Becoming-care: reframing care work as flesh work not body work

References

• Adamson, J., Y. Ben-Shlomo, N. Chaturvedi, and J. Donovan. 2003. “Ethnicity, Socio-Economic Position and Gender—Do They Affect Reported Health—Care Seeking Behaviour?” Social Science and Medicine 57 (5): 895–904. doi: 10.1016/S0277-9536(02)00458-6
   PubMed Web of Science ®Google Scholar
• Aldridge, J., and S. Becker. 1994. My Child, My Carer: the Parents’ Perspective. Loughborough: Loughborough University.
   Google Scholar
• Aubeeluck, A., and H. Buchanan. 2006. “Capturing the Huntington’s Disease Spousal Carer Experience.” Dementia (Basel, Switzerland) 5 (1): 95–116.
   Google Scholar
• Barad, K. 2003. “Posthumanist Performativity: Toward an Understanding of How Matter Comes to Matter.” Signs: Journal of Women in Culture and Society 28 (3): 801–831. doi: 10.1086/345321
   Web of Science ®Google Scholar
• Betcher, S. V. 2010. “Becoming Flesh of My Flesh: Feminist and Disability Theologies on the Edge of Posthumanist Discourse.” Journal of Feminist Studies in Religion 26 (2): 107–139. doi: 10.2979/fsr.2010.26.2.107
   Web of Science ®Google Scholar
• Buchanan, I. 1997. “The Problem of the Body in Deleuze and Guattari, Or, What Can a Body Do?” Body &Society 3 (3): 73–91. doi: 10.1177/1357034X97003003004
   Google Scholar
• Butler, J. 1993. Bodies That Matter. On The Discursive Limits of Sex. New York: Routledge.
   Google Scholar
• Cambridge, P. 1999. “The First Hit: A Case Study of the Physical Abuse of People with Learning Disabilities and Challenging Behaviours in a Residential Service.” Disability & Society 14 (3): 285–308. doi: 10.1080/09687599926154
   Web of Science ®Google Scholar
• Carlson, L. 2010. The Faces of Intellectual Disability, Philosophical Reflections. Bloomington: Indiana Press.
   Google Scholar
• Cluley, V. 2017. “Using Photovoice to Include People with Profound and Multiple Learning Disabilities in Inclusive Research.” British Journal of Learning Disabilities 45 (1): 39–46. doi: 10.1111/bld.12174
   Web of Science ®Google Scholar
• Cluley, V. 2018. “From ‘Learning Disability to Intellectual Disability’ – Perceptions of the Increasing Use of the Term ‘Intellectual Disability’ in Learning Disability Policy, Research and Practice.” British Journal of Learning Disabilities 46 (1): 24–32. doi: 10.1111/bld.12209
   Web of Science ®Google Scholar
• Deleuze, G., and F. Guattari. 1984. Anti-Oedipus. London: Continuum.
   Google Scholar
• Deleuze, G., and F. Guattari. 1987. A Thousand Plateaus. London: Continuum.
   Google Scholar
• Descartes, R. (1640) 1968. Discourse on Method and the Meditations. London: Penguin.
   Google Scholar
• Edwards, S. 1998. “The Body as Object Versus the Body as Subject: The Case of Disability.” Medicine, Health Care and Philosophy 1: 47–56. doi: 10.1023/A:1009985821964
   PubMedGoogle Scholar
• Foucault, M. 1989. Birth of the Clinic. London: Routledge.
   Google Scholar
• Fox, N. J. 2002. “Refracting ‘Health’: Deleuze, Guattari and Body-self.” Health 6 (3): 347–363. doi: 10.1177/136345930200600306
   Web of Science ®Google Scholar
• Goodley, D. 2007. “Becoming Rhizomatic Parents: Deleuze, Guattari and Disabled Babies.” Disability & Society 22 (2): 145–160. doi: 10.1080/09687590601141576
   Web of Science ®Google Scholar
• Gustafsson, L., and K. Bootle. 2013. “Client and Carer Experience of Transition Home From Inpatient Stroke Rehabilitation.” Disability & Rehabilitation 35: 1380–1386. doi: 10.3109/09638288.2012.740134
   PubMed Web of Science ®Google Scholar
• Harrington Meyer, M., ed. 2000. Care Work: Gender, Class and the Welfare State. London: Routledge.
   Google Scholar
• Hebsen, G., J. Rubery, and D. Grimshaw. 2015. “Rethinking job Satisfaction is Care Work: Looking Beyond the Care Debates.” Organisation Studies 29 (2): 314–330.
   Google Scholar
• Huxley, P., S. Evans, and T. Maegusuku-Hewet. 2007. “‘Social Care’, ‘the Care Ethic’, and ‘Care Work’: New Definitions, New Directions?” Research, Policy & Planning 23 (1): 3–11.
   Google Scholar
• Isaksen, L. W. 2002. “Toward a Sociology of (Gendered) Disgust: Images of Bodily Decay and the Social Organization of Care Work.” Journal of Family Issues 23 (7): 791–811. doi: 10.1177/019251302236595
   Web of Science ®Google Scholar
• Jackson, A. Y. 2010. “Deleuze and the Girl.” International Journal of Qualitative Studies in Education 23 (5): 579–587. doi: 10.1080/09518398.2010.500630
   Google Scholar
• McDougall, E., M. O’Connor, and J. Howell. 2018. “‘Something That Happens at Home and Stays at Home’: An Exploration of the Lived Experience of Young Carers in Western Australia.” Health and Social Care in the Community 26 (2): 572–580. doi: 10.1111/hsc.12547
   PubMedGoogle Scholar
• Merleau-Ponty, M. 1964. The Primacy of Perception. Evanston, IL: Northwestern University Press.
