Event

Beyond Bioethics

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12:00 pm - 2:30 pm
(Lunch will be served)

B-339 Rayburn House Office Building
Washington, DC

Featuring:

Francis Fukuyama
Bernard L. Schwartz Professor of International Political Economy
School of Advanced International Studies, Johns Hopkins University

Franco Furger
Professor, Foreign Policy Institute
School of Advanced International Studies, Johns Hopkins University

Comments:

Richard Hayes
Executive Director
Center for Genetics and Society

William A. Galston
Senior Fellow
The Brookings Institution

Shannon Brownlee
Schwartz Senior Fellow
New America Foundation

Moderator:

Steven Clemons
Senior Fellow and Director, American Strategy Program, New America Foundation
Publisher, www.TheWashingtonNote.com

Beyond Bioethics, a new report by Dr. Francis Fukuyama and Dr. Franco Furger, provides the most comprehensive examination to date of legislative and/or regulatory answers to the challenges raised by human biotechnologies in the United States. The report's premise is that reaping the benefits of medical progress offered by biotechnology while preventing possible abuses requires that we create a new regulatory agency. Dr. Fukuyama and Dr. Furger will discuss legislative developments at the national and international level and explore public attitudes towards controversial reproductive technologies.

Following their presentation, Richard Hayes of the Center for Genetics and Society, William Galston of The Brookings Institution, and Shannon Brownlee of New America Foundation will comment and discuss possible policy implications for biotechnology. Steven Clemons will moderate a question and answer session. Copies of the report will be available at the event.

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2007-03-02T12:00:00
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A Proposal for Modernizing the Regulation of Human Biotechnologies

Gender, Justice and the New Human Biotechnologies

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Wednesday, Nov. 15
9:15 am - 11:00 am
(Bagels and coffee at 9:00)


Moriah Fund
One Farragut Square South
1634 I Street NW, Suite 1000
Washington, DC

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PRESENTERS

Sujatha Jesudason
Dr. Jesudason's presentation [PDF]
Program Director on Gender, Justice and Human Genetics
Center for Genetics and Society
Richard Hayes
Executive Director
Center for Genetics and Society

New human biotechnologies hold potential for both great good and great harm.

How can we reap the benefits they offer while minimizing the risks they pose for women's health, social and racial justice, human rights, and our common humanity?

What policies need to be supported at the state, federal and international levels?

What political challenges do we face, and what responses are needed?

What organizations are currently working to bring these issues to the attention of key constitutencies, opinion leaders, and policy makers?

Come learn about and discuss:

  • New human biotechnologies: implications for social justice
  • Women's eggs for research and fertility treatments
  • Race-based medicine
  • "Designing" babies
  • Disablity de-selection
  • Choosing a child's sex
  • New eugenic ideologies
  • Ways to regulate stem cell research
  • Human experimentation

IF YOU HAVE QUESTIONS OR WOULD LIKE ANY OTHER ASSISTANCE, PLEASE CONTACT:
Leah Ottersbach
Center for Genetics and Society
510-625-0819 x 307


 

RESOURCES

Selected resources on gender, justice and human genetics are shown below. Search the CGS website for more.

CONFERENCE REPORTS AND PRESENTATIONS

Report on the historic conference, Gender and Justice in the Gene Age, May 2004, New York City

Background packet on Race, Gender and Justice in the Gene Age

Conference Report:Inequality, Democracy, and the New Human Genetic Technologies, June 2004, New York City

"Between Scylla and Charybdis: Reproductive Freedom after September 11," Keynote Address, Annual Convention, National Abortion Rights Action League, Washington, D.C., (November 9, 2001)

CGS Briefing for United Nations Delegates on human cloning, October 2002.

George J. Annas, "Genism, Racism, and the Prospect of Genetic Genocide," presented at the World Conference Against Racism (September 2001)

ARTICLES

The Future of Violence Against Women: Human Rights & the New Genetics
US Women Without Borders
| Feb. 23, 2006 Sujatha Jesudason

Eggs vs. Ethics in the Stem Cell Debate (The NationOnLine). November 2005.

Rupsa Mallik, "A Less Valued Life: Population Policy and Sex Selection in India," Newsletter of Center for Health and Gender Equity (October 2002)

Judith Levine, "What Genetic Modification Means for Women," World Watch (July 2002)

Civil Society Organizations Oppose Sex Selection Technologies. January 2002. This letter signed by over 150 women's health leaders and others demonstrates the depth and breadth of the concerns raised by proposals to commercialize "sex selection" techniques.

