Vaccine Ingredients Everyone Should Know
Vaccine Safety: Another Piece of the Puzzle. Information and documentation to help everyone understand vaccine safety, and to make print outs with and share.
Most people don't know what's in vaccines. To evaluate safety properly, it's very important to know about the ingredients. All FDA approved vaccines are required to include a package insert that includes information on ingredients, as well as other things like "Adverse Reactions". The ingredients are often in the "Description" section. All these package inserts are available on the FDA website.
Vaccines Licensed for Use in the United States
https://www.fda.gov/vaccines-blood-biologics/vaccines/vaccines-licensed-use-united-states
Most people believe vaccine ingredients are simple. I heard one doctor say they thought vaccines were just bits of virus and saline. That is not all what is actually in vaccines, at all.
Like many medicines, vaccines usually have main, primary ingredients, and then secondary ingredients. These secondary ingredients are often called “excipients”.
The CDC Pink Book has a summary chart of excipients. Here is a recent copy:
CDC -The Epidemiology and Prevention of Vaccine-Preventable Diseases, a.k.a. the “Pink Book,”
Appendix B for the Pink Book-Vaccine Excipient Summary 2021
https://vaccine.guide/wp-content/uploads/2023/03/cdc-vaccine-ingredient-and-excipient-summary.pdf
This summary makes an excellent print out to distribute and share with everyone.
Some excipients have unusual names, like Thimerosal. These can all be looked up. For Example:
“Thimerosal (an ethylmercury-containing compound used as a preservative in vaccines )…22 studies from 1971 to 2019 show that exposure to ethylmercury-containing compounds (intravenously, intraperitoneally, topically, subcutaneously, intramuscularly, or intranasally administered) results in accumulation of mercury in the brain. In total, these studies indicate that ethylmercury-containing compounds and Thimerosal readily cross the Blood-brain-barrier, convert, for the most part, to highly toxic inorganic mercury-containing compounds, which significantly and persistently bind to tissues in the brain, even in the absence of concurrent detectable blood mercury levels.”
Examining the evidence that ethylmercury crosses the blood-brain barrier. Janet K Kern, et al., Environ Toxicol Pharmacol. 2020 Feb;74:103312. doi: 10.1016/j.etap.2019.103312. Epub 2019 Dec 9.
https://europepmc.org/article/med/31841767
Triton X-100 is another excipient with a unrecognizable name. It is in several flu shots. Here are some documents on it:
"TRITON X-100 Synonyms: X-100; TRITON X-100 1; Octylphenol ethylene oxide condensate"
https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/160/855/t8532pis.pdf
"What is ethylene oxide?
At room temperature, ethylene oxide is a flammable colorless gas with a sweet odor. It is used primarily to produce other chemicals, including antifreeze. In smaller amounts, ethylene oxide is used as a pesticide and a sterilizing agent. The ability of ethylene oxide to damage DNA makes it an effective sterilizing agent but also accounts for its cancer-causing activity."
National Cancer Institute
https://www.cancer.gov/about-cancer/causes-prevention/risk/substances/ethylene-oxide
"As Octylphenol Ethoxylates are not placed on Annex XIV because of a concern to humans, the exposure of workers is not included in the exposure assessment. However, the human health hazard of Skin irritant 2 and Eye damage 1 is controlled by means of the same rigorous containment which prevents exposure to biological material and emission to the environment. In the production facility safety glasses are mandatory. In Figure 2 an example of gowning is shown"
https://echa.europa.eu/documents/10162/dd2e920b-d54f-3b49-4529-1f6d73fcb8b6
Aluminum may be more recognizable, but most peple don't know what would be the results of injecting it.
In fact, no one is completely certain, because it has never been properly studied.
But there is a lot of good information available about the lack of studies, and what evidence that is known.
