Cells That Save Lives Are Called A Mother 's Legacy

The Immortal Life of Henrietta Lacks is a novel written by Rabecca Skloot that outlines the life and story of a woman named Henrietta Lacks and her families struggle to discover the truth. Henrietta Lacks was and African American women who was diagnosed with cervical cancer at the age of thirty. A doctor at John Hopkins Hospital examined Henrietta and a biopsy of the cancerous tissue was retrieved. Henrietta received treatment for her cancer, but the cancer was too aggressive and she soon passed away at age of thirty-one, but her cells continue to live today. Henrietta Lack’s cells were unlike any other humans cells ever examined. The cells were able to grow, multiply, and divide outside of the human body in a lab (Skloot 2010). This was a major scientific discovery. Henrietta’s cells, more commonly known to the public as HeLa, aided in the creation of several scientific discoveries and are still used today. It is because of HeLa we have the polio vaccine, a better understanding of cancer, and cells in general. The cells have even been sent into space and have been exposed to nuclear testing and to toxins (BigPicture). Although Henrietta Lacks’s cells have done a lot good, many ethical issues surround her case such as privacy issues, monetary compensation, exploitation, and cell contamination to name a few. Perhaps the most important and controversial ethical issue in Hennrietta’s case resides around consent, or the lack there of.

The non-fiction book The Immortal Life of Henrietta Lacks, written by Rebecca Skloot, details the happenings and life of Henrietta Lacks, an African American woman and tobacco farmer who became a medical miracle in the 1950’s. The book is written in an attempt to chronicle both the experiences and tribulations of Henrietta Lacks and her family, as well as the events that led to, and resulted from, research done on Henrietta Lacks’ cells. Henrietta was a very average African American woman in this period; she had only a seventh-grade level education, and followed traditional racial and gender roles by spending her time has a mother and caretaker, as well as working on farms throughout her life until the involvement of the US in World War II brought her and her husband, “Day” Lacks, comparatively better work opportunities in industrial steel mills. However, after her death in 1951 Henrietta became much more than average to doctors at John Hopkins when the discovered that cells extracted from her cancerous tissue continued to live and grow much longer than any other tissue samples. Further investigation and isolation of these thriving cells led to the creation of the first ever immortal human cell line in medical history. The incredible progress in medicine made possible by Henrietta Lack’s tissue cells were not without downfalls, though. The treatments and experiences received by Henrietta and the effects it had on her and her family demonstrate both racial and gender

Many people would assume that, because of HeLa’s impact on society, the Lacks family is probably very wealthy and well informed about HeLa cells; unfortunately, that is not the case. Not only did the Lacks feel taken advantage of by the medical community, but it wasn’t until an article by Howard Jones in December 1971 that Henrietta’s real name was finally revealed. That same article was used to inform Bobbette Lacks, Henrietta’s daughter-in-law, that the immortal cells she had been reading about in the paper were Henrietta’s. Bobbette was the first member of the Lacks family to learn about the fate of Henrietta’s cells and she immediately ran to the family yelling, “Part of your mother, it’s alive!”(181). The family felt misinformed, confused, betrayed and most of all, angry. In 1976, Mike Rodgers published an article in Rolling Stone that informed the Lacks family that people were buying and selling Henrietta’s cells. The family immediately accused Hopkins of withholding money from them. Lawrence, Henrietta’s eldest son, was quoted saying, “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

The family connects the HeLa cells with poverty, racism, ethical issues, and tissue ownerships. They’re encouraging readers to read The Immortal Life of Henrietta Lacks to educate people about Mrs.Lacks.

The Immortal Life of Henrietta Lacks by Rebecca Skloot is a nonfiction book about Henrietta Lacks, an African American woman living in the 1920’s-1950’s. When she was thirty, doctors diagnosed Henrietta with cervical cancer. Doctors at John’s Hopkins took her cells without her permission and used these cells to create the first and most widely used cell line, named HeLa after Henrietta’s initials. Soon after the doctors took Henrietta’s cells, she died from her vicious cervical cancer, however her cells lived on in the hands of scientists around the world. Since then, her cells have been mass produced and used to test the polio vaccine, research cancer, AIDS, radiation, and human longevity, and develop drugs for treating herpes, leukemia, and hemophilia. Henrietta’s family did not know anything about the HeLa cell line until twenty-five years after Henrietta’s death, and even after HeLa cells created a multimillion-dollar industry, Henrietta’s family never received compensation. Even now, Henrietta remains widely unknown, and her family can’t afford health insurance.

In Rebecca Skloot’s pioneering non-fiction book, The Immortal Life of Henrietta Lacks, the complex story about the revolutionary HeLa cancer cells is told through the lives of the Lacks family and the multiple scientists and doctors that were part of one of the greatest breakthroughs of medical research in the twentieth century. The tale of the infamous and immortal HeLa cells was not just a scientific one, but one that involved struggle, confusion, ethical transgressions, and legal issues. Skloot writes about the life of Henrietta Lacks and her immortal cancer cells as well as her own research endeavor. Henrietta grew up with a very large family who all lived together and sometimes married internally. She eventually married and had kids with her first cousin, David. As an adult, Henrietta suffered from what she called a “knot” in her cervix, medically being cervical cancer. It all started when she started receiving cancer treatment from Johns Hopkins University in Baltimore, MD. John Gey had used cells from the tumor for medical research. At the age of 31, Henrietta died from her fatal disease, leaving her cells behind to continue her legacy. Despite the fact that her cells were researched throughout the world, the Lacks family was still living in extreme poverty with little to no opportunities for advanced education. Johns Hopkins conveyed limited information about Henrietta’s cells to her family to the extent that some family members did not even understand what a cell

