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The Degradation of Medical Ethics Concerning HeLa Cells
As a poor black woman from rural southern Virginia, no one would have thought Henrietta Lacks would hold the key to various medical advancements and the production of wealthy scientific industries. Henrietta Lacks had a sample of her cervical cancer cells taken from her to be cultured in 1951 and they were later named “HeLa” cells . Her cells were the first types of cells that were used continuously for experiments due to the fact that her cells were immortal. They never died and grew rapidly and uncontrollably due to their cancerous nature. Henrietta Lack’s cells have been used to create polio vaccines, have been exposed to space, have gone through nuclear testing, and have been used to understand cancer cells more effectively. Yet with all of the benefits her cells have provided to the scientific world and to those suffering from diseases, Henrietta never knew her cells were taken from her in the first place. In the book The Henrietta Lacks Legacy Grows, it was revealed that “Henrietta Lacks was not asked for permission to use samples of her tumour for research”(849 Greely & Cho). This meant that Henrietta’s family knew nothing of the cells being distributed and used around the world for research. The discovery opened up the complex, ethical issues of medical research. The distribution of Henrietta Lack’s cells not only invaded the privacy of the family but also defied human consent which is extremely unethical.
In January 1950, Johns Hopkins colored ward received a visit from a patient named Henrietta Lacks. She came from a poor background and being a mother of five children also did not help her financial situation. Lack’s was tested and it was revealed that she was suf...
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... it is possible to acknowledge the good that the HeLa cells provided while also keeping in mind a great injustice was done towards the Lacks family. Also, some will argue that Henrietta did give informed consent be that as it may, she consented to Johns Hopkins operative procedures not the stealing and the commercialization of her tissues.
The medical advancements and the good that was acquired due to the cells cannot overshadow the fact that immoral practices were the reason of such advancements. If such mindset were used then the Tuskegee Syphilis Study of 1992 and the unspeakable crimes committed by scientist towards the jewish, could all be excused. The information collected and the improvement of the scientific world could have occurred without the violation of informed consent and the callous treatment from the scientific world towards the Lacks family.
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 February 2010, author and journalist Rebecca Skloot published a book, "The Immortal Life of Henrietta Lacks," which included the stories surrounding the HeLa cell line as well as research into Henrietta Lacks' life. In 1951 a poor young black women, Henrietta Lacks was diagnosed with cervical cancer and at the time was treated in the “colored ward” or segregated division of Johns Hopkins Hospital. The procedure required samples of her cervix to be removed. Henrietta Lacks, the person who was the source of these cells was unaware of their removal. Her family was never informed about what had been accomplished with the use of her cells. The Lacks family has not received anything from the cell line to this day, although their mother’s cells have been bought and sold by many. This bestseller tells the stories of HeLa and traces the history of the cell while highlighting the ethical and legal issues of the research.
....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...
“Ah, the creative process is the same secret in science as it is in art,” said Josef Mengele, comparing science to an art. He was less of an artist and more of a curious, debatably crazy, doctor. He was a scientist in Nazi Germany. In general, there was a history of injustice in the world targeting a certain race. When Mengele was around, there were very few medical regulations, so no consent had to be given for doctors to take patients’ cells and other tests done on the patients’ bodies without their consent. This was the same time that Henrietta Lacks lived. Henrietta Lacks was an African American woman who went to the doctor because she had cervical cancer. Her cells were taken and are still alive in culture today (Skloot 41). Hence, her cells were nicknamed Immortal (Skloot 41). Although many, at the time, saw no issue with using a patient without consent issue with what?, on numerous occasions since then courts have determined that having consent is necessary for taking any cells. The story of Henrietta lacks is has similarities to an episode of Law and Order titled Immortal, which is an ethical conundrum. Despite this, the shows are not exactly the same and show differences between them. Both of these stories, one supposedly fictional, can also be compared to the injustices performed by Josef Mengele in Nazi Germany.
