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Person with dementia needing constant reassurance

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How do you deal with a person with dementia who needs constant reassurance about things? My grandma doesn't come across like she has memory problems, but she can, and will, ask the same question every 5 minutes.

She is very anxious, she's always been an anxious person but increasingly has become even more so. She needs reassurance about certain things over and over and over again. She forgets she's asked you for reassurance about a thing and will ask for it over and over again. Once a worry is in her head, it takes days for her to forget about it. She has never has therapy or ever learned any way to manage her anxiety or her mood. She has always looked to others to reassure her.

She is very old and has no hobbies. She doesn't socialise anymore or like to leave the house.

The constant reassurance-seeking would try the patience of a saint and I'll be honest I usually either get annoyed with her or I'll lie and say I'm busy and I'll tell her later. I find there is no point in offering reassurance as she forgets it anyway.

Is there a better way to deal with this other than just cave and reassure her about the same thing a 100 times? I honestly find it very stressful. Her anxiety feels contagious.

I am not her caregiver but am currently visiting. She is like this with everyone; her caregiver, her doctor, her few remaining friends. She has been prescribed an antidepressant which she takes, but doesn't really understand that it is an antidepressant (if you ask her she would say she is perfectly healthy).

Checklist to help older couple in CA with financial decisions?

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I am looking for a checklist or guide to help an older couple (relatives of mine) make basic but crucial financial decisions. This couple lives in California and owns a small business there. One of them (A) is experiencing some cognitive decline, and the other (B) is trying to figure out how much longer they can keep their business afloat--and how much longer they *have* to keep their business afloat, as they have basically no savings. B wants some support in figuring out whether / when / how to shutter their business, and I want to be able to help them with those decisions, though I have very little financial / elder care knowledge myself.

These people are in their 80s and have been working 7 days a week with no break for over 30 years. I have always taken them at their word that they’ve needed to work that much to stay afloat, but I’d like to get a better understanding of what that means, and whether it’s necessary or even feasible. Because of various health issues, they’re probably within a few years of a major medical event forcing them to stop this type of work anyway. Would love to help them get in front of that if I can.

I know some appropriate steps would be: bring them to a financial planner and maybe an elder care specialist. But I am out of state, and to even figure out what sort of help they’d most benefit from, I’d love to find a guide we could go through together. A and B both are proud, mistrusting, and indirect at the best of times, and they tend to be unrealistic and irresponsible in the face of crisis. When other relatives and I have asked about their finances, we've never gotten anything like a clear picture—I’m hoping to maximize this this rare moment when they’ve asked for some help, and I feel like having a basic checklist would help with that.

When looking online for elderly/retirement financial planning, most of what I find is about long-term investment strategies, which is emphatically not where they’re at. I believe they’re close enough to crisis, foreclosure, and homelessness that a sunny site with the terms “nest egg” or “tee time” won’t be so useful.

Would love specific online or published checklist-type resources rather than general advice here—Calfornia-specific would be especially useful. Thank you.

Cataracts and the elderly

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You are not my relative's doctor nor her ophthalmologist, this will not constitute medical advice. But I could use your help thinking this through. My family member "Beatriz" is 80 years old, and has diabetes and hypertension. She has astigmatism (worse in left eye) and cataracts (worse in right eye). She was told she needed cataract removal two years ago, and delayed treatment. During the most recent consult, the right eye had deteriorated further. She likes this ophthalmologist, and he's done thousands of surgeries.

Medicare covers standard removal and mono lens insertion. Beatriz agreed to pay $1,800 out of pocket (per eye) to cover laser removal, which was recommended due to her pre-existing conditions. Other specialists (endocrinologist, primary care physician) also said the laser technique was the better choice. The left eye procedure, which is expected to be less difficult, is scheduled for later this month, and the right eye procedure is next month.

Now the ophthalmologist is recommending a toric lens (an Alcon AcrySof IQ, per brochure attached to surgical coordinator's email) for the left eye, to correct the astigmatism. (The right eye would need a corrective lens, too.) These lenses would be discounted. Per the email, "Most patients will still need glasses for reading but not for the distance."

