The Woman Who Walked into the Sea and over one million other books are available for Amazon Kindle. Learn more

Buy New

or
Sign in to turn on 1-Click ordering.
or
Amazon Prime Free Trial required. Sign up when you check out. Learn More
Buy Used
Used - Good See details
$7.92 & eligible for FREE Super Saver Shipping on orders over $25. Details

or
Sign in to turn on 1-Click ordering.
 
   
Kindle Edition
 
   
More Buying Choices
Have one to sell? Sell yours here
The Woman Who Walked into the Sea: Huntington's and the Making of a Genetic Disease
 
 
Start reading The Woman Who Walked into the Sea on your Kindle in under a minute.

Don't have a Kindle? Get your Kindle here, or download a FREE Kindle Reading App.

The Woman Who Walked into the Sea: Huntington's and the Making of a Genetic Disease [Hardcover]

Alice Wexler (Author)
4.5 out of 5 stars  See all reviews (4 customer reviews)

List Price: $30.00
Price: $23.94 & eligible for FREE Super Saver Shipping on orders over $25. Details
You Save: $6.06 (20%)
o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o o
In Stock.
Ships from and sold by Amazon.com. Gift-wrap available.
Only 3 left in stock--order soon (more on the way).
Want it delivered Thursday, February 2? Choose One-Day Shipping at checkout. Details

Formats

Amazon Price New from Used from
Kindle Edition $9.99  
Hardcover $23.94  
Paperback $20.00  

Book Description

September 30, 2008

When Phebe Hedges, a woman in East Hampton, New York, walked into the sea in 1806, she made visible the historical experience of a family affected by the dreaded disorder of movement, mind, and mood her neighbors called St.Vitus's dance. Doctors later spoke of Huntington’s chorea, and today it is known as Huntington's disease. This book is the first history of Huntington’s in America.

 

Starting with the life of Phebe Hedges, Alice Wexler uses Huntington’s as a lens to explore the changing meanings of heredity, disability, stigma, and medical knowledge among ordinary people as well as scientists and physicians. She addresses these themes through three overlapping stories: the lives of a nineteenth-century family once said to “belong to the disease”; the emergence of Huntington’s chorea as a clinical entity; and the early-twentieth-century transformation of this disorder into a cautionary eugenics tale. In our own era of expanding genetic technologies, this history offers insights into the social contexts of medical and scientific knowledge, as well as the legacy of eugenics in shaping both the knowledge and the lived experience of this disease.

 

(20081218)

Frequently Bought Together

The Woman Who Walked into the Sea: Huntington's and the Making of a Genetic Disease + Learning to Live With Huntington's Disease: One Family's Story + Mapping Fate: A Memoir of Family, Risk, and Genetic Research
Price For All Three: $68.79

Show availability and shipping details

Buy the selected items together
  • In Stock.
    Ships from and sold by Amazon.com.
    Eligible for FREE Super Saver Shipping on orders over $25. Details

  • Learning to Live With Huntington's Disease: One Family's Story $20.90

    In Stock.
    Ships from and sold by Amazon.com.
    Eligible for FREE Super Saver Shipping on orders over $25. Details

  • Mapping Fate: A Memoir of Family, Risk, and Genetic Research $23.95

    In Stock.
    Ships from and sold by Amazon.com.
    Eligible for FREE Super Saver Shipping on orders over $25. Details



Editorial Reviews

Review

“Wexler provides an accessible account of a disease in history. A richness of context gives her study its strength and character.”—Charles E. Rosenberg, Harvard University
(Charles E. Rosenberg 20090301)

“This is a remarkable story of ‘St. Vitus'' Dance’ (Huntington''s Chorea) from many perspectives: personal, historical and social. Its meticulous history, drawn from archives and personal experience details how this late-onset hereditary disease was viewed not only medically but personally and socially by family members, neighbors and friends of afflicted individuals. This is a must read for anyone interested in the social history and policy surrounding hereditary disease.”—Garland Allen, Washington University in St. Louis
(Garland Allen )

“This is at once a riveting history of a deadly genetic disease and a sensitive rendering of how fear of the affliction shaped the lives of people at risk and affected their families and community. Wexler discerningly exposes the hereditarian values that made the victims outcasts yet unflinchingly makes clear that in its grim physical reality Huntington’s disease is independent of any social construction. In all, a brave and pioneering work.”—Daniel Kevles, author of In the Name of Eugenics: Genetics and the Uses of Human Heredity
(Daniel Kevles )

