The nature of self-help groups is discussed and considered with special reference to those composed of epileptics. Results of a preliminary survey of epilepsy self-help group members are presented, and effects relating to stigmatization, reasons for participation, asserted curative factors, and formal-only versus informal participation in the self-help group process are examined. Societal reaction to people with epilepsy is viewed as a major contributor to problems associated with this disability.
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