2018, Family Fun

03.20.18 Communicating in Alzheimer’s World, by Bob DeMarco, AlzheimersReadingRoom.com and other things

Tuesday, March 20, 2018 – I’ve written about how while Mama lived with us, the last few months we’d live in her bizarre little world.  She was not the mama I grew up with, nor the mama I’d known during my adult life.  Some times “my mama” would come out, but most of the time her world and ours varied widely from each other.  She’d talk about people long dead that were coming to visit or she wanted me to check on. We’d answer just like saying something that made sense and went along with what she thought was reality.  She thought we were the “couple who lives upstairs” and cooked for her (often it was food not fit for a dog, she’d say!!)  This article from Bob DeMarco, founder of AlzheimersReadingRoom.com explains that same concept, he just calls it Alzheimer’s World.  I’d call it Dementia World or the bizarre little world of the patient.
I am pleased to say I don’t have a bizzare little world I live in yet!!!
We celebrated Kallie (our teenage granddaughter’s) birthday Sunday.  She’s 17 now!!!
Roy has suddenly become quite busy with computer work and flooring work.  What we thought was going to be a quiet non eventful week, this week, has blown up with fun and other frivolities!  Roy is doing this work for a specific reason which we’ll share soon!
Madisyn’s school class had a field trip to Liuzza Land yesterday (Monday).  I went with Chip and her class and LOVED IT!!!  More on that in our next blog post.

Communicating in Alzheimer’s World , by Bob DeMarco, AlzheimersReadingRoom.com, July 31, 2017

You want to decrease both your stress as caregiver, and the stress of the person living with Alzheimer’s disease.

You want to reduce stress. You want to change the dynamic.

You want to change for the better — you want and need to change the way things are.

After repeatedly correcting my mother, telling her she just ate, and watching her get frustrated or angry, I finally realized something had to change and that something was me.

You might be wondering why I just repeated myself. Why? Because I believe it is necessary to get focused on what you want to accomplish, if you ever expect to accomplish.

It must become a deep and strong desire within you.

A goal.

For example, my mother, Dotty, continually tells me she is hungry. She does this repeatedly, just minutes after she has finished eating lunch or dinner. When a person says something that doesn’t make sense the natural tendency is to correct them. In this case, I would remind my mother over and over that she wasn’t hungry because she just ate.

Ever done that or something similar with a person who is deeply forgetful – raise your hand?

We do this because we have a problem accepting that a person living with Alzheimer’s does not remember. In the case of my mother, she does not remember that she just ate. She can’t remember she just ate, so she says she is hungry.

After the thousandth or so time of correcting my mother, telling her firmly she just ate, and watching her get frustrated or angry, I finally realized something had to change — this something was me.

I had to change.

I want to interject here that my mother even after years continued to tell me she was hungry right after eating. She frequently told me after breakfast and lunch that she hadn’t had a thing to eat all day. She told people on the telephone at night — I haven’t had a thing to eat all day. She — honestly — believed that what she is saying is true.

Why is it so hard to understand that a person living with Alzheimer’s forgets? A person living with dementia is deeply forgetful.

Why is it so hard to understand and accept they can no longer store the memory of what was just said, or what was just asked? They cannot store the answer to the question you just answered in memory, so they just keep on asking the same question over and over.

Like you and me, the deeply forgetful ask questions. The questions come from a different part of the brain then the part that is sick.

My guess is that you experience the frustration of hearing your loved one repeating words that you believe to be untrue over and over. You see and experience the same crazy behaviors over and over.

What you believe to be true, and what the person living with Alzheimer’s believes to be true are often diametrically opposed. The exact opposite.

Here is the one thing you need to understand.

Your view of reality and your loved one’s view of reality might be very different. This occurs because their brain is sick and they can’t remember simple things that are easy for you to remember.

Ask yourself, what are you doing and how are you reacting when someone living with Alzheimer’s says something you know to be incorrect or untrue?

What are you feeling when this happens? Are you constantly correcting them?

If you are constantly correcting a person living with dementia are you also experiencing enormous feelings of frustration and stress?

When you correct them do you you start to feel angry, stressed, and/or disconcerted?

Sooner or later you must make a decision.

Do I want to continue doing this? Do I want to continue feeling terrible? Or, is there an alternative?

This isn’t easy to do, but it is necessary — you need to start accepting that when a person who is deeply forgetful says something they believe to be true it is in fact a reality for them. It is their reality.

When they continually repeat themselves they do it because they can’t remember. There is no sinister plot here. Brain sick, Brain not functioning properly.

Don’t be afraid or reluctant to step into this new and very different world.

In Alzheimer’s World, reality takes on a different shape.

Reality in Alzheimer’s World is a reflection of what the person living with Alzheimer’s thinks and believes. It is this reality that you must focus on, not the way YOU think things are, or should be.


I feel confident when I say this — you won’t be able to convince a person who is deeply forgetful that they are wrong, and you won’t be able to convince them that your reality is the true reality. They can’t remember like you or me, so they really cannot comprehend your point of view.

When you do this you are asking the person who is deeply forgetful to come back into your world. They cannot do this.

Think about what I am saying here.

I am asking you to develop a frame of reference, a new and different behavior that is one hundred percent diametrically opposed to the way you think and act — the way you think and acted for your entire life.

This isn’t easy. It could be one of the hardest things you ever try to accomplish.

Even though I was well aware of what I needed to accomplish, trying as hard as I could, it still took years to get there — to get into and comfortable with Alzheimer’s World.

Once I made it into Alzheimer’s World I reaped rewards that are hard to describe.

When you make it to Alzheimer’s World you begin the process of redefining reality. Instead of trying to brow beat your loved one back into your reality, you start to interact with them based on their view of reality.

For example. When my mother said, I am hungry, I’m starving — I said OK, we will eat in a little while. Instead of telling her — you just ate, you can’t be hungry.

If my mother asks how long before we eat, I don’t say in two hours — I say, soon. The soon in this sentence means when it is time to eat. When it is time to eat. I resist the temptation to say, we just ate.

Instead of an argument, my mother now reacts positively to this response.

Over time, my mother started saying something she never said before, instead of saying I’m hungry, I am starving, she sometimes says — Bobby, what did I eat today?

When I answer by recounting our meals, she still makes a funny face, the face of disbelief, but she doesn’t get angry or upset, and neither do I.

When I answer my mother I am in Alzheimer’s World. I’m calm, and my voice is calm, I am not showing her that I am exasperated by these questions. Why? Because I am not. This is how you learn to communicate in Alzheimer’s World.

When I recount to her what she has eaten I have to be very careful. Careful to tell her with a smile on my face, and in a low calm voice. Not like a lecture. If she gets that bewildered look on her face — confusion — that is OK because I can then change the topic.

On the other hand, if I allow my mother to get angry and disconcerted then she will start going into the black hole of Alzheimer’s World.

When my mother goes into the black hole, I can feel the Alzheimer’s trying to drag me into the black hole. If this happens, I am the one that ends up with a sore heart or stomach ache.

By listening to her lament — I am hungry, I’m starving — and by responding to her reality rather than correcting her — the communication between my mother and me has improved. The amount of anger, stress and angst is greatly reduced. On both sides.

This new form of communication leads to the reduction of stress, anger, and angst. It seems to have a cumulative effect. Less stress build up across a series of situations, leads to less anger and nutty behavior from my mother.

Less conflict, fewer explosions. More happiness.

Better care giving result.

 The goal in all communications with a person living with Alzheimer’s disease should be to connect with the patient in a positive, constructive, effective way.
So instead of telling my mother — you just ate. I accept her reality that she is hungry and respond in a positive proactive way.

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