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Research with d/Deaf people

Abstract
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This paper explores the diverse experiences and identities of d/Deaf individuals, examining how deafness is understood in both physiological and cultural contexts. It highlights the need for researchers to pay close attention to the heterogeneity within the d/Deaf community, the importance of language and communication preferences in research methodologies, and ethical considerations unique to this population. Innovations in technology are noted as a means to enhance participation and representation of d/Deaf people in research.

Key takeaways

  • Each has a different relationship with 'not hearing' and a different understanding of what it is to 'be deaf'.
  • Consider for a moment the culturally Deaf social work professional (first language British Sign Language) who demands the most sophisticated digital hearing aids to assist in accessing the casual conversation of their hearing office colleagues, but who in formal meetings would prefer to make their point in their own first language and would want an interpreter.
  • For 'deaf' people the transition to hearing impairment is one that is often resisted and thus hearing aids rejected as visible markers of such transition (Jones et al. 1987).
  • However, for those who might have been deaf in childhood the crucial variable is the extent to which childhood deafness interfered with their acquisition of a spoken language.
  • For example, a hearing researcher, however experienced and skilled, has not had the personal experience of growing up as a deaf child.