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Jude, I reported nearly all of the rants as well. That's what the link is for. I remember very vividly back when I was relatively new on here and my mom was still with us, there was someone like this and they cut me to the core. It was not Shelly, but another person who insisted that 1. her caring for her loved ones was nothing but an honor and a privilege and she would never ever for a moment feel the same way we did about the caregiving tasks before us, or need to vent any kind of frustration...and 2. that if we found ourselves feeling that way, it meant simply that we were unfit caregivers. The (il)logic ran even to the idea that since you were an unfit caregiver, you should find someone else to care for your loved one, while also expressing the sentiment that finding someone else to care for your loved one meant you did not love them.

SO many of us feel unfit, feel guilty, feel selfish, constantly doubt every single decision, grieve the fact that all we can do is all we can do. But even if we could do more than that somehow, it would not make our loved ones happy, restore a relationship either ruined by dementia or one that never was, or let them live on as we so fervently wish. We are human beings, not God, and not without human limits. You will be stronger for having withstood this, and more sure that you absolutely can and must defend yourself from false guilt and the wishful thinking that if you really loved or cared enough, you could make it all better.

And, just a few posts later, this same person admitted they were terribly depressed and anxious. Yes - a hurting soul, and who could not give herself or anyone else a chance to be human and to feel what they felt. I subscribe to the view that there is a greater courage in the one who is afraid but runs towards the disaster anyways; there is a greater devotion in the one who feels dreadful things and yet does what must be done. There is even a book called "The Secret Strength of Depression" which tried to dispel the idea that the emotions of depression signal weakness and unworthiness - that there is really a great strength in feeling those things and yet carrying on. Our emotions tell us things - important things - sometimes we need to adjust our attitudes, sure; but sometimes we need to adjust our lives and our burdens, and get help either medically or materially in creating a just a bearable life for ourselves and our families. Even the most negative emotions in the world should not be allowed to tell us that we are bad people, ever. This storm is past; there will probably be another at some point, but wiser hearts (and a little good moderation - much appreciated, BTW) should prevail.
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OK screaming point for today is the bank. It is 3.23 am right now and I am doing the monthly finances for Mum should be weekly but hey I got behind with her being in hospital and then us taking her on holiday once she was well again. I cant log in and eventually it says please ring this number so I did. There has been unusual activity on your account says the voice. Now I am concerned so we go through all the security questions and finally the voice decides it is me and so I ask can you tell me the balance please £xxxxxx says the voice - but that is correct says I patiently (well only just patiently to be honest) So what is the unusual activity. Somone tried to log on at 3am. Deep breath, yes that would be me. Well you need to tell us if youre abroad. Deeper breath Im not abroad I am in the UK. And you are logging on to your bank at this time of night? Huge breath - well spotted its now 3.25 and I am talking to you so yes I am awake - I work nights (and days and evenings but never added that bit). I will reactivate you. Scream point - no apology nothing just I will reactivate you. So really sarcastically I said I am so sorry to have inconvenienced you to which the voice replied dont worry about it its fine truly. AAAAAAAAAAAAAAAAAAAAAARGH
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Vikki you were a star last night and again tonight thank you so much - I do feel much stronger today last night I just cried despite my vitriolic replies, but then thought you know what I am better than this. What annoys me most is that lines, taken out of context can have a really weird meaning. My friend who has a stoma bag explained in graphic detail the ue of stoma bag to someone who had name called her for using a diability toilet. I did see that as fair game and was it revenge on the idiot who said it ? Yep and she deserved it for not thinking about why people use them. We too have little and in some cases no control over our situations...they are not what we would have chosen to do and in my mums case she didnt want dementia either in fact she feared it more than anything but then who WOULD want dementia. I care for her out of a promise made to my Dad, out of duty, out of repayment for her raising me ..... something in the back of my head recalls this every so often......
A little boy went up to his mother and he handed her a piece of paper that he had been writing on. This is what it said:

