Raise the subject of medical history among parents of special-needs children, and the diagnosis stories can be heard in abundance. Perhaps parents learned of their child's differences in pregnancy, or at birth. Perhaps it was a slow dawning of awareness as an infant missed the usual developmental milestones – or a sickening sense that something was wrong as a toddler suffered a series of illnesses or crises. But what about the truly puzzling cases when something is obviously not right with a child – yet the constellation of symptoms is vague, and the maladies seem to come and go –...
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