I want to have a place to post pictures and stories about Grace and Owen for our family and friends to enjoy. So much happens with them and they grow so fast and many of you are far away and miss so much!
My other goal with this blog is to bring awareness and hope to other families that have a baby diagnosed with a Congenital Diaphragmatic Hernia (CDH). Our son Owen was born March 6, 2007 with CDH. He spent 25 days in the NICU and is very healthy now. When he was first diagnosed in-utero at 33 weeks the information that I found on the web was very scary. The first website that I found was for a baby that had died. Unfortunately, that is reality for many people, but I want people to know that babies do survive and can even be healthy despite this birth defect.
Thanks for reading!
darcy





sis-
it looks great! looking forward to all kinds of pictures and stories!
k
What a great idea!! You will probably bless more people than you will ever know. Since I will be one of those who live far away and don’t get to see them often, I will appreciate this site and connection with you. I will miss you, Darcy. I’m glad God allowed our paths to cross. God bless you and your family.
Donna
Such a precious family you have! Welcome to blogland.