My Mother has been in a conv. home since sept. She has alzheimers. She lived with me for 9 years. I really have to force myself to go see her and do not go very often at all. I am the only child and took care of her myslef while working until I finally got some help. Which seemed to take forever. It wasn't until she set my patio on fire that her doctor realized the extent of her disease since she always seemed fine at her visits. Its like I have a panic attack before I go to see her and it takes all I have to go there. Everytime she "never" remembers when I was there. I call her often but she does not ever remember the calls. Of course, I feel guilty not going. Actually haven't been there since Jan. But I find myself becoming physcially ill at the thought of going to see. My home is now peacful. I do have a 19 yr old daughter, but unfortunately she refuses to go see her. Only on the holidays. Does anyone else have this problem?
Pictures don't work, because he asks, "Who's that?" He doesn't remember being a pharmacist, or much of anything. A picture of his mom and dad produced a happy response: "That's mama and papa," for which I've never heard him address his parents that way before. His dad's been gone since 1962, and mom since 1985.
When mom visits, and kisses him, he doesn't seem to mind, but he won't leave my side to do what she wants... She's always been very controlling, and she's antagonistic toward me. He seems to prefer me to her. She has cognitive issues, and will never understand. The whole package is hard for me. Mixed emotions go with the territory. My comfort comes from elsewhere.
It wouldn't be so bad if she would just quit talking. But she yammers constantly. Most of it doesn't make sense or is a repeat of what she's already told me. Often it is some grudge against someone in her past like the way her father ran the family when she was growing up.
I really hate her. Why is she still alive?
I listen to her to try to determine if there is something different in her life which would signal a need for medical evaluation or a deterioration in her condition to the point that her living situation needs to be changed. I'm ready to step in but can't do it if she is still capable of being in charge of her life.
I take her on errands because she needs transportation and help carrying groceries. Fortunately she has given up driving on her own. The lady next door had two accidents before she decided not to drive. I think that was a deciding factor for my mother. Sometimes you get lucky.
Okay. Here I go. I can almost predict the conversation it's so repititious and boring. God help me.
She also yammers constantly and it is ALWAYS about some grudge or misconceived notion that she has, or crying about how my family doesn't like being around her, or that someone where she lives dresses weird or wears their hair weird or.... whatever it is... she NEVER has anything to nice to say about anything or anybody.
She has "yammered" consistanly for the last 10 years about wanting to move back to Colorado. Now that my husband has been transferred to Colorado, she thinks its a bad idea and doesn't want to go. I've told her, "Fine, stay here, but the rest of us are moving." She says maybe she'll just die and then we won't have to worry about. I have to bite my tongue to not tell her that she is right and we would be better off.
Now, I am on my way to do my weekly duties - groceries, medication, go through all her JUNK mail that I have told her a thousand times to just throw away (but she insists that I look at it first).... blah blah blah.... I dread it sooooo much.
So, MaggieSue, I COMPLETELY understand what you are saying and going through. I pray that we both can find peace with all of this soon.
Having vented here before I left made me feel more in control and I went in my mother's house with a sense of purpose that I don't usually have. I told her what we were going to do. Usually I let her muddle around and tell me.
The first thing she said to me was I was not talking loud enough. We go thru this every single time I enter her home. Then she remembers that she needs to put in her hearing aids. Usually she complains about the hearing aids but today I hustled her along and didn't listen to the story of how the audiologist ripped her off. Some of the reason she cannot hear is she can't comprehend more than five or six syllables at a time. All communication has to be dumbed down to her ability. So I wind up using hand signals and grunting a lot.
We went to the pet store and got her cat some flea & tick medicine. Mother stayed in the car but gave me her credit card. The girl at the store was kind enough to come out to the car to get a signature on the sale. Oh how much easier that was for all of us than me trying to get her out of the car and walking her to the back of the store.
Then we went to the hardware store where she insisted on coming in. She bought batteries for her hearing aids. I have to check those kind of purchases to make sure she gets the right size. She thinks the people at the hardware store remember her and treat her special. They remember her all right as she sometimes brings them old junk from my dad's workbench thinking they can sell it. It's embarassing for me, but they are kind enough about it and take the stuff.
