This online resource centre is updated regularly and has been designed as a one-stop shop for comprehensive information about all aspects of ALS. Use the filters to hone in on the specific information you’re looking for, or browse the full offering. Resources developed and/or offered by ALS Quebec are marked with an asterisk (*).
Be sure to bookmark this page and check in frequently as we are regularly adding new resources. If you’ve found a resource particularly helpful and don’t see it listed here, please recommend it to us by emailing info@sla-quebec.ca.
Please note there may be additional resources within the French section of our website. The FR icon means that the resource is also available in French.
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, […]
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).
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 […]
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. Other resources Important note This information is shared for informational purposes only. ALS Quebec cannot […]
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 is a unique new book of deeply personal letters from members of the amyotrophic lateral sclerosis (ALS) community. Presented as “Dear ALS” letters, […]
Real Kids Talk About ALS – Feeling Normal, Sad, and Different by Melinda S. Kavanaugh & Megan Howard
ALS Quebec does not endorse and is not responsible for the information contained on external sites. Should you have questions about any of the services or require additional information, please contact the organizations directly. These links are provided as a convenience and should not be construed as endorsements of any of the organizations.
