For many Canadians with neuromuscular disorders, the journey to diagnosis is long and frustrating, marked by uncertainty, misdiagnoses, and delays. Myotonic Dystrophy Type 1 affects not only mobility but also the heart, cognition, and the gastrointestinal system, yet many individuals spend years searching for answers before finally accessing genetic testing. These delays result in missed …READ MORE

Join us at one (or more!) of 30 in-person Walk & Roll events taking place across the country! At each event, you can look forward to an amazing, fun-filled day complete with games, snacks, crafts and interactive activities, the chance to connect with other members of the neuromuscular community, and opportunities to hear stories and …READ MORE

Every year, individuals and groups across the country raise money to support Muscular Dystrophy Canada in their own way by hosting their own special events, including everything from bake sales to bike rides, golf tournaments, dances, auctions, and head-shaving challenges. Each year our community has fun while giving back in all sorts of ways! Community …READ MORE

Thanks to the generosity of our donors, supporters, and Canadian Fire Fighters, students affected by neuromuscular disorders are now one step closer to achieving their dreams of higher education and building meaningful careers. This type of support makes a profound impact, enabling students to attend post-secondary institutions and overcome barriers that might have previously seemed …READ MORE

Breaking Barriers – Building Bonds Thanks to generous supporters, like you, Muscular Dystrophy Canada is thrilled to be hosting more than a dozen retreats in 2025. From Caregiver Retreats to Family Retreats and new this year, hybrid retreats there is something for everyone to enjoy this year. Caregiver Retreats offer anyone taking care of someone …READ MORE