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Phoenix Rising

A Community for People With Myalgic Encephalomyelitis / Chronic Fatigue Syndrome

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June 9, 2015 Sasha

Jen Brea launches mass-advocacy platform — #MEAction goes live!

Sasha gives you the tour and tells you what it’s all about… Jen Brea is a phenomenon. After working as a freelance writer in China and Africa, she enrolled for a PhD at Harvard in political science but, four years ago, got sick. She had a fever that lasted ten days. Her health collapsed, and she was forced to go

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Phoenix Rising myalgic encephalomyelitis / chronic fatigue syndrome community, forum, and blog. Content on Phoenix Rising is for informational purposes only and does not constitute medical advice. It is the user’s responsibility to seek medical advice from a licensed medical professional. Phoenix Rising is not liable for risks or injuries associated with using or acting upon information on this website.
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