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irishspirit
11th December 2010, 22:10
Imagine being the parent of a young child who is not acting normally and being told by your doctor that your child has autism, that there is no known cause, and there is no known treatment except, perhaps, some behavioral therapy. That is exactly what Jackson's parents were told as their 22-month-old son regressed into the non-verbal psychic prison of social withdrawal, disconnection, and repetitive behaviors typical of autism.

While we don't have all the answers, and more research is needed to identify and validate the causes and treatment of autism, there are new signs of hope. A study just published in The Journal of the American Medical Association by researchers from the University of California, Davis called "Mitochondrial Dysfunction in Autism" (i) discovered a profound and serious biological underpinning of autism -- an acquired loss of the ability to produce energy in the cells, damage to mitochondria (the energy factories in your cells), and an increase in oxidative stress (the same chemical reaction that causes cars to rust, apples to turn brown, fat to become rancid, and skin to wrinkle). These disturbances in energy metabolism were not due to genetic mutations, which is often seen in mitochondrial problems, but a condition the children studied acquired in utero or after birth.

Bottom line, if brain cells cannot produce enough energy, and there is too much oxidative stress, then neurons don't fire, connections aren't made and the lights don't go on for these children. In fact, this problem of energy loss is found in most chronic disease and aging -- from diabetes to heart disease to dementia. Brain function and neurodevelopment in particular are highly dependent on energy.

This is exactly the problem, I documented and found in Jackson when I first saw him. He had a profound loss of energy in his cells (particularly his brain cells), and indicators of severe oxidative stress. This is the same problem many other researchers have found in similar studies. (ii) Despite the evidence, most physicians don't test for mitochondrial dysfunction, oxidative stress or other myriad factors commonly found in autistic children.

Let's look more closely at what this new study in The Journal of the American Medical Association tells us about mitochondrial dysfunction, and how this may lead us to new methods of treatment -- methods similar to the ones I used to help reverse Jackson's autism.

http://www.huffingtonpost.com/dr-mark-hyman/autism-research-discovery_b_794967.html

In other words, do not give them the Jab.

Czarek
12th December 2010, 01:32
Imagine...child has autism, that there is no known cause, and there is no known treatment except, perhaps, some behavioral therapy..

I'd like to share one case with you that I had experienced. One of my patients came in for a check of his chronic foot infection. He already lost one foot due to a blister that got infected. (he is diabetic). We started talking about what he's doing to save his other foot. He switched from antibiotics tx to a total body heavy metal detox. i.e.chelation. It was working! The foot was getting better. No infection in the bone, marrow but surronding tissues still had slightly elevated levels of white blood cells. Some how we got onto a topic of children, and how his autistic son was cured with just that method. I was scheptical and he sensed that. He had to come back to see me again the next day and he offered to bring his son to meet me.
His son looked to be about 6-7 years old, but acted like he was 12!

Zook
12th December 2010, 04:18
Hi Irishspirit,



[...]
http://www.huffingtonpost.com/dr-mark-hyman/autism-research-discovery_b_794967.html
In other words, do not give them the Jab.

The article tries to mitigate the culpability of the FDA, JAMA and Big Pharma, IMHO.

Real science ... has revealed mercury to be the prime suspect in autism. Both as an environmental pollutant; and as a preservative in vaccines (e.g. thimerosal). Of course, the Huffington Post article tries to pretend that multiple factors are involved, e.g. in their explanation of the explosion of autistic cases in the past twenty years. While one of the effects may, indeed, be mitochondrial dysfunction in the neurons, as the article alleges ... the primary cause appears to be atrophy of the dendritic processes (as shown in the following video, e.g. due to receptor blockage by mercury in the construction of the dendrite's microtubules):


http://www.youtube.com/watch?v=85tgwh3HpsM

This link discusses the thimerosal link:
http://chetday.com/autismthimerosal.htm

Another link, this one describes a simple way of determing the role of mercury in autism.(e.g. through analyzing its presence or absence in hair):
http://www.rense.com/general41/merc.htm

***************** beginExcerpt *************************

The study, co-authored by Mark Blaxill, a director of Safe Minds, suggests a biological mechanism for the hypothesis first advanced by Safe Minds that autism is a form of mercury poisoning and that exposure to the mercury-based preservative thimerosal in vaccines has likely caused neurological damage to thousands of children.

Blaxill, along with co-investigators Amy Holmes, MD and Boyd Haley, PhD, assessed mercury exposure levels among 94 autistic children and 45 normally developing controls. They found higher pre- and postnatal exposures in the autistic group. Then they took a novel approach to measuring mercury distribution in the study subjects during infancy: they collected the first lock of baby hair that had been taken years earlier from each child to determine its mercury content. In a result that appears surprising at first, they found that the autistic hair mercury levels were only a fraction of the controls'.

"Our findings might seem counter-intuitive," says Blaxill, "but if you take into account the higher exposures of the autistic children, you quickly see that these reduced hair levels suggest that less mercury was being excreted by these babies. This is because mercury must be in the blood in order to be taken up by the hair follicle, and mercury must be in the blood in order to be eliminated from the body. If it's not in the hair, then it is not in the blood. And if it's not in the blood to be eliminated, more mercury is retained and available to cause neurological damage in infants who subsequently develop autism."

************ end ************************************


Humble opinions all around.

:typing:

ps: You're spot on, Irishspirit. The jab appears to be primarily responsible for autism; specifically, an accumulation of mercury through a multiplicity of jabs.

Houman
12th December 2010, 05:54
those children are the canaries in the coal mine... we should all be concerned about their fate...
http://www.youtube.com/watch?v=EbCKQ1JSgW0

http://www.ch3nutrigenomics.com/phpBB2/viewtopic.php?t=16274&sid=5bc25f8ad09db3b568c3e8f7bdc24d4d