The ALS Society of Alberta is a non-profit organization dedicated to making each day the best possible day for people living with and affected by Amyotrophic Lateral Sclerosis (ALS). It is the only non-profit organization in Alberta that provides support to those affected by the disease, and also invests in the most promising research initiatives in Alberta.

Our provincial office is in Calgary, and we have an additional office located in Edmonton. The Society also provides services in the Northwest Territories when needed.