You’re reading Part 6 of Coercive Care, a yearlong examination of the denial of reproductive autonomy for people with sickle cell disease. As a small
You’re reading Part 5 of Coercive Care, a yearlong examination of the denial of reproductive autonomy for people with sickle cell disease. ST. LOUIS —
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We generally don’t think of rare-disease advocacy as funny. But of the many qualities apparent to anyone who met Sammy Basso, a biologist and spokesperson
You’re reading Part 4 of Coercive Care, a yearlong examination of the denial of reproductive autonomy for people with sickle cell disease. Often, women with
She knew what it was to have pain she couldn’t put into words, but this was worse. As a child, Nana-Bilkisu Habib had felt it in
A diagnostics company has agreed to stop selling two questionable blood tests as part of a settlement with a consumer watchdog that accused the firm
DECORAH, Iowa — It was livestock check-in day at the Winneshiek County Fair, and the dairy barn was consumed with a kind of pre-prom anxiety.
You’re reading Part 3 of Coercive Care, a yearlong examination of the denial of reproductive autonomy for people with sickle cell disease. Sonya Borrero didn’t
Federal officials, medical organizations, and reproductive health advocacy groups have expressed outrage in response to STAT’s recent investigation revealing that women with sickle cell disease