Aluminum in the central nervous system (CNS): toxicity...

Discuss autism theories, media stories, and efforts to put ASD on the government agenda here.

Moderator: ModeratorBill

Forum rules
Please limit quotes from articles to five paragraphs. Also, researchers may post study information here.
lioralourie
Posts: 22
Joined: Sat Jan 18, 2014 12:35 pm

Re: Aluminum in the central nervous system (CNS): toxicity..

Postby lioralourie » Sat Jan 18, 2014 9:08 pm

I had to break up the 10 aluminum studies into two posts (too many url's)

here are the remaining 5

6) Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration.
J Inorg Biochem. 2009 Nov;103(11):1555-62. doi: 10.1016/j.jinorgbio.2009.05.019. Epub 2009 Aug 20.
FULL TEXT - free- BELOW
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819810/
original ncbi listing is here http://www.ncbi.nlm.nih.gov/pubmed/19740540





7) Adjuvants and autoimmunity.
Lupus. 2009 Nov;18(13):1217-25. doi: 10.1177/0961203309345724.
Israeli E, Agmon-Levin N, Blank M, Shoenfeld Y.
http://www.ncbi.nlm.nih.gov/pubmed/19880572

Abstract
Some adjuvants may exert adverse effects upon injection or, on the other hand, may not trigger a full immunological reaction. The mechanisms underlying adjuvant adverse effects are under renewed scrutiny because of the enormous implications for vaccine development. In the search for new and safer adjuvants, several new adjuvants were developed by pharmaceutical companies utilizing new immunological and chemical innovations. The ability of the immune system to recognize molecules that are broadly shared by pathogens is, in part, due to the presence of special immune receptors called toll-like receptors (TLRs) that are expressed on leukocyte membranes. The very fact that TLR activation leads to adaptive immune responses to foreign entities explains why so many adjuvants used today in vaccinations are developed to mimic TLR ligands. Alongside their supportive role, adjuvants were found to inflict by themselves an illness of autoimmune nature, defined as 'the adjuvant diseases'. The debatable question of silicone as an adjuvant and connective tissue diseases, as well as the Gulf War syndrome and macrophagic myofaciitis which followed multiple injections of aluminium-based vaccines, are presented here. Owing to the adverse effects exerted by adjuvants, there is no doubt that safer adjuvants need to be developed and incorporated into future vaccines. Other needs in light of new vaccine technologies are adjuvants suitable for use with mucosally delivered vaccines, DNA vaccines, cancer and autoimmunity vaccines. In particular, there is demand for safe and non-toxic adjuvants able to stimulate cellular (Th1) immunity. More adjuvants were approved to date besides alum for human vaccines, including MF59 in some viral vaccines, MPL, AS04, AS01B and AS02A against viral and parasitic infections, virosomes for HBV, HPV and HAV, and cholera toxin for cholera. Perhaps future adjuvants occupying other putative receptors will be employed to bypass the TLR signaling pathway completely in order to circumvent common side effects of adjuvant-activated TLRs such as local inflammation and the general malaise felt because of the costly whole-body immune response to antigen.

8) Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity.

FULLTEXT HERE
http://katlynfoxfoundation.com/wp-conte ... search.pdf

http://www.ncbi.nlm.nih.gov/pubmed/23609067


(PMID:23609067)

Shaw CA, Tomljenovic L
Neural Dynamics Research Group, Department of Ophthalmology and Visual Sciences, University of British Columbia (UBC), 828 W. 10th Ave., Vancouver, BC, V5Z 1L8, Canada, cashawlab@gmail.com.
Immunologic Research [2013]
Type: Journal Article
Abstract


We have examined the neurotoxicity of aluminum in humans and animals under various conditions, following different routes of administration, and provide an overview of the various associated disease states. The literature demonstrates clearly negative impacts of aluminum on the nervous system across the age span. In adults, aluminum exposure can lead to apparently age-related neurological deficits resembling Alzheimer's and has been linked to this disease and to the Guamanian variant, ALS-PDC. Similar outcomes have been found in animal models. In addition, injection of aluminum adjuvants in an attempt to model Gulf War syndrome and associated neurological deficits leads to an ALS phenotype in young male mice. In young children, a highly significant correlation exists between the number of pediatric aluminum-adjuvanted vaccines administered and the rate of autism spectrum disorders. Many of the features of aluminum-induced neurotoxicity may arise, in part, from autoimmune reactions, as part of the ASIA syndrome.



