Citations (35)
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Anne-Marie Callus, Isabel Bonello, Charmaine Mifsud & Rosanne Fenech. (2019) Overprotection in the lives of people with intellectual disability in Malta: knowing what is control and what is enabling support. Disability & Society 34:3, pages 345-367.
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Anna Dunér & Elisabeth Olin. (2018) Personal assistance from family members as an unwanted situation, an optimal solution or an additional good? The Swedish example. Disability & Society 33:1, pages 1-19.
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Heléne von Granitz, Ieva Reine, Karin Sonnander & Ulrika Winblad. (2017) Do personal assistance activities promote participation for persons with disabilities in Sweden?. Disability and Rehabilitation 39:24, pages 2512-2521.
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Elisabeth Olin. (2017) The clinical gaze – ascribed gender(ed) identities in a mental health service context. Scandinavian Journal of Disability Research 19:1, pages 45-55.
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Elisabeth Olin & Anna Dunér. (2016) A matter of love and labour? Parents working as personal assistants for their adult disabled children. Nordic Social Work Research 6:1, pages 38-52.
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Kamilla Peuravaara. (2015) Reflections on collaborative research: to what extent and on whose terms?. Scandinavian Journal of Disability Research 17:3, pages 272-283.
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Roy I. Brown, Virginie Cobigo & Whitney D. Taylor. (2015) Quality of life and social inclusion across the lifespan: challenges and recommendations. International Journal of Developmental Disabilities 61:2, pages 93-100.
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Julia Bahner. (2013) The power of discretion and the discretion of power: personal assistants and sexual facilitation in disability services. Vulnerable Groups & Inclusion 4:1.
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Dominique Van de Velde, Piet Bracke, Geert Van Hove, Staffan Josephsson, Ignaas Devisch & Guy Vanderstraeten. (2012) The illusion and the paradox of being autonomous, experiences from persons with spinal cord injury in their transition period from hospital to home. Disability and Rehabilitation 34:6, pages 491-502.
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Karen Christensen. (2009) In(ter)dependent lives. Scandinavian Journal of Disability Research 11:2, pages 117-130.
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Lars Grönvik. (2009) Defining disability: effects of disability concepts on research outcomes. International Journal of Social Research Methodology 12:1, pages 1-18.
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Borgunn Ytterhus, Christian Wendelborg & Hege Lundeby. (2008) Managing turning points and transitions in childhood and parenthood – insights from families with disabled children in Norway. Disability & Society 23:6, pages 625-636.
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Elizabeth Kendall & Anne Rogers. (2007) Extinguishing the social?: state sponsored self‐care policy and the Chronic Disease Self‐management Programme. Disability & Society 22:2, pages 129-143.
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Anneli Nyman & Maria Larsson Lund. (2007) Influences of the social environment on engagement in occupations: The experience of persons with rheumatoid arthritis. Scandinavian Journal of Occupational Therapy 14:1, pages 63-72.
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Kathryn Ellis. (2005) Disability rights in practice: the relationship between human rights and social rights in contemporary social care. Disability & Society 20:7, pages 691-704.
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Vera Chouinard & Valorie A. Crooks
. (2005) ‘Because they have all the power and I have none’: state restructuring of income and employment supports and disabled women's lives in Ontario, Canada. Disability & Society 20:1, pages 19-32.
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INGRID HELGØY, BODIL RAVNEBERG & PER SOLVANG. (2003) Service Provision for an Independent Life. Disability & Society 18:4, pages 471-487.
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Karin Barron. (2002) Who am I? Women with learning difficulties (re)constructing their self‐identity. Scandinavian Journal of Disability Research 4:1, pages 58-79.
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Articles from other publishers (17)
Õie Umb Carlsson & Päivi Adolfsson. (2022) No ordinary adult life: Living conditions from the perspective of adults with intellectual disabilities. Journal of Intellectual Disabilities 27:4, pages 944-963.
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P Femenias, E Punzi & K Granath. (2022) The voices of vulnerable tenants in renovation. IOP Conference Series: Earth and Environmental Science 1078:1, pages 012083.
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Susana Delgado Catalán, Andrés Arias Astray & Eva Sotomayor Morales. (2022) Jóvenes con discapacidad intelectual en la universidad: entre la sobreprotección y la autodeterminación. Siglo Cero Revista Española sobre Discapacidad Intelectual 53:2, pages 145-165.
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Kristina Eivergård, Ingela Enmarker, Mona Livholts, Lena Aléx & Ove Hellzén. (2021) Disciplined into good conduct: Gender constructions of users in a municipal psychiatric context in Sweden. Journal of Clinical Nursing 30:15-16, pages 2258-2269.
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Elisabeth Olin & Anna Dunér. (2019) Careful assistance? Personal assistance within the family as hybridization of modern welfare policy and traditional family care. Alter 13:2, pages 113-125.
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ANNA DUNÉR, PÄR BJÄLKEBRING & BOO JOHANSSON. (2017) Merely a rhetorical promise? Older users' opportunities for choice and control in Swedish individualised home care services. Ageing and Society 39:4, pages 771-794.
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Andrew D. Wormald, Philip McCallion & Mary McCarron. (2019) The antecedents of loneliness in older people with an intellectual disability. Research in Developmental Disabilities 85, pages 116-130.
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Õie Umb Carlsson & Päivi Adolfsson. (2018) Quality of Life Is to Experience Adult Social Status. Journal of Policy and Practice in Intellectual Disabilities 15:4, pages 272-283.
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Casey Fulford & Virginie Cobigo. (2018) Friendships and Intimate Relationships among People with Intellectual Disabilities: A Thematic Synthesis. Journal of Applied Research in Intellectual Disabilities 31:1, pages e18-e35.
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Virginie CobigoRoy BrownYves LachapelleRosemary LysaghtLynn MartinHélène Ouellette-KuntzHeather Stuart & Casey Fulford. (2016) Social Inclusion: A Proposed Framework to Inform Policy and Service Outcomes Evaluation. Inclusion 4:4, pages 226-238.
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Jessica Arvidsson, Stephen Widén, Carin Staland-Nyman & Magnus Tideman. (2016) Post-School Destination-A Study of Women and Men With Intellectual Disability and the Gender-Segregated Swedish Labor Market. Journal of Policy and Practice in Intellectual Disabilities 13:3, pages 217-226.
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Jami Petner-Arrey & Susan R. Copeland. (2014) ‘You have to care.’ perceptions of promoting autonomy in support settings for adults with intellectual disability. British Journal of Learning Disabilities, pages n/a-n/a.
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Julia Bahner. (2012) Legal Rights or Simply Wishes? The Struggle for Sexual Recognition of People with Physical Disabilities Using Personal Assistance in Sweden. Sexuality and Disability 30:3, pages 337-356.
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Antika Sawadsri. (2012) ‘Do I Look Like an Object?’ A Quest of Exploring Person – Place Relationship of Disabling. Procedia - Social and Behavioral Sciences 50, pages 418-428.
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Nicky Stanley & Jill Manthorpe. (2009) Small Acts of Care: Exploring the Potential Impact of the Mental Capacity Act 2005 on Day-to-Day Support. Social Policy and Society 8:1, pages 37-48.
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Peter Williams, Karen Bunning & Helen Kennedy. (2007) ICTs and learning disability: multidisciplinary perspectives on Project @pple. Aslib Proceedings 59:1, pages 97-112.
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R.N. Lisa Skär. (2003) Peer and adult relationships of adolescents with disabilities. Journal of Adolescence 26:6, pages 635-649.
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