The Fastest Growing Disability in the US

When it comes to autism and vaccines, people like to say that there's no proof - I don’t even need “proof.” There are THOUSANDS of parents who watched their child regress over night. There’s children who were developing normally or even ahead of schedule, who suddenly didn’t know things they had known for months. There’s parents who live with kids on all ranges of the spectrum that will tell you vaccines changed their child - parents know! Moms don’t lie.

According to the University of Calgary, there’s been an 1148% increase in Autism the last 10 years. Boys are 4-5 times more likely to receive an autism diagnosis than girls.

In April 2018, the Centers for Disease Control and Prevention (CDC) released a report estimating the prevalence of autism spectrum disorder. The study was based on a 2014 survey of eight-year-old children across 11 residential communities. Source: https://www.cdc.gov/mmwr/volumes/69/ss/ss6904a1.htm 

The children were born in 2004, studied in 2012 and it took two years to collect and process the data - so it was outdated before it was even published.  In 2017, the NCHS published health data for 2014-2016 which pegged the prevalence of autism for children aged 3-17 years at 1 in 36 in 2016, compared to 1 in 43 in 2015 and 1 in 45 in 2014. Source: https://www.cdc.gov/nchs/data/databriefs/db291.pdf

In the 1980s, it was 1 in 10,000. 

1990: 1 in 500

2000: 1 in 250

2004: 1 in 166

2009: 1 in 110

MIT Doctor Stephanie Seneff estimates that 1 in 2 children in the US will have autism by 2025. Her paper links glyphosate to the cause. Source: http://people.csail.mit.edu/seneff/glyphosate/Groton_Seneff.pdf

Here is the World Atlas of autism rates: 

http://www.worldatlas.com/articles/countries-with-the-highest-rates-of-autism As the vaccine schedule grew, so did the number of autism diagnosis. Please see our 101 unit post about vaccine schedules here: https://www.facebook.com/groups/VaccinationReEducationDiscussionForum/permalink/3180176728701820/

History of Autism 

There is no formal evidence that the condition existed before the 20th century. However, some historical figures, including Thomas Jefferson, Albert Einstein and Michelangelo are believed to have had autistic traits.

Between 1908-1912: Dr. Eugene Bleuler used the term autistic in reference to schizophrenic individuals who exhibited catatonic behaviors.

1938: Leo Kanner was a doctor from Johns Hopkins University who used the term autism to refer to a group of children who displayed withdrawn behaviors.

1940s: Freudian psychology suggested that children with autism were not given the proper love and attention they required in order to develop healthy interpersonal relationships.

1967: Bruno Bettleheim described refrigerator mothers in his book The Empty Fortress: Infantile Autism and the Birth of the Self. In the book, he compares autistic disorder to imprisonment in a concentration camp. The notion is that a cold and indifferent mother leads to the symptoms of autism

1970s: Interventions typically included removal from the family home. Many children were placed in institutions in order to receive care around the clock. Treatments included: D-Lysergic Acid Diethylamide (LSD), Electroconvulsive therapy (which is still under investigation as a treatment for autism), Behavioral approaches that used aversives (punishment)

1977: Research on twins finds that autism is largely caused by genetics and biological differences in brain development.

1980s: Autism was introduced to the Diagnostic and Statistical Manual

1987: UCLA psychologist Ivar Lovaas, Ph.D., publishes the first study showing how intensive behavior therapy can help children with autism--thus giving new hope to parents.

1991: The federal government makes autism a special education category. Public schools begin identifying children on the spectrum and offering them special services.

1998: A study published in The Lancet suggests that the measles-mumps-rubella (MMR) vaccine causes autism.

2000: Vaccine manufacturers remove thimerosal. 

2013: The DSM-5 folds all subcategories of the condition into one umbrella diagnosis of autism spectrum disorder. ASD is defined by two categories: 1) Impaired social communication and/or interaction. 2) Restricted and/or repetitive behaviors.

