So a few weeks ago, spurred by a family emergency, I made the first of two posts here asking for advice. Several of you responded generously with very thoughtful words and insights, which I appreciated. I had hoped to be in a different place now. But alas, things have reached a difficult crux, which is the inspiration for this final post on the matter. For the time being, anyway. I'm going to lay it out in a manner that doesn't require reading the others.
For the last couple of years, my parents (both in their 70s) have been stuck in a rut caused by marriage issues and mental health challenges. They've lived in a house that's unsuitable for aging, with lots of stairs and physical upkeep work, and this causes them stress that they vent to me and my sister about. But no matter how many times we try to persuade them to move and downsize to a safer place, nothing comes of it. My mom, who has untreated depression and anxiety, comes up with reasons why moving wouldn't be feasible. My dad doesn't push back, in the interest of mitigating conflict between them. And my sister and I throw up our hand and continue to worry about their well-being.
A few weeks ago, one of the scenarios we've dreaded finally happened. Our dad slipped on the exterior stairs and broke his hip. I was the first responder who got them both to the hospital, where a successful partial hip replacement surgery was performed. He was in the hospital for a week, and then physical rehab for another 10 days. During this whole time, my mom acted as the main caregiver and barely took any time for herself to recharge, despite my sister and I urging her to do this, with offers to step in and help more. (We still did help a lot, in our own ways.) This past Friday, at both of my parents' request, the rehab center discharged our dad to home. The idea was that he would receive PT/OT there, and my parents would also hire in-home help so that my mom could finally get a more sustained breather and recuperate. We also discussed the possibility of a short term respite care stay at assisted living for my dad, if being home this soon yielded too many challenges and home help didn't seem like enough.
Five days later, the in-home help has still not been hired, the respite care option has basically been shot down (they have the money to afford either), and my mom is still overworking herself. When she's overwhelmed, which is often these days, it's near-impossible for her to make proactive decisions. My sister and I learned this from the downsizing impasse, and now we're seeing the same thing play out here, in the context of our dad's recovery. He's actually doing very well with recuperation in a physical sense, but the missing in-home help is creating unneccessary and preventable stress for everyone. I've made calls, done vetting, and put all of the pieces in front of my parents, and still, they have not taken the next step of setting up home care or reconsidering respite care. If I offer to set it up myself, my mom gets overwhelmed and pushes back. And at that point, all I can do is step back.
After our last conversation about this, which devolved into an argument, I am giving my parents one more afternoon/night to talk this over, reach a decision, and move forward; at their request. If they shift gears by tomorrow, great. And if they don't, which is likely, I don't know what else I can do but throw up my hands, tend to my own life more, and wait for time and hardship to humble them. If that ever happens. In a way, this would feel like partially cutting off my parents. It's not that I would stop speaking with them or helping them at all, but I would be far more discerning about what I'm willing to do for them, if they don't take actionable steps to help themselves, and what I won't do; the lines that I would refuse to cross. Like listening to their venting, or helping them with ill-advised home projects.
I love them. This is tough to do. But I don't know what else I can do now.
In this case it is normal to step back a bit and realize they have their own lives and they can run them as they see fit. Until something changes (like they have demonstrable dementia), unless they agree to do something you can't make them do it. So it's also a kind of protection for you, because while it's scary, worrying will change nothing for you or them. You have to try to not be on "high alert" all the time.
This is very frustrating, I know. It becomes this dance between you and your parents, where you have to see what you can do and what you can't, and they can give up a little here and there, or refuse to give in. You are trying to take over parts of their lives so they will be safer, and yet you can't do it without them agreeing in some way. They might be willing to do more in the future, depending on what happens to them. It was hard to figure out when to step in with my mom, and how to say everything, and to not make her feel bad or embarrassed etc.
Please do keep us updated because this situation is so central to everything else that happens to the people who come to this forum. What can we do when they won't let us?
There is a time in everyone's life that needs outweigh wants. When the person can't or won't realize is very difficult because their safety becomes compromised. Been there and will be there again as my dad is becoming less independent. If I had not found this forum I would be in a major depression from trying to support, prop and enable my parents and uncle.
Wishing you good luck and emotional strength throughout this journey.
He had one of Mom's caregivers drive to the ER to take him home.
I backed way off for 6 months.
A great example for others to read in a similar situation .
Often the only way they realize they can’t manage on their own is to be left to do things themselves .
A wise social worker told me “ Stop helping “.
I don't see anywhere in your post that you or anyone else is their PoA? Is this correct? If so, you will need to have a conversation with them about this problem. They need to know what happens to seniors who eventually need the help of a PoA but don't have one assigned: they run a very high risk of becoming the ward of a 3rd party court-assigned guardian who may not be a family member. And not just that final outcome but all the drama and exhaustion that happens leading up to that point.
I had to explain this to my SFIL when he was declining from Parkinsons and Lewy Body dementia: Plan A was to assign someone, anyone, as his PoA. Plan B was he didn't do this and become a ward of the county. He chose Plan B and had a bad time, but that's the plan he willingly chose. No pity for him as he had made our lives hell up to that point. But it was still a solution in the situation and we were glad to have it.
Once you express your boundaries clearly to your parents, you must be very consistent in defending them so that you don't confuse them. You may not be able to get your other siblings on board, and they may not like it but you should not get dragged along for that messy ride. You can only control your own self, so be clear about it. It doesn't mean you don't love your parents but we experienced caregivers can tell you that it will be very unproductive to do anything else and it will bring about a sustainable solution much sooner.
Step back and wait for The Call. In the meantime, don't be their fix-it guy anymore, reminding them of their choice to hire no help or move to a suitable place. Love ya mom and dad, but this is YOUR DECISION.
Best of luck and stay connected with us.
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