Abstract

Article 19 of the UN Convention on the Rights of Persons with Disabilities requires states to ensure that disabled people can choose where and with whom they live with access to a range of services including personal assistance. Based on qualitative research of the implementation of Article 19 in Nordic countries, this paper focuses on Sweden, which was at the forefront of implementing personal assistance law and policy and has been the inspiration for many European countries. Instead of strengthening access to personal assistance, this study found that since the Swedish government ratified the Convention in 2008, there has been an increase in the numbers of people losing state-funded personal assistance and an increase in rejected applications. This paper examines the reasons for the deterioration of eligibility criteria for accessing personal assistance in Sweden. The findings shed light on how legal and administrative interpretations of “basic needs” are shifting from a social to a medical understanding. They also highlight a shift from collaborative policy making towards conflict, where courts have become the battleground for defining eligibility criteria. Drawing on the findings, we ask if Sweden is violating its obligations under the Convention.

Highlights

  • The United Nations Convention on the Rights of Persons with Disabilities1 opened for signatures in March 2007 and entered into force in May 2008

  • Sweden has been at the forefront of advocating for and developing wide ranging rights to personal assistance in Europe since the 1980s and has served as an inspiration to other countries

  • Instead we found that since Sweden ratified the CRPD in 2008 many disabled people have lost their personal assistance at a state-level or had their first application rejected

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Summary

Introduction

The United Nations Convention on the Rights of Persons with Disabilities opened for signatures in March 2007 and entered into force in May 2008. Article 19, in particular, “expresses the paradigm shift by outlining a series of tangible obligations to achieve independent living (something assumed for most people) and inclusion in the community” Under the heading “Living independently and being included in the community” it requires states to ensure that “persons with disabilities have access to a range of in-home, residential and other community support services including personal assistance necessary to support living and inclusion in the community”. The paradigm shift requires the involvement of disabled people’s organizations (DPOs) [3]. To comply with Articles 33.3 and 4.3, states need to involve

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