Do any of you have a live in caregiver in your parent's home?
My mom has been in memory care since spring, but I'm contemplating hiring a close friend who has been a caregiver for many years to live in my mom's home to take care of her. My mom is moderate severe in her dementia. She is able to feed herself, walk, and is still sociable. She is incontinent and is beginning to fall though. She fell in the spring and again this month. She was very sore, but no broken bones.
I'm not sure if this is a good idea because I know mom's dementia will get worse, but my sibling would prefer for her to be at home. My mother is doing a lot better physically and socially than her counterparts at memory care. It bothers me a little because she doesn't have anyone to talk with, but it doesn't seem to bother her. She keeps herself busy.
It also bothers me a little that the caregivers have too many people to take care of, the ratio is 1 to 6. It seems like they have to hurry to keep up with all the residents, and sometimes don't have time to change mom or get her teeth in. I have to go ahead of time to get her ready before any friends come to visit because she might not have her teeth in.
I wonder sometimes what my mom would have wanted for herself, and know she wouldn't want my sibling and I to be stressing. We both have young families. I'm afraid moving mom home might be more stressful to deal with bills, taxes, insurance, paperwork, moving, and what if it doesn't work and have to move her back to memory care again.
What do you think? Have you ever had to make the decision between selling your parents home, and moving to memory care, or keeping them at home and hiring a live in caregiver? If you have hired a private live in caregiver, who do you go to to do the paperwork? Or, would it be best to keep mom where she is in memory care so everything is already taken care of especially for when she progresses?
Thank you for any advice!
To be honest, since Mom is doing so well at the facility, I would hesitate to uproot her. Even though the care ratio is 1-6 ( which truthfully isn’t that bad), there is staff on duty all the time. Moving from place to place, even back to a familiar home, can be confusing and upsetting.
mom has been in memory care for 3 1/2 years - she is no longer mobile and while I would prefer she be comfortable at home, I know it isn't possible
wheelchair wouldn't fit
no way to shower her
caregivers get sick, have their own family emergencies etc
with dementia, things only get worse, so you will need a plan beyond just the near term especially around mobility and incontinance
6 to 1 is a very good ratio
i have private caregivers with mom in the facility
if mom has funds, maybe you can find someone to spend some time with her at the facility and provide those extra touches that staff can't
Live-in would become mom's employee. Taxes, Medicare, disability, all deductions would need to be paid for caregiver by mom. You would need a caregiver agreement prepared by an elder law attorney. You would need an accountant or payroll service to take care of salary. There is also consideration needed to labor law. Will caregiver be 24/7 or will there be three shifts of caregivers to provide breaks for the live-in?
If you were to use an agency, that would require three shifts of caregivers, 40 hours a week times three, 120 hours at $20.00 an hour or more. $2,400.00 a week plus expense of being in home with utilities, etc? Excess of $12,000.00 a month, easily.
Then a friendship that could be lost. Never hire a friend. She will not, necessarily, do things the way you want, then what? Or mom, with dementia, could decide she hates this woman. Leave mom where she is. 6:1 ratio is very good.
* No stairs
* Large bathroom for a wheelchair or other equipment? NO lip on the shower that she would have to step over or that you could not roll a shower chair into?
* No carpeting?
*No thresholds to get over going between rooms?
* Wide halls and wide doorways?
Just a few things to consider there are plenty others.
Are you ready to loose a friend?
How long will she work?
Who will care for your Mom when she is off? You can not expect someone to work 24/7/365 with no break.
You do not say how old your Mom is nor any other physical problems but this could go on for 5, 8, 10 years is your friend ready to commit to that? And are you willing to maintain the house for that length of time as well.
You will still have property taxes as well as all the household expenses (include added insurance for your friend in case she is injured, because she will get injured).
Personally I would leave her in Memory Care. She is with staff that is trained, she is in a facility that is set up for proper care.