There is a recent excellent documentary made in Europe called:
Injecting Aluminum
https://cinemalibrestudio.com/injecting-aluminum/
https://odysee.com/@Vaccine_Documentaries:1/injecting-aluminum-documentary:2
Here are some great quotes from the film:
“In fact, for almost everything else you can think of, you have to do that, you have to demonstrate that something is safe first. That has never been necessary for aluminum, it has never been demonstrated that aluminum is safe. No, there's never been any legislation in order to do that, and this is a historical thing.” - Dr. Christopher Exley
“Since the 1920s, aluminum salts have been used primarily as the adjuvant in most childhood vaccines to optimize the body's immune response to the injected disease. Aluminum is now known to be neurotoxic and the root cause of many serious illnesses including MS and Alzheimer. The aluminum adjuvant was only tested for 28 days, on two rabbits, and their remains have mysteriously disappeared. What the pharmaceutical companies don't make public is how the aluminum adjuvant was never rigorously tested before going on the market and there were alternatives albeit slightly more expensive--available.”
https://cinemalibrestudio.com/injecting-aluminum/synopsis.html
“The study cited as a reference on how the body absorbs the aluminum adjuvant in a vaccine dates from 1997. It was carried out by an American researcher named Flarend. His co-author is Stanley Hem, the pope of adjuvants. Their work consisted of injecting an aluminum isotope - radioactive aluminum - into two rabbits. Only two bunnies! These two rabbits received intramuscular injections.
Scientists then monitored the rate at which the rabbits could eliminate the radioactive aluminum, by measuring the levels of aluminum in the rabbits' urine. The result of this test, in itself, is quite alarming. Elimination, 28 days post-injection, was 6%. In other words, 94% of the aluminum remained in the animal's body. Despite this study, scientists still claim that it only takes a few weeks to eliminate aluminum injected into humans. Worse, the researchers “lost” the animals' bones. Bones are known to be one of the sites where the body stores aluminum. So, besides using only two rabbits, the researchers lost both femurs of both rabbits. Unfortunately, they were destroyed. How silly. The muscle that was injected was not examined. In other words, they couldn't determine whether the injected aluminum stayed there, or not. Moreover, we find ourselves with a study lasting only 28 days. Whereas now, there is no doubt that the adjuvant stays in the body for years. This study, which says, “Nothing's amiss; very little is absorbed by the brain.” Perhaps, after 28 days. But how about 6 months, a year, or 18 months post-injection? So this is the study that worldwide vaccinology takes as its reference. Two rabbits, whose organs were lost, and who were studied for 28 days. The study simply has to be done all over again, properly!
...Researchers checked for a link between multiple sclerosis and hepatitis B vaccine. An association between the two was found in the studies that looked at the vaccination in the long term, and saw a phenomenon. I mean Hernan's research, and Tardieu's work on childhood-onset MS. It took three years for the increase in risk to be visible. In the first few years, it was unobservable. No acute toxicity. When they say “the innocuity of these adjuvants has been proven,” beware of the semantics! Stop! They are innocuous - in the short term. But you can't say they are innocuous in the long term, because you don't know: no studies have been done.
The guiltiest act is that once it has been pointed out that the aluminum persists for much longer than a month, that it remains in the immune system for many years, no watchdog agency sat up and said, “Stop. Back to the laboratory, guys.” That should have been done in the early 2000s. And it was not. So we're fifteen years late, in terms of the natural reaction elicited by the normal application of intellectual discipline.” - Dr. Romain Gherardi
“...The thing about aluminum and what makes people complacent about aluminum is that you don't see acute events very often from aluminum. Aluminum is not like cyanide or lead, or cadmium. You don't suddenly feel ill and you don't suddenly get ill and die because you've had a single exposure to it. You can, but it would have to be a very high exposure. Aluminum is different, it's this silent visitor. Now, there is a proviso for that, an exception, and I believe the exception to that can be vaccination.”
“It is clearly not an exception in the vast majority of people, because the vast majority of people receive aluminum adjuvant and do not get severe adverse events, but if it's one percent of people, one percent of millions of people, young women having the HPV vaccine, is a huge number of people suffering severe adverse events. These severe adverse events are unquestionably due to the presence of that aluminum compound."
“Aluminum has this amazing ability to turn the body against things that were normally considered as self, so that's why, for example, I am not surprised that aluminum could be involved in something like multiple sclerosis. In multiple sclerosis, we know that the body starts to break down its own myelin, it produces anti bodies against its own myelin product. Why?”
“In fact, the adjuvant does not require clinical approval at all. It is the vaccine preparation which requires clinical approval, so you may put any adjuvant into a vaccine, it will then go through a clinical approval process and if it gets approved with that adjuvant, regardless of what it is, whether it's an aluminum adjuvant or another, then it's the vaccine that will be clinically approved, not the adjuvant.”