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
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
Doctors often would not inform their patients of everything they were doing to them and they did most things without a patient’s consent. In the book, Henrietta was not aware of many of the things the doctors were doing to her. They took samples of her tumor without her knowledge. The treatments that were given to her had negative side effects that she was not made aware of. The doctors’ and researchers’ actions had similar effects on Henrietta’s family. The family was never aware that her cells were being used in laboratories or that researchers were making millions of dollars off of them. Even when the Lackses were made aware of the research being conducted on the cells, it caused the family a great deal of confusion and distress. When they finally found out about the HeLa cells, it was because a doctor wanted to take their blood to test for genetic markers. The doctors did not explain this to the poorly educated Lackses, who thought they were being tested for cancer. This miscommunication caused Henrietta’s family to panic, for they thought they were going to die just like Henrietta. On the other hand, on the national level, HeLa cells served as a platform for research about many diseases, including cancer and polio. The cells progressed the scientific research on genetics and diseases further than ever thought
The novel The Immortal Life of Henrietta Lacks, by author Rebecca Skloot is about a black woman whose cells were used by doctors to study medicine without her knowledge or her permission. Rebecca Skloot first heard of Henrietta Lacks when she was 16-years-old in her college biology class. Her professor, Donald Defler, mentioned Henrietta briefly during his lesson about cells. Defler talked about how Henrietta’s cells helped scientists learn all they know about cell and cell culture today, and allowed them to develop disease-fighting drugs to combat herpes, leukemias, influenza, hemophilia and Parkinson’s disease. Although Defler did acknowledge the fact that it was Henrietta’s cells who helped change the future of medicine, all Defler added was that she was a black woman. Skloot was unsatisfied with this information and she wanted to know more about Henrietta Lacks, such as “Where was she from?... Did she know how important her cells were? Did she have any children?” (Skloot 4). The problem was, though, that no one cared to find out anything about the person whose cells were famous all over the world. Most people, in fact, did not even realize that her name was Henrietta Lacks, and not Helen Lane. All people knew about this woman was that her cancerous cells were referred to as HeLa cells. Thus, Skloot’s purpose was to inform people around the world about the life of the woman whose
In The Immortal Life of Henrietta Lacks, multiple cell research studies involving Henrietta’s cells are described. Author Rebecca Skloot writes about Henrietta Lacks’ journey through her cervical cancer and how her cells changed the lives of millions long after her death. Skloot relates the history of cell research, including those studies which were successful and those that were not so successful. It is necessary for the author to include the achievements and disturbing practices of scientists throughout this history to inform readers and focus on the way Henrietta’s cells were used. Truth always matters to readers and Henrietta’s family deserves the truth.
The story of Henrietta Lacks and her family is one that raises many questions about ethics, consent, medical treatment, and family rights. The decisions made by the scientists and doctors surrounding HeLa research have had lasting impacts in the Lacks family. The question I have chosen to address is what change would have helped the Lacks children the most. I feel the most influential piece to the Lacks children’s suffering was being raised by Ethel. This portion of their life was filled with physical and emotional abuse that led to destructive behavior. This behavior would also play a role in the anger toward HeLa researchers and anyone else who did harm to the family or left them in the dark. Although questions about their mother, financial
Nowadays, when patients are given consent forms, every step is explicitly stated so that there is no confusion or harm. All in all, Henrietta Lacks has contributed and made significant changes to the scientific, ethical, and political aspects of society.
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
Physician-assisted suicide refers to the physician acting indirectly in the death of the patient -- providing the means for death. The ethics of PAS is a continually debated topic. The range of arguments in support and opposition of PAS are vast. Justice, compassion, the moral irrelevance of the difference between killing and letting die, individual liberty are many arguments for PAS. The distinction between killing and letting die, sanctity of life, "do no harm" principle of medicine, and the potential for abuse are some of the arguments in favor of making PAS illegal. However, self-determination, and ultimately respect for autonomy are relied on heavily as principle arguments in the PAS issue.
The story about Henrietta Lacks is the evidence that the ethics of medical processes need to be improved. For a long time, many patients have been victims of malpractice. Sometimes, the doctors still can do anything without the agreement from patients. Any medical institution needs to hold the integrity on any consent form that is signed by a patient. To summarize, the story of Henrietta Lacks could be the way to improve the standardization and equality of medical institutions in the future.