Polio cases peaked around 1952 with just under 58,000 cases and 3,145 deaths. When the Polio vaccine was rolled out 3 years later Polio was already declining significantly with around half the amount of cases (28,985) and deaths (1,043). https://ourworldindata.org/grapher/reported-paralytic-polio-cases-and-deaths-in-the-united-states-since-1910?time=earliest..1962&country=~USA The OPV vaccine that is still used in many places has caused outbreaks of vaccine-associated paralytic poliomyelitis (VAPP) and polio outbreaks due to circulating vaccine-derived polioviruses. These outbreaks are not caused by the wild strain of polio virus. They are caused by the weakened virus used in vaccines that changes over time and begins to act like the wild virus. https://www.cdc.gov/vaccines/vpd/polio/hcp/vaccine-associated-paralytic-polio-faq.html https://www.cdc.gov/vaccines/vpd/polio/hcp/vaccine-derived-poliovirus-faq.html However, for the last 20 years in the United States we have used the inactivated polio vaccine (IPV) instead of OPV. Since it’s not a live virus it doesn’t carry the risk of VAPP. On the other hand, “IPV induces very low levels of immunity in the intestine. As a result, when a person immunized with IPV is infected with wild poliovirus, the virus can still multiply inside the intestines and be shed in the faeces, risking continued circulation.” Also “IPV does not stop transmission of the virus” https://polioeradication.org/polio-today/polio-prevention/the-vaccines/ipv/ -Recent data show that protection from acellular pertussis vaccines is not long-lasting. Antibody levels wane rapidly following vaccination. -Consistent with this T cell skewing, acellular vaccines did not prevent colonization or transmission following challenge in nonhuman primates. https://www.sciencedirect.com/science/article/abs/pii/S0952791515000813?via%3Dihub The DTP vaccine has been associated with a 5 fold higher mortality rate than being unvaccinated. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360569/ Those who receive the DTaP vaccine will be “more susceptible to pertussis throughout their lifetimes”. https://pubmed.ncbi.nlm.nih.gov/24277828/ Vaccination with varicella vaccine leads to an increased risk of shingles. https://pubmed.ncbi.nlm.nih.gov/22659447/ The International Agency for Research on Cancer found that individuals who never had measles had a 66% increased rate of non-Hodgkin lymphoma and a 233% increased rate of Hodgkin Lymphoma. https://seer.cancer.gov/statfacts/html/nhl.html https://seer.cancer.gov/statfacts/html/hodg.html A 22-year prospective study of over 100,000 individuals in Japan revealed that “measles and mumps, especially in case of both infections, were associated with lower risks of mortality from atherosclerotic CVD heart disease. https://pubmed.ncbi.nlm.nih.gov/26122188/ Vaccinated children are also at a higher risk for allergic rhinitis, eczema, learning disability, ADHD, neurodevelopmental disorder, and chronic illness than unvaccinated children. https://archive.is/PwUrN In 2011, HHS paid the IOM to conduct a study on vaccine safety. The IOM located science that “convincingly supports a causal relationship” for 14 of these serious injuries, including pneumonia, meningitis, hepatitis, MIBE (deadly brain inflammation a year after vaccination), febrile seizures, and anaphylaxis. The review found sufficient evidence to support “acceptance of a causal relationship” for 4 additional serious injuries. The IOM, however, found the scientific literature was insufficient to conclude whether or not those vaccines caused 135 other serious injuries commonly reported after their administration, including: Encephalitis, Encephalopathy, Infantile Spasms, Afebrile Seizures, Seizures, Cerebellar Ataxia, Ataxia, Acute Disseminated Encephalomyelitis, Transverse Myelitis, Optic Neuritis,  Neuromyelitis Optica, Multiple Sclerosis, Guillain- Barre Syndrome, to name just a few. https://www.nap.edu/read/13164/chapter/2#3 In a recent study comparing vaccinated vs unvaccinated children, they found children who were vaccinated were 5x more likely to have autism 4x more likely to have allergies 13.8x more likely to have gastrointestinal issues 17.6x more likely to have asthma 20.8x more likely to have ADHD 27.8x more likely to have chronic ear infections https://www.oatext.com/health-effects-in-vaccinated-versus-unvaccinated-children-with-covariates-for-breastfeeding-status-and-type-of-birth.php Another study done last year, looking at health outcomes of vaccinated and unvaccinated children, found, “We can conclude that the unvaccinated children in this practice are not, overall, less healthy than the vaccinated and that indeed the vaccinated children appear to be significantly less healthy than the unvaccinated.” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709050/#!po=1.51515 The rate of chronic illness in children in the United States is up from 12.5% in 1986 to 54% now. I am not saying it is all due to vaccines, but we went from giving kids 11 doses of vaccines by the time they were 18 to giving 72 doses now. We have the highest mortality rate of pregnant women than any other developed country in the world. “Despite spending more per capita of any country, the U.S. has one of the worst rates of infant mortality of all developed countries.” “Every year twice the number of U.S. babies die on their first day alive than in all 27 European Union nations combined, although 1 million more are born there (4.3 million versus 5.3 million respectively).” https://thevaccinereaction.org/2016/05/why-is-the-u-s-infant-mortality-rate-so-high/ We have a problem. And no, I don’t think vaccines are the entire cause of the problem. It’s many things, including our food. But Why would we blindly trust the industry that outspends oil and gas 2:1 in lobbying, that has paid out BILLIONS in lawsuits for knowingly misrepresenting their products, for bribing doctors, for withholding information about their products from the FDA? The industry that knew for decades the product they sold to us to use on our baby's bare skin every day contained asbestos. The only difference between vaccines and the other products produced and marketed by these companies is that vaccines don’t undergo the same standard of safety testing as other drugs. There are no double-blind placebo safety studies, and follow-up periods are as little as 48 hours. Vaccines are also the only product that can be produced. They are safety tested by the same company, mandated to every citizen in the country, and then held no liability for any damages caused. To say vaccines are safe and effective and that the science is settled without even taking the time to read the science is ignorant. The science is never settled, but so far, the science shows that vaccines are not always safe or effective.

