Families of Spinal Muscular Atrophy Launches New Fundraising Stars Blog.
March 8, 2010.

To recognize the amazing fundraising efforts made by our members nationwide which help advance research for a treatment and cure for Spinal Muscular Atrophy.

Families of SMA recently launched a blog called Fundraising Stars, which allows us to instantly recognize the many fundraising efforts made by members nationwide.  We’re pleased to have a forum that offers family and friends the ability to view and comment on their personal and inspirational contributions. 

Click here to view our Fundraising Stars!

The blog is linked to from our Families of SMA homepage and can also be viewed directly at http://www.spinal-muscular-atrophy.org/. 

A great feature of the blog is its social networking capabilities.  Each article automatically links to our Families of SMA Twitter and Facebook pages, and all pictures link to our Flickr account and videos to the FSMA YouTube page.  Overall, it’s a great way to connect with the Families of SMA community and for us to thank all our amazing families and volunteers.

To learn more about our Fundraising Stars Blog, please call us at (800) 886-1762 or email fundraising@fsma.org.

Thank you for your fantastic dedication and support to our mission to find a treatment and cure for SMA.
Families of SMA.