- A nutrional toolkit -
EVENTS
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Join us this summer, alone or as a team, and ride to Fight ALS
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This virtual support group provides a place to exchange, to promote a better understanding of the disease and its different stages, inspired by each person’s unique context and reality.
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This English-speaking support group is for people living with ALS and their caregivers; to share time together with others, as well as with one of our psychosocial counsellors.
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This conference, given by Elaine Clavet, will allow you to better understand the changing reality of caregiving and to better identify the caregivers around you.
NEWS
On Tuesday, March 29 2022, was held the conference To learn more about ALS with Dr. Geneviève Matte.
This presentation, given by Dr. Geneviève Matte (Clinical Assistant Professor, Department of Neurosciences, Faculty of Medicine, Université de Montréal, Research investigator, CHUM Research Centre) explains what ALS is, it’s history and where
*Description available in French only*
La Société de la sclérose latérale amyotrophique du Québec est un organisme à but non lucratif voué à l’amélioration des conditions de vie des personnes atteintes de la SLA (maladie de Lou Gehrig) et au soutien des membres de leur famille. Notre étroite collaboration avec
On Tuesday, March 29 2022, was held a conference on Medical aid in dying and organ donation presented by Sophie Villemaire, clinical nurse at the ALS Clinic, CHUM and Lysane Desrosiers, liaison nurse in organ donation for Transplant Québec.
You can watch the recording of the conference above or click
During the month of February, conferences were held on Tax credits for caregivers and for people living with disabilities, presented by representatives of Revenu Québec.
If you missed the conference on Tax credits for caregivers and would like to have more information on this subject, click here to view