9) http://www.ncbi.nlm.nih.gov/pubmed/23576057


Immunol Res. 2013 Jul;56(2-3):299-303. doi: 10.1007/s12026-013-8400-4.
Adverse events following immunization with vaccines containing adjuvants.
Cerpa-Cruz S, Paredes-Casillas P, Landeros Navarro E, Bernard-Medina AG, Martínez-Bonilla G, Gutiérrez-Ureña S.
Author information

Abstract
A traditional infectious disease vaccine is a preparation of live attenuated, inactivated or killed pathogen that stimulates immunity. Vaccine immunologic adjuvants are compounds incorporated into vaccines to enhance immunogenicity. Adjuvants have recently been implicated in the new syndrome named ASIA autoimmune/inflammatory syndrome induced by adjuvants. The objective describes the frequencies of post-vaccination clinical syndrome induced by adjuvants. We performed a cross-sectional study; adverse event following immunization was defined as any untoward medical occurrence that follows immunization 54 days prior to the event. Data on vaccinations and other risk factors were obtained from daily epidemiologic surveillance. Descriptive statistics were done using means and standard deviation, and odds ratio adjusted for potential confounding variables was calculated with SPSS 17 software. Forty-three out of 120 patients with moderate or severe manifestations following immunization were hospitalized from 2008 to 2011. All patients fulfilled at least 2 major and 1 minor criteria suggested by Shoenfeld and Agmon-Levin for ASIA diagnosis. The most frequent clinical findings were pyrexia 68%, arthralgias 47%, cutaneous disorders 33%, muscle weakness 16% and myalgias 14%. Three patients had diagnosis of Guillain-Barre syndrome, one patient had Adult-Still's disease 3 days after vaccination. A total of 76% of the events occurred in the first 3 days post-vaccination. Two patients with previous autoimmune disease showed severe adverse reactions with the reactivation of their illness. Minor local reactions were present in 49% of patients. Vaccines containing adjuvants may be associated with an increased risk of autoimmune/inflammatory adverse events following immunization.


10)Expert Rev Clin Immunol. 2013 Apr;9(4):361-73. doi: 10.1586/eci.13.2.
Autoimmune/inflammatory syndrome induced by adjuvants (Shoenfeld's syndrome): clinical and immunological spectrum.
Vera-Lastra O, Medina G, Cruz-Dominguez Mdel P, Jara LJ, Shoenfeld Y.

VIEW HERE but cannot download full text….
http://www.scribd.com/doc/94838202/Alum ... ne-Disease


Abstract
An adjuvant is a substance that enhances the antigen-specific immune response, induces the release of inflammatory cytokines, and interacts with Toll-like receptors and the NALP3 inflammasome. The immunological consequence of these actions is to stimulate the innate and adaptive immune response. The activation of the immune system by adjuvants, a desirable effect, could trigger manifestations of autoimmunity or autoimmune disease. Recently, a new syndrome was introduced, autoimmune/inflammatory syndrome induced by adjuvants (ASIA), that includes postvaccination phenomena, macrophagic myofasciitis, Gulf War syndrome and siliconosis. This syndrome is characterized by nonspecific and specific manifestations of autoimmune disease. The main substances associated with ASIA are squalene (Gulf War syndrome), aluminum hydroxide (postvaccination phenomena, macrophagic myofasciitis) and silicone with siliconosis. Mineral oil, guaiacol and iodine gadital are also associated with ASIA. The following review describes the wide clinical spectrum and pathogenesis of ASIA including defined autoimmune diseases and nonspecific autoimmune manifestations, as well as the outlook of future research in this field.
original link: http://www.ncbi.nlm.nih.gov/pubmed/23557271


and this is only the Aluminum studies regarding autoimmunity. Macrophagic Myofasciitis (MMF) and Chronic Fatigue Syndrome, there are more studies, too, I also ran across, and also a few for Al's possible role in Crohn's disease.

María Luján
Posts: 1345
Joined: Sun Jun 25, 2006 5:26 pm

Re: Aluminum in the central nervous system (CNS): toxicity..

Postby María Luján » Sun Jan 19, 2014 8:06 pm

Thank you very much for posting

Josie
Posts: 393
Joined: Mon Jun 11, 2012 1:35 am

Re: Aluminum in the central nervous system (CNS): toxicity..

