Please check out Duke's brand new CDH page (and Carter's picture)! This has been a long time coming and we're so excited to have been a part of it. Visit it again in the coming days for more pictures of our CDH friends. I'll post a link to it in the right-hand column for easy access.
http://www.dukechildrens.org/services/congenital_diaphragmatic_hernia
We started this blog in early 2008 to follow our first pregnancy. After our son was prenatally diagnosed with a Congenital Diaphragmatic Hernia (CDH), we turned to the blog to inform friends and family of Baby C's progress. There used to be 100s of posts, but it was overwhelming to sift through, so I've consolidated them into "Carter's Story," which you can read by clicking the link above.
November 10, 2009
Duke's CDH Page
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5 deep thoughts:
What a fabulous website and Carter is the perfect poster boy sporting his Duke T-shirt. Did you guys ever imagine that he would pull through, do so well and be the face that gives other families hope? It's amazing. I'm so happy for you.
What an awesome page, and it's even better because it has Carter's handsome little face on it!
Pretty awesome! I love that Carter made the page. He's famous! :)
Great page but it is all about the Carter ;-)
so happy to see how well carter is doing! our little cdh babies are fighters, huh?? =)
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