The Huntington Society of Quebec is a non-profit organization. Our mandate is to provide services to people affected with Huntington disease (HD) and their families. Being diagnosed with an incurable neurological, hereditary and degenerative disease requires tremendous support for the patient as well as the family and caregivers. The Huntington Society of Quebec offers services such as toll free lines for support and information, a summer camp for people with HD, a respite program for caregivers as well as documentation and training for families and health professionals. In addition, this year we would like to develop a program for young people living at risk for Huntington. In order to continue to offer these invaluable services free of charge, we need your support.