A few days ago I got my blood test results back. Not only have I been feeling really lousy in the deep of winter and my HHV6 levels never dropped and my EBV came back too. I recently only convinced my doc to put me back on 1800mg Valcyte. This dose is what I foresee myself to be on for the next few months. So for now no short-term/immdiate side effects on Valcyte. I have countered all of that with SLO. It seems to be working. Long term, I dont know. All the Lerner studies show his patients being on Valcyte for 6 months or more. I am not sure if I want to be on it for that long given what it can do cytotoxically. I am considering Vistide but that can screw my kidneys. Ah, I love my life and the decisions I have to make while living it. Cant wait for it to be over. I am functionable, as long as I dont exert myself. That also includes walking in the cold, I just break out into a sweat perspiring profusely. Proboost seems to help with this on days that I take it. Otherwise as long as I stay indoor-bound and dont excercise I am pretty ok. Mind fog is still there. I am also looking into Avonex. PR mentioned that Dr Chia supposedly cured his son with beta-interferon and AVs. I have thought of this combo myself but it was with Pegasys and Ribivirin. Chia's theory seems sound and worth looking into if my insurance will pay. This way I dont have to go hunting for all the pathogens that I maybe infected with and just hit them all with one therapy, much more preferable and much less poking. I like.