Postby Josie » Wed Jan 22, 2014 8:55 pm

It appears Monsanto is currently marketing an aluminum resistance gene. I wonder how they make a gene resistant to aluminum.

http://farmwars.info/?p=2927

What in the world are they spraying?

http://www.youtube.com/watch?v=QW8WycvZpr8

Full video

http://www.youtube.com/watch?v=ybWku-lJ ... video_user

lioralourie
Posts: 22
Joined: Sat Jan 18, 2014 12:35 pm

Re: Aluminum in the central nervous system (CNS): toxicity..

Postby lioralourie » Mon Nov 17, 2014 4:17 am

DOWNLOAD ALL THESE, READ THEM, AND SHARE THEM.



1) Aluminum adjuvant linked to Gulf War illness induces motor neuron death in mice.
 
FULLTEXT available here
http://www.mediafire.com/view/r4h8pb1l8 ... n_Mice.pdf

2) Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration.
J Inorg Biochem. 2009 Nov;103(11):1555-62.FULL TEXT BELOW
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819810/


3) Macrophagic myofasciitis lesions assess long-term persistence of vaccine-derived aluminium hydroxide in muscle. Brain. 2001 Sep;124(Pt 9):1821-31. 
FREE FULL TEXT HERE
http://www.ncbi.nlm.nih.gov/pubmed/11522584



4) Mechanisms of aluminum adjuvant toxicity and autoimmunity in pediatric populations.
Tomljenovic L, Shaw CA.
http://www.ncbi.nlm.nih.gov/pubmed/22235057
FULLTEXT AVAILABLE HERE
http://www.mediafire.com/view/potofd3o8 ... ations.pdf
published in the journal:
Lupus. 2012 Feb;21(2):223-30. doi: 10.1177/0961203311430221.


5) Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?

J Inorg Biochem. 2011 Nov;105(11):1489-99.

Abstract
Autism spectrum disorders (ASD) are serious multisystem developmental disorders and an urgent global public health concern. Dysfunctional immunity and impaired brain function are core deficits in ASD. Aluminum (Al), the most commonly used vaccine adjuvant, is a demonstrated neurotoxin and a strong immune stimulator. Hence, adjuvant Al has the potential to induce neuroimmune disorders. When assessing adjuvant toxicity in children, two key points ought to be considered: (i) children should not be viewed as "small adults" as their unique physiology makes them much more vulnerable to toxic insults; and (ii) if exposure to Al from only few vaccines can lead to cognitive impairment and autoimmunity in adults, is it unreasonable to question whether the current pediatric schedules, often containing 18 Al adjuvanted vaccines, are safe for children? By applying Hill's criteria for establishing causality between exposure and outcome we investigated whether exposure to Al from vaccines could be contributing to the rise in ASD prevalence in the Western world. 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 (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, particularly at 3-4 months of age (Pearson r=0.89-0.94, p=0.0018-0.0248). The application of the Hill's criteria to these data indicates that the correlation between Al in vaccines and ASD may be causal. Because children represent a fraction of the population most at risk for complications following exposure to Al, a more rigorous evaluation of Al adjuvant safety seems warranted.

FULLTEXT AVAILABLE AT
http://www.mediafire.com/view/b9g18txgx ... ejovak.pdf



6) Aluminum vaccine adjuvants: are they safe?
Tomljenovic L, Shaw CA.
http://www.ncbi.nlm.nih.gov/pubmed/21568886
FULLTEXT AVAILABLE HERE
http://www.mediafire.com/view/a2k0hknqs ... c_Shaw.pdf

7) Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity.

FULLTEXT HERE
http://katlynfoxfoundation.com/wp-content/uploads/2013/10/2013-Shaw-CA-LT-Imm-Res-CNS-Toxicity-of-alum-adjuvants-and-autoimmunity-Immunological-Research.pdf
 - see abstract here http://www.ncbi.nlm.nih.gov/pubmed/23609067
Last edited by lioralourie on Mon Nov 17, 2014 8:05 am, edited 2 times in total.

lioralourie
Posts: 22
Joined: Sat Jan 18, 2014 12:35 pm

Re: Aluminum in the central nervous system (CNS): toxicity..