"Women's Health and Reproductive Rights Leaders Call for Cloning Ban," Genetic Crossroads (#19, April 18, 2001)

"Human Rights in a Post-human Future." Chapter by CGS Associate Director Marcy Darnovsky's in the book Rights and Liberties in the Biotech Age, Sheldon Krimsky and Pete Shorett (Eds). She distinguishes between "social justice" rights and "individual autonomy" rights

Dorothy Roberts, "Race and the New Reproduction," in Killing the Black Body(New York: Pantheon, 1997), pages 104-149

 

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2006-11-15T12:00:00
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New Challenges for Equality, Human Rights and Social Justice

Which Comes First: The Woman or the Egg?

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Presentation at the Ethical Worlds of Stem Cell Medicine conference, San Francisco and Berkeley, CA

My title was inspired by this advertisement recruiting young women to provide their eggs for stem cell research. It was placed early this year in a free newspaper in Washington DC by Advanced Cell Technology, the company recently in the news for dubious claims about a new method of deriving embryonic stem cells.

It's a small ad, not very flashy, structured around marketing-style clichés: "Which comes first - the egg or the cure?", "It could happen to you or your loved one" and "Let your eggs be part of the cure." These slogans convey a threat of suffering and disease, and a promise of cures; both are in keeping with the hyperbole that characterizes so much of the stem cell debate. They also signal the resumption, after the Hwang debacle of late 2005 and early 2006, of what some U.S. scientists have described as a global "cloning race."

Exaggerated promises like the ones repeated in this ad, competition among researchers for patents and prizes, the increasing influence of the private sector in biomedical research - these are important features of what our conference title terms the "ethical worlds of stem cell medicine." They are part of the social context in which the procurement of eggs for research will take place, in which women will weigh the benefits and risks of providing their eggs for research, and in which policy makers are now deliberating about the sorts of rules, regulations and oversight that are needed.

My remarks today are an invitation to look at what might be called the "conditions of procurement" - that is, at the full social, political, economic and cultural context of egg procurement. This is a different approach than the risk-benefit calculus and individual focus that often characterize bioethical discourse.

Bioethics and biopolitics

Bioethics is good at examining the experience of the individual woman when she walks into a fertility clinic or medical facility to sign a consent document, undergo screening, or get her hormone injections. But I assert that we need to broaden our field of vision, to bring into focus the high-profile and politically polarized environment of stem cell research and stem cell discourse. We need to account for a complex and fraught set of social relationships outside the Petri dish, the laboratory, and the informed consent documents.

We need to think not just about bioethics - understood as a mostly expert endeavor centered in the thickening nexus between the academy and the biotechnology industry - but also about what is increasingly termed, especially outside the US, "biopolitics." This biopolitics is different from the Foucauldian notion of government control of populations through statistics and similar tools; it refers instead to an emerging public, policy, and civil society discourse about the social implications of genetic, reproductive and biomedical technologies.

Before turning to consider these conditions of procurement, I'll first say a few words about my organization, the Center for Genetics and Society, and our experience with the politics of stem cell and cloning research.  Then I'll give a brief account of  how the "missing persons" in the stem cell debate have recently begun to reappear.

CGS and Prop 71

 

The Center for Genetics and Society is a non-profit organization based in Oakland. We see ourselves as a biopolitical organization. Our mission is to encourage the responsible use and effective societal governance of new human biotechnologies. We work to promote social justice, the common good, and the public interest as guiding values for the use, development, and governance of those technologies; to build the influence of civil society constituencies who share these values; and to bring their voices and perspectives to bear on public understanding of and policy-making about human biotechnologies.

CGS supports embryonic stem cell research, and we want to see it publicly funded and publicly regulated. But we opposed Proposition 71 because of its many serious flaws including conflict of interest, unaccountable power over public funds, inadequate oversight.

Also opposing the initiative were the California Nurses Association, which characterized it as a corporate give-away, an ad hoc group of women's and reproductive health advocates called the Pro-Choice Alliance Against Proposition 71, and a few other progressive and liberal organizations. Most liberals and progressives, of course, understood Prop 71 as an up or down vote on the validity of embryonic stem cell research, and as a way to poke a stick at the Bush administration and its Christian fundamentalist base.

The disappearing woman in the stem cell debate

 

CGS and the other pro-choice and progressive groups opposed to Prop 71 raised the issue of women's eggs during the campaign. This was an interesting experience. When we first talked about it to reporters, most of them had no idea what we were talking about. It was simply outside of the dominant frame of reference - which of course was the moral status of human embryos - and so it didn't register.

In fact, the first half-decade of the public debate about stem cell research was dominated almost entirely by the politics of abortion and divisions about the moral status of human embryos. Other issues, including the welfare of the women who would provide eggs for cloning research, received little attention.

But the missing persons in the stem cell debate have lately reappeared. By 2004, a number of countries and the European Parliament had adopted rules about egg procurement, including a range of limitations or prohibitions on compensation. In April 2005, a National Academies committee issued guidelines on embryonic stem cell research that recommended reimbursing women who provide eggs for research for their direct expenses only. Though the NAS guidelines have no legal force and no sanctions, the recommendation put researchers on notice about the seriousness of this issue.

