How do you deal with your own negative responses to the actions of a loved one with dementia?

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I know they can't help it in my head.

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THANK YOU so much to everyone and anyone commenting here about this subject!
My mother is 96 1/2. She was the healthiest person I have ever met in my life, until at 92, she fell while we were riding bikes. She broke her ankle( which healed in 6 months) and skinned her shin badly and a few other things. Luckily her head landed in the grass not the pavement. I believe it was the anesthesia, the blood thinners and all the different drugs they give you while you are under anesthesia, that started to affect her mentality. She just started to change mentally after this accident.
Maybe it wasn't even that, maybe it's because she stopped exercising everyday. She walked 2-6 miles every single day of her adult life and then started riding her bike 2-3 times a day at about 80, instead of the walking. Things just started going down hill mentally. It started out slow, but suddenly six months ago, I noticed she was forgetting that we watched a movie on tv just days before, and she was mixing up events that happened. She insists something happened 20 years ago when it was just last year, etc. she blames me for everything that she can't find, and she gets very angry easily, has started loosing her hearing, and wants to sleep till at least 10 am every morning. I live with her.
Sorry for the long explanation. I've been going to the therapist once a week for 4 years. FINALLY the therapist said something that has helped me greatly! it's extremely helpful no matter who you are dealing with, when they act up and say negative things or are always trying to challenge what you say. JUST DONT TAKE THE BAIT! that one quote is helping me incredibly well. Here is an example:
Every time is say " oh it's a beautiful day outside, the sky is so blue, etc.", my mother will shoot me down and say: " well it's not really blue out." Or
Well they said it's going to rain today( even when the weather people haven't said a word about rain).
It's nothing but negativity and cutting comments.
So now, when she makes negative remarks, I have taught myself to just not respond and and not give her the satisfaction of commenting. I just let it go over my head and continue what I was doing. It's been extremely difficult to deal with 24 hours a day, and it took about 3-6 months to learn to be quiet and calm and NOT TAKE THE BAIT!
but it has helped so much! My mother has been so negative all her life and I have been there for her to abuse since I was 15, but now, she can't get a rise out of me ANY MORE!
It's a breath of fresh air!
Just remind yourself at breakfast , lunch and dinner: DONT TAKE HER BAIT! She will continue to try, but your life will be so much better once you practice this. Good luck and God bless! 😇
My mother is slowly declining into dementia--and it's really hard. Conversations with her are one sided, most days and she circles around and around until you simply cannot understand her--and she is considered to have VERY mild dementia. I cannot even fathom trying to talk with her as she progresses--but since I am with her a couple days a week, I can manage.

Mother will say the most outrageous things--just bigoted, racist, homophobic things--I don't know if this is just the "filter" lifting and she's always felt this way and covered it up. She will talk about people in the most embarrassing ways--has a 'friend' who is fairly heavyset, and refers to her as 'that fat girl I know'. Well--the 'fat girl' is 75, and she knows well and good she's heavy--and I'm sure mother makes comments to her. Shoot, she comments about my appearance every time I see her. Yesterday she actually said "you have aged really, really well". WHAT? Did she mean that? I mean, I'll take it since she hasn't given me a compliment in a long time! Usually it's a comment about how men only like slim women and I have never been slim!!

Dementia basically means 'broken brain'. People with it will say anything and everything. They usually don't mean it. You just can't be angry with them...even when they are yelling at you. They aren't 'them' anymore.

