Citations (46)
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Elizabeth Price, Liz Walker & Sara Booth. (2020) Feeling the benefit? Fluctuating illness and the world of welfare. Disability & Society 35:8, pages 1315-1336.
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Maria Berghs, Karl Atkin, Hilary Graham, Chris Hatton & Carol Thomas. (2017) Public health, research and rights: the perspectives of deliberation panels with politically and socially active disabled people. Disability & Society 32:7, pages 945-965.
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Heather Mack & Ian Paylor. (2017) The inclusion of people with hepatitis C within disability studies. Scandinavian Journal of Disability Research 19:1, pages 18-33.
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Anna Alanko & Sami Outinen. (2016) Dualising activation. Responses to unemployment and mental health-related disability retirement in Finland at the turn of the millennium. European Societies 18:5, pages 417-437.
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Kayleigh Garthwaite, Clare Bambra & Jon Warren. (2013) ‘The unwilling and the unwell’? Exploring stakeholders’ perceptions of working with long term sickness benefits recipients. Disability & Society 28:8, pages 1104-1117.
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Ruth Lewis, Lynn Dobbs & Paul Biddle. (2013) ‘If this wasn’t here I probably wouldn’t be’: disabled workers’ views of employment support. Disability & Society 28:8, pages 1089-1103.
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Chris Grover & Linda Piggott. (2013) Employment and Support Allowance: capability, personalization and disabled people in the UK. Scandinavian Journal of Disability Research 15:2, pages 170-184.
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Kayleigh Garthwaite. (2011) ‘The language of shirkers and scroungers?’ Talking about illness, disability and coalition welfare reform. Disability & Society 26:3, pages 369-372.
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Rossio Motta-Ochoa, Natalia Incio-Serra, Hélène Poliquin, Sue-Ann MacDonald, Christophe Huỳnh, Philippe-Benoit Côté, Jean-Sébastien Fallu & Jorge Flores-Aranda. (2022) “A place to be safe, feel at home and get better”: including the experiential knowledge of potential users in the design of the first wet service in Montreal, Canada. Harm Reduction Journal 19:1.
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Jennifer Remnant. (2021) Managing cancer in contemporary workforces: how employees with cancer and line managers negotiate post-diagnosis support in the workplace. Employee Relations: The International Journal 44:1, pages 229-243.
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김기태 & Seung-yoon Sophia Lee. (2018) Comparative Analysis of Sickness Benefits Abroad and Proposal for Its Introduction in Korea. Social Welfare Policy 45:1, pages 148-179.
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Aimee Grant. (2017) “I Don’t Want You Sitting Next to Me”. International Journal of Qualitative Methods 16:1, pages 160940691771239.
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Suzanne Moffatt & Emma Noble. (2015) Work or welfare after cancer? Explorations of identity and stigma. Sociology of Health & Illness 37:8, pages 1191-1205.
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Margrit Shildrick. (2015) Living On; Not Getting Better. Feminist Review 111:1, pages 10-24.
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Kayleigh Garthwaite. (2015) Becoming incapacitated? Long-term sickness benefit recipients and the construction of stigma and identity narratives. Sociology of Health & Illness 37:1, pages 1-13.
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