Negotiating health care : the social context of chronic illness

The findings of a large qualitative research project which studied the experiences of the chronically ill within the health care system are presented here. Thorne demonstrates the vast difference between chronic and acute illness in terms of their social and health care consequences. The book is divided into three sections: the first examines how patients handle the onset of diseases and acute episodes; the second explores the relationship with health care providers; and the final part focuses on the 'system' with its sociocultural and organizational agenda. The concluding chapter proposes future directions for health care organization, biomedical technology and social policy. 1. Background To The Chronic Illness Experience -- 2. Onset And Diagnosis -- 3. Acuity And Chronicity -- 4. Normalcy And Visibility -- 5. Relationships With Health Care Providers -- 6. Trust And Confidence -- 7. Confrontations With The Health Care System -- 8. Politics And Ideology -- 9. Response And Resolution -- 10. The Course Ahead. Sally E. Thorne. Includes Bibliographical References (p. 239-253) And Indexes.