If your friend wants to do something for you, and get paid, have her run all the errands you would have to do, bring Mom to the Dr, get any shopping done that she needs stop in for a visit on a few days you can't make it in.
Moving your mom back home is an unknown.....and to depend on 24/7 permanent private care is precarious at best. Also, with dementia being progressive, you would most probably need to move her back at some point. As MsMadge suggested.....hire a companion to visit with her a few days a week to ease whatever loneliness you think she might be experiencing. If that doesn't work, then nothing is lost....whereas a move would be an upheaval and could impact her dementia. Decisions concerning our LO's is not for the faint of heart.....best of luck with this one.
Please do not project your issues onto mom, nor your siblings preferences. This is about mom and her wellbeing, which sounds like she is being taken care of pretty good.
I would find out how her skin is doing if you believe they are leaving her in wet briefs. That can't be denied, our skin speaks for itself. Could it be a situation that she has gone after they changed her? Ask the DON to help you understand what the process is for dealing with wet ones.
There comes a time when it will take a village to care for a person, and with memory issues, that time will come quicker than you know it. Keep Mom where she is comfortable.
My Dad had around the clock caregivers, 3-full time shifts each day, that way each caregiver could have a good rest until her next day shift. But the cost was expensive, as in my area it was costing my Dad $20k per month. Eventually it was his decision to move to senior living and he was happy as a clam being there :)
You also have the benefit of the burden of care being spread out among many caregivers, in a good facility that means they are policing each other and picking up the slack when someone else is having a bad day or is ill, with a live in caregiver you place everything into a single pair of hands.
Then there is the whole headache of finding and keeping a good person, setting up contracts, withholding taxes, arranging alternate care for the caregiver's days off, vacations and sick days, as well as managing all the medical appointments, home maintenance, grocery shopping etc etc.
I guess you can already tell which would be my choice, leaving her where she is and working to improve any deficits you've identified would be a far better use of your time and resources.
I have to agree with your siblings. My 1 sibling lived with our Mom/stepfather for 10+ yrs. Even though I told her I'd help pay for respite help and some other things she would tell me Mom doesn't want strangers in her house. I was looking into in-home care even though my ugly step-sister took over without consulting me and expecting Mom to pay for it, the owner of the company FINALLY backed out and told ugly step-sister that in-home care CANNOT help with medications nor can they do anything but clean, take to appointments etc and are VERY WELL PAID BABYSITTERS.
Your friend CANNOT LEGALLY administer ANY MEDICATIONS EVEN ASPIRIN SPELLS LAW SUIT! IN-HOME-CARE CANNOT ADMINISTER EITHER.
My Mom/stepfather are in an assisted living group home. It was very very hard for about 2-3 months because they wanted to go home. We, the family and the caregivers tell my stepfather that Mom is very sick and the doctor will not let her go home yet. He says Oh that's right, I forgot. They now "call their suite home". Mom will tell a caregiver she's done eating (when she talks) she wants to go home, gets her walker, turns toward the hallway and goes "home". My stepfather has begun asking me if I'm his oldest daughter (UGH!) when I visit every month now.
This group home has Tuesday bingo day, a musician come from the manager's church for singing day, celebrate holidays, birthdays or just so something to surprise the residents. There is a resident who isn't there for mental issues, she's by her choice because she has to use a wheelchair, has fallen and her children live out of State like I do. The owner has 3 group homes, he as well has all of his employees are Romanian who fled Romania due to their Faith (Pentecostal, this is great as we were raised Pentecostal). They treat every resident as a family member. I asked why they took such great care of everyone, the answer OUR TRADITION WITH FAMILY IS YOU TAKE CARE OF YOUR FAMILY AS THEY AGE. It is the job of the YOUNGEST sibling to live with the parents EVEN AFTER THEY MARRY and take care of the grandparents/parents. The youngest receives the home as thanks for taking care of the grandparents/parents. The older siblings understand this are never angry about what the youngest receives for this family duty.
