Simply A Farmer’s Wife

The Jack Ryan Gillham Foundation
February 5, 2008, 10:25 am
Filed under: CDH, CDH Awareness, Congenital Diaphragmatic Hernia, Turquoise

Through this journey we have met so many wonderful people.  Each of them inspired to do things never thought imaginable before their diagnosis of Congenital Diaphragmatic Hernia (CDH).

Bethany and Matt are two of those people.   Their son, Jack Ryan, was born on July 6, 2007 and lived a short but wonderful 5 weeks.

This organization is one that will help change the face of Congenital Diaphragmatic Hernia (CDH).

They are joining hundreds of others in the  turquoise ribbon campaign and bringing awareness to Congenital Diaphragmatic Hernia (CDH).

Please take the time to read Jack’s story and pray for this family as they embark on this wonderful journey.


The Jack Ryan Gillham Foundation


2 Comments so far
Leave a comment

You’re awesome.

Comment by Bethany

thank you for sharing this story…

*~* :o) if you do not have a smile today… :o) I will give you one of mine… :o) *~*

Comment by Aimee

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