SMA DMD Support is a non-profit organization committed to improving the lives of children affected by Spinal Muscular Atrophy (SMA) and Duchenne Muscular Dystrophy (DMD). We provide families with access to essential medical care, physical therapy, and life-changing treatments.

Our mission is to offer hope, support, and practical solutions to those facing the daily challenges of living with neuromuscular disorders. We work closely with medical professionals, caregivers, and other organizations to ensure that each child receives the care they need — from diagnosis to treatment and beyond.

Through our programs, we help families cover the costs of therapy, assist with medical equipment, support surgical procedures, and guide them through the complex treatment landscape, including access to gene therapy and innovative medications. Every step we take is rooted in compassion, collaboration, and a belief in a better future for all children with SMA and DMD.