Feeling cheated
My husband is 14 years older than me and has had advancing dementia for years now. I am increasingly feeling guilty about anger and feelings of being cheated out of my own advancing years. I have family support but understandably, no one wants to spend too much time around him. Everybody tells me to get help,few times a week but I’m such a private person and I keep,feeling conflicted about leaving him while I just go to park or shopping. But these feeling re leading to little bouts depression and I need to stem them now.Any advice will be greatly appreciated
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@jeanadair123 All these golden nuggets from this coveted connect site. I stayed churned up over this, but this site actually helps anchor me every day, why I always try to post something of value. Many of us don't have enough friends - at this stage of our life - making it difficult to talk and get support. And even with friends or neighbors, I'm reluctant to say much about what's taking place with my husband's MCI. I found where I live it's a taboo subject, sad, since it happens to so many people that need friends, quality care and the love and compassion from others. Along with the caregiver, that needs that same love and compassion. So thank you for sharing about the daycare for seniors....I think we'll know when it's time to consider a day care. At least I hope so....
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8 Reactions@judimahoney Thanks so much for this tidbit. I have this folder as I move through this progression, of what I need to do. So much to consider.
Thanks for reaching out.
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2 Reactions@judimahoney I’ve said similarly awful things like I hate my life. I understand it’s worse for the partner with memory loss but I feel for all of us.
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4 Reactions@kjc48 Great words of wisdom you hit the nail on the head. I have a really close friend who I can tell anything, but for some reason, I never go into depth’s into my situation although in a way she would understand because her mother had dementia yet at the same time she lived next door to her and she also had a husband so she had moral support at home. I don’t want to say too much to her because she is my best friend and if I say anything negative, she worries about me and she is always on my side besides, I don’t want to say anything negative about my husband. He has been my rock for 40+ years, we just seem to have good days or I think we’re having good days and then all of a sudden things change in seconds today has been a good day apart from me, putting the laundry on the floor and he picked it up and started folding it to put it away. 😂😂 One can’t help me smile. It would be nice if we all knew where each other was located since we understand each other you never know In this small world, we could live around the corner from each other? Well I must continue with laundry, have a good day.
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8 Reactions@carolreid I understand where you’re coming from. I have all of the same feelings. I am not a saint and I am not able to fake being a saint. We get this disease thrown into our lives and feel like we’re expected to be stoic, pull the pieces together and be a wonderful example of the perfect caregiver. Not everyone is cut from that cloth. My husband likes to try and turn the tables on me. He comes to me all concerned and says “Are you alright? You spend so much time in your office all day and you’re so mad all the time”. I’m trying to keep my head above water with all of my new responsibilities, I’m so overwhelmed and I can’t even turn to him for condolences. I also set myself apart to avoid the constant announcements, narrations and surmising all day.
I’m just rambling now…. But you get the gist.
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3 Reactions@jeanadair123 oh my gosh, my husband puts everything away that I’m using or left out because I will be using it soon, too. He empties the dishwasher before I get to it and puts things away where I can’t find them and wonders what big deal is…
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2 Reactions@lkbous
I've only been reading these posts for a few days, but so far I do think it helps to know that I am not the only one feeling this way.
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5 Reactions@lkbous I am so glad to hear that I thought I was on my own because I never knew what to expect it’s reassuring to hear the same type of things? I’m wondering at what stage of dementia this is mild or medium and what would be the next steps to take? It’s tiring to be 10 steps ahead all the time I can never leave anything out because I’ll never know where it will end up? I don’t mean to take it lightly about what you said, but I totally understand .
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4 Reactions@lkbous Well said this is so far The most helpful thread I have been on so far I also get he must be mad at me.
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1 Reaction@jeanadair123 I agree about wishing we could all talk in person…. That would be a crazy gathering, and soo great. In support groups you get so many different stages and that isn’t always helpful. Picking and choosing a support group would be ideal.☺️ We, here in these threads, seem to be so much in the same place in our journeys.
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3 Reactions