“I think it's relatively clear that there are some questions in the field of aluminum research, which most would not like to see answered. I cannot sit here now and tell you, for example, that aluminum is a cause of Alzheimer's, but what I can tell you now is that aluminum does make Alzheimer's worse, aluminum does make Alzheimer's occur at an earlier age, and we know this because when we find such high levels of aluminum as we have in human brain tissue, it is inevitable that that aluminum will contribute to this disease, it is inevitable.”
“You know, the one thing I hope is this, I actually, like all of us, rely on people like the World Health Organization. I hope that in everything else, other than aluminum, they do consult experts, and they are correct, so when they're telling us about the levels of certain PCB's or something in the environment, I hope that they're not as wrong as they are with aluminum, because if they are, then this organization is totally corrupt and useless. In terms of aluminum, it is, and it always will be until they decide to actually talk to people who know.”
“....Yeah, right now, we're just accepting the consequences of taking this very biologically reaction metal, living with it, and accepting what it does, without any attempt to protect ourselves from it. Actually, opposite to that, really covering up the damage that we probably know that it does already, for example, in the recent EMA, European Medicine's Agency review of the HP vaccine, how many experts on aluminum did they consult? None. How can they get that aspect if they cannot consulted anybody, and this happens all of the time, all of the time.” - Dr. Christopher Exley
“In particular, as early as 1974, the Institut Pasteur developed calcium-phosphate adjuvants to replace aluminum salts in all of its products... Dr. Floret, president of the Vaccination Technical Committee admitted that the calcium phosphate adjuvant was no less effective than aluminum hydroxide, or aluminum salts. The adjuvant could be brought back. All it takes is a political decision. Then our vaccines would be safer.”
“So, in 1986, Institut Merieux decided to eliminate its calcium-phosphate vaccine line. But Institut Merieux also long manufactured a vaccine without any adjuvant at all. Sanofi, which bought out Institut Merieux decided to get rid of the adjuvant-free vaccine in 2008. In particular, the DTaP (Diphtheria, Tetanus, and Polio) which functioned well for forty years.”
“In late 2012, the Council of State acknowledged the link between our disease and the aluminum in the vaccines. They have handed down eight rulings since 2012. A strong legal precedent has been set.”
- Didier Lambert
https://cinemalibrestudio.com/injecting-aluminum/quotes.html
“7) Aluminum salts are identified as neurotoxic by the highest French health authorities. Many diseases, such as Alzheimer's, Parkinson's, Crown's, Sarcoidosis, development of allergies, cases of chronic fatigue, multiple sclerosis, amyotrophic lateral sclerosis, autism and many more could be caused by aluminum according to Professor Christopher Exley (GB), renowned international specialist in aluminum toxicity and a professor in inorganic chemistry at Birchall Centre at Keele University, Straffordshire, UK.
11) Two professors from the University of British Columbia, Dr. Christopher Shaw, a Professor in the Department of Ophthalmology and Visual Sciences and holds cross appointments with the Department of Experimental Medicine and the Graduate Program in Neuroscience, and Lucija Tomljenovic, from the Neural Dynamics Research Group at the University of British Columbia, have published a study called, "Aluminum vaccine adjuvants: are they safe?" In the study they assert, "Electron microscopy and microanalytical analysis showed that the appearance of MMF lesions was due to long-term persistence of aluminum adjuvants at the site of injections and concomitant ongoing local immune reactions [8, 83]. Aluminum was shown to persist at the site of injection from several months up to 8 years following vaccination [83, 85]. MMF lesions were subsequently also reproduced in rats by injection of aluminum adjuvants [86]."
In their study, which was published in the journal Current Medicinal Chemistry, Shaw and Tomljenovic contend that medical science's understanding of the metallic element's mechanisms of action in the body remains poor. They argue that experimental research shows that aluminum adjuvants have the potential to induce serious autoimmune disorders, long-term brain inflammation, and associated neurological complications.
12) The French court ruled that the Council of State (the highest French administrative jurisdiction) has acknowledged the link between Macrophagic Myofascite and aluminum in vaccines in court 8 times (2012, 2013, 2014, 2015).
