Bathing why it’s a struggle


I’m new to all this and the group. Yesterday was a bad day for me I have never reached out before but mum for the first time ever got so angry and nasty to me it was a shock never has she done this before in my whole life and I’m 52. All because I’m trying to get her to bathe. I hope and pray she doesn’t start to associate me with bathing and become a fear of me xx
Comments
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Hi Morag and welcome to the forum. Bathing is a really, really difficult thing for many people with alz and dementia. My mom would have no part of it and it is still a huge struggle. Thankfully she now has skilled caregivers who seem to find ways.
Have you thought about having someone come in to help? Maybe telling her it is a spa day? Others may have concrete suggestions.
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Bathing is a nightmare. For some reason they freak out with the shower or a bath. My mother would have no part of it. I was my mother's caregiver. But you will learn thru trial and error (so to speak) to find a way that works for you. I used to fill the sink up with hot, soapy water. I put bath mats and towels on the floor. Sometimes a basin on the floor as well with soapy water to cleanse her feet. She used to like to play in the soapy water - sort of like a child - while she was playing with her hands in the sink, I would take a wash cloth and wash Mom. I would give her a cloth also and tell her to wipe her face and her privates (sometimes it worked - sometimes it did not). Luckily she had short hair so it was easy to wash and care for. I would take a cup and rinse her - gently pouring it over her and her hair. Like bathing an infant. It was quite the ordeal and a long process. Lots of love and patience. Good Luck to you.
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Yes, this was one of the issues that eventually resulted in my mom going to memory care. She would refuse assistance for showers in assisted living and they would just let her stay unwashed in the same clothes for about 2 weeks. When I tried to take on the shower responsibility, I only got her into the shower twice. She was completely baffled about why I would ask her to sit naked on a bench in a booth and then pour water on her! Washing her hair seemed to scare her. In MC they seem to know how to get her bathed smoothly. Even so, they report to me that she will occasionally still refuse a shower but will allow them to use bathing cloths to wipe her down.
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My stepdad (PWD) is also now in MC because of agitation & progression, including this bathing battle. I think he gets premedicated before bathing now or is on an antipsychotic.
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Cathe: I am with you all on bathing. My husband starts yelling and screaming at me and bathing is so scary that I just have to pick a time he seems to have more cognition whatever time of day that might be, but it is never easy. The water is either too hot or too cold but once in the shower after a few minutes he is fine. He will not let anyone else see him naked so caregivers are unable to help! Any other suggestions would be gratefully accepted. Sponge baths are definitely out of the question as well.
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Hi Morag1212 - welcome to 'here', but sorry for the reason.
Bathing is also on the top of the list for us. "I've already washed" "I didn't do anything to get dirty" "Who are you to say I need to bathe". ugh! We were finally able to get someone in to help.
Many times, a PWD actually thinks they have washed already. Sometimes it is just too much that is involved. We wash without thinking about it. But if you break it down and do think about it, there are a lot of steps involved, and they just cannot do it themselves any longer. Another reason is that they can lose depth perception. There have been studies and some folks without anosognosia have said that the bathtub can look more like a deeeeep hole that they don't want to step into. Basically, it is all so confusing for some.
With some, it may help to warm the bathroom, maybe play some favorite low-key music, and get it all ready to go for them. It may not, but maybe worth a try. That didn't help us, but she would wash if we warmed up some water in the sink. As Regina312 mom, she kind'a liked to play in the water for a bit, but it worked, for a while.
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I have zero experience here, but I do remember seeing something about the person with dementia may not recognize themselves in the mirror. When seeing their reflection in the mirror they may feel uncomfortable that there is a stranger in the room with them. The suggestion was to cover the mirrors. It could be so many thing’s causing the problem. For those of you that do in home care I don’t know how you do it. I hope you can find something that works.
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My dh with mild Alzheimer’s suddenly stopped showering says he likes “washing up” better. But his hair is not getting washed. So? He does quite well with most things, he still drives well, this is new, any suggestions?
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They make dry shampoos have you tried that?
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I lack direct experience of this, but there is a geriatric psychologist, Natali Edmonds, who has useful videos about caring for PWD on YouTube. She has several videos that explain the fear of bathing and give advice about possible solutions:
This is a common problem. Hang in there!
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I currently am a caregiver for my 86 year old Mom and showering use to be a big issue with alot of resistance and strong words by my mother. Routine has improved this by showering on Wednesday and Saturdays every week. ( I do them currently with her). I put her schedule on a white board every night for the next day and we read it together (mainly me) out loud. Then in the morning when call her before coming over, I remind her of the schedule and I don't get any resistance anymore on the shower part. I also added music that she likes (Big Band) to the morning routine right when I get there. This has worked wonders as she loves music and it reminds her of her younger self and she seems to forget about the shower part with the music on.
On the shower part, I assist her where needed. She mainly does everything except her hair and scrubbing her back. Water coming down on her head is one of the fears with people with dementia, so we have her shower hose/head low on her body and when it is time to rinse her hair, I gradually let her know when it is going to come on her head and tell her to use the washcloth to cover her eyes. Then she lets me rinse her hair when ready. It is all trial and error as we walk this path and find our successes.0 -
I am having the same problem with my Dad. He drives still and works out but he forgets when he showered. He also forgets to change his clothes, especially his underwear. So I started putting clothes out everyday for him to change. But recently he has been putting the clothes I put out back in his drawers and then doesn't change. It's very stressful because he makes me feel like I am harassing him. He also will lie quite often. I don't think he means to but he will say things that aren't true.
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I'm new here too and this is one of the many issues we are experiencing as well. I'm my mother's caretaker.0
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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