Originally published on April 3, 2014. Thanks to so many amazing Chapter leaders and SMA Families, we are aiming to raise over $1.6 Million to fund advancements in SMA research and critical family support and patient care programs. Over the next four months, our Chapters and SMA families will be hosting over 60 events including […]
Originally published on February 27, 2013. Thanks to so many amazing Chapter leaders and SMA Families, we are aiming to raise over $1.6 Million to fund advancements in SMA research and critical family support and patient care programs. Over the next four months, our Chapters and SMA families will be hosting over 60 events including
Originally published on August 7, 2013. Several Major League Baseball teams are teaming up with Cure SMA to help raise awareness and funds for finding a treatment and a cure for spinal muscular atrophy. Cure SMA is excited to be a part of the game and provide SMA kids with chances to run the bases,
Join Cure SMA at the Ballparks to Raise Awareness for Spinal Muscular Atrophy Read More »
Originally published on July22, 2013. Thank you to our amazing Chapter Leaders and SMA families who spend countless hours planning these wonderful fundraising events in support of finding a treatment and a cure for spinal muscular atrophy. Together, we hosted over 32,300 participants at 222 events raising over $3.7 Million to help fund new SMA
Record Breaking Fundraising Year in Support of Cure Spinal Muscular Atrophy Read More »
Originally published on March 7, 2013. The Cure SMA spring event season is already making huge progress toward our goal of raising over $1.6 million to fund exciting new spinal muscular atrophy research and critical family support programs. Our Development Team here at Cure SMA is here to help you meet and exceed your personal
Meet Your Fundraising Goals with These Resources and Tips from Cure SMA Read More »
Originally published on December 17, 2013. Cure SMA and the entire SMA community mourn the loss of 35 year old David Cunniff of Duanesburg, NY. David was in a work related accident last night and passed away this morning. David is the father to Caleb, who has SMA type II and Zach, and husband to
SMA Community Mourns the Passing of David Cunniff Read More »
Originally published on June 25, 2013. Thanks to hundreds of SMA families across the country, families, researchers and medical providers are able to come together to share information on spinal muscular atrophy to better support the SMA Community. This year marked the 24th Annual SMA Conference hosted by Cure SMA. Over 1,300 SMA families, researchers
SMA Families Make The Annual SMA Conference Possible Read More »
Originally published on October 22, 2013. Cure SMA is excited to announce our continued partnership with BAYADA Pediatrics for the signature Walk-n-Roll Program. This year, Cure SMA Chapters and families will host 47 Walk-n-Roll events throughout the US. Walk-n-Rolls are the signature event for the organization by bringing SMA families together and raising huge awareness
BAYADA Pediatrics Renews $25,000 Sponsorship of the Cure SMA Walk-n-Roll Program Read More »
Originally published on September 4, 2013. Throughout the month of August, the SMA Community joined together to raise awareness of SMA and hosted dozens of awareness events across the country! The SMA Community officially recognizes August as Spinal Muscular Atrophy Awareness month, an effort that Cure SMA has been coordinating since 1996. Families worked together
Originally published on July 15, 2013. August is SMA Awareness month and families and friends around the country are joining together to help promote this devastating disease so that we can one day see a world where SMA is treatable and curable. So, how can you get involved? There are numerous ways to raise much
SMA Awareness Month: What You Can Do with Support From Cure SMA! Read More »
