Literature DB >> 25601066

Unstable terminality: negotiating the meaning of chronicity and terminality in motor neurone disease.

Sverre Vigeland Lerum1, Kari Nyheim Solbraekke, Trygve Holmøy, Jan C Frich.   

Abstract

This paper explores the meaning of chronicity and terminality in motor neurone disease (MND), also known as amyotrophic lateral sclerosis (ALS). There is no known cause or cure for MND, and expected survival is 2-5 years, but several interventions may improve or prolong life. This study draws on qualitative interview data with health professionals in hospitals and primary care, and family carers, in Norway. The actors emphasised chronic and terminal aspects in subtly different ways along the entire illness trajectory, also when recounting the trajectory in retrospect. As a consequence of improved health services and medical technology the distinction between chronicity and terminality has become more vague and sometimes ambiguous. We suggest the concept unstable terminality to describe this ambiguity. While MND is a fatal diagnosis; it may be contested, as contingencies and interventions create an indefinite time scope. The instability creates challenges for primary care which is dependent on prognostic information to organise their effort; hospitals tackle the instability by pre-scheduled consultations allowing for avoidance of an explicit prognosis. Some carers experienced what we understand as a disruption within the disruption, living with chronic and terminal illness simultaneously, which made the limbo phase more challenging to overcome.
© 2015 The Authors. Sociology of Health & Illness © 2015 Foundation for the Sociology of Health & Illness/John Wiley & Sons Ltd.

Entities:  

Keywords:  ambiguity; limbo; motor neurone disease; prognosis; unstable terminality

Mesh:

Year:  2015        PMID: 25601066     DOI: 10.1111/1467-9566.12182

Source DB:  PubMed          Journal:  Sociol Health Illn        ISSN: 0141-9889


  5 in total

1.  Ethical challenges in tracheostomy-assisted ventilation in amyotrophic lateral sclerosis.

Authors:  Morten Magelssen; Trygve Holmøy; Morten Andreas Horn; Ove Arne Fondenæs; Knut Dybwik; Reidun Førde
Journal:  J Neurol       Date:  2018-09-14       Impact factor: 4.849

2.  Family caregivers' accounts of caring for a family member with motor neurone disease in Norway: a qualitative study.

Authors:  Sverre Vigeland Lerum; Kari Nyheim Solbrække; Jan C Frich
Journal:  BMC Palliat Care       Date:  2016-02-24       Impact factor: 3.234

Review 3.  End of life care for long-term neurological conditions: A meta-ethnographic review of the experiences of informal carers.

Authors:  Michael Toze; Mo Ray; Thomas George; Kelly Sisson; David Nelson
Journal:  Palliat Med       Date:  2020-11-25       Impact factor: 4.762

Review 4.  Talking about the end of life: communication patterns in amyotrophic lateral sclerosis - a scoping review.

Authors:  Anke Erdmann; Celia Spoden; Irene Hirschberg; Gerald Neitzke
Journal:  Palliat Care Soc Pract       Date:  2022-03-15

5.  The nebula of chronicity: dealing with metastatic breast cancer in the UK.

Authors:  Cinzia Greco
Journal:  Anthropol Med       Date:  2022-03-11
  5 in total

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