Thousands of Canadians affected by neuromuscular conditions require essential medical equipment and assistive devices to enhance their quality of life. Unfortunately, government-supported Assistive Devices Programs do not cover the full cost of these devices. To help bridge this

We have 7 Walk & Roll events left this season and are looking for volunteers. For details, visit muscle.akaraisin.com/ui/WalkRollMDC…

What a memorable SMA Awareness month it has been! We have achieved 100% newborn screening across Canada thanks to your support! We would like to remind you that if you or a family member is affected by spinal muscular atrophy, please register muscle.ca/services-suppo…. We offer a

Fire Fighters have been dedicated partners with #MuscularDystrophyCanada since 1954. To celebrate an amazing partnership, 70 years in the making, Muscular Dystrophy Canada is pleased to be launching the 70th Anniversary National Fire Fighter Challenge! #FF70YearsChallenge

A huge shoutout to our Fire Fighter partners working to #FilltheBoot across the country this weekend! Your unwavering support and dedication is helping to break down barriers for the thousands of Canadians affected by a #NeuromuscularDisorder! Thank you! Are you interested in

Have you heard? In honour of Muscular Dystrophy Canada’s 70-year partnership with Fire Fighters, we are launching the 70th Anniversary National Fire Fighter Challenge! Not a Fire Fighter, but still want to show your support? Donate to your participating local or department today

Last month we launched the Canadian Neuromuscular Clinical Trial Database to provide reliable details about recruiting and not yet recruiting #neuromuscular clinical trials in Canada! 🍁🔍 Explore the database here: neuromuscularnetwork.ca/pillar-2-clini… CIHR-IMHA Community Muscular Dystrophy Canada #clinicaltrials

This week, Fire Fighters are hosting boot drives to raise critical funds and awareness for Muscular Dystrophy Canada. Come #FillTheBoot in your area, and help our Fire Fighter partners make a difference for Canadians affected by #NeuromuscularDisorders. filltheboot.ca

Please RSVP for virtual or in-person attendance to Pamela Musgrave at [email protected] or 613-218-7131.

September is Muscular Dystrophy Awareness Month, and while significant research progress has been made, there are still many unknowns. Muscular Dystrophy Canada is proud to support Dr. Reshma Amin, Dr. Lena Xiao, and their team on the James Lind Alliance Priority Setting project,

MDC offers the neuromuscular community various programs, including support of our Service Specialists. Donate today to provide life-changing support to those who need it most - muscle.ca/?form=GeneralD…

📣Muscular Dystrophy Canada will be at the 5th Western Canadian Neuromuscular Conference, bringing together neurologists, researchers, and academics dedicated to neuromuscular medicine and science! ❔Have you registered yet? Don’t miss out on this opportunity to connect,

September 7th is World Duchenne Awareness Day! We're committed to support those affected by Duchenne muscular dystrophy, and launched a survey to capture insights into their diagnosis experiences. Children/Youth: surveymonkey.com/r/DMDDiagnosis… Adults: surveymonkey.com/r/DMDDiagnosis…

The stage is set and the curtains are about to rise. The Muscular Dystrophy Canada Cabaret is making its grand return! Stay tuned!

🗓️ Mark Your Calendar! September 15 is Myotonic Dystrophy Awareness Day! To raise awareness and share valuable insights, we're hosting a special webinar focused on cognitive and neurobehavioral symptoms in #MyotonicDystrophy. 🗓: Monday, September 16, 2024 🕐: 1-2 pm EST 🔗:

Don't miss your chance to get your 2024 Walk & Roll for Muscular Dystrophy Canada t-shirt! This year's exclusive design is printed on a 100% cotton shirt and is sure to impress! Shop online today! 🔗 ow.ly/mw7j50TkwgN #WalkRollMDC