Do you know about Spinal Muscular Atrophy (SMA)? You should.

I'm passionate about fighting this disease. SMA is the #1 genetic killer of children. BIll and Victoria Strong created the Gwendolyn Strong Foundation to raise awareness and funds for research.

SMA has no cure - and there is no treatment. Children, babies - battle this terminal disease - their bodies fail them, while their minds stay strong.

The Gwendolyn Strong Foundation is hoping to win $20,000 for research from the Jimmie Johnson Helmet of Hope Contest - will you vote?

http://www.VoteForSMA.com - check the Gwendolyn Strong Foundation - you can vote every day until September 29th.

After the contest ends, you can be sure, Bill and Victoria will find a new way to fight this disease.

http://www.GwendolynStrong.com

Follow Bill on Twitter:
http://www.twitter.com/billstrong

Follow me on Twitter:
http://www.twitter.com/DanielleSmithTV

Visit me at:
http://www.ExtraordinaryMommy.com

Category:

People & Blogs

Tags:

• SMA
• Spinal Muscular Atrophy
• Gwendolyn Strong
• Gwendolyn Strong Foundation
• Jimmie Johnson Helmet of Hope
• VoteForSMA
• Danielle Smith
• ExtraordinaryMommy.com
• Genetic disease

[GoogooEyedChihuahua]

Hi I have SMA

[bishoujosteph]

Voted and posted it on my Facebook for my friends/family to vote. It's so sad.

[johnnybrazil01]

Thanks for the message. Im gonna check it out!