Rights to research: utilising the Convention on the Rights of Persons with Disabilities as an inclusive participatory action research tool

2013 ◽  
Vol 28 (5) ◽  
pp. 616-630 ◽  
Author(s):  
Janice Ollerton ◽  
Debbie Horsfall
2021 ◽  
pp. 104420732110554
Author(s):  
Benoît Eyraud ◽  
Iuliia Taran

In this article, we present findings from a participatory action-research program in France on the exercise of human rights and supported and substitute decision-making, inspired by the United Nations Convention on the Rights of Persons with Disabilities (“CRPD”). Bringing together persons with the lived experience of disability, academics, and health and social care and support professionals, the project used the method of “experience-based construction of public problem” to transform experience into collective expertise. This enabled the exploration of support that people in vulnerable situations, whose capacity to exercise their human rights has weakened, need to make decisions in their lives and participate meaningfully in public debate. The relationship between the awareness of rights and exercise of rights is discussed. We argue for the need to balance out the positions of different contributors in participatory action research, in a reasoned manner, by recognizing the scientific and citizen-based participation of all partners.


2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. 360-360
Author(s):  
Deborah O'Connor

Abstract Article 12 of the United Nations Convention of Rights of Persons with Disabilities (CRPD) affirms the rights of persons with physical and mental disabilities to be treated as equal, and deserving of state support to realize their full human potential. This focus on a ‘positive’ right to support (as opposed to the ‘negative’ right to non-interference) has established an important set of expectations around societal responses to people living with dementia(PLWD). This presentation examines the contributions of a rights-based approach to build community with and for PLWD. Data is drawn from Participatory Action Research (PAR) and bi-weekly online action groups with N=10 PLWD in urban and rural British Columbia. Two thematic targets were identified. First, it is important to bring together PLWD in ways that create a sense of solidarity and inclusion. Second, fostering community requires addressing the stigma and discrimination which often leave PLWD feeling isolated, excluded, and marginalized.


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