Hi Everyone,
A quick question. I've been caretaking my grandparents for about 4 years solid now and they are getting to the point where they need assisted living.
One has advanced dementia (asking the same question multiple times in a conversation, repeating same conversation multiple times a day), and is forgetting to bathe and take medication frequently, etc. The other can't cook for himself and will skip meals unless I'm there to provide them, and is often in need of assistance with dressing and other small tasks. Neither can drive, or leave the house without assistance.
I have tried twice to get an in-home caretaker and they have had meltdowns and tantrums each time, prompting me to placate and put an abrupt end to the arrangements in hope of finding another solution. I can't.
They need all of what assisted living provides, and they can afford it.
How can I get them to jump over this hurdle willingly and peacefully? And if not, perhaps more forcefully?
It's at a point far exceeding my ability to provide for or meet even some of their basic needs, let alone advanced ones.
They are terrified of outsiders, harbor a mentality that all long-term care facilities are low-level prisons where residents are tortured, and feel that any family members owe it to them as a debt of honor I guess to care for them.
I'm 34, the only family member involved, and it's just not possible. Parents have passed, two brothers are unable/unwilling/unfit to help (mental illness, substance abuse, identity theft).
I have navigated this whole thing really well, and have much awareness about all the nuances and facets of LTC leading up to this point but, man, am I struggling to figure this out...
One thing they have requested multiple times is to find a mature caregiver with life experience (not a timid younger person) as they would feel more comfortable with that. It's been difficult to always ensure that with home health providers. Not sure how I could accomplish this in the interim between living at home and moving to a dedicated LTC home.
I know it's more than one question,, but any creative thoughts would be greatly welcome!
Thank you😊🙏
Next idea: Simplify it for them.
They NEED assistance with their living arrangements. This is FACT.
At present they are living how they wish, in their own home, & YOU are providing all the assistance.
But the simple truth is their needs now outweigh what you can do. What ONE Person can do.
So these are their choices;
A. Age in Place: Stay home but MUST accept home help. Lots & lots of it.
B. Move: into an 'assisted living' community/facility & accept staff help.
C. Continue until a Crises: until illness or fall etc. Then be forced to accept change.
In each of these options notice the common thing? They will need to ACCEPT HELP, specifically *Non-Family* help.
Losing one's independence is hard, very hard. But it is denial to think because your relative does everything for you, that you are still independent.
Having one person (you), providing care for 2 people with lots of needs is just too much. At your young age, you should be able to enjoy life more, not be tied down to this caregiving routine.
We tried the aide route. The only good thing was the agency sent a nurse to mom's place to do an evaluation. Two of us were there. Being done in her own place with us present made it less threatening. It was paid for by Medicare (including some follow up.) She gave recommendations, one of which was a timed, locked medication dispenser. Aides were started at 1 hr/day, mainly as a sanity check and to check that she took meds. They can't dispense, but they can check and point it out. We also installed cameras, mainly to monitor in/out activity (already got rid of her car.) Mom was in the earlier stages of dementia, but in her mind she was perfectly fine! This is very common, as they aren't really aware of the changes. Repetition was the first real clue (hindsight did show a few minor ones that were missed, mainly accusing others of taking items.) Because I had to facilitate getting food and supplies, it became apparent she was no longer cooking anything (shriveled up veggies, freezer items unused other than microwave dinners, etc.) The plan was to increase time and help as needed.
Sadly, because she convinced herself she was fine, this didn't last 2 months. She refused to let them in. They even sent their "expert" to talk to mom. She's lucky mom wasn't able to throw her out bodily!!
Now, to the issue about getting them to move. Despite what others have said, POAs do NOT give you any authority to make them move or accept care-givers. When the aide plan failed, plan B was to move her to MC. She refused to consider moving anywhere, esp not AL, although that had been in her own plans before dementia. The Elder Law atty told me we CANNOT force her to move, even with POAs. POAs are mainly documents allowing you to help manage financial and medical issues when the person is no longer able to do so. To back this up, staff at mom's facility also said they aren't allowed to force any resident to do something they refuse to do (take medications, get medical care, bathe, etc.) They have to coax the person as best they can to get the resident's compliance/agreement.
