Literature DB >> 25520059

Social aspects of multiple sclerosis for Iranian individuals.

Shahla Abolhassani1, Ahmadreza Yazdannik, Fariba Taleghani, Ahmadreza Zamani.   

Abstract

PURPOSE: This study aimed to determine the social aspects of multiple sclerosis (MS) in the Iranian individuals.
METHODS: A qualitative case study approach was used for this study, which is a part of a larger qualitative study about health care delivery system of MS. Participants were selected on the basis of purposive sampling method. Semi-structured interviews regarding the social aspects of MS were conducted with 18 MS patients, 6 family members and 7 health care providers. Besides interviews with the participants, documents related to the aim of the study, including weblogs, MS magazines, special websites of individuals with MS and news agencies. Data analysis was performed using the qualitative content analysis technique.
RESULTS: Data obtained has been categorised into five main categories, including confronting stigma symbols, the outcome of stigma, walling-in due to stigma, disturbance in normal life and concern about job.
CONCLUSION: There are multiple social effects of MS on the afflicted individuals, which affect various dimensions of their life. Policy makers and health care providers must also consider these effects of MS on other dimensions of the individuals' life. Implications for Rehabilitation Multiple sclerosis (MS) is a disease which restricts social life for patients, in addition to physical impacts. Individuals with MS experienced stigma as well as problems with employment and marital life, due to improper information about MS in society. We recommend that health care workers offer proper information about MS to patients and their family members to minimise the social problems faced by them. We recommend that mass media offers proper information about MS to people in society to disseminate the correct picture of MS. We recommend that the rehabilitation team offers psychological support to patients and their families for their empowerment, to facilitate dealing with the impacts of the disease. We recommend that health care providers teach the family members about patient support and communication skills.

Entities:  

Keywords:  Family; interview; multiple sclerosis; nurses; physicians; social aspects; stigma

Mesh:

Year:  2014        PMID: 25520059     DOI: 10.3109/09638288.2014.918192

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  4 in total

1.  Psychometric Evaluation of the Persian Version of the Chronic Illness Anticipated Stigma Scale (CIASS).

Authors:  Ali-Akbar Nejatisafa; Sahar Mozafari; Ahmad-Ali Noorbala; Fatemeh Sadat Asgarian; Valerie A Earnshaw; Mohammad-Ali Sahraian; Farnaz Etesam
Journal:  Int J Behav Med       Date:  2017-08

2.  Psychometric Properties of the Persian Version of the PARADISE-24 Questionnaire.

Authors:  Amirreza Azimi; Rozita Doosti; Sara Mohammad Vali Samani; Bita Roostaei; Sara Hamtaei Gashti; Samira Navardi; Mahsa Ghajarzadeh
Journal:  Int J Prev Med       Date:  2021-05-27

Review 3.  Disabled in Society - A Scoping Review on Persons Living with Multiple Sclerosis and Disability.

Authors:  Daniel Ståhl; Ylva Bjereld; Anna Dunér
Journal:  J Multidiscip Healthc       Date:  2022-02-24

Review 4.  Stigma, Discrimination and Disclosure of the Diagnosis of Multiple Sclerosis in the Workplace: A Systematic Review.

Authors:  Bruno Kusznir Vitturi; Alborz Rahmani; Guglielmo Dini; Alfredo Montecucco; Nicoletta Debarbieri; Paolo Bandiera; Michela Ponzio; Mario Alberto Battaglia; Benedetta Persechino; Matilde Inglese; Paolo Durando
Journal:  Int J Environ Res Public Health       Date:  2022-08-02       Impact factor: 4.614

  4 in total

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