Can people with dementia have what they call "show-timer's?"

She ought to get an Oscar huh?

Oscar for sure, I read somewhere that it's very common. That's why they named this condition showetimers, I wish I could find where I read about it!

This brings a funny story to my mind.... I must share it!!! When I took Mom to the Doctor, who she liked very much, and even had a delusional wedding with Dr.B as her Groom (at a later time than this story) He was telling her at my request to eat veggies, and as he was going through the list and as he was saying each veggie she made a face like YUK!!! Was so cute and funny. I thought she would listen to him and I could say well Dr. B said you should eat veggies. Not that simple.... So one day we were in the store, and we were in the produce section, I saw the Dr. right behind her and I winked at him. Mom had no idea he was there. So I picked up broccoli and said, Do you want broccoli she says "Dr. B said I can't eat that." Then I picked up green beans..... "Dr. B said I can't eat that." He was smiling ... I said are you sure that's what he said , she said " Oh yes the veggies make me itch so I can't eat them." I said are you sure that's what he said , because he's right behind you. She says no he's not your lying...I said "turn around" he says Hello She said "OH Hello" She blushed and was speechless batted her eyes then said lets go. I love sharing these things because it makes all the badness turn into a goodness. I forget all the hard times I had and laff about the silly. BTW she still makes me laff.

Definitely. For company or for doctor visits, etc. early-to-moderate dementia patients can gather up all their composure and put on their best behavior and appear perfectly normal. It takes a great effort and they may be exhausted afterward, but for a limited time they can put on the "normal" show. This gets harder as the dementia progresses and eventually they can't do it. But for a while this can be very frustrating for the caregivers, who can't get anyone to take their concerns seriously!

thanks for sharing your story, it really helps to know this happens to other caregivers too, I keep getting looks from all the people she has fooled like Im so mean and lying about my mom! your story was funny I hope I can reach that point but right now its very frustrating, she tells everyone I have dementia not her!

Its allot better than sun Downers! LOL bad joke :/

Oh I love this.... S can only shuffle when he walks, but let a pretty RN or Aide come in and he is struttin' instead of shufflin'..... gonna remember this... thanks for sharing...

LUCKYDOG55 If you like that one lol I got more... this one might make you feel better about her accusations. Mom was already in NH but needed to go to Dermatologist the NH calls me to ask me to bring her. I said the whole reason she is there is she cannot be alone with me I am the bad guy to her. I want to go but an aid needs to go with us. So we are at the Dr. in waiting room with the aid. You could hear a pin drop. Mom was pleasant until I was chatting with the aid. Then like someone flipped a switch....Loud as can be Mom says.... "She's a thief, she stole my clothes, my money, she's crazy, etc." I buried my head in a magazine as if I didn't know her." It is obvious that I am her daughter we look a lot alike. So we then go into the Dr. and he's asking her questions she's telling him I get a rash when it rains out. I rolled my eyes he had no clue she has dementia. I pulled him aside to explain and he was repeating what she had told him, I said you can't believe what she say's she also thinks she's 17!! He said OOHHHH!!!

LUCKYDOG55. I completely know what you're going through. This site is comforting, because every day someone mentions a problem I'm dealing with related to my 88 year old mother who lives in denial about her dementia and I don't feel so alone and isolated.
My mom's split personality is a huge part of my stress and angst related to being her caregiver. She's so wacky, mean and abusive most of the time with me. She's basically miserable most of the time with me. With me, she has almost no short term memory. Then, whenever she goes out with me, she's like an entirely different woman, nice and sweet and jovial. I don't even recognize her. She's such a phony. But, my life is really hell because my brother and sister do nothing for my mother and see her maybe once a month for an hour. They tell me that she's fine and I must be losing it to say my mother's sick and has dementia. Also, when my mom goes to her doctor, she goes in alone and won't allow me to tell her doctor the truth about her condition, so she's getting no help for her severe mental problems.
Anyway, it's gratifying to know others are experiencing many of the difficulties I am.

So comforting to hear others go thru this same thing. My mother had her doc so fooled the doc decreased mom's psych meds and she's back to being a witch with me again.i called doc and asked for a conference next week.wish me luck.

deewayland,
Good luck and a hug.

