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This forum and many of the folks on it have been SO helpful in offering their own experiential insight as I posted about an escalating situation that my sister and I (37 and 34) have been dealing with, involving our aging parents (78 year old dad, 72 year old mom). Several of you have also urged me to share updates and in the hope that this might be helpful for people treading similar waters, here's the latest:

Short-ish background. Our dad was diagnosed with mild cognitive impairment in 2022. It mostly manifests as speech troubles and impulsivity. It has progressed, but he is still firmly in MCI territory. (His most recent neurology assessment was last week and I went to it with my parents, as I've done for the last few.) He gets frustrated by it sometimes but stays active and in good spirits. Our mom has struggled for a long time with untreated anxiety and depression, for which she has occasionally explored therapy and medication, without really committing to trying either for the long haul. Our dad's condition and looming questions about aging, such as needing to move to a more aging-suitable home, have made her mental health challenges much worse in recent years. My sister and I have tried to help them find a good place to move to, and we have encouraged our mom to avail herself of therapeutic and/or psychiatric support, which she has been vocally receptive to. But again, other than handful of therapy sessions here and there, she has never really followed through lastingly.

Three months ago, our dad slips on ice on the stairs up to their house and breaks his hip. A scenario my sister and I have feared. Surgery goes well, the inpatient rehab phase is tough but physically effective, but then the discharge to home happens and many of the issues we've dealt with pre-accident manifest again. Our mom feels burnt out as the sole caregiver but refuses to explore solutions that my sister and I research and put in front of our folks; such as respite care or in-home help. They have the money for either, just as they have the money to move to a good place that's better for aging. But our mom comes up with reasons why the solutions won't work, our dad doesn't push back (to mitigiate conflict between them), and my sister and I throw up our hands and give up.

I stepped back for a bit, to mentally recuperate, and by mid-May, once our dad was walking unassisted again and doing most of his usual things, the four of us all sat down with an eldercare consultant (my idea) to help us identify a plan for getting our folks into a better situation, while also underscoring the things my sister and I can do to help them, and where support from a friend, therapist, or medical provider would be more helpful. (Both of our parents have a habit of venting to my sister and I, which has forced us to draw harder boundaries.)

One thing I took on, which my parents had been meaning to do for years, was set up a meeting with an estate lawyer to finish up legal directives. (POA and such were set up in 2022.) The meeting went well and my folks agreed to follow up with the necessary financial documents to firm it up.

They have also stepped up their visits to new potential homes.

Another thing that happened around this time was that my dad had a near miss on the road, which triggered brewing concerns about his driving, and he has admirably decided to stop driving. My sister and I got him set up using Lyft and other ride services for times when he needs to go someplace and he doesn't want our mom to have to drive him. I also helped him get a new step-through bike. (His surgeon encouraged this.)

Our biggest challenge is still our mom's indecisiveness and mental health challenges, which negate our efforts to help our folks make decisions we can't make. We persuaded her to reconnect with a therapist she saw once and liked. But it took time to persuade her to make an appointment.

Overall, we have made progress. But I'm stepping back to recharge again.

You have made great strides as have your parents.
One of the moves they should consider is a move to a CCC (Continuing Care Community) This would enable mom to get help with dad in Assisted Living when she needs it but starting in Independent Living (if that is appropriate at this time) then as dad declines Memory Care if that becomes necessary.
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Reply to Grandma1954
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You are MUCH more successful than I have been. I was able to inch my parent forward with a few things - getting trust and estate documents updated given their spouse's declining state. For your family, if they have the finances, you might be able to "sell" them on how to best support your dad's possible cognitive decline in a dignified way: goal is to lessen the chance that he will be in a geriatric locked psych ward because her amazing care for him could precipitate a steep decline if she should get sick. My cautionary tale: my parent went to the hospital unexpectedly for two nights and that caused their spouse to go into a psychotic state (angry delusions, violent behavior where my parent had never seen any of that before - just thought their partner was getting a little "fuzzier" than before). Trying to make changes now before cognition gets "fuzzier" for your father can be a great way your mom can demonstrate her love for him as well as being a better way to stay strong for both their benefits. Helping parents through this is a "long con" - congratulate yourselves that you've gotten them to take some really smart decisions.
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Reply to CTSusan01
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It sounds like things are heading in a more positive direction. And it is an encouraging sign that your mother is willing to reconnect with her therapist. That is very important.

