Our Vision | 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.
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
|M.C. Kiselick, President||Charlotte Small||Phil Kiselick|
|Maggie Milnamow, Vice President||Brendan Milnamow||Peter Devore|
|Daniel Fendler, Treasurer||Brandon Pearson||Katie Papciak|
|Theresa Spelman||Lizzie Greene||Shravanthi Chidambaram|
|Amanda Polli, Celebration of Hope Chair||Michael Varner||Elizabeth Greene|
|Carol Baird, Team Hope Chair||Emily Rekstis|