I have ALS
*Educational Webinar – Kinesiology and ALS
Join us for the webinar Kinesiology and ALS with kinesiologist Billy-Ann Houle-Powers. Discover how adapted physical activity can help preserve functional abilities, reduce discomfort, and promote the well-being of people […]
*Zoom User Guide
A Zoom guide to facilitate access to ALS Quebec’s virtual activities. In order to help you with Zoom, we created a user guide. In the event of a technical issue, […]
Quebec.ca – Residential Adaptation Assistance Program (PAD)
The PAD provides financial assistance for home improvements that increase accessibility and safety, thereby helping individuals remain in their homes and maintain their independence (info only available in French).
*Educational webinar – ALSUntangled: Understanding alternative and off-label treatments (AOTs) for ALS
Have you ever been curious about possible ALS treatments you may have heard of or found online? ALSUntangled founder Dr. Richard Bedlack will explain how people living with ALS can […]
*Educational webinar: Spotlight on ALS Research and Q&A – June 9, 2026
Leading amyotrophic lateral sclerosis (ALS) researchers and clinicians shed light on their current clinical studies. Presentations are followed by a question-and-answer period. Dr. Richard Robitaille, Ph.D., Full Professor of Department […]
A selection of summer resources and activities for the ALS community and their loved ones
A selection of summer resources and activities for the ALS community and their loved ones. Other resources Important note This information is shared for informational purposes only. ALS Quebec cannot […]
*Educational webinar – Talking about ALS in the family: supporting children and adolescents
This panel and discussion is facilitated by Justine Hugh, social worker and clinical director at Deuil-Jeunesse, and Isabelle Lessard, former caregiver. Justine provides concrete guidance and practical tools for discussing […]
Letters to ALS: Our Journeys to Hope
Letters to ALS: Our Journeys to Hope is a unique new book of deeply personal letters from members of the amyotrophic lateral sclerosis (ALS) community. Presented as “Dear ALS” letters, […]