I feel that the re-analysis of the PACE trial by so many well placed experts is clear evidence that the BPS model is incorrect. How can we use it as a tool which benefits our cause? How can we use that to prevent the NHS, NICE and MRC pouring any more money into investigating any benefits of CBT and/or GET in adults or children with ME/CFS? In other words get those in BPS school out of research into ME/CFS. I understand that until there is a biomarker or chemical signature for ME/CFS this is difficult. The ME Association has launched an Xmas appeal to raise funds to find out if the Naviaux and Hanson et al metabolomics study can be replicated in the UK using the ME/CFSBIobank samples. See http://www.meassociation.org.uk/201...hristmas-appeal-starts-today-9-november-2016/ for appeal for any support anyone can give. How can we focus?