Acquisti, A., and Jens G. “Losses, Gains, and Hyperbolic Discounting: An Experimental Approach to Information Security Attitudes and Behavior.” In 2nd Annual Workshop on Economics and Information Security – WEIS ’03., (2003).
Adams, A., and M. A. Sasse. “Privacy in Multimedia Communications: Protecting Users, Not Just Data.” In People and Computers XV – Interaction without frontiers. Lille: Springer, 49–64. (2001).
Allen, A. L. Uneasy Access. Rowman & Littlefield, New Jersey, 1988.
Alonzo, A. A., and N. R. Reynolds, “Stigma HIV and AIDS: An Exploration and Elaboration of a Stigma Trajectory.” Social Science & Medicine 41, 3 (August 1995): 303–315.
Altman, Irwin. The Environment and Social Behaviour. Monterey, CA: Brooks/Cole Publishing Co, 1976.
Anthony, D., H. Tristan, and K. David. “Privacy in Location-Aware Computing Environments.” IEEE Pervasive Computing, 6, 4 (2007): 64–72.
Bakardjieva, M. Internet Society: The Internet in Everyday Life. Thousand Oaks, CA: Sage Publications Ltd, 2005.
Berger, M., T. H. Wagner, and L. C. Baker. “Internet Use and Stigmatized Illness.” Social Science & Medicine 61, (2005): 1821–1827.
Bury, M. “Illness Narratives: Fact or Fiction.” Sociology of Health & Illness 23, 3 (2001): 263–285.
Corona, R., M. K. Beckett, B. O. Cowgill, M. N. Elliott, D. A. Murphy, A. J. Zhou and M. A. Schuster. “Do Children Know Their Parent’s HIV Status? Parental Reports of Child Awareness in a Nationally Representative Sample.” Ambulatory Pediatrics 6, 3 (2006): 138–144.
Cunningham, S. D., J. M. Tschann, J. E. Gurvey, J. D. Fortenberry, and J. M. Ellen. “Attitudes About Sexual Disclosure and Perceptions of Stigma and Shame.” Sexually Transmitted Infections 78, 5 (2002): 334–338.
Department of Health. HIV and AIDS in African communities: A framework for better prevention and care. London, 2004.
Derlega, V. J., B. A. Winstead, K. Greene, J. Serovich, and W. N. Elwood. “Perceived HIV-Related Stigma and HIV Disclosure to Relationship Partners After Finding Out About the Seropositive Diagnosis.” Journal of Health Psychology 7, 4 (2002): 415–432.
Doyal, L., and J. Anderson. “My fear is to fall in love again” How HIV-positive African women survive in London. Social Science & Medicine 60 (2005): 1729–1738.
Elford, J., J. Anderson, C. Bukutu, and F. Ibrahim. “HIV in East London: ethnicity, gender and risk. Design and methods.” BMC Public Health 6, 150 (2006).
Elford, J., F. Ibrahim, C. Bukutu, and J. Anderson. “Disclosure of HIV status: the role of ethnicity among people living with HIV in London.” Journal of Acquired Immundeficiency Syndrome 47, 4 (2008): 514–521.
Flowers, P., M. Davis, G. Hart, M. Rosengarten, J. Frankis, and J. Imrie. “Diagnosis and stigma and identity amongst HIV positive black Africans living in the UK.” Psychology and Health 21, 1 (2006): 109–122.
Fortenberry, J. D., M. McFarlane, A. Bleakley, S. Bull, M. Fishbein, D. M. Grimley, C. K. Malotte, and B. P. Stoner. “Relationships of stigma and shame to gonorrhea and HIV screening.” American Journal of Public Health 92, 3 (2002): 378–381.
Foucault, M., and J. Miskowiec. “Of Other Spaces.” Diacritics 16, 1 (1986): 22–27.
Frank, A. The wounded storyteller: Body, Illness and Ethics. Chicago, IL: University of Chicago Press, 1995.
Freidson, E. “Client Control and Medical Practice.” The American Journal of Sociology 65, 4 (1960): 374–382.
Green, G. and R. Smith. “The psychosocial and health care needs of HIV-positive people in the United Kingdom.” HIV Medicine 5, 1 (2004): 5–46.
Greene, K., V. J. Derlega, G. A. Yep, and S. Petronio. Privacy and Disclosure of HIV in Interpersonal Relationships: A Sourcebook for Researchers and Practitioners. 1st ed. London: Routledge, 2003.
Haddon, L. Information and Communication Technologies in Everyday Life: A Concise Introduction and Research Guide. Oxford: Berg Publishers Ltd, 2004.
