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Goffman's (1963) theory of stigma holds that rejection by “normals” leads people with disabilities to adopt practices that help them to pass as normal or cover the immediate impact of their physical difference. However, such an attempt to mitigate the effects of stigma does not characterize the life histories of three adults with severe multiple congenital limb deficiences described in this paper. For them, self‐display, within the context of American culture in the 1980s, is a strategy for self‐empowerment in which the primary focus is the experience of the person with disabilities rather than the reactions of people who are “normal.” Their adaptations suggest some limitations to the applicability of Goffman's theory in a changing social context.
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