Muscular Dystrophy Canada

Muscular Dystrophy Canada (MDC) is a non-profit organization that provides support and resources to people affected by muscular dystrophy and related muscle diseases. The organization was founded in 1954 and is headquartered in Toronto, Ontario, Canada.

History[edit | edit source]

Muscular Dystrophy Canada was established in 1954 by a group of parents who had children affected by muscular dystrophy. The organization was initially created to raise funds for research into the disease, but has since expanded its mandate to include support services for individuals and families affected by muscular dystrophy.

Mission[edit | edit source]

The mission of Muscular Dystrophy Canada is to enhance the lives of those affected by neuromuscular disorders by continually working to provide ongoing support and resources. This includes funding research to find a cure, providing financial assistance for medical equipment, and offering educational programs and support groups.

Services[edit | edit source]

Muscular Dystrophy Canada offers a variety of services to individuals and families affected by muscular dystrophy. These include:

Financial Assistance: MDC provides financial assistance to individuals for the purchase of mobility equipment and assistive devices.
Education and Advocacy: The organization offers educational resources and advocates for policies that improve the lives of people with muscular dystrophy.
Support Groups: MDC facilitates support groups where individuals and families can share experiences and offer mutual support.
Research Funding: The organization funds research into the causes, treatment, and cure of muscular dystrophy.

Fundraising[edit | edit source]

Muscular Dystrophy Canada raises funds through a variety of events and campaigns, including the annual Walk for Muscular Dystrophy. The funds raised are used to support research, provide services to individuals and families, and advocate for policies that improve the lives of people with muscular dystrophy.