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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...

To start at the beginning of our story click here and scroll all the way to the bottom.

Monday, January 5, 2009

Please pray

Please pray for Ryann Smith's family. I have been following Ryann's blog and learned today that she passed away. Please keep her family- Jaime, David and Reggan in your prayers. You can find a link to Ryann's blog on the right if you would like to let her family know you are thinking of them, or to read about Ryann's story.
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1 comment:

Alex, Ingrid, Alina & Robbie Houchin said...

I just looked at Ryann's blog - very sorry to hear such devastating news for the family.

Our thoughts are with them.

January 7, 2009 at 3:50 AM

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