Should I leave a written note for my father with dementia, reminding him why he's in memory care? How can I help him better adjust to the move?

It can take up to 6 months. We have notes all over saying her address and this is where she lives, memory care. It also helps that the director writes out a note for her with who is on shift, if anyone is scheduled to visit, and the sentence this is my home
it also helps that all
staff say them same thing to her….this is your home. Memory care. 6 months and we still go through it but she has stopped packing her things. It is worth a try and just remember 6-8 months IT can take

Seems you need to talk with his neuropsych doctor about medication plan to help decrease his anxiety and agitation. He might need to start on injectable medication since he is refusing oral medication. He can be switched to oral medication once he is more stable. When he is more stable, those momentos and notes can be reassuring.

Don't waste your time. Your father lives in a world that is different than yours.

HonorAble: Imho, in your father's current state of cognitive impairment, it is highly unlikely that leaving him a note would help. He may conjure up any number of faux stories about the proposed note, confusing him even further. I do not advocate writing one. Prayers and love sent.

I hear you loud and clear! My mother is still home but is always thinking of ways to get rid of home health care aids/helpers. I don’t have any answers but understand how hard it is to see a parent unsettled daily. This forum is so helpful at calming me after I spend a few days with my mother who was such a nurturing mother over the years. I want her to feel safe but can’t seem to accomplish it.
I’m hopeful people will share their experiences with us.

Dementia behavior is extremely difficult & frustrating to deal with, that's for CERTAIN! Leaving dad a note is unlikely to help him 'remember' or understand why he's in Memory Care, not at his stage of dementia anyway.

I suggest you read this 33 page booklet (which is a free download) which has THE best information ever about managing dementia and what to expect with an elder who's been diagnosed with it. Medication isn't always the ONLY answer for 'behaviors', either; it's more about how YOU respond to HIM that makes all the difference.

Understanding the Dementia Experience, by Jennifer Ghent-Fuller 
https://www.smashwords.com/books/view/210580

She also has published a workbook entitled, “It Isn’t Common Sense: Interacting with People Who Have Memory Loss Due to Dementia.” For people to understand that reality and context as perceived and experienced by a person with dementia, is altered by the dementia; and, that their reality and context is continuously changing as the dementia progresses, requires learning and an attitude shift; it is not ‘common sense.’

Here is a list of useful tips from her e-book I found to be excellent:

The “Dont's”
· Do not reason and argue
· Do not demand that they reason or problem-solve
· Do not demand that they remember
· Do not demand that they get their facts straight
· Do not correct their ideas or scold them
· Do not reorient them
· Do not think that they are being uncooperative on purpose
· Do not think that they really do remember, but are pretending not to
· Do not use a “bossy” dictatorial attitude in care
· Do not act with impatience
The Do's
· Enter into their frame of reality, or their 'world'
· Be aware of their mood or state of mind
· Use few words and simple phrases
· OR use no words, just friendly gestures and simple motions
· Do everything slowly
· Approach from the front
· Wait for a slow response
· Constantly reassure them that everything is 'OK'
· Keep people with dementia comfortable 'in the moment' - every moment
· Maximize use of remaining abilities
· Limit TV or radio programs which they may feel are frighteningly real
· Maintain privacy
· Provide a safe physical environment
Language Needs
· Use short words
· Use clear and simple sentences
· Speak slowly and calmly
· Questions should ask for a “yes” or “no” answer
· Talk about one thing at a time
· Talk about concrete things; not abstract ideas
· Use common phrases
· Always say what you are doing
· If they repeat their question, repeat your answer as you did the first time · Give them a longer time to process information
· Wait patiently for a response
· Be accepting of inappropriate answers and nonsense words
· Speak softly, soothingly and gently

Care Needs
· Recognize that receiving personal care feels intrusive
· Reassure with your tone and manner
· Do one thing at a time
· Talk through the care “play-by- play”
· Be aware of your body language and use it to communicate relaxation and reassurance
· Be sincere
· Use a soft, soothing touch
· Be aware of the individual’s unique triggers
· Be aware that a person with dementia may not accurately judge whether a situation is threatening to them
· They may respond to fear, pain or anxiety by defending themselves with what we call “aggression”
· If they become distressed, stop immediately and allow them time to calm down – don’t try to restart the activity right away
You need to change your behaviour to adapt to the dementia because the person with the disease cannot.

Another good book is Living in the Labyrinth: A Personal Journey Through the Maze of Alzheimer's, by Diana Friel McGowin. Learn all you can about AD/dementia b/c knowledge is power!

Wishing you the best of luck with all you have on your plate.

