VictoriaGray United States

Victoria Gray was the 1st Sickle Cell Anemia patient in the world to be treated with CRISPR gene editing in 2019. After a lifetime of pain, treatments, and hospitalizations for Sickle Cell Disease, she is now symptom-free, working as a patient advocate and international speaker to spread the word about CRISPR and rare diseases to clinicians, scientists, patients, and students. Mrs. Gray is a wife and mother of four children and lives in Forest, Mississippi.