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PATIENT ORGANIZATIONS
Muscular Dystrophy Canada (MDC) has supported the neuromuscular community in Canada since 1954. MDC supports individuals impacted by neuromuscular disorders by providing support through all stages of disease progression. Their goal is to enhance the lives of those affected by neuromuscular disorders while relentlessly searching for a cure.
ALS Canada is a source of knowledge, support, and advocacy for people affected by ALS. ALS Canada works to improve the lives of Canadians affected by ALS through advancing care, research, and information.
The Myasthenia Gravis Foundation of America was founded by Jane Ellsworth, when her teenage daughter Pat, was diagnosed with the rare neuromuscular disease myasthenia gravis (MG). The MGFA is dedicated to improving the lives of people living with myasthenia gravis, and the foundation’s mission is to have “A World without MG”.
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