A new Twitter application is making it easy to contact legislators about the fight against spinal muscular atrophy (SMA), the leading genetic killer of children under two.
Online PR News – 17-September-2009 – – (Santa Barbara, CA) – With millions of people 'Tweeting' every day, Bill Strong knew there had to be a way to harness all of that online talk to help end a disease that is affecting him very personally. With a Twitter application called 'Tweet for a Cure' and the help of thousands of Twitter users, he’s making progress in his quest to find a cure for spinal muscular atrophy.
Bill and Victoria Strong’s daughter, Gwendolyn, was diagnosed with spinal muscular atrophy (SMA) at the age of six months. SMA is a neuromuscular disease that causes weakness and wasting of the muscles. In the most severe cases, it can rob its victims of the ability to crawl, sit, walk, breathe, eat, talk, or even smile. SMA is the leading genetic killer of children under two.
Not long after the SMA diagnosis, Bill and Victoria founded the Gwendolyn Strong Foundation to raise awareness of and money for SMA research. Bill also serves on the board of directors of Fight SMA, a larger organization with a mission of strategically advancing research for SMA.
Bill has harnessed the power of the Internet and social media for several campaigns that further his cause of raising much needed awareness of SMA. His latest effort is 'Tweet for a Cure'. The Twitter application helps users send a 'tweet' to their local legislators. The message asks the legislators to support the SMA Treatment Acceleration Act. The proposed legislation in the United States, written and backed by multiple SMA organizations, would help to clear the way for researchers to find a cure for the disease. Within one month of its launch, more than 2,600 people utilized “Tweet for a Cure”, reaching nearly two million Twitter users.
“Using social media, such as Twitter, Facebook, and even online petitions, organizations like ours can reach large numbers of people with less effort than it took just a few years ago,” said Strong. “We’re grateful for the individuals who have used ‘Tweet for a Cure’ and for those who have signed our online petition, and hope that they continue to support our efforts to help end spinal muscular atrophy.“
Bill’s online petition, which asks that legislators support the SMA Treatment Acceleration Act, can be found at http://www.petitiontocuresma.com. Since being created in July of 2008, it has gathered approximately 70-thousand digital signatures.
To find the 'Tweet for a Cure' application, go to http://www.endsma.org/twitter. To learn about the Gwendolyn Strong Foundation, go to http://www.endsma.org. For more about spinal muscular atrophy, go to Fight SMA’s website, at http://www.fightsma.org.
About Fight SMA
Headquartered in Richmond, Virginia, Fight SMA (also known as Andrew's Buddies) is an international nonprofit group dedicated to accelerating research for a treatment or a cure for spinal muscular atrophy (SMA), a neuromuscular disorder that kills more babies than any other genetic disease. For more information on spinal muscular atrophy and Fight SMA, please visit http://www.fightsma.org. The latest SMA news and research information is available at the Spinal Muscular Atrophy Blog, at http://www.fightsma/blog.