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Articles

Tortoise or hare? Supporting the chronotope preference of employees with fluctuating chronic illness symptoms

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Pages 695-714 | Received 28 Apr 2018, Accepted 16 Dec 2018, Published online: 29 Jan 2019
 

Abstract

Objective: Our aim is to understand how to facilitate the job retention of employees with chronic illness. We focus on multiple sclerosis (MS) as a criterion chronic illness.

Design: An opportunity sample of 20 individuals of working age (13 female; 7 male) were recruited who had been in paid employment for over 28 months with a concurrent diagnosis of MS. Participants took part in one of three focus groups with a topic guide comprising keywords: work, coping, performance, support, future, expectations, sharing and symptoms. Data were analysed using dialogical analysis.

Main outcome measures: As a qualitative study, no outcome measure was used. However, the specific focus of interest was to search for differential patterns of ‘timespace’ – chronotope – that people with chronic illness utilise to manage their condition in the workplace.

Results: Participants oriented to two distinct chronotope types: unsustainable epic (characterised by condensed time) and temporary idyll (characterized by condensed space). Perceived managerial discretion was identified as possibly influencing participants’ chronotope preference.

Conclusion: Identifying chronotope preference has practical implications for health psychologists and related professionals who provide and advise on support to facilitate people with chronic illness to thrive in the workplace.

Acknowledgements

We would like to thank Sookhoe Eng (Senior Research Nurse) for moderating the focus groups and coaching Amanda Stroud in her role as focus group facilitator. This research would not have been possible without the generosity of the people with MS who shared their experiences and we extend to them our sincere gratitude.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was supported by a Multiple Sclerosis Society grant (974/12).

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