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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.

Tuesday, August 25, 2009

Prayers please!

Just a quick note to ask for you to please, please pray for Ireland and Max (Maximus). They are both on ECMO now and need prayers!!! Links to their blogs are on the right.

2 comments:

Debby@Just Breathe said...

Praying for Ireland and Max. God hear my prayers. Amen

The Griffin Family said...

Hey girl, thanks so much for including us in your thoughts and prayers...it means a lot!