Student Union opens ‘hasbara’ room in effort to fill public diplomacy vacuum.
Above we see a chronically ill person who is wheelchair bound. His expression is one of sadness and dependence, and he seems to be uninvolved. He is even leaning away from his wife, who is standing next to him. She has a sort of forced semi smile (or perhaps it is just an absence of a frown). Her hand is on his shoulder for moral support. She looks unfocused, tired and overwhelmed. The title asks, “Who is the powerful one in this picture”? Below the picture, the cartoonist put some words in the man’s mouth. “Give me! Get me!” “Why do you have to go out?” “Where are you going? When are you coming back?” “Move me a little to the right.”
In a normal relationship, where there is a give-and-take, these words may not be as emotionally laden as they are in this situation. Note the lack of “please” and “thank you”. These woman felt that those little courtesies would have made a vast difference in what they were asked to do to assist their spouses. Their lack made them feel taken for granted, used and even abused. They told me that the demands and questions the cartoonist listed were things they heard all the time. They brought with them tremendous feelings of guilt. Guilt for being the healthy one, for being able to leave the house on their own and go where they wanted; when they wanted. As one woman said, “How do you say ‘no’ to someone who can’t do it for himself; no matter how you feel or how tired you are. Even if you think what he’s asking for is something he is capable of doing for himself, you can’t just say ‘get it yourself’ or ‘I’m busy now’. So, who does have the power in a relationship where you can never say ‘no’. Not me!”
There are many different kinds of power that we come across in our lives. Some are obvious. An employer who decides if we remain employed or not has power over us. So too is the power of a union that defends a person who is fired. But in these cases there is some recourse, someone to go to for help. But who does a well spouse go to to discuss the power his or her spouse has over them? Who would understand that a chronically ill person, who may not be able to move can still exert a great deal of power, even if it is only over the spouse?
About the Author:
If you don't see your comment after publishing it, refresh the page.
Comments are closed.
On his marriage, he wrote: “This is what I believe: something of the core, of the essence of this meaningful and life-affirming Judaism will not be absent from our home” (1882).
With the recent kidnapping by the Hamas and the barbaric murder of three children – Gilad Shaar, Eyal Yifrach and Naftali Frankel, we believe that the best answer to honor the memory of those murdered is to continue building those very communities – large and small – that our enemies are trying to destroy.
Adopting an ancient exegetical approach that is based on midrashic readings of the text, thematic connections that span between various books of the Bible are revealed.
While Lipman comes from an ultra-Orthodox background and is an Orthodox rabbi, he offers a breath of fresh air when he suggests that “polarization caused by extremism and isolationism in the religious community may be the greatest internal threat to the future of the Jewish people”
The Joys of Yiddish, Leo Rosten defines a mentch as “someone to admire and emulate, someone of noble character.”
Certainly today’s communication via e-mail, Facebook, Twitter and the like, including the ubiquitous Whatsapp, has reduced the need to talk with people and communicate at length.
These two special women utilized their incredibly painful experience as an opportunity to assist others.
Maybe we don’t have to lose that growth and unity that we have achieved, especially with the situation in Eretz Yisrael right now.
Sleepily, I watched him kissing Mai’s chubby thighs.
I have always insisted that everything that happens to anyone or anything is min Shamayim.
My teachers like me and they tell my parents that I am a great girl with good middos.
The chicken and waffle nuggets were fabulous and were like chicken in a dessert form.
When one is blind one learns to use Braille to read. When one cannot walk, a wheelchair gives mobility. Sign language allows a mute person to speak and ocular implants assist in hearing when one is deaf. These are all compensatory strategies that help a person function despite his disability. But compensatory strategies are not just for physical problems. Understanding our psychological weaknesses and setting up our lives to ensure that we are not tempted to repeat our past mistakes, is as necessary as any aid to the disabled.
Well spouses have often discovered that their friends and relatives, despite their closeness to the situation, often don’t realize the tremendous emotional impact living with chronic illness has on the family. With the best intentions, suggestions, ideas and criticism are offered, based on the non-experience of those with healthy families. Even when the good intentioned get a taste of the difficulties, it is sometimes not enough for them to then identify and understand what the family of the chronically ill must face on a constant basis.
Over the past two weeks I have shared letters from a therapist and a well spouse. Both of the letters gave personal insights into the process of losing hope, how we react when that happens and some ways of coping when test scores, diagnosis and just simple repetitive behavior indicate that change for the better is impossible.
I’ve read your last few articles on psycho-neurological testing (Oct.8-22) with interest. As a therapist who has counseled couples dealing with chronic illness, I’d like to give you another perspective.
Your articles on the Neuro-Psychological Testing were right on (October 8-22). My husband underwent testing twice and your articles explained it things exactly the way they were. Besides the test, we also tried therapy.
Very often when we can’t face our big hurts or big loses we focus on the little ones. We can discuss those. We can cry over the small loses, be angry at the smaller hurts even though it may look trite and sound ridiculous to others.
Over the last two weeks we have been discussing one way in which well spouses can determine whether behavior displayed by their ill partners is caused by their illness or is a way they have chosen to act. We have focused on Psycho-Neurological testing, what it can tell us, as well as its pros and cons.
Last week I discussed a question that haunts many well spouses: not knowing if the difficult and often inappropriate behavior frequently displayed by their partners are caused by the disease and therefore not-controllable, or if the behavior is a choice the spouse makes and can therefore be changed. This doubt can be the source of much frustration and many marital disagreements. One way of alleviating this doubt is by having a psycho- neurological work up done. But that path is not so simple.
Printed from: http://www.jewishpress.com/sections/magazine/a-picture-is-worth-a-thousand-words-part-2/2006/04/12/
Scan this QR code to visit this page online: