We are told they are bringing her up now. All we know is that she is now on a breathing tube.
-- Post From My iPhone
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!
I honestly can't imagine what you guys are going through right now. I don't think I will be able to sleep, because my heart is with you guys tonight.
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Allison N.
Lori and I are following your blog. Things have been going so well that it is hard to have setbacks, it seems like in the nicu it is ALWAYS one step forward and 2 steps back.....that is what i remember w/ my 32 weeker.....hang in there....we are all praying for you here in indiana!
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