• Welcome to Phoenix Rising!

    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

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Search results

  1. S

    Will the CAA support a name change to ME/CFS?

    Who cares if the CAA will support a name change to ME?CFS. They don't seem too relevant any more.
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    Article: The "A Time For Action" Campaign Is WORKING!

    It was clear what Dr. LeGrice was doing at the science presentation today, which was to insinuate that what really needed to be done was to clean out those test tubes and get over XMRV.
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    Watch US CFSAC meeting NOW!

    I'm new to all of this but it looked like his job was to discredit and cast doubt wherever possible. This serves the interests of the government very well. Above all, they don't want the public to freak out about a retrovirus that could be too close for comfort, and they can always come back...