Who We Are

Welcome to the Huntington's Disease Society of America's (HDSA) Minnesota Chapter. We are a part of HDSA's Upper Great Lakes Region.

Our Mission

To improve the lives of everyone affected by Huntington's disease and their families.

Our Vision

A world free of Huntington's disease.

About HDSA

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.​

HDSA Centers of Excellence

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

Mailing Address:
PO Box 16103
Minneapolis, MN 55416-6103

Social Worker:
For questions regarding support groups, genetic testing and medical referrals contact our social worker:

Jessica Marsolek
phone: 612.371.0904
email: jmarsolek@hdsa.org

HDSA Regional Development Officers
Peggy Cribbin
3286 Ivanhoe Avenue
St. Louis, MO 63139
p. (314) 293-4359

Camille Colletti
P.O. BOX 477
Mukwonago, WI 53149
P. (847) 849-0680

Take a moment and Like the Minnesota Chapter of HDSA on Facebook to connect with other members of the local HD community and stay informed of local news and details on upcoming events.

If you're interested in attending support groups, be sure to check out this link:

Minnesota HD Support Groups