What Is The Thesis For The Immortal Life Of Henrietta Lacks

Throughout the book The Immortal Life of Henrietta Lacks, many social justice issues were presented. One of them was racial discrimination, specifically in the medical world. Race was perceived in an extremely different way than it is now; it is clearly evident how it impacted the medical care that Henrietta Lacks received and what happened with the family as her cells were spread and studied. Today the situation would be handled differently. There are not segregated hospitals with people saying that since a person does not have enough money to pay for a hospital visit, taking tissues and cells from the body is okay. Racial discrimination in the medical world has changed a great deal since the time that the HeLa cells were first taken.

“The Immortal Life of Henrietta Lacks” is the story of Hela cells and the women and family behind them. HeLa cells are the cells that have helped scientists all around the world discover cures and vaccines that have saved thousands of lives. But before they did all those things, they were inside a woman, named Henrietta Lacks, and were taken from her without her knowledge. Her family would not know about her cells until years after her death and millions of dollars in revenue gained from the HeLa cells. At the time doctors did what was considered common practice but did they cross a line? Or were the amazing scientific achievements enough to excuse the violation of personal privacy? Despite good intentions doctors should never have taken Henrietta’s cells without her consent, and furthermore her family deserves compensation for the work those cells have helped accomplish, and the sometimes horrible circumstances they have had to deal with because of the 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

The Immortal Life of Henrietta Lacks is a true story of a poor, Southern African-American tobacco farmer who died in 1951 at the very young age of 31 years old from cervical cancer. Little did she know that cells harvested from her tumor, which were obtained without her consent have lived on and on and became one of the most important tools in medicine today. Despite Henrietta’s story being full of legal and ethical issues, the story was one filled with success and anguish. Success for science as her cells served as advancement in medical research and development; yet was sorrowful for Henrietta and her family. This story occurred during a time of segregation in the United States, when Henrietta Lacks believed she

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 story took place in Baltimore in the early and mid 1900s, when prejudice was prominent and black people were not treated fairly or equally by white people. Moreover, the entire black community was terrified of night doctors, who would kidnap black people for scientific testing, and the book states that “fear of the night doctors only increased in the early 1900s, as black people migrated north to Washington D.C., and Baltimore” (166). This shows that the setting of the story had a huge impact on the book, as black people were taken advantage of routinely against their will. This is what happened to Henrietta, as she had to drive miles and miles to go to the only hospital around that would serve black people just to have her cells were taken without her consent by white scientists and used for the benefit of others. The author also uses many changes in point of view in the story to provide more background and portray the many different ideas and views of different people. For example, Skloot starts off telling the story from Henrietta’s point of view, showing her family and her struggles through her time with cancer. Then, she switches over to the eyes of a scientist who was working with Henrietta’s cells in a lab and working to grow the cells to benefit the scientific world. Finally, the author tells the story through her own eyes as she had to acquire information about Henrietta’s personal life through Henrietta’s family and the struggle she went through to get it. The setting of the story and the changes in point of view used by the author improve the story

Henrietta Lacks was diagnosed with cervical cancer. Her doctor at Johns Hopkins hospital took her tissues without informing her and grew them. When she died her tissue became HeLa cells which became the key to science research creating vaccines and medications. Race In the Immortal Life of Henrietta Lacks was exploited by the doctors. It was a major issue and the doctors took advantage of their patients to receive what they wanted. It left people like Henrietta and her family uninformed because blacks were forbidden to ask questions.

It clearly obvious that to George Guy- the man who discovered HeLa cells- Henrietta was the same black women she was before she died and after she died. During this period of time, there were no set laws regarding that a patient must give permission or be notified if they cells were extracted from them. Even so, being African American and a woman during this extremely racist time period there was guarantee that she would even be told or lied to, similar to the 600 African Americans who were involved in the Tuskegee syphilis experimentation who were actually lied to.

The Immortal Life of Henrietta Lacks, by Rebecca Skloot, is a book about an African-American woman, Henrietta Lacks, who had cervical cancer in the early 1950s. Henrietta went to John Hopkins hospital, one of the only hospitals to treatment African-Americans, they derived part of her cancer cells from her cervix and tried to keep growing her cells for research to try and discover a cure for cervical cancer. They have tried this on many patients before, but Henrietta’s cells were special and kept growing, while the other patient’s cells would die. However, Henrietta Lacks and her family had no idea about the doctors taking her cells and medical records and sending them to other doctors around the world. In Skloot’s book there are many ethical

The Immortal Life of Henrietta Lacks is a very touching book; this book has really helped me take a new perspective on how patients were treated in hospitals in the 1950s. Also the book demonstrates how patients and research has changed drastically from how they are now compared to back when Henrietta’s cells were being used. Unfortunately Henrietta did not know that her cells were being used for research in the hospital labs, since she was unaware they were using her cells there was no way for her family to try to obtain money from the researchers to help them financially. Also, during this time period most people weren’t given the proper knowledge and consent rights to be used as research unlike today’s standards. Therefore, this leads me

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

When I first heard about the book "The Immortal Life of Henrietta Lacks", I thought it was just a reading assignment when I was in high school that I had to complete for a grade. As I began reading I became particularly interested in Henrietta Lacks and the HeLa cells. In "The Immortal Life of Henrietta Lacks", Rebecca Skloot talks about Henrietta Lacks and how her cells were taken without her permission, and how her family suffered afterwards. Skloot shows how medicine and science were seen back in the 1950's compared to now.

The effect the discovery and creation of the HeLa cells made on the science community and Henrietta’s family had a domino effect. Both had different opinions and beliefs on the matter; this led to some difficult questions asked of the family and of the medical community. Due to the new and advanced methods of experimentation, the HeLa cells made to to the field of science, the scientific community and the media failed to remember that Henrietta and her family were not abstractions but actual people. Rebecca Skloot, however, took into account the Lack’s family, she inquired both the history of the HeLa cells as well as the Lacks family, treating them as actual people with inalienable rights.