Postby lioralourie » Mon Nov 17, 2014 4:18 am

continuing on:

8. Autoimmune/inflammatory syndrome induced by adjuvants (Shoenfeld's syndrome): clinical and immunological spectrum.
Expert Rev Clin Immunol. 2013 Apr;9(4):361-73. doi: 10.1586/eci.13.2.
VIEW ALL HERE but cannot download full text….
http://www.scribd.com/doc/94838202/Alum-Autoimmune-Disease
NEW LINK updated - download all the screen shots here (that's the only way I could get this paper)
https://www.mediafire.com/#agwk730gzpwhu

9) Med J Aust. 2005 Aug 1;183(3):145-6.
Macrophagic myofasciitis associated with vaccine-derived aluminium.
FULL TEXT HERE
https://www.mja.com.au/journal/2005/183 ... -aluminium

10) Autoimmune or auto-inflammatory syndrome induced by adjuvants (ASIA): Old truths and a new syndrome?'

. Yehuda Shoenfeld, MD, FRCP, Zabludowicz Center for Autoimmune Diseases, Chaim Sheba Medical Center, Israel.

extract: Physicians are often puzzled by enigmatic medical conditions or the abrupt appearance of an immune-mediated disease. Such a story was recently presented to us by a young Sheikh. A Saudi Sheikh, who suffered at the age of 27 from joints pains, rash and serological evidence of anti-Ro antibodies, was diagnosed with probable systemic lupus erythematosus (SLE) at that time. He was treated with Plaquenil for a year, but as no signs of SLE were apparent, treatment was stopped and he remained disease free for the next 12 years. At the age of 39 years, 2 weeks after immunization with the flu vaccine, his disease reemerged. This time he presented with severe arthritis and pericarditis, which required treatment with high doses of steroids.
This patient’s story illustrates the acceleration of an autoimmune or immune-mediated condition following exposure to external stimuli. During the past year a new syndrome was introduced and termed ASIA, ‘Autoimmune (Auto-inflammatory) Syndrome induced by Adjuvants’.1 This syndrome assembles a spectrum of immune-mediated diseases triggered by an adjuvant stimulus.2 – 4 The use of medical adjuvants has become common practice and substances such as aluminum adjuvant are added to most human and animal vaccines, while the adjuvant silicone is extensively used for breast implants and cosmetic procedures. Furthermore, ‘hidden adjuvants’ such as infectious material or house molds have also been associated with different immune mediated conditions.1,5 The adjuvant effect has been recognized for years, and is broadly …
FULL TEXT HERE
xa.yimg.com/kq/groups/16063327/1870391070/name/ASIA3.pdf

11) ASIA or Shoenfeld’s Syndrome – An Autoimmune Syndrome Induced by Adjuvants

FULL TEXT ONLINE here
http://www.intmed.ro/attach/rjim/2013/rjim313/art02.pdf

abstract: Recently, reports have suggested grouping different autoimmune conditions that are triggered by external stimuli as a single syndrome called autoimmune syndrome induced by adjuvants (ASIA). This syndrome is characterized by the appearance of myalgia, myositis, muscle weakness, arthralgia, arthritis, chronic fatigue, sleep disturbances, cognitive impairment and memory loss, and the possible emergence of a demyelinating autoimmune disease caused by systemic exposure after vaccines and adjuvants. As there are no markers for ASIA, the authors intend to present ASIA, or Shoenfeld’s syndrome, as an autoimmune syndrome induced by adjuvants.
Key words: ASIA, Shoenfeld’s syndrome, autoimmune syndrome, adjuvants.

12)
HUMAN EXPOSURE TO ALUMINIUM
Christopher Exley, PhD
fulltext here: http://pubs.rsc.org/en/content/articlep ... c3em00374d



13) Aluminium adjuvants and adverse events in sub-cutaneous allergy immunotherapy
http://www.ncbi.nlm.nih.gov/pmc/article ... 2-10-4.pdf

14)
Long-term persistence of vaccine-derived aluminum hydroxide is associated with chronic cognitive dysfunction.
J Inorg Biochem. 2009 Nov;103(11):1571-8.
original abstract here http://www.ncbi.nlm.nih.gov/pubmed/19748679
Couette M, Boisse MF, Maison P
download HERE http://www.mediafire.com/view/ld8421b2r ... nction.pdf
Last edited by lioralourie on Mon Nov 17, 2014 10:03 pm, edited 2 times in total.

lioralourie
Posts: 22
Joined: Sat Jan 18, 2014 12:35 pm

Re: Aluminum in the central nervous system (CNS): toxicity..

