The Right to Science: Centering People With Intellectual Disability in the Process and Outcomes of Science

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Abstract

The right to science has been identified in multiple human rights treaties; however, there has not been a clear framework for how governments or research organizations can advance this right particularly ensuring equitable engagement of people with intellectual disability (ID) in the process of scientific research. Although the feasibility and impacts of engaging people with ID in the process of science have been repeatedly demonstrated there remain systemic barriers including ableism, racism, and other systems of oppression that sustain inequities. Researchers in the ID field must take steps to dismantle systemic barriers and advance participatory approaches that advance equity in the process and outcomes of science.

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Shogren, K. A. (2023). The Right to Science: Centering People With Intellectual Disability in the Process and Outcomes of Science. Intellectual and Developmental Disabilities, 60(2), 172–177. https://doi.org/10.1352/1934-9556-61.2.172

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