“font-family: Verdana; font-size: 13px; line-height: 14px;”>Best-selling

author Rebecca Skloot’s book

“mso-bidi-font-style: normal;”>The Immortal Life of Henrietta

Lacks

has developed an immortality of its own. The story about

a poor black woman whose cells were used for medical research

without her knowledge or permission is a riveting read that is

being taught in history and ethics classes. Now it will be the

topic of public discussion 6:30 p.m. Tuesday, March 1 at the

Missouri History Museum in Forest Park.

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>“Henrietta’s

Ghost” will be a panel discussion of race, ethics and medicine in

American history. The idea started from a book club hosted by Lorry

Blath, who wanted the story of Henrietta Lacks to become the topic

of public discussion. Blath secured 50 copies of the book that have

been distributed to the public for the upcoming

discussion.

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>Sowandé

Mustakeem, professor of African Studies at Washington University

Assistant, will moderate the discussion which will include Iris A.

Malone, a clinical trial analyst, and Dr. Ira Kodner, a medical

ethicist at Washington University.

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>“There

is a lot of conversation about this book,” Mustakeem said.

“Everyday people should be able to get access to this

story.”

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>She

also wants the broader community to dialogue and ask

questions.

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>“We

want to make sure it doesn’t happen again,” Mustakeem said, of the

unlicensed use of Lacks’ tissue in research. “Perhaps dispelling

some myths and really being able to have a deep conversation around

this.”

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>Lacks

was a 31-year-old mother of five who died of cervical cancer on

October 4, 1951 at Johns Hopkins Hospital in Baltimore. While her

disease was a devastating tragedy for her family, her cells became

a profitable marvel of medicine.

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>Cells

taken from her tumor while she was undergoing surgery – dubbed HeLa

cells (the first two letters of her first and last name) – have

been responsible for many important medical advances. Cancer cells

taken from Lacks’ body without her knowledge or her permission

became the world’s first replicating human cell line. In her book,

Skloot writes that HeLa cells were vital for developing the polio

vaccine; studying cancer, viruses, and the atom bomb’s effects; and

making important advances with in vitro fertilization, cloning and

gene mapping.

They also have “been bought and sold by the billions,” Skloot

writes, though Lacks’ descendents did not benefit from the

commercial use of her tissue.

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>The

fame of her cancer cells are juxtaposed to her obscurity. It took

20 years before her family learned her cells existed, and the

contribution of Henrietta Lacks remained unknown until Skloot

published her book in February 2010 and took it on the road for a

blockbuster reading tour. Lacks was buried in an unmarked grave in

Clover, Va. until Dr. Roland Pattillo of Morehouse School of

Medicine donated a headstone last May after reading Skloot’s

book.

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>The

March 1 Henrietta’s Ghost panel discussion is a preview to another

Missouri History Museum event three weeks later on Wednesday, March

23 at 6:30 p.m., when Skloot herself visits St. Louis.

“font-size: 10.0pt; line-height: 115%; font-family: Verdana;”>For

more information on both events, visit mohistory.org.

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