American College of Obstetricians and Gynecologists Still Pushing COVID Shots for Pregnant Women
Could Millions in Government Funding Explain Why?
By Brenda Baletti, Ph.D. | The Defender | May 2, 2024
The American College of Obstetricians and Gynecologists (ACOG) missed a May 1 deadline to explain why the organization recommends COVID-19 vaccines for pregnant women despite growing evidence that they pose a serious risk.
Reform Pharma, a Children’s Health Defense (CHD) initiative, sent ACOG a letter on March 22 outlining the extensive and mounting scientific research documenting the risks of the vaccines to mothers and infants.
The letter also addressed grant money ACOG accepted from the U.S. Department of Health and Human Services (HHS).
The funding was contingent on the organization’s full compliance with the Centers for Disease Control and Prevention’s (CDC) guidance endorsing the vaccine during pregnancy.
The grant also stipulated that ACOG admonish doctors who failed to follow CDC protocols and track women who declined the vaccine, then target them with follow-up pressure to get the shot.
Reform Pharma demanded ACOG end its practice of recommending COVID-19 vaccination for pregnant women and explain why it has continued to push the shot until now.
The letter stated:
“It’s time for ACOG to reconcile and admit its mistake. … Our team demands that ACOG stop intimidating and misleading both physicians and pregnant women. …
“It is imperative that ACOG take proper action now to prevent needless further injury and death, as it is under a legal, ethical, and moral obligation to stop the shots!”
After ACOG didn’t respond, Reform Pharma sent a follow-up letter on April 22 via certified mail and email to the ACOG president and its chief legal officer.
The letter gave ACOG until May 1 to explain, in writing, why it continues to push the COVID-19 vaccines.
ACOG President Verda J. Hicks responded by blocking Reform Pharma’s email.

An automated out-of-office reply was the only response from the organization’s chief legal officer, Molly Meegan.
“The fact that the ACOG president blocked us shows that they are not even willing to have a conversation to explain why they continue to push COVID-19 shots on pregnant women despite mounting scientific evidence of the safety risks,” Reform Pharma co-director Amy Miller told The Defender.
Reform Pharma continues working to publicize what it says is ACOG’s corruption.
“The American people need to know that ACOG is using its authority and influence to push dangerous COVID-19 shots on pregnant women but failed to disclose its backdoor deal with the CDC,” Justine Tanguay, an attorney and Reform Pharma’s co-director, told The Defender.
“Sacrificing the lives and health of pregnant women and their unborn babies in exchange for money is unacceptable,” she added.
Reform Pharma’s mission is to systematically end corruption in Big Pharma and restore integrity to the U.S. healthcare system.
“Reform Pharma is doing critically important work shining a light on organizations like ACOG which purport to represent the interests of their member physicians and the patients those physicians treat,” Kim Mack Rosenberg, CHD general counsel and a signatory to the letter, told The Defender.
“In reality, money talks, and it appears that payments and incentives from pharmaceutical companies may influence and capture such organizations.”
ACOG a ‘massively powerful’ organization that dominates maternal-fetal health
ACOG is a “massively powerful” organization with 60,000 members, maternal-fetal medicine expert Dr. James Thorp told The Defender.
The professional membership organization for obstetricians and gynecologists produces practice guidelines, educational materials and initiatives to improve women’s health, according to its website.
It is also — along with the Society for Maternal-Fetal Medicine (SMFM) and American Board of Obstetrics and Gynecology (ABOG) — a key gatekeeper organization for the field of obstetrics and gynecology, exercising tremendous power over the practices and norms among its members who are practitioners in women’s health, Thorp said.
According to Reform Pharma, ACOG takes its marching orders from Big Pharma and public health agencies.
“It functions primarily as a shill for the U.S. Department of Health and Human Services and, in particular, the Centers for Disease Control and Prevention — both lobbying arms for the pharmaceutical industry,” Reform Pharma wrote in its letter.
This became even more concerning once ACOG started promoting the COVID-19 vaccines, Reform Pharma said.
When the vaccines came on the market in December 2020, ACOG held a neutral position on vaccination during pregnancy, recommending pregnant women “be free to make their own decision regarding COVID-19 vaccination.”
That changed in July 2021, when the organization began encouraging its members to “enthusiastically recommend vaccination to their patients,” after accepting $11 million in grant money from HHS and CDC to adopt and promote the agencies’ positions on COVID-19 to its members.
“If ACOG should waver or fail to toe the line, ACOG would be required to return all the grant money it received,” according to Reform Pharma’s letter.
“ACOG made a deal with the devil and willingly sacrificed the health of pregnant women and their unborn babies in exchange for money,” Reform Pharma said.
Reform Pharma also accused ACOG of pressuring and intimidating doctors into strongly recommending the vaccine to their patients and directing them to “harass” women who refused until they capitulated.
Attorney Maggie Thorp, who last year identified the HHS grant funding — which she told The Defender is now up to $17 million since the COVID-19 pandemic period began — said she believes the CDC is just using ACOG as its mouthpiece.
Based on her analysis of the documents acquired through a Freedom of Information Act request, Maggie Thorp said the collaboration between the public health agency and the private organization is so tight that it was “hard to identify where CDC ended and where ACOG began.”
She said HHS is using ACOG to do what it cannot — “dictate the content of private conversations that happen between doctors and their pregnant patients.”
In that sense, Maggie Thorp said, HHS is “using ACOG to quell doctors’ free speech and their ability to express dissent.”
As a result, she said, patients don’t get access to the information they need to give “true, valid informed consent.”
James Thorp said that ACOG then collaborates with its partner organizations, SMFM, ABOG, and the Federation of State Medical Boards, which can take away doctors’ medical licenses or accreditation if they don’t comply, as the federation openly said it would in a July 2021 letter.
“They have the power to fire doctors or remove their accreditation from the medical board. That destroys an obstetrician,” he said. “So it’s extraordinarily intimidating.”
