Robert Bishop
Introduction
HD family tree
Why I do this
Family photos
What is HD?
Definition
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.
www.curehd.org
Last updated:
Oct 2008
huntington's disease
huntington's disease
huntington's disease
huntington's chorea
huntington's chorea
huntington's chorea
huntingtons disease
huntingtons disease
huntingtons disease
huntingtons chorea
huntingtons chorea
huntingtons chorea
huntington disease
huntington disease
huntington chorea
huntington chorea
hd, hd, hd, hd, hd
hd, hd, hd, hd, hd
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(50% at-risk for HD) |

(50% at-risk for HD) |

(50% at-risk for HD) |
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(50% at-risk for HD) |

(50% at-risk for HD) |
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(Bishop Family) |
PLEASE HELP SAVE MY KIDS!!!
My name is Robert Bishop. I am 46 years old and the father of five at-risk children
(ages 22, 19, 16, 13, and 11). In 1998, I sold my computer software business
to take up the cause of fund raising and public awareness for a terminal illness
called Huntington's Disease (HD). Unless a cure is found, 2 or 3 of my children
will tragically die from this disease. Each has a 50% chance of having inherited
a defective gene from their first mother, Amy (who became symptomatic for HD in her
mid-twenties).
Can you imagine growing up knowing you had a 50% chance of suffering 15-20 years
while the nerve cells in your brain slowly died? Can you imagine losing
everything that is you (from your personality and intelligence to your ability
to walk and speak) while in the prime of your life? It's no wonder my
eldest daughter has asked "Dad, how will I ever marry or have children?" or
that my eldest son has said "Dad, what's the point of school?... I'm just
going to get sick like Mom and forget everything anyway!" or that my
third-born son has said "I think I'm going to get the disease since I'm in the
middle!" Thankfully, the two youngest at-risk children don't know
what may lie ahead for them or their brothers and sisters.
While viewing the information on this site, please take the time to do two
things. First,
make a donation. All contributions are used to fund good
science in finding a cure for Huntington's Disease. Second,
spread the word. Send a personal note to 10 people you know
and ask them to do the same. Help make this the last
generation to suffer from this dreaded illness.
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