In fact, there is now wide agreement among policy makers that exposing women to the risks of egg retrieval for cloning research raises novel ethical concerns. Compensation is one of them, but not the only one. David Magnus and Mildred Cho are among the close observers who have called attention to the novelty of procuring eggs for stem cell research from healthy women. In a 2005 article, they called these women a "new category of research subject" - meaning that none of the available models of tissue donation are a good fit.

The Hwang scandal

 

The tipping point on media and public recognition of the eggs for research issue was late last year, when the cloning claims and rock-star status of researcher Hwang Woo-suk began to unravel. Hwang's fabricated data, fraudulent claims, and embezzlement of government funds garnered most attention. But accounts of ethical breaches, illegal conduct, and coercion of junior researchers in the procurement of eggs by Hwang and by his associates were also high profile.

When the counting was done, it turned out that Hwang had used over 2200 eggs collected from 119 women, many of whom reported that they had not been properly informed of the risks associated with the procedure. Twenty percent of the donors experienced OHSS and 16 were hospitalized. More than half of the women were paid for their eggs, and several said they agreed to provide their eggs because of dire financial situations.

In the immediate aftermath of the Hwang scandal, a number of US research teams announced that they would resume SCNT work that they had abandoned because Hwang had succeeded in being first. If the "cloning race" ramps up, and especially if SCNT becomes a widely used procedure, researchers will be seeking to procure eggs from many women - perhaps thousands of women.

Some have argued against drawing any general lessons from the Hwang scandal. But I don't think it makes sense just to consider him a single rotten apple in a distant foreign barrel. The atmospheres around stem cell and cloning in South Korea and in the U.S. - and especially here in California - are quite similar, and they comprise the social context, the conditions of procurement, in which women are being recruited to supply their eggs for cloning research.

Conditions of procurement

 

At this point I want to run quickly through a list of the conditions that I think are most relevant to a full understanding of the context in which women will decide whether or not to provide their eggs for stem cell and cloning research, and the context in which policy makers should be thinking about the appropriate rules and regulations for egg procurement.

The first condition of procurement is one that the bioethics framework should highlight: the inadequacy of existing data about the risks of egg retrieval. The many gaps in our knowledge are widely acknowledged - that's why CIRM asked the IOM to organize the scientific meeting about egg retrieval that's going on today in SF. But for now, the incomplete nature of our understanding of the risks creates a challenge to the possibility of meaningful informed consent.

The second condition of procurement is the speculative nature of the benefits of SCNT. Providing eggs for fertility treatments has a clearly established clinical value, as does providing an organ for transplant. SCNT and stem cell research do not.

It's also important to notice that the young women likely to be recruited to provide eggs for research may be drawn from a different population than those who typically provide eggs for other people's fertility procedures. Everyone knows that in the IVF context, the term "egg donor" is an oxymoron: women are paid from $5000 up to $50,000 or even reportedly $100,000 if they have the sought-after characteristics - usually high SAT scores, white skin, blonde hair and long legs.

When eggs are meant for research, on the other hand, the characteristics of the women who provide them are irrelevant - the DNA will be sucked out; all that matters is healthy eggs. The concern is that rather than going after young women from prestigious universities and competing with the sums that the high SAT scorers command, researchers will be tempted to recruit women for whom the floor-level payment - in the Bay Area, around $5000 - will be an inducement to accept the risks of egg retrieval.

Exaggerated promises, therapeutic misconception, and SCNT hype

 

The greatest ethical challenge to responsible egg procurement is what one commentator has called the "irrational exuberance" about the prospects of medical treatments based on stem cell and cloning research. Bioethicists speak of therapeutic misconception - that is, the tendency of research subjects to erroneously believe that their participation in early-stage clinical trials will benefit them. This is understood as a serious impediment to meaningful consent, and bioethicists try to design informed consent procedures to address this problem.

But in the case of stem cell and cloning research, there is no informed consent document that can do this trick. Women contemplating providing eggs for research won't be forming their beliefs about the benefits of SCNT on the basis of a legal document or an interview in a clinic. Instead, their understanding will have been previously shaped by:

  • The wildly overblown promises and endlessly repeated claims about the imminence of lifesaving cures made by research advocates, politicians, and sometimes researchers themselves;
  • the exaggerations about the number and kind of diseases that are likely candidates for stem cell treatments;
  • the inflated hopes that all this hype has produced.

This is the context in which women will weigh the benefits and the risks. It is therapeutic misperception on a grand scale, a social scale.

SCNT as a research tool; the "cloning race"

 

Another important aspect of the social-scale therapeutic misconception is the widespread belief that SCNT will produce cell-based therapies that can be genetically matched to an individual patient. More and more stem cell researchers are acknowledging that this is very unlikely. A still medically important but farm more modest role for SCNT is now foreseen: SCNT as a research tool, a way to produce stem cells against which candidate pharmaceuticals can be efficiently tested.