Per eye, Beatriz's options are:

Standard cataract surgery with an astigmatism lens for $1,800

Laser cataract surgery with an astigmatism lens for $2,500

I want Beatriz to heal as well as possible. I hope a toric lens might reduce overall fall risk. Beatriz was already annoyed about the laser technique cost, is reliably suspicious of newer technology and last-minute upsells, and will likely argue that her age makes the additional $1,400 for both eyes (thus making $3,600 into 5K overall out of pocket) a waste of money.

Is healing/adjusting post toric lens much different from the mono lens? Are there known issues with the AcrySof IQ? How significant are age and medical conditions in this process? Should I not even mention the toric lens rec, because she needs glasses for distance -- so, for driving, and the family is already trying to get her give that up? Any insight would really help, I have to present the new info midweek. Thanks so much.

Pacemaker in elderly person with dementia

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My dad was given a pacemaker, unfortunately he has dementia so doesn’t understand what’s happened. Any advice on helping him through recovery? Bradycardia (34-39), previously diagnosed a-fib, shortness of breath and fatigue led to this. I took him to the ER last Friday, he’s been here in the hospital since then, and had the procedure yesterday. Apparently he also now has mild heart failure.

He doesn’t know he had a procedure or why things hurt. He can’t remember not to fiddle with the wound or to avoid raising his head. Until tonight, they had a sitter with him.

(A nurse decided that a hesitant positive response to a single heavily leading question excluded confusion in an 89 y/o with baseline dementia on two kinds of painkillers… so the sitter who was going to be here was cancelled. Anyway.)

Recovery should take 6 weeks. The device is under the muscle to prevent him fiddling with or being confused by it. Doctor couldn’t say how long healing time might be exactly.

Usually he lives alone with support workers coming 3 x a day. Walks comfortably around his neighborhood. We have a camera and a GPS. I see him 3-4 times a week and he spends a few other days with very close friends who look after him well. Not going to cut it.

Either 1) I live with him for the six weeks, with occasional relief from family friends, or 2) he stays in a transitional care unit in town where he won’t have 1:1 support, will have wound cleaning, meals and meds. At home he’d have the same through home support but would be totally alone at least some of the time. I have things to do and one other person to care for who isn’t well (multiple organs going wrong, not urgently dire but needs care and advocacy because the GP is uh, whatever he needs advocacy). But I don’t know, maybe I can manage.

So far (day 2 after surgery) I’ve noticed his breathing is a little laboured and his shoulder jerked up twice. Will ask doc about this tomorrow morning.

He needs to be reminded to not raise his arm, a sling will help but obviously that won’t do it. Site needs to be checked daily for infection (and so does he for systemic signs). Exercises to avoid frozen shoulder.

I understand there’s a trade off between pain control and cognition, however it’s very hard to see your now-vulnerable dad you love cry and not know what happened to him.

He can’t wear t shirts obviously. Needs an updated medic alert bracelet. He will definitely lose the card with device information, I’ll have to sew something into his clothes.

What else do I need to be thinking about? Very anxious.

How to ensure a happy old age

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Older Mefites enjoying a happy, healthy older age, please share your secrets with me. I'm taking care of two elderly, sick relatives currently (ages: 67 and 88) and the whole question of health is weighing on my mind. They have diabetes, congestive heart failure, kidney disease and dementia.

It's gotten me thinking about my future, and what is in my power to ensure that I don't have the same issues at their age (should I reach it), as unlike them, I do not have younger relatives to take care of me.

I realise I don't have much control over this. But I want to think I may have a little, if I can make the right choices? So I was hoping to hear from older Mefites who are healthy and enjoying their lives, to hear about the choices you made to get to where you are.

Info about me:

I'm 40. Overweight. As far as I know, I am healthy. (Touch wood.) I do not smoke, do any drugs, I drink vanishingly rarely. I am very sociable but I am single and I feel lonely a lot. I am a very busy person, both with work and other commitments. I have a rewarding creative practice. I love eating. When I am happy, I overeat. When I am stressed, I can't eat at all. I TRY to cultivate a regular exercise regime. Some months are better than others. I am very conscious of my mental health and I try to educate myself, take responsibility, do the right things for myself; but in practice it is a constant struggle to do things like take time out for myself, not work myself to the ground, get enough sleep, eat when I am stressed out, etc. But again. The best I can say is that I try. All the time.

