Help with bringing in help


Hi All,
My DW is putting up a fight about brining in a caregiver in our home. Probably Stage 5 but I don't feel comfortable leaving her for extended times. I would like a break as well. Anyone have a good therapeutic fib for why So-n-So is coming in? Any stories that you've used to bridge the resistance? Thank you
Comments
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When my DH was at the point where I couldn't leave him alone AND I needed time away, I called my local "Family Means". The organization was a life-saver! They provided a volunteer to come for 2 hours once a week. The first two weeks, the 3 of us walked around our neighborhood together and had ice cream cones here. DH was fine with it (food always worked!). The third week, I was home but kept myself busy away from them. They walked around the neighborhood together. Fine. The fourth week, DH and the volunteer walked together—and I was away from the house. (I was two minutes away). From then on, the two became friends! Worked like a charm. Good luck!
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My DW was resistant to the idea as well when I presented it as a caregiver. I waited a week and brought it up again, but I presented it as help for me in cooking, cleaning and laundry. Anytime my DW brings up not having her come over, I can still remind my DW that the person coming is to help me, not her.
Good luck!
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My DW is generally good with people but I still took a cautious approach.
I hired the companion myself rather than using agency. Consistency of having the same person was very important to me and I believe I had a much better chance a finding a consistent companion if I hired them myself rather than going through an agency.
The first time we met the companion was for an interview at a public space. DW loves ice cream so we met companion for ice cream. I sort of played it as happenstance that we met this new "friend". Again, DW has always been good meeting new people.
For the first couple of visits I stayed at home with companion. Companion was generally quiet and a bit out of the way just watching and hanging out with us.
I started leaving for short periods of time. Fortunately DW gets along well with companion and it has worked out.
For me, it was important to take a gradual approach. I did not want to leave DW with some random stranger who just shows up.
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I have just started with a caregiver for DH for 2 hours a week. On her first meet and greet visit I just said it was an old friend. When she came for her scheduled time, I just let her in, said Hello {name} and pretended she was just visiting. I stayed in the house but said “I have to make some phone calls. Maybe you two could keep each other company?” The next time she came in I stayed a few minutes then left for an hour. He seemed ok with that. We’ll see how next week goes…
I would add that DH likes to have people come over so he can show them everything in the house - so that works well for this.
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Hi Pier Walker-
I’d been trying for a couple of years to get my wife comfortable with the idea of getting “help” in the house- and used the same excuse as Cindy Bum, that I could use the help with cooking etc. But she was very resistant to the idea. Then I got “lucky” and had a series of vertigo attacks and dizziness recently and became unable to drive. (Luckily I was prepared with just who to call to get someone in.) I became adamant at that point and insisted that there was no other way forward other than to have help! My wife had no choice but to go along with having our caregiver here, and she has been helping both of us. I wish I’d been more insistent before. I believe there is no real “fib” involved in any of us using the fact that we ourselves could use shopping and cooking help (or whatever it is) and insist on having the help for US. IT REALLY IS A FACT, WE NEED HELP! My wife has gotten used to the idea of having someone around and most of the time she barely notices that the caregiver is now mainly focused on her. In fact, she gets out and about more now with the caregiver than with me these days.
Good Luck, let us know!!Karen
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Thanks everyone. Couldn't get over how fast everyone was to respond…this was my first post. So thank you truly. DW doesn't buy the fact that I need help, she says she can do whatever to help me. Will be working a different angle.
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Karen - so sorry about the vertigo! That is not fun!! My DW has had that several times over the years. PT really helped. The last time when it didn't help and was getting worse…the PT sent us right back to the DR asap…turns out it was Leukemia. DW is doing well with the treatment and shortly after treatment started, 4 years ago, the vertigo symptoms disappeared. Hoping yours is GONE!
When I do get someone coming in I will let you know.
Pier Walker/Stephanie
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Pier Walker, the reason your PWD believes she can still do everything in the home is because she isn't aware of having dementia. This is a characteristic of dementia and is called anosognosia. Do not try to confront her with reality. Learn the work-arounds that the members discuss.
Iris
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A friend of mine was in the same boat. His wife hated the idea of needing a caregiver and wanted nothing to do with her for months. Finally, she has accepted her as a friend.
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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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