Showing posts with label aluminum. Show all posts
Showing posts with label aluminum. Show all posts

Thursday, November 29, 2012

Vaccine Autism Shocker: Study Reports Strong Evidence of Autism Connection to Aluminum and Acetaminophen Exposure

It is quite possible that a paper claiming that empirical data confirm autism symptoms are related to Aluminum and Acetaminophen exposure, and possibly to the MMR vaccine,  could put the research standing and careers of the authors in jeopardy.  The paper in the journal Entropy is tantamount to treason in some health circles and could invite serious retribution from those who have elevated vaccines to a level beyond criticism.  

The researchers, to my great surprise, did not try to sugar coat their findings in  Empirical Data Confirm Autism Symptoms Related toAluminum and Acetaminophen Exposure, published in Entropy, November 7, 2012: 

Abstract: Autism is a condition characterized by impaired cognitive and social skills, associated with compromised immune function. The incidence is alarmingly on the rise, and environmental factors are increasingly suspected to play a role. This paper investigates word frequency patterns in the U.S. CDC Vaccine Adverse Events Reporting System (VAERS) database. Our results provide strong evidence supporting a link between autism and the aluminum in vaccines. A literature review showing toxicity of aluminum in human physiology offers further support. Mentions of autism in VAERS increased steadily at the end of the last century, during a period when mercury was being phased out, while aluminum adjuvant burden was being increased. Using standard log-likelihood ratio techniques, 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. We propose that children with the autism diagnosis are especially vulnerable to toxic metals such as aluminum and mercury due to insufficient serum sulfate and glutathione. A strong correlation between autism and the MMR (Measles, Mumps, Rubella) vaccine is also observed, which may be partially explained via an increased sensitivity to acetaminophen administered to control fever.


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6. Conclusion 

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-aluminumcontaining vaccines, suggests that neuronal damage due to aluminum penetration into the nervous system may be a significant factor in autism. The fact that mentions of autism rose steadily concomitant with significant increases in the aluminum burden in vaccines, is highly suggestive. However, it is possible that other factors, such as more aggressive reporting or simultaneous increases in other environmental toxins, e.g., herbicides or pesticides, or aluminum in other products such as antiperspirants and antacids, may have contributed to these observed increases. We also observed a strong correlation between the MMR vaccine and autism, which we suggest could be explained by the effects of acetaminophen. 

We have proposed elsewhere that an impairment in cholesterol sulfate synthesis in the skin and in the vasculature may be causative in autism, and we argue here that vaccines can act synergistically with this impairment in the vulnerable child. We propose that simple corrective measures such as increased sunlight exposure and decreased use of sunscreen may help protect a child from a severe reaction to aluminum-containing vaccines, but we also feel that the vaccine industry should find a way to reduce or even eliminate the aluminum content in vaccines. 

As might be expected Dr. David H. Gorski, writing under the handle Orac has already spewed some venom on  one of the authors of the study in his blog commentary of November 20, 2012, Stephanie Seneff: Following the Geiers dumpster-diving in the VAERS database.  I am not sure why Gorski engages in the childish, self inflating style that he does. There is no question he has a loyal following but I doubt very much that he is persuading parents or others with vaccine concerns to abandon those concerns and vaccinate themselves and their children.   I suspect his venomous hostility is actually counter productive.

I have received the usual recommended vaccines and so have both of my sons. I have never suspected vaccines as contributing factors to my younger son's severe autistic disorder and profound developmental delays although I have not closed my mind on the possibility either should further research demonstrate such a connection.  I believe that more research is needed to persuade those with concerns and, if connections are shown, to recommend study and changes to eliminate those possible connections.

What I don't recommend is the strategy of attacking vaccine safety skeptics and expecting the attacks to change their minds.  That approach simply has not worked. A much better scientist than David Gorski, a gentleman named Albert Einstein, characterized "doing the same thing over and over again and expecting different results" as a form of insanity.   I don't expect Orac to change his approach. Nor do I expect the results of his attacks to yield different results.  What would be helpful is to have the Seneff study findings properly rebutted or, if confirmed, the problems they point to addressed.