I have a lot of anxiety about doctors so I avoid them like the plague, if you will. I'm trying to get over that.

Helping an elderly friend with one working arm

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An elderly friend has a broken arm. We'd like to drop off hot meals for her but she'd struggle to open a traditional thermos. Can you recommend a way of keeping food hot that's easy to open with one hand? More broadly, how can we improve the life of an elderly person with a broken arm? A few additional details:

• We are part of a group of people who are coming together to help her. All of us know her but none of us are her close relatives or best friends. It's not possible for any of us to move in with her or spend huge amounts of money.

• She welcomes our help and she'll tell us about anything that she knows she needs. But this is a new experience for her as well as us so we welcome suggestions of things we could propose to her.

• She does not have a microwave.

• She lives on her own and is used to being independent.

• She does not have much disposable income. Her home is small and rather full of stuff, and there probably isn't room for many additional objects. (Some of us are helping her declutter but that is probably a long-term project for a variety of reasons.)

• Everybody involved lives in the London area.

Echo device for relative with Alzheimer’s

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I’ve never used an Alexa/Amazon Echo device, so I don’t even know what they’re good at. Which of the countless devices out there would be most useful for my relative? She has very poor eyesight as well as memory problems and dementia. My relative is in her late 80s, but more relevant here is the Alzheimer’s or whatever else is going on. She can barely use a phone to call me; she can’t check voice mail. Between vision and memory problems, she can’t use email anymore. And dementia is playing such tricks on her mind that she no longer enjoys watching TV anymore (her brain tells her she’s seen everything before).

She hasn’t been able to use voice commands on her phone very well due to hesitation and her tendency to use full sentences that Google simply can’t understand. (“OK Google…would you please call my granddaughter Mary now?”)

So I don’t know if Alexa would be an improvement at all in that respect.

She does not shop at Amazon so that’s not a useful feature for her.

It would be helpful if she could use it to find out the date, day of the week, time, and whether it’s morning or evening, as she’s often confused about these things.

She might like listening to music (if she says “Alexa, play ‘Staying Alive’” will anything happen without a Google Play subscription?).

I don’t know if there are other entertainment options that might be useful for her. She is kind of starved for entertainment.

I heard about the “Drop In” feature, which might be useful? How easy would it be on her end?

Is there any way for me to access the device if it needs updating? (I don’t live nearby, so if it requires being on the same network, I’m out of luck.)

What could she use it for without additional subscriptions?

Any specific recommendations? I can’t imagine she’d be facing it all that often, but would one with a larger screen be useful? (or is a screen pointless for anything other than Drop In?)

Sorry for the scattershot question.

Recliner covers for 70yo incontinent woman?

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My mom just spent more money than she can really spare to get a La-Z-Boy Pinnacle rocking recliner. She is incontinent. I am worried the recliner will be ruined and she will be unable to afford a replacement. Snowflakes inside. She is about 5'3" and 225 pounds. She has scoliosis. She requires a walker. She is in assisted living.

She has already placed an incontinence pad (don't know what kind) on the chair seat, but is worried about sweating on the chair back during summer months.

I am in a different state and will not be able to help install anything, at least not immediately. It's okay if I have something shipped there and it sits a couple months before I can install it, though.

Attend big family event or stay with dying dog

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Should my wife and I travel to attend my nephew’s coming of age ceremony or stay with our long time dying dog? My wife and I are supposed to travel cross country to attend my nephew’s “becoming a man” ceremony in a few weeks. If u know about the Jewish religion you know what it is. My dog who is 13 doesn’t have long to live. Both my wife and I planned to go and be gone 6 days. We have a pet sitter scheduled to stay with the dog. One important note here…my elderly parents are attending the ceremony and my sibling wants me there to look after our parents since my sibling needs to be focused on her son and the event so I’m in charge of our parents….reason being is that one has Alzheimer’s and the other is overwhelmed with looking after the sick one.

