Our son Maxton was diagnosed with left-sided congenital diaphragmatic hernia (CDH) at his 19 week ultrasound. Maxton was born on 3/3/09 at Vanderbilt University. He fought hard for 18 days but earned his wings on 3/21/09. Maxton was an inspiration to many during his brief time on earth and has forever changed our lives. If your child is diagnosed with CDH, please feel free to contact us. Maxton may no longer live here on earth, but he will live forever in our hearts...

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Monday, May 18, 2009

Pray for Colin

I just wanted to request prayers for Colin. He is at UCSF. He was there when Kaden was there and you may have read a little about him on their blog. His mother, Hayley, is on breath of hope and I read tonight that Colin is not doing well. He reherniated last week and has surgery to fix it. (he had never made it home before reherniating, I believe he is about 7 weeks old). Anyway, tonight he has a fever and they cannot figure out exactly what is causing it. They have sent out for blood cultures and are thinking infection but aren't sure. His crit levels are off too. Anyways, just wanted to request a few extra prayers for him. I don't believe they have a blog.

1 comment:

Stephanie said...

Will definitely keep them in our thoughts and prayers. If you find out that they have a blog, will you forward it to me?

Also, I need to see about getting those bracelets from you. I wanted to order 2. How do I pay for them, and get them? It would be so neat to have them by the time Brooke and Kamryn are born.

Hugs to you my dear!

Love, Stephanie