Our group, the Mothers of Omphaloceles are using all our social networks to spread the word in order to spread awareness of this condition. We want to let other mothers that are being diagnosed now know that there is hope, and support for them. And also spread awareness to the general public that although a child being born with an Omphalocele has hope, it is important to support the family because the recovery isn't as easy and straight-forward as some might think.
This video is a compilation of pictures of Omphalocele children and adults. Please share!
http://m.youtube.com/#/watch?feature=share&list=FLss-1w6DO-csRBR0kuGepYQ&v=MiDHmKrtvXY&desktop_uri=%2Fwatch%3Fv%3DMiDHmKrtvXY%26feature%3Dshare%26list%3DFLss-1w6DO-csRBR0kuGepYQ
I think this is a worthy goal...to bring awareness of the condition to the public view. You know I wore my black and white...and my cute little "MOO" pin Kelly was so kind to send me :-)
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