The pregnancy has not been all doom and gloom. Today Amanda got to ride on a segway... The whole time I worried about her falling... But she didn't and smiled the whole time!
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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!
Hello. My name is Sarah and I came across your blog and wanted to introduce myself. We have a son who was born on September 16 with an omphalocele. We live in St. Louis and delivered at Barnes. After a very long and anxiety filled pregnancy, our little boy spent just a week in the NICU at Children's and is now home with us. Words can't describe how wonderful the doctors and nurses are at Childrens (Dr. Warner was our surgeon). We had such a positive experience and I would be happy to share anything with you. My email is sarahhellmann@yahoo.com. I will keep you and your family in our thoughts and prayers
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