Muscular Dystrophy Canada (MDC) is a non-profit organization seeking a cure for neuromuscular disorders. Founded in 1954 as Muscular Dystrophy Association of Canada, volunteers and staff nationwide have helped to provide support and resources to those affected. Since the founding year, over $64 million has been put towards research via collaborations, fundraising events, and donations. Muscular Dystrophy Canada provides various programs within five areas of service: Education, Information, Advocacy, Support and Equipment. In 2000, Muscular Dystrophy Canada joined with the ALS Society of Canada and the Canadian Institutes of Health Research in the Neuromuscular Research Partnership (NRP). In 2011, there were over 38 chapters and two affiliates across Canada.

History

Muscular Dystrophy Canada was founded in 1954 as the Muscular Dystrophy Association of Canada by Dr. David Green and Arthur Minden along with a number of parents whose children were affected by the disorder. The first President was Arthur Minden. Today Arthur Minden's humanitarian work is remembered by the Arthur Minden Pre-Doctoral Award, set up through Muscular Dystrophy Canada. Fire departments have continued to be Muscular Dystrophy Canada's strongest source of fund-raising support.

Fundraising

Muscular Dystrophy Canada hosts many events and initiatives to raise funds. The funds raised help provide research and services for people with neuromuscular disorders. Muscular Dystrophy Canada events also raise awareness about these disorders and get entire communities involved. Some of these fundraising efforts are: