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The ALS Society of Quebec is a non-profit organization dedicated to improving the quality of life for individuals living with Amyotrophic Lateral Sclerosis (ALS) and their families. Founded in 1983, the Society provides a wide range of support services, including technical aid, psychosocial support, and financial assistance programs. In addition to patient care, the organization is a significant funder of ALS research in Canada, collaborating with academic and clinical partners to advance the understanding and treatment of the disease. The Society also focuses on public awareness and advocacy to ensure better access to healthcare resources for the ALS community in Quebec. Through its fundraising efforts, it supports the ALS Canada Research Program to accelerate the discovery of a cure.
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