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Information, Communication & Society Volume 23, 2020 - Issue 11
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Articles

Enacting chronic illness with and through digital media: a feminist new materialist approach

Sarah Maslena Faculty of Business, Government and Law, University of Canberra, Bruce, AustraliaCorrespondence[email protected]
&
Deborah Luptonb Faculty of Arts & Social Sciences, Centre for Social Research in Health and Social Policy Research Centre, UNSW Sydney, Randwick, Australia
Pages 1640-1654 | Received 10 Jul 2018, Accepted 21 Mar 2019, Published online: 12 Apr 2019

Citations (11)

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Read on this site (2)

Kerstin Leder Mackley, Carey Jewitt & Sara Price. (2022) The re-mediating effects of bio-sensing in the context of parental touch practices. Information, Communication & Society 25:3, pages 341-358.
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Allegra Clare Schermuly, Alan Petersen & Alison Anderson. (2021) ‘I’m not an activist!’: digital self-advocacy in online patient communities. Critical Public Health 31:2, pages 204-213.
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Articles from other publishers (9)

Matthew Blaszka & Natasha A. Rascon. (2021) Wearable Fitness Devices: An Investigation into Co-constructed Meaning of Use. Communication & Sport 11:3, pages 570-591.
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Karine Wendrich & Lotte Krabbenborg. (2023) Negotiating with digital self-monitoring: A qualitative study on how patients with multiple sclerosis use and experience digital self-monitoring within a scientific study. Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine, pages 136345932311753.
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Laura Ann Chubb. (2023) Me and the Machines: Possibilities and Pitfalls of Using Artificial Intelligence for Qualitative Data Analysis. International Journal of Qualitative Methods 22.
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Elena Link, Eva Baumann & Christoph Klimmt. (2022) Understanding the importance of trust in patients’ coping with uncertainty via health information-seeking behaviors. Communications 0:0.
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Nihar Ranjan Pradhan, Siddhartha Suman Rout & Akhilendra Pratap Singh. (2021) Blockchain Based Smart Healthcare System for Chronic –Illness Patient Monitoring. Blockchain Based Smart Healthcare System for Chronic –Illness Patient Monitoring.
Deborah Lupton. (2021) ‘The Internet Both Reassures and Terrifies’: exploring the more-than-human worlds of health information using the story completion method. Medical Humanities 47:1, pages 68-77.
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Sharynne L. Hamilton, Sarah Maslen, Rochelle Watkins, Katherine Conigrave, Jacinta Freeman, Melissa O’Donnell, Raewyn C. Mutch & Carol Bower. (2020) ‘That thing in his head’: Aboriginal and non‐Aboriginal Australian caregiver responses to neurodevelopmental disability diagnoses. Sociology of Health & Illness 42:7, pages 1581-1596.
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Stine Lomborg, Henriette Langstrup & Tariq Osman Andersen. (2020) Interpretation as luxury: Heart patients living with data doubt, hope, and anxiety. Big Data & Society 7:1, pages 205395172092443.
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Sarah Maslen & Deborah Lupton. (2019) ‘Keeping It Real’: women's Enactments of Lay Health Knowledges and Expertise on Facebook. Sociology of Health & Illness 41:8, pages 1637-1651.
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