being continuously created to fill the space created as stars and galaxies move apart) was advocated by Fred Hoyle, one of the most eminent physicists of his generation, over more than 20 years, until the weight of empirical observations by radio astronomy brought about its demise. The debate was ended in the traditional way, whereby the predictions of the steady state theory were falsified.

The grand strategy of COVID-19 pandemic responses, which was supposed to end the pandemic and end excess deaths, has been contradicted by empirical observations. The pandemic did not end, almost everyone became infected, excess deaths have continued and there is no hard evidence especially from randomised controlled trials that the vaccines can prevent or reduce all-cause mortality. In Australia, the bulk of our excess deaths have come during the mass vaccination period.

And yet, the orthodox continue to have faith in the strategy and continue to ignore and suppress alternative strategies, believing that the science has been settled, when it seems to be decidedly unsettled.

This leads to the war against ‘disinformation and misinformation,’ which is in fact a war against contrarian viewpoints. Government has colluded with establishment scientists and social media companies to systematically censor alternative observations and strategies.

The straw-man arguments usually deployed to justify this highlight irrational ideas such as rumours that the vaccines contain microchips, etc. But they completely ignore the issues raised by serious scientists such as Doshi, Fenton, and Gøtzsche. The orthodox hold that sceptics are science denialists, whereas the reverse is true: the establishment denies the diversity of findings in the scientific literature.

The market in ideas should be the freest of all markets, as there is much to be gained and little to be lost by engaging with all ideas that derive from evidence-based analysis. By contrast, pandemic policy has been characterised by a kind of intellectual protectionism, in which orthodox ideas are privileged.

The fake consensus has been used as the basis for academic studies of ‘disinformation.’ There is no precise conceptual basis for the concept of disinformation, which is assumed to be ‘false or misleading information.’ Who determines what is false? This is usually defined derivatively as any information that goes contrary to the established narrative.

The self-appointed Aspen Commission in its final report on ‘information disorder,’ referred to some of these issues, by asking for example ‘who gets to determine mis-and disinformation?’ and acknowledging that ‘there are concomitant risks of silencing good-faith dissent’ – and then proceeded to ignore them. Without defining it, a key recommendation was: ’Establish a comprehensive strategic approach to countering disinformation and the spread of misinformation including a centralised national response strategy’ (p30).

A further recommendation is: ‘Call on community, corporate, professional, and political leaders to promote new norms that create personal and professional consequences within their communities and networks for individuals who willfully violate the public trust and use their privilege to harm the public.’ In other words, pursue and persecute those who step out of line, with no consideration of whether they may be relying simply on different information, not misinformation.

  1. They go on to make helpful practical suggestions on how to implement their vaguely worded recommendation:
  • Ask professional standards bodies like medical associations to hold their members accountable when they share false health information with the public for profit.
  • Encourage advertisers to withhold advertising from platforms whose practices fail to protect their customers from harmful misinformation.
  • Spur media organizations to adopt practices that foreground fact-based information, and ensure they give readers context, including when public officials lie to the public.

All of this assumes that there is a simple distinction to be made between ‘true’ and ‘false’ information, and underlying this, a naïve trust that only the health authorities are relying on ‘fact-based information’ and contrary views are self-evidently not fact-based. But, as we have seen, Doshi, Fenton, Gøtzsche and Demasi have published contrarian papers that are heavily fact-based.

In an academic extension of the ad hominem attack, there is even research into the psychological characteristics of dissidents, which brings to mind the worst excesses of the Soviet Union. Examples provided by ChatGPT of general studies on misinformation indicated that those of us who question established narratives are apparently led astray by confirmation bias, have a ‘low cognitive ability,’ and are biased by our political views. This implies that those who support conventional positions are unbiased, smart, and are never influenced by their political orientation. These assumptions should also be tested by research, perhaps?

In relation to COVID-19, it turns out that us dissidents are also prone to ‘epistemic vices such as indifference to the truth or rigidity in [our] belief structures,’ according to Meyer et al. This was based on testing people’s willingness to believe 12 patently ridiculous statements, such as ‘Adding pepper to your meals prevents COVID-19,’ which I have never heard of before. Willingness to agree with these statements was then stretched to equate with more serious issues:

People who accept COVID-19 misinformation may be more likely to put themselves and others at risk, to strain already overburdened medical systems and infrastructures, and to spread misinformation to others. Of particular concern is the prospect that a vaccine for the novel coronavirus will be rejected by a sizeable proportion of the population because they have been taken in by misinformation about the safety or effectiveness of the vaccine.

None of these issues were tested in the research, yet it was extended beyond the findings to justify these conclusions.

In an article back in 2020 for the Harvard Kennedy School Misinformation Review, Uscinski et al asked: Why do people believe COVID-19 conspiracy theories? They summarised their findings as:

  • Using a representative survey of U.S. adults fielded March 17-19, 2020 (n=2,023), we examine the prevalence and correlates of beliefs in two conspiracy theories about COVID-19.
  • 29% of respondents agree that the threat of COVID-19 has been exaggerated to damage President Trump; 31% agree that the virus was purposefully created and spread.

