Mom is currently visiting me in my city and agreed to look at assisted living communities. That agreement changes every 20 minutes because she is determined to live independently 400 miles away. I'm the only child/relative left. Mom is 90 with vascular dementia that is progressing...and neighbor caregiver who checked in on her says he can no longer provide assistance. "It's time." I have an appointment with an elder law attorney in three days. Am I the client because I need advice on my POA for Mom....or is she? I'm thinking I am. She has trust and wills and POA all set. I'm the one who needs legal advice. We have visited 2 lovely and new assisted living facilities...tours, lunch...great places and we had fun joining some other residents for lunch. Of course I have tried to include Mom (for over a year and a half) in ideas/plans to move to my city and be part of a senior community. Her cognitive ability, of course, has deteriorated to the point where agrees one minute and then insists she will never live her home a few minutes later. This is an excellent example of how impossible it is to reason with an elder who is living with dementia. What I get from her is...I can take care of myself...go live your life...forget about me...I'll be dead soon anyway....you don't want to come to Chicago to live...well, I don't want to live here....leave me alone and forget about me. .... etc., etc., etc. I do have POA that includes the recommendation of only one physician for me to take over decisions...and I have a copy of her neuropsych evaluation with the diagnosis and recommendation that she cannot make her own decisions with care. So...am I the client for the elder law attorney.....and if anyone has suggestions for how to proceed from here, I'm all ears....and believe me, I've even thought of getting her committed while I get her furniture and things relocated...the abduction scenario. She is grieving and full of fear and anger. My heart breaks for her.
Has she been seen by a geriatric psychiatrist? It sounds as though she might benefit from meds for depression and agitation. Vascular dementia often causes and exacerbates these conditions.
I think you are the lawyer's client. You want to know if you have the authority to determine where mom lives. But even if the answer is no, you are going to mske a good faith effort to move her to the AL, because that's what she needs.
Therapeutic fictions are helpful. "Oh mom, the foctor wants you to stay here for a while until you get stronger/until I get back from my trip/until your house is fitted with a new roof." With my mom, it was until the winter was over.
Apart from anything else - not to be grabby, just to be fair - that also means she's the one who gets the invoice! After all, the entire exercise is for her benefit, not yours.
I don't mean this to sound like a con either, but could you perhaps get her firm(er) agreement to give her choice of facility a "fair trial" of, say three months? For one thing, she might be more likely to agree if it doesn't mean making a final, irrevocable decision; and for another if, as seems likely, she's unable to make any kind of decision before long, it'll be a heck of a lot easier to make the move permanent if she's already placed.
Another point I want to make to any new folks reading/learning from our experiences is this: I've always visited Mom at home but this last visit, when we agreed to go visit where I live (Columbia, MO)...it was only then that I truly saw how impaired her thinking/confusion had become. She was in her element in her familiar home...but outside familiar territory it a whole other story...and terrifying. I'm the only child...so I am so grateful circumstances happened as they did. Also very grateful for all the folks who post questions/dilemmas on this site and the many responses of wisdom offered. I'm a daily reader.
I'd consider that while your mom may seem to be changing her mind about things. She likely has forgotten what she told you 20 minutes earlier and that's why she's telling you something different. It's more of memory loss of what she just said than mind changing. That would be my suspicion.
It's not likely that people with dementia are going to suddenly or gradually see the light, get on board, agree, be reasonable, etc. They can't continue to drive the train. It's nice to placate as suggested above, but, I'd get a reason that she's moving to the facility and reiterate as she is placed. With my LO her Primary told her she needed AL. Period. She would not let it go. So, my LO adjusted to the idea of going to rehab to get her physical therapy, medications, help with her memory, etc. temporarily. The professionals at the facility are skilled and are good at administering medications.
Do you know what level of care your mom needs? I'd explore that, so you know what type of facility you need to find. The neuropsychological evaluation may provide some information, but, I'm not sure if it will help with what daily activities she needs assistance with, like, bathing, food preparation, laundry, toileting, etc. I'd keep in mind that with an AL community, as she progresses with dementia, she may need a higher level of care. I'd consider if they have that available on site, like a Memory Care unit, so she doesn't have to move to a new facility later on. Also, I'd explore just how much the AL will provide in hands on care. It varies by state as to what they are allowed to do.
If Mom's current home could be maintained while she has a trial stay in AL that would be ideal because the ultimate decision could be 24 hour care at home or an AL in her current location if she has a good group of supportive friends, church etc there. 400 miles is a long way to go for a short visit but with proper local support could be done and then if necessary as she progresses move her closer to you.
i think the right first thing to do is wait and see what the lawyer has to say then proceed from there. Mom is never going to make a decision with the dementia.
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