My Mother needs 24/7 care. I myself take care of her on the weekends. I have a daughter that has a disability and have to care for her. My siblings do not want give up there weekends so they think they can force me by saying if something happens to mom its your fault.
Most of the best involve setting realistic, rotational limits on other's use of you and your resources.
Limit setting should be a learned skill from childhood, but, too often, instead of that, we get taught how to cave-in to being guilt-tripped.
Please look into respite care, or a senior day care center [if she's up/mobile].
Your local ages Agency on Aging might have some possible resources to help with home care for Mom, too.
Last resort is putting her into a facility, which is very costly, one way or another.
Maybe check with local churches to see if there might be any volunteers who could give some time-off from elder care.
Always background check the persons who might be coming to the house to do elder care.
Hope things go well for you; just know that, in families who use guilt-tripping tactics, it's fairly common for them to resist ever "working cohesively" together to accomplish Mom's care, because it's not about their busy weekends....it's really about them not wanting to do elder care...they'll think up any excuse, including refusing to sign for "return receipt requested" letters.
[I did that, to make sure they got them, asking them to work together---2 refused to pick up the letters; one waited until the last minute before it would have been sent back; none answered the letters. It was clear none wanted to participate in working together; all were inclined to emotionally tear each other to bits to avoid working together.]
If a person fails to set reasonable limits on others use of them, it makes it way too easy to end up in predicaments we cannot abide. Sometimes it requires getting help for ourselves to learn this skill, which a good councilor can help with.
PLEASE don't do it out of a sense of duty - it is NOT a duty. It is a commitment that can last years and if you decide to continue, you must take that into account.
HOWEVER, you can say NO. If it is too much for you - period- then you have to say time to change the arrangements, have a family meeting or if they really don't want to know then a Skype or email conversation.
When you say family I am not sure whether you mean siblings. Well meaning siblings who cannot/will not do the hands on care but see fit to criticise do my head in and (with the exception of my cousin who has dementia) I tell them to hold the criticisms until they have walked the walk.
Sometimes however the criticism is not of the care you give but is out of concern for the fact you are not coping and sometimes outsiders (even family outsiders) see that better than you can because you are so involved/stressed etc that you can't see the wood for the trees.
Let's shed a little light on that dark tunnel you're in. Repeat after me I am not worthless and I can change things. That is going to be your mantra every day. And every day you have to put a little extra in to establish your NEEDS - said it before will say it again - your NEEDS (not wants) MUST be met.
You NEED respite - you MUST have time away from your parents and I don't mean a couple of hours to do the grocery shopping - that is NOT time away - that is another chore. Time away means taking time out to stop and smell the flowers along life's journey. Respite should NOT be a couple of hours - it simply is not enough time to recharge batteries. Respite is NOT taking your parents out for the day or on holiday - thats just part of the care package
Real respite is having your parents cared for while you do WHAT YOU WANT TO DO and if you want to lie in bed and sleep for a week that's fine (not advisable but fine).
So having done that little extra to determine what your NEEDS are...now your next bit is to work out how to make that happen. Trust me the state doesn't want you to be ill - for then someone else has to do the care and that costs money. Apply a little pressure and see what's out there.. Charitable groups/the church/ grants/ plus all the usual Medicaid. Hassle social services/your doctor - they get PAID a handsome sum to very often do a piss poor job so make them earn their money.
If your parents have money then they must spend it. Lie if you absolutely have to and tell them your Blood Pressure is through the roof and the doc says you need to rest. Whatever you do get yourself that break - then perhaps you will see things differently. It may be you need them to go into some sort of AL or other care facility but right now you are not seeing the alternatives - day groups, afternoon teas etc.
Good luck Hoping - time for you to do some serious thinking and take action - if you don't change anything you won't get anything different and you NEED something different xxxx bless ya
We have well off family retired and non who flies all over but yet doesnt come here. So, this board said kids first( I did put them first but tried putting gpa and my died first too, it doesnt work) then any time then can help in whatever way you can. Its hard, the guilt and obligation to care for your mom, your child, and yes, you!!! They wont like that your putting your foot down, but you need help with your mom, you need to care for your daughter and you. Since January, I have been firm! My health got worse too, dont let this happen to you, take some time for you please.