In February 2021, I asked someone to show me a study that looked at the entire vaccine schedule and proved it didn’t increase the risk of autism. I was sent several studies and read through all of them. None of these studies examined more than one vaccine, and most only focused on one ingredient. Since that day, I haven’t stopped reading. I’ve gone through study after study, and the facts are undeniable: vaccines do contribute to autism. Beyond autism, they are linked to ear infections, type 1 diabetes, asthma, and more. Why are we letting pharmaceutical companies off the hook for the damage they cause? If any other product harmed or killed children at the rate vaccines do, it would be pulled without question. At the very least, it would have to be properly labeled, with the risks clearly listed for consumers. If your child is injured by a vaccine, the pharmaceutical company bears zero liability. They don’t even have to show up in court. It’s our tax dollars that pay for those injuries. So what incentive do these companies have to make their products safer? We are forcing parents to vaccinate their kids—vaccines that have never undergone double-blind placebo safety testing—in order for them to attend school. How are more people not outraged by this? Instead, I see the opposite. People get offended or angry when I speak the truth, or they ignore it completely. I don’t understand it. I want to share Isaiah’s story now that I’ve reviewed his medical records and notes. Isaiah’s first two months of life were normal. His well-child visits showed no concerns; everything seemed fine. Just before he turned two months old, I received IV and oral antibiotics for an infection. I was exclusively breastfeeding because I believed “breast is best,” not considering that the antibiotics could be passed to Isaiah. Antibiotics disrupt the gut microbiome, which plays a critical role in immune system function. A study on cephalexin, the antibiotic I was given, states that it passes through breast milk and can disrupt an infant’s gastrointestinal flora. At the end of my antibiotic treatment, I went in for a postpartum follow-up and was given a flu shot. I normally never get flu shots, but I did that year to protect Isaiah. I was told the best way to protect him was to ensure those around him were vaccinated. Now I know that I probably harmed him more than I protected him. Influenza vaccines still contain thimerosal, a preservative removed from most children’s vaccines in the early 2000s. Many studies link thimerosal to autism—at least 180 studies show its harmful effects. The flu vaccine insert even states, “data is not available to assess the effects on the breastfed infant.” I should never have been given that shot. A week later, Isaiah was vaccinated for rotavirus, diphtheria, tetanus, pertussis, hepatitis B, and polio—six vaccines at once, after just being exposed to an influenza vaccine that isn’t safe for children under six months, and after being exposed to antibiotics that weakened his immune system. How did no one stop and consider that this combination might not be safe? They don’t test the safety of multiple vaccines given together. They barely test the safety of one. That same month, Isaiah had a developmental assessment done. Studies have shown this screener to be accurate and reliable. Isaiah scored a 109. Fourteen months later, he was given the same screener and scored a 62. He went from being advanced in every area to being developmentally delayed in every area. He wasn’t born that way. After the two-month mark, his head began to grow significantly. In less than a year, he went from the 32nd percentile to greater than the 99th percentile for head circumference. He stopped eating and started screaming. Looking back at his medical records, the connection is clear: Isaiah would get vaccinated, and within a week, we’d end up in urgent care with no explanation. Every. Single. Time. By four months old, he was diagnosed with failure to thrive. Just over a year later, he was diagnosed with neurological impairment, macrocephaly, and developmental delay syndrome. He now also has diagnoses of Autism Spectrum Disorder, speech delay, dysphagia, anxiety, and OCD. I would much rather this be a genetic issue because the regret I live with is overwhelming. I’m working hard to find ways to help Isaiah, and he’s doing well, but I would give anything to go back and do things differently. I’ll never tell another parent what choices are best for their family. But I urge parents to please do your own research before deciding. I used to think there was no unbiased information available, but that’s not true. There are many scientific research articles out there. PubMed is a great place to start. The studies can be hard to read at first, but it’s so important to know the facts for yourself. No one else will look out for you and your family like you will. You wouldn’t make a large purchase without researching it first. If you’re buying a new home, you’d likely have an inspection done. If you’re buying a new car or appliances, you’d probably do some research to make sure they aren’t known for having issues. The same diligence should apply to something as critical as your child’s health.