‘Sad’ that ACOG ‘ignores the science’
Reform Pharma provided ACOG with an extensively footnoted overview of current science showing the risks COVID-19 shots pose to pregnant women and the general population.
For example, studies have shown that the vaccine can pass through the blood-brain barrier and the placenta.
Early reporting in 2021 by the CDC’s Dr. Tom Shimabukuro in the New England Journal of Medicine claiming the shots were safe based on the CDC’s own Vaccine Adverse Event Reporting System (VAERS) and Vaccine Safety Monitoring System (V-safe) data was statistically flawed, the letter stated.
Shimabukuro concluded there were no “obvious safety signals” among pregnant women who received the vaccine. However, he presented the numbers in a misleading manner that obscured the actual rate of spontaneous abortions.
According to Reform Pharma’s letter:
“Failure to disclose the true incidence of spontaneous abortion is at best gross incompetence and at worst malfeasance. The true incidence of spontaneous abortion [in his statistics, among first- and second-trimester pregnancies] is alarming, ranging between 82% to 91%.”
Early research also linked the shot to “autism-like behaviors” in newborn rats, indicating the shot could complicate neurodevelopment and underscoring the need for more studies.
Several studies in top journals have shown that nursing mothers shed the spike protein in their breast milk, causing potentially serious adverse reactions in their newborn babies.
And, according to the letter, the COVID-19 shots pose safety risks for all people that also extend beyond complications associated with pregnancy. That data has been published extensively in places ranging from VAERS to peer-reviewed studies and beyond — sources readily available to anyone at ACOG who cares to investigate.
Given the extensive evidence summarized in the letter, “It is sad that ACOG appears not to be doing a deep dive into all the science concerning COVID-19 injections, instead taking the word of the pharmaceutical companies themselves and the FDA and CDC, which similarly rely on pharma science,” Mack Rosenberg said.
“Particularly tragic is the failure of ACOG to acknowledge and investigate the important evidence from patients themselves of the tragic impact these injections have had on pregnant women, their babies and their families,” she added.
“Pregnant women should never take this vaccine,” said James Thorp, who also has extensively documented the literature on the dangers of the COVID-19 shots for pregnant women.
“It isn’t even really a vaccine,” he said. “It’s an experimental genetic therapy with absolutely zero long-term follow-up. This is unprecedented. This is a complete violation of the golden rule of pregnancy.”
‘Wrongdoers will be held accountable’
The “public health emergency” has been officially over since May 11, 2023, and it has been demonstrated that vaccines don’t stop transmission and that there is extensive evidence regarding risks to pregnant women and all people, Reform Pharma wrote.
That means, “the only explanation for ACOG continuing to push this poison on pregnant women and their unborn children is that the organization is ‘bought off,’” the letter said. “Wrongdoers will be held accountable.”
Reform Pharma reiterated its concerns in the second letter, but aside from the blocked email and out-of-office notifications, ACOG has not responded.
Brenda Baletti, Ph.D., is a senior 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.
IS A CLIMATE LOCKDOWN ON THE HORIZON?
The Highwire with Del Bigtree | May 2, 2024
A recent article by the LA Times editorial board claims that California is experiencing record high temperatures. Jefferey Jaxen does a fact check on their claims. As President Joe Biden mulls the idea of declaring a climate emergency, we look into the potential powers that could be gained from this move. Will we have a climate lockdown on our horizon?
UN Official Condemns Health “Misinformation,” Advocates for “Digital Integrity Code”
By Didi Rankovic | Reclaim The Net | April 30, 2024
The United Nations continues with an attempt to advance the agenda to get what the organization calls its Code of Conduct for Information Integrity on Digital Platforms implemented.
This code is based on a previous policy brief that recommends censorship of whatever is deemed to be “disinformation, misinformation, hate” but that is only the big picture of the policy UN Under-Secretary-General for Global Communications Melissa Fleming is staunchly promoting.
In early April, Fleming gave a talk at Boston University, and here the focus was on AI, whose usefulness in various censorship ventures makes it seen as a tool that advances “resilience in global communication.”
A piece on the Boston University Center on Emerging Infectious Diseases site first asserts that AI had a “major role” in helping spread misinformation and conspiracy theories “in the post-pandemic era,” while the UN is described as one of the institutions that have been undermined by all this, while “working to dispel these narratives.”
(The article also – helpfully, in terms of understanding where its authors are coming from – cites the World Economic Forum (WEF) as the “authority” which has proclaimed that “the threat from misinformation and disinformation as the most severe short-term threat facing the world today”).
You will hardly hear Fleming disagreeing with any of this, but the UN’s approach is to “harness” that power to serve its own agendas. The UN official’s talk was about how AI can be used to feed the public the desired narratives around issues like vaccines, climate change, and the “well-being” of women and girls.
However, she also went long into all the aspects of AI that she perceives as negative, throwing pretty much every talking point already well established among the “AI fear-mongering genre” in there:
“One of our biggest worries is the ease with which new technologies can help spread misinformation easier and cheaper, and that this content can be produced at scale and far more easily personalized and targeted,” she said.
Flemming said that with the pandemic, this “skyrocketed” around the issue of vaccines. But she didn’t address why that may be – other than, apparently, being simply a furious sudden proliferation of “misinformation” for its own sake.
Flemming then mentions a number of UN activities, basically along the lines of “fact-checking” and “pre-bunking” (like “Verified,” and #TakeCareBeforeYouShare”).
Some might refer to Flemming as one of the “merchants of outrage” but she has this slur reserved for others, such as “climate (change) deniers.”
And it wasn’t long before X and Elon Musk cropped up.
“Since Elon Musk took over X, all of the climate deniers are back, and (the platform) has become a space for all kinds of climate disinformation. Here is a connection that people in the anti-vaccine sphere are now shifting to the climate change denial sphere,” Flemming lamented.
But, the UN official reassured everyone that “she and her team are working to build coalitions and initiatives that leverage AI to promote exciting, positive, fact-driven global public health communications.”