For Cutting the grass $5.00
For cleaning my room this week $1.00
For going to the store for you $0.50
Baby-sitting my kid brother while you went shopping $0.25
Taking out the garbage $1.00
For getting a good report card $5.00
For cleaning up & raking the yard $2.00

Total Owed: $14.75

Well, his mother looked at him standing there expectantly, and you could see the memories flashing through her mind. So she picked up the pen, turned over the paper he'd written on and this is what she wrote:

- For the nine months I carried you while you were growing inside me, no charge.
- For all the nights that I’ve sat up with you, doctored and prayed for you, no charge.
-For all the trying times, and all the tears that you’ve caused through the years, there’s no charge.
-When you add it all up, the cost of my love is no charge.
-For all the nights that were filled with dread, and for the worries I knew were ahead, no charge.
-For the toys, food, clothes, and even wiping your nose, there’s no charge, son.
-And when you add it all up, the full cost of real love is no charge.

When he finished reading what his mother had written, there were great big tears in his eyes, and he looked straight up at his mother and said, “Mom, I sure do love you.” And then he took the pen and in great big letters he wrote: “ALREADY PAID.”

(original by M. Adams
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OH Jude, as a fellow night owl, I sympathize! As a fellow (half-) Brit, I even sympathise! I don't know how many times I could not get something done online for me or my folks because they all have a down time around midnight or so. You handled it well and you are entitled to the AAARRRRGGHHH (American English spelling)!!
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I need help these ghastly messages from Shelly are still on this discussion I have reported them twice do you think they will remove them ever for if not I dont think I want to stay
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You can write the admin or speak to them and ask that they be removed. I don't know if they will but it is worth a try. Here is a link to the "Contact Us" page. https://www.agingcare.com/ContactUs.aspx
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Yay no screaming. Melissa from the team has been brilliant she has removed everything for me. Go Melissa go melissa (said in true cheerleading fashion)
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THANK YOU MELISSA!!!
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Jude don't get cross with those lovely bank ladies - they live in Swansea, they have enough to cope with :)
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I go & sit on the floor in the dark beneith the hanging clothes in the walkin closet & eat cookies....often the only meal i have time to eat! althoug screaming in the garage sounds like an attractive alternative.
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Hmm, tired. Now that's weird. (Said with love and smile)
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My screaming point is when she repeatedly says all day she wants a particular food item. I go and get it from the store foolishly thinking that ive stopped the incessant nagging for the moment only to have her say "i dont want that! I hate that!" Or "you know i dont like such and such!"
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Jessiebelle...yes i think im starting to go nuts! Its so nice & peaceful in there...no angry rants from mom, demands or adventures in loopy land...but alas its only for a few brief restful moments & i must face reality again.
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Tonite its putting the cpap on mom for the 4th time. Getting someone with dementia to wear a cpap is a real treat
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says all day she wants a particular food item. I go and get it ....only for her to (sic) say "i dont want that! I hate that!" Or "you know i dont like such and such!" - Oh yes I know that one really well but not just food .....any and everything. the sad thing is she hated people who repeated themselves when she was fit and well
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Is dementia contagious? My brother finally answered the door when mom went over to his house. Mom was telling me about it yesterday and said she found out that he has not paid the car tags for his car because his fence is falling down. what? I ask her what the fence had to do with the car and she repeated herself and added that the 68 Dodge Dart car he has was actually made in 64 by Honda and got mad at me for not listening better. We spent the day together running errands and I was so confused from her ramblings that on my way home, I passed my own house and started pulling into someone else's driveway. Very confusing day.
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What do we really feel when we do the same thing, answer the same question time after time after time day after day after day? I have been through my mums handbag with her 14 times since she got up. She has asked me the same question again and again. I am not sure whether I am bored, frustrated, annoyed, irritated, tired or just danged worn out but I do want to burn that bloody handbag right now
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I can so relate, Jude! Mom's repetitive questioning revolves around what day it is, am I going to work/church/grocery shopping, is there anyone coming to see me today, is the door locked, and is dad dead. On the rear occasions we do go out, she goes through her hand bag every couple of minutes worrying if she has her keys or cards or money - even in the taxi! My sister says in jest that I should just record the answers on tape and play it back to her. Mom is quick to pick up any irritation in my voice, and then I feel guilty. Long ago and far away I used to think (and others did, too) that I was a patient person. How we change!

