Hamilton-West, Kate E., Quine, Lyn (2009) Living with Ankylosing Spondylitis: the patient's perspective. Journal of Health Psychology, 14 (6). pp. 820-830. ISSN 1359-1053. (doi:10.1177/1359105309341394) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:23315)
The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided. | |
Official URL: http://dx.doi.org/10.1177/1359105309341394 |
Abstract
Ankylosing spondylitis (AS) is a potentially debilitating chronic condition that necessitates a biopsychosocial approach for successful long-term management. However, the psychosocial consequences of AS are not well understood. In this study patients (N=68) reported impacts of AS across a wide range of life domains; negative impacts included physical effects of AS, changes in mood or personality, effects on social life and relationships with friends and family, low self-esteem, stigma, and worry about the future; positive impacts included increased exercise, feelings of achievement and empathy, stronger relationships, slower pace of life and a more positive perspective. Implications for treatment are discussed.
Item Type: | Article |
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DOI/Identification number: | 10.1177/1359105309341394 |
Uncontrolled keywords: | Ankylosing Spondylitis; benefit-finding; quality of life |
Subjects: | B Philosophy. Psychology. Religion > BF Psychology |
Divisions: |
Divisions > Division of Human and Social Sciences > School of Psychology Divisions > Division for the Study of Law, Society and Social Justice > School of Social Policy, Sociology and Social Research > Centre for Health Services Studies |
Depositing User: | Kate Hamilton-West |
Date Deposited: | 11 Nov 2009 15:12 UTC |
Last Modified: | 05 Nov 2024 10:02 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/23315 (The current URI for this page, for reference purposes) |
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