Read Online Rouse Up O Young Men of the New Age! by Kenzaburō Ōe - Free Book Online
Authors: Kenzaburō Ōe
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life.
Having realized this much, I felt certain that the face I had seen in the depths of the pool at the Couple, with the inverted V's for eyebrows, had indeed been my mother's face, and I felt I understood as well that she had angrily written me off at the moment of the accident as a person capable of stepping off the road to life intentionally. Looking back, I could identify a number of instances between my son's birth and his first operation when she had revealed this judgment about me.
Thanks to Dr. M and his assistants, the long operation was a success, my son was liberated from the glistening lump that was like a second head, and my wife and both our mothers were understandably overjoyed. As the young father, I was also very happy, but I recalled the conversation the night before the operation and felt constrained and embarrassed about demonstrating my joy.
A definition of death. I am not able to say that I have provided my handicapped son with a definition of death that is at once accurate, uncomplicated, and capable of encouraging him. What is worse, my wife and I have used the word carelessly in his presence. Looking back, I realized that this had been going on for more than two years until the crisis that made us aware of it, repeatedly. I am clear about how much time had passed because it was late in the spring two years ago—my experience has taught me to believe in the hidden link between the changing seasons, that is, the cycle of the universe, and events that occur deep inside our bodies—that my son experienced an epileptic seizure, an incident that was an unmistakable turning point in our daily life with Eeyore at its center. As we didn't consult a specialist at the time, it wasn't exactly the case that the seizure was diagnosed as epilepsy. Even so, when we informed Doctor M of what had happened, he did not object to my insistence on describing it as an epileptic seizure.
From the onset, my wife and I were of different minds about this. We weren't necessarily opposed—where my son was concerned we often faced in the same direction but took different views. There were times when my son lost his sight briefly and froze where he stood in the street. If this had happened at a railroad crossing or in a crosswalk it would have been dangerous. These events had been occurring intermittently for five or six years, and Dr. M had been controlling them with Hidantol, a drug that caused Eeyore's gums to swell to rosy redness until they protruded from the spaces between his teeth like kernels of red rice but had no other apparent side effect. Hidantol was an antiepileptic, and as such provided me with a basis for diagnosing my son's new seizure.
My wife had heard from her friends in the PTA at our son's special school that epilepsy was a different animal, and that if this were indeed epilepsy it was a very mild case. The term used on the report after the medical exam for middle school was “brain separation syndrome,” and although these words were more than adequate to strike terror into the hearts of our nonmedical family, the word “epilepsy,” as my wife insisted, did not appear. I searched a number of encyclopedias, looking under “epilepsy” for a subentry on “brain separation syndrome,” and failed to find it.
As it happened, my wife wasn't even home when my son had the first of these major new seizures. It began with an unusual atmosphere that felt like the concave underside of pro-truberant symptoms like screaming or spasms. We were in the living room; I lay reading on the couch as always, and my son was sprawled on the rug on the floor listening to a Mozart record at low volume. Presently, instead of putting on a new record, he pushed away from himself with both elbows, like an infant with no appetite weakly rejecting his food, the pile of records he had selected. This registered in my consciousness like a small thorn. But I continued to read. Before long, an impression of interruption reached
Having realized this much, I felt certain that the face I had seen in the depths of the pool at the Couple, with the inverted V's for eyebrows, had indeed been my mother's face, and I felt I understood as well that she had angrily written me off at the moment of the accident as a person capable of stepping off the road to life intentionally. Looking back, I could identify a number of instances between my son's birth and his first operation when she had revealed this judgment about me.
Thanks to Dr. M and his assistants, the long operation was a success, my son was liberated from the glistening lump that was like a second head, and my wife and both our mothers were understandably overjoyed. As the young father, I was also very happy, but I recalled the conversation the night before the operation and felt constrained and embarrassed about demonstrating my joy.
A definition of death. I am not able to say that I have provided my handicapped son with a definition of death that is at once accurate, uncomplicated, and capable of encouraging him. What is worse, my wife and I have used the word carelessly in his presence. Looking back, I realized that this had been going on for more than two years until the crisis that made us aware of it, repeatedly. I am clear about how much time had passed because it was late in the spring two years ago—my experience has taught me to believe in the hidden link between the changing seasons, that is, the cycle of the universe, and events that occur deep inside our bodies—that my son experienced an epileptic seizure, an incident that was an unmistakable turning point in our daily life with Eeyore at its center. As we didn't consult a specialist at the time, it wasn't exactly the case that the seizure was diagnosed as epilepsy. Even so, when we informed Doctor M of what had happened, he did not object to my insistence on describing it as an epileptic seizure.
From the onset, my wife and I were of different minds about this. We weren't necessarily opposed—where my son was concerned we often faced in the same direction but took different views. There were times when my son lost his sight briefly and froze where he stood in the street. If this had happened at a railroad crossing or in a crosswalk it would have been dangerous. These events had been occurring intermittently for five or six years, and Dr. M had been controlling them with Hidantol, a drug that caused Eeyore's gums to swell to rosy redness until they protruded from the spaces between his teeth like kernels of red rice but had no other apparent side effect. Hidantol was an antiepileptic, and as such provided me with a basis for diagnosing my son's new seizure.
My wife had heard from her friends in the PTA at our son's special school that epilepsy was a different animal, and that if this were indeed epilepsy it was a very mild case. The term used on the report after the medical exam for middle school was “brain separation syndrome,” and although these words were more than adequate to strike terror into the hearts of our nonmedical family, the word “epilepsy,” as my wife insisted, did not appear. I searched a number of encyclopedias, looking under “epilepsy” for a subentry on “brain separation syndrome,” and failed to find it.
As it happened, my wife wasn't even home when my son had the first of these major new seizures. It began with an unusual atmosphere that felt like the concave underside of pro-truberant symptoms like screaming or spasms. We were in the living room; I lay reading on the couch as always, and my son was sprawled on the rug on the floor listening to a Mozart record at low volume. Presently, instead of putting on a new record, he pushed away from himself with both elbows, like an infant with no appetite weakly rejecting his food, the pile of records he had selected. This registered in my consciousness like a small thorn. But I continued to read. Before long, an impression of interruption reached
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