In a desperate attempt to hold on to what the person feels is slipping away, which is frightful to them , I am sure that this is a survival tactic. Frustrating for the caregiver, I am sure that is AS frustrating to hold it together when needed for the person. It seems like a kind of "letting their hair down " when they return to their home base. Perhaps SLOWLY introducing help or support now is a way to do it instead of any drastic changes in threatening independence....

Since my aunt Ami (95) is 100% compliant in front of her doctor, I asked him to write her a "prescription" for a weekly bath. She gushed over it, thanked him profusely for the 'reminder,' and then, when we were in the car, ripped it to shreds. "Who is that idiot to tell me to take a bath? I take a bath every morning." Some days later, when I got her into the bathroom for a sponge bath, she was horrified. Oh, no, we'd have to wait till the weather was better, till she was well, on and on. I said the doctor called, he wants you to get cleaned up. Without missing a beat, Ami said, "I know. He called again. He said 'not yet.'" I fell down laughing. I know what you mean about how they fool others. At a dinner, Ami had an entire table of people convinced that she had cooked the meal. When she saw me smiling at her description of how hard the desserts had been, she grinned and shrugged as if to say, "Well, if they want to believe it. . ."

It always amazes me how so many people don't pick up on the dementia their family members have. I have several friends who tell me their mom's are very alert; but if you have spent much time with people with dementia, you can see the signs so clearly! And doctors are often slow to pick up on it because they don't realize that what the patient is telling them is not fact... My mom would tell her doctor that she spent her days reading, writing letters, working on the computer.. long after she was able to do any of those things!

I am so glad to read all of this. My mother drives me crazy when she acts normal to others and not to me. If I tell her something, it is wrong. If someone else tells her the same thing she does it and acts like they know everything. She also lies to everyone about everything in order have a good story and no one knows what is real. They think she is so adorable and sharp. They think she is sane and I am an idiot. When we get home, she has no clue what was happening or even who the people were or where we went. My mother is 92 and I take care of her 24/7.

As I'm reading this, I'm wondering if these talented parents are doing it on purpose. I'm just kidding, but it's aggravating to live with. My mother is absolutely adorable and charming around doctors and waiters, but put her in the car with me, and it's fireworks. I really don't understand why the split personalities develop. My guess is that it's easier to dump on those closest to you. My strategy is to exit as soon as possible and not to engage in any kind of debate. That becomes a lose-lose situation very quickly! Sometimes I call my Mom on her behavior, saying, "I don't feel respected when you talk to me that way." If she doesn't apologize (and often she doesn't), I say, "Well, I think I will have to leave now. Maybe we can talk later more calmly." It seems to be working. However, if I'm tired or stressed, it's much more difficult! I hope this help you.

I have to say how helpful it is for me to read all of the stories here. When I am alone with my mom in this, I sometime feel like she is the one who is really on top of things, smart and manipulative and I am the dim one. When I take a moment to read your stories I can see I share so many of the examples you have written here. Being in the waiting room, in the car with her after a doc appointment with a handsome man, etc, etc. My stories are so painful I hate to recall them, but if your stories were painful to recall... I just want to say a heartfelt thank you to you for sharing, because you made me feel less alone... and much more intelligent than I did before I read them! Thank you for being here with me... we all must be reassured that we are OK because the stories are so similar and we should be proud of being kind and helpful!!...

sounds like dad. he loves to throw me under the bus to make himself look good, everybody ' oh i cant see him behaving like that hes so nice' yeah till you live with him!
oh yeah, they still have brain cells, i think its kind of their only form of entertaiment anymore, theyre mind is shutting down and preparing to go to the other side, but on this side, it looks like they are reverting back to being a kid. so if they act like a kid, talk to them like a parent. stern, but dont punish them. unlike a kid, they wont learn from mistakes, all you can do is kind of clean up their mess.
what you can do, keep good notes, keep reciepts and pray for strength, you have to bite your tounge a lot, it goes with the job.. people seem to forget that elderly people do this, everyone acts like dad had full brain cell, the strentgh of a 50 year old and he doesnt! it takes all his energy to put on that face for others,but you would think people would listen to you, YOU are the one that sees the real person, and this happens with everyone. i dont get why people seem so shocked when a caregiver says their behavior is different behnd closed doors.hang in there, im learning as i go along too

