Suchergebnisse

Recent policies and government initiatives in many Western countries have strengthened the expectation that young disabled people have the right to be involved in decisions affecting their futures. Sonali Shah uses a comparative study of young disabled students within mainstream and special education to determine the influence these recent policies will have on the realization of their long term goals.

This article explores the methodological opportunities and challenges I encountered, as a disabled researcher, while doing research on the educational experiences and career aspirations of a group of young disabled people, still in full-time mainstream or special education. While the key barriers facing disabled researchers are recognized, they are challenged in this article and rather seen as opportunities. Further, they are diluted by the ontological privileges that are at the disposal of the disabled researcher, including the use of empathy, which provides a way of understanding other people's experiences in the context of both similarities and differences between the researcher and the researched. This article focuses on three methods of qualitative enquiry – namely, classroom observation, forum theatre workshops and individual interviews. It explores how they were employed to ensure the voices of young disabled people were captured by the research process in ways that reflect their views and recognize them as active social agents who are able to make decisions about their own futures.

Mass vaccination programmes mean that poliomyelitis is almost a forgotten memory in the Global North. But in reality its effects continue as many people who contracted paralytic polio in childhood may develop functional deterioration (Post-Polio Syndrome or PPS) in later adulthood; mass migration and escape from violence means that it is also re-emerging in contemporary societies. Thus it is crucial for different audiences to have opportunities to engage with, and understand the life histories of polio survivors and their personal experiences of disease and disability across biographical and historical time. This article discusses the process of using recorded delivery verbatim techniques, with disabled and non-disabled actors, to translate ethnographic research about social history of polio into a creative accessible medium for new generation audiences to learn about the hidden, often contested, histories of disability and disease that may collide with professional, medical and public discourse. Our contention is that ethnodrama can give a voice to the voiceless, and enable them to contribute to the production of new knowledge, health interventions and policy instruments that affect their lives.

The impact of childhood on success in adulthood has been much researched. This paper discusses how parental expectations, social class, childhood experiences and gender influenced the career success of disabled people. For respondents with congenital disabilities, disability was perceived as a primary factor influencing parental expectations, but those with acquired disabilities felt it was gender. Social class played a significant part in all respondents' childhood socialisation and parental expectations. Some experienced deprivation and trauma as children, encouraging them to master future life events. The findings highlight the importance of childhood socialisation to the career success of disabled people.