The last week has been an eye opener, I slowly watched as he scanned through the guide on the TV, then decided to scan channels one by one. I said nothing. Then he asked my daughter to read something to him after looking at it for several minutes. I said nothing. Yesterday he make a comment that Mom was hiding out at her sister's house, this is a dreaded loaded response.
"Daddy, Mom passed away almost a year ago now." He was silent.
"Did you hear me?"
"Yes, but you are lying." He rubbed his chin and raised an eyebrow.
I gave him her obituary, he starred at it for several moments, "It's dark in here and I can't read it." I turned the lights on.
Again he handed it to my daughter to read, he spat, "Why didn't anyone tell me?"
"Daddy I did, you were here when it happened. She passed here at home."
An argument ensued and I removed myself from the situation. Later returning to confront him about being able to read. He told me he could not read any longer and the words made no sense to him.
Keeping up with what he is losing is hard, people with ALZ can hide things very well, they think that no one will notice. No longer can you just hand him his meds to take. You must stand there and make sure just as you would with an obstinate child. All the while making sure you don't treat them as a child. You don't discount the fabricated stories they tell, you do not correct them or you are in for a battle. I decided to say, "Well, I never knew that."
It is his world, your world and the two will never be the same again. Roll with it, yes you will anger, but temper that anger by removing yourself. It is hard, if someone tells you it is not they are flat out lying or their parent is not as far along as my father. Another problem is severe paranoia over their money, I keep the checkbook handy to show him what is going on how his money is spent on his living expenses. He is angry that bread is no longer a quarter, and pants are no longer two dollars.
Keep all your receipts for everything so that they have them, it is a comfort and I can't tell you why. I have been called so many names I can't count them on one hand, screamed at, and made to feel as if I did not matter. Let it go, if you don't it will drive you insane, because in ten minutes he won't remember saying anything.
Endless days and Restless Nights - living with, caring for, and loving someone with Alzheimer's. Tips and tricks not told to you in any text book, crafts, and memory loss. Your emotions are important and I am sharing our emotions.
Showing posts with label disengage. Show all posts
Showing posts with label disengage. Show all posts
Monday, August 3, 2015
Friday, July 17, 2015
Another Endless Night
Sit back for a moment while I go get me
some more coffee. I have been awake since 11 pm last night after
coming off of a two day insomnia. Daughter is sick and so is her
fiance, so it was my turn to pick up the slack. Hold on....okay here
we go. Today I am sick, not sure if it is from running for two days,
or I have managed to pick up their bug.
Dad has been in rare form, God I love
him, but this is like having a child all over again. They don't tell
you that, pretty much no one mentions that BIG fact. He throws
tantrums out of the blue, forgets who you are and decides it is OK to
talk to you however he chooses.
Here are some hints on how to handle
that situation.
- Disengage from the situation
- Do not take it personal
- It is the disease not them
- Find him/her/yourself something else to do
- It will be fleeting just give it fifteen minutes and it will pass
He is certain that Christmas is next
week and I am too lazy to go buy some presents. I keep telling him
that his birthday has not come yet, that is mid summer and when the
leaves fall from the trees that is when I go shopping for the
holiday. This is not going well insert giggle here.
I was on the phone from 2am to 3am
trying to get him back to bed so he can get up this morning and take
his medications. Once he is off schedule his symptoms become worse.
The hopes that this will get better are gone, the medications do not
seem like they are helping any longer. Although using the new depends
pull up diapers are much more friendly for him.
He has many days he doesn't realize
that Mom is not coming back. I have attempted to do her room several
time, but even dusting sends him into a tizzy. I talked to his doctor
and he told me to leave it alone until he was ready to handle it. As
long as he can go in there and see her things it is a comfort and not
to take that away. I have to admit I too find comfort, but also
sadness. I will leave things as they are for now. I am just not so
sure other people that may happen by the house is going to
understand.
Life changes so quickly, and I find
myself afraid to open his door in the morning, because I am not ready
for the inevitable yet. I have not even grieved for Mom yet.
Tuesday, May 5, 2015
Another Day Repeated
I know how you feel, and I feel for you the angst, constant questions that are never answered so that your loved one can understand and exasperation begins to set in. Take a deep breath, realize this is not your loved one , this is his/her disease and it is not going anywhere, it is not going to get better, however it will get worse. ALZ is not your friend, it takes away all that you once knew leaving an empty hole.
Just another day in the life of ALZ. I will write more, I had planned on it, but my mother his primary caregiver passed away and I have been working on non stop days where there is no time to sit and write. I will promise to write more later.
One escape when I get an alone minute
Just another day in the life of ALZ. I will write more, I had planned on it, but my mother his primary caregiver passed away and I have been working on non stop days where there is no time to sit and write. I will promise to write more later.
One escape when I get an alone minute
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