Marciwriter, What my sister and I do is hand the nurse a note ahead of when the Dr. Comes in the room telling him what is really going on with my mom. He reads it before he gets into the room where my mother is waiting for him. Then we just sit there and keep quiet and he handles everything. This has worked out great........ so far. Good luck.

avidreader - I am so glad to hear your story. I have taken to not spending to much time with mother because she is always complaining. It has been quite some time since she has said much of anything positive. Sort of makes you feel like a "failure" when all she can do is complain about everything you are doing to make her comfortable and happy. Nothing seems to work. So - thank you for your story! It helps alot!

I work for a senior community. When adult children came in with their mom or dad for a tour, I used to be shocked by how often I would see unmistakable symptoms of dementia in their parent that they seemed completely unaware of.
Despite all the ALZ awareness campaigns, many people don't see the tell-tale signs that their own family member is having serious cognitive issues. I think it's because parents naturally put on their best face for their child. They instinctively go into parenting mode and that masks some of the behaviors that provide the clues that something is wrong.
I'm still no 'expert' in detecting dementia. Some people are so gifted in putting up a good facade. I once had a long conversation with a new resident about my son's college search. We chatted in detail. She even gave me advice and some good recommendations for essay topics. The next day I saw her and struck up a conversation again. She had no idea who I was or, even when reminded, that we had spoken.
One thing I've learned is that a person with dementia is like a snowflake; there are lots of similarities, but no two manifest the disease exactly alike.

My mother in law is soo good at this. She wont even allow my father in law to go into their Dr.'s office alone just in case he wants to discuss her memory loss with the Dr. It took 2 years for us to convince my brother in law that she had a problem. AND she is very good at deflecting. She will convince Dr.'s that her memory loss is because she is stressed because other family members are sick.

Momsdauhter2, that's exactly what I did with my mom- notes to the doctor "prime the pump" for understanding what's really going on with mom.

I think that's lot of times the elders don't purposely try to be difficult, but that they lose their "governor" and don't have the control of their behavior which they used to have and aren't capable of smoothly communicating what they need. I wish I had understand this when I was younger. Everyone stopped visiting my grandmother because she complained about nobody visiting her every time they visited. If I'd only known to say, "grandma, it sounds like you really get lonely", she would probably have agreed and been able to enjoy the visit!

Avid reader, I love how you used the "I" statement about your feelings with your mom. By communicating your feeling, instead of just saying you can't talk to me that way, it isn't so attacking to the other person. Good job! :-)

Thankfully, I'm not there yet, so the only thing I can think of is recording the behavior maybe.

WOW!!! I was thinking it was just me, others laugh when I tell them what Dad/Mom did or said but for me I took their actions as personal and serious. I guess I'll just laugh and not take my Parents behavior so personal and serious. Thanks for this post and thanks all for sharing.

I have to say that several times I have sat down with my mom and pointed out what she has done. I tell her that my only goal is to ask her to be kind and respectful. After sharing actual examples and telling her what I expect, she does try ... for a few days, sometimes for a few weeks. While I often think I need to suffer in silence, when I feel calm enough to address these issues with her unemotionally, I notice that she does try. I think that the conversation makes her attempt to bring the same energy to our interactions that she typically reserves for strangers and doctors. I'm guessing this will deteriorate over time, but for now, those calm conversations seem to be working. I also try not to do it often... only once in 3 to 4 weeks. The key is to remain calm, unemotional and to treat her with kindness and respect that I'm asking her for... (it's been a big mistake for me to address things immediately when they happen or when I'm hurt or upset... I should never, ever, ever talk to her in that condition... because then you could say I'm behaving just exactly the way I don't want her to behave.)

