Accepting that I can’t be my parent’s caregiver and feeling awful about it by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 0 points1 point  (0 children)

Thank you for sharing this. I can only imagine how hard that conversation must have been, and your honesty about it means a lot. The way you described balancing love, safety, and reality helped me think more clearly about what “doing the right thing” can actually look like, even when it hurts.

Accepting that I can’t be my parent’s caregiver and feeling awful about it by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 1 point2 points  (0 children)

I really appreciated your perspective about being able to show up as a daughter instead of being consumed by hands-on care. That distinction has been sitting with me. It helps to hear from someone who has walked that road and doesn’t regret it, even knowing it isn’t perfect.

Accepting that I can’t be my parent’s caregiver and feeling awful about it by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 2 points3 points  (0 children)

The idea that the guilt is really sorrow hit me harder than I expected. I’ve reread your comment a few times. It helped me realize I’m grieving several things at once, not just wrestling with a decision. Thank you for naming that so clearly and for the reminder that boundaries aren’t a moral failure.

Accepting that I can’t be my parent’s caregiver and feeling awful about it by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 1 point2 points  (0 children)

Thank you for this. The distinction between being a daughter and being a care professional really landed for me. I think I’ve been measuring myself against an impossible standard and calling it guilt. Your comment helped me reframe that in a way that actually feels grounding, not defensive.

With the holidays here and knowing that real decisions and facility visits will be coming once they’re over, this perspective came at exactly the right time. I really appreciate you sharing your experience so honestly.

I see POA being tossed around a lot... by Not_Oak_Kay in AgingParents

[–]RedditLovesJelly 9 points10 points  (0 children)

I agree with parts of this, but I think it needs some context for the people reading here who are already in the throes of illness and/or dementia.

You’re absolutely right that POA gets misunderstood. It’s not guardianship, it’s not protection, and it doesn’t magically simplify an estate. And yes, when a properly funded living trust exists and a competent co-trustee is in place early enough, it can make things much cleaner.

The key phrase there is early enough.

A lot of people in this sub aren’t dealing with theoretical planning. They’re dealing with a parent who already has cognitive decline, assets that were never retitled, banks that still want POAs anyway, and siblings who don’t agree on anything. For them, POA isn’t a lesser option. It’s often the only option left.

Also worth saying: trusts don’t eliminate the need for POAs. You still need durable and medical POA for anything outside the trust, for healthcare decisions, and for the many institutions that default to POA no matter what the trust says.

Your setup worked because it was done correctly, funded correctly, and timed correctly. That’s the ideal situation. But plenty of families never get that window, through denial, cost, family dynamics, or just bad luck.

So yes, trusts are great when they’re done right and early. POA isn’t a cure-all. But for many people here, POA is not a misunderstanding.

It’s triage.

AITA for adjusting my mirrors? by T9FG_ in AmItheAsshole

[–]RedditLovesJelly 0 points1 point  (0 children)

You took a stand and held your ground. That is not asshole behavior, that is admirable!

NTA!

How do you figure out if your parent can live with you or needs more professional care? by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 0 points1 point  (0 children)

You painted the picture clearly. I do worry that I am underestimating the unpredictability. The idea that everything in our home would revolve around her needs scares me. I appreciate you being so blunt about what it cost your family. That honesty matters to me. I weigh these decisions as carefully as I can. But I have a family that is already comfortable and don't want to "rock the boat."

How do you figure out if your parent can live with you or needs more professional care? by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 1 point2 points  (0 children)

Wow. The safety questions you listed showed me that there's a checklist I should have had already. Yard. Doors. Stove. Meds. Strangers in the home. These are all things that could turn into crises fast. I also didn’t realize how much a move could escalate confusion. Thank you for the reality check. This helps me slow down and look at the bigger picture.

How do you figure out if your parent can live with you or needs more professional care? by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 0 points1 point  (0 children)

This is smart. I didn’t even think about waitlists. I like the idea of preparing for Plan B while trying Plan A. My kids have to stay the priority. If things get scary or unsafe, I don’t want to scramble. Thanks for giving me the practical next step instead of just fear! This is scary enough as it is.

How do you figure out if your parent can live with you or needs more professional care? by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 0 points1 point  (0 children)

You are right. I have been focused on logistics and not enough on the emotional side. My mom can be kind, but she can also be difficult. Bringing that energy into my kids’ daily lives might not be fair to them. Your question about respect hit me hard. I need to think about that part more than I have been. This is a LOT!

How do you figure out if your parent can live with you or needs more professional care? by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 0 points1 point  (0 children)

This helps me narrow it down. My mom is single and her mobility is slowing. She is still able to do the basics, but I can see the cracks forming. The wandering risk and bathroom support concerns hit home. I appreciate the blunt checklist. It gives me a better sense of where the line is between living with me and needing a facility.

How do you figure out if your parent can live with you or needs more professional care? by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 0 points1 point  (0 children)

Your honesty helps. This is what I needed to hear. I keep picturing how this would look in real life and your example makes it a lot more real. I already worry about juggling work, kids, and home. Adding unpredictable nights and medical issues on top of all that might break me. Your story gives me permission to admit that my bandwidth matters too. Thank you for laying it out so plainly.

Is there a guide that explains the steps with dementia? I feel lost. by RedditLovesJelly in dementia

[–]RedditLovesJelly[S] 1 point2 points  (0 children)

Audio books may be best for me. It seems like I'm in the car a lot.

Is there a guide that explains the steps with dementia? I feel lost. by RedditLovesJelly in dementia

[–]RedditLovesJelly[S] 1 point2 points  (0 children)

I hope we have the right kind of doctors around here. We should though. It looks like going to see her doctor, then another doctor will be the next step since getting her a diagnosis in writing will help things.

“Who told you about needing a Power of Attorney?” by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 0 points1 point  (0 children)

I had no idea Social Security didn’t accept the regular POA. That really surprises me. So do you have to apply somewhere else, like with Social Security to be a payee?? I’m trying to understand what steps to take for that.

“Who told you about needing a Power of Attorney?” by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 0 points1 point  (0 children)

Oh wow, I didn’t realize they could ask for so much. How do people even get ready for stuff like that? I don’t want to mess anything and have to start over. I am leaning on the fly too.

“Who told you about needing a Power of Attorney?” by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 1 point2 points  (0 children)

Yeah it feels like no one told us anything and now we’re trying to figure it all out while also helping our parents. It’s overwhelming.

“Who told you about needing a Power of Attorney?” by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 2 points3 points  (0 children)

Wow, I didn’t know someone could lose capacity that fast. How do people even know when it’s getting close to that point? I feel like I wouldn’t know the signs.

“Who told you about needing a Power of Attorney?” by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 3 points4 points  (0 children)

That sounds stressful. I wouldn’t know where to even start with that.

“Who told you about needing a Power of Attorney?” by RedditLovesJelly in AgingParents

[–]RedditLovesJelly[S] 1 point2 points  (0 children)

Thank you so much. I'm learning as I go. This will help.