When I got back they had him sitting up with his glasses on and he was really trying hard to tell me something. I can't really understand him yet, so he is frustrated with that as well. Tomorrow he is going to have a stomach tube put in and maybe things will get a little better once he gets food in him.
Monday, December 7, 2009
Monday night
Matt had a pretty big day today while I was in Burlington closing on the house. Because of the swelling in his head and the fact that he is missing part of his skull (to allow for that swelling), they've had to fit him with a helmet in order to get him out of bed and doing PT. He really doesn't like the helmet and takes it off the second someone turns around, so they've also had to put a glove on so he can't use his hand. I think he likes this even less than the helmet, so I heard he was pretty grumpy most of the day. The nurses tell me this is a very natural part of the healing process - he doesn't understand yet what has happened and why he is here and what is going on, so his first reaction is frustration and anger.
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Keri, We have been following Matt's progress. I know it has been slow going but each day is a blessing. Keep strong and know there are lots of us praying for you two.
ReplyDeleteMark and Deb Peterson
(Kirk's Mom and Dad)
Keri!
ReplyDeleteWe are sitting here in Arizona reading your posts and trying to envision what you and Matt and all your wonderful family must be feeling. You are so brave and courageous!
We send warm wishes, prayers, hopes, optimism....
Love and Hugs,
Suzie and Blair
Hello Keri~
ReplyDeleteSo glad to hear Matt is coming up. I have a clear vision of next year's Christmas card with a photo of the two of you standing healthy and in love with your new successful tree farm, family and friends.
much love,
Suzy and staff at Cedar Wood