My latest screaming point is mom's reaction to the carpet that my siblings and I bought her for her birthday. She cannot deal well with change, so my sister emailed a picture of it while in the store and I showed it to mom, and she said yes, it's a lovely carpet. She agreed that we could buy it for her.

When my sister brought it over on Mother's Day, she complained that it was too light and would get too dirty. She wished people would stop buying her things she doesn't want. We thought after a few days she would get used to it, but no, I came home from work a couple of days later and she had the new carpet rolled up and the old one put down again. At first she agreed to put it in her room, then changed her mind. So I said I would put it in my room, but that didn't work because it was too small.

So I said I would clean the old carpet and sell the new one. When the carpet came back from the cleaners she complained it didn't look any cleaner and what a waste of money. When I came back from the groceries yesterday she had the old carpet rolled up and the new one put down. Since then she's been going on about wanting to put pieces of plastic down because it will get filthy with everyone walking over it (I don't know where all these people are coming from). So we are now playing musical carpets!
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Globetrotter, I thought I was the only one with carpet problems. I bought two big beautiful rugs for my mother because she said the floor was too cold. The rugs cover almost the entire rooms and are thick, lush, expensive pieces. She keeps the one in the bedroom covered with blankets -- a real trip hazard that I can't get her to stop doing. She first of all said that wind was coming up through the cracks in the floor. Then she said the floor was still too cold. Now she says she likes the feel of the blankets under her feet. Who knows why the blankets are on the rug in her bedroom? I sure don't. I don't think she does, either, but she won't stop doing it. If anyone were to come in, they would think I was terrible to leave the bedroom like that. They wouldn't know how hard I tried.

Someone needs to do a story on dementia and rugs. I wondered if your mother also rearranges furniture.
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JB Globe My mum rearranges everything. Did you ever play that game where 20 items were put on a tray then you had a minute to look at them . Then you closed your eyes and 2 items were taken away or added and you had to try and remember which 2 they were. Let me tell you dementia or no dementia mum would win this hands down every time. She knows exactly wha goes on that table and precisely where it goes on the table and how much of it goes on the table. Sometimes its like living with rain main.
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tired, have you seen the new tubeless cpap devices? They look a lot more comfortable than the ones commonly used now. I don't know how well they would work with someone with dementia, since they also look easy to yank off the face.
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I just checked. The CPAP device fits on the end of the nose -- very small. It is cordless and hoseless. It will be available next month from Airing. I wonder how well it will work.
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Thanks jessiebelle I'll check it out!
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OK brilliant idea really bad result. To stop mum driving me nuts with all her sorting a local hardware store owner brought me a huge bag of screws for mum to sort by size and then into tens. She was having a whale of a time this morning I didn't here a peep. I peeked in a few times and there she was using the measuring thingy he gave her (mini ruler in my opinion) and hse had virtually sorted the lot. I was impressed seriously impressed. I went in and said how you doing mum.

Why do we need all these screws - erm we dont mum they are for the nice man at the hardware store .

Are they why have we got them

You were sorting them for him??? remember??

Ah yes well I have done that and before I could stop her she scooped the lot back into the bag!
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My mom has always wanted to rearrange things, but it is much worse now. She spends all day rearranging the items in her bedroom...and I mean ALL DAY! We couldn't find her phone the other day, and it was off the hook (cordless but you know what I mean) and it took us an hour to find it. It was in the cushion of her recliner. We have found it under the bed, under the chair, in the fridge, etc.