Someone once told me that vaccines were safe and that I was just looking for something to blame for my son’s autism. But they had no idea what I was going through. Unfortunately, most people won’t recognize the truth until they are personally affected. Cognitive dissonance can blind us to the evidence that’s right in front of us. I had doubts about vaccinating my son. A few people hinted that vaccines might be harming him, but no one ever said it outright. I wish I had trusted my instincts. I wish someone had told me that vaccines can cause harm and that there are hundreds of studies proving it. I wish I had known that the issues we were seeing could have been caused by vaccines. So many parents live with this regret. It’s heartbreaking, and unless you’ve experienced it, it’s impossible to truly understand. Watching your child disappear—seeing a child who once spoke suddenly stop speaking, a child who was always happy stop smiling—is a pain beyond words. Unless you’ve seen your child struggle to speak, refuse to eat for weeks, or bang their head against the floor during a meltdown they can’t control, you can’t fully grasp the depth of this experience. Unless you’ve been in the backseat of your car, helpless as your child thrashes, screams, and cries because you exited the parking lot the wrong way, you just can’t understand. We would give anything to go back and make a different choice. The guilt is immense and difficult to bear. But we have no choice but to keep moving forward. When you have a child with disabilities and a future full of uncertainty, moving forward becomes essential. The fear of what will happen to them when we’re gone, of who will care for them if we’re not here, is overwhelming. And it weighs even heavier, knowing it didn’t have to be this way. I think most parents would agree with me when I say that I would rather it had been a genetic issue—something that was simply beyond our control. At least then, there would be some comfort in knowing that nothing I could have done would have changed it. But knowing that my son could have had a normal life, that he didn’t have to start therapy five days a week at just two years old, is a heavy burden to carry. It’s heartbreaking to think he didn’t have to be so sensitive that, at times, it was unbearable to even leave the house because the sound of the outside world was too much for him. To know these struggles could have been avoided if I had refused the Hepatitis B vaccine because it was only safety tested for 5 DAYS! Not even in babies who were just born but in adults . Also, he has a 0% chance of getting Hepatitis B at this point in his life, and studies have shown that boys vaccinated with the Hepatitis B vaccine in the first month of life have a 3-fold higher risk of autism than boys who aren't vaccinated until after one month. If I would have refused the rotavirus vaccine because most babies (who are the only ones at risk of dying from rotavirus) are protected against rotavirus with breastfeeding. Or because in the vaccine trials that compared the vaccine to the vaccine minus the antigen, 1 in 30 to 1 in 40 control group participants suffered a severe medical event . 43 infants in the Rotarix trial died , and 20 died in the RotaTeq trials . If I would have refused the DTaP vaccine because the Diphtheria mortality rate dropped 87% before the vaccine for Diphtheria was used widely, and the antitoxin used to treat diphtheria since 1891 has a clinical efficacy of 97%. On the other hand, "Receiving 3 doses of diphtheria toxoid vaccine is 87% effective against symptomatic disease and reduces transmission by 60%. Vaccinated individuals can become colonized and transmit; consequently, vaccination alone can only interrupt transmission in 28% of outbreak settings , making isolation and antibiotics essential." Because Tetanus rates have always been rare , with 500-600 cases annually before the vaccine. Among all persons with reported tetanus from 2001-2008, the CDC states that "in the multivariable model, comparing age ≥65 years versus <65 years, diabetes versus no diabetes, and no doses of vaccination versus 1 dose, neither diabetes nor vaccination were statistically significant." Because a study exposing baboons to pertussis showed that those who were vaccinated previously carried the bacterium for 5 days longer than the unvaccinated baboons and were able to infect other baboons with the bacterium. Conversely , the baboons who had previously been infected by pertussis were not able to spread the bacterium to other baboons following re-exposure. If I would have refused the Hib vaccine because death rates from Hib were 1 in 2 million prior to the vaccine. Also because studies show that vaccination with the Hib vaccine may induce diabetes related autoantibodies. My dad was the only diabetic in our family . He was diagnosed with type 1 diabetes after getting very sick following a vaccination he received at age 12. If I had refused the Pneumococcal vaccine, which protects against 13 of the 90+ different serotypes. In the clinical trials, there were 18 fewer cases than expected of Pneumococcal infection , but almost 1,200 infants in the vaccine group had emergency room visits, and 500 were hospitalized . Finally, if I would have refused the polio vaccine, one of which causes more cases of polio than wild-type polio itself, and because the other states in the vaccine insert, "Although no causal relationship has been established, deaths have occurred in temporal association after vaccination of infants with IPV." If I had taken the time to research vaccines, just as we carefully researched the reliability of a new car or the quality of a new TV, I would have known. I could have changed the course of my son’s life if I had just known. So, to the person who thinks I’m simply looking for something to blame for my son’s autism, you’re wrong. As parents, we would give our lives for our kids. Imagine, as a parent, realizing that you could have protected your child from something that would cause them lifelong harm, but you didn’t. You were supposed to be their voice because they couldn’t speak up for themselves. If they could have, they might have told you that their brain was on fire. You didn’t protect them from this harm, and now you have to live with that, watching your child struggle every day as a constant reminder. Why would we choose to blame our child’s pain on something we could have prevented? If we were simply looking for something to blame, I can assure you we wouldn’t choose this.

