. Does anyone have any Information about this new ME Org called 'ME/CFS International Alliance'? . . There does not appear to be any online background information about it, especially about its Policies or Governance. The only online information about the 'ME/CFS International Alliance' (that I could find) comes from the UK Charity Action for ME Website, referencing the ME/CFS International Alliance's recent Statement re the Edward Shorter NIH lecture, Here: https://www.actionforme.org.uk/news/me/cfs-international-alliance-protests-shorter-lecture/ 'ME/CFS International Alliance protests Shorter lecture' 'Current members of the International Alliance are: Sonya Chowdhury, CEO, Action for M.E., UK Carol Head, CEO, Solve CFS, USA Jen Brea, #MEAction, USA David Mann, President, FM-CFS, Canada Sally Missing, President, Emerge, Australia Christina Montane, Board Member, Platforma de Familiar FM-SFC ACAF, Spain David Cifre, Coordinator, Associació Catalana d'Afectades i Afectats de Fibromiàlgia i d'altres Síndromes de Sensibilització Central, Spain' ~~~~~~~~~~~~~~~~~ How long has the ME/CFS International Alliance been in existence? Who is its Chair? Who instigated the formation of the ME/CFS International Alliance? Was the Instigator Sonia Chowdhury, CEO of Action for ME? Why has there been no public announcement of the existence of the 'ME/CFS International Alliance', or details of its aims and objectives, or details of it's Governance/Policies? . . .