Sign in to wowOwow

Enter the email address that you used when registering at wowOwow.
The password field is case sensitive. Click here if you have forgotten your password.

Please register for wowOwow

Newsletter subscriptions
Sign up to receive wowOwow's weekly newsletter and get our best picks delivered right to your inbox. Our newsletter content is hand-picked by the wowOwow editorial team and provides the top features, news, and commentary from our site. Subscribing to our newsletter is free and safe. We will never share your email or other information with a third-party without your direct consent.
By registering, you indicate that you have read and agree
with our privacy policy and terms of service.

Sheila Nevins | 05/08/2008 12:00 am

The Dictator, The Farmer & The Professor

© Shutterstock

A Short Poem/Essay

How do you deal with aging parents facing dementia or Alzheimer’s disease? Read the poem and comment below.

The Dictator, The Farmer & The Professor

The DICTATOR thought
The orange
Was the world
And he squeezed the juice
All over
His hospital robe in the clinic
That bore his name
"Naughty, Naughty," said the nurse
To the man who had ruled a nation
"Yes, Naughty, boy," she repeated
As she changed his robe to a fresh one

The FARMER thought
The orange
Was a seat cushion
And he lifted his crippled body
Laboriously to
Sit on the orange
And the juice got all over his hospital-issued robe
"Naughty, naughty," said the day nurse.
"Naughty, boy," she repeated
And left him dirty
For the night orderly
To change that evening

The PROFESSOR thought
The orange
Was a book
Peeled it open
To read its contents
Juicing his shirt
"I’m a naughty boy, Nurse, I’m a naughty boy"
He said to his wife
And wept at the wet.
She had carefully ironed
And buttoned-on his fresh shirt
this once Sunday visit

And there they were three men
Divided by continents and duty
United in solidarity
Clearly as homage to the famous
Dr. Alzheimer
Who knew once
How to know an orange
For what it was
And told them
Who they were
Though they would never
Know.

 

