-- Post From My iPhone
Tuesday, November 3, 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!
She is still the cutest little thing ever. Darick- that was a great story from the girl named "Bayta". I have never heard of the books yall are talking about - but that doesn't mean anything- I am not a big reader..I am sure Bayta will go thru life just like the rest of us with a name that fits her just fine. There were not too many Doris' when I was growing up either..it is an old name and I used to get called "Doris Day" alot!!Is there any given reason why she is not gaining weight like she should?? If not she will on her own time. I know yall are tired of the hospital and miss the boys- but like your friend told you- you are in the right place now and if you get home and something happens- you want have that"team" there for you.Right now all you have is time - so take it!! Take care...
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