Despite Concerns About ‘Vaccine Fatigue,’ CDC Recommends Extra COVID Boosters, Including for Some Infants
By Brenda Baletti, Ph.D. | The Defender | October 24, 2024
Advisers to the Centers for Disease Control and Prevention (CDC) on Wednesday recommended two COVID-19 boosters during the 2024-2025 season for people ages 65 and older and for younger people who are moderately or severely immunocompromised.
The Advisory Committee on Immunization Practices (ACIP) also recommended that immunocompromised people ages 6 months and older take “additional doses” of the shot — three or more — based on shared clinical decision-making between doctor and patient.
The vote for all three new COVID-19 vaccine recommendations was unanimous.
The committee also voted 14-1 to recommend Pfizer and Merck’s pneumococcal conjugate vaccines — designed to protect against meningitis and pneumonia — for all adults who have never received the vaccine ages 50 and older, lowering the recommended age from 65.
The U.S. Food and Drug Administration in June approved Merck’s Capvaxive for prevention of invasive pneumococcal disease and pneumococcal pneumonia in adults.
The vote expands the market for both companies, who will now be able to market their vaccines to millions more eligible adults, boosting their annual revenues by hundreds of millions of dollars, FiercePharma reported.
CDC Director Mandy Cohen endorsed the recommendations after the meeting, making them official CDC recommendations.
“CDC will continue to educate the public on how and when to get their updated vaccinations so they can risk less severe illness and do more of what they love,” Cohen said.
“ACIP loves advising that people receive the most vaccines possible,” internist Dr. Meryl Nass told The Defender.
She added:
“When ACIP talks about shared decision-making, what they mean is this: ‘We lack the data to recommend this vaccine for this group, so we could be criticized (or worse) for making an unscientific recommendation. But we really want you to have it.’
“So we think the patient and doctor (who is much less educated about the minutiae regarding the vaccine than the ACIP members are) should together decide whether the patient should get it. That way we protect ourselves while maximizing the number of jabs.’”
Nass said that if ACIP members were serious about shared clinical decision-making, “They would put all their thoughts down so clinicians could become educated and then jointly evaluate the risks and benefits with patients.”
The committee also voted unanimously to add high-dose and adjuvanted flu vaccines to the Vaccines for Children Program — which provides free vaccines to children whose families can’t afford them — for transplant recipients taking immunosuppressive medications.
ACIP is described as an independent, nonfederal expert body of professionals with clinical, scientific and public health expertise. The committee decides which vaccines should be recommended to the public, who should take them and how often.
In practice, most members have financial ties to vaccine makers that they don’t consider to be conflicts of interest. For example, in Wednesday’s meeting, paid Merck consultant and researcher Noel Brewer, Ph.D., declared “no conflict” before voting to recommend Merck’s vaccine.
More recommendations may ‘exacerbate existing vaccine fatigue’
The CDC said that in the 2023-2024 COVID-19 season, only 8.9% of people over age 65 and 5.4% of immunocompromised adults age 18 and older had received two boosters.
The presenter, Dr. Georgina Peacock, said there was “obviously a need for additional education and recommendations,” but raised concerns that additional recommendations “may also exacerbate existing vaccine fatigue.”
Ruth Link-Gelles, Ph.D., presented COVID-19 vaccine efficacy data that provided the rationale for the new recommendations. Efficacy is affected by time since the last booster dose, changes in COVID-19 variants and the time since someone was last infected with COVID-19, she said.
Link-Gelles said those are hard to disentangle, especially given that all adults have high rates of infection-induced immunity. Infection-induced immunity rates ranged from 72% for people over age 65 to 89% for those ages 16-49 and 84% for those ages 50-64.
In adults over 65, she said protection waned to zero against emergency room visits and hospitalization by four to six months and was somewhat more effective against critical illness.
She also said that additional education alone wasn’t effective in increasing uptake.
Waning efficacy: an argument for more shots or proof of natural immunity?
Link-Gelles presented a slide that showed COVID-19 vaccine effectiveness waned significantly among people ages 18-64, beginning at 30% and dropping to negative 15% by six months post-vaccination.
When pressed on how to interpret the negative efficacy, she said, “There is no biological plausibility for the vaccine increasing your risk of disease.”
