Born in Roanoke, Virginia on August 1, 1920, Henrietta Lacks would one day unknowingly be the reason for one of the most important cell lines in medical research. Henrietta Lacks became the source of HeLa cells after her death on October 4, 1951 (aged 31), cells which were the first immortalized cell line in history; immortalized cells are cells that will reproduce indefinitely under specific conditions. While Henrietta’s cells were and continue to be used to treat many illnesses, there was never any consent given from Henrietta herself, or any of her family. To this day, no portion of the billions of dollars made from HeLa cells ever found it’s way to Henrietta’s family. The medical ethics in the 1950’s are very questionable in comparison …show more content…
After the death of her mother, Henrietta’s father moved her family to Virginia where each child was distributed among relatives. Henrietta ended up living in a cabin with her Grandfather sharing a room with her cousin David Lacks. Henrietta worked as a tobacco farmer at a young age, when Henrietta was fourteen she gave birth to her first child, Lawerence Lacks. Four years later, Henriette gave birth to her first daughter, Elise Lacks.By 1950, Henrietta and David Lacks had another three children. The beginning of 1951 is when Henrietta Lacks visited Johns Hopkins, the only hospital in the area that treated black patients because she felt a pain in her womb. She was told she was pregnant. However, after giving birth to her fifth child, Henrietta had a severe hemorrhage. After many tests were run, a hard mass was found on Henrietta’s cervix. During treatment, two samples were taken from Henrietta’s cervix, one healthy and one cancerous, without her knowledge. For the final months of her life, Henrietta remained in the hospital until her death on October 4, 1951. Cancer had spread throughout her entire …show more content…
All this of this testing on HeLa cells has led to thousands of new pieces of knowledge advancing scientific technology. The amount of HeLa cells that have been produced is so substantial that researchers estimate that if the cells were to be laid down all end-to-end, the cells would wrap around the planet at least three times. HeLa cells made it possible to expose the cells to conditions that wouldn't have been ethical if they were inside a human body. However it is quite strange that exposing cells inside a human body would be unethical, still there was no question of ethics when cells were taken and used from a dead body without the permission of the individual. At the time, the general standpoint of medical science is that cells are taken from an individual and used for research benefit the common good, therefore it is okay to use them. However, the case of Henrietta Lacks would state otherwise, as Henrietta’s cells were used to develops medical treatments, none of those treatments available to those who cannot afford medical
The Immortal Life of Henrietta Lacks is a novel written by Rebecca Skloot, a science reporter, depicting the lives of Henrietta Lacks’s family and their connection between them and Henrietta’s famous cancer cells “HeLa Cells”. Henrietta Lacks was diagnosed with cervical cancer in 1951 and was treated with radium and radiation therapy. During her treatment process, the tumor and other cancerous tissue that was removed from her body was sent George Gey's lab at Hopkins to be grown in test tubes all without Lacks’s consent or knowledge. The cells were successfully able to divide and give the scientific community a good supply of human cancer cells to experiment on. The Lacks’s family was never informed about the cells even when there were amazing
HeLa has helped our world in many ways, as many as 70,000 medical studies and even more till this day. Her cells have been very needful in the development of drugs for herpes leukemia influenza (flu) and Parkinson’s disease. They have been used in many things like lactose digestion and mosquito mating. Before HeLa cells scientists spent more time keeping cells alive than actual research, an endless supply of HeLa freed up time for that(Skloot, Rebecca. The Immortal Life of Henrietta Lacks.
The Immortal Life of Henrietta Lacks is written by Rebecca Skloot and it has proved to be a very fascinating and educational book. From the beginning I was amazed by how medical practices happened in the early 1900’s. I knew they weren’t what they are now, but to have radiation treatments that turned your skin black sounds terrifying. This book taught me how important this woman’s cells were and how important it is to make sure you get consent. Henrietta married her cousin David Lacks and together they had five children.
The doctors dehumanized Henrietta and used her cells to make millions and become famous. One of the themes of this book is
If they didn’t want to blood samples, the children probably would have never found out about the cells in the first place. Scientists started to make a profit off from HeLa cells as well. The family got nothing but stress because of them. “Everyone is making funds off Henrietta’s cells,” Lacks grandson, Ron Lacks, told the sun. “I am sure my grandmother is up in heaven saying,”Well, what about my
One of the ironies explored in The Immortal Life of Henrietta Lacks is the dichotomy between the vast value of the HeLa cell line—which has been used in the development of the polio vaccine, nuclear bomb testing, the
Henrietta was born Loretta Pleasant, and she later changed her name to Henrietta. She married her first cousin David “Day” Lacks, they shared a room together at her grandfather’s house. Henrietta and David had 5 children; Lawrence, Elsie, David Jr., Deborah, and Joseph. Henrietta was diagnosed with cervical cancer on January 29, 1951 at John Hopkins Hospital. During all her diagnosing and surgeries without Henrietta’s knowledge the doctors took two samples from her cervices.
Throughout the Rebecca Skloot’s book, The Immortal Life of Henrietta Lacks, she described her investigation into the life of Henrietta Lacks, her immortal cell line, the ethical violations surrounding her case, as well as the major contributions to modern medicine and research her case provided. During the time of Henrietta’s treatment, both medical and research ethics were quite different; many values such as autonomy, justice, and beneficence were not as enforced, and were applied differently throughout different institutions and individuals of different demographics. Though investigating her case and other important cases surrounding the use of HeLa cells, Skloot acknowledges the unethical circumstances which filled Henrietta’s case and
In the chapter we learned that Henrietta only had a sixth-grade education, then she started birthing her children. Most of her early life she spent time on a farm and rarely went to the doctor. After Dr. Howard Jones tested Henrietta he found a “tumor the
Henrietta later had 3 more children by the names of David jr., Deborah, and Joseph. On August 1st, 1951 Henrietta Lacks was experiencing a sharp knot in her abdomen so her husband decided to take her to John Hopkins hospital to figure out what was going on, little did they know that this little visit would not only change their lives but change the lives of people all around the world. After the doctors inspected her abdomen they quickly came to the conclusion that she had cervical cancer. Subsequently, the doctors conducted radiation tests and took two cervical cell samples without her knowledge.
Henrietta Lacks was an African American woman from the 1900s. She was diagnosed with cancer and had her cancer cells cultured without her consent. These cancer cell lines are known as HeLa cell lines and one of the first immortalized cell lines utilized in current medical research. The fundamental issue with Henrietta Lacks’ HeLa cells is that the researchers never obtained consent for the use of these cells; nevertheless, these cells have benefitted greatly for the area of research. Not only were the cells useful for finding treatments for diseases, but the cells were also utilized in space studies too.
Later, when Henrietta’s genome was published, it sparked up more drama, because this too was unethical. “That is private family information,” said Jeri Lacks-Whye, Lacks’s granddaughter. “It shouldn’t have been published without our consent” (The NY Times). I believe that the continued use of the HeLa cells would have been ethical if the scientists were given permission. “It was a big moment, a hopeful moment, sitting down with the family and bringing so many years of research without consent to an end” (NBC News).
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.
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.