I've spent countless hours working on this website. Every spare minute I had for months, because once I got started I was anxious to get it to a point where I could share it. Once I felt I had gotten to that point I took a break from it to work on other projects. I still have several pages to do on the website, covid vaccine, other effective treatments, and kids are sicker than ever. I also have some work to do on some of the published pages. One of the big things is explaining WHAT exactly autism is in laymen terms. I'm doing a lot of reading to understand the biological mechanisms and I want to have a good understanding of it before I write this part of the website. I'm also planning on adding resources for families who have autistic children and resources for those looking for information on vaccine exemptions as well as how people can help keep or expand the rights for exemptions in their state. Thankfully in Minnesota we currently have a conscientious exemption. Most people don't even know this is an option and they vaccinate their kids in order for their kids to go to school. I want to help people feel confident standing their ground for what they believe and knowledge is power! If you know the facts about vaccination and the facts about the laws in your state you are less likely to be pressured or coerced into making a decision you don't feel comfortable making. I've also made a planner, specifically for parents of autistic children. It has sections to keep your calendars, school information, medication information, therapy information, diet information, etc. It also has places to track behaviors and sleep and other things because once you track things you can typically find patterns of things that trigger the behaviors we want to minimize. I haven't figured out how I can distribute the planners yet but I'm working on possibly putting the pdf version on Etsy or publishing through Amazon. Unfortunately, I haven't found a cost effective way to print and distribute the planner in a way where you can just refill certain sections, like the calendar, without having to replace the whole book since some information will stay the same. If anyone has any ideas for this please let me know! I am really proud of the work that I've done to make this and I hope people find it useful and informative. If you have any suggestions for me on things to change or add I'd love to hear about it. Happy Sunday Everyone!

I once had someone tell me that vaccines were safe and I just needed something to blame my sons autism on. This person has no idea. Unfortunately, most people won't see the truth until they are personally affected by it. A sort of cognitive dissonance takes over and we refuse to see the evidence that is right in front of us. I had doubts about vaccinating my son. I even had a couple of people hint at the idea that vaccines might be harming him, though no one ever flat out said it. I wish I had listened to my gut. I wish someone would have told me that there ARE harms associated with vaccinating and that there are hundreds of studies that prove it. That the issues we were seeing were possibly being caused by vaccines. I wish I would have known. So many parents live in this regret. It is heartbreaking and impossible to understand unless you've experienced it. Unless you have seen your child disappear like so many parents have. A child who spoke stopped speaking, a child who was always happy stopped smiling. Unless you have seen your child struggle to speak, or refuse to eat for weeks, or bang their head against the floor because they are having a meltdown that they cannot control. Unless you have experienced your child completely fall apart in the backseat of your car, thrashing and screaming, trying to hit you while tears stream down their face, because you went out the wrong side of the parking lot when leaving Target.... You just can't possibly understand. You could not know that we would give anything to be able to go back and make a different choice. It is not an easy thing to carry, the guilt. But we have no options but to keep going forward. Because once you have a child with disabilities, with a future of uncertainty, it becomes critical that you, Keep. Moving. Forward. The fears of what will happen to them when we are gone. Who will take care of them if we aren't here? It's all very heavy. It weighs even heavier knowing that it didn't have to be this way. I think most parents would agree with me when I say that I would rather it have been a genetic issue. This was just the way it is and nothing I could have done differently would have changed it. To know that my son could have had a normal life. That he didn't have to go to therapy 5 days a week when he was only 2 years old. That he didn't have to be so sensitive that at times it was unbearable to leave the house because the SOUND of OUTSIDE was too much for him. To know these struggles could have been avoided if I would have refused the Hepatitis B vaccine because it was only safety tested for 5 DAYS! Not even in babies who were just born but in adults. Also because he has a 0% chance of getting Hepatitis B at this point in his life and studies have shown that boys vaccinated with the Hepatitis B vaccine in the first month of life have a 3 fold higher risk of autism than boys who aren't vaccinated until after one month. If I would have refused the rotavirus vaccine because most babies (who are the only ones at risk of dying from rotavirus) are protected against rotavirus with breastfeeding. Or because in the vaccine trials which compared the vaccine to the vaccine minus the antigen, 1 in 30 to 1 in 40 control group participants suffered a severe medical event. 43 infants in the Rotarix trial died and 20 died in the RotaTeq trials. If I would have refused the DTaP vaccine because Diphtheria mortality rate dropped 87% before the vaccine for Diphtheria was used extensively and, that the antitoxin used to treat diphtheria since 1891 has a clinical efficacy of 97%. Whereas "receipt of 3 doses of diphtheria toxoid vaccine is 87% effective against symptomatic disease and reduces transmission by 60%. Vaccinated individuals can become colonized and transmit; consequently, vaccination alone can only interrupt transmission in 28% of outbreak settings, making isolation and antibiotics essential." Because Tetanus rates have always been rare, with 500-600 cases annually before vaccine. Among all persons with reported tetanus, from 2001-2008 the CDC states that "in the multivariable model, comparing age ≥65 years versus <65 years, diabetes versus no diabetes, and no doses of vaccination versus 1 dose, neither diabetes nor vaccination were statistically significant" Because It has been shown in a study exposing baboons to pertussis, that those who were vaccinated previously carried the bacterium for 5 days longer than the unvaccinated baboons, and were able to infect other baboons with the bacterium. Whereas, the baboons who had previously been infected by pertussis were not able to spread the bacterium to other baboons following re-exposure. If I would have refused the Hib vaccine because death rates from Hib were 1 in 2 million prior to the vaccine. Also because studies show that vaccination with the Hib vaccine may induce diabetes related autoantibodies. My dad was the only diabetic in our family. He was diagnosed with type 1 diabetes after getting very sick following a vaccination he received at age 12. If I would have refused the Pneumococcal vaccine which protects against 13 of the 90+ different serotypes. In the clinical trials there were 18 fewer cases than expected of Pneumococcal infection but almost 1,200 infants in the vaccine group had emergency room visits and 500 were hospitalized. And finally, if I would have refused the polio vaccine, one of which causes more cases of polio than wild type polio itself, and because the other states in the vaccine insert, "Although no causal relationship has been established, deaths have occurred in temporal association after vaccination of infants with IPV." If I had taken the time to look into vaccines, just as we take the time to look into what vehicles are most reliable before purchasing a new car, or what brands give the clearest picture and best sound before purchasing a new TV, I would have known. I could have changed the course of my sons life if I had just known. So what I say to the person who thinks I am looking for something to blame my sons autism on is, you're wrong. As parents we would give our lives for our kids. So as a parent, try to imagine that you could have protected your child from something that would cause them lifelong harm but you didn't. You were supposed to be the voice for your child because your child could not speak up for themselves. If they could they might have told you that their brain was on fire. You didn't protect them from this harm and now you have to live with that. Watching your child struggle everyday as a constant reminder. Why would we choose to blame our child's pain on something WE could have protected them from? If parents were looking for something to blame their child's autism on, I can assure you we wouldn't pick this.

