Podcasts about The Hastings Center

This lecture discusses key ideas from the 20th and 21st century philosopher and moral theorist, Alasdair MacIntyre's short address "Designing Our Descendants: Seven Traits for the Future", a presentation to the 1978 general meeting at the Hastings Center. MacIntyre first discusses how intentionally designing descendants is a matter that has political dimensions, then sets out seven key traits that he thinks are most needed, and concludes with projections of what the lives of people in a society where these traits are widespread would look like. The seven traits in a "new table of virtues" MacIntyre identifies and discusses are: Ability to live with uncertainty (and an unpredictable environment) Roots in particularity (a capacity for finding a particular and local way of being a home in the world) A commitment to non-manipulative modes of relationship with people and nature Finding a vocation in one's work (an ability to find a work that is peculiarly our own to do in the world) Accepting one's death (recognition that there will come a time when one's life is complete) Hope (a spirit of hope for which there cannot be adequate empirical grounds) Willingness to take up arms (to go to war and to acquire the skill necessary to win a war) To support my ongoing work, go to my Patreon site - www.patreon.com/sadler If you'd like to make a direct contribution, you can do so here - www.paypal.me/ReasonIO - or at BuyMeACoffee - www.buymeacoffee.com/A4quYdWoM You can find over 3,500 philosophy videos in my main YouTube channel - www.youtube.com/user/gbisadler You can get MacIntyre's After Virtue here - amzn.to/2RiplGT

A newly available kind of genetic testing, called polygenic embryo screening, promises to screen for conditions that can include cancer, obesity, autism, bipolar disorder, even celiac disease. These conditions are informed by many genetic variants and environmental factors - so companies like Orchid and Heliospect assign risk scores to each embryo for a given condition. These tests are expensive, only available through IVF, and some researchers question how these risk scores are calculated. But what would it mean culturally if more people tried to screen out some of these conditions? And how does this connect to societal ideas about whose lives are meaningful? Brittany gets into it with Vardit Ravitsky, senior lecturer at Harvard Medical School and president of the Hastings Center, a non-partisan bioethics research center, and Katie Hasson, associate director of the Center for Genetics and Society, a nonprofit public affairs organization that advocates for responsible use of genetic technology.Learn more about sponsor message choices: podcastchoices.com/adchoicesNPR Privacy Policy

Happy holidays from BITM! We are delighted to share this episode with you this week. Kirk and Amelia sat down with Dr. Donald Carter III, assistant professor at Mercer School of Medicine. Dr. Carter earned his Doctorate in Bioethics from Loyola University after earning a Masters in Divinity from Vanderbilt and an MBA from Tennessee State. He is a Sadler Scholar with the Hastings Center and the co-chair of the Race and Culture and Ethnicity (RACE) affinity group of the American Society for Bioethics and Humanities (ASBH). Dr. Carter began his career as a musician after earning a BA in music from Fisk University, one of the many Historically Black Colleges and Universities (HBCUs) in the United States. This episode is a great one for those who are curious about pursuing a career in Bioethics. Dr. Carter shared how he explored several career paths before ultimately finding his professional home in Bioethics. Dr. Carted discussed his work exploring the impacts of the 1910 Flexner report, which, while contributing to creating uniform standards for medical education, also resulted in the closing of 5 of the 7 medical schools within HBCUs. This is one of the reasons for the shortage of Black physicians that persists today. He discussed the importance of diversifying the field of Bioethics and the positive changes he has observed within ASBH over the past few years. He shared how he views HBCUs as an important resource to tap to help diversify the field. He recommends building up bioethics education at HBCUs as a way of fostering lasting change. He also discussed the importance of humanities in medical education, sharing his experiences using visual training strategies (VTS) in medical education, reminding us that the arts have a way of returning us to a place where we can see each other as full humans again. Dr. Carter pointed out that one of the superpowers of the field of Bioethics is that we have a large tent. He examined specific ways in which racial, cultural and professional diversity can enhance the value our field brings to patients and communities.

When health care meets ethics, our choices reveal as much about our values as they do about our scientific advances. In this episode, Vardit Ravitsky, President and CEO of the Hastings Center, highlights the role of bioethics in navigating complex health care choices, especially those made prominent by the pandemic. She describes bioethics as interdisciplinary, involving collaboration across philosophy, sociology, and other fields to address ethical issues like justice, equity, and patient autonomy. Her journey into bioethics began with personal experiences that led her to explore the intersections of technology and core human values, such as family and kinship. Looking ahead, Vardit identifies artificial intelligence and climate change as the next major ethical challenges in health care, with AI potentially increasing access but presenting risks like bias and privacy concerns. Viewing bioethics as a guide for responsible innovation, she sees the Hastings Center as dedicated to public engagement, policy influence, and fostering diversity within bioethics. Tune in and dive into the heart of bioethics, exploring how our most challenging health care decisions reflect who we are and shape the future of medicine! Learn more about your ad choices. Visit megaphone.fm/adchoices

How do we keep technology from slipping beyond our control? That's the subtitle of the latest book by our guest in this episode, Wendell Wallach.Wendell is the Carnegie-Uehiro fellow at Carnegie Council for Ethics in International Affairs, where he co-directs the Artificial Intelligence & Equality Initiative. He is also Emeritus Chair of Technology and Ethics Studies at Yale University's Interdisciplinary Center for Bioethics, a scholar with the Lincoln Center for Applied Ethics, a fellow at the Institute for Ethics & Emerging Technology, and a senior advisor to The Hastings Center.Earlier in his life, Wendell was founder and president of two computer consulting companies, Farpoint Solutions and Omnia Consulting Inc.Selected follow-ups:Wendell Wallach Personal WebsiteWendell Wallach - Carnegie Council for Ethics in International AffairsThe Artificial Intelligence & Equality InitiativeNobel Peace Prize Lecture by Christian Lous Lange (1921)Thomas Midgley Jr. - WikipediaMontreal Protocol - WikipediaRobot Dog Highlighted at China-Cambodia Joint Military Exercise (video)For Our Posterity - essay by Leopold AschenbrennerCampaign by Control/AI against deepfakesMusic: Spike Protein, by Koi Discovery, available under CC0 1.0 Public Domain Declaration

In this episode I will be discussing the topic of abortion with a philosopher who has studied the moral arguments on both sides of the issue. I am interested in rational bases of moral decision making. I'd like to be able to work out moral rules from a set of socially acceptable first principles, but often I find that my moral intuition conflicts with what I derive as a rational morality. Is our morality wrong if it is not totally consistent, or is morality not derivable from precepts? I'd like to understand how these ideas apply to the topic of abortion ethics. Bonnie Steinbock is professor emerita of the Department of Philosophy at the University at Albany/State University of New York. A Fellow of the Hastings Center, she has been a visiting professor at Santa Clara University (2012), the Chinese University of Hong Kong (2015) and Monash University in Melbourne, Australia (2017). In addition to 70 articles, she is the author of Life Before Birth: The Moral and Legal Status of Embryos (Oxford University Press, 1992, 2011) and the editor or co-editor of several collections, including Killing and Letting Die (1980, 1994), New Ethics for the Public's Health (1999), Public Health Ethics: Theory, Policy, and Practice (2006), the Oxford Handbook of Bioethics (2008), and Ethical Issues in Modern Medicine, 4th - 8th editions. Her latest book, co-written with Paul Menzel, is Bioethics: What Everyone Needs to Know (Oxford University Press, 2023). Please support the podcast at patron.podbean.com/TheRationalView Join the Facebook discussion @TheRationalView Instagram @The_Rational_View Twix @AlScottRational

Amelia and Kirk chat with Dr. Mark Kuczewski, Professor of Medical Ethics at Loyola University, Chicago. In this episode, they discuss his recent article https://www.healthaffairs.org/content/forefront/nonprofit-health-care-behaves-badly-case-mission-leaders-ombudsmen in which Dr. Kuczewski elucidates the challenges nonprofit healthcare employees face as workplace culture becomes increasingly corporatized and the importance of counterweights– in the form of ombudsmen, better-designed incentive structures, and virtuous local board members– who can potentially help promote the nonprofit mission for patients. They also discuss Dr. Kuczewski's publication on organizational ethics and the importance of hiring for mission (https://www.researchgate.net/publication/6121839_Is_Organizational_Ethics_the_Remedy_for_Failure_to_Thrive_Toward_an_Understanding_of_Mission_Leadership).Dr. Kuczewski describes the “patchwork” of healthcare available to undocumented immigrants and the need to sever the tie between immigration status and healthcare access and talks about his work with Loyola University Chicago Stritch School of Medicine to accept DACA recipients into its program.Dr. Kuczewski is the Father Michael I. English S.J. Professor of Medical Ethics at Loyola University, Chicago, the director of the Neiswanger Institute for Bioethics and Health Policy, and a Fellow of the Hastings Center. His current interests include the bioethical issues related to immigration. He served as the project manager of the Loyola University Chicago Stritch School of Medicine effort to include Dreamers in medical education, wherein Stritch became the first medical school in the nation to welcome applications from Dreamers of DACA status. https://www.luc.edu/stritch/bioethics/aboutus/facultydirectory/profiles/kuczewskimark.shtml

Back in the 1960s, a committee of seven Seattle residents met regularly to decide which patients with chronic kidney disease were “worthy” of life-saving dialysis.  Whoever wasn't selected by the committee would likely die within months. An exposé of this so-called “God Squad” helped spark the formation of a new field: bioethics. In this prequel to playing god?, we'll find out how this committee made life-and-death decisions, and why something like it is unlikely to happen again.  Show Notes: This episode features interviews with:  Rick Mizelle, Jr., Associate Professor of History, University of Houston Kate Butler, Assistant Professor of Nephrology, University of Washington School of Medicine The God Squad was just one of many notable cases that led to the formation of the field of bioethics. The Hastings Center, a bioethics research institute, has compiled a timeline of many of the most famous cases and their impact. Check it out here.  The Berman Institute has also collected oral histories– first hand accounts of the doctors, philosophers, lawyers and other scholars who were involved in many of these cases. You can explore that collection here.  To learn more about the ethics issues raised in this episode, visit the Berman Institute's episode guide.  The Greenwall Foundation seeks to make bioethics integral to decisions in health care, policy, and research. Learn more at greenwall.org.See omnystudio.com/listener for privacy information.

