The story and core argument The Immortal Life of Henrietta Lacks tells the story of Henrietta Lacks. In the early 1951 Henrietta discovered a hard lump on the left of the entrance of her cervix, after having unexpected vaginal bleeding. She visited the Johns Hopkins hospital in East Baltimore, which was the only hospital in their area where black patients were treated. The gynecologist, Howard Jones, indeed discovers a tumor on her cervix, which he takes a biopsy off to sent it to the lab for diagnosis. In February 1951 Henrietta was called by Dr. Jones to tell about the biopsy results: “Epidermoid carcinoma of the cervix, Stage I”, in other words, she was diagnosed with cervical cancer. Before her first radium treatment, surgeon dr. Wharton removed a sample of her cervix tumor and a sample of her healthy cervix tissue and gave this tissue to dr. George Gey, who had been trying to grow cells in his lab for years. In the meantime that Henrietta was recovering from her first treatment with radium, her cells were growing in George Gey’s lab. This all happened without the permission and the informing of Henrietta Lacks. The cells started growing in a unbelievable fast way, they doubled every 24 hours, Henrietta’s cells didn’t seem to stop growing. Henrietta’s cancer cell grew twenty times as fast as her normal healthy cells, which eventually also died a couple of days after they started growing. The first immortal human cells were grown, which was a big breakthrough in science. The HeLa cells were spread throughout the scientific world. They were used for major breakthroughs in science, for example the developing of the polio vaccine. The HeLa-cells caused a revolution in the scientific world, while Henrietta Lacks, who died Octob... ... middle of paper ... ...and the great scientific achievements that followed were very interesting to me and very well written by Rebecca Skloot. But what made it all so real for me, was the personal story of Henrietta and her family. The frustration of the family and the lack of information that was given by the scientists really made me angry. These people suffered from so much injustice, why did no one made a small effort to explain it to them all? Reading about the health problems The story of the Lackes really visualizes the problems in science before, and the need to resolve them. In the end, the most important lesson learnt is that human tissue used for research shouldn’t be used in such a materialistic way, but it should be handled with in a respectful and ethical way. Rebecca Skloot has done a marvelous job telling the story of Henrietta Lacks; the woman who changed science!
The book The Immortal Life of Henrietta Lacks by Rebecca Skloot is the result of years of research done by Skloot on an African American woman with cervical cancer named Henrietta Lacks. Cells from Lacks’ tumor are taken and experimented on without her knowledge. These cells, known as HeLa cells, are the first immortal human cells ever grown. The topic of HeLa cells is at the center of abundant controversial debates. Despite the fact that her cells are regarded as, “one of the most important advancements in the last hundred years” (4), little is actually known about the woman behind the cells. Skloot sets out on a mission to change this fact and share the story of the woman from whom the cells originate and her family as they deal with the effects these cells have on them.
An abstraction can be defined as something that only exists as an idea. People are considered abstractions when they are dehumanized, forgotten about, or segregated and discriminated against. The scientific community and the media treated Henrietta Lacks and her family as abstractions in several ways including; forgetting the person behind HeLa cells, giving sub-par health care compared to Caucasians, and not giving reparations to the Lacks family. On the other hand, Rebecca Skloot offers a different perspective that is shown throughout the book. Rebecca Skloot’s book The Immortal Life of Henrietta Lacks describes the trials and tribulations the Lacks family has gone through because of HeLa cells and shows how seeing a person as an abstraction is a dangerous thing.
Henrietta’s cells were being inaugurated with space travel, infused into rat cells, and even being used to make infertile hens fertile again. However, these are only a few of the many accomplishments that Henrietta’s immortal cells made possible: “The National Cancer Institute was using various cells, including HeLa, to screen more than thirty thousand chemicals and plant extracts, which would yield several of today’s most widely used and effective chemotherapy drugs, including Vincristine and Taxol,”(pg.139). This example of logos from the text again shows just how important these Henrietta’s cells were to the future developments in
All I can say is amazing information of your glorious and late Henrietta Lacks. This incedible women bettered our society in ways no common human could understand at the time because of how complex this matter was and still very much indeed is. I know there is much contraversy with the matter of how scientists achived immortal cells from your late relative, and I do strongly agree with the fact that it was wrong for these researches to take advantage of this incredible women, but I know it is not for me to say nonethless it must be said that even though it was wrong to take Lacks’ cells when she was dying sometimes one must suffer to bring joy to the entire world.
In the novel The Immoral Life of Henrietta Lacks by Rebecca Skloot, the author tells the miraculous story of one woman’s amazing contribution to science. Henrietta Lacks unknowingly provides scientists with a biopsy capable of reproducing cells at a tremendusly fast pace. The story of Henrietta Lacks demonstrates how an individual’s rights can be effortlessly breached when it involves medical science and research. Although her cells have contributed to science in many miraculous ways, there is little known about the woman whose body they derived from. Skloot is a very gifted author whose essential writing technique divides the story into three parts so that she, Henrietta
Henrietta lacks name was purposely mis-published numerous times -as Helen Lane-, which further took away the chances of her family being financially compensated for the usage of their mothers cells. It is in the strongest belief of the family that scientist and media purposely published the wrong name to hide information about Henrietta from her family. The deceit constantly thrown at Henrietta's family by the scientist community and how the media responded proved that the media also viewed Henrietta as a concept and not as a living breathing human being because they too did not care to know or tell Henrietta's true story.
