Articles show that for decades big pharma has prioritized profits over safety. Some unethical practices they use include hiding safety studies that show the dangers of their products, bribing doctors & scientists, fraud, & unethical testing including testing their products on vulnerable populations. 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 I Don't Trust Big Pharma A collection of articles showing that for decades the pharmaceutical industry has prioritized profits over safety. Some of the Big Pharma Corruption includes hiding safety studies that show the dangers of their products, bribing doctors and scientists, scientific fraud, and unethical testing including testing their products on vulnerable populations. Democracy Now Nigerian Attorney General Play Video pharma deception Play Video I Don't Trust Pharma Watch Now Share Whole Channel This Video Facebook Twitter Pinterest Tumblr Copy Link Link Copied Share Channel Info Close GlaxoSmithKline to Plead Guilty and Pay $3 Billion to Resolve Fraud Allegations and Failure to Report Safety Data Largest Health Care Fraud Settlement in U.S. History Read More Justice Department Announces Largest Health Care Fraud Settlement in Its History Pfizer to Pay $2.3 Billion for Fraudulent Marketing Read More Johnson & Johnson to Pay More Than $2.2 Billion to Resolve Criminal and Civil Investigations Allegations Include Off-label Marketing and Kickbacks to Doctors and Pharmacists Read More Abbott Labs to Pay $1.5 Billion to Resolve Criminal & Civil Investigations of Off-label Promotion of Depakote Company Maintained Specialized Sales Force to Market Drug for Off Label Purposes; Targeted Elderly Dementia Patients in Nursing Homes Read More Eli Lilly and Company Agrees to Pay $1.415 Billion to Resolve Allegations of Off-label Promotion of Zyprexa $515 Million Criminal Fine Is Largest Individual Corporate Criminal Fine in History; Civil Settlement up to $800 Million Read More U.S. Pharmaceutical Company Merck Sharp & Dohme to Pay Nearly One Billion Dollars Over Promotion of Vioxx® Merck to Pay $950 Million for Illegal Marketing Read More Amgen Inc. Pleads Guilty to Federal Charge in Brooklyn, NY.;Pays $762 Million to Resolve Criminal Liability and False Claims Act Allegations Biotech Giant Pleads Guilty to Illegally Introducing Drug into Market for Uses That the Fda Declined to Approve; Will Pay $612 Million to Resolve False Claims Act Suits and $150 Million in Criminal Penalties and Forfeiture Amerisourceberge Read More Pharmaceutical Giant AstraZeneca to Pay $520 Million for Off-label Drug Marketing Read More Drug Maker Actelion Agrees to Pay $360 Million to Resolve False Claims Act Liability for Paying Kickbacks Read More Johnson & Johnson knew for decades that asbestos lurked in its Baby Powder Facing thousands of lawsuits alleging that its talc caused cancer, J&J insists on the safety and purity of its iconic product. But internal documents examined by Reuters show that the company's powder was sometimes tainted with carcinogenic asbestos and that J&J kept that information from regulators and the public. Read More List of largest pharmaceutical settlements Read More Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial Revelations of poor practices at a contract research company helping to carry out Pfizer’s pivotal covid-19 vaccine trial raise questions about data integrity and regulatory oversight. Paul D Thacker reports Read More Pfizer Hit with Largest Criminal Fine in US History Read More Pfizer Has a Long History of Fraud, Corruption and Using Children as Human Guinea Pigs Pfizer’s CEO Albert Bourla claimed during a November 2021 interview that a small group of “medical professionals” who are intentionally circulating “misinformation” critical of the Pfizer vaccine narrative are “criminals,” but Bourla didn’t mention the criminal history of his own company. Read More Learn about how the media, our educational institutions, and our regulatory agencies are involved in Big Pharma Corruption CONFLICTS OF INTEREST Home Page BACK TO TOP Conflicts of Interest

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 Covid-19 Vaccines The response by public health authorities and governments around the world to the novel corona virus in 2020 and throughout the following years had devastating effects on the population. Start Now Covid Sign in Covid Play Video Share Whole Channel This Video Facebook Twitter Pinterest Tumblr Copy Link Link Copied Search video... All Categories All Categories Now Playing covid death rates austrailia and niger 00:42 Play Video Now Playing Maddie de Garay Injured in vaccine trials 00:30 Play Video Now Playing ‘Colossal_Failure’_Did_This_Just_Become_the_Worst_Public_Health 01:53 Play Video Now Playing Jessica Rose discussing vaccine ingredients 02:13 Play Video BACK TO TOP

There is no better place to find the actual risks associated with a vaccine than the vaccine insert. These are the vaccines given to our children. Starting with vaccines they are exposed to while in utero through 18 years. 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 The Vaccine Inserts There is no better place to find the actual risks associated with a vaccine than the vaccine insert. These are the vaccines given to our children. Starting with vaccines they are exposed to while in utero through 18 years. Find Out How Vaccines Are Tested For Safety The CDC recommends that pregnant women receive TDap (Tetanus, Dihptheria, Pertussis), Influenza, and Covid 19 vaccines. They also list "other" vaccines, "Other vaccines- Some women may need other vaccines before, during, or after they become pregnant. For example, if a pregnant woman works in a lab or is traveling to a country where she may be exposed to meningococcal disease, her doctor or healthcare professional may recommend meningococcal vaccination." Hepatitis B: A baby whose mother has hepatitis B is at highest risk for becoming infected with hepatitis B during delivery. Moms, talk to your healthcare professional about getting tested for hepatitis B and whether or not you should get vaccinated. Hepatitis A: For pregnant women who have a history of chronic liver disease, doctors or healthcare professionals may recommend the hepatitis A vaccine. Vaccines for travel: Pregnant people planning international travel should talk to their doctor or healthcare professional at least 4 to 6 weeks before their trip to discuss any special precautions or necessary vaccines. See Traveler’s Health for additional tips on how to prepare to travel safe Table 1 shows the CDC vaccine schedule from birth to 18 years. You can find a full list of vaccines currently approved for use by the FDA along with the package inserts, patient information sheets, and licensing documents here VIEW ALL Hepatitis B Rotavirus DTP Haemophilus Infenzae Type B Pneumococcal Polio Influenza (IIV4) Measles, Mumps, Rubella Varicella (VAR) Hepatitis A Tetanus, Diphtheria, Pertussis Human Papillomavirus (HPV) Meningococcal Dengue Covid Hepatitis B Birth, 1-2 months, 6-18 months Recombivax-HB Click Here Engerix-B Click Here Rotavirus 2 months, 4 months, 6 months ROTARIX Click Here RotaTeq Click Here Diphtheria, Tetanus, Acellular Pertussis 2 months, 4 months, 6 months DAPTACEL Click Here PEDIARIX DTaP, hepatitis B, and inactivated poliovirus vaccine Click Here Pentacel® DTaP, inactivated poliovirus, and Haemophilus influenzae type B vaccine Inactivated Poliovirus component grown in Vero cells Click Here Quadracel® DTaP and inactivated poliovirus vaccine Inactivated Poliovirus