I never realized what this disease can do to people. It can be terrorizing. It is very difficult to deal with a person who truly believes their hallucinations. I can’t calm my mom down when she thinks she is in jail surrounded by police or people keep moving her around from one building to another. It’s scary to her and she doesn’t understand why I am not doing something about it. She gets angry at me. Why does this disease have to exist? I don’t understand it. To think my mom lives in this horrific world is very disturbing and upsetting. There’s nothing I can do to help her.
Are you sure it’s a hallucination?
Ie:if the “careworkers” are uncaring and aggressive in nature,it can very much feel/perceive to a vulnerable and confused person with Dementia that she is in a jail surrounded by prison warden like people.
What is it that is making your mum miserable?
Is it that she has surroundings devoid of stimulation or is it she doesn’t like the staff and feels they are short/aggressive/dominating towards her or is depression due to the illness itself or reactive depression due to knowing what she’s lost?
It’s extremely important that you listen to your mums feelings and that she is treated with dignity.
Having minimal stress is very important too and if she’s in an environment being treated poorly that’s the last thing she deserves/needs on top of everything else.
I think first it’s important to ascertain whether she really is having hallucinations or whether the staff actually are moving her around and treating her poorly and the right person to ask is your mum and not the carestaff.
You should always believe your mums version over their opinion of her state/circumstances unless what she tells you is obviously bizarre/highly unlikely-eg:if she said she thought she was 15 years old and abducted by 20 foot aliens last night.
Your mums emotional and mental comfort is what’s most important and sometimes these care homes are actually the opposite of caring and very traumatic for the person.
Some people with Dementias or even some forms of Schizophrenia,become very fearful in the face of staff that treat them aggressively as they are no longer necessarily able to perceive the full picture of what’s going on around them or why they are being moved to another room for example or that the nurse that treats them bad that it’s the nurses problem and that she’s just a nasty individual.
Instead then can respond with confusion,fear,hysterical crying,hitting the careworker etc.
It’s a natural reaction in their situation and it’s important your mum and others are treated with respect,kindness and much gentleness.
Alternatively,if the home is not the problem and your mum actually is hallucinating,then the best thing you can do is comfort and reassure her as Antipsychotics have been found to make quality of life worse not better.
In my view,safety shouldn’t come at the cost of quality of life.
Physical safety gives reassurance to the family but what does it due for the person to be physically safe but living in misery/“hell”?
There are ways for people with Dementia to stay living with family but it involves modifications like locking doors,removing sharp knives,cigarette matches,safety proofing electricity etc,making the stove not usable etc…
Having your mum live with you might be an option but first you’d need carer support etc to help you.
At the end of the day,your mum should be involved in whatever decisions are regarding her to the best capacity that she has and if something is making her miserable needs to be changed to improve her quality of life because it’s a often devastating illness and she needs as much happiness and autonomy as she can get out of life.
fightdementia.org.au/understanding-dementia/behaviour-changes.aspx
fightdementia.org.au/services/safety-issues.aspx
I wish the parishes had more fundraising to help families keep their loved one at home as it’s often money that’s a barrier.