References
- Amaze 2013. Parent and Carer Survey. Amaze, Brighton. http://amazebrighton.org.uk/resources/publications/fact-sheets/
- Atkinson, Sarah. 2013. “Beyond Components of Wellbeing: The Effects of Relational and Situated Assemblage.” Topoi 32 (2):137–44. doi:https://doi.org/10.1007/s11245-013-9164-0.
- Baker-Ericzén, Mary J., Melissa M. Jenkins, and Lauren Brookman-Frazee. 2010. “Clinician and Parent Perspectives on Parent and Family Contextual Factors That Impact Community Mental Health Services for Children with Behavior Problems.” Child & Youth Care Forum 39 (6):397–419. doi:https://doi.org/10.1007/s10566-010-9111-9.
- Banks, Pauline, and Maggie Lawrence. 2005. “Transparent or Opaque? Disabled People in Scotland Describe Their Experience of Applying for Disability Living Allowance.” Journal of Social Work 5 (3):299–317. doi:https://doi.org/10.1177/1468017305058937.
- Becker, K., M. Reiser, S. Lambert, and C. Covello 2014. Photovoice-conducting community-based participatory research and advocacy in mental health. Journal of Creativity in Mental Health, 9, 2, 188.
- Bray, Lucy, Bernie Carter, Caroline Sanders, Lucy Blake, and Kimberley Keegan. 2017. “Parent-to-parent Peer Support for Parents of Children with a Disability: A Mixed Method Study.” Patient Education and Counseling Vol 100 (8):1537–43.
- Cabot, Heath. 2016. “Contagious’ Solidarity: reconfiguring Care and Citizenship in Greece's Social Clinics: ‘Contagious’ Solidarity.” Social Anthropology 24 (2):152–66. doi:https://doi.org/10.1111/1469-8676.12297.
- Carrabregu, Gent. 2016. “Habermas on Solidarity: An Immanent Critique: Habermas on Solidarity: Gent Carrabregu.” Constellations 23 (4):507–22. [Mismatch] doi:https://doi.org/10.1111/1467-8675.12257.
- Cooke, M. 1995. “Selfhood and Solidarity.” Constellations 1:337–57.
- Dewey, Deborah, Susan G. Crawford, and Bonnie J. Kaplan. 2003. “Clinical Importance of Parent Ratings of Everyday Cognitive Abilities in Children with Learning and Attention Problems.” Journal of Learning Disabilities 36 (1):87–95. doi:https://doi.org/10.1177/00222194030360011001.
- Dixon, Lisa B., Alicia Lucksted, Deborah R. Medoff, Joyce Burland, Bette Stewart, Anthony F. Lehman, Li Juan Fang, Vera Sturm, Clayton Brown, and Aaron Murray-Swank. 2011. “Outcomes of a Randomized Study of a Peer-Taught Family-to-Family Education Program for Mental Illness.” Psychiatric Services 62 (6):591–7. doi:https://doi.org/10.1176/ps.62.6.pss6206_0591.
- Duff, Cameron. 2012. “Exploring the Role of 'enabling Places' in Promoting Recovery from Mental Illness: A Qualitative Test of a Relational Model.” Health and Place 18 (6):1388–95. doi:https://doi.org/10.1016/j.healthplace.2012.07.003.
- Fiks, A., C. C. Hughes, A. Gafen, J. P. Guevara, and F. K. Barg. 2011. “Contrasting Parents and Paediatricians Perspectives on Shared Decision Making in ADHD.” Pediatrics 127 (1):e188.
- Foucault, M., and C. Gordon. 1980. Power/knowledge: selected interviews and other writings, 1972–1977. New York, London: Harvester Wheatsheaf.
- Harper, David, and Ewen Speed. 2013. “Uncovering Recovery: The Resistible Rise of Recovery and Resilience.” Studies in Social Justice 6 (1):9–26. doi:https://doi.org/10.26522/ssj.v6i1.1066.
- Haslam, C., J. Jetten, and S. A. Haslam 2012. The social cure: identity, health and well-being. Hove: Psychology Press.
- Hochschild, Arlie Russell. 2012. The Managed Heart: commercialization of Human Feeling. Updat ed. London;Berkeley, Calif;: University of California Press.
- Hout, van A., J. Pols, and D. Willems. 2015. “Shining Trinkets and Unkempt Gardens: on the Materiality of Care.” Sociology of Health & Illness 37 (8):1206–17. doi:https://doi.org/10.1111/1467-9566.12302.
- Hung, J.-W., Y.-H. Wu, Y.-C. Chiang, W.-C. Wu, and C.-H. Yeh. 2010. “Mental Health of Parents Having Children with Physical Disabilities.” Chang Gung Medical Journal 33 (1):82–91.
- Joseph Rowntree Foundation. 2014. https://www.jrf.org.uk/sites/default/files/jrf/migrated/files/MPSE-2014-FULL.pdf
- Klein, O., and C. Walker 2013. Distress in the parents of children labelled with complex needs: replacing psy professionals with something more useful. Journal of Critical Psychology Counselling and Psychotherapy 13(4).
- Knight, K. 2013. “The Changing Face of the "Good Mother': Trends in Research into Families with a Child with Intellectual Disability, and Some Concerns.” Disability & Society 28 (5):660–73. doi:https://doi.org/10.1080/09687599.2012.732540.
- Luckstead, A. 2012. “Sustained Outcomes of a Peer-taught Family Education Program on Mental Illness.” Acta Psychiatr Scand 127:279–86.
- Marabelli, Marco, Sue Newell, Chantal Krantz, and Jacky Swan. 2014. “Knowledge Sharing and Health-care Coordination: the Role of Creation and Use Brokers.” Health Systems 3 (3):185–98. doi:https://doi.org/10.1057/hs.2014.8.
- McGrath, Laura, and Paula Reavey. 2015. “Seeking Fluid Possibility and Solid Ground: Space and Movement in Mental Health Service Users' Experiences of 'crisis'.” Social Science and Medicine 128:115–25. doi:https://doi.org/10.1016/j.socscimed.2015.01.017.
- Moen, Ø. L., M. L. Hall-Lord, B. Hedelin, O. Avdelningen För, Samhälls-. Fakulteten För, L. Och, and U. Karlstads. 2011. “Contending and Adapting Every Day: Norwegian parents' lived experience of having a child with ADHD.” Journal of Family Nursing 17 (4):441–62. doi:https://doi.org/10.1177/1074840711423924.
- Papataxiarchis, Evthymios. 2016. “Unwrapping Solidarity? Society Reborn in Austerity.” Social Anthropology 24 (2):205–10. doi:https://doi.org/10.1111/1469-8676.12309.
- Pols, J. 2015. “Towards an Empirical Ethics in Care: relations with Technologies in Health Care.” Medicine, Health Care and Philosophy 18 (1):81–90. doi:https://doi.org/10.1007/s11019-014-9582-9.
- Pols, Jeannette. 2016. “Analyzing Social Spaces: Relational Citizenship for Patients Leaving Mental Health Care Institutions.” Medical Anthropology 35 (2):177–92. doi:https://doi.org/10.1080/01459740.2015.1101101.
- Pols, Jeannette, and Hans Kroon. 2007. “The Importance of Holiday Trips for People with Chronic Mental Health Problems.” Psychiatric Services 58 (2):262–5. doi:https://doi.org/10.1176/ps.2007.58.2.262.
- Rakopoulos, Theodoros. 2016. “Solidarity: the Egalitarian Tensions of a Bridge-concept: Solidarity.” Social Anthropology 24 (2):142–51. doi:https://doi.org/10.1111/1469-8676.12298.
- Reid, D. Kim., and Jan Weatherly Valle. 2004. “The Discursive Practice of Learning Disability: Implications for Instruction and Parent—School Relations.” Journal of Learning Disabilities 37 (6):466–81. doi:https://doi.org/10.1177/00222194040370060101.
- Rozakou, Katerina. 2016. “Socialities of Solidarity: revisiting the Gift Taboo in Times of Crises: Socialities of Solidarity.” Social Anthropology 24 (2):185–99. doi:https://doi.org/10.1111/1469-8676.12305.
- Ryan, Sara. 2005. “People Don't Do Odd, do They?' Mothers Making Sense of the Reactions of Others towards Their Learning Disabled Children in Public Places.” Children's Geographies 3 (3):291–305. doi:https://doi.org/10.1080/14733280500352920.
- Ryan, Sara. 2010. “Meltdowns’, surveillance and Managing Emotions; going out with Children with Autism.” Health and Place 16 (5):868–75. doi:https://doi.org/10.1016/j.healthplace.2010.04.012.
- Solomon, Michael, Nancy Pistrang, and Chris Barker. 2001. “The Benefits of Mutual Support Groups for Parents of Children with Disabilities.” American Journal of Community Psychology 29 (1):113–32. doi:https://doi.org/10.1023/A:1005253514140.
- Stephens, J. R., J. Farhall, S. Farnan, and K. M. Ratcliff. 2011. “An Evaluation of Well Ways, a Family Education Programme for Carers of People with a Mental Illness.” Aust N Z J Psychiatry.Jan 45 (1):45–53.
- Swain, J., French, S., Barnes, C., and Thomas, C. 2014. Disabling barriers - enabling environments. (3rd ed.). London: SAGE.
- ter Meulen, Ruud. 2015. “Solidarity and Justice in Health Care. A Critical Analysis of Their Relationship.” Diametros 43 (43):1–20. doi:https://doi.org/10.13153/diam.43.201.710.
- Walker, Carl, Angie Hart, and Paul Hanna. 2017. Building a New Community Psychology of Mental Health: spaces, places, people and Activities. London: Palgrave Macmillan.
- Walker, C., and J. Streatfield 2012. The Amaze disability living allowance project and the experiences of the parents who use the service. University of Brighton.
- Walker, Carl, and Klein Orly. 2015. The children's disability living allowance form: policing dependency with a boundary object. In Craig Newnes (ed.) Children in Society: politics, policies and Interventions. Monmouth: PCCS Books
- Weatherly Valle, J., and Elsie Aponte. 2002. “IDEA and Collaboration: A Bakhtinian Perspective on Parent and Professional Discourse.” Journal of Learning Disabilities 35 (5):469–79.
- Woodcock, J., and C. Tregaskis. 2008. “Understanding Structural and Communication Barriers to Ordinary Life for Families with Disabled Children: a Combined Social Work and Social Model of Disability Analysis.” British Journal of Social Work 38 (1):55–71.