Surgeon Appointment
1 year ago
This is our story of our son Kaden. We found out at 18 weeks that Kaden had a 'congenital diaphragmatic hernia', CDH. Even though our outcome was not what we prayed for, we hope within Kaden's story you will find information, hope, support and links to others who can make the difficult journey a little easier. We are "The CDH Family"...
Praying for Maxton and his family. Maxton was such a warrior. (((HUGS))) Kristi, for I took Maxton's passing hard too and I know it must be very difficult to watch other's go through this loss, when Kaden will be here in several weeks. Sending you and Maxton's family much love and support in the weeks to come.
ReplyDeleteTracy - mom to Ian
Kriti. Thanks for thinking of Maxton. I hope that his passing doesn't upset you too much. I know what it was like to read of other babies passing while I was pregnant. Just remember that God has a plan for your Kaden. He will be such a warrior and change your lives, as I am sure he already has. I just wanted to say that I am thinking of you and hoping/praying for you and Kaden and your family.
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