August 5, 2009
A new scientific study proves that the mercury-based compound used as vaccine preservative — known as ‘thimerosal’ — induces neural damage similar to that seen in autism patients.
According to the study, thimerosal-induced cellular damage caused concentration- and time-dependent mitochondrial damage, reduced oxidative-reduction activity, cellular degeneration, and cell death. Thimerosal at low concentrations induced significant cellular toxicity in human neuronal and fetal cells.
Thimerosal was found to be significantly more toxic than the other metal compounds examined.
Dr. Mercola’s Comments:
I’m always pleased to see another study confirming what vaccine-safety advocates have tried to get across for so long—that the mercury-based preservative thimerosal is seriously bad news and should never be injected. I don’t know how much proof will be required take to get the truth to finally get through, but a mountain of evidence is apparently still not enough for some nay-sayers.
This latest study confirms that damage does occur in human neuronal and fetal cells, even at low concentrations.
As you’ve likely heard by now, rates of autism in the U.S. have increased nearly 60-fold since the late 1970s, rising right along with the increasing number of vaccinations added to the childhood vaccination schedule.
This oftentimes debilitating neurological disorder now affects about one in 150 U.S. children, but an article in the Daily Mail two years ago reported the rate of autism in Great Britain could be as high as 1 in 58.
Although autism may be apparent soon after birth, most autistic children experience at least several months, or even a year or more of normal development — followed by regression, defined as loss of function or failure to progress.