But researchers and research advocates still repeat the claim about personalized stem cell treatments as part of the stem cell hype engine, and part of the political polarization that makes assessing the potential of stem cell research even more confusing. Many people may remember Ron Reagan, Jr. at the last Democratic Party presidential convention saying that SCNT would produce "your own personal repair kit standing by at the hospital."

There have been hyped treatments before - consider the snake oil. Or more recently, consider gene therapy, also hailed as a medical miracle, also controversial. But there has never before the stem cell debate been a biomedical technology that has generated political wedges, headlines in newspapers across the land, meetings in church basements, presidential vetoes, and state constitutional amendments.

All these aspects of hyperbole around stem cell research foster an over-estimation of the benefits.

There is one final aspect of the overheated stem cell atmosphere that could increase the actual risks to women who undergo egg retrieval. The "cloning race" atmosphere in which SCNT efforts are taking place could encourage the kind of ethical and technical corner-cutting that we saw in Woo Suk's Hwang's work. Without clear standards and effective oversight, it's all too possible that what happened in Hwang's work can happen here.

Unfortunately, existing standards for egg retrieval in the US are for the most part voluntary guidelines, not enforceable in any meaningful way.

SB 1260

An exception to that, and hopefully a harbinger of things to come, is a set of regulations that was signed into law just two days ago by California's governor. The bill was authored by Deborah Ortiz, the Sacramento Democrat who was an early supporter of stem cell research and of Prop 71 but who began working immediately after its passage to fix what she called its "serious flaws." My organization worked closely with Senator Ortiz's office on the bill, along with Planned Parenthood Affiliates of California, and the Pro-Choice Alliance for Responsible Research. It was opposed by the American Society for Reproductive Medicine, the professional organization of the assisted reproduction industry.

SB 1260, which applies to research not funded by CIRM, ensures that any research efforts in California to produce embryonic stem cells using techniques that require women's eggs will meet certain minimum standards to safeguard women's health. Among other things, it mandates that no woman who needs treatment for an adverse reaction will have to pay for it herself, sets some rules to minimize conflicts of interest between the cloning researchers and the medical personnel who conduct the egg retrieval procedures, and in accordance with the NAS guidelines limits compensation to reimbursement for direct expenses.

What is to be done

 

SB 1260 is a small step toward the kind of comprehensive policies that we need in the US on stem cell and cloning research, assisted reproduction and other human biotechnologies. On egg procurement specifically, there are also other ways to minimize the risks, and to increase women's control over and power in the situation:

  1. First: In standards enacted by guidelines, by IRB reviews, by regulations and law, we can ramp up consent procedures, strengthen conflict of interest rules, and limit payments to avoid a market in eggs.
  2. Second: We need better data - on best protocols, on outcomes short and long term.
  3. Third: We need creative outside-the-box thinking about tissue and gamete donors, and the structures that might be set up to give them more influence and power. David Winickoff, for example, has proposed a public biorepository and trust structure that would establish a "commons" rather than a market approach, and that would include representatives of egg providers on its governing board.
  4. Finally, I believe that we need biopolitics. Like other technologies, the human biotechnologies can deeply influence people's lives and life chances, and shape social arrangements and power relations. They are appropriately the subjects of democratic processes.

Many stem cell researchers insist that their job is "just to do the science," and many stem cell advocates decry the intrusion of "values" into the scientific arena. But science and values are never separate. Religious opponents of ESCR have their values (non-destruction of embryos); we have ours (health equity, protecting women, preventing misuse). These values - or the lack of them - are unavoidably being built into stem cell program at many levels of decision making: about particular research projects, about research standards, etc. Without democratic control and public participation, these are values that are all too likely to fall by the wayside.

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Marcy Darnovsky
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2006-09-29T12:00:00
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Missing Persons in the Stem Cell Debate

Democratizing Biopolitics

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Presentation at The Future of Bioethics in a Divided Democracy conference, organized by the Alden March Bioethics Institute, Albany, NY, July 13-14, 2006.

My organization, the Center for Genetics and Society, was founded because of the recognition at the end of the 1990s that liberal and progressive civil society voices were almost completely missing from ongoing discussions among policy makers, bioethicists, and others about the social meanings of human biotechnologies - discussions that were quickly growing more urgent as the pace of technological development accelerated. We called this situation a "civil society deficit," and began working to remedy it.

