United Hatzalah program honors our survivors, war veterans with specialized medical care
Fraidy and Chaim were married for 10 years. They were still in love. They cared for and respected each other. They had weathered the last five years since Chaim’s diagnosis pretty well. Counseling had helped. Chaim learned to accept that he had as much responsibility to be there for Fraidy, not only despite his illness, but because of it. He learned that his illness made it even more important to be an emotional support for Fraidy just as she was a physical support for him. They were the best of friends.
The couple had been trying to have children for years. Finally, seeking genetic counseling, they learned that Chaim’s illness had probably made it impossible for him to father children. Fraidy desperately wanted children. She was still young enough, if she remarried, to have children. And so they divorced. To this day, they remain good friends.
Mini and her husband had also remained good friends and lovers throughout the 15 years of his chronic illness. However, as his condition deteriorated, she began to become ill herself. First she was diagnosed with fibromyalgia, then chronic fatigue syndrome. She became ill with shingles and chronic headaches. Her blood pressure soared.
Her doctor first put her on tranquillizers, then antidepressants. Nothing seemed to help. Both Mini and her doctor knew that unless she got her stress under control, chances were she would not outlive her husband. Then, who would care for him?
Mini could never adjust to the perpetual state of crisis chronic illness leaves in its wake. She couldn’t cope with the constant sleepless nights and fears of one disaster following another during the day.
Finally, the couple divorced. Within weeks, Mini’s health improved. She is still there for her husband. She is by his bedside when he is hospitalized. They remain best friends. But not living with him gave her enough relief from the constant stress that the illness brings to still be there for him. For Mini, leaving him was the only way she could manage to be there for him.
A few months after their marriage, a young couple was in a terrible accident. The boy was left a quadriplegic. Despite his insistence, the bride refused to leave him. She felt her place was to be with her husband and care for him for the rest of their lives. The young man, full of love for his beautiful bride, insisted that they divorce. He wanted her to have a life other than caring for him into her old age.
He wanted her to be the wonderful mother he knew she could be. He could no longer give her children. He wanted her to be happy and full of laughter as she had been before the accident. But, she refused. Finally, they agreed to talk to a rabbi and abide by whatever he would tell them to do. Today, she is a mother, raising a large family. She keeps in touch with her first husband and visits often. Seeing her this way gives him joy.
Coping with chronic illness is very hard. The lives of those coping with it are complicated. More complicated then most of us can even imagine. Some people stay in the marriage because of the children. Some leave for the very same reason. Many leave so they can have children. Many leave simply so that they can both survive the stress the illness brings.
We should not presume to judge anyone in that situation for making the decision to stay or leave the marriage. Our job is to lend support. Everyone coping with chronic illness − the one who is ill, the spouse, all members of the family and even close friends, all need our support. They do not need our criticism or our uninformed advice, just our support. And that is the only thing we should feel compelled to give.
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During the Second World War, a million and a half Jewish soldiers fought in the Allied armies, the Partisan units in Eastern Europe, and the anti-fascist underground movements in Western Europe and North Africa. These Jewish fighters won over 200,000 medals and citations. The Museum of the Jewish Soldier in World War II in Latrun, […]
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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.
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/choosing-divorce-part-two/2007/02/07/
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