Back in the 1960s, a committee of seven Seattle residents met regularly to decide which patients with chronic kidney disease were “worthy” of life-saving dialysis.  Whoever wasn't selected by the committee would likely die within months. An exposé of this so-called “God Squad” helped spark the formation of a new field: bioethics. In this prequel to playing god?, we'll find out how this committee made life-and-death decisions, and why something like it is unlikely to happen again.  Show Notes: This episode features interviews with:  Rick Mizelle, Jr., Associate Professor of History, University of Houston Kate Butler, Assistant Professor of Nephrology, University of Washington School of Medicine The God Squad was just one of many notable cases that led to the formation of the field of bioethics. The Hastings Center, a bioethics research institute, has compiled a timeline of many of the most famous cases and their impact. Check it out here.  The Berman Institute has also collected oral histories– first hand accounts of the doctors, philosophers, lawyers and other scholars who were involved in many of these cases. You can explore that collection here.  To learn more about the ethics issues raised in this episode, visit the Berman Institute's episode guide.  The Greenwall Foundation seeks to make bioethics integral to decisions in health care, policy, and research. Learn more at greenwall.org.See omnystudio.com/listener for privacy information.

In our Mental Health Mini-Series we have our friend Dr. Sammy Kim join us! Rev. Dr. Sam D. Kim is the Co-founder of 180 Church, near Union Square in downtown Manhattan. Dr. Kim is a Yale-Hastings Scholar at the Hastings Center exploring the crisis of physician burnout in academic medicine and health care from an ethical perspective in partnership with the University of Pennsylvania. He was appointed as a research Fellow in Global Health and Social Medicine at the Center for Bioethics at Harvard Medical School and part of Harvard catalyst, where he explored and taught on inequities surrounding health, immigration and social policies. He is also the author of the book "A Holy Haunting" available here: https://amzn.to/3G0p8Bc www.fyi-podcast.com | www.youngadults.today 

Discusses ethical and policy considerations for xenotransplantation clinical trials.Our guest today is Karen Maschke, a Senior Research Scholar at The Hastings Center and editor of The Hastings Center's journal Ethics & Human Research. Her work focuses on ethical, regulatory, and policy issues associated with developing and using new biotechnologies.Additional resource:· The Hastings Center “Ethical and Policy Guidance for Translational Xenotransplantation Clinical Trials:” https://www.thehastingscenter.org/who-we-are/our-research/current-projects/ethical-and-policy-guidance-for-translational-xenotransplantation-clinical-trials/

Dr. Rosemarie Garland-Thomson, Professor Emerita of English and bioethics at Emory University and senior advisor at the Hastings Center, talks about rethinking visibility, identity, and access for those with disabilities, and the implications for everyone. Listeners can keep up with ICS happenings by following us on Twitter and Instagram at icsbgsu, and on our Facebook page. You can listen to big ideas wherever you find your favorite podcasts. Please subscribe and rate us on your preferred platform. For more information or to suggest an episode topic, visit us at bgsu.edu/bgideas.

In this podcast, we cover - 1. Nuances of biochemical interventions into love and relationships  2. Ethics of deciding which medications should be a part of our society 3. The art of calibration within yourself to negotiate with your ideals of self worth Brian is a Senior Research Fellow in the Uehiro Centre for Practical Ethics at the University of Oxford, Associate Director of the Yale-Hastings Program in Ethics and Health Policy at Yale University and The Hastings Center, and Associate Editor of the Journal of Medical Ethics. Brian's work is cross-disciplinary, following training in philosophy, cognitive science, psychology, history and sociology of science and medicine, and ethics. A co-recipient of the 2018 Daniel M. Wegner Theoretical Innovation Prize from the Society for Personality and Social Psychology, Brian was also one of four named finalists for the 2020 John Maddox Prize for “standing up for science” (awarded by Sense about Science and Nature). Brian is also recipient of both the Robert G. Crowder Prize in Psychology and the Ledyard Cogswell Award for Citizenship from Yale University, where, as an undergraduate, Brian was elected President of the Yale Philosophy Society and served as Editor-in-Chief of the Yale Philosophy Review. Brian then conducted graduate research in psychological methods as a Henry Fellow of New College at the University of Oxford, followed by a degree in the history, philosophy, and sociology of science, technology, and medicine as a Cambridge Trust Scholar and Rausing Award recipient at Trinity College at the University of Cambridge. After spending a year in residence as the inaugural Presidential Scholar in Bioethics at The Hastings Center in Garrison, New York, Brian was appointed Benjamin Franklin Resident Graduate Fellow while completing a dual Ph.D. in philosophy and psychology at Yale University. Brian's essays have been translated into Polish, German, Italian, Spanish, French, Portuguese, Japanese, and Hebrew.

Professor Larry R. Churchill, Emeritus Professor of Medical Ethics at Vanderbilt, discusses “Biotethics Reenvisioned,” a just-published book he co-authored with Wake Forest Professor Nancy M. P. King and UNC Professor Gail E. Henderson. The authors, appropriately, argue “bioethics needs an expanded vision” or beyond one that has predominately focused on patient autonomy, beneficence and nonmaleficence.  The field needs to take “a more robust role” they write and begin to address upstream issues including social determinants, health disparities, structural racism, or in sum begin to meaningfully address social or distributive justice.  The field needs to move beyond what the authors' term “lifeboat ethics” or “lifeboat framing” where issue beyond the bedside are largely if not completely ignored. The impetus for their thinking is largely, no surprise, the COVID pandemic that according the CDC has to date been responsible for 1.35 million excess deaths. During this 31-minute interview Professor Larry Churchill begins by defining “lifeboat ethics.” He discusses the harm or damage caused by the failure by the bioethics filed to address upstream justice issues resulting from social determinants, He briefly discusses scholars, e.g., Charles Taylor and Norman Daniels, who have productively commented on the social dimensions of justice and his sense of how their lifeboat framework criticism been received by the profession. We discuss at some length the book's last and lengthiest chapter “Bioethics and the Global Warming Crisis” and what bioethicists working on issues of social justice can do to educate, improve public literacy and inform policy. Larry R. Churchill is Professor of Medical Ethics Emeritus, Vanderbilt University Medical Center. Prior to Professor Churchill taught at the University of North Carolina at Chapel Hill where he was Chair of the Department of Social Medicine. Professor Churchill is a member of National Academy of Medicine and a Fellow of The Hastings Center. He is the author of seven books, including Ethics for Everyone: A Skills-Based Approach (2020, Oxford University Press). Churchill's work has been featured in popular media such as USA Today, The New York Times, Bill Moyers' Journal, and the Alex Gibney documentary Money-Driven Medicine. Information on the book is at: https://uncpress.org/book/9781469671581/bioethics-reenvisioned/. This is a public episode. If you would like to discuss this with other subscribers or get access to bonus episodes, visit www.thehealthcarepolicypodcast.com

In this episode of the COVID Ethics Series Podcast, Dr. Bryan Pilkington speaks with Dr. Joel Reynolds, Assistant Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Senior Bioethics Advisor to and Fellow of The Hastings Center, and Faculty Scholar of The Greenwall Foundation. Dr. Reynolds is especially concerned with the meaning of disability, the issue of ableism, and how philosophical inquiry into each might improve the lives of disabled people and the justness of practices in medicine, science, politics, and law.Joel Reynolds can be found at https://joelreynolds.me/Works mentioned:Binkley, C. E., Reynolds, J. M., & Shuman, A. (2022). From the Eyeball Test to the Algorithm - Quality of Life, Disability Status, and Clinical Decision Making in Surgery. The New England journal of medicine, 387(14), 1325–1328. https://doi.org/10.1056/NEJMms2207408Reynolds, J. M. Three Things Clinicians Should Know About Disability. AMA J Ethics. 2018;20(12):E1181-1187. doi: 10.1001/amajethics.2018.1181Reynolds, J. M., & Wieseler, C. (Eds.). (2022). The Disability Bioethics Reader. Taylor & Francis Group.Reynolds, J. M. (2022). The life worth living: disability, pain, and morality. U of Minnesota Press.