• One of the most famous (and the FIRST autism court award)  cases regarding vaccines and autism involves Hannah Poling. When Hannah was 19 months old, she received nine vaccines DPT, MMR, IPV, Varicella, and HIB. had been developing normally, according to her parents—her father, Jon, is a Johns Hopkins–trained, practicing neurologist, her mother is an attorney and registered nurse—but in the months after the shots, she developed a fever and litany of other symptoms… She regressed and was diagnosed with “mitochondrial disorder.” Hannah's parents believed that vaccines had triggered her encephalopathy. They sued the Department of Health and Human Services (DHHS) for compensation under the Vaccine Injury Compensation Program (VICP) and won. https://www.cbsnews.com/news/family-to-receive-15m-plus-in-first-ever-vaccine-autism-court-award/  "We showed there was a plausible mechanism. We showed that an injury occurred shortly after her vaccination. Her growth curve went flat for months." (Hannah’s dad) According to US Division Of Vaccine Injury Compensation, the shots “significantly aggravated and underlying mitochondrial disorder” and resulted in a brain disorder, “with features of autism spectrum disorders.” 

• Here are 83 cases reviewed by lawyers regarding autism and vaccines  http://digitalcommons.pace.edu/cgi/viewcontent.cgi?article=1681&context=pelr

• Hannah Brusewitz case and how she was harmed by DTP  https://www.law.cornell.edu/supct/cert/09-152

• The government and vaccine makers have already admitted legally that vaccines have and do cause Autism. http://bit.ly/2E5IXYR

• Vaccines caused autism here in this federal court case:http://www.uscfc.uscourts.gov/sites/default/files/opinions/ABELL.ZELLER073008.   and here, page 2: http://www.uscfc.uscourts.gov/sites/default/files/opinions/CAMPBELL-SMITH.MOJABI-PROFFER.12.13.2012.pdfAnd here - https://ecf.cofc.uscourts.gov/cgi-bin/show_public_doc?2012vv0423-91-0

