I have overheard my father on the phone with a couple of different doctor's offices and he lies to them about his diet, exercise, pretty much everything. To the point where I called one back last week and told them the truth, that he is mostly sedentary when he had her convinced he works out daily. I try to go to as may of their appointments as I can because I know they aren't honest but I cant make every single one. We've told them numerous times that the doctors can't help if they aren't telling them the truth but it doesn't matter.
Of course not one of us for fear we would set the record straight
I would call his Doctor and give him a heads up mostly so he could draw important blood tests and other tests for surveillance of liver disease, kidney failure, Diabetes and other effects of alcohol abuse Then the doctor has “guilty knowledge “ and then has to investigate the effects of alcohol abuse. It preserved my relationship with my father.
- Understand that they are re-acting out of fear of change and losing independence - and what this will (eventually) mean to them, i.e., deteriorating health, needing more care/givers, relocation-moving, At the least or most - SOME KIND OF CHANGE. Older people in decline (or not) do not want to change.
- When you understand their motivation, you can express compassion and understanding (not acceptance of their behavior (i.e., not sharing the truth with their MDs or others). You can talk to them about their fears of change - without judgment. Offer reflective listening, i.e., "I hear you saying XXX" - this gives them an opportunity to get their feelings out and share, and know it is okay to feel scared and it is okay to share with you how they feel.
- Do take time to listen to their needs, without judgment or confrontation.
- The goal is to give them space to freely talk about how they feel.
- The more you try to change them the more they will resist. It can be a tricky situation although take a step at a time.
You, too, be vulnerable / self-disclose how YOU feel. i.e., say "I feel scared at times when I ... xxx or when XXX happens . . . (When are the times when you) / Are there times when you feel scared, too?"
Medical Providers / Chart _____________________________
1) I would recommend that you put your concerns in writing to each medical provider so it is in your parents' chart 'on the first page.'
2) Ensure that paperwork in done re their medical records / chart giving you the legal right / authority to be informed, and as possible - a part of decision making of their heatlhcare (would mean a diagnosis of dementia).
Keep a journal of medical / cognitive changes. This kind of ongoing dated information is very helpful to MDs/providers. [I did / do this all the time with my clients: track changes.]
You need to be able to
1) talk to their medical providers (legally);
2) be with them during appts.
3) As you can, ask the medical providers to ONLY speak to your parents on the phone when you are also there. This needs to be in their chart, otherwise it sounds like a revolving door of mis-truths and likely / possibly mis-diagnoses, and VERY IMPORTANT: follow-up care.
In m own experience (w a client), I accompanied her into an exam and she lied about how much alcohol she was drinking daily. As this woman is an alcoholic, she certainly didn't want to share the truth. Drinking as she was could result in serious medical consequences due to falls, breaking bones, etc., and poor decision making, esp if dementia is involved.
It is not unusual that older people will lie to medical providers due to wanting to maintain the status quo of their life / lives. In some ways, we all want that - no or minimal day-to-day upsets or changes. We have enough stressors just surviving. No one wants to add 'more changes' to an already challenging or overwhelming life. Still, it is for their benefit to ensure they are getting the health/care they need which ultimately depends on how they speak to medical professionals, and to you.
None of this is easy. It is a process of learning as one goes.
Get the support YOU need to keep going. Take respites, try to eat healthier than not, get enough sleep and exercise. And, know I'll take my own advice and do my own PT exercises.
Gena / Touch Matters
Most doctors probed further and he would slowly open up.
I’d stand behind her & shake my head or speak to the dr alone after the visit.
Best wishes to you!
I worked in one small hospital that serviced primarily Latinos who spoke no English.
They consistently denied any health problems . What you conclude is they just never went to a doctor , its obvious. Not picking on Latinos, just my experiences. At some point , you realize people exert their own will and follow an ingrained belief system .
This has caused severe depression, anxiety, insomnia, and terrible health issues for me.
I know we all read and see the comments about how bad this disease is, but it also affects the one that takes care of them even worse in my opinion. I’m working on trying to change my own thought processes to not feel guilty for not being able to help. I know she is one of those that even before this disease that no one could ever please.
