I’ve been blogging for five (5) and for the first time I’m asking American’s, directly from my
HD is one of 7,000 Rare Diseases in the world with NO CURE. In the U.S., HD affects a small population; approximately 41,000 Americans live the disease and 200,000 live at risk. I’m a volunteer and Chair for HDSA San Francisco Bay Area Affiliate, having lost my three (3) sisters-in-law to HD complications.
I’m reaching out to you because it has been an unusual year with the pandemic which has affected everything in our lives. Please consider making your year-end donation to HDSA so the nonprofit can continue supporting Huntington’s disease (HD) families across the U.S. DONATE TO HDSA
Resources/programs funded by HDSA are: 50 Centers of Excellence (HD) clinics, local HD support groups, Disability Chats, Telehealth Program, National Youth Alliance Program, education and research. HDSA also funds two yearly fellowships, Berman Topper Fellowship Donald King Summer Research Fellowship , and the Human Biology Project.
HDSA has high ratings as a nonprofit. Please see HDSA’s Charity Navigator ratings.
To make a donation, please visit: HDSA Donation Page
Thank you in advance for your generosity.
Below are HDSA accomplishments:
We Can Never Lose HOPE……………
No Comments