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Latest News
August 22, 2014   Exciting Weekend for Families of Spinal Muscular Atrophy Fundraising Events
 
August 21, 2014   Research Funding Connection between ALS and Spinal Muscular Atrophy from Families of SMA.
 
August 20, 2014   Families of Spinal Muscular Atrophy Awards Second Year of Research Funding to Dr. Lyndsay Murray for a Total of $80,000.
FSMA will be committing $1.8 million to new research funding over the coming year.
 
August 18, 2014   Thank You to the FSMA Medical Advisory Council and Scientific Advisory Board for a Great Spinal Muscular Atrophy Conference
At our Annual SMA Conference in June, we asked families to write short notes of thanks to our Medical Advisory Council and Scientific Advisory Board for all the hard work they’ve put into planning the conference.
 
August 15, 2014   NeuroNEXT Recruitment Update: 25 infants with SMA Have Enrolled in the Study with 2 More Infants Needed.
 
August 15, 2014   Call Congress and Urge Passage of The ABLE Act
 
August 14, 2014   Families of SMA provides critical services to families recently diagnosed with Spinal Muscular Atrophy
 
August 12, 2014   SMA Researchers Talk About the Importance of the Spinal Muscular Atrophy Research Group Meeting
 

 
 
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