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Hi @lorrie272, My husband has moderate Alzheimer's Disease. He was diagnosed in 2019, but I noticed changes in him a couple of years earlier. I sometimes go down a depressing road when I compare the changes in him, from who he was in the past to who he is now. It's better to live in the moment, as @IndianaScott suggested.
Last week I was frustrated and angry because my husband discontinued Physical Therapy, post surgery about seven months, for a broken hip. He was belligerent to the therapist, a very nice guy, who was trying to get him to do stretches. My husband was so elated when he fired the PT that I came round to thinking he felt empowered when he took action to leave PT. He has so little control of his life now and is so dependent on me that it must scare him. Long story short, at home, he'll do the stretches if I ask him, with some coaxing.
Luckily, he goes to bed early and sleeps well so I can relax at night and have some time to myself.
One nugget I picked up from somewhere, that I keep reminding myself, is never argue with someone with Alzheimer's Disease. If my husband gets adamant or angry about something, I let it go or move on to the next thing. The doctor told us to shorten his shoelaces so he wouldn't trip, and he became very angry with me when I tried to correct how he was tying them. Later that night, I shortened the shoelaces in a way he hasn't noticed, so that problem is solved.
Wishing you and your wife the best. You will always find a sympathetic ear here.

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Replies to "Hi @lorrie272, My husband has moderate Alzheimer's Disease. He was diagnosed in 2019, but I noticed..."

Thank you for the encouraging words. It’s hard to stay in the moment. I find myself looking too far into future. It is terrifying.

You just said a mouthful! It is so easy for me to argue with him because he can get very mean and almost to the point of being combative
Instead of insisting he make a right hand turn at the stoplight, I should not say anything and let him make the wrong turn and help him figure out what happened (if he asks for help). He is very sensitive about his Dementia and is always losing things. He lost thousands of dollars in cash somewhere in our apartment, and haven’t found it after 3 days of hunting. I should have put the cash in our bank right away. My fault too!
So much to learn about Dementia and how it affects everyone he comes in contact with, in person or on the phone.
I am getting a social worker to help us on this journey. I admit we need help.