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Not liking me or DH much these days

JC5
JC5 Member Posts: 239
250 Care Reactions Third Anniversary 100 Comments 25 Likes
Member

It’s very apparent to me that everything and I mean everything my DH does or doesn’t do these days annoys the heck out of me! Trying to get him to shower or change his clothes or eat a decent meal (and not sweets) is always a battle. I take him out everyday and no matter what we do he complains about something. If I leave him home he complains about that and proceeds to call our children wanting his truck back. He called one daughter 5 times, her husband twice, their son 3 times! On to daughter 2 which he called 14 times consecutively and then my son 7 times!

I can’t stand the way he looks, smells, behaves! I’m tired I’m tired of being nice, understanding, the distraction expert , the newly crowned fiblet queen, the pleasant encouraging person only to get yelled at it’s exhausting! I know I need a break which I get when I take him to adult care 2x a week. He doesn’t like it and calls me several times while he’s there but it’s my only break. It’s heaven - my stomach doesn’t hurt, my head doesn’t hurt but I am exhausted and just want to crawl into bed on those days. Tell me how do you cope, how do you keep going, how do you have a day where you don’t cry? Tks for your advice

Comments

  • Jeff H
    Jeff H Member Posts: 157
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    I'm sorry you have to go through that. Not that medications are always the answer but there are medications for agitation and anxiety. Is your DH seeing a neurologist?

  • Sunfish47
    Sunfish47 Member Posts: 55
    25 Care Reactions 25 Likes 10 Comments 5 Insightfuls Reactions
    Member

    I’m so sorry you are going thru this !!! Yes you must get him onto some med to calm him down, for your sake.
    YOUR health is the most important at this point. And as the disease progresses he won’t be able to use his phone to call/annoy family members (this eventually happened with my husband).

  • Russinator
    Russinator Member Posts: 315
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    Is placing him in a MCF possible?

  • WIGO23
    WIGO23 Member Posts: 284
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    Your exhaustion description is spot on and describes caregiver overload. All I can offer is understanding and caring. I have no idea how this is done day after day, year after year. But I am going into year three and still standing.

  • Michele P
    Michele P Member Posts: 389
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    Member

    Can you bring in a caregiver to help him shower and make him a meal? This could be a few hours a day several days a week to give you a break. Maybe he would be more responsive to another person and not argue. I would talk to his neurologist about medication. You have to take care of yourself before you can take care of him. Come back here for support.

  • BethL
    BethL Member Posts: 1,346
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    I don't think you should live this way! The stress will sicken or kill you. Ideas: Try getting him on medication as others have suggested. Hire someone to help you and give you a break. Put him in an MCF for respite, and if it works out for you, place him.

  • BPS
    BPS Member Posts: 465
    500 Care Reactions 250 Insightfuls Reactions 250 Likes 100 Comments
    Member

    From what I have been told hospice is treated differently for dementia because for most diseases they are treating the disease trying to cure it but with dementia having no treatment available the six month thing is not treated the same. My wife has been on hospice for over 6 months and her physical condition did improve after getting on hospice, I think because they made some medication changes, but there has been no talk of her what they call "graduating" off hospice. I was told that "graduating" does sometimes happen, but they can be reassessed and get back on when things change again. My wife is in MC but hospice has still been a great help.

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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