component grown in Vero cells Click Here Kinrix® DTaP and inactivated poliovirus vaccine Click Here INFANRIX Click Here Pentacel® DTaP, inactivated poliovirus, and Haemophilus influenzae type B vaccine Inactivated Poliovirus component grown in MRC-5 cells Click Here Quadracel® DTaP and inactivated poliovirus vaccine Inactivated Poliovirus component grown in MRC-5 cells Click Here Vaxelis® DTaP, inactivated poliovirus, Haemophilus influenzae type b, and hepatitis B vaccine Click Here Haemophilus Inflenzae Type B (Hib) 2 months, 4 months, 6 months, 12-18 months ActHIB® Click Here PedvaxHIB® Click Here Hiberix® Click Here Pneumococcal 2 months, 4 months, 6 months, 12-18 months Prevnar 13® Pneumococcal 13-valent conjugate vaccine Click Here Pneumovax® 23 Pneumococcal 23-valent polysaccharide vaccine Click Here Inactivated Poliovirus (IPV<18yrs) 2 months, 4 months, 6-18 months, 4-6 years IPOL® Click Here Influenza 6 months- 8 years annual vaccination of 1-2 doses, 9 years or older annual vaccination of 1 dose only Influenza Virus Vaccine, H5N1 Click Here Flucelvax Quadrivalent Click Here FluLaval Quadrivalent Click Here FluLaval Click Here Fluzone Click Here FluMist Quadrivalent Click Here AUDENZ Click Here Fluarix (3+ Years) Click Here Fluvirin (4+ years) Click Here FluLaval Click Here Fluarix Quadrivalent Click Here Measles, Mumps, Rubella (MMR) 12-15 months, 4-6 years M-M-R-II Click Here ProQuad Package Insert - Frozen Formulation - Recombinant Human Albumin (RHA) - ProQuad Click Here ProQuad Package Insert (Frozen) - ProQuad Click Here ProQuad® Package Insert - Refrigerator-Stable Formulation - ProQuad Click Here ProQuad Package Insert - Frozen Formulation - Human SerumAlbumin (HSA) - ProQuad Click Here ProQuad Package Insert (Refrigerated) - ProQuad Click Here Varicella (VAR) 12-18 months, 4-6 years Varivax® Package Insert - Varivax (Frozen) Click Here Varivax® Package Insert - Varivax (Refrigerator) Click Here Hepatitis A (Hep A) 2 dose series 12-23 months Havrix® Click Here Vaqta® Click Here Tetanus, Diphtheria, Pertussis 1 dose during each pregnancy between weeks 27-36, one dose 11-12 years, every 10 years Adacel® Click Here Boostrix® Click Here Human Papillomavirus (HPV) If started between ages 9-14 give 2 dose series, Age 15 years and older give 3 dose series GARDASIL 9 Click Here Meningococcal 11-12 years, 16 years Menactra® Click Here MenQuadfi® Click Here Trumenba® Click Here Menveo® Click Here Bexsero® Click Here Dengue Age 9-16 years living in endemic areas and have lab confirmed previous infection Dengvaxia® Click Here Covid COMIRNATY Gray Cap Click Here Home Page BACK TO TOP Inadequate Safety Testing

So what is in vaccines? 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 So what's in vaccines? Aborted Fetal Tissue Cells Aluminum Formaldehyde Thimerosal 2-Phenylethanol Polysorbate 80 Ingredients by vaccine & manufacturer Here I will look at some of the ingredients of vaccines. What their purpose is. Most importantly what potential adverse effects they might have on our health. Also, please watch the video below to get an inside look at how Maurice Hilleman, who is described as "one of the greatest microbiologists/ vaccinologists of all time", views the vaccine industry he helped create over six decades. View More on Maurice Hilleman Here " I think vaccines have to be considered the bargain-basement technology for the 20th century" -Maurice Hilleman What are the different types of ingredients in vaccines and what is their purpose? ADJUVANTS ANTIBIOTICS ANTIGENS INACTIVATING MATERIALS CELL CULTURE MATERIALS PRESERVATIVES STABALIZERS OTHER MATERIALS Adjuvants are ingredients put in vaccines in order to create an immune response in the body. To help keep outside germs and bacteria from growing in the vaccine. Weakened, Killed, or parts of a virus or bacteria. Added to vaccines in order to create an immune response to that specific substance. Antigens or viruses for the vaccines are grown in cell culture materials. This could be anything from eggs to human embryonic cells. Used to kill viruses or inactivate toxins Added to multi-dose vials of vaccines to prevent contamination. Added to vaccines to help the active ingredients in vaccines continue to work while the vaccine is made, stored, and moved. Stabilizers keep the active ingredients in vaccines from changing because of something like a shift in temperature where the vaccine is being stored. Residual substances not added to vaccines but left behind from the manufacturing process. Aborted Fetal Tissue Cells The use of aborted fetal tissue cells in the manufacture and production of vaccines is not uncommon. Vaccines currently in use that were developed using fetal cells include Hepatitis A, Rubella, Varicella, Zoste r, Adenovirus and Rabies. The use of fetal tissue in the production o f vaccines comes with an obvious religious issue for some but even for those who are not religious there are serious moral issues as well. Babies used are all 3 months or older gestation. In an interview published on LifeSite News for the pod cast, The John-Henry Westen Show, Pamela Acker who is an author and biologist states that “They will actually deliver these babies via cesarean section. The babies are still alive when the researchers start extracting the tissue; to the point where their heart is still beating, and they’re generally not given any anesthetic, because that would disrupt the cells that the researchers are trying to extract. So, they’re removing this tissue, all the while the baby is alive and in extreme amounts of pain. So, this makes it even more sadistic.” You'll often hear that the fetal cells used in vaccines come from two aborted babies from the 1960s, MRC-5 and WI-38. It is said or is made to sound as if these are the only two babies that were used or are used in the productions of vaccines. However, this is untrue. There are several other cell lines that have been made as backups or for research purposes. WI-38: Developed from the lung tissue of an aborted baby in 1962. The WI stands for Winstar Institute where the cell line was created, and 38 is because it was developed from the 38th fetus they used. MRC-5: Developed in 1965 from lung tissue of an aborted fetus HEK-293: From a baby aborted in 1973. HEK stands for Human Embryonic Kidney which means the cells came from the babies kidneys. This cell line was produced from the 293rd experiment done by Frank Graham. PER.C6: Produced from human embryonic retinal cells from an 18 week fetus aborted in 1985 Walvax-2: There were 9 aborted fetuses used to find the one with the best cell line to make vaccines from. The cells came from a 3 month female who was delivered in China using the "waterbag method" used to deliver the fetus intact. MRC-9: From the lungs of a female aborted in 1974 developed for research and as a back-up for vaccines. IMR-90: From the lungs of a female aborted in 1975 for research and related activities Publications that go into the details of how babies are delivered and used for research can be found here. Full deposition found here. In this clip from The Highwire you can hear Stanley Plotkin, The Godfather of Vaccines, discuss the use of aborted fetuses during a deposition by lawyer Aaron Siri. You can find the full interview here. Aluminum Aluminum Play Video Play Video Public Health Committee Public Hearing Play Video Play Video IS ALZHEIMER’S LINKED TO ALUMINUM EXPOSURE? Play Video Play Video IS ALUMINUM EXPOSURE LINKED TO AUTISM? Play Video Play Video CDC STUDY FINDS ALUMINUM IN VACCINES IS ASSOCIATED WITH ASTHMA The FDA states (a) The aluminum content of large volume parenteral (LVP) drug products used in total parenteral nutrition (TPN) therapy must not exceed 25 micrograms per liter ([micro]g/L). and must contain a warning label that reads, WARNING: This product contains aluminum that may be toxic . Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature , and they require large amounts of calcium and phosphate solutions, which contain aluminum. Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 [micro]g/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration. View More The math is calculated for us in 1,200 Studies - Examples of weight and corresponding maximum dose of aluminum per the FDA guidelines of 5 mcg per 2.2lb of body weight. 8lb baby = 18.16 mcg aluminum 15lb baby = 34.05 mcg aluminum 30lb toddler = 68.1 mcg aluminum 50lb child = 113 mcg aluminum 150lb adult = 340.5 mcg aluminum 350lb adult = 794.5 mcg aluminum Within hours of being born our babies are given a hepatitis B vaccine that contains 250mcg of aluminum. At 2 months old they receive another hepatitis B vaccine- 250mcg Rotavirus (RV)- 0mcg Diphtheria, tetanus, acellular pertussis- 500mcg-1,500mcg! Haemophilus influenzae type b (Hib)- 0mcg-225mcg Pneumococcal conjugate (PCV13)- 125mcg Inactivated poliovirus (IPV <18 yrs)- 0mcg OR combination vaccines such as DTaP, hepatitis B, and inactivated poliovirus vaccine- 850mcg DTaP, inactivated poliovirus, and Haemophilus influenzae type b vaccine- 1,500mcg DTaP and inactivated poliovirus vaccine- 500mcg-1,500mcg DTaP, inactivated poliovirus, Haemophilus influenzae type b, and hepatitis B vaccine- 319mcg At a MINIMUM an 8lb baby is getting approx. 14x the FDA limit of Aluminum on the first day of life, and 24x the FDA limit at 2 months old. Depending on the combination a baby can receive up to 115x the FDA limit in one day. This will be repeated at 4 months, and at 6 months. Acute exposure and chronic retention of aluminum in three vaccine schedules and effects of genetic and environmental variation Read More By Jefferey Jaxen STUDY: CDC VACCINE SCHEDULE LIKELY INDUCES ALUMINUM TOXICITY IN NEWBORNS Read More Learn more about the harms of Aluminum HERE. Formaldehyde The Center for Disease Control Describes Formaldehyde Formaldehyde (CH₂O) is a colorless, highly toxic, and flammable gas at room temperature. It is used in the production of fertilizer, paper, plywood, and some resins. It is also used as a food preservative and in household products, such as antiseptics, medicines, and cosmetics. Exposure to formaldehyde can irritate the skin, throat, lungs, and eyes. Repeated exposure to formaldehyde can possibly lead to cancer. Workers may be harmed by exposure to formaldehyde. The level of exposure depends upon the dose, duration, and work being done. See More Here A search on PubMed for "Formaldehyde adverse health effects" returned 1,124 articles Find Studies on Formaldehyde Here Vaccines that contain Formaldehyde Td (adult)/ DT DTaP (Daptacel®, Infanrix®) DTaP-Hep B IPV (Pediarix®) DTaP-IPV (Kinrix®, Quadracel®) DTaP-IPV-Hib (Pentacel®) Hepatitis A (Havrix®, Vaqta®) Hepatitis A - Hepatitis B (Twinrix®) Hib (ActHIB®, HIBERIX®) Hepatitis B (RECOMBIVAX®) Meningococcal vaccines Polio (IPOL®) Japanese encephalitis vaccine (IXIARO®) Tdap (ADACEL®, Boostrix®) Influenza Thimerosal From the FDA website, "Thimerosal, which is approximately 50% mercury by weight, has been one of the most widely used preservatives in vaccines. It is metabolized or degraded to ethylmercury and thiosalicylate. Ethylmercury is an organomercurial that should be distinguished from methylmercury, a related substance that has been the focus of considerable study. Methylmercury is the type of mercury found in certain kinds of fish. At high exposure levels methylmercury can be toxic to people. In the United States, federal guidelines keep as much methylmercury as possible out of the environment and food, but over a lifetime, everyone is exposed to some methylmercury." "Methylmercury is a highly toxic substance; a number of adverse health effects associated with exposure to it have been identified in humans and in animal studies. Most extensive are the data on neurotoxicity, particularly in developing organisms." Environmental Protection Agency (EPA) recommended guidelines for safe intake of methylmercury. Environmental Protection Agency (EPA) recommended guidelines for safe intake of methylmercury. Environmental Protection Agency (EPA) recommended guidelines for safe intake of methylmercury. Environmental Protection Agency (EPA) recommended guidelines for safe intake of methylmercury. 1/19 The FDA states, "Thimerosal has a long record of safe and effective use in preventing bacterial and fungal contamination of vaccines, with no ill effects established other than hypersensitivity and minor local reactions at the site of injection." and that, "There is a robust body of peer-reviewed, scientific studies conducted in the United States and countries around the world that support the safety of thimerosal-containing vaccines. The scientific evidence collected over the past 15 years does not show any evidence of harm, including serious neurodevelopmental disorders, from use of thimerosal in vaccines." However, the U.S. Environmental Protection Agency Chemical Assessment Summary shows that mercury does have developmental effects on children exposed in utero. Vaccines and Autism Play Video Politics of Thimerosal Play Video Rep Dan Burton Play Video Thimerosal Play Video Thimerosal Watch Now Share Whole Channel This Video Facebook Twitter Pinterest Tumblr Copy Link Link Copied Share Channel Info Close 1/3 The CDC says that thimerosal was removed from all childhood vaccines in 2001 . However, around the same time period they began recommending flu shots to every pregnant woman and also began giving flu shots to babies in two doses at 6 months followed by one dose annually . Not only has the safety of flu shots given during pregnancy never been established , about half of the flu shots on the market continue to use thimerosal as a preservative. The South Dakota Department of Agriculture & Natural Resources (DANR) Waste Management Program/Hazardous Waste Section,Management Guidelines for Vaccines Containing Thimerosal , describes the process for disposing vaccines that are expired or no longer usable. "State and federal hazardous waste regulations establish that any waste containing 0.2 milligrams per liter (mg/L) or more of mercury, as determined using the EPA-mandated Toxicity Characteristic Leaching Procedure (TCLP) , requires management as hazardous waste "as opposed to a non-hazardous pharmaceutical waste. This document goes on to state that some vaccines labeled “ preservative- or thimerosal-free ", " may contain trace amounts (less than or equal to 1 microgram/0.5 mL dose) because thimerosal was used during the manufacturing process". So a vaccicne labeled Preservative or thimerosal free may actually contain 1 microgram of thimerosal or 0.5 micrograms of Hg. Recommended upper limit of mercury intake "The FDA has proposed 0.4 µg per kg of body weight per day as the acceptable daily intake of methyl mercury, on the basis of the threshold at which paresthesia occurs in adults (11) . However, the foetus and infants are particularly susceptible to mercury toxicity, and long-term studies in Iraq have shown language delays among infants exposed to mercury (12) . On the basis of the findings of the Iraq studies, the Environmental Protection