These beliefs are certainly debatable and are held to be founded once again in denialism: ‘a psychological predisposition to reject expert information and accounts of major events.’ Denialism was further broken down to these:

  • Much of the information we receive is wrong.
  • I often disagree with conventional views about the world.
  • Official government accounts of events cannot be trusted.
  • Major events are not always what they seem.

Are you telling me these statements are not true?! I will have to rethink everything!

These studies all equate dissident views with ‘conspiracy theories.’ They assume that dissident views are self-evidently contrary to the scientific record, invalid and plain wrong; and they do not see any need to support this with references. They are insufferably superior and patronising, resting on immense confidence in their unfalsifiable academic findings.

The scientific method contains many valuable tools for counteracting confirmation bias – the tendency we all have to interpret all data as favourable to our pre-existing ideas. Pandemic science has shown that these tools themselves can be misused to reinforce confirmation bias. This leads to a kind of objectivity trap – the sages become blind to their own bias because they think they are immune.

They are founded in a belief that dissidents must be fundamentally anti-social since they are ‘anti-science.’ They must be either bad actors or gullible and misled. These authors do not consider the positive attributes that could be associated with dissident beliefs: a proclivity for independent thinking and the critical thinking that is supposed to be inculcated by higher education.

Establishments have been trying to suppress rebels and dissidents for hundreds if not thousands of years. But every society needs (non-violent) rebels to challenge beliefs that are not well-founded.

The establishment consensus on COVID-19 is built on sand and should be challenged. It arose from premature closure of the scientific debate, followed by suppression of contrarian evidence-based analysis. Dissidents include scientists, who are clearly not anti-science but are opposed to flawed science based on ‘low cognitive ability’ and confirmation bias in favour of establishment ideas. They are pushing for better science.

The most reliable policy arises from open science and open debate, not from protectionism and closed science.

Let a hundred schools of thought contend – or we are all lost!

Michael Tomlinson is a Higher Education Governance and Quality Consultant. He was formerly Director of the Assurance Group at Australia’s Tertiary Education Quality and Standards Agency, where he led teams to conduct assessments of all registered providers of higher education (including all of Australia’s universities) against the Higher Education Threshold Standards. Before that, for twenty years he held senior positions in Australian universities. He has been an expert panel member for a number of offshore reviews of universities in the Asia-Pacific region. Dr Tomlinson is a Fellow of the Governance Institute of Australia and of the (international) Chartered Governance Institute.

April 29, 2023 Posted by | Full Spectrum Dominance, Science and Pseudo-Science, Timeless or most popular | , | Leave a comment

D.C. Doctors Gone Wild

It is shameful to pressure and coerce a minor to receive a vaccine

BY AARON SIRI | INJECTING FREEDOM | APRIL 28, 2023

A recently filed lawsuit alleges that a pediatrician who works at MedStar in Washington, D.C., forcibly vaccinated two minors without parental consent. According to the lawsuit:

two minor children were held in a room by Defendant until she overcame their will and forcibly vaccinated them while physically preventing them from consulting with their mother, who was right outside the room.

As if that weren’t bad enough, the lawsuit further alleges:

Minor children W.M. and K.M. were additionally provided with false and fraudulent information in order to obtain purported consent to a procedure in the absence of actual or freely given consent. Specifically, Dr. Rethy told the children that they were required to be vaccinated against COVID-19 to attend school and that they had no lawful option to decline such vaccination.

What makes this story even more incredible is that this is the same pediatric practice that sought to vaccinate a minor child in the lawsuit we brought to strike down the “Minor Consent for Vaccinations Amendment Act of 2020” passed by Washington D.C. in 2020. We succeeded in winning an injunction which resulted in the repeal of that law.

Before being repealed, the law permitted doctors in D.C. to vaccinate a child, 11 years of age or older, without their parent’s consent or knowledge, and created an elaborate and deceitful scheme in which the healthcare provider, insurance company, school, and health department all participated to hide from those parents the fact that their child had been vaccinated. According to the law, a child did not even need to be a resident of the District of Columbia in order to be vaccinated without parental consent!

In this previous case, the minor was subject to intense pressure and coercion to get vaccinated by a doctor and her staff at MedStar in D.C. When she eventually refused the vaccines, the doctor and staff took physical positions in the room that made her feel trapped! Thankfully, she was eventually able to escape without getting vaccinated.

These lawsuits expose a deeply concerning trend that must be stopped dead in its tracks. And these lawsuits should hopefully have that exact effect.

To any doctor out there who injects a minor without parental consent, you should know this: if that child’s parent contacts our firm, expect to receive an unwanted injection of justice in return.

For now, I am pleased to celebrate the repeal of the D.C. law that permitted vaccination of minors without parental consent and thank ICAN for making that lawsuit possible!

April 29, 2023 Posted by | Timeless or most popular, War Crimes | , , | Leave a comment