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    The paradox of haemodialysis: the lived experience of the clocked treatment of chronic illness

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    Author
    Burton, James O
    Hull, Katherine L
    Keyword
    chronic illness
    chronic time
    crip time
    end stage kidney disease
    time
    Date
    2024-03
    
    Metadata
    Show full item record
    DOI
    10.1080/14461242.2024.2319189
    Publisher's URL
    https://www.tandfonline.com/doi/full/10.1080/14461242.2024.2319189
    Abstract
    Studies exploring the relationship between time and chronic illness have generally focused on measurable aspects of time, also known as linear time. Linear time follows a predictable, sequential order of past, present and future; measured using a clock and predicated on normative assumptions. Sociological concepts addressing lifecourse disruption following diagnosis of chronic illness have served to enhance the understanding of lived experience. To understand the nuanced relationship between time and chronic illness, however, requires further exploration. Here, we show how the implicit assumptions of linear time meet in tension with the lived experience of chronic illness. We draw on interviews and photovoice work with people with end-stage kidney disease in receipt of in-centre-daytime haemodialysis to show how the clocked treatment of chronic illness disrupts experiences of time. Drawing on concepts of 'crip' and 'chronic' time we argue that clocked treatment and the lived experience of chronic illness converge at a paradox whereby clocked treatment allows for the continuation of linear time yet limits freedom. We use the concept of 'crip time' to challenge the normative assumptions implicit within linear concepts of time and argue that the understanding of chronic illness and its treatment would benefit from a 'cripped' starting point.
    Citation
    Cluley, V., Burton, J. O., Hull, K. L., & Eborall, H. (2024). The paradox of haemodialysis: the lived experience of the clocked treatment of chronic illness. Health sociology review : the journal of the Health Section of the Australian Sociological Association, 33(1), 24–42. https://doi.org/10.1080/14461242.2024.2319189
    Type
    Article
    URI
    http://hdl.handle.net/20.500.12904/18561
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