14) The safety of aluminum has been debated since 1891. Two German scientists claimed that aluminum was dangerous. They said it could start to break down, and dissolve into food. To settle court cases, manufacturers hired scientists on both sides to do research. Some tried to show aluminum was harmless, others, that it was toxic. A commission was appointed by Roosevelt in 1908 to consider the safety of aluminum further. High economic and scientific stakes were attached to aluminum. Certain researchers published incriminating evidence and alleged that aluminum was harmful. Ernest Ellsworth Smith was recognized as a scientist. He published a book in 1928, to weigh all the pros and cons of aluminum. The book was extremely biased and omitted any findings that aluminum was harmful. The anti-aluminum side, Smith's opponents, had much less funding, and couldn't afford to publish a book like this one. Both sides had scientists doing serious, legitimate work but the pro-aluminum group had sponsorship and was able to quash all legitimate concerns from the other side.
15) The study cited as the main reference on how the body absorbs the aluminum adjuvant in a vaccine was done in 1997. It was carried out by an American researcher named Flarend. His co-author is Stanley Hem, the pope of adjuvants. Their study comprised of injecting radioactive aluminum into two rabbits. They then monitored the rate at which the rabbits could eliminate the radioactive aluminum, by measuring the levels of aluminum in the rabbits' urine. Elimination, 28 days post-injection was 6%. In other words, 94% of the aluminum remained in the animal's body. The animals were only studied for 28 days, no long-term studies were ever done. Despite this study, scientists still claim that it only takes a few weeks to eliminate aluminum injected into humans.
16) Aluminum hydroxide became available in 1927. The exact same compound is still used today in vaccines, vaccinology continues to use aluminum in the same form as it was originally used in 1927 with no new scientific developments.”
https://cinemalibrestudio.com/injecting-aluminum/facts.html
Aluminum Found in Vaccines Are Neurotoxic
by Dr Hagmeyer/ June 5, 2014
“Aluminum Hydroxide: This form of aluminum is a protoplasmic poison and a potent neurotoxin that is completely unnatural to the biochemical process of any life form on earth. The American Academy of Pediatrics has stated that aluminum is now being implicated as interfering with a variety of cellular and metabolic processes in the nervous system and other tissues. Aluminum toxicity is known to cause encephalitis (brain swelling), bone disease and anemia.
“Aluminum hydroxide is used in vaccines to increase the body’s production of antibodies, though no one knows how it works,” says Purdue researcher Stanley Hem, professor of industrial and physical pharmacy.
Antigens are protein molecules that stimulate the immune system. Antibodies are protein molecules made by the immune system to defend against foreign substances. In the 1930′s vaccine researchers tested a number of ingredients to see what would effectively bring antigens into the body so the immune system of the individual would produce antibodies. Aluminum was proved to be an effective adjuvant or substance that irritates the immune system and causes antibody production.
The FDA limits the dosage to 0.85 mg of aluminum per vaccine to minimize exposure. Children following normal vaccine protocols receive up to 3.75-4 mg of aluminum in the first 6 months of life. The kidneys normally eliminate aluminum from the body. People with strong, healthy kidneys should be able to excrete the aluminum in vaccines. Most research has shown that about 50% of aluminum in vaccines or food is eliminated within 24 hours and 85% is eliminated in 2 weeks. However, infants have reduced renal function and may not be able to excrete ample amounts. Kidney function is very low at birth and does not reach maturity until 1-2 years of age.
A 1992 study showed that aluminum based vaccine injected into mice caused a transient rise in brain tissue aluminum levels that peaked around the 2nd -3rd day after injection. This is particularly concerning because aluminum does its greatest damage in the brain. This study showed that it is possible for aluminum to cross over the blood brain barrier and lodge into areas of the brain. A 1997 study published in the New England Journal of Medicine showed that premature babies injected with aluminum build up toxic levels in the bones, blood and brain. This aluminum toxicity can lead to very serious mental handicaps by 18 months of age.
Aluminum is found in the DTP, Haemophilus Influenza, Pneumococcal, Hepatitis A, Hepatitis B, Human Papillomavirus, Anthrax, & Rabies vaccines. A 2004 article published by the FDA states, “Research indicates that patients with impaired kidney function including premature neonates who receive aluminum at greater rates than 4-5 mcg per kilogram of body weight per day accumulate aluminum at levels associated with central nervous system and bone toxicity.”
