Hello Duncan:
I am aware that the Spooky2 delivers its effects through four different modes called plasma, contact, PEMF, and remote. Are you using the Spooky2 (made in China)?
Is the Phanotron your plasma device? Is the gas truly in a plasma state and only so when pulsed?
I assume that the Phillips bulb is for the PEMF mode or am I mistaken? What normally is used for the PEMF mode?
I believe that the signal is strictly DC. Right? Have you tried using an antenna and scoping the signal to look at the wave form? I am curious about ringing transients. Careful if you have not done it and are going to try it. I have blown up a small circuit in an oscilloscope because I didn't do the math before doing the experiment. After blowing up the sweep generator in the oscilloscope I decided to do the math and discovered that I had put about a 70kV spike into it that lasted maybe a microsecond. The circuit limit was maybe 50 volts. The test apparatus was a pulsed DC circuit which probably isn't unlike what is used in Rife. It was 25 years ago and don't remember the details.
I know a few people with Lyme Disease and success varies.
Dr Holly Ahern (a microbiologist) did in-vitro experiments of bioresonance combined with low level antibiotics and her team observed that death rates of a number of different species of bacteria is accelerated. She hypothesizes that the biofilm that the bacteria hide in is broken up to allow the antibiotics in.
https://www.youtube.com/watch?v=Z1EdRYFPDWM&t=1170shttps://www.youtube.com/watch?v=wm04_5AneBcAlso, I have a friend that had a 10-year old skin infection all over his body that doctors could not budge using topical antibiotics, steroids and other potions. Needless to say it was ruining his marriage. He worked at a biomedical lab that happened to make biofilm busters and so they made a special soap for him that contained one of their biofilm buster compounds. Within three months of use his own immune system was able to irradiate all of the infection with the help of the biofilm buster; he didn't need any antibiotics.
He and I believe part of my problem is that my illness is hiding in biofilms and my immune system can't get at it. I have tried using N-acytl cystine (NAC), EDTA and serripeptase. If I take the two affore mentioned ones before bed, as recommended (empty stomach), I get sick -- a Herxheimer reaction. It seems that my detox pathways are rather slow. I have stopped using them because I feel that I am just stirring up dust and spreading it.
I feel that my infections are primarily intracellular. I've never heard of intracellular biofilms but can not see why they can not exist.
Klebs is a common entity among AS victims but one hypothesis I have is that it is working synergystically by sending signals to other species of microbes that are in the collagen and interfering with the protein folding when the body is trying to repair damage from inflammation. Some researchers are obsessed with why the protein misfolds in the special case of HLA-B27. Perhaps that is not important and it is best just to get rid of the microbe that is in the collagen which not only interferes with the protein folding but the cause of the inflammation. If the microbe wasn't in the collagen then the Klebs would have no effect. I get this idea from how HPV interferes with the DNA self-correcting mechanism during mitosis. Perhaps it's really a virus in the collagen. How to work in the effects of biologics isn't impossible. Sometimes ignorance is bliss.
May the Force be with you!
Robin