April 19 | Food For Thought’s Unequal Healthscapes in California’s “Biohub”

Wednesday, April 19th
5:30-7:30 pm
Namaste Lounge

Hosted by the College Nine and Ten CoCurricular Programs Office, SJRC Assistant Director, Kate Weatherford Darling will present her research centering social justice and health inequalities in the discussion of biomedicine and US healthcare and policy. Asking the question: What would it take to build new California “healthscapes” (Clarke 2010) with visions of disability justice and health equity?

Unequal Healthscapes in California’s “Biohub”

California’s recent Tech Boom buoyed the Bay Area economy and transformed the political geography of the state and a global center of wealth. Venture capital / philanthropic investment along with public policies to promote “entrepreneurism” are rapidly changing the spaces, places of biomedical science and healthcare practice. In this talk, Kate offers an incomplete map of our unequal “healthscapes” (Clarke 2010), the cultural, economic and political terrains of health. Drawing on findings from her current and forthcoming research, she asks: What would it take to build new California healthscapes with visions of disability justice and health equity?

Katherine Weatherford Darling is Assistant Director at the Science and Justice Research Center and faculty in UCSC Sociology Department. Her research and teaching bridges Sociology of Health, Illness and Disability and Feminist Science Studies. Her current projects span diverse topics including: Post-Genomic epidemiology and HIV/AIDS science and health policy in the U.S. With UCSC and Bay Area collaborators, her new projects examine how the social and built environments of Bay Area’s tech and biotech economies are impacting the health of low-income Californians.

Flyer for Food for Thought

Flyer for Food for Thought

Digital Dreams and Their Discontents: Where do we go from here?

Wednesday, April 20, 2016 | 4:00 – 5:30PM | SJRC Common Room (Oakes 231)

A conversation with Erin McElroy (PhD Candidate, Feminist Studies, UCSC) and Sara Tocchetti (SJRC Visiting Scholar, Postdoctoral Fellow, Centre Alexandre Koyré, Paris, France).

Erin McElroy on the Digital Nomad

With the emergence of Silicon Valley’s “Tech Boom 2.0,” so too has emerged the figure of the “digital nomad”—a type of transient technologic worker tethered to Silicon Valley corporations yet able to embody new mobilities vis-à-vis the globalization of high-speed fiber-optics and sharing economy infrastructure. From San Francisco to new global outposts such as Romania, which boasts the world’s fifth fastest internet speed due to postsocialist technologic economization, the arrival of the digital nomad often incites contexts of gentrification, manifesting as increased rental prices, eviction rates, and forced homelessness/nomadism. Critical of this correlation as well as formative histories of nomadic racial fantasy, I also question what other uses of digital technology, such as that of the Anti-Eviction Mapping Project, emerge not just to critique technologies of displacement, but also to fight for other futures of the digital?

Erin McElroy is a Doctoral Student in Feminist Studies at UC Santa Cruz and cofounder/director of the Anti-Eviction Mapping Project, a digital cartography and oral history collective documenting the ecology of “Tech Boom” induced gentrification. McElroy brings a spatial analysis and collective ethos to their research, which studies materializations and histories of dispossessive technologies in Romania, employing ethnography, literary/cultural analysis, and archival work, and utilizing postsocialist analytics and feminist science and technology studies. McElroy holds a MA in Cultural Anthropology from CIIS and a BA in Cultural Studies from Hampshire College, and is an active anti-eviction organizer with Eviction Free San Francisco.

Sara Tocchetti on DIYbio and the Possibility of Critical Life Sciences

Drawing from the analogy with the personal computer and other personalized technologies, DIYbio members envision biology and biotechnology as a creative and personal technology to be made available to everyone. Such ideology of a ‘personal biology’ can be understood as a variation of ‘digital utopianism’ and seems especially attractive for young and/or disenfranchised students and researchers. Working through several case studies of DIYbio initiatives and engaging with a general sense of enthusiasm for such practices expressed in the STS literature, this presentation questions what type of critical space does digital utopianism occupies in the life sciences and STS and what forms of alternative practices we might need to recollect and/or imagine.

