I have tried for 10 years to get my brother and sister to help with my mother who is very physically disabled. In the past 3 years, it has gotten much worse, and they seem unaffected. She has almost died many times, and I have been the only one there for her. I have always helped with her shopping, cleaning, etc. Recently, she had a very serious neck injury (chronic spinal cord compression) which made her mobility almost zero, and she became incontinent. I changed her diapers, fed her, did laundry, shopping, held her when she cried, everything. All I asked my brother and sister to do was to call her 1 or 2 times per week to keep her spirits up... they could not even manage to do that! She had the surgery, almost died, but did make it through. She is slowly getting a little better, but has been in a nursing home for quite some time. I am moving her to assisted living near me when she gets out. I have asked my brother and sister to help me many times with cleaning out and moving her apartment items. They continue to ignore my emails, texts and phone calls, or make amazing excuses. I have fully given up on my brother and sister to help physically, and really need them to help financially. I keep asking for help, but they keep avoiding me. My new plan is to do everything, and to start keeping receipts and billing them for each and every thing I pay out for my mother. I am tempted to start billing them for a portion of my caregiving hours just to prove a point to them. I have started keeping a log of exactly what I do, and how many hours I help her because I am not sure they know exactly how much I do for her.
I truly hate my brother and sister, and when my mother passes, I am going to let them know just how much I hate them. I am only being nice to them out of consideration for my mother at this point. I can't wait to tell them how much I hate them for putting me through 10 years of ABSOLUTE HELL.
What tends to happen so often, is that such arrangements evolve informally, and because it seemed to be just an evolving form of family relationship, that sib who is involved directly end up seeing the needs as they emerge, and so they don't feel OK just ignoring them. Needs grow, and they end up giving lots of their time.
They should talk to other sibs at that point, and say, Mom needs this level of care. If she can pay, then her finances (or inheritance) should be allocated for care, whether it's to an assisted living program or to a live in sibling, likely at a reduced rate, but not insignificant.
The difficulty I found, being caregiver for my disabled brother - is that when I was the closest geographically to him and began to help him, I saw the risks and needs, but my other sibs were off leading their own lives, and it was not possible or was lots of trouble to let them know of every need that came up. I didn't begrudge them doing so, but I wrongly assumed that they understood how much care my brother needed - but they did not. Being far away, as I prevented crises, for I learned how they would set him back in massive ways, and this could be prevented with attention and help - if I complained and demanded help, they said, "What's the problem? He's doing fine, he has no crises." .Of course not, for I was working to prevent them. My sibs knew I was doing that, and they didn't worry, for suddenly the major problems disappeared, as I handled them well. They didn't even notice how much time passed, so they minimized how much was needed and done and for how long, and after the fact, argued about it..
The kind of care and risks and plan should be quantified for the siblings who are not close enough to the situation, to realize that major risks are being addressed.
Sibs need to request/demand an objective family research process to study options with written costs. Informal caregiver should track and write up hours spent in helping, or number of chunks of days disrupted, for it's not just the time of doing care, but of disrupting one's life to be available on call. An elder care professional can help add some reality to considerations of all the siblings, for care costs money, and you don't have just one person aware of the needs because they see them close up, and handle them, while the others are not paying attention.
As children we have often been taught that it's our responsibility to watch and help each other in families. Some sibs take that message to heart, while others either believe it's not a valid expectation, or else they don't know what's needed, or minimize how much is needed as disabilities of a parent grow over time. They need some expert to inform them that crises can be prevented, but it takes attention to see all the things that go into facilitating a quality life for person losing memory, vision, mobility.
It took me years to keep clarifying to my distant sibs, what was needed and what I did, and that it was not easy for me, and that I helped out at a cost. My doing so, meant that they never had to worry. They could have chosen a different plan, but nobody stepped up to suggest it, and what I did worked well..
If it works out well for the fragile person (based on their safety and cleanliness and health and getting to MDs and to some day activities), it's worth making an effort to share information and come to an agreement that feels fair to all sibs. I finally got a monthly stipend of $300 from my disabled brother's funds, right through my own retirement - not much but it's something, and the recognition means a lot to me.
Yeah, cuz some kids in the alcoholic home do fine and only a couple get of kids are selected for damage. Hervbalizer is doing her part care giving for others, that's enough. The other reason for not helping your folks sounds like a pity party ALL the children of alcoholics would like to have. Those of us who show up only have one reason for doing so much: you aren't carrying your part of the load so we have to.
Your brother, with 2 cars, asking for the car is beyond unconscionable. I often think, these lowlife siblings have jobs and and families and function in the real world?!?!?.....are they complete as$h0les to their families and co-workers too?
one of my brothers has a very important job at a big company and some days I want to call and leave a message with an assistant like, "just wondering why you haven't called, written a card or seen Mom in 3 years. " I know that is small and petty but, it is what it is.
I took care of my husband for 10 years. He died on advanced Alzheimer's at the age of 62. His own mother didn't spend much time with him and she knew he would die. Screw all the selfish ones. They are all dead to me!
I would like for them to at least provide some support...even just a caring phone call now and then. I always feel like my parents are my problem...completely.
And yes..if there is still an inheritance left..they are in the will equally with me...even the sister that calls about once a year...she is there favorite by the way.
You're right, it does "bite". And the kicker is once the parent is gone they suddenly appear. The very people who couldn't be bothered to offer any help or even call once in awhile, manage to show up after the parent is gone.
My brother couldn't be bothered even at the end with my dad(we had a great father)to come see him(and to support me) as he lay dying in the hospital for four days, but his ass was on a plane the day after. It was all about $$$$$. I can't get over that one.
He even had the audacity to ask about the car. He had two cars in his home state, I moved in with my parents(and this involved a cross country move) and gave up my car. I couldn't even believe that one, I said "am I supposed to walk to the stores now to shop"...unreal.
I am firm believer that the parent if they have any means, should consider that adult caregiver child be taken care of. Many times they give up a job(as you mentioned earning potential) which also impacts your SS benefits.
But the do nothings who can't be bothered make a beeline for the house once the parent is gone. You can count on it.
As others have said the answer you get when you get frustrated is "well you chose to do this"(no, someone had to step up to the plate and those who have a conscious do so), and "they're too busy to help"(yet when the parent dies they manage to show up).
Let's tell like it is, it isn't a misunderstanding, it's an "on purpose".
I found when I stepped up, that I felt encouraged and inspired by the positives in close range care - but could not communicate about those to distant, non-involved siblings. I think we learn best by experience, and the far-off sibs, don't get the same experiences, so their assumptions that the experts and professionals have all the best answers, and that delegating care to those people is all that's needed - they don't understand what is missing in their view, and yes, they do avoid learning more details, but partly because they believe that getting emotionally involved is a quagmire of endless sorrow and obligation that will drag down their efforts to sustain themselves and their families. It's a major cultural lack of awareness of the positives and potential of close-up care, and it's so important that our complaints as caregiver siblings, our sense of being abandoned with our many insights, is real.