I am not sure whether or not I should ask about this here as there seems to be a an almost non-existent discussion on XMRV at this time. Anyone here who would consider or not consider getting the blood work done now? My doctor filled out the paper work for me to get the work done. I just cannot sift through all the different opinions about whether XMRV is still a factor in CFIDS/ME. Any input will be appreciated and thanks in advance.