The ALS Society, founded in 1977, is the only national voluntary health organization dedicated solely to the fight against ALS. Our mission is to provide care and find a cure for ALS. One of the
important ways we work to accomplish this mission is by promoting awareness and understanding of ALS and the role and work of the ALS Society of Canada and its regional partners across
the country.
The ALS Society of Canada offices are in Toronto. Regional Units (make list live) are located in every province. Units develop local chapters and support groups and provide direct support to
people with ALS and their families and caregivers.
The ALS Society of Canada raises funds for research into the cause a cure for ALS. It also works to raise public awareness and supports units in providing patient care. ALS Society Units
support patient care through information and referrals, patient and care giver support, equipment programs and advocacy.
ALS Society of Canada leadership includes
Who is the official spokesperson for the ALS Society of Canada?
The ALS Society draws on the knowledge of numerous experts to speak on various aspects of ALS and the role of the ALS Society. To arrange an interview please contact Susan Graham
Walker, Director of Communications and Program – 800-276-4257 ext 208, sgw@als.ca
Does the ALS Society advertise to the general public?
The ALS Society is fiscally responsible and therefore does not pay for advertising to promote the organization. Rather, we build partnerships with organizations who share our vision for a
cure for ALS and who will enable public awareness opportunities. Als, the ALS Society produces public service announcements and other material for placement in the media. Media outlets
are encouraged to run these announcements free-of-charge, pending space availability. To discuss this opportunity please contact Susan Graham Walker, Director of Communications and
Program – 800-276-4257 ext 208, sgw@als.ca
