In its zeal to promote universal vaccination, @gavi, the Vaccine Alliance has neglected the key issue of vaccine safety. When vaccine safety issues have come before GAVI, it has treated them not as a patient health problem, but as a public relations problem.
During the COVID-19 pandemic, GAVI partnered with the World Health Organization to recommend best practices for social media companies to silence dissenting views and to stifle free speech and legitimate questions during that period.
GAVI should consider the best science available, even when that science contradicts established paradigms. It should define success not just in terms of the number of vaccines delivered, but on their rigorously measured overall impacts.
I call on GAVI to re-earn the public trust and to justify the $8 billion dollars that America has provided in funding since 2001. Until that happens the United States won’t contribute more to GAVI. Business as usual is over.
In conformance with the pharma-financed mainstream media’s mantric ritual of dutifully parroting the propaganda tropes spoon-fed them by vaccine makers and their captive regulators, @guardian on Friday pronounced thimerosal, the ethylmercury-based vaccine preservative, “safe.” Opining under the headline, “CDC vaccine panel to review ingredient RFK Jr has targeted for removal,” The Guardian authoritatively assures: “The preservative has been deemed safe.” The Guardian did not bother to cite any peer-reviewed study.
Journalists don’t seem to read those anymore. Instead, it referenced a fact check website operated by the Pharma-funded American Academy of Pediatrics. @AmerAcadPeds likewise cites no peer-reviewed study to support this claim or its equally terse assertion that “Thimerosal has been removed from all routine childhood vaccines.”
This is another treadworn lie of the vaccine industry. There are high bolus doses of mercury in flu shots, which CDC recommends to pregnant women in any trimester of pregnancy and as a routine vaccine for children at six months and in every year of life. Between conception and age 18, a compliant American child today could get a cumulative load of as much as 500 mcg of ethylmercury from multidose flu shots—nearly double of what they were once getting from all the childhood vaccines put together.
Now let’s look at The Guardian claim that thimerosal is safe.
A quick search at the National Library of Medicine’s PubMed and PubChem websites nets thousands of studies on search terms such as: mercury neurotoxicity,[1],[2] mercury and development,[3],[4] and mercury and brain,[5],[6] and hundreds that identify thimerosal as a potent neurotoxin, carcinogen, mutagen, and endocrine disruptor. There has never been a study that proves thimerosal safe.
In early 2001, Director of the FDA Office of Vaccine Research and Review, the late William Egan, admitted under oath before Congress that thimerosal’s safety had never been studied in human beings.[7],[8] I leave it to the reader to speculate as to why CDC has not performed such studies in the intervening 24 years as it dosed hundreds of millions of American children and pregnant moms with mercury-laden flu shots. Furthermore, CDC has no existing guidelines for safe exposure to ethylmercury.[9]
But let’s put all that peer-reviewed science aside and just look at what the government and the vaccine industry say about thimerosal. Thimerosal’s label advises against its use during pregnancy, pointing out that thimerosal has never been shown to be safe and that it causes mutations in mammals.[10],[11] Thimerosal’s material safety data sheet (MSDS) acknowledges that thimerosal is “toxic,” has “Nervous System and Reproductive Effects,” and is “mutagenic in mammalian cells,” and that exposure to mercury in thimerosal “in utero and in children can cause mild to severe mental retardation and mild to severe motor coordination impairment.”[12]
The MSDS lists a grim inventory of dozens of other devastating injuries from thimerosal exposure.[13]
In 2001, the National Institute for Environmental Health Sciences (NIEHS) revised its thimerosal toxicity statement, warning that thimerosal is “toxic by ingestion and inhalation.”[14]
The California EPA recognizes thimerosal as a reproductive toxicant in the clearest possible language: “Thimerosal dissociates in the body to ethyl mercury. The evidence for its reproductive toxicity includes severe mental retardation or malformations in human offspring who were poisoned when their mothers were exposed to ethyl mercury or thimerosal while pregnant, studies in animals demonstrating developmental toxicity after exposure to either ethyl mercury or thimerosal, and data showing interconversion to other forms of mercury that also clearly cause reproductive toxicity.
The US EPA, the authoritative body relied on when mercury and mercury compounds were listed under California’s Proposition 65, currently identifies mercury and mercury compounds as causing reproductive toxicity.” The amount of ethylmercury in a flu shot is 25,000 times EPA’s safety level for drinking water.[15],[16]
Federal and state laws provide that whenever expired thimerosal vaccines are disposed of, they constitute a hazardous waste.
