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What Is Looking After Yourself

This might seem a bit silly but it’s said to me often by medical staff “look after yourself” Could I ask what does everyone do to look after themselves. Apart from getting enough sleep which is hard, is it a frame of mind, time out on your own once or twice a week and then where do you go. When you have a baby you never stop thinking, caring and planning your life around this new child, I can’t stop planning around our new set of circumstances. Maybe a change in my mental approach.

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  • Lgb35
    Lgb35 Member Posts: 174
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    this is a great question. I am on the path trying to figure this out now. I am starting therapy. She has a lot of experience with dementia and the impact on caregivers. I am hoping she will give me some ways to release stress.

  • Denise1847
    Denise1847 Member Posts: 923
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    Hi Biggles,

    Based on my own experience, the medical staff have seen the destruction/deterioration of caregivers and is warning us to take our plight seriously. My physician has said multiple times how he has seen what the disease does to the patient and the caregiver. My caregiver experience has been akin to the frog in the pot of water slowly coming to a boil. My DH would not accept someone coming in so that I could leave for a few hours or attend an adult day care. The confinement, social alienation, mind-numbing routines, fatigue etc. took its toll on me physically and mentally. Fortunately, I was able to get counseling, meds for depression and the strength to place my DH in memory care.

    Biggles, I share this with you to encourage you to do whatever it takes to protect your peace and sanity. Get a therapist who specializes in depression, grief and Alzheimer's. Try journaling. Think about writing your experiences/feelings etc. down to help sort out things mentally, exercise, learn something new, meditate, reach out to friends/family on the phone, learn about grief (anticipatory grief) and how it affects you. Caregivers are grieving the life we planned to have, the experiences we cannot do and our loved one's eventual death. Please be as vigilant with helping yourself as you are with your loved one.

  • BethL
    BethL Member Posts: 1,212
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    Don't neglect dr., dentist and vision checks for you. Have suggested screenings appropriate to your age.

  • howhale
    howhale Member Posts: 160
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    Had people tell me that same phrase countless times as if there was something magic I should be doing to "take care of yourself". When the burden became so great that I just could not physically handle it alone any longer, I hired caregivers to sit with my wife each day. It started at 4 hours per day for 5 days and eventually grew to 7 hours per day 7 days a week as her condition progressed. Caregivers allowed me at least time to take care of grocery shopping, critical doctor appointments, etc. It also allowed me the chance for just some private quiet time to read, nap or whatever helped that day. It became important because when alone with my wife I was "on duty" every second of every minute because that is just what it takes. You have to find what will work for you to allow you to recover some, definitely not all, of what we lose as caregivers. Also, I had to find people as caregivers who I could trust with my wife alone and who had experience or understanding of caring for someone with this disease. Some caregivers did not last long because, while very good at caring for a physically impaired person, they failed miserably at being adaptable enough for memory care. They could not adapt on the fly to my wife's ever changing needs or condition. In all honesty, home health services proved to very poor at providing the right people and I fired them all. Besides the fact that you will pay a premium per hour for their service and the caregiver receives a pitifully low rate, they were just bad at providing people I would trust with my wife.

  • Chris20cm
    Chris20cm Member Posts: 118
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    Thank you for this response, I find it very encouraging because DW in stage six, has barely let me out of her sight for eight years and will not accept home care, and will likely have a meltdown when she goes to memory care. I am burned out and am considering counseling, medication, whatever creative ideas might help make the transition before I blow a circuit board.

  • Biggles
    Biggles Member Posts: 598
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    ha ha a 2am bike ride sounds just the thing.🤣

  • MPmom02
    MPmom02 Member Posts: 1
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    I wish I could get the VA to help us. They denied my husband because they said, he was JUST in the Army Reserves. My husband literally had to hold me back.
  • Biggles
    Biggles Member Posts: 598
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    Thank you so much you have all opened my eyes to taking care of myself unreservedly. Still not sure how I’ll do this but I I’ll use all the resources I can find.

  • SDianeL
    SDianeL Member Posts: 2,596
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    shame on them for saying that!

    • Federal Active Duty: Reservists who were called to active duty by a federal order and completed the full period of that order are generally eligible for VA health care benefits. 
  • Biggles
    Biggles Member Posts: 598
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    Good stuff and you made me smile your turn to do your thing.

  • ARIL
    ARIL Member Posts: 264
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    Agreed absolutely. Sometimes being told to look after myself sounds like criticism and that oh, right, here’s one more thing I am failing at. If I would just try harder, they could get back to their lives and not think of me. Or that’s how I think when I am grumpy.

    At the same time I know that some people want to express concern and don’t know what to say.

    And I am trying: I maintain regular doctor and dentist visits, I try to exercise, I see friends. But a full-time job plus caregiving is getting to me. My LO is in a facility, but the amount of effort is still very great (laundry, supplies, visits, medical appts, finances, communicating with his family and friends), and the worry and sadness about the decline are persistent.

  • jennybeeay
    jennybeeay Member Posts: 27
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    I can sense the challenge you faced with caring for your wife. I imagine this progression while caring for my newly-diagnosed husband with Alzheimer’s. Did you ever find in-home care that worked for you long-term? I am wondering if trying to find a caregiver through “referral “ is better that through an agency. Do you have thoughts on this?


    Thank you for your time.

  • persevere
    persevere Member Posts: 78
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    OMG, I’m laughing so hard, ‘the drywall boy’. Thanks so much for this lighthearted break! We need more of this. As for me, the whole ‘take care of yourself’ is their way of making themselves feel good. They don’t know jack about what we’re doing.

  • Chance Rider
    Chance Rider Member Posts: 129
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    I’ve found deep breathing exercises to be very helpful. I started after watching a video by Teepa Snow where she described the affect it can have on stress and cortisol.
    My Apple Watch has a customizable Mindfulness feature where I set timers.
    A bonus is that I’m teaching myself to breath deeply when things are challenging with my husband’s ALZ.

  • lenbury
    lenbury Member Posts: 49
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    I think hearing this from friends and family made it easier for me to bring in outside help to give me a break. For a while I felt it would be an imposition to have strangers in our home but they were life savers.

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
Read more