• If we use the correlation as fact that vaccines are safe and effective. then we could also use the correlation where the countries with the highest vaccination rates also have the highest rates of autism. Here is the WHO's data on vaccination rates:http://www.who.int/immunization/monitoring_surveillance/data/en/
• Our results show that: (i) children from countries with the highest autism spectrum disorder (ASD) prevalence appear to have the highest exposure to aluminum from vaccines; (ii) the increase in exposure to aluminum adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades; and (iii) a significant correlation exists between the amounts of aluminum administered to preschool children and the current prevalence of ASD in seven Western countries. Source: http://www.ncbi.nlm.nih.gov/pubmed/22099159
• ”The present study provides new epidemiological evidence supporting an association between increasing organic-Hg exposure from Thimerosal-containing childhood vaccines and the subsequent risk of ASD diagnosis.” Source: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878266/
• “A positive association found between autism prevalence and childhood vaccination uptake across the U.S. population” Source: http://www.ncbi.nlm.nih.gov/pubmed/21623535
• Did British scientists just solve the autism puzzle?Five clear, replicable, and related discoveries explaining how autism is triggered have formed an undeniably clear picture of autism’s causation, and possibly ways to alleviate the symptoms, too. Most of the research that has created this understanding has been published in the last 36 months, and largely from international scientists in the United Kingdom, Canada, France, Israel, and China. immune activation and is far more neurotoxic than previously thought. Source: https://medium.com/@jbhandley/did-british-scientists-just-solve-the-autism-puzzle-5a7eacc77415
• ”It is biologically plausible that mercury toxicity in genetically susceptible persons may contribute to the numbers with autism and ASD. However there is no clear proof linking the mercury in Thimerosal to the spurt in cases seen in recent years. The apparent linkage of autism to the MMR vaccine (which is Thimerosal free) seems to suggest that mercury exposure through Thimerosal-containing vaccines is not the only factor that may be responsible for the subsequent “autism” and “ASD” diagnoses in developing children.”  Source: http://ijme.in/articles/commentary-controversies-surrounding-mercury-in-vaccines-autism-denial-as-impediment-to-universal-immunisation/?galley=html
• Canadian study released online 9/18/17 for their upcoming December 2017 issue of the Journal of Inorganic Biochemistry, titled, "Subcutaneous injections of aluminum at vaccine adjuvant levels activate innate immune genes in mouse brain that are homologous with biomarkers of autism.” Source: www.sciencedirect.com/science/article/pii/S0162013417300417
• What is regressive autism and why does it occur? Is it the consequence of multi-systemic dysfunction affecting the elimination of heavy metals and the ability to regulate neural temperature?: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/
• Brian Hookers famous paper: “As seen in this review, the studies upon which the CDC relies and over which it exerted some level of control report that there is no increased risk of autism from exposure to organic Hg in vaccines, and some of these studies even reported that exposure to Thimerosal appeared to decrease the risk of autism. These six studies are in sharp contrast to research conducted by independent researchers over the past 75+ years that have consistently found Thimerosal to be harmful. As mentioned in the Introduction section, many studies conducted by independent investigators have found Thimerosal to be associated with neurodevelopmental disorders.” https://www.hindawi.com/journals/bmri/2014/247218/
• “Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism” http://www.ncbi.nlm.nih.gov/pubmed/12145534
• Boys vaccinated as neonates had threefold greater odds for autism diagnosis compared to boys never vaccinated or vaccinated after the first month of life.” http://www.ncbi.nlm.nih.gov/pubmed/21058170
• ”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 (Pearson r=0.92, p<0.0001); and (iii) a significant correlation exists between the amounts of Al administered to preschool children and the current prevalence of ASD in seven Western countries” Ironically this author still suggested it was a “casual” link. http://www.ncbi.nlm.nih.gov/pubmed/22099159 And: https://www.sciencedirect.com/science/article/pii/S0162013411002212?via%3Dihub
• “In the developed world, there is an estimated 0.1-0.3% risk of mortality from measles which compares with a 0.6% risk and rising (with some estimates at 1-2%) of autism” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364648/
• A case series of children with apparent mercury toxic encephalopathies manifesting with clinical symptoms of regressive autistic disorders: http://www.ncbi.nlm.nih.gov/pubmed/17454560
• A comprehensive review of mercury provoked autism: http://www.ncbi.nlm.nih.gov/pubmed/19106436
• Thimerosal Exposure and the Role of Sulfation Chemistry and Thiol Availability in Autism: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774468/
• ”ASD is a disorder caused by a problem in brain development. If the B-cells from the families in the AGRE collection are at all representative of the neurons in the brains of the cell donors, we can say that a third of them have a sensitivity to thimerosal that would restrict cell proliferation at levels that were/are typically found after vaccination” http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3697751/
• Hypothesis: Conjugate vaccines may predispose children to autism spectrum disorders: https://www.sciencedirect.com/science/article/pii/S0306987711004117?via%3Dihub
• Autism: a novel form of mercury poisoning: https://www.sciencedirect.com/science/article/pii/S0306987700912817?via%3Dihub
