They have POA set up and no heroic directives in place. I am grateful as their daughter for this as well as their financial pieces in place. Here’s what is missing… we never talked about what it really means to ‘stay in your own home’ . It sounds dandy and doable until you’re in the depths of declining physical, emotional and brain health and them desperately trying to hold on to control and independence. My mom’s decline is significant, my dad doing all for both but mom calling the shots. So hard to be a bystander. Neither my sister or I live nearby. I’m not sure if we could have made a further plan, but here we are. The private home helper we’ve waited for to become available is now available. My mother’s pushback and confusion is enough to make moving forward difficult. Do we take control? Do we put our foot down? Do we continue to let things happen as they may??
Who has been here and how did you manage? Thank you.
Many people love the idea of aging in place, but never really assess if they have the resources to make this a reality. If it is only a matter of your mom's care, then you have a couple of options: privately paid aide, home health care aide through an agency, and volunteers of qualified family/friends/members of faith community. Usually the paid staff will need to be paid from your parents resources unless they have long term care insurance (few folks do since it is very expensive). If your father becomes overwhelmed, you can also consider day programs that are usually Monday through Friday during business hours to care for your mom and give your dad a break. Please also consider services that help take tasks off of your father - housecleaning, lawn service, grocery shopping/delivery services...
Does she pass urine when she is gotten up to the toilet most every time? If yes, ask her MD to work up for UTI, and consider urologist evaluation.
This behavior can be anxiety based - fear of having an accident or smelling bad. Can you sometimes distract her with TLC and diverting her attention to something pleasant?
Sometimes the need to void becomes the words used whenever there is discomfort somewhere in her body. (Like kids have a stomach ache when they are scared.) Is she acting like she is uncomfortable? Does she need to have a BM? Does she need to change position?
Or this just may be the way agitation shows itself in her. A low dose of antidepressant (trazodone and mirtazapine are well tolerated by elders) or a low dose of quetiapine (an antipsychotic and the only one of that class that is supported by research for use in dementia) or a mood stabilizer (such as divalproex) can all help to adjust the brain to decrease the agitation that is driving her behavior.
These meds are not always helpful and antipsychotics have a very bad reputation. Treating agitation in patients with dementia is an art as well as a science..we dont know enough about what is happening in her brain as the disease progresses.
See if there is some way to reduce her distress....at home....partly to prepare for move to a care home setting.
It's a hard job, caring for your partner with this disease. Support groups and social workers can help...ask your MD for referrals.
Take good care .
Your dad is going to have to speak up for himself. He will only be able to make that tough decision if he knows you and your sister back him and will support him in the decision. Take him to look at care options for her or at least look into home health care to take some of the burden off of him. Maybe they come in to bathe her or to watch her for the day so he can get away. If her care is still too much, definitely look at nearby facilities. He can visit her as often as he likes!
When a person feels guilty about something they did, there's a reason.
For me, I believe moving an elder out of their home into a care facility should be last not first. An AL facility is different than an independent senior community. It's one thing to downsize into a smaller place that's easier to get around and maintain. No one is deprived of their liberty in an independent senior community. They are free to live as they wish and come and go as they please. That is not true in an AL facility. I've known and worked for many elders who were coping well enough in their original homes or in independent senior housing with some help coming in who were placed in care facilities against their will. Or seniors who had to go into the hospital for something or who were supposed to be temporarily receiving therapy in a rehab that never went home again and for no other reasons than they were an inconvenience to their family or there was an overly zealous nurse or social worker involved who wanted that company bonus.
Of course many elders do have to go into facility care because their needs cannot be met at home anymore.
I think it's wrong for someone to persuade a family into placing a senior into facility care before even trying the homecare option or live-in caregivers. Sure sometimes it doesn't work out and a care facility is the only other option. Try it anyway though. Everyone's "independent days" are numbered.
I hope I never have a friend like AnnReid. A friend that will persuade my family to deprive me of my home and liberty by dumping my a$$ in a care facility as the first and only care plan.
If you let things happen as they may, then the decisions get made FOR you by hospitals and rehabs. Elders who are either mentally or physically incompetent are not permitted to live alone or w/o full time caregivers helping them out at home.
Whatever you decide to do, no judgement here. Wishing you the best of luck with trying to do the right thing and getting judged for it, no matter WHAT
I said...no, I will have to be an adult, be watchful and proactive in assessing my abilities to stay in my home independently when I'm your age. I don't have children or close relatives so that means I'm completely on my own and will have to make an adult decision. If I can't drive etc etc....I won't be living in my own home but will have to move into a more appropriate situation.
Sometimes the truth hurts mother.
Unfortunately, if he doesn't initiate a change time/fate will intervene and an event will force a change at no one's convenience.
Is dad showing some cognitive changes himself?
the inevitable happenws and they wer both in the hospital at the same rime.
the begged to move to assisted living at that point and have been fone. My Dad passed at the end of September but Mom is stable
Unfortunately this is the way they eventually get the wakeup call when they are stubborn
My dad needed a sitter while he was in rehab and he loved this lady so much she transitioned to his home when he was discharged.
Dad passed and now almost 2 yrs later mom still has the same part time evening sitter.
We also have a part time morning sitter two days a week. Sister and I take a day or two each week as we can. For now it is perfect.
Many chores are done online like banking, med refills and grocery delivery. Other supplies come via Amazon.
Mom has a visiting physician and we have just started palliative care as another layer of support.
ASL paperwork is done should we need to move her.
OK I said. What are your options? Dye them? "no" Learn to love em? "no way!" Pluck? "spose so.."
So when you have plucked bald patches from the sides & top of your head, I suppose if you don't like that look you can re-evaluate 😂
(She now dyes her hair).
I see aging, downsizing, needing help, needing help from strangers as a similar process.
https://www.mycareprints.com/elderly-products-review/wireless-led-lights