FightSMA Marks 20th Birthday with New Home on the Web

February 18, 2011

FightSMA Marks 20th Birthday with New Home on the Web

Press Release | February 18, 2011

(Richmond, Virginia) – Parents fighting spinal muscular atrophy (SMA), the leading genetic killer of children under two, need help and information. Recognizing that need, FightSMA, an international nonprofit organization dedicated to finding a cure for SMA, is announcing the launch of its all new website, FightSMA.org.

“When we set out to redesign FightSMA.org, we looked at the enormous amount of information we have for SMA parents, and hoped to make it more accessible and easy to find,” said FightSMA co-founder and president, Martha Slay. “The new website features better categorization and a more flexible design that will help us in our fight, and a new website is a great way to celebrate our birthday!”

Click HERE or on the image below to read more…

Advertisement

Dr. Kaspar In The Lab

November 23, 2010

Dr. Kaspar In The Lab

FightSMA Blog | November 22, 2010

It’s not often that we get to see SMA researchers in their labs.  That’s why the picture to the left is such a treat.  It shows Dr. Brian Kaspar and one of his colleagues hard at work on gene therapy research that could some day yield a treatment or cure for spinal muscular atrophy.  To get a better look, click on the image for a larger version.

Click HERE or on the image below to read more…