The Heart of Climate Deception Temperature
Climate Realism by Paul Burgess | April 26, 2024
Links coming shortly
Link to IPCC table in AR6 https://www.ipcc.ch/report/ar6/wg1/do… Go to page 1856.
Link to USA Standard Reference Network – you can set what graph you want to see https://www.ncei.noaa.gov/access/moni…
Bird Flu Outbreaks & the WHO/IHR Pandemic Treaty Push
By Barbara Loe Fisher | The Vaccine Reaction | April 22, 2024
Even as U.S. health agencies and the United Nations World Health Organization (WHO) are being heavily criticized for their botched response to the COVID-19 pandemic,1 2 3 WHO officials are ramping up pressure on all nations to sign a WHO pandemic treaty and amendments to the WHO’s International Health Regulations (IHR), which will give them more authority to track, quarantine, force vaccine use and censor free speech during WHO declared pandemics.4 5 The WHO’s Director General has been blaming opposition to the UN agency’s epic power grab on “a torrent of fake news, lies and conspiracy theories.”6
On Apr. 19, 2024, the United Nations sent out a press release declaring that the “ongoing global spread of ‘bird flu’ infections to mammals including humans is a significant public health concern,” pointing to an outbreak of H5N1 viral infections in dairy cows in the U.S. and warning that the virus could evolve and cause human-to-human transmission with “extremely high” mortality.7 The implication was that a potentially deadly global bird flu pandemic was a clear possibility.
The CDC website describes symptoms of H5N1 bird flu infections, and they sound very similar to seasonal influenza or SARS-CoV-2 infections associated with COVID-19 disease:
“The reported signs and symptoms of bird flu virus infections in humans have ranged from no symptoms or mild illness [such as eye redness (conjunctivitis) or mild flu-like upper respiratory symptoms], to severe (such as pneumonia requiring hospitalization) and included fever (temperature of 100ºF [37.8ºC] or greater) or feeling feverish*, cough, sore throat, runny or stuff nose, muscle or body aches, headaches, fatigue, and shortness of breath or difficulty breathing. Less common signs and symptoms include diarrhea, nausea, vomiting, or seizures.”8
Warnings That Egg and Milk Supplies May Be Contaminated with Bird Flu Virus
Mainstream media have been joining the UN in characterizing bird flu outbreaks in cattle as a significant public health concern, with news outlets breathlessly reporting that cattle were infecting each other with H5N1 and some experts questioning whether raw or even pasteurized milk containing high levels of the avian virus is safe.9 Although H5N1 bird flu was first detected in 1996, since 2020 there have been more outbreaks in poultry farms, wild bird and land and marine animals.10 11 Americans were warned in early April that the eggs from chickens potentially infected with the avian virus should be well cooked,12 and then the media reported that a U.S. dairy farm worker in Texas had been infected with bird flu.13
The same day the UN issued their press release, Agence France Presse again reminded readers that a person working on a dairy farm in Texas was recovering from bird flu. A WHO official was quoted as stating that, “The case in Texas is the first case of a human infected by an avian influenza by a cow.”14
U.S. Plan to Drive the Global “Health Security” Agenda If WHO Treaties Fail
Three days earlier, on Apr. 16, the White House announced a five-year “Strategy to Strengthen Global Health Security” plan citing the COVID-19 pandemic as the need to put the U.S. in the driver’s seat via bi-lateral financial investment partnerships with 50 to 100 countries to “drive global action toward shared goals” and “mitigate the impact of health security threats” in order “to prevent, detect and contain them at their source.”15 The new plan “articulates a whole-of-government science-based approach to strengthening global health security.”
The current U.S. administration is in favor of the WHO pandemic treaty and IHR amendments proposed by the world’s largest public health agency.16 However, the WHO is getting pushback from lawmakers and citizens in the U.S. and in other nations, who do not want to go along with the UN/WHO power grab that many critics say threatens human rights and national sovereignty.17 18 19 A respected Japanese scientist posted a video message to the world online,20 and there was a massive demonstration In Japan this month against the WHO pandemic treaty.21
The U.S. “Global Health Security” plan would ensure that if the WHO treaties fail to be signed by enough countries to become international law, the U.S. will make sure there is a global “rapid response to global health emergencies.” According to the U.S. plan, the core of that “rapid response” are “efforts to transform international financial institutions, such as the World Bank, and to accelerate “manufacture, procurement and delivery” of medical countermeasures like vaccines.22
Even though there is Increasing public opposition to the WHO’s plan to expand its legal authority to tell eight billion people what to do whenever WHO officials declare a “public health emergency” – which includes eliminating freedom of speech and electronically monitoring everyone’s vaccination status and requiring people to carry a digital “vaccine passport” in order to travel or enter public spaces23 – it looks like the U.S. government is going to get the job done whether the WHO manages to get enough countries to sign the WHO/IHR treaties or not. The lucrative public-private business partnerships that have been expanded over the past four decades between the WHO, pharmaceutical corporations, governments and other institutions is paying big dividends for the Public Health Empire.24
Bird Flu Vaccines Being Developed and Stockpiled
Is the latest well-publicized specter of a deadly global bird flu pandemic, which is so reminiscent of the well-publicized specter of a deadly coronavirus pandemic in early 2020,25 a harbinger of things to come or just a coincidence?
Whatever it is, the preparations for delivery and approval of H5N1 “vaccines,” which includes mRNA bird flu shots, is well underway.
On Apr. 20, Barrons reported that the U.S. government “says it could distribute enough [bird flu] vaccines within four months to inoculate a fifth of the U.S. population” (68 million people) if the H5N1 strain infecting cattle began to spread among humans.26 Healthcare workers, law enforcement and other first responders, military personnel pregnant women, infants and high risk children would get the shots first.