In the early 1970s, researchers called the Lacks family requesting blood samples from Henrietta’s family so as to determine which cells were HeLa cells as they had begun contaminating other cell cultures in labs. One has to wonder if the need to identify HeLa cells from other cells hadn’t arisen, than perhaps the Lacks family would have never been told of impact of their mother’s cells. As it is, the researchers who contacted the Lacks family didn’t make much effort to explain the situation to Day Lacks, Henrietta’s husband, or her children. Mr. Lacks had only a third grade education, so he didn’t know

The Immortal Life of Henrietta Lacks by Rebecca Skloot is an amazingly captivating book about an African American woman who died in 1951 of cervical cancer, whose cells became the first in history to be able to survive and replicate endlessly outside of the human body. Skloot covers the true story on the impact Henrietta’s cells, also known as HeLa cells, had on her family and the world of science. Although I was intrigued by the entire book and the concept of HeLa cells, what truly provoked me to want to further research the topic was the injustice Henrietta’s family was forced to face, and how they learned to cope with it.

In 1951, Henrietta Lacks was diagnosed with cervical cancer at John Hopkins Hospital. Henrietta complained of a knot in her womb that caused her pain so she decided to visit the hospital in search of diagnosis. After being diagnosed with cervical cancer, the doctor recommended a biopsy be done on her cancerous tissue. Without any consent, Henrietta’s doctors took tissue samples from her cervix and attempted to grow them and keep them alive. These cells were known as HeLa cells, they began to grow at an unbelievable rate; The HeLa cell became vital for the development of vaccines and other scientific research. However because of Henrietta’s race and economic standpoint, Henrietta Lacks and the rest of the Lacks family was exploited by doctors. The exploitation of the family allowed the doctors and researchers to benefit scientifically and monetarily.

In 2010, Rebecca Skloot published her book The Immortal Life of Henrietta Lacks, a result of her discovery and findings devoted to Henrietta’s life story along with her family members, and revived the real person behind tremendous scientific accomplishments sprung of immortal HeLa cells’ exploitation. The research involving HeLa cells has changed the landscape of medical study, leading to scientific and medical breakthroughs that continues today. HeLa cells were vital for developing the polio vaccine; uncovered secrets of breast cancer and leukemia; helped lead to important advances in vitro fertilization, cloning, genetic hybrids, gene mapping in virology, scientific standards, live cell transport, for profit distribution of cells, space

Henrietta Lacks was an African American woman who had cervical cancer and had tissues taken from her body without her consent. This, along with her death, affected the lives of everyone in her family, especially her kids. Even though the children had wanted to sue Johns Hopkins for what they did, Deborah was able to help them come to peace with the situation- as much as they could. Deborah’s insistence to learn more about their mother helped them to turn their focus on Henrietta’s cells and how they majorly contributed to science. Rebecca Skloot was able to gain the family’s trust, because she wanted to learn more about Henrietta Lacks and her family, not only the cells that the whole world had known them to

Can you imagine doctors stealing your cells and using them for scientific medical experiments without you or your family’s consent, and for your cells to be sold worldwide without anyone knowing, even your family, that you are the woman whose cells became immortal and helped in fascinating scientific and medical discoveries? This is the story of a woman named Henrietta Lacks whose immortal cells are known as HeLa. The book, “The Immortal Life of Henrietta Lacks,” written by Rebecca Skloot is a scientific biography about Henrietta’s life before and after her death and the effects it had on others. In the book she explains her journey of discovering the truth behind Hela, she talks about the Lacks family, and the events caused by the HeLa cells.

The story of Henrietta Lacks and HeLa cells is one to remember. It is truly amazing how one person’s cancerous cells could impact science and the lives of so many. In the book sections of “The Immortal Life of Henrietta Lacks”, Rebbeca Skloot did a wonderful job portraying how Henerietta’s cells have had a positive affect on scientific studies. She described what HeLa cells have done and how studies with these cells have evolved over time. The movie “The Immortal Life of Henrietta Lacks” provided good insight on Henrietta’s family and described what they have been through since the passing of their mother.

The medical community did not explain to or inform the Lacks family of the HeLa cells; along the way the scientists altogether forgot that Henrietta and her family were not abstractions but actual people. The family felt that this was unethical; they felt their mother was robbed and taken advantage of. Despite the spread of HeLa cells and the whirlwind of new research that followed, there were no recent news or stories about “the birth of the amazing HeLa cell line” (Skloot 58). In the beginning, when Gey had kept the origin of the cells- or Henrietta - a secret, no one knew where the cells had came from and no one cared to ask.

The book The Immortal Life of Henrietta Lacks by Rebecca Skloot, was a nonfiction story about the life of Henrietta Lacks, who died of cervical cancer in 1951. Henrietta did not know that her doctor took a sample of her cancer cells a few months before she died. “Henrietta cells that called HeLa were the first immortal human cells ever grown in a laboratory” (Skloot 22). In fact, the cells from her cervix are the most important advances in medical research. Rebecca was interested to write this story because she was anxious with the story of HeLa cells. When she was in biology class, her professor named Donald Defler gave a lecture about cells. Defler tells the story about Henrietta Lacks and HeLa cells. However, the professor ended his