In 1998, FDA banned thimerosal in all over-the-counter products, ending its use in creams, eye medicine, and disinfectants like mercurochrome. It’s ironic that CDC still recommends its injection into babies.
A 2000 study by the National Research Council found that prenatal and infant mercury exposures cause multiple impacts to basic brain development by disrupting the division and migration of neuronal cells.[17],[18],[19]
According to a National Toxicology Program PowerPoint presentation entitled “Comparative Toxicity of Ethyl and Methyl Mercury”: “Ethylmercury is a neurotoxin. Infants may be more susceptible than adults. Ethylmercury exposure from vaccines (added to dietary exposures to methylmercury) probably caused neurotoxic responses (likely subtle) in some children.”[20]
A 2005 NIH study commissioned by FDA’s Center for Biologics Evaluation and Research (CBER) and performed by the National Toxicity Program (NTP) obliterated the industry claim that the ethylmercury in vaccines is less toxic than the heavily regulated methylmercury in fish, finding that the ethylmercury in thimerosal crosses the blood-brain barrier, lodges in the brain, and metabolizes into the most toxic form of mercury at double the rate of methylmercury.[21] A subsequent study found that this highly toxic mercury remains in the brain for over 27 years.[22]
A 2000 study in Neurotoxicology by Dr. William Slikker Jr., former head of the FDA’s National Center for Toxicological Research, directly foretold the results of a 2005 NIH-funded study, reporting that “Thimerosal (sodium ethylmercurithiosalicylate) crosses the blood-brain and placental barriers and results in appreciable mercury content in tissues including brain.”[23]
A 2017 NIH/CDC study links miscarriage to flu vaccines, particularly in the first trimester. Pregnant women vaccinated in the 2010/2011 and 2011/2012 flu seasons had two times greater odds of having a miscarriage within 28 days of receiving the vaccine. [24]
In women who had received the H1N1 vaccine in the previous flu season, the odds of having a miscarriage within 28 days were 7.7 times greater than in women who did not receive a flu shot during their pregnancy. These results are all the more significant when considering the fact that 7 of the 13 authors on the study had potential conflicts of interest such as having received research support from GlaxoSmithKline, Sanofi, Pfizer, Merck, Novartis, Novavax, and other Big Pharma companies. One author, Frank DeStefano, was head of CDC’s immunization Safety Branch.
It’s noteworthy that these authors chose not to differentiate outcomes between thimerosal-containing flu shots and those that did not contain thimerosal. Around half the flu shots available at that time contained thimerosal.
On October 1, 2001, the Institute of Medicine of the National Academy of Sciences Immunization Safety Review Committee (ISR) issued a report concluding that the link between thimerosal and the rise of neurological injuries in children, including autism, is “biologically plausible,”[25] and recommended the termination of all thimerosal-preserved vaccines.
An entire bibliography of pharmacokinetic studies by independent scientists, prestigious universities, and prominent research institutes published in high-gravitas journals, attest to thimerosal’s powerful neurotoxicity, and show that mercury tends to accumulate (and remain for considerable periods of time, years to decades) in the brains of primates and other animals after injection of thimerosal-containing vaccines.[26]
It’s worth noting just one of these, a well-known Russian study from 1977 led by Dr. N.D. Mukhtarova, found that the majority of adults exposed to much lower concentrations of ethylmercury than those currently given to American children in vaccines were still suffering neurological injury and neuropathology several years after the exposure. These symptoms included decreased vision, hearing, memory, vertigo, and pain and numbness in the hands and feet.[27],[28]
The Guardian is blind and scientifically baseless repetition of empty industry assurances about thimerosal safety is yet another proof that journalists, and particularly science journalists, have now devolved into obsequious stenographers for Big Pharma.
This is why RFK Jr. Retired Every Member of ACIP
This clip from a 2018 ACIP meeting illustrates exactly why ACIP reform is necessary.
----
"Is there any comment on using this vaccine at the same time with other adjuvanted vaccines?"
"We have no data to make a recommendation one way or the other."
"Just to sort of put this in context of other vaccines, while preclinical studies were not done using these vaccines simultaneously, our general approach to immunizations is that they should be given... they can be given at the same time in different limbs."
"Are adjuvanted, multiple-adjuvanted vaccines used in Europe or other markets?"
"Not to my knowledge."
"Okay. I think unless there's any further discussion, we will take a vote on this recommendation."