It is key to know when to step back. It's great that you realize that you will
have to be doing that from time to time.
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Reply to Hothouseflower
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Thank you for the update. I'm glad things are headed in a better direction.
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Reply to JustAnon
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Congratulations on taking care of yourselves and setting boundaries. Our family is in a similar situation with our sister and her husband ( 66 and 70), After 9 weeks in rehab she moved to assisted living . She just wants to go home so she doesn’t take advantage of the nursing help, food and activities at this lovely facility. It is so exhausting.
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Reply to Sister1956
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Thanks for the update!
I'm happy you are enforcing boundaries, while still remaining actively engaged with your parents. I'm sure your mother's lack of taking action is frustrating for you.

If you feel your parents are both open to making a change, especially to moving, but you are letting them take the lead on this, some people are just not good at taking action. They hem and haw, they make excuses, they procrastinate. For them, you could possibly take charge of this for them, even without activating POA status. If they are open to moving, and just don't want the trouble of making it happen, you and your sister take charge and make it happen.
Or Make virtual appointments for your mother with a therapist she likes, and remind her of the appointment times. Don't leave it to her if she doesn't follow through.

Of course, you don't need to do any of this! Choosing to step back and let them manage their life on their own is an admirable step for you to take if you need to preserve your mental energy.
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Reply to CaringWifeAZ
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Overall, this is an admirable and hopeful update. Kudos to you— also to your father for voluntarily giving up driving.
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Reply to Suzy23
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Good for you for stepping back and identifying boundaries. However, the one this I would still push for is the completion of their PoA paperwork. When my in-laws were falling apart, I had a stack of printouts that I'd take with me and discuss the importance of the PoA with them every time. They hemmed and hawed. Eventually, my MIL filled it out in a rehab facility during a family meeting with the staff and it was notarized right there. My SFIL never would fill it out and he eventually had to have a court-assigned guardian who then put him directly into a facility (which is where he needed to go with his Parkinsons and Lewy Body dementia and no money whatsoever).

I would download the paperwork for your parents' home state and go over there with a notary and tell them that if they don't take care of this one piece of very important business that you and your sister will simple keep reporting them to APS whenever they have a problem and will not accompany them to their next ER visit. Eventually they will also be assigned a court-appointed 3rd party guardian and then you and your sister will have no control and no insight into their management and care. If this truth doesn't budge them, then they may be well into cognitive impairment and guardianship may be something you and your sister would consider, if you wish. But there's only 1 other solution to no PoA and no family guardian and it's court-assigned guardianship.
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Reply to Geaton777
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What an interesting and encouraging update! I definitely admire your father for giving up driving without putting you all through a horrible struggle. I’m frankly not surprised your mom doesn’t want to commit to therapy for her issues. It is so hard to change!

Anyway, all in all this is great to read and I hope you’ll update us again. We learn from each other, for sure.
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Reply to SnoopyLove
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Thank you for the update. It will be valuable to others here navigating similar issues. I’m glad you have the wisdom to step back and take breaks from a stressful, frustrating situation. Seems like the time for the POA to kick in and make decisions in their best interests is drawing nearer. One day indecision and cognitive/mental health struggles won’t be able to rule anymore. I wish you peace
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Reply to Daughterof1930
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heinrich57 Jul 3, 2026
I think you’re right that we are approaching the juncture where POA will kick in. Whether we are months or years away from that happening is the unanswered question, but in the absence of our mom changing her mind about mental health support (and knowing that our dad’s condition is not going to reverse itself) I think it’s safe to be ready for this outcome.

My sister and I are not totally giving up on them. We will remind them that we are ready and willing to help them make any of these moves to improve their situation if they are willing to do their part too. But otherwise, we are stepping back from trying to save our parents from the consequences of their decisions, or lack thereof.

This doesn’t mean cutting them out. We will still create nice experiences that we can all share. (We’ve had good times amidst the hard times of late.) But it does mean that we aren’t going to engage with them about their anxieties and arguments about this stuff unless they’re willing to work with us to make tangible changes.
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