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Art of Flourishing: Conversations on Disability [Mīkstie vāki]

Edited by (Associate Professor of Philosophy and Disability Studies, Georgetown University; Senior Research Scholar, ), Edited by , Edited by (Assistant Professor of Bioethics and Humanities at SUNY Upstate Medical University; Presidential Schilar, The Hastings Center), Edited by
  • Formāts: Paperback / softback, 228 pages, height x width x depth: 201x135x15 mm, weight: 227 g, 10 b/w
  • Izdošanas datums: 09-Aug-2025
  • Izdevniecība: Oxford University Press Inc
  • ISBN-10: 0197625711
  • ISBN-13: 9780197625712
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  • Cena: 19,59 €
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  • Formāts: Paperback / softback, 228 pages, height x width x depth: 201x135x15 mm, weight: 227 g, 10 b/w
  • Izdošanas datums: 09-Aug-2025
  • Izdevniecība: Oxford University Press Inc
  • ISBN-10: 0197625711
  • ISBN-13: 9780197625712
Citas grāmatas par šo tēmu:
The Art of Flourishing offers a window into the innumerable and varied ways scholars, artists, writers, and thought leaders with disabilities understand what it means to "flourish." Based on a series of public talks hosted by The Hastings Center, a bioethics research institute, and funded by the National Endowment for the Humanities, this volume demonstrates the incredible range of priorities, practices, and possibilities that characterize disabled experience.

Disabled people are experts in innovation and adaptation, experts in building networks of support and knowledge sharing, and experts in navigating a world that is not built for them. This expertise is not a niche form of knowledge, but one that speaks to a fundamental question about how we should live together--and even thrive together--amid the vast landscape of human difference. In pieces discussing everything from moving with guide dogs to hiking on wheels to nurturing chosen family, The Art of Flourishing offers a window into the innumerable and varied ways scholars, artists, writers, and thought leaders with disabilities understand what it means to "flourish."

For some, it means contesting the medical establishment's narratives of technological salvation that attempt to "fix" people who don't need fixing. For others, it means cultivating interdependent networks of artistic collaboration, or it means having agency in choosing how one appears in and navigates public space. Based on a series of public talks hosted by The Hastings Center, a bioethics research institute, and funded by the National Endowment for the Humanities, this volume demonstrates the incredible range of priorities, practices, and possibilities that characterize disabled experience. It also invites both scholarly and public audiences to imagine what it would take to build a world in which everyone gets to exercise their own capacities in ways they find meaningful.
1 Belonging: On Disability, Technology, and Community
Featuring: Haben Girma, Rachel Kolb, Teresa Blankmeyer Burke

2 Navigating: On Disability, Technology, and Experiencing the World
Featuring: Yomi Sachiko Young, Rod Michalko, Kim Q. Hall

3 Disrupting Ableism with Artful Activism
Featuring: Lateef McLeod and D.J. Savarese

4 Questioning Cure: Disability, Identity, and Healing
Featuring: Anand Prahlad, Ann Millett-Gallant, and Karen Nakamura

5 Enjoying: Disability as a Creative Force
Featuring: Julia Watts Belser, Georgina Kleege, and Jerron Herman

6 We Belong to One Another: Disability and Family-Making
Featuring: Jina B. Kim, Jess Waggoner, Sami Schalk, Joseph A. Stramando,
Leah Smith, and Mia Mingus


References
Index
Liz Bowen is Assistant Professor of Bioethics and Humanities at SUNY Upstate Medical University and a Presidential Scholar at The Hastings Center. She is a disability studies scholar and clinical ethicist trained in literary studies, whose research explores how cultural narratives of disability shape public perceptions of ethical responsibility. She has published widely in both scholarly and popular venues including Scientific American, The Believer, Boston Review, Public Books, English Literary History, and Disability Studies Quarterly.

Joel Michael Reynolds is Associate Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Faculty in the Georgetown University School of Medicine and Medical Center, and Senior Bioethics Advisor to and Fellow of The Hastings Center. Reynolds is the author or co-editor of six books as well as over sixty scholarly publications. They founded The Journal of

Philosophy of Disability and co-founded the book series Oxford Studies in Disability, Ethics, and Society.

Rosemarie Garland-Thomson is professor emerita of English and bioethics at Emory University. She is a Hastings Center Fellow and senior advisor, a National Endowment for the Humanities Public Scholar, a Phi Beta Kappa Visiting Scholar, and a member of the American Academy of Arts and Sciences. She is co-editor of About Us: Essays from the New York Times about Disability by People with Disabilities and author of Staring: How We Look and several other books.

Erik Parens is a Senior Research Scholar at The Hastings Center and Director of the Center's Initiative in Bioethics and the Humanities. He is the author or editor of several books in bioethics, including Shaping Our Selves: On Technology, Flourishing, and a Habit of Thinking, as well as numerous articles and commentaries for academic journals and general-interest publications.