Everyday my Mother who is 86 and living alone calls me everyday and asks "what am I supposed to do today?" I tell her she needs to make herself a cup coffee, get the newspaper from the front door, make herself some breakfast and take her morning medication. She then calls and asks me if she "is safe at the place where she is". She is at home, a home she has lived in for 18 years. She thinks she is in someone else's home and I have to describe to her furniture, carpeting, etc., to assure her it is her home and she can relax.
These calls repeat throughout the day. She is treated by various doctors but she is keen enough to get past their mini tests and will not accept any discussion about her having dementia. She has lots of alternatives, such as long term home health insurance, money to move to assisted living, or live with me in a new home. She always says why do I have to make that decision know, I'm fine. In the meantime, I'm working all day and speed home to see her after work, make her dinner or take her out and then spend hours afterwards paying her bills, looking for things that don't make sense like paying $10,000 for dating service or refinancing home , purchasing crazy TV productions, cleaning her house or watching TV and trying to explain what is happening as she cannot follow any storyline or news.
I'm 60 and can't keep up the pace and my house is falling apart. My husband is working and takes care of two homes, four cars and all the animals. He is wonderful and supportive but I don't know how to move forward for all of us. She lives in a deed restricted community that will not permit us to live with her and my home is too tiny for all of us. I think we need a house with 3 bedrooms where we can live together and have room for a nurse in the future if necessary.
I have a POA but I don't know how or when to activate it. I'm doing all the finances and I'm the executor of her estate and will inherit her home so combining our assets for one bigger home seems reasonable, but is it? She says everyday that she is confused and asks me to do everything for her, but resists any long term changes. How do I begin? Where do I begin? Any suggestions????
Otherwise, since your husband sounds as if he is having to manage so many things, your idea of getting into a house for the three of you might be good, if he agrees. And if you haven't "activated" the POA, it sounds like now is definitely the time! But Mom is going to have adjustment problems to any changes she has to make.
Never mind Lymie61 answers.
While there can be some differences state to state, in general a POA is in effect as soon as it’s signed because it gives you the ability to act legally at your mother’s direction. So she needs help getting bill payment set up on-line, paying bills or that it’s time to sell her house, you can take care of all of that, sign for all of that on her behalf, which is why you want someone you can trust to have POA. DPOA or springing POA is the type that goes into effect under specified requirements when she is no longer able to make decisions for herself, some states have one document that is both others do not. There are also separate legal authorities for medical decisions but under the circumstances it sounds like that may be included in the POA document created for you and your mom. My guess is you have all of those legal authorities spelled out in the POA document so reviewing that may clarify your fears about when and how to “activate” what. If not consult the attorney that drew it up.
If she has been seeing her PCP for a long time and especially if that person has a geriatric practice her reluctance to discuss a dementia diagnosis or test probably doesn’t matter, she may have that diagnosis or some form of it in her records anyway. Some people cover every little complaint and others don’t want to complain, usually a pattern throughout life so it may not be such a copious thing but rather moms instinct to rise to the occasion and pull it together with others. A good provider is accustomed to this. Their reluctance to push a diagnosis may very well simply be an effort to keep mom happy and trusting them, no real point in forcing her to hear a diagnosis she is resisting and may not remember anyway unless the time has come and you need that to put the durable or springing part of a DPOA or they don’t know if all your paperwork is in order and are giving you time and room to make that happen before having to go through the courts because they have made a diagnosis and you don’t have the authority to take over decisions for her rather than just carry out hers.
It sure sounds like it’s time to make sure all of your legalities are in order and talk to her doctors with that authority about what’s happening and what the options are. You are very fortunate that she is set up so you both have such options and while it may take some time over several conversations it’s probably time to talk to her in her more lucid times about why she prepared the way she did, what does she picture the next step looking like “when the time comes”. Give her some ownership of the decision making, it doesn’t mean that will be the best thing in the end but getting her to talk about it and knowing what her ideal is will at the very least help you feel good about your decisions, “yes I can make that happen for now or no but I can come close” because ultimately her safety and your piece of mind and health come first. I have to agree that it sounds as though she is past the point where moving you all in together makes sense, it will likely mean an additional big move sooner rather than later when you can no longer be her full time hands on caregiver. Since she has LTHC policy that might be the thing to explore first but weigh it with some sort of IL/AL situation where she has her own place perhaps on a campus that also offers MC and NH care should she need it. I would urge you again to consult her medical professionals as well as elder care professionals to help you come up with the ideal path and then B, C and even D plan options while including her in that as best you can. After all she did some of the important planning, how to pay for options, ahead of time so this isn’t unchartered territory for her, even if it was actually her husband who did the financial planning. We find laughter helps a lot too with Mom, lucky 2 have U.
Also, you don't say if she is driving. I hope not! If so, you need to address this with an appropriate evaluation by OT certified to determined if she can still drive safely. Fortunately, we have Lyft and Uber to allow her to move around without needing to drive. You can always manage that for her remotely.
Make arrangements for her to spend part of her days in a senior program if there is one available nearby. COVID-19 shut many programs down, but some are opening with limited enrollment. This is really a huge problem - most seniors are isolated and bored. If they have lost executive functioning they cannot plan, learn, make timely or appropriate decisions, but may have normal speech and motor skills thus appearing OK for short periods of time.
Does Mom have any hobbies? Can you hire someone to come in for a few hours each day to work with her? Does she have neighbors that she is friendly with?