"I want to remind everyone to please check your voting whatever machine thing... I don't know what it is. Voting is open."
"Thank you very much. So the voting is completed, and it is unanimous to support this recommendation. Thank you all."
"Does anybody have any comments they wish to make about their vote?"
"So just a slight reservation. I think this is a huge advance and a step forward. I am concerned about that signal, that myocardial infarction signal. I am concerned about the use of this new adjuvant and certainly urge us to continue to look at the postmarketing data carefully. Thank you."
"Just a question about that. How soon would we be getting that postmarketing data update here?"
"There's two kinds of data. The Vaccine Safety Datalink data will require people to be using the vaccine to develop a substantive database. And, Doctor…do you want to comment on the postmarketing data that FDA is requiring?"
"I think for the myocardial infarction study, we’re seeing that the data for likely completion is May 20th, May 31st, 2020. There will also be studies looking at autoimmune diseases as well as herpes zoster. And there will be a pregnancy registry as well. So that’s all included in the postmarketing surveillance."
"Thank you."
#ACIPreform #ACIP @delbigtree@ICANdecide@AaronSiriSG
Yesterday, I retired 17 members of the Advisory Committee on Immunization Practices or ACIP, the @CDCgov external panel that wields the grave responsibility of adding new vaccines to the recommended childhood schedule. Over the coming days, I will use this platform to announce new members to populate ACIP. None of these individuals will be ideological anti-vaxxers. They will be highly credentialed physicians and scientists who will make extremely consequential public health determinations by applying evidence-based decision-making with objectivity and common sense.
I will also be tweeting examples of the historical corruption at ACIP to help the public understand why this clean sweep was necessary.
The most outrageous example of ACIP’s malevolent malpractice has been its stubborn unwillingness to demand adequate safety trials before recommending new vaccines for our children. Today, a compliant American child receives between 69 and 92 routine vaccines (depending on brand/dictated dosage) from conception to 18 years of age. This is up from 11 shots in 1986. ACIP has recommended each of these additional jabs without requiring placebo-controlled trials for any of them. This means that no one can scientifically ascertain whether these products are averting more problems than they are causing.
Many vaccine promoters have challenged this assertion. They are always wrong. Last week, @CNN, which has devolved into a shameless propagandist for Big Pharma, triumphantly announced that it had proof that my pronouncement that “there have been no placebo-controlled safety trials for any routine vaccines” was false. CNN gleefully proclaimed that it had found 257 placebo-controlled studies for routine vaccines.
So, allow me a moment to deconstruct CNN’s claims. Warning: this post may only be sufferable for science geeks like myself.
CNN is wrong. No routine injected vaccine on CDC’s schedule was licensed for children based on a placebo-controlled trial. In instances where a vaccine was used as a control, it too was never licensed based on a placebo-controlled trial. That is not conjecture. It is a fact based on FDA’s clinical trial data. (See https://t.co/q1xAtVxJ4N). As Secretary of @HHSGov, acknowledging this lamentable truth is part of my promise of radical transparency.
The 257 studies cited by CNN unwittingly reflect the lack of safety trials underpinning CDC’s schedule. Despite CNN’s worldwide effort to crowdsource trials with a placebo control (per @US_FDA/@CDCgov, an “inert substance”*), this list, on its face, reflects that 236 of the studies clearly did not use an “inert” safety comparator in a trial to license an injected routine vaccine for children on CDC’s schedule.**
For the remaining 21 studies CNN’s list claims used an inert injection, 9 plainly did not:
• RCT 251, 252 (Varivax) injected an antibiotic, neomycin – not inert.
• RCT 84, 97 (HPV-16 and 16/18) injected aluminum adjuvant – not inert.
• RCT 215 (Almevax) injected another vaccine – not inert.
• RCT 55 (Lyophilized PedvaxHIB) injected lactose, aluminum adjuvant, and thimerosal – not inert.
• RCT 197 (Salk vaccine) injected 199 solution, synthetic tissue culture, ethanol, phenol red, antibiotics, and formalin – not inert.***
• RCT 168 (Dow’s MMR) injected full vaccine minus virus, including all stabilizers, antibiotics, diluent, preservative, and buffers – not inert.****
• RCT 189 (Menveo) injected Tdap+saline or Menveo+saline – not inert.
