Double my gift The Amyotrophic Lateral Sclerosis Society of Quebec is dedicated to improving the lives of people living with ALS as well as their caregivers. We're here for you! Stronger together More info Download now! Culinary Care in ALS

- A nutrional toolkit -
See who is part of our team to #StrikeOutALS! WHAT ACTION WILL YOU TAKE? June is ALS Awareness Month Learn more
I AM

living with ALS

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a caregiver

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a healthcare professional

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willing to help

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EVENTS

Date :

Join in on the fundraising bracelet sale organized by Valerie and her daughters!

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Ann-Marie Léporé, occupational therapist, will explain what you should expect once you have a file opened at the CLSC.

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This group is for people living with ALS in Quebec and the surrounding areas, as well as their friends, families, and caregivers. If you wish to discuss, obtain information or be in the company of others who know what you’re going through, please join us! 

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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.

NEWS

During the month of November 2022 was held the Conference: The shock of diagnosis with Mia Lanno (in English and in French).
This conference with Mia Lanno, social worker, explores the shock of receiving a diagnosis of ALS.
To watch the recording of the conference in English: click here.

NATIONAL CAREGIVER APPRECIATION WEEK
FROM NOVEMBER 6-12 2022
In celebration of National Caregiver Appreciation Week, we are sharing some inspiring stories and words
from our beloved community!

Chantal Lanthier

“Providing

On Tuesday, October 18 2022, was held the Conference: Communication disorders – Speech Therapy.
This conference addresses the context of the management of communication disorders in a hospital setting within an ALS clinic (assessment, interventions/monitoring, support, etc.), and then addresses the context of management in a rehabilitation center, including technological

On Tuesday, June 14 2022, was held the conference by Tracey Palmer – Sexuality and ALS.
The purpose of offering this presentation to people living with the disease is to help them recognize that they are still sexual beings with a need for connection and love and to share methods