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I had the worst realization this weekend. I realized that my mom lives her life in fear. She is like someone who gets hit over the head, kidnapped, taken to a strange place with strange people. She knows she used to have people but she can't remember who they are. She doesn't know what is going to happen to her or if anyone she used to know is going to find her or if they know where she is. She has been at her memory care for almost 2 years and they are very good to her but of course she is declining and now the fear is evident. All day. I can't give her any relief that lasts longer than 30 seconds now. My sister and I see her every day. And until the last couple of weeks or so we were able to comfort her. Now everytime i leave her it feels like I am abandoning her and it kills me. It is so freaking painful to not have any way to make her feel safe. I can understand why so few of the other residents get any visits. Most of the residents (10/12) are completely zombie like which I almost find myself wishing for her just to relive her stress. There is one other lady who talks and reminds me of my mom a year ago. This is 10 years of thinking that this has got to be the rock bottom. Things can't possibly get any worse. And yet they do. I pray for my mom to be free of this horrid disease knowing there is only one way out of it. I love her so much. I am so sad and I am so mad and I just needed to vent to people who could possibly understand the trauma that infects the entire family with this disease.

Dementia is such a terrible disease. Is your mother on any kind of medication that may lessen her anxiety and help her relax a bit?

Lealonnie in the comments wrote that the drug Ativan helped her mother. It really can. Talk to the DON at the memory care and ask about it for your mother.

That's kind of you and your sister to visit her every day, but have you ever had your mother observed in the memory care by someone you know but she doesn't? I ask this because I worked as a caregiver to clients with every kind of dementia for many years. In many instances the person in memory care or assisted living does just fine until their family shows up for a visit or calls. For some reason this triggers them into the panicking, hysterics, or negativity and complaining. It's no one's fault. Their minds often do this. Have someone you know but your mother doesn't go and visit her. It may bring some comfort to you and your sibling to know she may not be panicking and flipping out all day long.

Good luck, and please ask about getting her some medication.
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I just want to say that your "venting" is an honest and beautiful (albeit heartbreaking) expression of your feelings and what many people experience. Although not your intention, I'm sure that others reading this post will feel seen and not as alone. I've learned that writing is a powerful tool when dealing with grief and I thank you for sharing with us.
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My FIL had Parkinson's related dementia. It came on gradually and I don't think his family wanted to admit it was a problem. They insisted on including him in our very boisterous family gatherings for holidays, etc., with lots of kids, people and activity. There were times when he just looked lost and scared. The group photos at these times makes me sad. He was definitely fearful and they were not thinking rationally about his presence. They just keep forcing the routine because they could not accept that he wasn't the same and things were changing. The important thing is that you recognize what is happening to your mom and you want to help her. Please talk to her dr about adjusting her meds to add or increase her anti-anxiety meds.
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Yes it sucks. My father is unresponsive when I try to make conversation. I want this to be over. I feel bad because I am impatient for the end to finally arrive. He’s been like this for two years and is already gone as far as I am concerned.
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If mom lives in constant fear, she needs meds to calm her nervous system down. Stat. Ativan worked pretty well for my mother and once hospice was on board, it was scheduled every few hours. Ativan took her from looking in the closets for her dead relatives where "I hid them" to being much more relaxed in general. Hospice was a huge blessing and I suggest you ask her doctor for a referral.

This whole journey is awful, and I feel your pain. I did a lot of crying myself over the years. Mom finally died at 95 very peacefully, thanks to hospice, and I was very relieved she was at peace after all the struggles. Wishing you good luck and Godspeed with a difficult situation.
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Have you spoken with your Mom's doctor?
Many are helped by a low dose anti-depressant.
In Austin, Tx. a friend's mother was helped enormously by prescribed marijuana in small doses. She went from paranoia and fear with almost zero appetite to calm, relaxed and eating.

I think this is something to discuss with medical team for your mom's comfort at this end of life stage. There is nothing to lose in trying things.
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It is so very very sad. Thank you for sharing and please know you are not alone. Hugs and prayers.
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I know. It is one of the saddest things to witness our loved ones lose their ability to remember. It broke my heart when it happened to my mom. And with some of my patients, I would cry on the way home. I am hoping and praying that new medications and new discoveries will continue to be made... I retired 8 years ago and they know so much more about Alzheimer's and dementia than they did back then. All we can do is our best in making our loved ones as happy as we can for when we are with them. Hugs.
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