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, April 5, 2010

Will Max have a brother or sister?

We had an ultrasound on Sat, at 15 weeks, to see if they could tell the sex of the baby. We are fairly certain Maxton will have a little.... BROTHER!!!! Let me know what you think!

I am excited. We will have an ultrasound in May to confirm this and more importantly to make sure the little one is healthy! We are planning to name him Gatlin Grant!

In other news, I have decided to start a new blog about our life. I do not want to continue to post about this pregnancy here as I want this blog to be used for CDH awareness and to be seen by families who need it. Our new blog is-

Please visit the new blog for updates about the pregnancy and our lives. I plan to only post things related to Max and CDH here.

Thanks for checking in on us!