The aim of this study was to explore how women who were diagnosed with autism spectrum disorder as adults described their existence before and after the diagnosis. The study was conducted by analysing four women’s autobiographical texts. The texts deal with their experiences growing up without awareness of their disability, how they got diagnosed as adults and how the diagnosis impacted their lives. The study used a qualitative approach and a theoretical framework consisting of social constructionism and crip-theory. Through a thematic analysis of these women’s stories this study found that women who are diagnosed late in life experience challenges such as mental health problems, feelings of exclusion and confusion around one’s own identity. Findings also highlight the importance of early diagnosis to prevent previous mentioned challenges. Further research should be made to explore how new national guidelines for support and treatment impact individuals with autism spectrum disorder.
| Identifer | oai:union.ndltd.org:UPSALLA1/oai:DiVA.org:mau-65067 |
| Date | January 2024 |
| Creators | Schultz, Emelie |
| Publisher | Malmö universitet, Institutionen för socialt arbete (SA) |
| Source Sets | DiVA Archive at Upsalla University |
| Language | Swedish |
| Detected Language | English |
| Type | Student thesis, info:eu-repo/semantics/bachelorThesis, text |
| Format | application/pdf |
| Rights | info:eu-repo/semantics/openAccess |
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