Follow
Share
Read More
This discussion has been closed for comment. Start a New Discussion.
Find Care & Housing
We call yogurt "pudding" and dad eats it right up!
(2)
Report

We went to her doctor today. I discussed the problem with floor and towels. The doctor prescribed Celexa. She started it this evening. I hope that it agrees with her and we'll see some improvement with time.

Her new bed arrives tomorrow. She has been wanting it off and on for a while. She is in her anti-bed frame of mind today, resenting the fact that I ordered it for her when she didn't want it. I wish she had started on the Celexa a while back. I fear that she will make herself dead-set against the bed and it will become a source of her woes. She started on it tonight, saying because the bed we couldn't do house repairs that needed doing so badly. I just smiled and said, "Don't worry. Be happy." I was talking more to myself, I believe.
(2)
Report

Hugs to you, Jessie. I hope the new medication is very successful.

You say, "She is still in the moderate dementia category, with most of her memory intact," and therefore don't think she is ready for hospice. That may be perfectly true. But Coy had most of his memory intact right to the day he died. And though the autopsy revealed a very severe case of LBD, his dementia was in mostly in the moderate category to the end. Your mother may not be even close to needing hospice, but don't look to just her memory and dementia symptoms to determine that. See how the new drug works. Since you do intend to use hospice services, it is better to have an evaluation too early than to late. Just keep it in mind.
(2)
Report

Jeanne, when I woke up this morning, I was thinking of how the life has begun to fade rapidly from my mother's eyes. Her body has slowed down to near-stop. One hope I've had for my mother was that her mind held out as long as her body. I realize that she may be nearing the end of her life faster now, and it is not just depression and anxiety. I don't know what the next few months will bring. Maybe I will try to put together some things to make the end of her life richer. My out-of-state brother is visiting in April, so it's a good time to plan.

We have an appointment with my mother's doctor in a month. Maybe the Celexa will pick her up some. If not, I may talk about bringing in hospice. My mother still likes to get out some, but maybe we can just go out to eat, instead of going to the doctor. My mother was opposed to hospice for my father until the last day of his life. Hospice to her meant letting go. I don't know how she will feel about it for herself. I hope that she will welcome it.
(1)
Report

Jessie, glad she started on the celexa..... it is a great medicine. I don't think antipsychotics should be used unless used as a last resort. Good job!
(1)
Report

Jessie, you are sensing a downward turn in your mother, and who would know better than you. I do hope the Celexa will help her mood and general functioning and also make care giving a little easer for you. (((((((hugs)))))
Let us know about the bed and if she accepts it.

Jeanne, your insights from your experience with Coy are very helpful.
(2)
Report

Hope things work out. Hugs!!!
(2)
Report

Her doctor told her no towels and blankets on the floor. It worked for a day, but today they were back on the floor, so I took them up. She has decided her new bed is all wrong and she can't sleep on it. Then there was another crazy-making incident. I had put down a secure floor covering in the hall -- the rubber pieces that fit together like a puzzle. She decided she couldn't walk on it, so I took them up and put them in the rabbit room. This morning she said I needed to put them back in the hall, because it made it easier to walk. I told her they were no longer available, which is true because I'm not going to move them again.

I had decided yesterday to do things to make her life happier until she died. I realize, of course, that it was wishful thinking. There's really no way to make her happy. She is already stressing over my brother's visit in April. She is pressing me on cooking a huge feast and inviting everyone. Today I'm hiding out in my room, trying to put a little order to the chaotic hoard that is accumulating. Clutter drives me crazy. I wish I could get a little bulldozer and go through the house, pushing everything out the doors. That would feel good. My mother is a hoarder. I was able to get everything manageable, but it is still too cluttered to clean. It drives me crazy, because I am just the opposite.
(1)
Report

JB I know what you mean about eyes. My mother has a blank look a lot of the time and a little evil manic smile when she's cooking up some manipulative lie or story. I've tried to figure out what stage of dementia she's at but I can't find anything definitive. She's totally irrational, demanding, accusatory and delusional. I don't visit too much now as it was affecting my health.

When the hospital returned her to the NH after another stroke a few months ago they deemed her "palliative". She can't sit up or stand alone and will never walk again. She weighs less than my big labrador. I can't get a prognosis from anyone and the nurses/doctors just say we have to take things one day at a time.

I backed away almost 2 weeks ago after having a TIA due to the years of stress. Since then, apart from basic chores, I've been resting and sleeping a lot and I'm starting to feel better. Almost 2 p.m. and once the dishes are done I'm going back to bed with my dogs and taking a nap.
(3)
Report

JB I can't and will not deal with the looney tunes any more for the sake of my own health.
(2)
Report

I can understand that, Ashlynne. Whether they are ill or not, being jerked around is no fun. I do wonder at myself and the need to make her happy, knowing that it is not possible. It must be that stupid inner child again. I'm going to have to locate that inner child and tell her to knock it off before she drives the adult me crazy. :)
(3)
Report

JB it never occurred to me until a mutual friend said some time ago "Well, your mother's never been happy with anything" and she was so right. Looking back as far as I can remember, nothing was ever big enough, good enough or grand enough and she was never happy in her life. Never mind keeping up with the Jones's, she had to have more and be better than the Jones's. It never occurred to her that a big fancy house can be mortgaged to the hilt, an expensive car leased and that those she so admired were likely in debt up to their eyeballs.

When you find your inner child have her look back over how your mother has been all her life. Some folks just are never happy and nothing can make them happy. {{{huggs}}}
(3)
Report

To you all who are dealing with what appears to be end stage dementia and narcissism, my best wishes. Something that I found works for us, is never telling Mom about anything beforehand. Not visits, not weddings, not nothing! When it happens, it's a nice surprise. We started doing this to save OUR sanity because she'd obsess over everything for months on end; last summer, before my son got married and she had declared that she wasn't going to the wedding, her doctor said to me "please don't try to talk her into it now; she'll drive us ALL crazy all summer long!" he was right. Mom had a stroke (I'm convinced it's because of the 90th birthday party we gave, where the very few guests brought small gifts. She obsessed over the thank you notes and stroked out). On a more sobering note, in September, when she was already in memory care, she broke her hip. they did a scan of her skull/brain to make sure there was no concussion; the picture was sobering. There's more space than brain at this point, so we "get" why her reasoning isn't there anymore. Something to keep in mind.
(3)
Report

Something that helps me at times is to step outside the situation and look at it like a sit-com. It makes it all not seem so serious and depressing. If we need to live it, may as well try to make it more live-able.
(1)
Report

We too do not mention appointments to my MIL. She too obsesses. It does wonders!
(1)
Report

My mom doesn't have dementia, but I've learned not to tell her we're going somewhere ahead of time or I'll get a litany of reasons why she doesn't want to go and isn't up to it. Now I just go over and say, "We're going" and get her dressed and we go. MUCH easier on both of us!
(4)
Report

This discussion has been closed for comment. Start a New Discussion.
Start a Discussion
Subscribe to
Our Newsletter