www.smafoundation.org

The mission of the Spinal Muscular Atrophy Foundation is to accelerate the development of a treatment for SMA, the number one genetic killer of infants and toddlers.

www.mdausa.org

The Muscular Dystrophy Association is a voluntary health agency -- a dedicated partnership between scientists and concerned citizens aimed at conquering neuromuscular diseases that affect more than a million Americans.

www.fightsma.com

We continue to need your help with this important legislation. Every vote will be critical! For more information, read the House of Representatives version and the Senate version. Also, please indicate YOUR support by clicking on the banner below and signing the Petition to Cure SMA!

We are an all-volunteer, non-profit, 501(c)(3) tax-exempt organization dedicated to providing information and support to family, friends, individuals and caregivers on all aspects regarding the devastating genetic disease called Spinal Muscular Atrophy.

Families of SMA. Research. Support. Hope.