Consult with Elder Law atty is advised as a starting point. This situation may require obtaining guardianship, which can allow one to make that awful decision to move them. Of course they will still object, but it gives you the authority, if the courts agree, that this needs to be done.
Meanwhile, see if the agency you used can send a nurse to do the evaluation. What this nurse did was more than a doc office will do (their cognitive test is so minimal it really isn't very useful, esp in the very early stages.) Be there when it is done, to help them - pass it off as a Medicare necessity if you have to! For grandma, with dementia, facilitating compliance can be a bit easier, as you can use little white lies to assuage her anxiety or refusal to work with anyone. It sounds likely that grandpa is also in the early stages of dementia and might be "pliable" as well.
Our attorney told me that we'd need guardianship to move mom, but the place chosen wouldn't accept "committals", so we needed a ruse - she helped a bit by injuring her leg and developing cellulitis. YB used a fake letter from 'Elder Services' that gave her 2 choices: move to the place we choose or they will choose. She was VERY angry, but she went.
Hopefully you've been checking out places (MC.) EL atty can help if Medicaid is needed. While it's nice if one can manage home care, it isn't always possible, despite what some say.
See atty. Ask for nurse eval. Check MC places. Let us know how things are going! Come back if you need other suggestions. Don't feel alone - we hear you!
"My two brothers resent them too much to be able to actually help, and instead add great deals of negativity and grief to my life through constant venting of their repressed resentment and other emotion."
First order of business - block these clowns. Don't answer calls. Don't respond to texts or other modes of communication. Since the "...two brothers are unable/unwilling/unfit to help...", there's no point to putting up with anything from them.
I also have 2 brothers. Not as bad as yours. There were different issues, but nevertheless, I moved on to take care of what needed doing without consulting them. I'd either get a lot of flak, abuse or no response (sometimes well after the fact, which wasn't helpful - some decisions need to be made NOW!) It made my life easier to just put them out of my mind and do what mom needed.
A little daily cleaning and food prep to cover all the meals is a good place to start. Limit personal phone use for the employee while they are on the clock. I can tell you that older people believe in working during the hours you are paid to be on the job - not staring at a phone or sending texts while being static.
If there is a separate room in the house that could be set up as a sitting area for an employee, you might do that. The employee would not be in their face all day, but there to handle tasks that arise. If they can afford 8-10 hours a day - then go for it. Increase hours as need arises and add a couple more people to work out the schedules. If they want to stay home and they have money to pay for the care, it can be managed.
I have no sage advice on their feelings of entitlement for your time and care, aside from being blunt and honest. It seems the types that feel this way don't ever suddenly see the light. They have to be told and forced. It's exhausting.
But to their fears that facilities are like torture chambers- you may be able to change that some by showing them some virtual tours. Many facilities are like staying at a nice hotel. An all inclusive hotel. Since they have resources they can likely go to one of the nicer places.
After Covid isn't an issue maybe you could even do an in-person tour, and have lunch at the facility.
An aunt in my extended family moved to a nice facility, and when I was in town my son and I went to have lunch with her. I was amazed at how nice the place was, like a mini-resort. The dining hall was like a restaurant. Her apartment was lovely. So.... today's seniors need to be brought up to speed on modern day facilities. Many are very nice.
Aa far as their thoughts on LTC, they aren't that far off. Sure theur are homes that look pretty and the people overseeing the home tells you exactly what you want to hear to make the sell but then the reality if living there is not fun at all! Usually they are all under staffed, they over medicate if your loved one gives resistance or problems with anything.
Living in them, makes your loved one feel lonely, scared, unloved, bored, they lose all their rights, they have to get up at a certain time, take bath at a certain time which can be very early in the morning because there are only so many aides and they have to go thru so many Seniors to get them all bathed..
eat when their told to, go to bed when their told to.
They can't have any visitors during the Covid.
