Nothing dramatic to report - mainly the aftereffects of the Medicaid transition still rumbling through the landscape. On Wednesday's visit there were the usual signs that he's getting worse - speech gets progressively less coherent, people get progressively more conflated. The borders between objects are coming down. I showed him his new electric razor and he expressed mild interest and then said he had something better and handed me one of the television remotes. He showed me how you can press the buttons and affect what's on the screen. This, of course, explains why the television is continually getting mis-tuned. I'd be happier if the aides could come in and re-set it - ideally to a baseball game - but they clearly don't know how, or don't care, or both.
E would have done it better but she's gone. Except that she isn't. She visited him on Wednesday and again on Thursday - and, seeing the condition he's in and the way the aides neglect him, did what anyone would do. She jumped in and bathed him and helped him shave and changed his clothes. As soon as I heard about it I had to intervene. Only the Medicaid aides are allowed to perform aide services. A civilian like me could help out. But if another aide does it, that breaks the Medicaid rules and we lose the coverage. A shame, but that's the system I've got to live in. E wasn't pleased. She called me this morning and told me all about what she'd seen of the awful condition of elderly people who had Medicaid coverage - soiled clothing and roaches on the floor "and the women don't care. But I know how it is," she added. "You're trying to save some money. We've all gotta do that." None of this was really helpful. She told me again that she's a responsible person and the proof is she owns a house. I told her again that I don't own a house and probably never will because I can't afford one. She got quiet all of a sudden and stayed that way.
A few years ago she got my father involved in some sort of legal guardianship for her son. This requires that he sign court papers every year. I mentioned to her that he's no longer able to write his signature. Note to self - tell the family lawyer about that, too.
Apart from all that, the machine is running, more or less. There was a new aide Wednesday night that I liked - she seemed to be alive, and actually sat at the dinner table with us and joined in the conversation, and he asked her questions and listened to her answers. He said later that she wasn't any good, but that could be the hangover effect from E's visit. Unfortunately, the new aide turned out to be temporary, and judging by his phone comments, it sounds like we've gone back to the Night of the Living Dead Home Health Care Workers...
We'll see how it all shakes out. It could be that, apart from the human drama, we're making progress - Medicaid is in place, we've been through the staffing changes, he's got 24-hour coverage (it's amazing to think about this but a few months ago, he didn't), he has a gerontologist, there's a care manager overseeing everything... At the beginning of the year, all those things were goals, and we've achieved them. So that's something. The overall trend is downward, of course. But then, it always was.
Am thinking at the moment less of myself than of Shu, whose mother went through surgery for a melanoma yesterday. I hope that went well and I'll be looking for her next post. On the surface, the situation sounds similar to what we went through with my father in May. I hope in her case the outcome is better. As, of course, it could be. That's the thing with Alzheimer's - it's always the same, and it's always different.
As long as you remember that, you'll be OK.

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