HART response to incorrect statements from Fraser Myers, published by Spiked
Health Advisory & Recovery Team | May 12, 2023
Spiked has published a spiteful article by Fraser Myers that claims HART is “notorious for its anti-vax statements”. This follows a debate between him and Andrew Bridgen MP on GB News in which Bridgen brought along facts and Myers repeated the phrase “anti-vax conspiracy theory” numerous times. In turn, the debate had come about after Myers had published a shoddy attack — short on facts and heavy on invective — on Bridgen a week previously. The Spiked article was brutally dismembered by Will Jones at Daily Sceptic.
Perhaps stung by this, Myers produced the offending article, bringing HART into the picture after we asked for clarification about funding that Spiked had previously received from Pfizer. Nick Dixon, also of Daily Sceptic, has attempted to triangulate the state of play. We have written a longer piece about this episode; numerous others have opined on the matter. David Paton stated that Myers “would have more credibility in this debate if Spiked addressed their inexcusable support for sacking unvaccinated care workers” having supported this policy in July 2021.
Myers’ unpleasant statement about HART sits alongside various incorrect facts. We are happy to put the record straight and — as Myers has stated that this is his final word on the matter — we are pleased that this debate can be put to bed… unless, of course, Myers was just shooting from the hip with that statement and intends to continue the discussion.
- Myers claims it is wrong to call the vaccines experimental. The injections were always experimental, which was why Pfizer’s Chief Scientific Officer described Israel as a “sort of laboratory” for the covid vaccines and why the world eagerly awaited evidence that they might work. The Pfizer phase 3 trial for safety does not officially conclude until 31st December 2023, but they destroyed the control by offering them the vaccine so the proper phase 3 safety studies will never complete. The safety aspect of Pfizer’s pregnancy, immunocompromised and myocarditis/pericarditis studies do not complete until 31st March 2026. The appropriate phase 0 pre-clinical work to measure the amount of spike protein produced in the body and how long it lasts has still not been done, or has not been made public.
- Myers claims it was wrong to call the injections a gene therapy simply because they are not thought to alter a person’s DNA. According to Moderna’s filing in June 2020 “mRNA has been characterised as a Gene Therapy Medicinal Product.” BioNTech agreed in a filing in March 2020 saying, “mRNA therapies have been classified as gene therapy medicinal products.” Do these companies not know what they’re talking about?
- Myers quotes early safety data saying that there were 139 adverse reactions in the vaccine arm and 97 in the placebo arm, claiming that it “isn’t an enormous difference”. These figures are from table 2 of the paper he references but he has not read the whole of table 2. This works out at an extra 12.5 events per 10,000 participants, which is 1 in 800 and exactly what Bridgen claimed. In the UK that would account for 52,000 such injuries after the second dose alone and would be properly defined as “uncommon” not “rare”. It is worth remembering that this terminology is designed for describing the harms from drugs given for treating people who are already sick. Serious harm caused to healthy people at a rate of 1 in 800 is totally unacceptable. Remember these were only the worst adverse events – life changing events, hospitalisations or deaths – which had all occurred during the short period of follow up at the very beginning of the safety trials. There had only been a median of 2 months follow-up at that point. For some participants the ink was metaphorically still wet on their consent forms. Any events that occurred after the cut off were not included in the study. He is right that others have criticised that paper but none of the critics have attempted their own analysis to estimate the scale of harm. It is also worth noting that this is a very high rate of serious adverse events — more frequent than 1 in 1,000 is properly termed ‘uncommon’ rather than ‘rare’ and certainly not ‘very rare’. Assuming a similar adverse reaction rate for later doses, such a rate would amount to over a hundred thousand such serious adverse events in the UK after 151 million jabs.
- Myers then complains that 1 in 800 refers to the number of events, not the number of people affected. The same paper points out that the published trial data is inadequate to make that assessment. FDA data showed twice as many vaccine recipients had multiple adverse events as placebo participants which further suggests a genuine issue here.
- Myers then claims the number needed to vaccinate (“NNV”) calculations from UKHSA were based on 2023 data. That is not correct: they were based on data from July 2022. At the time vaccines were still being pushed on the whole population. The estimates they calculated of thousands to hundreds needing to be vaccinated to prevent a serious hospital admission tally well with the estimates HART carried out for the NNV to prevent a single death from the Delta wave, using UKHSA’s own data.
