{"id":38,"date":"2010-08-18T23:23:43","date_gmt":"2010-08-19T03:23:43","guid":{"rendered":"http:\/\/www.chloegkatkins.com\/?page_id=38"},"modified":"2020-01-30T04:02:55","modified_gmt":"2020-01-30T08:02:55","slug":"publications","status":"publish","type":"page","link":"https:\/\/www.chloegkatkins.com\/?page_id=38","title":{"rendered":"Publications & Presentations"},"content":{"rendered":"

Books<\/u><\/strong><\/p>\n

My Imaginary Illness: A Journey into Uncertainty and Prejudice in Medical Diagnosis<\/em><\/strong>. ILR-Cornell University Press, The Culture and Politics of Health Care Work Series, 2010. E-book publication February 2015.<\/p>\n

Peer- reviewed articles<\/u><\/strong><\/p>\n

\u201cWhy Bioethics Should Pay Attention to Patients Who Suffer Medically Unexplained (Physical) Symptoms \u2013 a Discussion of Uncertainty, Suffering and Risk.\u201d The American Journal of Bioethics<\/em><\/strong>, 26 April 2018. 18:5, 20-22, DOI: 10.1080\/15265161.2018.1445319.<\/p>\n

\u201cA Qualitative Study of the Role of Model Clinical Practitioners yields a Framework for the Management of Patients with Medically Unexplained Physical Symptoms.\u201d British Medical Journal<\/em><\/strong> Vol 6, Issue 12; 23 Jan 2017; (BMJ Open 2016;6:e012379. doi:10.1136\/bmjopen-2016-012379).<\/p>\n

\u201cThe Meaning of Patient Experiences of Medically Unexplained Symptoms.\u201d Qualitative Health Research<\/em><\/strong> 1-10. 1049732314566326, first published on January 12, 2015.<\/p>\n

\u201cSilos of Silence, Stress and Suffering: Patient and Physician Experiences of MUPS and Diagnostic Uncertainty.\u201d Special issue of American Journal of Bioethics: Neurosciences<\/em><\/strong> 4:3 (July-Sept 2013).<\/p>\n

\u201c<\/em>Two Mothers\u2019 Choices: Disability, Gender, Sexuality and Prenatal Testing.\u201d Cultural Studies – Critical Methodologies<\/strong>, <\/em>Volume 8; No. 1; 2008; pp. 106-129.\u201cCritical Disability Theory<\/em>.\u201d (Review) Canadian Journal of Law and Society<\/em><\/strong> Vol 22, No 1, pp. 145-148 (2007).<\/p>\n

\u201cA Cripple at a Rich Man\u2019s Gate: A Comparison of Disability, Employment and Anti-discrimination Law In the United States and Canada.\u201d Canadian Journal of Law and Society<\/em> <\/strong>Vol 21-2, January 2007 pp. 87-111.<\/p>\n

\u201cThe Failure of Formal Rights and Equality in the Clinic: A Critique of Bioethics.\u201d Ethics & Medicine<\/em> <\/strong>Volume 21:3, Fall 2005.<\/p>\n

Book- Chapters<\/u><\/strong><\/p>\n

\u201cThe Limits of Liberal Values in the Ethical Assessment of Genomic and Technologic Innovation.\u201d Chapter in Democracy, Public Participation and Genomic and Technologic Innovation<\/em>, Edited By Edna Einseidel and Kieran O\u2019Doherty; University of British Columbia Press, 2013.<\/p>\n

\u201cTrading Patients.\u201d In Telling Stories Out of Court: Narratives about Women and Workplace Discrimination.<\/em><\/strong> Ruth O’Brien (Editor); Liza Featherstone (Foreword). Ithaca, ILR-Cornell University Press. Ithaca, N.Y.: 2008.<\/p>\n

\u201cCivil Rights Backlash: An Examination of the US ADA and of Canadian Law on Disability,\u201d Encyclopedia of Disability<\/strong><\/em>, Sage Publications, 2006.<\/p>\n

\u201cCovering My Tracks.\u201d In Disabled: Faculty and Staff in a Disabling Society. Multiple Identities in Higher Education. <\/em><\/strong> Mary Lee Vance. Association of Higher Education and Disability, Huntersville, North Carolina, 2007.<\/p>\n