I never worry about Mom/stepfather being there. Mom's Alzheimers has become more aggressive in this past year and stepfather's Alzheimers/dementia is becoming worse also. Mom fell about 4 months ago, she got up from bed without pressing the button for help, so no one knew or how long she had been on the floor. She was fine after taking her to hospital and neither she nor stepfather remember it.
You can walk into this group home and EVERYONE is happy. There isn't that OMG hold your nose smell. What you do smell is delicious home cooking going on. The caregiver's parents come to US on a visa, Momma does the cooking, Pappa takes care of the property while they're visiting their children!! This is Romanian tradition at work.
I'm happy when I get a smile from Mom, a look on her face that I know she recognizes who I am or my favorite "what the hell are you doing here"? She tells me she loves me after I tell her I love her.
Memory Care is just an oxymoron.
No one can ever care for their memory, it's gone when it's gone and WE as their children have to accept it no matter how hard that is to do.
My Mom is just sleeping more and more now. Not as in needing hospice, just something that happens with Alzheimers which is different with every single person. Like snow flakes, no 2 are alike.
I hope this helps you and something to help discuss with your siblings too.
They can not if you hire through an agency.
If you hire privately and not through an agency you can instruct them to do anything that you can do.
I personally have not experienced that diagnosis and I have read here from many others that have been changing incontinence products for a great deal longer.
Very interested in where you get that.
A year ago I had to go home regarding Mom and other issues of which I was never made aware.
I took Mom to the Dr as she had not seen him for over a year, my sister lived with Mom/stepfather and she moved out without my knowledge!
I told the Dr after he explained her issues with me immediately she would stay in her home for as long as possible BECAUSE I PROMISED. My promise only lasted 1 month. Both Mom/stepfather have Alzheimers, keeping them in Mom's house was TOO DANGEROUSE FOR BOTH. There's a swimming pool 3-4 steps just outside the patio door. Front street is extremely busy with traffic and speeders. In-home-care babysitters cannot administer meds, cannot touch the bottles. What if either one of them "thought" they needed their meds or took the wrong one? Mom is also diabetic, in-home cannot inject her insulin. Stepfather gets lost, drives the car, has hit other vehicles; what if he killed someone doing this?
As the Dr told me, the children all have good intentions, but with our lives being as they are today; those intentions don't always work the we had hoped.
I don't know your age, but those of us from the baby boomer generation are facing these decisions more and more. It isn't we no longer love our parents or do not want to personally care for them, but we wish this day would never come as "our" life decisions have made caring for our parents more than difficult due to distance, jobs, time available as well as being guilt ridden because we don't want to make this decision.
The worse part of it is that gap in age between parent-child becomes less of a canyon to just a jump over a crack.
OUR day is coming closer and our children will be making this same decision for us.
My siblings and I followed our mom’s wishes. Several years, before being diagnosed with
dementia, she told us that she does not want us to take care of her in our homes. She knew it’s hard on marriages and family (she took care of grandma). Years forward, when the doctor/psychiatrist told us mom had dementia we put her in an assistant living facility with memory care. She complained but eventually adjusted in the Assistant Living side. The caregivers were marvelous. She made friends and enjoyed the outings. Mom has passed on. Not from the dementia but pancreatic cancer (we caught it to late).
Now I’m helping my husband with his parents. MIL has been-diagnosed with Alzheimer’s (2 years now). My FIL (1 year). We researched Assisted living facilities in our area but couldn’t put her in because my MIL was aggressive/combative with all who tried to help. She refused all medications. The Al facility told us they would accept them with a private caregiver for her. Way to expensive. We then researched home care. We now have 24/7 care for them. They hated it the first year but adjusting now. They wanted to know why there are people in their house, We just tell them Kaiser (their health insurance) said so or they have to be in a hospital. They accept care because “Kaiser” said.
I hope my experiences help you.
Stillhere1
We are struggling with same situation with my 88 yr mom. The 24/7 is running higher than or close to the assisted living in area of GA.
