Home > Archive > Neurological Disorders > September 2005 > Huntingtons desease





You are viewing an archived Text-only version of the thread. To view this thread in it's original format and/or if you want to reply to this thread please [click here]

Author Huntingtons desease
Cliff fisher

2005-09-25, 10:35 am

Hi
My name is Cliff, my wife has been diagnosed with HD.
I'm interested in finding out as much as I can, so if anyone can help point
me in the right direction to discusion groups or info on HD I'd VERY
greatful.


Jerry Story

2005-09-25, 10:35 am

Cliff fisher wrote:
> Hi
> My name is Cliff, my wife has been diagnosed with HD.
> I'm interested in finding out as much as I can, so if anyone can help point
> me in the right direction to discusion groups or info on HD I'd VERY
> greatful.


I did a Google search on "Huntington's Disease" and got 1.4 million
hits.

The little bit of information that I read is not encouraging. They say
it's genetic. But doctors usually don't try very hard to find causes of
diseases. I would get Blaylock's books and I would stay strictly off
all excitotoxins, the same as for ALS.

Copyright 2003 - 2008 pahealthsystems.com