The Immortal Life Of Henrietta Lacks

In 1951, Henrietta Lacks went to John Hopkins Hospital because of pain and bleeding in her abdomen and was diagnosed with cervical cancer. During one of her radiation treatments, doctors took samples from Henrietta’s cervix without her knowledge to see if her cells would grow in culture and it did. Her cells were the first immortal cells to grow in culture. From there everything changed. Henrietta’s cells were used to create the polio vaccine, they went in space to what would happen to human cells in zero gravity, and many more. But as HeLa cells were bought, sold, and used for these scientific researches her family did not receive any money from it. Many people think that they should receive financial compensation but they should not.

The Immortal Life of Henrietta Lacks is a book written by Rebecca Skloot that touches on many important issues. Of the dozens of issues referenced in the book, the one that stands out the most to me is bioethics. Bioethics is “the study of the typically controversial ethical issues emerging from new situations and possibilities brought about by advances in biology and medicine.” Bioethics plays a huge role in the story of Henrietta Lacks.

A researcher George Gey was given the cells of Henrietta’s tumor for research. George Gey discovered that Henrietta’s cells were unique and did something by no means seen before; they could be kept alive and grow. Before Henrietta’s cells, cultured cells would only be able to survive a few days. More time was spent on observing and preserving Henrietta’s cells than actually using them for research. It was

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

Skloot's book includes primary sources and insightful stories with interviews from the family. When the samples were taken neither Henrietta nor her family knew that her cells were being experimented on. The doctors never informed them even after the cells began growing in the cultures. At the age of thirty one Henrietta died after rounds of radiation treatments and removed cervical samples. Henrietta and her family were poor tobacco growing farmers.

Henrietta Lacks was a poor, black woman who died of cervical cancer in the fifties. Her cells were taken from her during surgery, without her knowledge. However, back then there were no laws about informed consent and the mindset was entirely different. Researchers knew little about cells and how they function. Her immortal cells allowed researchers to have an ample amount of resources to be able to study cells and later on develop vaccines and treatments for many diseases. Even though her cells were cancerous, they still shared many basic characteristics of a normal cell, which allowed researchers to learn a lot about a cell’s basic function. Her story explains how medical research has developed and how health care has progressed over the past sixty years.

After seeking treatment 20 miles away at Johns Hopkins Hospital, her biopsy came back showing that she was in stage I of cervical cancer. Henrietta decided to keep this saddening news from her family. David or “Day” who was Henrietta’s husband and also cousin, drove her back to Johns Hopkins for treatment. Her treatment involved inserting radium into her cervix, then closing her up. What her doctor, Howard Jones, didn’t mention however, was that he took a sample of tissue from her tumor without mentioning it to Henrietta before or after he operated. Back in this era, doctors ran experiments on black women to compensate for them not having a pay a medical bill. The tissue sample was sent to George Gey, the man in charge of all culture and tissue samples who was eagerly looking for a way to separate cells and get them to grow to be able to make infinite amounts of cells that can be used for future experiments. Gey found that Henrietta’s cells were growing at a miraculous rate, like nothing he had ever seen before. This finding was exactly what Gey had been looking for that led him to a discovery that medical technology had never seen

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 a poor African American that became one of the most vital tools in developing medicines like polio vaccine, cloning, gene mapping, and much more. She was a loving mother of five, wife, sister, and friend to many that was taken on October 4, 1951 at the age of thirty-one to cervical cancer. Henrietta’s cells were taken without her knowledge to develop the first ever immortal line of cells.

“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.

Rebecca Skloot’s bestseller, The Immortal Life of Henrietta Lacks, begins with a quote from World War II concentration camp survivor Elie Wiesel, “We must not see any person as an abstraction. Instead, we must see in every person a universe with its own secrets, with its own treasures, with its own source of anguish” (Wiesel qtd. in Skloot n. pag.). This quote serves as a preview of the book and its underlying moral purposes, as Henrietta Lacks and her family are continually treated as objects without rights to their privacy and without regards to their worth or feelings. The dehumanization of the Lacks family by the media and scientific community not only resulted in consequences for the family, but influenced society, as well.

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

Although she was taken from the world too soon, Henrietta Lacks was a warm hearted woman, and though unbeknownst to her, she would pave the way for the medical field and greatly expand our understanding of one of the nation’s

Clearly, these researchers had their own agenda to acquire a medical breakthrough that would change the history of science and contribute to the greater good of society. However, their authority was used in an unwarranted manner to accomplish their goals, regardless of their respectable intentions in wanting to make medical progress. In reviewing these researchers and medical practitioners’ actions during the 1950’s which entails series of unethical behaviors and violation of human right, it develops an essential need to establish guidelines in the attempt to protect patient’s rights and privacy. Furthermore, due to the alternatives that arise throughout this case, there are many possible outcomes to be considered that could have a significant impact on stakeholders if these courses of action are fallowed. These solutions consequences may involve the tentative research, an advance way of life for the Lack’s family, political turmoil, economic health impact and a society whose cells may have similar experience.

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