I dont know if I have CFS or not. How do you define it? I did not start off with a virus or viral feeling. I started with POTS diagnosed after birth of my child, but my symptoms were not worse.. just got tested because my sister was sick and bedridden and diagnosed with severe dysautonomias. Did not take medication for 8 years or so. Had an elevated pulse. No problems exercising, standing that I was aware of.. that effected me adversely. Had an attack one night with chills, cold sweats, raging pulse and BP. Lasted few hours. It was like my body was in shock. Then on clonapin and toprol since. Down hill over the next few years.. babesia diagnosis and clinical diagnosis of lyme. 6 months of abx, anti-malarial. Aches, neuro symptoms, fibro. Got worse after a short round of flagyl and have not improved. Getting worse. Pain (can be overwhelming), fatigue, cannot recover well esp from anaerobic exercise, feeling of O2 loss, peripheral neural pain, etc. Lots of metals in my urine. Low amino acids, almost none. Methylation genes messed up. Low glut, low folates. ??? No viral counts show up except high IgG antibodies around 4000 to EBV. No CP and other bacterias except in my gut where I have a stew going on. CFS? Thank you.