Discusses chimeric research, why it is important to scientific progress, and current recommendations for addressing the ethical and policy issues raised by chimeric research.Our guest is Josephine Johnston, LLB, MBHL who is the Director of Research and a Research Scholar at The Hastings Center, and a Lecturer at The University of Otago's Bioethics Centre. Her research addresses ethical, legal, and policy issues in medicine and science, with a focus on emerging biotechnologies in human reproduction and genetics.Additional Resources:· Research report discussed in this podcast: https://www.thehastingscenter.org/centerreports/clarifying-the-ethics-and-oversight-of-chimeric-research/· The National Academies guidelines for human embryonic stem cell research: https://www.nationalacademies.org/our-work/guidelines-for-human-embryonic-stem-cell-research· The National Academies consensus report on the emerging field of human neural organoids, transplants, and chimeras: https://www.nationalacademies.org/our-work/ethical-legal-and-regulatory-issues-associated-with-neural-chimeras-and-organoids· The International Society for Stem Cell Research guidelines for stem cell research and clinical translation: https://www.isscr.org/guidelines· CITI Program provides an online module on human-animal chimera research: https://about.citiprogram.org/course/technology-ethics-and-regulations/

Nonhuman Animals Containing Human Cells: Ethics and Oversight Karen Maschke, PhD, Research Scholar at The Hastings Center Website | Twitter @hastingscenter This presentation focuses on ethical and oversight issues as they relate to the insertion of human cells into nonhuman animals, e.g., “chimeric research.” Abstract Research involving the insertion of human cells into nonhuman animals at various stage of development – referred to here as chimeric research – has helped scientists learn how human cells behave in a living environment. Advances in human stem cell science and gene editing are enabling scientists to more extensively and precisely insert human cells into nonhuman animals at any stage of development. Scientists have conducted in vitro experiments with chimeric embryos and in vivo studies that create chimeric animals. The goals of these studies include developing more accurate models of human diseases, creating inexpensive sources of human eggs and embryos for research, and developing sources of tissues and organs suitable for transplantation into humans. Yet concerns have been raised that by biologically altering nonhuman animals with human cells – particularly at an early stage of the chimeric animal's development – scientists may end up changing them in morally relevant ways, especially if the chimeric animals exhibit “humanlike” behaviors or capacities that they previously lacked. An NIH-funded interdisciplinary research project of The Hastings Center and Case Western Reserve University examined the ethical, oversight, and policy issues regarding research that involves the transfer of human embryonic or induced pluripotent cells, or cells derived directly from them, into nonhuman animals or nonhuman animal embryos. This presentation highlights three of the project's recommendations: scientists, journalists, bioethicists and others writing about chimeric research should use precise and accessible language that clarifies rather than obscures the ethical issues at stake; animal welfare is a primary ethical issue and should be a focus of ethical and policy analysis as well as the governance of oversight of chimeric research; and enhanced communication between institutional committees involved in oversight of chimeric research is needed, as well as a mechanism for a national discussion amongst those in oversight of these studies. Related links: Clarifying the Ethics and Oversight of Chimeric Research, Josephine Johnston, Insoo Hyun, Carolyn P. Neuhaus, Karen J. Maschke, et. al., 2022 Composite Animals: Then and Now, Amy Hinterberger, 2022 Human, Nonhuman, and Chimeric Research: Considering Old Issues with New Research, Jeff Sebo, Brendan Parent, 2022 Threats to Benefits: Assessing Knowledge Production in Nonhuman Models of Human Neuropsychiatric Disorders, Carolyn P. Neuhaus, 2022 Moral Status and the Oversight of Research Involving Chimeric Animals, Patricia Marshall, Kaitlynn P. Craig, Insoo Hyun, 2022 A Conversation with Chimeric Animal Researchers, Kaitlynn P. Craig, 2022 How Chimeric Animal Research Impacts Animal Welfare: A Conversation with Animal Welfare Experts, Kaitlynn P. Craig, 2022 Speaker Bio Karen J. Maschke, PhD is a Research Scholar at The Hastings Center and the editor of the Center's journal, Ethics & Human Research. As a researcher with training in political science and bioethics, she focuses on policy and ethical issues related to the introduction, use, regulation, and oversight of new biomedical technologies. She recently completed two projects: the NIH-funded project, “Actionable Ethics Oversight for Human-Animal Chimera Research” (co-Principal Investigator) and the NSF-funded project, “Public Deliberation on Gene Editing in the Wild” (co-Investigator). She is currently the lead co-Principal Investigator of the NIH-funded project, “Informing Ethical Translation of Xenotransplantation Clinical Trials.” She is interviewed frequently by the media, appearing in AP, New York Times, Wall Street Journal, NPR, Washington Post, Kaiser Health, STAT News, Reuters, and Bloomberg Law. Her recent book (co-authored with Michael K. Gusmano), is Debating Modern Medical Technologies: The Politics of Safety, Effectiveness, and Patient Access (Praeger, 2018). GES Colloquium (GES 591-002) is jointly taught by Drs. Jen Baltzegar and Dawn Rodriguez-Ward, who you may contact with any class-specific questions. Colloquium will generally be live-streamed via Zoom, with monthly in-person meetings in the 1911 Building, room 129. Please subscribe to the GES newsletter and Twitter for updates . Genetic Engineering and Society Center GES Colloquium - Tuesdays 12-1PM (via Zoom) NC State University | http://go.ncsu.edu/ges-colloquium GES Mediasite - See videos, full abstracts, speaker bios, and slides https://go.ncsu.edu/ges-mediasite Twitter - https://twitter.com/GESCenterNCSU GES Center - Integrating scientific knowledge & diverse public values in shaping the futures of biotechnology. Find out more at https://ges-center-lectures-ncsu.pinecast.co

In this episode of the COVID Ethics Series Podcast, Dr. Bryan Pilkington speaks to bioethicist, Dr. Nancy Berlinger. Berlinger is a Research Scholar at The Hastings Center, an independent bioethics research institute based in Garrison, NY. Her current research focuses on ethical and societal challenges arising from population aging; the bioethics of migration, and responding to and learning from the Covid-19 pandemic.

Dr. Vardit Ravitsky is a Professor of Bioethics at the University of Montreal and at Harvard Medical School. She is Immediate Past-President and currently Vice-President of the International Association of Bioethics. She is the Director of Ethics and Health at the Center for Research on Ethics and holds a Research-Creation Chair on the Re-appropriation of Maternity. She is a 2020 Fellow of the Pierre Elliott Trudeau Foundation and chaired the Foundation's COVID-19 Impact Committee. She is also a Fellow of the Canadian Academy of Health Sciences and of the Hastings Center. Listen until 27:27 to hear Vardit talk about growing up and her early curiosity.  “I grew up in Jerusalem in a very homogeneous orthodox Jewish community. I didn't speak English or French. I could only speak Hebrew. The first time I left the country I was 13, so I had very little exposure to otherness, and I think already at that early age, I was tremendously curious about diversity. How do people live in other countries, other culture, what is it like to speak another language?What are other people's norms and values and how are they different? I was drawn to diversity before I even knew what it was, or before I could put any content into it.”Check out the book! - Fearless: Girls with Dreams, Women with VisionThe Fearless Women Podcastfearlesswomenpodcast@gmail.comThe Beacon Agency

Pluck brings together the spirit of courage, taking of roads-less-traveled, and living with a mindset focused on possibility that we can all call upon to improve everyday life. It inspires hope and collaboration, as well as meaningful change and actions.Alfred Sadler and Blair Sadler, a doctor and a lawyer, who are also twin brothers, worked together on the early laws concerning organ donation and the first heart transplants, the emergence of the physician assistant profession, the birth of bioethics, and the creation of emergency medicine including 9-1-1. In this compelling and stirring book, they take us on a fascinating journey through the National Institutes of Health, Yale University Medical School, The Hastings Center on Bioethics, and the Robert Wood Johnson Foundation. Dr. Sadler visits with Mark Alyn.

Pluck brings together the spirit of courage, taking of roads-less-traveled, and living with a mindset focused on possibility that we can all call upon to improve everyday life. It inspires hope and collaboration, as well as meaningful change and actions.Alfred Sadler and Blair Sadler, a doctor and a lawyer, who are also twin brothers, worked together on the early laws concerning organ donation and the first heart transplants, the emergence of the physician assistant profession, the birth of bioethics, and the creation of emergency medicine including 9-1-1. In this compelling and stirring book, they take us on a fascinating journey through the National Institutes of Health, Yale University Medical School, The Hastings Center on Bioethics, and the Robert Wood Johnson Foundation. Dr. Sadler visits with Mark Alyn.

