At a time when some schools across the U.S. are rethinking their names or mascots, one high school in Vancouver is driven by its name.
You can read the headlines about schools ditching Confederate-inspired names from the Civil War. Or swapping out names of presidents who favored prejudiced policies. But Henrietta Lacks Health and Bioscience High School, isn’t only comfortable with its name, it’s proud of it, said Julie Tumelty, the school’s principal since it opened in 2013.
The high school is the first public building in the country named after Lacks, a black cancer patient who had cells taken from her body without consent in 1951. She died at age 31 that same year. Her cells ended up as the most widely used human cells in scientific research. The high school chose her name instead of Mother Joseph.
“We’re a school who wants to honor the legacy of this woman, who never had a chance to be honored when she was alive,” Tumelty said.
Tumelty called Lacks’ story “fascinating,” since it carries the complexity of unethical medical research that helped lead to medical advancements.
Lacks visited Johns Hopkins Hospital in 1951 in Maryland, complaining of vaginal bleeding. She had a large, malignant tumor on her cervix. That’s when her cells were harvested without her consent. Dr. George Gey, a cancer researcher, collected cells from patients at Johns Hopkins, but each time, the cells died quickly. Lacks’ cells were different. They doubled every 20 to 24 hours.
The cells taken from Lacks’ cancerous cervical tumor became the first naturally “immortal” cell line from a human, which means the cells don’t die after a set number of cell divisions and can reproduce indefinitely under the right conditions.
They were the first cells to live outside the body in a glass tube, according the Washington Post. The cells are named HeLa, and were crucial to the development of the polio vaccine and “are used to study the effects of toxins, drugs, hormones and viruses on the growth of cancer cells without experimenting on humans,” according to Johns Hopkins University.
Lacks’ family wasn’t made aware of HeLa’s existence until 1975, and they haven’t received any compensation. Johns Hopkins has said there was no precedent for consent of taking cells at the time. Lacks story fits into the history of African Americans being experimented on without consent.