HART can cite multiple other sources to evidence the claim that the covid injections were harmful and caused deaths, but what do we know? Myers has, after all, declared that HART is “notorious for its anti-vax statements”. But at least we’ve looked into the matter and attempted to shed light on some very iffy claims made by the authorities. If that has saved one person from suffering an unnecessary adverse effect, our consciences are clear — we will sleep well knowing we did what we could.
Others, however, will have to look themselves in the mirror for evermore and know what they have done.
Florida’s Letter to the CDC and the FDA Exposes Vaccine Quackery
BY IGOR CHUDOV | MAY 11, 2023
Florida’s Surgeon General Joseph Ladapo sent an open letter to the FDA and the CDC. The letter asks all the right questions about COVID vaccines – and exposes the FDA and the CDC as charlatans engaging in medical quackery.
Here’s the letter:
A very nice statement at the bottom summarizes the state of things:
Ladapo: Your organizations are the main entities promoting vaccine hesitancy – Florida promotes the truth. It is our duty to provide all information within our power to individuals so they can make their own informed health care decisions. A lack of transparency only harms Americans’ faith in science.
Vaccine Medical Quackery
Reminder: promoting unproven, untested, and non-working medications is called medical quackery, and promoters of such are called charlatans.
Ladapo exposes this medical quackery by asking several questions, each showing that the FDA (and the CDC) attempted to hide facts that reveal the dangers and ineffectiveness of Covid vaccines. Summary follows:
- Why were randomized clinical trials not conducted for “Covid boosters” (such trials were necessary to establish that they are safe and effective)
- Why did the FDA ignore many subclinical myocarditis reports and allow Pfizer to postpone its report on subclinical myocarditis?
- Why were vaccine side effects intentionally ignored in V-Safe?
- Why did the FDA allow Pfizer to hide the results of its clinical trial of Covid vaccines in pregnant women, that ended in 2022?
- Why are the FDA and the CDC hiding negative effectiveness of Covid vaccines?
All these questions demonstrate that the FDA and the CDC intentionally conspired with vaccine manufacturers to hide adverse events of Covid vaccines and violated their own rules.
Covid Reckoning Instead of “Pandemic Amnesty”
The questions, growing more pointed daily, show that the long-hoped-for Covid reckoning is coming, as I explained:
Florida’s Surgeon General, Dr. Ladapo, is working hard to protect Floridians from Covid vaccines. However, he is not stupid and probably angling to become the next United States Surgeon General.
Asking questions such as the above will hopefully help enact “regime change” and allow new players, not tarnished by reckless “Warp Speed” vaccine programs or by vaccine mandates, to take over.
While I do not expect an honest answer from the FDA or the CDC, I wish Dr. Ladapo all the best and hope to see him appointed the US Surgeon General in 2024.
FDA ordered to produce all Moderna C-19 vaccine & Pfizer adolescent C-19 vaccine data by mid-2025
BY AARON SIRI | INJECTING FREEDOM | MAY 12, 2023
As you may recall, we obtained a court order in January 2022 forcing FDA to produce all of its data on Pfizer’s covid vaccine for those 16 years and older at a rate of 55,000 pages per month, as opposed to the 75 years FDA sought. That production should be completed in a few more months.
In a second lawsuit we brought, the same judge just ordered FDA to produce the documents it relied on to license and Moderna’s covid vaccine AND Pfizer’s covid vaccine for 12-to-15-year-olds at an average rate of at least 180,000 pages per month.
In this second lawsuit, this time also on behalf of the parents of Maddie de Garay, a young girl grievously injured in Pfizer’s clinical trial for 12-to-15-year-olds, we explained to the Court the importance of timely production. Once again, FDA claimed it would be “impractical” to release the estimated 4.8 million pages at more than between 1,000 to 16,000 pages per month, or in other words at least 23.5 years. We countered, demanding FDA produce all documents by mid-2025.
The federal judge, in an amazing decision, started by stating that “Democracy dies behind closed doors” and ordered them to produce the files – millions of pages – in just 2 years, amounting to a rate of at least 180,000 pages per month.
Indeed, it is another blow for transparency and accountability. The Judge’s decision is just that good that I am including below a copy of the entire decision – it is a short four pages.