Vaccine effectiveness data is relative, meaning it’s a measure of how much more protection a vaccinated person has than an unvaccinated one, she said. Therefore, “what we think is happening” is that unvaccinated people were getting natural immunity during that time, giving them more robust immunity and skewing the baseline for comparison.
Because vaccine efficacy is a comparison of the disease in the vaccinated versus the unvaccinated, if the efficacy is negative, “then the unvaccinated have more protection than the vaccinated,” Karl Jablonowski, Ph.D., senior research scientist at Children’s Health Defense, told The Defender.
Jablonowski pointed out that Link-Gelles suggested the unvaccinated are exposed to wild-type COVID-19 and then gain immunity, compared with the vaccinated who would not gain that same wild-type immunity.
“What Dr. Link-Gelles is not entertaining, that which she sees ‘no biological plausibility,’ is the possibility of diminishing immune health of the vaccinated,” he said.
Jablonowski added:
“Both scenarios reduce the infections in the unvaccinated relative to the vaccinated. Either scenario points to the same conclusion, that the unvaccinated have superior long-term (180-299 days) immune health when facing the COVID-19 pandemic.
“More broadly, you cannot present VE [vaccine efficacy] analysis as a valid assessment of how well a vaccine works and then disregard the analysis when it shows the vaccine is not working.
“It is clear, from CDC’s own data and presentation, that the vaccinated had a higher long-term incidence of disease than the unvaccinated.”
Watch the Oct. 23 ACIP meeting here
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.
Fluoride Finally Declared an “Unreasonable Risk”
A look at the ruling that will have a widespread impact on the health of all American children
By Aaron Siri | Injecting Freedom | October 25, 2024
A seven-year battle between the EPA and the public interest regarding the fluoridation of public drinking water has finally concluded. This is an excellent result by Siri & Glimstad partner Michael Connett in securing a court order against the EPA. Great job, Michael!
U.S. District Court Judge Edward Chen concluded the following in his ruling:
“[T]he Court finds that fluoridation of water at 0.7 milligrams per liter (“mg/L”) – the level presently considered “optimal” in the United States – poses an unreasonable risk of reduced IQ in children… [A] risk sufficient to require the EPA to engage with a regulatory response…”
“There is little dispute in this suit as to whether fluoride poses a hazard to human health. Indeed, EPA’s own expert agrees that fluoride is hazardous at some level of exposure. And ample evidence establishes that a mother’s exposure to fluoride during pregnancy is associated with IQ decrements in her offspring. The United States National Toxicology Program (“NTP”) – the federal agency regarded as experts in toxicity… concluded that fluoride is indeed associated with reduced IQ in children, at least at exposure levels at or above 1.5 mg/L (i.e., “higher” exposure levels)…”
“In all, there is substantial and scientifically credible evidence establishing that fluoride poses a risk to human health; it is associated with a reduction in the IQ of children and is hazardous at dosages that are far too close to fluoride levels in the drinking water of the United States. And this risk is unreasonable under Amended TSCA. Reduced IQ poses serious harm. Studies have linked IQ decrements of even one or two points to e.g., reduced educational attainment, employment status, productivity, and earned wages.”
The NTP report referred to above can be found here. While we wait for the EPA to take the next step, many municipalities have already acted to remove fluoride from their water systems.
NIAID Declares Mpox Vaccine ‘Safe’ for Teens, Opening the Door for Vaccine’s Approval for Kids as Young as 12
By Michael Nevradakis, Ph.D. | The Defender | October 18, 2024
The National Institute of Allergy and Infectious Diseases (NIAID) this week announced Bavarian Nordic’s mpox (monkeypox) vaccine is “safe and generates a robust antibody response in adolescents.”
The announcement drew criticism from doctors and scientists who cited the lack of any evident control group in the clinical trials and any publicly available data.
The results of the NIAID study, funded by the National Institutes of Health, could open the door for the vaccine’s approval for 12- to 17-year-olds in the U.S., a month after European regulators approved the vaccine for the same age group.
According to the Oct. 16 announcement, the modified vaccinia Ankara-Bavarian Nordic (MVA-BN), marketed as Jynneos in the U.S., “generated antibody levels in adolescents equivalent to those observed in adults at day 43 and found that the vaccine was well tolerated through study day 210.”
The results are based on a pair of Phase 2 clinical trials of the MVA-BN vaccine. One trial included 229 participants between 18 and 50 years old, while the other trial tested the vaccine on 315 adolescents between ages 12 and 17.
