The positive effects of socialization, initiative, and motivation on the part of Alzheimer's sufferers and their caregiver should not be overlooked. I believe these are as important as the medication......
My name is Bob DeMarco, I am an Alzheimer's caregiver. My mother Dorothy, now 93 years old, suffers from Alzheimer's disease. We live our life one day at a time.
I can't tell you how many times I either heard or read these words -- I can't take him/her out because she eats with her hands. I know this -- it is a big problem among Alzheimer's caregivers.
To be honest, I never worried about this. My attitude more or less is -- so be it.
I am not the kind of person that wants to give someone else we are around in public 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.

The problem -- they eat with their hands.
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 now understand that this does make me a bit unique.
I can assure you by this time, 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, there is Alzheimer's world where things are not like they are in Real world. Once you accept that you live in Alzheimer's world even thought 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.



Hi Bob, I'm somewhat new to this site and pleased to see that with you and Bill, I'm not alone as a male caregiver or care coordinator, as things currently stand. My mother with "unspecified dementia" has some other eating habits that are a challenge for dining out. She has a habit of knocking over her drink due to constant fidgeting with other objects on the table. Worse perhaps, is when she spits out a mouthful of food onto her plate or napkin. On a recent occasion, she had been eating prime rib that I had carefully cut up for her into small bites with some Brussels sprouts. Ten minutes into the meal, she leaned forward and spit out a golf ball sized lump of well chewed food. This completely ruined the meal of a person dining nearby. To be fair, I do have to be considerate of others when dining with mom in public. I don't want her to be embarrassed by someone else's misunderstanding about her behavior. She is confused enough without dealing with potentially awkward public situations. The outdoor meal at a fast food restaurant is a very good suggestion. I will certainly give it a try, although mom is likely to want to dine in a much nicer establishment! It will have to wait until warmer weather, though. Good post! -- Joe
Hi...thanks for commenting.
Did you know that 41 person of Alzheimer's caregivers are men? Not there is a well kept secret.
Boy oh boy, you have your hands full with your mom. I had not heard that problem before but I am sure it is out there.
If I found myself in you shoes I would have to do some serious thinking to come up with any kind of workable solution. Good luck.
Weather wise, I am down here in south Florida which is a big advantage for getting my mother out. However, if I take her out and the temperature falls under 70 I Have to put gloves on her.
It isn't easy.
Bob DeMarco
http://www.alzheimersreadingroom.com
Thanks for your answer to my reply. I did see the AARP male caregiver article that shows guys at 40-41%. That is a surprise to me, but there's no reason to dispute it.
I just wanted to point out that some issues are legitimate for not taking a parent with dementia into a public dining situation. I liked your fast food suggestion. However, I'm in the Pacific Northwest and outdoor daytime temperatures are in the mid forties right now! Florida, on the other hand, would be great this time of the year! -- Joe