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The Difference
Not knowing all the information you need to fully access a situation, or not being able to see the good being done because it hasn’t happened yet can lead you to feel a certain way about a topic. I am trying to show you in these next few how different your opinion can be based on the knowledge you have. Henrietta Lacks had cells taken from her without her or her family's knowledge; little did they know the positive impact it would have. The public interpretation would be different if the book had been published in 1951 because of the lack there of information, biased judgment, and ethical reasoning.
One way that the public interpretation would be different in 1951 would be the lack of information views on the doctors taking the cells. “But first- though no one had told Henrietta that TeLinde was collecting samples or asked if she wanted to be a Donor-Wharton picked up a sharp and shaved two dime-sized pieces of tissue from Henrietta’s cervix: one from her tumor, and one from the healthy cervical tissue” (pg. 33). This example states that the doctor deliberately took Henrietta’s cells without consent. From the public’s viewpoint in 1951, they could see this as the doctors violating her rights to her body and knowing what goes on in and around it. Today, we believe that this was a bold move for that doctor and we know that, by him taking those
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“During this time, we were not considered as humans, I guess. They could do what they liked” (Phelps Page 3). This is a prime example in showing, that during these times, black people were not considered human beings. So being that during the 1950s most of the community was white, they would not see any harm being done in a white doctor taking a black woman’s cells. That is how biased judgement could cause the public to interpret their feelings towards the doctor
The initiative wasn’t taken to learn about the family or the origin of the cells. Roland H. Berg, a press officer at the NFIP, sent George Gey, head of tissue-research at John Hopkins, a letter saying, “ An intrinsic part of this story would be to describe how these cells, originally obtained from Henrietta Lakes, are being grown and used for the benefit of mankind” (pg. 106). This letter is a very clear representation of the lack of knowledge from society. Berg referred to Henrietta as “Henrietta Lakes” on multiple occasions in the letter. The correct form of her name wasn’t even known. A name is such a distinct representation of identity and Henrietta’s was so commonly mixed up and misspelled. An opposing view could argue that the scientists’ job was to work with the cells. Their goal was not to learn the family tree of the individual, but to make discoveries using the cells. It wasn’t until the autopsy of Henrietta Lacks, that people started to face reality: HeLa is not just a cell line. HeLa was a mother, a daughter, a sister, and a best friend. Mary Gey, George Gey’s wife and research assistant, viewed Henrietta’s body once it was being used for tests in the autopsy room. She noticed that Henrietta had her toenails painted with a bright red polish. Mrs. Gey said, “When I saw those toenails, I nearly fainted. I
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.
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
...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.
In 1951, the sickness of a poor African American woman named Henrietta Lacks -also know as HeLa- would go on to change the face of scientific research; without her consent. Henrietta Lacks went into John Hopkins Hospital in hopes of medical treatment, but instead her cells were unlawfully stolen from her and used for scientific advances in the world of medicine for the creations of the polio vaccine, cell cloning, vitro fertilization, and gene mapping. Long after Henrietta's death, Henrietta's family was forced to live a life of poverty without medical insurance simply because they could not afford it although their mothers cells had yielded billions of dollars due to its advances in the medical world. The scientific community and the media
The Belmont Report identifies three core principles that are to be respected when using human subjects for research. The three ethical principles are: respect for persons, beneficence and justice. In the case of Henrietta Lacks each of these fundamental components are violated. The consent that Henrietta provided was not sufficient for the procedures that were conducted.
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
Most people live in capitalist societies where money matters a lot. Essentially, ownership is also of significance since it decides to whom the money goes. In present days, human tissues matter in the scientific field. Rebecca Skloot, author of The Immortal Life of Henrietta Lacks, shows how Henrietta Lacks’s cells have been used well, and at the same time, how they have been a hot potato in science because of the problem of the ownership. This engages readers to try to answer the question, “Should legal ownership have to be given to people?” For that answer, yes. People should be given the rights to ownership over their tissues for patients to decide if they are willing to donate their tissues or not. Reasons will be explained as follows.
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
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 ...
Though it wasn’t illegal at the time, it was completely wrong of the doctors to segregate her because of her ethnicity. Henrietta wasn’t treated properly as a patient and was discriminated against at the Hopkins hospital, like when a nurse labeled her blood sample as ‘colored.’ Henrietta would have most likely supported doctors taking her cells if it meant it was going to help countless people, if only she had the knowledge of
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.
Her name was Henrietta Lacks, also known as HeLa is credited for the huge advancements in the medical industry such as for polio, cancer, and many viruses
The Immortal Life of Henrietta Lacks is a wholesome story about hope, science, and coming together as a family in a new, strange environment. The story consists of the author: Rebecca Skloot, endeavoring on a lifechanging journey which spans states, as well as time periods. The main struggle of the story is John Hopkin’s use of Henrietta’s Lacks’ cells without her knowledge. After Henrietta’s death, the scientific community receives these cells, and begins to make groundbreaking advances in the fields of medicine, cancer research, and virology. The main conflict in the story is what the family should receive in terms of compensation for Henrietta’s cells. The plot continues to thicken when Henrietta’s daughter: Deborah, begins to discover more about her mother’s past, as well as her mother’s cells effects on most, if not all of humanity.