Based on the findings, the European Medicines Agency (EMA) last month approved the MVA-BN, marketed as Imvanex in Europe and the United Kingdom, for 12- to 17-year-olds.
“The immune response in adolescents was similar to adults. … According to the submitted data, the safety profile of Imvanex in adolescents was comparable to that seen in adults and no additional risk has been identified,” the EMA stated in its Sept. 19 announcement.
Last month, the World Health Organization (WHO) approved MVA-BN for adults — and said it can be used for babies, children, teens and pregnant women if they are in “outbreak settings where the benefits of vaccination outweigh the potential risks.”
The U.S. Food and Drug Administration (FDA) in September 2019 approved the Jynneos vaccine for adults, for the prevention of both mpox and smallpox and added it to the Strategic National Stockpile.
The approvals went through even though no data on the MVA-BN clinical trial results for the 12-17 age group have been publicized.
‘The complete void of any transparency in this clinical trial is stunning’
Critics of the vaccine cited the lack of data for 12- to 17-year-olds, the lack of a control group in the clinical trials, and questioned the necessity and safety of administering the mpox vaccine to children.
“The complete void of any transparency in this clinical trial is stunning,” said Brian Hooker, Ph.D., chief scientific officer for Children’s Health Defense. He added:
“Also, the clinical trial had no unvaccinated control group for comparison, which is a fatal flaw even if they would have made the trial results public. These are supposedly the premiere clinical researchers worldwide, yet they make 9th-grade mistakes in running their experiments.”
A spokesperson for NIAID who spoke with The Defender directed the public to the study protocol for the two clinical trials. However, the protocol does not indicate a control group and contains no findings.
“Short-term antibody responses in a study with an undisclosed sample size and no reported safety data are not sufficient for an NIAID press release,” cardiologist Dr. Peter McCullough told The Defender.
McCullough said:
“The Jynneos monkeypox vaccine has been used for years and carries a risk of myocarditis or heart damage. This study is not reassuring on safety or theoretical efficacy. The NIAID should take this post down and wait for the full peer-reviewed manuscript to be published.”
Internist Dr. Meryl Nass questioned the need for the MVA-BN clinical trials and NIAID’s claims of insufficient data for people 18 and younger. She told The Defender the studies were performed “after the U.S. government already gave hundreds of thousands of Americans both doses in mid-2022 and collected data on them.”
“One wonders what the purpose of this tiny trial was,” Nass said.
Data indicate a potentially high risk of severe adverse events
According to the NIAID announcement, “The overall frequency of adverse events was comparable between the study groups. Reports of dizziness were more common in adolescents than adults, but similar to the frequency of dizziness reported when other vaccines are administered in adolescents.”
The study results for the 18- to 50-year-old group indicated a rate of severe adverse events exceeding 1%. For Nass, a “1% SAE [severe adverse event] rate for a vaccine is very high,” though she added, “We need to know more to make any safety judgment.”
Nass suggested the actual number of severe adverse events may have been underreported.
“NIAID claims that only two of the 229 subjects had a serious adverse event. However, their definition of serious has been made more and more restrictive over the years,” Nass said.
According to Nass, while NIAID’s definition of a serious adverse event once “included an ER [emergency room] visit after vaccination,” the current NIAID definition is narrower, referring, in part, to “inpatient hospitalization or prolongation of existing hospitalization” instead of an ER visit.
The two reported severe adverse events in the 18-50 age group involved cases of cystitis — an inflammation of the bladder — and euglycemic diabetic ketoacidosis, an “uncommon diabetic complication.”
Nass also noted that severe adverse event data were “collected only for the first 57 days of the study.” In the event NIAID determined the adverse event was related to vaccination, further data were collected through day 181 — even though “blood was drawn at day 365 also.”
“Why were SAEs not collected through day 365 for everyone? That is how you learn what the SAEs related to a vaccine actually are,” Nass said.
Data from the U.S. government’s Vaccine Adverse Event Reporting System (VAERS) as of Sept. 27 indicate 2,115 reports of adverse events related to MVA-BN, including 19 reports for people under 18.
According to Managed Healthcare Executive, “Bavarian Nordic is preparing for a clinical trial to assess the safety of MVA-BN in children 2 to 12 years of age.”
