I just typed this long post about what is going on and I lost the whole thing. So now you just get the short version.
Damon had to go back on oxygen this morning so we wont be going home today. They are going to observe him the rest of the day and slowly wean him back off. The docs think it might be the new medicine he's started so they aren't going to plan on doing another cath or anything like that yet. We're still now sure when we are going to come home. We really want to but we also want to make sure he's 100% ready before we leave.
Please keep praying for Damon and also for Jeremy and Myles. Jeremy's work schedule is crazy so Myles can't stay at home and he's being passed around. They both want to be up here and it's really hard on all of us, I miss them so much. I'll update when I know more. Talk to you all later.
Sarah
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About Me
- Cochran Family
- CJ, MO, United States
- Damon was born on Nov 16, 2006 in St. Louis, MO. He has a congenital heart defect called Hypoplastic Left Heart Syndrome. Damon has had 2 of the 3 surgeries he will need to repair his heart. We glorify God for all he has done for Damon so far and will continue to do. God bless all of you who check this site; we love you so much and thank you for your prayers and support.
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Growler
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McDonald's Cheeseburgers
Barney
Drums
The Wiggles
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1 comments:
Hey Sweetie!
I wish I could come up there and be with you. We are continuing our prayers and we know God will heal Damon. If you need me to watch Myles at all next let me know. We have Spring Break and Wed. is the only day we are doing anything special. I could take him and Alivia to a movie or something. Anything you need let me know! I am here for you babe:)
Lacey
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