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20 days agoGrassroots efforts and work on Capitol Hill is fully underway to support the SMA Treatment Acceleration Act in the 111th Congress.
27 days agoGrassroots Update for Families and Friends: Please Schedule District Meetings during Upcoming Recess! On June 29, 2009, the 111th Congress
189 days agoThe Petition to Cure SMA was profiled on the popular blog Post Secret. Bill and Victoria Strong started the petition in support of the SMA
243 days agoA big thanks to Bill Strong from PetitionToCureSMA.com for passing along a link where you can vote your approval or disapproval for proposed
259 days agoFrom the Delaware County Times in Pennsylvania: Elizabeth Vandiver never heard of Spinal Muscular Atrophy (SMA) until her sister’s baby,
261 days agoAre you one of the thousands and thousands of people who have signed the Petition to Cure SMA ? If not, it’s about time you joined the
285 days agoGreetings SMA families, researchers and friends: We would like to extend our deepest thanks for your dedication and all you have done to
300 days agoA petition created by an SMA family to show the U.S. Congress the support for the SMA Treatment Acceleration Act has hit a big milestone.
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