The Life Worth Living: Disability, Pain, and Morality (U Minnesota Press, 2022) investigates the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Building on decades of activism and scholarship, Joel Michael Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. More than 2,000 years ago, Aristotle said: "let there be a law that no deformed child shall live." This idea is alive and well today. During the past century, Supreme Court Justice Oliver Wendell Holmes Jr. argued that the United States can forcibly sterilize intellectually disabled women and philosopher Peter Singer argued for the right of parents to euthanize certain cognitively disabled infants. The Life Worth Living explores how and why such arguments persist by investigating the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Joel Michael Reynolds argues that this history demonstrates a fundamental mischaracterization of the meaning of disability, thanks to the conflation of lived experiences of disability with those of pain and suffering. Building on decades of activism and scholarship in the field, Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. The Life Worth Living is the first sustained examination of disability through the lens of the history of moral philosophy and phenomenology, and it demonstrates how lived experiences of disability demand a far richer account of human flourishing, embodiment, community, and politics in philosophical inquiry and beyond. Joel Michael Reynolds is an Assistant Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Senior Bioethics Advisor to The Hastings Center, Faculty Scholar of The Greenwall Foundation, and core faculty in Georgetown's Disability Studies Program. He is the founder of The Journal of Philosophy of Disability and co-founder of Oxford Studies in Disability, Ethics, and Society from Oxford University Press. Dr. Reynolds' work explores the relationship between bodies, values, and society. He is especially concerned with the meaning of disability, the issue of ableism, and how philosophical inquiry into each might improve the lives of people with disabilities and the justness of institutions ranging from medicine to politics. These concerns lead to research across a range of traditions and specialties, including philosophy of disability, applied ethics (especially biomedical ethics, public health ethics, tech/data ethics, and ELSI research in genomics), 20th c. European and American philosophy (with an emphasis on phenomenology and pragmatism as practiced in connection with the history of philosophy), and social epistemology (particularly issues of epistemic injustice as linked to social ontology). Autumn Wilke works in higher education as an ADA coordinator and diversity officer and is also an author and doctoral candidate with research/topics related to disability and higher education. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network

The Life Worth Living: Disability, Pain, and Morality (U Minnesota Press, 2022) investigates the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Building on decades of activism and scholarship, Joel Michael Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. More than 2,000 years ago, Aristotle said: "let there be a law that no deformed child shall live." This idea is alive and well today. During the past century, Supreme Court Justice Oliver Wendell Holmes Jr. argued that the United States can forcibly sterilize intellectually disabled women and philosopher Peter Singer argued for the right of parents to euthanize certain cognitively disabled infants. The Life Worth Living explores how and why such arguments persist by investigating the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Joel Michael Reynolds argues that this history demonstrates a fundamental mischaracterization of the meaning of disability, thanks to the conflation of lived experiences of disability with those of pain and suffering. Building on decades of activism and scholarship in the field, Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. The Life Worth Living is the first sustained examination of disability through the lens of the history of moral philosophy and phenomenology, and it demonstrates how lived experiences of disability demand a far richer account of human flourishing, embodiment, community, and politics in philosophical inquiry and beyond. Joel Michael Reynolds is an Assistant Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Senior Bioethics Advisor to The Hastings Center, Faculty Scholar of The Greenwall Foundation, and core faculty in Georgetown's Disability Studies Program. He is the founder of The Journal of Philosophy of Disability and co-founder of Oxford Studies in Disability, Ethics, and Society from Oxford University Press. Dr. Reynolds' work explores the relationship between bodies, values, and society. He is especially concerned with the meaning of disability, the issue of ableism, and how philosophical inquiry into each might improve the lives of people with disabilities and the justness of institutions ranging from medicine to politics. These concerns lead to research across a range of traditions and specialties, including philosophy of disability, applied ethics (especially biomedical ethics, public health ethics, tech/data ethics, and ELSI research in genomics), 20th c. European and American philosophy (with an emphasis on phenomenology and pragmatism as practiced in connection with the history of philosophy), and social epistemology (particularly issues of epistemic injustice as linked to social ontology). Autumn Wilke works in higher education as an ADA coordinator and diversity officer and is also an author and doctoral candidate with research/topics related to disability and higher education. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/intellectual-history

The Life Worth Living: Disability, Pain, and Morality (U Minnesota Press, 2022) investigates the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Building on decades of activism and scholarship, Joel Michael Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. More than 2,000 years ago, Aristotle said: "let there be a law that no deformed child shall live." This idea is alive and well today. During the past century, Supreme Court Justice Oliver Wendell Holmes Jr. argued that the United States can forcibly sterilize intellectually disabled women and philosopher Peter Singer argued for the right of parents to euthanize certain cognitively disabled infants. The Life Worth Living explores how and why such arguments persist by investigating the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Joel Michael Reynolds argues that this history demonstrates a fundamental mischaracterization of the meaning of disability, thanks to the conflation of lived experiences of disability with those of pain and suffering. Building on decades of activism and scholarship in the field, Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. The Life Worth Living is the first sustained examination of disability through the lens of the history of moral philosophy and phenomenology, and it demonstrates how lived experiences of disability demand a far richer account of human flourishing, embodiment, community, and politics in philosophical inquiry and beyond. Joel Michael Reynolds is an Assistant Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Senior Bioethics Advisor to The Hastings Center, Faculty Scholar of The Greenwall Foundation, and core faculty in Georgetown's Disability Studies Program. He is the founder of The Journal of Philosophy of Disability and co-founder of Oxford Studies in Disability, Ethics, and Society from Oxford University Press. Dr. Reynolds' work explores the relationship between bodies, values, and society. He is especially concerned with the meaning of disability, the issue of ableism, and how philosophical inquiry into each might improve the lives of people with disabilities and the justness of institutions ranging from medicine to politics. These concerns lead to research across a range of traditions and specialties, including philosophy of disability, applied ethics (especially biomedical ethics, public health ethics, tech/data ethics, and ELSI research in genomics), 20th c. European and American philosophy (with an emphasis on phenomenology and pragmatism as practiced in connection with the history of philosophy), and social epistemology (particularly issues of epistemic injustice as linked to social ontology). Autumn Wilke works in higher education as an ADA coordinator and diversity officer and is also an author and doctoral candidate with research/topics related to disability and higher education. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/public-policy

The Life Worth Living: Disability, Pain, and Morality (U Minnesota Press, 2022) investigates the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Building on decades of activism and scholarship, Joel Michael Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. More than 2,000 years ago, Aristotle said: "let there be a law that no deformed child shall live." This idea is alive and well today. During the past century, Supreme Court Justice Oliver Wendell Holmes Jr. argued that the United States can forcibly sterilize intellectually disabled women and philosopher Peter Singer argued for the right of parents to euthanize certain cognitively disabled infants. The Life Worth Living explores how and why such arguments persist by investigating the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Joel Michael Reynolds argues that this history demonstrates a fundamental mischaracterization of the meaning of disability, thanks to the conflation of lived experiences of disability with those of pain and suffering. Building on decades of activism and scholarship in the field, Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. The Life Worth Living is the first sustained examination of disability through the lens of the history of moral philosophy and phenomenology, and it demonstrates how lived experiences of disability demand a far richer account of human flourishing, embodiment, community, and politics in philosophical inquiry and beyond. Joel Michael Reynolds is an Assistant Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Senior Bioethics Advisor to The Hastings Center, Faculty Scholar of The Greenwall Foundation, and core faculty in Georgetown's Disability Studies Program. He is the founder of The Journal of Philosophy of Disability and co-founder of Oxford Studies in Disability, Ethics, and Society from Oxford University Press. Dr. Reynolds' work explores the relationship between bodies, values, and society. He is especially concerned with the meaning of disability, the issue of ableism, and how philosophical inquiry into each might improve the lives of people with disabilities and the justness of institutions ranging from medicine to politics. These concerns lead to research across a range of traditions and specialties, including philosophy of disability, applied ethics (especially biomedical ethics, public health ethics, tech/data ethics, and ELSI research in genomics), 20th c. European and American philosophy (with an emphasis on phenomenology and pragmatism as practiced in connection with the history of philosophy), and social epistemology (particularly issues of epistemic injustice as linked to social ontology). Autumn Wilke works in higher education as an ADA coordinator and diversity officer and is also an author and doctoral candidate with research/topics related to disability and higher education. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/law

The Life Worth Living: Disability, Pain, and Morality (U Minnesota Press, 2022) investigates the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Building on decades of activism and scholarship, Joel Michael Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. More than 2,000 years ago, Aristotle said: "let there be a law that no deformed child shall live." This idea is alive and well today. During the past century, Supreme Court Justice Oliver Wendell Holmes Jr. argued that the United States can forcibly sterilize intellectually disabled women and philosopher Peter Singer argued for the right of parents to euthanize certain cognitively disabled infants. The Life Worth Living explores how and why such arguments persist by investigating the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Joel Michael Reynolds argues that this history demonstrates a fundamental mischaracterization of the meaning of disability, thanks to the conflation of lived experiences of disability with those of pain and suffering. Building on decades of activism and scholarship in the field, Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. The Life Worth Living is the first sustained examination of disability through the lens of the history of moral philosophy and phenomenology, and it demonstrates how lived experiences of disability demand a far richer account of human flourishing, embodiment, community, and politics in philosophical inquiry and beyond. Joel Michael Reynolds is an Assistant Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Senior Bioethics Advisor to The Hastings Center, Faculty Scholar of The Greenwall Foundation, and core faculty in Georgetown's Disability Studies Program. He is the founder of The Journal of Philosophy of Disability and co-founder of Oxford Studies in Disability, Ethics, and Society from Oxford University Press. Dr. Reynolds' work explores the relationship between bodies, values, and society. He is especially concerned with the meaning of disability, the issue of ableism, and how philosophical inquiry into each might improve the lives of people with disabilities and the justness of institutions ranging from medicine to politics. These concerns lead to research across a range of traditions and specialties, including philosophy of disability, applied ethics (especially biomedical ethics, public health ethics, tech/data ethics, and ELSI research in genomics), 20th c. European and American philosophy (with an emphasis on phenomenology and pragmatism as practiced in connection with the history of philosophy), and social epistemology (particularly issues of epistemic injustice as linked to social ontology). Autumn Wilke works in higher education as an ADA coordinator and diversity officer and is also an author and doctoral candidate with research/topics related to disability and higher education. Learn more about your ad choices. Visit megaphone.fm/adchoices

