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Dr. Lisa Sanders crowdsources diagnoses for mysterious and rare medical conditions in a documentary series based on her New York Times Magazine column.
2019
The once-athletic Angel, 23, suffers from episodes of muscle pain so severe she often can't move. As she begins a nursing career, she needs answers.
The parents of bright and charming, Sadie, 7, seek alternatives to the devastating brain procedure doctors propose to treat her frequent seizures.
Day by day, Willie, 46, loses pieces of himself. He has memory loss, seizures, mood sings, a brain lesion -- but no diagnosis. Can the crowd help?
Six-year-old Kamiyah suddenly and briefly go limp dozens -- sometimes hundreds -- of times a day. Now the search is on to find others like her.
Lashay, 17, can't hold anything down that she eats or drinks. But negative interactions with previous doctors leave her family leery of the crowd's advice.
Matt, 20, experiences fainting spells that stop his heart, each one preceded by a sense of déjà vu. But is the issue with his heart -- or his head?
Two very different people are desperate for a diagnosis to their unexplained paralysis: textbook "good patient" Joe, 61, and more skeptical Ann, 44.