I’ve had this dog since he was 7 months old. It’s hard to even fathom not being there to say goodbye. It’s very possible he could pass away soon. Possibly Weeks…maybe a couple months. So I’m really feeling anxious about leaving him. But…my sister is really applying pressure for me to come because of my parent’s situation. One option is to have my wife stay back with the dog since this is my family. At least if he passed she’d be with him. But still I’m waaay closer to the dog then my wife…if my dog were to pass while I’m gone that would be rough. Should both my wife and I go and risk it with the pet sitter? Should my wife stay back? Should we both stay back to be with the dog? In some ways I feel like I’m being asked to put my human family before my dog. Rough situation to be in. Any thoughts here are appreciated.

Personal experiences with Alzheimer's/dementia clock?

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I'm looking for a clock for an elderly relative with dementia (probably Alzheimer's) and vision problems. It needs to 1. plug in 2. have battery backup 3. have very large and clear text. 4. spell out the day of the week 5. display the time of day (e.g. morning, night) 6. automagically update for DST. I'd prefer backlit LCD or e-ink for improved viewing angles, but I'll take what I can get. Does not need to speak, have lots of settings, have color, or be atomic.

Reviews online are hard to trust. There are a million products from nonsensically-named manufacturers with thousands of sketchy positive reviews, huge markups, and it's just frustrating. So I would really like to hear from you if you've actually given one to a relative, worked in a facility where someone used one of these clocks, or otherwise had experience with one.

Taxes, elderly parents edition

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My parents are struggling to do their taxes, and I am struggling to help them during visits and at a distance. One of my parents, who is (and has always been) a slow, methodical person, has historically been responsible for most of the family finances. This parent has a progressive condition that causes memory issues, and they are now struggling to complete paperwork (lose track of what they are doing partway through). But, they are also resistant to change and are not comfortable with financial forms that they haven't personally verified. One thing is that my parents' tax accountant sends them a program into which they are supposed to enter all their tax forms. I have worked with a couple of tax people, and I think I've always sent them my forms and they enter the numbers into their software themselves.

So, questions:
1. Is it normal for a tax accountant to operate this way (and what are you paying for then?)

2. If I want to help them find a new tax person, how do I go about finding someone who will be patient with a slow and possibly confused senior citizen?

3. Any advice for convincing my parent to allow somebody else to take over this task would be appreciated. We haven't been pushing it because we don't want to take away their agency unnecessarily, but honestly it's at the point where I could probably do it for them in a couple of hours as opposed to many days of frustration trying to help them do it.

Best practices for setting up computer systems for elderly parents?

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I need to set my mom up with some updated computer systems, including a password manager. If you've been doing tech support for elderly family members, what are your go-tos? What's worked well and been accepted and used? I don't mind throwing money at this problem if required. I'm trying to get my mom some better computer systems that she feels more confident and comfortable with. She's all on Apple products - iPhone, MacBook, and iMac. Is there a password manager than plays particularly well with Apple (or should I just stick with the Keychain function)? Complication that most of the passwords on the iMac are under my dad's AppleID. My dad just passed away, hence this question, but my mom's been managing all of the household accounts for the last few years of his declining health. She's been essentially logging in as him, but it would be better to have everything under her AppleID or another centralized password/account.

The iMac has plenty of space but is glacially slow. I'm running diagnostics and will try to clean a bunch of stuff off of it. My mom's smart but not comfortable or confident with technology. I'm trying to make things as easy as possible for her. Stuff that will help her maintain systems (or should I set up remote monitoring?) would be great, too.

Helping an older person back from the edge

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An older member of our community suffered a painful and embarrassing incident last year and has since turned to the bottle. Is there anything we can do to help? I belong to a loose-knit group of retired expats. Last year one of the central people got caught up in an affection con -- not a lot of financial damage in the end, but they came very close to losing everything. In retrospect it's clear that our friend was purposefully separated from our social group and since it came to a head there have a few months of silence -- but recently they've started reaching out again. That's the good news; the bad news is that they are drunk a lot of the time and it's clear that their very sharp mind is not what it once was. I'm pretty sure this falls under "they'll have to find their own way" territory, but it's painful to watch so I thought I'd ask if anyone had advice.

Good buy - by - phone cust serv experiences in '23? which retailers?

