The story of Henrietta Lacks is a very tragic story. Many ethical issues are present in the story. It is also a very great story, because of all the accomplishments that were possible because of her cell line. The main issue in the story is that the family was never compensated, while other companies, who have no relations to Henrietta and might not even know who she is, are making millions, if not billions, off of her cell line. The family struggled in life while other people were living better and better because they were making money off of Henrietta’s cell line. The family deserved to be compensated, and have still not to this day been paid any money at all.
Henrietta Lacks was born in Roanoke, VA on August 1, 1920. She had five children
…show more content…
George Gey didn’t take the cells to make money. He gave the samples to anyone who wanted them, and had a reason to have them, for free. He never made a cent off of Henrietta’s cells. “Johns Hopkins never patented HeLa cells, and therefore does not own the right to the HeLa cell line. John Hopkins also did not sell or profit from the discovery or distribution of HeLa cells” (McDaniels 1). The people who got free samples of the cells were the people who made money of the cells. They started to produce the cells themself. Even though John Hopkins Hospital never made any money they aren’t innocent. They took the cells without Henrietta’s consent. They also lied to the family about taking blood samples from them. They had an asian woman call the family, and tell them that they were going to take blood samples from them to see if they were at risk of getting cancer. First off, the asian woman wasn’t good at speaking english so the family had a hard time understanding what they were actually doing. Second, they weren’t actually testing to see if they were at risk of getting cancer. They were actually using them for studying Henrietta’s cell line. The children’s cell line could help to compare the Henrietta’s cell line because they kids have some of the same cells that she has (McDaniels
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.
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.
....S. Public Health Service advanced medical technology, it came at a high cost. A high cost that resulted in many African-Americans dead and a breach of trust for medical professionals. In the notable experiments of Henrietta Lacks, The Tuskegee Syphilis Men, and The Pellagra Incident, medical professions in no way protected the lives of these individuals. In fact, they used the medical advances discovered as a result of the human experimentations as a shield to mask the unethical decisions. Medical professionals targeted the African-American population and used their ignorance as a means to advance medical technologies. This in no way upholds the ethics that medical professionals should display. The Immortal Life of Henrietta Lacks vividly exhibits the how the United States Public Health Service used, abused, and ultimately destroyed the African-American community.
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...
The Immortal life of Henrietta Lacks is a book about the women behind the scientific revolution of using actual cancer cells to perform cancer research. Henrietta Lacks was an African American woman who was barely educated and worked as a tobacco farmer. At the age of thirty she was diagnosed with cervical cancer. In Lacks’ time being uneducated, African American, and a woman was not a great mix. They were often undermined and taken advantage of. When Lacks started to become very ill she went to the nearest hospital that would accept black patients. There the doctor, George Gey, misdiagnosed her illness and took a tissue sample without her consent. After suffering through her illness and trying to keep up with her five children Henrietta died
Although she was taken from the world too soon, Henrietta Lacks was a warm hearted woman, and though unbeknownst to her, she would pave the way for the medical field and greatly expand our understanding of one of the nation’s greatest killers; cancer. In 1951 people did not talk about cancer lightly; cancer was a very touchy subject, especially for those who knew they couldn’t receive treatment once they had been diagnosed. When Lacks went to the hospital because of a “knot on her womb” she never thought that it would grow into a full fledge tumor that would end up taking her life. Henrietta lived a simple yet happy life which consisted of working on the farm, loving her husband, and raising children, and she was not going to ruin the lifestyle she knew so well by telling her family that she had cancer; it was just unheard of.
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.
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.
On the concept of feasibility, disputes regarding practicality make reparation impossible. The fundamental definition of “family” yields the question of deciding which members of the Lacks family should be eligible for remuneration. Would compensation conclude with Lacks’s immediate kin or expand to extended family? Her children Lawrence Lacks, Sonny Lacks, and Zakariyya Bari Abdul Rahman would undoubtedly receive restitution, but the passing of daughters Elsie Lacks and Deborah Lacks complicate the case for direct descendants. Hence, no just method exists to determine which relatives would qualify for restitutions. Additionally another hindrance to compensation arises: who should be held accountable for repaying the Lacks family? The default culprit Johns Hopkins merely freely distributed HeLa to other laboratories, never garnering any profit from the cells. Hundred of research institutions across the globe have received samples of HeLa; thus, tracking down each individual laboratory would be next to impossible. Even if that feat was feasible, what monetary value should be compensated? No single individual or organization has the authority to dictate an appropriate amount that can simultaneously satisfy both family and compensator as well as solve the ethical
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 ...
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.
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.
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
...ave. They have been through a lot by people asking over and over about the HeLa cells. I think the least the doctors could do is tell them the actual truth about how they used those cells and stop making them guess or always wonder. I think they should have told them when they come to get the blood what they were actually using it for. They may not have understood, but the least they could do is tell them. They could have told them they wasn’t taking their blood to see if they had cancer they should have told them they were taking it for the HeLa cells. I think it was a good thing when I found out that Gey was actually doing research on the cells and not actually trying to get money. I thought this whole time he was probably getting money from it. I think when he was doing his research he was actually trying to help people, not put the Lack’s family through so much.
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.