For the remaining 12 listed studies which may have had an inert injection, none was a trial relied upon to license a routine vaccine on CDC’s childhood schedule:
• RCT 170, 171, 172 (MMR VaxPro), 228 (PCV11), 136 (Vaxigrip), 242 (Antitetanus), and 122 (Chinese flu shots) trialed vaccines never licensed in the U.S. nor relied upon to license a U.S. vaccine.
• RCT 124 (Fluzone IIV3), 102 (WVV/SPV), and 188 (Menveo) trials occurred after each respective vaccine was licensed, hence were not relied upon for their licensure.
• RCT 176 (Mumps vaccine) was not relied upon by the FDA to license the current MMR vaccine. (See MMR-II clinical trial report in link above.)
• RCT 53 (PRP-D) was for a vaccine withdrawn soon after its introduction and not relied upon by the FDA to license any U.S. vaccine.
While these 12 studies were not relied upon to license a routine vaccine on the CDC’s schedule, they do reflect that a placebo-controlled trial of a vaccine is possible. They also reflect what can be learned when a placebo trial is performed. For example: RCT 136 found the vaccine ineffective; RCT 122 found that “severe adverse effects occurred in 69 (0·6%, 95% CI 0·5–0·8) recipients of vaccine compared with one recipient (0·1%, 0–0·2) of placebo.”; and RCT 124 found “the rate of hospitalization was actually higher in the [Fluzone IIV3] vaccine group than in the placebo group.”
The unfortunate reality is that placebo-controlled trials, however, do not occur and have not been relied upon when FDA licenses vaccines for injection during childhood or ACIP recommends the shot for addition to the CDC’s routine schedule.
CNN would have reached the same conclusion had it reviewed the FDA documentation for each vaccine, instead of relying upon a random, crowd-sourced list from the internet. CNN’s list ironically proves the lack of adequate safety trials for routine childhood vaccines.
It is time to stop playing games, such as CNN’s false gotcha. We have gone from 3 routine injections by age one in 1986 (the year the National Childhood Vaccine Injury Act passed) to 25 routine injections by age one in 2025 (which now does not include Covid-19 vaccine). Because of the 1986 Act, every one of these products, save one, was developed by companies knowing they would almost never be liable for serious harm. During this same period, chronic diseases in our children exploded, most of which are caused by immune system dysregulation. If we are to identify the exposures that are causing this epidemic of autoimmune diseases, we need to rule out products given dozens of times to young children, specifically to modify the immune system, as potential culprits.
Our infants and children deserve the best safety trials possible to keep them safe. We should care as much about every child who could be injured by one of these products as we do every child who could be injured by an infectious disease. We must protect all children.
Notes:
* https://t.co/o6PtXJVxrv (“Placebos, defined as inert substances with no pharmacologic activity, are commonly used in double-blind, randomized controlled clinical trials.”); https://t.co/KwvrlZSkok (“the placebo control design, by … including a group that receives an inert treatment…”); https://t.co/8eJ0PNI5Mp (“Placebo: A substance or treatment that has no effect on living beings, usually used as a comparison to vaccine or medicine in clinical trials.”).
** While the above addresses injected vaccines, CNN’s cited list also includes 10 trials for rotavirus vaccine, given by oral drops, but none of these trials used saline only drops. Instead, RCT 205, 207, 208, 209, 210, 213 (Rotarix) contained dextran, sorbitol, amino acids, dulbecco’s modified eagle medium, calcium carbonate, and xanthan; RCT 211, 212 (RotaTeq) contained polysorbate 80, sucrose, citrate and phosphate; and RCT 206, 214 (Rotavac) included neomycin sulphate, kanamycin acid sulphate, trehalose, lactalbumin hydrolysate, human albumin, potassium dihydrogen orthophosphate, dipotassium hydrogen orthophosphate, and trisodium citrate dihydrate. The list also included three trials of an inhaled flu vaccine; the controls in RCT 104 were OPV+saline or LAIV (a vaccine), hence neither inert; in RCT 106 the control “consisted of normal allantoic fluid harvested from uninfected eggs stabilized with sucrose–phosphate–glutamate”; and, in RCT 109, the control was “intranasal spray of egg allantoic fluid containing sucrose-phosphate-glutamate.”
*** Note that the current polio vaccines used in the U.S. are a different product than the polio vaccine developed by Jonas Salk in the 1950s—which was discontinued in the 1960s—including because the currently-used polio vaccines are “grown in vero cells, a continuous line of monkey kidney cells cultivated on microcarriers.”
