Does anyone know if the Cleveland Clinic is doing anything with the CFS piece of XMRV? I know the research there came out of the cancer department but I wondered if any of their autonomic or infectious disease or mitochondrial doctors are involved in XMRV research or treating CFS patients? Are there any CFS friendly doctors at the Cleveland Clinic? I may be heading there this summer for another appt. and thought it worth checking. I've heard there are some good dysautonomia doctors there and would love to know their names.