DefeatDuchenne
One in every 5,000 boys is born with Duchenne muscular dystrophy, the most common fatal form of muscular dystrophy. The disease is relentless. It slowly weakens the body’s muscles, deteriorating function of vital organs and ultimately - shortens their life. Although there are medical treatments that may help slow its progression, there is currently no cure.
Defeat Duchenne Canada is the country’s only national charity dedicated to ending Duchenne muscular dystrophy. We have provided leadership in research, advocacy, and support since 1995. We‘ll continue until a cure is found to ensure our boys can live long and active lives.
Industry Update: Avidity
We're Stronger Together: Meet Henry
We're Stronger Together: Meet Brayden
Family Forum 2025: Solid Biosciences
Family Forum 2025: REGENXBIO
Family Forum 2025: Duchenne Treatment Landscape Part 2
Family Forum 2025: Navigating School and Employment
Family Forum 2025: Rick Hanson Accessibility Training
Family Forum 2025: Financial Resources and Planning for the Future
Family Forum 2025: The Canadian Drug Approval Process and Where Your Voice Matters
Family Forum 2025: Advocacy from the Heart
Family Forum 2025: Illness & Emergencies
Family Forum 2025: DMD Childhood Care (Ages 9-15)
Family Forum 2025: Teen and Adult Care (Ages 16+)
Family Forum 2025: Navigating Clinical Trials
Family Forum 2025: Wave Life Sciences
Family Forum 2025: Avidity Biosciences
Family Forum 2025: Dyne Therapeutics
Family Forum 2025: Edgewise Therapeutics
Family Forum 2025: Kye Pharmaceuticals
Family Forum 2025: Duchenne Treatment Landscape Part 1
Family Forum 2025: Navigating Your New Diagnosis (Ages 0-8)
Family Forum 2025: Adjusting to a New Diagnosis
Family Forum 2025: Community the Heart of Care
Family Forum 2025: Weekend Welcome
The Journey Continues: John's Walk 2025
Industry Update: REGENXBIO
2025 Annual General Meeting
2025 Walk - Fundraising Update
2025 Walk - Remarks from CEO