Sara Tocchetti recently received her PhD from the London School of Economics working on the DIYbio network, socio-technical utopias, theories of technology driven social change, and her own professional identity. Feeling stuck as an ex-biologist-not-yet turned into a science and technology studies scholar, she has moved on to study the history and present of radical science movements and is currently based at the Centre Alexandre Koyré in Paris on an Early Post-doc Scholarship from the Swiss National Fund. Her recent publications includes Is an FBI Agent a DIY Biologist Like Any Other? A Cultural Analysis of a Biosecurity Risk (Tocchetti and Aguiton, 2015) and Quelles tactiques critiques sur le terrain des promesses scientifiques [Which critical tactics in the field of scientific promises] (Aguiton, Bovet and Tocchetti, 2015).

Fixing the Pathological Body

fixing-the-pathological-body-potserThe medical industry leans heavily upon a distinction between the “normal” and the “pathological.” How and why do we continue to define this distinction, and for whom are these categories useful?  What are some alternative ways to organize the lived experiences of human bodies and/or minds?

A Panel Discussion with Janette Dinishak (Assistant Professor of Philosophy at UCSC) Kelly Ormond (Professor of Genetics and Genetic Counselor at Stanford University) Matthew Wolf-Meyer (Associate Professor of Anthropology at UCSC and author of The Sleeping Masses).Organized by Science & Justice Training Program Fellows Sandra Harvey (Politics), Linda Dayem (Philosophy) and Jessica Neasbitt (History of Consciousness). Co-Sponsored by UCSC Departments of History of Consciousness, Literature, and Philosophy, as well as the Institute for Humanities Research.

Read Rap Report > Fixing the Pathological Body – Report by Jess Neasbitt 

Janette Dinishak is an Assistant Professor of Philosophy at the University of California, Santa Cruz. Her research interests include philosophy and history of psychology and psychiatry (especially autism), Wittgenstein, philosophy of mind, disability, and ethical theory.

Kelly Ormond is a Professor of Genetics at the Stanford School of Medicine. While Ormond’s primary role is to direct the MS in Human Genetics and Genetic Counseling program, her research focuses on the intersection between genetics and ethics, particularly around the translation of new genetic technologies (such as genome sequencing or non-invasive prenatal diagnosis) into clinical practice. She is especially interested in patient decision making, informed consent, and the interface between genetics and disability.

Matthew Wolf-Meyer is an Associate Professor of Anthropology at the University of California, Santa Cruz. He received his Ph.D. from the Department of Anthropology at the University of Minnesota, specializing in medical anthropology, the social study of science and technology, and neuroscience. He is author of The Slumbering Masses: Sleep, Medicine and Modern American Life (UMN Press, 2012), which focuses on sleep in American culture and its historical and contemporary relations to capitalism. His second book, What Matters: The Politics of American Brains, focuses on the ethical and epistemological practices in contemporary neuroscience, cybernetics, disability activism, and psychoanalysis in American society. Currently he is in the early stage of a new project focused on the neurological turn to the gut as an extension of the nervous system, the history of shit in the United States, and the therapeutic uses of human excrement in modern medicine.

April 22, 2015

Trust in Genomics: A challenge for scientists and ethicists alike

Rap Report > Trust in Genomics: A Challenge for Scientists and Ethicists Alike

Access to data and the quality of data depend partially on the quality of trust between physicians, researchers and many different patients.  When trust breaks down, patients and research subjects may request that their samples be withdrawn, or they may not provide samples and data in the first place. Technological developments that enable biomedical institutions to bank vast quantities of tissues and data today introduce new challenges to this critical project of creating and maintaining trust.  Any tissue now given for research or routine medical care technically could be used for an indefinite amount of time for entirely unforeseen purposes. In such a situation, it is hard to say that anyone understands what they are consenting to, even the researchers and physicians collecting samples and running trials.  Under these conditions, trust based in mutual understanding faces new challenges.

How to address these novel challenges will be at the center of the Science & Justice Working Group meeting on April 16, 2014, “Trust in Genomics: A Problem of Knowledge and Ethics”, 4:00-6:00PM in Engineering 2 599 on the UCSC campus. In this discussion, respected medical geneticist Wylie Burke (University Washington) and cultural anthropologist and bioethicist Barbara Koenig (UCSF) will share their experiences working with biobanks, researchers and patients to build better data sets by attending to matters of trust and respect.

