The lived experiences of patients with spinal muscular atrophy: A phenomenological study

Context: Spinal muscular atrophy (SMA) is a neuromuscular disease which, in addition to physical disability, causes psychological and social problems for patients and their families. If physiological and mental disorders continue to persist for a long time, it leads to serious deterioration in the p...

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Main Authors: Ali-Asghar Jesmi, Leila Jouybari, Akram Sanagoo
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Journal of Nursing and Midwifery Sciences
Subjects:
Online Access:http://www.jnmsjournal.org/article.asp?issn=2345-5756;year=2019;volume=6;issue=2;spage=57;epage=62;aulast=Jesmi
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spelling doaj-aa6cb318d3444cadb4015c19cc99386d2020-11-25T03:16:55ZengWolters Kluwer Medknow PublicationsJournal of Nursing and Midwifery Sciences2345-57642019-01-0162576210.4103/JNMS.JNMS_59_18The lived experiences of patients with spinal muscular atrophy: A phenomenological studyAli-Asghar JesmiLeila JouybariAkram SanagooContext: Spinal muscular atrophy (SMA) is a neuromuscular disease which, in addition to physical disability, causes psychological and social problems for patients and their families. If physiological and mental disorders continue to persist for a long time, it leads to serious deterioration in the patient's physical condition, influences the treatment process, and prevents the outcome of the therapies. Aims: The aim of this study was to explore the lived experiences of patients with SMA. Setting and Design: In this qualitative study, a total of six participants (five patients and one patients' wife) were selected by purposive sampling method. Material and Methods: Data were collected by semi-structured interview. Eleven interviews were conducted and analyzed by Colaizzi's descriptive phenomenological approach. Statistical Analysis Used: Data were analyzed by One Note soft ware version 14.0 with Colaizzi's descriptive phenomenological approach. Results: Two main themes – “tragic life” and “vague future” – emerged from data analysis. They had four categories including “physical and psychological problems,” “limitations and lost opportunities,” “concerns,” and “uncertain future.” Conclusions: These patients experienced a lot of physical and psychological impairments in their life. They have many concerns and lost some opportunities. Therefore, policymakers and authorities should support these patients for participating as an effective members in the society, consequently their feeling improve by getting independent.http://www.jnmsjournal.org/article.asp?issn=2345-5756;year=2019;volume=6;issue=2;spage=57;epage=62;aulast=Jesmilived experiencesqualitative researchspinal muscular atrophy
collection DOAJ
language English
format Article
sources DOAJ
author Ali-Asghar Jesmi
Leila Jouybari
Akram Sanagoo
spellingShingle Ali-Asghar Jesmi
Leila Jouybari
Akram Sanagoo
The lived experiences of patients with spinal muscular atrophy: A phenomenological study
Journal of Nursing and Midwifery Sciences
lived experiences
qualitative research
spinal muscular atrophy
author_facet Ali-Asghar Jesmi
Leila Jouybari
Akram Sanagoo
author_sort Ali-Asghar Jesmi
title The lived experiences of patients with spinal muscular atrophy: A phenomenological study
title_short The lived experiences of patients with spinal muscular atrophy: A phenomenological study
title_full The lived experiences of patients with spinal muscular atrophy: A phenomenological study
title_fullStr The lived experiences of patients with spinal muscular atrophy: A phenomenological study
title_full_unstemmed The lived experiences of patients with spinal muscular atrophy: A phenomenological study
title_sort lived experiences of patients with spinal muscular atrophy: a phenomenological study
publisher Wolters Kluwer Medknow Publications
series Journal of Nursing and Midwifery Sciences
issn 2345-5764
publishDate 2019-01-01
description Context: Spinal muscular atrophy (SMA) is a neuromuscular disease which, in addition to physical disability, causes psychological and social problems for patients and their families. If physiological and mental disorders continue to persist for a long time, it leads to serious deterioration in the patient's physical condition, influences the treatment process, and prevents the outcome of the therapies. Aims: The aim of this study was to explore the lived experiences of patients with SMA. Setting and Design: In this qualitative study, a total of six participants (five patients and one patients' wife) were selected by purposive sampling method. Material and Methods: Data were collected by semi-structured interview. Eleven interviews were conducted and analyzed by Colaizzi's descriptive phenomenological approach. Statistical Analysis Used: Data were analyzed by One Note soft ware version 14.0 with Colaizzi's descriptive phenomenological approach. Results: Two main themes – “tragic life” and “vague future” – emerged from data analysis. They had four categories including “physical and psychological problems,” “limitations and lost opportunities,” “concerns,” and “uncertain future.” Conclusions: These patients experienced a lot of physical and psychological impairments in their life. They have many concerns and lost some opportunities. Therefore, policymakers and authorities should support these patients for participating as an effective members in the society, consequently their feeling improve by getting independent.
topic lived experiences
qualitative research
spinal muscular atrophy
url http://www.jnmsjournal.org/article.asp?issn=2345-5756;year=2019;volume=6;issue=2;spage=57;epage=62;aulast=Jesmi
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