 

I'm going to

 

  1. first say a few words about how CGS got its start and what we've learned about that civil society deficit
  2. second, talk just a bit about how it is beginning to change, as liberal and progressive constituencies become involved in human biotech debates, and
  3. third, of particular interest at a conference aimed at exploring the divide between liberal and conservative bioethics, talk about some important differences and tensions that are becoming apparent among liberals and progressives on human biotechnology issues

 

CGS and the civil society deficit

 

Before the formal establishment of the Center for Genetics and Society, we convened a series of meetings. We brought together several multi-disciplinary groups of people who were knowledgeable and concerned about the social and political implications of new reproductive and genetic technologies, and who were committed to social, economic, and racial justice; to reproductive rights; and to socially responsible science and environmental protection.

 

At those meetings, we discussed

 

  • the speed with which human biotechnologies were developing,
  • the inadequacy of the rules and regulations in place to guide their development and use,
  • the increasingly commercialized environment in which these developments were taking place, and
  • the fact that both the technical and policy situation were not on the radar of the general public, opinion leaders, or policy makers.

 

There was general agreement that some human biotechnologies were likely to yield beneficial applications in the diagnosis and treatment of disease, and that we wanted to support these. But we were also concerned about the potential of these technologies to greatly exacerbate human inequality, both through increasing our already shameful global health disparities; and depending on how the techniques developed, through the potential use of new human genetic and reproductive technologies for eugenic purposes.

 

We were already seeing that the prospect of powerful new reproductive and genetic technologies was triggering a revival of eugenic ideologies by a small but disturbing number of influential scientists and others, including some bioethicists. This was a vision of "better breeding" not through government mandate or authoritarian decree, but as a supposedly inevitable technical advance and the natural play of free markets.

 

When we set up CGS in 2001, we defined our mission as one of "working to encourage responsible uses and effective societal governance of the new human genetic and reproductive technologies." A large part of our work has been aimed at increasing the participation of civil society constituencies in public and policy debates about biomedical, genetic, and reproductive technologies. Toward that end, we have organized or participated in hundreds of conferences, workshops, meetings and briefings, the majority of them with liberal and progressive individuals and organizations, including those working for women's health and reproductive rights; GLBT and disability rights; racial justice and civil rights; environmental protection and animal welfare; consumer advocacy and good government.

 

In nearly all these encounters, we've found a keen interest in the issues raised by human biotechnologies, but uncertainty about how to participate in shaping them, and deep concern that developments are moving at a pace and in a manner that leaves the great majority of people excluded from the debate.

 

[Bioethicists, civil society, inclusion]

 

On the topic of exclusion: I can't help but remark on the demographic imbalances of this conference. I appreciate the organizers for bringing together people across the left-right political spectrum, but it's disappointing to see the lack of diversity and balance among the plenary speakers. The roster of invited speakers is pretty overwhelmingly dominated by - not to put too fine a point on it - white men from academia. I'd thought we were well past the days of counting, but I confess to comparing the numbers of women and people of color among the plenary speakers to the numbers in George Bush's cabinet. By that measure, it doesn't look good for the bioethicists.

 

It's obviously important to address lack of racial and gender balance wherever it occurs. There also seems to be an imbalance here in the types of expertise represented. Most of us are technical or academic experts, but there are many other types of relevant expertise, including social constituency expertise.

 

Given that an important part of the project of bioethics consists of setting the rules for the development and use of powerful, future-shaping technologies, it's clearly important to be as inclusive and democratic as possible. Bioethicists have often functioned as surrogates for democratic participation in decisions about biotechnologies, and in so doing have perhaps perpetuated the civil society deficit on the issues. Though bioethicists typically present themselves as experts rather than as spokespeople, there is a tendency to believe that they are minding the store for the rest of us - which they may or may not be doing, and which of course they have no mandate to do.

 

Bioethical expertise is in some ways a peculiar kind of expertise. Here's what I mean: Think about the kind of involvement we have come to expect in the politics of other powerful technologies. Think, for example, about controversies over what kind of energy technologies to develop - should we emphasize nuclear power or solar power? Should we build large hydro-electric dams? Should we drill for oil in the Arctic?

 

On these issues, we don't consult energy ethicists. We consult academic and policy experts, yes. And we also recognize these as political issues, as decisions that will transform the way many people live and work, that will create winners and losers, that involve some people making decisions that will shape the lives and life chances of others, perhaps on the other side of the world or in future generations.

 

We expect, at the beginning of the 21st century, that these issues will be widely debated, that environmental, consumer protection, and human rights groups are likely to weigh in, sometimes quite vociferously, that these civil society actors will be cited in the media and participate in conferences, that they will be included in policy debates and decisions.

 

We need similar robust debate, democratic participation, and broad inclusiveness of civil society constituencies in decisions about human biotechnologies. This is a crucial endeavor, but a challenging one. Our democratic processes are imperfect; the mechanisms by which civil society constituencies assert themselves are often messy, we are operating in a politically polarized environment that makes thoughtful deliberation about human biotechnologies difficult, and the combined power of techno-science and the market is daunting.

