Correspondingly, social exclusion frequently occurs for disabled people, such as from being absent of employment, and often disabled people only have their family as their main supporting social network (Joly & Venturiello 2012, p. 334; O’grady et al. 2010, pp. 265-29; Wynne & McAnaney 2009, p. 95). Another facet of being disabled, which I too have experienced, is being regarded as public property - where doctors and other healthcare professionals feel as though they know the patient’s condition, quality of life, and level of happiness better than the patients themselves (Edwards 2013, pp. 189-191; Tomlinson 2006, p. 30). Conversely, is has been found that disabled people often report higher levels of happiness than what objective assessments identify (Edwards 2013, pp. 191-192). Remarkably, I too feel that after several years adjusting to my condition, I am happier than what I was prior to my …show more content…
We have seen that disability is rooted in social structures including capitalism and media. We have identified risk as one of many barriers that have limited my opportunities and social inclusion. Additionally, transitions into adulthood, such as acquiring employment, has been identified as one of many limited opportunities disabled people face. We have seen how disability has removed many of my identities, whilst also becoming formed as an identity for me and many other people with disabilities. Likewise, epilepsy has also been developed as a part of my identity. Through exploring education and employment chances for people with disability we find justification for why I withheld disclosing my condition during education and the effects of having a disability during employment. We have analysed the extent of social exclusion, and feelings of being public property. The conflict between masculinity and disability was explored, as well as the effects of losing physical activities and sports from my identity. Finally, we examined how I, like most disabled people, have lost consumerism as an