• A prospective study of thimerosal-containing Rho(D)-immune globulin administration as a risk factor for autistic disorders: https://www.tandfonline.com/doi/abs/10.1080/14767050701228057?journalCode=ijmf20
• “Medical hypothesis that autistic disorders, in fact, represents a form of testosterone mercury toxicity,” https://www.sciencedirect.com/science/article/pii/S0306987704006152?via%3Dihub
• “Based on the levels of this toxin that children receive through routine immunization schedules in the first years of life, it has been postulated that thimerosal may be a potential triggering mechanism contributing to autism in susceptible individuals.” https://www.sciencedirect.com/science/article/pii/S0161813X06001665?via%3Dihub
• “This mechanism explains the link between excessive vaccination, use of aluminum and ethylmercury as vaccine adjuvants, food allergies, gut dysbiosis, and abnormal formation of the developing brain. It has now been shown that chronic microglial activation is present in autistic brains from age 5 years to age 44 years. A considerable amount of evidence, both experimental and clinical, indicates that repeated microglial activation can initiate priming of the microglia and that subsequent stimulation can produce an exaggerated microglial response that can be prolonged. It is also known that one phenotypic form of microglia activation can result in an outpouring of neurotoxic levels of the excitotoxins, glutamate and quinolinic acid. Studies have shown that careful control of brain glutamate levels is essential to brain pathway development and that excesses can result in arrest of neural migration, as well as dendritic and synaptic loss. It has also been shown that certain cytokines, such as TNF-alpha, can, via its receptor, interact with glutamate receptors to enhance the neurotoxic reaction.” https://www.ncbi.nlm.nih.gov/m/pubmed/19043938/
• The role of mercury in the pathogenesis of autism: https://www.nature.com/articles/4001177
• ”Compared with placebo group, the eye opening time of thimerosal-treated mice were apparently delayed (Fig. 1b), suggesting that early neonatal exposure to thimerosal led to a delayed neural development.” https://academic.oup.com/toxsci/article/139/2/452/2511500
• Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism. http://www.ncbi.nlm.nih.gov/pubmed/12145534
• Autoimmunity to the central nervous system (CNS), especially to myelin basic protein (MBP), may play a causal role in autism, a neurodevelopmental disorder. Because many autistic children harbor elevated levels of measles antibodies, we conducted a serological study of measles-mumps-rubella (MMR) and MBP autoantibodies.….over 90% of MMR antibody-positive autistic sera were also positive for MBP autoantibodies, suggesting a strong association between MMR and CNS. autoimmunity in autism. Stemming from this evidence, we suggest that an inappropriate antibody response to MMR, specifically the measles component thereof, might be related to pathogenesis of autism. Serological association of measles virus and human herpes virus-6 with brain auto-antibodies in autism. Source Source:http://www.ncbi.nlm.nih.gov/pubmed/9756729
• This study is the first to report an association between virus serology and brain auto antibody in autism; it supports the hypothesis that a virus-induced autoimmune response may play a causal role in autism. Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders. http://www.ncbi.nlm.nih.gov/pubmed/21993250 Conjugate vaccines fundamentally change the manner in which the immune systems of infants and young children function by deviating their immune responses to the targeted carbohydrate antigens from a state of hypo- responsiveness to a robust B2 B cell mediated response. This period of hypo-responsiveness to carbohydrate antigens coincides with the intense myelination process in infants and young children, and conjugate vaccines may have disrupted evolutionary forces that favored early brain development over the need to protect infants and young children from capsular bacteria.
• Hepatitis B vaccination of male neonates and autism diagnosis, NHIS 1997-2002. http://www.ncbi.nlm.nih.gov/pubmed/21058170
• Findings suggest that U.S. male neonates vaccinated with the hepatitis B Vaccine prior to 1999 (from vaccination record) had a threefold higher risk for parental report of autism diagnosis compared to boys not vaccinated as neonates during that same time period. Nonwhite boys bore a greater risk. Immunological findings in autism. http://www.ncbi.nlm.nih.gov/pubmed/16512356 The immunopathogenesis of autism is presented schematically in Fig. 1. Two main immune dysfunctions in autism are immune regulation involving pro-inflammatory cytokines and autoimmunity. Mercury and an infectious agent like the measles virus are currently two main candidate environmental triggers for immune dysfunction in autism.
•  “To the best of our knowledge, these results are the first to show that Al, a highly neurotoxic metal and the most commonly used vaccine adjuvant, may be a significant contributing factor to the rising prevalence of ASD in the Western world.... We also show that children from countries with the highest ASD prevalence appear to have a much higher exposure to Al from vaccines, particularly at 2 months of age.” Source: http://omsj.org/reports/tomljenovic%202011.pdf
• Our results show that: (i) children from countries with the highest autism spectrum disorder (ASD) prevalence appear to have the highest exposure to aluminum from vaccines; (ii) the increase in exposure to aluminum adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades; and (iii) a significant correlation exists between the amounts of aluminum administered to preschool children and the current prevalence of ASD in seven Western countries. Source: http://www.ncbi.nlm.nih.gov/pubmed/22099159
• “In summary, research data suggests that vaccines containing Al may be a contributing etiological factor in the increasing incidence of autism.” Source: http://link.springer.com/referenceworkentry/10.1007%2F978-1-4614-4788-7_89