Based on these FDA toxicity thresholds a 6lb baby could not handle more than 11-14 mcg of aluminum. The Hepatitis B vaccine which is given at birth contains 250 mcg which is 20x the toxicity threshold. The average baby weighs close to 12 lbs at 2 months of age when they are injected with 1,225 mcg of aluminum in their vaccines which is 50 times the toxicity threshold.”
https://www.drhagmeyer.com/aluminum-found-in-vaccines-are-neurotoxic
“There is also growing evidence that co-exposure to multiple metals can result in increased neurotoxicity compared to single-metal exposure, in particular during early life.”
https://pubmed.ncbi.nlm.nih.gov/26231505/
“What the data from several studies clearly shows is that no one can state what is a “safe” level of mercury exposure without knowing the concentration of all other factors that may synergistically exacerbate mercury toxicity.
Synergistic effects on ethylmercury is demonstrated by the dramatic enhancements of thimersosal toxicity against neurons in culture by aluminum cation (Al3+), antibiotics and testosterone. Al3+ is another component of vaccines and dramatically increases the killing of neurons by thimerosal. Testosterone, at low nanomolar levels is not noticeably toxic to neurons. However, if testosterone is present with low nanomolar levels of thimerosal the rate of neuron death is greatly enhanced, more so than with Al3+. This likely explains the 4 to 1 ratio of boys to girls that become autistic and the fact that most of the severe cases of autism are boys. This involvement of testosterone in autism is further supported by the work of Dr. Baron Cohen of England who studied the amniotic fluid of mothers who gave birth to autistic children. The only abnormality he found was that their amniotic fluid contained elevated testosterone. It is likely that this early elevated testosterone level rendered these children at enhanced risk for ethylmercury neurotoxicity.”
https://www.mercurypoisoned.com/hearings/mercury_toxicity_from_dental_amalgams_and_thimerosal.html
Since there are different types of vaccines, the main ingredients can vary significantly. Many conventional viruses use attenuated viruses as one of their main ingreduents.
Viruses cannot reproduce themselves, they need a host cell to reproduce. Since many vaccines use attenuated viruses, they need to produce many attenuated viruses to put in each vaccine. They use "cell lines" to reproduce the viruses in, and originally used animal cells, like monkey kidney cells for some of the most common cell lines. Unfortunately, when gathering the viruses they were reproducing intentionally in animal cells, other viruses that had already been in the animal cells were gathered also. These were effectively impossible to filter, since they were the same size as the intended viruses.
One of these monkey viruses was found to be very dangerous, and has become quite notorious. It's called SV40.
“In 1959, Dr Bernice Eddy who was conducting polio vaccine safety studies discovered that an extract of monkey kidney cells used to propagate the polio vaccines was causing tumors in newborn hamsters. She surmised that the monkeys carried a cancer-causing virus which would later become known as
SV40 – the 40th simian (monkey) virus discovered. Despite efforts to silence her new revelations, as it’s public knowledge would threaten vaccine confidence, she went ahead and presented her data at an annual Cancer Society conference in New York in October 26, 1960. The NIH actively blocked her from publishing her findings and eventurally she was eliminated from vaccine research. Her treatment was considered a scandal. [3]
She did manage in 1962 to publish in the journal of the Federation of American Societies for Experimental Biology reporting that the Salk polio vaccine contained SV40, which was confirmed to be the cause of cancer tumors in hamsters. [1, 2]
Prior to this in 1955 when the Salk polio vaccines were launched, Dr Eddy ‘s screening of polio vaccines revealed they inconveniently contained amounts of live polio virus, in an alledged “inactivated” vaccine, she was demoted and fired for this finding!
Soon after, Dr. Maurice Hilleman, Merck’s Chief vaccine expert, published similar tumor results, leading Merck voluntarily withdrawing its killed-virus polio vaccine.”
This problem is the main reason scientists switched to using human cell lines, instead of animals, for vaccine research and development. These are now usually from fetuses.
SV40 has been studied a lot since it was discovered, and has been found it can be used as a "promoter", helping DNA get into the nuclues. It is sometimes used in genetic engineering for that purpose.
The genetic sequence for SV40 is also listed on the description of the plasmid on the ingredients list for some COVID shots, but it isn't labeled distinctly.
That is a regulation violation, but so far no agency has enforced it.
