A Qualitative Inquiry: Parental Approaches and Expectations, What Role Does Disability Play?

Persistent Link:
http://hdl.handle.net/10150/626168
Title:
A Qualitative Inquiry: Parental Approaches and Expectations, What Role Does Disability Play?
Author:
Ficchi, Gabrielle
Issue Date:
2017
Publisher:
The University of Arizona.
Rights:
Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
Abstract:
Parenting a child with a disability is a unique experience, and both parents and children need to find the most effective parenting strategies. The purpose of this qualitative study is to gain a better understanding of the experiences associated with raising a child who has a disability. Specifically, this study examines what factors parents feel influence them in making decisions about their child and the expectations they have for them. In addition, it assesses how parents perceive they have modified their childrearing approaches and expectations for their child with a disability. To collect qualitative data, the investigator used narrative inquiry. This methodology was appropriate as eliciting specific stories and examples from participants allowed the team to capture the authentic experience of each one. The primary investigator collected qualitative data through multiple interviews with parents who have children with disabilities. For purposes of this study, sampling methods were a mix between convenience and non-probability sampling. Parents included were those of children whose disability is primarily physical. The researcher conducted a semi-structured interview to examine the feelings, thought processes, challenges and overall life experience surrounding parenting a child who has a physical disability. Data was analyzed using a "constant comparative" method whereby the researcher constantly compares within the study the data being collected. Periodic review of the data, as well as summaries, helped identify trends warranting further analysis. Overall, the results of this study indicate that parents and families perceive that they have needs that are not being met, empowering them to make certain parenting decisions. Based upon these perceptions, it would appear that there is a need for change in the types of services and information parents are receiving. While medical support is necessary, parents are also expressing a need for more practical forms of assistance. This study explores several ways in which rehabilitation professionals might implement changes in order to accommodate these needs. Families whose children have disabilities expressed both a strong desire to provide the best possible care. What appears to be currently lacking is sufficient education and emotional support to channel their loving energy into setting higher expectations for their children, knowing how to effectively plan for and reach milestones, while being confident enough in their child’s abilities to afford them opportunities to take control of their own lives.
Type:
text; Electronic Dissertation
Degree Name:
Ph.D.
Degree Level:
doctoral
Degree Program:
Graduate College; Special Education & Rehabilitation
Degree Grantor:
University of Arizona
Advisor:
Shaw, Linda

Full metadata record

DC FieldValue Language
dc.language.isoen_USen
dc.titleA Qualitative Inquiry: Parental Approaches and Expectations, What Role Does Disability Play?en_US
dc.creatorFicchi, Gabrielleen
dc.contributor.authorFicchi, Gabrielleen
dc.date.issued2017-
dc.publisherThe University of Arizona.en
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en
dc.description.abstractParenting a child with a disability is a unique experience, and both parents and children need to find the most effective parenting strategies. The purpose of this qualitative study is to gain a better understanding of the experiences associated with raising a child who has a disability. Specifically, this study examines what factors parents feel influence them in making decisions about their child and the expectations they have for them. In addition, it assesses how parents perceive they have modified their childrearing approaches and expectations for their child with a disability. To collect qualitative data, the investigator used narrative inquiry. This methodology was appropriate as eliciting specific stories and examples from participants allowed the team to capture the authentic experience of each one. The primary investigator collected qualitative data through multiple interviews with parents who have children with disabilities. For purposes of this study, sampling methods were a mix between convenience and non-probability sampling. Parents included were those of children whose disability is primarily physical. The researcher conducted a semi-structured interview to examine the feelings, thought processes, challenges and overall life experience surrounding parenting a child who has a physical disability. Data was analyzed using a "constant comparative" method whereby the researcher constantly compares within the study the data being collected. Periodic review of the data, as well as summaries, helped identify trends warranting further analysis. Overall, the results of this study indicate that parents and families perceive that they have needs that are not being met, empowering them to make certain parenting decisions. Based upon these perceptions, it would appear that there is a need for change in the types of services and information parents are receiving. While medical support is necessary, parents are also expressing a need for more practical forms of assistance. This study explores several ways in which rehabilitation professionals might implement changes in order to accommodate these needs. Families whose children have disabilities expressed both a strong desire to provide the best possible care. What appears to be currently lacking is sufficient education and emotional support to channel their loving energy into setting higher expectations for their children, knowing how to effectively plan for and reach milestones, while being confident enough in their child’s abilities to afford them opportunities to take control of their own lives.en
dc.typetexten
dc.typeElectronic Dissertationen
thesis.degree.namePh.D.en
thesis.degree.leveldoctoralen
thesis.degree.disciplineGraduate Collegeen
thesis.degree.disciplineSpecial Education & Rehabilitationen
thesis.degree.grantorUniversity of Arizonaen
dc.contributor.advisorShaw, Lindaen
dc.contributor.committeememberShaw, Lindaen
dc.contributor.committeememberHartley, Michaelen
dc.contributor.committeememberKroeger, Sueen
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