Hello, and welcome to our website. We have started this website in memory of our daughter, Jenna Jean.  On July 28th, 2009, our six month old baby girl went to be with Jesus after a ten week long struggle at Peyton Manning Children's Hospital in Indianapolis, with complications from surgery on a congenital heart defect.

In result of the pain and grief we have went through, my wife and I have decided to start a support group and web ministry.  We want to reach out to other parents who have or had children with a congenital heart defect (CHD).  We want to offer hope to those who have or will go through some of the same situations that we have.

We invite you to read Jenna's story by clicking the link on the left of this page.  We also want to offer resources on this site as well to help you understand your child's condition. Those can be found under the "resources" tab.

Also, please be sure to visit our blog. Please be sure to send us your e-mail if you wish to be notified when there is a new entry.

By clicking on the "Contact us" link, you will be able to send us your story by using a convenient web form.  We would very much appreciate the opportunity to be able to offer encouragement to you from a couple who has been there.