Just a quick note to say hi ! Thanks for the note... I was sort of worried about you. A CFS diagnosis is a bitter pill to swallow. I hope that you will read my journal entry about the history of CFS and politics.... because you'll need to know this and the potential problems that this could cause for you in the future. I hope you also checked out the healthcare pages in the EBV and fibro/CFS forums. There are treatments for CFIDS that involve supplements and some medications only. There are also NATURAL formulas that I actually prefer to antibiotics and antivirals... they give me herxing symptoms. If you want more info, send me a PM.
Just a quick note to say hi ! I was wondering if you read my response in the EBV forum ?? Hope you are having a good day.
Let me know when you hear back.
Patti
Hi, I wanted to check out your experiences with Lyme and some of your history is close to mine. I have parasthesias, neuropathy, floaters, migraines (only if on birth control pill?), tinnitus, fatigue, heat intol. high HSV-1 and positive IgM for Lyme on WB(by Igenex and CDC standards) but mostly negative IgG. One lesion of unknown etiology on several MRIs. I am trying to be brave and go ahead with PICC line antibiotics, but I'm struggling with the political aspects of my diagnosis. Any advice would be greatly appreciated and I was wondering what, if any treatment you have tried? Thanks!!