| Naam | Muscular Dystrophy Canada |
|---|---|
| Website | http://muscle.ca |
| Samenvatting | You are not alone. Muscular Dystrophy Canada is here to support individuals and families living with neuromuscular disorders. |
| Vrijwilligers | Geinteresseerd om als vrijwilliger voor Muscular Dystrophy Canada aan de slag te gaan? Kijk op hun website: https://muscle.ca/get-involved/volunteer-or-work-with-us/ |
| Socials |
Muscular Dystrophy Canada, in partnership with the Neuromuscular Disease Network for Canada (NMD4C), is pleased to announce the recipients of the national post-doctoral fellowships funding competition. These awards supp...
As we close out 2025, we want to extend a heartfelt thank you to the more than 600 volunteers who helped make this year such a success. Your generosity, passion, and commitment have strengthened the neuromuscular commun...
As we look back on the year, we are deeply grateful for our incredible community. Thanks to our donors, supporters, partners, sponsors, and volunteers, Muscular Dystrophy Canada continued to provide vital programs, equi...
Thanks to generous supporters like you, Muscular Dystrophy Canada is proud to have hosted 6 retreats in 2025. From Caregiver Retreats to Family Retreats, there was something for everyone to enjoy. These retreats help br...
Message from Stacey Lintern, CEO, Muscular Dystrophy Canada This past year has been a powerful reminder of what we can achieve when we work together with determination, compassion, and a shared vision. Our 2024–2025 Ann...
Intravenous immunoglobulin, known as IVIG, and subcutaneous immunoglobulin, known as SCIG, are plasma-derived treatments that are essential for many people living with immune-mediated neuromuscular conditions. Because C...
Life with a neuromuscular disorder in Canada is expensive. Individuals and families face not only the daily challenges of managing a complex, often progressive condition, but also the rising financial strain of mobility...
On November 22nd, 2025, Muscular Dystrophy Canada proudly gathered with volunteers, Fire Fighters, clinicians, researchers, donors, and partners from across the country for the 2025 Dr. David Green Awards Banquet, an in...
This holiday season, we’re thinking of Julie’s family. When Julie’s husband, Michel, was diagnosed with myotonic dystrophy (DM1), their world shifted overnight. Soon after, two of their children — Alexandra and Nicholas...
Julie’s family knows firsthand how myotonic dystrophy (DM1) can change lives. Her husband Michel was the first to be diagnosed. Within a year, two of their three children, Alexandra and Nicholas, received the same diagn...