67 Reader Comments (so far…) Sign In or Register to comment

doll lady
Oh my ~~~~ this subject is so close to my heart. Not my parent but my wonderful sister. I have mentioned my wonderful younger sister before who was born as a downs syndrome child. I didn’t know that 99% of downs children will suffer the horrible affects of alzheimers. Many times these wonderful children of God don’t live long enough to even have to go through this. Right now is a very trying time for her and the family. I normally wouldn’t tell all of my business to people I don’t know but in a short time “knowing you”, I feel you all are my sisters in life. Patty has begun to have seizures. A month ago her heart stopped but she was revived and needed a pacemaker. Then she unknowingly pulled the pacemaker out and another had to be inserted. Luckily her heart was not perforated. Two nights ago she began to choke while chewing. Her dentures were caught in her throat. The caregiver got them out. She is having tremors and her seizure medicines are continually upgraded. Some of your might think….where do you go from here? You might think ….. why revive her? But when it’s family and she has some recognition, it is so hard to “pull the plug” and place her in a do not revive status. I know that things will get worse. But it breaks my heart. This disease is horrible. I pray that your families will be lucky and will not have to suffer through the horrible ravages of this disease.
By doll lady on 05/08/2008 8:51 am
Diana T
During WW2, (I think it was during the London Blitz) Winston Churchill said something that has always stuck with me: ” When you are going through Hell, keep going.” That is all I could do when I was caregiving both parents in the nursing home. Dad had a stroke and was paralyzed on the right side. Mother, a bi-polar and not too stable a person even in the good times, had dementia. One day at a time. Lots of prayers and faith in myself that I was always doing the right thing. Luckily Dad was the leader until the end, and even though he had terrible Aphasia, he would let me know what to do next. My late husband’s mother had to go into a nursing home for a few months during this time, because of a debilitating stroke. Husband and I cooperated with each other fully, communicated our feelings constantly and took it a day at a time, no matter how hard things got. We were very fortunate in that somehow he managed to get my parents into a small non-profit Catholic facility whereupon they received the best possible care. We were very fortunate because Dad had planned for this financially and the funds were there. And back in the 80’s-early 90’s, the expenses were staggering. I can only imagine what it is like now. The families enduring this kind of hell have to face the huge care costs, and I can’t see how it is done nowdays. What is the national answer? What can be done when people can’t take care of themselves and do not have the funds to get help when it is needed?
By Diana T on 05/08/2008 10:34 am
Jeannot Kensinger
Diana, I am in the middle of this. My husband was diagnosed 10 years ago. He is a great artist and made a living as such, still, this means feast and famine. So a stacked portfolio is not in our possibilities of dealing with this financially. For 7 years I paid 600 to 700 a month in medicine. Medicine which we did not know if they would work. I tell myself that they did. Now I would love to have him in day care a few days a week. Cost at our hospital is 45.00 a day. I can’t afford that. I went back to work at 76 as an auditor in a clothing shop. It is part time, it is grocery money if I am careful. The finances are not the worst part. The daily routine of things disappearing , my 2400 hearing aids are gone for instance, the mail, my underwear, his medicine, everything is being held hostage until I find it. He was a mild mannered man but now he kicks the dogs. I am concerned when it could become my turn. This man is nothing like my husband, he is a stranger, after 40 years I live with a stranger, what is worse , he does too. He tells my son to get out of the house. He tells me to get out of his bed he is waiting for his wife. It never ends. Most of the day he walks within a few steps behind me. I lost him a thought at the time. I get angry, I get furious, and then when he looks at me and for a moment I know that he knows me and I melt and we hug and hug and I know that inside this brave soul is my best friend. I try and do this all with grace but I am not doing a good job of it. My mother always told me to just DO IT, some days I just CANT and I sit on the pitty pot and hate myself for it. Yes Churchill was right. This is hell and I we will make it but I would not wish this on my worst enemy if I had one.
By Jeannot Kensinger on 05/08/2008 12:07 pm
Gianna Bracco
JMK Singer …. Please don’t be so hard on yourself. I can’t imagine there is anyone out there that could endure this experience without a visit to the pity pot every now and then. I’ll keep you in my thoughts and prayers. Take Care and Happy Mother’s Day.
By Gianna Bracco on 05/08/2008 1:07 pm
Star Lawrence
I think you are doing a wonderful job! Tears sprang to my eyes. My sister and I have taken care of Mom for almost 20 years—she is in assisted care (private accredited home, 4 people, 2 caregivers). We have had many experiences, mostly negative. But that poem? Those caregivers would have been sooo fired if we had anything to say. And we do.
By Star Lawrence on 05/08/2008 2:15 pm
Diana T
JMK, I deeply hope that you are in an area that has a support group because that is so important for you NOW. It is essential that you regulary take time out for yourself and let someone else do the dirty work. This situation is when the medical system in our country is so cruel. There is no reason that our country can’t have a system that lets families get the help they need without bankrupting them. Sadly, if you own property, you can’t get Medicaid and Medicare simply does not help. So, I hope you seriously (a.) consider getting as much help as you can from the support group, and (b)never hesitate to ask you kids if they are nearby to get over there and help you nno matter how much your husband objects. I am sure you have heard the saying that Alzheimers has 2 victims…the one with the disease and the one taking care of him/her. You cannot and should not expect to do this all by yourself, ever. Good luck and my prayers are with you. p.s. If you Google in Alzheimers Support Groups, I would think you can find one near you.
By Diana T on 05/08/2008 3:15 pm
Diana T
JMK, I just Googled: ALZ.ORG is the website. It has an easy to find way of finding support groups in your area. The 24/7 toll free hot-line is 800-272-3900. They offer support on that also. It is a very comprehensive website. Good luck.
By Diana T on 05/08/2008 3:24 pm
Estimada C
doll lady, my heart goes out to you and the sister you love so much. We never know what sorrow we must bear. Strength, Dear One, and much love.
By Estimada C on 05/08/2008 11:27 am
Ms. Dee
Great verse, Sheila. Sad, sad.
By Ms. Dee on 05/08/2008 11:31 am
Blue Circle Girl
Doll, Oh, my. How terrible this must be for your family and for your sister. Our prayers are with you and I am sorry for this terrible struggle you are suffering. Love, Blue
By Blue Circle Girl on 07/23/2008 4:53 pm
Dr. Mark Klein
Atlzheimer’s is an issue in the presidential election. http://thecaucus.blogs.nytimes.com/2008/05/07/mccain-fields-questions-on… Comment #18 is particularly on point.
By Dr. Mark Klein on 05/08/2008 9:26 am
MaryPage Drake
Poignantly beautiful. Beautifully poignant.
By MaryPage Drake on 05/08/2008 9:48 am
G T
The way I delt with my mother who had dementia, was to love and care for her as best I could until she died. I was a very revealing experience to see someone you knew and loved as they lost their identity..We tend to identify ourselves by things outside ourselves..our job, our role in life, wife, sister, etc. As her awareness of these roles faded slowly you could see who she thought she was was vanishing. When at the end of life we are faced with withdrawing our Spirit from the body and from all those identifying roles, it sure helps if you have some close aquaintence with who you REALLY are. This gift my mother gave to me was one of the most loving things she had ever done. Its like she said ‘now, pay close attention, and watch what happens, it is enlightening”.. And bless her, she was correct.
By G T on 05/08/2008 11:21 am
Estimada C
Diana and GT, My post above to you, also. Have you seen “The Notebook” or read the book by the same title? It is a beautiful, heartwarming story (true) dealing with alzheimers.
By Estimada C on 05/08/2008 11:35 am
beth toni kruvant
In this poem I see long term memory defining the behavior of the three men. It is amazing for me to see my mother who has lost so much of her short term memory relate to the moment because that is all she can relate to. Like a small child without a past to which she can define herself. She is rootless until she sees the photos on her door which ground her and comfort her to know she is in the right place.
By beth toni kruvant on 05/08/2008 11:57 am