Muscular Dystrophy Canada

Muscular Dystrophy Canada

Muscular Dystrophy Canada (MDC) (French: Dystrophie musculaire Canada) is a non-profit organization that strives to find a cure for neuromuscular disorders. Founded in 1954 as Muscular Dystrophy Association of Canada, volunteers and staff nation-wide 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.[1]

Muscular Dystrophy Canada provides various programs within five areas of service: Education, Information, Advocacy, Support and Equipment.

Muscular Dystrophy Canada joined with the ALS Society of Canada and the Canadian Institutes of Health Research in the Neuromuscular Research Partnership (NRP).[when?][citation needed]

Currently, there are 38 chapters and two affiliates across Canada.[2]

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.[3]Today Arthur Minden's humanitarian work is remembered by the Arthur Minden Pre-Doctoral Award, set up through MDAC.[4]

References

External links


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