Literature DB >> 17056769

Individuals' descriptions of living with fibromyalgia.

Margaret Mui Cunningham1, Carol Jillings.   

Abstract

Fibromyalgia (FM) is a chronic pain syndrome with no known etiology, cure, prognosis, or clear diagnostic criteria. This interpretive descriptive study was focused on the experience of living with FM. Using a constant comparative inductive analytic method, the researcher collected and analyzed data from in-depth, semistructured interviews with eight participants. This study's findings offer insights into the experience of living with and managing FM and identify social, policy, and health care issues that profoundly affect those suffering from it. Participants believe that people with FM would benefit if more health care professionals, as well as family and friends, would validate their condition and provide them with better support. More research could clarify ways in which health care providers may provide more effective interventions, appropriate care, and ongoing support for those affected with FM.

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Year:  2006        PMID: 17056769     DOI: 10.1177/1054773806291853

Source DB:  PubMed          Journal:  Clin Nurs Res        ISSN: 1054-7738            Impact factor:   2.075


  22 in total

1.  Impact of invalidation and trust in physicians on health outcomes in fibromyalgia patients.

Authors:  Carroline P Lobo; Andrea R Pfalzgraf; Vincent Giannetti; Gibbs Kanyongo
Journal:  Prim Care Companion CNS Disord       Date:  2014-10-09

2.  [Restrictions in participation in women with fibromyalgia syndrome. An explorative pilot study].

Authors:  A Ullrich; E Farin; W H Jäckel
Journal:  Schmerz       Date:  2012-02       Impact factor: 1.107

3.  Fatigue in fibromyalgia: a conceptual model informed by patient interviews.

Authors:  Louise Humphrey; Rob Arbuckle; Philip Mease; David A Williams; Bente Danneskiold Samsoe; Claire Gilbert
Journal:  BMC Musculoskelet Disord       Date:  2010-09-20       Impact factor: 2.362

Review 4.  Self-management support from the perspective of patients with a chronic condition: a thematic synthesis of qualitative studies.

Authors:  Jolanda Dwarswaard; Ellen J M Bakker; AnneLoes van Staa; Hennie R Boeije
Journal:  Health Expect       Date:  2015-01-26       Impact factor: 3.377

5.  Patients' and professionals' views on managing fibromyalgia.

Authors:  Erica Briones-Vozmediano; Carmen Vives-Cases; Elena Ronda-Pérez; Diana Gil-González
Journal:  Pain Res Manag       Date:  2013 Jan-Feb       Impact factor: 3.037

6.  Evaluation of the impact of fibromyalgia on patients' sleep and the content validity of two sleep scales.

Authors:  Susan Martin; Arthi Chandran; Laurie Zografos; Gergana Zlateva
Journal:  Health Qual Life Outcomes       Date:  2009-07-10       Impact factor: 3.186

7.  Life impact of urologic pain syndromes.

Authors:  Lena Hatchett; Mary Pat Fitzgerald; Jeannette Potts; Abigail Winder; Keith Mickelberg; Ted Barrell; John W Kusek
Journal:  J Health Psychol       Date:  2009-09

Review 8.  Fibromyalgia: A Critical and Comprehensive Review.

Authors:  Andrea T Borchers; M Eric Gershwin
Journal:  Clin Rev Allergy Immunol       Date:  2015-10       Impact factor: 8.667

9.  Patient perspectives on the impact of fibromyalgia.

Authors:  Lesley M Arnold; Leslie J Crofford; Philip J Mease; Somali Misra Burgess; Susan C Palmer; Linda Abetz; Susan A Martin
Journal:  Patient Educ Couns       Date:  2008-07-21

10.  Patients' experiences of living with and receiving treatment for fibromyalgia syndrome: a qualitative study.

Authors:  Heidi K Lempp; Stephani L Hatch; Serene F Carville; Ernest H Choy
Journal:  BMC Musculoskelet Disord       Date:  2009-10-07       Impact factor: 2.362

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