Sorry to make this long, I didnt read through all the replies but I do know they all gave you great advice and support already so I cant add much. Just wanted to say your not alone and I understand as well as lend you my support. Being firm and sticking to it is hard, but needed. I just wanted to let you know Im going through it and you can do this too. This forum is wonderful and honest, will give the the best support you can get. Many hugs!!
When your siblings do pitch in to help thank them specifically for what they have done. "Peter, thank you for going to Mom's and replacing the light bulbs and organizing the mail. I know Mom appreciates seeing you and I appreciate having more time to maintain my own home. Thanks again."
Those used to using us badly, can turn ugly if we suddenly change what we allow...which is their problem--they either see their part in the issue and choose to change, to be allowed to stay in your life, or, they find others who allow them to stay the same.
You can't make them change their attitudes / perspectives, except by choosing to
improve yourself. What they do in response to that, is up to them.
Did I miss who takes care of mom during the week?
Is she on her own M - F? How's that work?
OR...could those providing care on weekdays, also help on weekends??
Things you can do might include: Create a data packet to send, return-receipt-requested registered mail, which includes things like [not in this in order, and not limited to]:
--pamphlets and other information on at least 2 viable facilities which could appropriately serve mom's needs;
--state what your needs and those of your family are [disabled child, work, limited funding, wear-and-tear on your vehicle, etc--what fits your situation].
Putting it in print allows you to edit it to be concise, and they can reread as needed. It should state facts only, about your needs relative to your family, and mom's needs, in the fewest, most concise words.. This is part of necessary legal paper trail.
--could start making 911-well-check calls on mom, as this is also part of a legal paper trail. This is important, when elders might be in a grey-area, not yet diagnosed as being unable or incompetent. Officers observe and document if the living conditions are deficient or untenable.
--include copies of things like in-home evaluation by social worker/home-health nurse, about mom's actual level of care needs; copies of the well-check notes; list her habits/behaviors which substantiate why/how she needs full-time care [hoarding? filth? bills unpaid? no groceries? wandering? acting-out inappropriately? cold? heat? health/fire hazards? etc.].
Why? Because adult children of fading elders often cannot, or refuse to, admit mom needs more care than is realistic for family member[s] alone to provide, until, maybe, they see it in writing.
Also, making a paper-trail protects you: you are performing due-diligence on behalf of your elder who cannot. THAT shows you are trying to do what's needed, and trying to get siblings on-board to work together on it...if they refuse, that is their own neglect, not yours.
I did something like this, trying to get my sibs to at least add their voice to decision-making, so we could work together on it.
Copies of letter were sent listing mom's needs, brief of her behaviors, care facilities which might work for her [or not], and let them know I really wanted all of them to work together on making choices for mom's care. I also let them know mom had signed paperwork to donate her body to medical research and cremation.
[2] brothers refused to sign for their letters; those got returned.
[2] sisters signed for theirs, but refused to communicate rationally or reasonably about it. One of those devolved to calling me a b**ch; the other one, with mom's dysfunctional goading and collusion, eventually pulled-off a "secret-squirrel -007" maneuver,to extract mom from our house to theirs, 3 states away.
The letter sent all of them, was the best way I could think of to avoid confusion of verbal communications; AND it motivated them to do something....it was not necessarily the best thing, or in the best way, and it was done in hurtful ways.
...but it got mom out of our home, which was catastrophically necessary at that point.
They all showed their worst behaviors, though managed to keep civil tongues at least while hauling out mom's hoardings.
This final episode helped me understand to just give them, with love and forgiveness, what their behaviors and words had repeatedly, loudly indicated for years....that they wanted me out of their lives.,
They have communicated very little...mostly silence; a little verbal acting-out...which I ignore.
They seem to have quit making snotty assaults, but likely will fire-off more volleys when mom dies, for my refusal to contact any except via print.
If they email anything that actually needs a response, I answer in the fewest words, just to that question.
And wish them well.
Unless and until they show consistent loving, inclusive and respectful behaviors, and willingness to hold actual sane conversations, I have no other way to understand their decades of repellant behaviors.
Behaviors speak more volumes than words; but mean words sure can ice-the-cake.
Are you willing to keep accepting/putting-up-with, the current situation?
What might you expect to gain by continuing as things are?
Are you willing to make constructive changes? I hope you can! It's tough tasks for those who aren't used to it.
We're rooting for you to handle it for the best outcomes! Keep us posted!
Carol