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At the 2014 Annual Meeting in San Francisco, Executive Officer Sally Hillsman, met with the Committee on Professional Ethics (COPE) and suggested that it was time to revise the Code of Ethics. Revisions were last made to the Code 20 years ago, and a great deal of change had taken place. Regulatory and technological advances have had striking impacts on the field. At the time, the Department of Health and Human Services was about to announce changes to The Common Rule, which governs the vast majority of human subjects research efforts.
The unequal impacts of COVID-19 demonstrate an urgent need for sociological interrogations of disability as a social category and axis of inequality commensurate with race, class, and gender and intersecting with them. While disability can be a marker of health status, it is also a unique social category with particular politics structuring disabled people’s lives and reflecting interlocking systems of oppression. We provide examples of how the pandemic reveals disability is a societally mediated category of existence that is (de)valued in particular ways.
Jessica Collett, University of California-Los Angeles
Interpreting physiological responses is a key part of emotional experience. Imagine a father who tells a child about to start kindergarten that what they describe as feeling sick is actually a sign of nervous excitement—what some call butterflies—and not illness. His emotional vocabulary, combined with an understanding of situational cues, help him interpret his child’s experience (and stops him from searching for the pediatrician’s number).