
Alzheimer’s disease en.wikipedia.org
By Larry Peterson
What follows is some insight for those who have never been a primary caregiver. This is more like “a day in the life” of someone living and caring for an Alzheimer’s patient who is usually a spouse or a son or daughter. Many folks have seen people with Alzheimer’s or have relatives or friends with the disease and think they “get it.” Still, unless you, as a caregiver, live it, day after day after day, year after year, up until the end, you do not “get it.” You just can’t.
Simple memories triggered
My thoughts and I were sitting together reflecting the other night, just floating back to days long gone. The trigger for the thoughts was my wife, Marty, who passed away from cancer and Alzheimer’s Disease five years earlier on March 27. The thoughts kept bouncing around, and the “little things” that used to happen frequently began to dominate the memory flow. Anyway, I would like to share some of those simple memories. This is from an evening I remembered well. It was when I promised I would call her in sick for work.
It began like this. After dinner (I had turned into a pretty good cook), Marty asked me, “What time is my show on?”
Sundowning
Reflexively I would ask her, “Which one?” I knew she had no favorite show. I also knew she had stepped into what is known in Alzheimer’s disease as “sundowning.” I called it, ‘Uh-oh time.’ I called it this because these were the moments when she would unexpectedly become frustrated and agitated.
I could see her tensing. Then she would look at me and, raising her voice a decibel or two, would say, “You know what show. Just tell me what time it comes on.”
I had become a guilt-free liar
As a Catholic who loves his faith, I do not lie. However, the fact was, in my caregiver world, I had become a guilt-free, therapeutic liar. It was about survival, mine and hers. My justification was that without me, she was alone, and she was no longer able to survive on her own. “Sorry, sweetie, your show is not on tonight. There is a special about sharks on, and sharks scare you, right?”
“You know I don’t like sharks. I am scared of sharks. But that’s okay. I can watch the news, right?’
“Absolutely.” I had lied to my wife, Marty. I felt no guilt. It was a necessary tool for me to use in my role as her caregiver.
She headed to the sofa, sat down, and picked up her puzzle book. She always was good at doing the anachrostics (I find them incredibly difficult). Still, she would sit and look at the page, holding the pencil on it, which never moved. Then she said, “Do I have to go to work tomorrow? I’m so tired. I really could use a day off.”
Liar’s Hat on
Two years earlier, I might have tried to explain that she did not have a job and had not worked in seven or eight years. She still may have understood. Those days were gone. So, with my “Liar’s Hat” still in place, I answered, “You’re right. You do look tired. I think you need a day off too. Don’t worry. I’ll call in for you and tell them you’re sick.”
“You would do that for me?
“Of course, I would do that for you.”
That’s’ so nice. I’m so glad I don’t have to get up and go in. Is today Sunday?”
Whew, a relief question. I could tell the truth. “No, it’s Wednesday.”
“Wednesday, are you sure?”
“Yes, it’s Wednesday.”
Things were quiet for a while It was about 9 p.m. when I walked back to the bathroom. Suddenly I hear smashing and banging coming from the utility room off the kitchen. I head in there, and in a matter of minutes, Marty had pulled out of the wall cabinet all of the plastic containers, glasses and cups, and other things inside and stacked them all on the washer and dryer below. “Hey hon, what are you doing?”
We have to get rid of the junk
She looks at me, and I can tell she is agitated. “We have all this junk. We have to get rid of it. Why do we have all this junk? We have to throw it out.”
Immediately, I switch back to my ‘Liar’s Hat’. “Okay, when should we throw it all out?”
“I don’t know, maybe right now?”
“Well, it is kind of late. Maybe we can do it in the morning.”
“I don’t feel like putting it all back tonight.”
“Don’t worry about it. I’ll do it.”
“Oh, thanks. I’m too tired
There was one final comment. She looks at me and asks, “We are married, right?”
“Yes Marty, we are married.” (That was not a lie)
She got into bed about 9:30 and was asleep in about two minutes. I was mentally worn out but I looked at her and realized that an innocence had come from an unknown place and embraced her. I also knew that when she awoke in the morning, she would not remember anything of what had happened.
I was blessed
Since I do not “punch a clock” I have the joy of being able to attend daily Mass at 8 a.m.. Marty will wake up at about 7 a.m. and always ask me, “Are you going to church?”
I answer, “Yup.”
She will ask, “Will you take me with you?”
“Of course.”
From 1 Corinthians 13:4-5
Love is patient, love is kind. It does not envy, it does not boast, it is not proud. It does not dishonor others, it is not self-seeking, it is not easily angered, it keeps no record of wrongs.
As a caregiver to a child of God, I was blessed.
Copyright©LarryPeterson 2022
2 thoughts on “A Caregiver Remembers; Living with Alzheimer’s”