This will be an ongoing post with resources I've found helpful throughout my journey of learning. Check back for updates! Powerful & Informative Documentaries Trace Amounts- Autism, Mercury, and The Hidden Truth (1hr33min) After recovering from a devastating sickness that brought him to the edge of despair, Eric Gladen would quit his career, move into an RV, and travel the country for years trying to piece together one of the biggest childhood epidemics of all time. This investigative documentary tackles the science and controversies around autism and the mercury based preservative used in vaccines. https://www.michaelfosterfilms.com/traceamounts VAXXED - FROM COVER UP TO CATASTROPHE (2016) (1hr30min) Interviews with pharmaceutical insiders, doctors, politicians, and parents of vaccine-injured children reveal an alarming deception that has contributed to the skyrocketing increase of autism and potentially the most catastrophic epidemic of our lifetime. Buy or Rent Here- https://vaxxedthemovie.com/watch/ Watch free on Bitchute- https://www.bitchute.com/video/WBzD7RKTmYlv/ Vaxxed II: The People's Truth (2019) (1h30min) In 2016, a media firestorm erupted when Tribeca Film Festival abruptly censored its documentary selection, VAXXED: FROM COVER-UP TO CATASTROPHE, amid pressure from pro-pharmaceutical interests. In response to media silence on CDC whistleblower, Dr. William Thompson, who admitted to fraud on a pivotal vaccine safety study, VAXXED catapulted to notoriety and became a worldwide trending topic, opening to sold out theater audiences nationwide. Stunned by the immense volume of parents lining up outside the theaters with vaccine injury stories to share, VAXXED producer Polly Tommey began to livestream worldwide reaching millions, and a community that had once been silenced were empowered to rise up. In VAXXED II: THE PEOPLE'S TRUTH, Polly and the team travel over 50,000 miles in the USA and around the world. Interviews of parents and doctors with nothing to gain and everything to lose exposed the vaccine injury epidemic and asked the question on every parent's mind, "Are vaccines really as safe and effective as we've been told?" Buy or Rent Here- https://www.vaxxed2.com Watch free on Bitchute- https://www.bitchute.com/video/KzREp2RwrMn5/ 'Vaccine Secrets’: What Parents Should Know Before They Vaccinate Their Kids (2021) (22min) “Vaccine Secrets,” an animated video created by parents of vaccine-injured children, fact checks the many statements used to convince parents that vaccines are safe and effective. https://childrenshealthdefense.org/defender/vaccine-secrets-parents-should-know-before-vaccinate/ Who is Bill Gates? (Full Documentary, 2020) (2h5m) Part One: How Bill Gates Monopolized Global Health Part Two: Bill Gates' Plan to Vaccinate the World Part Three: Bill Gates and the Population Control Grid Part Four: Meet Bill Gates https://www.corbettreport.com/gates/#part2 Websites PubMed PubMed® comprises more than 35 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to full text content from PubMed Central and publisher web sites. https://pubmed.ncbi.nlm.nih.gov National Vaccine Information Center NVIC is dedicated to preventing vaccine injuries and deaths through public education and securing informed consent protections in public health policies and laws. NVIC has a lot of great educational information and links to other helpful resources. The most unique thing about NVIC is the Advocacy Portal. By signing up to be a user of the free online Advocacy Portal, you will be able to directly contact YOUR lawmakers through your smart phone, tablet or computer. Once registered, you will receive action alerts for your state. They also have tips on how to talk to your legislators. https://www.nvic.org/resources/frequently-asked-questions/protecting-expanding-exemptions The Highwire Del Bigtree is one of the preeminent voices of the vaccine risk awareness movement around the world. He is the founder of the non-profit, Informed Consent Action Network, and host of a rapidly growing internet talk show The HighWire, boasting over 33 million views to date. Del’s multi-pronged approach incorporates legal, legislative, and media actions to expose the fraud, lies, and conflicts of interest that have allowed the pharmaceutical industry to evade standardized safety testing for vaccines. When you sign up for their news letter you'll receive an email following each weekly broadcast with all of the science and articles discussed that week. You can also find editorials, white papers, and information on current and previous lawsuits. https://thehighwire.com/ More information on lawsuits, FOIAs, legal letters, scientific and education resources from the nonprofit that supports the Highwire https://icandecide.org/get-informed/ Children's Health Defense The Defender is Children’s Health Defense’s news and views website. It features content aligned with the organization’s mission to end childhood health epidemics.The Defender provides open, honest discussion about issues systematically ignored by the majority of media outlets, either because the topics are considered taboo, or because corporate advertisers are allowed undue influence over content. The Defender is a unique platform for frank, civil, nonpartisan discussions of evidence-based science and medicine. The site hosts a space where writers of every viewpoint may safely air contrary science-based views. There are many videos, podcasts, interviews. Along with information on legal actions, current events, educational information. https://childrenshealthdefense.org/?_ga=2.37390816.1541660914.1675902055-1520254113.1675238519&_gl=1 Physicians For Informed Consent Physicians for Informed Consent is a 501 (c)(3) nonprofit organization focused on science and statistics. PIC delivers data on infectious diseases and vaccines, and unites doctors, scientists, healthcare professionals, attorneys, and families that support voluntary vaccination. Physicians for Informed Consent empowers the public with scientific information about infectious diseases and vaccines.https://physiciansforinformedconsent.org Alliance For Human Research Protection Advancing Voluntary, Informed Consent to Medical Intervention AHRP’s mission is to ensure that the moral right of voluntary medical decision-making is upheld. To accomplish that mission, we engage in an educational campaign, providing relevant factual information including ethical, legal, technical reports, and media reports. We endeavor to counter widely disseminated false claims that exaggerate the benefits of medical interventions, while minimizing risks. https://ahrp.org/ Books/E-Books Turtles All The Way Down: Vaccine Science and Myth (2022) If you are reading this, you are probably aware of the fierce debate surrounding vaccination and looking for information that will allow you to make the best decisions for yourself and your loved ones. Whether you are a parent or a parent to be, sorting through the many arguments on vaccines can be daunting. Still, you need an answer, a definitive one, to the crucial question: Who has it right in the great vaccine debate – the critics, who claim that vaccines often cause serious harm, or the medical establishment, which tells us that vaccines are safe and effective and the science is settled? Available in Hardcover, Paperback, and Kindle versions and can be purchased here- https://www.amazon.com/Turtles-All-Way-Down-Vaccine/dp/9655981460/ref=nodl_?dplnkId=7c226d19-bbd1-4d Truth Will Prevail: 1,200 Studies [PDF]... by Dr. Alan Palmer (2021) ****There is SO much information in this ebook! Awesome Free Resource!**** The contents of this e-Book are evidence based and substantiated by extensive research published in medical and scientific journals. It contains SEVERAL HUNDRED LINKS that you can click on, giving you instant access to the actual studies, corroborating everything reported in this document. In addition, the references contained in the excerpts from these studies consist of thousands of additional studies that also corroborate that evidence. Download Free E-Book Here https://archive.org/details/truth-will-prevail-1200-studies-dr-alan-palmer

From The Children's Health Defense- "In February 2017, Children’s Health Defense collected 89 peer-reviewed published articles linking autism, mercury and thimerosal. Each of these article abstracts are presented here along with a short annotation in layman terms about what the researchers found and how the findings are linked to autism. The science continues to accumulate that mercury and thimerosal are potent drivers of the autism epidemic." https://childrenshealthdefense.org/wp-content/uploads/autism-mercury-abstracts-2.27.20.pdf