The Life Worth Living: Disability, Pain, and Morality (U Minnesota Press, 2022) investigates the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Building on decades of activism and scholarship, Joel Michael Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. More than 2,000 years ago, Aristotle said: "let there be a law that no deformed child shall live." This idea is alive and well today. During the past century, Supreme Court Justice Oliver Wendell Holmes Jr. argued that the United States can forcibly sterilize intellectually disabled women and philosopher Peter Singer argued for the right of parents to euthanize certain cognitively disabled infants. The Life Worth Living explores how and why such arguments persist by investigating the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Joel Michael Reynolds argues that this history demonstrates a fundamental mischaracterization of the meaning of disability, thanks to the conflation of lived experiences of disability with those of pain and suffering. Building on decades of activism and scholarship in the field, Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. The Life Worth Living is the first sustained examination of disability through the lens of the history of moral philosophy and phenomenology, and it demonstrates how lived experiences of disability demand a far richer account of human flourishing, embodiment, community, and politics in philosophical inquiry and beyond. Joel Michael Reynolds is an Assistant Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Senior Bioethics Advisor to The Hastings Center, Faculty Scholar of The Greenwall Foundation, and core faculty in Georgetown's Disability Studies Program. He is the founder of The Journal of Philosophy of Disability and co-founder of Oxford Studies in Disability, Ethics, and Society from Oxford University Press. Dr. Reynolds' work explores the relationship between bodies, values, and society. He is especially concerned with the meaning of disability, the issue of ableism, and how philosophical inquiry into each might improve the lives of people with disabilities and the justness of institutions ranging from medicine to politics. These concerns lead to research across a range of traditions and specialties, including philosophy of disability, applied ethics (especially biomedical ethics, public health ethics, tech/data ethics, and ELSI research in genomics), 20th c. European and American philosophy (with an emphasis on phenomenology and pragmatism as practiced in connection with the history of philosophy), and social epistemology (particularly issues of epistemic injustice as linked to social ontology). Autumn Wilke works in higher education as an ADA coordinator and diversity officer and is also an author and doctoral candidate with research/topics related to disability and higher education. Learn more about your ad choices. Visit megaphone.fm/adchoices

The Life Worth Living: Disability, Pain, and Morality (U Minnesota Press, 2022) investigates the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Building on decades of activism and scholarship, Joel Michael Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. More than 2,000 years ago, Aristotle said: "let there be a law that no deformed child shall live." This idea is alive and well today. During the past century, Supreme Court Justice Oliver Wendell Holmes Jr. argued that the United States can forcibly sterilize intellectually disabled women and philosopher Peter Singer argued for the right of parents to euthanize certain cognitively disabled infants. The Life Worth Living explores how and why such arguments persist by investigating the exclusion of and discrimination against disabled people across the history of Western moral philosophy. Joel Michael Reynolds argues that this history demonstrates a fundamental mischaracterization of the meaning of disability, thanks to the conflation of lived experiences of disability with those of pain and suffering. Building on decades of activism and scholarship in the field, Reynolds shows how longstanding views of disability are misguided and unjust, and he lays out a vision of what an anti-ableist moral future requires. The Life Worth Living is the first sustained examination of disability through the lens of the history of moral philosophy and phenomenology, and it demonstrates how lived experiences of disability demand a far richer account of human flourishing, embodiment, community, and politics in philosophical inquiry and beyond. Joel Michael Reynolds is an Assistant Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Senior Bioethics Advisor to The Hastings Center, Faculty Scholar of The Greenwall Foundation, and core faculty in Georgetown's Disability Studies Program. He is the founder of The Journal of Philosophy of Disability and co-founder of Oxford Studies in Disability, Ethics, and Society from Oxford University Press. Dr. Reynolds' work explores the relationship between bodies, values, and society. He is especially concerned with the meaning of disability, the issue of ableism, and how philosophical inquiry into each might improve the lives of people with disabilities and the justness of institutions ranging from medicine to politics. These concerns lead to research across a range of traditions and specialties, including philosophy of disability, applied ethics (especially biomedical ethics, public health ethics, tech/data ethics, and ELSI research in genomics), 20th c. European and American philosophy (with an emphasis on phenomenology and pragmatism as practiced in connection with the history of philosophy), and social epistemology (particularly issues of epistemic injustice as linked to social ontology). Autumn Wilke works in higher education as an ADA coordinator and diversity officer and is also an author and doctoral candidate with research/topics related to disability and higher education. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/book-of-the-day

The HBS hosts talk with Dr. Joel Michael Reynolds about what bodies are afforded and denied. As we come to recognize more and more the occlusions that occur in, and often constitute, philosophy and its history, attention to an ableist presupposition in philosophy has come to the fore. Much as with feminist theory or queer theory or race theory, disability theory not only works to expose the ableist presuppositions of philosophy but also to alter philosophy for the better by the inclusion of the formerly excluded. Why are affordances-- social, political, moral, and physical-- made for some types of bodies, but denied to others? Have we yet grasped what different types of bodies can really do? What is the difference between a "disability" and an "impairment"? To what degree is our category "disability" more philosophical than it is corporeal?Our guest for this episode, Dr. Joel Reynolds, is the perfect person with whom to talk about these questions and issues! Dr. Reynolds is an Assistant Professor of Philosophy and Disability Studies at Georgetown University, Senior Research Scholar in the Kennedy Institute of Ethics, Senior Advisor to The Hastings Center, Faculty Scholar of The Greenwall Foundation, and core faculty in Georgetown's Disability Studies Program. He is the founder of The Journal of Philosophy of Disability and co-founder of Oxford Studies in Disability, Ethics, and Society from Oxford University Press. In 2022, he published The Life Worth Living: Disability, Pain, and Morality.You can read/download a transcript of this episode at this link. Full episode notes are available at this link:http://hotelbarpodcast.com/podcast/episode-67-rethinking-disability-with-joel-michael-reynolds-------------------If you enjoy Hotel Bar Sessions podcast, please be sure to subscribe, submit a rating/review, and follow us on Twitter @hotelbarpodcast.You can also help keep this podcast going by supporting us financially at patreon.com/hotelbarsessions. 

Sustainable Development Goal 16: Peace, Justice, and Strong Institutions focuses on promoting peaceful and inclusive societies for sustainable development, providing access to justice for all and building effective, accountable, and inclusive institutions at all levels.Dr. Ross Upshur is currently the Dalla Lana Chair in Clinical Public Health and Head of the Division of Clinical Public Health at the Dalla Lana School of Public Health, Scientific Director, Bridgepoint Collaboratory for Research and Innovation and Associate Director of the Lunenfeld Tanenbaum Research Institute, Sinai Health. At the University of Toronto, he is a Professor in the Dalla Lana School of Public Health and the Department of Family and Community Medicine, affiliate member of the Institute for the History and Philosophy of Science and Technology, Member of the Centre for Environment and Adjunct Senior Scientist at the Institute for Clinical Evaluative Sciences. He is a Staff Physician at Bridgepoint Active Healthcare, Sinai Health. In 2015, he was named one of the Top 20 Pioneers in Family Medicine Research in Canada by the College of Family Physicians of Canada and was a Tier 2 Canada Research Chair from 2005-2015. He is an elected Fellow of the Hastings Center and the Canadian Academy of Health Sciences. During COVID-19 he has served as the co-Chair of the WHO Ethics and COVID-19 Working group and is a member of the WHO ACTA Ethics and Governance Working Group.Rushay Naik is an MSc student in Health Policy & Global Health at the University of Toronto. His research centres on health service delivery in conflict-affected states, and has conducted fieldwork for research initiatives in Greece, Mongolia, and Switzerland. Rushay has held research fellowships at UofT's School of Cities, at the Center for the Study of the Presidency & the Congress in Washington, D.C., and at the University of Oxford's COVID-19 Government Response Tracker. Rushay previously worked for Health Canada's Climate Change and Innovation Bureau, and is now an incoming intern to the Health Division at the OECD in Paris. CREDITS: This podcast is co-hosted by Dr. Erica Di Ruggiero, Director of the Centre for Global Health, and Ophelia Michaelides, Manager of the Centre for Global Health, at the DLSPH, U of T, and produced by Elizabeth Loftus. Audio editing is by Sylvia Lorico. Music is produced by Julien Fortier and Patrick May. It is made with the support of the School of Cities at U of T. 

George Estreich is an award-winning writer whose work includes poetry, memoir, and non-fiction. He is also a musician who plays with the band Mule On Fire. In addition to writing and music. George is an activist, storyteller, husband, and father to Ellie and Laura.  George talks about raising his daughter, Laura, who was born with Down syndrome. And then he talks about biotechnology, disability, and the stories we tell ourselves. He discusses how all people are more than a single identity and not only are stereotypes untrue, but they are also incomplete.For more information about Down syndrome, see here.Find and follow George: https://georgeestreich.com/Listen to Laura's episode here: https://wisdom-shared.simplecast.com/episodes/laura-eFROM THIS EPISODE:The Shape of the Eye by George EstreichFables and Futures: Biotechnology, Disability, and the Stories We Tell Ourselves by George EstreichUnexpected: Parenting, Prenatal Testing, and Down Syndrome by Alison Piepmeier with George Estreich and Rachel AdamsNo Pity: People with Disabilities Forging a New Civil Rights Movement by Joseph P. ShapiroWhat Can a Body Do?: How We Meet the Built World by Sara HendrenAlison PiepmeierUnified Sports - Special OlympicsIndividuals with Disabilities Education Act (IDEA)Report from the Hastings Center about the marketing of NIPT: Bias and Inaccuracy in Marketing Noninvasive Prenatal Tests 

The impacts of climate change on our health are growing, as surely as global temperatures and sea levels are rising. So how can we strive to live as healthy people on an increasingly sick planet? What are the major ways global warming is threatening human health?  

The impacts of climate change on our health are growing, as surely as global temperatures and sea levels are rising. So how can we strive to live as healthy people on an increasingly sick planet? What are the major ways global warming is threatening human health?  