\u201c<\/em>A Chair Unseen.\u201d In Voices from the Edge: Narratives about the ADA.<\/strong><\/em> Edited by Ruth O\u2019Brien.\u00a0 Oxford University Press, 2004.<\/p>\n

Non-refereed publications<\/u><\/strong><\/p>\n

\u201cWhose Death is It Anyway?\u201d opinion editorial https:\/\/ipolitics.ca\/2016\/06\/03\/whose-death-is-it-anyway\/<\/a> 3 June 2016.<\/p>\n

Book review: Elizabeth Neill, Rites of Privacy and the Privacy Trade.<\/em> \u00a0University of Toronto Quarterly<\/em><\/strong>. Fall 2002.<\/p>\n

Book review: Radha Jhappan, ed., Women\u2019s Legal Strategies in Canada<\/em>. Labour\/Le Travail<\/em><\/strong>, Spring 2003.<\/p>\n

Book review: Ruth O\u2019Brien\u2019s Crippled Justice<\/em>. The Ragged Edge Magazine<\/em><\/strong>, 2001.<\/p>\n

Various opinion editorials and articles in trade newspapers and journals. 1999 \u2013 present.<\/p>\n

NYD- Not Yet Diagnosed<\/em>, NFB (English) documentary, Workweek Television Productions, 48 min; 1997.<\/p>\n

 <\/p>\n

Publications Under Construction <\/u><\/strong><\/p>\n

Books:<\/u><\/strong><\/p>\n

The Ethics of Everyday Life: A Memoir<\/em>. Book manuscript being drafted. Book proposal, draft outline of 8 chapters and, 2 chapters with book agent.<\/p>\n

I is for Illness \u2013<\/em> a book length monograph tapestry\/collage of genetic and medical research, genealogy and archival research, historical fiction and memoir which explores the incidence of inherited neurologic disease in the Quebec Founder Population which arrived in North America in the early1600s and whose descendants bear the names, genes, social mores and behaviours of their ancestors in the 21st<\/sup><\/p>\n

Peer-reviewed articles<\/u><\/strong><\/p>\n

\u201cDisability Sucks.\u201d A socio-legal reflection on the difficulty of pursuing equality and autonomy using disability as an identity framework.\u00a0 Being drafted for Disability and Society or DisabilityZ Studies Quarterly.<\/p>\n

\u201cA Reflection on the Legalization of Physician-Assisted-Dying in Canada.\u201d Being drafted for submission to Health Law. <\/em>Proposes that physician assisted dying is less a question of medical diagnosis and more one of the social\/relational\/financial\/environmental context of individual patients which determines whether their conditions constitute \u2018intolerable suffering.\u2019<\/p>\n

\u201cVulnerability, Human Rights and Canadian Constitutionalism: An Exploration of Martha Fineman\u2019s Vulnerable Subject.\u201d Being drafted for Canadian Journal of Law and Society<\/p>\n","protected":false},"excerpt":{"rendered":"

Books My Imaginary Illness: A Journey into Uncertainty and Prejudice in Medical Diagnosis. ILR-Cornell University Press, The Culture and Politics of Health Care Work Series, 2010. E-book publication February 2015. Peer- reviewed articles \u201cWhy Bioethics Should Pay Attention to Patients … Continue reading →<\/span><\/a><\/p>\n","protected":false},"author":3,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"","meta":{"footnotes":""},"class_list":["post-38","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.chloegkatkins.com\/index.php?rest_route=\/wp\/v2\/pages\/38","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.chloegkatkins.com\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.chloegkatkins.com\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.chloegkatkins.com\/index.php?rest_route=\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.chloegkatkins.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=38"}],"version-history":[{"count":13,"href":"https:\/\/www.chloegkatkins.com\/index.php?rest_route=\/wp\/v2\/pages\/38\/revisions"}],"predecessor-version":[{"id":279,"href":"https:\/\/www.chloegkatkins.com\/index.php?rest_route=\/wp\/v2\/pages\/38\/revisions\/279"}],"wp:attachment":[{"href":"https:\/\/www.chloegkatkins.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=38"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}