I have POA for my father, he lives in our guest house. Sister lives out of state. She used to call him once a week now she calls him everyday since he fell. She is in denial over his dementia and constantly argues with me on the subject. I finally had to set ground rules and asked her not to talk about our father's care as I am extremely stressed out and stress brings on my seizures. Well that didn’t work. Everyday she tries to micromanage my caring for him. I was sick in bed today and she said get your butt up and go check on dad. Which I find strange as she didn’t even want him to live with her. Maybe it’s her way of feeling like she is helping him? I don’t know. I had always hoped she could be supportive from a distance and we could be a team in our fathers care. I’m finally seeing she is more of a burden than a help. It’s so sad. We’ve never argued this much in our lives. Sure we are sisters and we have had our disagreements but nothing like this.
I hate to say it but my father is driving a wedge between us, even if in his dementia state he doesn’t know he is. He calls her and complains about me. He also calls his sister (my aunt) and complains about me. How I’m trying to take his license away (I currently have his keys) etc etc. I feel like I have everyone against me and I just can’t deal with the stress of him on top of everyone else. I finally had to block my sister from texts and phone calls. I first told her I really hate that it has come down to this but I have to do this for my own health. Nothing else has worked.
* Provide details of a medical diagnosis of dementia. If you don’t have that, give details of the symptoms you are seeing, and ‘official’ information about dementia that confirms your own diagnosis.
* Find some information about dementia that includes the fact that it will include many many criticisms, many lies, and a lot of misinformation.
* Send the same information to your aunt, who may have more experience. If she understands, ask her to contact your sister, who presumably is also her niece.
* Make sure your information also tells her about ‘show-timing’, so she doesn’t make judgements based on just a short exposure (like a phone call).
* Ask if your sister can visit to see things for herself, preferably for a week to give you a break.
* Look up the information on ‘care topics’ (top RHS of your screen) for D for Driving, and send it to her in an email – the danger to father and other road users, how common this problem is, and how dreadful it will be if father kills an innocent person in another car and the family has to deal with the legal fall-out.
Many people have found that it is really hard for relatives to understand and accept the implications of dementia. We regularly have new posters who use this site to educate themselves. You may have to educate your sister, who can’t even see for herself.
Good luck! Margaret
Ask his physician to recommend a PROFESSIONAL (psychiatrist, neurologist, psychologist, social worker) TRAINED in GERIATRICS, and request that that specialist’s report include your father’s ability to manage ADL, ESPECIALLY from the standpoint of PERSONAL SAFETY and ability to function independently in a familiar environment.
When you have gotten your copy of the report, MAIL A COPY to your sister.
The relationship between you and your sister may or may not survive this. It may be fractured but not permanently disrupted. Once she has read the professional report, the ball will be in HER COURT.
I myself learned to avoid ANY VERBAL INTERACTIONS when there was hostility between my fellow POA and me. I communicate now ONLY by text or email, because I keep records of everything he accuses me of.
Many relationships among siblings/mutual caregivers are disrupted during caregiving. You, as the hands on caregiver AND POA, have the ABSOLUTE RIGHT to being a conscientious and responsible caregiver TO YOURSELF.
For the time being, you MUST place your father’s needs and YOUR NEEDS far FAR beyond whatever needs your sister THINKS SHE HAS, whatever has caused them.
“More of a burden than a help” describes what a sibling of mine was in the care of my dad. What I quickly decided was that only one person can argue and I wasn’t having any part of it. I distanced myself from his tirades, hired extra help for my dad so I didn’t depend on his non-helpful help, and communicated on a need to know basis only. I wasn’t rude, just didn’t participate in his mess.
Not sure any kind of documentation or information is going to be useful for the sister or the aunt. Some people just don't get it.
So, yes, focus on self-care and dad-care. As POA we don't own ANY explanation to anyone. POAs are to allow you to function while helping the person in need. It's nice when we can share at least some info with our siblings, but not this one!