Influenza Vaccine Fails to Stop Hospitalization and Death
Large Japanese Study Shows No Benefit on Hard Outcomes
By Peter A. McCullough, MD, MPH | Courageous Discourse | May 12, 2023
Influenza vaccination has become a mainstay in American medicine largely as measure to protect the elderly. However in recent decades the FluShot has been pushed on healthcare workers, the general adult public, and starting in 2017 the CDC ACIP Panel stated: “Routine annual influenza vaccination is recommended for all persons age 6 months and older who do not have a contraindication.” I wondered if the FluShot even did what it was supposed to do originally in the elderly — protect against hospitalization and death. I was disappointed by real world data.
Uemura and coworkers from the Department of Biostatistics & Bioinformatics, Interfaculty Initiative in Information Studies, University of Tokyo, Japan reported on 83,146 individuals who were aged 65 years or older at baseline and were followed up between April 1, 2014 to March 31, 2020.
Uemura K, Ono S, Michihata N, Yamana H, Yasunaga H. Duration of influenza vaccine effectiveness in the elderly in Japan: A retrospective cohort study using large-scale population-based registry data. Vaccine. 2023 May 5;41(19):3092-3098. doi: 10.1016/j.vaccine.2023.03.066. Epub 2023 Apr 10. PMID: 37045684.
The multivariable analysis showed a lower incidence of influenza in vaccinated individuals (hazard ratio [HR], 0.47; 95% confidence interval [CI], 0.43-0.51; P < 0.001), however the incidence of hospitalization for influenza did not differ significantly by vaccination status (HR, 0.79; 95% CI, 0.53-1.18; P = 0.249). Protective effectiveness against incidence waned quickly after 4 or 5 months.
These data suggest the massive effort on vaccination in the general population is a waste of time and effort. If the frail and elderly get no overall direct reduction in hospitalization and death, influenza vaccination should be individualized based on pulmonary and systemic risks.
FBI Contractor Created Fake Online IDs to Join Chatrooms Run by Groups Organizing Against Vaccine Mandates
By Brenda Baletti, Ph.D. | The Defender | May 12, 2023
An FBI surveillance contractor infiltrated the chatrooms of two airline industry groups opposed to vaccine mandates to collect intelligence on the groups’ organizing activities, investigative journalist Lee Fang reported.
The contractor, Flashpoint, which in the past infiltrated Islamic terror groups, now focuses on “anti-vaccine” groups and other domestic political organizations, according to Fang.
In a webinar presentation for clients last year, which Fang analyzed on his Substack, Flashpoint analyst Vlad Cuiujuclu demonstrated his company’s methods for identifying and entering encrypted Telegram chat groups.
He explained how the company attempted to join chatrooms of transportation workers resisting the COVID-19 vaccine mandates.
Fang described the presentation:
“‘In this case, we’re searching for a closed channel of U.S. Freedom Flyers,’ said Cuiujuclu. ‘It’s basically a group that opposed vaccination and masks.’
“As he clicked through a database, Cuiujuclu showed a chat group on Telegram sponsored by Airline Professionals For Justice, another group formed by airline industry workers opposed to the mandate. The forum, he added, provided useful insights, including Zoom links for meetings of the grassroots organization.
“‘Private chats,’ said Cuiujuclu, ‘require for you to have an invite link,’ which he noted can often either be found by scrolling through public forums or by ‘engag[ing] the admin of that channel.’”
Flashpoint also offers clients artificial intelligence and internet scraping tools.
According to Fang, the firm is a leader in the “threat intelligence industry,” a growing number of security and surveillance firms that create fake online identities to infiltrate Discord chats, WhatsApp groups, Reddit forums and dark web message boards to gather information for clients, including corporations and the FBI, to monitor potential threats.
Joshua Yoder, president of US Freedom Flyers, said he is aware that Flashpoint infiltrated private chat groups associated with his organization.
Yoder told The Defender :
“Tradecraft and other strategies are often used to gain inside knowledge of conservative organizations with the intent to disrupt, mislead and otherwise thwart effective campaigns.
“Infiltration is a tactic used by the deep state to prevent the truth from being told by attempting to destroy the advancement of the message. The team at US Freedom Flyers has been successful in recognizing these attacks and we have taken decisive actions to protect the organization and our members.”
Aviation industry workers were some of the most vocal and organized against COVID-19 vaccine mandates.
They wrote an open letter to the aviation industry signed by thousands of organizations, physicians and pilots. They also organized research on the risks of vaccines for pilots, spoke publicly about the “culture of fear and intimidation” around the mandates in the industry, and filed multiple lawsuits in Canada, the Netherlands, and the U.S.
