I am, Henrietta Lacks, and this is my story. My personal war on cancer was lost. I have died in pain, tormented by the tumors covering my body like a web, at the John Hopkins Hospital. But my life didn’t end at that point. Unexpectedly, the cancer tissue, which was taken from me by Dr. Gey, continued on living. Even though I was dead, my cells were alive - full of miracles to unfold and misery to cause. The wonderful abilities of my cells were praised all over the world – they were a hope of finding the cures for the diseases that never though to be found. Even cancer didn’t seem so undefeatable. Medicine triumphed on the yet to be started war on cancer. But my cells were not only about science and potential medical progress that …show more content…
No one, even I, couldn’t retell this story better than she did. As I was lying on my deathbed in agony waiting for the end, Dr. Gey came to me and said: “your cells will make you immortal” (p.66) and that’s where it all started.
Dr. Gey named my tissue He-La cells claiming that it stands for the name of one of his patients – Helena Lane. He preferred keeping the information of the cell’s origins in a secret. Even though, I am still struggling to understand why he would not want to show his gratitude for my contribution to science through acknowledgement of my name, Rebecca has offered her explanation to that. According to her findings, Dr. Gey was simply afraid that my family would halt the research and start demanding their rights for the cells, which I think on the one hand would be a justifiable action to take considering my family’s poor financial circumstances. But at the same time, I see, Dr. Gey’s aspirations about the future of the medical progress, where He-La could facilitate his research on cancer and research of other scientists on various diseases. Perhaps, If my family knew about the value of my cells they would either demand a price so high that a scientific community wouldn’t have an easy and cheap access to these tissues, or my family wouldn’t let using the cells at all. Although, I can’t dismiss the sufferings that my family went through as the truth about my cells
But even more important than that was the fact that no one even told her family that the cells existed until the ‘70’s. Her children were used in research without their consent and without answering their simple questions about the cells. This was scary especially for her daughter, Deborah. She worried that there were clones of her mother wandering around. Her family was also upset that at one point
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
Should people put the value of life into monetary value or should life be kept solely as an emotional quantity? People and societies throughout the ages have been trying to answer the problem of putting the value of life into terms of dollar bills. The ancient Egyptians buried their dead with all of their worldly belongings. They believed a person’s monetary worth on Earth was over, and they should take all of that earthly worth with them to the afterlife. Modern day Americans are different from the Egyptians. Today people believe that the families of the dead should be compensated for “their” loss.
Claiborne, Ron; Wright IV, Sydney (2010). "How One Woman's Cells Changed Medicine". ABC World News.
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.
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
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
In her book, The Immortal Life of Henrietta Lacks, Rebecca Skloot discusses how one woman’s unfortunate diagnosis of cancer resulted in the discovery of the first immortal human cell line, HeLa. The establishment of the HeLa cell line has proven to be one of the most influential breakthroughs in the biomedical sciences because these cells have played a major role in some of the largest breakthroughs in since they were first cultured in the 1950s. In addition to an examination of the science behind HeLa cells, Skloot also provides a look at the lives of Henrietta Lacks’s descendants. One characteristic that all members of the family share is a dedication to religion and spirituality. This juxtaposition between science and religion presents the body and its constituent cells in a unique way. It provides multiple dimensions to how people can view bodies. Specifically, Skloot’s depiction of HeLa cells presents the body and its individual cellular components as entities that exist as both scientific and spiritual beings simultaneously.
Skloot’s powerful message and use of literary devices should make her book common in a high–school classroom. Unlike the labs who classified her as simply “HeLa”, Skloot took the initiative to reveal who the woman of the immortal cells truly was. As stated by her daughter Deborah,“[e]verything [is] always just about the cells and [people] don’t even worry about her name and [if] HeLa was even a person” (Skloot 52). In order to achieve her purpose of revealing the immortal life of not only the cells but the person, Skloot uses ethos, pathos, and logos within her research of the Lacks and scientific community, to write her book accurately and sufficiently. Skloot is able to justify her story based on years of research and interviews, which a student can mock to write a research paper (to note, at the end of the book Skloot has 21 pages of notes to validate all sources of information). A example of this is regarding the Lacks family who questioned, “if our mother cells done so much for medicine, how come her family can’t afford to see no doctors?” (9). In order to complete this book, Skloot had to explain herself and her research to them, while simultaneously forming “a deep personal bond” (7). Similarly, the author had to sift through medical journals and family reflections to
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.
In the book “The Immortal Life of Henrietta Lacks” the author, Rebecca Skloot, discusses many important points. The main point of this informative novel is how doctors from Hopkins hospital captured cells from an African American woman to study possible outcomes to many new ideas. This main point unfolds an analysis of how this event made many new discoveries, immortal memories, and prevented Henrietta’s family from varies negative situations. Firstly, this event helped unfold many new discoveries to medicine and to the medical revolution.
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.
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