Parents with dementia, how dealing with that has gone.

   / Parents with dementia, how dealing with that has gone.
  • Thread Starter
#41  
Thanks to all for their kind words. 🥰 We were there about 2 years ago and did a modest "clean out" and this is why its not all that bad now. We took a bunch of things we thought elderly shouldn't be using anyway, like a leg hold coon trap. They'd never had coon troubles before! And a month later he was asking "where it had gone"" and other tools a 85yo shouldn't be using. This place will be cleaned up and put on the market ASAP.
 
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   / Parents with dementia, how dealing with that has gone. #42  
I have LOTS of stuff too. I am only 49 so I have plenty of time to use this stuff. But how can we live more mindfully as we age to not leave our offspring in this same situtation? I know you guys have shops full of stuff too.
Tag your “treasures. If it hasn’t been used in a year, odds are pretty good you will not. Time for a new home. When you bring in anything new, the old goes out (boots, shoes, drills, w/e)
 
   / Parents with dementia, how dealing with that has gone. #43  
Tag your “treasures. If it hasn’t been used in a year, odds are pretty good you will not. Time for a new home. When you bring in anything new, the old goes out (boots, shoes, drills, w/e)
That is a great plan. I have been trying to implement that lately.
 
   / Parents with dementia, how dealing with that has gone. #44  
Unless hazardous or toxic one call to a disposal company will quickly dispose of anything not titled…

The hazardous and/or toxic use to be simple but now requires extra steps… chemicals, batteries, liquids, meds, electronics, etc.

My CPA leased a copier and it has given years of good service but the company says a part no longer available.

He said ok… lease is up end of May so come and pick it up and lease company says $400 disposal fee!

Lease after 5 years has a $1 buyout… he said he never pd the dollar but Toshiba says they waived the buyout and gifted the copier…
 
   / Parents with dementia, how dealing with that has gone.
  • Thread Starter
#45  
The county they reside in has a free hazardous material drop off an hour drive away. We couldn't believe the 1/2 used and unopened containers we found around there. Seems every spring he purchased another set of garden chemicals he already had. In the first cleaned up we did, we found about 5 partial bags of lawn fertilizer that was still granular and usable.
 
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   / Parents with dementia, how dealing with that has gone. #46  
One of the bigger mistakes we made was not getting my Dad committed when he started losing his mind. We took his drivers license from him and his Doctors told him that he couldn't drive anymore, and I sabotaged his car, so that worked at keeping him home. Before that, he drove to town and didn't come back for three hours. It should of been 45 minutes. He didn't know where he went, he denied he was gone that long, and we realized that we had a potential problem.

Once he was stuck at home, he started calling people. He would get a wild idea, get on the phone to make it happen, and not tell anybody what he was doing. People showed up to take him to other states. He decided that Stanford had a cure for Dementia, but it was kept secret and the only way to get them to treat him was to go there in person. He called friends to pick him up so he could rent a car in another state. He figured that he would outsmart us that way. He booked airline tickets that we had to cancel. We took his wallet, but that freaked him out really bad, so we gave it back to him, but canceled all his cards.

Anytime he got a crazy idea, he acted on it. Most of them we where able to stop. But just yesterday we found out that he made changes to his medical insurance that now affects my mom. We don't know how bad it is yet, but it's not good.

It was hard to realize that his brain was gone, and he really had no idea what he was doing. Before he got really bad, he would have periods of sanity, and his biggest concern was to not be put in a home. We agreed to that, and it never happened, but it was VERY TEMPTING.

Another thing that he did that we didn't know about was messing up the Will. Fortunately, nothing permanent was done since my Mom is still alive and the lawyer was able to fix it, but it still cost her a couple of grand to undo his mistakes. It wasn't like he was trying to give anything away, he was more focused on keeping everything after he passed away so nobody would take it from him. Paranoid about money was a huge issue.

Once it happens, it only gets worse. Having a solid plan, and everything done and in writing for what happens afterwards is very important. Dealing with his stuff is easy, getting everything into Mom's name has been the challenge because of his never ending changes.
 
   / Parents with dementia, how dealing with that has gone.
  • Thread Starter
#47  
One of the bigger mistakes we made was not getting my Dad committed when he started losing his mind. We took his drivers license from him and his Doctors told him that he couldn't drive anymore, and I sabotaged his car, so that worked at keeping him home. Before that, he drove to town and didn't come back for three hours. It should of been 45 minutes. He didn't know where he went, he denied he was gone that long, and we realized that we had a potential problem.

Once he was stuck at home, he started calling people. He would get a wild idea, get on the phone to make it happen, and not tell anybody what he was doing. People showed up to take him to other states. He decided that Stanford had a cure for Dementia, but it was kept secret and the only way to get them to treat him was to go there in person. He called friends to pick him up so he could rent a car in another state. He figured that he would outsmart us that way. He booked airline tickets that we had to cancel. We took his wallet, but that freaked him out really bad, so we gave it back to him, but canceled all his cards.

Anytime he got a crazy idea, he acted on it. Most of them we where able to stop. But just yesterday we found out that he made changes to his medical insurance that now affects my mom. We don't know how bad it is yet, but it's not good.

It was hard to realize that his brain was gone, and he really had no idea what he was doing. Before he got really bad, he would have periods of sanity, and his biggest concern was to not be put in a home. We agreed to that, and it never happened, but it was VERY TEMPTING.

Another thing that he did that we didn't know about was messing up the Will. Fortunately, nothing permanent was done since my Mom is still alive and the lawyer was able to fix it, but it still cost her a couple of grand to undo his mistakes. It wasn't like he was trying to give anything away, he was more focused on keeping everything after he passed away so nobody would take it from him. Paranoid about money was a huge issue.

Once it happens, it only gets worse. Having a solid plan, and everything done and in writing for what happens afterwards is very important. Dealing with his stuff is easy, getting everything into Mom's name has been the challenge because of his never ending changes.
We agreed to not let him drive and have his auto keys and plan to sell their car asap. Gosh, so many things it do.
 
   / Parents with dementia, how dealing with that has gone. #48  
Anytime he got a crazy idea, he acted on it. Most of them we where able to stop. But just yesterday we found out that he made changes to his medical insurance that now affects my mom. We don't know how bad it is yet, but it's not good.
Discuss with attorney, but could try to get this reversed due to mental incapacity and see what happens.
 
   / Parents with dementia, how dealing with that has gone. #49  
My Grandma was starting in on dementia to where we couldn’t take care of her. In the assisted living she told us God told her to stop eating and go. The place forced her to eat and she lived another 8years not knowing who people were being generally pissed off the whole time.

That was 20 years ago and I still think about it often.
 
   / Parents with dementia, how dealing with that has gone. #50  
My Grandma was starting in on dementia to where we couldn’t take care of her. In the assisted living she told us God told her to stop eating and go. The place forced her to eat and she lived another 8years not knowing who people were being generally pissed off the whole time.

That was 20 years ago and I still think about it often.
I would say that is most if not all old people's worst nightmare, I know it's my dads.
 

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