US Freedom Flyers brought a lawsuit against Atlas Air, one of the largest air cargo carriers in the aviation industry, in May 2022.
Fang told The Defender the targeting of American citizens resisting the vaccine mandates fits into a long history of surveillance being used to subvert democracy. He said:
“There is a long sordid history of informants and surveillance contractors working to undermine democratic engagement in this country.
“The push against regular citizens opposed to COVID-19 vaccine mandates has come in many forms: censorship, demonization and in this case, surveillance.”
The growing market for spying on domestic dissent
Flashpoint advertises its surveillance success on its website, providing examples of its work undermining environmental activism, G20 protests and protests against the aviation industry.
The webpages describing these activities were taken down after Fang published his investigation, but they can be found on the Wayback Machine internet archive.
For example, Flashpoint described its capacity to monitor activists organizing against pollution and the aviation industry. The website said:
“By monitoring the situation and assessing tactics, techniques, and procedures (TTP’s), Flashpoint was able to assess the impact of upcoming protests, and determine that these groups would likely continue to protest and attempt to impede airport construction and expansion projects through direct action. …
“Based on this information, Flashpoint customers were able to take actions to help control the impact to business operations, and to ensure the safety of their employees and facilities as well as the safety of those protesting.”
Flashpoint was founded by Evan Kohlmann, former NBC News contributor who investigated Islamic terror groups and whom The Intercept described as “the U.S. government’s go-to expert witness in terrorism prosecutions.”
Jack Poulson of Tech Inquiry, a group that researches the surveillance industry, told Fang that “Flashpoint has been selling its chatroom infiltration services to companies and governments for years.”
But, he said, it has shifted its focus from “surveilling Muslims after September 11” and “followed the money into both the Pentagon’s information warfare programs and the business of monitoring domestic protest groups.”
Last year, Flashpoint acquired Echosec Systems, another intelligence contractor, and last month it formalized a partnership with Google Cloud.
These acquisitions come in addition to “a steady stream of contracts to Flashpoint in recent years from the FBI, the Department of Defense, Treasury Department, and Department of Homeland Security, among other agencies,” Fang wrote.
Fang also spoke to Jay Bhattacharya, M.D., Ph.D., professor of medicine at Stanford University, research associate at the National Bureau of Economics Research and one of the authors of the Great Barrington Declaration.
Bhattacharya said:
“This kind of domestic spying violates the implicit protection Americans have in these kinds of settings.
“This isn’t terrorism, this doesn’t have anything to do with national security.
“This is a private set of employees, workers who are trying to maintain their jobs in the face of unscientific demands for COVID vaccinations.”
Brenda Baletti Ph.D. is a reporter for The Defender. She wrote and taught about capitalism and politics for 10 years in the writing program at Duke University. She holds a Ph.D. in human geography from the University of North Carolina at Chapel Hill and a master’s from the University of Texas at Austin.
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.
Robert Kennedy Jr. is the only presidential candidate to still be banned from Instagram
By Tom Parker | Reclaim The Net | May 12, 2023
Robert Kennedy Jr., a Democratic candidate for the 2024 United States presidential election, revealed that his account is till banned from Instagram and accused the tech giant of preventing him from accessing the site, despite him being a contender for the White House.
This makes him the only 2024 US presidential candidate that’s unable to post to the influential social media platform and currently being subjected to direct Big Tech censorship.
Former President Donald Trump, who is running for president in 2024 as a Republican candidate, was suspended from Instagram on January 6, 2023 and banned on January 7. However, his ban was lifted on January 25, 2023.
The other 2024 presidential candidates, Joe Biden (D), Marianne Williamson (D), Larry Elder (R), Nikki Haley (R), Asa Hutchinson (R), Vivek Ramaswamy (R), and Corey Stapleton (R), all have active Instagram accounts.
Kennedy was banned from Instagram in February 2021 for violating the platform’s strict speech rules related to the coronavirus and vaccines. The ban came after several Democratic senators and 12 state attorneys general demanded that Kennedy and other Covid vaccine skeptics be deplatformed by Big Tech. Before the ban, Kennedy had over 800,000 Instagram followers.
Instagram’s failure to reinstate Kennedy since announcing his presidential campaign means that he won’t be able to directly post his message to the social media platform’s sizeable audience of two billion monthly active users.