Why I Won't Vax Home I Don't Trust Big Pharma Conflicts of Interest No Liability The Vaccine Inserts Inadequate Safety Testing Ingredients The Risks Outweigh The Benefit Unvaxxed are Healthier Decline in Illness Prior to Vaccines Vaccine Failure & Shedding Autism Vaccines Dont Cause Autism Vaccines Do Cause Autism Search Results BACK TO INGREDIENTS Polysorbate 80 Dietary emulsifiers consumption alters anxiety-like and social-related behaviors in mice in a sex-dependent manner Holder MK, Peters NV, Whylings J, Fields CT, Gewirtz AT, Chassaing B, de Vries GJ. Dietary emulsifiers consumption alters anxiety-like and social-related behaviors in mice in a sex-dependent manner. Sci Rep. 2019 Jan 17;9(1):172. doi: 10.1038/s41598-018-36890-3. PMID: 30655577; PMCID: PMC6336787. Dietary emulsifiers carboxylmethylcellulose (CMC) and polysorbate 80 (P80) alter the composition of the intestinal microbiota and induce chronic low-grade inflammation, ultimately leading to metabolic dysregulations in mice. Importantly, emulsifier treatment altered anxiety-like behaviors in males and reduced social behavior in females. It also changed expression of neuropeptides implicated in the modulation of feeding as well as social and anxiety-related behaviors. Read More Polysorbate 80 increases the susceptibility to oxidative stress in rat thymocytes Tatsuishi T, Oyama Y, Iwase K, Yamaguchi JY, Kobayashi M, Nishimura Y, Kanada A, Hirama S. Polysorbate 80 increases the susceptibility to oxidative stress in rat thymocytes. Toxicology. 2005 Feb 1;207(1):7-14. doi: 10.1016/j.tox.2004.07.020. PMID: 15590117. Polysorbate 80 at clinically-relevant concentrations increases the cytotoxicity of hydrogen peroxide under the in vitro condition. Result suggests that polysorbate 80 may increase the susceptibility of cells to oxidative stress. Read More Dual effects of Tween 80 on protein stability Wang W, Wang YJ, Wang DQ. Dual effects of Tween 80 on protein stability. Int J Pharm. 2008 Jan 22;347(1-2):31-8. doi: 10.1016/j.ijpharm.2007.06.042. Epub 2007 Jul 3. PMID: 17692480. Tween 80 increased the rate of oxidation in general but also altered the temperature-dependency of IL-2 mutein oxidation. Read More Polysorbate 80-induced leaky gut impairs skeletal muscle metabolism in mice Nishimura S, Aoi W, Kodani H, Kobayashi Y, Wada S, Kuwahata M, Higashi A. results suggest that daily PS80 intake induces intestinal permeability, leading to glucose intolerance and mitochondrial dysfunction in the skeletal muscle. Read More Consumption of Select Dietary Emulsifiers Exacerbates the Development of Spontaneous Intestinal Adenoma Viennois E, Chassaing B. Consumption of Select Dietary Emulsifiers Exacerbates the Development of Spontaneous Intestinal Adenoma. Int J Mol Sci. 2021 Mar 5;22(5):2602. doi: 10.3390/ijms22052602. PMID: 33807577; PMCID: PMC7961571. Overall, our findings further support the hypothesis that emulsifier consumption may be a new modifiable risk factor for colorectal cancer (CRC) and that alterations in host-microbiota interactions can favor gastrointestinal carcinogenesis in individuals with a genetical predisposition to such disorders. Read More Polysorbate-80 modified neurotoxin nanoparticle with its transport and cytotoxicity against blood-brain barrier Zhao YM, Xia AX, Wei YH, Ruan YP, Li FZ. [Polysorbate-80 modified neurotoxin nanoparticle with its transport and cytotoxicity against blood-brain barrier]. Yao Xue Xue Bao. 2010 Oct;45(10):1312-6. Chinese. PMID: 21348312. polysorbate-80 modified neurotoxin nanoparticles can transport across the BBB Read More Dietary emulsifier polysorbate-80-induced small-intestinal vulnerability to indomethacin-induced lesions via dysbiosis Furuhashi H, Higashiyama M, Okada Y, Kurihara C, Wada A, Horiuchi K, Hanawa Y, Mizoguchi A, Nishii S, Inaba K, Sugihara N, Watanabe C, Komoto S, Tomita K, Miura S, Hokari R. Polysorbate-80 enhances the vulnerability of the small intestine to indomethacin-induced injury by inducing ileal dysbiosis. Direct enhancement of the motility of specific flagellated microbiota by P80 might be related to dysbiosis and intestinal injury. Read More Flow-cytometric analysis on adverse effects of polysorbate 80 in rat thymocytes Hirama S, Tatsuishi T, Iwase K, Nakao H, Umebayashi C, Nishizaki Y, Kobayashi M, Ishida S, Okano Y, Oyama Y. Polysorbate 80 increases membrane permeability and decreased glutathione content. Read More Dietary Emulsifier-Induced Low-Grade Inflammation Promotes Colon Carcinogenesis Viennois E, Merlin D, Gewirtz AT, Chassaing B. Dietary Emulsifier-Induced Low-Grade Inflammation Promotes Colon Carcinogenesis. Cancer Res. 2017 Jan 1;77(1):27-40. doi: 10.1158/0008-5472.CAN-16-1359. Epub 2016 Nov 7. PMID: 