Hi, I've been looking around to see if currently there is an active public database for which patients with ME/CFS can enter their lab results anonymously so that they can be used to make graphs that could help us to see pseudo scientific trends. I haven't found one and so I've been trying to start one. If anyone is interested in helping me I would love that! Right now, based on the premiss that a site like this doesn't exist, I'm starting to put together an outline of how one would work and I'd love to hear your input. 1. As of 2016 do we have an official-up to date international diagnostic criteria list? 2. My thought is that to start, we can ask a list of questions to loosely evaluate if the participant meets the most current diagnostic criteria. Those who meet/say they meet the criteria will continue with the questionnaire. 3. What questions do we want to ask? Age, gender, diagnosis/es, how long have you been ill?, What was the age of onset.... 4. Which lab results do we want to plot into the public data graphs? (lab results will need to be entered in a standard unit of measure with a single reference range.) Thanks!