Apparently, two clinical trials of bird flu vaccine have been underway since last year and CSL Sequiris and GlaxoSmithKline (GSK) are under contract to test the vaccines targeting a strain of avian influenza closely related to the H5N1 strain currently infecting U.S. dairy cows. Another major manufacturer of influenza vaccine, Sanofi, would also likely be involved in bird flu vaccine production.
H5N1 Vaccine Production Could Be Ramped Up to Vaccinate the Entire U.S. Population
An FDA spokesperson reportedly told Barrons that the approval process to quickly distribute a new H5N1 bird flu vaccine for Americans would be similar to the accelerated process used to create annual flu vaccines. A spokesperson for Administration for Strategic Preparedness & Response (ASPR) also commented that, if needed, the agency would work with bird flu vaccine manufacturers “to ramp up production to make enough vaccine doses to vaccinate the entire [U.S.] population.”
Oil in Water Adjuvants in Vaccines and Autoimmunity
Both Sequirus and GSK have developed “oil in water” emulsion adjuvants added to influenza vaccines, including bird flu vaccines, to stimulate hyper-inflammatory responses in the body that generate high levels of antigen-specific antibodies in an effort to make the vaccines more “effective.” Squalene adjuvants have been associated with development of autoimmune disorders.27 28 29
GSK’s AS03 adjuvant contains a-tocopherol, squalene and polysorbate 80,30 and some European children and adults, who got GSK’s AS03 adjuvanted H1N1 “swine flu” vaccine in 2009, developed cases of narcolepsy, a neurological autoimmune disorder.31 The Sequiris influenza vaccine contains MF59,32 the first squalene oil in water emulsion adjuvant added to influenza vaccines in the 1990s.33 According to the Apr. 20 Barrons’ report, large quantities of both of these squalene adjuvants are stored in the U.S. government’s special pandemic influenza vaccine stockpile, which was created in 2005, along with premade influenza antigens.
A 2023 article published by Chinese researchers the medical literature promoted the “remarkable success” of mRNA coronavirus vaccines and the need to use three types of specific adjuvants to make mRNA vaccines more effective: (1) RNA with self-adjuvant characteristics; (2) components of the delivery system [such as lipid nanoparticles]; and exogenous immunostimulants (such as squalene).34
As with squalene adjuvants, the lipid nanoparticles, which envelop and deliver synthetic RNA in COVID shots to body cells to produce the SARS-CoV-2 spike protein, are highly inflammatory to stimulate a strong immune response, but also have been associated with allergy and autoimmunity.35
Europe Already Has Approved Two H5N1 Bird Flu Vaccines
Earlier this year, the European Medicines Agency (EMA) approved two H5N1 avian flu vaccines made by Sequiris, although neither one are mRNA products. Medscape reported on Feb.23, 2023 that Celldemic had been approved for use in infants six months of age and older if public health officials anticipate a bird flu pandemic, and Incellipan had been approved for use when a bird flu pandemic has been declared.36
mRNA Bird Flu Vaccines A Quick Way to Produce Bird Flu Vaccines
A year ago, Scientific American reported that “vaccine makers are preparing for bird flu,” with one pediatric infectious disease doctor quipping “It’s a really dangerous time to be a bird.” Another expert warned “None of us know when the next influenza pandemic will emerge… At the outset, you have to say there is uncertainty, with one exception: there will be a pandemic.”37 In that article, the reliance on U.S. stockpiled egg-based flu vaccines to produce an H5N1 vaccine was called into question and mRNA technology to produce bird flu vaccine was highlighted because it offers “speed of production” so an mRNA vaccine targeting a new influenza strain can be created in a matter of weeks.
Also in 2023, there was a report in the medical literature that University of Pennsylvania researchers had created an H5N1 mRNA lipid nanoparticle vaccine being tested on mice and ferrets.38 In March 2024, Chinese researchers announced they had created a 10-valent mRNA nanoparticle vaccine encoding proteins from four seasonal influenza viruses, two avian flu viruses with pandemic potential, and spike proteins from four SARS-CoV-2 variants. They said two doses of FLUCOV-10 “elicited robust immune responses in mice” against all 10 vaccine-matched viruses.39
Only Time Will Tell
Amendments to the WHO’s International Health Regulations (IHR) will be voted on at the end of May. Only time will tell whether the latest publicity warning the public about a potentially imminent bird flu outbreak in humans is real or just another bit of propaganda being used to create fear and put pressure on governments to give up sovereignty for the illusion of safety.
1 Bell D. Pandemic preparedness and the road to international fascism. The American Journal of Economics and Sociology July 30, 2023.
2 Nuccio D. Public health agencies must be reined in before next pandemic. Washington Examiner Mar. 29, 2024.
3 Schaefer B, Groves S. The WHO Pandemic Treaty Fails Again. The Heritage Foundation Apr. 19, 2024.
4 Fisher BL. Stop the World Health Organization Power Grab To Mandate Vaccines & Censor Free Speech. National Vaccine Information Center Apr. 11, 2024.
5 Door to Freedom. WHO International Health Regulations Compendium. April 2024.
6 AFP in Geneva. Global pandemic agreement in danger of falling apart,WHO warns. The Guardian Jan. 22, 2024.
7 United Nations. Pandemic experts express concern over avian influenza spread to humans. UN Press Release Apr. 18, 2024.
8 U.S. Centers for Disease Control & Prevention (CDC). Bird Flu Virus Infections in Humans. Apr. 11, 2024.
9 Branswell H. USDA faulted for disclosing scant information about outbreaks of H5N1 avian flu in cattle. STAT News Apr. 18, 2024.
10 Parpia R. Bird Flu Outbreak in Oregon Leads to Mass Euthanization of Poultry. The Vaccine Reaction Feb. 5, 2024.
11 Singler E. H5N1 influenza: From avian to bovine to feline and beyond. AAHA Apr. 19, 2024.
12 Camero K. Is it safe to eat runny eggs amid the bird flu outbreak? Here’s what the experts say. USA Today Apr. 4, 2024.
