Tuesday, September 6, 2011

Monday, September 6: Day 2 Home

Kevin's mood continues to get better. I'm not sure about his body. His drainage is increasing (from 15mls in the hospital to 100mls daily at home) and we don't know what that means. I will call the Dr tomorrow when he is back in his office to discuss.

His blood pressure continues to go down a bit, too, so that's good. He's eating well but I want him moving more. I am threatening to make him walk down the driveway and back.

IVs at 2:00am and 3:30am are still killing us but I'm getting used to it.

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