This looks like a good opportunity to get a voice in relation to Cochrane reviews, which affect us all (especially BPS-proponent-produced reviews of the efficacy of GET & CBT). There'll be a one-hour live tweetchat session on each day. http://www.evidentlycochrane.net/cochraneforall-tweetchat/ In this discussion, we would like to hear your thoughts on the following: What would make the conference appealing? Think about things you’d like to do, hear or discuss at the conference What would make it easy for you/others to attend and participate? This might include practical considerations, access issues, cost etc What are the different ways people could work together at the conference? Have you any suggestions for speakers who bring a patient/carer perspective? What are your main hopes and worries for this event? (BTW, I'm not putting that in quotes so that people don't have to click to expand and read it.) How can we take advantage of this? @Esther12, @Dolphin, @Woolie, @Jonathan Edwards, @Simon M... who else to tag?