Her tremoring is also getting worse. She told me this morning she wants to go back to the doctor and I told her I would make an appointment to see her neurologist (who we just saw in late January) but he is 4 hours away. She then said she wanted to see her regular doctor and we just saw him Monday. I told her "You have Parkinson's you are going to shake". Wish we knew what her triggers were other than overdoing (she won't slow down) and getting upset. She is already on so many medications for anxiety and tremoring. I don't want her to be on "Planet Mimi, Population 1" or a complete wackadoodle, but I also don't like seeing her shaking so hard she turns red.
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Well, I wanted to just try to be witty again and comment on how therapeutic it can be to rearrange a room, but she actually sounds agitated. And an interim visit on the tremor sounds appropriate. If it is just Parkinson's progressing and changing over time as it usually and unfortunately does, medication changes could help a great deal. Usually it is not really 'triggered" type of condition like migraine. On the other hand, maybe she's got something else like a dystonia or serotonin syndrome going on - the "shaking so hard she turns red" is not quite how most people describe the typical Parkinson resting tremor.

You might want to consider checking on clinicaltrials.gov to see if there is anything she'd qualify for - direct benefit is not promised with becoming a subject, but it could be interesting and treatment and symptom logs could be a far better thing to obsess over. Just a thought!
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The only thing that will help you understand what the triggers are is geolocating although you may all call it something different in the USA.

However I have to say that everything I know about Parkinsons would seem to indicate that not so ver much actually triggers it - this site might help you : https://www.parkinsons.org.uk/sites/default/files/publications/download/english/fs94_tremorandparkinsons_0.pdf

If you have a problem that you believe is started by a trigger then geolocating might help

You need to have a diagram of the rooms first and foremost and then when something kicks off you need to put an x on the place she is AT THE POINT OF STARTING . If for example it always happens when she is on the loo (mum is much worse on the toilet an if anything is going to go wrong it is usually toilet associated) tou have the makings of a pattern then you start to whittle down the options.

If there isnt a location pattern you can still try to drill down as long as you recognise there may be no trigger just a symptom - not all problems have triggers

To drill down you need to write down who was there, what happened, what was on tv, what was the conversation etc. its not easy to do, its time consuming but it can result in triggers being forthcoming for some people but only if there are similarities emerging.

Example there is a war programme on person starts screaming and trembling
Bonfire night person starts screaming and trembling

Aha you think something to do with fire/death/destruction

Eating in the dining room and someone drops a plate in the kitchen and it breaks person starts screaming and trembling
Out for a walk past the sports ground person starts screaming and trembling
Now you start to see that the only thing that links all these is loud noises and it is perhaps those that are the triggers.

At this point you limit access to noise and see if that has a positive effect

I hope that made sense
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Jude - love the story! Maybe you can get her to do it again tomorrow.

Sometimes, as noted in private messages, we really are hitting our head on the wall - but there are times when that feels kind of good for some strange reason. It may be therapeutic to either sharpen or counter the dull ache of something else going on - better to laugh or cry than feel utterly lost and drifting!
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She's bloody doing it as we speak V 10:53 at night and shes sorting screws ffs
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My new screaming point: the constant, unceasing noise from Mom's oxygen condenser. WsssshhhhhhKA-THUDwsshhhhhhKA-THUDwshhhhhhhhh

When I turn it off to change the tubing once a week, it's like I've gone stone deaf all of a sudden. And it makes the living room incredibly hot. It's like walking into the 7th level of h*ll some days.

Some nights, I am ever, ever so grateful to be able to retreat to my bedroom - where I can still hear the O2 running, but it's not nearly so loud, and I can open my bedroom window and not worry about freezing Mom out because of her blood thinner making her feel cold all the time. I don't even care that I sleep in what is now the laundry room. It's my only escape from the noise!
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