Initial Psychological Experiences of Parents toward Recent Disclosure of Diagnosis for Children with Special Needs
Main Article Content
Abstract
This study aimed to examine the psychological experiences of parents toward recent disclosure
of the diagnosis of their children with special needs. Key informants were 7 parents whose children were
diagnosed with special needs by child and adolescent psychiatrists and pediatricians specialized in child
development and behavior which involves Autistic Spectrum Disorder (ASD), Down Syndrome, and Cri-du-chat
syndrome. Data was collected via in-depth interviewing, and then analyzed using phenomenological analysis
method. Findings revealed three main themes: (1) Factors related to disclosure of the diagnosis and medical treatment, including child rearing problems, an observation and perception of children's abnormality, and
readiness for help seeking, (2) Disclosure of the diagnosis, including information received from health professionals, rejection of the diagnosis results, and acceptance of the diagnosis results and readiness for child rearing, and (3) Adjustment and overcoming myriad obstacle process, including difficulties in parenting
children with special needs, receiving support from family members, receiving support from health professionals, inspirations from other parents of children with special needs, and commitment to child rearing. Understanding psychological experiences of the parents will make related individuals and institutes better provide appropriate support to a family whose child has special needs.
Article Details
References
ประภัสสร ฉันทศิริเวทย์. (2556). ประสบการณ์การฟื้นคืนได้ของครอบครัวที่มีบุตรเป็นออทิสติก. วิทยานิพนธ์ปริญญา ศิลปศาสตรมหาบัณฑิต สาขาวิชาจิตวิทยาการปรึกษา คณะจิตวิทยา จุฬาลงกรณ์มหาวิทยาลัย.
ศนิ พงษ์สุระนันทน์. (2558). ประสบการณ์ทางจิตใจของมารดาที่บุตรได้รับการวินิจฉัยภาวะดาวน์ก่อนคลอด. วิทยานิพนธ์ ปริญญามหาบัณฑิต สาขาวิชาจิตวิทยาการปรึกษา คณะจิตวิทยา จุฬาลงกรณ์มหาวิทยาลัย.
Ansari, N. J. R., Dhongade, R. K., Lad, P. S., Borade, A., Suvarna, Y. G., Yadav, V., Kulkarni, R. (2016). Study of parental perceptions on health & social needs of children with neuro-developmental disability and it’s impact on the family. Journal of Clinical and Diagnostic Research, 10(12), SC16-SC20.
Canbulat, N., Demirgöz, M., & Çoplu, M. (2014). Emotional reactions of mothers who have babies who are diagnosed with Down Syndrome. International Journal of Nursing Knowledge, 25(3), 147-153.
Collins, T., & Coughlan, B. (2016). Experiences of mothers in Romania after hearing from medical professionals that their child has a disability. Journal of Policy and Practice in Intellectual Disabilities, 13(1), 4–14.
Corrigan, P. W., & Watson, A. C. (2002). The paradox of self-stigma and mental illness. Clinical Psychology Science and Practice, 9, 35-53.
Dillon-Wallace, J. A., McDonagh, S. H., & Fordham, L. A. (2014). How stable is the well-being of Australian mothers who care for young children with special health care needs? Journal of Child and Family Studies, 23(7), 1215–1226.
Fareo, D. O. (2015). Counselling intervention and support programmes for families of children with special educational needs. Journal of Education and Practice, 6(10), 103-109.
Fernández-Alcántara, M., García-Caro, M. P., Pérez-Marfil, M. N., Hueso-Montoro, C., Laynez-Rubio, C., & Cruz-Quintana, F. (2016). Feeling of loss and grief in parents of children diagnosed with autism spectrum disorder (ASD). Research in Developmental Disabilities, 55, 312-321.
Graungaard, A. H., & Skov, L. (2006). Why do we need a diagnosis? A qualitative study of parents’ experiences, coping and needs, when the newborn child is severely disabled. Child: Care, Health and Development, 33(3), 296–307.
Green, S. E. (2007). "We’re tired, not sad": Benefits and burdens of mothering a child with a disability. Social Science and Medicine, 64, 150–163.
Koydemir-Özden, S., & Tosun, Ü. (2010). A qualitative approach to understanding Turkish mothers of children with autism: Implications for counselling. Australian Journal of Guidance and Counselling, 20(1), 55–68.
Kübler-Ross, E., & Kessler, D. A. (2007). On grief and grieving: Finding the meaning of grief through the five stages of loss. NY: Scribner.
Lazarus, R. S., & Folkman, S. (1984). Stress, appraisal, and coping. NY: Springer.
Reichman, N. E., Corman, H., & Noonan, K. (2008). Impact of child disability on the family. Maternal and Child Health Journal, 12(6), 679-683.
Watson, S. L., Hayes, S. A., & Radford-Paz, E. (2011). “Diagnose me please!”: A review of research about the journey and initial impact of parents seeking a diagnosis of developmental disability for their child. In R. M., H. (Ed.), International review of research in developmental disabilities (Vol. 41, pp. 31-71). San Diego, CA: Elsevier Academic Press.