I have a parent that has said from the beginning, they would not move in with a relative due to them not wanting to be a burden. They took very good care of themselves and are financially capable of going into a facility today. However, I do not think they are ready for the restrictions of a facility. The person of whom I speak was diagnosed with Alzheimer's 8 years ago and the last doctor visit determined that living alone was no longer an option. I have the means to provide the care and my family is all on board with this plan, however the parent is making up reasons to not move in. I have done countless hours of research on the disease and facilities that do and do not care optimally for Alzheimer's sufferers. I have one in my area that is certified and a lovely facility. However, I feel that if they were to go to this facility tomorrow, they would be miserable because they are still high functioning enough to go to the senior center and do swim classes and such. Therefore, when do I overrule their desire to move to a facility now vs. later? Any help would be greatly appreciated.
Some assisted living facilities will accept high functioning dementia residents with the acceptance that they will eventually move to memory care when needed. This is a very common practice where my mom lives. I think this would make the move much easier if the parent is willing to go.
Or your parent can live with you and go to adult day care - during the day. That worked for us, for awhile. Mom lived with me for 2 years, she went to a day center that specialized in dementia. The place was fabulous and she loved going. She believed she worked there. Since she didn't have any concept of time, she didn't live with me, she was just visiting. That may be a good alternative; I am not sure what services are in your area.
When I moved mom to assisted living - it was hard - since she was high functioning and many of the residents were not. I moved her because her health was declining and I knew her dementia would also. Look at what services are provided in your area for people with dementia.
It's never easy.
The person of whom I speak understands the reasons behind why I do not think they are ready and that when the time comes, yes I will move them to the facility. However, at the end of the conversation, they have forgotten everything that was talked about. All they can remember is that they don't want to move in because they don't want to be a burden.
As for the POA, yes they have been established and finances/trusts/will have all been finalized. Arguing with them to where they will move immediately, is what is on the horizon.
Let him know that the minute he needs more care than you can properly give him, you'll put him in a facility but for now, he's no bother and you would rather he lives with you. A compromise.
My mother has a personality disorder and developed vascular dementia the past few years. She became paranoid about staff at the very nice ALF where she lived, and was very well cared for, and found another ALF she wanted to live in. I (POA medical and financial) looked into it and found that services were less than she had where she was and it would not be a suitable place for her. For example, there was no nurse on call on her floor, just a security guard. This was not enough for a 100 year old! She was quite upset at me when I said I could not stop her from moving, but I would not support or help that move, as I felt it was not in her best interests. In time and after many difficulties, she was hospitalized and diagnosed with the vascular dementia, treated and placed in a facility very suitable to her needs.
Moving slowly and methodically as you have has given you the chance to check our several places. Now take dad and mom to visit.
My old 'Client" when I worked in elder care, was ready to go---but she didn't know it! It took slow, gentle persuasion and MANY trips to the new "facility" to acclimate, before long, she accepted the family request that she move--and she thought it was her own decision!
As far as outings, ALF patients can come and go. My client routinely went to parties, luncheons, family activities...no big deal. Had she wanted to go swimming I am sure they would have made that happen.
I will add---her place was the nicest, most posh ALF I've ever been in. The food was amazing, the staff, top notch and her little apartment, just delightful. Her family spared NO expense, and often told me it was worth every penny.
Within a year of being moved, her dementia worsened, she would not have done so well in that condition, being moved from home. Eventually she did wind up in a lockdown type area of the same ALF. Still nice, but dedicated to keeping the patient safe--and from wandering.
I'd strike while the iron is hot. We waited to long to "push" Mother along and now she doesn't have the ability to make the decision and as kids, we can't do it for her, as we cannot all agree, and never will.
Good luck.
Early onset Alzheimer's can be controlled with medication. My father was considered early onset for the 7.5 years I took care of him but it never progressed. He was on Aricept at the time. His passing had nothing to do with the Alzheimer's - it had to do with his stopping Dialysis at the age of 88. He was on the lower dosage of Aricept and it never never progressed.
If your parents can still manage well, leave them be.
For my dad who was 100% against ANY nursing home, the tipping point was when he had an incident that involved any harm or injury. Lacking that I, my brothers and mother, felt it was still his decision. It didn't matter that dementia was taking hold, that he could no longer decipher the microwave instructions on the box, that we had to lay his medicine out and he would pick and choose which to take, we felt the time was just not right. He still had reasoning to control his destiny. But when he lost his way coming home from the $ store, [6 blocks from home]- ran the car over a curb 18 miles from home, it was time.
He still periodically asks why he is there, and we tell him. He promptly forgets then later, maybe that visit or the next one, he asks all over again. He is now getting the care and safe living quarters he needs.
I hope someone has been appointed as POA and he has an up to date will made. Too late now to put any real property into a trust.
Since you are asking about making this decision, take cues from the doctor and your parent's wishes. Take him/her to the facility and explore that option, discuss the option of having care in his/her home, as well as coming to live with you. Give your parent time to think about it. It may help to try in home care first, especially if he/she is safe at night, before moving on to another option. Each person is different, but having doctor input and considering your parent's needs and wishes as well as your peace of mind, is important.
Best wishes for making this decision.
The nice part of a facility is that your loved one will have built in socialization possibilities that won't easily exist in your home. The sooner you make the transition, the longer your loved one has to adjust, which is important for someone with dementia. Good luck with whatever you choose.
Lucky that you have a parent that does NOT want to be taking in and taken care of by their family. In particular- one of their children. Lucky that you have a parent that has the means to finance their choice of living arrangements and lifestyle. And lucky that your parent has remained active both physically and mentally- as well as being active and perhaps practical in their own decisions.
While you look at this choice to move into a facility as a potentially over restrictive one - could it be that your parent views it as a step in maintaining some independence - not having to be "taken care of" by their child. Perhaps they are not willing to let the often occurrence of role reversal with the child taking care of the parent take place any sooner than it needs to when dementia is involved.
As well, could dignity and respect factor into this choice. Of course you would treat your parent with both dignity and respect - but perhaps your parent is not willing or wanting you and your family to witness their deminishing skills and abilities. And deminish they will.
To your parent this move may be in their eyes the best shot and keeping your relationship one of family - of parent and child verse caregiver and "patient".
There are multiple smaller issues as well. Maybe they'd like to remain in their own generational peer group. Maybe they believe there will be more activities available to them for keeping busy. Maybe they would like more personal space verse having family around all day, everyday.
There are a whole lot of maybes. But if this is your parents choice - personally, I think you ought to give them their earned right to make it. After all, if it doesn't work out you could always bring them to your home.
Since the doctor is worried about him living alone, I take it there is no spouse involved. Is that correct?
There are 3 options:
1. Continue living at home, with round-the-clock care. This option tends to be the most expensive.
2. Move in with a family member. This is an option he has specifically rejected in the past.
3. Move into a care facility with the appropriate level of care and supervision. Apparently this is the option your parent would prefer.
Surprisingly, living with family members is not always the best option. Sometimes it is, of course, but not as often as you might suppose.
If he were in the care center you have in mind, could a family member take him to the swim classes? Go on outings with him often? Consider that he probably wouldn't be the only high-functioning person there, and those residents tend to find each other.
When should the decision be made? Now. He is no longer safe to live alone.
What can you do to make the decision for him? Persuasion only. He is high-functioning enough to make his own decision.