News

Some doctors told him he'd live with the disease forever, but Khaled Alsheebani never stopped believing treatments would advance one day.
BEAM-101, a genetically modified cell therapy for sickle cell, is designed to turn on HbF to counteract mutated adult ...
India faces a critical shortage of 41 million blood units annually. Doctors stress that the country needs lifelong donors for ...
In a world often divided by politics, borders and beliefs, this is one thing that unites us all. The same blood that flows ...
Victoria Gray, the first person cured of sickle cell using CRISPR gene editing therapies, spoke in Fargo about her journey and the need to lower the $2M treatment cost.
One of the largest nonprofits supplying blood to hospitals and health centers is urging African Americans to donate more ...