After reading what you wrote at the bottom of this post, that your sister doesn't even think that dementia is real, has to be one of the most ignorant things I've ever read. Perhaps if she would actually do her homework, and learn about dementia, she could better assist you in the care of your father.
So if your sister thinks she can do a better job caring for your father, tell her that she can come and get him. I'm guessing that that will shut her up in heartbeat.
But honestly and realistically, you probably need to place your father in the appropriate facility, as the stress is taking its toll on you, and with you having seizures, that's not good in any way shape or form. Seizures can kill you, as you already know, and I'm not sure all this is worth losing your life over. So please take care of you first, and do whatever is necessary to cut down on the stress in your life. God bless you.
The boundaries you have set for your sister have been ignored. You are now going to have to enforce them. Say a letter telling her how often she is allowed to contact you unless there is an emergency. You are correct in supposing that this has a very real chance of changing your relationship for the rest of your lives, and in all truth I would rather have this sister, in her own denial and hence believing everything Dad chats with her about, calling an assisted living which WILL control her actions.
Only you can make the decisions about how much you can take in terms of continuing to care for Dad. I would make it clear to your Sis that her continuing in this manner will leave HER responsible to Dad's entering into LTC, and that then she can both chew on that for a lifetime, and can attempt to bother ALF or NH in the same manner she adds to your burdens.
I am so sorry all of this continues with problem upon problem piled onto your already full plate. I know you are here often, participating in the forum, so the one thing you can recognize is that you are not alone; that doesn't make it easier.
Just because your sister said he can't go into a care home and he can't live with her (read that in one of your previous posts) doesn't mean that YOU have to provide the care for your father.
What are his finances? How would a facility be paid for? Would he be Medicaid-eligible? Just how much care are you providing for him?
PLEASE PLEASE put yourself FIRST and do not be a martyr.
Take a vacation from all this drama. Get your own health in order. You don’t have to explain anything to anyone why you are doing this. It’s your business.
With a calm mind and better health, you can make well-considered decisions. Good luck!
It can be a nightmare and you need to do what you can to protect your sanity.
Things may get better later (they have between me and mine) especially if you had a good relationship before.
Remember none of it is your fault. You can only do your best.
Good luck! x
I really, really hope you don’t jeopardize your own health for your father. As much as you love and care for him, you have to take care of yourself mentally, emotionally and physically.
Maybe try to think things through and get some help.
Best wishes.
What i do now through text and zoom meetings ONLY is act as if this is a corporation. I give everyone the platform to vent and and if they have issues with care - i ask THEM to go out and resource the solution. Not just complain, you need the solution or together we come up with a middle ground that satisfies both sides.
YOU are POA and were selected to be POA because your father saw something in you to take care of his best interests and that is your job at this time.
I suggest you get help at least 4 hours a day possibly a shared cost. It is easy to tell someone who lives with a sick parent while they have their feet up watching tv and relaxing with a bottle of wine.
Tell her she can be supportive by paying for your dads care of x amount of hours per week and e-transfer $ to the caregiver. (she may not but see) This way she can tell that person to do whatever she wants done during those hours. Also you can take reasonable $ monthly for caring for him in your home.
If you express concern privately to his doctor regarding dementia - and have the doctor deem him incapable of making decisions. (if he truly can't -they will make an assessment) you can enforce the POA and no one can interfere with your decisions - and he will not get his license - blame it on the doctor. What you will find is that everything will be blamed on you so you need to be strong. Just stay strong. I have the same problem and had to keep telling myself that this is about dad NOT us.
see a lawyer and seek advise - see what your rights are -
keep all documents with you and share nothing. You can answer questions but are not obligated to show anything.
You are the chosen one so do what you know is right. Put your dads bank account in both your name if you still can so you can easily make financial decisions.
TALK TO YOUR LAWYER - BANKER and listen to your heart - Dementia has broken tones of families - try and listen to all and get the family to come up with their own solutions to their complaints because its easy to complain.
Good luck.
