Founded in 1977, the ALS Society of Canada (ALS Canada) and our provincial partners are dedicated to supporting Canadians living with ALS and investing in research to make ALS a treatable, not terminal, disease. We are a registered charity that receives no government funding – all of our services and research are funded through the generosity of our donors.

Through the ALS Canada Research Program, we fund peer-reviewed research grants, foster collaboration and build capacity within Canada’s ALS research community, and participate in new areas of research where we are well-positioned to have an impact.

Within Ontario, ALS Canada has a role similar to that of the provincial ALS societies providing services and support to help meet the needs of people living with ALS.

ALS Canada advocates federally, provincially and locally for better government support and access within the healthcare system for people touched by ALS.

Charity

Health Care

Humanitarian

ALS Society of Canada

ALS Society of Canada's headquarters in Toronto, Canada

Description

People (17)

Tammy Pighin Moore

Christopher K. Pon

Justin Edmonstone

Jennifer Asselin

Monique Dannell

David Taylor

Colleen Doyle

Carolina Jung

Anthony Battista

Rabia Shah

Paulenia Ramlingum

Ilayda Ulgenalp

Sonila Elezi

Mike Etuhoko

Lisa Flaifel

George Hubbard

Rachel Curran

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