“After The Genome” – A Conference on the Language of Our Biotechnological Future. Presented by Wake Forest University & Baylor University. 12 & 13 April 2013

 

An exploration of the intersection of biotechnology, ethics, language, religion, and science is both timely and critically important. This national forum will provide a location for leading scholars from a variety of disciplines to discuss the vital topic of how language is shaping medical ethics, religion, and competing visions of our biotechnological future.

Interview with Nancy King, JD, Co-Director for the Center for Bioethics, Health & Society and a speaker at the conference:  http://www.youtube.com/watch?v=kZzCXUkt1ik.

9:00 AM April 12th – 7:00 PM April 13th

Wake Forest University, Benson University Center, Pugh Auditorium.

 To register please go to the following link:  http://afterthegenome.provost.wfu.edu/.

SCARRED FOR LIFE: The Legacy of Forced Sterilization at Home & Abroad – Film Screenings (20 & 27 March) & Discussions (4-5 April)

 

SCARRED FOR LIFE: The Legacy of Forced Sterilization at Home and Abroad

Film Screenings (7:00-9:00, DeTamble Auditorium, Tribble Hall)

Wednesday, March 20: Gattaca (dir. Andrew Niccol, 1997)

Wednesday, March 27: Tomorrow’s Children (dir. Crane Wilbur, 1934)  

 

SCARRED FOR LIFE: The Legacy of Forced Sterilization at Home and Abroad

4 – 5 April 2013

Location: Annenberg Auditorium, Carswell, Wake Forest University

Thursday April 4, 2013:  Focus on North Carolina

5:00-5:45: Welcome and general introduction.

5:45-7:00: Panel Discussion and Reception

Simone Caron, Professor and Chair of the Department of History, WFU, a leading expert on reproductive history

Kevin Begos, journalist who has written extensively on NC’s eugenics program in the Winston-Salem Journal’s 2002 series Against Their Will and a 2011 series in the Indy in Chapel Hill

Charmaine Fuller Cooper, former director of the NC Justice for Sterilization Victims Foundation established by the then Gov. Bev Perdue in 2010 to provide justice and compensate victims who were forcibly sterilized by the State of North Carolina

 

Friday April 5, 2013, Focus on National and International Contexts

2:00-2:50: Dan Kevles, Professor of History, Yale University—A review of the history of the eugenics movement in the United States and its implications for the future of genetics.

3:00: Panel Discussion and Reception

Angela Kocze, Hungarian visiting Fulbright scholar with Women’s and Gender Studies

Adam Stein, North Carolina lawyer who filed suit on behalf of sterilization victims in the 1970s

Nancy King, Professor in the Department of Social Sciences and Health Policy, WFU School of Medicine and Co-Director, Center for Bioethics, Health and Society

Dan Kevles; Professor of history, Yale University   

For the further information please contact Dr. Wanda Balzano, Program Director & Assoc. Professor, Women & Gender Studies - balzanow@wfu.edu, or Phoebe Zerwick, Lecturer, The Writing Program, Dept of English – zerwicp@wfu.edu.

“The End of Sex: The Future of Human Reproduction” – Bioethics Seminar Series – 28 March 2013

 

Hank Greely, JD, Deane F. and Kate Edelman Johnson Professor of Law and Professor, by courtesy, of Genetics at Stanford University       

5:00 – 6:00 pm, Thursday 28th March 2013                     

Room 308, Greene Hall, Reynolda Campus, Wake Forest University

“Biobanks & Databases: Challenges for Research Ethics (& Researchers)” – Research Ethics Grand Rounds – 28 March 2013

 

Hank Greely, JD, Deane F. and Kate Edelman Johnson Professor of Law and Professor, by courtesy, of Genetics at Stanford University

Thursday, 28th March 2013

12:00 – 1:00 PM

G28,  G Floor Hanes Building, Wake Forest School of Medicine.

To Register please contact Andrea Nance:  anance@wakehealth.edu

“Clinical Rationality: Lessons from Doctor Dolittle” – Bioethics Seminar Series, Thursday 28 February, 5:00-6:00 pm.

Kathryn Montgomery, Julia & David Uihlein Professor of Medical Humanities and Bioethics Professor of Medicine,  Northwestern University Feinberg School of Medicine

Doctors, like all humans, exercise their reasoning and judgment through stories, not merely through numbers.  Dr. Montgomery draws on her exploration of clinical thinking, from her books Doctors’ Stories: The Narrative Structure of Medical Knowledge (Princeton 1991) & How Doctors Think: Clinical Judgment and the Practice of Medicine (Oxford 2006), to examine clinical reasoning in medicine.

