Benefit-finding among young adults with spina bifida

Author:

Kritikos Tessa K1ORCID,Stiles-Shields Colleen2,Shapiro Jenna B3,Holmbeck Grayson N1

Affiliation:

1. Loyola University Chicago, Chicago, IL, USA

2. Rush University Medical Center, Chicago, IL, USA

3. Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL, USA

Abstract

The purpose of the current study was to examine benefit-finding in a sample of young adults with SB and assess relationships between demographic and medical variables and benefit-finding. Young adults with SB ( N = 329), ranging in age from 18 to 30 ( M = 23.44 ± 2.93), completed the Benefit-Finding Scale (BFS), a 17-item self-report questionnaire, and reported on demographic and medical information related to their SB diagnosis. Participants endorsed a range of benefits associated with living with SB. The most frequently endorsed benefits were related to personal strengths, interpersonal relationships, and life philosophy. Younger age, majority race, higher education level, and employment were significantly associated with higher BFS scores. Young adults with SB report benefits associated with their chronic condition. Future research should examine these benefits in relation to psychosocial outcomes.

Funder

National Institute of Nursing Research and the Office of Behavioral and Social Sciences Research

National Institute of Child Health and Human Development

March of Dimes Birth Defects Foundation

Publisher

SAGE Publications

Subject

Applied Psychology

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