So even though Biden declared a month ago that the pandemic was over, HHS renewed the public heath emergency this month extending it another 3 months https://aspr.hhs.gov/legal/PHE/Pages/covid19-13Oct2022.aspx Then last week CDCs ACIP committee voted 15:0 to add the Covid-19 vaccine to the childhood immunization schedule starting early 2023. What this means is that the Covid-19 vaccine manufacturers will go from having liability protection  from the Emergency Use Authorization to having liability protection under the National Childhood Vaccine Injury Act. https://www.nytimes.com/1986/11/15/us/reagan-signs-bill-on-drug-exports-and-payment-for-vaccine-injuries.html Most states follow the CDC Vaccine Schedule as requirements for kids to enter daycares, private, and public schools. https://www.cdc.gov/phlp/docs/school-vaccinations.pdf Why would we require kids to be vaccinated against a virus they have a 0.0027% risk of dying from? https://www.medrxiv.org/content/10.1101/2021.07.08.21260210v1 Despite being told otherwise by both our current and former presidents, the director of the CDC, and basically all mainstream media outlets, vaccines do not provide protection from catching or spreading covid- Pfizer clinical trial documents submitted to the FDA show that “Among 3410 total cases of suspected but unconfirmed COVID-19 in the overall study population, 1594 occurred in the vaccine group vs. 1816 in the placebo group.” Making the vaccine efficacy 12% compared to the 95% effectiveness they claimed. https://thevaultproject.org/was-pfizers-95-vaccine-efficacy-claim-fraudulent-from-the-start-data-show-staggeringly-low-12/ Even against the original strain the effectiveness was misrepresented as being 95% effective which was referring to relative risk reduction. The absolute risk reduction was 0.7% for Pfizer and 1.1% with moderna. https://pubmed.ncbi.nlm.nih.gov33652582/ This article explains the difference. https://www.canadiancovidcarealliance.org/wp-content/uploads/2021/08/Relative-VS-Absolute-Rate-of-Effectiveness.pdf Basically, you’re about 99% just as likely to get Covid after being vaccinated as someone who wasn’t vaccinated. And again, these are the numbers from the original strain. Against omicron the data is even worse- “Among those with Omicron infection, the risk of symptomatic infection did not differ significantly for the 2-dose vaccination status vs unvaccinated status and was significantly higher for the 3-dose recipients vs those who were unvaccinated (327/370 [88.4%] vs 85/107 [79.4%]; OR, 2.0 [95% CI, 1.1-3.5])“ https://jamanetwork.com/journals/jama/fullarticle/2797418 Does anyone else think it's crazy that according to FDA Emergency Use Authorization documents Pfizer based their claim of 75% efficacy for babies 6-23months off of 3 confirmed covid cases???  One in the vaccine group and two in placebo group. The 82% efficacy in 2-4 year olds was based on seven cases- two cases in vaccine group, five cases in the placebo group. COVID-19 cases occurring at least 7 days post-Dose 3 among participants with and without evidence of SARS-CoV-2 infection prior to 7 days after Dose 3 (Dose 3 evaluable efficacy population) included three COVID-19 cases in participants 6-23 months of age, with 1 COVID-19 case in the BNT162b2 group compared to 2 in the placebo group, corresponding to an estimated VE of 75.6% (95% CI: −369.1%, 99.6%), and 7 COVID-19 cases in participants 2-4 years of age, with 2 cases in the BNT162b2 group and 5 in the placebo group, corresponding to an estimated VE of 82.4% (95% CI: −7.6%, 98.3%). Meanwhile, according to the same documents, looking at all covid positive cases following at least one dose- more kids in the vaccinated groups met the criteria for severe covid than in the placebo groups. Among all COVID-19 cases accrued from Dose 1 through the data cutoff of April 29, 2022, 1 placebo recipient 6-23 months of age and 7 participants 2-4 years of age (6 BNT162b2 recipients and 1 placebo recipient) met the protocol-specified criteria for severe COVID-19 during both blinded and open-label follow-up. Less than a year into the vaccination campaign the data was already showing that the amount of people vaccinated in a population did not decrease the covid cases in the area. They actually saw the opposite “In fact, the trend line suggests a marginally positive association such that countries with higher percentage of population fully vaccinated have higher COVID-19 cases per 1 million people.” https://link.springer.com/article/10.1007/s10654-021-00808-7 One study looking at the viral loads in vaccinated and unvaccinated people “detected infectious virus in nearly everyone: from 88 percent of unvaccinated individuals and 95 percent of vaccinated people.” “If vaccinated people can still produce a lot of infectious viruses, it means they can spread the virus as easily as those who are not vaccinated.” https://www.nationalgeographic.com/science/article/evidence-mounts-that-people-with-breakthrough-infections-can-spread-delta-easily https://www.medrxiv.org/content/10.1101/2021.07.31.21261387v4.full.pdf More data looking at vaccinated and unvaccinated “Peak viral load did not differ by vaccination status or variant type “ “Between week 39 and 42, a total of 100.160 COVID-19 cases were reported among citizens of 60 years or older. 89.821 occurred among the fully vaccinated (89.7%), 3.395 among the unvaccinated (3.4%) [3]. “ “The US Centres for Disease Control and Prevention (CDC) identifies four of the top five counties with the highest percentage of fully vaccinated population (99.9–84.3%) as “high” transmission counties “ https://www.sciencedirect.com/science/article/pii/S2666776221002581 Not only do kids have a zero risk of dying from covid, and not only are the vaccines ineffective at stopping infection or transmission of covid, but there are serious risks of harm from these vaccines. Especially for kids. “This prospective cohort study enrolled students aged 13–18 years from two schools, who received the second dose of the BNT162b2 mRNA COVID-19 vaccine.” “Cardiovascular manifestations were found in 29.24% of patients, ranging from tachycardia or palpitation to myopericarditis.” https://www.mdpi.com/2414-6366/7/8/196 For boys 12-15 without medical comorbidities receiving their second mRNA vaccination dose, the rate of CAE is 3.7 to 6.1 times higher than their 120-day COVID-19 hospitalization risk as of August 21, 2021 (7-day hospitalizations 1.5/100k population) and 2.6-4.3-fold higher at times of high weekly hospitalization risk (7-day hospitalizations 2.1/100k), such as during January 2021. https://www.medrxiv.org/content/10.1101/2021.08.30.21262866v1 Pfizer and Moderna mRNA COVID-19 vaccines were associated with an increased risk of serious adverse events of special interest, with an absolute risk increase of 10.1 and 15.1 per 10,000 vaccinated over placebo baselines of 17.6 and 42.2 (95% CI -0.4 to 20.6 and -3.6 to 33.8), respectively. Combined, the mRNA vaccines were associated with an absolute risk increase of serious adverse events of special interest of 12.5 per 10,000 (95% CI 2.1 to 22.9). The excess risk of serious adverse events of special interest surpassed the risk reduction for COVID-19 hospitalization relative to the placebo group in both Pfizer and Moderna trials (2.3 and 6.4 per 10,000 participants, respectively). https://papers.ssrn.com/sol3/papers.cfm?abstract_id=4125239 There is a robust and statistically significant association between the weekly CA and ACS call counts, and the rates of 1st and 2nd vaccine doses administered to this age group. https://www.nature.com/articles/s41598-022-10928-z Moderna covid vaccine co-developed by Moderna and NIAID https://www.nih.gov/news-events/news-releases/statement-nih-barda-fda-emergency-use-authorization-moderna-covid-19-vaccine In a 2002 survey of 3247 National Institutes of Health scientists, 15.5% admitted to changing the design, methods, or results of a study in response to pressure from a funding source 231 (58%) principal investigators had financial ties. https://www.bmj.com/content/356/bmj.i6770 Acip members who voted to approve covid shot EUA last year for 5-12 year olds had huge financial conflicts of interests https://childrenshealthdefense.org/defender/cdc-acip-pfizer-pediatric-covid-vaccine-big-pharma/ Because I think its extremely important, I have made a separate Blog Post specifically summarizing the conflicts of interest of those serving on the ACIP committee.