A virtual event presentation by Dr. Paul Root Wolpe ABOUT THE EVENT: Two paradigms of human-created ‘monsters' have reverberated through modern history as models for considering everything from genetic safety, to scientific hubris, to man's relationship to the material world and G-d. In this talk we compare these two legends and discuss why they portray Humankind so differently and teach such different lessons. ABOUT THE SPEAKER: Paul Root Wolpe, Ph.D. is the Raymond F. Schinazi Distinguished Research Chair in Jewish Bioethics, Professor of Medicine, Pediatrics, Psychiatry, Neuroscience, and Sociology, and the Director of the Center for Ethics at Emory University. He is the Editor-in-Chief of the American Journal of Bioethics – Neuroscience, and sits on the editorial boards of over a dozen professional journals. Dr. Wolpe served for 17 years as Senior Bioethicist for the National Aeronautics and Space Administration (NASA). He is Immediate Past-President of the Association of Bioethics Program Directors, a past President of the American Society for Bioethics and Humanities, a Fellow of the Hastings Center, the country's oldest bioethics institute, and a Fellow of the College of Physicians of Philadelphia, the country's oldest medical society. Dr. Wolpe publishes widely in sociology, medicine, and ethics, and has contributed to a variety of encyclopedias on ethical and bioethical issues. Trained as a social scientist – a rare background for an ethicist — Dr. Wolpe's work focuses on the social, religious, ethical, and ideological impact of medicine and technology on the human condition. A founder of the field of neuroethics, which examines the ethical implications of neuroscience, he also organized BEINGS, “Biotechnology and the Ethical Imagination: A Global Summit,” which brought together thought leaders to reach consensus on ethical principles and standards for human cellular genetics and biotechnology. He has also been a leader in the national bioethical conversation on COVID-19 and vaccine distribution. -- DONATE: www.bit.ly/1NmpbsP​​​​​​​ For podcasts of VBM lectures, GO HERE: www.valleybeitmidrash.org/learning-library/ www.facebook.com/valleybeitmi...​ Become a member today, starting at just $18 per month! Click the link to see our membership options: www.valleybeitmidrash.org/become-a-member/

Kirk and Amelia interview our very own sound editor Nicole Strand, JD, MBE, MPH. @Nicolle_Strand is the Assistant Director for Research at the Center for Urban Bioethics at Temple University. Her work is on structural determinants of health, racism, health equity, advocacy, and culture change. We discuss critical race theory, the use of race in biomedical research and more. Professor Strand's comments on the Hastings Center blog can be found here: Bioethics Must Resist Attacks on Critical Race Theory. She also recently published Racial Myths and Regulatory Responsibility in the Journal of Law, Medicine and Ethics.

Dr. Farhat Moazam is Professor and founding Chairperson of the Centre of Biomedical Ethics and Culture (CBEC) of the Sindh Institute of Urology and Transplantation in Karachi, Pakistan. She is an American board-certified pediatric surgeon with an MA in Bioethics and a doctorate (2004) from the Department of Religious Studies, University of Virginia, USA. Dr. Moazam is also Fellow of the Institute of Practical Ethics and Visiting Professor, Centre for Humanism in Medicine, UVA, and International Fellow of The Hastings Center, Garrison, New York. Camille Castelyn interviews Dr. Moazam about the promise of precision and genomic medicine and what the next step may be in order to ensure just and equitable access in the near future. Challenging the narrative that precision medicine will only be accessible to an elite few, they discuss the importance as described by the United Nations in Sustainable Development Goal #3 that health should be seen as a public good and that we must leave no one behind in the pursuit of healthy lives and well-being for all ages.

Gone Missing in Harlem by Karla FC Holloway (TriQuarterly 2021) tells the story of an African American family trying to survive the early decades of the twentieth century. The Mosbys leave their life in Sedalia within hours after six-year-old Percy loudly notes that his father's boss has made a mistake in calculating what is owed. Percy's parents know what would happen if they stayed. They settle in Harlem, but the Spanish flu is raging around the globe, and Percy's father doesn't survive. His mother, DeLilah, is pregnant with Selma. Years later, Percy witnesses a murder in New York, and DeLilah sends him back to Sedalia. She does her best to make a home for her daughter, but Selma's childhood is cut short when a brutal rape leaves her pregnant. After her baby is kidnapped, the city's first ‘colored policeman', Weldon Haynie Thomas, vows that this kidnapping will not end like the Lindbergh kidnapping. Gone Missing in Harlem touches upon many things, including African American soldiers coming home from WWI, the Great Migration north, and the world of 1930's Harlem. Gone Missing in Harlem is historical, African American literary fiction and a mystery, but it's ultimately a novel about the lengths a mother will go to protect her family. Karla FC Holloway, Ph.D., M.L.S., is James B. Duke Professor Emerita of English and Professor of Law at Duke University. She is former Dean of Humanities and Social Science Faculty at Duke. Her research and teaching focused on African American cultural studies, bioethics, literature, and law. Her national and institutional board memberships have included the Greenwall Foundation's Advisory Board in Bioethics, the Trent Center for Bioethics and Humanities, the North Carolina Humanities Council, the College Board, and the Hastings Center. She is a co-founder of Duke University's John Hope Franklin Center for International and Interdisciplinary Studies and founding co-director of the John Hope Franklin Humanities Institute. Professor Holloway is the recipient of national awards and foundation fellowships including the Rockefeller Foundation's Bellagio Residency Fellowship and the Sheila Biddle Ford Foundation Fellowship at Harvard University's Du Bois Institute. Professor Holloway is the author of over fifty essays and ten books including Codes of Conduct: Race, Ethics and the Color of Our Character (1995), Passed On: African American Mourning Stories (2002), BookMarks: Reading in Black and White (2006), and Legal Fictions: Constituting Race, Composing Literature (2014). In her emerita years she has shifted to fiction and has published A Death in Harlem (2019) and Gone Missing in Harlem (2021) both with Triquarterly. She's at work on the final book in the “in Harlem” series, A Haunting in Harlem, and tweets on bioethics, law, society, and popular cultures from @ProfHolloway. When she's not tweeting, or writing, she's deep into reading fiction or painting miniature acrylic landscapes and abstract compositions. Anything, she says, with colors that swirl into cerulean. G.P. Gottlieb is the author of the Whipped and Sipped Mystery Series and a prolific baker of healthful breads and pastries. Please contact her through her website (GPGottlieb.com) if you wish to recommend an author (of a beautifully-written new novel) to interview, to listen to her previous podcast interviews, to read her mystery book reviews, or to check out some of her awesome recipes. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/historical-fiction

Gone Missing in Harlem by Karla FC Holloway (TriQuarterly 2021) tells the story of an African American family trying to survive the early decades of the twentieth century. The Mosbys leave their life in Sedalia within hours after six-year-old Percy loudly notes that his father's boss has made a mistake in calculating what is owed. Percy's parents know what would happen if they stayed. They settle in Harlem, but the Spanish flu is raging around the globe, and Percy's father doesn't survive. His mother, DeLilah, is pregnant with Selma. Years later, Percy witnesses a murder in New York, and DeLilah sends him back to Sedalia. She does her best to make a home for her daughter, but Selma's childhood is cut short when a brutal rape leaves her pregnant. After her baby is kidnapped, the city's first ‘colored policeman', Weldon Haynie Thomas, vows that this kidnapping will not end like the Lindbergh kidnapping. Gone Missing in Harlem touches upon many things, including African American soldiers coming home from WWI, the Great Migration north, and the world of 1930's Harlem. Gone Missing in Harlem is historical, African American literary fiction and a mystery, but it's ultimately a novel about the lengths a mother will go to protect her family. Karla FC Holloway, Ph.D., M.L.S., is James B. Duke Professor Emerita of English and Professor of Law at Duke University. She is former Dean of Humanities and Social Science Faculty at Duke. Her research and teaching focused on African American cultural studies, bioethics, literature, and law. Her national and institutional board memberships have included the Greenwall Foundation's Advisory Board in Bioethics, the Trent Center for Bioethics and Humanities, the North Carolina Humanities Council, the College Board, and the Hastings Center. She is a co-founder of Duke University's John Hope Franklin Center for International and Interdisciplinary Studies and founding co-director of the John Hope Franklin Humanities Institute. Professor Holloway is the recipient of national awards and foundation fellowships including the Rockefeller Foundation's Bellagio Residency Fellowship and the Sheila Biddle Ford Foundation Fellowship at Harvard University's Du Bois Institute. Professor Holloway is the author of over fifty essays and ten books including Codes of Conduct: Race, Ethics and the Color of Our Character (1995), Passed On: African American Mourning Stories (2002), BookMarks: Reading in Black and White (2006), and Legal Fictions: Constituting Race, Composing Literature (2014). In her emerita years she has shifted to fiction and has published A Death in Harlem (2019) and Gone Missing in Harlem (2021) both with Triquarterly. She's at work on the final book in the “in Harlem” series, A Haunting in Harlem, and tweets on bioethics, law, society, and popular cultures from @ProfHolloway. When she's not tweeting, or writing, she's deep into reading fiction or painting miniature acrylic landscapes and abstract compositions. Anything, she says, with colors that swirl into cerulean. G.P. Gottlieb is the author of the Whipped and Sipped Mystery Series and a prolific baker of healthful breads and pastries. Please contact her through her website (GPGottlieb.com) if you wish to recommend an author (of a beautifully-written new novel) to interview, to listen to her previous podcast interviews, to read her mystery book reviews, or to check out some of her awesome recipes. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/african-american-studies

