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Becoming mean

My mom is 90, currently in independent living apartment. She picked the facility 10 years ago so she could access transitional help as she aged. I believe she is in the latter part of early stage dementia. The last year she bas become very argumentative with everyone … fired one cleaning service and “hates” the new one. The food service is “disgusting” …. The social worker called me concerned because now mom is sending nasty notes. She had seen a counselor late last year but says she doesn’t need that now. Saw doctor last week after I called him with concern with growing anger and unhappiness with everything. He prescribed new meds but she won’t take them. It’s been cycles of crisis (sobbing) and then ignoring it happened. I am frustrated because trying to calmly discuss things, she brushes it off and the we move on to the next “incident” or issue. Vicious circle that I cannot find a way out of. She refuses outside help.

Comments

  • SDianeL
    SDianeL Member Posts: 2,426
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    welcome. Sorry about the reason you are here. Your Mom has Anosognosia which is a condition in which a person with a disability is cognitively unaware of having it. As I learned here, you can’t reason with someone whose reasoner is broken. Many PWDs refuse outside help. Try a fib that she may accept. Like the person needs a job or is working their way through school or needs credits. Talk to the pharmacist to see if her meds can be crushed and put in her food. Applesauce works great for that. Will the facility do that? It may be time to consider moving her to MC. They are better trained to care for PWDs. Read the book “The 36 Hour Day” which helped me understand the disease.

  • H1235
    H1235 Member Posts: 1,299
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    Member

    Welcome. Anosognosia is the worst! At one point mom’s doctor prescribed medication for her anger, mom says “ I don’t have a #$@& anger problem and I’m not taking that @#&$ medication.” She had so many medications for other things that she didn’t even notice when we included it with her other pills. Could you tell her the new medication if for high blood pressure, or a vitamin ( make something up). Medication can take a while to really figure out. The type of medication the dose when she takes it, it takes time to figure out. But the right medication can make all the difference. I agree that it sounds like it’s time for more care. When a person with dementia is faced with something that is uncomfortable, hard for them or stressful they often lash out to blame those around them. Food may not taste the same anymore- so she blames the food service, she miss places things and blames the cleaning service, if she has problems using the phone she will tell you the phone needs to be replaced. I could go on and on. Here is how most try to deal with this. If it doesn’t matter just agree with her (yes Elvis is alive), distract or change the subject (offer a treat, a drive or turn on a favorite tv show), do what needs to be done be done without consulting her or even telling her and last use a therapeutic fib ( telling her the medication for anxiety is a vitamin). She will never admit she needs more care and will probably fight you on it, making things even more difficult and heartbreaking for you. Do you have DPOA? If not this is very important!

    https://www.agingcare.com/topics/295/anosognosia

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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