Postby lioralourie » Mon Nov 17, 2014 6:25 am

more: still only FullText! (I have even more just abstracts)

15) Adverse events following immunization with vaccines containing adjuvants.
http://www.ncbi.nlm.nih.gov/pubmed/23576057
Cerpa-Cruz S1, Paredes-Casillas P
Immunol Res. 2013 Jul;56(2-3):299-303. doi: 10.1007/s12026-013-8400-4.
download Fulltext HERE
http://www.mediafire.com/view/st884flaf ... uvants.pdf


16)
Why industry propaganda and political interference cannot disguise the inevitable role played by human exposure to aluminum in neurodegenerative diseases, including Alzheimer’s disease
Christopher Exley, PhD
Front. Neurol., 27 October 2014 | doi: 10.3389/fneur.2014.00212
full text here http://journal.frontiersin.org/Journal/ ... 00212/full


17) Aluminum’s Role in CNS-immune System Interactions leading to Neurological Disorders
download it HERE
http://www.researchgate.net/publication ... _Disorders
published in: Immunome Research 01/2013; 9(069):1. DOI: 10.4172/1745-7580.1000069

ABSTRACT Multisystem interactions are well established in neurological disorders, in spite of conventional views that only the central nervous system (CNS) is impacted. We review evidence for mutual interactions between the immune and nervous systems and show how these seem to be implicated in the origin and progression of nervous system disorders. Well-established immune system triggers leading to autoimmune reactions are considered. Of these, aluminum, a known neurotoxicant, may be of particular importance. We have demonstrated elsewhere that aluminum has the potential to induce damage at a range of levels in the CNS leading to neuronal death, circuit malfunction, and ultimately system failure. Aluminum is widely used as an adjuvant in various vaccine formulations and has been implicated in a multisystem disorder termed “autoimmune/inflammatory syndrome induced by adjuvants” (ASIA). The implications of aluminum-induced ASIA in some disorders of the CNS are considered. We propose a unified theory capturing a progression from a local response to a systemic response initiated by disruption of water-based interfaces of exposed cells.


AND new from Oct. 2014
18) in Journal of Toxicology 10/2014; Shaw, C.A., Seneff, S., Kette, S.D., Tomljenovic, L.

2014.Aluminum-Induced Entropy in Biological Systems/ Implications for Neurological Disease
full text here
http://www.researchgate.net/publication ... al_Disease


ABSTRACT Over the last 200 years, mining, smelting, and refining of aluminum (Al) in various forms have increasingly exposed living species to this naturally abundant metal. Because of its prevalence in the earth's crust, prior to its recent uses it was regarded as inert and therefore harmless. However, Al is invariably toxic to living systems and has no known beneficial role in any biological systems. Humans are increasingly exposed to Al from food, water, medicinals, vaccines, and cosmetics, as well as from industrial occupational exposure. Al disrupts biological self-ordering, energy transduction, and signaling systems, thus increasing biosemiotic entropy. Beginning with the biophysics of water, disruption progresses through the macromolecules that are crucial to living processes (DNAs, RNAs, proteoglycans, and proteins). It injures cells, circuits, and subsystems and can cause catastrophic failures ending in death. Al forms toxic complexes with other elements, such as fluorine, and interacts negatively with mercury, lead, and glyphosate. Al negatively impacts the central nervous system in all species that have been studied, including humans. Because of the global impacts of Al on water dynamics and biosemiotic systems, CNS disorders in humans are sensitive indicators of the Al toxicants to which we are being exposed.

lioralourie
Posts: 22
Joined: Sat Jan 18, 2014 12:35 pm

Re: Aluminum in the central nervous system (CNS): toxicity..

Postby lioralourie » Mon Apr 20, 2015 12:27 pm

adding to the full text list above

19 ) J Toxicol. 2014;2014:491316. doi: 10.1155/2014/491316. Epub 2014 Oct 2.

Aluminum-induced entropy in biological systems: implications
for neurological disease.

