Having epilepsy : the experience and control of illness /

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Bibliographic Details
Author / Creator:Schneider, Joseph W., 1943-
Imprint:Philadelphia : Temple University Press, 1983.
Description:xiii, 280 p. ; 22 cm.
Language:English
Subject:
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/572191
Hidden Bibliographic Details
Other authors / contributors:Conrad, Peter, 1945-
ISBN:0877223181 : $24.95
Notes:Includes indexes.
Bibliography: p. [253]-268.
Table of Contents:
  • Preface
  • 1. The Sociology of Illness
  • Medicine, Sociology, and Illness: Outsider Perspectives
  • The Experience of Illness: Toward an Insider's Perspective
  • Studying Epilepsy: Data, Sample and Method
  • Outline of the Book
  • 2. The Historical and Social Realities of Epilepsy
  • Historical Notes
  • Three Myths About Epilepsy
  • Myth 1. Epilepsy Is an Inherited Disease
  • Myth 2. Epilepsy Creates Psychopathology and Leads to Mental Illness
  • Myth 3. Epilepsy Causes Aggression and Crime
  • The Social Response to Epilepsy: A Stigmatized Illness
  • The Medical Reality of Epilepsy
  • Diagnosis
  • Etiology
  • Epidemiology
  • Prognosis and Treatment
  • 3. Discovery
  • Definitions, Diagnosis, and Discovery
  • Making the Strange Familiar: Lay Definitions
  • Medical Uncertainty: Delaying Discovery
  • Self Diagnosis and Pessimistic Accounts
  • The Impact of a Medical Label
  • 4. The Other Side of Care: Parents and Family Life
  • Parents, Children, and Epilepsy
  • Setting the Stage: Open and Closed Parental Styles
  • The Open Style: Epilepsy as a "Normal" Medical Problem
  • The Closed Style: A Route to Disability and Dependence
  • Worry, Protection, and Control
  • 5. Seizures and Self
  • Having a Seizure: Losing Control
  • Seizures as Social Events: Trouble for Others
  • Embarrassment
  • "Call an Ambulance": Seizures as Medical Emergencies
  • Seizures, Responsibility, and Social Competence
  • 6. Controlling Seizures, Protecting Face
  • Toward Regaining Control: Seizure Theories and Preventive Work
  • Seizure Theories
  • Preventive Work
  • Some Lines of Defense
  • Anticipatory Defenses
  • Emergency Measures
  • After a Seizure: Attending to Face
  • 7. The Problem of Stigma: Managing Information
  • Stigma and Epilepsy
  • The Perception of Stigma
  • Strategies of Selective Concealment
  • Instrumental Telling: Disclosing as a Management Strategy
  • 8. Ties That Bind and Free: The Paradox of Medical Care
  • Seeking Information
  • Information: A Scarce and Valuable Resource
  • Obtaining Information
  • Gaining Control
  • 9. The Meaning of Medications
  • A Ticket to Normality
  • Taking Medications
  • Self-Regulation: Grounds for Changing Medication Practice
  • Social Meanings of Regulating Medication Practice
  • Testing
  • Controlling Dependence
  • Destigmatization
  • Practical Practice
  • Asserting Control
  • 10. Having Epilepsy: The Experience and Control of Illness
  • Illness and Epilepsy: General Concerns and Particular Insights
  • Managing Uncertainty
  • Knowledge of Disease and Illness as a Resource
  • Relationships with Medical Professionals
  • Managing Regimens
  • Symptom and Crisis Control
  • Family Relationships
  • Friends and Associates
  • Illness, Social Meanings, and Identity
  • Suggestions for Change
  • Changes in Society: The Public Image and Control of Epilepsy
  • Changes in Medical Practice: Doctors and Patients as Partners
  • Changes in the Life: Owning Epilepsy and Realizing Self
  • Appendix
  • Doing the Study: Issues, Problems, and Strategies
  • Studying the Experience of Illness
  • Who to Study: Sampling
  • How to Collect Data: Interviewing
  • Making Sense of the Data: Analysis
  • Roads Not Taken
  • Interview Guide
  • Letter Passed to Anonymous People with Epilepsy
  • References
  • Index