Andy should have celebrated his 15-month birthday today, if not for SMA. Please think of him – and all of the children with this disease – and please sign the Petition to Cure SMA at www.PetitionToCureSMA.com.
This petition is in support of the SMA Treatment Acceleration Act, which was initially introduced in Congress in 2007 and was reintroduced in 2009. The passage of this legislation will help researchers cross the finish line and END SMA, while providing groundbreaking data for SMA and other disorders.
Your signature on this petition will let our lawmakers know that finding a cure or treatment for SMA is IMPORTANT and that their support of this legislation is CRITICAL.
PetitionToCureSMA.com is a grassroots effort started by our friends Bill and Victoria Strong, whose daughter Gwendolyn also has SMA.