Here is a summary of an article by The Childrens Health Defense outlining the conflicts of interest between the ACIP members who approved the use of covid vaccines in children and the pharmaceutical companies. I have taken the parts of the article I found most important and included them here. These are the writings of the Children's Health Defense Team and not my own. You can find the full article here https://childrenshealthdefense.org/defender/cdc-acip-pfizer-pediatric-covid-vaccine-big-pharma/ ACIP Chair Dr Grace Lee has been associate chief medical officer for practice innovation at Stanford Children’s Health and a pediatrics professor at Stanford School of Medicine since 2017. ·         Stanford receives extensive funding from the Gates Foundation, including for the development of 3D-printed vaccine micro needle patches (a strategy that would allow “vaccination without a shot”). University today announced that it has received a grant from the Bill and Melinda Gates Foundation to accelerate efforts in vaccine development. The $50 million grant over 10 years will build on existing technology developed at Stanford and housed in the Human Immune Monitoring Core, and will establish the Stanford Human Systems Immunology Center. ·       Stanford is the second largest university beneficiary of funding from the David and Lucile Packard Foundation, which is aggressively funding COVID vaccination of U.S. Latinos. The University of California, Berkeley received the largest sum from the Foundation ($15.4m), followed by Stanford University ($14.4m) and University of California, San Francisco ($11.9m). Beth Bell is a clinical professor in the Department of Global Health at the University of Washington (UW) School of Public Health ·       UW not only benefits from close ties with and extensive funding from the Gates Foundation Purpose To accelerate globally-informed and pregnancy-specific modeling to support drug development for maternal health Date OCTOBER 2021Committed amount$222,593 ·       but also enjoys extensive support from Microsoft. Microsoft Research, to announce a founding gift of $1.7 million from Microsoft for the new Lab Oliver Brooks is chief medical officer and a member of the executive team at Watts Healthcare Corporation in Los Angeles ·       During the pandemic, Watts Healthcare has received millions in funding from Kaiser Permanente to promote COVID vaccination in L.A.’s Hispanic and African American communities. Kaiser Permanente will spend $5 million in grants to support dozens of nonprofit and community-based organizations across the country – including two in Southern California – which will provide direct assistance to at-risk populations who are most impacted by COVID-19 The two local nonprofit organizations receiving funds from Kaiser Permanente are L.A.-based NALEO Educational Fund and Watts Healthcare, which will assist the Hispanic and African American communities respectively. ·       In March 2021, Watts Healthcare also received $4.3 Million via the American Rescue Plan to increase the federally qualified health center’s “ability to get more shots in arms.” ·       Since 2014, Brooks has received $118,439 (350 general payments primarily for consulting or speaking engagements) from biopharmaceutical companies that include Pfizer as well as Sanofi Pasteur, Novartis, Seqirus, Gilead, GlaxoSmithKline, Merck, Meda, AbbVie and Theratechnologies. Wilbur Chen is a professor at the University of Maryland School of Medicine ·       Chen is co-investigator for two entities funded by the Anthony-Fauci-led National Institute of Allergy and Infectious Diseases (NIAID) ·       In 2020 alone, Chen accepted $437,251 from vaccine makers GlaxoSmithKline (GSK) and Emergent BioSolutions ·       Chen’s payments since 2014 total over $476,880 and include monies from Janssen, Seqirus, MedImmune, Astellas Pharma, Valneva Austria and BioFire Diagnostics in addition to the two companies already mentioned ·       Chen also receives research funding from the Gates Foundation and from the Seattle-based global health organization PATH. Sybil Cineas a Harvard Medical School graduate, is an associate professor of medicine, pediatrics and medical science at Brown University, and, as associate program director of Brown’s combined residency program in internal medicine and pediatrics ·       CDC has given Brown researchers $4.9 million to study COVID vaccine effectiveness in seniors Matthew Dale  is a senior investigator and practicing pediatrician at Kaiser Permanente Colorado Camille Kotton is clinical director for Transplant and Immunocompromised Host Infectious Diseases at Massachusetts General Hospital and an associate professor at Harvard Medical School ·       Since 2014, Kotton has received over $304,000 in general payments and associated research funding from companies like Merck, GSK, Roche, Quiagen Sciences, Oxford Immunotec, Astellas Pharma, Shire, Takeda Pharmaceuticals, BeiGene and Biotest. James Loehr owns Cayuga Family Medicine in Ithaca, New York. ·       In 2015, Loehr authored an article with detailed instructions telling physicians how to “minimiz[e] costs and maximiz[e] reimbursement” to “make immunizations profitable.” Describing how Cayuga Family Medicine “enjoys steady revenue from immunizations, with vaccine reimbursement sometimes exceeding that for the rest of the visit,” Loehr outlined a series of strategies to improve a practice’s financial viability through vaccination, including becoming a “savvy vaccine shopper,” taking advantage of manufacturer discounts and doing “a bit of additional work” when coding for the service to obtain extra reimbursement for “brief counseling” and multiple vaccine components. Sarah Long is a professor of pediatrics at Drexel University College of Medicine and a physician at St. Christopher’s Hospital for Children in Philadelphia ·       Drexel University received half a million dollars from the Gates Foundation in June 2020 “to evaluate the use of a digital health platform to make care for COVID more accessible to marginalized populations.” ·       The Gates Foundation is also supporting the work of other Drexel researchers in areas such as diagnostic test development . Katherine Poehling is a professor of pediatrics and epidemiology at North Carolina’s Wake Forest University School of Medicine ·       Poehling has published on “ethics and acedemic pediatrics” but apparently sees no conflict in sitting on ACIP while receiving, according to Open Payments, over $523,000 in general payments and associated research funding from MedImmune and AstraZeneca since 2014. Pablo Sanchez ·       Sanchez’s 80-page self-congratulatory curriculum virtae reveals that he is a consummate insider fluidly bridging academia, public health agencies and private industry. Sanchez’s invited participation and lectures include appearances at public health agencies like CDC, the World Health Organization (WHO) and the Pan American Health Organization (PAHO); COVID-vaccine-promoting trade groups like the AAP and March of Dimes; and biopharma companies like AbbVie, GSK (formerly Smithkline Beecham), ICN Pharmaceuticals, Inhibitex, MedImmune and Ross Laboratories. ·       Sanchez also lists hundreds of thousands in research monies received from these same entities. ·       Since the 1990s, Sanchez has been funded by Abbott Laboratories, American Lung Association, BioStar, Biosynexus, Burroughs Wellcome, CDC, F. Hoffman-La Roche, Gerber Foundation, MedImmune, NIAID, NICHD [National Institute of Child Health and Human Development], Pediatric AIDS Foundation, Ross Laboratories and Smithkline Beecham/Glaxo/GSK. ·       According to Open Payments, since 2014, Sanchez has pocketed roughly $221,000 in general payments and associated research funding from AbbVie, AstraZeneca, F. Hoffmann-La Roche, MedImmune, Medtronic, Merck, Novartis, Sanofi