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I like to multitask while driving. I also have some older friends that get frustrated easily by online processes.. sometimes it would be faster if they could just place an order 90s style. especially some relatives who are .. ahem.. a tad difficult to provide tech support for. So, I'd like to hear about good experiences you've had recently with retail companies that still allow you to buy by phone (and, for purposes of older folks part of question, still have print catalogues. tho open to those who do not as well.) I'll start - swanson vitamins. really good customer service, open late. Others? thanks in advance : )

Are there self-adhesive motion sensor hallway lights that actually work?

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Family is now on a third brand of motion detecting hallway lights similar to these for an elderly relative’s hallway and stairway. All of them are crap - either eating through batteries or the switch suddenly doesn’t work leaving us with a dead light. Has anyone had a consistent positive experience with any brand or model? Requirements are motion detecting, pointing down only so said relative doesn’t get blinded while walking, bright enough to light 2-3 steps each, and no wires or cords, which would add to the tripping hazards. At this point, I’m ok with something we have to mount with screws, tho self sticking is preferred.

Zurich for the Elderly

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I will be meeting up with my elderly parents in Zurich where they will be staying for a week in late September. Looking for suggestions on the best area for them to stay and what to do with elder folks who can't walk for too long. My parents decided to stay a week in Zurich after their tour in Scandinavia ends, before heading back to the US. I think this will be their first time staying in a place without a tour group, and they really just want to take it easy and do some standard sightseeing. Coincidentally I will also be in Europe at that time, so I want to pop by and spend a few days with them and help them see the city.

They are old Chinese Americans and my mom has joint problems so they can only do so much walking in a day. No particular interest except the standard sightseeing and eating good food, etc. Would love all suggestions on best area to stay and things to do. Danke schön!

Locked-down Ubuntu for the elderly?

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My elderly relative uses Ubuntu on his desktop, and he keeps breaking it. I would like to lock it down in a way that I can manage remotely. He likes to tweak stuff and install random things from the internet, so it's always getting corrupted. Then he reinstalls various versions of the OS which sometimes fails. This is only getting worse, so I want to give him a sandbox where he can screw up Ubuntu distros to his heart's content.

I would need to occasionally administer this remotely. Basically, Ubuntu remote managed desktop for seniors. Features I'd like:

* OS snapshot/rollback
* Remote access
* Mount folders on external drive or RAID (he will fill up all available partitions)

Things that won't work: Windows, Mac, Chromebook, unless they run Ubuntu transparently in a VM (he has an iPad and iPhone but he really wants to use Ubuntu)

I was thinking something like Proxmox but it might be overkill. Maybe some other VM-based solution would be practical? I would also consider buying a new system for this, his is pretty old.

You blew it up! Ah, Danube! Danube you all to hell!

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My MIL, whom I love dearly, wants to take a cruise down the Danube. I want to make this the best experience possible for her. Cost is not a consideration, schedule is wide open, and we have no idea what we're doing. She's pretty fit for an 87 year old. She can walk a mile with no problem, right now. That may change with no notice, but we can accommodate. What is the best cruise line for a Danube cruise? What is the best itinerary for a Danube cruise? When is the best time of year to take a Danube cruise? Thank you MetaFilter, you're my only hope!

How to tell narcissistic Dad he has to go to memory care?

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My Dad has Alzheimer's disease and lives alone. His doctor has said he has to go to memory care. We have power of attorney, a decent facility, and money to pay. But Dad doesn't think he needs care. He is a legit narcissist. How can we make this easier? Dad is in his 80s and in perfect health except for his brain. He CAN do all the things he needs to do to live alone, like cooking, housework, bathing, etc. But he hasn't been doing well and has become unsafe.

I live far away and there is no one else who can provide live-in support.

He of course doesn't realize this and thinks he's doing fine. He is very ego driven and HATES being told what to do. He is a legit narcissist but not malicious at all. He just believes he's doing fine and doesn't remember all the times he's gotten sick from rotten food, forgotten to eat, wandered off, made devastating financial decisions, etc.

We have a facility and the move-in date is in a few days. He has to go or the doctor will hospitalize him. We haven't told him yet.

A lot of the advice I've seen involves tricking the person, telling them it's an apartment, telling them it's a free trial stay, etc. Dad still has very good reasoning, it's just his short-term memory that's gone. He's not going to be fooled by a simple trick like this.

The facility is one of the better ones in his town and we were thinking to play up the exclusivity and independence they offer to assuage his ego. But we just found out the spot that opened up is a smaller and less nice room that doesn't look AT ALL like an exclusive place for the well off.

