I am not the kind of person that wants to give someone a bad day. In others words, I understand if I were to take my mother out in public, and she ate with her hands, it might be disconcerting to others.
It is not likely they would assume my mother is suffering from Alzheimer's, and as a result, they would likely conclude she is -- (you fill in the blank).
When I first met someone in person that lamented that they couldn't take their loved one out because they ate with there hands I was disturbed. I doubt anyone understands better than I do how a trip out into the 'real' world can benefit a person suffering from Alzheimer's.
There is also a big benefit for the Alzheimer's caregiver -- they get to leave Alzheimer's world, and reattach themselves to the 'real world'. This is vitally important.
I am willing to bet that at least a handful of you have heard the lament -- I can't take him/her out.....
Time for a trip into the Alzheimer's bunkhouse.
Bunkhouse logic solution -- eat finger food.
Many of you know that when I take my mother out we usually go to an open air bar/restaurant. A place where we can mingle with other people, and where there is a good amount of social interaction.
When we go out we usually eat things like chicken wings, burgers, chicken fingers, fries, and shrimp. You can eat all of these foods with your hands, and nobody is going to conclude that you failed Etiquette 101.
I never spent one second worrying about what other people would think about my mother or me. I understand this does make me a bit unique.
I can assure you, I am not going to be embarrassed by anything my mother does in public, and I am not going to be embarrassed for her.
Sooner or later you have to accept and understand that it is easier to accept Alzheimer's World then do the impossible and change Alzheimer's World into Real world. Once you accept that you live in Alzheimer's World even though you don't have Alzheimer's, it will change your perspective. It will give you a strength and courage to accept the ways things are -- and stop fighting yourself.
As many of you know, on my trip down Alzheimer's lane I finally realized it was time to start living our life as we always had. One day at a time. One activity at a time. The same way we lived before the Alzheimer's diagnosis came.
As a result, I started taking my mother out to eat and into public venues. I learned early on how much this benefited her. It took me a while to figure out it also benefited me in my role as a Alzheimer's caregivers.
What can I say -- try it, you'll like it.
Here is tip that might help you get started.
Most McDonald's have tables and umbrellas outside the restaurant. You can sit around having a burger, fries, a coffee, or an ice cream cone. It is likely that there will be others sitting out there also. If you are lucky there will be some kids around. An added benefit.
You might get lucky like we do. Often a little bird flies up and lands on the ground. My mothers finds this fascinating, and it gives us something to talk about.
Some people might call this thinking outside the box. I call it bunkhouse logic. Keep it simple. More often than not, simple is the best of all possible solutions.
Please feel free to comment and share this article with someone that can benefit from the information.
More Insight and Advice for Caregivers
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- What is Alzheimer's Disease?
- What is Dementia?
- What’s the Difference Between Alzheimer’s Disease and Dementia
- Communicating in Alzheimer's World
- How the Loss of Memory Works in Alzheimer’s Disease, and How Understanding This Could Help You
- Learning How to Communicate with Someone Suffering From Alzheimer's Disease
- Alzheimer's World -- Trying to Reconnect with Someone Suffering from Alzheimer's Disease
- Does the Combination of Aricept and Namenda Help Slow the Rate of Decline in Alzheimer's Patients
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