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.
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3 comments:
I know we don't know you personally, but Jamie and Eric have been gracious to share your story with us. Your family has touched us in a very special way, and we continue to pray that God gives you strength, hope and peace that is only conceivable because of the great God we serve. I can't wait to continue to read about the awesome ways God is caring for your precious daughter, Jillian!
no need to apologize. you are loved and prayed for my friends...
I agree with Bennett :) We all love you and we're praying for you so that you can focus your time and energy on your family...no apologies necessary! :)
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