Cure Spinal Muscular Atrophy funds and directs the leading spinal muscular atrophy research programs to develop a treatment and cure for the disease.

NSF is a patient-led nonprofit organization dedicated to helping children, parents, adults and healthcare providers to understand the complexities of spinal deformities.

The mission of the SMA Foundation is to accelerate the development of a treatment for spinal muscular atrophy, the number one genetic killer of infants and toddlers.