I am sure she will outlive me because she is actually in better physical health than I am. What is pathetic is I let this happen. When you are programmed at birth to be a slave it’s hard to get away from that mindset. No one should ever feel guilty for wanting to have a little life for themselves.
My step-mother who has dementia doesn't have a clue so I write an outline and give it to the doctor either before or when I get there with her.
I would do that with your parents and leave it at that.
Hopefully someone is their DPOA, so they can step in when necessary.
I go with my Mom to her appts. I take her to them. There isn't a lot they can do for them at this point. My Mom tells the tall tales also.
I haven't yet but next visit I be handing over a note about things are being done or not done in between visits. Hoping Mom will be able to get a few more weeks of PT. I fear the immobility part of this so called journey. I know it's coming, though.
My best thoughts to you.
However, another LO has learn the lingo. Rarely 'falls' now.. but has had 'slips', 'trips' & 'lowered to the floor'. Love that one. It was a WALL that provided the lowering to the floor, not a person.
Reminds me of the old story about a car accident.. It wasn't my fault at all. A pole just came out of nowhere & ran into my car.
Is your angst over this situation less about your parents lying to their doctors and more about your parents' unwillingness - at least as far as you can see - to keep themselves as healthy and fit as possible? If so, that is an understandable and justified frustration, especially due to the fact that they live with you, and presumably the bulk of the caregiving responsibilities falls/will fall onto your shoulders.
If that's the case, there is nothing wrong with telling your parents some hard truths: "mom, dad, ever heard the expression 'use it or lose it'? Because if you lose too much, we're going to have to have a serious conversation about just how far and how much caregiving I am able and willing to do. For example, if you end up in a wheelchair, this house isn't equipped for that. I am not strong enough to help you in and out of bed/bathtub/toilet. If it gets to that point, we are going to have to consider at least an assisted living facility." or some such version of that conversation. There is nothing wrong with laying your cards on the table, rather than wishing mom and dad would get with "the program" and make themselves as fit as they can out of respect and consideration for YOU.
Chances are, your parents have never really considered the "what ifs?" scenarios, at least not since they have moved in with you. It seems to me, the longer a parent lives with an adult child, the less those thoughts seem to come under consideration in their minds - or at least, that's what I saw happen with my mom. Every once in a while, I had to remind her that if something were to happen to me, she would have to figure out what to do then. When Covid was in full swing with no vaccine yet and no real treatment options, she once said to me (after chiding me about not going to the grocery store more than once a week) "oh, well I don't care if I get Covid." And I told her "That's great mom, but *** I *** don't want to get Covid. Besides, what would YOU do if I and all my family got it? We would be in quarantine and wouldn't be allowed to go near you. What would you do then?" She really had no good answer to give, because there really was no good solution at that point. But it got her thinking that there was more to the equation to consider that just HER getting sick, she had to take into consideration MY health as well, because my being able to take care of her would be directly related to my own health.
That's also something to remind your parents of. That your ability - never mind your willingness - to caretake for them is directly affected by your well-being. And their seeming disregard for their health also directly affects YOU, because you are likely going to be the one to deal with whatever fallout occurs.
In my very humble opinion, if they are in "reasonable" health as you describe, and they are lying about the amount of exercise they do, or what they eat, then leave it. I mean, really, if your parents are in their 80's, for instance, then what the heck does the doctor really care about their every day diet at this point? Unless one or the other is suffering from, say, congestive heart failure and they are eating loads of salt, which is contributing to edema, which is leading to ER visits/hospital admissions, then I think maybe just leave it be. Sometimes doctors just give the rote speech about diet and exercise without considering the age of their patient, their ability and willingness to watch their diet and/or exercise, and just how beneficial that will actually be at whatever age that patient is.
When my mom had CHF, she had doctors at the hospital telling her she should exercise more! It was actually one of her PT's in rehab that just rolled her eyes and told mom "Oh, they always say that. Then we have to tell the patient and family that it might be more dangerous for the patient to exercise because of the likelihood of falls or threat of stroke or something of that nature."
Now, if mom or dad are lying about something more significant, such as "yes, I can always remember where I live when I go out of the house" or "yes, or course I remember to turn off the flames on the stove when I cook" or "yes, I always take my medication exactly as prescribed and don't over/under-dose myself" then that's an entirely different story, and one where you should absolutely intervene and let the doctor know what exactly is going on.
