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Medical treatment of women with Lupus: the case for sharing knowledge and decision-making
- Authors:
- WHITEBREAD Kate, WILLIAMS Jennie
- Journal article citation:
- Disability and Society, 16(1), January 2001, pp.103-121.
- Publisher:
- Taylor and Francis
Few women patients in this study were found to be active partners in the medical management of systemic lupus erythematosus (SLE). Despite the growing emphasis on doctors and patients sharing knowledge and decision-making power, most of the women were struggling to have their symptoms and needs taken seriously, and appeared relatively powerless in relation to the medical profession. Acknowledging patient expertise requires that doctors share some of their power, and we suggest this may be especially problematic when medical resources and power are primarily located in the hands of white men, and when the patients are typically women and often from the black community. Implications for action that are considered include maximising the influence of women with SLE on research, training and practice.
Ethnicity, disability and chronic illness
- Editor:
- AHMAD Waqar I. U.
- Publisher:
- Open University Press
- Publication year:
- 2000
- Pagination:
- 154p.,bibliog.
- Place of publication:
- Buckingham
Brings together work on ethnicity, disability, chronic illness and caring. Examines the conceptualisation of disability or chronic illness and the implications of particular definitions; looks at everyday living with a disability or chronic ill health; and examines the role of services in providing support to disabled people and carers. Highlights the continued problems experienced by minority ethnic disabled and chronically ill people and their families.