Skip to main content

Improvements!

Image
By
Abby spent most of the afternoon sleeping or crying as the sedation wore off and she became more aware of her pain. 


 But this evening, she started becoming more alert, watched a little of Annie on the iPad, and even sat up a bit!



Her face is still pretty swollen, so it's hard for her to open her eyes very wide.  But she's perking up!  She enjoying skyping tonight and I'm hoping to get her out of bed tomorrow. 

Her oxygen levels have been great and she's no longer needing any!  They did a blood gas to test CO2 levels and they were perfect!  Yay!!

Sadly, she got sick a little while ago and her stomach really hurts from all the meds and because she was still for so long. They're going to do some mean things to get things <ahem> going in a little while.  This one is a new experience for us, so it should be...uh....fun?

All in all, though, this was a great day!  We are praising God for how well she has done.  SO thankful!!


Labels:

Comments

RicKim said…
Praise God!! Go Abby!!!
November 11, 2014 at 12:38 AM
Mary Lou said…
Julie....
"Her oxygen levels have been great and she's no longer needing any! They did a blood gas to test CO2 levels and they were perfect! Yay!!" Thanks be to God!! ;-D
Love you later, Raelyn
November 12, 2014 at 12:30 AM
Post a Comment

Popular posts from this blog

Cerebrocostomandibular Syndrome

By
If you happen to pick up the latest Reader's Digest, there is an article in there about Piper Breinholt , a four year old with CCMS.  If you've been around here a while, you'll remember wayyyyyy back when we first received Abby's diagnosis that I was able to speak to Piper's mom, Reagan.  The article is more about their story and not as much about the ins and outs of CCMS, but I think it's probably enough to get some people googling it and I'm hoping a few will end up here. Every once in a while, I give a blog post the title of Cerebrocostomandibular Syndrome so that it would show up in Google.  My ever-present hope is that people will stumble across my blog and 1) be encouraged by the hope we have in Christ, 2) feel a connection with someone in a similar situation as them, or 3) get excited over the miracles that have been performed in Abby's life!!  (a combination of all 3 is great too!)  :)   Notice that it's not to get famous and it ...
10 comments
Read more

Bath Time Photos!!

By
As promised, here are lots of photos of Abby's first bath. Caleb was supposed to be in bed, but the bathroom is right next to his room... "I'm not too sure about this..." Once she learned how to splash, she was all smiles! Her first good hair wash! Gotta protect the trach! She really liked getting water poured on her head.  It was cute! Smiley (and bubbly) for Daddy while he dried her off. All clean!!  (Note the Lysol wipes in that last picture.  They are NEVER far away!)
Post a Comment
Read more

Imagination Movers Photo Recap

By
Seriously, The Imagination Movers were so much fun!  They played lots of their own music, with some classic rock mixed in for the adults.  There were also quite a few jokes and references to Baltimore, which was kind of fun.   The whole night centered around this robot named Rock-o-Matic, or "Rocko."   This is Mover Scott, and he wears Wobble Goggles that help him see new ideas.  Caleb and Abby have a pair of goggles too.  :) There are 4 main Movers that are part of the TV show, but they have 2 extra movers to play instruments and do back-up vocals in their live tour. Abby finished up her feed before the show started so that she would be free to dance! My dancing queen did NOT want to sit in my lap.  The row in front of us was empty, and that is where she stood almost the entire show--dancing the night away. My Imagination Movers  Caleb did his share of singing and dancing too.  He knows m...
13 comments
Read more