Agency lowered its reference dose for methyl mercury exposure to 0.1 µg per kg per day." Indian Journal of Medical Ethics February 15, 2017- Robert F. Kennedy Jr announced $100,000 challenge in which Children's Health Defense would pay $100,000 to the first journalist, or other individual, who could find a peer-reviewed scientific study demonstrating that thimerosal is safe in the amounts contained in vaccines currently being administered to American children and pregnant women. The challenge was open for submissions from February 15th, 2017 until August 15th, 2017. During that six month period not one submission was made that could assure the safety of injecting thimerosal into pregnant women, infants and children. You can see a summary of the research that was submitted along with a summary response from CHD HERE . Read More About Thimerosal & Autism Here 2-Phenoxyethanol Toxicity Summary Adverse Effects 2-Phenoxyethanol (PhE) has been shown to induce hepatotoxicity, renal toxicity, and hemolysis at dosages ≥ 400 mg/kg/day in subchronic and chronic studies in multiple species. The major hazards encountered in the use and handling of 2-phenoxyethanol stem from its toxicologic properties. Toxic by all routes (inhalation, ingestion, and dermal contact) , exposure to this very faintly aromatic, colorless, oily liquid may occur from its use as a fixative for cosmetics, perfumes, and soaps; as a bactericide and insect repellant; as a solvent for cellulose acetate,dyes, stamp pad, ball point, and specialty inks; as a chemical intermediate for carboxylic acid esters (eg, acrylate, maleate) and polymers (eg, formaldehyde, melamine); and as a preservative for human specimens used for dissection and demonstrations in anatomical studies. Effects resulting from exposure to this substance can include eye irritation, headache, tremors, and central nervous system depression . If contact with the eyes occurs, irrigate exposed eyes with copious amounts of tepid water for at least 15 minutes, and wash exposed skin thoroughly with soap and water. 2-Phenoxyethanol must be preheated before ignition can occur. Neurotoxin - Acute solvent syndrome Occupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation. Nephrotoxin - The chemical is potentially toxic to the kidneys in the occupational setting. Reproductive Toxin - A chemical that is toxic to the reproductive system , including defects in the progeny and injury to male or female reproductive function . Reproductive toxicity includes developmental effects . See Guidelines for Reproductive Toxicity Risk Assessment. Skin Sensitizer - An agent that can induce an allergic reaction in the skin. FDA Warns Consumers Against Using Mommy's Bliss Nipple Cream Product can be harmful to nursing infants Polysorbate 80 What is Polysorbate 80? Why is Polysorbate 80 in Vaccines? This description and explanation from TheDermReview.com explains Polysorbate 80 is produced by the ethoxylation of a molecule called sorbitan. Sorbitan is the dehydrated form of sorbitol, a sugar alcohol that can naturally be found in some fruits. Ethoxylation is a chemical reaction in which ethylene oxide is added to a substrate, in this case, sorbitan. Sorbitan is reacted with 80 units of ethylene oxide, which is where the 80 in polysorbate 80 comes from. Polysorbate 80 exists as a thick, water-soluble yellow liquid. Polysorbate 80 is also an emulsifier. As an emulsifier, polysorbate 80 is often used in formulations that contain both water and oil components. Mixing water and oil together creates a dispersion of oil droplets in water. However, the oil and water can separate if the product is left to settle. To address this problem, an emulsifier like polysorbate 80 can be added to help the droplets remain dispersed and so that the product remains mixed and doesn’t separate. Emulsifiers improve the consistency of a product, which enables an even distribution of the benefits of the key ingredients. Studies on the adverse effects of Polysorbate 80 According to the Material Safety Data Sheet from Merck, Polysorbate 80 seems to have very little hazards. Although, testing seems to be incomplete "Reproductive toxicity No data available Specific target organ toxicity - single exposure No data available Specific target organ toxicity - repeated exposure No data available Aspiration hazard No data available 11.2 Additional Information To the best of our knowledge, the chemical, physical, and toxicological properties have not been thoroughly investigated." Material Safety Data Sheet From 1,200 studies Vaccines that contain Polysorbate 80 DTaP (Infanrix) + aluminum DTaP IPV (Kinrix) + aluminum DTaP IPV (Quadracel) + aluminum DTaP Hep B IPV (Pediarix + aluminum DTaP IPV Hib (Pentacel) + aluminum HPV (Gardicil 9) + aluminum Influenza (Fluad) + squalene, neomycin, kanamycin Influenza (Fluarix) + b-propiolactone Influenza (Flulaval) + thimerosal Meningococcal (MenB-Tumenba) + aluminum Tdap (Boostrix) + aluminum Vaccines that contain Polysorbate 20 Hep A (Havrix) + aluminum Hep A/Hep B (Twinrix) + aluminum (2 types) Polysorbate 80 is not only found in vaccines. It serves a number of purposes and is found in many things. It is used as a surfactant in cosmetics and as an emulsifier in foods. It is also used to help drugs cross the blood brain barrier for the treatment of neurological disorders. The blood-brain barrier serves a filter, controlling which molecules can pass from the blood into the brain. Because the endothelial cells are positioned so closely together, they keep out any harmful toxins or pathogens from reaching your brain. In 1995 the first successful delivery of a drug across the blood brain barrier occurred using Polysorbate 80 to transport an anti-nociceptive peptide that cannot cross the BBB alone. This could be beneficial if your goal is to target the brain for a specific treatment. However, in the case of vaccines it can become problematic. Vaccines contain ingredients that intentionally illicit an immune response. Some of the ingredients are very toxic to the brain. While Polysorbate 80 is added to vaccines as an emulsifier it also still has the ability to not only cross the blood brain barrier but to help other substances cross the blood brain barrier as well. Home Page BACK TO TOP Risks Outweigh Benefits

By removing liability through NVICP & PREP Act, then making products mandatory we have created a very lucrative business model for vaccine makers.  There is no longer an incentive for manufacturers to invest in making their products safe. 