the grieving process
My husband is in the late stages of early onset alzheimers. I feel that I have been saying goodbye slowly for 10 or more years. I feel more detached from him emotionally all the time while at the same time feel so sad watching him disappear. It is a struggle and it seems that no one else really understands. How are some other caregivers who are losing the love of their life coping?
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Thank you for sharing your story. Like SallySue, I hope you find peace.
The gift of listening is a profound gift of love.
This is my 20th year as a family caregiver, and I am very isolated. Although friends know my story, and sympathize with me, I rarely see them because of the demands of caregiving. To make contact with others, I write articles and books, write for three websites, and give talks about caregiving. These steps help to reduce my feelings of isolation.
Thank you for your words regarding the gift of listening. I find that one very challenging for me right now . He is in so much fear of the future when I am around him he criticises my actions on simple daily life stuff, like how much water I use to wash dishes and throwing away a small end of a bread loaf. The micro managing is a form of anxiety I’m told. He’s on antidepressants but I feel this situation is getting harder for me to mentally tolerate. I have a carers break when he’s go into the hospital for a couple days of treatment. I’m sleeping in another room. I think I’ll call my cancer counsler and ask for help. He’s becoming less and less of the man I use to know and it’s frightening me.
Thank you for your words. I too, feel isolated in a small country town. I will try writing more too.
Getting some help sounds like a good idea. When my mother criticized me, I realized it was dementia talking, not the amazing mother of my childhood. I also realized, yet again, that her life had become a confusing maze. Mom felt lost and scared. Reversing roles mentally with my mother helped me to cope with her behavior.
Writing helps in many ways. I think writing affirmations helps family caregivers. First, it makes us focus on the blessings in our lives. Second, it changes our thinking from negative to positive. Third, it creates a framework for our lives. I recommend one-sentence affirmations because they are easier to write and remember. Your first affirmation: I can write affirmations!
Thank you. I will ask for help. I will try to remember to not react but to think he’s unwell in a way I don’t understand. I don’t feel safe around him when he’s like this. He hasn’t become verbally aggressive in about 8 months but I guess I fear it may happen again. I find feeling unsafe very difficult to manage. I feel unsafe because when I try to explain or talk it through it turns into an irrational argument , that’s when I realise there’s nothing to argue about. Really. Like how much water is too much to wash dishes.
Good morning @mnina Caregiving is often nothing short of a brutal assignment for which we receive no training and no ’employee manual’! Remember we only find super heros in the comic books and not in caregiving! Often what we are confronted with is simply beyond our abilities. You show great strength in seeking assistance!
While I know each patient is unique on their journey, but in the case of my wife, she too lashed out at me the most. Her neuro-oncologist explained to me it was because she felt the very safest with me so she could vent, rant, etc. and know my love would still be there afterwards. Her anxiety was never able to be corralled by the doctors in her case and that was a highly challenging situation for me. She couldn’t focus on anything for longer than a few seconds at a time. I agree this can be an incredibly exhausting aspect of caregiving! In cases such as your water and dishes, I would simply say ‘ok, I’ll watch that. Thanks for letting me know.’ More often than not that ended that particular concern — for that moment until it came back up again.
My wife, too, showed very different personalities during the course of her war. I say while I was married to one woman for 41 years I was married to about a dozen different people. Chronic disease and longtime disease fighting takes its tolls in some very challenging ways for sure.
Sending strength, courage, and peace!
Thank you. I do feel better , especially knowing that I’m not the only one and I’m not going to lose my common sense over this, With Gods Grace. Thank you.
Thank you for your honest post. I think you’re so right when you say your wife had about a dozen different personalities. It’s hard for caregivers to adapt to these changes.
Demented loved ones can say confusing things and, every once in a while, say something profound. When my mother became more difficult, I could usually calm her by saying “I love you.” After a while that didn’t work. One day I told her I was doing my best. “You may be doing your best,” she replied angrily, “but it isn’t good enough.” What a hurtful comment. Later I realized my mother was right. My best wasn’t good enough to make her young again. My best wasn’t good enough to restore mental functions. My best wasn’t good enough to make her happy. All I could do was continue to love her, manage her finances, and provide the best possible care.