Abstract
Through the creation of safe spaces to explore and challenge negative, dominant views of disabled children and young people, this co-written paper presents unique insight into the meaning and impact of medical lenses and deficit models of disability upon disabled young peoples lives and its resonance within dominant debates in medical sociology, disability studies and childhood studies. Such bodies of work have so far largely overlooked the experiences and positioning of disabled children and young people and have rarely involved them in the development, or discussion, of theory. Drawing on empirical data, and through a series of creative, reflective workshops with a UK-based disabled young researchers’ collective (RIP:STARS), this paper discusses areas of theoretical importance identified by the disabled young researchers collective; the validation of their lives, negotiation of their identity and acceptance in society. The implications, and possibilities, of platforming disabled children and young people’s voices in theoretical debates are discussed, and are achieved through the yielding of privileged academic voice, and the development of a symbiotic, genuine partnership with disabled young people recognising them as experts in their own lives.
| Original language | English |
|---|---|
| Pages (from-to) | 1376-1392 |
| Number of pages | 17 |
| Journal | Sociology of Health & Illness |
| Volume | 46 |
| Issue number | 6 |
| Early online date | 21 Jun 2023 |
| DOIs | |
| Publication status | Published - 1 Jul 2023 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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SDG 10 Reduced Inequalities
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SDG 16 Peace, Justice and Strong Institutions
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SDG 17 Partnerships for the Goals
Keywords
- disability
- youth
- theory
- voice
- disabled young researchers
- children's rights
- youth activism
- co-production
- illness
- social justice
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