Pasteur, Seqirus and Sobi. The database lists AstraZeneca, MedImmune and Merck as the “top companies" making associated payments,” with notable payments from Merck in Fall 2020. ·       In 2010, Sanchez served as a “Pfizer visiting professor.” Helen Keipp Talbot  is associate professor of medicine at Nashville’s Vanderbilt University ·       Talbot’s research and publications  (sometimes co-authored with fellow ACIP member Poehling) center on adult vaccination, influenza vaccination, human coronaviruses and vaccine trials for respiratory illnesses such as RSV. The focus on coronaviruses pre-dates COVID; from 2007–2009, Talbot was principal investigator on an NIH-funded study on the “epidemiology of human coronaviruses.” ·       According to Talbot’s curriculum vitaeher recent research funding comes from both the federal government (CDC, National Institutes of Health [NIH]) and Sanofi Pasteur, primarily for the study of pandemic preparedness (in 2015) and influenza vaccination. ·       Open Payments lists Talbot’s receipt of roughly $1.4 million in research payments and associated research funding since 2014 (417 total payments) from these companies, along with 29 general payments totaling $17,000. ·       In 2008, Talbot received a Sanofi Pasteur Advanced Vaccinology Course travel grant. Rochelle Walensky  CDC Director ·       As reported by independent media outlet RedState (but not by the mainstream media), Walensky’s husband, Loren Walensky, became scientific co-founder and board member of early-stage biotech company Lytica Therapeutics in October 2019. ·       In December, the Biden administration announced Rochelle Walensky’s pending appointment as CDC director, and in February 2020, Lytica received the first installment ($5.3 million) of a $16.9 million grant from HHS, representing the “only funding this new company [had] received to date — nearly two years after its founding.” Lynn Bahta is an immunization program clinical consultant for the Minnesota Department of Health, with a 25-year career focused on promoting vaccination. ·       When ACIP deliberated over Covid booster shots in September, Bahta was willing to recommend boosters for adults age 50 and up and individuals with underlying conditions but not for some groups of younger adults. At the time, Bahta argued for the need to “stay with the science,” stating, “I don’t think we have the data.” ·       By November, Bahta apparently was untroubled by the paucity of safety data available for the 5–11 age group, stating, “We know more than what we don’t know.” Veronica McNallyHaving lost an infant to pertussis, McNally describes herself as a “public health advocate” in addition to being an attorney.founded the I vaccinate campaign, which, on November 16, excitedly reported that “nearly 1 million kids ages 5-11 will have their first COVID shots by the end of today.

A collection of information regarding Aluminum https://www.atsdr.cdc.gov/toxguides/toxguide-22.pdf Aluminum is poorly absorbed following either oral or inhalation exposure and is essentially not absorbed dermally. Approximately 1.5–2% of inhaled and 0.01–5% of ingested aluminum is absorbed. https://www.wqa.org/Portals/0/Technical/Technical%20Fact%20Sheets/2014_Aluminum.pdf Aluminum limits in drinking water Secondary Maximum Contaminant Level US EPA SMCL* = 0.05 to 0.2 mg/L WHO† Guideline = 0.1 to 0.2 mg/L Health Canada OG** = 0.1 to 0.2 mg/L https://www.atsdr.cdc.gov/ToxProfiles/tp22-c1-b.pdf “Oral exposure to aluminum is usually not harmful. Some studies show that people exposed to high levels of aluminum may develop Alzheimer’s disease, but other studies have not found this to be true. We do not know for certain that aluminum causes Alzheimer’s disease.” “Some people who have kidney disease store a lot of aluminum in their bodies. The kidney disease causes less aluminum to be removed from the body in the urine. Sometimes, these people developed bone or brain diseases that doctors think were caused by the excess aluminum.” • Vaccines may contain small amounts of aluminum compounds, no greater than 0.85 mg/dose. ***(Note that safe drinking limits are 0.05-0.2mg/L and that aluminum is not easily absorbed orally. Yet vaccines contain up to 0.85mg/dose in each vaccine. This is being injected directly into the body bypassing our bodies filtration systems)*** https://pubmed.ncbi.nlm.nih.gov/11259180/ The healthy human body has effective barriers (skin, lungs, gastrointestinal tract) to reduce the systemic absorption of aluminum ingested from water, foods, drugs, and air. The small amount of aluminum (<1%) that is systemically absorbed is excreted principally in the urine and, to a lesser extent, in the feces. No reports of dietary aluminum toxicity to healthy individuals exist in the literature. Aluminum can be neurotoxic, when injected directly into the brains of animals and when accidentally introduced into human brains (by dialysis or shrapnel). https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=201.323 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. https://www.sciencedirect.com/science/article/pii/S0946672X19305784 None of the individual vaccines violates the guidance of a maximum of 850 μg of aluminum for an adult (Table 1). However, because of multiple vaccines typically given together at 2, 4, and 6 months, the CDC schedule violates this limit even assuming an adult weight ([27]; 29,773,196). Adjusting the safe dose limit based on a child’s weight at these ages therefore results in doses that far exceed the estimated safe limit of acute toxicity (Lyons-Weiler and Ricketson, 29,773,196). The CDC schedule crosses the recommended limit of aluminum for an adult by recommending multiple vaccinations containing aluminum being delivered together. Note that on all days of injection the safe limit for a child is exceeded for all three schedules; this points to acute toxicity Fig. 2. All of these schedules greatly exceed the weight-adjusted limit for aluminum from Lyons-Weiler and Ricketson (29773196). The CDC schedule has the largest violation at 15.9 times the recommended safe level. This occurs at 2 months, when four recommended vaccinations containing aluminum are simultaneously administered. In addition, modeling the time to clear aluminum from the body using Priest’s equation estimates that for this schedule a child will be over the safe level of aluminum in the body for 149 days from birth to 7 months, constituting about 70 % of days in this period (Fig. 3). This points to chronic toxicity. Over the first two years of life, days over the estimated limit are estimated as 176 days or 24 % of the days in this period. https://www.atsdr.cdc.gov/ToxProfiles/tp22.pdf Occupational studies in workers exposed to aluminum dust in the form of McIntyre powder, aluminum dust and fumes in potrooms, and aluminum fumes during welding provide suggestive evidence that there may be a relationship between chronic aluminum exposure and subclinical neurological effects such as impairment on neurobehavioral tests for psychomotor and cognitive performance and an increased incidence of subjective neurological symptoms. Neurodegenerative changes in the brain, manifested as intraneuronal hyperphosphorylated neuro­ filamentous aggregates, is a characteristic response to aluminum in certain species and nonnatural exposure situations generally involving direct application to brain tissue, particularly intracerebral and intracisternal administration and in vitro incubation in rabbits, cats, ferrets, and nonhuman primates. Significant alterations in motor function, sensory function, and cognitive function have been detected following exposure to adult or weanling rats and mice or following gestation and/or lactation exposure of rats and mice to aluminum lactate, aluminum nitrate, and aluminum chloride. https://www.sciencedirect.com/science/article/abs/pii/S0946672X21000547?via%3Dihub •There is a parallel rise in AlAd in vaccines for infants and ASD. •Injected Al induces behavioral changes in mice. •Brains in ASD patients contain more Al than control. •Numerous mechanisms exist that can explain Al neurotoxic effects. •The consilience of evidence supports AlAd as an etiologic factor in ASD. https://childrenshealthdefense.org/defender/aluminum-exposure-brain-alzheimers-disease-cola/?utm_source=salsa&eType=EmailBlastContent&eId=b10ab12a-9145-457a-a009-beb7a8ae8a07 When aluminum was first approved for use in vaccines, it was approved based on its efficacy. It was never actually tested for safety. It was simply assumed to be safe. Aluminum has been shown to cause mitochondrial dysfunction and depletion of adenine-triphosphate, which sets the stage for virtually any chronic disease. Aluminum salts can increase levels of glial activation, inflammatory cytokines and amyloid precursor protein within the brain. Recent research found the Centers for Disease Control and Prevention’s (CDC) vaccine schedule — when adjusted for body weight — exposes children to a level of aluminum that is 15.9 times higher than the recommended “safe” level.

Polio cases peaked around 1952 with just under 58,000 cases and 3,145 deaths. When the Polio vaccine was rolled out 3 years later Polio was already declining significantly with around half the amount of cases (28,985) and deaths (1,043). https://ourworldindata.org/grapher/reported-paralytic-polio-cases-and-deaths-in-the-united-states-since-1910?time=earliest..1962&country=~USA The OPV vaccine that is still used in many places has caused outbreaks of vaccine-associated paralytic poliomyelitis (VAPP) and polio outbreaks due to circulating vaccine-derived polioviruses. These outbreaks are not caused by the wild strain of polio virus. They are caused by the weakened virus used in vaccines that changes over time and begins to act like the wild virus. https://www.cdc.gov/vaccines/vpd/polio/hcp/vaccine-associated-paralytic-polio-faq.html https://www.cdc.gov/vaccines/vpd/polio/hcp/vaccine-derived-poliovirus-faq.html However, for the last 20 years in the United States we have used the inactivated polio vaccine (IPV) instead of OPV. Since it’s not a live virus it doesn’t carry the risk of VAPP. On the other hand, “IPV induces very low levels of immunity in the intestine. As a result, when a person immunized with IPV is infected with wild poliovirus, the virus can still multiply inside the intestines and be shed in the faeces, risking continued circulation.” Also “IPV does not stop transmission of the virus” https://polioeradication.org/polio-today/polio-prevention/the-vaccines/ipv/ -Recent data show that protection from acellular pertussis vaccines is not long-lasting. Antibody levels wane rapidly following vaccination. -Consistent with this T cell skewing, acellular vaccines did not prevent colonization or transmission following challenge in nonhuman primates. https://www.sciencedirect.com/science/article/abs/pii/S0952791515000813?via%3Dihub The DTP vaccine has been associated with a 5 fold higher mortality rate than being unvaccinated. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360569/ Those who receive the DTaP vaccine will be “more susceptible to pertussis throughout their lifetimes”. https://pubmed.ncbi.nlm.nih.gov/24277828/ Vaccination with varicella vaccine leads to increased risk of shingles. https://pubmed.ncbi.nlm.nih.gov/22659447/ International Agency for Research on Cancer found that individuals who never had measles had a 66% increased rate of Non-Hodgkin Lymphoma and a 233% increased rate of Hodgkin Lymphoma. https://seer.cancer.gov/statfacts/html/nhl.html https://seer.cancer.gov/statfacts/html/hodg.html A 22-year prospective study of over 100,000 individuals in Japan revealed that “measles and mumps, especially in case of both infections, were associated with lower risks of mortality from atherosclerotic CVD heart disease. https://pubmed.ncbi.nlm.nih.gov/26122188/ Vaccinated children are also at a higher risk for allergic rhinitis, eczema, learning disability, adhd, neurodevelopmental disorder and chronic illness than unvaccinated children. https://archive.is/PwUrN In 2011 HHS paid the IOM to do a study on vaccine safety. The IOM located science which “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, an anaphylaxis. The review found sufficient evidence to support “acceptance of a causal relationship” for 4 additional serious injuries. The IOM, however, found the scientific literature was insufficient to conclude whether or not those vaccines caused 135 other serious injuries commonly reported after their administration, including: Encephalitis, Encephalopathy, Infantile Spasms, Afebrile Seizures, Seizures, Cerebellar Ataxia, Ataxia, Acute Disseminated Encephalomyelitis, Transverse Myelitis, Optic Neuritis,  Neuromyelitis Optica , Multiple Sclerosis, Guillain- Barre Syndrome, to name just a few. https://www.nap.edu/read/13164/chapter/2#3 In a recent study comparing vaccinated vs unvaccinated children they found children who were vaccinated were 5x more likely to have autism 4x more likely to have allergies 13.8x more likely to have gastrointestinal issues 17.6x more likely to have asthma 20.8x more likely to have ADHD 27.8x more likely to have chronic ear infections https://www.oatext.com/health-effects-in-vaccinated-versus-unvaccinated-children-with-covariates-for-breastfeeding-status-and-type-of-birth.php In another study done last year looking at health outcomes of vaccinated and unvaccinated they find “We can conclude that the unvaccinated children in this practice are not, overall, less healthy than the vaccinated and that indeed the vaccinated children appear to be significantly less healthy than the unvaccinated.” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709050/#!po=1.51515 The rate of chronic illness in children in the United States is up from 12.5% in 1986 to 54% now. I am not saying it is all due to vaccines but we went from giving kids 11 doses of vaccines by the time they were 18 to giving 72 doses now. We have the highest mortality rate of pregnant women than any other developed country in the world. “Despite spending more per capita of any country, the U.S. has one of the worst rates of infant mortality of all developed countries.” “Every year twice the number of U.S. babies die on their first day alive than in all 27 European Union nations combined, although 1 million more are born there (4.3 million versus 5.3 million respectively).” https://thevaccinereaction.org/2016/05/why-is-the-u-s-infant-mortality-rate-so-high/ We have a problem. And no I don’t think vaccines are the entire cause of the problem. It’s many things including our food. But Why would we blindly trust the industry that outspends oil and gas 2:1 in lobbying, that has paid out BILLIONS in lawsuits for knowingly misrepresenting their products, for bribing doctors, for withholding information about their products from the FDA. The industry that knew for decades the product they sold to us to use on our babies bare skin everyday contained asbestos. The only differences between vaccines and the other products produced and marketed by these companies is that vaccines don’t go through the same standard of safety testing as other drugs. No double blind placebo safety studies, and follow up periods as little as 48 hours. Vaccines are also the only product that can be produced and safety tested by the same company, be mandated to every citizen in the country, and then hold no liability for any damages caused. To say vaccines are safe and effective and that the science is settled without even taking the time to read the science is ignorant. The science is never settled, but so far the science shows that vaccines are not always safe, nor are they always effective.

