For those that didn't know the National HD Team Hope web page recently got its final approval from HDSA and is now live and running at http://www.walk4hd.org....
I made a memorial page for my Mom. She died of HD when I was 17. I wanted to do one for a while now. There is one now. I will try and be as brave as my Mom was...
I made a memorial page for my Mom. She died of HD when I was 17. I wanted to do one for a while now. There is one now. I will try and be as brave as my Mom was...
See links to both the AP & Reuters news coverage articles. The below are excerpts only and not the full article. Dr. George Daley and his colleagues at the...
Mike Brown wrote about the new HD support group and he said it was okay if I shared a little more information on this group. If you're receiving individual...
Can you give me some information if you have any on support groups in North Louisiana For all have sinned, and come short of the GLORY OF GOD Romans 3:23 ...
Ooops I sent out the old one with a bad email for Mike. The below & attached is correct, sorry about that! Mike Brown wrote about the new HD support group and...
H.R. 6259: Huntington's Disease Parity Act of 2008 On-line Petition http://www.petitiononline.com/HR6259/petition.html As of this morning, August 16, 2008,...
The Canadian HD Society is having their annual HD Amaryllis Campaign. Buy the flowers. My family does this every year. They want to raise a million dollars...
Almost everyone knows and loves Jimmy Pollard and everything he has done over the past 20+ years helping caregiver's and care facilities understand what having...
There is a Canadian program here that will fly you down to California for stem cell treatment. They will pay for someone to go. It takes six months. Trevor...
More than 5 long years into President Bush's short-sighted, cruel policy restricting stem cell research, America once again has the chance to reverse it -- and...
Hello everyone, The Huntington's Disease Society of America is a national non-profit voluntary health agency dedicated to finding a cure for Huntington's ...
Vitamin B-12 deficiency should be checked for periodically in HD patients, especially in the mid to later stages when the person may not be consuming enough...
I have done my stem cell research. I found one of the world's best stem cells companies in the world. They are called Beike Biotechnology. They are on the...
Nancy Fiore, Mark Smrtnik's Mom, asked me to share this with everyone, writing: This just shows what a wonderful community we live in! My son touches so many...
For those who are receiving individual messages, attached is the brochure for this event. Subject: Annual Ultimate Hollywood Experience drawing Open to: All...
Marsha Miller has published two new articles on HDSA's website. Thank you Marsha & HDSA for keeping us up-to-date! The Hereditary Disease Foundation's...
There are three new articles up on the HDDW website written by Dr. LaVonne Veatch Goodman. The first talks about what CHDI is up to and provides some insight...
I'm a careseeker and I have found the ideal match on http://carecenter.bravehost.com/,It is a really trustworthy site.they identify your family's needs and...
Having problems with message search?
Fill out this form to ensure your group is one of the first to be migrated to the new message search system.
