The Immortal Life of Henrietta Lacks by, Rebecca Skloot

In April 2011, I watched a C-SPAN show interviewing the author of a book about Henrietta Lacks, her name: Rebecca Skloot.

Henrietta’s story starts August 1, 1920, and her birth and life ended sometime in the early fifties, 1951. This story has just come into the light of day and while I cried again because it’s sad, and unacceptable by some, it reminds us of how life is treated when you have no or less power than the “average Joe” which is code for being white.

After having several children and years and years of reports by “the Media”, publicity, and whatnot, Henrietta’s family seems to be the only ones who didn’t benefit from the story of this woman whose cells were used to create a cell line for medical research but got nothing in return. I don’t know when everyone else heard of this story, but Oprah and some associates decided to make a movie…hopefully, some or ALL of the revenue will be given to the family. It is a story that makes you gasp, gets you upset, or mad, it will make you cry and wonder how the science community got away with not paying Henrietta Lacks and or her family for her contribution. If I understood the interviewer, Henrietta’s family has recently gotten more PR about their Mother’s story, but it’s unclear if anyone paid money for all the stories, books, and or TV programs about her. It is a story that appears to be on the surface, one of unintentional theft, that became just that, and if you are willing to dig deeper you realize it is theft and a secret kept quiet for years.

It becomes apparent her cells are used by an immoral scientist who did not tell her or her family even after it was evident that the cells were rare, viable, unusual, and priceless…worth an astronomical amount in my opinion.  The fact that they were used and what effects they all would eventually have on science today, in 2011, was not evident then, but those scientists probably had some idea. I understand that back then technology may not have been as advanced, but it did advance and still is and if the reports are correct, the science community gave Henrietta nothing to her or her family for the wonderful things those rare cells she had that changed the lives of so many. It happened in a time when minorities were treated very poorly and again, even if the reports state that standard procedure was this that, and or the other, the ’70s gave way to new ways to handle science technologies; it’s time to pay Henrietta Lacks and her family back.

First posted 4/13/11