   Google Scholar
• Morgan, A. 2008. Being Human: Reflections on Mental Distress in Society. Ross-on-Wye: PCCS Books.
   Google Scholar
• Paterson, K., and B. Hughes. 2006. “The Social Model of Disability and the Disappearing Body: Towards a Sociology of Impairment.” In Overcoming Disabling Barriers, edited by L. Barton, 101–117. London: Routledge.
   Google Scholar
• Shakespeare, T. 2014. Disability Rights and Wrongs Revisited. London: Routledge.
   Google Scholar
• Sheehan, R., K. Kimona, A. Giles, V. Copper, and A. Hassiotis. 2018. “Findings From an Online Survey of Family Carer Experience of the Management of Challenging Behaviour in People with Intellectual Disabilities, with a Focus on the use of Psychotropic Medication.” British Journal of Learning Disabilities 46 (2): 82–91. doi: 10.1111/bld.12216
   Web of Science ®Google Scholar
• Shildrick, M. 1997. Leaky Bodies and Boundaries: Feminism, Post-Modernism, and Bio Ethics. London: Routledge.
   Google Scholar
• Shildrick, M. 2018. “Re/membering the Body.” In A Feminist Companion to the Posthumanities, edited by C. Asberg and R. Braidotti, 165–174. London: Springer.
   Google Scholar
• Shilling, C. 2011. “Afterword: Body Work and the Sociological Tradition.” Sociology of Health and Illness 33 (2): 336–340. doi: 10.1111/j.1467-9566.2010.01309.x
   PubMed Web of Science ®Google Scholar
• Shutes, I. 2012. “The Employment of Migrant Workers in Long-Term Care: Dynamics of Choice and Control.” Journal of Social Policy 41 (1): 43–59. doi: 10.1017/S0047279411000596
   Google Scholar
• Skills for Care. 2017. “The State of the Adult Social Care Sector and Workforce in England.” www.skillsforce.org/stateof.
   Google Scholar
• Stacey, C. L. 2005. “Finding Dignity in Dirty Work: The Constraints and Rewards of Low-Wage Home Care Labour.” Sociology of Health and Illness 27 (6): 831–854. doi: 10.1111/j.1467-9566.2005.00476.x
   PubMed Web of Science ®Google Scholar
• Stayt, L. C. 2009. “Death, Empathy and Self Preservation: The Emotional Labour of Caring for Families of the Critically Ill in Adult Intensive Care.” Journal of Clinical Nursing 18 (9): 1267–1275. doi: 10.1111/j.1365-2702.2008.02712.x
   PubMed Web of Science ®Google Scholar
• Thanem, T. 2004. “The Body Without Organs: Nonorganizational Desire in Organizational Life.” Culture and Organization 10 (3): 203–217. doi: 10.1080/14759550412331297147
   Google Scholar
• Timonen, V., and M. Doyle. 2010. “Caring and Collaborating Across Cultures?” European Journal of Women’s Studies 17 (1): 25–41. doi: 10.1177/1350506809350859
   Web of Science ®Google Scholar
• Turner, B. 2008. The Body & Society. 3rd ed. London: Sage.
   Google Scholar
• Twigg, J. 2000. “Carework as a Form of Bodywork.” Ageing and Society 20 (4): 389–411. doi: 10.1017/S0144686X99007801
   Web of Science ®Google Scholar
• Twigg, J., C. Wolkowitz, R. L. Cohen, and S. Nettleton. 2011. “Conceptualising Body Work in Health and Social Care.” Sociology of Health & Illness 33 (2): 171–188. doi: 10.1111/j.1467-9566.2010.01323.x
   PubMed Web of Science ®Google Scholar
• Walmsley, J. 1993. “Contradictions in Caring: Reciprocity and Interdependence.” Disability & Society 8 (2): 129–141. doi: 10.1080/02674649366780111
   Google Scholar
• Walmsley, J. 1996. “Doing What Mum Wants Me to Do: Looking at Family Relationships from the Point of View of People with Intellectual Disabilities.” Journal of Applied Research in Intellectual Disabilities 9 (4): 324–341. doi: 10.1111/j.1468-3148.1996.tb00118.x
   Web of Science ®Google Scholar
• Wang, C., and M. A. Burris. 1997. “Photovoice: Concept, Methodology, and Use for Participatory Needs Assessment.” Health Education & Behaviour 24 (3): 369–387. doi: 10.1177/109019819702400309
   PubMed Web of Science ®Google Scholar
• Wendell, S. 1996. The Rejected Body. New York: Routledge.
   Google Scholar
• Williams, V., and C. Robinson. 2002. “‘He Will Finish up Caring for Me’: People with Learning Disabilities and Mutual Care.” British Journal of Learning Disabilities 29 (2): 56–62. doi: 10.1046/j.1468-3156.2001.00111.x
   Google Scholar
• Wolkowitz, C. 2002. “The Social Relations of Body Work.” Work, Employment and Society 16 (3): 497–510. doi: 10.1177/095001702762217452
   Web of Science ®Google Scholar