Please share your experience and any tips that can help our family get through this transition.

Help me keep my mother-in-law occupied with her KDP-published novel

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Short version: My mother-in-law wrote a YA/kids novel many years ago. My husband and I scanned it and have laid it out and produced a custom-designed (i.e. non-template) cover for it. We plan to give her the book and hand over the Amazon KDP account to her so that she can do whatever she likes with it. But here's the real question: What can an 80-year-old with decent, but limited mobility, do to promote her book? Bonus: She isn't especially tech-savvy. (more inside) Longer version: My mother-in-law has been in desperate need of a project to keep her busy. She's becoming isolated and has lost some of her interest in engaging with the world. But she has always wanted to share her writing with people (and she's also still writing).

She wrote the book that we've put on Amazon KDP about 35 years ago, and weirdly, it reads like a contemporary, retro-80s YA book. I think that works well for her, as there's some real nostalgia still around kids' lives in that period.

When we hand over the account to her, we want to help her schedule some projects that might help boost the book's readership. But they can't be too difficult (in terms of technology), nor should they be too expensive.

She lives in South Florida, in a pretty populated area. So library readings, community center events, etc. are a possibility for her. She'd also love these, as she enjoys interacting with people.

[Side note: Printing copies of the book to take to a signing might also make this feel more legit to her, so don't shy away from proposing things that might require hard copies (it's actually a paperback now, but you get the idea).]

What other things can she do?

How should I support my elderly Mum, who has Alzheimer's?

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How can I support my elderly Mum, who has Alzheimer's? She lives at home with my Dad and my brother (who is nearly 50) who cultivates a toxic, even unsafe, environment that is detrimental to my Mum's care but also makes it difficult to provide support? (More inside, inevitably) I'll try to keep this as short as I can. Sorry if some of these details seem irrelevant. I share in the hopes the context is useful, but I'm not sure that, from the inside, I can see the edges to a situation decades in the making.

My brother and I come from a dysfunctional family background. Angry shouting and screaming were the norm. The threat of violence loomed more or less intensely as other family members came (sometimes for extended periods) and went. I have myself been recently diagnosed (in my 40s) with bipolar disorder and I'm convinced behavioural disorders are present in other close family members (including my Mum and brother). I have reason to think my brother was sexually abused as a child by another family member (not a parent). My mental health providers refer to my own childhood as emotionally abusive. So for Britain in the 1970s and 1980s, all fairly normal.

My Mum was diagnosed with Alzheimer's a few years ago. She is now in her early 80s. This was, in my opinion, a late diagnose due to a resistance on my Dad's part to seek timely medical help. My family has always been reclusive, suspicious of the authorities, and resistant to outside help. During my latest visit I could see that my Mum's long-term memory is starting to crumble, after years of worsening short-term memory problems.

My brother, several years older than me, has lived with Mum and Dad his whole life. He has never made a financial contribution to his own upkeep, my parents', or the house. If he uses the oven or washing machine on occasion, it is only for himself. He has more or less shut himself in his room (which is a no-go area) for decades. Over those decades on and off he has used strong forms of cannabis. For many years he was an avid night-time gamer. In the last decade or so, a long-term flirtation with conspiracy theories has descdended into what I believe to be alt-right radicalisation. I can only infer this from what my parents have reported of these outbursts, but territory he has veered into includes holocaust denial and, more recently, the darkest kind of conspiracy theories about the current US president.

My brother goes months without talking to my parents. The cycle swings around to being on good terms with them, but after that he uses current affairs and his conspiracy theories to bait my Mum (who has always been politically engaged) into arguments which frequently end up with him shouting agressively. From his point of view, perhaps this is normal. But he doesn't seem to see that our parents are old now. On one occassion (that I only found out about much later – Dad tends not to relay concerning information) he placed a hand on Mum's neck in a show of intimidation (she reports that he didn't hurt her). He actively tells her there is nothing wrong with her, and discouraged my parents to get COVID vaccinations (although they did anyway, which is a minor miracle in itself).