Yes, Memory Care is the right place! The staff have seen it all before and know how to deal with things that crop up.
The idea that people are stealing belongings is extremely common with dementia patients, so it is quite "normal" for your father to be suspicious. And a regular reaction is to hide things to keep them safe. And then forget where, or even that they hid it. Essentially they have the whole MC center to hide things. It's amazing how creative someone can get when hiding things! My friends mother used a paper clip to hang her hearing aid on a coat hanger, then hung a seldom worn sweater on the same hanger. It was months before it was discovered!

You can't change or fix the behavior. But you can be sure he doesn't have anything valuable in his room that could be hidden so well it is never found. Jewelry, watches, collectibles etc.

Thinking he is in the military is his new reality. Go with the flow. His brain is unable to learn anything new, so explaining to him is fruitless. Distraction and changing the subject could be helpful.

And YES watch Teepa Snow. A lot of her videos are available on YouTube so you can watch if you have internet access.

One thing that may be comforting is that he may move into a completely different reality as the disease progresses. Hopefully it will be a more comforting place than the army!
Best of luck to you.

I'm sorry for what you and your father are experiencing! We have found some success in having a written log, for my father, that he can access and read for himself. In our case, the log is primarily notes from doctor visits, since dad tends to challenge "who said I need to...?" for any new medication, diet, physical therapy, etc. Reading it for himself is important in his case. We keep the notes in a formal looking 3 ring binder, front & center on his bookshelf.

Your father is in the right place! He’s in the ‘adjustment period’ which may last a long time since he has an awareness of what has happened. His anger, hallucinations and delusional episodes (being detained by the military for questioning) are common symptoms for a dementia patient. Following his neuro-psych evaluations, did you receive a copy of his treatment plan going forward? If he’s on meds and they’re not working, speak to the doctor and ask if the dose can be increased or if he could benefit from a change of medications. My Dad – who outsmarted many a physician and firmly denied that he had dementia to the end - exhibited similar symptoms and benefited greatly from medication.

Leaving a written rationale as to why he’s been moved to MC is likely to further agitate him (why rub it in?). Instead, you could leave a note telling him when to expect your next visit to reassure him that you’re coming back. Be patient. He’s struggling. So are you. Give yourself a break.

He wont remember a note. He'll lose it or forget where he puts it. It's easier just to keep repeating yourself.

I like the military idea. It’s cheap and easy to try. Maybe an American flag, a foot locker, pictures of Uncle Sam and Norman Rockwell, patriotic music - things that make dad feel safe and. Things the enemy would never allow. Maybe he can reframe his thinking to military base and the lockdown is to evade the enemy or because the general said so. Good luck and God bless..

Just a thought…if he thinks he is in the military and feels his “stuff” is being stolen, maybe a footlocker or a locking cabinet will give him some peace? I keep hearing that we need to go to their world, not force them back to ours.

As far as meds, maybe introduce some of his nurses as “Captain” or other such nomenclature. If it works, he’ll think they have authority to help him.

im just kibitzing here, hope it helps.

Have you had a chance to watch any of Teepa Snow’s videos on YouTube? They have helped me understand so very much, since my mother needed to move to Memory Care.

Teepa says that with a dementia, a person’s field of vision can change.

So, if we write notes for our loved ones, many times, they cannot even see them, let alone remember that they’re there.

Best wishes to you.

No, a note won't help. He will read it and probably forgot within minutes what he read.

Your Dad is in his own little world and you play along. If he thinks he is in the military his mind is telling him he is in the military. IMO they go back in time. My Mom forgot my Dad. When asked about her kids, she had none. I think she thought I was her Mom. My GFs father did the same thing your Dad is doing, packed up everyday.

There is really nothing you can do. Seems he is on meds to help with some of his problems. They staff have ways of getting him to take his meds. Putting it in pudding or yogurt.

Everything you have described is someone suffering from a Dementia. He is in the best place he can be.

Oops meant to reply to Cappuccino

Hmm I initially wrote notes and / or instructions for Mum (she even had a white board) but then realised a few months later that she was no longer able to read. She loves flicking through magazines still but I became aware it was only to look at the pictures and she’d get impressions from them. If his imagining his being detained / forgetting what he has packed, how confident are you in his reading ability? Mum still has full on conversations with me but can’t read or write, she knows she’s home but has those similar attributes of thinking someone has snatched something of hers. You can give it a go but it may only work a few months. I use video suirvaillance for Mum these days. Each morning despite being in the same house I give her a little talk via that,.. like good morning, it’s Tuesday it’s a nice sunny day, open your curtains, coffee is ready, will you please look for some cool clothing. There are some ready on the chair, I will come check on you shortly. That way it gives her a little independence and assurance and time to wake up before I get there to assist with anything that is left to do. I just find it easier because she can be a bit grumpy first thing in the morning and slow. I’m trying to fit full time work in with all this caring so if she can start on the process on her own, it’s of benefit and as I said,.. helps her feel independent, like it’s all her ideas. Could you reassure via video?