A world free of Huntington's disease.
The Huntington's Disease Society of America (HDSA) is the premier nonprofit organization dedicated to improving the lives of everyone affected by Huntington's disease. From community services and education to advocacy and research, HDSA is the world's leader in providing help for today, hope for tomorrow for people with Huntington's disease and their families. In the battle against Huntington's disease no one fights alone. At HDSA, family is everything.
The HDSA Centers of Excellence provide an elite multidisciplinary approach to Huntington's disease care and research. HDSA currently has 50 Centers of Excellence across the United States.
At these world-class facilities, patients benefit from expert neurologists, psychiatrists, therapists, counselors and other professionals who have deep experience working with families affected by HD and who work collaboratively to help families plan the best HD care program throughout the course of the disease.
For the exact address of each HDSA Center of Excellence, click here for our Locate Resources page
Peggy Cribbin, HDSA Regional Development Officer
3286 Ivanhoe Avenue
St. Louis, MO 63139
p. (314) 537-1539
f. (314) 645-5754
Peggy Cribbin joined the Huntington’s Disease Society in June 2002. She has over 18 years of experience in the arena of fundraising for Huntington’s Disease. She is deeply interested and committed to educating the public about HD. Peggy resides in St Louis, MO with family.
Camille Colletti, HDSA Regional Development Officer
PO BOX 14252
Chicago, IL 60614-0252
P. (847) 849-0680
Camille Colletti joined HDSA as the Development Manager in December 2017. She has over 5 years of fundraising experience, and is committed to exceeding fundraising goals for HDSA in the coming years. Camille currently resides in Lincoln Park, Chicago.