I was looking through the CDC CFS website and while it is mentioned the last changes on the site were done this week, I cannot see what changes have been made. Correlation with sexual abuse is still showing in the front page and this is what our doctors are seeing when they check out CFS. . Looking good for the retrovirologists wanting to learn more about ME/CFS, or perhaps this would be a crash course in political illness? XMRV page is still only 2 pages long, a brief explanation of what is XMRV and a FAQ, updated from February 2010- old news if you will. I wonder if anybody not working full time at the CDC on the CFS program? Couldn't they update the website and not send the wrong messages to all the people interested to research CFS and XMRV? Another question I have : since the CDC is bound by the FOI law, what secret documents would you like to put your hand on? Personally I would like to see all the letters that have been written from nurses and doctors that have contracting the disease while working in hospitals, and I want to know what the CDC did with these letters. I am curious of what people would like to know. And perhaps even explore the possibility of class action as we are getting closer to prove causalty.