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As I continue to share the cartoons from a well spouse group I interviewed, I’d like to share one that illustrates a common bone of contention to well spouses and their partners. Have you ever noticed how people tend to talk louder to people whose first language is not English? Clearly they know that saying the same words, just louder, will make no difference in helping someone understand them. Yet, they persist. Have you ever noticed how people who are disabled are also treated to louder voices when they are spoken to? Do people really think that the source of their disability is in their ears or that they must be hard of hearing, since they can’t walk or see or stand? Yet, this is a common practice that we all tend to do. For the most part, it is harmless, sometimes even amusing. But there is one common habit, illustrated by the next cartoon that is neither amusing nor benign. It is very common for well spouses to be asked about their partner’s condition. After all, when a person is chronically ill, people are concerned. It is just as common for a person to ask their spouses how their partner is, right in front of the person they are inquiring about. It is not that the ill people they are enquiring about cannot hear, nor are they cognitively delayed, so that they don’t understand the question. They are not mute, and are capable of dealing with an inquiry about their health, directed at them when they are alone. However, as soon as they are in the company of their spouse, they are treated as less then a child and are totally ignored. Then the simple question of “How are you?” becomes the whispered inquiry of “How is he?” Further, as soon as the well spouse has the audacity to answer, “Fine.” the answer is usually not accepted and tends to be followed by the question, “Really, how is he?” The woman in the support group jokingly decided that people see them all as either pathological liars, or just as a spouses, reluctant to discuss their partner’s condition. If indeed, they are trying to avoid talking about the health of the person to whom they are married, why would anyone insist on pursuing it? Yet, this was a common experience to every woman in the group. They told me that people just would not accept “Fine” as the answer, and they felt as if they were being harassed until they came up with something negative to say. As for their spouses, they hated being ignored and dreaded having someone else be asked how they were, especially when they were sitting right there. Many of their wives told me that their partners found it insulting and demeaning. The wives, on the other hand felt that, bypassing the sick persons when making a simple inquiry about their health and directing it to them instead, just gave them added responsibility. Not only do they have to care for their spouses, often in ways people really don’t want to know about, but they are also now responsible for regular updates on their condition. This is something their chronically ill spouses are not only capable of giving, but might really benefit from handling. It would let them know someone else cares. Imagine for a moment someone coming up to your well spouse, leaning over to him/her, conspiratorially and in a hushed voice say, “Really, how is your husband/wife.” What would your reaction be? What would be the reaction of your spouse? I think the cartoon says it all.
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Rewind sixty years to 1953.
Television was considered kosher by most and featured the likes of Desi Arnaz, Lucille Ball, Jack Benny, George Burns, Red Buttons, Perry Como, Arthur Godfrey, Clayton Moore as The Lone Ranger, Dinah Shore, Red Skelton, Danny Thomas, Jack Webb as Joe Friday on “Dragnet” and many others who provided great memories.

Yet all are part of one neshamah, planted in rich, verdant soil, determined to grow. May our garden continue to produce a glorious assortment of flowers and trees, each attached firmly to its roots. Our diverse southern vegetation flourishes and grows into different trees, flowers, and fruits, and a rainbow of glorious shades and hues appears. Yet each shoot is rooted in the same soil, stretching its branches and blossoms heavenward in an endless pursuit of growth and connection to the One above.

This past Lag B’Omer, we were blessed to make our first upsherin, where we celebrate our son’s first hair cut. It’s a wonderful milestone that mimics the three years that we refrain from plucking a tree’s first fruits and symbolizes the entry of the child into the world of Torah learning. It’s a clear sign to everyone; this boy is no longer a baby.
Although there are more direct and faster routes to Beer Sheva and Eilat and all the sites and towns in-between, the Basor River is one of the beauties of the Negev that defiantly justifies a diversion.
The importance of death customs has been ingrained in me since birth. When I served as a shomeret for my grandmother, I was instructed not to eat, drink or perform a mitzvah in the same room. In the shock of death, it seemed rather inane to be told it would be considered mocking the dead. My grandmother was gone; she couldn’t do those things because she didn’t exist anymore, a fact that still makes me tear up.
I would have to say that one of the most annoying things about having a newspaper advice column, aside from all these people writing to me and asking for advice, is that they frequently don’t tell me WHY they’re asking.
Rav Yosef Shalom Elyashiv zt”l, who passed away on 28 Tammuz, (July18) this year at age 102, spent all of his days and most of his nights learning Torah. He was the paramount leader of our generation, and inspired tremendous awe and reverence in everyone who knew him. Now, every woman has the stunning opportunity to do something in his memory. A Sefer Torah is being written in his memory and women around the world have the chance to dedicate a letter.
Due to her family situation, it is understandable that she will have more responsibilities than other girls her age, but she would benefit from having some free time and receiving more appreciation for her hard work.
For children, summer means outdoor sports, picnics, and of course, no school! Teachers and students work hard all year long – and everyone deserves a break from education over the summer. However, this two-month break can often have some pretty devastating consequences.
It was only after we celebrated the great news that we were expecting twins that we saw the first sign of problems. First of all, my wife was losing, not gaining weight, even as the babies continued to grow normally. Soon after, routine blood work revealed that my wife was suffering from gestational diabetes.
Rabbi Pinchas Gruman is the new rav of the Minyan at Aish Tamid.
One of the most respected Torah figures in Los Angeles, Rabbi Gruman has been described as “The Los Angeles link in the mesorah of the yeshiva world” by Rabbi Nachum Sauer. As a talmid in Lakewood in the 1950s, Rabbi Gruman received semicha from Rav Aaron Kotler, zt”l, and Rav Moshe Feinstein, zt”l. Soon after, he moved to Los Angeles.
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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.
Dear Ann,
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.
Dear Ann,
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-3/2006/04/19/
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