For many years I've been encouraging my parents to ask my brother to move out for their own good. For years my Dad makes the same noises – that he will deal with it, that progress is being made. You can pin this "progress" onto the cycles of my brother's behaviour. My Dad is very loving and wants to take care of everyone – to a fault, as he has certainly cultivated – perhaps inadvertantly – my Mum's agoraphobic tendencies. I think he needs to be needed, by my brother as well as my Mum. In reality, my brother needs help as much as anyone, but right now my Mum is the priority.

On my most recent visit the house was dirtier than I've ever seen it. Walls, doors and light switches are covered in sticky black grime as a result of my brother's dirty fingers (which could be because of the warehouse jobs he is sometimes able to hold down, or the residue from cannabis resin, or both.) My Dad's own clothes were filthy – and we're not talking the good kind of DIY/gardening/car repair sort of muck. At face value he has his wits about him, but his ability to cope and make good decisions is much diminished.

The upshot of all this is I visit less than I should. I feel terrible about it, but it just doesn't feel like a safe environment to visit. My brother's more-predictable work patterns (for the time being) make it a bit easier at the moment. I try to clean up the worst of the dirt when I do, but my parents refuse to have a cleaner visit, and the filth and grime returns quickly anyway. I don't feel able to confront my brother. We've had violent flare ups in our early adulthood, initiated by him. Given his more recent tendencies, I genuinely don't know what he's capable of if pushed. Or perhaps I'm a coward looking for excuses.

I've tried raising safe-guarding concerns with the local authorities, but these don't progress because my parents front that everything is OK. When I last spoke to my psychiatrist (since discharged from their specialist care) they felt compelled to raise a safeguarding concern on behalf of my parents, but I don't know what came of it. I have tried once more to raise a concern, and request an urgent care needs assessment. We'll see what happens but my expectations are low. I've sought advice from Age UK who are deeply concerned by the circumstances but can provide no actual help.

I have just given Dad an ultimatum that, unless my brother leaves, I won't be able to visit or provide other help. I don't think I mean it, but out of desperation, it seems worth a try. A last resort might be going to the police about my brother's physical intimidation, or the ongoing verbal, emotional and financial abuse (as I see them). My Dad has given my brother tens of thousands of pounds to encourage him to leave – he has the means to do so. But last time my Dad made noises in this direction, my brother's response was to quit his job. I am skeptical that the police will act without cooperation from my parents, which I doubt they'll get. My Dad asks me not to involve authorities so it feels like a betrayal of him and my brother when I do.

This has been spiralling for years, but the trend is only ever downwards. I can see that this is a situation of my parents’ making. Home wasn't a safe environment for me or my brother, and understanding and support wasn't there in the aftermath. And fundamentally, they have decided over many decades to let him stay. But I think my parents have always done the best they know how. And it's them that need the help now.

The last few years it's had a significant affect on my own mental health (which my doctors and immediately family want me to prioritise). Mainly this is out of desperation of not knowing what to do and feeling powerless to help. I'm struggling to sleep again with the worry since my last visit. But of course my Mum's wellbeing is my top priority. What can I do? Thank you.

Abusive parent needs care

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How do my sister and I come to grips with having to help our Abusive Father who is now having cognitive issues? My father who is in his mid 70's recently had a brain hemorrhage. Up until this happened which was about a month and a half ago he was independent. To add to the equation, my mom has Alzheimer's and he was her caregiver for about 4 years until she was placed in a memory facility where she's actually doing very well.

My dad was abusive to me, my sister, and for sure my mom. The abuse was verbal and psychological, not physical. But it absolutely took it's toll on all of us. I believe my mom's Alzheimer's was accelerated because of the daily barrage of abuse from my dad for many years including after she was diagnosed.

I wanted to also provide some more info...I live on the west coast. My mom and dad are on the east coast. My sister lives on the east coast, about an hour and a half away from mom and dad.

I have spent the last month living with my father and helping out with driving him places and taking him to doc appointments and trying to take care of bills, etc. My sister, while she never ever physically stays at my father's house, has tried to help him with logistical things like getting my mom into a home, and helping with bills. But she has, and for good reason, kept her distance from my dad. When my mom went to a home several months ago, she virtually cut off contact with our dad unless absolutely necessary.

