Hello and welcome to my website! I am an Assistant Professor of Philosophy at the University of Massachusetts Lowell and the 2017-19 Rice Family Fellow in Bioethics and Humanities at The Hastings Center.
My work centers on the relationship between bodies, values, and society, and their effects on wellbeing. I am especially concerned with the meaning of disability and the issue of ableism, and how philosophical inquiry into each might improve the lives of people with disabilities and the justness of social institutions ranging from medicine to politics. Towards this aim and working to bring reflective and empirical studies together, my research revolves around five key areas:
- Ableism in the History of Ideas
- Epistemic Injustice in Healthcare
- Philosophy of Disability (Continental and Analytic)
- Phenomenology and Medicine
- ELSI (Ethical, Legal, and Social Implications) Research in Genomics
Accordingly, the majority of my scholarship occurs at the intersection of bioethics, philosophy of disability and disability studies, 19th-20th century American and European philosophy (esp. phenomenology), and applied epistemology. I also draw heavily from feminist philosophy (esp. care ethics), philosophy of medicine, and medical humanities.
I am the author of Ethics After Ableism: Disability, Pain, and the History of Morality, forthcoming with The University of Minnesota Press in 2019. With Christine Wieseler, I am co-editor of The Disability Bioethics Reader, currently under proposal review with Routledge. It will be the first general introduction to bioethics through the lens of critical disability studies and philosophy of disability. I am also co-editor, with Erik Parens, of a special issue of The Hastings Center Report on “The Gift and Weight of Genomic Knowledge: In Search of the Good Biocitizen,” forthcoming in winter 2019 and based upon a co-organized conference held on that theme at Brooklyn Law School in late 2018. In addition to a series of articles, my current research is developing into a new book, Justice and the Future of Health. Other ongoing projects include studies on the intersection of hermeneutic phenomenology and narrative medicine, epistemic injustice and ableism, care ethics and the “duty to know,” the history of modern medicine and bioethics, disability-related ELSI research in genomics, and the role of epistemologies of ignorance in healthcare delivery.
Articles and commentaries of mine have appeared in the American Journal of Bioethics, AJOB Neuroscience, Hypatia: A Journal of Feminist Philosophy, The Hastings Center Report, AMA Journal of Ethics, Chiasmi International, The Review of Communication, and Philosophy, Ethics, and Humanities in Medicine. Book chapters of mine have or will soon appear in volumes including The Handbook of Genetic Counseling, Applying Nonideal Theory to Bioethics, 50 Concepts for a Critical Phenomenology, Philosophy of Disability: New Perspectives, Disability and American Philosophies, UnMuted: Conversations on Prejudice, Oppression, and Social Justice, and Disability in American Life. My public philosophy has been featured in TIME, HuffPost, AEON, and Tedx.
I received my PhD and MA in Philosophy from Emory University and my BA in Philosophy as well as Religious Studies from the Robert D. Clark Honors College at the University of Oregon. My doctoral research was supported by fellowships from Emory University, the Andrew W. Mellon Foundation, and the Howard Hughes Medical Institute.