Then we went to a grocery store where she sent me in to get her donuts. They we went to another grocery store to get lunch from the deli and other groceries.
After that we ate, I dosed the cat with flea and tick medicine, paid the bills and turned her mattress and made up her bed. She delayed me by telling me she was too tired to sign the checks for the bills. Once I got her to do that, I stopped by the post office and mailed them and came home and ate ice cream.
I feel pretty good now that it's over for a week. I still call her every evening just to make sure she's still able to answer the phone. If she doesn't answer, I go over there and check on her.
I decided to make a list of all the things she will say when I visit on Sunday. I can make a game out of predicting the repititous "conversation". It's not really conversation because I don't get to say more than 5 syllables at a time.
She will always tell me about her money. She is convinced that she is wealthy and is very proud that it gives her a step up in life where she can look down on the "little people". In reality she is not wealthy but has enough that I don't have to chip in.
Also she will comment about my hair. I keep it sort of short. Mother doesn't like short hair and thinks I should not wear short hair. Her personality disorder is such that she can't tell the difference between me and her. She says she "lives through me" and expects me to relate the details of my life to her everyday. Then she picks thru what I tell her and decides what is acceptable for her. You can be sure I don't tell her much anymore. She's got enough of my life as it is.
She's about as close to psychotic as you can get without being truly out of touch with reality. And now she's ancient and living in her dream world. Her brain is slow, but she doesn't seem to have dementia.
It's just tough to have to spend time in her fairytale world.
I fully sympathize with not wanting to go. My Dad also has Alzheimer's, and lives 500+ miles away. I dread driving to the airport for another visit, dread making the phone calls. It truly hurts to give up control of one's life, but they do need oversight.
My GP put me on Celexa because it is an antidepressant with some amount of anti-anxiety activity. This has helped, and I also have Klonopin (anti-anxiety) which I take on the actual visits.
Other things that have helped - forcing myself to take time to walk on a regular basis, especially when I am at my Dad's home. Talking to friends and to my pastor.
I wish you all the best.
Life is so the drama - and I see that the drama has continued for all of us. OH - and he even called all of the relatives b/c I was missing in action (I let the answering machine pick up!) Do you know how annoying it is to be in Wal-Mart shopping and have your cell phone go off fifty times? GRRR!
Oh my! How I have missed you all!
Secret Sister, you are so right - it's all about BALANCE! And how I needed a break !!! A few days away and a few more hiding out at home with my family - it was wonderful!
Both my parents would have hated to see themselves in chairs, wearing diapers and unable to feed themselves. They were proud strong people married seventy years. I get physically nauseated before my visits and deeply depressed after. The only other relatives are elderly and living in Florida. The nurses and cna's are great people. My parents were always clean and dressed properly when I visited. It's Mother's Day tomorrow and i'm in the fetal position sucking down ice cream. My life sux right now and I want to be free from the pressure.
I'm so glad you posted on this site. I hope that helps a little. If I were there, I'd offer you a cup of coffee and a hug. I'd attend a dementia support group with you. Know you're not alone. God cares, and I'm saying a prayer for you. Please keep writing. And please take care of yourself. You deserve to live free, and at peace. Hugs for all you're going through.
you can do this, we arent given things in life we cant handle...
I love my dad, and spend as much time at the nursing home as I can, but his wife (mom) rarely goes, and only for show. That is the worst part of all. Yes, it's difficult watching dad decline, and all the behaviors associated with Advanced Stage Alzheimer's, but the horrendous family dynamics are the biggest heartbreak of all. Thank God some people see it for what it is, but some do not, and they are part of the problem. Wednesday's child is full of woe, and I was born into adversity. I'm asking for strength to endure. Mom is declining in her cognitive abilities, and worsening in her envy and hate. My sister's greed and bitterness knows no bounds. I grieve. At least my dad still gives me hugs. No pity party here, just stark reality, and it's not pretty.
Ultimately, we stand before God. And he knows our heart, and who is doing right, and who is doing wrong. Ultimately, I hope to hear, "Well done, good and faithful servant. Now, enter into thy rest." That is my great hope. Until then, I'll appreciate all the prayer support I can get. Thank you, and God speed, fellow caregivers.