Our mission is to make each day the best possible day for people living with and affected by ALS. We achieve our vision by providing support, facilitating the provision of care, promoting awareness, helping find a cure and advocating for change.


The Amyotrophic Lateral Sclerosis Society of Alberta was incorporated as a non profit organization in 1986 and helps those living with and affected by ALS. We provide programs and services for clients, families, caregivers and health care providers. Our Programs and Services include: Information and Education; Equipment and Assistive Technology; Support Groups; Care Coordination; Referrals; and Home Visits. The work of the Society is funded through special events, foundations, bequests, memorial contributions, general donations and corporate gifts.


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