COVID Was Not Dangerous to Unvaccinated Pregnant Women
BY IGOR CHUDOV | MAY 11, 2023
Remember the endless media hysterics about COVID being “dangerous to unvaccinated pregnant women”?
A recent report MBRRACE-UK throws doubt on such statements. It covers 2018-2020, so the year of 2020 was a part of the COVID pandemic.
In the UK, in 2020 (before COVID vaccines), only NINE women died from (or with) COVID-19 during pregnancy or up to six weeks after giving birth.
Remember that in 2020, all pregnant women in the UK were unvaccinated. COVID was at its worst in 2020.
COVID was quite rampant in the UK at the time. According to Our World in Data, the UK had 94,194 COVID deaths in 2020. However, only nine deaths out of those involved pregnant women.
ONS reports that England and Wales had 613,936 live births in 2020.
So,
- Pregnant women’s COVID deaths (9 total) were less than one in ten thousand overall COVID deaths.
- Pregnant women’s deaths (9 total) were less than one in 68,000 (sixty-eight thousand) births.
- In other words, for every pregnant woman who died of COVID in 2020, over 68,000 did NOT die.
Every death is a tragedy, especially those of future mothers. Those nine deaths were tragic for the families involved. I am very sorry for each of the nine women who died with COVID in the UK in 2020. I am relieved, however, that the number of deaths among pregnant women was far less than what the media intimated.
Was COVID a great danger to pregnant women? The numbers above suggest that the chance of dying from COVID for unvaccinated women in 2020 was very remote, as there was less than one COVID death per 68,000 births.
To me, this cannot be considered “particularly dangerous.” Pregnant women are young (most are under 40), and Covid is not particularly deadly to that age category.
So, those who believed that COVID-19 puts future mothers’ lives at tremendous risk were lied to. Pregnant women were given false information to nudge them to get vaccinated.
We finally have the proof.
Pfizer trial data showed danger for babies but health czars recommended jabs to pregnant women anyway
By Guy Hatchard | TCW Defending Freedom | May 11, 2023
A PREPRINT paper published this month highlights just how many unknowns we are dealing with when it comes to assessing the long-term outcomes of mRNA vaccination. It shows that IgG4 antibodies are present in umbilical cord blood of infants born to vaccinated mothers, meaning a theoretical risk to newborns of an ineffective response to Covid infection.
But was this really unknown to those recommending that mRNA vaccination was safe for pregnant women? Documents released by Pfizer under court order reveal that Pfizer and the US Food and Drug Administration (FDA) were well aware of clinical trial results indicating appalling outcomes for babies of pregnant women.
Watch this 20-minute video where dozens of so-called experts in New Zealand are recorded telling us that the mRNA Covid vaccines are completely safe for pregnant women in direct contradiction of Pfizer trial results available in April 2021. These results indicated an unfolding disaster for babies including miscarriage, premature birth, cardiac arrest, toxic breast milk and spike protein crossing the placenta.
In the video, their comments are juxtaposed with scientists exposing the highly disturbing content of the Pfizer trials of pregnancy outcomes.
Was the NZ government aware of this information? Certainly the contractual arrangements that our government had made with Pfizer would have required Pfizer to fully inform the Ministry of Health of all the results of vaccine trials. But the MoH has completely ignored the information which has become public knowledge. Since the start of this month they are again encouraging pregnant and breastfeeding mothers from 16 and up to get a further booster shot. Why? Especially considering the increased incidence of miscarriages and stillbirths since the NZ vaccine rollout began.
I can’t imagine at this time a more important video to watch than this 20-minute film of our experts lining up to misinform prospective mothers of safety. Were they misled by Pfizer, by the MoH, by politicians, by the FDA, or by all of the above? Or did they just decide to promote a safety rating without any evidence to back up their statements? We may never know, but the lesson of this video is clear: we will not be able to trust the medical czars again.
Covid jabs the big picture: Part 1
Overview of evidence prior to rollout
Health Advisory & Recovery Team | May 10, 2023
HART have been asked to submit evidence to module 3 of the Covid-19 Public Inquiry. That module is about the impacts on healthcare but we were specifically asked to include evidence around deaths in males aged 15-18 years of age and so provided an overview of the full impact these novel products have had on the healthcare system. What follows are some of the highlights. There will be three parts to this series. Here the evidence on what was known before rollout will be presented. Part two covers the evidence after rollout (excluding deaths) and part three the evidence on deaths.