Many Seniors will actually lose their will to live.
I understand it would be better for you not to have this on your shoulders but not for your Grand Parents.
You should have cameras installed at their home so you can check on them 24 7 with your computer or cell phone.
Order their groceries to be delivered.
Order easy things for them to fix and eat like microwaveable items.
They have breakfast items from Jimmy Dean's Sausage egg on a biscuit, frozzen pan cakes and waffles to cook in a toaster to all kinds of easy good and nutritious frozen dinners that only need heated in the microwave.
There are also easy things like soup and Crackers for a meal.
Easy snacks like Apleasure, Instant Oatmeal, Yogurt, breakfast bars. Ect.
Bup 1/2 gal drinks like milk and juice to make it easier for them to handle or by the individual single drinks.
The deli even has baked beans, potato Salad, baked chicken ect that one can eat.
They can even order out food once a week as a treat.
Besides the cameras being installed, set up bars in their bathroom so they can go to the toilet and take a bath/shower easier.
Hire a cleaning service to come once or every other week.
Bit a few easy clothing for them to wear if they're having problems getting dressed.
Forget all the button up clothes. Go for pull overs a size a little larger than they normally wear to make it easier to put on or clothes that zip or pants that only have elastic waist.
It's not hard to find an older Caregiver if that's what your Grandparents feel more comfortable with, just tell the Service.
You might also check with your Grandparents and see what they think about having a Live In which would require a bedroom for them but that person would take care of the house, meals and look after them.
Please let your Grandparents live their remaining life however they want, even if you think it's not the way you think it should be. After all, It is in fact their life not yours.
I would rather be free snd make my own choices than put somewhere and do what everyone else says to do as that sounds like being in prison to me.
Prayers
6 bed, are more conscientious and intimate, cozy than the larger facilities.
Having 2 staff to care for 6 residents 24/7, vs 1 staff to 10? residents is simple math. This is an option available in most communities, pre-Covid.
Start with a trip to a lawyer with your grandparents that specializes in family law, or better yet elder law. If you can get your grandparents to name you as their advocate for medical power of attorney and financial power of attorney. Make sure that each has a will written. Talk to them about advanced directives (whether to take heroic measures or not) and get a document for this as well for each grandparent. Then, you will be legally covered to act in their best interest.
After you have these legal documents, get your grandparents to their doctor. Sometimes, seniors are more willing to listen to an authority, like the doctor, telling them that there needs to be changes. Write down a list of problems each grandparent has and the resources to meet their challenges (basically that you are the only source of help) Ask the doctor to evaluate each for mental competence. He/She can "order" that this arrangement needs to change. My grandmother needed to hear that my grandfather needed to go to a residential facility rather than caring for him at home. I am fairly positive that the doctor will do the same in your situation.
When one is deemed mentally incompetent, you make invoke the powers of attorney for that person. You can then make arrangements for their care even if they are fearful or argumentative. Getting extra care can take several forms:
home health care aides when you are not there, sitters in the evenings when you need to sleep if grandparents tend to be "up" at night, assisted/senior living apartments that phase to total care when necessary, and full care residential facilities. It seems you are leaning in the direction of residential facilities, especially since your grandmother appears to need memory care placement. Find a place where they can be together and avoid calling it a nursing home.
If the court decides it’s appropriate to award guardianship, you can take whatever steps you must to ensure their safety. This doesn’t mean trample on their preferences...if they want to be at home, and the support is available, arrange that and pay for it with their money. If they have to go to a nursing home they will have to spend all their savings anyway, so there’s no point trying to save money. Some parents fight this because they want to leave an inheritance, but their own well being is more important. If they can’t be maintained at home, and there is a safe AL option, you will be able to arrange it.
The judge will order regular accounting and updates. You will need to retain your good elder law attorney. The fees for the attorney, home care, etc, can be paid from your parents’ assets but you must keep good records. Be prepared for your parents to contradict you in court and to sound very convincing. Be prepared for siblings to contradict you in court out of fear of losing inheritance or access to your parents’ money. Take many videos and document everything in advance,
This is truly a last resort, and if your parents are able to stay home, and can manage it - even if it seems a low quality of life - that’s their right. They have the right to make their own decisions, but they don’t have the right to demand support from anyone. If one of their lives is really endangered by living without help, it’s time for a hard look.