Hui, K.-L., H. H. Teo, and S.-Y. T. Lee. “The value of privacy assurance: A field experiment.” MIS Quarterly 31, 1 (2007): 19–33.
Joinson, A., C. Paine, T. Buchanan, and U.-D. Reips. “Measuring self-disclosure online: Blurring and non-response to sensitive items in web-based surveys.” Computers in Human Behavior 24, 5 (9, 2008): 2158–2171.
Kearns, R. A. and A. E. Joseph. “Space in its place: Developing the link in medical geography.” Social Science & Medicine 37, 6 (September 1993): 711–717.
Kivits, J. “Researching the ‘Informed Patient’: The case of online health information seekers.” Information, Communication & Society 7, 4 (2004): 510–530.
Kleinman, A. The illness narratives: Suffering, healing, and the human condition. New York, NY: Basic Books, 1989.
Lee, M. B., and M. J. Rotheram-Borus. “Parents’ disclosure of HIV to their children.” AIDS 16, 16 (2002): 2201–2207.
Mackinnon, C. “Toward a Feminist Theory of the State.” Women’s Rights Law Reporter 12 (1990): 205.
MacKinnon, C. A. “Feminism, Marxism, Method, and the State: Toward Feminist Jurisprudence.” Signs 8, 4 (Summer 1983): 635–658.
MacKinnon, C. A. Toward a Feminist Theory of the State. 2nd ed. Cambridge, MA: Harvard University Press, 1991.
Margulis, S. T. “On the Status and Contribution of Westin’s and Altman’s Theories of Privacy.” Journal of Social Issues 59, 2 (6, 2003): 411–429.
McKinlay, J. B. “Social Networks, Lay Consultation and Help-Seeking Behavior.” Social Forces 51, 3 (1972): 275–292.
Mechanic, D. Medical Sociology. New York, NY: Free Press, 1968.
Milligan, C. “Location or dis-location? Towards a conceptualization of people and place in the care-giving experience.” Social & Cultural Geography 4, 4 (2003): 455.
Nettleton, S., R. Burrows, and L. O’Malley. “The mundane realities of the everyday lay use of the internet for health, and their consequences for media convergence.” Sociology of Health & Illness 27, 7 (2005): 972–992.
Nissenbaum, H. F. “Privacy as Contextual Integrity.” Washington Law Review 79 (2004): 119.
Nissenbaum, H. F. Privacy in Context: Technology, Policy, and the Integrity of Social Life. Stanford, CA: Stanford University Press, 2009.
Orgad, S., “The cultural dimensions of online communication: a study of breast cancer patients’ internet spaces.” New Media & Society 8, 6 (2006): 877–899.
Paine, C., U.-D. Reips, S. Stieger, A. Joinson, and T. Buchanan. “Internet users’ perceptions of privacy concerns and privacy actions.” International Journal of Human-Computer Studies 65, 6 (June 2007): 526–536.
Pateman, C. The Disorder of Women: Democracy, Feminism and Political Theory. Polity Press, Cambridge, 1990.
Petronio, S. S. Boundaries of Privacy: Dialectics of Disclosure. Illustrated edition. Albany, NY: State University of New York Press, 2002.
Prost, A., J. Elford, J. Imrie, M. Petticrew, and G. J. Hart. “Social, Behavioural, and Intervention Research among People of Sub-Saharan African Origin Living with HIV in the UK and Europe: Literature Review and Recommendations for Intervention.” Aids Behaviour 12 (2008): 170–194.
Scambler, A., G. Scambler, and D. Craig. “Kinship and Friendship Networks and Women’s Demands for Primary Care.” Journal of the Royal College of General Practitioners 26 (1981): 746–750.
Schoeman, F. D. Privacy and Social Freedom. 1st ed. Cambridge, MA: Cambridge University Press, 1992.
Shapiro, S. “Places and Spaces: The Historical Interaction of Technology, Home, and Privacy.” The Information Society 14 (1998): 275–284.
Sillence, E., P. Briggs, P. R. Harris, and L. Fishwick. “How do patients evaluate and make use of online health information?” Social Science & Medicine 64 (2007): 1853–1862.
Warren, S. D., and L. D. Brandeis. “Right to Privacy.” Harvard Law Review 4 (1890): 193.
Wellman, B., and C. Haythornthwaite. The Internet in Everyday Life. Oxford: Blackwell, 2002.
Westin, A. F. Privacy and Freedom. New York, NY: Atheneum, 1970.
Westin, A. F. “Social and Political Dimensions of Privacy.” Journal of Social Issues 59, 2 (6, 2003): 431–453.