27821485; PMCID: PMC5214513. Here, we demonstrate in a preclinical model of colitis-induced colorectal cancer that regular consumption of dietary emulsifiers, carboxymethylcellulose or polysorbate-80, exacerbated tumor development. Enhanced tumor development was associated with an altered microbiota metagenome characterized by elevated levels of lipopolysaccharide and flagellin Read More Preparation and therapeutic efficacy of polysorbate-80-coated amphotericin B/PLA-b-PEG nanoparticles Ren T, Xu N, Cao C, Yuan W, Yu X, Chen J, Ren J. Preparation and therapeutic efficacy of polysorbate-80-coated amphotericin B/PLA-b-PEG nanoparticles. J Biomater Sci Polym Ed. 2009;20(10):1369-80. doi: 10.1163/092050609X12457418779185. PMID: 19622277. The prepared nanoparticles were spherical with homogeneous distribution. Drug concentration in mice brain was greatly enhanced, which indicated that the coated nanoparticles could get across the BBB Read More Macromolecules in polysorbate 80 for injection: an important cause of anaphylactoid reactions Li Y, Duan J, Xia H, Li Y, Shu B, Duan W. macromolecular impurities may cause strong anaphylactoid reactions, passive cutaneous anaphylactoid (PCA) reactions, pulmonary capillary permeability, vasodilation, and severe hemolysis Read More Dietary emulsifiers impact the mouse gut microbiota promoting colitis and metabolic syndrome Chassaing B, Koren O, Goodrich JK, Poole AC, Srinivasan S, Ley RE, Gewirtz AT. relatively low concentrations of two commonly used emulsifiers, namely carboxymethylcellulose and polysorbate-80, induced low-grade inflammation and obesity/metabolic syndrome in wild-type hosts and promoted robust colitis in mice predisposed to this disorder. Emulsifier-induced metabolic syndrome was associated with microbiota encroachment, altered species composition and increased pro-inflammatory potential. Read More

Why I Won't Vax Home I Don't Trust Big Pharma Conflicts of Interest No Liability The Vaccine Inserts Inadequate Safety Testing Ingredients The Risks Outweigh The Benefit Unvaxxed are Healthier Decline in Illness Prior to Vaccines Vaccine Failure & Shedding Autism Vaccines Dont Cause Autism Vaccines Do Cause Autism Search Results Return to Ingredients Aluminum Do aluminum vaccine adjuvants contribute to the rising prevalence of autism? Tomljenovic L, Shaw CA. Do aluminum vaccine adjuvants contribute to the rising prevalence of autism? J Inorg Biochem. 2011 Nov;105(11):1489-99. doi: 10.1016/j.jinorgbio.2011.08.008. Epub 2011 Aug 23. PMID: 22099159. Our results show that: (i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines; (ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades Read More Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure Seneff, S.; Davidson, R.M.; Liu, J. Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure. Entropy 2012, 14, 2227-2253. https://doi.org/10.3390/e14112227 In this paper, we have presented some analyses of the VAERS database which strongly suggest that the aluminum in vaccines is toxic to vulnerable children. While we have not shown that aluminum is directly causative in autism, the compelling evidence available from the literature on the toxicity of aluminum, combined with the evidence we present for severe adverse reactions occurring much more frequently following administration of aluminum-containing vaccines as compared to non-aluminum-containing vaccines, suggests that neuronal damage due to aluminum penetration into the nervous system may be a significant factor in autism. Read More Experimental Epilepsy in the Monkey Following Multiple Intracerebral Injections of Alumina Cream Joseph G. Chusid, Lenore M. Kopeloff, Ph.D. and Nicholas Kopeloff, Ph.D. The Bulletin, 1953. Aluminum caused tics and grand mal seizures in monkeys. Read More Macrophagic myofasciitis lesions assess long-term persistence of vaccine derived aluminum hydroxide in muscle R.K. Gherardi, M. Coquet, P. Cherin, L. Belec, P. Moretto, P.A. Dreyfus. Brain, 2001, 124, 1821-1831. French scientists tie aluminum adjuvant in vaccine to macrophagic myofasciitis. Read More Long-term persistence of vaccine-derived aluminum hydroxide is associated with chronic cognitive dysfunction Maryline Couette, Marie-Françoise Boisse, Patrick Maison, Pierre Brugieres, Pierre Cesaro, Xavier Chevalier, Romain K. Gherardi, Anne-Catherine Bachoud-Levi, François-Jérôme Authier. Journal of Inorganic Biochemistry, 2009. French scientists report aluminum from vaccines causes chronic cognitive dysfunction. Read More Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity Shaw C, Tomljenovic L. Immunologic Research. 