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No Support From My Kids

As expected, this was the worst Christmas ever. My DW goes to the Alzheimer’s Activity Centre  7 hrs a day 5 days a week , however , they are now closed for the Christmas Holidays… reopening on the 2nd Jan 2025 as such It has been very tough for me. Keeping her occupied is brutal . Watching TV for hours is all she does and I have to sit with her. I have put on Sound Of Music which she enjoys 4 times already . I have driven to the Mall twice as we could not take our usual 40 min walk as it has been raining here the past few days. During this Festive Season we visited ( 3 hours ) each of our 3 kids once at their respective homes . That’s it . None of them ever ask me how their mom is doing yet I know they love her very much . I feel they do not want to know .Today my son calls and I could not help telling him how tough it has been for me all these past few days ( 2 more to go ) . I got the usual response “ WE TOLD YOU TO GET MORE HELP.” I got really pissed off and hung up. I also know that behind my back the 3 of them discuss between themselves what’s happening and how their dad is not doing enough to help their mom yet they each spend only 2 hours a week with her.
BTW …I do have a PSW come in once a day every evening to give my DW a shower . Still debating if I should press the send button. Aw well …

Comments

  • SDianeL
    SDianeL Member Posts: 1,080
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    Member

    so sorry. Someone posted on here The Calvary Isn’t Coming” which for many caregivers is true. Maybe it’s time for memory care? Or can you hire more help? We understand what you are going through. Hugs.

  • BPS
    BPS Member Posts: 138
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    Member

    Your kids and most people think they are helping with their "wisdom" but unless they have spent real time in the trenches they just don't get it. The people here have put in a lot of time to be able to give ideas that are based on real life. Sometimes it is hard to be polite to those that don't have any experience but want to tell you all they think they no.

  • Quilting brings calm
    Quilting brings calm Member Posts: 2,579
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    Member
    edited December 2024

    The reason your children don’t ask is because they feel they know the answer.

    For whatever reason, 2 hours a week is all they can do. The only available answer then to give you relief is to hire more help. Normally you are getting 7 hours a day most days plus an hour at night. That’s actually quite a lot of help for at home. The next step would be MC. It sounds as if your children would be supportive if you went that route.

    Caregiving is hard. I knew I wasn’t suited for it 24/7 so I placed my parents in AL.

  • illusion62
    illusion62 Member Posts: 5
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    Member

    I don't think kids really know how to help. In my opinion all that's needed is for them to call for 5mins a day to see how YOU the caregiver is doing. They don't need to do anything for the one suffering with AD as I don't think there's really anything they can do, unless they have lots of time and patience to get physically involved. I'm a newbie to this, but for the past year have seen DH short term memory deteriorate and it has pulled the rug from under my feet. Our children will ask how we are every few months via WhatsApp because they all live so far, only visit once year. But I know I would have appreciated talking on the phone for just 5 mins daily with one of them!

  • jfkoc
    jfkoc Member Posts: 3,967
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    Member

    Please, always press the send button. We truly understand and we really do care!

  • Russinator
    Russinator Member Posts: 57
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    Member

    Sadly The Calvary Isn’t Coming

  • cavenson
    cavenson Member Posts: 36
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    Member

    As disappointed as you may be when kids don't show up to help, trying to dish out guilt just makes things worse. My DH has 4 adult children and 5 grown grandchildren in the area. I wish they gave DH more attention, but I show heartfelt gratitude for the attention they do give him. I'd rather be pleasantly surprised when they do visit or take DH out than feel resentment when they don't.

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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