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-- Post From My iPhone
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!
Darick and Amanda!
ReplyDeleteYou will continue to learn that little "O" babies are a true miracle! They are so strong and such little fighters! I'm SO thankful that you were able to bring your little miracle home in such a short amount of time. Treasure the no shower taking and the busy schedule. I know it sounds crazy, but some people truly take it for granted!
Great big hugs and I'm SO glad you were finally able to post!
Hugs - Tiff
glad to get an update but even better is that you are enjoying the "normal" part of a newborn now! and what a perfect little outfit for Bayta!
ReplyDeleteSo glad to hear little Bayta is doing so well. Have not talked to Judy - I guess she has gone home by now!!!I pray for Bayta's & Amanda's continued progress and health. Amanda don't forget about you!! take care and try to get you some rest and you to Daddy!! Take care--hope to see you all real soon!!!
ReplyDeleteHey... how's everything going? We haven't heard from ya'll lately! :)
ReplyDeleteHugs - Tiff