Tell you sister she is right....you can't care for dad so you are bringing him to her house so she can take over. Then watch her attitude change. Lol. I joke that I am going to leave my mother on sisters porch, ring the bell and run. At least I think it's a joke. 🤔😏. Hang in there pal.
The decision was theirs to cut me off, so if they can live with it so can I. My dad would be very disappointed with them. He passed 9 years ago. It's a sad situation but I had to accept it.
#1. My sisters and I have a scheduled weekly conference call. We have done this for many years, since my younger sister had cancer (now in remission). We talk about ALL the things going on in our lives, including our parents health.
#2. I take their ideas seriously enough to research them and sometimes act on them. For instance recently, my older sister had concerns about my mom getting the Covid-19 vaccination. My first reaction was to go on the defensive, but I know my sisters want the best for my mom, so I read the article she had seen, googled for more information, talked to my mom's hospice nurse, talked again to my sisters, and we all decided that it would be best for my mom to get the vaccine. It can be a little more trouble, but it is worth it to me to have my sisters on my side.
#3. I really really listen to my sisters. We talk about how what I see visiting twice a week, what they get from phone calls and infrequent, but longer visits and what my mom's caregivers see is different, and all provides valuable insight to my mom's condition.
Finally, I will say that our relationship began in childhood with our parent's encouragement, so encourage your children and grandchildren to get along with each other so when things get difficult, they will have each other.
Try again to mend fences and tell them you are trying, stories he has relayed are not the truth but he can't help it. Invite sister/aunt to come and spend a couple of weeks with him to observe on their own. Lastly, let them know you are doing the best you can, given his condition, and you completely understand that if they aren't there to see things first hand, they can't possibly know what is going on. Without being angry, ask if either of them would prefer that he come to stay with either of them to ensure he gets the quality of care that they may believe he does not get from you.
If dad has money, hire some people to help you out with his care to take some of the burden off (if his other family is not wiling to help out). If he has no money, ask sister and aunt if they would like to donate to his cause to hire some additional help for his care.
In closing, if neither of them offers any help or to come stay with him for a few weeks, then sum up the conversation with them - as I understand it, neither of you can help so my only request as I try to do this alone is that you support my efforts and have some belief in what I tell you about his condition instead of assuming what he says is a problem. You might also ask, if you really believe I am not giving him adequate care, why haven't either of you been here to help him?
Doubt either will help. If they honestly thought you were not treating him right, they would/should have already shown up to see for themselves. But you have given them option to help. Any more comments from them?? - just reply with what can you do to help me? When they suggest something you should be doing? What can you do to help me with that.
You are doing your very best and don’t need your father pitting your sister against or your aunt against you. They should be interested in hearing your side.
I have my own experience with a mom who stirred the pot with my siblings when I was the one who did all the heavy lifting! They wanted to remain mom’s favorites so they weren’t interested in hearing my side.
I developed health issues from all of the stress, not to mention not being able to eat because of nerves being unstrung and depression.
I couldn’t take anymore and got so tired of scrutiny that I ended up telling my mom that since she and my brothers felt like they could do better, than they could take over her care!
I had mom for 15 years in my home. Now my brother has her.
Mom’s doctors said that I took excellent care of her and that is all that matters to me.
I am no longer interested in what my brothers’ opinions are and I am finally at peace.
You’ve heard the expression, ‘Consider the source.’ Do not allow them to degrade you. I am glad that you blocked your sister’s number.
Your sister should know better than to push you. You can push back harder!
Most likely you have already tried to remedy this situation and ended up at this forum as a result from frustration and exhaustion.
Wishing you all the best as you tackle this heart wrenching situation.
I think the division of siblings is far more common than you realize. It was discussed many times at a local support group. Then there are the others who have NO siblings to share the burden...that too is not good.
