To hospital.
-- Post From My iPhone
Saturday, October 24, 2009
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This Blog was created to help us tell the story of our daughter Bayta and her batles with a rare birth defect called Omphalocele. She is now home but has an even rarer diagnosis of Pentology of Cantrell. It is our desire that this blog, the good the bad and the ugly parts, can be used by other families to help guide them through the scariest experiences of their lives!
It brakes my heart that one so little has to go thru a battle such as this. But with loving parents as you two are and a BIG family that loves you all so much and prayers ringing in from all over, I know little Bayta will come thru this cause she is so loved. We pray every minute for her and you and Amanda.
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