It is worth remembering how cautious people were about any novel products that might claim to prevent covid. In February 2020, Chris Whitty said,
“The rate limiting steps are late clinical trials for safety & efficacy, & then manufacturing. For a disease with a low (for the sake of argument 1%) mortality a vaccine has to be very safe so the safety studies can’t be shortcut. So important for the long run.”
He was right.
The belief that vaccines were safe had led to a circular belief that vaccines required fewer safety checks than other novel therapies. Novel vaccines take a decade or more to go through safety checks. Flu vaccines don’t. These novel drugs were treated like flu vaccines for regulatory purposes.
The regulators failed us in numerous ways as set out in The Perseus Report. Examples include:
- Companies were allowed to skip testing for gene and cancer toxicity and even studies showing how much spike is produced, for how long and where in the body it reaches. Pfizer said these studies were “not considered necessary.” Even while their trial info sheet said “Due to the urgent need for a vaccine against Covid-19, with agreement from the MHRA, some of the tests usually required for a newly manufactured vaccine have been modified, in order to make the vaccine available more quickly for assessment.”
- They did not demand these studies were done after rushed emergency approvals either. No human studies were carried out to see what happened to the synthetic modified RNA – no-one knows how long it takes to be removed from the body. There is evidence that in some it lasts between at least 28 days and 4 months in the blood.
- The regulators let the pharma companies get away with terminating the placebo arm of the study after ~3months by offering them all the novel products.This was despite us knowing that narcolepsy caused by Pandemrix vaccine took on average of 8 months to be diagnosed.
- The lipid nanoparticles that deliver the modified synthetic mRNA are themselves toxic. This mechanism of delivery was shelved in 2016 for gene therapy to treat inherited genetic conditions because of the multiple doses needed. It was claimed it could still be used in vaccine technology because that only requires one dose…
- The viral vector used for delivering the AstraZeneca DNA message was reported in 2007 to cause platelet activation, which can lead to blood clots.
- There were many more points made including failings in investigating deaths, failing to listen to patients, problems with manufacturing processes and problems with accountability and governance all of which are in the report.
Since 2005 there have been concerns about the regulator losing “sight of the need to protect and promote public health.” The CEO of the MHRA, Dame June Raine, claims the MHRA is now an “enabler” not a “watchdog.” Even before there was political capture there were pre-existing conflicts of interest.
The spike protein is the most toxic part of the virus. It damages lungs, vessel walls and causes clots. Part of the sequence is identical to a region of a bacterial sequence that can bind directly to a particular type of white blood cells resulting in lethal cytokine storms. This part of the sequence was heavily mutated in the Omicron variant making it less lethal. However, even the most recent injections contained the original Chinese spike sequence with this dangerous sequence.
The manufacturers decided to use the WHOLE chinese spike sequence rather than parts of it, or peptides, which have been shown to be safer for vaccine design. Some manufacturers modified the spike so that it could not bind to the receptor and enter a cell. This might have reduced some harm from receptor binding but not from the action of spike within cells. The spike was delivered into cells so spike was produced INSIDE the cells in the first place. AstraZeneca did not modify the sequence. From November 2020 it was clear that parts of AZ spike could be shed outside of cells.
The Pfizer and Moderna clinical trial data shows a higher rate of serious adverse reactions from the treatment group (12.5 per 10,000) than any reduction in serious events from covid (2.3 and 6.4 per 10,000 for Pfizer and Moderna respectively). Yet the claim of 90%+ efficacy was all that was reported and all that Dame June Raine claimed she needed to see in order to approve the drugs.
AZ issued a press release claiming 100% efficacy against hospitalisation and death after only two severe covid hospitalisations and one death in the placebo arm. This claim was repeated widely and was believed.
At the time, the priority was to protect the old and vulnerable who accounted for 98% of covid deaths. There were going to be 15 million jabs to freedom:
The evidence presented is damning. The failures of the regulators to adequately test the safety and efficacy of these novel vaccines are shocking. The circular belief that vaccines required fewer safety checks than other novel therapies is a dangerous assumption that has put the lives of millions at risk. The fact that serious adverse reactions were higher in the treatment group than any reduction in serious events from covid is deeply concerning. We must demand accountability from the regulators and demand that the safety and wellbeing of the public is always the top priority, not profit or political gain. There was total regulatory failure in allowing these products to be given to anyone, which was compounded by not withdrawing them promptly once evidence these issues were clinically relevant became clear.