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 There Is No Liability For Injuries. With most products on the market consumers have the ability to bring litigation against the manufacturer if that product causes injuries. If your seatbelt is faulty and you are injured in a crash because of it, you can sue the car manufacturer for those injuries This is true for any of the products that we as consumers buy and use. Despite Bidens claim that gun manufacturers are the only industry in America that can't be sued , even they can and have been sued. According to an article in Forbes, "Plaintiffs do not need to prove that the defendant acted negligently or intentionally in product liability cases. That’s because a legal doctrine called “strict liability” applies in these types of claims. Under strict liability rules, plaintiffs can prove their case and prevail in court if they simply show that the problem with the product was the direct cause of unexpected harm." In the medical industry you can sue if you are injured due to physician negligence, or faulty medical devices . For example, thousands of lawsuits have been filed against manufacturers who made metal on metal hip replacements . More than $7 Billion has been paid out in settlements for these lawsuits. If you are injured due to taking a medication you can sue the pharmacuetical companies. Currently there are over 13,000 open lawsuits in New Jersey for those injured by proton pump inhibiters such as prilosec. Claims allege that companies failed to warn consumers about the drugs potential risks of kidney failure, kidney disease , and other injuries . Having the ability to file a lawsuit for injuries is important for a number of reasons. The thing that usually comes to mind for people is the financial compensation that those who are injured may need for medical bills, missed work, and compensation for pain and suffering. Another important part of litigation is that it creates a system in which manufacturers must search for and produce products that are safe for their own survival. It gives them an incentive to invest into the safety of their products or face litigation that could potentially bankrupt the company. The incentive to invest money into safety is reduced greatly when a company understands that they do not have to be accountable for damages. However, a company may still consider safety testing important if they want consumers to purchase their products. With vaccines, consumers are required to take this product to enter schools and daycares. Often they must continue to get vaccines as adults to work in certain career fields. By removing liability and then making the products mandatory for every person in the country we have created an extremely lucrative business model for manufacturers. There is no longer an incentive for manufacturers to invest in making their products safe. Why Is There No Liability For Vaccine Manufactureres? The National Vaccine Injury Compensation Program (NVICP) The National Vaccine Injury Compensation Program (NVICP) was establised by congress in 1986 as a no-fault alternative to the traditional legal system. Prior to this there were concerns that potential liablity for injuries caused by vaccines threatened the vaccination program and acted as a deterrant to vaccine manufacturing. The United States was facing a vaccine shortage that was thought to threaten public health. These concerns led to the establishment of The Committee on Public-Private Sector Relations in Vaccine Innovation by the Institute of Medicine in 1983. The committee was asked to do a comprehensive study of vaccine research and development, production and supply, and utilization. Their report and reccommendations were published in 1985. You can find that full report HERE. In their report they state that, "A manufacturer is not liable for harm caused by a nondefective product due to its inherent or unavoidable dangerousness . Thus, if a properly manufactured vaccine will cause harmful side effects in some portion of the recipient population, the manufacturer of the vaccine is not liable for those side effects." They go on to state that some products are " Unavoidably unsafe products. There are some products which, in the present state of human knowledge, are quite incapable of being made safe for their intended and ordinary use. " The report notes that those injured by vaccines should recieve compensation and that the traditional legal system can be complex, expensive and time consuming. Therefore, the committee recommends the development of a compensation program where claims should be processed without regard to "fault". They recommend the establishment of a schedule of events for which scientific evidence indicates a plausible association with vaccination. The goal of the NVICP was to encourage investment in vaccine development and manufacturing and to compensate those who are injured in a timely mannor. The program seems to have been effective at encouraging vaccine development. With the threat of liability off the table the vaccination program has exploded. In 1986 children recieved 12 doses of 8 vaccines. In 2023 we are up to 58 doses of 18 vaccines from birth-18 years, plus 2 injections for 4 vaccines in-utero. This chart from Children's Health Defense shows vaccine schedules from 1986 compared to 2019. We have since added 3 doses of Covid-19 vaccinations to the schedule. However, the program has not been as successful when it comes to making sure those who are injured are compensated for their injuries. The program has a table of covered vaccines and injuries that will qualify for compensation if they fall within a certain time frame of being vaccinated. For injuries that are not listed on the table the burden of proof lies with the petitioner. The program also has a very strict time limit of 3 years from the time of injury to file a claim. Since 1988 there have been 25,961 claims filed and 9,664 of those were compensated. Considering there have been 2,439,553 reports of injury to VAERS following vaccination , and that a report by Harvard Pilgrim Health noted, "fewer than 1% of vaccine adverse events are reported" to VAERS , there seems to be a very small number of individuals with injuries actually filing a claim with the NVICP. (See What Is VAERS?) The program has also not been a timely process for petitioners. A report from the U.S. Government Accountability Office looked at the data for claims filed between 1999-2014 and found that most claims took multiple years to process. View More "Every year, a number of children are seriously injured by adverse reactions to vaccines. When such a tragedy befalls a family, they are faced with devastating emotional and financial consequences. As the devastation of adverse reactions can lead to paralysis, permanent disability and death, families without adequate insurance can face enormous expenses, including residential care, therapy, medical equipment, and drugs." -COMMITTEE ON GOVERNMENT REFORM, SIXTH REPORT Public Readiness and Emergency Preparedness Act (PREPA) The Public Readiness and Emergency Preparedness Act (Prep Act or PREPA) was enacted by Congress in 2005. Health & Human Services describes the PREP Act on their website , "The Public Readiness and Emergency Preparedness Act (PREP Act) authorizes the Secretary of the Department of Health and Human Services (Secretary) to issue a PREP Act declaration. The declaration provides immunity from liability (except for willful misconduct) for claims: of loss caused, arising out of, relating to, or resulting from administration or use of countermeasures to diseases, threats and conditions determined by the Secretary to constitute a present, or credible risk of a future public health emergency to entities and individuals involved in the development, manufacture, testing, distribution, administration, and use of such countermeasures A PREP Act declaration is specifically for the purpose of providing immunity from liability, and is different from, and not dependent on, other emergency declarations." Immunity means that courts must dismiss claims brought against any entity or individual covered by the PREP Act. Claims that courts must dismiss include claims for any loss that is related to any stage of design, development, testing, manufacture, labeling, distribution, formulation, labeling, packaging, marketing, promotion, sale, purchase, donation, dispensing, prescribing, administration, licensing or use of a countermeasure recommended in a Declaration. This