It might be better to present a few alternatives instead of an open question. “Please agree to AL” is too open ended and too easy to reject. Try “We haven’t been able to find caregivers that meet the standards. Your choices are AL, in which case I will help you find the best place, or take whatever caregivers we can find. Having me continue to be responsible is not an option. Which is it going to be?” Maybe they will come up with something. Maybe you can insist on video check-ins, having them show the med containers, food eaten, etc.
My parents and aunt at first were very opposed to someone in their home. We placed a lockbox on the door so the caregivers could come and go.
Give them an option of starting with home care or moving to AL.
In Jacksonville, Fl we used Concierage Care and were very satisfied.
My relative still gets away with this a lot too. A mixture of denial & lack of insight.
'I do all my own shopping & cooking myself'. A nurse will buy that over a quick chat but more thorough needs assessment questioning revealed 'shopping' actually meant just eating the food 😆. Family actually shopped, paid & put away the groceries. 'Cooking' was actually a toasted sandwich & microwave reheats.
Her situation was relabeled 'indepenant' to 'dependant' very quickly.
I would suggest getting a needs assessment done to see what care is required compared to what is available. Is it going to be enough? A social worker experienced with geriatrics would be a good resource.
The usual place to start is with home help.
My relative DOES have a few mature aides, who have become like good friends, this is a huge plus. But the negative is this set up requires a lot of management. Set days & times are good but there are many extras needed too, eg extra support for illness, at appointments plus if late/cancellations, fill-ins are required or she goes without. Calls, unmet needs, it's far from perfect.
When dementia is involved, this can be harder - starting with not opening the door to let the aide in. So sometimes this option doesn't even get started.
I've seen success with continuum care places where couples either share a room, or, if the memory issues are becoming too hard, one partner is in a memory care room & the other in an assisted living room. They may meet up for the whole day, or part day. I would support this option for my own folks so they can spend time together but also get a break from each other's needs (especially memory/behavioural issues).
It might be a wonderful opportunity to have frank chat with your Grandparents about what they want, what they value. And what they would sacrifice or compromise on? Is staying together the most important thing? (So together in AL an acceptableoutcome?) Or staying in their own home, even if this is with aides/strangers. Would one want to stay in the home if the other has a health crises & is hospitalized/unable to return home?
Good luck finding the path forward. There may be no *right* path, but roads that change direction as the needs change.
You may want to talk to a lawyer well versed in Medicaid. Lets say Gma needs to be placed but you feel u can still care for Gpa. He will become the Community Spouse. Their assets split with hers being spent down then applying for Medicaid, He gets to stay in the home and have a car and is given enough money to live on. There's more to this, but this is basic.
When you were 16 and wanted to go on a date and stay out late and mom and dad said "no" and you got all upset and stomped your foot and said "you never let me do anything...I hate you!" did they give in?
Most of the "no's" in your life were for your best interests, to keep you safe. Not because they wanted you to have a miserable life, not because they hated you, but because they loved you and part of life is hearing "NO" once in a while.
Time to stop letting grandma and grandpa throw temper tantrums.
Time to make sure they are safe.
The 2 options I see are :
They accept help IN THEIR home
The transition to Assisted Living or possibly Memory Care. (it sounds like they would both be better in MC than AL due to the level of care both need, and they would not have to be separated)
This is their choice. They can choose one or the other.
Do you have POA?
Are they both "competent" if not do they need a Guardian?
Are there other family members that you can talk to about this?
Apparently, there are no other family members suitable or available to help OP "willpower".
One received Medicaid in home services and was told it was a special program for seniors that they all get to help with cleaning and cooking. The other got a bath aide for an hour 2 days a week through a different program.
So who controls the finances? Can they hire a "maid" service?