Your life, like many other has probably at some point been touched by Henrietta lacks and most likely you didn’t even know it.
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.
In The Immortal Life of Henrietta Lacks, author Rebecca Skloot tells the true story of the woman who the famous HeLa cells originated from, and her children's lives thereafter. Skloot begins the book with a section called "A Few Words About This Book", in which a particular quote mentioned captured my attention. When Skloot began writing Henrietta's story, one of Henrietta's relatives told Skloot, "If you pretty up how people spoke and change the things they said, that's dishonest. It’s taking away their lives, their experiences, and their selves" (Skloot). After reading that quote, an array of questions entered my mind, the most important being, "Do all nonfiction authors take that idea into consideration?" Nonfiction is a very delicate and
Rebecca Skloot’s novel, The Immortal Life of Henrietta Lacks, depicts the violation of medical ethics from the patient and researcher perspectives specifically when race, poverty, and lack of medical education are factors. The novel takes place in the southern United States in 1951. Henrietta Lacks is born in a poor rural town, Clover, but eventually moves to urban Turner Station. She was diagnosed and treated for cervical cancer at Johns Hopkins hospital where cells was unknowingly taken from her and used for scientific research. Rebecca Skloot describes this when she writes, “But first—though no one had told Henrietta that TeLinde was collecting sample or asked she wanted to be a donor—Wharton picked up a sharp knife and shaved two dime-sized pieces of tissue from Henrietta's cervix: one from her tumor, and one from the healthy cervical tissue nearby. Then he placed the samples in a glass dish” (33). The simple act of taking cells, which the physicians did not even think twice about, caused decades
..., the name of Henrietta Lacks needs to be introduced to the world since she is the woman who generated HeLa cells, because the name of the person who generated HeLa cells is still unknown. By doing this, her family will be honored and respected by others.
Henrietta Lacks was born on August 18, 1920 in Roanoke, Virginia. She stayed with her grandfather who also took care of her other cousins, one in particular whose name is David (Day) Lacks. As Henrietta grew up, she lived with both her Grandpa Tommy and Day and worked on his farm. Considering how Henrietta and Day were together from their childhood, it was no surprise that they started having kids and soon enough got married. As the years continued, Henrietta noticed that she kept feeling like there was a lump in her womb/cervix and discovered that there was a lump in her cervix. Soon enough, Henrietta went to Johns Hopkins Medical Center to get this check and learned that she had cervical cancer. But here is where the problem arises, Henrietta gave full consent for her cancer treatment at Hopkins, but she never gave consent for the extraction and use of her cells. During her first treatment TeLinde, the doctor treating Henrietta, removed 2 sample tissues: one from her tumor and one from healthy cervical tissue, and then proceeded to treat Henrietta, all the while no one knowing that Hopkins had obtained tissue samples from Henrietta without her consent. These samples were later handed to ...
Lacks lived in Virginia from childhood to marriage, until her and her husband, David, had to move to Maryland in search for work. In 1951, she was diagnosed with cervical cancer; concerned for her health, she went to Johns Hopkins to be diagnosed by doctors. After being probed and scraped and having her privacy waived aside, the doctors realized her condition and took particular interest in her cancer cells, which reproduced continuously. This kind of cellular division promised the possibility of immortality for humans. As a result, her cells were taken and used by scientists and doctors to make significant advances in the medical field; her cells live on today and continue to be the key to opening more doors to cure diseases and help sick humans. Despite the manner in which Ehrlich phrased it, Lacks’ cells were taken from her and used without her consent. Recognition years later counts for little when her and her family were awarded no money they desperately needed and, in a sense, were entitled to. Though Henrietta Lacks’ privacy was taken from her when her cells were used and passed around without her consent, some have tried to make it seem as though Henrietta was a consenting
...d syndromes, such as Down and Turner Syndrome. Along with the discovery of having 46 chromosomes, scientists and researchers were able to map genes tracing back diseases. The production of the cells to test all these different diseases increased as more cell factories were built and cells could be shipped safely. This led to a multi-million industry, but also led to a loss of money along the way when HeLa cells infected many crucial experiments. HeLa led to many patient consent rules and regulations, including her family. These regulations included the government coming up with a commission and the Common Rule. Nowadays, when patients are given consent forms, every step is explicitly stated so that there is no such confusion or harm. All in all, Henrietta Lacks has contributed and made significant changes to the scientific, ethical, and political aspects of society.
...or instance, hepatitis C virus), biological molecules (such as cyclic adenosine monophosphate), and Human Immunodeficiency (HIV) virus (Bauman et. al. 2011). Rosalyn had went farther in the world of science than anyone including her self thought was possible (Bauman et. al. 2011). Rosayln and Berson changed history, altered the way science was perceived and their time, and how today we see and research science.