The Immortal Life of Henrietta Lacks

The truth is the doctors that took Henrietta’s cells were doing it for a good cause. They didn’t do it to ruin her and her family’s life, they did it to help people and save lives. There were no laws prohibiting the taking of one’s cells, in fact in a later Supreme Court of California ruling, it was actually defended. When tissues are removed from your body, with or without consent, any claim to ownership

The scientific community is culpable of viewing Henrietta Lacks as an abstraction rather than a human being in that they disregarded her right to privacy in extracting her cells

The main ethical issues in this case is that researches at Johns Hopkins Hospital used Henrietta’s cell in multiple researches and send her cells to other researchers around the world without her family’s consent. Moreover, the Lackes themselves were used in medical research without informed consent, and Henrietta’s medical records were release to journalists without her family knowing.

Henrietta Lacks is not a common household name, yet in the scientific and medical world it has become one of the most important and talked names of the century. Up until the time that this book was written, very few people knew of Henrietta Lacks and how her cells contributed to modern science, but Rebecca Skloot aimed to change this. Eventually Skloot was able to reach Henrietta’s remaining family and through them she was able to tell the story of not only the importance of the HeLa cells but also Henrietta’s life.

The non-fiction book The Immortal Life of Henrietta Lacks, written by Rebecca Skloot, details the happenings and life of Henrietta Lacks, an African American woman and tobacco farmer who became a medical miracle in the 1950’s. The book is written in an attempt to chronicle both the experiences and tribulations of Henrietta Lacks and her family, as well as the events that led to, and resulted from, research done on Henrietta Lacks’ cells. Henrietta was a very average African American woman in this period; she had only a seventh-grade level education, and followed traditional racial and gender roles by spending her time has a mother and caretaker, as well as working on farms throughout her life until the involvement of the US in World War II brought her and her husband, “Day” Lacks, comparatively better work opportunities in industrial steel mills. However, after her death in 1951 Henrietta became much more than average to doctors at John Hopkins when the discovered that cells extracted from her cancerous tissue continued to live and grow much longer than any other tissue samples. Further investigation and isolation of these thriving cells led to the creation of the first ever immortal human cell line in medical history. The incredible progress in medicine made possible by Henrietta Lack’s tissue cells were not without downfalls, though. The treatments and experiences received by Henrietta and the effects it had on her and her family demonstrate both racial and gender

With the numerous legal, ethical and moral issues that were highlighted in Henrietta Lacks case, two major ones to note: 1) the Lacks never specifically consented to providing samples of Henrietta’s cervical tissue for research, and 2) Johns Hopkins University releasing Henrietta’s name and medical records to third parties without her or her family’s

While performing the treatment Dr. Lawrence Wharton Jr. collected Henrietta’s normal and cancerous cell and sent them to George Gey, who was the researcher collecting any type of cells that the hospital would provide for his research, this was all done without Henrietta’s knowledge. In the 1950’s segregating still existed, and “Many scientist believed that since patients were treated for free in the public wards, it was fair to use them as research subjects as a form of payment.” (Pg. 30) Henrietta had a painful death in 1951, due to all the tumors that had spread throughout her body, leaving her 5 children without a

Neither Lacks nor her family gave her physician permission to harvest the cells. At that same time, however, permission was neither required nor usually sought. (Washington, 1994) In the early 1970’s, the family of Henrietta Lacks began getting

Henrietta Lacks is woman, whose cells have been used for 63 years after her death in 1951, and will continue to be used as long as they are continue to grow. Henrietta Lacks was an African American woman who was born in the south, who married her cousin and moved up north. After giving birth to her last child, she finds that she has cancer. The doctors took a sample of her cancer cells without her permission, and now have millions of dollars but the family is still hasn’t received the money they are rightfully entitled to. Many of healthcare and entitlements that are around today, are due to the ill treatment of Henrietta and her family. Still to this day, there is very little known about Henrietta Lacks, even with the book out, and she has

"The Immortal Life of Henrietta Lacks", by Rebecca Skloot, is about an African American woman born and raised in Roanoke, Virginia, and later dying in Baltimore, Maryland. Through her a life she battled a cancer that was often called a cervical cancer, and she later died in Baltimore, Maryland. Henrietta Lacks, born as Loretta Pleasant, is commonly known for her cancer cells called, HeLa, which is a name made from the first two letters of her first and last name. This book was very informational, not only for family purposes, but for science too. It has a lot to relate to science, whether readers realize it or not.