13 Hendler C. Texas Man and Dairy Cattle Test Positive for Bird Flu. The Vaccine Reaction Apr. 16, 2024.
14 Agence France Presse. H5N1 Strain of Bird Flu Found in Milk: WHO. The Barron’s Daily Apr. 19, 2024.
15 White House. Fact Sheet: Biden-Harris Administration Releases Strategy to Strengthen Global Health Security. Apr. 16, 2024.
16 Staver M. Biden’s Amendments Hand U.S. Sovereignty to the WHO. Liberty Counsel 2023.
17 Human Rights Watch. Draft “Pandemic Treaty” Fails to Protect Rights. Apr. 17, 2024.
18 Webster A. WHO pandemic amendments threaten national sovereignty. Mail Guardian Apr. 17, 2024.
19 NTD. U.S. Representatives speak on “Surrender of U.S. Sovereignty to WHO.” Press Conference Apr. 18. 2024.
20 Professor Massayasu Inoue, MD, PhD video message to the world on harms of mRNA COVID “genetic” vaccine and the WHO pandemic treaty threat to freedom and human rights. NVIC Rumble Channel Apr. 10, 2024.
21 The Gateway Pundit. Massive protests break out in Japan in Opposition to WHO’s proposed pandemic treaty. Apr. 13, 2024. Twitter video of protest in Japan.
22 White House. Fact Sheet: Biden-Harris Administration Releases Strategy to Strengthen Global Health Security. Apr. 16, 2024.
23 Fisher BL. G20 Leaders Pledge to Require Global “Digital Health Certificate” Vaccine Passport. The Vaccine Reaction Nov. 22, 2022.
24 Fisher BL. WHO, Pharma, Gates & Government: Who’s Calling the Shots? National Vaccine Information Center Jan. 27, 2019.
25 Fisher BL. Coronavirus Vaccines on Fast Track as WHO Declares Global Public Health Emergency. National Vaccine Information Center Feb. 5, 2020.
26 Kazis JN. U.S. Could Vaccinate a Fifth of Americans in a Bird Flu Emergency. Barron’s Apr. 20, 2024.
27 Autoimmune Technologies. Gulf War Syndrome: Anti-Squalene Antibodies Link Gulf War Syndrome to Anthrax Vaccine.
28 Kuroda Y, Nacionales DC et al. Autoimmunity induced by adjuvant hydrocarbon oil components of vaccine.Biomed Pharmacother 2004; 58(5): 325-327.
29 Guimaraes LE, Baker B, Perricone C, Shoenfeld Y. Vaccines, adjuvants and autoimmunity. Pharmacological Research 2015; 100: 190-209.
30 Garcon N, Vaughn DW, Didierlaurent AM. Development and evaluation of AS03, an Adjuvant System containing a-tocopherol and squalene in an oil-in-water emulsion. Expert Rev Vaccines 2012; 11(3): 349-366.
31 Miller E, Andrews N et al. Risk of narcolepsy in children and young people receiving AS03 adjuvanted pandemic A/H1N1 2009 influenza vaccine: retrospective analysis. BMJ 2013; 346.
32 Patel SS, Bizjajeva S, Heijnen E, Oberye J. MF59-adjuvanted seasonal trivalent inactivated influenza vaccine: Safety and immunenicity in young children at risk of influenza complications. Int J Infect Dis 2019; 85 (Suppl): S18-S25.
33 Black S. Safety and effectiveness of MF-59 adjuvanted influenza vaccines in children and adults. Vaccine 2015; 33 (Suppl 2): B3-B5.
34 RxLisXie C, Yao R, Xia X. The advances of adjuvants in mRNA vaccines. Npj Vaccines 2023; 8:162.
35 Lee Y, Jeong M, Park J et al. Immunogenicity of lipid nanoparticles and its impact on the efficacy of mRNA vaccines and therapeutics. Exp Mol Med 2023; 55: 2085-2096.
36 Agarwal D. Europe Greenlights Two Avian Flu Vaccines. Medscape Feb. 23, 2024
37 Docter-Loeb H. Vaccine Makers Are Preparing for Bird Flu. Scientific American Mar. 2, 2023.
38 Furey C, Ye N, Kercher L et al. Development of a nucleoside-modified mRNA vaccine against clade 2.3.4.4b H5 highly pathogenic avian influenza virus. bioRxiv Apr. 30, 2023.
39 Wang XC, Ma Q, Li M et al. A 10-valent composite mRNA vaccine against both influenza and COVID-19. bioRxiv Mar. 5, 2024.
Why won’t Chris Packham have a real debate on climate?
By Paul Homewood | Not A Lot Of People Know That | April 25, 2024
On Sunday, the BBC did something unusual. It invited Luke Johnson, a climate contrarian, to join a panel with Laura Kuenssberg to discuss net zero. As followers of this debate will know, the BBC’s editorial policy unit issued guidance to staff in 2018 saying: ‘As climate change is accepted as happening, you do not need a “denier” to balance the debate.’ Although it did allow for exceptions to this rule: ‘There are occasions where contrarians and sceptics should be included within climate change and sustainability debates.’ Presumably this was one such occasion.
The other two people on the panel – Chris Packham and Layla Moran – are members of the climate emergency camp, so there was no pretence of ‘balance’. At one point, the exchange between Johnson and Packham became heated and when the latter invoked the recent downpour in Dubai as well as extensive wildfires in the ‘global south’, as evidence of the effect of anthropogenic global warming, Johnson challenged him to come up with evidence that extreme weather was caused by carbon emissions.
‘It doesn’t come from Toby Young’s Daily Septic [sic], which is basically put together by a bunch of professionals with close affiliations to the fossil fuel industry,’ replied Packham. ‘It comes from something called science.’ This was hailed by Packham’s side as a slam-dunk rebuttal of Johnson’s argument. The Canary wrote up the exchange under the following headline: ‘Chris Packham just humiliated Kuenssberg’s preposterous climate-denying guest.’ The London Economic, which describes itself as ‘a digital newspaper with a metropolitan mindset’, summarised it as follows: ‘With science on his side, Chris Packham was able to deliver a devastating put-down when challenged on the evidence of climate change.’