Mom wants neither but our stress, managing caregiving, changes in staffing and mom’s lack of social interaction — leads us to looking more closely at assisted living with memory care available as needs increase.
This forum is helping us to learn and to not feel alone or that we are being
uncaring when examining the best options for mom and her kids (all in our 60’s)!
What would an in home caregiver, one person, be able to offer your mother on a day to day basis, by comparison, and what would the cost be? When my cousin hired an in home caregiver for her father so he could stay in his own home, she wound up filling up suitcases with all of the valuables in his home and having a truck pull up front to load it all up. I'm sure that's not a standard story, but one of many nevertheless. I'm sure there are horror stories out there with facilities as well, so be sure to make your choice based on informed decisions. In my experience, I 100% believe that my mother is still alive at 92 BECAUSE she's been in Assisted Living and Memory Care vs. at home with me. The ALF caught her first bout of pneumonia immediately, had the in house doc prescribe antibiotics right away, and saved us a hospital trip and possible death from the #1 killer of the elderly. We've had many such instances where the ALF or the MC stepped in to ward off disaster.
Best of luck!
Talk to the Social worker over there. If there is one. Or get one. I agree mom is maaybe better off there right now, But there is alot Riding on her Finacial deal and there is much to consider. Dad is staying Home, My sister helps him and is His POA. He would have had to do a Spend time down the line to get Medicaid and didn't want to do this, Thank God he is doing okay.
God bless you and See what is Best, I agee though, She is probably bet left There for Better care.
Lots of people got there before me: hire this close friend to supplement the care your mother receives in the facility; but *don't* take her away from the safe, fully-staffed, fully-equipped environment she's doing so well in.
Even if you took your mother home and everything worked out well with the friend for the time being - and the friend has endless stamina, never needs a break and is in perfect health - you know that the time will come when one person cannot meet your mother's needs and you will have to get her readmitted to a facility. By that time your mother will not be functioning well enough to adjust, and it will mean another big change just as she's become completely unable to cope with it. And that is if everything goes *well*.
What's your brother's main reasoning? Is it financial, social, a bit of both?
A live in caretaker will probably not be able to hold up to 24/7 duties, so you're not going to be able to do it with only one person. Family members get strapped with 24/7 and accept what they can't do anything about, but a friend is not the same. You're going to need back up caregivers to allow for days off, vacations, illness, personal time away from the house. The other thing is, if this friend moves in and gives up her own residence and things don't work out, she's going to be looking for another home within a, possibly, short period of time. Not worth having issues destroy a friendship.
No situation is perfect, but in memory care, your Mom has the best care, access to staff, activities, drs come to see her(no getting in /out of the car!), PT, OT, etc..
With my Mom’s moderate/severe dementia, we know additional care will be on the horizon..We will bring in a part time private CNA, in due time..
Your love, & providing the best for Mom, is a Blessing..She “senses” that, even if her communicative skills decline..Prayers for you, Mom & the family🙏🏻❤️
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I agree with commenters who say staying at home with 1 person is a sterile environment. Unless your friend has prior experience, she may be shocked at how boring care taking can be.
Unless your friend has a medical certification, she can't (or shouldn't) be administering any medications to her, even pills. Does she even have any first aid training? What if she's not as good as you thought...then you're going to ruin a friendship letting her go. What happens when your friend is sick or goes on vacation? Who will tend to your mom then?
If I were you I'd have your mom in long term care where there are many eyeballs on her and they are trained and there are things they can do with her socially. I also agree with hiring a companion to hang out with her for a few hours on a few days per week. But it begs the question: if your mom doesn't remember that she was visited, is it of any benefit to spend the extra money and hire someone for this? Is it really for your own guilt? I've had this dilemma with my MIL. No short term memory. We visit her because we love her but she forgets we were ever there 5 minutes later and gets no other benefit from our visit..
Make sure the facility she is in also has hospice care so that she won't need to be moved when "that" time comes.
Good luck!