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Phoenix Rising

A Community for People With Myalgic Encephalomyelitis / Chronic Fatigue Syndrome

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Tag: stakeholders meeting

May 19, 2012 Phoenix Rising Team

Fighting For a Stake! FDA Cold Shoulder = More Action On Treatments For ME/CFS

Posted by Cort Johnson (This was never going to be easy….ME/CFS has been ignored by every federal agency for over 2 decades and its going to take time and work to break down those walls.  Let’s send a message that we are no longer willing stand for being ignored…Thanks to Mary Dimmock, Bob Miller and others for standing up for

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