I first heard about Henrietta Lacks story after noticing and advertisement of Oprah Winfrey directing or possibly playing the role of Ms. Lacks. Reading the caption underneath the picture posted I decided to inquire more about the Henrietta Lacks. Ms. Lacks was an African American woman who found out in 1951 after a biopsy, Lacks was diagnosed with cervical cancer. The manifestation of the tumor was unlike anything that had ever been seen by the examining gynecologist Dr. Howard Jones. Henrietta Lacks was treated at the segregated John Hopkins Hospital with radium tube inserted and sewn into her body, a standard treatment at that time sewn in her body. However, a few days after doctors removed the tubes and performed an X-Ray exam. The doctors, took two samples, a noncancerous and a cancerous part of her cervix without her permission. These cells would ultimately develop into the HeLa immortal cell line, a universally used cell line in biomedical research. My immediate reaction to the ethical issue with Henrietta Lacks cell taken without her permission disturbed me because I felt if she was a White woman doctors would have asked for permission and would have given credit …show more content…
Many Supreme Court precedent cases have assisted in the battle for civil right for people of color. Therefore, the attempt to harvest someone cells without permission is less likely to happen now unless persons live in a third war country which human rights is an irrelevant concern or issue. Henrietta Lacks’ story violates and impact research today because her treatment desecrated her individual rights since she was a woman of color. The effects of Henrietta Lacks’ mistreatment makes me question society views on “black lives matter” if we’re not violating people of color on a slab table were currently mistreating them within the criminal justice
HeLa cells were taken from Henrietta unbeknownst to her by George Gey, a cell biologist at Johns Hopkins hospital, when she went in for a biopsy of the tumor growing inside of her. Today, those cells have been crucial in the development of the polio vaccine, aided scientists in learning more about the secrets of cancer, helped in cloning and gene mapping, and have ultimately, been sold by the billions. Even still, Henrietta was buried in an unmarked grave.
Although many are unaware of it, scientific ethics have always been a major issue, especially in the United States. This was especially the case of Henrietta Lacks and her family through the early 1950s to present day. Henrietta Lacks hurried into John Hopkins Hospital in Baltimore, Maryland to find out why there was a lump on her cervix. When doctors diagnosed her with cervical cancer, she filled out a form giving consent to let the doctors perform any surgery they deemed necessary. Soon after Henrietta died in October of 1951, her husband, David (Day) Lacks, signed a consent form to let them perform an autopsy on her corpse.
On the topic of respect, there was also a lack of respect related to her family. The Lacks family were not all on board for the usage of HeLa cells. Infact, not until about 20 years later did the scientist have the audacity to mention it to them. When Henrietta’s children were informed that her mother's cells are still living today, they were very rudely informed. The scientists wanted more information about Henrietta, so they went to her children to collect more blood samples.
The Immortal Life of Henrietta Lacks is a book that includes her biography, then her childhood to her tragic death; the story of her family over various decades; Skloot’s research and her relationship with the Lacks family, especially Deborah; and the story of the HeLa cells. Henrietta Lacks was known by scientists as HeLa was a poor black tobacco farmer whose cells were taken without her knowledge in 1951, and then became one of the most important tools in medicine. They were necessary for the development of the polio vaccine, cloning, and much more scientific developments. A doctor at Johns Hopkins took a piece of her tumor without her consent and then sent it down to scientists who been trying to grow tissues in culture for decades. Henrietta's
“The historic dream of public health…is a dream of social justice” (Health Affairs, Vol. 25, Number 4). In the story of Henrietta Lacks, it is hard to say that the use of her cervical tissue is ethical, because it is not. Henrietta was diagnosed with cervical cancer and Dr. Gey decided to isolate those cells. When he found that these cells could grow in a culture medium and last, he shared them with the world of science.
