Words are powerful. As a result, changing one word in a sentence can make the biggest of differences. The quote above is part of a statement by Honorable Robert L. Ehrlich, Jr. of the house of representatives commemorating Henrietta Lacks. Ms. Lacks was whom the HeLa cells that have been used since their discovery came from. The use of the word “provided” in Ehrlich’s statement is controversial, as Henrietta Lacks’ cells were taken from her and used regardless of her opinion. Her privacy was taken from her and used by the public without her consent. This turns attention to other women have had their privacy brushed aside, such as Frieda Kahlo. Lacks’ cells were made public, much like Kahlo’s diary was made public. The manner in which authors …show more content…
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 …show more content…
His piece, however, honored Lacks and explicitly mentioned that no one asked for her or her family’s permission to take her cells, stating that “without … permission … , doctors at Johns Hopkins had collected and saved samples of tissue from her cancerous tumor”. Though both political figures with no personal ties to Henrietta Lacks or her family, it is clear that Hon. Perriello and Hon. Ehrlich had different understandings of the situation and Lacks’ role in it, as made evident by their explanation of it. Once more, it is proven not only that Lacks’ privacy was taken from her when her cells were passed around without her consent, but diction plays a highly significant role in recreating
While doctors and scientists were making millions of dollars through HeLa research, Henrietta’s family was living in poverty. Lawrence Lacks, Henrietta’s firstborn child, says, “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 science, why can’t we get health insurance?” (pg.168). Someone who disagrees with this standpoint may argue that scientists had been trying for years to develop the perfect culture medium and had a much more hands on experience with the cells (pg.35), therefore, they should be receiving the earnings from any outcomes the HeLa cells may produce. While the scientists were in fact the brains behind the scientific advances, the family should be acknowledged on behalf of Henrietta Lacks. These successes in science would not have been possible without the origin of the cells: Henrietta Lacks. For some of the family, the primary focus was not even the profit. “Since they gone ahead and taken her cells and they been so important for science, Deborah thought, least they can do is give her credit for it.” (pg. 197). Here, Deborah Lacks, Henrietta’s fourth born child, makes it clear that her primary concern is getting her mother the recognition that she deserves for her
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.
In the novel, The Immortal Life of Henrietta Lacks, the author, Rebecca Skloot, tries to convince the audience that her argument regarding, Henrietta and her cells is worth thinking about. Skloot argues that the woman whose body contained these life-changing cells deserved to be recognized. While trying to prove her side of the argument, Skloot uses logos within the novel to emphasize to the audience just how important her cells are, by providing the science behind the cells and their accomplishments.
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
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...
At the time the tissue samples were collected from Henrietta Lacks she was an individual capable of deliberation about personal goals and of acting under the direction of such deliberation (Belmont Report, 1979). By collecting the samples without Henrietta’s sufficient consent she was denied of her freedom of choice. She was not given the opportunity for her decisions
To have something stolen from you is devastating and can change your life. But what if what was taken from you will save billions of human lives? In the book The Immortal Life of Henrietta Lacks by Rebecca Skloot, we see a woman named Henrietta had a biopsy of a cancerous tumor, and the cells from the tumor were able to live and grow outside of her body; and even better, the cells go on to find the cure for diseases such as polio. The catch is this: she signed a document giving her hospital permission to perform any medical procedure they find necessary to help her treatment, but she never gave specific permission for the cells in that biopsy to be tested and cultured. Now the big debate is over whether or not it was legal for her doctors
People trust doctors to save lives. Everyday millions of Americans swallow pills prescribed by doctors to alleviate painful symptoms of conditions they may have. Others entrust their lives to doctors, with full trust that the doctors have the patient’s best interests in mind. In cases such as the Tuskegee Syphilis Experiment, the Crownsville Hospital of the Negro Insane, and Joseph Mengele’s Research, doctors did not take care of the patients but instead focused on their self-interest. Rebecca Skloot, in her contemporary nonfiction novel The Immortal Life of Henrietta Lacks, uses logos to reveal corruption in the medical field in order to protect individuals in the future.
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 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 lecture when he said that Henrietta Lacks was a black woman. In this book, Rebecca wants to tell the truth about the story of Henrietta Lacks during her medical process and the rights for Henrietta’s family after she died.
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 ...
What is privacy? Well, it’s the state or condition of being free from being observed or disturbed by other people. In terms of information, it is the right to have some control over how one’s own personal information is collected and used. This is a right that has been inherently protected by the U.S Constitution, agreed upon by the Supreme Court, and yet, issues around this very topic arise every day. In The Immortal Life of Henrietta Lacks, the author Rebecca Skloot, addresses this issue in her story of the women behind the infamous HeLa cells. Her story shows that although privacy is a right that is inherently protected by the law, situations of injustice can still occur. Examples of this in the book include when Henrietta’s cells were given to Dr. Gey without any consent from Day, the situation in which Mr. Golde’s spleen was sold without his permission, as well as when the Lacks family were recontacted and mislead about the reasons they were tested years after Henrietta’s death.
And even though the Lacks family learns for the first time in 1973 that Henrietta’s cells are still alive, it wasn’t until 1991 that it became illegal for research to be done without informed consent (The Common Rule).The family of Henrietta Lacks had not been informed because there were no laws requiring it. This can lead us to believe that at the same time, many other individuals were not being fully informed as to what they were getting into. Today “many bioethicists question why the family [of Henrietta Lacks] was left in the dark.”
Once the Lacks family found out, they were none too happy. They were “angry—angry that Henrietta’s cells were being sold for twenty-five dollars a vial” and their anger was justified. “Hopkins say they gave them cells away,” Lawrence yelled, “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 science, why can’t we get health insurance?” Henrietta’s family’s lack of compensation is one of the unethical portions of this story. It’s possible, if the Lacks family was given compensation for their loved ones cells, this whole ordeal would be justifiable. But because the Lacks family is not living in a mansion on a hill with a large settlement, this is still up for debate. Henrietta’s family lives in poverty, while there loved one is one of the most important people to have ever lived. This is one of the stronger, pathos driven arguments against the ethics of this