Navigating Hope: A Journey with Sickle Cell Disease

Last May, a 12-year-old with sickle cell anemia was the first person to receive a new gene therapy to treat the disease. The process is painful, expensive, and still frightening and uncertain, but biomedical researchers are cautiously calling it a “cure.”

Guests:

Gina Kolata, medical reporter for the New York Times

Deb and Keith Cromer, parents to Kendric Cromer, the first person in the world to go through a commercially approved gene therapy for sickle cell anemia.

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Podcast production by Evan Campbell, Patrick Fort, and Cheyna Roth.

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