Literature DB >> 18578274

Understanding chronic pain complicating disability: finding meaning through focus group methodology.

Clint Douglas1, Carol Windsor, Judy Wollin.   

Abstract

Although extensive literature exists on the experiences of people living with chronic nonmalignant pain as a primary condition, little is known about the phenomenon of pain as it is experienced by the person with a chronic disabling condition. This focus group study explored the experience of disability-related pain among 32 people with multiple sclerosis (MS) living in the community. Thematic analysis of transcripts revealed 4 broad conceptualizations of the experience of living with chronic MS-related pain. The first theme, pain is pervasive, described the overwhelming and intrusive presence of pain in daily life. Participants related the physical, emotional, and social consequences of living with chronic, disability-related pain, which caused them great loss and restriction. The second theme resonated around feelings that nobody understands. The participants sought understanding and validation of their pain experiences by family, friends, and healthcare professionals and struggled with difficult issues concerning the legitimacy and invisibility of their pain. The third theme, I'm fine, referred to the propensity of participants to keep pain private from others. In part because of its contested nature, participants at times concealed their pain from others to avoid conflict and maintain some semblance of their former lives. The final theme that emerged was always a factor in the equation. The participants shared how MS had transformed their worlds into ones in which pain and discomfort had become a normal part of everyday life, requiring careful negotiation and planning to undertake activities and prevent exacerbation. It is vital that healthcare providers give people with MS opportunities to talk about pain and pain-related concerns, validate their experiences, and provide interventions that enable self-management. Clinicians are encouraged to challenge their own meanings and expectations about disability-related pain so that therapeutic interventions can be facilitated.

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Year:  2008        PMID: 18578274

Source DB:  PubMed          Journal:  J Neurosci Nurs        ISSN: 0888-0395            Impact factor:   1.230


  5 in total

1.  Patients as collaborators: using focus groups and feedback sessions to develop an interactive, web-based self-management intervention for chronic pain.

Authors:  Sarah K Moore; Honoria Guarino; Michelle C Acosta; Ian David Aronson; Lisa A Marsch; Andrew Rosenblum; Michael J Grabinski; Dennis C Turk
Journal:  Pain Med       Date:  2013-07-16       Impact factor: 3.750

2.  Validity of an observation method for assessing pain behavior in individuals with multiple sclerosis.

Authors:  Karon F Cook; Toni S Roddey; Alyssa M Bamer; Dagmar Amtmann; Francis J Keefe
Journal:  J Pain Symptom Manage       Date:  2012-11-15       Impact factor: 3.612

3.  The use of focus groups to characterize symptoms in persons with multiple sclerosis.

Authors:  Pamela K Newland; Florian P Thomas; Marguerite Riley; Louise H Flick; Arleen Fearing
Journal:  J Neurosci Nurs       Date:  2012-12       Impact factor: 1.230

4.  Living with Chronic Pain: A Qualitative Study of the Daily Life of Older People with Chronic Pain in Chile.

Authors:  Iyubanit Rodríguez; Esmeralda Abarca; Valeria Herskovic; Mauricio Campos
Journal:  Pain Res Manag       Date:  2019-04-01       Impact factor: 3.037

5.  Narratives reflecting the lived experiences of people with brain disorders: common psychosocial difficulties and determinants.

Authors:  Sally Hartley; Maggie McArthur; Michaela Coenen; Maria Cabello; Venusia Covelli; Joanna Roszczynska-Michta; Tuuli Pitkänen; Jerome Bickenbach; Alarcos Cieza
Journal:  PLoS One       Date:  2014-05-07       Impact factor: 3.240

  5 in total

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