And that's fine if you aren't intertwined anymore and are just treating them as a baby. In the beginning stages though you don't really know what is going on and it's confusing what's happening because they can be fine for 5 days and then completely off. |
Yes, dementia is memory issues and memory loss. They don't understand. They are trying to cover it up as they don't get what is happening to them. |
The big thing with my mom was “lying” about her continued abilities. She thinks she still has the ability to drive and go places herself even though two doctors have told her she no longer had the physical or mental capacities to do so. I’ve had them put it in writing so I can refer her to it when she thinks I’m making it all up. Not only shouldn’t she drive, she doesn’t know the area, she can’t lift any weight (or her walker), she can’t get into or out of a car independently, can’t navigate a step up over a curb, open doors, etc. It would be a complete nightmare yet she would do it in a second without regard to her or anyone else’s safety. |
It's not gaslighting, it's reframing in a way that can make it a lot easier to deal with (or, really, not deal with -- you can't fix this, you can't even make it better, so just do what you can and get out). Your parents aren't aware of facts but telling you something different: They genuinely do not know what's going on. Someone's personality doesn't change from sweet and appreciative to hostile and accusatory because they have suddenly discovered pleasure in being a biotech: They don't know what's going on and the narrative they've come up with makes sense to them. The more you try to make them aware of facts, the more frustrated they get, and the more they'll take it out on you. I'm surprised that a PP's mother actually accepts the written documents from her doctors saying she shouldn't drive any longer. My mom would have said she'd never seen them before and spun a nonsensical conspiracy before she'd ever acknowledge that maybe she just didn't remember. Did you ever take lifeguard classes? I remember being told that when you get close enough to a drowning person, you have to be careful because in their desperation, they will push you under in their efforts to get their heads above water. It makes no sense -- you're there to save them -- but all they can think of is how to breathe. |
Yes that's it. Making no sense because she doesn't want to admit she doesn't remember. |
That may be true for some people, but my mother actually was dealing with both in the early stages. She knew she was declining and was terrified and upset, because her father had Alzheimer’s. She would cry about it and confide to my father how afraid she was. To me that was the one of the saddest aspects — her retention of awareness that she was experiencing cognitive decline, for a long time. |
+1 Perfect example. |
On some level they are aware there are gaps in their cognition/memory, this causes discomfort, the solution is "lying". |
PP whose mother ‘lied’ to cover up/deny her decline. One problem with this is that it was actually pretty successful in fooling other people, some of whom may have been willfully in denial (like my dad), which delayed getting a diagnosis. Other relatives thought I was overreacting when I tried to sound alarm bells about cognitive decline and it took almost a year to convince them that it wasn’t ’normal aging.’ I don’t blame her, but it was very frustrating and undermined our ability to get her on medications that had some benefits in the early stages. |
What medications are given in early stages? |
Yes. I have one sister that called me and said my mother, who is in a rehab after breaking her knee was very sad because the sister that lives near her (we are 3K miles away) “never visits her and the staff hates her”. My sister goes there at least every other day and I call constantly, but my mother won’t pick up the phone if she doesn’t want to. The staff doesn’t hate her either - they are just encouraging her to be able to transition from bed to toilet, etc, so she’s not bedridden for her entire rest of her life. She’s always HATED exercise and refused even 20 years ago after a car accident, to do the PT needed, so now she’s much worse off as a result. She’s also called the nurses in during the night to check on my father, who she said is dead in the bed next to her. My father died last August. She also speaks of my father constantly poking her and not letting her get any rest. Could be the pain pills, could be sundowning, could be a lot of things. She’s lost 50 lbs and is fairly anemic and I suspect that she has something else undiagnosed going on, but she has refused to go to her regular doctor and the staff can only do so much. She was refusing to be transferred in a wheelchair to the orthopedist to check on her knee but the rehab doesn’t give her a choice like her assisted living place did, which is actually a good thing. NOW my mother wants to move back East where there is more family, but of course, now it’s too late to make that transition because flying would be too difficult, and she’s too afraid, even with medication, to let the staff transfer her from wheelchair to plane chair. I feel sad for my mother, but after five years of trying to get her to move back East and being refused, I don’t have any guilt. I’m still upset that the last time there was a crisis and I went out, I couldn’t leave for 2 months and our old dog had to be put to sleep and I couldn’t be there to say goodbye. Bottom line is the more siblings, the more disagreement, the more misery, esp when it comes to memory issues, which often brings out stubbornness in those who were previously in denial. |
My husband was called a slumlord by my aunt, telling relatives that he would not fix up the house she rented. In truth, he was the legal bank for her mortgage 20+ years earlier, and she welched on the loan, never paying him a dime, and lying about her income (said the company cut off her pension, which wasn’t true). I found all this out when I was at her home, helping her hospice, because relatives were “so surprised I showed up”. My husband is much nicer than me and just rolled his eyes and chuckled. I wanted to put a pillow over her face, and pride myself on not doing so. |
So hard to reconcile with. I feel badly for your friend. It’s very hard |
I agree with you - it’s devastating and so hurtful, esp. when other family members believe it. |
This is not always true. My mother told me my sister had not visited and I said “Mom, she was just there yesterday; I spoke with both of you on the phone”. Her next statement was “Oh, yeah, I wasn’t in a very good mood”, which was actually the truth. We were told by a neurologist after my father’s stroke, that his personality could change and he could become a lot more difficult. And that dementia can make people mean. That does not make things easy on the family members, whether or not the person can’t help it. |