“This book is an engaging chronicle of how the lived experience of illness in a family and community transforms over centuries into an intensely monitored and medicalized hereditary disease. Wexler does what historians do best: she folds what we take now to be a straightforward phenomenon, Huntington’s disease, back into the story of its making. By doing so, she tells us something profound about how we imagine ourselves and how we are connected to one another.”—Rosemarie Garland-Thomson, author of Extraordinary Bodies: Figuring Physical Disability in American Literature and Culture
(Rosemarie Garland-Thomson )

“A brave and pioneering work.”—Daniel Kevles, author of In the Name of Eugenics: Genetics and the Uses of Human Heredity 
(Daniel Kevles )

"[A] detailed and evocative portrait. . . . Using a range of sources—including diaries, letters, business ledgers, whaling logs and local newspapers—Ms. Wexler re-creates a picture of a long-ago place where doctors lived next-door to their patients and where generation after generation of a community''s most prominent members struggled with a crippling disease."—Amy Dockser Marcus, Wall Street Journal
(Amy Dockser Marcus Wall Street Journal )

"Highly recommended."—Choice
(Choice )

“Alice Wexler has once again accomplished the near impossible by writing a fascinating academic page-turner. Filled with truth and brilliance throughout, The Woman Who Walked into the Sea is an amazing book that leaves the reader not only better informed, but materially enriched, moved by the experience, and not wanting it to end.”—Carole Browner, University of California, Los Angeles
(Carole Browner )

About the Author

Alice Wexler is a research scholar at the UCLA Center for the Study of Women and the author of Mapping Fate: A Memoir of Family, Risk, and Genetic Research. She lives in Santa Monica.


Product Details

  • Hardcover: 288 pages
  • Publisher: Yale University Press; 1 edition (September 30, 2008)
  • Language: English
  • ISBN-10: 0300105029
  • ISBN-13: 978-0300105025
  • Product Dimensions: 9.3 x 6.1 x 1.1 inches
  • Shipping Weight: 1.2 pounds (View shipping rates and policies)
  • Average Customer Review: 4.5 out of 5 stars  See all reviews (4 customer reviews)
  • Amazon Best Sellers Rank: #1,019,677 in Books (See Top 100 in Books)

More About the Author

Discover books, learn about writers, read author blogs, and more.

 

Customer Reviews

4 Reviews
5 star:
 (3)
4 star:    (0)
3 star:
 (1)
2 star:    (0)
1 star:    (0)
 
 
 
 
 
Average Customer Review
4.5 out of 5 stars (4 customer reviews)
 
 
 
 
Share your thoughts with other customers:
Most Helpful Customer Reviews

7 of 7 people found the following review helpful:
5.0 out of 5 stars A must read for anyone interested in medicine and humanity, May 28, 2009
Amazon Verified Purchase(What's this?)
This review is from: The Woman Who Walked into the Sea: Huntington's and the Making of a Genetic Disease (Hardcover)
Read through the media, and you'll find all sorts of opinions about what diseases deserve more research dollars. Sadly, I can't recall any major media pieces in recent years stressing the need for more focus on Huntington's disease. While it may be a rare condition, there is no illness I can think of that creates more dread in those at risk for developing it and creates more havoc on those who do develop it. Significantly more resources and compassion are needed to fight this illness.

The quick facts:

1) A child born to a parent with Huntington's disease has a 50% chance of developing the illness later in life (if the child inherits a mutant form of the Huntington's gene from his/her parent, he/she has approximately 100% odds of developing the disease later in life).
2) Symptoms of Huntington's disease often develop around age 30 or later--after one has already had children--and late enough in life so that the children can see what happens to their affected parent.
3) Huntington's disease causes an progressive, unrelenting movement disorder (chorea) with progressive mental decline and death.
4) In the past (and no doubt today, too), patients with Huntington's disease and their blood relatives have been stigmitized and ostracized. Within the past century, attempts (some successful) have been made to sterilize patients and prevent them from marrying (in Germany and the US).
5) The disease may be so stigmitizing and physically destructive that children of Huntington's patients who start to develop symptoms are at risk for suicide. In fact, this book is based upon the story of a woman who develops symptoms and literally walks into the sea to end her life.