I this same problem sometimes. My mom seems to do this when my siblings are around. She can sound perfectly sane.... the problem is, she will sometimes say horrible things, about getting hit or other bizarre things. Fortunately she only says these things around my dad and brother. My brother knows better and my dad's hearing is so bad he can't tell WHAT she is saying 1/2 the time. My sister thinks I made her this way?? That if we just took her off ALL of her medications, she would be fine. First of all, I am not her doctor. I can't prescribe medications for her! She is on very few medications at that. She is diabetic, and controlled by oral meds and diet. Other than diabetes medications, she is on one for her heart, one for cholesterol, vitamins, a stool softener, and one med to help with her insomnia as well as a herbal supplement ~ How are those causing dementia symptoms? She is totally convinced that I am using meds to control her and keep her "sick" so that I can just "hang out" and take care of her. Trust me. It would be easier to have a normal 8-5 Job!! People don't get how it is being a caregiver! I am glad I am able to do this, but wow! It is a challenge~

Also, working in a nursing home, there were people that would come in and be totally confused! The families of a couple couldn't wait to get them back home...ALONE! I was like, are you serious?? I guess at home in their normal environment they were almost completely normal~ It was only in new situations that you even noticed the behaviors or dementia~

Go figure.

Sooozi, LUCKYDOG55,

Yep--our elders can really fool people who are not around them,
and even some they are around!

You are in such great company here!
So right:
we NEED validation, to help keep our sanity intact.

If we have no support persons who can do that for us,
or worse, if family, friends, etc. get sucked into the demented person's manipulations, thinking the caregiver is the wicked one,
the caregiver can lose what sanity they had, in fairly short order.

Mom has suffered from undiagnosed [to her kids' knowledge] mental illnesses all her life, triggered by her early childhood traumas, etc.
These conditions are things her family knew of, but tried to work around, while continuing to worry about her, and struggling to avoid having her labeled--in those days, it was really really bad, to have a psych tag.

She herself, admitted to one of my friends, while here, that she felt she was "a little bipolar" [really? like "a little pregnant"?!],
but would never admit that to a Doc or other family,
as she was terrified of the treatments she might be forced to take
[she was remembering electroshock therapy, frontal lobotomies, and the nasty drug side effects from the 1950's and before].
She also exhibited split personalities with fear and anger issues.

She refused to see Docs unless there was something drastically, physically wrong; no one diagnosed her, and she got no constructive help for any of it.
Compounded by substance abuses and other problems.

So I finally got her convinced to see a Doc, for an annual exam a second time, because we'd gotten notice her previous one from previous year had moved elsewhere--- "...good idea, because of how insurance is, to have a Primary Care Doc updated".

I wrote a letter to be entered into her chart, described Mom's behaviors, addictions, etc.,
and to PLEASE avoid giving her narcotic pain pills, since she has, in the past, been suicidal; has, for years, spoken about being about to die, and while staying with us, spoken of suicide again.
I made this a letter, instead of trying to buttonhole the Doc before her appointment, since I wished to preserve what was left of Mom's sense of self, etc.; I have always known how sensitive she has been about all these things--not to mention how epically angry and violent she can become when she feels crossed in any way.