The Immortal Life of Henrietta Lacks focuses on many issues that Henrietta and her family have faced over the years resulting from the discovery of HeLa cells. One such issue that was recurrently present was the ethical issue of informed consent, or the lack of it, in the Lacks’ case. In the beginning when Henrietta was first being treated with radium to kill her cancerous tumor, her primary doctor, Dr. TeLinde, took a sample of the tissue and sent it to Dr. Gey, head of tissue

Rebecca talks about whether or not people should have the rights to their own tissues. She points out two issues, consent and money. In the past there was no informed consent, so the doctors and researchers felt free to use tissues in whatever way they wished, with little concern for patients' rights. Nowadays there is a different system, and it's required by the law to ask for a patient's informed consent.mThe money issue is a question of whether doctors should be required to tell patients if their cells or tissues are going to be used for commercial research, and what rights those donors should have. Later on, “scientists sequenced Henrietta Lacks's genome and made it public, without asking the family's permission” which was just another way in which the family was violated and looked over (Silver). Apparently Henrietta didn't get her rights, and neither did her children. Any way we look at it, if the family had received any benefits from the cells, it

This research paper is based on the findings from the book “The Immortal Life of Henrietta Lacks”. What you will read and come to know is nonfiction. I wish I could put the pictures of what I have seen and read together here for you to perhaps get a better understanding. A story based on not Henrietta’s life being that of immortality, but rather cancer cells removed from her body without her knowledge. These were the first cancer cells to reproduce outside of her body. You will come to know about Henrietta, her cancer, her cells, and her immortal life. Perhaps we can all learn to appreciate life in greater means of appreciation after reading and knowing the life and immortal afterlife of Henrietta Lacks. You will learn about a woman, who like us, had a family, and ended up not being able to truly live life to its fullest. Making us all realize just how cancer is and the amazing research that came from being able to reproduce her cells. Not just for cancer but for various other illnesses that plague so many of us. My hope is that you take away from this a better understanding of a time we do not know, for the ups and downs of science and the possibility of immortal life.

After Gey succeeded to find the immortal human cells, he started to sell HeLa cells without Henrietta’s consent. “Gey sells HeLa cells to researchers in Texas, India, New York, and many others place” (Skloot 84). He did not give any credit to Henrietta. He only told Henrietta that her cells will help many people in the future. “In fact, in the future HeLa cells were contribute into polio vaccine; develop drugs for treating herpes, leukemia, influenza, hemophilia, and Parkinson’s disease” (Skloot 22). Hela cells were also used in cancer treatment and were the first cells that were shot into space.

“The Immortal life of Henrietta Lacks” written by Rebecca Skloot exposes the truth about a colored woman, Henrietta Lacks, who died from cancer leaving five children and a husband behind. Before her death doctors took her cells,without her or her family consent, to do there own research and experiments. They discovered that her cells were immortal, they became the first immortal cells known as the HeLa cells..After the discoverment the Lacks family were never told that Henrietta Lacks cells were used, bought and sold. Through the HeLa cells the scientist had made money while Henrietta kids were mistreated and were in poor situations.It wasnt till 25 years later that the Lacks family found out about the HeLa cells doing miracles. Rebecca Skloot though “The immortal Life of Henrietta Lacks” was able to explain the unethical situations that the Lacks family faced after Henrietta’s death.