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Normally, confused and very forgetful, when on the phone my mom seems far less confused and to know what is going on. This is frustrating as my siblings seldom see the side of her that I do...with very little short term memory and signs of dementia.

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LOL! I think you'd have some "takers" with the trade.
Carol
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LOL mip66 you made me laugh!
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I have similar with my Mom on Phone. With her, it is partly because she can hear better on phone. But it is so frustrating to be told how "cute" your parents are. Having friends in similar situations help, as they know the "cover up" is only an act. Sometimes I think we should all trade parents for a while since Other people's parents foibles are just cute.
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Well, the neurologist said it couldn't be reversed only slowed. She at the stage where she still knows what's happening and of course it is depressing to her. And to me. Mostly she does take her meds and supplements when I give them to her (she pretty much won't on her own). Thankfully, I am staying with her so that she can live at her own house.

I need to go about finding outside seniors activities for her. That can't hurt and ahe said she'd be interested when I asked. She also needs exercise. That has to be beneficial as well I should think. I mean, look at Jack LaLane, eh.
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Yes. Alzheimers is one form of dementia and there is no cure. There are other forms that, with proper treatment and care, can be reversed. However, Alzheimers is more widely known by both doctors and the public. Yet it is still not correctly diagnosed or even suspected by family members until it has reached later stages. Many families go into total denial when faced with dementia. This is easier to do with non-alzheimer type dementia because the patient can have some good days and some bad days. Alzheimer's patients get progressively worse without treatment and sometimes even with treatment. But those with treatable dementia will only improve if they follow doctor's orders carefully. That is a Catch-22 because without family support, the patient is often incapable of following doctor's orders and tries to hide that fact from the family. I know a person who missed 3 full weeks of medication but family caregivers did not find out until they came to reorder prescriptions and found excess pills in the old bottles.
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Dear pcvs, At first it starts as only forgetting things which is the Alzheimers, then at times the dementia, of which the total confused person. it is not there fault but I told the doctor in NT many times about her actions he did not believe me at first . however each time she fell he would note on the release report about Alzheimers/dementia, but no medicine was given to her until I demanded a neurologist test. Then he put her on medicine. But it was to late. she mixed up all her medicine. Yes New York sent out social workers, protacted service, nurses, aides to help. They did nothing that is why I made over 30 trips back and forth even when i wasa working. The house was a mess. the urine smell was bad. and also no help from all her hold roolers from the church or neighbors...............
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But it isn't just Alzheimer's. The neurologist even said it wasn't Alzheimer's that she has. With all this preoccupation with Alzheimer's folks tend to forget there are other forms of dementia to be dealt with.

Patricia
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Wow, what a fantastic doctor! Can they clone him/her?
Carol
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Carmarlein,
I think you have hit on an aspect of Alzheimer's disease that needs much more investigation. My mom was diagnosed in 1996 by a doctor who had a lot of elderly patients. He was clever enough to engage my mom in a normal conversation in which she held her own then he gradually slid in questions like "Do you think Jimmy Carter is going to get a second term?" and "Does your son graduate college in June? (I was 50 yrs old at that time) Of course mom gave the "expected" answers without any sign of confusion or contradiction :-) After a short discourse, the doctor asked my mom to wait in the waiting room because my father had to sign some paperwork for the Medicare billing. Then he broke the news to my dad and told him not to confront mom with the bad news but prepare himself to deal with it first. He also prescribed a new drug that slowed the progression of the disease so mom was blessed to have a gradual decent rather than crash and burn like many who-due to denial-are not brought in for evaluation til it is too late.
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My mother is also 78 and like yours, has to be urged to participate in life. I have found that she does enjoy going to the local Senior day care for 2 mornings a week and you are right, her memory is much better when she is engaged in something interesting. She has no problems recounting what she did at the center. But recently she just wants to nap on the couch all afternoon and uses going out in the morning as an excuse to be on the couch for the rest of the afternoon. It is partly depression but now she is on medication for that...hopefully, it will help. I try not to expect too much in the way of memory (short-term memory that is) but it definitely comes and goes. As I said, she is most clear when she is on the phone, esp. when talking to someone she hasn't seen in quite a while, like an old friend or one of her children who live farther away. It is tough to be patient when it sometimes seems within her control, but I know that is is not.
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This is very interesting because I was starting to think my M-I-L was faking her memory lapses. She can no longer remember how to write out a check for a bill and when she trys to help out by putting dishes away I find them everywhere but where they belong.

