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 31, 2011
Cannula Free: Day 41
Garrett came off his oxygen today. He still breathes fast.It is weird to be able to see his face.VERY WEIRD.
OHMYGOSH! Such exciting news! I love that last pic- he's looking at Paul like "Hey Dad, what's new with you?!"
ReplyDeleteYay! Good job Garrett.
ReplyDeleteRose
SO great to see his cute little face!!!!! :) Fingers crossed....
ReplyDeleteWow! How great to see his little face.
ReplyDeleteit's a beautiful face...
ReplyDeleteIt's so great to see his beautiful face. He has got to be loving no tubes! I can't wait to see him.
ReplyDeleteAWWW Janna he's so handsome, it's so great to see him without all the tubes around his face.
ReplyDeleteHow amazing and overwhelming. What a tough little man.
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