My mom is 85. She keeps pretending to be sicker than she is. She also pretends that she can't speak well. Some would ask, "How do I know." It's easy . She gets sick every Saturday, when home health doesn't come. She does this to frustrate me and make me stay home. My sister nearby is a drunk. The one downtown doesn't care too much. The one in Alabama just sends texts telling me what to do. I'm seeing a counselor . For a while I just prayed for death to come to me. I still don't enjoy living. I lost my best sister in January. My mom faked a heart attack to avoid the funeral. Does anyone have any suggestions ? I live with her but I need to move out but don't want a guilty conscious when she dies, if she precedes me in death. Any thoughts ?
The second thing is your md needs to know what she is doing and you should ask for some help from them The US lasses and lads will tell you what they are - I am in UK so it is different for us.
She can pretend she is as sick as she likes every Saturday but I would frustrate that by asking the home health to come one Saturday and not on a Friday or some other day - you only have to play that card once or twice to have proof that she is playing you up.
Siblings aren't always supportive for whatever reason and I would just ignore them for the most part. I would however ask the downtown one if she could spare you a morning as you HAVE to do something really important - doesn't matter what just something. Then when Mum plays up say its fine Mum xxxxx is here see you later and go. I agree with Pam on your Mums medication.
Finally - you DO NOT HAVE TO LIVE WITH HER - if you are not of the type that CAN CAREGIVE then DONT - Caregiving and caring are two entirely different things - to be a caregiver you have to care but to care you DO NOT have to be a caregiver. Do not LET your mum play the guilt card on you - you will be effectively laying the guilt on yourself. - easy to say extremely hard to do.
She SHOULD precede you in death - she is your Mum when all is said and done - and that is the way of life and death. If you find the best option for care for her that DOES NOT include you then you will be able to visit her in a totally different mode and maybe the anxieties will go away for you. Once your mother comes to terms with her loss of control she will turn to other ways but don't let that impact on you - you have a right to a life too.
It's going to be a really bumpy road hun but once travelled the sun will shine on you once more and you will feel far better placed to cope
Saying they are sick is common confabulation.. Speech will go for real… Blame Alheimer's... add in manipulation as a controlling device and go bonkers
Everyone and particularly medical personnel and caregivers must understand!
Confabulating and Confabulations
In psychology, confabulation (verb: confabulate) is a memory disturbance, defined as the production of fabricated, distorted or misinterpreted memories about oneself or the world, without the conscious intention to deceive.
Key factors in confabulations are there is no intent to deceive, second the person being unaware that the information is blatantly false. Confabulating is distinct from lying because there is no intent to deceive, and the person being unaware that the information is blatantly false.
Carers challenge: is what they say true? Confabulations become a far greater concern in the later stages, because confabulations are much more likely to be acted upon.
It is difficult for everyone to accept a mind is damaged.
Confabulations are a major annoyance and can be dangerous- when we the take everything in a discussion at face value. Confabulating is very frequently observed in people with Alzheimer's.
Alzheimer's is without doubt frustrating for anyone who comes into contact with it - for the person because they KNOW the information is in there they just can't connect the dots and for the non Alzheimer's person for they just can't get to understand what the real issues are. For the person with it because their carers aren't meeting their needs and for the carers who know there is something they are missing.
I have said it before and I will say it till I am blue in the face - I HATE ALZHEIMER'S.
However in this case no mention of Alzheimer's has been made so I wonder if an assessment perhaps is required so that everyone knows what they are dealing with
As children of an emotionally dependent, narcissistic parent(s) we are struggling to become adults. Our parents didn't know how to make the distinction between their roles as our parents and their left-over emotional needs as children who were probably abused and neglected themselves. I know exactly why my mother is so broken emotionally! Some of it is of her own doing. When we were young, she could suppress the feelings of hopelessness more because she had small children to distract her from the memories of emotional loss and abuse. She developed very ineffective coping mechanisms, but luckily didn't subject herself to addictive habits, just extreme codependency. My mother made me her substitute spouse from a young age. I have always felt emotionally responsible for my mother and I was pulling away from her because I was angry with her for burdening me with that. She controlled me and manipulated me until about 4 yrs ago when she had a mild stroke. She has been over-playing this stroke like you wouldn't believe. The stroke was her only hope of pulling me back in.
I haven't had a life for about 4 years now. I want to be in a relationship and deeply value family. I plan to take my life back and in doing so, i will have to make some very hard emotional decisions where my parents are concerned.
A few good things that I have learned through all of this are:
1) you can't want more for someone than they want for themselves.
2) I have a choice in exactly how much I want to give and take from this situation. That doesn't mean that I won't have to make sacrifices to be there for them, but I don't have to sacrifice "ME" to help them.
3) Helping my parents doesn't mean that I have to conform to their dysfunctional way of dealing with things. Helping them means keeping them as independent as they can be, for as long as they can be.
I will not do things for them that they can do for themselves. That is the problem with co-dependence. Codependent people look for others to save them when in reality they don't really need saving. This is very hard and emotionally taxing, but knowing that there are a lot of other people dealing with the same issues helps. The advice that I've gotten from others has been comforting and has helped me grow stronger each day. Learn how to set boundaries with your mother and don't feel bad about having to do that. I have so many people trying to make me feel guilty about drawing boundaries because they don't know how to do it. Learn to draw boundaries Nia!
I loved Jude's wise (as always) answer. Her idea that you change days for the caregiver to take off is terrific. If possible, vary the day so that your mother is kept off guard. That is counter to what I'd normally suggest but your case does sound like one of manipulation.
You mother needs to move into an assisted living facility or have a caregiver move in with her. Your siblings won't help and you've done this too long on your own. There's no need for guilt. She's supposed to predecease you. That's natural.
