IDEAS home Printed from https://ideas.repec.org/a/eee/socmed/v165y2016icp246-254.html
   My bibliography  Save this article

The politics of health mobilization in the United States: The promise and pitfalls of “disease constituencies”

Author

Listed:
  • Epstein, Steven

Abstract

A critical review of recent literature on U.S. social movements concerned with matters of health and illness prompts reconsideration of the prevailing conception of such movements as necessarily isolated and particularistic. With a focus on disease-constituency-based mobilization—presently the most potent model of efficacious activism to be found in the domain of health and illness in the United States—I argue that such activism may tend in two directions: a specific response to an imminent disease threat, and a bridging of collective action frames and identities that can lead to connections across differences and broader mobilization. Case studies have demonstrated how patient activism has affected the management of illness, attitudes and practices of health professionals, research practices, processes of innovation, state policies, and corporate behavior. Through close analysis of patient group mobilization and its distinctive orientation toward knowledge and expertise, I argue that patient groups in practice may connect with or influence one another or a range of other forms of mobilization in relation to health, and I examine the “linkage mechanisms”—spillover, coalition, and frame amplification—by which this can occur. Rather than imagine a stark opposition between particularistic, single-issue health politics, on the one hand, and universalistic efforts to transform the meaning and practice of health and health care in the United States, on the other, I propose closer attention to the potentially Janus-faced character of many health movement organizations and the ways in which they may look either inward or outward.

Suggested Citation

  • Epstein, Steven, 2016. "The politics of health mobilization in the United States: The promise and pitfalls of “disease constituencies”," Social Science & Medicine, Elsevier, vol. 165(C), pages 246-254.
  • Handle: RePEc:eee:socmed:v:165:y:2016:i:c:p:246-254
    DOI: 10.1016/j.socscimed.2016.01.048
    as

    Download full text from publisher

    File URL: http://www.sciencedirect.com/science/article/pii/S0277953616300491
    Download Restriction: Full text for ScienceDirect subscribers only

    File URL: https://libkey.io/10.1016/j.socscimed.2016.01.048?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    References listed on IDEAS

    as
    1. Brown, Phil & Mayer, Brian & Zavestoski, Stephen & Luebke, Theo & Mandelbaum, Joshua & McCormick, Sabrina, 2003. "The health politics of asthma: environmental justice and collective illness experience in the United States," Social Science & Medicine, Elsevier, vol. 57(3), pages 453-464, August.
    2. Landzelius, Kyra, 2006. "Introduction: Patient organization movements and new metamorphoses in patienthood," Social Science & Medicine, Elsevier, vol. 62(3), pages 529-537, February.
    3. Aronowitz, R. & Deener, A. & Keene, D. & Schnittker, J. & Tach, L., 2015. "Cultural reflexivity in health research and practice," American Journal of Public Health, American Public Health Association, vol. 105, pages 403-408.
    4. Rabeharisoa, Vololona, 2003. "The struggle against neuromuscular diseases in France and the emergence of the "partnership model" of patient organisation," Social Science & Medicine, Elsevier, vol. 57(11), pages 2127-2136, December.
    5. Anglin, Mary K., 1997. "Working from the inside out: Implications of breast cancer activism for biomedical policies and practices," Social Science & Medicine, Elsevier, vol. 44(9), pages 1403-1415, May.
    6. Rabeharisoa, Vololona, 2006. "From representation to mediation: The shaping of collective mobilization on muscular dystrophy in France," Social Science & Medicine, Elsevier, vol. 62(3), pages 564-576, February.
    7. Hoffman, Beatrix, 2012. "Health Care for Some," University of Chicago Press Economics Books, University of Chicago Press, number 9780226348032, September.
    8. Hoffman, B., 2003. "Health care reform and social movements in the United States," American Journal of Public Health, American Public Health Association, vol. 93(1), pages 75-85.
    9. Baggott, Rob & Jones, Kathryn, 2014. "The voluntary sector and health policy: The role of national level health consumer and patients' organisations in the UK," Social Science & Medicine, Elsevier, vol. 123(C), pages 202-209.
    10. Lupton, Deborah, 1997. "Consumerism, reflexivity and the medical encounter," Social Science & Medicine, Elsevier, vol. 45(3), pages 373-381, August.
    11. Crossley, Michele L. & Crossley, Nick, 2001. "Patient' voices, social movements and the habitus; how psychiatric survivors 'speak out," Social Science & Medicine, Elsevier, vol. 52(10), pages 1477-1489, May.
    12. Zavestoski, Stephen & Brown, Phil & McCormick, Sabrina & Mayer, Brian & D'Ottavi, Maryhelen & Lucove, Jaime C., 2004. "Patient activism and the struggle for diagnosis: Gulf War illnesses and other medically unexplained physical symptoms in the US," Social Science & Medicine, Elsevier, vol. 58(1), pages 161-175, January.
    Full references (including those not matched with items on IDEAS)

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Morse, Jaimie, 2019. "Legal mobilization in medicine: Nurses, rape kits, and the emergence of forensic nursing in the United States since the 1970s," Social Science & Medicine, Elsevier, vol. 222(C), pages 323-334.
    2. Numerato, Dino & Honová, Petra A. & Sedláčková, Tereza, 2021. "Politicisation, depoliticisation, and repoliticisation of health care controversies: Vaccination and mental health care reform in the Czech Republic," Social Science & Medicine, Elsevier, vol. 277(C).

