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Toward a phenomenology of congenital illness: a case of single-ventricle heart disease

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Abstract

Phenomenology has contributed to healthcare by providing resources for understanding the lived experience of the patient and their situation. But within a burgeoning literature on the characteristic features of illness, there has not yet been an account appropriate to describe congenital illnesses: conditions which are present from birth and cause suffering or medical threat to their bearers. Congenital illness sits uncomfortably with standard accounts in phenomenology of illness, in which concepts such as loss, doubt, alienation and unhomelikeness presuppose prior health. These accounts reflect, in different ways, Maurice Merleau-Ponty’s assumption that the ways of living of the ill contain allusions to fundamental, healthy functions. The originality of congenital illness complicates this assumption and demands its own original phenomenology. In this paper, I sketch my personal experience living with a single-ventricle heart condition. While some of this story may reflect my own idiosyncratic experience, I hope that much of it will resonate with the congenital illness experience. I argue that the phenomenological literature on illness, grounded in the notion of loss, does not describe the congenital illness experience. I show how a number of other patient-centred theories of health and illness which have been influential on phenomenology can and cannot elucidate congenital illness. In particular, I consider Georges Canguilhem’s account of the normal and the pathological; debates in disability; and the notion of illness as biographical disruption. I show that congenital illness results in the preadmission of its patients to a paradoxical logic of medical palliation, one product of which is existential maturity.

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References

  • Berghammer, Malin C., Eva Brink, Annika M. Rydberg, Mikael Dellborg, and Inger Ekman. 2015. Committed to life: Adolescents’ and young adults’ experiences of living with fontan circulation. Congenital Heart Disease 10 (5): 403–412.

    Article  Google Scholar 

  • Bury, Michael. 1982. Chronic illness as biographical disruption. Sociology of Health & Illness 4 (2): 167–182.

    Article  Google Scholar 

  • Canguilhem, Georges. 1989. The Normal and the Pathological. Trans. Carolyn R. Fawcett, and Robert S. Cohen. New York: Zone Books.

    Google Scholar 

  • Carel, Havi. 2016. Phenomenology of illness. Oxford: Oxford University Press.

    Book  Google Scholar 

  • Carricaburu, Danièle, and Janine Pierret. 1995. From biographical disruption to biographical reinforcement: The case of HIV-positive men. Sociology of Health & Illness 17 (1): 65–88.

    Article  Google Scholar 

  • Ciesemier, Kendall and Jameson Rich. 2019. The Dystopian World of Diabetes feat. Maris Kreizman. Podcast. That That Don't Kill Me.

  • Clare, Eli. 2015. Exile and pride: Disability, queerness, and liberation. Durham: Duke University Press.

    Book  Google Scholar 

  • Cordina, Rachael, Karin du Plessis, Derek Tran, and Yves d’Udekem. 2018. Super-Fontan: Is it possible? The Journal of Thoracic and Cardiovascular Surgery 155 (3): 1192–1194.

    Article  Google Scholar 

  • DeMaso, David R., Johanna Calderon, George A. Taylor, Jennifer E. Holland, Christian Stopp, Matthew T. White, David C. Bellinger, Michael J. Rivkin, David Wypij, and Jane W. Newburger. 2017. Psychiatric disorders in adolescents with single ventricle congenital heart disease. Pediatrics 139 (3): e20162241.

    Article  Google Scholar 

  • du Plessis, Karin, Rebecca Peters, Ingrid King, Kirsty Robertson, Jonathan Mackley, Rachel Maree, Tracy Stanley, et al. 2018. “How long will I continue to be normal?” Adults with a Fontan circulation’s greatest concerns. International Journal of Cardiology 260: 54–59.

    Article  Google Scholar 

  • Faircloth, Christopher A, Craig Boylstein, Maude Rittman, Mary Ellen Young, and Jaber Gubrium. 2004. Sudden illness and biographical flow in narratives of stroke recovery. Sociology of Health & Illness 26 (2): 242–261.

    Article  Google Scholar 

  • Parsons, Talcott. 1951. The social system. London: Routledge and Kegan Paul.

    Google Scholar 

  • Parsons, Talcott. 1975. The sick role and the role of the physician reconsidered. Milbank Memorial Fund Quarterly Health and Society 53 (3): 257–278.

    Article  Google Scholar 

  • Rabinow, Paul. 1996. Georges Canguilhem: A vital rationalist. In Essays on the anthropology of reason. Princeton: Princeton University Press.

    Google Scholar 

  • Rychik, Jack, Andrew M. Atz, David S. Celermajer, Barbara J. Deal, Michael A. Gatzoulis, Marc H. Gewillig, Tain-Yen. Hsia, et al. 2019. Evaluation and management of the child and adult with fontan circulation: A scientific statement from the american heart association. Circulation 140 (6): e234–e284.

    Article  Google Scholar 

  • Rychik, Jack, and Yuli Kim. 2018. The adolescent and adult with a fontan circulation: “Unnatural” selection and survival of the fittest. Journal of the American College of Cardiology 71 (9): 1018–1020.

    Article  Google Scholar 

  • Shilling, Chris. 2002. Culture, the ‘sick role’ and the consumption of health. The British Journal of Sociology 53 (4): 621–638.

    Article  Google Scholar 

  • Svenaeus, Fredrik. 2011. Illness as unhomelike being-in-the-world: Heidegger and the phenomenology of medicine. Medicine, Health Care, and Philosophy 14 (3): 333–343.

    Article  Google Scholar 

  • Toombs, S. Kay. 1992. The meaning of illness: A phenomenological account of the different perspectives of physician and patient. Dordrecht: Kluwer Academic Publishers.

    Book  Google Scholar 

  • Toombs, S. Kay. 2001. Reflections on bodily change: The lived experience of disability. In Handbook of phenomenology and medicine, ed. S. Kay Toombs, 247–261. Dordrecht: Kluwer Academic Publishers.

    Chapter  Google Scholar 

  • Wendell, Susan. 2001. Unhealthy disabled: Treating chronic illnesses as disabilities. Hypatia 16 (4): 17–33.

    Article  Google Scholar 

  • Zaner, Richard M. 1981. The context of self: A phenomenological inquiry using medicine as a clue. Athens: Ohio University Press.

    Google Scholar 

  • Zeiler, Kristin, and Lisa Folkmarson Käll. 2014. Feminist phenomenology and medicine. Albany: State University of New York Press.

    Google Scholar 

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Funding

This research is supported by an Australian Government Research Training Program (RTP) Scholarship.

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Correspondence to Pat McConville.

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McConville, P. Toward a phenomenology of congenital illness: a case of single-ventricle heart disease. Med Health Care and Philos 24, 587–595 (2021). https://doi.org/10.1007/s11019-021-10026-3

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