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We went through a lot million-question-marathons of argument/denial at the beginning until I learned how to answer once then postpone the discussion. I chose not to lie (I'm bad at it, don't want to, & he's a human lie detector). I did learn to answer once, then answer with "maybe" to a lot of stuff rather than arguing. The hardest thing for me was not to try to "fix" the dementia by correcting the mistake. I realized this is what I was doing -- I somehow thought if I could just CONVINCE HIM of the truth he would be OK...not rational on my part, but there you are.
The "follow their reality" thing IS hard, and dementia isn't across the board - sometimes they know "our" reality, sometimes not, sometimes they have the sneaking suspicion that something is wrong from reading social cues from others ( like kids ---"Mom's mad...does she know about the vase?"). Especially aggravating is that once a "wrong" idea is in place it is IMPOSSIBLE to dislodge (no matter how unlikely/impossible/etc), while the "right" ideas seem to slip away like they are teflon....for us logic-based personalities it is crazy-making!
So...explain things patiently, and sympathetically. Be consistant, it IS a test. Early dementia patients KNOW something is wrong, and often their memory can be better than they let on. In our best discussion I spent a lot of time explaining (simply) that what his brain was doing was normal (even the denial), and that his brain was trying to protect him (which made sense to him). I found it helped both of us if we talked about his brain in the 3rd person, the same way you might talk about kidney disease or your liver, rather than referring to "him", as it helped make it a bit more clinical and not accusatory. He had studied human thought, philosophy, etc, as a hobby in the past, so that helped. We even discussed that the hallucinations might be his subconscious' way of communicating to him. Am I SURE what's going on in his synapsis? No, but it's as good an explanation as any, made sense to him, comforted him and made him less afraid of them.
Whatever it takes, STOP HER FROM DRIVING. Backing into a friend's car was bad enough. What if she'd backed into a neighbor's child? Contact DMV to get her license revoked. Remove the car from the premises, take the keys away -- yes, she'll be furious and her anger is likely to last a long time. But it has to be done. No more driving. This means other means of transportation must be arranged. Her not driving is certainly not something you'd do for your own convenience but you must do it for public safety.
Your descriptions sounds like early stages to me (though I am far from trained in this area). Use this time to make sure all the proper paperwork is completed. POA, medical authority, someone's name on accounts, etc. My Mom was demonstrating "cognitive impairment" at the beginning of 2011. By June, she would have been considered unable to sign papers. I just made it through with paperwork at the bank that has made things 1,000 times easier.
Make sure there isn't a medical reason (UTI or thyroid issue) or drug interaction before you just accept the behavior.
If your mother has dementia she will have it the rest of her life, and it will progress. Waiting a few weeks for a formal diagnosis, aggravating as it is, won't change anything. In addition to the paperwork geewiz suggested, you might use some of this time to read up on dementia. Odd behavior is really much easier to deal with when you can put it in context and understand how it fits the disease.
Best wishes to you on this bumpy caregiving road!
My mother agreed to move into the home of my sister who was just retiring, but then she balked at the last minute. Another sister took Mom aside. "You know, Mom, Sis and BIL are having a harder time paying their mortgage now that they both are retired. They have been thinking about renting out their lower level. You would be doing them a huge favor if you could move in." And she went on to list the benefits, not the least of which is my sister's excellent cooking!
This helped Mom think of the move in a whole new way, and got her through the transition period. She stayed with Sis for 14 months, until her care needs increased. She is now thriving in a nursing home (Age 96, dementia.)
The "they need financial help" message was a total fabrication, by the way. But Mom did pay the same rent she'd been paying for her subsidized apartment. I think all adults should have the dignity of paying their own way. Not necessarily at full market value, but at a reasonable level they can afford.
I guess my point is, if there is some way you make the move more palatable to Mom, do it, even if it means lying through your teeth!
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