Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Click here for more information

SAGETRACK

Sign In to gain access to subscriptions and/or personal tools.
Qualitative Health Research
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Baker, L. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Baker, L. M.
Social Bookmarking
Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Sense Malking in Multiple Sclerosis: The Information Needs of People during an Acute Exacerbation

Lynda M. Baker

Library and Information Science Program, Wayne State University, Detroit, Michigan, LBaker{at}cms.cc.wayne.edu

Chronic illness has been described as a major disruption in one's everyday life. Studies have shown that people seek and use information to help them cope with their disease. Using the micro-moment time-line interview technique, this study focused on the information needs of people with multiple sclerosis (MS) who had recently experienced an exacerbation of their disease. The results revealed gaps in people's knowledge about physical symptoms they were experiencing, emotions they felt, and drugs. Various sources of and barriers to obtaining information were identified. The results suggest that health professionals need to be aware of the continuing need for relevant, current, and specific information to help people with MS retain their independence and to empower them to make informed decisions.

Qualitative Health Research, Vol. 8, No. 1, 106-120 (1998)
DOI: 10.1177/104973239800800108
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
 J Health PsycholHome page
K. I. Pakenham
Making Sense of Illness or Disability: The Nature of Sense Making in Multiple Sclerosis (MS)
J Health Psychol, January 1, 2008; 13(1): 93 - 105.
[Abstract] [PDF]

Home page
 Qual Health ResHome page
A. E. Kurz, N. Saint-Louis, J. P. Burke, and M. G. Stineman
Exploring the Personal Reality of Disability and Recovery: A Tool for Empowering the Rehabilitation Process
Qual Health Res, January 1, 2008; 18(1): 90 - 105.
[Abstract] [PDF]

Home page
 Mult SclerHome page
K. Lode, J.P. Larsen, E. Bru, G. Klevan, K.M. Myhr, and H. Nyland
Patient information and coping styles in multiple sclerosis
Multiple Sclerosis, July 1, 2007; 13(6): 792 - 799.
[Abstract] [PDF]

Home page
 J. Neurol. Neurosurg. PsychiatryHome page
J Greenhalgh, H Ford, A F Long, and K Hurst
The MS Symptom and Impact Diary (MSSID): psychometric evaluation of a new instrument to measure the day to day impact of multiple sclerosis
J. Neurol. Neurosurg. Psychiatry, April 1, 2004; 75(4): 577 - 582.
[Abstract] [Full Text] [PDF]

Home page
 Qual Health ResHome page
S. Thorne, A. Con, L. McGuinness, G. McPherson, and S. R. Harris
Health Care Communication Issues in Multiple Sclerosis: An Interpretive Description
Qual Health Res, January 1, 2004; 14(1): 5 - 22.
[Abstract] [PDF]