Hence, the Salk trial was not relied upon to license any current polio vaccine.
https://t.co/ko1RUVXSYi; https://t.co/FnwWUZulTF;
https://https://t.co/jWbEOEXKIGmedia/122249/vero-cell-line-profile.pdf; https://t.co/dg7R93iqT2.
**** Dow Chemical’s MMR vaccine used different strains than any licensed U.S. MMR vaccine and also, after 14 days of safety review, this trial vaccinated all participants.
Today, the COVID vaccine for healthy children and healthy pregnant women has been removed from @CDCgov recommended immunization schedule. Bottom line: it’s common sense and it’s good science. We are now one step closer to realizing @POTUS’s promise to Make America Healthy Again.
Tim Walz’s daughter goes on a bizarre rant about ‘running,’says her dad told her “running is a privilege” and it’s causing climate change and destroying the planet.
Kennedy left Bill O’Reilly speechless—something that rarely happens to the longtime host.
O’Reilly: “That was an excellent answer.”
“Most political appointees are pinheads.”
“They don't care about improving things. They care about their job title, their prestige, and their expense account.”
“You had an answer that everybody could understand, and that's what more people should do.”
“Kennedy, you know I wouldn't kiss your butt at all.
RFK: “You never have Bill.”
This is really terrible. AHA: please give us one justification for sugary soda in service to health. Nutritious food and drink is what people especially children need most. No legitimate cardiologist would support this. No pediatrician. Will keep amplifying. Bravo @travelingenes
HOLY CR*P 🚨
- Democrats did give MILLIONS of illegals Social Security Numbers
- They were REGISTERING TO VOTE
- Elon Musk has confirmation THEY DID VOTE
- Democrats qualified illegals for MAX SOCIAL SECURITY BENEFITS
- They enrolled in Medicaid with their new Social Security Numbers
See graph in video:
“Then you'll notice there's a strange, what jumped out at us when we saw these numbers. We're like, what is this? In 2021, you see 270,000 people, it goes all the way to 2.1 million and 2024. These are non-citizens that are getting social security numbers.
This is a mind-blowing charge. This literally blew us away.”
“If I hadn't seen this myself, I'm not sure I believed it. I went through it myself and mapped it. And Elon is right. This is true. The defaults in the system from social security to all of the benefit programs have been set to max inclusion, MAX PAY for these people and minimum collection.
We found 1.3 million of them already on Medicaid as an example. We've gone through on every benefit program we went through, we found groups from this particular group of people, this 5.5 million people in those benefit programs.
And then what was really, really disturbing us was why we're asking ourselves why.
So we actually just took a sample and looked at voter registration records and we found people here registered to vote in this population. Yes.
Who did vote? We found some by sampling that ACTUALLY DID VOTE.
We have referred them to prosecution at the Homeland Security Investigation Service. Yeah. Already, already. That is already happening right now. The truly disturbing thing though, I just want you to know this, a truly disturbing thing to me, and the darkest thing about this, to me, the voter fraud is terrible.”
@TheChiefNerd I treated one of Mel Gibson's friends with Ivermectin & Fenbendazole
I'm glad he's shining a light on the cancer successes of repurposed drugs.
We must insist on having Ivermectin, Fenbendazole and Mebendazole made available over the counter, to every American! 💪
@joerogan
The most important video on X today.
RFK Jr: “Food is medicine.”
“There was a recent study that showed that when prisons switched to whole food diets, violence went down by about 70%.”
“When they switched the diet in juvenile detention centers to a whole food diet, violence went down 100%.”
“There's a scientist at Harvard now who is curing schizophrenia with a carnivore diet.”
"It was the job of a professional [and] it's NOT Natural"
Nobel Prize winner for HIV research, Luc Montagnier (RIP), said someone "inserted small sequences of HIV" into the original covid Pandemic virus. He died after he presented the findings aired here on a French mainstream media platform.
He said it was a "very meticulous job".
Remember.....Pharmaceutical companies based the manufacturing process of their mRNA covid vaccines from this VERY sequence. And then on top of that, as [@Kevin_McKernan] points out, SV40 sequences have been found in vials of Pfizer mRNA covid vaccine
Dr. Patrick Soon-Shiong: “we have to face reality”
“For the first time in my career, I’ve seen an 8-year old, 9-year old, 10-year old with colon cancer [and] for the first time in my career, I’ve had a 13-year old child in our clinic d*e of metastatic pancreatic cancer”