includes, but is not limited to, claims for: death; physical, mental, or emotional injury, illness, disability, or condition or fear of any such injury, illness, disability, or condition; any need for medical monitoring; or property damage or loss, including business interruption loss. The only exception is for claims of willful misconduct. From the U.S. Department of Health & Human Services A Declaration may provide liability immunity for covered persons. Covered persons may include, at the Secretary’s discretion: Manufacturers of countermeasures; Distributors of countermeasures; Program planners , i.e., individuals and entities involved in planning, administering, or supervising programs for distribution of a countermeasure (e.g., State or local governments, Indian tribes, or private sector employers or community groups that establish requirements or provide guidance, technical or scientific advice or assistance, or provide a facility); Qualified persons, i.e., persons who prescribe, administer, or dispense countermeasures such as healthcare and other providers or other categories of persons named in a Declaration, e.g., volunteers; Officials, agents, and employees of any of these entities or persons; and The United States. A “covered countermeasure” may be: A qualified pandemic or epidemic product ; A security countermeasure ; An unapproved drug , biological product , or device used under an Emergency Use Authorization (EUA) issued by FDA; An approved drug , biological product , or device used pursuant to Federal law in conditions that are in consistent with its approval ; or An unapproved drug , biological product , or device , or an approved drug, biological product , or device intended for an unapproved use, that is intended for emergency use and shipped and held by a government agency or someone working on that agency’s behalf for use only when that use is authorized. The PREP Act states that those who are seriously injured, described as an injury that warranted hospitalization (whether or not the person was actually hospitalized) or that led to a significant loss of function or disability, by a declared countermeasure may file a claim with the Countermeasures Injury Compensation Program (CICP) within one year of the injury. " If no funds have been appropriated to the compensation program, or the Secretary does not make a final determination on the individual’s request within 240 days, or the individual decides not to accept the compensation, the injured individual or his representative may pursue a tort claim in the United States District Court for the District of Columbia, but only if the claim involves willful misconduct and meets the other requirements for suit under the PREP Act . If the individual accepts compensation from the CICP, or if there is no willful misconduct, the individual does not have a tort claim that can be filed in a United States Federal or a State court. Any award is reduced by public or private insurance or worker’s compensation available to the injured individual. Awards for non-economic damages, such as pain, suffering, physical impairment, mental anguish, and loss of consortium are also limited ." CICP may compensate for medical expenses, lost employment income, and survivors benefits. However, it is a last resort and will only pay for expenses that are not compensated by other means such as health insurance and workmans comp. Unlike the NVICP, the CICP will not cover lawyer fees. Since 2010 there have been only 30 claims compensated through the CICP CICP Data for Fiscal Years 2010 – 2023 (As of March 1, 2023) Total CICP Claims Filed: 11,765 Pending Review or In Review: 10,629 Decisions: 1,136 Claims Found Eligible for Compensation: 61 Claims Compensated: 30 Claims Pending Benefits Determination: 21 Claims with No Eligible Reported Expenses: 10 Denied: 1,075 Requested Medical Records Not Submitted: 182 Standard of Proof Not Met and/or Covered Injury Not Sustained: 324 Missed Filing Deadline: 248 Not CICP Covered Product/Not Specified: 321 There Is Also No Mandated Reporting For Injuries In a research project conducted by Harvard Pilgrem Health over a span of three years and funded by a grant from Health and Human Services, it was noted that "fewer than 1% of vaccine adverse events are reported. " The team at Harvard Pilgrem Health developed a way to electronically monitor medical records and notify physticians of possible adverse events following reciept of vaccinations. This would prompt the physician to review the records and submit the event to the VAERS system, along with any optional notes or to note in the record reasons for not submitting to VAERS. The team concludes that after three years of collecting data and development of the automated system they were unable to move forward with implementing the program, "Unfortunately, there was never an opportunity to perform system performance assessments because the necessary CDC contacts were no longer available and the CDC consultants responsible for receiving data were no longer responsive to our multiple requests to proceed with testing and evaluation." More information can be found HERE One report describes VAERS as a spontaneous surveillance system and explains, " Spontaneous surveillance means that no active effort is made to search for, identify and collect information, but rather information is passively received from those who choose to voluntarily report their experience. Therefore, VAERS relies on the intuition and experience of healthcare professionals in particular, but likewise for patients, parents and caregivers, to recognize and report unusual or unexpected events following vaccination or suspected vaccine safety problems. " This same report notes that, "During 2011-2014, VAERS averaged around 30,000 U.S. reports annually, with 7% classified as serious." If VAERS is only representiong 1% of adverse events that would mean the number of actual adverse events during that 3 year period was closer to 3,000,000 annually with about 210,000 a year being serious. Some might say that is a small number compared to the number of vaccine doses administered each year, but when its your child who is injured the number isn't small at all. Another important point to consider is "Vaccines are generally given to healthy individuals to prevent disease, whereas drugs are primarily given for treatment of illness. Sick patients, or parents of sick children, might be more willing to accept safety risks of drugs used to treat illnesses compared to vaccines used to prevent possible future illnesses." 210,000 serious injuries a year starts to seem like a lot when you consider many of these injuries happened in perfectly healthy children. Looking back on our own personal experience my son was seen in urgent care 3 times in the 30 days following his first round of vaccines. None of these visits were reported to VAERS. Not one of the doctors, nurses, or other medical professionals (such as those at the WIC office or our public healt h nurse who came out to visit us weekly) ever mentioned that vaccines could have been related to the issues we were having. Sadly, I was unaware that it was even possible for vaccines to cause these problems. Then dealing with a sick baby who would not eat or sleep and screamed non-stop, I was sleep deprived and stressed out and not able to see clearly the connection that is so obvious to me when looking back. Whether is was caused by the vaccine or not those urgent care visits should have been reported to VAERS so that it could be used to look for signals. If there are a high number of urgent care visits with similar complaints following the same vaccinations that would raise a flag for our regulatory agencies to look at it further. If things are not reported then they can't find possible connections. Home Page BACK TO TOP The Vaccine Inserts

