6:45pm 4/12/16
Test Passed and the tube is out. He has said a few words and answered some
questions(name, first and last, hospital, month-he thought May, nickname -Mac
and step dude). He asked if he got a new heart and seemed pleased when we told
him he did. He is pretty exhausted now,
so is sleeping. We've been swabbing his
mouth with cool water which he likes and is swallowing well. He'll get his ice when he is more alert. He has good strength in his legs and feet. His right hand is pretty strong, much more
than his left hand. They are keeping an
eye on that. His hands are no longer
restrained, so he is able to itch his nose with his right hand. He is on a bit of oxygen. The surgeon, Dr Smith just visited for a few
minutes. He is also very happy with the
results.
They weaned him off of the propophal just before they did
the breathing test. Twice in the
afternoon they slightly rolled him so he won't get sore spots. The one they did about 6pm was painful, so
they got him a some IV pain which should take the edge off
We don't have to gown up anymore. Just masks and gloves. Tiny steps but in the right direction.
I'm going home after Maria, his night nurse comes on. It's time to water Johns flower pots and
baskets, get some laundry done and get a good night sleep. More tomorrow.
Colleen

2 Comments:
John, you were the topic of conversation at the Children's Garden today! We are all just ecstatic about how well you are doing.
Colleen, we so appreciate all your posts. Karen the clinic director sent the blog site out to everyone so we can keep up to date.
You both are in all our thoughts. Jinny
Colleen, thank you so much for taking the time to do these updates. You've got a lot going on so thank you for doing this. Tell John I'm thrilled he's doing so well, as I've still never gotten him back for pushing me out of that truck. He's on my list. �� Give him my best and perhaps we'll be able to meet up some day. Take care
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