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.
Janna, thanks for updating all of us who aren't there with you guys! Love Grant's Honey Bear! I am sure that over the next few days, you'll make Garrett's room into a home for him! Let us know if you need anything!
Wow! Such great news so far. Keep the posts coming and we'll keep the prayers coming your way. Garrett is such a doll by the way. He looks like a fighter!
And I dont see any ECMO, so Im kinda loving this picture!! =0)
ReplyDelete(((hugs))) Thanks for updates!!! cont prayers....
Janna, thanks for updating all of us who aren't there with you guys! Love Grant's Honey Bear! I am sure that over the next few days, you'll make Garrett's room into a home for him! Let us know if you need anything!
ReplyDeleteYes, thank you for the updates! I feel like I'm right there with you guys. Hope to see you soon.
ReplyDeleteThank you for keeping us updated on how Garrett and the rest of you are doing. He looks like a cute little guy.
ReplyDeleteLove,
Aunt Linda
Wow! Such great news so far. Keep the posts coming and we'll keep the prayers coming your way. Garrett is such a doll by the way. He looks like a fighter!
ReplyDeleteAnne