Deborah states, "Truth be told, I can 't get mad at science because it help people live, and I 'd be a mess without it. I 'm a walking drugstore! I can 't say nuthin bad about science, but I won 't lie, I would like some health insurance so I don 't got to pay all that money every month for drugs my mother cells probably helped make". This explains how Deborah has to spend all her money on not even all her medication because she can 't even afford health insurance that will cover her medicine. African Americans who were
Jasmine Poole The Immortal Life of Henrietta Lacks by Rebecca Skloot is about a women who has cervical cancer that went to the doctor to get better. But instead of just getting better, the doctors took a sample of the cancer cells. The doctor used her cells to help other people with the same cancer get better. In this case, Henrietta and her family didn’t know that her cells were being sold all around the world to reporters/doctors.
Henrietta Lacks was a black tobacco farmer from the south who, in 1950, at the age of 30, she was diagnosed with aggressive cervical cancer. Lacks went to John’s Hopkins medical center for treatment for her cancer. In April of 1951, she underwent surgery to remove the larger tumor on her cervix. Henrietta Lacks, died three days following the surgery. Even though Henrietta Lacks died, her cells from the tumor have lived on and have made a major impact on the biomedical community.
Bushra Pirzada Professor Swann Engh-302 October 4th 2015 Rhetorical Analysis: The Immortal Life of Henrietta Lacks The Immortal Life of Henrietta Lacks written by Rebecca Skloot tells the story of a woman named Henrietta Lacks who has her cervical cancer. It further goes to tell the audience how Henrietta altered medicine unknowingly. Henrietta Lacks was initially diagnosed with cervical cancer in 1951; however, the doctors at John Hopkins took sample tissues from her cervix without her permission. The sample tissues taken from Henrietta’s cervix were used to conduct scientific research as well as to develop vaccines in the suture.
In 1951, at the age of 31 Henrietta Lacks was diagnosed with cervical cancer. Henrietta was under treatment at Johns Hopkins University in Baltimore, where cells from her malignant tumor were removed. Neither Henrietta nor any of her family members knew about the tissue sample and nor did the Hopkins ever informed them of the situation. Unfortunately after Henrietta’s radiation treatment, her condition continued to worsen and soon she lost her battle to cancer on octomber 4th 1951. Henriettas cells left the Hopkins what they discovered to be known to be the first immortal human cell line.
Participation Portfolio 1 Asst 3: Henrietta Lacks Discussion Questions Please answers each of the following questions, and be prepared to discuss in class 1. Please outline the history of Henrietta Lacks 's tissue cells. Who did what with the cells, when, where and for what purpose? Who benefited, scientifically, medically, and monetarily?
The seemingly endless battle for civil rights was one fought long and hard and during the 20th century a time of fruition occurred that allowed for concrete and tangible progress though the efforts of many, including key black intellectual revolutionaries. The call to freedom, and the fight for civil liberties to be bestowed upon people of color, who for hundreds of years were perceived as subordinate was happening. Change was fought through self-determination, and a burgeoning of powerful ideologies that laid the foundation for movement to be made. The admirable actions of women have been slighted, as they are almost non-existent in the pages of our history books. The contributions of the civil right movement have many a time excluded the contributions of prominent African American woman who tirelessly fought.
Racism in The Immortal Life of Henrietta Lacks Imagine your mother, sister, wife, or cousin was diagnosed with cervical cancer and you believed the doctors were doing everything in their power to help her. Only later you discovered her cells were used for research without consent and she was not properly informed of the risks of her treatment due to her race. This story happened and is told by Rebecca Skloot in The Immortal Life of Henrietta Lacks. Skloot use of narrative and her writing style enhances the understanding of the story. Henrietta Lacks was a young black woman who was diagnosed with cervical cancer at John Hopkins Hospital.
Despite the wrongdoings Henrietta Lacks was put through her cells did a lot to help advance science. Her cells helped develop different types of vaccines, which such as her daughter faced. A lot of good and bad came out of Henrietta’s
The origination of HeLa cells, used in biomedical research for a potential cure for cancer, had made many ground breaking discoveries in science; all thanks to one woman, Mrs. Henrietta Lacks. The history of Mrs. Lacks’s contribution to these studies raised many ethical issues concerning healthcare practice. In the short film, The Way of All Flesh, we learn how these cells were revealed by direct violation of ethical principles. During the 1950s, matters regarding informed consent practices were in their beginning stages of implementation.