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Full-Text Articles in Social Work
The Experiences Of Huntington’S Disease Caregivers, Alisa Kanuit
The Experiences Of Huntington’S Disease Caregivers, Alisa Kanuit
Master of Social Work Clinical Research Papers
Huntington’s Disease (HD) is a genetic, inherited, and terminal neurological disorder that affects both physical and mental capacities. The most recent estimates state that 1 in every 10,000 Americans has HD and more than 250,000 are at risk of inheriting the disease from a parent (Huntington’s Disease Society of America, 2013). Caregivers can be defined as informal or formal. Informal caregivers are typically family members such as spouses, children, or siblings. Formal caregivers are paid, professional caregivers. Family members often become caregivers for diagnosed individuals, however, the need for formal and paid care increases as the disease continues to progress. …
Caregivers’ Perceptions Of Day Treatment Programs, Julie Lochen
Caregivers’ Perceptions Of Day Treatment Programs, Julie Lochen
Master of Social Work Clinical Research Papers
This paper addresses the mental health concerns of millions of children across the United States; especially those with diagnosis of Emotional and Behavioral Disorders. This researcher used a qualitative research design to obtain the perceptions of caregivers who have children placed in day treatment programs. This researcher used an exploratory design with action research theory. Action research theory was used in the hopes that clinicians would empower clients, caregivers, and families. The researcher used an open-ended interview technique to collect data through a qualitative questionnaire with participants, lasting about 15 minutes. The questions that were asked pertained to the perceptions …
The Experiences Of Latino Parents As They Navigate Care For A Child With Autism, Emily Tibbetts
The Experiences Of Latino Parents As They Navigate Care For A Child With Autism, Emily Tibbetts
Master of Social Work Clinical Research Papers
This qualitative study explored the experiences of Latino caregivers as they navigate care for a child with autism spectrum disorder (ASD). Six caregivers participated in a semi-standardized interview containing 14 questions. The data obtained was analyzed using a phenomenological approach to find common themes in the participants’ experiences. Findings were organized into two broad themes and sub-themes of positive experiences with service access and delivery and negative experiences with service access and delivery. The sub-themes of positive experiences were as follows: communication, support systems, collaboration, education, and luck. The sub-themes of negative experiences were language access and interpretation, lack of …