Disease Information from NORD, National Organization for Rare Disorders, Inc.

The National Organization for Rare Disorders (NORD)

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This is the list of diseases currently covered in the Rare Disease Database.

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This is the list of organizations in NORD’s Organizational Database.

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Read about more than 2,000 patient organizations and other sources of help.

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**IMPORTANT** The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.

ALS Society of Ontario
a/k/a: ALS Society of Canada

Address:
402-3100 Steeles Ave E
Markham
Ontario, Intl L3R 8T3
Canada

Phone: 905--24-8-2101
Fax: 905--24-8-5620
800 Number: 866--61-1-8545
TDD: --
Email Address: info@alsont.ca

The ALS Society of Ontario is a national, non-profit organization dedicated to providing information and support to individuals and family members affected by ALS and to promoting research to find a cure for the disorder. Amyotrophic lateral sclerosis (ALS), also known as "Lou Gehrig's disease," is a rapidly progressive neuromuscular disease characterized by degeneration of the motor neurons responsible for transmitting electrical impulses from the brain to the voluntary muscles throughout the body. Established in 1977, the ALS Society, which operates in many locations across Canada, provides support and counseling for people with ALS, their families, and caregivers; raises funds to support research into the cause of and a potential cure for ALS; engages in patient advocacy; offers networking services; and provides equipment such as wheelchairs.

Website: http://www.alsont.ca

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Last modified Tuesday, September 07, 2010