A Year In, 1st Patient To Get Gene-Editing For Sickle Cell Disease Is Thriving

Victoria Gray, who underwent a landmark treatment for sickle cell disease last year, has been at home in Forest, Miss., with her three kids Jadasia Wash (left), Jamarius Wash (second from left) and Jaden Wash (right).

Since receiving a landmark treatment with the gene-editing tool CRISPR, a sickle cell patient has the strength to care for herself and her children — while navigating the pandemic.

(Image credit: Victoria Gray)

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