About 60 years ago, before African Americans had much respect at all, there was a woman named Henrietta Lacks who was diagnosed with cancer in her cervix. Without asking for permission, Henrietta’s doctors took some of her cells from her cervix, and they took them to do more research on them and tried to grow them for the first time outside of a persons body. Because she was African American, she and the rest of her family were not respected by doctors, or many other people at this time. These cells later became very critical to medical advancements and scientific research for the rest of the world. But, the injustice of this situation raises a large controversy over whether or not this is justified. Should the doctors be able to have done this without her consent? Rebecca Skloot wrote the book The Immortal Life of Henrietta Lacks to talk about this in more depth.
These doctors took her cells, and used them for research and
…show more content…
There are many reasons for this; because the cells weren’t ‘part of” Henrietta anymore so it shouldn’t matter whether the doctors did what they did or not. The problem however, is that Henrietta was not informed on any of this and were not given a real opportunity to give ‘informed consent’ about her cells and tissues on her body. Because of the pressure that they felt from the doctors, they were vulnerable. They weren’t told that tissues were taken from her body, and now, these cells and tissues made many people other than the Lacks family rich, when the Lacks family still struggled to keep their heads above water and to just make it by. “The biggest payday any of the Lacks children ever saw...Day got a check for $12,000 and gave $2,000 to each of his children” (Skloot 208). This isn’t fair to the family that their family members cells are still alive and doctors are making money when the family is
Patients have no rights to samples taken from them as they become biological waste. Yet it is not necessary for doctors to obtain consent to store the same tissues that are supposed to be biological waste and use the samples for research. The lines in bioethics are blurred and there should be stricter guidelines on how research should be conducted and exactly who should benefit from. I believe the tissue donor should receive some sort of compensation because it not for said cells, the research would not exist. As with HeLa cells, without Henrietta Lacks, there would be no HeLa cells nor any
In Rebecca Skloot’s novel “The Immortal Life of Henrietta Lacks” , she informs readers about “HeLa” aka Henrietta and also about her journey discovering the many traits of Lack’s past . Henrietta Lacks , known in the medical world as “HeLa” died in 1951 due to cervical cancer . She experienced frequent bleeding from her genital parts , due to a tumor that was in her womb . She wasn’t known for going to the doctor whenever she had a health problem , but in the book Skloot said that HeLa explained the tumor as a “ lump in her in womb” and had a feeling that she needed a doctors help. After being looked at by her doctor and being tested for possibly having syphilis , she was redirected to a gynecologist .
Henrietta Lacks was a poor black tobacco farmer,born in Roanoke, Virginia on August 1 ,1920.Henrietta’s mother died when Henrietta was very young, her dad did not wanted to take care of her and her siblings, so they were sent with different relatives. She grew up with her grandfather. Henrietta died at age of 31 years old of cervical cancer, on October 4, 1951. At the age of twenty-nine she felt a “knot” inside of her. In the year of 1950, she had a full-fledged tumor just three months after she had felt the knot.
After eight months of treatment and excruciating pain from the tumors that kept appearing everywhere, Henrietta passed away. During that time scientists were developing a factory to mass produce her cells. As new developments with her cells kept occurring, her family was oblivious to it all until one day when Bobette, Henrietta's daughter in-law, ran into someone who shed some light on the subject. A brother of a friend unveiled how Bobette’s mother in-law’s cells were in his lab right now being tested for different things. Bobette then told the family which made Deborah, Henrietta’s daughter ver curious and worried about what they were doing.
Henrietta Lacks was a thirty-one year old African American who had five kids and married her cousin David Lacks. Henrietta was diagnosed with cervical cancer, the doctors never informed Mrs. Lacks that her cells were to be tested on. The Lacks family was certainly not advised that Henrietta 's cells were growing at an incredible rate. Because of this, the cancer cells were shipped and bought across the world. The last 8 months of Henrietta’s death became a piece of history nobody would ever want to forget.
First of all, Henrietta was an African American woman at the time when there was still inequality and segregation towards African Americans. This was really evident when she went in for her checkups at Hopkins and how she was never asked for her consent with her cell tissue. Also, the medical treatments at that time were not very safe or effective. An example would be when they used radium to try and treat her cervical cancer. Little did they know that radium destroys any cells it touches and it can also cause cancer.
When Henrietta went to John Hopkins Hospital she soon found out that she had Cervical Cancer. While she was under anesthetics they took some cells without her knowledge and gave them to a lab. If she had been a white women I feel as if they would have asked her for a sample of her cells and respected her decision whether it be yes or no. The hospital continued to do things that she did not know of.
The Immortal Life of Henrietta Lacks is a strong illustration of the interplay between race and medicine. After reading this book, I thought that I probably owe Henrietta Lacks for my some of the medications or treatments I have received in my life. It is unfortunate that Henrietta and her family were treated
In the reading of “The Immortal Life of Henrietta Lacks”, the author Rebecca Skloot makes it well known that Henrietta Lacks, while a patient at John Hopkins Hospital samples of her cells was taken from her without her or her family’s knowledge or consent. We are made aware of this on page 33 “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 knife and shaved two dime sized pieces of tissue from Henrietta’s cervix”. As a health professional, you are violating that patients’ rights and in this case the Lacks right to privacy were violated. The way that the lacks family’s right to privacy was the fact that Henrietta’s cells often referred to as the HeLa cells
What would you do if a doctor took your cells without consent and shortly after, your cells went viral, being sent all over the world to millions of different scientists? Well, I can’t say that Henrietta Lacks lived through this, but I can say that her cells did. Bioethics, the ethics of medical and biological research, has been a controversial issue throughout the U.S. for years. Different laws have been formalized to help tame the fire on the topic of consent and mortality. In the year of 1951, Henrietta Lacks was diagnosed with cervical cancer and had too many tumors to count inside her rotting body.
Is it right for one's life to be manipulated for the use of scientific research or is it just a evasion on the person's privacy. Henrietta Lacks was a African American with cells that intrigued many people, she was diagnosed with cancer leaving her to be cared for at her local hospital, where she would later die due to the extremity of the illness. While at the hospital she was unaware that the doctors there were experimenting on her taking cell samples from her body, to help find a resolution to multiple diseases. The people who examined Henrietta manipulated her and the rest of her family to gain information on her cellular structure to be ahead of others looking to achieve the same objective. Henrietta Lacks cells should have never been evaluated because it's an evasion of her freedom, a danger to her personal health, and cause conflicts.
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.
The Immortal Life of Henrietta Lacks tells the story of Henrietta, an African-American woman whose cells were used to create the first immortal human cell line. Told through the eyes of her daughter, Deborah Lacks, aided by journalist Rebecca Skloot. Deborah wanted to learn about her mother, and to understand how the unauthorized harvesting of Lacks cancerous cells in 1951 led to unprecedented medical breakthroughs, changing countless lives and the face of medicine forever. It is a story of medical arrogance and triumph, race, poverty and deep friendship between the unlikeliest people. There had been many books published about Henrietta’s cells, but nothing about Henrietta’s personality, experiences, feeling, life style etc.
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