Part two of, The Immortal Life of Henrietta Lacks, once again submerges the reader in to the world of HeLa cells. This section emphasizes what occurred with Henrietta’s immortal cells after her death. Along with the many medical discoveries made from these miracle cells, part two delves into the physical and emotional abuse that Henrietta’s children were forced to live with after her passing all while struggling financially while their mother’s cells are being sold for millions of dollars. Skloot continues her phenomenal synopsis of the life of Henrietta Lacks and the stories her cells continue to tell. One of the utmost riveting and critical scenes of this section occurs in the first few pages. Day agrees to allow for an autopsy to be performed on Henrietta and on page 90 Skloot describes what Mary told her years later. After seeing Henrietta’s painted red toenails Mary thought to herself, “Oh jeez, she’s a real person.” This simple sentence has a massive story to it and reflects what many readers are bothered with while reading this book. It is difficult to learn about what this woman …show more content…
Millions of people have these cells to thank for their health and researchers owe their life’s work to them. Yet, the Lacks family cannot even afford to go to the doctor and are completely unaware of everything their mother’s cells have done for the wellbeing of people all around the world. Gey would not even publish or release her real name. In chapter 22, the reader sees the family’s reaction to being kept in the dark about these cell, Bobbette says, “Everybody always saying Henrietta Lacks donated those cells. She didn’t donate nothing. They took them and didn’t ask.” This quote ties together much of the story behind the ethical issues surrounding these cells and the importance of informed consent, a privilege we now take for granted
She had took him to many doctors appointments, and everything for the study. So when her professor begun talking about the HeLa cells, it sparked a similarity with her own father. In Rebecca Skloot’s 2010 tribute, The Immortal Life of Henrietta Lacks, to reveal the troubles the Lacks family had finding out information of a deceased love one, whose cells have contributed to medical history. Throughout her writing Rebecca uses a southern vernacular, to help re-create the time with Henrietta Lacks family.
Table of Contents Title Page Abstract Review of Literature Introduction Henrietta Lacks The Knot Doctor Jones and TeLinde Doctor Grey and Treatment Birth of HeLa Cells Henrietta’s Death A Cure for Polio Other Contributions Immoral Practices
The doctors dehumanized Henrietta and used her cells to make millions and become famous. One of the themes of this book is
The book “The Immortal Life of Henrietta Lacks” written by Rebecca Skloot revolves around an African American woman who began life as a poor tobacco farmer, but soon after being diagnosed with cervical cancer in 1951 would unknowingly become one of the most important people in history. Unfortunately many would come to simply know her as “HeLa” the first “immortal” human cell line instead of another human being who had the right to know what doctors would soon do to her. She was strong woman and great mother to five unique children; Elsie, Lawrence, David (Sonny), Deborah, and finally Zakariyya (born Joe). The story itself tends to transition between the past and the present day. It gives us the story from both the perspective of Henrietta’s
The Immortal Life of Henrietta Lacks is a novel by Rebecca Skloot detailing the life of Henrietta Lacks and her family. In her 2010 narrative, Skloot explores the scientific discoveries made through the use of the so-called HeLa cells obtained from Henrietta in her final years, as well as the results of malpractice within segregated hospitals and the effects on the Lacks family. The importance of these topics was only amplified with each new advancement and each new onus transferred to the Lacks family. Consequently, strong held beliefs by both the scientific community and Henrietta’s ancestors clashed. The story of Henrietta Lacks began on a plantation in Virginia in 1920, but the most impactful years of her life came at the end of her time.
Henrietta Lacks Honor Essay “The reason Henrietta's cells were so precious was because they allowed scientists to perform experiments that would have been impossible with a living human. They cut HeLa cells apart and exposed them to endless toxins, radiation, and infection. They bombarded them with drugs, hoping to find one that would kill malignant cells without destroying normal ones.” (58)”Throughout the book “The Immortal Life of Henrietta Lacks” there are many examples of how the HeLa cell of Henrietta Lacks provided cellular information and examples that helped mold many cellular discoveries and experiments.
In August of 2013, Talha Khan Burki wrote “Righting a Long-standing Wrong for Henrietta Lacks” for Lancet Oncology. Burki’s purpose was to highlight the problem with the sequence data of patients’ cells (namely, Henrietta Lacks) being publicly released and to inform people of the privacy risks involved. Burki did a very good job at explaining what the issue was, what had been done about it and what needed to happen. Generally, readers struggle and become overwhelmed when they see a large sum of information all at one time. However, while this article provides the reader with several facts, it makes the reader think and Burki did a very well at writing in a manner that prior knowledge of certain terms or concepts are not critical to comprehending.
This was really touching to read because it really did show that Henrietta Lacks was a selfless woman and the only thing in the world she cared about was her family. We can also see the immense love between the Lacks family all throughout the authors reporting journey. In the beginning when no one wanted to talk to her, they weren't doing it to be mean. They were doing it because they didn't know who to trust anymore with their family’s situation since they had been lied to so many times. This shows tremendous love and respect for their mother since they wouldn't just talk to anyone randomly about what they were going through.
The absence of empathy extends to the Lacks family. When it was found that HeLa cells contaminated many of the cells lines around the world scientists scrambled for a definite marker unique to the HeLa so they might contain the HeLa infestation. For this they turned to Henrietta’s family. Genetic researcher Victor McKusick and assistant Susan Hsu began to take blood from Henrietta’s children and husband, David Lacks, without having the decency to fully explain the situation to Henrietta’s closest family members (Skloot, 2011). Mourning is a physically, mentally, and psychologically draining experience.
McLaurin writes that “the life of Celia demonstrates how slavery placed individuals, black and white, in specific situations that forced them to make and act upon personal decisions of a fundamentally moral nature” (xiii). This provides the overview of what Celia endured and the actions she took,
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.
#3-Examining how death and the losses were addressed within my African American family is openly discussed and always some one’s fault. The experience of my grandmothers death relates to the statistics of the life expectations of African America. According to (Walsh 2004 p. 56) African American woman life expectancy for older adults is 70.2 years and African American men life span is 66.1 according to the national Vital Statistics Report (Volume, 47 NO.28). My grandmother died young
Nonfiction books can often expand ones knowledge, especially in the subject of science. In the book, The Immortal Life of Henrietta Lacks, writer of the book and journalist Rebecca Scloot finds herself looking at an image of an African American whom had a tumor growing in her body without knowledge of it. This woman in the photo, Henrietta Lacks, although her name was unknown by most scientist and teachers, helped change the face of medicine back then and even today. Henrietta Lacks started getting treatment for cervical cancer at Johns Hopkins Hospital at age 31. The physicians at the hospital cut a dime size piece of her tumor and sent it into the lab where George Gey then put it on clots of chicken blood to see if the cells would grow.
What are the specific issues raised in the book—legally and ethically? Think about the 1980s John Moore case: the appeal court decision and its reversal by the California Supreme Court. Issues that raised in the book are race issues, the legality of taking adventage of patients who’s family aren’t able to fight for the rights and benefit of their cells. According to California supreme court, Under the duty to obtain informed consent, “a doctor must disclose his intent in using a patient for research and economic gain.” 6.
Her doctor collected cancerous cells and healthy cells from her cervix and gave them to the cancer researcher, George Otto Gey, who was trying to keep cells alive for more than a couple days. Henrietta endured intense radium treatments, but she still died at the age of 31, leaving her husband and five children behind. An amazing discovery was made Henrietta’s cell were immortal. Racism is prevalent in this book through the limited availability of healthcare, unethical behaviors of the doctors, and how racism affected her family. During this time, there was an extensive lack of medical care for colored people.