Wednesday, August 12, 2009

More Autism on the Way? Swine Flu Vaccine Adjuvants, Thimerosal and Autism

Pregnant women will be at the front of the line for the Swine Flu vaccine in many countries. Mercury in thimerosal crosses the placental barrier. So thimerosal will not be used in the Swine Flu vaccine right? WRONG!. Thimerosal will be used and its negative effects, including possibly autism in some of the women's children, could be enhanced by the aluminum adjuvants used in the vaccines.

Australian scientist Vera Scheibner Ph.D., has described the effects of aluminum adjuvants including the enhancement of mercury toxicity and possible autism implications amongst a host of other health issues in The Terrifying World Of Vaccine Adjuvants:

Adjuvants are formulated compounds, which when combined with vaccine antigens intensify
the body’s immune response. They are used to elicit an early, high and long-lasting immune
response. “The chemical nature of adjuvants, their mode of action and their reactions (side
effect) are highly variable in terms of how they affect the immune system and how serious their adverse effects are due to the resultant hyperactivation of the immune system. While
adjuvants enable the use of less *antigen to achieve the desired immune response and reduce vaccine production costs, with few exceptions, adjuvants are foreign to the body and cause adverse reactions”, writes Australian scientist Viera Scheibner Ph.D, (1) The most common adjuvant for human use is an aluminum salt called alum derived from aluminum hydroxide, or aluminum phosphate. A quick read of the scientific literature reveals that the neurotoxic effects of aluminum were recognized 100 years ago. Aluminum is a neurotoxicant and has been linked to Alzheimer’s disease and other neurological disorders.

The article cites Boyd Haley for the proposition that vaccines which contain both aluminum adjuvants and mercury based preservative, greatly magnify the neurotoxic effects. The article comments on squalenes used in vaccines and a process called molecular mimicry and ties molecular mimicry to the autism epidemic:

Tying molecular mimicry to the autism epidemic, many children have regressed into autism spectrum disorders after injection with the triple live virus MMR (measles,mumps,rubella) vaccine. Dr.Vijendra Singh’s research at Utah State University suggests that auto-antibodies are attacking myelin in these children. He has shown that many autistic children have auto-antibodies to brain myelin basic protein (MBP) as well as elevated levels of measles virus antibodies. “Immunoblotting analysis showed the presence of an unusual MMR antibody in 60% (75 of 125) of autistic children, but none of the 92 normal children had this antibody. In addition, there was a positive correlation (greater than 90%) between MMR antibody and MBP auto-antibody, suggesting a causal association between MMR and brain autoimmunity
in autism. This is one of the most important findings in autism to date, which prompted us to link measles virus in the etiology of the disorder”, writes Dr. Singh. (8,9,10)

These excepts are a small selection of the information contained in this article which I recommend for reading by anyone who is interested in reading beyond the standard public health authority assurances about the possible consequences of the still not tested Swine Flu Vaccines. Although I have extracted sections directly referencing autism the article covers many other issues associated with vaccine adjuvants.




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Thursday, March 13, 2008

Autism Rising in Oregon



More than 7,000 Oregon students have autism, triple the count 10 years ago and 11 percent higher than just a year ago, the state reported Wednesday."

The Oregonian, March 13, 2008

Neurodiversity believers will automatically state that increases in autism in Oregon are due to changes in the definition, diagnostic criteria , and increased public awareness of autism disorders. They are partly correct in that such factors have occurred. And it is very reasonable to assume that such factors account for some of the increases in Oregon and elsewhere. But it is not reasonable to assume that the startling increases in autism disorder diagnoses is attributable entirely to definition change and social factors.

The belief that these increases are due entirely to changes in how we view autism is a faith based belief unsupported by credible studies or data. It amounts, without evidence, to a rejection of the possibility that environmental factors, not just thimerosal, but any environmental factors, are causing or contributing to the rise, across Canada, the US, and Europe to the startling increases in autism diagnoses. The presence of mercury, lead, aluminum, and a long list of chemicals and plastic components in our drinking water, and our environment generally, are ruled out as possible causes or contributing factors to the rise of autism.

The true believers of the neurodiversity movement are free to cling to their beliefs. I prefer to keep an open mind and, until more study is done, and more information is available, work on the assumption that the very dangerous substances in our environment might be having harmful effects on our children. Increases in autism disorder diagnoses might be one of those harmful consequences of our increasingly toxic environment.