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Volume 7, Issue 3 (2019)
Health Educ Health Promot 2019, 7(3): 147-154 |
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History
Received: 2019/02/8 | Accepted: 2019/04/10 | Published: 2019/06/21
Received: 2019/02/8 | Accepted: 2019/04/10 | Published: 2019/06/21
How to cite this article
Rahimi T, Khazir Z. Perceived Experiences of Life Problems for Parents with a Down Syndrome Child. Health Educ Health Promot 2019; 7 (3) :147-154
URL: http://hehp.modares.ac.ir/article-4-30286-en.html
URL: http://hehp.modares.ac.ir/article-4-30286-en.html
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1- Public Health Department, Health Faculty, Jiroft University of Medical Sciences, Jiroft, Iran
2- Health Education & Health Promotion Department, Health Faculty, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
2- Health Education & Health Promotion Department, Health Faculty, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
Abstract (10248 Views)
Aims: Down syndrome (DS), as the most common cause of mental retardation causes many health problems for families. This study aimed to investigate the experiences of life problems for parents with a DS child.
Participants & Methods: This qualitative research was conducted using the conventional content analysis method on 21 Iranian parents with a DS child of over one year of age. Data were collected using online asynchronous interviews in 2017. Snowball sampling was continued until the data saturation was reached. Data collection and analysis were conducted simultaneously by qualitative content analysis.
Findings: Participants included 21 parents of children with DS in the age range of 28-49 years old. The analysis of qualitative data led to the extraction of three main themes, including continuation of a difficult life, inappropriate atmosphere of the community for acceptance of a child with DS, and perceived future concerns.
Conclusion: The findings showed that parents of children with DS had major common concerns about taking care of their children. It is necessary for health policymaker and healthcare providers to pay more attention to the implementation of medical care and education programs for children with DS. Also, informing the community about DS helps to raise awareness and appropriate social interactions among the families and community members.
Participants & Methods: This qualitative research was conducted using the conventional content analysis method on 21 Iranian parents with a DS child of over one year of age. Data were collected using online asynchronous interviews in 2017. Snowball sampling was continued until the data saturation was reached. Data collection and analysis were conducted simultaneously by qualitative content analysis.
Findings: Participants included 21 parents of children with DS in the age range of 28-49 years old. The analysis of qualitative data led to the extraction of three main themes, including continuation of a difficult life, inappropriate atmosphere of the community for acceptance of a child with DS, and perceived future concerns.
Conclusion: The findings showed that parents of children with DS had major common concerns about taking care of their children. It is necessary for health policymaker and healthcare providers to pay more attention to the implementation of medical care and education programs for children with DS. Also, informing the community about DS helps to raise awareness and appropriate social interactions among the families and community members.
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