ALS Society of Canada

A national voluntary health organization, together with Provincial Partners, dedicated to supporting Canadians living with ALS (amyotrophic lateral sclerosis) also known as Lou Gehrig’s disease, by investing in research, so ALS will be a treatable, not terminal disease.

This group has an Ontario chapter, but those with ALS or their caregivers must be registered with the Canadian-wide organization.

Contact
Melissa van Tuyl, Regional Manager, Hamilton, Niagara, Haldimand, Brant and Halton, ALS Society of Canada
Agency Status
Registered Charity
Last Full Update
January 21, 2021