 

The overall trends are sobering. But the increasing involvement of civil society organizations and opinion leaders in the politics of human biotechnology is a hopeful sign. I'll just mention a few of the constituencies that are beginning to weigh in on these issues.

 

Liberals and progressives in the politics of human biotech

 

First, women's health and reproductive rights advocates. The fact that many human biotechnologies involve reproduction, and that the most controversial biomedical technologies involve human embryos, means that women's health and reproductive rights are inescapably affected by biopolitics. The first impulse of some mainstream feminists has been to embrace these technologies, but this has been far from stable and far from uniform.

 

In 2004, CGS, OBOS and CWPE held a meeting at the Ford Foundation that gathered together 65 women and a few men to discuss the full array of the new reproductive and genetic technologies and their impact on women and communities of color. This meeting connected academics to advocates, and feminist, disability rights and social justice organizations. Many attendees went on to lead their groups to become more involved on these issues.

 

Another example is the California Coalition for Reproductive Freedom's recently established Reproductive Technologies subcommittee, set up as a safe space for CA leaders to debate and explore these issues. One more: CGS worked with PPFA and Smith College on their Reproductive Justice for All Conference so that one of the four major topics of focus was Assisted Reproductive and Genetic Technologies. About 100 people spent two days discussing and debating politics and policies in this area.

 

Stem cells in California. CGS was one of a small number of progressive or liberal groups in California that support ESCR but opposed Proposition 71, the $3 billion stem cell initiative of 2004.

 

The other progressive organizations that opposed Prop 71 were an ad hoc network of women's health and reproductive rights advocates working under the name Pro-Choice Alliance Against Prop 71, and the California Nurses Association - an important ally, with 65,000 members in the state and a public approval rating that consistently stays above 80%.

 

At first it was pretty lonely, and our positions were often misunderstood. But within weeks of the initiative passing, a buyers' remorse began to develop. Now, almost two years later, our criticisms of Prop 71 and its implementation have been not just reported on but editorially echoed in every major newspaper in the state. We've worked with women's health groups and a Democratic state senator on a bill to ensure that women who provide eggs for research are treated as research subjects, and not compensated beyond direct expenses so as to avoid creating a market in eggs. We've worked with good government groups including Common Cause and CalPIRG, with racial justice groups including the Greenlining Institute, with consumer protection groups including the Foundation for Taxpayers and Consumers Rights, and others.

 

Others: Disability rights groups have been out in front on these issues, acutely aware of the history of eugenic targeting of people with disabilities, and concerned that norms of "perfection" could all too easily displace values of care and respect. We co-sponsored a series of events at the New York GLBT Center. Environmentalists have opposed portrayals of efforts to clone endangered species as conservation measures. Animal welfare advocates including the Human Society of America have sharply criticized pet cloning.

 

Liberal values and human biotechnologies

 

As liberals and progressives begin to consider human biotech issues and become involved, differences among them have started to become apparent. These differences or tensions turn on the different emphases they place in three areas:

 

  1. balancing personal liberty and individual autonomy with social justice and the common good;
  2. determining the kind and amount of enthusiasm or caution appropriate to various genetic, reproductive, and biomedical technologies;
  3. deciding whether regulation in these areas is best centered in government or market mechanisms.

 

None of these are absolutes - each requires a balancing act. And these differences are not exclusively about biotechnologies or biopolitics - they crop up in other areas as well. Sometimes, they are tensions not just among those of us to the left of center, but within ourselves.

 

However - the United States is a place where the combination of techno-science and the market is especially powerful, where the commitment to perpetual progress - defined as technological progress - is strong, and where the emphasis is on individual and market-based solutions to social problems. Add to this the polarized politics that have developed as the religious Right stakes out a ground of absolutism around protecting human embryos, and liberals and progressives react, sometimes reflexively, to defend freedom on inquiry. Under these conditions, the skewed and incomplete conversation that has developed around human biotechnology is perhaps no surprise. As Dan Sarewitz puts it:

 

The result is a highly restricted domain of permissible conversation, and an increasing willingness to stake the future of humanity not on our admittedly imperfect processes of negotiating competing values and interests in light of our moral foundations, but instead on the accelerating capacity of science and technology to remake the world in any and every way that it can.

 

All this conspires to create a situation in which social justice, a precautionary sensibility, and a commitment to crafting government regulation and oversight tend to be slighted. I'll conclude with a very few brief remarks about what each of these values counsels on issues of responsible development and use of human biotechnology.

 

Social justice and personal liberty. To promote social justice in the gene age, we need ways to apply needed brakes on two very slippery slopes: one that leads to "designer medicine" and the other that leads to "designer babies."

 

By designer medicine, we mean high-tech therapeutics that will almost certainly be unaffordable except for the very wealthy - for example, the kind of treatments envisioned in the notion of "personal repair kits" that has been used to promote stem cell and cloning research.

