News

Being a caregiver for someone living with ALS can be emotionally and physically exhausting, isolating, and overwhelming. Families need consistent guidance, resources, and support to manage both the disease and the strain it places on them. ALS Canada’s Community Leads…

The ALS Society of Canada (ALS Canada) is proud to launch the Children and Youth Resource Hub to provide children, youth, and families with important educational materials that support the understanding of amyotrophic lateral sclerosis (ALS) – a disease that…

From December 2 to 8, 2024, the ALS Society of Canada (ALS Canada) and the ALS Society of Quebec (ALS Quebec) co-hosted a series of events that brought more than 1,500 delegates from around the world to Montreal to…

ALS Canada is proud to recognize and celebrate Dr. Richard Robitaille, a leader in ALS research and a professor at Université de Montréal, who has received the prestigious Drs. Ayeez and Shelena Lalji & Family ALS Endowed Award for Innovative…

ALS Canada Buck-A-Puck for ALS is back! This event unites young athletes and their passion for hockey with fundraising and awareness building for amyotrophic lateral sclerosis (ALS) – a disease that affects nearly 4,000 Canadians and their families. The concept…

The ALS Society of Canada (ALS Canada) is committed to Canada’s contribution to global ALS research. We’re excited to share our involvement in the Accelerating Medicines Partnership® in Amyotrophic Lateral Sclerosis (AMP® ALS), led by the Foundation for the National…

The ALS Society of Canada (ALS Canada) is proud to share that the Canadian ALS Learning Institute (CALI) program has received the Silver Leaf Award of Merit in the Community Relations category from the International Association of Business Communicators (IABC)…

Participants can choose from three scenic routes and unite to raise funds for ALS research and community-based supports HAMILTON, September 17, 2024 – On Sunday, September 22, cyclists will unite for the ALS Canada Revolution Ride in the scenic…