It looks like you're using an Ad Blocker.
Please white-list or disable AboveTopSecret.com in your ad-blocking tool.
Thank you.
Some features of ATS will be disabled while you continue to use an ad-blocker.
The Undeniable Evidence: Proven and Peer Verified
Here are just a few of the studies that you're not supposed to know about, which show a definitive correlation between mercury and autism:
Cell Biol Toxicol. 2010 Apr;26: Induction of metallothionein in mouse cerebellum and cerebrum with low-dose thimerosal injection.
"As a result of the present findings, in combination with the brain pathology observed in patients diagnosed with autism, the present study helps to support the possible biological plausibility for how low-dose exposure to mercury from thimerosal-containing vaccines may be associated with autism."
Hepatitis B Vaccination of Male Neonates and Autism
"Findings suggest that U.S. male neonates vaccinated with hepatitis B vaccine had a 3-fold greater risk of ASD; risk was greatest for non-white boys."
Toxicology & Applied Pharmacology 214 (2006) 99–108: Porphyrinuria in childhood autistic disorder: Implications for environmental toxicity (This French study finds that heavy metal toxicity is a cause of autism.)
"A subgroup with autistic disorder was treated with oral dimercaptosuccinic acid (DMSA) with a view to heavy metal removal. Following DMSA there was a significant (P = 0.002) drop in urinary porphyrin excretion. These data implicate environmental toxicity in childhood autistic disorder."
Toxicological & Environmental Chemistry, Volume 91: 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.
This study showed the effects of exposure to ethyl mercury on cells, a component that vaccine advocates claim is harmless (unlike methyl mercury which is found in dental fillings, etc).
Journal of American Physicians and Surgeons Volume 11: Early Downward Trends in Neurodevelopmental Disorders Following Removal of Thimerosal-Containing Vaccines
"Holmes et al. examined first baby haircuts and determined that autistics had significantly higher body burdens of mercury in comparison to nonautistic matched controls, by demonstrating that the mercury level in hair, and thus the ability to excrete mercury, was inversely proportional to the severity of autism and overall much lower in the autistic group."
Med Hypotheses. 2001 Apr;56(4):462-71: Autism: a novel form of mercury poisoning.
"A review of medical literature and US government data suggests that: (i) many cases of idiopathic autism are induced by early mercury exposure from thimerosal."
While we could easily continue citing studies to show that ethyl mercury has an effect on causing developmental capabilities and autism, it would be pointless to do so. Those who would ignore all of these studies would also find a way to deny anything else that we might provide, because the facts contradict their zealous institutional dogma. It would cost them their jobs to believe otherwise.
What The Parent Of An Autistic Child Needs To Know Now
The truth is that autism can sometimes be cured, but only if it is caught in time. There is not enough data to make a statement about what percentage of cases are curable; even for those who begin the treatments early. Fast action is prudent because vaccine-injected mercury does tremendous damage to the brain, and to the central nervous system. If the mercury is not removed in time, recovery will not be possible. Mercury poisoning for autistic children is a ticking time-bomb, and its payload is permanent brain damage. Younger children are the most receptive to a full recovery, but the clock is ticking for them too.
Thousands of families are currently using DMSA, a substance that was F.D.A.-approved for the removal of lead. Studies are now beginning to show that it is likewise effective for mercury removal, which explains why this therapy helps autistic children.
Skeptics deny the effectiveness of this protocol based only on the fact that they do not believe that any vaccine-autism link exists. This bias stems from the fact that successful treatments further prove that autism was caused by mercury poisoning, and therefore by vaccines. Accepting this link would mean committing a career ending sacrilege, and nobody wants that. So, they ignore data showing the benefits of this therapy, and deride proponents (who are often parents that saved children) for being "unscientific". We have repeatedly found that the whole vaccine debate is much more about business and politics than science. It's what we call F.D.A. science ― in all its glory.
When the DMSA cure became popular, James Adams, Ph.D, Professor in the Division of Clinical Sciences at S.C.N.M. began a study, largely because his own daughter has autism. Surprisingly, N.B.C. covered the story.
Young, male colony CD-1 mice were injected with the adjuvants at doses equivalent to those given to US military service personnel. All mice were subjected to a battery of motor and cognitive-behavioral tests over a 6-mo period postinjections. Following sacrifice, central nervous system tissues were examined using immunohistochemistry for evidence of inflammation and cell death. Behavioral testing showed motor deficits in the aluminum treatment group that expressed as a progressive decrease in strength measured by the wire-mesh hang test (final deficit at 24 wk; about 50%). Significant cognitive deficits in water-maze learning were observed in the combined aluminum and squalene group (4.3 errors per trial) compared with the controls (0.2 errors per trial) after 20 wk. Apoptotic neurons were identified in aluminum-injected animals that showed significantly increased activated caspase-3 labeling in lumbar spinal cord (255%) and primary motor cortex (192%) compared with the controls. Aluminum-treated groups also showed significant motor neuron loss (35%) and increased numbers of astrocytes (350%) in the lumbar spinal cord. The findings suggest a possible role for the aluminum adjuvant in some neurological features associated with GWI and possibly an additional role for the combination of adjuvants.
Originally posted by Raelsatu
We have over 3 times as many vaccines per child, and our autism rate from 2011 is 1 in 91. Countries like Iceland have a rate of 1 in __ thousand, which is a significant difference. Also, take a look at the lifespan ratings and notice how the U.S. has been in a steady decline.
Originally posted by Raelsatu
Well according deathbyvaccine stats.
We have over 3 times as many vaccines per child, and our autism rate from 2011 is 1 in 91. Countries like Iceland have a rate of 1 in __ thousand, which is a significant difference. Also, take a look at the lifespan ratings and notice how the U.S. has been in a steady decline.
Originally posted by research100
good response, dj....I recently read a study where the drs decided to look at the younger siblings of older siblings with autism, this was before the younger siblings had any vaccines..... they examined them very closely and they were already showing signs of autism.
If the vaccines were the cause some of these children should have been nornal.. I will have to look to find the link but I wanted to share the story.
that dr who started this whole, autism/vaccine connection was totally discredited.