The trial will be partially funded by the Coalition for Epidemic Preparedness Innovations, which previously announced its intention to develop “pandemic-busting vaccines in 100 days.”
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.
‘Childish Temper Tantrums’ – Australian Councilor Fires Back at Pressure From Authorities
By Anatoly Donstov – Sputnik – 24.10.2024
Following his powerful interview with Sputnik, Adrian McRae, businessman and member of the Town of Port Hedland Council in Australia, has been urged to resign by Western Australia Premier Roger Cook in a desperate attempt to silence him.
“Earlier this week, before the Premier had heard I was in Russia, he suggested that the entire Town of Port Hedland Council should get back to “knitting” when we demanded him to show us evidence that the Covid-19 vaccines were safe… So, instead of acting like a true leader, … he attacks me personally and resorts to ad-hominem – the last refuge of a failed argument. I feel sorry for him actually. I don’t know what I’d do if I was in his shoes,” McRae told Sputnik, explaining Cook’s “contempt” towards him and “all West Australian Councilors.”
On Wednesday, the Premier called for the resignation of McRae, labeling him “an embarrassment” after his interview with Sputnik, ABC reported. In the interview, the businessman criticized Australian and Western media for biased coverage of Russia and challenged the narrative portraying Moscow as the enemy.
McRae warned that free speech is under threat in the West, while BRICS countries still offer hope for its protection. As an observer in the 2024 Russian presidential election, McRae praised the transparency of the process, drawing heavy criticism from Australian media.
“It’s simple. The Premier is using the boogeyman of Russia to attempt to ruin my character in hopes of people forgetting about the important questions my entire Council has asked him regarding the mRNA vaccine contamination. He is deflecting the subject to the best of his very limited ability and making an absolute fool of himself in the process,” McRae told Sputnik, explaining why Cook has gone to such lengths to smear him.
Despite the Premier’s desperate attempts to suppress the council member, McRae remains a strong voice against Western censorship and political corruption, with Sputnik delivering the uncensored truth that the West fears.
“Sadly for the Premier, I have truth and science on my side. He, on the other hand, has nothing but a dying prostitute media and a really poor scriptwriter. So no, I am not too concerned about the Premier and his childish temper tantrums,” McRae said confidently, undeterred by the threats from the Western Australia Premier.
Dark Money, Darker Motives: Why is Bill Gates Backing Kamala Harris Using Shady Super PAC?
By Ilya Tsukanov – Sputnik – 23.10.2024
Tech billionaire, philanthropist and WEF cheerleader Bill Gates has given Kamala Harris’s campaign a $50 mln boost using dark money super PAC Future Forward. The donation was intended to remain secret, but was uncovered by NYT this week.
What’s Future Forward?
Set up in 2018 by former Obama campaign staffers and coming out of left field in the final weeks of the 2020 race to fund a massive pro-Biden media blitz, Future Forward is a super political action committee funded mostly by Big Tech and venture capital firms, including Meta, Google, disgraced crypto financier Sam Bankman-Fried, Bain Capital and Bridgewater Associates.
The super PAC has raised a whopping $700 mln for the 2024 election cycle, rolling out $75 mln in pro-Harris ads last week.
What’s Behind Gates’ Electoral ‘Generosity’?
2024 is at least the second election cycle where Gates has used a dark money vehicle to support the Democratic Party’s candidate. In 2020, the Bill and Melinda Gates Foundation contributed nearly $70 mln to the New Venture Fund, a nonprofit belonging to DC consultancy Arabella Advisors, which bankrolls the Sixteen Thirty Fund, a goliath of undisclosed donations for Democratic politicians and liberal causes which raised nearly $390 mln four years ago. Publicly, Gates and his now former wife also gave $500,000 to Biden’s inaugural committee.
Mr. Gates has been an active supporter of Democratic candidates since at least 2008, contributing financially to and praising the campaigns of Barack Obama and Hillary Clinton.
Gates’ ties to the Clintons are deeply rooted, with the billionaire becoming a top donor to the Clinton Foundation, and forging partnerships with the organization for global projects since at least 2013.
In a telling interview in 2016 in which he explained his preference for Clinton, Gates said “there have been questions about vaccines in general where some of the candidates have shown that they’re not as up to date about vaccines in general, and that’s got to be a concern.”
“Science in general, whether it’s GMOs or vaccines, there’s a lot of people out there who don’t give science the benefit of the doubt. In terms of experience, Hillary Clinton and Bill Clinton have more experience in global health,” Gates said at the time.