 

One problem here comes down to the allocation of the significant resources-talent and money, much of it public funds-that high-tech enhancement would entail. Budgeting is not a zero-sum game, but oughtn't we be prioritizing clean drinking water for the third of the world's population that doesn't have it, or health insurance for the 46 million Americans who don't have that?

 

By designer babies, we mean inheritable genetic modification - the production of children who are genetically "enhanced." This is another kind of procedure that, if successfully developed, would almost certainly be disproportionately available to the wealthy, and would create increased social division, discrimination, and conflict.

 

However far off the technical accomplishments that would permit such experiments, we're faced now with the impact of the stories we tell ourselves about how to improve the human condition. We can tell ourselves, and encourage politically engaged people to believe, that we should be expending our efforts to the production of children with wings and gills and superior intelligence. Or we can commit ourselves to creating social conditions that will improve the life chances of children: clean air to breathe, vaccinations for infectious illnesses, good educations. I believe that the transhumanist story of a glittery techno-utopianism reflects the tragic withering of our collective confidence in human improvement through social change, and makes that withering worse.

 

Techno-enthusiasm vs "critical optimism." The way I understand it, honest skepticism is in fact a hallmark of good science; and I would argue that careful assessment is a hallmark of good technology.

 

It is of course largely meaningless to declare oneself either "for" or "against" technology. Instead, we need to understand and shape how technologies are used, who they benefit, who controls them and whom they control, and, upstream, how they are developed - because social relations are actually built into many technologies.

 

Of course, we enjoy the benefits of many biotechnologies - my eyeglasses, my kid's protection against many infectious diseases, my friends' knee replacements. We also live with the knowledge of the great civilizations that have collapsed because of misuse of contemporaneous technologies, in the shadow of Hiroshima, with severe environmental degradation in many parts of the world, and with the prospect of catastrophic climate change.

 

Human biotechnologies give us - or some of us - the capacity to change our own bodies at a molecular level. Doesn't it make sense to try very hard to get the balance right between progress and precaution?

 

That's not what we're seeing. In the case of stem cell research, we have far too many researchers and their supporters, echoed by politicians and the media, indulging in a level of hype and over-promising that is scientifically embarrassing and ethically irresponsible. In the case of advocates of genetic enhancement and tanshumanism, we have glib dismissal of risks. In his, Introduction to Transhumanism, for example, Nick Bostrom writes this about enhancement technologies, "It would be tragic if the potential benefits failed to materialize because of technophobia and unnecessary prohibitions.

On the other hand, it would also be tragic if intelligent life went extinct because of some disaster or war involving advanced technologies."

 

Government regulation versus market mechanisms or voluntary guidelines.

How do we react to the fact that human biotechnologies are increasingly being developed in an intensely commercial environment?

 

Fifty years ago, Jonas Salk became famous for developing the polio vaccine that put an end to a horrible disease that caused enormous suffering. When news broke that the field trials of the vaccine had been successful, Salk was interviewed by Edward R. Murrow on "See It Now." "Who owns the patent on this vaccine?" Murrow asked. Salk replied: "Well, the people, I would say. There is no patent. Could you patent the sun?"

 

That was then. But even 15 or 20 years ago, scientists were far less likely than they are today to be involved with private industry as consultants, stakeholders, founders. We're now seeing the first generation of biomedical science that's being developed by a cadre of researchers with anything like this level of direct interest in profit-making and corporate gain. This has created a raft of widely acknowledged problem: conflicts of interest, adverse reactions unreported because of proprietary concerns, patent blockages, and most important, a serious under-representation of the public interest.

 

Most scientists remain ethical, responsible, and devoted to expanding knowledge and developing tools to benefit humanity. But in an age of corporate biotechnology, we need to confront conflicts of interest forthrightly. We need to acknowledge that biomedicine is a business, that assisted reproduction is a business, and that progressives historically have championed government oversight and regulation as a necessary means of protecting the public interest. The idea that scientists can regulate themselves doesn't hold up.

 

We have a far greater chance of reaping the benefits of human biotechnologies and avoiding their risks if we strengthen our commitments to social justice and the common good, to a precautionary optimism and what Jonathan Moreno calls "critical optimism," and to responsible government regulation. Whether or not we manage to do this is one of the most consequential questions we face.

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Marcy Darnovsky
Date
2006-07-12T12:00:00
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Civil Society and Human Biotechnology

Progressive Values and Stem Cell Research at Take Back America

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CGS Associate Director Marcy Darnovsky spoke on a key panel about progressive values at Take Back America, the Campaign for America’s Future’s award-winning annual conference. The gathering brought together more than two thousand progressives from around the country. The other speakers on the panel were Cecile Richards, President, Planned Parenthood Federation of America; Joe Solmonese, President, Human Rights Campaign; and, Wade Henderson, President, Leadership Council on Civil Rights.

