Hey, All,
I'm finally getting back into my old Lyme tests. I must call contact my ex fms/CFS Dr that tested me Lyme Positive in 2012 thru IGeneX for those test results again. No Co Infection tests were done at that time. I'm going to try to get a full panel done thru my PCP- primary Dr for Mats Lindstrom. I can only inform from my own experiences. I've got Medicare/Medicaid which should cover it, as well as C4 tests and CD 57 tests. It is my understanding that a low CD57 test indicates a Lyme presence due to low numbers of 57NK cells. That would be a next step. Mine in 2011 was 23, in 2012 was 33. Below 200 (the range is 0-350) indicates chronic Lyme presence. A C4a test came out high, mine was 12,279, a reference range is 0-2830. I was told this would infer Lyme, mold, yeast and neurotoxins. My present treatment choice is a Rife machine, a GB-4000 with a SR4 amplifier. From what I'm reading the Cowden herbs can drill the spirochetes deeper, and put it into dormancy but it's still there. The same for hyperbaric oxygen. But the Rife signals are like a stealth strike, the buggers don't anticipate the incoming. Varicella reproduces rapidly, so at least ok initially it has to be rifed on at least 1X every day. You can check Bryan Rosners site. Also LymeNet Flash has an already 65 page message board for its Rife community.