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Hi, I am a long-time caregiver for a mom who has had BPD all her life (untreated by her wishes) and now has dementia. I took care of her by myself for as long as I could, the BPD presenting significant challenges to which dementia was added, perhaps 10-12 years ago based on signs I'm seeing in retrospect. She's been mostly bedridden for the last 7 years, with me nursing her, basically her full-time CNA. I never left the house during the COVID years. Ten months ago, she could still walk a little and I couldn't stay awake 24 hours a day (there was never anyone to help me). She got out of bed in the middle of the night, terrified intruders were in the house. Before I could wake and get to her, she was down and had broken several bones. Her next stop, after the hospital, was a rehab facility where she refused to have anything to do with physical therapy. After about a month, she was transferred upstairs to the SNF, where she has been ever since.



I'm going to come right out and say it, I let her manipulate me for decades before the dementia. Her BPD meant she was terrified of abandonment and she constantly threatened suicide if she couldn't be with me ALL the time. I tried, unsuccessfully, several times to get away and have my own life, but she parentified me from an early age and programmed me to feel guilty if I tried to escape. I knew I was being manipulated, yet I couldn't get myself to abandon her because she could never figure out to do anything on her own, couldn't hold a job, has never had a friend that I know of, and it felt wrong to ditch someone who is family who can't take care of themselves. My life has not been the greatest.



Since her admission to the facility, I have visited her every day. I tried getting a part-time job and working my visits around the work schedule (never the same hours) I was given, but without me there on a consistent basis, she stopped eating and lost so much weight the decision was finally made to place her in hospice care. I quit my job and now visit her at the same hour staying with her 2-1/2 to 3 hours daily. I haven't missed a day in months, even when the entire facility came down with COVID, including my mom.



To make things worse, my mom has recently become violent and abusive, screaming, cursing, hitting, and pinching people. She spits out any medication she's given because she thinks it's poison. I'm told she can scream my name for hours and throws things to get attention. I hadn't seen this myself, but tonight, she let it all hang out, throwing, cursing, and—when the nurses wanted to talk to me out in the corridor—she proceeded to tear up a handwritten notebook I'd created for her, wadding pieces and flinging them around.



When it was time for me to leave she pleaded, begged hysterically for me to stay. I told her I was sorry, but I couldn't, I really needed to get home (I'm trying to build an online business and that requires work). She grabbed me and wouldn't let me go. I told her I loved her and gently freed myself. As I left, I was treated to her screams following me down the corridor.



The nurses today let me know that since she refuses meds they will need to give her injections in her rear end, which is fine with me. I don't want her hurting herself, her roommate, or any of the staff. However, I'm not sure what to do to help her. Her emotional state, her clinging, and the same fears I have to calm every few minutes because she forgets, her constantly telling me "I loved you," (past tense to dramatically demonstrate to me that she's dying), make me wish I could just leave and never go back. She's my mom. I love her, I know none of this is her fault. Still, I'm exhausted.



Has anyone been in this position? How did you cope? What is the responsible way to handle this?

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So, I went over there today at the normal time. My mom was sound asleep from the drugs to calm her. I let the staff know that I would be cutting back to twice a week and will see her four days from now when we have her quarterly care meeting. I didn't try to wake, or hug my mom to let her know I was there. I didn't want to upset her and cause a scene. I feel awful, like a horrible person, but I did it.
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ZippyZee Apr 2023
You did the right thing

Stay stong!
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Have you read the memoir by Liz Scheier called Never Simple? If not, do order it from your library. Ms. Scheier, like you, spent decades attempting to provide for her mentally ill mom. Most of this time spent to no avail.

Can you not now understand that these daily visits of yours may actually be harming your mom? That they are causing her to feel desperate and out of control?

Do speak to the team at your Mom's facility. Tell them that you are cutting back for three or four visits a week. Then assess how she's doing with that If OK, then you try for 2 or three visits; that would be a good thing, reassesseding each time.

Meanwhile you need a GOOD psychologist, perhaps a licensed social worker in private counseling practice to help comb out the enmeshment that has happened with so many years of care. You need to be shaken up out of habitual ways of acting and reacting that are not working. At this point you two are so joined at the hip that what one feels is almost instantly mirrored in the other. Not a good thing.

I am so sorry. You didn't cause your mom's mental illness and there is no way you can fix it. As you can see, your trying to make things better may be having the opposite affect. Your mom has had an unhappy life, likely through no fault of her own, and CERTAINLY through no fault of yours. The end of her life, like all the rest of it, shall just have to be endured. Happiness cannot be a goal for her. My heart goes out to you.
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Stop visiting daily.

At the very least, go back to work. You have just one life and she has taken up all of it. Now it’s YOUR life and YOUR time. She is mentally ill. You can’t help her with that. She is getting care she needs and there is no need to rush to her aid daily.

The last thing you want is to be mom’s age and feel like you never had your own dreams or accomplishments. That would be the most tragic thing of all.
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I HAD to leave my beautiful, previously active, semi-independent LO in her Memory Care unit after I’d determined in EVERY WAY I could, that her condition was progressive and ultimately, without any sense of when, would be at least in part responsible for her demise.

YOU have a responsibility towards HER, AND towards yourself, to address the emotions that you have that have linked you to her as you are linked now.

I have not only been in YOUR situation as it is NOW, but I have been this enmeshed TWICE, with 2 of my dearest LOs, and slightly less so in a THIRD situation with another.

And from these situations, I have learned that you MUST allow the caregivers in the facility to become MORE IMPORTANT, as you become LESS, and that ths transfer CANNOT HAPPEN until you sever it.