Dr. Thompson is a CDC whistle blower who came forward and admitted that the CDC had omitted and destroyed evidence in their final report which revealed a causal relationship between the MMR vaccine and autism, particularly in black boys.The CDC Autism/MMR Files Released By Dr. William Thompson https://www.vaxxed.com/thompson-file-releases/ 

A few articles:

• https://sharylattkisson.com/2016/06/cdc-scientist-we-scheduled-meeting-to-destroy-vaccine-autism-study-documents/ 
• https://thefreethoughtproject.com/cdc-scientist-admits-destroyed-data-showed-vaccines-caused-autism-children/
• https://www.ecowatch.com/cdc-vaccines-autism-2051536402.html 

Here is a quote from biologist Dr. Brian Hooker, which you can read in full in this PDF to download (jpands.org/vol22no4/hooker.pdf):

When the CDC team responsible for the paper by Destefano et al. originally completed the analysis regarding MMR timing and autism in black male children, an odds ratio of 2.56 was obtained when comparing those children receiving the MMR vaccine before 36 months of age with those who didn’t receive MMR until after 36 months of age. This result was statistically significant, with a p-value less than 0.01. This result alarmed Dr. Thompson’s co-authors on the paper, especially those who were in leadership positions at CDC.In order to dilute this association, Dr. Thompson was asked to eliminate any children in the sample who did not possess a valid State of Georgia birth certificate. This eliminated children living in the Atlanta area but not born in Georgia—about 40 percent of the sample. When this was done, the odds ratio was reduced to 1.68 but more importantly, statistical significance was obviated (i.e., p > 0.05). In the final paper, only the result for the “birth certificate” sampling was reported. In addition, according to Dr. Thompson, all data showing the original effect for African-Americans were destroyed in the September 2002 meeting, despite the fact that the original analysis plan for the study explicitly stated: “The only variable available to be assessed as a potential confounder using the entire sample is child’s race.” DeStefano et al. deviated from the original analysis plan, expressly to avoid reporting the statistically significant finding.”

The VAXXED movie is a documentary created to expose this https://www.vaxxed.com/home/  

Yes, vaccines can cause autism. This is an absolutely unavoidable reality, if you are open-minded enough to consider the studies and clinical data from the last 30 years. The CDC claims vaccines do not cause autism, but the data they publish does not support this claim. As Dr. Richard Kelley, one of the foremost experts on autism says, he disagrees with the CDC claims about the vaccine-autism link, but does not disagree with the CDC data.

Please understand this one concept, if you understand nothing else about vaccines and autism. The only vaccine that has been studied for a link to autism, is MMR; the only vaccine ingredient that has been studied for a link to autism is thimerasol. It is not true that vaccines and autism have been studied. Only about 4.1% of the vaccines/ingredients in the CDC schedule have been studied.

THE SCIENTIFIC BASIS THAT VACCINES CAUSE AUTISM 

There are 11 scientific discoveries that make the link clear between vaccines and an autism diagnoses. They have all been published in peer-reviewed journals by scientists across disciplines.

1. Discovery #1: In 2004 Dr. Carlos Pardo-Villamizar at Johns Hopkins University discovers that autism brains are permanently inflamed.

· The study is titled “Neuroglial Activation and Neruoinflammation in the Brain of Parients with Autism.”[1]

· It was the first time the brains of people with autism were looked at.

· We learn that autism brains have an immune system in a permanent, active state. We also learn that certain cytokines are highly elevated. They are biomarkers for inflammation.

· They were the first to study microglial activation in the brains of children with autism, and this has been replicated in several other studies.

2. Discovery #2: In 2005 Dr. Paul Patterson at the California Institute of Technology discovers that immune activation events lead to autism.

· The paper is titled “Pregnancy, Immunity, Schizophrenia, and Autism.”[2]

· If a pregnant woman becomes sick while pregnant—an event that activates her immune system—that activation can impact the neurodevelopment of the fetus, potentially leading to neurological problems after birth.

· Dr. Patterson tied the immune system and the brain together in ways not previously understood.

· His work was replicated many times. In 2012, he produced a paper titled, “Maternal Immune Activation Yields Offspring Displaying Mouse Versions of the Three Core Symptoms of Autism.”[3]This work was replicated in monkeys in 2014.[4]

3. Discovery #3: Dr. Paul Patterson discovered that the cytokine interleukin-6 is the key biomarker for immune activation.

· Maternal Immune Activation was producing offspring with neurological disorders (in the mouse model) and they wanted to find out exactly what was causing the altered brain development. The theorized it was a cytokine, but hadn’t figured out which one. They injected interleukin-6 and observed the same changes in the offspring.

· Dr. Patterson produced more evidence in 2012 in a study titled, “Brain IL-6 Elevation Causes Neuronal Circuitry Imbalances and Mediates Autism-Like Behaviors.”[5]

· These, along with other studies, proved that when IL-6 level is elevated, we know that immune activation is present.

4. Discovery #4: In January 2018, a study discovered that Immune activation can take place after birth.

· Dr. Patterson had never bridged the gap between a child in gestation and a child during infancy. If immune activation events after birth could also trigger the development of autism, then something besides the mother would have to trigger the immune activation.

· A 2018 study from McLean Hospital shows that these events can happen after birth.[6]

5. Discovery #5: In 2009, Dr. Christopher Shaw discovered that aluminum adjuvant in vaccines produces behavior and motor function deficits.

· They were examining the potential toxicity of aluminum hydroxide in male, outbred CD-1 mice injected subcutaneously in two equivalent-to-human doses.[7]

· They quickly discovered that behavioral symptoms emerged shortly after injecting the aluminum. This manifest not only in behavior, but in motor functions and cognitive deficits. They found massive damage to motor neurons after they dissected the mice.

