Promoting the role of patients and the patient voice in all areas of health care.
Multiple Sclerosis Society of Canada
Our two major programs provide hope for the future through the support of MS research into the cause, treatment and cure of the disease and hope for today through our many services that assist people with MS and their families.
Since our founding in 1948, the core support of the MS Society has been from tens of thousands of dedicated individuals, companies and foundations in communities across Canada. The Society receives almost no funding from government.
The MS Society of Canada has a membership of 28,000. It is the only national voluntary organization in Canada that supports both MS research and services for people with MS and their families. The MS Society is governed by a National Board of Directors comprised of 13 volunteer members who are elected annually. The seven regional divisions and nearly 120 chapters are also governed by elected volunteer boards of directors.
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