Hi I assume you mean the patient advisory for CRMC? - I'm not at liberty to reveal names (although there was a link at one point on AfME's CMRC section; I can't seem to find it now....),
but we comprise at present: one carer (of a very sick child), one recoveree (me), and six sufferers (includign one with a child with ME) who range from the moderately affected to on-the-border of severe. We will be looking to recruit further members this autumn, if people wish to get involved & have a chance to influence the future.
In terms of our approach, we are all firmly in the need-for-more biomedical research camp, and are 100% anti-PACE, and anti-any more funding going to BPS research (if that helps!). the CMRC board are fully behind us with this approach. So if you support, in any way, the PACE Trial, GET, or CBT as primary interventions for this disease, you'll be unlikely to be a good fit.