Gone Missing in Harlem by Karla FC Holloway (TriQuarterly 2021) tells the story of an African American family trying to survive the early decades of the twentieth century. The Mosbys leave their life in Sedalia within hours after six-year-old Percy loudly notes that his father's boss has made a mistake in calculating what is owed. Percy's parents know what would happen if they stayed. They settle in Harlem, but the Spanish flu is raging around the globe, and Percy's father doesn't survive. His mother, DeLilah, is pregnant with Selma. Years later, Percy witnesses a murder in New York, and DeLilah sends him back to Sedalia. She does her best to make a home for her daughter, but Selma's childhood is cut short when a brutal rape leaves her pregnant. After her baby is kidnapped, the city's first ‘colored policeman', Weldon Haynie Thomas, vows that this kidnapping will not end like the Lindbergh kidnapping. Gone Missing in Harlem touches upon many things, including African American soldiers coming home from WWI, the Great Migration north, and the world of 1930's Harlem. Gone Missing in Harlem is historical, African American literary fiction and a mystery, but it's ultimately a novel about the lengths a mother will go to protect her family. Karla FC Holloway, Ph.D., M.L.S., is James B. Duke Professor Emerita of English and Professor of Law at Duke University. She is former Dean of Humanities and Social Science Faculty at Duke. Her research and teaching focused on African American cultural studies, bioethics, literature, and law. Her national and institutional board memberships have included the Greenwall Foundation's Advisory Board in Bioethics, the Trent Center for Bioethics and Humanities, the North Carolina Humanities Council, the College Board, and the Hastings Center. She is a co-founder of Duke University's John Hope Franklin Center for International and Interdisciplinary Studies and founding co-director of the John Hope Franklin Humanities Institute. Professor Holloway is the recipient of national awards and foundation fellowships including the Rockefeller Foundation's Bellagio Residency Fellowship and the Sheila Biddle Ford Foundation Fellowship at Harvard University's Du Bois Institute. Professor Holloway is the author of over fifty essays and ten books including Codes of Conduct: Race, Ethics and the Color of Our Character (1995), Passed On: African American Mourning Stories (2002), BookMarks: Reading in Black and White (2006), and Legal Fictions: Constituting Race, Composing Literature (2014). In her emerita years she has shifted to fiction and has published A Death in Harlem (2019) and Gone Missing in Harlem (2021) both with Triquarterly. She's at work on the final book in the “in Harlem” series, A Haunting in Harlem, and tweets on bioethics, law, society, and popular cultures from @ProfHolloway. When she's not tweeting, or writing, she's deep into reading fiction or painting miniature acrylic landscapes and abstract compositions. Anything, she says, with colors that swirl into cerulean. G.P. Gottlieb is the author of the Whipped and Sipped Mystery Series and a prolific baker of healthful breads and pastries. Please contact her through her website (GPGottlieb.com) if you wish to recommend an author (of a beautifully-written new novel) to interview, to listen to her previous podcast interviews, to read her mystery book reviews, or to check out some of her awesome recipes. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/new-books-network

Gone Missing in Harlem by Karla FC Holloway (TriQuarterly 2021) tells the story of an African American family trying to survive the early decades of the twentieth century. The Mosbys leave their life in Sedalia within hours after six-year-old Percy loudly notes that his father's boss has made a mistake in calculating what is owed. Percy's parents know what would happen if they stayed. They settle in Harlem, but the Spanish flu is raging around the globe, and Percy's father doesn't survive. His mother, DeLilah, is pregnant with Selma. Years later, Percy witnesses a murder in New York, and DeLilah sends him back to Sedalia. She does her best to make a home for her daughter, but Selma's childhood is cut short when a brutal rape leaves her pregnant. After her baby is kidnapped, the city's first ‘colored policeman', Weldon Haynie Thomas, vows that this kidnapping will not end like the Lindbergh kidnapping. Gone Missing in Harlem touches upon many things, including African American soldiers coming home from WWI, the Great Migration north, and the world of 1930's Harlem. Gone Missing in Harlem is historical, African American literary fiction and a mystery, but it's ultimately a novel about the lengths a mother will go to protect her family. Karla FC Holloway, Ph.D., M.L.S., is James B. Duke Professor Emerita of English and Professor of Law at Duke University. She is former Dean of Humanities and Social Science Faculty at Duke. Her research and teaching focused on African American cultural studies, bioethics, literature, and law. Her national and institutional board memberships have included the Greenwall Foundation's Advisory Board in Bioethics, the Trent Center for Bioethics and Humanities, the North Carolina Humanities Council, the College Board, and the Hastings Center. She is a co-founder of Duke University's John Hope Franklin Center for International and Interdisciplinary Studies and founding co-director of the John Hope Franklin Humanities Institute. Professor Holloway is the recipient of national awards and foundation fellowships including the Rockefeller Foundation's Bellagio Residency Fellowship and the Sheila Biddle Ford Foundation Fellowship at Harvard University's Du Bois Institute. Professor Holloway is the author of over fifty essays and ten books including Codes of Conduct: Race, Ethics and the Color of Our Character (1995), Passed On: African American Mourning Stories (2002), BookMarks: Reading in Black and White (2006), and Legal Fictions: Constituting Race, Composing Literature (2014). In her emerita years she has shifted to fiction and has published A Death in Harlem (2019) and Gone Missing in Harlem (2021) both with Triquarterly. She's at work on the final book in the “in Harlem” series, A Haunting in Harlem, and tweets on bioethics, law, society, and popular cultures from @ProfHolloway. When she's not tweeting, or writing, she's deep into reading fiction or painting miniature acrylic landscapes and abstract compositions. Anything, she says, with colors that swirl into cerulean. G.P. Gottlieb is the author of the Whipped and Sipped Mystery Series and a prolific baker of healthful breads and pastries. Please contact her through her website (GPGottlieb.com) if you wish to recommend an author (of a beautifully-written new novel) to interview, to listen to her previous podcast interviews, to read her mystery book reviews, or to check out some of her awesome recipes. Learn more about your ad choices. Visit megaphone.fm/adchoices Support our show by becoming a premium member! https://newbooksnetwork.supportingcast.fm/literature

The Social Contract and Our Bodies The pandemic has given us a glimpse into the ways our health is woven into the social contract. The high number of deaths from COVID are the result of the government's failure to collaborate with international organizations and with our own state lawmakers. We leaned on essential care workers, many of whom are people of color. And yet, they often lacked PPE, challenging what it really means to be “essential.” The Inequality of Health Racism is a preexisting health condition in the United States. COVID unveiled the institutional and infrastructural inequalities that have existed in our healthcare system for decades, which we see with the alarming rates of death among Black and Latino children. These inequalities and social stereotypes affect every corner of healthcare. For example, Black adults are 2 to 6 times more likely to suffer an amputation than a white adult, especially for common conditions like diabetes. Women's Health Increasingly, aspects of women's health, such as reproduction, pregnancy, abortion, birth, and motherhood have been criminalized in the United States. Criminalization especially affects Black and brown women so that medical care has become a weapon to turn health issues like a stillbirth into a criminal offense. However, in creating these sorts of precedents, all women—regardless of race—are then subject to suffering under this weaponization of healthcare, which we see happening across the country right now. FIND OUT MORE: Michele Goodwin is a Chancellor's Professor at the University of California Irvine and founding director of the Center for Biotechnology and Global Health Policy. She is the recipient of the 2020-21 Distinguished Senior Faculty Award for Research, the highest honor bestowed by the University of California. She is an elected member of the American Law Institute, as well as an elected Fellow of the American Bar Foundation and the Hastings Center (the organization central to the founding of bioethics). She is an American Law Institute Adviser for the Restatement Third of Torts: Remedies. Goodwin has won national awards for excellence in scholarship, outstanding teaching, and committed community service. Gov. Paul Patton of Kentucky commissioned her a Colonel, the state's highest title of honor for her outstanding contributions to K-12 education. She's the recipient of the Be The Change Award, the Sandra Day O'Connor Legacy Award by the Women's Journey Foundation, and was named Teacher of the Year by the Thurgood Marshall Bar Association in 2018. Goodwin received a commendation from the United States House of Representatives for Outstanding Teaching.  You can follow Michele Goodwin on Twitter at @michelebgoodwin

In this episode, I speak with Brian Earp. Brian is the Associate Director of the Yale-Hastings Program in Ethics and Health Policy at Yale University and The Hastings Center, and a Research Fellow for Practical Ethics at the University of Oxford and is currently finishing a joint Philosophy and Psychology PhD at Yale University. Given Brian's wide experience, this conversation traverses a wide range of topics. We first speak about graduate school: its promise, problems, and our experiences with it. We then transition into a discussion about ethics and social science, taking up what's been called the replicability crisis in social science as well as some of the perennial questions within the subfield of bioethics. The combination of these two elements leads us to a topic that is close to Brian's heart: circumcision. We speak about male and female circumcision, why the latter is often called female genital mutilation but the former is rarely spoken of at all, as well as some of the myths and bad science that surround this topic. As you will see toward the end of our conversation, we seemingly have just begun to explore some of these topics when the reality of time intervenes in our conversation. Brian was tremendously gracious with his time and I hope to speak with him again soon, picking up from where we left off here. Find Love and Other Drugs here. Brian's other work can be found here. He can also be found on Twitter here.  Introductory music was written by Alex Yoder. Find him here Please consider supporting the podcast here and following it on Twitter. Thank you for your support! --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app Support this podcast: https://anchor.fm/struggletounderstand/support

Rosemary Gibson of the Hastings Center is back in the Economic War Room with specific next steps to help close the executive order being worked on to get our pharmaceutical business back in the U.S. In addition to the national security and health issues we have covered before, she shares about the real economic and job impact America was hit with after we gave China the ability to control 80% to 90% of the core chemicals of our pharmaceutical industry.