Sometime in the middle of February 2021, I had asked if someone could show me a study on the entire vaccine schedule showing that it doesn’t increase risks of autism. I was sent several studies, and I read through all of them. None of the studies sent to me looked at more than one vaccine, or in most cases one ingredient. Since that day, I haven’t stopped reading. I have read study after study and the facts are undeniable that vaccines do contribute to autism. Besides autism they contribute to ear infections, type 1 diabetes, asthma. The list goes on and on. Why are we letting pharmaceutical companies off the hook for the damages when they are caused? If any other product hurt and killed children at the rate vaccines do it would be pulled without question. At the very least the product would have to be properly labeled, with the risk listed very clearly for consumers to see. If your kid is hurt from a vaccine injury the pharmaceutical company has zero liability. They don’t even have to show up to court. Our taxes pay for those injuries. So what incentive do these companies have to make their products safer? We are forcing parents to give their kids vaccines that have NEVER been through safety testing with double blind placebo (not even one) in order to allow their kids to go to school. How are more people not outraged by this? Instead I see the opposite. People are offended and angry when I speak the truth or they ignore it completely. I don’t understand it. I want to share Isaiahs story now that I’ve gotten his medical records and been able to go through all of the notes. Isaiah’s first two months of life he was developing normal. There were no complaints listed at any of his well child visits, all was fine. Just before he was two months old I received IV antibiotics and oral antibiotics for an infection. I was also exclusively breast feeding because I thought “breast was best” and wasn’t even thinking about the antibiotics being passed to Isaiah. Antibiotics kill gut microbiome which play a role in immune system function. A study on cephalexin which is what I was given states that it is passed through breast milk and there may be “disruption of the infants gastrointestinal flora”. At the end of my treatment of antibiotics I went in for a postpartum follow-up where I was given a flu shot. I normally never get flu shots but I did this year because I wanted to protect Isaiah.  I was told the best way to protect Isaiah from getting sick was to make sure those close to him were vaccinated. Now I know that I probably hurt him more than I protected him. Influenza vaccines still contain thimerasol which was removed from most children’s vaccines in the early 2000s. There are many studies showing connections between thimerasol and autism. There are at least 180 studies showing harm from thimerasol. Not to mention the influenza insert even states “data is not available to assess the effects on the breastfed infant”. I should have never been given that shot. A week later Isaiah was vaccinated for rotavirus, diphtheria, tetanus, pertussis, hep b, and polio. Six vaccinations at once after just having been exposed to an influenza vaccine not safe for children under 6 months old. After having been exposed to antibiotics that weakened his immune function. How did no one stop and think this combination might not be safe? They don’t look at the safety of a combination of vaccines. They hardly look at the safety of one! That same month Isaiah had a developmental assessment done. Studies have been done proving this screener to be accurate and reliable. Isaiah scored a 109. Fourteen months later, he was given the same screener, only this time he scored a 62. He went from being advanced in every area to behind or developmentally delayed in every area. He wasn’t born that way. Another thing that happened after that 2 month mark was his head began to grow significantly. He went from 32nd percentile to greater than 99th percentile for head circumference in less than a year. He stopped eating and started screaming. Looking back at his medical records is so easy to see the connection. Isaiah would get vaccinated then bam we are in urgent care within a week with no explanation being found. Every. Single. Time. By 4 months old he was diagnosed failure to thrive. At just over one year old, he was diagnosed with Neurological Impairment, Macrocephaly, and Developmental Delay Syndrome. He now also has diagnosis of Autism Spectrum Disorder, Speech Delay, Dysphagia, Anxiety, and OCD. I would much rather this be a genetic issue because I can’t explain the regret that I live with. I’m working so hard to find ways to help Isaiah and he’s doing so good! But what I wouldn’t give to be able to go back and do things different. I will never tell another parent what choices are best for their family. But I’m asking for parents to PLEASE do some research of your own before deciding!! I always thought there was no unbiased information available but that’s not true! There are a ton of scientific research articles out there. Pubmed is a great website to start. They can be hard to read and comprehend at first, but it’s so important to know the facts for yourself. No one else is going to look out for you and your family the way you would.

