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.
The author shares her personal experience caring for her father who has ALS, in order to help others in a similar situation.
A palliative care educator and volunteer living with ALS (also known as MND) provides insight to her colleagues. Part of a series.
Support your loved one with ALS and take care of yourself by learning about available home care options.
Information about programs available through the Quebec government to support people with disabilities.
This comprehensive guide covers a range of topics about living with the disease and what to expect.
A booklet to help teens cope with a parent’s ALS diagnosis.
How to deal with feelings of grief and loss following an ALS diagnosis and as the disease progresses.
Learn about home care and what to expect once you have a file opened at the CLSC. Hosted by ALS Quebec for newly diagnosed people and their families.
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.
