In November 2007, our unborn daughter was found to have a condition called Congenital Diaphragmatic Hernia (CDH), which occurs in 1 out of every 2,500 pregnancies. Basically, our daughter’s diaphragm had a hole in it that had allowed her stomach, liver, and some intestines to pass into the upper regions of her chest cavity. Her chest was too overcrowded to allow her lungs to fully develop. She was given slim odds to survive and worse odds to thrive.
Our daughter, Jillian Olivia, was born in the Spring of 2008. Since her birth, Jill had two surgeries during her first year and has since thrived.
We started this site to chronicle our experiences throughout this journey and to keep our family members and friends up-to-date on Jill's condition. Now we use this site to update others on what's going on in our lives.
Friday, November 30, 2007
Coping
I (Bryan) took Thursday and Friday off from work to be with Judy and help each of us to cope with the news from Wednesday. It gave us a chance to run some much needed errands. We just moved to Boise and still need to get our lives in order here. We got our car insurance set up, got pre-approved for a home loan, and continued looking for a home to purchase. Luckily, Judy's brother, Jay, is allowing us to live at his house until we find a place of our own.
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