TED: What happens when you have a disease doctors can't diagnose | Jennifer Brea

Jennifer Brea shares her journey from being a healthy PhD student to living with myalgic encephalomyelitis (ME), commonly known as chronic fatigue syndrome. She discusses the challenges of being misdiagnosed, the historical context of hysteria, and the gender biases in medicine. Despite the lack of research and support, she finds hope in emerging scientific discoveries and the resilience of the patient community. Brea emphasizes the need for change in medical research and the importance of listening to patient stories.

How did Jennifer Brea's perception of her health change after her initial illness?

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What were some of the initial symptoms experienced by Jennifer Brea after her fever?

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What diagnosis did Jennifer Brea receive from her neurologist?

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What are some of the challenges faced by patients with myalgic encephalomyelitis according to Jennifer Brea?

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What historical context did Jennifer Brea provide regarding the diagnosis of hysteria?

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What does Jennifer Brea suggest about the funding and research for myalgic encephalomyelitis?

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In what ways does Jennifer Brea express hope for the future of myalgic encephalomyelitis research?

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How did Jennifer Brea describe the impact of her illness on her daily life?

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What role did the internet and community play in Jennifer Brea's journey with her illness?

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What message does Jennifer Brea convey about the importance of listening to patients' stories?

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