In my case, I have been seeing a therapist for years. She has helped me to overcome my atrocious childhood and now I actually have an OK relationship with mother. In big part, b/c I don't take what she says personally. It's hard, don't get me wrong, but for me to be angry w/her at this stage is pointless.
It's hard, a caregiver is always on the edge of burn out some days more so, it makes thing's worse and dose no good to argue or explain why they shouldn't say thing's or defend yourself if they accuse you of doing thing's like stealing key's or anything they hide and forgot where they hide them. Or complain about the food. It's hard to hold it in. a support group is a must. You have to talk to someone to blow off steam. Facebook, talk to a spouse, friend, someone or you'll hasten burnout. My advice hold it in but not forever. it helps to know you have some one to tell what happened. It hurts and vary hard to not think bad thoughts and this hurts but you're just human and you have to fight harder some days to hold it in. Trying to change the subject a lot of times doesn't work as dose trying to distract them. Every case is different just got to do what you got to do to get through it
I'm not sure what you mean by negative responses, but, if you know that the LO has dementia and can't be blamed, held responsible or punished for things they may say, I'd try to keep that in mind and practice my own responses to them in advance.  I'd try to have a pre-planned reaction that is appropriate, so I'd know what my response is going to be in advance. Just having a knee jerk (figuratively speaking) isn't helpful and can be hurtful. If it's something that you can't seem to get past, I'd explore other options for her care. It's very stressful to be with a person who has dementia around the clock. I'd explore alternate caregiver options. Everyone is not cut out for this kind of thing.
Also, getting plenty of respite time may help.  If you don't get a chance to recharge your own batteries, you might be overwhelmed. That can contribute to burnout, which lowers our ability to respond as thoughtfully. 
Why, oh why do caregivers feel they have to tred on thin ice when they are lashed out at and otherwise abused. I don't care what the reasons are, dementia, old age, etc It is unacceptable and must never be tolerated beyond the point where the caretaker can take it. Remember, without the caretaker, the patient is going to be a l o n e. The caretaker must be diplomatic, funny, change the subject, etc. but when it gets to the point where the caretaker is being affected very negatively, IT HAS TO STOP. If that means "letting them have it" - no they won't understand but YOU will feel better OR YOU HAVE TO REMOVE THEM. There is no other choice if the caretaker wants a life and I assume they are much younger and should have a life ahead. Sorry this is so harsh but I have been through it all.
I am also dealing with a very negative mother. She has always been that way, but now it's increasing dramatically....along with the paranoia. Nevertheless, your suggestion to not take the bait is the perfect way to describe how to handle it. I just remain silent during her rantings. It's one of the hardest things I ever had to do in terms of self control. I also set a boundary with small doses of her. I can't do more than two hours in her presence. I will call her every day...she has a FB account...so I will message her through there to check in. These are all coping mechanisms I've adapted for myself to deal with her.
midkid: "...the 'filter' lifting..." yes, along the same lines as my sister's husband's term for this. mom blames others for stealing and calls police for the little things she misplaces, even when i find them, at which point she says they snuck back and returned it!
his term is 'DISTILLED'. i love the oddly poetic explanation. she always did blame others and never took responsibility for anything negative - for which it would have been so right and easy and honest to simply say "oops, sorry" and laugh about the messy fridge or some misplaced item. this behavior compromised our respect for her and luckily we haven't 'inherited' this behavioral flaw.
so, yes, she always did have this 'blame thing' going, but it is certainly distilled with dementia.
I don't know how you deal with it, honestly. It's tough. My FIL is still sweet and kind even though he has dementia (and believe me, I count my blessings on that one!!), but even so, hearing the same things over and over and over does get on your nerves. He'll say good morning to me 20 times in 5 minutes, and if I don't respond each and every time with a cheery "Good morning to you too!" as if it's the first time I've said it, then he gets offended. (I'm not a morning person, by the way. I need awhile to wake up.) I know this is tiny compared to what others on this forum endure, but I'm a quiet introvert, and I can never even walk through my own house in peace - my FIL comments about EVERYTHING that I do. It's affecting my health (I now have ulcers), and I'm not sure how to deal with it.

That said, again, I know that it could be way worse! Sorry for those of you who are getting yelled at a lot - that's awful. :(
Dementia is so hard! 5 1/2 years in and here it is Monday morning trash day. I snuck her trash can out last night. For the 3 rd. Week, she snuck it back in and it did not get dumped. So I brought the whole can to our store and dumped it. I'm just waiting for her to wake up and later call and ask where is my trashcan? I'm sitting here breathing deep and laughing! Outwitted by the 84 year old. Again lol! Sometimes you just have to roll with it.
I don't get many neg remarks from alz hubby but the latest has been in bed he has maybe slept 30 min. He gets up to straighten my covers making sure I'm on my back. All creases out of my side gets in bed makes sure no creases. I have learned to do what he wants so no problems & wait for him to fall asleep. We have king bed thank goodness. I used to try telling him it's my side & I'll take care of it. Well forget that. I was thinking last nite he's like putting a baby to bed. I found when I argued I felt my adrenalin going up. A caregiver in my support group just had heart attack & died. His wife didn't seem to far gone but until you live w them....Support grps are so valuable to let it all out as those there care & understand. Weekly mtgs are best as you engage more w caregivers.

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