Monday, June 19, 2006

I've been following the story of a boy named Corbin who has been in the hospital following his Fontan on April 13th. I don't know the family at all, I've never spoken to any of them butI have been very concerned about him, because so many of his after surgery complications have sounded familiar, and realistically speaking, the longer the hospital stay, the more difficult things tend to become. He's had his ups and downs, but last week he seemed to be doing very well. Yesterday the news was not so good, they're even discussing undoing what was done to repair his heart because his pressures are too high and to be honest, today I'm afraid for him. He has a carepage, but you have to sign up to be able to read it, it's free if you'd like to read his whole story. Anyway, all of your thoughts and prayers and well-wishes sure couldn't do any damage eh?

posted by Erin @ 9:45 PM   4 comments

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Donovan "Nova" LeClair

Monroe, North Carolina
Nova was our second child to be born with congenital heart defects. We lost our daughter at 12 days after open heart surgery in 2001. Nova was born 12/2/05, with Pulmonary Atresia with VSD. He lived 6 weeks after surgery, and passed away on April 6th, 2006. This blog is his story, and the on-going story of how our family is dealing with the loss of our beautiful boy.
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