Literature DB >> 18041660

The fibromyalgia diagnosis: hardly helpful for the patients? A qualitative focus group study.

Merete Undeland1, Kirsti Malterud.   

Abstract

OBJECTIVE: To explore experiences and consequences of the process of being diagnosed with fibromyalgia.
DESIGN: Qualitative focus-group study.
SETTING: Two local self-help groups.
SUBJECTS: Eleven women diagnosed with fibromyalgia. MAIN OUTCOME MEASURES: Descriptions of experiences and consequences of the process of being diagnosed with fibromyalgia.
RESULTS: Many participants had been suffering for years, and initial response of relief was common. For some, the diagnosis legitimized the symptoms as a disease, for others it felt better to suffer from fibromyalgia rather than more serious conditions. Nevertheless sadness and despair emerged when they discovered limitations in treatment options, respect, and understanding. Some patients keep the diagnosis to themselves since people seem to pay no attention to the name, or blatantly regard them as too cheerful or healthy looking. The initial blessing of the fibromyalgia diagnosis seems to be limited in the long run. The process of adapting to this diagnosis can be lonely and strenuous.
CONCLUSION: A diagnosis may be significant when it provides the road to relief or legitimizes the patient's problems. The social and medical meaning of the fibromyalgia diagnosis appears to be more complex. Our findings propose that the diagnosis was hardly helpful for these patients.

Entities:  

Mesh:

Year:  2007        PMID: 18041660      PMCID: PMC3379768          DOI: 10.1080/02813430701706568

Source DB:  PubMed          Journal:  Scand J Prim Health Care        ISSN: 0281-3432            Impact factor:   2.581


  10 in total

1.  Turning points and protective processes in the lives of people with chronic disabilities.

Authors:  Gillian King; Tamzin Cathers; Elizabeth Brown; Jacqueline A Specht; Colleen Willoughby; Janice Miller Polgar; Elizabeth MacKinnon; Linda K Smith; Lisa Havens
Journal:  Qual Health Res       Date:  2003-02

2.  Experiencing chronic illness: cocreating new understandings.

Authors:  Pamela M Ironside; Martha Scheckel; Constance Wessels; Mary E Bailey; Sharon Powers; Deana K Seeley
Journal:  Qual Health Res       Date:  2003-02

3.  Creating meaning in fibromyalgia syndrome.

Authors:  Sue Madden; Julius Sim
Journal:  Soc Sci Med       Date:  2006-09-01       Impact factor: 4.634

4.  "I am allowed to be myself": women with chronic muscular pain being recognized.

Authors:  Sissel Steihaug; Birgitte Ahlsen; Kirsti Malterud
Journal:  Scand J Public Health       Date:  2002       Impact factor: 3.021

5.  Women's experiences of stigma in relation to chronic fatigue syndrome and fibromyalgia.

Authors:  Pia Asbring; Anna-Liisa Närvänen
Journal:  Qual Health Res       Date:  2002-02

6.  What's in a name? An experimental study of patients' views of the impact and function of a diagnosis.

Authors:  Jane Ogden; Ruben Branson; Annie Bryett; Amaryllis Campbell; Alberto Febles; Ian Ferguson; Hilary Lavender; Jacques Mizan; Robin Simpson; Michael Tayler
Journal:  Fam Pract       Date:  2003-06       Impact factor: 2.267

7.  Naming the illness: the power of words.

Authors:  M L Wood
Journal:  Fam Med       Date:  1991 Sep-Oct       Impact factor: 1.756

8.  Avoiding humiliations in the clinical encounter.

Authors:  Kirsti Malterud; Hanne Hollnagel
Journal:  Scand J Prim Health Care       Date:  2007-06       Impact factor: 2.581

9.  It is hard work behaving as a credible patient: encounters between women with chronic pain and their doctors.

Authors:  Anne Werner; Kirsti Malterud
Journal:  Soc Sci Med       Date:  2003-10       Impact factor: 4.634

10.  Diagnosis in chronic illness: disabling or enabling--the case of chronic fatigue syndrome.

Authors:  R V Woodward; D H Broom; D G Legge
Journal:  J R Soc Med       Date:  1995-06       Impact factor: 5.344

  10 in total
  20 in total

1.  In a unique position or squeezed out? The professional roles of general practitioners in cancer care in general and of young adult cancer patients in particular.

Authors:  Bibi Hølge-Hazelton; Inge Christensen
Journal:  J Cancer Educ       Date:  2009       Impact factor: 2.037

2.  Fragility, uncertainty, and healthcare.

Authors:  Wendy A Rogers; Mary J Walker
Journal:  Theor Med Bioeth       Date:  2016-02

3.  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

4.  General practitioners' experiences with provision of healthcare to patients with self-reported multiple chemical sensitivity.

Authors:  Sine Skovbjerg; Jeanne Duus Johansen; Alice Rasmussen; Hanne Thorsen; Jesper Elberling
Journal:  Scand J Prim Health Care       Date:  2009       Impact factor: 2.581

Review 5.  Ketamine in the Past, Present, and Future: Mechanisms, Metabolites, and Toxicity.

Authors:  Eric S Schwenk; Basant Pradhan; Rohit Nalamasu; Lucas Stolle; Irving W Wainer; Michael Cirullo; Alexander Olsen; Joseph V Pergolizzi; Marc C Torjman; Eugene R Viscusi
Journal:  Curr Pain Headache Rep       Date:  2021-07-16

Review 6.  Patients' experiences of chronic non-malignant musculoskeletal pain: a qualitative systematic review.

Authors:  Francine Toye; Kate Seers; Nick Allcock; Michelle Briggs; Eloise Carr; JoyAnn Andrews; Karen Barker
Journal:  Br J Gen Pract       Date:  2013-12       Impact factor: 5.386

7.  Living with a double burden: Meanings of pain for women with fibromyalgia.

Authors:  Päivi Juuso; Lisa Skär; Malin Olsson; Siv Söderberg
Journal:  Int J Qual Stud Health Well-being       Date:  2011-07-13

8.  The lived experience of fibromyalgia in female patients, a phenomenological study.

Authors:  Francesca Wuytack; Peter Miller
Journal:  Chiropr Man Therap       Date:  2011-09-19

9.  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

10.  In their own words: qualitative study of high-utilising primary care patients with medically unexplained symptoms.

Authors:  Francesca C Dwamena; Judith S Lyles; Richard M Frankel; Robert C Smith
Journal:  BMC Fam Pract       Date:  2009-09-21       Impact factor: 2.497

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.