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“Ethical and Bioethical Issues in Medicine
Medical ethics
“Ethical and Bioethical Issues in Medicine
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There is a saying, usually associated with acts of war. This saying is “the ends justify the means,” which means although bad things may be done to reach an end goal, the end goal may be so good that the means of reaching it are justifiable. But do the ends truly justify the means in all cases? This is something that can be debated in the story of a loving mother who lost her life while battling cervical cancer. Her name was Henrietta Lacks. Her doctor, without her true knowledge, took her cells. While Henrietta sadly died, those extracted cells lived on, continuing to split, and grow. The ethical debate is whether it was right for her doctor to extract, and sell, Henrietta’s cells without her true knowledge. The debates cover sub topics such as the doctor’s choice to extract and sell the cells, Henrietta’s lack of knowledge, Henrietta’s families …show more content…
lack of compensation, or say, and about the ends, that may or may not justify the means. “Like many doctors of his era, (Richard Wesley) TeLinde often used patients from the public wards for research, usually without there knowledge. Many scientists believed that since patients were treated for free in the public wards, it was fair to use them as research subjects as a form of payment” because this was a common practice of the time, TeLinde probably didn’t give it a second thought. This in and of itself seems immoral, but there are always factors that have to be addressed. In some cases, the testing that doctors did on patients probably did hurt them. But in the case of Henrietta, there was not truly any harm done to her, not physically. Other than the pain the extraction may have caused, any testing done was not advancing her cancer, or killing her in any other way. In this aspect, there was not ethical wrong doing. “No harm no foul” as some would say. And her cells were reproducing. “They reproduced an entire generation every twenty-four hours, and they never stopped. They became the first immortal human cells ever grown in a laboratory.” Which was very helpful to the advancement of science, one of the “ends.” Henrietta’s cells were given to George Gey, head of tissue research at Hopkins. He was the first to grow HeLa cells. “Gey was able to isolate one specific cell, multiply it, and start a cell line.” This was the start to many advancements, all because Henrietta’s cells survived. “But Henrietta's cells weren't merely surviving, they were growing with mythological intensity … Soon, George told a few of his closest colleagues that he thought his lab might have grown the first immortal human cells. To which they replied, Can I have some? And George said yes” this may seem harmless, just a scientist sharing his discoveries, and the product of them, but there are a few issues with this exchange. One of the main issues, is Henrietta’s lack of knowledge about what she was agreeing to. She had no idea what her cells would become, or that they would be sold for millions. Henrietta was given a paper to sign at the beginning of her treatment, one that said “I hereby give consent to the staff of The John Hopkins Hospital to do any operative procedures and under any anesthetic either local or general that they may deem necessary in the proper surgical care and treatment of, under which she signed her name, a witness signing as well. Due to the fact that she signed this, it was legal for the doctors to extract her cells, but did Henrietta fully understand to what extent the “operative procedures” would advance? Most likely not. Henrietta most likely did not understand that she was giving consent to experimentation on her cells that did not involve her specific case of cervical cancer. She also probably didn’t know that any extracted cells and any reproduction of them could be sold. She was completely unaware of what she was truly signing, or what this would mean for her or the future generations of her family. She most definitely did not know what her cells would do for science. This, is the aspect of the story of Henrietta lacks that can be truly deemed unethical. She was not thoroughly informed, and thus made an uninformed and ignorant decision. This was not her own fault, and this will cause turmoil for the future generations of her family. Henrietta’s family was totally oblivious to the extraction and selling of her cells, while the doctors who sold Henrietta’s cells after her death were making millions.
