Culinary Care in ALS – A nutritional toolkit
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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 WHAT ACTION WILL YOU TAKE? ALS doesn't stop - neither do we Learn more June 2: Lou Gehrig Day
This June, we will Strike Out ALS, together. 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 :

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.

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You are invited to an evening for those who have been touched by the loss of a loved one to ALS.

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Join the ALS Quebec team on Saturday, June 19th, 2021, for our Virtual Walk to End ALS.

NEWS

We are pleased to present this bilingual presentation on current ALS Research, held on February 24th, 2021. A Q&A follows the conference.
Speakers:
1. Dr.  Richard Robitaille, PhD, Full Professor, Neurosciences Department, Université de Montréal
2. Dr. Angela Genge, Neurologist and Director of the ALS Clinic and the Clinical Research

The Canadian ALS Research Network (CALS) offers you an explanatory document in which you will find the answers to the following questions:

Is the vaccine safe?
Should people living with ALS be considered a vulnerable population?
Should I receive the vaccine?
When and where can I get the vaccine?

⛄ During the confinement and all winter long, enjoy the beautiful weather and inspire your family and friends by building a snowman in honor of a loved one with ALS. Send us your story and photos at [email protected]!
🎨 For the chilly days indoors, have fun with the kids doing this

“With change comes adjustment and resilience.” – Odette Lacroix
Back in 2001, when my husband Pierre was diagnosed with ALS, the outlook for people living with the disease was very different. At the time, there was only one support group in the entire province, so we had to travel to