English
SpanishTrusted Resources: People & Places
Healthcare providers, researchers, and advocates
The mission of the SMA Foundation is to accelerate the development of treatments for Spinal Muscular Atrophy. SMA is the leading genetic cause of death in young children. The SMA Foundation was established in 2003 by Loren Eng and Dinakar Singh, parents of a child with SMA.
BookmarkRelated Content
-
Spinal Muscular Atrophy 2020: SMA Medications for Treatment Updateshttps://www.youtube.com/watch?v=dnSXnvrO...
-
Boston Children’s Hospital – Spinal Muscular Atrophy ProgramThe Spinal Muscular Atrophy Program at B...
-
Nonrespiratory Complications of Nusinersen-Treated Spinal Muscular Atrophy Type 1 PatientsBackground: Emergence of new treatments ...
-
Mass General Spinal Muscular Atrophy (SMA) Multidisciplinary ClinicThe Mass General Spinal Muscular Atrophy...
-
A Dallas Startup Aims to Build a Big Business—and Transform Lives—by Curing Rare DiseasesBabies born with spinal muscular atrophy...
-
SMA Treatments and Continuing the FightFor so many years, patients and their fa...
-
An Interview With Muscular Dystrophy Association President Donald S. WoodLarry Luxner, senior correspondent for R...