Oddly, when she talks about things in her past or when she gets a phone call from a friend she hasn't talked to in a while she can remember things from when she was 6 years old.

I've noticed on the occassions when she gets out of the house and participates in life her memory seems to improve. The problem is she always has an excuse why she doesn't want to go anywhere. She's only 78 and I think to young to just give up. I'm wondering if I should point out the memory improvement to her after she's been socially engaged. I don't want to hurt her feelings.
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This happens to me as well. My mama is so lucid and bright at the doctor's and even on the phone, but she can't keep it going for any length. I suspect the adrenaline upsurge might be part of it. It might also be responsible for the fact that she eats better when we go out for lunch than at home.

Is there any way to use this to keep her mental acuity closer to what it used to be?
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I also have the same issue. I take my mom to my sister's for the weekend and all I hear is that she is doing great and she doesn't act that way here! Well, live in my house with her and then maybe you will see. As for the doctors, I agree it seem's good. I was just there yesterday and he said well she looks good, yeah, I gave her a shower, dressed her and she is walking fine, but as the visit went on, OUT it came, he finally GOT it. I swear I heard music playing when he got it....
People who don't walk in our shoes think we are the ones, but we all know that is not the case, we have to stay focused and be the bad guy if need be, but we all know what is right.... All of use have earned wings in some way or another. United We Stand...... And, please don't foget to laugh, it is what keep's me sane most of the time..... :~)
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Thanks for your comments...this has been a major source of frustration for me. And you are right, even the doctors don't really "see" it...one nurse said to me "she seems quite happy"...this is so far from the truth that I just looked at her bewildered and said, "No, not really..." Mom hides the dementia and depression from others very well. Even when visiting my sister for several hours, she holds it together quite well, except for repeating a few questions. Minor, compared to her behavior at home. I don't think anyone can appreciate how difficult it can be to be the caregiver for someone with dementia until they have done it for a fair amount of time. I have been caring for my mom now for over 1 year. I am feeling burned out but need to hold it together for mom...it's good to talk to others who truly "Understand"!
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I have the same thing happen with my mother. She suffered a stroke which impaired her speech. She has difficulty speaking with my husband and myself, yet when she talks to someone on the phone she has no difficulty. I am sure that they think we have the problem and not my mother. To bad none of them ever see her struggling to get her words our with us.
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It's most likely adrenaline. One of the biggest frustrations of hands-on caregivers is to get visitors and others (even on the phone) who seldom see the elder - even doctors - to "get it." The elder gets so excited when talking with someone they haven't seen for awhile that they seem quite normal. Then, when it's over, they crash and it's your problem.

My mother covered her dementia like a wizard. People who talked to her occasionally on the phone or people who visited every few weeks wondered why we said she had dementia. I suffered greatly from the "bad daughter syndrome." It's humiliating and infuriating to find that your efforts to care for your mother in the best way possible are viewed as suspect by others. If they'd just stick around awhile, they would see what you see.

I'm sorry you have to deal with this, but unfortunately, it's not unusual.
Take care,
Carol
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I have the same experience with my mother. It really frustates me. It seems like when I explain some of the behaviors mom is diplaying, they think I'm nuts because they dont get that over the phone. They think she sounds great and I'm blowing the situation out of proportion. I have taken care of mom for 2 1/2 yrs thus far and they haven't a damn bit... "I KNOW DEMENTIA as I 'm sure you do...I know exactally where you are coming from.
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