ABSTRACT
We analyze interviews with participants in a COVID-19 vaccine trial to show how Americans navigate conflicting discourses of individual rights and collective responsibility by using individual health behavior to care for others. We argue that interviewees drew on ideologies of “collective biology” – understanding themselves as parts of bio-socially interrelated groups affected by any member’s behavior – to hope their participation would aid collectives cohering around kinship, sex, age, race and ethnicity. Benefits (protecting family, representing one’s group in vaccine development and modeling vaccine acceptance) existed alongside drawbacks (strife, reifying groups), to illustrate the ambivalence of caregiving amid inequality.
Acknowledgments
We are grateful to the participants who kindly volunteered to be interviewed. We thank trial PI Dr. Patricia Winkour for providing access, and Michelle Rodenburg and the trial staff for their assistance.
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No potential conflict of interest was reported by the author(s).
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Notes on contributors
Emily Wentzell
Emily Wentzell is an Associate Professor of Anthropology at the University of Iowa. She uses approaches from medical anthropology, gender/sexuality studies, and science and technology studies to investigate how patients and providers experience emerging health interventions amid societal change.
Ana-Monica Racila
Ana-Monica Racila is a postdoctoral research fellow and medical anthropologist at the University of Iowa Carver College of Medicine. Their research foci include infectious disease prevention and LGBTQ healthcare delivery.