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Social Science & Medicine
Available online 10 June 2025, 118313Chronicity rhetoric in health and welfare systems inhibits patient recovery: a qualitative, ethnographic study of fibromyalgia care
Caroline Cupit 1, Teresa Finlay 1, Catherine Pope 1
For the PACFiND Team2
Rosemary Hollick 2, Gareth T. Jones 2, Louise Locock 2, Gary J. Macfarlane 2, Paul McNamee 2, Kathryn R. Martin 2, Peter Murchie 2, Ernest Choy 3, Sue Ziebland 4, Karen Walker-Bone 5, Chris Eccleston 6, David A. Williams 7, Neil Basu 8
2University of Aberdeen
3University of Cardiff
4University of Oxford
5University of Monash
6University of Bath
7University of Michigan
8University of Glasgow
1University of Oxford
Received 22 January 2025, Revised 8 April 2025, Accepted 6 June 2025, Available online 10 June 2025.
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Handling Editor: Medical Sociology Office
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https://doi.org/10.1016/j.socscimed.2025.118313Get rights and content
Highlights
- •
Biopsychosocial services offer valuable and holistic care - •
Experiential evidence indicates that improvement/recovery is possible - •
Chronicity rhetoric arises from Biomedical Research and Welfare Benefits systems - •
Chronicity rhetoric inhibits biopsychosocial healing work - •
Systems-level intervention is needed to roll out effective biopsychosocial services
Abstract
Fibromyalgia is a leading cause of disability in the UK and worldwide, but is difficult to diagnose and treat due to unclear pathogenesis and diverse and fluctuating symptoms.Although various treatment modalities are recommended, no treatments have been proven to effect sustainable improvement or recovery, and patients are typically dissatisfied with their care.
Increasingly, biopsychosocial services are being developed, that aim to take a multifaceted, holistic approach.
In this paper, we draw on a qualitative, ethnographic study of biopsychosocial services in the UK (including 59 interviews, 200 hours observation, document review, and stakeholder workshops), that are providing new and promising forms of support. Drawing on Smith’s Sociology for People as our analytic framework, we explore the work that is undertaken in these services.
We discover chronicity rhetoric that interrupts practitioners’ and patients’ efforts to promote healing and recovery.
We show that chronicity rhetoric is produced and reinforced through Biomedical Research and Welfare Benefits systems.
Our findings are likely to have wider applicability to services for other difficult-to-treat conditions that are having increasingly problematic impacts on health, wellbeing and economic productivity worldwide (e.g., chronic pain, Chronic Fatigue Syndrome (CFS), Myalgic Encephalomyelitis (ME)).