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Description: Documents the story of how scientists took cells from an unsuspecting descendant of freed slaves and created a human cell line that has been kept alive indefinitely, enabling discoveries in such areas as cancer research, in vitro fertilization and gene mapping. (science).
Description: #1 NEW YORK TIMES BESTSELLER • “The story of modern medicine and bioethics—and, indeed, race relations—is refracted beautifully, and movingly.”—Entertainment Weekly NOW A MAJOR MOTION PICTURE FROM HBO® STARRING OPRAH WINFREY AND ROSE BYRNE • ONE OF THE “MOST INFLUENTIAL” (CNN), “DEFINING” (LITHUB), AND “BEST” (THE PHILADELPHIA INQUIRER) BOOKS OF THE DECADE • ONE OF ESSENCE’S 50 MOST IMPACTFUL BLACK BOOKS OF THE PAST 50 YEARS • WINNER OF THE CHICAGO TRIBUNE HEARTLAND PRIZE FOR NONFICTION NAMED ONE OF THE BEST BOOKS OF THE YEAR BY The New York Times Book Review • Entertainment Weekly • O: The Oprah Magazine • NPR • Financial Times • New York • Independent (U.K.) • Times (U.K.) • Publishers Weekly • Library Journal • Kirkus Reviews • Booklist • Globe and Mail Her name was Henrietta Lacks, but scientists know her as HeLa. She was a poor Southern tobacco farmer who worked the same land as her slave ancestors, yet her cells—taken without her knowledge—became one of the most important tools in medicine: The first “immortal” human cells grown in culture, which are still alive today, though she has been dead for more than sixty years. HeLa cells were vital for developing the polio vaccine; uncovered secrets of cancer, viruses, and the atom bomb’s effects; helped lead to important advances like in vitro fertilization, cloning, and gene mapping; and have been bought and sold by the billions. Yet Henrietta Lacks remains virtually unknown, buried in an unmarked grave. Henrietta’s family did not learn of her “immortality” until more than twenty years after her death, when scientists investigating HeLa began using her husband and children in research without informed consent. And though the cells had launched a multimillion-dollar industry that sells human biological materials, her family never saw any of the profits. As Rebecca Skloot so brilliantly shows, the story of the Lacks family—past and present—is inextricably connected to the dark history of experimentation on African Americans, the birth of bioethics, and the legal battles over whether we control the stuff we are made of. Over the decade it took to uncover this story, Rebecca became enmeshed in the lives of the Lacks family—especially Henrietta’s daughter Deborah. Deborah was consumed with questions: Had scientists cloned her mother? Had they killed her to harvest her cells? And if her mother was so important to medicine, why couldn’t her children afford health insurance? Intimate in feeling, astonishing in scope, and impossible to put down, The Immortal Life of Henrietta Lacks captures the beauty and drama of scientific discovery, as well as its human consequences.
Description: Summary of The Immortal Life of Henrietta Lacks Rebecca Skloot, a specialist in science and medicine, authored The Immortal Life of Henrietta Lacks, which has become one of her best-selling books. The book was published in 2010 and it remained on The New York Best seller list for a long time. This book is about the subjects of science and medicine, focusing on the story of a young woman who is struggling hard against cervical cancer. The story shows how this young patient and all around her are affected by the disease, and the benefits to scientific research that result from her disease. The book also brings into focus the social class and racism perspective which made the book a best seller. The author writes in the book that she got most of the information by studying the journal of the young woman’s daughter. Because this did not provide enough information to produce the book, she did more research on other content so she could find enough detail to present the whole story. In addition, Oprah Winfrey came up with the idea to turn the story into a Home Box Office movie. Overall, the book is an interesting read, which revolves around social and race issues, highlighting the plight of African-American people who have suffered considerably in the United States. Here is a Preview of What You Will Get: ⁃ A Full Book Summary ⁃ An Analysis ⁃ Fun quizzes ⁃ Quiz Answers ⁃ Etc. Get a copy of this summary and learn about the book.
Description: Please note: This is a companion version & not the original book. Book Preview: #1 On January 29, 1951, David Lacks sat behind the wheel of his old Buick, watching the rain fall. He was parked under a towering oak tree outside Johns Hopkins Hospital with three of his children—two still in diapers—waiting for their mother, Henrietta. She had been telling her closest friends something was wrong with her sex life, but she still said no when she was pregnant with Joe, her fifth child. #2 Henrietta was diagnosed with a tumor on her cervix, but when she went to the hospital, she was treated for syphilis. She had six children with her husband, and she was never able to travel. She was asymptomatic neuro syphilitic, and her husband had no liking for sexual intercourse. #3 Henrietta was a prime example of how little black patients knew about their health. She had never heard of cervical cancer, and when she went to the hospital, she was sent home with a diagnosis of no abnormality of the cervix. Three months later, she had a fullblown tumor. #4 Henrietta Lacks was a woman whose cells were taken and sold by the thousands without her consent. She was born in 1920 in Virginia, and her cells were taken and sold by the thousands without her consent.
