Your support changes the lives of families living with neuromuscular diseases
Your generous gift of any amount today will empower people living with neuromuscular diseases by:
- Pursuing new treatments through dozens of research grants every year, constantly improving care protocols
- Providing a trusted voice through our MDA Resource Center for families seeking answers about life with a neuromuscular disease
- Advocacy goals such as making air travel more accessible for people with neuromuscular diseases, preventing injury and damage to wheelchairs and other expensive devices.
Thank you for being a caring friend of the Muscular Dystrophy Association (MDA) and for all the ways you’re changing lives.
Enter a duration between 2 and 99 months.