
Mary Kubicek, a 21 year old research assistant at Baltimore’s Johns Hopkins Hospital, had never seen a dead body before she attended Henrietta Lack's autopsy. Determined not to faint, she avoided looking into Henrietta’s lifeless eyes. Instead, she focussed on handing petri dishes to the pathologist as he cut tissue from the cancerous tumours that littered Henrietta’s body. Then Mary noticed Henrietta’s feet and the chipped red nail polish on her toes, and gasped. “When I saw those toenails I nearly fainted,” Mary recalled. “I thought oh jeez she’s a real person.”
Gey was soon sending the cells to virtually any scientist who asked for them. In 1954, Jonas Salk developed the polio vaccine with the help of HeLa cells. Since then the cells have been mass produced and used in countless research projects all over the world including ones relating to cancer, AIDS and the effects of radiation. It’s estimated that by 2009 more than 60,000 scientific articles about HeLa cells had been published. That number is increasing by more than 300 per month.
In The Immortal Life of Henrietta Lacks, author Rebecca Skloot looks beyond the science. She asks who was the woman with the flaking red toenail polish. And what happened to the five children left motherless by her death at the age of 31?
Skloot vividly evokes Henrietta’s early life living and working in the family’s Virginia tobacco fields – the same fields which her ancestors had worked as slaves. Later, after Henrietta, her husband Day and their five children move to Baltimore , Skloot describes how Henrietta would sneak out to dance halls with her cousin Sadie after her husband had gone off to work. As Sadie recalls: “We used to really swing out heavy. We couldn’t help it. Hennie made life come alive – bein with her was like bein with fun.”
At the heart of the book is Henrietta’s daughter Deborah, who was just two years old when her mother died. Deborah and her three brothers didn’t even know about the HeLa cells until 22 years after their mother's death. Skloot helps Deborah and her brothers try to answer the questions that have been gnawing at them ever since. As Deborah says: “If our mother cells done so much for medicine, how come her family can’t afford to see no doctors? Don’t make no sense. People got rich off my mother without us even knowin about them takin her cells, now we don’t get a dime.”
Skloot’s brilliant, fascinating book deals with poverty, racism and the medical ethics that determine who owns the cells our bodies are made of.
But most of all this is a book about Henrietta’s family and especially Deborah who “just wants to know who my mother was.” When a scientist atJohns Hopkins Hospital invites Deborah and her brother Zakariyya to look at some HeLa cells under a microscope it’s so moving you would think they had been reunited with their mother after 50 years. “They’re beautiful,” Deborah whispers, "I never dreamed this day would come.”
But most of all this is a book about Henrietta’s family and especially Deborah who “just wants to know who my mother was.” When a scientist at