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Uncertain Suffering
by
Carolyn Moxley Rouse
in
african americans
/ ambivalence
/ american healthcare system
/ Anthropology
/ community based health programs
/ cultural assumptions
/ Discrimination in medical care
/ Discrimination in medical care -- United States
/ disease
/ doctor
/ health disparity
/ Health services accessibility
/ Health services accessibility -- United States
/ healthcare
/ healthcare services
/ HISTORY / Social History
/ human condition
/ life and death
/ MEDICAL / Diseases
/ Medical care
/ medical treatment
/ medicine
/ mental suffering
/ Minorities
/ Minorities -- Medical care -- United States
/ national policy
/ pain and suffering
/ Patients
/ physical suffering
/ politics of racism
/ Race discrimination
/ Race discrimination -- United States
/ race in america
/ resource limitations
/ sicker
/ Sickle cell anemia
/ Sickle cell anemia -- Patients -- United States
/ sickle cell patients
/ sickness
/ Social medicine
/ Social medicine -- United States
/ SOCIAL SCIENCE
/ SOCIAL SCIENCE / Anthropology / General
/ symptoms
/ United States
/ united states of america
/ wealth disparity
2009
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Uncertain Suffering
by
Carolyn Moxley Rouse
in
african americans
/ ambivalence
/ american healthcare system
/ Anthropology
/ community based health programs
/ cultural assumptions
/ Discrimination in medical care
/ Discrimination in medical care -- United States
/ disease
/ doctor
/ health disparity
/ Health services accessibility
/ Health services accessibility -- United States
/ healthcare
/ healthcare services
/ HISTORY / Social History
/ human condition
/ life and death
/ MEDICAL / Diseases
/ Medical care
/ medical treatment
/ medicine
/ mental suffering
/ Minorities
/ Minorities -- Medical care -- United States
/ national policy
/ pain and suffering
/ Patients
/ physical suffering
/ politics of racism
/ Race discrimination
/ Race discrimination -- United States
/ race in america
/ resource limitations
/ sicker
/ Sickle cell anemia
/ Sickle cell anemia -- Patients -- United States
/ sickle cell patients
/ sickness
/ Social medicine
/ Social medicine -- United States
/ SOCIAL SCIENCE
/ SOCIAL SCIENCE / Anthropology / General
/ symptoms
/ United States
/ united states of america
/ wealth disparity
2009
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Do you wish to request the book?
Uncertain Suffering
by
Carolyn Moxley Rouse
in
african americans
/ ambivalence
/ american healthcare system
/ Anthropology
/ community based health programs
/ cultural assumptions
/ Discrimination in medical care
/ Discrimination in medical care -- United States
/ disease
/ doctor
/ health disparity
/ Health services accessibility
/ Health services accessibility -- United States
/ healthcare
/ healthcare services
/ HISTORY / Social History
/ human condition
/ life and death
/ MEDICAL / Diseases
/ Medical care
/ medical treatment
/ medicine
/ mental suffering
/ Minorities
/ Minorities -- Medical care -- United States
/ national policy
/ pain and suffering
/ Patients
/ physical suffering
/ politics of racism
/ Race discrimination
/ Race discrimination -- United States
/ race in america
/ resource limitations
/ sicker
/ Sickle cell anemia
/ Sickle cell anemia -- Patients -- United States
/ sickle cell patients
/ sickness
/ Social medicine
/ Social medicine -- United States
/ SOCIAL SCIENCE
/ SOCIAL SCIENCE / Anthropology / General
/ symptoms
/ United States
/ united states of america
/ wealth disparity
2009
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eBook
Uncertain Suffering
2009
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Overview
On average, black Americans are sicker and die earlier than white Americans. Uncertain Suffering provides a richly nuanced examination of what this fact means for health care in the United States through the lens of sickle cell anemia, a disease that primarily affects blacks. In a wide ranging analysis that moves from individual patient cases to the compassionate yet distanced professionalism of health care specialists to the level of national policy, Carolyn Moxley Rouse uncovers the cultural assumptions that shape the quality and delivery of care for sickle cell patients. She reveals a clinical world fraught with uncertainties over how to treat black patients given resource limitations and ambivalence. Her book is a compelling look at the ways in which the politics of racism, attitudes toward pain and suffering, and the reliance on charity for healthcare services for the underclass can create disparities in the U.S. Instead of burdening hospitals and clinics with the task of ameliorating these disparities, Rouse argues that resources should be redirected to community-based health programs that reduce daily forms of physical and mental suffering.
Publisher
University of California Press
Subject
/ community based health programs
/ Discrimination in medical care
/ Discrimination in medical care -- United States
/ disease
/ doctor
/ Health services accessibility
/ Health services accessibility -- United States
/ medicine
/ Minorities -- Medical care -- United States
/ Patients
/ Race discrimination -- United States
/ sicker
/ Sickle cell anemia -- Patients -- United States
/ sickness
/ Social medicine -- United States
/ SOCIAL SCIENCE / Anthropology / General
/ symptoms
ISBN
0520259122, 9780520259126, 0520259114, 9780520259119, 0520945042, 9780520945043
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