This book contains an interesting compilation of stories of the doctors who characterized the disease in the United States of America. A few highlights of the book:

The disease had been characterized by others well before George Huntington's major publication in 1872. However, Huntington meticulously demonstrated the autosomal dominant pattern of the disease--with about complete penetrance. At that time in history, perhaps only one form of blindness had been shown to have a similar strict, heritable pattern, but Huntington was unaware of that. Huntington also published his article only a few years after the Austrian Monk Mendel published his study on the heritable traits of peas--but Huntington was unaware of that paper too.

Huntington's disease also goes by the name St. Vitus's dance and "the Magrums." I have no idea where the name "Magrums" comes from--maybe I should reread the book. However, St. Vitus is a patron saint of dancers. Apparantly, epileptic and chorea patients used to pray to St. Vitus to try and cure their diseases.

Doctors used to try and treat Huntington's disease with herbs, medicines such as opium & digitalis, and a healthy diet.

William Osler was very interested in Huntington's disease, and admired Huntington's 1872 paper greatly. He even wrote to Huntington to try and arrange a trip to East Hampton to observe patients. He was initially rebuffed because the patients in East Hampton were extremely sensitive about their illness and didn't want to be observed.

Huntington's patients became a target of the eugenics movement in the 20th century.

Help other customers find the most helpful reviews 
Was this review helpful to you? Yes No


2 of 2 people found the following review helpful:
5.0 out of 5 stars rare glimpse, February 9, 2010
Amazon Verified Purchase(What's this?)
This book is a rare glimpse into the history of a genetic disesase that has been moving to the front and center of genetic research ever since the gene for Huntington's disease was discovered in the early 1990's. This is a dense book, yet I was amazed at the speed with which I read it. Writers and editors must have worked hard to get this distillation of material that enlightens and informs in a way that keeps the reader absorbed and fascinated. I am from an HD family but I think if I were an MD interested in research, or an MD with a highly creative mind or simply a person with a curiosity about genetics as it unfolds in the context of community, this is a stimulating and exciting read.

I expected to be interested, but am astounded, really, at what this book reveals about disease and community. Thank you Alice Wexler and to all those who supported you in this effort. I wish the whole medical community would read your book!

Nancy Hess
Hummelstown, Pennsylvania
Help other customers find the most helpful reviews 
Was this review helpful to you? Yes No


0 of 1 people found the following review helpful:
3.0 out of 5 stars interesting book, July 26, 2010
Amazon Verified Purchase(What's this?)
This review is from: The Woman Who Walked into the Sea: Huntington's and the Making of a Genetic Disease (Hardcover)
This is good book for people with an interest in chorea. The book has some excellent information and fasinating history. However, it does seem like it has been expanded beyond the information the authors have. For example, the story of the women and the sea is told 4-5 times and get repetitive.
Help other customers find the most helpful reviews 
Was this review helpful to you? Yes No

Share your thoughts with other customers: Create your own review
 
 
 
Most Recent Customer Reviews


Only search this product's reviews



Inside This Book (learn more)
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
ordinary chorea, hereditary chorea, childhood chorea, chronic chorea, eugenic family studies, social course, town trustee, choreic movements
Key Phrases - Capitalized Phrases (CAPs): (learn more)
East Hampton, George Huntington, New York, United States, Phebe Hedges, New England, Abel Huntington, Long Island, Inventing Hereditary Chorea, Eugenics Record Office, Elizabeth Muncey, George Lee, Cold Spring Harbor, Main Street, William Osler, The Eyes of Elizabeth, Smith Ely Jelliffe, Hiram Hedges, Captain David Hedges, Clarence King, Sag Harbor, North American, Civil War, Charles Davenport, Phebe Tillinghast
Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Surprise Me!
Search Inside This Book:


Suggested Tags from Similar Products

 (What's this?)
Be the first one to add a relevant tag (keyword that's strongly related to this product).
 
(5)

Your tags: Add your first tag
 

Customer Discussions

This product's forum
Discussion Replies Latest Post
No discussions yet

Ask questions, Share opinions, Gain insight
Start a new discussion
Topic:
First post:
Prompts for sign-in
 


Active discussions in related forums
Search Customer Discussions
Search all Amazon discussions
   
Related forums





Look for Similar Items by Category


Look for Similar Items by Subject