Abstract
Over the last 200 years, mining, smelting, and refining of aluminum (Al) in various forms have increasingly exposed living species to this naturally abundant metal. Because of its prevalence in the earth's crust, prior to its recent uses it was regarded as inert and therefore harmless. However, Al is invariably toxic to living systems and has no known beneficial role in any biological systems. Humans are increasingly exposed to Al from food, water, medicinals, vaccines, and cosmetics, as well as from industrial occupational exposure. Al disrupts biological self-ordering, energy transduction, and signaling systems, thus increasing biosemiotic entropy. Beginning with the biophysics of water, disruption progresses through the macromolecules that are crucial to living processes (DNAs, RNAs, proteoglycans, and proteins). It injures cells, circuits, and subsystems and can cause catastrophic failures ending in death. Al forms toxic complexes with other elements, such as fluorine, and interacts negatively with mercury, lead, and glyphosate. Al negatively impacts the central nervous system in all species that have been studied, including humans. Because of the global impacts of Al on water dynamics and biosemiotic systems, CNS disorders in humans are sensitive indicators of the Al toxicants to which we are being exposed.

lioralourie
Posts: 22
Joined: Sat Jan 18, 2014 12:35 pm

Re: Aluminum in the central nervous system (CNS): toxicity...

Postby lioralourie » Wed Nov 18, 2015 1:05 am

New full text to add into this list

20. Administration of aluminium to neonatal mice in vaccine-relevant amounts is associated with adverse long term neurological outcomes
fulltext FREE here
http://www.researchgate.net/publication/259653608_Vaccine_aluminium_injections_associated_with_adverse_behavioural_outcomes_JIB_LTShaw_2013

Abstract

Our previous ecological studies of autism spectrum disorder (ASD) has demonstrated a correlation between increasing ASD rates and aluminium (Al) adjuvants in common use in paediatric vaccines in several Western countries. The correlation between ASD rate and Al adjuvant amounts appears to be dose-dependent and satisfies 8 of 9 Hill criteria for causality. We have now sought to provide an animal model to explore potential behavioural phenotypes and central nervous system (CNS) alterations using s.c. injections of Al hydroxide in early postnatal CD-1 mice of both sexes. Injections of a “high” and “low” Al adjuvant levels were designed to correlate to either the U.S. or Scandinavian paediatric vaccine schedules vs. control saline-injected mice. Both male and female mice in the “high Al” group showed significant weight gains following treatment up to sacrifice at 6 months of age. Male mice in the “high Al” group showed significant changes in light–dark box tests and in various measures of behaviour in an open field. Female mice showed significant changes in the light–dark box at both doses, but no significant changes in open field behaviours. These current data implicate Al injected in early postnatal life in some CNS alterations that may be relevant for a better understanding of the aetiology of ASD.
Graphical abstract

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.

Image for unlabelled figure

Keywords

Autism; Aluminium; Adjuvants; Vaccines; Neurotoxicity; Neurodevelopmental disorders

apraxiaincanada
Posts: 9
Joined: Tue Jun 16, 2015 11:14 am

Re: Aluminum in the central nervous system (CNS): toxicity...

Postby apraxiaincanada » Thu Mar 24, 2016 9:07 am

Hi, I am an amateur autism researcher, like a lot of other autism parents.

I have actually been studying the link between autism and magnesium deficiency.

I was never looking for a link between autism and vaccines, but in studying the link between autism and magnesium, I realized the inevitable:

Anyone who is magnesium deficient will also, be default, be aluminum toxic.

This is because aluminum can actually pose as magnesium and take its place in cells, when magnesium is deficient.

Problem is, aluminum doesn't do the same job as magnesium.

Dr. Christopher Exley has shown that silica removes aluminum. Silica removes aluminum for the same reason that aluminum can pose as magnesium - silica, aluminum, and magnesium, are all of a similar atomic number. There is quite a bit of attention on Dr. Exley and silica in water right now (just based on the number of comments about it on the Recovering Kids facebook group) but zero attention on magnesium, since benefits from magnesium can happen more slowly.

Anyway I also have an autism theory centering around the lack of ionic magnesium (in water), and the lack or imbalance of minerals in water, if anyone would like to review it, I would be grateful.

I also have a facebook group on the topic, it is called pubmed parents - autism, apraxia viewed as a magnesium deficiency. I post a lot about aluminum, since you cannot discuss magnesium and autism without discussing aluminum and autism, and vice versa.

Thanks.


Return to “Autism Articles, Studies & Politics”