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Your child and scoliosis

by Janet Lohmeyer

Created on: April 27, 2008

Scoliosis: Walk a Crooked Mile

None of my sons have scoliosis. I had it as a child, worse than any of my relatives with it, and still have it today. Mine is the progressive kind, and causes pain and height loss even now, some fifty years later. My childhood was affected in every way by this condition, and the lessons I learned may help others.

Because of the early onset, doctors were concerned about a rapid decline, resulting in my becoming crippled. So they were aggressive in their treatments. At the age of seven, I wore a lift on the heel of my left shoe. I did exercises, 100 repetitions per day in 1958, a time when working out was definitely not in vogue. At the proper time, and because previous measures had failed to stop the curve progressing, doctors prescribed a Milwaukee brace. That technology was new to the United States in 1964, and I was the second patient in the entire Chicago metropolitan area to receive one. So no one had seen a brace like this no matter where I went and frequently I was the object of stares.

Fear of the unknown does strange things to people. Sometimes strangers would cross the street to avoid coming too close to me. That hurt my feelings.

On the playground, again fear created some odd behaviors in my classmates. They would tease me daily about the odd shoes I wore. When they learned about the exercises I had to do, they teased me about that, too. Later, in high school, when the brace caused my boat-necked blouses to gap away from my body; my classmates would throw eraser bits and spit wads at me whenever they could get away with it. They quickly became very accurate.

All this unwelcome attention made me feel sad and unwanted. Especially when everyone groaned when I had to be on their team. I was so uncoordinated I was terrible at sports. All this rejection was very hard to accept.

In those days, no one gave any thought to a patient's emotional needs. We were supposed to realize 'all this' was being done for our own best interest, and we were not to complain about anything.

But in reality, for the child with scoliosis who is forced to be different from their peers, who is compelled to endure burdensome and sometimes uncomfortable therapies, there is much to complain about. Parents and other adults can do a lot to alleviate the emotional pain the child feels.

Combating lack of knowledge and awareness at school by scheduling a time in the classroom to talk openly about scoliosis, what it is and what it is not, and the funny ways it is sometimes


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