Thirty million people live with a rare disease in the United States. And for many of them, it often takes years to get a diagnosis.
For one Chicago woman, those years were marked by uncertainty and doctors’ dismissal of her growing pain as she experienced lung collapse after lung collapse. She was eventually diagnosed with a rare form of endometriosis.
Reset sits down with her to hear her story and to talk about how women navigate physical pain and the medical system.
GUEST: Britt Julious, Chicago Tribune music critic
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