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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Tuesday, April 21, 2009

Kaden Alex Kuehl

It is with a very heavy, sad heart that I wanted to inform you all that Kaden passed away yesterday. Please continue to pray for Kristi and Craig on the road this jounrey has taken them. Pray for peace and understanding and healing. I understand far too well what they are going through and it is so difficult to imagine another family suffering from this stupid defect! I was so angry this morning when I read the news. Please also spread awareness in Kaden's memory!!!


Marion said...

It seems that Kaden's passing has brought back all the memories of the day Addison passed. I am sure that you are going through the same thoughts and feelings. Lots of love coming to you from Atlanta.

Rhonda in KY said...

Lots of love to all CDH families right now. Even though I only read about these tough little ones it is so hard not to get attached to to them. I can't help but root for them to make it. I pray for a cure so no one else has to say goodbye too soon.

Love. Prayers. Peace.