- CureHD Foundation -
Dedicated to funding a cure for Huntington's Disease.

Robert Bishop
HD family tree
Why I do this
Family photos

What is HD?
The HD secret
How many have HD
The cruelest illness

The HD nightmare
My experience
Other experiences

HD research
Hope for a cure
North America

How can I help?
Make a donation
Contact the media
Ask legislators...

News & events
Articles & stories
I need your help

Contact info
CureHD Foundation
CureHD sponsors
HD web sites
Other info

Content 1999-2009
CureHD Foundation
All Rights Reserved.


Why haven't I heard about HD?
Although HD is a very compelling illness, it's not very well known because families who are affected by HD are often afraid to speak out. Genetics is relatively new and our society is not very well suited to protect individuals who are predisposed to get a terminal illness, nor to assist those who already have it. I don't blame people for their fears. I've personally experienced an unbelievable amount of discrimination and judgment which almost buried our family, both financially and otherwise. But for some reason, we were saved from all of that. Now I have a unique opportunity to assist in finding a cure so that families with HD (including my children) can have a chance at something other than life-long misery.