Long COVID and Society

This edited book focuses on the social aspects and impacts of Long COVID from an international perspective, including contributions from researchers in the UK, Italy, Switzerland, the Netherlands. USA and Australia. The book highlights how Long COVID affects people's identities, social relationships, life opportunities and inclusion in society. Long COVID, like COVID itself, is a social and political as well as a medical phenomenon. People with Long COVID, from young children to older adults, are confronting ableism, social stigma, exclusion, invisibility and gaslighting. The book throws a spotlight on the struggles over the legitimacy of lay expertise versus medical authority and addresses how people with Long COVID are supporting and learning from each other and engaging in activism and advocacy initiatives. Crucially, most of the authors are themselves living with or caring for someone with Long COVID or work closely with Long COVID patient communities and others with lived experience.

Chapters 1 and 14 are available as Open Access under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License via link.springer.com.

The first book to focus on the social aspects and impacts of Long COVID Highlights how Long COVID affects people's identities, relationships, opportunities and inclusion in society Brings together social and political theory alongside international insights offered from lived experience

Autorentext

Deborah Lupton is SHARP Professor in the Faculty of Arts, Design & Architecture, University of New South Wales (UNSW) Sydney, Australia. She is located in the Centre for Social Research in Health and the Social Policy Research Centre. She is a leading health sociologist and has been awarded two honorary doctorates for her outstanding achievements in research.

Inhalt

Introduction.- The Social Aspects and Impacts of Long COVID.- Part I: Knowledge-Making.- Long COVID: The Critical Role of Patient Advocacy-Research in Disease Recognition.- Long COVID Times: An X/Twitter Informed Rhythmanalysis of Pacing.- Part II: Medical Responses.- 'Just Because You Didn't Detect It, Doesn't Mean It's Not There': Long COVID, ME/CFS and the Social Dynamics of Biomedical Knowledge Production.- Long COVID Services between Medical Clinics and Healing Rituals: A Case Study in Switzerland.- Part III: Biopolitics and Social Determinants.- Long COVID and the Biopolitics of Pandemic Timings and Endings.- The Profound Societal Impacts of Long COVID and Pandemic Non-Interventionism.- Equity Amidst Uncertainty: A Comparative Critique of Multiple Stakeholder Perspectives about Health Equity for People with Long COVID.- Part IV: Lived Experience.- We Will Not Be Silent: The Australia Long COVID Community Speak out About the Role of Epistemic Injustice in Erasing Evidence of Long COVID in Australia.- Living with the Virus: An Autoethnography of Long COVID as Multilayered Traumatisation.- The Double Bind: Gaslighting, Cultural Violence and the Post-Acute COVID Experience.- Part V: Specific Social Groups.- 'I Have Disappeared': Long COVID, ME/CFS and Inclusion in Church Communities.- The Debilitating Discourses of Long COVID: The Public Pedagogies of Sporting Bodies.- Long COVID in Children, Young People and Families.- Coda.- My Strange Revelations from Grief and Long COVID: How Caring for My Wife Showed Me the Horror and Beauty of Loss from Disease.