The Autism Catastrophe
Health Impact News Editor Comments:

One of the real tragedies in vaccine damaged children is that because the U.S. Government denies any link in vaccines causing autism, no research is ever conducted to find out why certain children suffer from autism after being vaccinated, even when the Vaccine Court rules in their favor. So as a result, the vaccines causing the problem continue to be marketed to all children, regardless of pre-existing conditions, and the rate of autism continues to climb. The government and medical system wants you to believe that vaccines are safe for everyone, and they refuse to examine or research why some children react differently to vaccines.

Research like this one published recently in the International Journal of Environmental Research and Public Health, therefore, must be done with private funds and no help from the government. This study has identified key markers that make certain children more susceptible to the toxic effects of mercury in vaccines, which could help doctors determine who should be receiving certain vaccines, and who should not due to increased risk. Sadly, you are not likely to read this in the mainstream media, nor learn of it from your doctor.

Thimerosal Exposure and the Role of Sulfation Chemistry and Thiol Availability in Autism

International Journal of Environmental Research and Public Health – August 2013

Abstract

Autism spectrum disorder (ASD) is a neurological disorder in which a significant number of the children experience a developmental regression characterized by a loss of previously acquired skills and abilities. Typically reported are losses of verbal, nonverbal, and social abilities. Several recent studies suggest that children diagnosed with an ASD have abnormal sulfation chemistry, limited thiol availability, and decreased glutathione (GSH) reserve capacity, resulting in a compromised oxidation/reduction (redox) and detoxification capacity. Research indicates that the availability of thiols, particularly GSH, can influence the effects of thimerosal (TM) and other mercury (Hg) compounds. TM is an organomercurial compound (49.55% Hg by weight) that has been, and continues to be, used as a preservative in many childhood vaccines, particularly in developing countries. Thiol-modulating mechanisms affecting the cytotoxicity of TM have been identified. Importantly, the emergence of ASD symptoms post-6 months of age temporally follows the administration of many childhood vaccines. The purpose of the present critical review is provide mechanistic insight regarding how limited thiol availability, abnormal sulfation chemistry, and decreased GSH reserve capacity in children with an ASD could make them more susceptible to the toxic effects of TM routinely administered as part of mandated childhood immunization schedules.

Read the Full Study online FREE: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774468/

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