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Organization: ALS Canada  
Phone Numbers: 905-248-2052
Toll-Free: 1-800-267-4257
Fax: 905-248-2019
Website: www.als.ca
Address:
3000 Steeles Ave E, Ste 200
Markham, ON
L3R 4T9
Intersection: Woodbine Ave and Steeles Ave E
Location: Markham
Accessibility: Wheelchair Accessible    Wheelchair Accessible
Executives: Tammy Moore - Chief Executive Officer
1-800-267-4257 ext 200 * tm@als.ca
Lisa Droppo - Vice President, Client Services
1-800-267-4257 ext 215 * ldroppo@als.ca
Service Description: Information and support to those with ALS (Lou Gehrig's disease) and their families * support groups (where available) * peer support * volunteer home visitors (where available) * information guides for the health care community * education materials * funds resesearch

Assistive Equipment Program - Loans or assists with the purchase of equipment designated by the society

Regional Services


Support Groups
  • Durham
  • Kingston
  • Kitchener
  • London
  • Niagara Region
  • North Bay
  • Ottawa
  • Ottawa-Caregiver
  • Peterborough
  • Scarborough
  • Simcoe County
  • Sudbury
  • Toronto - Caregiver
  • York Region

Application: Call * no referral required
Eligibility - Population(s) Served: Persons with ALS and their families * general public
Languages: English ; French
Language Note: French publications and website
Area(s) Served: Canada
See Also: Amyotrophic Lateral Sclerosis (ALS)

This information was last completely updated on 7/4/2016

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© 2016, thehealthline.ca Information Network




About Us
The ALS Society of Canada was founded in 1977. Together with our Provincial Partners, we are dedicated to supporting Canadians living with ALS (amyotrophic lateral sclerosis), and investing in research for the future, so ALS will be a treatable, not terminal disease. ALS Canada is a national organization responsible for the ALS Canada Research Program – funding peer-reviewed research grants and fostering collaboration amongst Canadian researchers, helping to nurture new ideas and build capacity. ALS Canada has a role in Ontario, similar to that of the Provincial Societies, providing services and support for people living within our provinces – we help fill the gaps between the healthcare system and needs of people living with ALS. We advocate federally, provincially and locally on behalf of people and their families for better government support and access within the healthcare system.