The Immortal Life Of Henrietta Lacks (Thorndike Press Large Print Nonfiction Series)

This is a historically significant book that captures three important points: (1) the lack of ethics in medical research, particularly informed consent; (2) how this lack of medical consent affected a simple African-American family of relatively no sophistication; and (3)that the family of Henrietta Lacks cannot afford health insurance, notwithstanding the enormity of her contribution to science.During 1951, Henrietta Lacks went to Johns Hopkins with a "knot" in her cervix. The biopsy revealed cancer. Tissue was removed and cultured. The cancer was unique in that it continued to grow in a laboratory setting, and were named HeLa cells for their source, Henrietta Lacks. These particular cells were unique in that they do not observe the Hayflick limit, which is the usual lifetime of cancerous cells.These cells were used in the testing by Jonas Salk for his polio vaccine, and are used so regularly in the scientific community that it is estimated 300 scientific papers a month are written on the basis of research performed with HeLa cells. Neither Lacks nor her family gave the physician permission to harvest the cells. When the family, who was relatively unsophisticated, learned that "she was being kept alive," they were extremely concerned, and engaged counsel. They did not understand that it was her tumor only.