2013;56:304–316. Canadian researchers: aluminum in vaccines can cause both autoimmunity and neurological damage. Read More Autoimmune/inflammatory syndrome induced by adjuvants (ASIA) 2013: Unveiling the pathogenic, clinical and diagnostic aspects Perricone C, Colafrancesco S, Mazor RD, Soriano A, Agmon-Levin N, Shoenfeld Y. Journal of Autoimmunity. 2013;47:1-16. Israeli and Italian researchers demonstrate that exposure to aluminum in vaccines can lead to autoimmune and brain dysfunction. Read More Aluminum exposure and toxicity in neonates: a practical guide to halt aluminum overload in the prenatal and perinatal periods. Fanni D, et al. World Journal of Pediatrics, 2014 May; 10(2):101-7. Newborns have been overexposed to aluminum. Read More Neuroprotective effect of Allium cepa L. in aluminium chloride induced neurotoxicity Tanveer Singh and Rajesh Kumar Goel. NeuroToxicology, 49 (2015) 1–7. Chronic aluminium administration resulted in significant motor incoordination and memory deficits, which were also endorsed biochemically as there was increased oxidative stress as well as elevated aluminium levels in the brain. Read More Assessment of hair aluminum, lead, and mercury in a sample of autistic Egyptian children: Environmental risk factors of heavy metals in autism El Baz Mohamed F, Zaky EA, Bassuoni EI-Sayed A, et al. Behavioural Neurology. 2015, Article ID 545674. Autistic children accumulate metals at a much higher level than children who do not have a diagnosis of autism. Read More On vaccine’s adjuvants and autoimmunity: Current evidence and future perspectives Pellegrino P, Clementi E, Radice S. Autoimmunity Reviews. 2015;14(10):880-888. The specific mechanism of action of each vaccine adjuvant may have different effects on the course of autoimmune conditions resulting from vaccination Read More Aluminum in Childhood Vaccines Is Unsafe Neil Z. Miller. Journal of American Physicians and Surgeons, Winter 2016. Aluminum in vaccines is highly neurotoxic and exposure levels given to infants have dramatically increased. Read More Behavioral abnormalities in female mice following administration of aluminum adjuvants and the human papillomavirus (HPV) vaccine Gardasil Inbar R, Weiss R, Tomljenovic L, Arango M-T, Deri Y, Shaw CA, Chapman J, Blank M, Shoenfeld Y. Immunologic Research. 2017;65(1):136-149. Israeli, Canadian and Colombian scientists show that the Gardasil vaccine triggers brain inflammation and autoimmunity in mice. Read More Combined subchronic toxicity of aluminum (III), titanium (IV) and silicon (IV) oxide nanoparticles and its alleviation with a complex of bioprotectors IA Minigalieva, BA Katsnelson, LI Privalova, et al. International Journal of Molecular Sciences, March 2018;19(3):837. Aluminum nanoparticles are toxic on their own and in combination with other metal nanoparticles. Read More Synergism in aluminum and mercury neurotoxicity Peter N Alexandrov,1 Aileen I Pogue,2 and Walter J Lukiw Aluminum and mercury sulfates may contribute to neurodegeneration and progressive age-related functional decline such as Alzheimer’s disease. Read More Reconsideration of the immunotherapeutic pediatric safe dose levels of aluminum James Lyons-Weiler 1, Robert Ricketson 2 The levels of aluminum present in individual vaccines and in the modern vaccine schedule as a whole are problematically high. Read More Aluminium in brain tissue in multiple sclerosis Matthew Mold,1 Agata Chmielecka,2 Maria Raquel Ramirez Rodriguez,1 Femia Thom,2 Caroline Linhart,3 Andrew King,4 and Christopher Exley1,* The first-ever measurements of aluminum in the brain tissue of donors with multiple sclerosis detected pathologically significant levels of aluminum in every single individual. Read More Immunoexcitotoxicity as the central mechanism of etiopathology and treatment of autism spectrum disorders: a possible role of fluoride and aluminum Strunecka A, Blaylock RL, Patocka J, Strunecky O. Surgical Neurology International. 2018;9:74. Fluoride and aluminum, alone or in combination, can produce the condition of “immunoexcitotoxicity” that leads to the pathological changes seen in autism. Read More Unraveling the enigma: elucidating the relationship between the physicochemical properties of aluminium-based adjuvants and their immunological mechanisms of action Emma Shardlow, Matthew Mold & Christopher Exley Aluminum adjuvants in vaccines produce toxic effects ranging from benign to fatal, depending on the physicochemical properties of the adjuvant and the physiological response of the vaccine recipient. Read More Aluminium toxicosis: a review of toxic actions and effects Ikechukwu Onyebuchi Igbokwe, Ephraim Igwenagu, Nanacha Afifi Igbokwe. Interdiscip Toxicol. 