I can’t help thinking Packham’s ‘devastating put-down’ would have been more effective if it had been true. The people who put together the Daily Sceptic, a news publishing site I’ve edited since 2020, have no connections to the fossil fuel industry. If Packham and his allies are so convinced of the rightness of their cause, why invent reasons to discredit their opponents? A clip from the show including this claim was posted on Twitter by BBC Politics and retweeted by Laura Kuenssberg, getting, at last count, 845,000 views. And to think the BBC launched a multi-million-pound department last year to ‘address the growing threat of disinformation’.
What about Packham’s claim that ‘something called science’ provides all the evidence we need that extreme weather events are caused by burning fossil fuels? There’s really no such thing as ‘the science’, as in a consensus viewpoint among scientists that’s so incontrovertible no serious debate is possible. All scientific theories are just hypotheses and, as such, subject to challenge. Indeed, if it were illegitimate to challenge these theories, progress in science wouldn’t be possible. To pretend that the science of what causes extreme weather is ‘settled’ when it’s the subject of ongoing dispute suggests that Packham and his pals aren’t capable of having a proper grown-up discussion.
Full story here.
Toby Young actually understates his complaint, as there is no evidence that weather is actually becoming more extreme – something the IPCC admit.
It is very easy for these conmen to claim it is, and simply justify it with a statement that “scientists say”. But as Toby points out, they are unable to back it up with actual data and evidence.
The idea, fraudulently circulated by grant funded climate scientists, that global warming means extreme weather has always been by definition absurd. After all, does this mean that the Earth’s climate was ideal during the Ice Age, which would be the logical conclusion?
The simple fact is that there has always been unpleasant weather, storms, floods, droughts, and glaciation. If Chris Packham can provide evidence that these have all gotten worse in recent times, then let him present it.
If he can’t, the BBC should apologise for broadcasting false statements, exclude him from all future debates on climate change, and ban him from making any further such political comments if he wishes to remain as an employee.
‘A Dangerous Vaccine for a Nothing Disease’: U.S. Stockpiling Bird Flu Vaccines
‘Why is it called a biodefense project?’
By John-Michael Dumais | The Defender | April 24, 2024
With the recent spread of H5N1 bird flu to dairy cows in eight states — and the infection of a Texas dairy worker marking the second known human case in the country — public health officials are raising concerns over the adequacy and safety of stockpiled vaccines meant to protect against a potential pandemic, according to Barron’s.
The Centers for Disease Control and Prevention (CDC) maintains bird flu is a low risk to humans — the infected dairy worker only contracted a case of conjunctivitis (pink eye) — and that there is currently no known mechanism for human-to-human transmission.
According to the World Health Organization (WHO), avian flu is responsible for 463 deaths worldwide over the past 20 years. The CDC reports only two U.S. cases of bird flu, and both were mild. No Americans have died from the virus.
Still, government agencies and Big Pharma manufacturers are building their capacity for bird flu vaccine production.
The U.S. government holds three U.S. Food and Drug Administration (FDA)-approved H5N1 vaccines in its National Pre-Pandemic Influenza Vaccine Stockpile.
The vaccines, manufactured by pharmaceutical giants Sanofi, GSK and CSL Seqirus, all contain mercury, a known neurotoxin, according to product inserts.
The same companies — plus Moderna — are working to develop new bird flu vaccines.
Federal officials said they supply several hundred thousand doses within weeks and 10 million more using materials on hand, and expect to produce 125 million doses within four months.
Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, suggested the agency has a “pretty low threshold” to deploy the stockpiled vaccines.
“We believe that, if we needed to, [our vaccines] would be reasonably good matches,” Marks said on April 1 at the World Vaccine Congress in Washington, D.C.
Given that all stockpiled vaccines were made for an earlier strain of H5N1, it’s uncertain how effective they would be against the strains that are circulating now, former FDA scientist Luciana Borio told STAT News.
“The FDA-approved H5N1 vaccines — licensed in 2013, 2017, and 2020 — do not elicit a protective immune response after just one dose,” Borio said. Even after two doses, “It is unknown whether the elicited immune response is sufficient to protect against infection or severe disease.”
A spokesperson for the U.S. Department of Health and Human Services’ Administration for Strategic Preparedness and Response (ASPR) program told Barron’s the agency could “ramp up production to make enough vaccine doses to vaccinate the entire U.S. population.”
A portion of the stockpile consists of “chunks” of premade antigens — good for training the immune system against specific strains — and adjuvants, the ingredients used to activate the human immune system when vaccines are administered.
However, despite its assurances of rapid vaccine delivery, ASPR did not detail its plans beyond claiming it could vaccinate about 68 million people, or one-fifth of the country’s population — using the two-dose regimen — within four months of an outbreak.
Internist and epidemiologist Dr. Meryl Nass, appearing with James Corbett on the April 20 episode of “Good Morning CHD,” said, “You’ve got a dangerous vaccine for a nothing disease,” noting the low number of human H5N1 cases reported thus far.
“It’s supposedly for a life-threatening illness,” she said. “Of course, pink eye is not life-threatening,” she said.
“The whole purpose of bird flu is to make you think the pandemics are out there, they’re coming for you all the time, and you need them [the health bureaucracy] to save you,” Nass said.
Sanofi vaccine contains thimerosol, PEG
Sanofi’s H5N1 vaccine, approved for adults in April 2007, was developed from a virus strain isolated from a Vietnamese patient in 2004.
“Our egg-based vaccine supply would well contribute to support a global influenza pandemic response should it arise either from A/H5N1 or any other influenza strain,” a Sanofi spokesperson told MedPage Today.