What really got me is that here I am doing my best to balance looking out for the elders and all that involved, bill paying, advocating, locating resources, shopping for the house or groceries, planning meals, cooking, working part-time, cleaning, laundry...and on. Then in late Sept I had the aortic dissection, which is often fatal and my snot sister had the nerve to BLAME ME. Never mind my balancing act sparing her out of state self any of the burden. She blames me for having high blood pressure I should have known about which is a potential contributing factor. And while she is unemployed did she even try to stay here longer to potentially be of assistance to the elders or to me? NOPE. ZERO sense of obligation or commitment to family. ZERO. She owes them NOTHING. ANd if I had died? I guarantee you she would have found a way to conserve her own physical energy as much as possible, and put the house on the market and the elders in a nursing home or assisted living, fooling herself that she just had to wait to get the grand inheritance by default, without realizing how much assisted living or the nh costs. To top the cake off she expected to be reimbursed for her travel expenses and incidentals when she came in see me while i was still alive, and later told me she hoped I "survived".
Truly clueless they are!!!
I knew it was going to be expensive. I set up appts to check 2 places near me. Last minute, YB comes up with a place 5 min from his place. Like HE was going to oversee anything? But, humored him anyway. We went there first. It was new, just about to open. The room they showed us was 2 BR with a shared bath. Mom would NEVER like that! Plus, the view was a parking lot and 4 lane busy roadway! ALL that for 8k/month! He suggested we meet down the road for a bite to eat and discussion. When they both got out of their cars, their first words were "For that kind of money, I'll take her in!" Neither had the first inkling of anything about dementia. I just said sure, if that's what you want, but you'd better know what you're getting into. OB isn't local, so if he took her, he'd be on his own. He has ZERO patience so that would not have ended well. YB is still working and sometimes I wonder if his head it stuck on right (I've often suggested perhaps he needs the room next to mom in MC!!)
OB and I went to another place the next day - I was NOT impressed with the facility or the "tour", if you could call it that. The last place, which had been my first choice, was still being rebuilt. It was non-profit, had endowments and from the pictures seemed like a great place. The deposit was refundable, so I went with that and when it was open enough to tour, it was VERY nice! Without going into other details, the care was very good and mom did very well there for almost 4 years. They cared so much that when she was moved to an empty AL room so we could be with her at the end, staff were coming up to see her and some even came in on their day off!
But I digress... the sticker shock those two showed how clueless they were. Their ideas of taking her in showed even more how clueless they were. OB's last trip here to help with the condo (almost 2 years of my life, a few weeks for him, 1-2 trips for YB), I sent him to visit her, bring coffee and DD. When I suggested another visit, he refused, saying he "didn't know what to do with her." Annnnd you were going to take her in????
He never came back to visit her again and I don't believe YB was visiting her either. They can go pound sand.
Bad enough when they don't help, but when they criticize you instead of offering to help or making suggestions to make things better, who needs them? The verbal abuse was bad enough, name calling, yelling at me, telling me more or less that I'm an idiot, but when it came to physical abuse, I'm done with OB. Until mom's stroke before Labor Day, I didn't have any contact with OB. None with YB except to coordinate her eye treatments with him - 4 times/year, which you'd think was weekly if you heard all his complaining! Never mind that I took care of it for about 4+ years before that.
Siblings, who needs them?
When I had to manage everything, which initially included ensuring the bills for the condo were paid, get it cleared out, cleaned up and repaired, ensure all paperwork needed for sale was done while managing her income and the trust (needed to be aware how much was needed each month, as it could vary a bit), keep receipts and bills, get taxes done for her and the trust, pay her rent, schedule and take her to appts, buy supplies and medications, etc etc etc... If I said it was too much and needed help, OB just bellowed at me to GIVE IT UP! No alternative. No offer to take some of the load. Jerk. Later when I said it was too much to YB, his response was "They take care of everything." Duh. No they don't. Jerk II, The Sequel.
Visits? OB couldn't handle the last one he had, about 10 m and hasn't been back in over 2.5 years. I don't believe YB visited in about 2 years or more. I was the only one consistently visiting with her.
