
Our mission is our everyday journey as an organization. We work with the ALS community to improve the lives of Canadians affected by ALS through advancing research, care, advocacy, and information.
Our vision is a world free of ALS. Open and honest with the challenges before all of us, we are determined to transform the reality of the disease.
ALS Canada (Amyotrophic Lateral Sclerosis Society of Canada) is a national charitable organization dedicated to supporting people living with ALS and funding research toward a cure.
Founded in 1977, it works closely with provincial ALS societies to provide community-based support services, education, and resources for individuals and families affected by the disease. The organization also invests in research to better understand ALS and advance treatments, while raising public awareness and advocating for improved care and access across Canada.