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Thanks to your support and interventions, your father is safely at home in the correct setting for his needs. So that's good: you need do nothing to ensure his actual wellbeing.
Handling his behavioural and emotional needs, next, is a team effort, and there are numerous strategies you can try. Perhaps step one is to stop looking on your conversations with your father about driving and money management as though these were real conversations leading to a real agenda. You're not going to get him a car, he can't drive, and he is no longer able to handle money. That is why the DPOA - which HE gave YOU, remember - is now in force.
But that doesn't mean that you can't have meaningful conversations with him about driving and about his personal finances. These are likely to be circular, and may get tedious for you, but the benefit is that he feels you're listening and is able to express himself. Perhaps you'll be able to divert him onto less controversial topics, such as cars in general, his memories of life on the road, cars he loved, cars that were a pain, Greatest Car of All Time, that kind of thing. And with money management, it might be helpful to have a basic document showing income, outgoings, budget and so on to reassure him that everything is under control.
Masterly inactivity is what you're aiming for, without subjecting him to the confusion and humiliation of being told to his face that he's incapable. He already did the responsible thing in giving you the authority to act for him when he could no longer act for himself. That's all you're doing. Be comforted.
Most of all, there are so many people in this world who are caring for elderly loved ones with all types of care needs. If nothing else, this site lets the world know that there are spouses, children, grandchildren, relatives, and wonderful friends who are taking on huge responsibilities for their loved one. Some of these folks have walked through the "valley of the shadow of death" with their dear one(s), and know what that feels like. Their input is greatly appreciated. Some are holding the hands of a confused parent or spouse (with Alzheimer's, dementia, or one who is confronted with cancer). Getting "feedback" from those who have been in this journey is comforting and clearly a blessing.
So come back often and gain insight into many care topics that can help and influence decisions that you may be faced with or that one of your dear friends will be faced with in the future.
You can tell him the doctor said he can not drive, he can not live alone..but again he will forget.
You can tell him that he can drive "when he gets better"..but he will forget that as well.
And I would expect that "acting up" is normal for someone entering into a new place, one that they have had no control over selecting. Being moved from a home that you have been in for sometimes most of your life.
I actually like the idea that they placed him in Memory Care almost right away. Less of a chance he will leave the facility. Also he will not have to adjust to another move in what might have been a month or two..or even a week depending on how fast he declines.
Just tell him he is safe where he is. Tell him that you love him and you want to keep him safe.
My father is in Memory care and I keep having to repeat myself as he forgets anything I say a half hour later. He's not violent but speaks his own mind.
Tell him that you love him and try to please him .
My LO’S first catastrophic failure was realizing, on her own, that she was no longer able to reconcile her check book. I had begun saying a few months earlier that I knew she was a capable driver (she still was), but that the traffic in her neighborhood was so congested and disorderly that it was getting too hard for her to navigate it.
She ultimately agreed, but continued to discuss missing her independence with the car even before and after making a reasonably good adjustment to placement on a memory care unit.
She also has difficult days, and days when she says she can’t remember her own name. We attempted to give voice to the losses that she was aware of experiencing, as she experienced them, without referring directly to a named diagnosis, and that seemed to work well for her.
As far as the car, I told my father that I'm so sorry but his driving days are over - it's just not safe for him to be out there alone anymore. Is there someplace he wants to go/visit?
This is a difficult transition. Try to be firm but kind in your language with Dad and shift the focus from what he cannot do anymore to what it is that he is really wanting. My father really likes ice cream sundaes (in my childhood we drove to the local Dairy Cream for treats almost every Sunday) so I make sure I bring one each Sunday when I visit. He might not have the car to get his treat himself, but he accepted just having someone bring it to him.
With my mom, I’ve been repeating things like ‘you're just slower now,’ trying to convey that being upset about it could be the only thing wrong, and ‘you don’t have to worry about this or that issue, isn’t it a relief.’ I tell her the brain does this, it’s not your doing or your fault. I may need more phrases, but these are helping for now.
Some people can accept these life changes better than others. Some people still have enough cognitive skills to evaluate what is being told to them. Some people will not understand no matter how much you try to tell them. However, all people deserve to be loved and treated kindly, whether or not they understand our words—believe me, they will understand our tone of voice and our actions. Holding a hand, a gentle pat on the back, bringing a treat, giving a hug, praying with or singing to, or just listening to whatever is being said can all demonstrate loving concern for our dear ones.
my dad has dementia, had his license suspended, but continued to drive... and LIE about it!(we were 3 states away)
He went to four different doctors (geriatric, neurologist, cardiologist, and neuropsychologist) to try to get his license back. Because of his dementia and OCD, he fixates on “getting his license back.” All 4 doctors told him NO- he cannot drive. He argues with them all, but none of them said “dementia”... they all told him he is “not safe at this time”... I got copies of his paperwork, so when he starts talking about his license, I refer to the “highlighted section” where it says “no driving.” It takes me out of the equation and since he doesn’t know to go about reapplying for his license himself ( never used a computer) he has no options. His cars are gone and we moved him closer to me in a 55+ apartment complex. My only regret is that we moved him SO fast (right from the hospital 3 states away) that AL was not an option. It would’ve taken too long, so he’s now on his own refusing help. You are VERY fortunate that he is in AL already!
my suggestion is to let the doctors tell him what is going on. Instead of saying “you have dementia” they only addressed my dad’s concerns about his limitations... managing his finances, driving, and medication management.
i wish you the best! It’s a tough journey!
He still tells me he can drive and always asks if he can when I take him out. My answer to that is that we are going someplace new and I'm not sure how to get there and I don't want him to stress out. Basically, I luck out that he goes with the flow... Most times I agree with him and try to redirect the conversations. Just so sad and heart breaking.
Rather than trying to orient him to his situation, try redirection. When he talks about getting his checkbook back or buying a car, change the subject. Ask him a question that will shift his concentration. Like, "Dad, I was trying to think of the name of that street where you and mom lived when you first got married." or "How do you think the Giants (fill in name of favorite in-season sports team) will do this Sunday?" Then, keep it going until he's completely off the topic. Works for me with my stubborn 'give me back my car and checkbook' Dad. Sometimes I don't have the energy for it, so I just let him ramble and I don't say a word. Other times, when I've really had it, I snap at him and feel guilty later. Dementia is a b*tch.
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