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To be a leader in finding a cure for multiple sclerosis and enabling people affected by MS to enhance their quality of life.
The MS Society provides services to people with multiple sclerosis and their families and funds research to find the cause and cure for this disease. We have a membership of 28,000 and are the only national voluntary organization in Canada that supports both MS research and services.
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 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.
Some 1,500 volunteers serve on MS Society national, division and chapter boards and committees. An estimated 13,500 women and men are volunteers for service programs, fundraising events, public awareness campaigns and social action activities.
The head office of the MS Society is located in Toronto, Ontario. The Saskatchewan Division offices are located in Regina and Saskatoon.
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