Negotiating Health Care
The Social Context of Chronic Illness
- Sally E. Thorne - University of British Columbia, Canada
Other Titles in:
Public Health
Public Health
May 1993 | 280 pages | SAGE Publications, Inc
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.
Background to the Chronic Illness Experience
PART ONE: THE INDIVIDUAL EXPERIENCE
Onset and Diagnosis
Acuity and Chronicity
Normalcy and Visibility
PART TWO: THE INTERPERSONAL EXPERIENCE
Relationships With Health Care Providers
Trust and Confidence
PART THREE: THE INSTITUTIONAL EXPERIENCE
Confrontations With the Health Care System
Politics and Ideology
Response and Resolution
The Course Ahead