Line up care or, if need be, turn her over the adult protective services so they can force something through. Then move on with your own life. You can visit as you feel that you are able, but you can't let your mother end your life which could happen without change.
Please read this whole thread. There's a lot of wisdom here.
Carol
No one wants a turn, even for one day.
I am sure, and I hope, that you are very proud of the work you do to save lives. It sounds to me, from the little of what I have read of your postings, and the anger and contempt that comes across, that you need someone to save YOUR life.
I hope that you can find a bit of compassion for the patients in your care--and for yourself. I urge you to do something about your OWN pain.
This Friday, tell her that you have commitments of Saturday and must be out of the house. Say you will leave at, say, 8 AM. Before you leave, put breakfast on the table. Also, put lunch into the fridge, sandwich, whatever.
When she pulls the sick act, just smile and say she will just have to wait until tomorrow to be sick because you must keep your appointments...Do not try to explain what the appointments are when asked.
Now, if she is incapable of getting out of bed, then that is another matter.
You know, willingness is a big key to satisfaction in life as I see it. I see you reaching out for advice..that means to me that you are willing and have a desire to live more normally. Thus, it is encouraging to me that you may feel like you don't want to live, but your communication to the group shows that you do, but on a happier footing.
I am sorry I cannot be more helpful...More facts from your end might help. For example, if you do move out, do you have a place to stay? If mom is unable to be left alone, could you possibly hire a person to come in midday on days when now caregiver is at the house to spell you for four hours or so?
Try to think outside the box.
I wish you well....Please keep us informed of your progress and status as time goes along.
Grace + Peace,
Bob
As far we the "weekend-only" illnesses, you may need to practice saying, "I'm sorry you're not feeling well, mom, but Norma is here to take care of you. If you feel you need to go to hospital, call Emergency Services, they'll find me and I'll meet you there."
I joined this group because of the overwhelming stress so I could vent. My patience wore thin a couple of times dealing with my mom being so incapacitated, and having so little support from family, and I was very often depressed.
My mom passed away four months ago. She wasn't a saint, but she was still my very best friend, and I miss her terribly every single day.
Even though I know I did my absolute best, I still wish I could take back that time and relive it. I would spend as much time as possible with her, talk with her more, and be more patient.
Please try to realize your loved ones won't be here forever, and even though now caregiving might sometimes feel like a life sentence, you really won't regret the time you spent caring for them. I know it seems hard to believe it now, but the day will come too soon when you'll wish you could have had more time with them.
On the issue of you don't have to be a caregiver per se - I do believe that but you have to be able to live with the alternatives and that sit always easy either.
Some people simply are NOT cut out to be caregivers and caregiving requires a hell of a lot of mental physical and emotional strength that NOBODY will recognise - so don't hope for the impossible.
I personally think it is a d*mned sight harder to say I can't do caregiving than it is to go with the flow and do it because it is expected of you INITIALLY.
However once you are a caregiver and you want to stop being one then it gets really tough. Everyone (I call them the grey they because we all know they are there but no-one knows who they are) will say but you have done it so well or your mum loves the care you give.
Stay strong and say she might be happy but I am miserable and I have a right to a life. That is not narcissistic in any way - you do have a right to a life so don't lose sight of that EVER.
Therefore, I was "it". I didn't have the option of saying no and could see no way out.
My mom was lucky to have me, but I was also lucky to have had her. It's true that you never fully realize what you had until it's gone. That's all.
I had a great-aunt who had to have both knees replaced. The first one was fine and she did the required therapy but with the second she refused to make much effort; we found she liked the attention she received while she was recuperating and having others respond to her every command while "incapacitated". So she gave up doing physical therapy on the second knee knowing she'd get more attention. Unfortunately, she ended up in a nursing home where she passed away after a couple of years. She was in her 80s. My aunt was very overweight and her husband, also in his 80s, couldn't pick her up and care for all of her needs after a certain point . Her sister, my grandmother, a strong, proud, responsible woman, who for most of her life did not want to inconvenience anyone, passed at 95. For most of her life, she used to "do" for others. For the last 10-15 years of her life, she became increasingly needy (much unlike her younger self). It's like a switch flips in their brain at some point and some elders revert to more toddler-like behavior. Trying to reason with them doesn't usually work as they may nod in agreement and then keep doing what is meeting their emotional needs. The difficulty comes in that they are not 3 and you would feel bad treating the person who gave birth to you the same way you would handle a 3-year-old child. It's like a role reversal where you are now the parent and they are the child. It's hard to handle. It was easier for me knowing that the changes in their elderly brain was responsible for their behavior and to not take the criticisms, etc. personally. However, at times, this is easier said than done.
Most people don't want their parents to die. As others have pointed out: she is your mother, she is 85, and in nature's scheme of things, it would be normal for her to pass before you do. If that happens, I don't see that you have anything to feel guilty about.
Try to take some solace in knowing you are not alone and the world won't end if you don't meet your mom's every need. I worked for a micro-managing, narcissistic, perfectionist for several years. When I figured out the personality type, I began to have less stress as I did the best job I could manage to do; and, at the end of the day, if I was happy with my efforts, then I really didn't care what the manager thought because no one's efforts really pleased him. So I suggest you do what you would want done if you were in your mom's shoes and be satisfied with those efforts. It sounds as if they are certainly more than any of your remaining siblings are doing.
I know some areas have senior daycare services or companion services. If possibly, perhaps you could get someone to come in on the Saturdays...or switch days around (if feasible) with the healthcare giver.
That said my daughter does come and take us out - but she rarely offers to stay so I can go out alone.
I would be a politician if I thought anyone could address the issue of whose rights come first theirs or ours....it does always seem to be theirs and sometimes at great costs to our rights.