References
- Abramowitz, J. S., and L. Reuman. 2020. “Obsessive Compulsive Disorder.” In Encyclopedia of Personality and Individual Differences, edited by V. Zeigler-Hill & T. K. Shackelford. Cham, CH: Springer. https://doi.org/10.1007/978-3-319-24612-3_919
- Cefalu, P. 2009. “What’s so Funny about Obsessive-Compulsive Disorder?” PMLA/Publications of the Modern Language Association of America 124 (1): 44–58. https://doi.org/10.1632/pmla.2009.124.1.44
- Cole, K. L. 2021. “The Paradox of Patient Consent: A Feminist account of Illness and Healthcare.” Health Communication 36 (8): 982–991. https://doi.org/10.1080/10410236.2020.1724645
- Cole, K. L. 2022. “Selling a Cure for Chronicity: A Layered Narrative Analysis of Direct-to-Consumer Humira® Advertisements.” Rhetoric of Health & Medicine 5 (2): 212–239. https://doi.org/10.5744/rhm.2022.5011
- Crohn’s & Colitis Foundation 2022, February 2. “What is Crohn’s Disease?” https://www.crohnscolitisfoundation.org/what-is-crohns-disease#:∼:text=Crohn's%20disease%20is%20an%20inflammatory,inflammation%20of%20the%20gastrointestinal%20tract.
- Cummins, M. W., and G. E. Brannon. 2022. “Implicating Ourselves through Our Research: A Duoethnography of Researcher Reflexivity.” Journal of Contemporary Ethnography 51 (1): 85–102. https://doi.org/10.1177/08912416211021898
- Defenbaugh, N. L. 2008. “Under Erasure”: the Absent Ill Body in Doctor-Patient Dialogue.” Qualitative Inquiry 14 (8): 1402–1424. https://doi.org/10.1177/1077800408322579
- Defenbaugh, N. L. 2013. “Revealing and Concealing Ill Identity: A Performative Narrative of IBD Disclosure.” Health Communication 28 (2): 159–169. https://doi.org/10.1080/10410236.2012.666712
- Evans, H. D. 2019. “Trial by Fire’: forms of Impairment Disclosure and Implications for Disability Identity.” Disability & Society 34 (5): 726–746. https://doi.org/10.1080/09687599.2019.1580187
- Fennell, D. F., and M. Boyd. 2014. “Obsessive-Compulsive Disorder in the Media.” Deviant Behavior 35 (9): 669–686. https://doi.org/10.1080/01639625.2013.872526
- Gibbons, H. M., and C. M. Gibbons. 2016. “Siblings with Disabilities: A Duoethnography on the Intersections between a Sibling Relationship and Disability.” Disability & Society 31 (6): 820–837. https://doi.org/10.1080/09687599.2016.1203291
- Goering, S. 2015. “Rethinking Disability: The Social Model of Disability and Chronic Disease.” Current Reviews in Musculoskeletal Medicine 8 (2): 134–138. (https://doi.org/10.1007/s12178-015-9273-z
- Goodley, D. 2014. Dis/Ability Studies: Theorising Disablism and Ableism. New York, NY: Routledge.
- Hughes, B. 2007. “Being Disabled: Towards a Critical Social Ontology for Disability Studies.” Disability & Society 22 (7): 673–684. https://doi.org/10.1080/09687590701659527
- Malacrida, C. 2010. “Income Support Policy in Canada and the UK: Different, but Much the Same.” Disability & Society 25 (6): 673–686. https://doi.org/10.1080/09687599.2010.505739
- Malacrida, C., and S. Duguay. 2009. “The AISH Review is a Big Joke’: Contradictions of Policy Participation and Consultation in a Neo-Liberal Context.” Disability & Society 24 (1): 19–32. https://doi.org/10.1080/09687590802535360
- Mukherji, R. 2023. “Chronic Illness is not Widely Viewed as Disability. This Needs to Change.” Harvard University Graduate School of Education Office of Student Affairs. https://osa.gse.harvard.edu/chronic-illness-not-widely-viewed-disability-needs-change.
- Norris, J. 2008. “Duoethnography.” In The Sage Encyclopedia of Qualitative Research Methods, edited by L. M. Given, 234–237. Thousand Oaks, CA: Sage.
- Norris, J., and R. D. Sawyer. 2012. “Toward a Dialogic Method.” In Duoethnography: Dialogic Methods for Social, Health, and Educational Research edited by J. Norris, R. D. Sawyer, & D. Lund, pp. 9–39. Walnut Creek, CA: Left Coast Press.
- Osborne, T. 2019. “Not Lazy, Not Faking: Teaching and Learning Experiences of University Students with Disabilities.” Disability & Society 34 (2): 228–252. https://doi.org/10.1080/09687599.2018.1515724
- Owens, J. 2015. “Exploring the Critique of the Social Model of Disability: The Transformative Possibility of Arendt’s Notion of Power.” Sociology of Health & Illness 37 (3): 385–403. https://doi.org/10.1111/1467-9566.12199
- Pavelko, R. L., and J. G. Myrick. 2020. “Measuring Trivialization of Mental Illness: Developing a Scale of Perceptions That Mental Illness Symptoms Are Beneficial.” Health Communication 35 (5): 576–584. https://doi.org/10.1080/10410236.2019.1573296
- Reeve, D. 2012. “Psycho-Emotional Disablism: The Missing Link?.” In Routledge Handbook of Disability Studies, edited by N. Watson, pp. 78–92. New York, NY: Routledge.
- Reeve, D. 2015. “Psycho-Emotional Disablism in the Lives of People Experiencing Mental Distress.” In Madness, Distress, and the Politics of Ableism, edited by H. Spandler, J. Anderson, and B. Sapey, 99–112. Bristol, UK: Policy Press.
- Shakespeare, T. 2013. “The Social Model of Disability.” In L. J. Davis (Ed.), The Disability Studies Reader (4th ed.) (pp. 214–221). New York, NY: Routledge.
- Thomas, C. 2007. Sociologies of Disability and Illness: Contested Ideas in Disability Studies and Medical Sociology. London: Palgrave MacMillan.
- Thompson, A. I. 2013. “Sometimes I Think I Might Say Too Much”: Dark Secrets and the Performance of Inflammatory Bowel Disease.” Symbolic Interaction 36 (1): 21–39. https://doi.org/10.1002/symb.50