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Henrietta Lacks: Sued To Share Profits From His Cells

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Henrietta Lacks John Moore was a leukemia patient that died at the age of 56 years old. He had his spleen removed because with the infection the doctor was worried that it was going to explode. Once his spleen was removed the tissue was then used in research by Dr. David Golde a researcher for UCLA (John Moors, 56; Sued to Share Profits from His Cells). John was never told about the research being done on his tissues, he was just asked by Dr. Golde to return to the UCLA medical center for follow up checkups, where doctors would take blood every time and still never mentioned anything about research to John. John was asked to sign a consent form, to allow Dr. Golde to patent his research on John’s tissues, and this is when John finally got …show more content…

In 1951 Henrietta went to John Hopkins hospital to help her overcome the cancer with radiation treatments. While she was going in for treatments and checkups her doctor took some tissue from her tumor in her cervix and sent it to lab to be research, none of this she told Henrietta that he was doing. In lab Henrietta’s cell grew in culture and actually stayed alive, unlike any other cells they tried to culture. This cells were called “Immortal” because they grew so fast and to such a huge amount that they could separate them and send them to all different doctors for their own research. They were eventually named HeLa cells, from the first two letters of Henrietta and the first two letter of Lacks (History, Travel, Arts, Science, People, Places/ Smithsonian). HeLa cells were used in all kinds of research and cure many diseases. They were used in the first mission to space to see what would happen to cells in zero gravity, they were a very important part to finding the polio vaccine, they were used in cloning, gene mapping and also in vitro fertilization (History, Travel, Arts, Science, People, Places/ Smithsonian). Henrietta never had claim to her cell and what they did until 20 years after she died and finally, even after efforts to keep it hiding, in 1970s her real name started to leak out into the

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On Henrietta’s deathbed Gey tells her that her cells will make her immortal. The tuskegee institute began giving cells for polio research but soon after began sending cells to any scientist who wanted them The hela cells were used to create many scientific breakthroughs and understanding of cells such as the use of freezing cells for delivery and the standardization of cell culturing Skloot and Deborah 1990 1999 Skloot reaches out to Roland Pattillo after coming across a collection of scientific papers compiled by Pattillo about Henrietta, after she decides she wants to write about

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With Henrietta the doctors took a sample from her tumor and started experimenting with it. After all the experiments they did,  the cells turn out to be the first cell line that did not died within days. One thing doctors fail to tell Henrietta was

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The HeLa cells not only survived, they grew intensely and kept right on growing as much as their given space would allow. It seemed like the cells would never stop growing, thus came the label of the immortal cells (Skloot, 2010). HeLa cells became a very important part of scientific research, and Henrietta’s name became well-known among Gey’s colleagues. On November 2, 1953, the real name behind the HeLa cells was leaked by the press, but they got it wrong, Henrietta Lakes was reported as the source of the cells in the Minneapolis Star. Gey and Dr. TeLinde, the cervical cancer specialist at John Hopkins, decided to allow their story about Henrietta to be told in a more accurate account, but they wanted to withhold her name.

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People did not know the truth about HeLa because Hopkins hospital hid the fact that they took living samples of Henrietta’s cells without consent. “-Add quote-“they did it to continue and advance in their research. From HeLa the scientific world was booming with questions. “–Add quote-“they asked questions such as where was HeLa from and who’s the patient was with the cells. Not to mention Hopkins did not release Henrietta name because they did not want people to find out who she really was.

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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

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And somewhere along the line, HeLa cells came from Helen Lane. Whether this was done to keep Henrietta’s identity a secret or not, give credit to Henrietta Lacks, who was an African American woman during the 40’s, Henrietta’s identity was kept a secret. Apart from that, I have already mentioned the hundreds of innovations brought about by Hela cells. Only for Henrietta’s children and spouse to never receive any credit, or compensation for that matter. The Lacks family has paid large amounts for medical coverage and

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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.

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Participation Portfolio 1 Asst 3: Henrietta Lacks Discussion Questions   Please answers each of the following questions, and be prepared to discuss in class   1. Please outline the history of Henrietta Lacks 's tissue cells. Who did what with the cells, when, where and for what purpose? Who benefited, scientifically, medically, and monetarily?

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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

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The Immortal Life of Henrietta Lacks is a book that includes her biography, then her childhood to her tragic death; the story of her family over various decades; Skloot’s research and her relationship with the Lacks family, especially Deborah; and the story of the HeLa cells. Henrietta Lacks was known by scientists as HeLa was a poor black tobacco farmer whose cells were taken without her knowledge in 1951, and then became one of the most important tools in medicine. They were necessary for the development of the polio vaccine, cloning, and much more scientific developments. A doctor at Johns Hopkins took a piece of her tumor without her consent and then sent it down to scientists who been trying to grow tissues in culture for decades. Henrietta's

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Lacks’ Cells Alive for Medical Industry Benefits The story of Henrietta Lacks in this reading is fascinating. By using Ms. Lacks’ cells, medical science has developed many cures. By one woman contributing her cells decades ago without her knowledge, on an involuntary basis, the impact has become mind-boggling. At the same time, it is disheartening and shaming to know that Henrietta’s family was unable to pay for medical attention for her.

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The injustice of taking Henrietta’s cells and using them for research without her consent or of her family for that matter; until 20 years later is incomprehensible. Many believe that the history of medical ethics such as the Hippocratic Oath and complying the federal law in protecting human research and confidentiality wasn’t yet recognized. All the same, the Lacks’ family isn’t given credit or acknowledgement for what Henrietta, has contributed to science, known as the HeLa cell line. Henrietta’s

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1020 Words | 5 Pages

In 1951, at the age of 31 Henrietta Lacks was diagnosed with cervical cancer. Henrietta was under treatment at Johns Hopkins University in Baltimore, where cells from her malignant tumor were removed. Neither Henrietta nor any of her family members knew about the tissue sample and nor did the Hopkins ever informed them of the situation. Unfortunately after Henrietta’s radiation treatment, her condition continued to worsen and soon she lost her battle to cancer on octomber 4th 1951. Henriettas cells left the Hopkins what they discovered to be known to be the first immortal human cell line.

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The final violation of ethical principles, in the story of Henrietta Lacks, was the violation of justice. Without the contribution of Henrietta’s cells, many discoveries and vaccines, such as the vaccine that conquered Polio, would not have made their pivotal breakthroughs in biomedical research. Her direct and unknowingly, supportive contribution helped save many people’s lives all over the world. Unfortunately, her named did not receive the recognition it deserved, and her family never received any compensation for profits made from direct use of her

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Bushra Pirzada Professor Swann Engh-302 October 4th 2015 Rhetorical Analysis: The Immortal Life of Henrietta Lacks The Immortal Life of Henrietta Lacks written by Rebecca Skloot tells the story of a woman named Henrietta Lacks who has her cervical cancer. It further goes to tell the audience how Henrietta altered medicine unknowingly. Henrietta Lacks was initially diagnosed with cervical cancer in 1951; however, the doctors at John Hopkins took sample tissues from her cervix without her permission. The sample tissues taken from Henrietta’s cervix were used to conduct scientific research as well as to develop vaccines in the suture.

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