Friday, October 23, 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!
So, what was the outcome of the surgery? Did they find a blockage? What's the plan for the immediate future? How are you both doing? It's hard, but you have to remember to take care of yourselves...
ReplyDeleteAllison N.
I've been reading the blog at least every other day and keeping people at Wesley up to date on Bayta's progress. You're also included in our prayers on the Wednesday mornings. But you two have certainly been ministering to others too. I look forward to Darick's observations, inspirations, and his humor. Ted said he could just imagine Amanda saying "MOO." I'm sure you miss the boys soooo much. We'll be so glad to have you back here in Springfield. Everyone needs to stay strong.
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