So in her appointment, she suddenly flips into her "flirty girl" personality, full-tilt.
Manipulating for pain killers,
"just in case; after all, I am over 80 years old, I should be able to have some on hand, just in case!"
[she started to slip into her "end of the world as we know it" schpiel, but cut herself off just in time.].
[[eyelashes batting, head tilted down looking out from under her thinned eyelashes, coy smiles and chuckles, higher-pitched teen girl voice, swinging feet, etc]].
She never mentioned narcotics, but danced all around it, so I told the Doc,
"I think she means narcotic pain killers, Doc";
Mom didn't skip a beat, just continued with her show.
Doc excused himself for a moment to check on something.
He returned and wrote her a script, showing it briefly to me, then handing it to Mom.
She kept up the flirting.
She thanked him.
She thot she was getting a narcotic pain reliever.
[[when she was not looking, I faced the Doc and mouthed words "thank you!!!!" for his not writing a narcotic script]]
We went to the car.
She shoved the script at me, suddenly a different personality, saying "I do not know what this is, do you?"
Stupid here, so easy to get the truth out of,
---I shoulda played dumb.
But I failed to grab that moment
....instead, I told her it was "a non-steroidal anti-inflammatory--kinda like ibuprofen".
She immediately flipped into her angry-betrayed-bully-mode,
yelling, cussing, and crumpling that script into a wad and throwing it on the floorboards [she was unable to manage turning the handle to open the window, or it woulda been litter].
She continued to erupt anger the rest of the afternoon; when we got home, she cloistered in her room for a couple days, barely coming out to get food or let her potty get dumped..
Much muttering.
After 2 days, she occasionally came out to ask a question/opinion to see if I thot it was inappropriate the Doc refused her request.
I told her, I thought the Doc was being entirely appropriate,
after all, those pills he scripted were able to help with pain, which was what she'd asked for.
I later found she had rescued that script, and carried it in her purse for over a year-when it became expired....
THEN she asked if we could get it filled---
I had to tell her, now she'd need to go back to the Doc to get another one, as this was expired.
"WHAAAT?! Since when do these things expire?!?!? THEY NEVER EXPIRED WHEN I WAS IN NURSING!!!"
"Sorry, Mom, prescriptions expire at most, in 1 year, or less, depending on what it is for, and scripts have had expiration dates for over 40 years. "
She refused to go back to the Doc.

Sometime later in her stay here, the State made Medicinal MJ more easily available.
Since people cannot commit suicide on that,
and since it controls pain,
and helps with sleep, breathing, etc., which helped her do a bit more physical mobility; and
after much study on it, I asked if she wanted to try that.
She said she might, so we went thru the hoops required to get it. .
In small bottle, in liquid form.

The good part:
She got relief from all her physical and some emotional ailments with that: --pain, short breath, sleep disorder, anxiety, gastrointestinal troubles, etc..
Her mood lifted: she no longer talked of being about to die, or about stockpiling pills "to have a way out" [she could be a drama queen epic "Eeyore", but since she had tried suicide at least once that I knew of, it is to be monitored ever after].
BUT,
it failed to stop her dementia getting worse,
the only relief from her angry outbursts was when she was actually using the drops.
When not using it, she continued to flip from one personality to another, as well as cycle fairly fast between depressive and manic states,
as well as having repeated and escalating anger episodes that could last for hours.
Those did get relief, WHEN she was using that liquid.

AND, for a bit, she felt like she was in control...
--she was getting away with something
--she felt a little bit more autonomous

While this might not be something others might try,
it worked for Mom, for the rest of the time she was at our house.
She moved out of State, so can no longer get it.
Since she usually and historically, refuses regular pharmaceuticals, or fails to use them properly, that liquid was a good option for her-
--she got relief, yet caused no harm doing it.
I have yet to hear from anyone else's experience with it, so can only share her results with it.

Blessings on Caregivers!
A task not for the faint of heart.
The more we can help each other learn to do the job better,
the better we can validate,
the better we ourselves can survive to tell the tails.

{{{hugs!}}}
Chi

Darcy123,
I totally get what you are saying!
Been thru that, too.
Sometimes, there is just no good way to resolve other family members who think they know better.
Keep sticking to the bit about letting the Doc decide what is best for Mom, since it is his business to know her health issues and how to best help those.
IT is fairly common for other family to blame the caregiver for causing the health issues, causing the trip to the ER, causing the [insert problem].
YET, those same family members will most often refuse to be a caregiver for that elder.
It is VERY common for an elder to become more confused upon moving to a different care venue
...whether it is a group home, a facility, another family member's home, or to a different room in the same house..
SOME elders gradually get better, but others remain worse in their dementia progress once moved.
It is a rotten thing to happen, but it is NO-one's fault.
It is the fault of the dementia.

If a Doc or other professional has said an elder needs cared for in a facility, or group home, etc., due to dementia, ==take their word for it==!!!
It is fairly hard to get professionals to diagnose it in the first place
--it has to be serious enough for professionals to even notice it for them to diagnose it, and recommend a move to a care home facility.

I use this quote all the time - it will become more and more valuable to all of us as we progress down this difficult path with our elders: Blessed are the flexible, for they shall not get bent out of shape.