Abstract
Palliative care professionals often speak of the importance of forming meaningful relationships with patients and their families. Trust and rapport, usually established over extended periods of time through face-to-face interactions, and a ‘gentle honesty’ regarding end-of-life and death are key aspects of developing a sense of intimacy with people who are approaching the end of their lives. A fundamental feature of this intimacy is conveying a sense of ‘being with’ a patient. However, these ways of working were greatly challenged by the im-pact of COVID-19. This article explores how intimacy both was and was not established at the height of the pandemic, and it describes the extent to which shared concerns functioned as a new means to create a sense of a common experience.
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Driessen, A., Borgstrom, E., & Cohn, S. (2021). Ways of ‘being with’ caring for dying patients at the height of the COVID-19 pandemic. Anthropology in Action, 28(1), 16–20. https://doi.org/10.3167/AIA.2021.280103
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