The Huntington’s Disease Society of America is the largest 501(c)(3) non-profit volunteer organization dedicated to improving the lives of everyone affected by Huntington’s Disease. Founded in 1968, the Society works to provide the family services, education, advocacy and research.
The purpose of the Wisconsin chapter is:
• To help individuals affected by Huntington's Disease and their families through support and services
• To educate both the public and health care professionals about Huntington's Disease
• To promote and support research directed at discovering a treatment and ultimately a cure for Huntington's Disease.
For questions regarding support groups, genetic testing and medical referrals contact their social worker:
Jean Morack, ACSW, MSW