2019; Vol. 12(2): 45–70. doi: 10.2478/intox-2019-0007 With the preliminary literature search starting in 2013 and looking backwards in time, research publications revealed a myriad of toxic actions of Aluminum causing pathological conditions. Read More Acute exposure and chronic retention of aluminum in three vaccine schedules and effects of genetic and environmental variation Journal of Trace Elements in Medicine and Biology Among the three schedules presented here, the CDC schedule exceeds the recommended dose limit for an infant (inferred from FDA adult “safe” levels) as a result of the simultaneous administration of multiple ACVs and insufficient spacing of ACVs. Read More Imaging of aluminium and amyloid β in neurodegenerative disease Christopher Exley∗ and Matthew J. Mold We suggest that complementary aluminium-specific fluorescence microscopy may reveal important information about the putative toxicity of aluminium in neurodegenerative and neurodevelopmental disorders. Read More Association Between Aluminum Exposure From Vaccines Before Age 24 Months and Persistent Asthma at Age 24 to 59 Months Academic Pediatrics In a large observational study, a positive association was found between vaccine-related aluminum exposure and persistent asthma. While recognizing the small effect sizes identified and the potential for residual confounding, additional investigation of this hypothesis appears warranted. Read More Aluminum and Alzheimer's Disease: After a Century of Controversy, Is there a Plausible Link? IOS Press The hypothesis that Al significantly contributes to AD is built upon very solid experimental evidence and should not be dismissed. Immediate steps should be taken to lessen human exposure to Al, which may be the single most aggravating and avoidable factor related to AD. Read More Aluminum adjuvant linked to gulf war illness induces motor neuron death in mice Springer The findings suggest a possible role for the aluminum adjuvant in some neurological features associated with GWI and possibly an additional role for the combination of adjuvants. Read More Administration of aluminium to neonatal mice in vaccine-relevant amounts is associated with adverse long term neurological outcomes Journal of Inorganic Biochemistry Repetitive administration of aluminium to neonatal mice in amounts comparable to those to children receive via routine vaccinations significantly increases anxiety and reduces exploratory behaviour and locomotor activities. The neurodisruptive effects of aluminium are long-lasting and persist for 6 months following injection. Read More STUDY: CDC VACCINE SCHEDULE LIKELY INDUCES ALUMINUM TOXICITY IN NEWBORNS Jefferey Jaxen A new study published in the Journal of Trace Elements in Medicine and Biology concluded the U.S. Centers for Disease Control and Prevention’s (CDC) vaccine schedule was 15.9 times over the recommended safe level of aluminum when researchers adjusted for body weight. Read More

Why I Won't Vax Home I Don't Trust Big Pharma Conflicts of Interest No Liability The Vaccine Inserts Inadequate Safety Testing Ingredients The Risks Outweigh The Benefit Unvaxxed are Healthier Decline in Illness Prior to Vaccines Vaccine Failure & Shedding Autism Vaccines Dont Cause Autism Vaccines Do Cause Autism Search Results BACK TO INGREDIENTS Polysorbate 80 Dietary emulsifiers consumption alters anxiety-like and social-related behaviors in mice in a sex-dependent manner Holder MK, Peters NV, Whylings J, Fields CT, Gewirtz AT, Chassaing B, de Vries GJ. Dietary emulsifiers consumption alters anxiety-like and social-related behaviors in mice in a sex-dependent manner. Sci Rep. 2019 Jan 17;9(1):172. doi: 10.1038/s41598-018-36890-3. PMID: 30655577; PMCID: PMC6336787. Dietary emulsifiers carboxylmethylcellulose (CMC) and polysorbate 80 (P80) alter the composition of the intestinal microbiota and induce chronic low-grade inflammation, ultimately leading to metabolic dysregulations in mice. Importantly, emulsifier treatment altered anxiety-like behaviors in males and reduced social behavior in females. It also changed expression of neuropeptides implicated in the modulation of feeding as well as social and anxiety-related behaviors. Read More Polysorbate 80 increases the susceptibility to oxidative stress in rat thymocytes Tatsuishi T, Oyama Y, Iwase K, Yamaguchi JY, Kobayashi M, Nishimura Y, Kanada A, Hirama S. Polysorbate 80 increases the susceptibility to oxidative stress in rat thymocytes. Toxicology. 2005 Feb 1;207(1):7-14. doi: 10.1016/j.tox.2004.07.020. PMID: 15590117. Polysorbate 80 at clinically-relevant concentrations increases the cytotoxicity of hydrogen peroxide under the in vitro condition. Result suggests that polysorbate 80 may increase the susceptibility of cells to oxidative stress. Read More Dual effects of Tween 80 on protein stability Wang W, Wang YJ, Wang DQ. Dual effects of Tween 80 on protein stability. Int J Pharm. 