6. Discovery #6: In 2013, Drs. Romain Gherardi and Josette Cadusseau discovered that aluminum adjuvant in vaccines, injected into the body, can be carried to the brain by macrophages.

· The study was titled, “Slow CCL2-Dependent Translocation of Biopersistent Particles from Muscle to Brain.”[8]

· When aluminum adjuvant enters the body, it’s not recognized by the body because it is foreign. The macrophages grab it, but they don’t have the means to eliminate it, so they carry it, and bring it to soft tissue places in the body, like the brain. When encounted by the brain, it triggers an immune activation.

7. Discovery #7: In 2015, the same doctors discovered that aluminum adjuvant stays in the brain much longer than anyone realized.

· The study is titled, “Biopersistence and brain translocation of aluminum adjuvants of vaccines.”[9]

· They discovered that the biopersistence of the adjuvant means it stays in our brains a long time, and potentially produces an ongoing activation event.

8. Discovery #8: In 2016, a study discovered that small doses of aluminum adjuvant are actually more dangerous than large doses.

· The study is titled, “Non-linear dose-response of aluminium hydroxide adjuvant particles: Selective low dose neurotoxicity.”[10]

· They disputed the FDA and CDC thinking about aluminum, saying that they were comparing other “non-relevant” aluminum exposures to injected aluminum adjuvant.

9. Discovery #9: In 2015, a study[11]discovered that aluminum causes immune activation in the brain.

· This study showed that aluminum triggers an elevated level of IL-6 in the brain, which is a biomarker for an immune activation event. Therefore, aluminum itself can cause an activation event in the brain.

10. Discovery #10: In 2016, a Chinese study discovered that Hepatitis B vaccine induces Interleukin-6 in postnatal rats.

· The studies are titled, “Neonatal vaccination with bacillus Calmette–Guérin and hepatitis B vaccines modulates hippocampal synaptic plasticity in rats”[12]And “Neonatal hepatitis B vaccination impaired the behavior and neurogenesis of mice transiently in early adulthood.”[13]

· This study demonstrates that vaccines can affect brain development via immune activation. The Hep B vaccine was shown to increase IL-6 in the hippocampus (the only brain region analyzed for cytokines).

· An important find was that many of the effects of the Hep B vaccine did not appear until 8 weeks. Since most vaccine studies do not observe nearly that far out, this is significant.

· They replicated their work again in 2016, focusing just on the biological effects of Hep B and confirmed their findings.

11. Discovery #11: In 2017, Dr. Christopher Exley discovered that high levels of aluminum are uniquely located in brain tissue of people with autism.

· The study is titled, “Aluminium in brain tissue in autism.”[14]

· They looked at the brain tissue of subjects with autism to measure aluminum for the first time.

· They found “shockingly high” amounts of aluminum in their brains. They found a high amount of monocytes at the injection site, and one kind of monocyte is a macrophage. He believes these macrophages are transporting the aluminum to the brain.

· Dr. Exley believes that they proved “that aluminum adjuvant could be transported to the brain from a vaccine injection site.”

To summarize these studies in a four-step process:

1) Aluminum adjuvant injection

2) Aluminum adjuvant particles travel to the brain

3) IL-6 production and microglial activation in the brain

4) Autism

[1] https://onlinelibrary.wiley.com/doi/abs/10.1002/ana.20315

[2] http://vaccinepapers.org/.../Pregnancy-Immunity...

[3] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322300/

[4] https://www.ncbi.nlm.nih.gov/pubmed/24011823

[5] https://www.ncbi.nlm.nih.gov/pubmed/...

[6] https://www.nature.com/articles/npp2017243

[7] https://link.springer.com/article/10.1385%2FNMM%3A9%3A1%3A83

[8] https://www.ncbi.nlm.nih.gov/pubmed/...

[9] https://www.ncbi.nlm.nih.gov/pubmed/25699008

[10] https://www.ncbi.nlm.nih.gov/pubmed/27908630

[11] https://www.sciencedirect.com/.../pii/S0162013417303380

[12] https://www.sciencedirect.com/.../abs/pii/S0165572815300291

[13] https://www.sciencedirect.com/.../abs/pii/S0306453016305145

[14] https://www.sciencedirect.com/.../pii/S0946672X17308763