My husband passed a little over 2 weeks ago. He was only age 63, but had a myriad of chronic conditions that affected him both physically and cognitively. The last 10 months, in particular, were ... rough.
His 92-year-old father (FIL) is in "Independent" Living.
I'm still in shock over my husband's death, and miss him horribly. But life, and its necessities, go on.
My FIL has dementia. He can only move far enough to get himself in trouble. His delusions cause him to get into lots and lots of trouble.
My 2 SILs have taken to staying with him overnight, every night. Nobody's pressuring me ... but I feel I need to step up, too.
That said, the whole purpose of placement seems to have been defeated. And, to be candid ... my Inner Monster Brat does NOT want to sign up for more caregiving. My Inner Adult, however, wants me to get a grip. After all, this is not the full-time caregiving I'd been doing.
What would you do?
If your SIL's want to take turns staying with their father, I think you let them and don't feel like you need to participate. He is not independent obviously and should be in memory care. That will not kill him. What will kill him is. his progressing dementia and the things that brings. like bone-breaking falls, lack of adequate nutrition and overall failure to thrive. That will happen anywhere but you will not convince them. He literally could be moved to the memory care area of his facility and he will do as well (or as poorly) as he is doing now. But you probably won't convince them.
My inlaws finally moved to independent living in their 90's. They really needed to be in memory care but my FIL thought he was fine so we started with IL. My husband is POA and we lived in Illinois near the inlaws; my SIL's live in California. They also said that leaving their home of almost 70 years would kill them. SIL's wanted home care. Inlaws needed 24 hour supervision; they were ambulatory so having care givers in the house just would not have worked and I was not willing to supervise them. I told SIL's if they wanted to hire and agency and handle staffing from afar, they could do that. Of course, they did not want to do that.
So inlaws went to IL which went well for 2 months. Then he started to fail, and he ended up in hospital. We did get 24 care for her but only until we could get them both into memory care. MIL fell and broke her hip, which was only a matter of time until it happened, she would not use a walker. She died a year after moving from house and he died without 18 months of moving. Moving did not kill either of them. The falls, the confusion, the lack of eating, the incontinence and UTI's killed them. And that would have happened anyway.
Had my SIL's been here, my husband would have let them take over if they wanted to keep them at home but I would not have involved myself in that even though I am a retired nurse. As it was, I managed their care, took them to doctors until we began using the facility doctors, and handled all of their issues. We saw them weekly at least but my husband, their son, is alive and participated, although I still did more than he did. I probably would have done it anyway, since they were very nice people and great inlaws.
I say this story so you know that you don't have to feel like you need to participate in this. As you say, no one is pressuring you. So do only what you want to do with an eye to how you will feel afterward when FIL does die. If you value your relationship with your SIL's, then help them as you feel you can. But only if you want to.
I can tell you, though, that taking care of our father for three years before he passed from COPD and moving directly into taking care of mom with Alzheimer's for the next seven years changed my brother and me in ways we didn't anticipate.
Year 1 with mom was trial and error until we finally realized that she could not be left alone. She was never alone at night from the start. Years 2 - 6 my brother and I alternated mornings, evenings, and weekend days and took her to Adult Daycare during the week. Year 7 she needed to be at home as her condition was quite advanced which required hiring sitters during the day rather than taking her to Adult Daycare; my brother and I kept the same pattern.
If your FIL is in Independent Living even with delusions, he is likely in the early years. If you can describe his condition more specifically and what "getting into trouble" means, that would be helpful. It will also help to judge how long you would need to provide changing types of support. Mom went through each stage until she could no longer swallow in the final stage. This was the most accurate delineation of mom's progression, even down to timeframes, and it may be helpful for you if he suffers from ALZ.:
https://www.alzinfo.org/understand-alzheimers/clinical-stages-of-alzheimers/. If he suffers from another type of dementia, there are other guides out there.
Taking care of your FIL will probably feel like going back to work at the same job that robbed you of energy, hope and joy. Two weeks is also not enough time to process your loss. In retrospect, I went back to work way too soon after both dad and mom passed. Don't make my mistake. And don't feel guilty.
I know that you want to help, and you will, but there are other possible combinations that would not require you to be there every third night or to dive in immediately. That requirement will also morph into greater needs, and even three people alternating full time may not be enough, regardless of will or physical, emotional, or spiritual strength.
First, it would be good to start to work through your grief. I went to a hospice grief recovery group and the book we used was "The Grief Recovery Handbook" by John W. James and Russell Friedman. You can read the book and work through the exercises yourself, or see if there are groups in your area that offer this program. I went through Crossroads Hospice and it was excellent. It took me the full 10 weeks to even begin to process the loss and listening to and talking with others was helpful. My personal physician did not understand and felt that I shouldn't be taking that long to "get over it" and there will be others who may urge you to push past and ignore your feelings. Don't.
Second, I would recommend that you have a talk with your sisters-in-law about the reality you are all facing and come up with a plan. It might be time to move FIL into Assisted Living, which will afford you all some assistance and oversight. But if you read through the stages of dementia, you will see that more assistance than that will be needed at some point, and may even be needed now.
Third, you need to be honest with them about what you need to do for yourself, how they can help you, and what you all need to do for one another in this continued odyssey.
I can tell that you're a truly good soul in pain. Your feelings are your own and you need to protect your right to feel them, regardless of the internal messaging you may be giving yourself to "get over it" and "move on." You matter. You are important. And your loss is very real and very big. Don't downplay it, even to yourself.
Please take care of yourself.
My vote is along the lines of notgoodenough. If you feel up to helping, help the sisters. It seems to me from what you said, he needs more care, hard for children to process sometimes. So, my vote is don't keep bailing out a sinking boat. He needs to move to someplace where he can get more care.
I vote for taking care of yourself right now. Allow yourself the time to grieve the loss of your husband. I'm sure the SIL's have things under control or will figure things out. I'm sure they also more than understand your need to grieve.
Don't isolate yourself. Seek grief counseling. Practice self-care.
I know I take a long time to heal. One day you might even remarry. Or when covid is over you could go away pn a vacation. If you step in now that all might not be possible.
I'm Catholic, so I would talk to a priest and get into the grief support at my church and probably psychological counseling to help me work through it all.
Oh, I forgot, I would also cry. Alot.
Please allow yourself to just be human and feel. To cry, to be angry, to be lonely, to be relieved . I can't process those emotions as a caregiver, and I don't do much.
If they approach you for help, I give you permission to say "No, I now need a caregiver for myself."
God bless you. You will be fine. It will take time.
Of course not. That would be cruel.
In fact, I would say that that person will need care for a long time. And I would be right about that. God bless.
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Let yourself grieve before thinking about anything else.
Right now and for the foreseeable future you have the right to just grieve.
FIL passed away last night. My younger SIL was there, as was his 24/7 hospice nurse.
Many thanks to you all for helping me get through this time!
The last I'd heard, they'd adjusted his meds so that he was comfortable and peaceful. Hope he stayed that way until the end.
Before his passing, I asked SIL about UTI. She said the care team had discussed it, but ruled it out. Not sure what that meant as far as testing goes.