1 person in 40 are carriers of the abnormal gene that causes SMA

Picture

Raising awareness for Spinal Muscular Atrophy

Picture
Picture

Grimes Family Raises over $16,000 for Families of SMA 
and counting!

Picture

Annie Makes FSMA Headlines!
Check out these featured pages
53, 62, 63, 74, 75 & 85
Thank you to Familes of SMA!  This issue featured a lot of great families out there!  Together we can find a cure!

THIS IS SMA!

This is SMA. Spinal Muscular Atrophy (SMA) kills more young children than any other inherited disease. There is currently no treatment or cure. Research, however, is extremely advanced but is in desperate need of increased funding. The Gwendolyn Strong Foundation (GSF) is a 501(c)(3) nonprofit organization focused on increasing awareness of SMA and accelerating research towards a cure. Together we can END SMA! www.gwendolynstrongfoundation.com
Picture

Donate Now
 in Annie's memory to 
Families of SMA!
**Be sure to choose "Type of Donation: In Memory of"

Upcoming Events:

If you have a fundraising idea or opportunity to raise awareness, we want to hear from you.  Please contact us so we can plan for upcoming events!
Visit our Facebook Page:  3rd Annual Crop 4 Annie

SMA Friends

Families affected by SMA become very close through their journey.  Having the support of those who truly understand are a God send!  Meet some of our special friends who have/are having this journey with us.

 

Picture
 

 Nora Gooden

Picture
 

 

Picture
 

 

Picture
 
Picture

Connect with Our Annie Girl:

Picture

Connect with Families of SMA:

Picture

Thank You for Visiting & Helping Us Raise SMA Awareness!