The CDC states that, "Vaccines do not cause autism."  What evidence do they use to make that claim?  It goes on further to state that, "Some people have had concerns that ASD might be linked to the vaccines children receive, but studies have shown that there is no link between receiving vaccines and developing ASD." 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 Autism Vaccines Do Cause Autism >>> What Evidence Is Used To Conclude That Vaccines Do Not Cause Autism? The CDC website states that, "Vaccines do not cause autism." What evidence do they use to make that claim? It goes on further to state that, "Some people have had concerns that ASD might be linked to the vaccines children receive, but studies have shown that there is no link between receiving vaccines and developing ASD. The National Academy of Medicine, formerly known as Institute of Medicine, reviewed the safety of 8 vaccines to children and adults. The review found that with rare exceptions, these vaccines are very safe." I have linked the report from the IOM below. Using the search tool at the top of the report I did a search for the word "autism" which made it easy to find each instance autism is referenced in the report. Quickly I could see that the statement made by the CDC was deceptive and misleading . Again, the statement made by the CDC is that the IOM reviewed the safety of 8 vaccines . However, the IOM only looked at the evidence available for two vaccines in relationship to autism. The committee reviewed 22 studies to evaluate the risk of autism after the administration of MMR vaccine . Twelve studies were not considered due to passive surveillance data used in the studies. Six studies were not considered due to "very serious methodological limitations". Based on the FOUR remaining studies IOM determined "The evidence favors rejection of a causal relationship between MMR vaccine and autism ". The IOM also looked at a possible relationship to DTaP vaccines and autism. The committee reviewed ONE study to evaluate the risk and the study "was not considered in the weight of epidemiologic evidence because it provided data from a passive surveillance system and lacked an unvaccinated comparison population." The IOM concluded that, "The epidemiologic evidence is insufficient or absent to assess an association between diphtheria toxoid–, tetanus toxoid–, or acellular pertussis–containing vaccine and autism." Further misleading the CDC stated that according to this review, "with rare exceptions, these vaccines are very safe" . When in fact the IOM reviewed available literature for 158 of the most common injuries thought to be related to vaccination, in which they found the science “ 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 was unable to find sufficient evidence to conclude or deny the relationship of 135 other serious injuries. Institute of Medicine Report The second reference used by CDC to support their claim that VACCINES DO NOT CAUSE AUTISM is a CDC study published in 2013 that focused on the number of antigens received during the first two years of life. They concluded that, " increasing exposure to antibody-stimulating proteins and polysaccharides in vaccines during the first 2 years of life was not related to the risk of developing an ASD. " This study in no way evaluates whether VACCINES cause autism. They don't look at how many vaccines each child received or which vaccines. Antigens have never thought to have been the issue in regards to autism and vaccines. Using this study on their website as proof that VACCINES do not cause autism is an insult to our intellegence. It also shows the CDCs overall lack of concern about children and families who are impacted by autism. If they wanted to prove that vaccines do not cause autism once and for all they would use the data they already have on millions of Americans and they would compare the rates of autism in the vaccinated against the rates in the un-vaccinated. They refuse to do this study, and have gone a step further by moving these records into a private company making it impossible for anyone else to access these records. Why? If they truly believe that VACCINES do not cause autism, why not do the study on vaccinated vs completely unvaccinated and end the debate once and for all??? I am not able to say the intentions of others but it certainly feels like they actually don't truly believe vaccines do not cause autism. It seems as though they care more about protecting the vaccine program and pharma profits, than they do about 1 in 44 kids who are having their chance at a normal life stolen from them. CDC Study on Autism & Antigens These are the only studies referenced on the CDC website in support of the claim that VACCINES DO NOT CAUSE AUTISM. They only reference TWO vaccines. One of which, DTaP, the report could neither acce pt OR deny a relationship between the vaccine and autism. THIS IS PATHETIC. But lets see what else they have to say. CDC goes on to state that, " vaccine ingredients do not cause autism". Lets look at the research they have used to support that statement. The first reference they use to support that claim is a 2004 scientific review by the IOM that concluded “the evidence favors rejection of a causal relationship between thimerosal–containing vaccines and autism.” In the review the IOM describes the five studies used to make that conclusion. 1. Hviid et al., 2003; Association between thimerosal-containing vaccine and autism Compared autism rates in those who received vaccines containing thimerosal with those that received thimerosal free vaccines. The mean age of diagnosis was 4.7 years old. However, the study included cases and controls as young as 1 years old . Meaning many of the subjects would later go on to receive an autism diagnosis . Also, instead of counting "persons" the authors counted "person-years of follow-up" meaning each age group was considered equially despite the fact that younger age groups were much less likely to have been diagnosed with autism as those in older groups. 2. Miller, 2004; Thimerosal exposure in infants and developmental disorders: a retrospective cohort study in the United kingdom does not support a causal association A retrospective cohort study completed using records from a database in the United Kingdom, where autism prevalence rates were compared for children receiving Thimerosal-containing DTaP and DT vaccines. Numerous statistical errors by correlating thimerosal exposure with year of birth. The authors of this study never released the raw data so that a valid single-variable analysis could be conducted to ascertain the probability of an association between Thimerosal exposure and the risk of autism. Also important is that the amount of thimerosal exposure in the UK was not comparable to that in the United States where children were getting larger exposures during younger periords of life. 3. Verstraeten et al., 2003 Safety of thimerosal-containing vaccines: a two-phased study of computerized health maintenance organization databases A cohert analysis of records from the Vaccine Safety Datalink done by the CDC. This study had at least 5 phases. Results from the first phase showed that infants who