Chronic sorrow in mothers of adult children with cerebral palsy: an exploratory study

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dc.contributor.author Masterson, Marilyn K.
dc.date.accessioned 2010-05-06T02:44:03Z
dc.date.available 2010-05-06T02:44:03Z
dc.date.issued 2010-05-06T02:44:03Z
dc.identifier.uri http://hdl.handle.net/2097/3906
dc.description.abstract Chronic sorrow has been defined as a permanent and reoccurring experience of pervasive sadness and loss which underlies the life experience and which recurs over time for the parent of a child with developmental, medical, or behavior issues that prevent him from participating in society in a way previously anticipated by parents. The functional question asked of the mothers was: “Some parents have described a sadness that can occur when they think about their child with a disability. Parents can believe they are functioning well, but have times where they feel the loss for their child.” To date, little research has targeted chronic sorrow among parents of adult children who have a disability. Neither is it known how chronic sorrow exists and has changed over the years since the initial diagnosis for this specific sample. This exploratory, qualitative study focused specifically on mothers of adult children with cerebral palsy. Snowball sampling was utilized to recruit six mothers in northeastern Kansas who were primary caregivers to their adult children with CP. Data were gathered with face-to-face mixed self-report surveys, including the Kendall Questionnaire on Chronic Sorrow; two surveys which assessed demographic, potential complications from cerebral palsy, and available resources; and a standard schedule open-ended interview targeting: personal experiences of chronic sorrow, chronic sorrow triggers (developmental milestones), and losses (including support, roles and responsibilities, and quality of life). Two-coder analyses of interview responses were conducted within cases and comparisons were made across cases. Common themes identified in the narratives included sense of isolation, fear for the future, frustration, loss of hope, exhaustion, sadness, financial challenges, guilt, and anger. For example, isolation was another theme that changed over time depending on if the mothers were providing full-time care. Also, fear for the future was a universal theme when the children were much younger, but it changed into loss of hope for some of the mothers when the child was the age of an adult. The relevance of the findings was discussed, with particular focus being the subjective meanings of chronic sorrow for this sample. Recommendations for advancing research, practice, and policy are offered. en_US
dc.language.iso en_US en_US
dc.publisher Kansas State University en
dc.subject Chronic sorrow en_US
dc.subject Cerebral palsy en_US
dc.subject Mothers en_US
dc.subject Adult children en_US
dc.subject Loss en_US
dc.title Chronic sorrow in mothers of adult children with cerebral palsy: an exploratory study en_US
dc.type Dissertation en_US
dc.description.degree Doctor of Philosophy en_US
dc.description.level Doctoral en_US
dc.description.department Department of Family Studies and Human Services en_US
dc.description.advisor Rick J. Scheidt en_US
dc.subject.umi Health Sciences, Nursing (0569) en_US
dc.subject.umi Psychology, Developmental (0620) en_US
dc.subject.umi Sociology, Individual and Family Studies (0628) en_US
dc.date.published 2010 en_US
dc.date.graduationmonth May en_US


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