The book is also widely used in advanced degree programs in a wide range of disciplines for courses on human subject research ethics. Many epidemiology classes (study of incidence, distribution, and control of disease) and labs now require students and scientists to read The Immortal Life of Henrietta Lacks to understand the ethical and legal issues involved in research using human tissue. Skloot's book raises bioethical issues, including informed consent, corporate profiteering, and the treatment of poor and African American patients and their families. With the release of The Immortal Life of Henrietta Lacks, Skloot starts a foundation to help Henrietta Lacks's relatives and others who are exploited and neglected by the medical industry. ![]() Scientists also involved Henrietta's children in their research through medical testing without any explanation or compensation. Skloot develops a close relationship with the Lacks family, who never knew scientists were using Henrietta's cells and received no compensation for their use. Blending the line between nonfiction and narrative, The Immortal Life of Henrietta Lacks is the story of Henrietta Lacks, her family, and the reporter who sought to uncover her story. Many decades later, science journalist Rebecca Skloot investigates the story of Henrietta Lacks, whose cells were taken without her permission. The Immortal Life of Henrietta Lacks is the first and bestselling book by science journalist Rebecca Skloot. ![]() These cells, nicknamed HeLa after the patient, turned out to be the first immortal cells scientists had encountered, and they used the cells to launch a multimillion-dollar industry that provides human biological products, including cells and tissue, to researchers. When doctors biopsied or removed groups of cells from her tumor (an abnormal growth of cells that destroys body tissue) to study, they used the removed tissue to grow more cells. The book's story starts in the 1950s, when doctors at Johns Hopkins Hospital, in Baltimore, Maryland, operated on Henrietta Lacks, an African American woman in her 30s who had cervical cancer. Lacks, a tobacco farmer from Virginia, died in 1951 from cervical cancer, but not before her cells were harvested without her knowledge or consent for scientific and medical use.
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