Don't forget to share our stories by following & forwarding our blog, following us on Twitter, Facebook and Tumblr @ Bellabenefit and Like us on Facebook.com/bellabenefit! The more people who are aware of SMA, the less babies are born with SMA, together we can make a difference and find a cure! Help us spread our stories and get a routine prenatal testing for SMA to happen!
Our Mission to spread the word to the world about this horrible incurable disease:
In an effort to raise awareness and funds for Spinal Muscular Atrophy, our foundation, Bella Benefit has teamed up with Families of Spinal Muscular Atrophy (FSMA)! We are in the process of organizing our first annual 5K run, we couldn't be more excited for our journey ahead. We are in the planning process and would hope to get on the local news to tell our story. We would love to be heard and take our story to the next level to aware everyone and also try to get genetic testing for SMA mandatory for pregnant mothers. The benefit date has been reserved for 9/29/2012 in Arlington, Texas at River Legacy Park !!! PLEASE "LIKE" OUR FACEBOOK PAGE AND SHARE ON YOUR PAGE. Your support is greatly appreciated.
Please visit our Facebook page and help us spread the word:
www.facebook.com/BellaBenefit
Please share our blog after reading this and help us spread awareness about this horrible incurable disease. No one should ever have go to thru a horrible tragedy like this. We would like the world to know that a genetic testing for this disease should be mandatory to all expecting mothers!
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