were exposed to greater than 25𝜇g of Hg in vaccines and immunoglobulins at the age of one month were 7.6 times more likely to have autism diagnosis than those not exposed to any vaccine-derived organic Hg. The second phase they compared exposure from 3 months old instead of one month and found that children exposed to the maximum amount of organic Hg in infant vaccines (62.5𝜇g) were 2.48 times more likely to have autism diagnosis compared to those exposed to less than 37.5𝜇gof Hg in vaccines. The third phase used different inclusion/exclusion criteria stratisfying the data the relative risk of autism for children at three months of Thimerosal exposure dropped to 1.69. The fourth and fifth phase of the study used records from only two of the original HMOs and incorporated a third HMO, Harvard Pilgrim, into the analysis. The HMO used different diagnostic codes and in this study they included children from 0-3 years old even though the average age of autism diagnosis was 4.4 years. There was a lot of contraversy around the Verstraeten study. Emails obtained through FOIA requests show that Verstraeten was receiving pressure from the CDC to use methods to deny a casual relationship between thimerosal and autism. 4. Madsen et al., 2003; Thimerosal and the occurrence of autism: negative ecological evidence from Danish population-based data CDC sponsored study that looked at whether discontinuing the use of thimerosal in vaccines in Denmark lead to a decreased rate of autism. The study examined the data from 1971 to 2000 and reported that rate of autism increased with the removal of Thimerosal from vaccines starting in 1992. However, autism rates only included those who were diagnosed in an inpatient setting from 1971-1994. In 1995 the inclusion of those diagnosed in an outpatient setting were added . The authors state that the outpatient setting had 4-6x that of the inpatient . In a previous publication the same authors using the same data reported 93.1% of children were treated only as outpatients. The inclusion of the outpatient population would explain why the numbers of autism cases continued to rise after phase out of thimerosal. Also inflating the numbers was the inclusion of a large clinic in the dataset starting in 1993. This clinic accounted for as many as 20% of a utism patients nationwide. Last, the diagnostic criteria for autism changed in 1994 resulting in an increased incidence by up to 25x what it was using previous diagnostic criteria . 5. Stehr-Green et al., 2003; Autis m and thimerosal-containing vaccines: lack of consistent evidence for an association Compared the prevalence/incidence of autism in California, Sweden, and Denmark with average exposures to thimerosal containing vaccines. This study used the same data from Denmark as the previous study. There was an artificial increase in autism rates by 20x following removal of thimerosal due to inclusion of outpatients starting in 1995 , the inclusion of a large clinic accounting for 20% of cases in 1993, change in diagnostic criteria in 1994. This study also used data from Sweden but looked at only inpatient cases of autism counting only a small portion of the actual cases of autism. Also, children in Sweden received a maximum 75 micrograms of Hg by age two. Children in California received up to 237.5 micrograms of Hg by 18 months. T his same report by the Institute of Medicine also states that, "Absent biomarkers, well-defined risk factors, or large effect sizes, THE COMMITTEE CANNOT RULE OUT , based on the epidemiological evidence, the possibility that vaccines contribute to autism in some small subset or very unusual circumstances." Your can veiw the IOM report H ER E . Read more about the flawed methods and manipulation of data- Methodological Issues and Evidence of Malfeasance in Research Purporting to Show Thimerosal in Vaccines Is Safe Study Misses Link Between Thimerosal and Neurodevelopmental Disorders Letter to the Editor M. Geier , D. Geier; Published 2004; Medicine Summarized conflict of interest issues, manipulated data, and suppression of initial findings in the Verstraeten study. Read It Here "Since 2003, there have been nine CDC-funded or conducted studies that have found no link between thimerosal-containing vaccines and ASD. These studies also found no link between the measles, mumps, and rubella (MMR) vaccine and ASD in children." 1 Thimerosal exposure in early life and neuropsychological outcomes 7-10 years late Ֆ Barile JP, Kuperminc GP, Weintraub ES, Mink JW, Thompson WW Conflicts & Issues- Overmatching phenomena meant that cases and controls had very little difference in thimerosal exposure. More Info 2 Prenatal and Infant Exposure to Thimerosal From Vaccines and Immunoglobulins and Risk of Autism Price CS, Thompson WW, Goodson B, Weintraub ES, Croen LA, et al. Conflicts & Issues: Overmatching phenomena meant that cases and controls had very little difference in thimerosal exposure. Prenatal thimerosal effect was hidden by cherry-picking data. More Info 3 Neuropsychological Performance 10 Years After Immunization in Infancy With Thimerosal-Containing Vaccines Tozzi AE, Bisiacchi P, Tarantino V, De Mei B, D’Elia L, et al. Conflicts & Issues: Study was completed using Italian vaccine schedule with much lower thimerosal exposure than U.S. schedule. No zero exposure control was use. More Info 4 Thimerosal-containing vaccines: evidence versus public apprehension DeStefano F. Destefano relied on flawed epidemiology studies from the U.K. and Denmark which follow different vaccination schedules compared to the U.S. Data from California show clear correlation between thimerosal uptake and autism incidence. More Info 5 Inactivated influenza vaccine (IIV) in children <2 years of age: Examination of selected adverse events reported to the Vaccine Adverse Event Reporting System (VAERS) after thimerosalfree or thimerosalcontaining vaccine McMahon AW, Iskander JK, Haber P, Braun MM, Ball R. The definition of an adverse event was limited to site reactions and fever. No data were collected regarding any type of neurological outcome. More Info 6 Early Thimerosal Exposure and Neuropsychological Outcomes at 7 to 10 Years Thompson WW, Price C, Goodson B, Shay DK, Benson P, et al Overmatching phenomena meant that cases and controls had very little difference in thimerosal exposure. More Info 7 Safety of Thimerosalcontaining vaccines: a two-phased study of computerized health maintenance organization databases Verstraeten T, Davis RL, DeStefano F, Lieu TA, Rhodes PH, et al Effects were diluted through five separate iterations of the study. Numerous exclusion criteria were erroneously applied and data cherry-picking was done to dilute statistically significant effects. More Info 8 Autism and thimerosalcontaining vaccines: lack of consistent evidence for an association Stehr-Green P, Tull P, Stellfeld M, Mortenson PB, Simpson D. Wrongfully dismissed autism rates in California as inclusion of milder ASD cases to obviate the rise in cases. More Info 9 Autism and thimerosalcontaining vaccines: lack of consistent evidence for an association Stehr-Green P, Tull P, Stellfeld M, Mortenson PB, Simpson D There was an artificial increase in autism rates by 20x following removal of thimerosal due to inclusion of outpatients starting in 1995 , the inclusion of a large clinic accounting for 20% of cases in 1993, change in diagnostic criteria in 1994 . More Info BACK TO TOP

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

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