My mother has moderate to severe dementia. She has occasional incontinence with her usual caregivers. When the fill in caregiver comes, my mom has all day incontinence. My mom verbalized she doesn’t like the fill in caregiver because she doesn’t talk to her and watches too much TV.
I think the fill in caregiver talks too fast and it’s hard for my mom to process the rapid speech. When the caregiver doesn’t get a response from my mom the caregiver takes it as if my mom wants quiet time. Sometimes my mom doesn’t answer my questions, but I don’t shut down and stop talking to her.
I have very few options for fill in caregivers, so I want to make the best of this situation and try and address the caregiver directly and sensitively. Any suggestions?
Look, if you have regular caregivers who work a schedule and occasionally a fill-in has to be sent if one of the regulars is sick or on vacation, just deal with it.
I was an in-home caregiver for 25 years and I'm going to tell you truthfully. It's never in a client's best interest or their family's to get fussy and knit-pick.
If your mother has good aides who are doing right by her, don't carry on about her peeing herself too much when there's a fill-in.
The aides need to be taking her to the toilet regularly. Every two hours or even every hour if needs be.
The cause of her peeing herself all day could also be because there's a disruption in her daily routine because a new face is there. The slightest disruption in a daily routine when you're dealing with someone that has severe dementia can make huge setbacks.
Anytime I brought additional caregivers onto a position with me, I required we all make a client note in the same book at the end of shifts of exactly what you're saying. How many times the diaper was changed. Hoe many times toileted. If the client ate or what they're general mood and condition was.
This is gold for any caregiver that works a position where the client has other caregivers.
Tell her caregivers to face her, talk slowly and don’t speak as they are walking away from her. I hope this will help her situation.
Best wishes to you and your mother.
Does not matter if she has to go or not, the caregivers should take her. (they should all do this not just the fill in caregiver)
Are you there when the caregiver is talking to mom If so if you hear that she is talking fast and not allowing mom enough time to respond you can say something.
Some of the things I made a point of doing with my Husband is:
Lowering my voice, not the volume but talking a bit deeper if that makes sense.
I think the higher pitched voices are more difficult to hear and understand.
Speak more slowly and enunciate.
I read a while ago that it can take someone with dementia 45 seconds to hear a question, process the question and formulate a response. I don't know about you but most of the time in 45 seconds I am onto a totally different subject. So to slow things down requires some thought.
Your replacement caregiver might not have the experience with people with dementia and if you help clue her in it might help.
See All Answers