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Original Articles

Private Tragedy in Social Context? Reflections on Disability, Illness and Suffering

Pages 255-267 | Published online: 01 Jul 2010

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (7)

Elizabeth Price, Liz Walker & Sara Booth. (2020) Feeling the benefit? Fluctuating illness and the world of welfare. Disability & Society 35:8, pages 1315-1336.
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Heather Mack & Ian Paylor. (2017) The inclusion of people with hepatitis C within disability studies. Scandinavian Journal of Disability Research 19:1, pages 18-33.
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Harriet Clarke & Stephen McKay. (2014) Disability, partnership and parenting. Disability & Society 29:4, pages 543-555.
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Patricia de Wolfe. (2012) Reaping the benefits of sickness? Long-term illness and the experience of welfare claims. Disability & Society 27:5, pages 617-630.
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Penny Rhodes, Andrew Nocon, Neil Small & John Wright. (2008) Disability and identity: the challenge of epilepsy. Disability & Society 23:4, pages 385-395.
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Articles from other publishers (16)

Dorothee Marx. (2023) Sanitizing Chronic Illness?. Journal of Literary & Cultural Disability Studies 17:2, pages 217-232.
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Yvonne Wechuli. (2022) Between cripping and reclaiming: epistemological implications of Disability Studies’ feeling strategies1. Emotions and Society 4:2, pages 142-160.
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Thurka Sangaramoorthy. (2019) Liminal Living: Everyday Injury, Disability, and Instability among Migrant Mexican Women in Maryland's Seafood Industry. Medical Anthropology Quarterly 33:4, pages 557-578.
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Loren E. Wilbers. 2019. New Narratives of Disability. New Narratives of Disability 151 167 .
Marwan Habiba. (2019) Controversies in applying the Abortion Act to Down syndrome. Clinical Ethics 14:2, pages 57-62.
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Felicity K. Boardman & Rachel Hale. (2019) “I didn’t take it too seriously because I’d just never heard of it”: Experiential knowledge and genetic screening for thalassaemia in the UK . Journal of Genetic Counseling 28:1, pages 141-154.
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Anna Wood. 2019. Artificial Intelligence and Inclusive Education. Artificial Intelligence and Inclusive Education 135 148 .
Emma Sheppard. (2018) Using Pain, Living with Pain. Feminist Review 120:1, pages 54-69.
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Felicity K Boardman & Rachel Hale. (2018) How do genetically disabled adults view selective reproduction? Impairment, identity, and genetic screening. Molecular Genetics & Genomic Medicine 6:6, pages 941-956.
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Silke Hoppe. (2017) A Sorrow Shared is a Sorrow Halved: The Search for Empathetic Understanding of Family Members of a Person with Early-Onset Dementia. Culture, Medicine, and Psychiatry 42:1, pages 180-201.
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Felicity K. Boardman, Philip J. Young & Frances E. Griffiths. (2017) Impairment Experiences, Identity and Attitudes Towards Genetic Screening: the Views of People with Spinal Muscular Atrophy. Journal of Genetic Counseling 27:1, pages 69-84.
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Felicity Boardman. (2013) Experiential knowledge of disability, impairment and illness: The reproductive decisions of families genetically at risk. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine 18:5, pages 476-492.
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Alex I. Thompson. (2013) “Sometimes, I think I might say too much”: Dark Secrets and the Performance of Inflammatory Bowel Disease * . Symbolic Interaction 36:1, pages 21-39.
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Katrina Arndt & Maia Van Beuren. (2013) The Speed of Dark and This Alien Shore . Journal of Literary & Cultural Disability Studies 7:1, pages 89-104.
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Nichola Hutchinson. (2016) Disabling Beliefs? Impaired Embodiment in the Religious Tradition of the West. Body & Society 12:4, pages 1-23.
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Wayne Paris & Connie White-Williams. (2005) Social Adaptation After Cardiothoracic Transplantation. The Journal of Cardiovascular Nursing 20:Supplement, pages S67-S73.
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