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.

Friday, May 1, 2009

Maxton's Memorable Moments

After a few weeks of planning and starting to get the project going, I have made Maxton's Memorable Moments it's very own blog. I am very excited about this project and it has been very therapeutic for me. I hope that the families that it can help will be touched by Max's story and also be able to remember their beautiful angel whenever they look at it. :-) I added a link on the right side of this page (see the pretty butterfly at the top) to the blog for MMM. Anyways, I just wanted to thank everyone for their support. I have received great feedback on this project and look forward to helping many families in the future. I also have received good feedback on the book and am working on trying to find a way to publish it. Not sure if it will happen anytime in the near future or not, but I am hoping so!


sharon said...

Ashley, you & David are such a great couple. We pray for you constantly. You are doing wonderful
things in the name of Maxton. We miss him every day as you do. CDH is an awful birth defect. God bless
what you are doing.
Love, Sharon

FaithCDH said...

I tried to check out your link again, but it says that you have to be invited. Could you add me Thanks!

I was wondering if you could do one for my nephew who was stillborn in January.