Cite

Arnstein, S. R. (1969). A ladder of citizen participation. Journal of the American Institute of Planners, 35(4), 216-224.10.1080/01944366908977225 Search in Google Scholar

Bennett, W. L., & Segerberg, A. (2012). The logic of connective action. Information, Communication & Society, 15(5), 739-768.10.1080/1369118X.2012.670661 Search in Google Scholar

Bruns, A. (2008). The Future Is User-Led: The Path towards Widespread Produsage. Fibreculture, 11. Search in Google Scholar

Carpentier, N. (2011). The concept of participation. If they have access and interact, do they really participate? Communication Management Quarterly, 21, 13-16. Search in Google Scholar

Carpentier, N. (2015). Differentiating between access, interaction and participation. Conjunctions: Transdisciplinary Journal of Cultural Participation, 2(2). Search in Google Scholar

Dijck, J. v., Poell, T., & Waal, T. d. (2018). The Platform Society. Public Values in a Connective World. New York: Oxford University Press.10.1093/oso/9780190889760.001.0001 Search in Google Scholar

Eeckman, E. (2015). Power to the patient? Studying the balance of power between patient and GP in relation to Web health information. In F. M. e. a. Murru (Ed.), Communication as the intersection of the old and the new. London: Lumière. Search in Google Scholar

Fuchs, C. (2014). Social media. A critical introduction. London: Sage. Search in Google Scholar

Gerlitz, C. (2016). What Counts? Reflections on the Multivalence of Social Media Data. Digital Culture and Society, 2(2), 19-38.10.14361/dcs-2016-0203 Search in Google Scholar

Gerlitz, C., & Helmond, A. (2013). The like economy. New Media and Society, 15(8), 1348-1365.10.1177/1461444812472322 Search in Google Scholar

Gerlitz, C., & Lury, C. (2014). Social media and self-evaluating assemblages. Distinktion: Scandinavian Journal of Social Theory, 15(2), 174-188.10.1080/1600910X.2014.920267 Search in Google Scholar

Hardey, M. (2001). Doctor in the house: the Internet as a source of lay health knowledge and the challenge to expertise. Sociology of Health and Illness, 21(6), 820-835.10.1111/1467-9566.00185 Search in Google Scholar

Høybye, M. T., Dalton, S. O., Christensen, J., Ross, L., Kuhn, K. G., & Johansen, C. (2010). Social and psychological determinants of participation in internet-based cancer support groups. Support Care Cancer, 18, 553-560.10.1007/s00520-009-0683-6 Search in Google Scholar

Ishii, K., Lyons, M. M., & Carr, S. A. (2019). Revisiting media richness theory for today and future. Human Behavior and Emerging Technologies, 1(2), 124-131.10.1002/hbe2.138 Search in Google Scholar

Jenkins, H. (2006). Convergence culture. Where old and new media collide. New York: New York University Press. Search in Google Scholar

Kingod, N., Cleal, B., Wahlberg, A., & Husted, G. R. (2017). Online Peer-to-Peer Communities in the Daily Lives of People With Chronic Illness: A Qualitative Systematic Review. Qualitative Health Research(1), 89-99.10.1177/1049732316680203 Search in Google Scholar

Lagerkvist, A. (2017). Existential media: Toward a theorization of digital thrownness. New Media and Society, 19(1), 96-110.10.1177/1461444816649921 Search in Google Scholar

Lupton, D. (2013). The digitally engaged patient: Self-monitoring and self-care in the digital health era. Social Theory and Health, 11(3), 256-270.10.1057/sth.2013.10 Search in Google Scholar

Lupton, D. (2016). The Quantified Self. Cambridge: Polity. Search in Google Scholar

McCosker, A. (2013). Intensive Media: Aversive Affects and Visual Culture. Basingstoke: Palgrave.10.1057/9781137273512 Search in Google Scholar

Mol, A. (2008). The logic of care. Health and the problem of patient choice. London, New York: Routledge.10.4324/9780203927076 Search in Google Scholar

Morden, A., Jinks, C., & Ong, B. N. (2012). Rethinking “risk” and self-management for chronic illness. Social Theory & Health, 11(3), 78-99.10.1057/sth.2011.20 Search in Google Scholar

Nettleton, S. (2004). The emergence of e-scaped medicine? Sociology, 38(4), 661-679.10.1177/0038038504045857 Search in Google Scholar

Orgad, S. (2005). Storytelling Online. Talking Breast Cancer on the Internet. New York: Peter Lang. Search in Google Scholar

Papacharissi, Z. (2015). Affective publics: Sentiment, technology, and politics. New York: Oxford University Press. Search in Google Scholar

Pateman, C. (1970). Participation and democratic theory. Cambridge: Cambridge University Press.10.1017/CBO9780511720444 Search in Google Scholar

Rose, N. (2006). The Politics of Life Itself. Biomedicine, Power, and Subjectivity in the Twenty-First Century. Princeton: Princeton University Press. Search in Google Scholar

Stacey, J. (1997). Teratologies. A cultural study of cancer. London: Routledge. Search in Google Scholar

Stage, C. (2017). Networked cancer. Affect, narrative and measurement. Basingstoke: Palgrave.10.1007/978-3-319-51418-5 Search in Google Scholar

Stage, C. (2019). The participatory patient. Exploring the platformed multivalence and public value of cancer storytelling on social media. In B. Eriksson, B. Valtysson, & C. Stage (Eds.), Cultures of Participation. New York: Routledge. Search in Google Scholar

Stage, C., Hvidtfeldt, K., & Klastrup, L. (2020). Vital media. The affective and temporal dynamics of young cancer patients’ social media practices. Social Media + Society, April-June, 1-13. Search in Google Scholar

Swan, M. (2012). Health 2050: The realization of personalized medicine through crowdsourcing, the quantified self, the participatory biocitizen. Journal of Personalized Medicine, 2(3), 93-118.10.3390/jpm2030093 Search in Google Scholar

Terranova, T. (2000). Free Labor: Producing Culture for the Digital Economy. Social Text, 18(2), 33-58.10.1215/01642472-18-2_63-33 Search in Google Scholar

eISSN:
2246-3755
Idioma:
Inglés
Calendario de la edición:
2 veces al año
Temas de la revista:
Arts, general, Cultural Studies, Media Studies, Media Theory, General Cultural Studies, Social Sciences, other