Now, given my dad's condition there is a TON on our plate. Both my sister and I are sacrificing a huge amount of time away from our families, losing time and work with our careers, and taking the blows of an abusive person who not only belittles us at every turn, but shuts us down from trying to help unless we really push him hard. And then he yells at us for not helping him. He is behind on bills, and is extraordinarily aggressive about telling us we're lying to his doctor to stop him from driving.

My sister is close to just stopping helping him all together. To be fair she has dealt with more since she's closer geographically. I've been consistent with talking to my dad on the phone every day for a long time and trying to be in his life. I've also come home almost every other month this year...even before this happened. I was mostly coming for my mom. And as much as I hate my dad, I never wanted to cut him off. But now, I think we're both starting to question our future with an abusive parent who now needs our help... it's torture trying to help him. It was torture having him in our lives. All the while, our family and work lives beginning to to unravel.

When I found out what happened to my dad and I booked my flight come home I almost had a nervous break down because I knew what was coming and what will be needed for who knows how long. I have had borderline suicidal thoughts since being home with my dad.

I know this is a very hard situation and no one has a solution. My sister seems very close to throwing in the hat. My dad's recent brain scan says the swelling has gone down and he is potentially going to get better but tough to say if that will really happen or when. I'm not sure I could fully turn my back on my dad. But my mental health as well as my sister's mental health is really fragile right now. We have part time caregivers in place to drive my dad places and help out around the house once I leave which will be soon. The driving for him is really the biggest concern. But I'm feeling pretty hopeless and helpless right now. I know I'll need to come back to help out in a couple months. But not sure if my sister and I have it in us to continue, but don't know what choice we have. Any words of wisdom or advice is greatly appreciated.

How to reduce pain and swelling in my elderly mother's ankles?

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Mom is 83 and back to walking with a walker after being bedridden for 1.5 years due to a now-healed stage 4 pressure wound. She is sore all over for known and unknown reasons and is on major pain meds. She has pre-existing back issues and a repaired hip fracture. The problem is that her ankles are sore and swollen and it is discouraging as well as stalling her progress. She has compression socks and takes a daily diuretic. My 83 year old mother was bedridden for almost 1.5 years and started walking again about a year ago today. It was slow going and painful and her PT team was confoundingly bad. They told us that she would probably never walk again, but here she is. She has spinal stenosis, a repaired hip fracture, and potentially arthritis. She walks very slowly with a walker.

Mom is incredibly motivated, is on a number of pain meds (and regular epidural steroid injections) and has a decent doctor. She is now almost fully mobile but swollen and painful ankles are interfering with further progress. Her legs hurt too but only the ankles are swollen.

Doc prescribed a daily diuretic and elevated feet. She wears light compression socks. Some days are better than others.

We keep bringing this up to nurses, caregivers, doctors and are not getting any concrete or helpful feedback except to keep using the socks. They think it's just strain from all of the movement after so much time in bed.Obviously YANMD but has anyone here run into this kind of thing with an aging parent and have you found anything that works? Massage? Diet? I'm at a loss. I am a part time caregiver for mom and also her point person with the medical world. None of her docs/nurses are able to help us get things under control although the diuretic appears to be working most days.

Can you help? I will be around to answer any questions. Thank you!

Pimp my walker

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So my mother just brought home one of these bad boys and other than the obvious racing stripes we’re looking at what accessories would be best. Off the top of my head a cup holder and some sort of collapsable tray (netting?) seem useful. Suggestions from experienced users would be welcome!

Support group for caregivers of elderly with abusive histories

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A friend is looking for a support group for caregivers of elderly with abusive histories. Online preferably, or Boston area. Details below the fold. My friend writes
I’m currently the only living relative of my 91 year old grandmother who is in the hospital in Estonia recovering from Covid & pneumonia. She is unlikely to be able to return to independent living but also resisting any attempts to suggest assisted living.

There is a lot of intergenerational trauma moving through this situation, some of which is manifesting as emotional abuse in my direction. This is a chronic dynamic between us, currently in a particularly acute phase due to her diminished lack of agency and cycles of anxiety.

While the details are individual, I imagine my situation itself is not unique.

I would love to find a support group in addition to my individual therapy. Online would be best, though I'm not opposed to in person in the Boston area

So far I’ve tried psychology today, cha, groupfind and nsgp




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