Dr. Mildred Solomon, President of the Hastings Center, joins Bonnie and Nick to discuss her leadership at the Center and how it relates to disability issues. She reviews several historical and current projects on bioethics. Additionally, Dr. Solomon explores COVID-19 and disability, particularly her piece in the New England Journal of Medicine around crisis triage and disability rights. Episode transcripts can be found at http://disabilityhealth.jhu.edu/included/ Learn more about the Hastings Center here: https://www.thehastingscenter.org/   Read her article in the NEJM: https://www.nejm.org/doi/full/10.1056/NEJMp2008300  

When it comes to pharmaceuticals, you have heard the list of complaints. Drug prices are too high. Drug prices are not transparent. My insurance plan won't cover X medication. Perhaps the complaint which should be raised but isn't relates to China. Author Rosemary Gibson has rung a fire bell in the night with her book, China Rx: Exposing the Risks of America's Dependence on China for Medicine.Well over 90% of the active ingredients of antibiotics in the U.S. are manufactured abroad. The vast majority of them are produced in China. Learn about the national security threats and quality oversight issues involved with the outsourcing of pharma manufacturing. This important episode will shock you.Rosemary Gibson serves as Senior Advisor at The Hastings Center and a Section Editor for “Less is More,” in JAMA Internal Medicine. Ms. Gibson is an award-winning author, inspirational speaker, and advisor to organizations that advance the public's interest in health care.www.rosemarygibson.orgChina Rx: Exposing the Risks of America's Dependence on China for Medicinehttps://www.amazon.com/ChinaRx  

Earlier this week, researchers from the Hastings Center published an article in the journal Health Affairs in which they make the argument that patients should not be considered consumers. The concept of patient-centered care has increasingly merged with the concept of patients as consumers, which “is conceptually confused and potentially harmful,” the authors contend. Joining me now to look at this paper is G. Keith Smith, MD. Dr Smith is the medical director, CEO and managing partner of the “free market” outpatient surgery center, Surgery Center of Oklahoma.

Listen NowDuring this 31 minute discussion Rosemary Gibson unpacks her latest work, co-authored with Janardan Prasad Singh, titled, China, Rx, "Exposing the Risks of America's Dependence on China For Medicine.  As the title suggests the authors discuss the problems with relying on China for the production of essential ingredients for thousands of medicines, or the implications of relying on China regarding the quality and availability of essential drugs.  Rosemary Gibson is Senior Adviser at The Hastings Center.  She is also board chair of the Altarum Institute, a non-profit health system research organization, she is a board member of the Accreditation Council for Graduate Medical Education, she serves on the MedStar Health System Institute for Quality and Patient Safety advisory board, is faculty for the Academy for Emerging Health Care Leaders and for the Dartmouth Summer Symposium on Quality Improvement.  While at the Robert Wood Johnson Foundation, Rosemary was the chief architect for it's $250 million, decade-long national strategy to establish inpatient palliative care programs that now number over 1,600.  She is also author of Medicare Meltdown (2013), Battle Over Health Care (2012), Treatment Trap (2010) and Wall of Silence (2003).  Among other awards, Rosemary is the recipient of highest honors from the American Medical Writers Association for her contributions to the field of medical communication. Information on China Rx is at: https://www.penguinrandomhouse.com/books/566043/china-rx-by-rosemary-gibson-and-janardan-prasad-singh/9781633883819/ This is a public episode. If you would like to discuss this with other subscribers or get access to bonus episodes, visit www.thehealthcarepolicypodcast.com

Image Credit: Maria Martin The Seekers, is the first in a two-part documentary series that examines the experiences of Central American migrants seeking asylum in the US. El Salvador, Honduras, and Guatemala are among the most dangerous countries in the world for women. Each year, thousands of women flee from these Northern Triangle Countries to escape the brutality that stem from drugs and gangs. Now, many Central American migrants are being returned to their countries of origin with their hopes of finding a lasting refuge from violence dimmed. In this episode of Making Contact, we look at what this means for some women who have tried to flee the violence in one of those Northern Triangle Countries— Guatemala. Featuring: Albertina Gutierrez, US asylum seeker, mother of two, from Guatemala; Denise Gilman, San Antonio-based immigration attorney; Alessandra, recently arrived from Guatemala to the US; Sister Consuelo, backpack volunteer with RAICES in San Antonio, Texas; Lynn Stephen, Oregon-based anthropologist and president-elect of the Latin American Studies Association; Lucia, US asylum seeker from Guatemala.   Resources: Trump's rigorous asylum proposals endanger domestic abuse survivors, by Molly Redden https://www.theguardian.com/us-news/2017/apr/10/domestic-violence-trump-asylum-immigration-guatemala RAICES Refugee and Immigrant Center for Education and Legal Services https://www.raicestexas.org/ University of California, Hastings – Center for Gender and Refugee Studies https://cgrs.uchastings.edu/ Music Credits:   “Assobio”, Z Trigueiros “Saez”, Z Trigueiros “Fast”, Z Trigueiros “Fater Lee”, Black Ant   The post The Seekers, Pt. 1: Freedom from Violence appeared first on KPFA.

Dr. Sheldon Krimsky is Professor of Urban and Environmental Policy and Planning at Tufts University and adjunct professor in the Department of Family Medicine and Community Health at Tufts University School of Medicine. He's a Fellow at the Hastings Center and author of, "The GMO Deception: What You Need to Know about the Food, Corporations, and Government Agencies Putting Our Families and Our Environment at Risk."   Krimsky discusses the social, political, and ethical implications of genetically modified foods, including who really controls the power structure of food production and why it's so difficult to get genetically modified foods labeled in the U.S. He shares where Ralph Nader stands in this debate. He also discusses how Vermont's new GMO law will affect the food industry.    Sheldon Krimsky is professor of Urban & Environmental Policy & Planning in the School of Arts & Sciences and Adjunct Professor in Public Health and Family Medicine in the School of Medicine at Tufts University. He received his bachelors and masters degrees in physics from Brooklyn College, CUNY and Purdue University respectively, and a masters and doctorate in philosophy at Boston University.     Professor Krimsky's research has focused on the linkages between science/technology, ethics/values and public policy. He is the author of ten books: Genetic Alchemy: The Social History of the Recombinant DNA Controversy (MIT Press) 1982, Biotechnics and Society: The Rise of Industrial Genetics (Praeger) 1991, Hormonal Chaos:The Scientific and Social Origins of the Environmental Endocrine Hypothesis(Johns Hopkins University Press, 2000), Science in the Private Interest: Has the lure of profits corrupted biomedical research? (Rowman & Littlefield Pub.) 2003. He is co-author of Environmental Hazards: Communicating Risks as a Social Process (Auburn House) 1988 and Agricultural Biotechnology and the Environment: Science, Policy and Social Values (University of llinois), 1996, co-editor of a collection of papers titled Social Theories of Risk (Praeger) 1992, and Rights and Liberties in the Biotech Age: Why We Need a Genetic Bill of Rights (Rowman & Littlefield Pub.) 2005.Genetic Justice: DNA Databanking, Criminal Investigations and Civil Liberties, 2011 with Tania Simoncelli, published by Columbia University Press, 2011; Race and the Genetic Revolution with Kathleen Sloan, published by Columbia University Press, 2011. His forthcoming book edited with Jeremy Gruber to be published by Harvard University Press is titled Genetic Explanations: Sense and Nonsesene. Professor Krimsky has published over 180 essays and reviews that have appeared in many books and journals.     Professor Krimsky served on the National Institutes of Health's Recombinant DNA Advisory Committee from 1978-1981. He was a consultant to the Presidential Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research and to the Congressional Office of Technology Assessment. He participated on a special study panel for the American Civil Liberties Union that formulated a policy on civil liberties and scientific research. Professor Krimsky was chairperson of the Committee on Scientific Freedom and Responsibility for the American Association for the Advancement of Science for 1988-1992. Currently he serves on the Board of Directors for the Council for Responsible Genetics, as a Fellow of the Hastings Center on Bioethics and on Committee A of the American Association of University Professors.   

For the past several decades, Dr. Daniel Callahan has been involved in addressing a wide range of fundamental ethical issues that include: care and decision-making at the end of life, public health priorities, and new and emerging technologies. He is the president emeritus of the Hastings Center and a co-director of the Yale-Hastings Program in Ethics and Health Policy. Dr Callahan has served as a Senior Lecturer at the Harvard Medical School. Along with a doctorate in philosophy from Harvard, he has been awarded several honorary doctorates. He is an elected member of the Institute of Medicine, National Academy of Sciences. Additional honors include being the recipient of  the 1996 Freedom and Scientific Responsibility Award of the American Association for the Advancement of Science. He is the author or editor of 41 books and his articles have graced the pages of many distinguished periodicals, such as Daedalus, the New England Journal of Medicine, the Journal of the American Medical Association, and Health Affairs. In this interview, Mr. Callahan discusses serious problems facing Medicare, the difference between medicine and health, obesity and social pressure, and the "health care pyramid", among others.