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Copelton, Denise A. & Valle, Giuseppina, 2009. ""You don't need a prescription to go gluten-free": The scientific self-diagnosis of celiac disease," Social Science & Medicine, Elsevier, vol. 69(4), pages 623-631, August.
    2. Madeleine Akrich & Maire Leane & Celia Roberts & João Arriscado Nunes, 2012. "Practising childbirth activism: a politics of evidence," CSI Working Papers Series 023, Centre de Sociologie de l'Innovation (CSI), Mines ParisTech.
    3. Claire Edwards & Etaoine Howlett & Madeleine Akrich & Vololona Rabeharisoa, 2012. "Attention deficit hyperactivity disorder in France and Ireland: parents' groups' scientific and political framing of an unsettled condition," CSI Working Papers Series 024, Centre de Sociologie de l'Innovation (CSI), Mines ParisTech.
    4. Vololona Rabeharisoa, 2013. "Evidence-based activism: Patients’ organisations, users’ and activist’s groups in knowledge society," CSI Working Papers Series 033, Centre de Sociologie de l'Innovation (CSI), Mines ParisTech.
    5. Rabeharisoa, Vololona, 2006. "From representation to mediation: The shaping of collective mobilization on muscular dystrophy in France," Social Science & Medicine, Elsevier, vol. 62(3), pages 564-576, February.
    6. Dimond, Rebecca & Bartlett, Andrew & Lewis, Jamie, 2015. "What binds biosociality? The collective effervescence of the parent-led conference," Social Science & Medicine, Elsevier, vol. 126(C), pages 1-8.
    7. Kofahl, Christopher & Trojan, Alf & Knesebeck, Olaf von dem & Nickel, Stefan, 2014. "Self-help friendliness: A German approach for strengthening the cooperation between self-help groups and health care professionals," Social Science & Medicine, Elsevier, vol. 123(C), pages 217-225.
    8. Kaiser, Karen, 2008. "The meaning of the survivor identity for women with breast cancer," Social Science & Medicine, Elsevier, vol. 67(1), pages 79-87, July.
    9. Katharina Hauck & Aki Tsuchiya, 2010. "Health mobility: implications for efficiency and equity in priority setting," Monash Econometrics and Business Statistics Working Papers 6/10, Monash University, Department of Econometrics and Business Statistics.
    10. Setti Rais Ali & Paul Dourgnon & Lise Rochaix, 2018. "Social Capital or Education: What Matters Most to Cut Time to Diagnosis?," Working Papers halshs-01703170, HAL.
    11. Baggott, Rob & Jones, Kathryn, 2014. "The voluntary sector and health policy: The role of national level health consumer and patients' organisations in the UK," Social Science & Medicine, Elsevier, vol. 123(C), pages 202-209.
    12. Dyer, Thomas Anthony & Owens, Janine & Robinson, Peter Glenn, 2014. "The acceptability of care delegation in skill-mix: The salience of trust," Health Policy, Elsevier, vol. 117(2), pages 170-178.
    13. Ewa Malchrowicz-Mośko & Joanna Poczta, 2018. "Running as a Form of Therapy Socio-Psychological Functions of Mass Running Events for Men and Women," IJERPH, MDPI, vol. 15(10), pages 1-15, October.
    14. Jeremy Mennis & Gerald J. Stahler & Michael J. Mason, 2016. "Risky Substance Use Environments and Addiction: A New Frontier for Environmental Justice Research," IJERPH, MDPI, vol. 13(6), pages 1-15, June.
    15. Duran, Eduardo, 2021. "Diagnostic slippage: Medical uncertainty and engaged patienthood in the case of atypical disorders," Social Science & Medicine, Elsevier, vol. 280(C).
    16. Steffensen, Mette B. & Matzen, Christina L. & Wadmann, Sarah, 2022. "Patient participation in priority setting: Co-existing participant roles," Social Science & Medicine, Elsevier, vol. 294(C).
    17. Prussing, Erica & Sobo, Elisa J. & Walker, Elizabeth & Kurtin, Paul S., 2005. "Between 'desperation' and disability rights: a narrative analysis of complementary/alternative medicine use by parents for children with Down syndrome," Social Science & Medicine, Elsevier, vol. 60(3), pages 587-598, February.
    18. Sarradon-Eck, Aline & Sakoyan, Juliette & Desclaux, Alice & Mancini, Julien & Genre, Dominique & Julian-Reynier, Claire, 2012. ""They should take time": Disclosure of clinical trial results as part of a social relationship," Social Science & Medicine, Elsevier, vol. 75(5), pages 873-882.
    19. Alison Kenner, 2021. "Emplaced care and atmospheric politics in unbreathable worlds," Environment and Planning C, , vol. 39(6), pages 1113-1128, September.
    20. Rodrigues, Carla F., 2021. "Communicative trust in therapeutic encounters: users’ experiences in public healthcare facilities and community pharmacies in Maputo, Mozambique," Social Science & Medicine, Elsevier, vol. 291(C).

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:eee:socmed:v:165:y:2016:i:c:p:246-254. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Catherine Liu (email available below). General contact details of provider: http://www.elsevier.com/wps/find/journaldescription.cws_home/315/description#description .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.