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
story. The “ends” of this story though, are very important to note. Because of the distribution of Henrietta’s cells, “In 1952, the worst year of the polio epidemic, HeLa cells were used to test the vaccine that protected millions.” And “Before HeLa cells, scientists spent more time trying to keep cells alive than performing actual research on the cells. An endless supply of HeLa cells freed up time for discovery.” And because “Some cells in Lacks' tissue sample behaved differently than others, Scientists learned to isolate one specific cell, multiply it, and start a cell line. Isolating one cell and keeping it alive is the basic technique for cloning and in-vitro fertilization.” and “A scientist accidentally poured a chemical on a HeLa cell that spread out its tangled chromosomes. Later on, scientists used this technique to determine that humans have 46 chromosomes—23 pairs—not 48, which provided the basis for making several types of genetic diagnoses.” Also, “It was discovered that Lacks' cancerous cells used an enzyme called telomeres to repair their DNA, allowing them, and other types of cancer cells, to function when normal cells would have died. Anti-cancer drugs that work against this enzyme are currently in early clinical trials.” “They also knew that there was a string of DNA at the end of each chromosome called a telomere, which shortened a bit each time a cell divided, like time ticking off a clock. As normal cells go through life, their telomeres shorten with each division until they’re almost gone. Then they stop dividing and begin to die. This process correlates with the age of a person: the older we are, the shorter our telomeres, and the fewer times our cells have left to divide before they die. By the early nineties, a scientist at Yale had used HeLa to discover that human cancer cells contain an enzyme called telomeres that rebuilds their telomeres. The presence of telomeres meant cells could keep regenerating their telomeres indefinitely. This explained the mechanics of HeLa’s immortality: telomeres constantly rewound the ticking clock at the end of Henrietta’s chromosomes so they never grew old and never died.” This could very well not only solve organ failure, but halt death all together. And in the case of Henrietta herself, like the author of “the immortal life of Henrietta lacks,” “I’ve tried to imagine how she’d feel knowing that her cells went up in the first space missions to see what would happen to human cells in zero gravity, or that they helped with some of the most important advances in medicine: the polio vaccine, chemotherapy, cloning, gene mapping, in vitro fertilization. I’m pretty sure that she—like most of us—would be shocked to hear that there are trillions more of her cells growing in laboratories now than there ever were in her body.” So, because of the amazing ends, I feel the means are justifiable (though the lacks family should be thoroughly compensated.) because of Henrietta’s immortal cells, many important life altering discoveries have been made. Not only have they advanced medical sciences and biology, but also astronomy, and many other areas. Her cells have advanced the human race, and we would be far behind where we are now without them. Of course, her family was not treated fairly, and that wrong should be righted, but her cells have helped millions of people. I think, if there was such a way, Henrietta is (or would be) happy that this happened. Shed see what her cells have done for others and shed be thankful that her cells were distributed. I know this, because getting to know who she was through what her family had to say in “immortal life,” she was a truly good person, and her contribution, no matter how uninformed it was, has helped humanity to continue to strive towards a more advanced version of ourselves. In part, at least, we have Henrietta to thank for that.
The family first heard that Henrietta’s cells were alive and being sent around the world, twenty-two years after Henrietta’s death. After discovering that Henrietta’s cells were in circulation, the family began to blame John Hopkins for taking Henrietta’s cells without permission and commercializing the cells to make multi-million dollar industry, while her family was living in poverty without health insurance. The John Hopkins Hospital has made various statements stating that the hospital never received funds for the HeLa cells specifying that Gey donated all of his HeLa cells samples to fellow researchers. Therefore, the sole benefactors of the HeLa cells profits are the biotechnology companies, which sell vials of HeLa cells for up to ten thousand
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.
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.
The Immortal Life of Henrietta Lacks by: Rebecca Skloot has a lot of themes, but one that is most relevant in my opinion is the racial politics of medicine. Throughout the chapters, there were examples of how Henrietta, being African American, prevented her from receiving the same treatment as the white woman sitting right next to her in the waiting room. The story begins with Henrietta going to Johns Hopkins Hospital and asking a physician to check a “knot on her womb.” Skloot describes that Henrietta had been having pain around that area for about a year, and talked about it with her family, but did not do anything until the pains got intolerable. The doctor near her house had checked if she had syphilis, but it came back negative, and he recommended her to go to John Hopkins, a known university hospital that was the only hospital in the area that would treat African American patients during the era of Jim Crow. It was a long commute, but they had no choice. Patient records detail some of her prior history and provide readers with background knowledge: Henrietta was one of ten siblings, having six or seven years of schooling, five children of her own, and a past of declining medical treatments. The odd thing was that she did not follow up on upcoming clinic visits. The tests discovered a purple lump on the cervix about the size of a nickel. Dr. Howard Jones took a sample around the tissue and sent it to the laboratory.
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
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.
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.
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
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 ...
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.