But for the sake of a few more Hostess Ring Dings and a few less sit-ups? I would let it go. Much like raising children, when you are taking care of aging parents you need to pick your battles and decide which hills you're willing to die on.
If not you could set one up and communicate concerns that way.
HOWEVER if you are not listed on HIPAA forms as a person they can share information with they can not legally discuss things with you. They CAN take the info and sue that though.
If your dad has already set up the Portal you could ask him for access and send the doctors notes.
If he does not want you doing this you can send a letter. Like write it out and put it in the mail or drop it off. You can not email since that would not be "secure". A call might work, someone would take a message and relay it to the medical team.
Another however....
If your dad/parents are cognizant they are aware that not informing the doctors of current conditions is not in their best interest. there is not much you can do. It is their choice to keep the doctors uninformed.
If they are not cognizant then someone should be with them at every appointment. So that correct information is relayed to the doctors and you are aware of the information the doctors say to them.
I do hope someone is POA for Health and Finances
Has your Father assigned you as his Medical Representative? This is a HIPAA form that you request at the doctor's office and they keep on file. This allows the medical staff to legally discuss your Father's private medical information with out him being present or providing any further approval. Every doctor or clinic needs its own signed form and you have to sign one every year.
Then this will also allow you to *give* actionable information to your Father's doctor as well.
The portal may be an option but if you're not your Father's MPoA or MR you shouldn't be discussing things with his doctor... but I totally understand your concern.
I used the patient portal all the time for my late husband and his doctors always said how much they appreciated me doing that.
Unless your father has given the doc permission to, they can’t discuss info with you, but nothing can stop them from reading your letter.
Didn't expect to hear back (as no medical permission) & I didn't. Maybe my info was useful as question starters..? idk.
Made me feel better, like I had done what I could.
How about this? How about you are talking to your doc and I overhear it and think you fudged your good eating habits a bit. Omitted a few episodes of extra large pizza and Trader Joe's Old Fashioned Potato Chips? How about I call your doctor and say you just lied to him or her and I saw you eating blah blah.
I think that you should examine the amount of enmeshment in your parent's private lives that you have sneaking up here. Just take a solid look at it. You have not now become the parent. I say this as an 81 year old with a 61 year old daughter, who--while she is a wise woman for certain--is not now my keeper. Not YET my keeper.
If I want to fib to my doc that's on ME. If I don't exercise or eat right or if I listen to too many true crime podcasts that still remains MY BUSINESS. Not hers.
The sad day may come if I am forced to live so long, that I will be quite dotty and my daughter will NEED to speak to my caregivers, need to put into active duty the POA ready for her, NEED to get me placement in care, etc. We both know that. And we both talk together about it. Both fear and dread it. Both hope I DIE first. But that's not within our control unless we go to plan B.
I will repeat. WE TALK TOGETHER, my daughter and I.
She doesn't call my MD. She talks with ME. I don't call her MD either now she is a grown up. I TALK to her. And we discuss it ONCE. We don't badger one another.
Honestly, I say this as respectfully as I can, it isn't your business. You can give advice. But the day may come when your parent tells you "enough advice". And it isn't your business YET. They will make their own decisions. The time comes soon enough when they cannot.
As I said. Examine it. It isn't easy. When things descend into a demented person able to confabulate enough to visit the MD (and this is rare) without getting "caught" into the trap of "Can you draw me a clock set at 11:10", you may need to call the doctor to discuss the level of forgetfulness, wandering, the hazards, when you act. A confusing and difficult time, that I suspect is not yet here for you.
I worry also at the amount of caregiving you are taking on. Have an honest talk with your folks about their plans. Let them know it may become too much for you, and the time to think about a move to independent living, etc may be more near than either of you like.
Good luck. None of this is easy to be certain. Just some things to think about above. You can ignore me. So many people do and live quite nicely, hee hee.
I pretty much am the parent since they both live with us and have for four years now. I oversee all of their medications and go to as many appointments as I can, and I do have the POA. We do talk with him/ them but he has zero qualms about outright lying.