Each 90 microgram (µg) dose includes influenza virus hemagglutinin, 500 milligrams (mg) of porcine (pig) gelatin and approximately 98 µg of thimerosal, a mercury derivative (equaling approximately 50 µg of mercury/dose).
Other ingredients used in the development of the vaccine include embryonated chicken eggs, formaldehyde, polyethylene glycol and sugar.
Polyethylene glycol, or PEG, has been linked to the anaphylactic reaction in the COVID-19 vaccines.
The product warnings cited adverse events related to the 1976 swine flu vaccine, which included Guillain-Barré syndrome and other neurological disorders such as encephalopathy, optic neuritis/neuropathy, partial facial paralysis and brachial plexus neuropathy, as well as vasculitis and altered immunocompetence.
The initial clinical trial, conducted by the National Institute of Allergy and Infectious Diseases, featured an experimental group of 452 healthy adults ages 18-64, of which 103 were given two 90 µg doses administered 28 days apart, resulting in 44% of recipients developing a protective immune response.
The other adults in the vaccine group received 45 µg, 15 µg or 7 µg doses. The product information does not indicate their immune responses. However, given that the 90 µg/dose version is the one stockpiled, it’s likely the lesser amounts were ineffective.
Experts at the time expressed concern over the large doses, compared to the standard 15 µg dose used in seasonal flu vaccines, according to the Center for Infectious Disease Research and Policy at the University of Minnesota.
The trials didn’t include anyone under age 18, which would indicate that the safety and efficacy of the vaccine for this age group are undetermined.
GSK vaccine approved for 6-month-olds
GSK’s H5N1 vaccine, approved in 2013 for people as young as 6 months, was made from the same virus strain as Sanofi’s.
According to GSK’s package insert, each adult dose also contains the adjuvant AS03, made of 11.86 mg DL-α-tocopherol (vitamin E), 10.69 mg squalene (wrongly blamed for Gulf War syndrome, according to Nass) and 4.86 mg of an emulsifier called polysorbate 80. The insert also lists 5 µg of thimerosal, which equates to less than 2.5 µg mercury.
Other elements used in the production of the vaccine — and still present in the doses — include ovalbumin or embryonated hen eggs (at least 0.083 µg), formaldehyde (at least 12.5 µg) and sodium deoxycholate (at least 3.75 µg).
Pediatric doses contain about half the adult amounts of each ingredient, according to the product information.
In the clinical trial of about 2,000 adults 18 and older, 91% of those between 18 and 64 and 74% of those over 65 who received a two-dose (0.5 milliliters each) regimen of the GSK vaccine developed an adequate level of antibodies, according to the FDA.
The package insert warns of adverse events like Guillain-Barré syndrome, fainting and “cerebral vascular accidents” and notes one case of pulmonary embolism.
Three subjects developed thyroid cancer on days 21, 29 and 223 after administration. Two subjects developed polymyalgia rheumatica, two developed psoriasis, and one of each developed autoimmune hepatitis, celiac disease, cranial nerve 4 palsy, Crohn’s disease, facial paralysis and other symptoms.
A pediatric age group of 838 subjects ages 6 months through 17 years participated in a clinical trial. In addition to frequently reported symptoms of injection site pain, swelling, muscle aches, headache, fatigue, gastroenteritis, fever and other symptoms, serious adverse events included one report of a febrile convulsion and one case of alopecia within seven days of administration.
In a randomized control trial in eight countries outside the U.S. for children 6 months through 9 years old, one death was reported (day 42) along with one case of hepatitis and nasopharyngitis (day 385), three cases of appendicitis (on days 8 or 9) and one case of thyroid cancer (day 84).
Other adverse events included alopecia areata (2 subjects), glomerulonephritis (2 subjects), hypothyroidism (2 subjects) and idiopathic thrombocytopenic purpura (1 subject).
GSK recently said it could provide at least 200 million doses to governments worldwide in the event of a pandemic, according to Barron’s.
CSL Seqirus vaccine: 1 in 200 died during clinical trials
The most recent addition to the U.S. government stockpile of bird flu vaccines is CSL Seqirus’ Audenz for H5N1, approved in 2020 for infants and adults 6 months old and up.
The vaccine contains CSL’s MF59 adjuvant, which includes 9.75 mg squalene, 1.175 mg polysorbate 80, 1.175 mg of sorbitan trioleate, 0.66 mg of sodium citrate dihydrate and 0.04 mg of citric acid monohydrate.
Nass considers MF59 dangerous because it can stimulate autoimmunity. “This adjuvant has not been approved for most other vaccines,” she said. She noted that the FDA is willing to take more risks for a vaccine needed in a dire emergency.
Other ingredients from the production process include MDCK cell protein (at least 3.15 µg) and MDCK cell DNA (at least 10 nanograms), both from dog kidneys, cetyltrimethylammonium bromide (at least 4.5 µg) and ß-propiolactone (at least 0.1 µg).
Each 5 milliliter (mL) multidose vial contains 0.5 mL of thimerosal as a preservative, providing 25 µg of mercury per dose.
Fatality from the clinical trials included 11 (0.5% or 1 in 200) from the experimental group, compared to 0.1% or 1 in 1,000 for the placebo group.
In a trial with children ages 6 months through age 17, 8% of vaccine recipients developed upper respiratory infections within 21 days of vaccination.
Among the adverse events noted in post-marketing reports were swollen lymph nodes, swelling, anaphylaxis, Bell’s palsy, convulsions, demyelination, encephalitis and Guillain-Barré syndrome.
“So 1 in 200 died [and] you want to take this vaccine for a case of pink eye,” Nass said. “This is an example of how … one bad decision sort of goes and rolls down a hill and snowballs to another.”
New bird flu vaccines in development
As concerns mount over the effectiveness of stockpiled vaccines, pharmaceutical companies and government agencies are racing to develop new H5N1 vaccines better matched to currently circulating strains.
Barron’s reported that the U.S. government has been working with GSK, CSL Seqirus, Sanofi and Moderna to develop vaccines that better match the latest H5N1 strains.
