I'm wondering if you have been tested for XMRV if so when were you tested and did you get your results? For some reason people feel that their results should be private. I'm waiting for my results and will post if positive or negative and how I feel about my out come. On WPI facebook page a gal posted that her test result came back negative, which made me want to ask her a bunch of questions like, who tested you, when were you tested, do you have classic cfs/me symptoms or fibromyalgia etc... I guess my point is, where are all the people who have been tested and why aren't they posting about it on one of the many cfs/me sites? When I get my results if they are negative then I'm going to have a few things to say about my results. I have the classic CFS symptoms there are no gray areas, I didn't have any other health issues before I became sick and my health issues now are classic CFS symptoms. So if I'm negative, then in my mind XMRV isn't the puppet master, just another virus that CFSers catch. Unless my blood testing procedure was inaccurate and I need to be tested later when better testing comes available. I sent my blood to VIPDX and spent $650. And if my results are possitive then once again, In my mind I would think that XMRV is the cause of CFS. I know, I know, CRAZY LADY....But that is how my mind works.