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The Celle Seminars_Page 325

Celle Seminar I, Case 12: Muscular Dystrophy

Case 12: Muscular Dystrophy

INTERVIEW

(Someone): He is very shy, so his parents will speak for him. (G. V.): You only have one child? (father): We also have a sixteen year old daughter. (Therapist): The patient is a boy, born in May, 1982. At the age of four years progressive muscular dystrophy was diagnosed. The patient has suffered from several attacks of bronchitis following pneumonia in 1985. These attacks were always accompanied by high fever. He shows an allergic reaction to dust and mites and has a fear of dogs and cats.
History in chronological order: His mother had a normal pregnancy without complications; birth normal, no complications. As an infant he suffered from eczema on his face, knees, and in the folds of his joints. Teething late, at the age of 8 months, with small teeth. In his first year he had a fracture of the skull which healed without complications. He learned to walk at the age of one, however, his parents noticed that he couldn’t stand up or get up without holding on to something. He started talking at the age of eighteen months. In 1985, he had severe pneumonia; since that time there have been numerous infections of the respiratory organs accompanied by bronchitis for which antibiotics were very often given. Also in 1985, the first hint leading to the diagnosis of progressive muscular dystrophy was uncovered through a blood test taken while he had pneumonia. In November, 1988, an operation was planned to prevent contractions of the muscles. But shortly after the operation began, it had to be discontinued due to a general urticaria. He finally underwent the operation in January, 1989. While he was in the hospital he developed tonsillitis, for which he was treated with antibiotics.
Findings following homeopathic interrogation: He sleeps restlessly, turns around often, covers himself up and perspires; he

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