Hi, I'm not sure where to put my post so if it needs to be moved, that's quite alright. Like all of you, I've tried (and continue) every supplement, vitamin, herb, gluten free diet, juicing, bio identical hormones, and the list goes on. Pre CFS, i was healthy and use to be a runner. I cringe when I think of all the money I've spent. I want go as far as to say wasted. The B12 has helped me. I have never been on any medications prior to the CFS I steered clear of doctors and medications. So, I have come to a fork in the road. I have been ill since Aug 09 and found a doctor who wants me to start on Valtrex for reactive EBV This has been a very difficult decision for me, a constant struggle. Most people would jump at the chance. However, I wrestle with making the decision. I'm not sure why. Fear perhaps. Here comes the hokey part. Have any of you read or heard about the Rife machine? People w/lyme have had success and like everything else, others have slight improvement and some have none at all. I would appreciate your input. I have ordered the machine and I should have it very soon. I guess some might view this as being desperate or naive but other than spending few bucks.....I will let you all know how this goes.