You not only CAN “just leave”, you MUST do so. Every extended (and non-productive) visit you make to her is like applying g the bandaid, then ripping it away, for you BOTH.

By the time my mother finally entered residential treatment, I weighed 265 pounds (5’4”, SMALL FRAME). Trust me, it was not “Happy Weight”. It was an outward symbol of my misery.

You have PAID YOUR DUES, and you deserve better. You have placed her in a safe environment that can comprehensively care for her many issues.

Good caregiving NEEDS balance. Take some time to think about where “the balance” is FOR YOU. Then PLEASE take steps to find it.
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DemDaughter Apr 2023
Thank you so much for the thoughtful words of support and for sharing your story. Believe me, I am well-acquainted with the drive to self-soothe with food. I am trying to eat healthier now, though I won't say it's been a success just yet.
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Hospice needs to PROPERLY MEDICATE your mother to stop all this unhinged behavior! What other purpose do they serve but to provide comfort care??? Who cares about other meds via a shot in the behind with end if life issues at play?? Shoot that Ativan or whatever into her and she'll calm down with enough in her.

Please stop spending SO much time subjecting yourself to such a thing. There's nothing you can do BUT speak to her hospice team about calming her down FOR BOTH OF YOUR SAKES. Then leave this issue in God's hands to resolve as He sees fit, hopefully sooner than later.

Good luck to you
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Give yourself a break, and staff too, stop seeing her every day. Give her a chance to adjust to someone else caring for her. Did the facility request you not visit for a period of time? Most do to allow the resident to get acclimated to their new home.

If each time you leave she is acting as in your description, then your visits are very hard for staff as well.
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When my daughters were small - my youngest would absolutely refuse to eat - what WE ate. We now know it was because she is high functioning Autistic, has ADHD and Sensory Processing Disorder, but we didn't at the time. BUT that being said, her pediatrician would remind me of two things.

First, that if she gets hungry - she will eat. And second, that it is not necessarily important that a person get every single nutritional requirement in in every single meal - as long as it balances out over say a week or two.

I'm not saying that texture, temperature or taste are your mother's issue here of course- I'm just saying what others have said - if she is hungry enough - she will eat.

Dementia or not, your mother has a long history of manipulative behavior to keep you in line. And YOU are used to staying in line to keep her behavior under control. You completely changed your entire life to make sure that HER life was regulated. That carries over into the current situation - and now because of the dementia - there is little that YOU can do to control it. And there is also little that she can do to control it either - as you said, but dementia exacerbates in many cases the behaviors of personality disorders.

She is where she needs to be now. You can breathe a little bit.

As others have mentioned- I'm going to take this back to my daughters when they were young - because I think the elderly- especially with dementia - are very childlike in so many ways. When they started daycare- we could stay a day or two with them for a few minutes each morning to allow them to adjust at drop off. Then after that - we were expected to hug and kiss and mommy/daddy will see you this afternoon, we love you, wave and out the door. Did they cry? Sometimes when we were walking out the door. But they usually calmed down as soon as we were out of sight. I guarantee you though if we had stayed for several hours every single day - that they would have cried the entire time we were gone. And that the longer we did that, the harder it would have made it - for all of us - to finally just start hugging, waving and leaving at drop off.

I know it is not exactly the same thing - but in many ways it is. It is hard for both of you. But you aren't giving her time to adjust to depending on them. And dare I say, you are at loose ends and don't really know what to do either. But you've got to stay away and let her get used to being there without you. Many places don't want family visiting for a week or two AT ALL to give their loved one time to get used to the care facility and the caregivers without the family being around.

You ask what is the responsible way to handle this? I know you are worried that you are doing something wrong by leaving her there - first - let go of THAT notion. You aren't. And then take a break. Let them do their jobs. Talk to them about how long would be a good amount of time to NOT come to give her time to adjust. Let them do what THEY need to do. You do what YOU need to do. So that SHE can do what she needs to do.

Caregiving has very few right or wrong answers absolutely. You learn as you go. But one of the absolutes is if you don't take care of you, there won't be anyone to take care of them. Take a step back. She is where she is so that you don't have to be taking care of her every minute of every day. Now it is time for YOU to actually realize that you can do that.
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You’re handling it responsibly. The only thing I’d suggest is not to visit so often. It seems that your visits aren’t helping anything and are causing further problems.

She is being cared for by professionals, and you need to take care of yourself. So sorry.
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Oh my gosh, if anyone deserves to have a break and some peace of mind, it’s you!

You have given so much of your time and energy to your mom. It’s time for you to give yourself the same amount of attention that you gave to her. You have earned it!

Please give yourself permission not to visit as often. She has a staff overseeing her care and she will receive medication. Trust their judgment.

You’re a loving and caring person. Of course, you love your mom and realize that she has a mental disorder which is the root cause of her behavior.

You say that it isn’t ‘her’ fault. It’s not ‘your’ fault either. It’s not anyone’s fault. Her behavior still needs to be addressed and treated.

Hopefully, she will respond reasonably well to her meds and once her symptoms are manageable, you will be able to have a peaceful visit.
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You need to read two books:

"Boundaries" by Townsend and Cloud.

"Never Simple" by Liz Scheier. Liz's mom had BPD.

Stop visiting every day. Go once a week. Same time, for predictability. Bring a treat for her to eat. Massage her neck, give her a manicure and then leave.

Get a job. Get a therapist. Take back your life.
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DemDaughter Apr 2023
Thank you for those titles. I've been reading a lot about BPD lately, and will add these to my list.
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