Attendees are invited (but not required) to read Sir Arthur Conan Doyle’s “A Study in Scarlet” before the seminar.  The story may be downloaded, at no cost, as an ebook or PDF, from project Gutenberg <www.gutenberg.org>.

Thursday, 28th February – 5:00-6:00 pm

Greene Hall, Room 308, Reynolda Campus, Wake Forest University

Reception to follow.

Research Ethics – articles from Wake Forest University Conference in the latest edition of The Journal of Law, Medicine & Ethics.

Ana Iltis, PhD and Nancy King, JD, Co-Directors of the Center for Bioethics, Health & Society edited a group of articles in the Winter 2012 Journal of Law, Medicine & Ethics, published by the American Society of Law, Medicine and Ethics.   

The articles resulted from the Center for Bioethic ’s sponsoring of the November 2011 “Research Ethics Conference:  Re-Examining Key Concerns”.  James H. Jones was the keynote speaker in honor of the 30th anniversary of the publication of his book “Bad Blood”.

“One Chaplain’s Story: The Use of Narrative in Clinical Ethics Consultation” – Bioethics Seminar Series, Thursday, February 14th, 5:00-6:00pm

Jay Foster, D.Min, BCC, NC LPC, Associate Director,

Department of Chaplaincy & Pastoral Education, Wake Forest Baptist Medical Center

5:00 – 6:00 PM

Room 308, Greene Hall, Reynolda Campus, Wake Forest University

Reception to Follow.

“Bioethics, Public Moral Argument, And Social Responsiblity” – December 2012 review of book co-edited by Nancy M.P. King, JD and Michael J. Hyde, PhD

Please click on the following link to read the review published by JAMA:  Bioethics, Public Moral Argument, And Social Responsiblity

Tuesday, December 4 – “A Defining Error” – A Performable Case Study with Discussion, part of the Bioethics Seminar Series

Presented by bioethics graduate students, directed by Professor Richard Robeson

This case study is inspired by events surrounding the 1989 creation and implementation of the Medical University of South Carolina’s policy of drug-testing pregnant women suspected of crack cocaine use.  The case considers a number of ethical questions, including involuntary urine drug screening for patients, substance abuse treatment imperatives, maternal-fetal conflict, and the appropriateness of involving the criminal justice system to implement healthcare policy.

Performable case studies are dramatic readings created from bioethics case prompts, research, and creative engagement with the human, ethical, social, and policy implications of the facts and issues under consideration.  They are designed to promote discussion; therefore, audience discussion after the reading is an integral part of the performance.

7:00-8:00 pm  -  Reception to follow.

Room 409, Benson University Center, Reynolda Campus, Wake Forest University

“Individualized Genomic Medicine: Is It Fair?” Co-Director of the Center for Bioethics, Health & Society to speak at Trent Center for Bioethics, Duke University

Nancy M. P. King, JD, Professor, Dept of Social Sciences & Health Policy, Wake Forest School of Medicine; Co-Director, Center for Bioethics, Health & Society, Wake Forest University to speak as part of the “Humanities in Medicine Lecture Series”.
 
Wednesday, December 5, 2012
12:00-1:00 pm
Duke Hospital Lecture Hall 2003
Lunch provided at NOON
Talk begins at 12:15 PM
 
Much has been made of the thousand-dollar genome and the impact that individualized genomic medicine could have on medicine and health care. But should everybody’s genomes be sequenced? It is critically important for individuals, health care providers, and society to consider the scientific, ethical, and policy promises and pitfalls of genomic sequencing information.
 
Professor King’s scholarship focuses on a range of bioethics issues, including informed consent in health care and research; ethical issues in large-scale genetic research and biobanking, gene transfer research, and regenerative medicine; and connections between science, ethics, design, and policy in biotechnology research. She is co-editor of The Social Medicine Reader (2nd ed., Duke University Press, 2005) and Beyond Regulations: Ethics in Human Subjects Research (UNC Press 1999). She has served on numerous hospital ethics committees, IRBs, DSMBs and on the NIH Recombinant DNA Advisory Committee.
 
Lecture Hall 2003 is one floor directly above the main lobby of Duke Hospital. 
For more information, please contact Trent Center for Bioethics us at (919) 668-9000 or trent-center@duke.edu