Changing personality
This is my 1st time on here. I needed to vent. My wife has early onset and has mild cognitive impairment. She is still high functioning but has become very anxious. She gets riled up fast and takes it out on me. I am finding that I lose my temper when she is angry at me. Afterward, I feel bad cause “I should know better.” My mantra is to repeat the word “deescalate,” but I often forget in the throws of it. Have others dealt with this and how do you keep a neutral stance in the middle of “an argument.”
Comments
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welcome. Sorry about your wife’s diagnosis and anxiety. First I would ask her doctor for medication for her anxiety. Remember it’s not her talking, it’s the disease. I learned 2 things on this forum. Never argue with someone with dementia and “You can’t reason with someone whose reasoner is broken” I repeated that many times throughout the day. It also helped me to think of my husband as my patient and me his nurse rather than thinking of him as my spouse. We no longer had that relationship. Dementia took it from us. Lastly, give yourself grace. You’re human. With practice you will become a better caregiver. 💜
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I suspect most of us have been there. You know what you are supposed to do but sometimes we fail. I vacillate between thinking of my DH as a patient and thinking of him as my husband of many years. A lifetime of behavior isn't going to magically change over night.
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Welcome. Feel free to vent at anytime. I think we have all been there to one degree or another. It's the sickening disease talking. It makes it worse to argue or get mad. It's hard, but try and keep your cool. Sometimes it's easier said than done. You are not alone.
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Thank you for your thoughtful and kind reply.
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Venting here is always a good idea! We know what you’re going through and as others have said, we have all most likely done this ourselves. I think for me, the more I accepted what was happening to him, the more I was able to control my reactions to the things he said or did. It took some time, but it did get easier, as with most of the challenges of caregiving.
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My DH was diagnosed with Dementia last June. This is my first time on here and reading this has helped me a lot. It's really hard to know I don't have my husband anymore. He changes from one hour to the next. I never know when he's going to get upset and blame me for things. I find myself arguing with him and I know I shouldn't. I'm still trying to figure out how not to argue with him but I end up doing it anyway. I've developed a lot of medical problems due to stress. I need help. How do you learn to communicate with them without upsetting them more. He gets very agitated.4
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Welcome to our forum. I'm sorry that you are here but I am glad that you found us! Vent away. Mostly, you just have to agree with your DH on any issue. If you argue or deny it can get worse. It's very tough to come up with replies for many situations without upsetting your DH so just try to agree if you can. Trying to deflect to another subject may work but can often not. For agitation, check with your DH neurologist for medications to curb that. Ask your doctor for antidepressants for you if needed. Your health is primary also. You are not alone in this. We are all here for you.
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Yes, this forum is a great place to vent away. We are all in the same boat, more or less, and good advice, as well as needed empathy can be found here. I would recommend reading The 36-Hour Day by Nancy Mace and viewing videos on YouTube by Teepa Snow and Tam Cummings. Educating oneself on this wrenching disease is really important in helping us all cope better.
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I keep remembering that dear old Nun Mother Angelica, foundress of a Catholic TV Network, who used to say: “ we don’t know what we’re doing, but we’re getting better at it”.
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I can definitely understand the need to vent. I found mom has a few complaints that come up regularly. She often demands answers regarding things she would not understand the explanation for or the explanation would unset her. Why won’t I bring her to her house, why can’t she live in her house alone, how much money does she have, why won’t I take her to the store….. I have found it helpful to have a few very vague generic responses ready for when I might need them. Her interrogations stress me out and I find I don’t know what to say. The pre planned responses help a lot. I often claim to have forgotten, I’ll have to look into that, I didn’t know that, I’m really busy today I can’t. I think I’m getting better with time. It’s so easy to fall into the trap of trying to give normal real explanations. I’m glad you found our group.
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There are some issues that I can go along to get along with, but there are a couple of things I just can't go along with so for them I find a reason to leave the room for a little while and when I come back the subject is not brought up again. It works most of the time as long as I can stick with the plan which I don't always.
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Welcome. If there is a Mayo Clinic near you, request a referral for The Habit Program. The program is excellent and is designed to help you and your wife deal with this disease. We were told not to argue. It gets you nowhere and escalates the behavior. Take blame for everything you never did and apologize for it. Their reasoning is broken, and they will never understand that they are wrong or that you did nothing. Keep structure and routine as much as possible. A break in these causes confusion and anxiety. This is what also helped me: I put myself in his shoes and asked myself what life was like for him. Once I did this, I had more empathy for what he is going through.
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My DH was 58 when his behavior started changing and I had no idea what was going on! He has an MBA and held a high-level position with global responsibility; he ended up putting us in financial ruin (bankruptcy) and refused to find a job. The arguments were horrible, we had never said such awful things to one another during our 30 years of marriage. I sought out an attorney; but we were literally too broke to get a divorce. I'm embarrassed to say I was so naive about what was happening, we didn't get a full diagnosis until he was 67 (AD + VD).
Whether you have a diagnosis or not, I think those first MCI years are mentally/spiritually the most difficult. Her actions are from illness while your responses are from your 'truth'. You have not had enough time to indoctrinate your 'gut reactions' to align with her illness. It takes time and energy to stop being your true-self. You have to learn what works for the two of you (and then it will change).
My DH is now 70 and we've settled into a relationship that is loving & caring, but not husband and wife. He is beginning to need more physical assistance, and this forum has taught me there are some tough times ahead. After years of practice, I no longer allow my reactions to reflect how I really think or feel.
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Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
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