Such experiences can be difficult to even acknowledge, let alone talk about publicly. To find them, Eric spoke with as many people as he could who have sickle cell disease and who'd been pregnant. Sometimes, it took weeks to set up an interview, if someone was in and out of the hospital with pain crises — in and of itself, a powerful window into the reality of living with this condition.
Part 1, published today, zeroes in on the doctor-patient power dynamic that can blur the line between medical pressure and advice. It also paints a powerful portrait of these women — not as patients, but as people. It's a story about bioethics, race, and inequality, but it's also a story about parenting, faith, and love. It's the kind of narrative that can only emerge from months of deep, and patient, reporting.
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