Guest guest Posted November 7, 2003 Report Share Posted November 7, 2003 Beck, what Rife did you use? There is this cheapie rife a few on lyement are using, norift rife that only costs $65--in fact, if one were handy, there is freeware on the net one can get if you knew how to hook up yoru stereo and computer which I don't. I was skeptical about this so I took a wait and see approach but a few months later the same lymies are claiming it is really helping. I tried some " big " rifes (rifebare, and doug machine) and did badly with the fields, way too strong. I'm currently using hyperbaric at home, which is helpful; and will be getting an ozone sauna which a few lymies have used and had major recovery after years of abx and illness. > Gayu, > > This is exactly the protocol I use. I came to it from Dr. Les Simpson's > work, which helped me overcome a 16 year depression, and my own natural > observation that when I ate lots of dairy, eggs and some lean meat, > including natural beef, I simply felt much better. I've been doing this the > last two years, along with undenatured whey. > > I attribute my increasing recovery from Lyme to be shape my immune system > was in when it was discovered. Couldn't have done it without Rich and Rife, > also. > > Beck Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 7, 2003 Report Share Posted November 7, 2003 P.S. Beck do you take the oral phoschol? This appeals to me and I am planning to get around to trying it sooner or later. > Gayu, > > This is exactly the protocol I use. I came to it from Dr. Les Simpson's > work, which helped me overcome a 16 year depression, and my own natural > observation that when I ate lots of dairy, eggs and some lean meat, > including natural beef, I simply felt much better. I've been doing this the > last two years, along with undenatured whey. > > I attribute my increasing recovery from Lyme to be shape my immune system > was in when it was discovered. Couldn't have done it without Rich and Rife, > also. > > Beck Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 17, 2004 Report Share Posted September 17, 2004 > I just wanted to check up on those doing Kane's protocol to find out > how they are doing in the long-term. Peggy, I did the Kane protocol completely and longer than the rxd duration earlier this year for my diagnosis of CFIDS. No improvement. Not a hint occurred. I also found out from my doc who rxd the protocol and who flew back east for the most direct in depth training from Kane herself that in general this protocol is not working in those dxd with CFIDS. Every single patient with this dx in his clinic I directly verified had as of July stopped the protocol and feel it was not worth the time, financial, etc cost. One patient did find some modest benefit from the IV glutathione pushes but even this feeling fizzled out after a while. IMO, whatever is creating the neuropsychiatric symptoms which are confirmed by Cheney et al to be in 99% of this patient population is what is keeping most of us so unmoveably stuck. It seems given the results of her treatment that Kane's neurotoxic model must be in error, but perhaps further insight will move us forward from the Marshall Protocol or whomever can figure out why CFIDS patients are via the CDC gene profiles testing to possibly be in the brain effected trinucleotide repeat protein family of diseases like Hungtington's, Parkinson's, etc.. Regards, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 17, 2004 Report Share Posted September 17, 2004 Thanx for the Kane protocol report. I think like all therapies, initial " pilot " studies often give one inflated expectations. It probably works in some cases. But it seemed very expensive and they seemed in it at least partly for the $--and it seemed to me you could do low tech versions of it, for instance, using ayurvedic methods or raw fats etc. Quote Link to comment Share on other sites More sharing options...
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