Description: Please note: This is a companion version & not the original book. Sample Book Insights: #1 On January 29, 1951, David Lacks sat behind the wheel of his old Buick, watching the rain fall. He was parked under a towering oak tree outside Johns Hopkins Hospital with three of his children—two still in diapers—waiting for their mother, Henrietta. She had been telling her closest friends something was wrong with her sex life, but she still said no when she was pregnant with Joe, her fifth child. #2 Henrietta was diagnosed with a tumor on her cervix, but when she went to the hospital, she was treated for syphilis. She had six children with her husband, and she was never able to travel. She was asymptomatic neuro syphilitic, and her husband had no liking for sexual intercourse. #3 Henrietta was a prime example of how little black patients knew about their health. She had never heard of cervical cancer, and when she went to the hospital, she was sent home with a diagnosis of no abnormality of the cervix. Three months later, she had a full-blown tumor. #4 Henrietta Lacks was a woman whose cells were taken and sold by the thousands without her consent. She was born in 1920 in Virginia, and her cells were taken and sold by the thousands without her consent.
Description: Henrietta Lacks was a beautiful African American woman who always painted her toenails red. She loved to dance. She had a big laugh and mischievous eyes. She had five children whom she loved with every inch of her soul. No one knows what her favorite color was. Henrietta Lacks was full life, but she died in 1951, her body consumed by tumors that had started in her cervix. She was buried in an unmarked grave and even though she was greatly loved, no one talked much about Henrietta after she died. The winds of time would have quickly swept away all signs of this vivacious woman had it not been for one thing: her cells were immortal.
Description: The Immortal Life of Henrietta Lacks: by Rebecca Skloot | A 15-minute Key Takeaways & Analysis Preview: Rebecca Skloot’s book, The Immortal Life of Henrietta Lacks, chronicles the life, death, and immortality of Henrietta Lacks, a young black woman whose cervical cancer cells became one of the most important factors in bringing about important scientific and medical advancements in the twentieth century. Her family, however, did not know until much later that researchers were using Henrietta’s cells in their experiments. When the family learned the truth, they endured turmoil and heartache in the decades that followed… PLEASE NOTE: This is key takeaways and analysis of the book and NOT the original book. Inside this Instaread of The Immortal Life of Henrietta Lacks: • Key Takeaways of the book • Introduction to the important people in the book • Analysis of the Key Takeaways
Description: So much to read, so little time? Get an in-depth summary of The Immortal Life of Henrietta Lacks, the #1 bestseller about science, race, and medical ethics. For decades, scientists have been using “HeLa” cells in biological research, from developing the polio vaccine and studying the nature of cancer to observing how human biology behaves in outer space. This famous cell line began as a sample taken from a poor African American mother of five named Henrietta Lacks. A cancer patient, Henrietta Lacks went through medical testing but never gave consent for the use of her cells. She died of cervical cancer in 1951, without ever knowing that the samples were intended for extensive medical research. This summary of the #1 New York Times bestseller by Rebecca Skloot tells Henrietta’s story and reveals what happened when her family found out that her cells were being bought and sold in labs around the world. With historical context, character profiles, a timeline of key events, and other features, this summary and analysis of The Immortal Life of Henrietta Lacks is intended to complement your reading experience and bring you closer to a great work of nonfiction.
Description: This book is a theoretical inquiry into alternative pedagogies that challenge current standardized practices in the field of science education. Through Mandy Hoffen, a fictional persona, Dana McCullough, the author, explores how stories of Henrietta Lacks become part of a conspiracy to change science education. Mandy Hoffen, however, never expected to find herself in the middle of a conspiracy. As a science teacher of 20 plus years, she worked diligently to meet the needs of her charges, who are currently ninth and tenth grade biology students in an age of standardized testing. The author also creates imaginary dialogues which serve as the theoretical framework for each chapter. Each chapter unfolds in a form of a play with imaginary settings and events that bring Henrietta Lacks back from the grave to participate in conversations about science, society, and social justice. The imaginary conversations are based on the author’s experiences in graduate courses, direct quotations from philosophers of science, historians of science, science educators, curriculum theorists, and stories of students in their study of Henrietta Lacks in a high school biology classroom. The play describes the journey of a graduate student/high school teacher as she researches the importance of the philosophy of science, history of science, science curriculum and social justice in science education. Through reflections on fictional conversations, stories of Henrietta Lacks are examined and described in multiple settings, beginning in an imaginary academic meeting, and ending with student conversations in a classroom. Each setting provides a space for conversations wherein participants explore their personal connections with science, science curriculum, issues of social justice related to science, and Henrietta Lacks. This book will be of interest to graduate students, scholars, and undergraduates in curriculum studies, educational foundations, and teacher education, and those interested in alternative research methodologies. This is the first book to intentionally address the stories of Henrietta Lacks and their importance in the field of curriculum studies, science studies, and current standardized high school science curriculum.
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