ADVOCACY, INTERVENTION, AND COPING: A QUALITATIVE STUDY OF HIGH FUNCTIONING AUTISM FROM A MOTHER'S POINT OF VIEW.

Mothers' views of their experiences with their child with high functioning autism (HFA) have not been thoroughly investigated in previous research. Thirty mothers of children with high functioning autism participated in a semi-structured interview in the present qualitative study. The collected data...

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Publicado en:Journal of Ethnographic & Qualitative Research Vol. 15; no. 3; pp. 231 - 245
Autores principales: Rausch, John L., Pascoe, Alicia
Formato: Artículo
Publicado: Ethnographic & Qualitative Research, LLC Spring2021
Materias:
Acceso en línea:Ver este registro en EBSCOhost
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        atl: ADVOCACY, INTERVENTION, AND COPING: A QUALITATIVE STUDY OF HIGH FUNCTIONING AUTISM FROM A MOTHER'S POINT OF VIEW.
      aug:
        au:
          Rausch, John L.
          Pascoe, Alicia
        affil: John Carroll University
      su:
        Autistic children
        Psychological adaptation
        Social dynamics
        Autism
        Social interaction in children
        Social services
        Family relations
      sug:
        subj:
          Autistic children
          Psychological adaptation
          Social dynamics
          Autism
          Social interaction in children
          Social services
          Family relations
          Other Individual and Family Services
      ab: Mothers' views of their experiences with their child with high functioning autism (HFA) have not been thoroughly investigated in previous research. Thirty mothers of children with high functioning autism participated in a semi-structured interview in the present qualitative study. The collected data were generally coded into five broad categories: diagnosis, intervention, social dynamics, advocacy, and coping skills. Diagnosis of HFA typically was not made until ages nine to 13. The participants created individualized interventions that were reality and strengths-based. Social dynamics included both the child's social interactions with peers and the social dynamics within the family system. The participants related having to advocate for their children with HFA with school, social service, and medical professionals. The participating mothers also found their own techniques for coping. The present study provides insights into mothers' experiences with each of these areas that would be useful for professionals to understand when working with families who have children with HFA.
      pubtype: Academic Journal
      doctype: Article
      src: R
    language: English
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