Our results show that: (i) children from countries with the highest ASD prevalence appear to have the highest exposure to Al from vaccines; (ii) the increase in exposure to Al adjuvants significantly correlates with the increase in ASD prevalence in the United States observed over the last two decades

In this paper, we have presented some analyses of the VAERS database which strongly suggest that the aluminum in vaccines is toxic to vulnerable children. While we have not shown that aluminum is directly causative in autism, the compelling evidence available from the literature on the toxicity of aluminum, combined with the evidence we present for severe adverse reactions occurring much more frequently following administration of aluminum-containing vaccines as compared to non-aluminum-containing vaccines, suggests that neuronal damage due to aluminum penetration into the nervous system may be a significant factor in autism.

Aluminum caused tics and grand mal seizures in monkeys.

French scientists tie aluminum adjuvant in vaccine to macrophagic myofasciitis.

French scientists report aluminum from vaccines causes chronic cognitive dysfunction.

Canadian researchers: aluminum in vaccines can cause both autoimmunity and neurological damage.

Israeli and Italian researchers demonstrate that exposure to aluminum in vaccines can lead to autoimmune and brain dysfunction.

Newborns have been overexposed to aluminum.

Chronic aluminium administration resulted in significant motor incoordination and memory deficits, which were also endorsed biochemically as there was increased oxidative stress as well as elevated aluminium levels in the brain.

Autistic children accumulate metals at a much higher level than children who do not have a diagnosis of autism.

The specific mechanism of action of each vaccine adjuvant may have different effects on the course of autoimmune conditions resulting from vaccination

Aluminum in vaccines is highly neurotoxic and exposure levels given to infants have dramatically increased.

Israeli, Canadian and Colombian scientists show that the Gardasil vaccine triggers brain inflammation and autoimmunity in mice.

Aluminum nanoparticles are toxic on their own and in combination with other metal nanoparticles.

Aluminum and mercury sulfates may contribute to neurodegeneration and progressive age-related functional decline such as Alzheimer’s disease.

The levels of aluminum present in individual vaccines and in the modern vaccine schedule as a whole are problematically high.

The first-ever measurements of aluminum in the brain tissue of donors with multiple sclerosis detected pathologically significant levels of aluminum in every single individual.

Fluoride and aluminum, alone or in combination, can produce the condition of “immunoexcitotoxicity” that leads to the pathological changes seen in autism.

Aluminum adjuvants in vaccines produce toxic effects ranging from benign to fatal, depending on the physicochemical properties of the adjuvant and the physiological response of the vaccine recipient.

With the preliminary literature search starting in 2013 and looking backwards in time, research publications revealed a myriad of toxic actions of Aluminum causing pathological conditions.

Among the three schedules presented here, the CDC schedule exceeds the recommended dose limit for an infant (inferred from FDA adult “safe” levels) as a result of the simultaneous administration of multiple ACVs and insufficient spacing of ACVs.

We suggest that complementary aluminium-specific fluorescence microscopy may reveal important information about the putative toxicity of aluminium in neurodegenerative and neurodevelopmental disorders.

In a large observational study, a positive association was found between vaccine-related aluminum exposure and persistent asthma. While recognizing the small effect sizes identified and the potential for residual confounding, additional investigation of this hypothesis appears warranted.

The hypothesis that Al significantly contributes to AD is built upon very solid experimental evidence and should not be dismissed. Immediate steps should be taken to lessen human exposure to Al, which may be the single most aggravating and avoidable factor related to AD.

The findings suggest a possible role for the aluminum adjuvant in some neurological features associated with GWI and possibly an additional role for the combination of adjuvants.

Repetitive administration of aluminium to neonatal mice in amounts comparable to those to children receive via routine vaccinations significantly increases anxiety and reduces exploratory behaviour and locomotor activities. The neurodisruptive effects of aluminium are long-lasting and persist for 6 months following injection.

A new study published in the Journal of Trace Elements in Medicine and Biology concluded the U.S. Centers for Disease Control and Prevention’s (CDC) vaccine schedule was 15.9 times over the recommended safe level of aluminum when researchers adjusted for body weight.