Henrietta Lacks Families Website

The media was also involved in neglecting to recognize Lacks as a person rather than a concept. The media bereaved Lacks of her identity as they called her by the name Helen Lane instead of using her real her real name. The use of the fictitious and more Caucasian name to identify Lacks in the media further dehumanized her and her family’s memory of her. They did not whatsoever consider Lacks’ family, their ordeal and whether or not the assumptions of Lacks being made were accurate. Moreover, the media did not provide any remuneration to Lacks’ family for using her story for their benefit. For example, an episode on the very popular television show Law and Order was based on the story of Henrietta Lacks however, no credit nor payment was given to the family. Apparent here is further display of the media’s view of lacks as an abstraction rather than a person.

The impact of any solution to the Lacks situation could be far-reaching. Stakeholders in any identified solutions include the dignity and memory of Henrietta Lacks’ herself, her family and descendents, the community in which she lived, medical researchers, medical practitioners, medical institutions and organisations, pharmaceutical companies and the financial world, governments and the

Although she was taken from the world too soon, Henrietta Lacks was a warm hearted woman, and though unbeknownst to her, she would pave the way for the medical field and greatly expand our understanding of one of the nation’s

The Henrietta Lacks Foundation is a non-profit organization founded by Rebecca Skloot, author of The Immortal Life of Henrietta Lacks, who is donating a portion of her book’s proceeds to the Foundation. Henrietta was a poor black farmer whose cancer cells had damaging consequences for her family who today can’t afford access to the health care advances their mother’s cells helped make possible. The Foundation strives to provide financial assistance to needy individuals who have made important contributions to scientific research without personally benefiting from those contributions, particularly those used in research without their knowledge or consent. The Foundation gives those who

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 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

Her family had realized that Henrietta had suffered and died, but her cells lived on and that her cells have helped so many people. Henrietta’s son said “I just hope Hopkins and some of the other folks who benefited off of her cells will do something in honor of her and make right with the family”(Skloot, pg. 328). Henrietta is finally getting recognized, which brought unwanted attention to the family from the media, doctors, and researchers that wanted a piece of the HeLa gene line. That affected her daughter, Deborah negatively because she never really knew her mother, but when Deborah first heard of the book she was very excited that the world would finally get to know her mother’s story.

I think this book adds a lot of value to ethical, biological and scientific education. The book gives you a very good view on how the HeLa-cells were grown, but also especially on the human behind these cells, Henrietta Lacks. Not only is the story of the discovery of HeLa relevant for (scientific) biological education, but also for scientific research education in general. The book adds value to scientific education, in a way that the story of HeLa makes you realize what the importance of research ethics is and how complicated and unfair issues about human tissue used in research are. You secretly hear the voice of Rebecca Skloot through her writing, telling the world to threat the “donors” with dignity and justice by making decent agreements and laws about human tissue used in research. She shows her readers how big the

When the family expressed concerns about privacy, the scientists removed the sequence from the Internet. Hudson and other NIH leaders then met with the Lacks family. Together, the family and the NIH came to an agreement. Researchers can use the HeLa genome by applying to the NIH for access. A group of scientists and Lacks family members review the applications. From now on, when a scientist publish a research conducted using HeLa cells, it must include a thank you note to the Henrietta Lacks and her family for their everlasting gifts to science (Barone 2). Science has used HeLa cells in many ways. For example, HeLa cells are used to study HIV, the virus that causes AIDS, HeLa cells prove that HPV can cause cervical cancer, there is a vaccine that protects against some strains of the virus now, and HeLa cells are also tested to see how quickly they can absorb nanoparticles, which can suggest new methods for delivering drugs to cancer cells. It’s crazy that Henrietta is technically alive after being dead for 60+ years. Her cancerous cells continue to thrive and multiple till this day, around the world. Her cells have help further the medical field, such as find vaccines and doing further studies for HPV and HIV (Barone 3-4). I’m so happy that Henrietta’s family and Henrietta get the acknowledgement they deserve, but still very disappointed that

After her death in 1951, for six decades, Henrietta Lacks did not exist in the eyes of the society, but her cells did. How? Well, the answer is quite simple. HeLa Cells are the first immortal human cells. These cells never die and multiply every twenty-four hours. After spending 10 years to perfect her first book, author of The Immortal Life of Henrietta Lacks, Rebecca Skloot essentially captured the life, the death, and aftermath of Henrietta Lacks’ life. With controversial issues regarding science, ethics, race, and class Skloot takes us on an extraordinary journey. From the “colored” ward of Johns Hopkins Hospital in the 1950s to stark white laboratories with freezers full of HeLa cells, from Henrietta’s small, dying hometown of Clover,

The Immortal Life of Henrietta Lacks is a very touching book; this book has really helped me take a new perspective on how patients were treated in hospitals in the 1950s. Also the book demonstrates how patients and research has changed drastically from how they are now compared to back when Henrietta’s cells were being used. Unfortunately Henrietta did not know that her cells were being used for research in the hospital labs, since she was unaware they were using her cells there was no way for her family to try to obtain money from the researchers to help them financially. Also, during this time period most people weren’t given the proper knowledge and consent rights to be used as research unlike today’s standards. Therefore, this leads me

Henrietta Lacks: an unknown name up until recent years. A name that had been known to the world only as HeLa; The first two letters of a name that belonged to a poor African American tobacco farmer that unknowingly changed science and life as we know it today. Her life has finally been portrayed in a very intimate story that not only does her life some justice but also transcendentally brings to mind the philosophical issues concerning medical ethics both of the past, present, and the future. In a world of constantly evolving medical advancement, science is a pivotal force that propels ideas forward. Although most will agree that the knowledge and cures found are a positive aspect, there is also a necessary evil that is involved, including

When I first heard about the book "The Immortal Life of Henrietta Lacks", I thought it was just a reading assignment when I was in high school that I had to complete for a grade. As I began reading I became particularly interested in Henrietta Lacks and the HeLa cells. In "The Immortal Life of Henrietta Lacks", Rebecca Skloot talks about Henrietta Lacks and how her cells were taken without her permission, and how her family suffered afterwards. Skloot shows how medicine and science were seen back in the 1950's compared to now.

The effect the discovery and creation of the HeLa cells made on the science community and Henrietta’s family had a domino effect. Both had different opinions and beliefs on the matter; this led to some difficult questions asked of the family and of the medical community. Due to the new and advanced methods of experimentation, the HeLa cells made to to the field of science, the scientific community and the media failed to remember that Henrietta and her family were not abstractions but actual people. Rebecca Skloot, however, took into account the Lack’s family, she inquired both the history of the HeLa cells as well as the Lacks family, treating them as actual people with inalienable rights.

In this case, it also seems that the doctors who treated Henrietta had something more important for research in mind rather than saving her from her cancer.