This is commonly referred to as “plasmid gate”
“Dr. Kevin McKernan, a genomics researcher, authored a pre-print study in April 2023 that found higher levels of SV40 than regulations allowed. Dr. McKernan posted on X that “no prior vaccine in Canada has been approved with such a sequence contaminant.”
Health Experts Raise Alarm: SV40 Enhancer in Pfizer/BioNTech Vaccines
https://thehighwire.com/news/health-experts-raise-alarm-sv40-enhancer-in-pfizer-biontech-vaccines/
COVID vaccine adulteration w/Kevin McKernan, Byram Bridle, Chris Martenson, Steve Kirsch
“..a snapshot of Kevin McKernan’s interviews and publications from... to his discovery of unexpected DNA contamination (and other concerning anomalies) in the Pfizer-BioNTech and Moderna mRNA COVID-19 vaccine vials. His work has been repeated by many labs around the world which have confirmed his findings, and together they’re learning more and more about the glaring dangers of these genetic products.
Kevin McKernan PhD is a highly published microbiologist with a long history in genomic science, he is the former research and development leader at the Human Genome Project and is the founder and CSO Medical Genomics where you can find out more about him.”
https://totalityofevidence.com/kevin-mckernan/
“How is it that Kevin McKernan, and not any world health authority, found the contamination in April 2023? And why are the FDA, CDC, and the mainstream media still silent about this?”
For very interesting perspective and first hand testimony of the research being done at the time of the discovery, there is a great new documentary interviewing Judyth Vary Baker, who was a young biology student working as an intern with several noteworthy scientists. The research she worked on included research on SV40, including with Dr. Mary Sherman, a world renowned expert in cancer research. Baker was also recruited to work on experiments funded by the CIA, being directed to assist in developing what she was told was a method to be used to assassinate Fidel Castro.
KILL SHOT: The CIA's SV40 Cancer Weapon - Full Story w/ Shannon Joy
https://rumble.com/v3mroia-kill-shot-the-cias-sv40-cancer-weapon-full-story-w-shannon-joy.html
“Other researchers linked the first CFS outbreak to a polio vaccine given to doctors and nurses that resulted in the “1934 Los Angeles County Hospital Epidemic.” That vaccine was cultivated on pulverized mouse brains. Retroviruses from dead animals can survive in cell lines and permanently contaminate vaccines.
Retroviruses from those dead animals can survive in cell lines and permanently contaminate the vaccines.
XMRV is so hazardous that the mere presence of mouse tissue in a laboratory can contaminate other tissues in the same room.
Dr. Mikovits’ studies suggested XMRV is present in the MMR and polio vaccines given to American children and the Japanese encephalitis vaccine given to military personnel.
The dangers of mouse brain derived vaccines are now widely acknowledged.
“… mouse brain derived vaccine has been associated with serious allergic and neurologic adverse events.” –American Academy of Pediatrics”
In addition to extraneous viruses being able to get into vaccines, pieces of regular animal or human DNA can also get into vaccines with the reproduced intended virus from the host cell. Much DNA is also often about the same size as viruses, and effectively can't be filtered out.
Some people are very concerned about the safety and ethics of this.
OPEN LETTER TO LEGISLATORS REGARDING FETAL CELL DNA IN VACCINES
April 8, 2019
“My name is Dr. Theresa Deisher. I am Founder and Lead Scientist at Sound Choice Pharmaceutical Institute, whose mission is to educate the public about vaccine safety, as well as to pressure manufacturers to provide better and safer vaccines for the public. I obtained my doctorate from Stanford University in Molecular and Cellular Physiology in 1990 and completed my post-doctoral work at the University of Washington. My career has been spent in the commercial biotechnology industry, and I have done work from basic biological and drug discovery through clinical development. I am writing regarding unrefuted scientific facts about fetal DNA contaminants in the Measles-Mumps-
Rubella vaccine, which must be made known to lawmakers and the public.
Merck’s MMR II vaccine (as well as the chickenpox, Pentacel, and all Hep-A containing vaccines) is manufactured using human fetal cell lines and is heavily contaminated with human fetal DNA from the production process. Levels in our children can reach up to 5 ng/ml after vaccination, depending on the age, weight and blood volume of the child. That level is known to activate Toll-like receptor 9 (TLR9), which can cause autoimmune attacks.”
https://soundchoice.org/wp-content/uploads/2021/01/open-letter-legislators.pdf