This blog will follow our family's journey with CDH. Our second child was diagnosed with a congenital diaphragmatic hernia at a routine ultrasound around 17.5 weeks. I started this blog to not only document our journey, but hopefully help those that may have to go through this same journey in the future.
Tuesday, May 10, 2011
With everything that has happened to you, you can either feel sorry for yourself or treat what has happened as a gift. Everything is either an opportunity to grow or an obstacle to keep you from growing. You get to choose. - Dr. Wayne Dyer
Janna~ Just wanted to let you know we're continually praying for Garrett, you, Paul, and Grant! Garrett is an absolute doll! So glad that you are getting to hold that sweet baby boy on a daily basis. I can't imagine what you are going through right now. Will continue to pray! Keep the faith! And Happy 3 Week Birthday, Garrett! Jennifer Ellis & Family
LOVE THIS! And I am so proud of your family- you have chosen to share your journey with others. Garrett is touching more lives than you can even imagine!
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ReplyDeleteJanna~
ReplyDeleteJust wanted to let you know we're continually praying for Garrett, you, Paul, and Grant! Garrett is an absolute doll! So glad that you are getting to hold that sweet baby boy on a daily basis. I can't imagine what you are going through right now. Will continue to pray! Keep the faith! And Happy 3 Week Birthday, Garrett!
Jennifer Ellis & Family
LOVE THIS! And I am so proud of your family- you have chosen to share your journey with others. Garrett is touching more lives than you can even imagine!
ReplyDelete