Tourette Syndrome Foundation of Canada / La Fondation canadienne du syndrome de la Tourette

The Tourette Syndrome Foundation of Canada provides support, education, and advocacy for people living with Tourette syndrome and their families. The organization funds research to better understand the neurological condition, offers educational programs in schools and workplaces across the GTA and beyond to reduce stigma, and connects individuals with resources and peer support networks. The foundation works to improve access to diagnosis and treatment while advocating for greater awareness among healthcare providers and the public. By combining direct support services with broader community education initiatives, the organization helps people with Tourette syndrome live fuller lives while advancing understanding of the condition in Canada.