When I tell her that she needs to take he cane with her to the store she fights against it but then the next time she will suggest it and its a good idea. Ask her if she knows where something of mine and every answer no matter what is I don't know and then I find it down stairs on her table. She also blames the animals on lots of things like turning my bathroom faucet on and it running over so much as to go all the way to the basement but the dog jumped up on the counter and turned it on. When I am sure what happened is she was giving the dogs some water and forgot and left it running. Tell her to stop wearing shorts cause she is always cold but she tells me she has to wear shorts. Ask her to straighten out the pantry which I was over half way done with it and she just took and threw everything back in with no rhyme or reason. Do they not understand anything any more or is she trying to get sympathy or at least get out of the chore. Its mind boggling to me how she comes up with every excuse to get out of something I ask her to do. Is this normal? I would love to hear any suggestions on how to handle this behavior.
You will be doing yourself and your mother both a favor if you accept that a person who is losing her ability to reason cannot be consistently rational. Expecting rational behavior and accurate answers is just asking for high-level frustration.
(I know. I've been there, done that, and have the scars to prove it.)
Why ask her what happened with the faucet? An answer won't change anything. How about "Oh dear! The faucet got left on. We'll need to clean this up fast. Can you help me? I'll get some rags and a bucket." If she explains that the dogs did it, say, "That's OK. I am sure it was an accident."
Don't ask if she knows where anything is. Of course she doesn't. She has dementia, remember? You might try, "I am so sad. My red-handled scissors is missing and I need it now. Will you help me look for it?" That gives her a chance to be a hero if she has a vague memory of where it might be, and no reason to get defensive about it. Remember the goal. You want the scissors, not to establish guilt.
Dressing inappropriately for the season or the occasion is extremely common in dementia. Help her pick out her clothes the night before. Or comment "That is my favorite pair of shorts on you. It is such a nice color. If you get a little cold, though, I have put a pair of warmer pants on your bed." Try not to have a contest of wills. Same with the cane. "Let's see. You have your purse, and your scarf. That is good. What else do you usually like to have in the store?"
She may never again be able to help you with chores that involve organizing things. Just can't do it. She might be able to arrange the pantry WITH you, but not alone. Try to find tasks that give her something to accomplish that she can succeed at. Matching socks from the laundry, folding towels, possibly polishing silverware are examples.
Adjusting to living with someone who has dementia is very, very hard. It will always be hard, but it can be a little easier if you accept that your mother's behavior is limited by physical flaws in her brain (plaques or tangles or protein deposits, etc.) She can't help her behavior. You'll have to adjust yours.
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It is important that Alzheimer's caregivers understand the difference between a hallucination and a delusion. Each of these symptoms can affect your loved one in different ways:
Delusions.Delusions are false beliefs caused by the deterioration of cognitive processes in the brain of the Alzheimer's patient, and are often influenced by misunderstandings or misinterpretations. Patients might think they are being followed, or might accuse a family member of stealing from them or plotting against them.
Hallucinations. These involve false perceptions, and are also caused by changes in the brain due to Alzheimer's. Patients can literally "sense" - see, hear, smell, taste, or feel - something that isn't there. They might see and talk with old friends who aren't there, or watch ships floating through the sky outside the window, or smell foods they enjoyed as a child.
end quote
Confabulations are a major annoyance - when listeners take everything at face value, no matter how false their statements. The danger is when banks, adult protective services, police, friends, family, and other listeners take everything our loved ones say at face value and react based on the statements. Know that confabulating is distinct from lying because there is no intent to deceive. The statements can be coherent, internally consistent, and reasonable.
Be aware there are similarities between confabulation and delusions; e.g., both involve unintentional false statements. Realize delusions are frequently observed in Alzheimer's patients may include beliefs about theft, the patient's house not being his home, a spouse, is an impostor, belief an intruder is in the house, abandonment, spousal infidelity, and paranoia.
--
It is difficult to accept the mind is damaged by Alzheimer's Disease. develop boundless patience. Forget about
rational responses.
Enhanced Moments, "Touch Many ... radiate your warmth." --
Jolene Brackey
Author of "Creating Moments of Joy" Perdue University
Press.
Bottom line: Don't get sucked into her game playing, manipulations, lies, demands for attention, etc. Otherwise you'll get exhausted, if you aren't already. Focus on something positive, do the necessary work and talk as little as possible. Easier said than done, particularly with the emotional hooks our mothers have into us, but practice will pay off.
Meanwhile, you may want to consider asking her doctor to evaluate her for possible intervention with medications. If the first drug doesn't work, keep trying. Good luck and blessings to you both for a peaceful solution to this challenge.
People with dementia need to be reassured. They live in a world that they don't understand. It's far better for their self-esteem, as well as our sanity, to agree with them. Or as Jennie suggested, when there's a problem include the person with dementia in the solution if at all possible.
The main thing is to remind ourselves repeatedly that this person has dementia. This is the disease. They aren't trying to punish us or make our lives miserable. It's hard to be the caregiver, but it's got to be harder to be the person with the disease.
Wonderful tips from all of you in this great community.
Carol
Point being, it was only the beginning,,,the phone tv n microwave abilities left shortly after.....it was a battle of our wills, us being healthy in mind unable to understand how one could just pick n choose what they can and cannot remember/do. and we plain old don't want it to be the case, hoping we could will it better with our nudging/reminders, so to speak. When I finally began letting go of my wants and expectations is when life got a little easier!
Wishing everyone the patience and strength it takes to manage our loved ones!
A nursing home is sometimes the best solution. I would never use it as a threat.
Those of us who can tell the difference between normal aging and dementia are not necessarily wimps, my friend.
(I agree about not threatening NH - seriously, below the belt).
Phil413 has it right. "Correcting or scolding is not going to restore the person my mother used to be."
Not all old people have dementia. But this thread is specifically about dealing with people who do. Caring for someone who has dementia is challenging and heartbreaking. Calling those trying to meet the challenge "wimps" is demeaning.
Their minds cannot except blame because their short term memory is not working correctly as in out of sight out of mind...have you had her diagnosed by a neurologist? You would hate to do anything blindly like take care of someone, that has dementia...without some of the right tools for coping and getting along...trust me you will need a baseline to work off of for the future it is a long road that can last years, you do not want to get worn out unnecessarily.
MIL has agreed to go into a home but she will go bonkers if they try to place her in a dementia unit. I'm not sure how its going to go. I guess we'll find out next week.