-- Post From My iPhone
Thursday, October 29, 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 is that cundiff hall??? wow....what a makeover....no more RED!
ReplyDeletei just logged on and read all of your posts today, ....i am so excited to see all the good news...and the talk about a "go home" date. I remember showing up at the nicu one morning and them telling me blake could go home with me....i was terrified!! glad they are letting you try it out first w/ the 24-48 hours thing....wish they had given us that option! hope amanda is feeling better!
I know the BOYS will be glad to see you all when you are able to go home. Harrison and Jackson will probably be Halloweening on Saturday night (how's the grandparents holding up?) Bayta is still the cutest ever!!! Glad things are going so smoothly!! Take care...
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