Andrew Bridgen MP Joins Reclaim Party and Announces He is Suing Matt Hancock for Defamation
BY WILL JONES | THE DAILY SCEPTIC | MAY 10, 2023
Ex-Tory MP Andrew Bridgen, who was expelled from the party for criticising the Covid vaccines, has announced he’s joining Laurence Fox’s Reclaim Party, making him its first member of Parliament. At a press conference today Bridgen said he would be standing at his North West Leicestershire constituency at the next General Election. He also confirmed he would be suing Matt Hancock MP for defamation over an allegation of antisemitism.
At the press conference this morning Bridgen confirmed he has decided not to appeal his expulsion and blasted the Conservative Party. He said:
Even if I were to be given a fair hearing, which I doubt, I would not wish to rejoin the party after the treatment received by myself and my family over the past few years.
I feel now that the party no longer represents the people of this great country. If I am to represent my constituents and countrymen it must be from outside the party which I have served dutifully for many decades.
I will be standing again in North West Leicestershire at the next election. Not as a Conservative, but as a Member of the Reclaim Party. More than anything, the Reclaim Party stands for freedom of speech.
I will cross the floor today, Wednesday May 10th, and sit on the opposition benches as the first Member of Parliament for the Reclaim Party. I say first because I have no doubt I will not be the last. This is just the beginning.
If the Conservative Party wishes to contest my seat it can do so at the next General Election.
I have more confidence that I will win my seat than the vast majority of sitting Conservative MPs, so I welcome the challenge should the Prime Minister and Parliamentary Party wish to take it.
Bridgen was accused of antisemitism for agreeing in a tweet with an anonymous heart doctor he quoted that the Covid vaccine rollout was “the biggest crime against humanity since the Holocaust”.
He has denied the allegation – which we at the Daily Sceptic agree is spurious and an example of a weaponised antisemitism allegation to achieve political ends. This morning Bridgen confirmed that he will be suing ex-Health Secretary Matt Hancock for defamation after the Conservative MP tweeted in January that he was spouting “antisemitic, anti-vax, anti-scientific conspiracy theories”.
In a YouTube video Bridgen said he has submitted a “defamation claim to the Royal Court of Justice against Matthew Hancock MP”. The basis of the claim is that Hancock’s accusation of antisemitism is “a false slur to deliberately try and shut down valid concerns raised by me on behalf of constituents and thousands of others around the world about the safety and efficacy of the experimental COVID-19 injections”.
Matt Hancock in the dock: that’s a court case to look forward to.
You can donate to Andrew Bridgen’s legal fund here.
Andrew Bridgen and Fraser Myers clash in fiery debate on Covid vaccine harms
GBNews | May 8, 2023
Andrew Bridgen, a Member of Parliament in the UK, has been vocal about vaccine harms and the origins of Covid.
Fraser Myers, deputy editor of Spiked online, published an article called “The delusions of Andrew Bridgen – Conspiratorial thinking corrodes reason, democracy and humanism”.
The pair joined Andrew Doyle on GB News in a fiery debate.
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From the Archives
Alarmist climate science as a textbook example of groupthink
By Paul MacRae | May 1, 2012
A while ago, I received an email from a friend who asked:
How can many, many respected, competitive, independent science folks be so wrong about [global warming] (if your [skeptical] premise is correct). I don’t think it could be a conspiracy, or incompetence. … Has there ever been another case when so many ‘leading’ scientific minds got it so wrong?
The answer to the second part of my friend’s question—“Has there ever been another case where so many ‘leading’ scientific minds got it so wrong?”—is easy. Yes, there are many such cases, both within and outside climate science. In fact, the graveyard of science is littered with the bones of theories that were once thought “certain” (e.g., that the continents can’t “drift,” that Newton’s laws were immutable, and hundreds if not thousands of others).
Science progresses by the overturning of theories once thought “certain.” … continue
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- Reality Check: Maldives Have Actually Grown In Size Or Remained Stable Over Recent Decades
- Abrupt Climate Change Also Occurred NATURALLY In The Past …25 Times During Last Ice Age
- Cave Discovery Reveals Today’s Desert Climates Were Recently Far Warmer, Wetter, Teeming With Life
- German Expert: Heat Dome Led To Record Temps In Western USA…Warmer In 1934, 1936
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