Read the full text of Darnovsky’s talk, "Stem Cell Politics and Progressive Values," in PDF format.

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Date
2006-06-29T12:00:00
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Genetic Crossroads

Reception for Publication of "Stem Cells and Public Policy"

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The Century Foundation and

The Center for Genetics and Society

will discuss the issues raised in the new publication

Stem Cells and Public Policy

Friday, June 16
12:00 noon - 1:30 pm
Lunch will be served


The Century Foundation
41 East 70th Street
New York City, New York

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As the US Senate prepares to vote on stem cell legislation, a new title in The Century Foundation Basics series, Stem Cells and Public Policy, offers informed lay readers a comprehensive overview of the complex scientific, ethical and policy issues that stem cell research raises.

Join authors Richard Hayes, Executive Director of the Center for Genetics and Society, and Leif Wellington Haase, Senior Program Officer and Health Care Fellow at the Century Foundation, to discuss how we can ensure that stem cell research proceeds in a manner consistent with the public interest.

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Date
2006-06-16T12:00:00

Gender, Justice and the New Human Biotechnologies

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Thursday, June 15
10:00 am - 12:00 noon
Lunch & continued discussion, 12:00-1:00

Ford Foundation
320 East 43rd Street
New York City, New York

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PRESENTERS

Dorothy Roberts
Professor of Law, Northwestern University
Author, Killing the Black Body
Sujatha Jesudason
Program Director on Gender, Justice and Human Genetics
Center for Genetics and Society
Richard Hayes
Executive Director
Center for Genetics and Society

New human biotechnologies hold potential for both great good and great harm. How can we reap the benefits they offer while minimizing the risks they pose for women's health, social and racial justice, human rights, and our common humanity?

What political challenges do we face, and what responses are needed?

What organizations are currently working to bring these issues to the attention of key constitutencies, opinion leaders, and policy makers?

Come learn about and discuss:

Stem cell research and human cloning
Choosing a child's sex
Eggs for research and fertility
Race-based medicine
"Designing" babies
Disablity de-selection
Human experimentation
Dangers of new eugenic ideologies
 

IF YOU HAVE QUESTIONS OR WOULD LIKE ANY OTHER ASSISTANCE, PLEASE CONTACT:
Leah Ottersbach
Center for Genetics and Society
510-625-0819 x 307


 

RESOURCES

Selected resources on gender, justice and human genetics are shown below. Search the CGS website for more.

BOOKS

Killing the Black Body: Race, Reproduction, and the Meaning of Liberty, by Dorothy Roberts (Vintage Books, 1998).

Undivided Rights: Women of Color Organize for Reproductive Justice by Jael Silliman, Marlene Gerber Fried, Loretta Ross, and Elena Gutiérrez (South End Press, 2004).

CONFERENCE REPORTS AND PRESENTATIONS

Report on the historic conference, Gender and Justice in the Gene Age, May 2004, New York City

Background packet on Race, Gender and Justice in the Gene Age

Conference Report: Inequality, Democracy, and the New Human Genetic Technologies, July 2004, New York City

"Between Scylla and Charybdis: Reproductive Freedom after September 11," Keynote Address, Annual Convention, National Abortion Rights Action League, Washington, D.C., (November 9, 2001)

CGS Briefing for United Nations Delegates on human cloning, October 2002.

George J. Annas, "Genism, Racism, and the Prospect of Genetic Genocide," presented at the World Conference Against Racism (September 2001)

ARTICLES

The Future of Violence Against Women: Human Rights & the New Genetics
US Women Without Borders
| Feb. 23, 2006 Sujatha Jesudason

Eggs vs. Ethics in the Stem Cell Debate (The NationOnLine). November 2005.

Rupsa Mallik, "A Less Valued Life: Population Policy and Sex Selection in India," Newsletter of Center for Health and Gender Equity (October 2002)

Judith Levine, "What Genetic Modification Means for Women," World Watch (July 2002)

Civil Society Organizations Oppose Sex Selection Technologies. January 2002. This letter signed by over 150 women's health leaders and others demonstrates the depth and breadth of the concerns raised by proposals to commercialize "sex selection" techniques.

"Women's Health and Reproductive Rights Leaders Call for Cloning Ban," Genetic Crossroads (#19, April 18, 2001)

"Human Rights in a Post-human Future." Chapter by CGS Associate Director Marcy Darnovsky's in the book Rights and Liberties in the Biotech Age, Sheldon Krimsky and Pete Shorett (Eds). She distinguishes between "social justice" rights and "individual autonomy" rights

Dorothy Roberts, "Race and the New Reproduction," in Killing the Black Body (New York: Pantheon, 1997), pages 104-149

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Date
2006-06-15T12:00:00
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New Challenges to Equality, Human Rights and Democracy
Source
Ford Foundation Briefing