Henrietta Lacks Conclusion

The Immortal Life of Henrietta Lacks written by Rebecca Skloot is a book filled with drama and ethical dilemmas. The book is broken into three sections which focus not only on the story of Henrietta Lacks, but the life of her family following her death. Part one, Life introduces readers to Henrietta and her family before she was officially the woman behind HeLa. In this section, it is discovered that Henrietta was born in Roanoke, Virginia, but due to her mom dying while she was young she relocated to Clover, Virginia. While in Clover, she fell in love with her cousin Day and they went on to get married and had five children. The Lacks children are Lawrence, Elsie, Sonny, Deborah, and Zakariyya who were all greatly affected by the loss of their

In the year 1951, an African American woman known as Henrietta Lacks died of cervical cancer. Unknowingly, her cancerous cells would later be discovered as the first immortal human cells. These cells were then referred to as HeLa by Doctor Gey, who was a tissue expert at the Hopkins Hospital. Her cells were discovered as the first human cells without her ever knowing they had been removed from her body and cultured. Rebecca Skloot, a journalist, and author of The Immortal Life of Henrietta Lacks embarked on a journey to discover more about Henrietta Lacks’s struggle, pain, and efforts to get treatment. Henrietta nor her family members were ever told of the cultured cells, but would later find out and be very upset. They would be shocked

Henrietta Lacks died never knowing the impact her life would have on the world of medicine. A poor, black woman living in Baltimore, Maryland in the 1950s, Henrietta was diagnosed with cervical cancer and died only nine short months after her diagnosis at the age of thirty-one. The mother of five children, Henrietta most likely died thinking her family would be her legacy. Little did she know her doctor at John Hopkins hospital, George Gey, had taken some of her cells before she died. With Henrietta’s cells, Dr. Gey was finally able to achieve a goal he had been working toward for decades – creating the first line of immortal cells (Freeman). These cells have been used for countless scientific research and have solidified Henrietta Lacks’ place

In the novel, the immortal life of Henrietta Lacks by Rebecca Skloot. Henrietta was a young black woman of 5 children whose cancerous cells were taken out without her knowledge. Those cells later became one of the most important tools in medicine. The case of John Moore vs. Regents of the University of California has similar ethical issues as present in the novel.

Due to the fact that Henrietta’s cells were the first human cells grown in a lab that did not die after a few cell divisions, they could be used for conducting many experiments. Her cells were considered “immortal”. This was a major breakthrough in medical and biological research. One major breakthrough was the development of a vaccine for polio. To test the vaccine the cells were quickly put into mass production in the first-ever cell production factory. Another enormous breakthrough was the successful cloning of human cells in 1955. Demand for the HeLa cells grew quickly. Since they were put into mass production, Henrietta’s cells have been mailed to scientists around the globe from “research into cancer, AIDS, the effects of radiation and toxic substances, gene mapping, and countless other scientific pursuits.” (Smith, 2002, "Wonder Woman: The Life, Death, and Life After Death of Henrietta Lacks, Unwitting Heroine of Modern Medical Science".) HeLa cells have been used to test human sensitivity to tape, glue, cosmetics, and many other products. Scientists have grown some 20 tons of her cells, and there are almost 11,000 patents involving HeLa cells. (Batts, 2010)

Racism is immortal just like Henrietta’s cells it will always be around. People would do anything to be the first to discover something. At the end of the day it’s all about the money. The Mississippi appendectomies and the Tuskegee experiments were similar in the way that the government forced treatment upon minorities without consent. Henrietta’s case was different than Mississippi and Tuskegee because the doctor in Johns Hopkins didn’t experiment on her actual body but on her cells without consent. Henrietta’s case the Tuskegee experiments and the Mississippi Appendectomies are all different cases in different locations but serve the same purpose which is to take advantage of poor and uneducated minorities to

This is a book that tells a story of an African-American woman and the Scientific journey of her cells, it also goes in depth about how her daughter came to find out about her immortal cells. The Immortal Life of Henrietta Lacks is divided into three layers and each part discusses different event that happened during the course of Henrietta’s life, death, and immortality. If the story was written in a chronological order would it had made it easier or harder to understand the more important things?

The book The Immortal Life of Henrietta Lacks by Rebecca Skloot, was a nonfiction story about the life of Henrietta Lacks, who died of cervical cancer in 1951. Henrietta did not know that her doctor took a sample of her cancer cells a few months before she died. “Henrietta cells that called HeLa were the first immortal human cells ever grown in a laboratory” (Skloot 22). In fact, the cells from her cervix are the most important advances in medical research. Rebecca was interested to write this story because she was anxious with the story of HeLa cells. When she was in biology class, her professor named Donald Defler gave a lecture about cells. Defler tells the story about Henrietta Lacks and HeLa cells. However, the professor ended his

Henrietta Lacks was born on August 1, 1920, in Roanoke, Virginia. Lacks died of cervical cancer on October 4, 1951, at age 31. Cells taken from her body without her knowledge were used to form the HeLa cell line. Lacks's case has sparked legal and ethical debates over the rights of an individual to his or her genetic material and tissue.

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

Henrietta Lacks: an unknown name up until recent years. A name that had been known to the world only as HeLa; The first two letters of a name that belonged to a poor African American tobacco farmer that unknowingly changed science and life as we know it today. Her life has finally been portrayed in a very intimate story that not only does her life some justice but also transcendentally brings to mind the philosophical issues concerning medical ethics both of the past, present, and the future. In a world of constantly evolving medical advancement, science is a pivotal force that propels ideas forward. Although most will agree that the knowledge and cures found are a positive aspect, there is also a necessary evil that is involved, including

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.

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.

Ethics, in our society, are the moral principles that govern our behavior, dictating what is right from wrong. The specifics of ethics changes as values in our society change and evolve. This occurs in Rebecca Skloots book, The Immortal Life of Henrietta Lacks. One major reoccurring theme in the book is the lack of informed consent and autonomy. Fortunately, now there are safeguards which protect human rights in regard to health care and research. The Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, now part of the Department of Health and Human Services, created The Belmont Report, which is one such safeguard establishing principles for all human research (USDHHS, 1979). This paper will discuss the ethical issue of informed consent within The Immortal Life of Henrietta Lacks, the disregard to parts of the Belmont Report, as well as compare the role of the nurse in charge of Henrietta’s care versus the standards of care set for modern nurses.

In the example with the HeLa cells, a great debate was raised when the book The Immortal Life of Henrietta Lacks was published. The debate centered around the lack of information of where the cells came from, who should have known about the original harvesting, and the lack of compensation for Henrietta’s family once the cells started generating income. Also discussed was the tendency of the medical community to