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1. I blocked his number as others have suggested. It's not cruel, it's survival. Calls go to my voicemail and I scan through them when I'm awake and can deal with it. It's not cruel -- it's survival.
2. I found out (on this forum) about a cell phone for people with memory problems (RAZ Memory Phone). You can Google it for more info. It's been a lifesaver. As the caretaker, you can set up her contacts, you can decide who is allowed to call her (if you want to), and you can set Quiet Hours, during which the caller gets a very friendly message that you are not available but will be excited to hear from you at a later time (something like that). Honestly, it's made all the difference in the world to us, and I wish I had known about it sooner.
Boundaries are not cruel, they are necessary for both you and your mom. Best of luck to you.
I placed my mother in Memory Care because she needed 24/7 care. She didn't want to be there, as 95% of elders don't want to be in such a position. So let's ALSO take their phone away, shall we, b/c it's "irritating" they're calling us a lot? Which also prevents them from calling their other family members or GETTING calls from friends and family members, too.
How about we give them some DIGNITY and some freedom, folks?
Just turn your phone off if you don't want calls, or on vibrate like I did.
And Joann is further advocating the staff not "allow" this OPs mother to MAKE any outgoing calls once her phone is taken away! Really? So now she's in prison? SMH. It's not funny Cover, its CRUEL imo.
I used to turn my phone to vibrate in the evenings so I could get some rest when my mother lived in Memory Care AL. One phone call a day is plenty. Ativan helped her a LOT with all the anxiety she was suffering with the dementia.
I suggest you read this 33 page booklet (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.
Understanding the Dementia Experience, by Jennifer Ghent-Fuller
https://www.smashwords.com/books/view/210580
Jennifer is a nurse who worked for many years as an educator and counsellor for people with dementia and their families, as well as others in caring roles. She addresses the emotional and grief issues in the contexts in which they arise for families living with dementia. The reviews for her books are phenomenal b/c they are written in plain English & very easy to read/understand. Her writings have been VERY helpful for me.
The full copy of her book is available here:
https://www.amazon.com/Thoughtful-Dementia-Care-Understanding-Experience/dp/B09WN439CC/ref=sr_1_2?crid=2E7WWE9X5UFXR&keywords=jennifer+ghent+fuller+books&qid=1657468364&sprefix=jennifer+ghent%2Caps%2C631&sr=8-2
She also has published a workbook entitled, “It Isn’t Common Sense: Interacting with People Who Have Memory Loss Due to Dementia.”
https://www.amazon.com/Isnt-Common-Sense-Interacting-Dementia/dp/1481995995/ref=sr_1_4?crid=2E7WWE9X5UFXR&keywords=jennifer+ghent+fuller+books&qid=1657468655&sprefix=jennifer+ghent%2Caps%2C631&sr=8-4
She will discuss lots of Do's and Don'ts and other tips (including the 'going home' mantra) in her booklet & other publications and you may get some good insight into dealing with your mom.
I know how hard all this is, truly. Dementia affects everyone in the family, not just our mothers. It's hard for US too, and we all suffer as a result. Wishing you the best of luck with all you have on your plate.
My step-mother is in MC, the facility does not allow any phones in the rooms as patients would call 911 and do what you are experiencing.
Time to disconnect.
I would talk to staff and get that phone removed. That is way to many times to be calling you. Why is the staff allowing that? My dad was in a nursing home, and they didn't have phones in their room. He called 1 time, and had to get staff help bc he didn't know my number.
Is staff helping her? She must have a great memory. I would get to the bottom of it right quick. That is way to many times. And it is extremely stressful.
Call them right away and say enough. They need to remove that phone or getting staff to keep dialing the phone. I'm surprised they would have time to do that.
Did you give her a phone? Then you need to take it away when she isn't looking, or delete the number out of it.
But either way you need to stop it. Don't feel guilty. That is way to many times to be calling.
Discuss specific incidents at specific times and dates with the director if necessary. Most states will investigate places, as will medicare, for serious patterns of lapses in care. This results are usually publicly available.The facilities worry about it. But keep that powder dry, and it might not provide quick or specific help for your Mom. Better for after you move her if no improvement.
I think it is very helpful for dementia people to know there is someone they can count on being there for them. It's difficult for them to trust the care givers, as they can't remember who the care givers are. Your mom will hopefully eventually stop wanting to go home. What I did was make up some stories about why my mom couldn't go home just yet. I learned to enjoy making up stories, since she never remembered the story I told her the day before. I told her once that her old tree fell down on her house and there were repairs to be done. She remembered the tree. It was true that her tree fell, but it actually fell on the neighbor's house. This tactic would get her mind working in other directions, as she liked to give advice on solving whatever problem I made up.
It's difficult for you and I know how frustrating it is. Hang in there and make sure the director of the facility knows what's happening. They might have suggestions or can divert her themselves.
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