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Muscular Dystrophy Canada

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Recent News

  • 100% of Canada is now screening infants for spinal muscular atrophy (SMA)

    100% of Canada is now screening infants for spinal muscular atrophy (SMA)

    December 11, 2024
    Muscular Dystrophy Canada is thrilled to announce that after three years of working with each Canadian province and territory, all babies born in Canada can now be tested for spinal …READ MORE
  • The 2024 Walk & Roll for Muscular Dystrophy Canada was a huge success thanks to you!

    The 2024 Walk & Roll for Muscular Dystrophy Canada was a huge success thanks to you!

    December 11, 2024
    The Walk & Roll for Muscular Dystrophy Canada 2024 season is officially over, and it was a huge success, raising more than $1,089,000! Through 30 in-person events, we hosted more …READ MORE
  • Donor support makes a difference

    Donor support makes a difference

    December 11, 2024
    When Sally and Cy Elston were approached by their longtime friend, Lloyd Lawrence, about supporting Muscular Dystrophy Canada, they rose to the challenge. Initially supporting a Dragon Boat Race fundraiser …READ MORE
  • Muscular Dystrophy Canada’s Annual Report is now available

    Muscular Dystrophy Canada’s Annual Report is now available

    December 11, 2024
    2023-2024 marked another year of Muscular Dystrophy Canada “Breaking Down Barriers” for the Canadian neuromuscular community. If you would like to review Muscular Dystrophy Canada’s 2023-2024 Annual Report, please visit …READ MORE
  • Clinical Trials in Canada for Neuromuscular Disorders Are on the Rise

    Clinical Trials in Canada for Neuromuscular Disorders Are on the Rise

    December 11, 2024
    In recent years, the number of clinical trials available in Canada for individuals with neuromuscular disorders has increased significantly, with opportunities doubling or even tripling in some cases. This is …READ MORE
  • Opening Doors: Navigating University with Neuromuscular Conditions

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    December 11, 2024
    Choosing the right university or college is always a big decision, filled with considerations about programs, campus life, and future goals. But for students living with neuromuscular conditions, the decision …READ MORE
  • Help families, like Danielle’s, get the answers and support they so desperately need.

    Help families, like Danielle’s, get the answers and support they so desperately need.

    October 31, 2024
    Danielle has defied all odds throughout her life. As a world-record holding Paralympian, Danielle challenged herself to win a medal, and not only did she win one, but over the …READ MORE
  • 100 percent of Canada is now screening infants for spinal muscular atrophy, a potentially fatal disorder

    100 percent of Canada is now screening infants for spinal muscular atrophy, a potentially fatal disorder

    August 20, 2024
      Muscular Dystrophy Canada and partners deliver on goal outlined in Canada’s Rare Disease Strategy Toronto, Ontario, Canada, August 20, 2024 – Muscular Dystrophy Canada is thrilled to announce that after …READ MORE

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