Funny that even now, with nothing for them to do except say how they want their share I can't even get an answer. One did, but asked me how one withdraws - gah!!! TALK to the Trust people, don't ask me. YB took 11 days to respond, despite getting FIVE emails and a text message.
I can't wait for all the paperwork to be done and the last checks to go out!!! Maybe I'll even have some kind of celebration, hmmm, what shall I call it? Good Riddance to Bad Brothers? Bad Boys Bad Boys, whatcha gonna do when I'm done with you!!! Because I AM done with them both.
bless you for all that you’re doing.
PARTY TIME COMING UP!!!
One of two others have suggested already but I think it could be an idea to let her know that if she does not like how the care is being done then she can take him in and do it herself. And then ask her if she wants to do that.
For now, your health and care for your dad should be your only concerns. What she or auntie cook up, they can eat. It is fairly clear sis isn't going to listen to anything you have to say (doesn't believe in dementia??? Quacko?) Auntie is in her own little world too. Focus on yourself and dad.
Rely on your "sisters" and "brothers" here on the forum for your moral support! Keep those shields up Scotty! Blocking her calls and texts at least keeps her diatribes at bay. There isn't much you can do to stop your dad from calling those 2 and making all kinds of complaints and accusations. As someone else pointed out, it takes 2 to argue, so if you won't she's just blaring into the wind! You asked her to back off, and she didn't, so you did the right thing by blocking her.
BTW, having POA does NOT require you to share ANYTHING with her - actually it's the opposite, it's none of her business. So she can't even argue that.
The dad complaints and accusations are also very common. They are generally directed at the person closest to them, care-giver, whether family or not. Since the other 2 won't listen to you and I doubt they will take the time and effort to learn anything, they will only hear his side and will likely believe him. It doesn't sound like she would step up to take on his care, even for a week or two, so perhaps you can plant a bug in dad's head for him to ask her to take him? Leave notes around that he'll see to remind him to ask, as he'll likely forget. Maybe if he starts asking her, she'll back off and stop calling him, for fear of him moving in??
Does he have enough income or assets to hire some help for you to care for him? Is there enough for any kind of facility? If not, are his income/assets low enough to qualify for Medicaid? Eventually you may have to consider placement, for your own well being, but you also need to have a plan in place in the event of a medical emergency for you. As POA, you need to have medical and financial plans for any situation, plan ahead! You know she's not the one to take care of it!
"I hate to say it but my father is driving a wedge between us..."
It's not likely his intention, but it is the end result, especially when the others allow it. Not a lot you can do about that, you can't control him or them, only yourself and your reactions to it all. Cutting off contact with the other side is about all you can do, but it should help. You know you are trying to do you best for dad. Keep those 2 at bay and try to ignore things he says about you - it is the dementia talking, not him.
I've posted various replies to others regarding my brothers and their inability to understand or help, plus the verbal and physical abuse. Suffice it to say that when all is said and done, I will be an only child. We can't divorce siblings, but we CAN cut them out of our lives. I'd already had no contact with OB in over 2.5 years. YB almost does it for me... takes SO long to respond, if he even does, but when the ink dries and the checks are mailed, I'm SO done with both of them. I have no plans to try to rebuild a bridge, that time is over for me. I *may* send a final letter, and plan to say the worst of all was that neither of you could be bothered to visit your mother. She used to ask about them, but eventually stopped. Live with that, you 2 jerks!
I think it will be cathartic to get the final words off my chest. In fact, I've been working on that letter since before my father passed last year. Definitely blocking and cutting toxic 'family' out of my life for good.
Now we can concentrate on our own health and try to recover from the betrayal. {{{Hugs}}}
She likes to act mom isn't any work at all and then imply criticism like I'm not taking care of her well. I've recently started to ask her for help financially when things come up that mom wants or needs, not because I think she'll help but so she knows that mom costs money and I spend money on her all the time. It really changes how you see your siblings, makes you resent them. I don't even want to be around her anymore. I've started to notice how most of the time when she calls me it's because of something she needs or wants. I don't really like her as a person anymore .