The Immortal Life Of Henrietta Lacks By Rebecca Skloot

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.

Have you ever been bullied or even discriminated against? Imagine that feeling of embarrassment, shame, and self-consciousness. Although I never have experienced the type of discrimination that Henrietta did, I still understand how it feels whenever you feel cheated because of another's actions and the pain that comes with self-doubt as a affect from the society. Seeing how I am affected by discrimination, it is easy to see that the theme of discrimination in "The Immortal Life of Henrietta Lacks" is relevant in today's world.

They don’t even give her a postcard” (164). This is just one instance of the media taking advantage of the Lacks family. Michael Gold, a Science 85 reporter, released a book about Henrietta Lacks. Deborah got a copy and discovered that Gold included vivid details from her mother’s medical records, even though Hopkins had not gotten permission from the family. The book then goes on to explain Henrietta’s decline and details of her autopsy (210). It haunted Deborah with images of her tumor ridden mother.

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

Imagine having no rights in life. Imagine one day you get sick, and you go to the hospital to get better, but you get taken advantage of. How would all that make you feel? Henrietta Lacks was an African-American woman. During her time, women didn’t have equal rights like men did, and African-Americans didn’t have equal rights like white people did. Since Henrietta was an African-American woman she had it rough, there were times that everyday tasks were a struggle. In 1951 she was diagnosed with terminal cervical cancer. She was treated at John Hopkins University, where doctors didn’t do all they could even if they said that was the case, and were Doctor George Gey took her cells from her cervix without consent. I watched the Law and Order episode titled “Immortal”, I found it to be extremely similar to a book I read titled The Immortal Life of Henrietta Lacks by Rebecca Skloot even though the show said in the beginning that this was not based on a true story.

The scientific community’s careless mistreatment of the Lacks family began with dehumanizing Henrietta’s cells in the very first lab. Generalizing people can especially be easy when one is working with their cells in a lab. The many scientists working on Henrietta’s cells must have found it easy to separate the cells from the person and reduce them to tools to aid them in the task at hand. This view may be harmless when it comes to the individual scientist, and the individual cell, but this view extended to the entire Lacks family and caused them much harm. “Meanwhile, Victor McKusick and Susan Hsu had just published the results of their research in

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

Henrietta was an African American woman who grew up in Clover, Virginia and was raised by her grandfather, Tommy Lacks because her mother died after giving birth to her 10th child. Henrietta worked with her cousin in the family’s tobacco farm, went to school until 6th grade, and had her first child with Day Lacks (her cousin) at the age of 14, and they got married when she was 20 years old and he was 25. After giving birth to her 5th child, Deborah, Henrietta goes

Henrietta Lacks is woman, whose cells have been used for 63 years after her death in 1951, and will continue to be used as long as they are continue to grow. Henrietta Lacks was an African American woman who was born in the south, who married her cousin and moved up north. After giving birth to her last child, she finds that she has cancer. The doctors took a sample of her cancer cells without her permission, and now have millions of dollars but the family is still hasn’t received the money they are rightfully entitled to. Many of healthcare and entitlements that are around today, are due to the ill treatment of Henrietta and her family. Still to this day, there is very little known about Henrietta Lacks, even with the book out, and she has

"The Immortal Life of Henrietta Lacks", by Rebecca Skloot, is about an African American woman born and raised in Roanoke, Virginia, and later dying in Baltimore, Maryland. Through her a life she battled a cancer that was often called a cervical cancer, and she later died in Baltimore, Maryland. Henrietta Lacks, born as Loretta Pleasant, is commonly known for her cancer cells called, HeLa, which is a name made from the first two letters of her first and last name. This book was very informational, not only for family purposes, but for science too. It has a lot to relate to science, whether readers realize it or not.

The story took place in Baltimore in the early and mid 1900s, when prejudice was prominent and black people were not treated fairly or equally by white people. Moreover, the entire black community was terrified of night doctors, who would kidnap black people for scientific testing, and the book states that “fear of the night doctors only increased in the early 1900s, as black people migrated north to Washington D.C., and Baltimore” (166). This shows that the setting of the story had a huge impact on the book, as black people were taken advantage of routinely against their will. This is what happened to Henrietta, as she had to drive miles and miles to go to the only hospital around that would serve black people just to have her cells were taken without her consent by white scientists and used for the benefit of others. The author also uses many changes in point of view in the story to provide more background and portray the many different ideas and views of different people. For example, Skloot starts off telling the story from Henrietta’s point of view, showing her family and her struggles through her time with cancer. Then, she switches over to the eyes of a scientist who was working with Henrietta’s cells in a lab and working to grow the cells to benefit the scientific world. Finally, the author tells the story through her own eyes as she had to acquire information about Henrietta’s personal life through Henrietta’s family and the struggle she went through to get it. The setting of the story and the changes in point of view used by the author improve the story

Henrietta Lacks was diagnosed with cervical cancer. Her doctor at Johns Hopkins hospital took her tissues without informing her and grew them. When she died her tissue became HeLa cells which became the key to science research creating vaccines and medications. Race In the Immortal Life of Henrietta Lacks was exploited by the doctors. It was a major issue and the doctors took advantage of their patients to receive what they wanted. It left people like Henrietta and her family uninformed because blacks were forbidden to ask questions.

In 1951 there was a young black lady who was named Henrietta Lacks. Henrietta Lacks was a tobacco farmer in Clover, Virginia. Her mother died giving birth and her father moved the family to Clover, where the children were distributed among some of the close relatives. In January of 1951 she went to John Hopkins hospital, which was the only place close to her that treated black patients at the time. Lacks described a “knot” in her stomach that ended up being cervical cancer. During her treatments two samples from her

Henrietta Lacks was a black woman that grew up in the rural segregated south; her lifespan was from 1921 to1951. She grew up on her grandfather Lacks tobacco farm after her mother died giving birth to her tenth child. From the time she was four years old, she picked, cleaned, and harvested tobacco leaves, spending little or no time in school; she had at most a 6th grade education. By the time she was fourteen, Henrietta had given birth

Rebecca talks about whether or not people should have the rights to their own tissues. She points out two issues, consent and money. In the past there was no informed consent, so the doctors and researchers felt free to use tissues in whatever way they wished, with little concern for patients' rights. Nowadays there is a different system, and it's required by the law to ask for a patient's informed consent.mThe money issue is a question of whether doctors should be required to tell patients if their cells or tissues are going to be used for commercial research, and what rights those donors should have. Later on, “scientists sequenced Henrietta Lacks's genome and made it public, without asking the family's permission” which was just another way in which the family was violated and looked over (Silver). Apparently Henrietta didn't get her rights, and neither did her children. Any way we look at it, if the family had received any benefits from the cells, it