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 woman reflects on the experience of caring for her husband after his ALS diagnosis and the ups and downs of their time navigating the disease.
A novel about the ALS diagnosis of a celebrated concert pianist and its effect on his family, including his ex-wife.
Lessons in how to live, based on discussions between author Mitch Albom and his former college professor Morrie Schwartz who is dying of ALS.
This comprehensive guide covers a range of topics about living with the disease and what to expect.
A caregiver shares the range of complex feelings she has experienced since the death of her husband.
A series of fact sheets providing quick information on a range of ALS-related topics.
Caring for a person with ALS is an important but demanding role. Learn how it can affect you and tips for self-care.
This fact sheet offers first steps you can take if you or your loved one has been diagnosed with ALS.
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.