It is easier to ask forgiveness than get permission from someone who is cognitively limited. Explain that she asked you to do all of this so that she doesn't have to keep track of every little thing. Then, as recommended, meet with an elder attorney and start planning for her LTC. It will be easier to move her now to a facility that can accommodate increasing needs. She will have time to make friends, get involved in activities, and will feel taken care of. That leaves you freer to take care of your own family, which will also be a priority of any loving parent.
The best thing you can do for her and your marriage is to convince her to go to a nearby facility where you can still see her as often as you want (I know, difficult with COVID) but where you won't have to constantly worry that she has forgotten to do something like eat or turn off the stove (we had both).
Best of luck and hugs!
I think you should talk to a doctor. It may be possible to get her tested at home not sure.
To become her P.OA. do you not have to prove she can't manage herself. The crazy bills you had to pay can you not find out how they came about? Is it scammers or would she know how to do these things herself. I really do believe you should seek both legal advice and a doctors. Best wishes as you get things sorted. For yourself too you can't go on the way you are. I hope i have been of some help 🙏💗
You might check with the deed restrictions on her house if that's a bigger place for you to live. It may be you can't rent rooms making it a multifamily residence. Moving in, as a family member, to provide her care may be something totally different if you'd rather do that.
if she is lonely and scared at home put her in AL. We did this with my dad and he surprised us by loving it. He even got a lil better b/c of socialization. Now he he has a girlfriend and is very happy.
My widowed sister moved to assisted living a few years ago and loves it. So many things she and the family no longer need to be concerned about. She is safe, activities, no longer has house upkeep, one meal a day with more if wanted, shopping bus, etc. Believe me, it will be a gift to both of you. Seeing she is interested in dating services, she might find someone in the assisted living.
I am an independant Elder care companion. You can find people like me on sites.
Agencies are horrible. !!!!!!!
I have been a companion for several wonderful people for over 6 years. I visit, games, crafts, make meals, go off on adventures with them, help with light chores and doctor appointments etc. I recently started paying bills etc. (At Family's request)
If your Mom is hesitant, as they can often be. When you find the RIGHT person introduce her as a friend of yours. Little fibs are sometimes needed.😊
Start slow, twice a week for a few hours until your Mom starts to look forward to her visits.
Always interview people off property. Check background!!!!!
Hopen this helps
Bobie D
I had some very good caregivers from agencies.
There are advantages and disadvantages of hiring through an agency and there are advantages and disadvantages of hiring privately.
There were some instances where I HAD to hire privately and there were some where I HAD to have a caregiver from an agency. Not all circumstances are the same.
I know it seems like if she could move in with you and your husband it would be much easier and it would be for a while because currently you are spread so thin. But as she declines, it will get much worse. In home care for an nurses aide costs $10,000 a month for 24 hours. A live in would be cheaper but still costly. A nice assisted living facility with option for memory care would cost about that much and would provide all her needs, with in house doctors, activities etc. Covid will not be around forever. This would also give you your life back so you and your husband can plan your own lives while making sure she is cared for.
A move to Assisted Living or if necessary memory Care might be the safest option for her.
It sounds like she is past the point of getting to make decisions so she will have to deal with long term changes.
A move to a new house would be a long term change just as a move to Assisted Living or Memory Care would be a long term change, she will not be happy with any of it.
Has she been diagnosed with Dementia of any type? Has she seen a doctor? Might be time to make a yearly appointment and also request a neurologist evaluation as well.
If you want to keep her in/at home this might be a long haul for you and your husband. Are you both willing to care for her as she declines over what might be another 5 or 10 years?
Before you make any decisions to buy a larger house you might want to discuss the future with an Elder Care Attorney and see what the best options might be.
Looking for a suitable hose might not be easy to find. You would want one that is accessible. Wide halls, wide doors, large enough bathroom to get equipment in (Hoyer Lift or at least a wheelchair) as well as at least 3 people. (possible need for 2 people to help with showering) and a roll in or zero threshold shower, no stairs or at least ramps in place, no carpeting. These are just a few things.
I would suggest having her move into independent living with the option to move to memory care later if needed.
My sis and I hired one after being referred to one by our county’s area of agency. What a Godsend she was. She helped us relocate my parents to a wonderful place that she was familiar with. My sis and I struggled through so many visits to facilities to find the right fit but ended with a board and care home where our parents received the best care. I would highly recommend it to people with dementia because it’s only 6 people. The good ones have two caregivers so there’s more help. They loved our parents like their own.
It would be a wise investment to spend 2 hours talking about possibilities with an elder law attorney who did estate and Medicaid planning. Laws in each state differ so please don't make any financial moves until you get professional advice from someone who will learn of your and your mom's entire financial landscapes.
My MIL lived 6 miles from us and we were checking in on her daily, although not always in person. We discovered that she was not remembering to eat or take her meds, even when we were prompting her by phone. She'd hang up and immediately forget. We transitioned her into AL and soon after that she needed LTC. There is no point in exhausting yourselves trying to keep her out of a facility if it results in your own burnout. Please read (on this forum) some of the thousands of posts by well-intentioned adult children trying avoid the very difficult decision to place their parent somewhere they don't want to go but badly need to be for everyone's sake. You will get excellent insights and advice here...I hope you listen to it. I wish you all the best and much wisdom and peace as you work through it all.
Do not co-mingle your assets! This could be a death knell for future care decisions. Bring this up with your atty.
Finally, make an appt with her PCP. There is some cognitive decline going on.