“It's education to the communities themselves, to the…” — Airing Pain at 24:52
“It's education to the communities themselves, to the potential patients, to the carriers. Absolutely. I meet many patients who could be carriers of the disease and you ask them, do you have sickle cell disease or sickle cell trait? And they look at you blankly. It's got to be spread. People have to know, just I think…”
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