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Experiences among children and adolescents of living with spina bifida and their visions of the future
Linköpings universitet, Institutionen för medicin och hälsa. Region Östergötland, Närsjukvården i östra Östergötland, Habilitering Norrköping. Linköpings universitet, Medicinska fakulteten.
Linköpings universitet, Institutionen för medicin och hälsa, Avdelningen för samhällsmedicin. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Närsjukvården i västra Östergötland, Forsknings- och utvecklingsenheten för Närsjukvården i Östergötland.
Linköpings universitet, Institutionen för klinisk och experimentell medicin, Avdelningen för neuro- och inflammationsvetenskap. Linköpings universitet, Medicinska fakulteten. Region Östergötland, Närsjukvården i västra Östergötland, Forsknings- och utvecklingsenheten för Närsjukvården i Östergötland. Region Östergötland, Hjärt- och Medicincentrum, Hudkliniken i Östergötland.ORCID-id: 0000-0001-8336-9767
Linköpings universitet, Institutionen för teknik och naturvetenskap, Medie- och Informationsteknik. Linköpings universitet, Tekniska högskolan.ORCID-id: 0000-0003-1032-2145
2017 (engelsk)Inngår i: Disability and Rehabilitation, ISSN 0963-8288, E-ISSN 1464-5165, Vol. 39, nr 3, s. 261-271Artikkel i tidsskrift (Fagfellevurdert) Published
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Abstract [en]

Purpose: Transitioning to independence may be problematic for persons with spina bifida (SB). Experiences of young persons with SB may provide insights into this group's needs for support. Therefore, the aim of this study was to investigate children'€™s and adolescents' experiences of living with SB, their social and emotional adjustment, and their thoughts about becoming independent adults. Method: Semi-structured interviews were conducted with young persons with SB (N = 8, age range 10 - 17 years). Social and emotional problems were assessed using Beck Youth Inventories. The interview transcripts were analyzed using qualitative content analysis. Results: Three main themes were found: being a person with SB; everyday living as a person with SB; and preparing for life as an adult with SB. Indications of emotional and social problems were most prominent among participants with milder physical disability. Conclusions: The findings indicate that young persons with SB may overestimate their independence. Other potentially problematic areas were lack of motivation, planning and preparedness for becoming independent. Research on transition to independence in this group should consider assistance at an early age in planning and executing strategies for independence. In addition, the potentially difficult situation for young persons with mild SB should be investigated further.

sted, utgiver, år, opplag, sider
Taylor & Francis, 2017. Vol. 39, nr 3, s. 261-271
Emneord [en]
spina bifida, independence, qualitative content analysis, children, adolescents, adjustment
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Identifikatorer
URN: urn:nbn:se:liu:diva-125792DOI: 10.3109/09638288.2016.1146355ISI: 000392480400006PubMedID: 26939640Scopus ID: 2-s2.0-84961209745OAI: oai:DiVA.org:liu-125792DiVA, id: diva2:909055
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Funding agencies: Swedish Inheritance Fund, County Council of Ostergotland; Research Fund of the Linkoping University Hospital

Tilgjengelig fra: 2016-03-04 Laget: 2016-03-04 Sist oppdatert: 2025-04-11bibliografisk kontrollert

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Wilhelmsson, SusanFalk, LarsHöst, Gunnar E.

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