GSK, recipient of multi-year pandemic preparedness contracts to supply a bird flu vaccine to the U.S., Canada, the European Union and the WHO, said it would be ready to supply 200 million doses globally, “updated with the latest circulating strains,” according to MedPage Today.
In October 2022, CSL Seqirus announced it was developing another vaccine based on the “pre-pandemic” H5N8 A strain, as part of ASPR’s Biomedical Advanced Research and Development Authority (BARDA) program.
The new vaccine also uses the MF59 adjuvant.
One of the surface proteins of H5N8 is reportedly similar, according to Barron’s, to the strain of H5N1 that infected the Texas dairy worker.
According to MedPage Today, CSL Seqirus said it could scale up production at its California facility — built in a private-public partnership with BARDA — to deliver 150 million vaccine doses during an outbreak.
Sanofi also partnered with BARDA in 2019 to “expand pandemic influenza preparedness” using the same recombinant technology as Sanofi’s Flublok Quadrivalent vaccine. Leveraging its existing technology would allow the company to more rapidly deliver a pandemic vaccine.
Moderna said in March 2023 that it planned to develop a bird flu vaccine, stating its COVID-19 vaccine was developed from its H10N8 pandemic flu vaccine research. Moderna didn’t mention the bird flu vaccine in its March 2024 announcements.
However, the company reported on its seasonal flu vaccine, mRNA-1010, saying it had “demonstrated consistently acceptable safety and tolerability across Phase 3 trials.”
“Early studies done by mRNA vaccine companies on seasonal flu are promising, which could be good news here since mRNA vaccines can be made more quickly than vaccines using eggs or cells,” said Borio.
‘Why is it called a biodefense project?’
Linking to a 2023 Global Biodefense article discussing BARDA’s work with CSL Seqirus, Dr. Peter McCullough tweeted on April 23, “Why is the bird flu (highly pathogenic avian influenza, H5N1) human vaccine a US @NIH @BARDA project with CSL? Why is it called a ‘biodefense’ project?”
The Daily Mail raised similar concerns about the U.S. Department of Agriculture (USDA) collaborating with the Chinese Academy of Sciences — which oversees biodefense labs like the Wuhan Institute of Virology — to develop more virulent strains of bird flu viruses, ostensibly to aid in the development of vaccines.
The White Coat Waste Project disclosed details of the USDA-China program in a February post showing numerous research project agreements beginning in April 2021.
A bipartisan group of Congress members on April 12 sent USDA Secretary Tom Vilsack a letter stating, “This research, funded by American taxpayers, could potentially generate dangerous new lab-created virus strains that threaten our national security and public health.”
Dr. Richard Bartlett, an emergency room director and former Texas Department of Health and Human Services advisory council member, in the April 10 episode of “The Defender In-Depth,” suggested gain-of-function research on bird flu viruses may be responsible for the current outbreak or could cause a future pandemic.
“After everything we just experienced and all the loss of life and bankruptcy and damage to the economy, families destroyed with COVID, why would you continue gain-of-function research?” he asked.
Nass told Corbett she was skeptical of the push for bird flu vaccines. “Every single time we’ve had an emergency and vaccines have been rolled out quickly, it’s resulted in disaster,” she said.
Nass cautioned against relying on centralized solutions pushed by public health authorities.
“They want you only to be able to get the solution they have made for you,” she said. “They don’t want it widely distributed where you have agency to decide whether you want it for yourself or not. … Don’t be scared. This is a scam.”
John-Michael Dumais is a news editor for The Defender. He has been a writer and community organizer on a variety of issues, including the death penalty, war, health freedom and all things related to the COVID-19 pandemic.
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.
Rumble Defies Global Censorship Trends, Takes Stand Against New Zealand’s Free Speech Crackdown
By Didi Rankovic | Reclaim The Net | April 25, 2024
The CEO of Rumble, a free-speech YouTube competitor, says that global censorship levels are on the rise, but that what’s particularly noticeable are censorship demands coming from Australia and New Zealand – who seem to be following in the controversial, to say the least, footsteps of France and Brazil.
On the one hand, this is surprising, given these countries’ formal democratic provenance.
On the other hand, their actions over the last years, including site blocking at ISP level, constant demands for more stringent regulation to facilitate social media content removal, and even the draconian Covid – and post-Covid era measures, tell a different story.
Chris Pavlovski told Mat Kim that the FreeNZMedia channel has now become a deplatforming target in New Zealand, for reporting about leaked data from the National Vaccination Database, that a whistleblower, former Health New Zealand IT employee Barry Young, made available.
And the data Young gave to reporters and activists concerns Covid vaccine-related deaths and claims that these facts are being covered up.
For referring to Young, and referring to the data he provided to the public, a letter has been sent to Rumble to remove FreeNZMedia. It came from the National Health Authority.
However, Pavlovski said that the company has decided to refuse to do that, or to withdraw from the country, and will instead “challenge it and see what happens.”
Pavlovski went on to refer to this particular New Zealand case as “absurd” and “disgusting” – in that it bears resemblance to the Pentagon Papers. At that time, journalist Daniel Ellsberg emerged as a hero of free speech that was protected by the courts in the US.
But that was nearly 50 years ago, and things have clearly changed not only in faraway lands, but in the US itself, and whistleblowers face anything from deplatforming to life in prison.
Speaking about the case of Young, and FreeNZMedia, Pavlovski said that the whistleblower “has a statistics background, went through all the data, found the different batches of vaccines that had an irregular high death rate and published that, and gave out different interviews on doing it.”
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Pavlovski said that he saw nothing that merits censoring the Rumble channel for basing its reporting on Young’s data, and called on the US State Department to “get involved immediately and start protecting US assets and businesses around the world.”
That would be an interesting turn of events, seeing as how the US treats those “assets and business” at home, where censorship is rampant; nevertheless, Pavlovski in this way essentially challenged them to react.


