The Spinal Muscular Atrophy Foundation, based in New York, NY, is dedicated to supporting individuals and families affected by spinal muscular atrophy (SMA). Through advocacy, research funding, and community outreach, the foundation strives to improve the quality of life for those impacted by this rare genetic disorder.
By raising awareness and providing resources, the Spinal Muscular Atrophy Foundation works to advance research efforts and promote access to care for individuals living with SMA. With a focus on collaboration and education, the foundation plays a vital role in the SMA community's journey towards better treatment options and ultimately a cure.
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