Literature DB >> 10207829

The journey to multiple sclerosis: a qualitative study.

W Koopman1, A Schweitzer.   

Abstract

The diagnosis of multiple sclerosis (MS) often creates more questions than answers. It is not uncommon to hear about individuals who receive the diagnosis with relief and surprise, However, the implications of being diagnosed with a chronic illness like MS is complex. There is no known cure for this disease that has remissions, relapses and possible continued progression. For individuals diagnosed with MS, responding to the physical and psychological stresses of a condition with an unknown cause and no cure is challenging. The purpose of this study was to explore the individual's experience of having symptoms for a period of time and then to be told they have MS. The phenomenological qualitative research method was used to illuminate the nature of their experiences. The time course spanned before diagnosis, at diagnosis and following diagnosis. Interviews were conducted with five purposefully selected participants. The process of data analysis highlighted common threads and patterns among informants. Four major themes emerged: Whispered Beginnings, Echoes of Silence, The Spoken Words, and Recreating Voice. The experiences of individuals recently diagnosed with MS are illuminated in order to provide insight and information to health care providers who are faced with telling a person the diagnosis of MS.

Entities:  

Mesh:

Year:  1999        PMID: 10207829     DOI: 10.1097/01376517-199902000-00003

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


  11 in total

1.  The path to self-management: a qualitative study involving older people with multiple sclerosis.

Authors:  Michelle Ploughman; Mark W Austin; Michelle Murdoch; Anne Kearney; Marshall Godwin; Mark Stefanelli
Journal:  Physiother Can       Date:  2012-01-31       Impact factor: 1.037

Review 2.  Multiple sclerosis: diagnosis and the management of acute relapses.

Authors:  S M Leary; B Porter; A J Thompson
Journal:  Postgrad Med J       Date:  2005-05       Impact factor: 2.401

3.  Unmet needs of patients feeling severely affected by multiple sclerosis in Germany: a qualitative study.

Authors:  Maren Galushko; Heidrun Golla; Julia Strupp; Ute Karbach; Claudia Kaiser; Nicole Ernstmann; Holger Pfaff; Christoph Ostgathe; Raymond Voltz
Journal:  J Palliat Med       Date:  2014-02-14       Impact factor: 2.947

4.  Understanding self-management behaviors in symptomatic adults with uncertain etiology using an illness perceptions framework.

Authors:  Cristina Leos; Cynthia M Khan; Christine Rini
Journal:  J Behav Med       Date:  2015-12-08

5.  The MS Symptom and Impact Diary (MSSID): psychometric evaluation of a new instrument to measure the day to day impact of multiple sclerosis.

Authors:  J Greenhalgh; H Ford; A F Long; K Hurst
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-04       Impact factor: 10.154

Review 6.  Accuracy of magnetic resonance imaging for the diagnosis of multiple sclerosis: systematic review.

Authors:  Penny Whiting; Roger Harbord; Caroline Main; Jonathan J Deeks; Graziella Filippini; Matthias Egger; Jonathan A C Sterne
Journal:  BMJ       Date:  2006-03-24

7.  Meanings of being received and met by others as experienced by women with MS.

Authors:  Malin Olsson; Lisa Skär; Siv Söderberg
Journal:  Int J Qual Stud Health Well-being       Date:  2011-03-07

8.  PICO, PICOS and SPIDER: a comparison study of specificity and sensitivity in three search tools for qualitative systematic reviews.

Authors:  Abigail M Methley; Stephen Campbell; Carolyn Chew-Graham; Rosalind McNally; Sudeh Cheraghi-Sohi
Journal:  BMC Health Serv Res       Date:  2014-11-21       Impact factor: 2.655

9.  Cerebellar ataxia and intrathecal baclofen therapy: Focus on patients´ experiences.

Authors:  Shala Ghaderi Berntsson; Anne-Marie Landtblom; Gullvi Flensner
Journal:  PLoS One       Date:  2017-06-27       Impact factor: 3.240

Review 10.  'It struck at the heart of who I thought I was': A meta-synthesis of the qualitative literature examining the experiences of people with multiple sclerosis.

Authors:  Jane Desborough; Crystal Brunoro; Anne Parkinson; Katrina Chisholm; Mark Elisha; Janet Drew; Vanessa Fanning; Christian Lueck; Anne Bruestle; Matthew Cook; Hanna Suominen; Antonio Tricoli; Adam Henschke; Christine Phillips
Journal:  Health Expect       Date:  2020-06-24       Impact factor: 3.377

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