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Just an update - she's still sleeping most of the time... Monday PM

she was alert, eating, said my name; Wednesday the social worker said

she will be ready to go back to the dementia floor on Friday;

Wednesday PM she was asleep the whole time; Thursday AM received the

call that the room she was to get is now not available so she won't

move until next week; Thursday PM received the call that they're

concerned with a temperature and she was having a 'bad day', and she

is drooling and not swallowing and they have a machine next to her to

clean out her mouth so she won't choke. This is such a roller coaster

ride. She only has a few more days left of the meds she's on. She's

finished the med that prevents swelling. And just a few more days of

the anti-seizure meds and antibiotics... If she could just hold out a

few more days she won't have to deal with being over medicated

anymore. It's a 'no win, no win' - I can't say take away the meds b/c

it's to prevent the possibility of something worse, but at the same

time she's so overly medicated she can't open her eyes - she tries -

but she just can't do it...

I'm visiting this AM - before work... With Haagen-Daz...

Poor Mom... :(

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