News

The ALS Society of Canada is pleased to welcome Kyle Thompson to its Board of Directors. Kyle is no stranger to ALS Canada or the ALS community. Over the last two years, he has served on the Finance and Audit…

Our bimonthly Fundamental Research Update keeps you informed about the latest advances in lab-based ALS research. We break down new studies using cellular and animal models, highlight progress on promising preclinical targets, breakdown trending research news, and showcase Canadian led science.  For other news on clinical research and trials, read our Clinical Research & Trials Updates.  ALS…

Members of the ALS community meet with MPPs and policymakers to highlight how the Ontario government’s investment is improving care and support for people affected by ALS across the province TORONTO, April 21, 2026 – The ALS Society of…

This week is National Volunteer Week (April 19 – 25), ALS Canada is honoured to recognize, celebrate, and thank our incredible volunteers who support our mission, raise funds, and help move the needle toward a world free of ALS.  This year’s theme is Ignite Volunteerism, highlighting the power…

From the Research Desk highlights recent updates from the ALS Canada Research Team, along with highlights from the broader ALS research community.  By staying connected with researchers around the world, supporting meaningful advances in ALS research, and sharing knowledge with our community, we are grateful…

Virtual program connects caregivers to mental health support anywhere in Canada TORONTO, ON, April 7, 2026 – In recognition of National Caregivers Day, caregivers for people living with amyotrophic lateral sclerosis (ALS) across Canada will have access to an…

Our bimonthly Clinical Research & Trials Update keeps you up to date on what’s happening in ALS clinical research. We unpack trial press releases, flag upcoming studies, and highlight important new publications, including care guidelines, long-term therapy data, and off…

People living with ALS, caregivers, and bereaved families are encouraged to share their lived experiences to help inform healthcare decision-making and strengthen advocacy efforts Toronto, ON, March 9, 2026 – Living with amyotrophic lateral sclerosis (ALS) affects every part…