My mother and I share a house. She has dementia which is worsening daily and every time I bring up the assisted living (memory care) issue, we get in a huge fight. It is absolute hell dealing with this and I can feel my years ticking away (58 years old). I'd go, if they would take me!
The place my Dad moved, it was so great, that I wanted to move there, too :)
I read this idea on the forum not to long ago... tell your Mom that you are able to get a free lunch, and she is invited to go. Set up an appointment at the facility and tell them what you are doing. You could also tell Mom you are searching out places for a friend, and they would want your Mom's opinion. Moms like to help [I realize your Mom has dementia, but would she be able to still go out for lunch and a short tour?]. She might be pleasantly surprised.
Wouldn't it be great if she spotted an old friend who now lives at the facility?
Somewhere on this forum I read a post from a caregiver who put mom in respite for one week every three months, and it was a sanity saver. Think of it as an investment in your health.
I'm so sorry to hear what you are going through. Its so tough. Even though your mom doesn't want to go to assisted living. I think Dana has an excellent suggestion.
Have you considered talking to social worker, counselor, family therapist, family doctor? Maybe someone can come to the house to speak with your mom about her options.
I know we want to do right by our parents, but I fear if you continue trying to appease her it will only lead to more anger and resentment and that is not good for anybody. No one likes change at any age, but as your mom's care escalates, its better to start looking at options now.
Take care and I hope your mom will come around. If not, make that tough choice for yourself and preserve your own well being. I know its easier said than done, but don't let the guilt control you. Its not fair.
The mother you are dealing with now is not your Mother you are dealing with a disease that knows no bounds in the way it erodes the person. Both the person with Dementia and the people close to that person.
She may say she hates you...she may say that you must not love her....but.
If you can not safely handle your Mom both physically and mentally it is time.
She will get used to having help round the clock, she will get used to a new room, a new routine and new friends. Best of all she will regain the Daughter that she is fast loosing. And you will be a better Daughter and a better advocate for her.
do your due diligence. Contact every facility that's within driving distance. I personally contacted 22 and toured 17 before applying on my mother's behalf. After all that, I only felt good enough about 4 to apply. Of those, one 1 accepted her. There are vast differences among facilities. For example, my mom already had Medicaid when she entered the facility. She got into a unit with all private rooms. At another facility, for the same Medicaid money, by mom could have been in a room with 3 other residents. So you must shop around. Don't just take your mom there and drop her off. The facilities I was interested in, I visited 3-4 times, both formally and informally, just dropping by. I talked to visiting family members as asked, "is this a nice facility? are you happy with the care your loved one receives?" When they answer, take it from there.
As much as you love your mom, you don't owe her your blood. What you do owe her is to get her into the best possible facility and to stay on top of her care, visiting often. Good luck.
As for
When I was doing my touring of NH, I would linger outside for a few minutes & ask anyone coming/going if they had a family member in it & how happy everyone was with it
A friend whose mom was about to be going into a NH said the one too close too home would mean he would take a real long way around so she didn't realize how close to home it was - maybe if taking mom to 'free lunches' say that it wouldn't be any good for her as it is too far from you - that may spark the 'contrary note' that she will then praise it - you may say if she is happy then you'll sacrifice yourself with longer drive as long as she is happy - remember to occationally say how far it is after she moves in even if 2 minutes away ... make it 38 minutes - might be time well wasted
You have to remember that it is now you in the 'parent' role not the 'child' role - also parents of that age think of NH as 'places for those with no body to love them' to quote my mother - good luck
If you worried that she will always hold it against you if she moves, reconsider, because her memories of this will fade.
"one size fits all". If you have always had a loving relationship and it was mutually based and if you are physically, mentally, emotionally - and financially - able to care for them and you WANT to be the caretaker, then do it. But do NOT feel you must if it is destroying YOU or your life or your family or your work or whatever. You have a life to live too and you must before you go to pieces and have no future life and nothing to fall back on in your old age. It is extremely difficult to go into a facility - especially if you have your full mental abilities but are physically damaged. It is horrible to be around people with mental issues. This makes it difficult to make good friends and she may fear the loneliness and the uncertainty of what is to come. You may just simply have to make the arrangements and then on a certain day have professional people come and take her, along with you, to the new home and then immediately within a day or two move her special belongings to the new home. She will never willingly go with you - just won't work. There is no real easy answer.
Oh, she was plenty upset and that last week of packing and moving her stuff was the worst. I tried reasoning with her, and she would have a few lucid moments and agree, especially when I told her that I could not do this any longer, that she would end up burying me due to the stress of my constant worrying about her.
She is adjusting (it's been only 10 weeks) and the staff tells me they are surprised at how well she is getting along. Of course when I visit, I get the full act of how she never wanted to live in a place like this, never expected her daughter to whisk her away into a "home" after she gave up her home to come help me (that was her reasoning for moving 1500 miles away to live with me 4 years ago). I'm doing my best not to get sucked into the sad mental and emotional state that she is in due to the dementia.
Now I just tell her whenever she asks (and it's often) if she can come "home" is that she is not safe being alone and I have to work.
Good luck!
Then, they tested her for intake. Suddenly, all those wonderful activities...not available to her because she would be in their lock down memory care unit. No freedom of movement. Dependent upon them to provide everything...even a cup of coffee..etc. not even close to acceptable,
I understand not wanting to be in that place. We opted for in home 24/7 caregivers instead.
I have toured and checked out NH all over this area. They look nice...but, they are understaffed, and minimum wage teenagers do not care. Without mobility, being stuck waiting endlessly for any attention is horrible.
The only nice places are seriously expensive and do not take Medicaid.
Maybe this is better than years ago....but, I see the only difference is in the remodeling of the buildings...same lousy care...same uncaring staff
All of the Memory Care facilities that I have encountered in my state, are required by law to provide daily scheduled activities for the residents. They have a secure outdoor area, activity room, dining room, etc. They don't lack any of the amenities that the regular AL unit has. Just more supervision and one on one assistance with needs. Of course, they are geared to protecting the resident from things like hot beverages, sharp objects, toxic substances, etc. It's for safety purposes. I'd explore them with that in mind.