Dr. Barbara Koenig, professor of medical anthropology and bioethics in the UCSF School of Nursing, is the co-Director of a newly launched research institute at UCSF dedicated to understanding the ethical, legal and social implications of translational medical genomics, The Center for Transdisciplinary ELSI Research in Translational Genomics (CT2G). By bringing together a broad, multidisciplinary range of expertise, CT2G is endeavoring to ask, and answer, questions about how genomic information will be used in a manner that benefits researchers, patients and broader publics. “A decade after the human genome was fully mapped,” Koenig argues, “figuring out how to translate genomic findings into prevention and clinical care has become a public health priority.”

Dr. Wylie Burke, Professor of Bioethics and Humanities at the University of Washington and Principal Investigator of the University of Washington Center for Genomics and Healthcare Equality, co-authored an article in Science (Trinidad et al., 2011) that highlighted the potential benefits of approaching consent (and re-consent) as an opportunity to engage with donors beyond legal formalities. She and her co-authors examine the downstream consequences of not thoroughly consenting donors for the use of their biological materials and data. Drawing on cases that have appeared in the headlines, such as the sequencing of the HeLa cell line, they examine the wide range of opinions about how best to protect patient privacy and dignity in an age when even experts cannot anticipate how biological samples might be used in the near future. In the article, they propose that “researchers and IRBs consider how the informed consent process could be used to foster respectful engagement, rather than merely mitigate risk.”

This discussion is the second in a series of discussions that the SJRC is hosting on Data Justice (see Science and Justice in an Age of Big Data: A Conversation with Peter Yu and David Haussler for a description of the first meeting held on January 22, 2014).  The meeting is co-sponsored by the Department of Molecular, Cellular, and Developmental Biology, the Center for Biomolecular Sciences and Engineering, and the GENECATS and CANCERCATS research groups.

April 16, 2014 | Engineering 2 Room 599    

 

When does personhood begin? The Science and the Rhetoric

Renowned developmental biologist Scott Gilbert (Swarthmore) joins us to discuss the science and rhetoric of personhood from a cross-disciplinary perspective. The argument that a potential human adult should be given the status of “person” from the moment of conception is being frequently made by people who wish to make abortion and human stem cell research illegal. While “personhood” is a cultural and not a scientific category, biology is often being used to justify such claims. Biologists, however, have not reached consensus on this issue, and this talk will discuss some of the places where different groups of biologists have claimed “personhood” begins. These include fertilization, individuation/gastrulation (when the embryo can no longer form twins), the acquisition of the human-specific EEG pattern, and birth. The rhetoric surrounding the fertilization issue concerns the photographs of prenatal life and the cultural representation of DNA as our soul or essence.

Rap Report Scott Gilbert: When Does Personhood Begin? The Science and the Rhetoric

Paper available for pre-reading: Gilbert – When Does Personhood Begin?

Cosponsored by the Molecular, Cellular, and Developmental Biology Department

November 13, 2012 | 4:00-6:00 PM |Engineering 2, Room 599

Modelling pigs and humans: Exploring the practices of models across sciences

Wednesday October 19, 2011

Engineering 2, Room 599

PhD Fellow Vibeke Pihl, Medical Centre for Science and Technology Studies, Department of Public Health, University of Copenhagen.

Vibeke Pihl’s research addresses how connections between humans and animals are shaped in contemporary biomedical research on human health. During an ethnographic multi-sited fieldwork, Vibeke has followed a group of Danish biomedical researchers working to establish a pig model for human obesity surgery. In biomedicine, the pig is increasingly established as a preferred model organism in biomedical research on human obesity due to an argued biological resemblance between pigs and human anatomy and physiology. The topic of the SJWG event concerns an analysis of how the use of pigs as models for humans does not rest solely on biological connections, but requires social, moral, economical and cultural connections to support the choice of the pig as the appropriate model for obese human bodies. In addition, the presentation will address how models are practised in biomedical science and social science. Drawing upon fieldwork, the presentation will focus on how the analysis of the biomedical researchers’ establishment of a pig model prompt a simultaneous crafting of a social scientific model of human-animal relations. Vibeke asks which connections between humans and pigs are included and excluded in the research practices of biomedical scientists’ and the practices of social scientists like her own. With this presentation, Vibeke wants to provide an opening for a stronger mutual engagement between researchers across sciences working with animals as models of humans.