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 palliative care educator and volunteer shares what it’s like physically to live with ALS (also known as MND). Part of a series.
A palliative care educator and volunteer living with ALS (also known as MND) provides insight to her colleagues. Part of a series.
A palliative care educator and volunteer living with ALS (also known as MND) shares her emotional journey. Part of a series.
A palliative care educator and volunteer living with ALS (also known as MND) shares her spiritual journey. Part of a series.
A guide to help people living with ALS and those supporting them to improve their everyday quality of life.
Information about programs available through the Quebec government to support people with disabilities.
How to deal with feelings of grief and loss following an ALS diagnosis and as the disease progresses.
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.
