Help us promote!

 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!

We are in the beginning stages of planning our first annual SMA benefit! We are so excited about making others aware of the existence of the terrible neuromuscular disease that so viciously took our daughters from us. More importantly, we are looking forward to financially aid families who are currently experiencing the devastation of SMA Type 1. Please like and share our page to help promote this important event. Thank you for your support ♥



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!