How has Gates profited off the Dems’ agenda?
With Harris’ presidential bid expected to broadly continue the Biden/Clinton line on foreign and domestic policy, it makes sense for Gates to throw his influence behind the VP, given the perceived threat of the Trump brand of red-pill MAGA Republicans and their anti-vax, anti-tech, and anti-interventionist leanings.
“This election is different, with unprecedented significance for Americans and the most vulnerable people around the world,” Gates said this week after info about his $50 mln donation leaked out.
“I think it’s great to have somebody who’s younger, who can think about things like AI and how we shape that in the right way, and I certainly offer up my opinions to the politicians who are interested,” Gates said this summer after Biden dropped out and named Harris his successor.
The Gates Foundation’s fortunes got a big boost under Biden, with its endowment growing from $69 bln in 2020 to $75.2 bln in 2023.
Gates enjoyed a profits bonanza off mRNA coronavirus vaccines mandated by the Biden administration. In 2022, he sold off shares of BioNTech stocks he bought in 2019 as sales slowed. His foundation has also owned shares in Pfizer, CureVac and Vir Biotech going back to well before the pandemic.
The billionaire’s foundation supports the Global Virome Project – an ambitious initiative created in 2018 to predict pathogens that could trigger lethal pandemics, but accused of weaponizing viruses from a network of 150 biolabs worldwide.
Gates has also backed a broad array of World Economic Forum-affiliated initiatives, including projects to reduce emissions and create synthetic meat and dairy. In 2022, The Seattle Times revealed Gates’ secret lobbying to save Biden’s signature $2+ trln Build Back Better social and climate spending package.
Gates has also been a top backer of the Biden administration’s battle against media and online ‘misinformation’, with an explosive MintPress investigation from 2021 revealing that his foundation had bankrolled some $319 mln in media, including CNN, the BBC, Le Monde, the Financial Times, Der Spiegel and others to ensure favorable coverage of his agenda and that of his allies.
EU President Likens Free Speech to Infectious Disease
Ursula von der Leyen advocates “pre-bunking” in the public forum to “vaccinate” people against “disinformation”
By John Leake | Courageous Discourse | October 23, 2024
EU President Ursula von der Leyen just joined the ranks of former Senator John Kerry and other globalist ghouls in declaring war on free speech by perversely proclaiming that the EU citizenry needs to be “vaccinated against disinformation.”
Like every censor in history, she characterizes her censorship program as a means of expunging erroneous information and ideas from public discourse. By using the word “disinformation,” she implies that she and her clique are already the sole possessors of the truth about everything, and that everyone who has and shares heterodox ideas is necessarily in error.
Her entire premise is FALSE for the following reasons:
1). Knowledge about the world is constantly evolving through constant inquiry, discussion, and dissemination. Knowledge is NOT a static thing. This is why countries with stifling censorship regimes have experienced intellectual, scientific, and artistic stagnation. Their rulers try to freeze the human mind in its state at their moment in history.
2). NO state, university, or ecclesiastical committee has ever been in possession of the full truth of any matter. Official orthodoxies have always been challenged by heterodox thinkers. Indeed, virtually every major advance in human insight has been performed by heterodox thinkers.
3). As John Milton observed in his 1644 pamphlet, Areopagitica, contending with error is an intrinsic part of learning and discovery. We literally learn by making mistakes and correcting them. If free speech is suppressed for the objective of preventing the propagation of erroneous thought—or “vaccinating against it”—it will become extremely difficult if not impossible for people to learn and discover.
4). Without a single exception in history, the people who hold power always advocate the orthodoxy that sustains and extends their power and that of their friends and supporters.
Ursula von der Leyen is the quintessence of this principle. As president of the EU, she conducted secret negotiations with Pfizer CEO to purchase a 20 billion Euros of Pfizer’s fraudulent and dangerous vaccine so that it could be inflicted on all the citizens of the European Union. She is currently under criminal investigation for her conduct in this affair that has come to be known as Pfizergate.
It takes a special kind of chutzpah for a powerful state official who is probably guilty of committing a major crime—a crime that has been systematically and ruthlessly concealed—to lecture the public about the need for censorship. The time has come for the citizens of Europe to rid themselves of Ursula von der Leyen and her clique of corrupt tyrants.
