Summary Of The Immortal Life Of Henrietta Lacks

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

The HeLa cells (the name for Henrietta Lacks cells) led to the discovery of polio vaccines, genetic medication, HPV vaccine, and much more. Still today, these HeLa cells are being researched and used to protect the public from life-threatening diseases such as cancer and tuberculosis. The public health response to new medical advancements and research from the HeLa cells has had many positive and negative consequences on the individuals, families/communities, and the nation.

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

I think this book adds a lot of value to ethical, biological and scientific education. The book gives you a very good view on how the HeLa-cells were grown, but also especially on the human behind these cells, Henrietta Lacks. Not only is the story of the discovery of HeLa relevant for (scientific) biological education, but also for scientific research education in general. The book adds value to scientific education, in a way that the story of HeLa makes you realize what the importance of research ethics is and how complicated and unfair issues about human tissue used in research are. You secretly hear the voice of Rebecca Skloot through her writing, telling the world to threat the “donors” with dignity and justice by making decent agreements and laws about human tissue used in research. She shows her readers how big the

Many people would assume that, because of HeLa’s impact on society, the Lacks family is probably very wealthy and well informed about HeLa cells; unfortunately, that is not the case. Not only did the Lacks feel taken advantage of by the medical community, but it wasn’t until an article by Howard Jones in December 1971 that Henrietta’s real name was finally revealed. That same article was used to inform Bobbette Lacks, Henrietta’s daughter-in-law, that the immortal cells she had been reading about in the paper were Henrietta’s. Bobbette was the first member of the Lacks family to learn about the fate of Henrietta’s cells and she immediately ran to the family yelling, “Part of your mother, it’s alive!”(181). The family felt misinformed, confused, betrayed and most of all, angry. In 1976, Mike Rodgers published an article in Rolling Stone that informed the Lacks family that people were buying and selling Henrietta’s cells. The family immediately accused Hopkins of withholding money from them. Lawrence, Henrietta’s eldest son, was quoted saying, “Hopkins say they gave them cells away, but they made millions! It’s not fair! She’s the most important person in the world and her family living in poverty. If our mother so important to

Henrietta Lacks, a woman whose cells have made millions of dollars, but most people don’t know her name, or her story. “She’s usually identified as Helen Lane, but often she has no name at all. She’s simply called HeLa, the code name given to the world’s first immortal human cells – her cells cut from her cervix just months before she died. Her real name is Henrietta Lacks,” (Skloot 1). Through the last few months of her life, she had major struggles with hospitals and scientists. Henrietta was in serious pain throughout the last few months, and the doctor treated her as a specimen. “Henrietta is still a miserable specimen,” (Skloot 66). Another major flaw in Henrietta story is the fact that her family was barely told of her condition of cervical

In this semester’s book club, I have enjoyed the book called The Immortal Life of Henrietta Lacks. This book describes a true and famous cell line in the medical research field, that is the first immortal cell line in the world, HeLa cells. Not until I finished reading this fantastic book, I know that the HeLa cells were taken from a cervical cancer patient, Henrietta Lacks, without letting her know the truth about using her cells in research, even though she died. What more surprising to me was that her family lived a hard life without health insurance while the researchers make many profits from developing HeLa cells, they were never informed about their family member’s devotion to the scientific research.

In 1951, Henrietta Lacks was diagnosed with cervical cancer at John Hopkins Hospital. Without any consent, Henrietta’s doctors took tissue samples from her cervix and attempted to grow them and keep them alive. These cells, known as HeLa cells, began to grow at an unbelievable rate; The HeLa cell became vital for the development of vaccines and other scientific research. However because of Henrietta’s race and economic standpoint, Henrietta Lacks and the rest of the Lacks family was exploited by doctors. The exploitation of the family allowed the doctors and researchers to benefit scientifically and monetarily.

Her family would later find out Henrietta was misdiagnosed. Henrietta went to John Hopkins for treatment due to it being the only hospital in her area who would treat African Americans. Many doctors during this time would use the public for research without the patient’s consent, and this happened to Henrietta. Without Henrietta’s permissions, a doctor treating Henrietta’s tumor proceeded to take tissue from her cancer tumors and her healthy cervical tissue. Her tissue ended up in Gey’s lab which were named HeLa. Two days later Henrietta’s cells began growing, and soon after Gey began giving samples of HeLa to his closest colleagues (Skloot 41). Henrietta never knew of her cells growing in the lab. Unfortunately, Henrietta’s cancer began to spread throughout her body. Treatment was not working for Henrietta, and she passed away October 4th, 1951 (Skloot 86). No one knew who Henrietta was for a long time, and she lost a lot of time of receiving credit for her cells. Henrietta’s cells ended up being sold for a profit by a manufacturer. Her family did not receive anything from Henrietta’s cells being used. Henrietta’s cells helped changed the medical world. Her cells were used for creating a polio vaccine and IVF. They also helped understand HPV, HIV, and AIDs. Henrietta’s cells have done a lot for cancer research. However, Henrietta’s family suffered deeply after her death, and

Due to severe pains, on January twenty-ninth, nineteen fifty-one, Henrietta went to Johns Hopkins Hospital in Baltimore, Maryland where she was diagnosed with cervical cancer by Dr. Howard Jones. She was a patient in the “colored ward”. During her eight month long radiation treatments, doctors removed two dime-sized samples of her cancer-ridden cervix without ever informing her, asking her permission and letting her family know. Henrietta Lacks died of cancer a few months after her diagnosis on October fourth, nineteen fifty-one, at Johns Hopkins Hospital at the age of thirty-one, leaving behind her husband

The National institute of Health, Rebecca Skloot, and John Hopkins Hospital have distorted Henrietta Lacks Legacy. In 1951, the Johns Hopkins Hospital took cervical cancer cells from Henrietta Lacks, and developed the HeLa cell line. Neither Henrietta nor her family gave the hospital permission to use her cells at the time. Her cells contributed to major medical discoveries, including the development of polio vaccine. Henrietta’s family was never compensated for the money that they made off of her cells. It was not until 1973 that her children discovered, by accident, that their mother's cells, now immortalized, had become a major boon to medicine and that many people had become rich from marketing them. Ron Henrietta’s

Bringing Henrietta to Life: Creating Dialogue on Disparities across Disciplines Henrietta Lacks was a woman who made an eye-opening breakthrough in medicine in the early 1950s. Her cells were the first immortal cells to be discovered which paved the way for developing the polio vaccine, cloning, gene mapping, in-vitro fertilization, and more. Unfortunately, there are two sides to every story. Although, modern medicine would not be where it is today without Hela cells, Henrietta’s family continued to struggle with her legacy because of the health disparities associated with ethics, race, and medicine. Henrietta’s cells were taken without her knowledge and used to cure various medical conditions.

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.

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