Abstract:Parental grief reactions have typically been examined in situations where parents have a child diagnosed with a major medical or mental health condition. This study used the grief and loss model as conceptualized by Kubler-Ross (1969), Lamb (1988, and Kubler-Ross and Kessler (2005) as a foundation in examining parental reactions when a child has been referred for special education services. The model was expanded to include definitions of the concepts as applied to a special education setting and incorporated … Show more
“…While the American School Counselor Association (2016) addresses the family's role in assisting their family member with a disability in receiving the appropriate modifications and adaptations necessary to meet the needs of the student to further their educational growth, there is limited attention to the family's role in assisting their family member with a disability in navigating higher education with their disability. In a K-12 school setting, families of individuals with disabilities are expected to be highly involved in their educational process as they cooperatively authorize accommodations or changes in the curriculum (Haley et al, 2013). Family involvement is the result of the individualized education plan, a process in which families serve as advocates for their family member with a disability to ensure that their family member with a disability receives the best, specialized education possible to meet their needs (Burke, 2013).…”
Section: Students With Disabilities In K-12 Settingsmentioning
Family counselors at times work with families in which a family member with a disability is transitioning into higher education settings. Frequently, these counselors are unaware of the federally protected rights of all students and they may not know how to access this information. This article explains the differences between laws for students with disabilities in K–12 school settings and the components of the Americans with Disabilities Act (ADA) and its subsequent ADA 2008 Amendments to inform family counselors on how to support clients and their families in the transition to higher education. In this article, the authors discuss the ADA and the ADA 2008 Amendments, which dramatically impacted the college experience of all students with disabilities. With record numbers of students with disabilities now attending college, counselors, as they advocate for families, should be aware of federal guidelines that require physical access to educational facilities, the use of universal design, electronic accessibility, and the provision of academic accommodations and modifications in college classrooms. Through family counselors’ awareness of these significant changes in the higher education experience, they can more fully assist families with students with disabilities who are transitioning from high school to higher education. This article describes each of these four facets of the ADA 2008 Amendments as well as the impact each major facet of the amendment has on the higher education landscape for students with disabilities.
“…While the American School Counselor Association (2016) addresses the family's role in assisting their family member with a disability in receiving the appropriate modifications and adaptations necessary to meet the needs of the student to further their educational growth, there is limited attention to the family's role in assisting their family member with a disability in navigating higher education with their disability. In a K-12 school setting, families of individuals with disabilities are expected to be highly involved in their educational process as they cooperatively authorize accommodations or changes in the curriculum (Haley et al, 2013). Family involvement is the result of the individualized education plan, a process in which families serve as advocates for their family member with a disability to ensure that their family member with a disability receives the best, specialized education possible to meet their needs (Burke, 2013).…”
Section: Students With Disabilities In K-12 Settingsmentioning
Family counselors at times work with families in which a family member with a disability is transitioning into higher education settings. Frequently, these counselors are unaware of the federally protected rights of all students and they may not know how to access this information. This article explains the differences between laws for students with disabilities in K–12 school settings and the components of the Americans with Disabilities Act (ADA) and its subsequent ADA 2008 Amendments to inform family counselors on how to support clients and their families in the transition to higher education. In this article, the authors discuss the ADA and the ADA 2008 Amendments, which dramatically impacted the college experience of all students with disabilities. With record numbers of students with disabilities now attending college, counselors, as they advocate for families, should be aware of federal guidelines that require physical access to educational facilities, the use of universal design, electronic accessibility, and the provision of academic accommodations and modifications in college classrooms. Through family counselors’ awareness of these significant changes in the higher education experience, they can more fully assist families with students with disabilities who are transitioning from high school to higher education. This article describes each of these four facets of the ADA 2008 Amendments as well as the impact each major facet of the amendment has on the higher education landscape for students with disabilities.
“…Turnbull, Turnbull, Erwin, and Soodak (2006) asserted that many parents of students with disabilities felt disempowered while working with educators. When parents perceive that their contributions are not valued, they develop an understandable sense of disenfranchisement (Haley et al, 2013).…”
Section: The Negative Impact Of Kübler-ross' Grief Model: the Disempowerment Of Parentsmentioning
confidence: 99%
“…This article asserts that the Haley et al (2013) article exemplifies the deficit model of disability in regard to how parental response to disability is framed. In light of the challenges associated with the grief lens, the Haley et al assumptions and conclusions deserve further examination.…”
Section: Revisiting Haley Et Al (2013)mentioning
confidence: 99%
“…For well over 40 years, the expectation among policy makers and school administrators in the United States and most Western nations has been that parents and professionals should work collaboratively so that students with disabilities obtain maximum benefit from their education (Knight, 2010). However, as Haley et al (2013) documented, too often parents have not had positive experiences while working with school professionals to develop and implement programs for their children (Fish, 2006; Hammond, Ingalls, & Trussell, 2008). Some researchers have reported that the underlying message that parents perceived from educators was that parental input was unwelcome if not actively discouraged (Turnbull & Turnbull, 1997).…”
Section: The Negative Impact Of Kübler-ross’ Grief Model: the Disempowerment Of Parentsmentioning
confidence: 99%
“…In a recent issue of Improving Schools , Haley, Hammond, Ingalls, and Marvin (2013) asserted that parents of students who had recently been diagnosed with disability and were entering into a special education program experienced a variety of responses that the authors associated with grief and the traditional stages of grief as outlined in the Model of Parental Response to Disability proposed by Kübler-Ross (1969). This article responds to the deficit model of disability by (a) addressing the viability and utility of the stage model of grief as it pertains to 21st century parents of children with disabilities and (b) presenting an emergent, empowering model of parental response to disability.…”
Educators in many Western nations have used the Kübler-Ross stage model of grief for five decades as a lens to explain parental response to disability. A recent article in Improving Schools, representing this deficit model, asserted that the grief lens is useful in understanding parent's response to learning that their child qualified for special education services. Implicit assumptions in such a perspective unintentionally undermine parent-educator relations. This article describes that phenomenon and notes an emerging 'transformational', empowering model of parental response to disability based on a social-ecological conceptualization of disability. Educators' intent on improving 21st century schools must confront belief perseverance regarding the grief lens and adopt a more empowering strength-based approach in order to effectively engage parents of students with disabilities in strong collaboration relationships.
Difficulty learning to read presents many struggles for children and their families, and evaluation of parental perspectives of the dyslexia assessment process within the United States represents an under-researched area. This study sought to investigate how parental perspectives change during their child's dyslexia assessment. Six hundred one parents of children experiencing reading difficulties provided both Likert scale and open-ended responses to an online survey regarding their experiences throughout the dyslexia assessment and diagnosis process. Participants' responses were analyzed through thematic coding, sentiment analysis, and regression analysis. Parent perspectives were largely positive but revealed three important areas for investigation: shift in parental perspectives and lifestyles, assessment timelines, and parental advocacy and support. The assessment timeline predicted parental satisfaction. Results indicate a desire for clarity in the assessment process and ongoing needs for advocacy, support, and intervention. Implications for educational assessments, parent/family support, and suggestions for future research are discussed.
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