Literature DB >> 11464341

Seeing the glass half full: living with Sjogren's Syndrome.

N Schoofs1.   

Abstract

The purpose of this qualitative research was to explore the lived experiences of women with Sjogren's Syndrome (SS), a chronic autoimmune syndrome in which invading lymphocytes attack moisture-producing glands of the body. This syndrome, affecting 4 million Americans, involves extreme dryness of the eyes and mouth and other systemic complications such as fatigue and muscle and joint pain. Ten women, ranging in age from 27 to 83, with SS were interviewed to understand their coping strategies and attitudes. This study used Strauss' framework to view the quality of life of the chronically ill-specifically, those with SS. Nine questions were asked to elicit information on limitations with daily living, relationships, emotions about lifestyle changes, and comparisons with others living with chronic disease. In addition to SS, 8 of the 10 women also had fibromyalgia, and 4 had other conditions such as lupus and rheumatoid arthritis (secondary Sjogren's). Their responses were categorized into four groups: helping, hindering, hoping, and hurting. This led to the development of the 4H Model of Chronic Autoimmune Disease with subcategories such as: supporting, joining, comparing, coping, health promoting, fearing, becoming a chronic sufferer, feeling, wishing, appearing, impeding, restricting, isolating, suffering, doctoring, and diagnosing. J Prof Nurs 17:194-202, 2001. Copyright 2001 by W.B. Saunders Company

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Year:  2001        PMID: 11464341     DOI: 10.1053/jpnu.2001.24863

Source DB:  PubMed          Journal:  J Prof Nurs        ISSN: 8755-7223            Impact factor:   2.104


  3 in total

1.  What impact does written information about fatigue have on patients with autoimmune rheumatic diseases? Findings from a qualitative study.

Authors:  Ruth I Hart; Wan-Fai Ng; Julia L Newton; Katie L Hackett; Richard P Lee; Ben Thompson
Journal:  Musculoskeletal Care       Date:  2016-11-18

2.  Activity interference in patients with Sjögren's syndrome: a cross-sectional study of 149 patients in the UK.

Authors:  Hannah Schoon; Emma Slack; Mark Pearce; Wan-Fai Ng; Katie L Hackett
Journal:  Rheumatology (Oxford)       Date:  2022-10-06       Impact factor: 7.046

3.  The lived experience of Sjögren's Syndrome.

Authors:  Di Ying J Ngo; William M Thomson; Anita Nolan; Shelagh Ferguson
Journal:  BMC Oral Health       Date:  2016-02-01       Impact factor: 2.757

  3 in total

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