Prenatal-Testing Books

This fascinating and thought-provoking book should be read by anyone interested in disability rights. It presents a variety of views on a challenging topic. The book deals with philosophical issues in understandable terms, and argues for a new paradigm for consideration of prenatal testing.

Different chapters are written by various authors from different backgrounds. Physicians, professors, parents, those with disabilities, therapists and lawyers all contribute to this multifaceted approach to whether or not prenatal testing devalues those with disabilities. Social factors and medical factors are discussed with clarity. This book will cause the reader to question the basis for their pre-concieved beliefs about what it means to have a disability, and will encourage them to look at this issue in a more thoughtful way.

I found this book difficult to put down, and have recommended it to several friends.

(A longer version of this review ran in the January 2001 issue of Ragged Edge magazine.) Does prenatal testing for genetic defects "send a message" to disabled people? Adrienne Asch, the Henry L. Luce Professor of Biology, Ethics and Reproduction at Wellesley College, insists that it does. For two years, Asch and Hastings Center bioethicist Eric Parens engaged a group of scholars, philosophers, ethicists, biologists, physicians, sociologists and educators under the auspices of the Hastings Center to grapple with that question, and the disability rights perspective on prenatal testing in general. This book is the product of that project.

After listening to all the opinions expressed by project members, Asch writes in an essay late in the book that she has not changed her mind. She says that people who choose to abort based on a diagnosis of disability are "allowing a single trait to stand in for the whole, to obliterate the whole." People like Baily -- and they are in the large majority in society -- simply do not believe that aborting a fetus because it will likely have a disability "sends a message" that is bigoted; most do not believe that it sends any message at all. Many do not agree that the provision of more accurate information about disabilities or about living with particular disabilities would make any great difference in their decision to abort a fetus they feared carried a "defect." Even knowing about disabled people and their lives, she would still not want to bear a disabled child if it could be avoided, says Baily. Nor do they buy the "any/particular" distinction articulated by Asch, who has been writing about the disability perspective on reproductive choice for decades. The "any/particular distinction" refers to the difference between the decision to simply not have any child at all at the time -- the decision of someone who becomes pregnant when they were not planning a family and thus seeks an abortion, for example -- and the decision to abort a particular fetus, even when the woman in fact wants a child, when prenatal testing has revealed disability in the fetus. The project, funded in part by a grant from the National Institute on Disability and Rehabilitation Research, did not reach unanimity on any of the "major claims" of the disability rights movement -- not after five intense two-day intense meetings, not despite ongoing email correspondence among participants, notwithstanding meetings with members of the Society for Disability Studies. So are we simply at that juncture in history in which almost no one outside one's tiny community of thought believes one's critique; before one's ideas are accepted? Is this what it was like in the 1800s to hear perfectly nice, logical people say things which we now we see as hopelessly racist? It's hard to tell. This is an important, though academic, book. It lays out both the disability rights critique from Asch, Marsha Saxton and others, and the reasons why people just don't "buy" the argument that life with a disability is alright, which is really what it comes right down to.

"Using prenatal tests to prevent the births of babies with disabilities seems to be self-evidently good to many people," Asch writes. No matter that critics argue that these beliefs stem from unexamined attitudes about disability; this project shows that when the attitudes are examined they are often found to be fine attitudes -- by those who hold them. In her piercingly honest essay "Somewhere A Mockingbird" (which also appeared in the anthology Bigger Than The Sky: Disabled Women on Parenting (Ragged Edge, Jan./ Feb. 2000), Deborah Kent reports what happens when she and her husband begin to plan having a child, knowing it may be born with Kent's genetic blindness: Despite the closeness of the couple, writes Kent, she had failed to convince her husband, even after their years together, "that it is really okay to be blind." "I will always believe that blindness is a neutral trait, neither to be prized nor shunned. Very few people, including those dearest to me, share that conviction... They cannot fully relinquish their negative assumptions...." "Though they dread blindness as a fate to be avoided at almost any cost," she writes of her family and friends, "they give me their trust and respect. I don't understand how they live without discomfort amid such contradictions."(emphasis ours.) Yet many of the project's participants live with this contradiction seemingly quite well and without question. If there is a theme to be taken away from this volume, it is that society can quite easily live without examining such contradictions. In one of the most sobering essays in the book, Nancy Press writes that "certain silences in the public discourse have actually enabled the routinization and rapid growth of prenatal testing,.... by obscuring or limiting the need for public debate about two topics about which Americans are deeply conflicted but which lie at the heart of prenatal testing: abortion and disability." This book arrives at a time in our society when prenatal testing is becoming routine -- and a duty. As tests for finding ever more genetic traits and predispositions become ever easier to administer, our country's legal hubris being what it is, women will be told to get them done, or else. Sociologist Dorothy Wertz contends that "even if some lines might be drawn in practice they will not make a difference since market and political forces will determine which prenatal tests are offered and in what kind of an atmosphere they will be offered." Biologist Pilar Ossorio points out that "when prenatal tests become part of routine [medical] practice, courts will find that physicians have a duty to offer them." Detailing the strange and horrific outcome, today's "wrongful birth" and "wrongful life" lawsuits (in which the disabled child argues before the court "that her life is worse than non-existence"), Ossorio's chapter is a sober reminder of the road we head down when we reject the disability rights critique of prenatal testing.

With increased pre-natal genetic testing comes the knowledge to know of disabilities that the chile will face later. This book is a series of papers describing the ethical and social issues this raises. A second theme is a discussion of the quality of life for disable persons.

This book came from a working group that the editors convened. Papers were presented on the subject, and then afterwards they were revised in light of the deliberations at the conference. The contents range from the social contract under which we all live to the right of the individual woman to terminate a pregnancy for any reason what so ever (as defined by Roe v. Wade).

"We are not born knowing how to be parents." That in a nutshell, motivated the Wexler's to produce this up to date guide for parents to be, both eager and anxious. They cover every important question regarding diagnostic techniques and results, and pay special attention to the latest technology and parental issues. "Not all of these (technological) advances have been positive. They may raise more questions than answers." Parents can discuss their concerns with their doctors. But at least they're here in this very current book. The authors guide the reader through adoption, AFP, amniocentesis, chromosomes, CVS, ectopic pregnancy, fetal growth, infertility, Down syndrome, lab tests, miscarriage, ultrasound and even insurance in a thorough, non-judgemental discussion.

"One of the most painful and difficult times is when
the joy of being future parents is burst by the prospect of an abnormality." That is always a possibility, and the Wexler's deal with it sensitively but honestly. They include a Family Genetic Profile for parents to complete. It is easily removed for sharing with a doctor. A very caring, informative and modern look at issues facing all prospective parents!

(As Reviewed by the Book Reader - America's Most Independent Review of New Books)

If I were only interested in genetic testing and genetic defects, I would have given this book at least a four star. (Would have been a five if it had a better index!)

But I wanted information on birth defects, open and closed cord defects also. I thought this book was a little weak in that area. As an example, the book didn't contain any statistics about the nuchal fold translucency ultrasound and results, etc.

It's not FUN reading about negative aspects of pregnancy like this, but the authors did a good job in making it readable and informative.