To be sure, there is increasing evidence that the Biden Administration has been exerting pressure on Germany—which remains an American vassal state—and the EU to step up its censorship regime. I will cover this strange development in a subsequent post.
Fired for Free Speech: Alison Morrow’s Battle Against Government Censorship
By Dan Frieth | Reclaim The Net | October 19, 2024
Alison Morrow (formally Westover), an accomplished journalist, found herself in the throes of a legal battle over her right to free speech. Represented by the Silent Majority Foundation, Morrow has filed a lawsuit against the Washington State Department of Natural Resources (DNR) and its top officials, citing wrongful termination after she was dismissed for airing an interview on her YouTube channel. The channel, a personal project crafted during her tenure as an environmental reporter at KING 5 in Seattle, became the subject of controversy following her post featuring a highly censored doctor, Dr. Aaron Kheriaty, and his views on COVID-19.
We obtained a copy of the lawsuit for you here.
Morrow’s career at KING 5, which spanned from 2013 to 2019, was marked by significant accolades, including two Emmy awards. Recognized for her independent journalism, DNR was fully aware of her YouTube activities when they recruited her as a communications specialist. Initially, her independent media pursuits were supported by DNR, but the tide turned with her decision to feature Dr. Kheriaty. DNR’s leadership warned Morrow that her continued interviews could lead to termination, a threat she met with a staunch refusal to abandon her First Amendment protections.
Determined to uphold her freedoms of speech, press, and association, Morrow chose to defy DNR’s directive to adhere to approved narratives. This act of resistance ultimately led to her dismissal, prompting her to seek legal assistance from the Silent Majority Foundation, which took up her case to safeguard these fundamental rights.
“The 1st Amendment is one of the most sacred rights of Americans. It is what differentiates our country from most others, that we have the freedom to question our government. It is also central to a free press. I was willing to lose my job – and all that it provided for our family – in order to stand up against the encroaching erosion of this right that I was witnessing at the time, not just in my case but in thousands of others across the country during the pandemic,” Morrow stated. “There was no way to do science or journalism, in the culture of censorship that was driven by our government at the time. That meant millions of people made decisions without informed consent. Given my commitment to seeking truth wherever it leads, I was unwilling to acquiesce to a demand that I remain silent.”
Doctors win libel case against British tabloid

Malcolm Kendrick MD and Zoë Harcombe PhD win libel case
By Maryanne Demasi, PhD | October 13, 2024
In a David and Goliath battle, two doctors have won a libel case against a British tabloid and journalist Barney Calman, in what the judge described as “the most significant piece of defamation litigation” he had seen in a very long time.
The UK’s High Court found that Calman and his publishers, Associated Newspapers Ltd, had falsely accused Malcolm Kendrick MD and Zoë Harcombe PhD of deliberately making false statements about statin drugs and putting many people at risk of heart attacks and strokes, with far graver consequences than the MMR scandal.
Further, Calman’s article inappropriately branded the two doctors as dishonest brokers, who were focused on the business of selling books that downplay the role of cholesterol in heart disease.

Barney Calman, journalist at Associated Newspapers Ltd
Calman and his publishers refused to apologise, remove or alter the offending articles which were published in March 2019, so Kendrick and Harcombe sued for libel arguing the articles “caused serious harm” to their reputations.
Calman and his publishers claimed the articles were “honest opinion” published in the public interest, and therefore protected under the Defamation Act 2013. But Justice Matthew Nicklin denied them a public interest defence in June 2024. (See previous coverage)
Since then, the publishers decided not to appeal the decision.
Today, the Mail Online issued an apology to Kendrick and Harcombe, conceding that the allegations it printed were “untrue and ought not to have been published.”
It added, “We are happy to set the record straight, and apologise to Dr Harcombe and Dr Kendrick for the distress caused. We will not repeat the allegations and have agreed to pay substantial damages and costs.”
In response to the announcement, Dr Zoë Harcombe said, “I’m delighted to say it’s finally over. Malcolm and I are so grateful to those who made this possible – especially our legal team Claire & Dominic at Carter-Ruck and Adrienne & Godwin at 5RB.”
The offending articles have been removed from the website. The case serves as a stark warning to journalists who use their platform to try and discredit those who challenge orthodoxy.
See the full apology (below).
























