We did have a glimmer of good news last night when I was talking with John (who happens to be the brother-in-law of one of the premier neuropsychiatrists in the country). He indicated that we should be evaluating Dad for low dopamine/stimulant levels and a full cognitive assessment to determine if the radiation damaged the brain sooner or more than previously thought. This would cause very low energy levels, no motivation, tremors/shakes, and confusion. We have an appointment tomorrow with a psychiatrist locally to get part of that evaluation done.
In the meantime, we're taking shifts playing the "mean" caregiver and forcing fluids and nutrition. I scared Dad straight a bit tonight with the news that if he didn't start eating/drinking on his own, a home health care nurse would do it for him via an NG tube. He told Mom upon going back to bed that tomorrow he was going to "hit it hard; walk more, drink and eat more, too."
He's pretty confused, and has no concept of time. I asked him tonight what year it was, and he said, "Eighty-something? I don't know." Just before this though, he looked much improved for a few minutes and actually ran the electric shaver himself with me holding the mirror. Glimmers of progress, but then it's short-lived.
I'm talking with the social worker tomorrow at the cancer center on next steps of getting to another location (Mayo's/MD Anderson) for more options on finding out what's going on. If he can fly, we may see if we can get a flight arranged to get him there.
I'll keep you updated when I can. It's been pretty busy talking to the ensemble of doctors and health care workers (and a stint in the ER yesterday where all tests were normal!), but we're determined to find out what's going on.
Tracy brought Sam out tonight for a little visit/boost. Sam was really happy to see Grandpa, and kept going back to the bedroom to "show Grandpa this shell with the ocean in it." It did offer a boost for us all, I think.
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