2008 Jan 22;347(1-2):31-8. doi: 10.1016/j.ijpharm.2007.06.042. Epub 2007 Jul 3. PMID: 17692480. Tween 80 increased the rate of oxidation in general but also altered the temperature-dependency of IL-2 mutein oxidation. Read More Polysorbate 80-induced leaky gut impairs skeletal muscle metabolism in mice Nishimura S, Aoi W, Kodani H, Kobayashi Y, Wada S, Kuwahata M, Higashi A. results suggest that daily PS80 intake induces intestinal permeability, leading to glucose intolerance and mitochondrial dysfunction in the skeletal muscle. Read More Consumption of Select Dietary Emulsifiers Exacerbates the Development of Spontaneous Intestinal Adenoma Viennois E, Chassaing B. Consumption of Select Dietary Emulsifiers Exacerbates the Development of Spontaneous Intestinal Adenoma. Int J Mol Sci. 2021 Mar 5;22(5):2602. doi: 10.3390/ijms22052602. PMID: 33807577; PMCID: PMC7961571. Overall, our findings further support the hypothesis that emulsifier consumption may be a new modifiable risk factor for colorectal cancer (CRC) and that alterations in host-microbiota interactions can favor gastrointestinal carcinogenesis in individuals with a genetical predisposition to such disorders. Read More Polysorbate-80 modified neurotoxin nanoparticle with its transport and cytotoxicity against blood-brain barrier Zhao YM, Xia AX, Wei YH, Ruan YP, Li FZ. [Polysorbate-80 modified neurotoxin nanoparticle with its transport and cytotoxicity against blood-brain barrier]. Yao Xue Xue Bao. 2010 Oct;45(10):1312-6. Chinese. PMID: 21348312. polysorbate-80 modified neurotoxin nanoparticles can transport across the BBB Read More Dietary emulsifier polysorbate-80-induced small-intestinal vulnerability to indomethacin-induced lesions via dysbiosis Furuhashi H, Higashiyama M, Okada Y, Kurihara C, Wada A, Horiuchi K, Hanawa Y, Mizoguchi A, Nishii S, Inaba K, Sugihara N, Watanabe C, Komoto S, Tomita K, Miura S, Hokari R. Polysorbate-80 enhances the vulnerability of the small intestine to indomethacin-induced injury by inducing ileal dysbiosis. Direct enhancement of the motility of specific flagellated microbiota by P80 might be related to dysbiosis and intestinal injury. Read More Flow-cytometric analysis on adverse effects of polysorbate 80 in rat thymocytes Hirama S, Tatsuishi T, Iwase K, Nakao H, Umebayashi C, Nishizaki Y, Kobayashi M, Ishida S, Okano Y, Oyama Y. Polysorbate 80 increases membrane permeability and decreased glutathione content. Read More Dietary Emulsifier-Induced Low-Grade Inflammation Promotes Colon Carcinogenesis Viennois E, Merlin D, Gewirtz AT, Chassaing B. Dietary Emulsifier-Induced Low-Grade Inflammation Promotes Colon Carcinogenesis. Cancer Res. 2017 Jan 1;77(1):27-40. doi: 10.1158/0008-5472.CAN-16-1359. Epub 2016 Nov 7. PMID: 27821485; PMCID: PMC5214513. Here, we demonstrate in a preclinical model of colitis-induced colorectal cancer that regular consumption of dietary emulsifiers, carboxymethylcellulose or polysorbate-80, exacerbated tumor development. Enhanced tumor development was associated with an altered microbiota metagenome characterized by elevated levels of lipopolysaccharide and flagellin Read More Preparation and therapeutic efficacy of polysorbate-80-coated amphotericin B/PLA-b-PEG nanoparticles Ren T, Xu N, Cao C, Yuan W, Yu X, Chen J, Ren J. Preparation and therapeutic efficacy of polysorbate-80-coated amphotericin B/PLA-b-PEG nanoparticles. J Biomater Sci Polym Ed. 2009;20(10):1369-80. doi: 10.1163/092050609X12457418779185. PMID: 19622277. The prepared nanoparticles were spherical with homogeneous distribution. Drug concentration in mice brain was greatly enhanced, which indicated that the coated nanoparticles could get across the BBB Read More Macromolecules in polysorbate 80 for injection: an important cause of anaphylactoid reactions Li Y, Duan J, Xia H, Li Y, Shu B, Duan W. macromolecular impurities may cause strong anaphylactoid reactions, passive cutaneous anaphylactoid (PCA) reactions, pulmonary capillary permeability, vasodilation, and severe hemolysis Read More Dietary emulsifiers impact the mouse gut microbiota promoting colitis and metabolic syndrome Chassaing B, Koren O, Goodrich JK, Poole AC, Srinivasan S, Ley RE, Gewirtz AT. relatively low concentrations of two commonly used emulsifiers, namely carboxymethylcellulose and polysorbate-80, induced low-grade inflammation and obesity/metabolic syndrome in wild-type hosts and promoted robust colitis in mice predisposed to this disorder. Emulsifier-induced metabolic syndrome was associated with microbiota encroachment, altered species composition and increased pro-inflammatory potential. Read More