Published studies on Autism Neurodevelopmental disorders, maternal Rh-negativity, and Rho(D) immune globulins: a multi-center assessment Geier 2007 "Results: There were significant and comparable increases in maternal Rh-negativity among children with Neurodevelopmental disorders, (Clinic: A=24.2%), autism spectrum disorders (Clinic: A=28.3%, B=25.3%), and attention-deficit-disorder/attention-deficit-hyperactivity-disorder (Clinic: A=26.3%) observed at both clinics in comparison to both control groups (Clinic: A=12.1%, B=13.9%) employed. Children with NDs born post-2001 had a maternal Rh-negativity frequency (13.6%) similar to controls." The results show that prior to 2001 there was a significant number of kids who had autism who's mothers received Rhogam shot while pregnant compared to those who did not receive Rhogam shot. However, after 2001 there is no longer a significant difference in mothers who did verses did not receive a Rhogam shot. The difference they highlight is that the Rhogam shot was reformulated in 2001 to remove the ingredient Thimerisol. https://pubmed.ncbi.nlm.nih.gov/18404135/ Neurodevelopmental disorders following thimerosal-containing childhood immunizations: a follow-up analysis David Geier et al. Int J Toxicol. Nov-Dec 2004. "It was determined that there were significantly increased odds ratios (ORs) for autism (OR = 1.8, p < .05), mental retardation (OR = 2.6, p < .002), speech disorder (OR = 2.1, p < .02), personality disorders (OR = 2.6, p < .01), and thinking abnormality (OR = 8.2, p < .01) adverse events reported to the VAERS following thimerosal-containing DTaP vaccines in comparison to thimerosal-free DTaP vaccines." https://pubmed.ncbi.nlm.nih.gov/15764492/ A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population Gayle Delong. J Toxicol Environ Health A. 2011. "A positive and statistically significant relationship was found: The higher the proportion of children receiving recommended vaccinations, the higher was the prevalence of AUT or SLI. A 1% increase in vaccination was associated with an additional 680 children having AUT or SLI." https://pubmed.ncbi.nlm.nih.gov/21623535/ The association between mercury levels and autism spectrum disorders: A systematic review and meta-analysis "Results of the current meta-analysis revealed that mercury is an important causal factor in the etiology of ASD. It seems that the detoxificationand excretory mechanisms are impaired in ASD patients which lead to accumulation of mercury in the body. Future additional studies on mercury levels in different tissues of ASD patients should be undertaken." https://www.sciencedirect.com/science/article/abs/pii/S0946672X17306089?via%3Dihub Thimerosal: Clinical, epidemiologic and biochemical studies "July 7, 1999, the US Public Health Service (USPHS) and American Academy of Pediatric (AAP) called for the elimination of Thimerosal from all vaccines in the US as soon as possible. As more of the reduced-Thimerosal and no-Thimerosal vaccines became available in the early 2000s in the US, the assumption was that the exposure to Thimerosal would sharply decrease. However, this expecttion proved to not be accurate because of recommendation changes in the vaccination schedule. Therefore, the approximate maximum lifetime exposure to Hg from Thimerosal-preserved vaccines has increased compared to the lifetime exposure under the US CDC's pre-2000 recommended vaccination schedule. It is estimated that it is now more than double what it would have been had the pre-2000 vaccination schedule been maintained." "Conclusion: The culmination of the research that examines the effects of Thimerosal in humans indicates that it is a poison at minute levels with a plethora of deleterious consequences, even at the levels currently administered in vaccines" https://www.sciencedirect.com/science/article/pii/S0009898115001023?via%3Dihub Toxic Heavy Metals and Autism Spectrum Disorder; Is There a Link???!!! "They concluded that the limited ability of autistics to excrete heavy metals as well as the increased environmental exposure at key points of fetal and infantile development seems to have a significant role in the occurrence of ASD." "Autistic children are defective in metabolizing sulfur compounds which results in significant reduction of their abilities to detoxify heavy metals and increases their toxicity. Also, they have impaired methylation and redox homeostasis with increased vulnerability to oxidative stress; like what occurs in cases of exposure to heavy metals intoxication, with subsequent negative impact on the development of the brain and normal CNS functions [6]." https://www.omicsonline.org/open-access/toxic-heavy-metals-and-autism-spectrum-disorder-is-there-a-link-2375-4494-1000336.pdf Hair mercury in breast-fed infants exposed to thimerosal-preserved vaccines https://link.springer.com/article/10.1007/s00431-006-0362-2 DO THE BRIGANCE SCREENS DETECT DEVELOPMENTAL AND ACADEMIC PROBLEMS? " Overall, sensitivity w a s found to be 72% to 100% across Forms while specificity ranged from 73%to 100%.The findings suggests that the use of the cutoffs identified in this study greatly improves the value of the Brigance in the early detection of children with developmental problems." https://citeseerx.ist.psu.edu/viewdoc/download?doi=10.1.1.923.9929&rep=rep1&type=pdf Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure "Our results provide strong evidence supporting a link between autism and the aluminum in vaccines " "we identify several signs and symptoms that are significantly more prevalent in vaccine reports after 2000, including cellulitis, seizure, depression, fatigue, pain and death, which are also significantly associated with aluminum-containing vaccines." "A meta-study involving oxidative-stress related biomarkers present in association with autism identified a consistent deficiency in reduced glutathione [17], an important sulfur-based antioxidant that also plays a role in detoxifying aluminum." "Glutathione [23] and sulfate [24] are also essential for the detoxification of xenobiotics and commonly administered drugs like acetaminophen in the liver. Selenium, a trace metal in the same column of the periodic table as oxygen and sulfur, has been shown to protect against acetaminophen toxicity [25], and it has also been shown to be severely depleted in hair and nail samples from individuals on the autism spectrum [26]." "It has recently been proposed that aluminum, commonly used in vaccines as an adjuvant, may be the most significant factor in adverse reactions, and, furthermore, that the nervous system is especially vulnerable to aluminum toxicity [45]. Vaccine clinical trials often include aluminum in the placebo, at the same or greater concentrations than the amount found in the vaccine [46–49]." "The Food and Drug Administration (FDA) has set an upper limit of 5 micrograms Al/kg/day for neonates and individuals with impaired kidney function [51]. children today receive a cumulative aluminum burden from vaccines that may exceed the FDA limit by a factor of 50." https://res.mdpi.com/d_attachment/entropy/entropy-14-02227/article_deploy/entropy-14-02227-v2.pdf The Relationship Between the Level of Copper, Lead, Mercury and Autism Disorders: A Meta-Analysis "There is, nevertheless, a significant relationship between mercury concentration and autism. Thus, the concentration of mercury can be listed as a pathogenic cause (disease-causing) for autism." https://pubmed.ncbi.nlm.nih.gov/33061742/ Immunoexcitotoxicity as the central mechanism of etiopathology and treatment of autism spectrum disorders: A possible role of fluoride and aluminum "Studies of autistic patients have confirmed the presence of a number of immune dysfunctions" "Importantly, this research indicates that ASD children experience increase reactiveness of their peripheral immune system to immune activation and that they also experience priming and activation of their brain microglia in conjunction with systemic immune activation." "Prolonged and repeated systemic immune activation appears to be central to ASD etiopathology. With subsequent, especially closely spaced immune stimulation, full activation of the overactive primed microglia occurs, leading to progressive pathological changes in the developing brain. This is especially so if the episodes of systemic immune stimulation are closely spaced together." "Many investigations show that Al3+ can elicit impairment of development and immunity; that it acts as a hormonal disruptor, a neurotoxin, and elicits intense and prolonged activation of brain inflammation." "In an extensive review, Tomljenovic and Shaw pointed out that 18 Al3+-containing adjuvanted vaccines are included in the current pediatric vaccine schedule.[256] They found that (1) children from countries with the highest ASD incidence appear to have the highest exposure to Al3+ from vaccines; (2) the increase in exposure to Al3+- adjuvants significantly correlates with increase ASD in the United States over the last two decades; and (3) a significant correlation exist between the amounts of Al3+ administered to preschool children and the current prevalence of ASD in seven Western countries, particularly at 3-4 months of age. The data satisfied Hill's criteria for causation." https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909100/?report=classic