Transitions and health trajectories of parents caring for children with intellectual disabilities

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Publication Type dissertation
School or College College of Nursing
Department Nursing
Author Eldredge, Alison Lee
Title Transitions and health trajectories of parents caring for children with intellectual disabilities
Date 2015-05
Description Little is known about transitions and lifetime health trajectories of parents caring for children with intellectual disabilities (ID). Parental health is important because of its far-reaching effects on parents themselves, their children, and society at large. The purpose of this qualitative study was to describe (1) how parents in mid- and later life (≥55 years of age) caring for children with mild to moderate ID narrate the transitions of this experience, and (2) parental perceptions of the influence of raising a child with ID on their health trajectories. Through a series of three in-depth, semistructured interviews, one of which included a lifeline illustration of their personal health trajectory, 6 couples and 6 additional mothers (n=18) shared their experiences raising children with ID and its relation to their life transitions overall. Parents narrated unique stories of resilience containing individual variations in both the content and prominence of the following challenges: (1) discovering, receiving, and accepting my child's limitations and diagnosis of ID, (2) caring for my child's health issues, (3) managing behavioral issues, (4) facilitating attainment of early developmental milestones, (5) ensuring a good education for my child, and (6) increasing my child's autonomy. In response to these challenges, parents initially took action to provide for their children. Over time, they learned to reflect over their experiences and utilize additional coping mechanisms for support. As parents adapted, they gained skills and learned lessons greatly enriching their lives. iv Parents could not link personal, physical health problems to their child's disability; however, they reported receiving benefits to their emotional, social, and spiritual health. Many parents initially experienced negative feelings, but over their lifespan, these feelings were replaced with increased love and gratitude for their child. Marriages and families became stronger as families worked together. Most parents found strength and/or meaning in their religious and spiritual practices. Based on the narratives of raising a child with ID, social actions can be undertaken to decrease risk factors and strengthen protective factors in order to maintain or improve parents' resilience and consequently their overall health. Early and continued professional and interpersonal support and resources are crucial.
Type Text
Publisher University of Utah
Subject MESH Intellectual Disability; Resilience, Psychological; Parents; Child; Parent-Child Relations; Adaptation, Psychological; Down Syndrome; Personal Autonomy; Social Support; Child Welfare; Self-Help Groups; Socioeconomic Factors; Healthcare Disparities; Quality of Life; Human Rights
Dissertation Institution University of Utah
Dissertation Name Doctor of Philosophy
Language eng
Relation is Version of Digital version of Transitions and Health Trajectories of Parents Caring for Children with Intellectual Disabilities
Rights Management Copyright © Alison Lee Eldredge 2015
Format Medium application/pdf
Format Extent 1,926,145 bytes
Source Original in Marriott Library Special Collections
ARK ark:/87278/s67d63gm
Setname ir_etd
ID 197349
Reference URL https://collections.lib.utah.edu/ark:/87278/s67d63gm
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