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Heredity and Hope: The Case for Genetic Screening

Heredity and Hope: The Case for Genetic Screening

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Author: Ruth Schwartz Cowan
Publisher: Harvard University Press
Category: Book

List Price: $27.95
Buy New: $15.75
You Save: $12.20 (44%)



New (22) Used (7) from $15.75

Avg. Customer Rating: 2.5 out of 5 stars 2 reviews
Sales Rank: 280893

Media: Hardcover
Edition: 1
Number Of Items: 1
Pages: 304
Shipping Weight (lbs): 1
Dimensions (in): 8.4 x 5.5 x 1

ISBN: 0674024249
Dewey Decimal Number: 616.042
EAN: 9780674024243
ASIN: 0674024249

Publication Date: May 20, 2008
Availability: Usually ships in 1-2 business days

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Editorial Reviews:

Product Description

The secrets locked in our genes are being revealed, and we find ourselves both enthused and frightened about what that portends. We look forward to curing disease and alleviating suffering?for our children as well as for ourselves?but we also worry about delving too deeply into the double helix. Abuses perpetrated by eugenicists?from involuntary sterilization to murder?continue to taint our feelings about genetic screening.

Yet, as Ruth Schwartz Cowan reveals, modern genetic screening has been practiced since 1960, benefiting millions of women and children all over the world. She persuasively argues that new forms of screening?prenatal, newborn, and carrier testing?are both morally right and politically acceptable. Medical genetics, built on the desire of parents and physicians to reduce suffering and increase personal freedom, not on the desire to “improve the human race,” is in fact an entirely different enterprise from eugenics.

Cowan’s narrative moves from an account of the interwoven histories of genetics and eugenics in the first half of the twentieth century, to the development of new forms of genetic screening after mid-century. It includes illuminating chapters on the often misunderstood testing programs for sickle cell anemia, and on the world’s only mandated premarital screening programs, both of them on the island of Cyprus.

Neither minimizing the difficulty of the choices that modern genetics has created for us nor fearing them, Cowan bravely and compassionately argues that we can improve the quality of our own lives and the lives of our children by using the modern science and technology of genetic screening responsibly.

(20080522)



Customer Reviews:

4 out of 5 stars Reducing Suffering Through Genetic Screening   August 17, 2008
 0 out of 1 found this review helpful

Ruth Schwartz Cowan's book is well written and exceptionally insightful. She makes a strong argument for allowing families to make informed decisions when there is the risk of having a child with a devastating disease.

This book is a thoughtful examination of the emergence of genetic screening as a method to reduce profound human suffering. It is certainly not an argument for using genetic screening to eliminate undesirable individuals or to avoid the challenges of life with a manageable disease. It does provide solid background and support for the widely held belief that until definitive therapies or cures are available, genetic screening provides the best method for allowing families to make informed decisions about how to deal with devastating diseases.

"Heredity and Hope: The Case for Genetic Screening" not only shows why genetic screening should be adopted as a means to reduce the frequency of new cases of debilitating and fatal diseases, it also explains how genetic screening is the key to helping at-risk individuals have healthy children.

Ruth Schwartz Cowan's research is thorough, her conclusions are sound, and her advice should be taken to heart. A comprehensive genetic screening effort, properly managed and administered, will reduce human suffering and will increase the likelihood that children will be born with the best possible chances for survival.



1 out of 5 stars Eugenics Re-Packaged   July 30, 2008
Ruth Schwartz Cowan's "Heredity and Hope" rejects classic eugenics with its lofty goal of "improvement of the race" and instead advocates a new micro-eugenics with a smaller, more selfish chief goal: protecting the comfort and independence of the parents of children prenatally diagnosed with genetic abnormalities by ending the life of the child.

Dr. Cowan eagerly advocates 21st century genetic testing, prenatal diagnosis, and pregnancy termination, yet clings to an outdated and discriminatory early 20th century view of those with disabilities, calling those with Down Syndrome "chronically dependent" and "suffering."
I'd like Dr. Cowan to meet Karen Gaffney, the remarkable woman with Down Syndrome who recently swam the nine miles across Lake Tahoe. And I'd like her to meet Sujeet Desai, a musician who plays six instruments, and his wife Carrie Bergeron, a community college graduate and national speaker; both have Down Syndrome. And I'd like her to meet my son Caedon, age 2, who experiences advantages in medical treatment, developmental therapies, and educational inclusion that were unavailable to children with Down Syndrome even a decade ago. We've yet to see what great things Caedon and others of his generation will contribute to society given these new advantages.

Far removed from the forced institutionalization of earlier generations, many people with disabilities now live meaningful and increasingly independent lives. Life is indeed challenging for those with Down Syndrome and other genetic abnormalities and for their families, and I am thankful for the advances that allow this increased achievement and independence. Further, I welcome additional advances in medical genetics that will cure or reduce the severity of these abnormalities.

We should all reject Dr. Cowan's outdated and discriminatory view that death is the appropriate outcome for those with prenatally diagnosed genetic abnormalities.


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