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The ALS Society of Alberta operates province-wide support programs and research initiatives for individuals affected by Amyotrophic Lateral Sclerosis. Based in Alberta, the organization coordinates three signature fundraising events: the "Side by Side for ALS" walk marking its 30th anniversary, "Cycle for ALS" rides in Edmonton, Calgary, and Lethbridge, and virtual book clubs featuring medical memoirs like "When Breath Becomes Air." ALSAB maintains active partnerships with CORDSAS and regional healthcare providers. The organization's programming spans three core areas: direct patient support, community education, and research advancement. Regular events include research symposiums, patient education sessions, and fundraising galas featuring presentations from neurological specialists and clinical researchers. Local volunteer networks coordinate support across Alberta's major urban centers. ALSAB's service model integrates clinical care coordination, equipment lending programs, and family support resources. The organization facilitates connections between ALS researchers, healthcare providers, and community members through structured programs and events. Research initiatives focus on understanding neurodegenerative disease mechanisms while developing enhanced care protocols.