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.

Wednesday, June 17, 2009

This was a picture done by Carly, a mother of an angel baby at Names in the Sand. ( Thank Carly!!! This turned out awesome.


FaithCDH said...

I love those pictures! I found one of Faith's name and downloaded it. Maxton's name looks beautiful on a beach in Australia with a perfect sunset.

Hope all is going well.



Kenny and Jennifer Miller said...

This is beautiful!!

April said...

I saw your sunset photo on To Write Their Names in the Sand. I was drawn to your blog because I am waiting for Carly to post my request for my baby brother that passed in 1988 of CDH. When I saw the photo of your precious Maxton with the tube taped to his little face, I started crying because that is the exact same photo I have of Adam, the only photo in fact that I have when he was alive. He would be turning 21 this June 27th and I plan to honor him with a special post on my blog.

I am sorry for your loss. I think your projects to recognize and support other families who have experienced the same tragedy is a wonderful thing to do. God Bless,


Marion said...

This is amazing!