• 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 (FM), long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

    To become a member, simply click the Register button at the top right.

Action for ME research

Messages
68
Location
Wales uk
can anyone tell me where I can find out more about there research arm? I got a letter today about it but it doesn't seem to actually explain how it's funds are spent. I have asked on there FB wall but I expect like in the past when I have asked difficult questions it will be removed. Any help appreciated to links etc
 
Messages
13,774
No idea. They're doing that study with Peter White that they took over from another group. That's all I can think of.