(Sorry I made a mistake when I sent this the first time) Hello all! :0) I have been using CS for about 5 weeks now..I am QUITE sure I am herxing. More tired brain fog and concentration are even WORSE as if I thought that were ever possible.;0/ LOL I have had Lyme for 3 years..I was only on doxy for about 10 days until I found CS thanks to Marsha;0). Now since I have had Lyme SOO long before getting any treatment at all I am sure I have a long way to go? I am ONLY taking CS for my treatment now. My question is to those of you who may have been in a similar Lyme situation. How long did you herx?? I know we are all different, but am just wondering how many weeks or months until I start to feel better so I can get on with my life you know? Just an idea so I know if this is normal or not? When I FIRST began the CS I noticed a little improvement which lasted about 3 days (mostly some ENERGY)...then I think the herx started to set in;0/. I guess I take about 6 oz of 20ppm CS a day. A! ny advice out there??? Should I increase? I don't mind the herx..I figure I will feel good once I have the worst behind me and just want to do that as fast as I can! ;0) I don't mind feeling bad as long as RECOVERY is around the corner! FINALLY!! I have had Lyme since I was 14..:0/. Also did anyone else have problems with their ears?? Like you feel like there is fluid/pressure in there and ringing at times? Also I think I have some hearing loss..ESPECIALLY my right ear..did these things improve as your Lyme got better??? ANY help or advice would be GREATLY appreciated!!! ;0) Nicole:O)
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