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Showing posts with label thimerosal. Show all posts
Showing posts with label thimerosal. Show all posts

7.30.2009

Washington Post admits [nonchalantley]- 'Flu vaccine has mercury'

http://www.washingtonpost.com/wp-dyn/content/article/2009/07/29/AR2009072903607_2.html?wpisrc=newsletter&wpisrc=newsletter&wpisrc=newsletter&sid=ST2009072903827
http://www.prisonplanet.com/images/november2007/151107vaccine.jpg
[...]
Some of the vaccine will be stored in multi-dose vials containing thimerosal, an antibacterial additive that contains mercury. But there will also be single-dose syringes without thimerosal, a substance that some assert is harmful to children.
Among the many unanswered questions is whether two doses[!!!] will be necessary to provide full protection, how close in time two shots can be given and how big the dose will be. Vaccination programs may start before the answers are known.
Clinical trials in which the prototype vaccine will be tested in hundreds of children and adults are just beginning[!!!!!]. Data on the effectiveness of one shot will be available in mid-September; [!]two shots[!], in late September.
Please, read more...

[It seems we don't have to wait that long! Look...]
Homeless people die after [an illegal?] bird flu vaccine trial in Poland
·Three Polish doctors and six nurses are facing criminal prosecution after a number of homeless people died following medical trials for a vaccine to the H5N1 bird-flu virus.
Read more of this...
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7.13.2009

Landmark Study Finds: Thimerosal Causes Autism Brain Pathology

·New Study Proves Thimerosal Induces Autism-like Neurotoxicity.
·Mitochondrial dysfunction, impaired oxidative-reduction activity, degeneration, and death in human neuronal and fetal cells induced by low-level exposure to thimerosal and other metal compounds.

http://charlieinwonderland.com/?p=1380
http://dprogram.net/2009/07/10/new-study-proves-thimerosal-induces-autism-like-neurotoxicity/
http://www.informaworld.com/smpp/content~content=a910652305~db=all~jumptype=rss
http://www.helpyourautisticchildblog.com/wp-content/uploads/2008/12/auti.gifhttp://www.whale.to/vaccines/thimerosal_infants.jpg
A new study, “A Mitochondrial Dysfunction, Impaired Oxidative-Reduction Activity, Degeneration, and Death in Human Neuronal and Fetal Cells Induced by Low-Level Exposure to Thimerosal and Other Metal Compounds”, published in the most recent issue of the peer-reviewed journal of Toxicology & Environmental Toxicology, confirms a causal connection between Thimerosal and the brain pathology found in patients diagnosed with an autism spectrum disorder (ASD).
[...]
This study showed Thimerosal-induced cellular damage in human neuronal and fetal-cell model systems in a concentration- and time-dependent fashion using Thimerosal at low nanomolar (parts-per-billion) concentrations. These concentrations are comparable to those found in fetal and early infant exposure to mercury from Thimerosal-containing biologics and vaccines in the 1990s and, in some instances, today. These levels induced significant cellular toxicity in the human neuronal and fetal cells studied. The Thimerosal-induced cellular damage was consistent with that found in pathophysiological studies of patients diagnosed with an ASD. In both instances, the studies found significant mitochondrial dysfunction, reduced cellular oxidative-reduction activity, cell degeneration, and cell death.
The present study also revealed that Thimerosal is significantly more toxic than the other metal compounds studied (e.g., aluminum sulfate, methylmercury hydroxide, lead acetate, and mercuric chloride). The explanation for Thimerosal’s greater toxicity than even methylmercury hydroxide (MeHgOH) appears to be the fact that Thimerosal was chemically engineered in the 1920s to be a more highly toxic alkylmercury compound, whose biological transport and intracellular delivery properties were enhanced. Compared to MeHgOH, Thimerosal has: 1) higher aqueous solubility (i.e. ability to dissolve in water and water-based systems); 2) higher solubility in cell membranes (i.e. ability to dissolve in cell membranes); and 3) higher intracellular toxicity (i.e. ability to inactivate essential cell processes) and mercury retention.
Read more...
[Here, the article from dprogram.net]
[And here the study, as published on informaworld.com]
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