LYME DISEASE
&
FREQUENCY
Also, is there always a relationship between a frequency and its "ten times higher" brother. For example, if you find a "hit" on a square frequency of 300, does it NECESSARILY FOLLOW that 3000 in sine is also a hit? I guess I'm wondering what the physics is that says that 432 is somehow related to 4320, etc. Why is a multiplication factor of 10 mean anything. What if you multiply 432 by something random, like 14? Are they related? See my question? What about the 10x relationship connects 432 with 4320? If 432 is a "hit" in square wave, and a hit in sine at 4320, would it also be a hit in SQUARE at 4320?
Only that the Crane squares were totally developed 1/10 from
the originals. These were the ones that were getting results, rather
than 1/7, 1/5, etc. So, his entire area of development was at that
fixed multiple of the Frequency sine. Yes, multiplying 423 by 14 will
give you a multiple of 14x 432. But, if there is zero effect when applied
it is useless. Squares at 1/10, do have an effect, and reconverting
back to sines at 10x also have an effect. Therefore, the denominator
is the type of wave. And the physics would be that there's a workable
fixed relationship of sine and square being 10x apart. This I actually
saw demonstrated by some material off the net where a guy was speculating
it was the type of device that determined the result - i.e. a frequency
on one machine would work but on another type it wouldn't. He ran a
plasma for candida on a woman suffering from it at 4340 (10x the common
434 [Crane] for candida) and she got major hit. But I know the type
of device he was using was putting out a sine, so in a way he was right,
but it was the wave form not the device. But more importantly, he inadvertently
demo'd the sine/square relationship.
When adjacent protein clumps oscillate 180 degrees out of phase, one protein clump is moving upward while its adjacent clumps are moving downward and visa versa. At maximum displacement of the protein clump from their equilibrium position, the stress at where the adjacent protein clumps are joined become a maximum. If the stress becomes large enough the bonding between adjacent protein clumps breaks down and the essential or critical structure for holding and delivering the virus genetic material is critically damaged or destroyed. This means the virus can not infect a new cell. Also, viruses that are forming and budding off of infected cells can be destroyed by this same method. This destruction / disintegration of forming and budding off viruses leaves holes in the infected cell's membrane, which can be fatal to the infected cell, which is actively producing viruses.
Viruses are miniscule compared to bacteria, but the same structural problems occur with them.
As the Lyme spirochete desperately mutates into different forms in the presence of antibiotics, the antibiotics can quickly be rendered ineffective. However, with the machines, slight changes in bacterial structure can easily be accommodated by changing the frequency slightly. For example, if the MOR for a spirochete is 400hz, and the spirochete changes its form slightly to avoid being “nuked,” the new MOR, for the changed spirochete might be 398, or 402hz. By “sweeping” through frequencies, you will effect these mutated forms. Even if the spirochete continues to change it’s body structure, you can continue to vary the frequency.
There are limits beyond which the spirochete would be unable to change....for example, a spirochete cannot change into a frog! Therefore, there are certain ranges of frequencies that work well when doing applications as regards Lyme. Instead of using one simple frequency, such as 400hz, you will apply with a sweep around that frequency. An example would be a sweep from 390 – 410hz. This “sweep” accounts for the various forms the spirochetes may have mutated to.
Although understanding of the technical aspects of frequency
technology are not necessary to getting well, I have included some
information for those who are interested in digging deeper into the “why” behind
the approach.
9. Live spirochetes. Facilities to cultivate them. After observing the spirochetes for some time, I applied 625 Hz and noticed a number-of unusual reactions from the
a. Vibrated tail and appeared broken.
b. Bent back and forth from center.
c. Spinning (100rpm).
d. Straightened out.
The spirochetes that reacted did die in 20 minutes to 2 hours.
600 Hz had the same effect. I knew that the response curve for resonance
was symmetrical, so I went to the midpoint of 612 and found this frequency
to be more effective. 920 seemed to be another kill frequency, and
it occurred to me that I was on a harmonic of 306. I tested 306 and
found it to be the most effective for killing spirochetes - in fact,
my wife and I had a "Herxheimer" for three days, from looking
in the microscope when its coil was running at that frequency.
Frequency: Start 625--611--305--and 20 Hz. Reaction: As with antibiotic treatment, there was a Jarisch-Herxheimer response with symptoms becoming worse before they went away. 20 Hz was also found to be effective, later tests show 27 Hz may be better.
The treatment continued once a month for six months before most
symptoms disappeared. NOTE: Care should be taken in start-up treatment
because of large Jarisch-Herxheimer reactions. Expect two years for
complete recovery.
Instead of using one simple frequency, such as 400hz, you will apply with a sweep around that frequency. An example would be a sweep from 390 – 410hz. This “sweep” accounts for the various forms the spirochetes may have mutated to
The electronic hardware set-up and frequencies have been added to over the years, and the latest frequencies are 27, 300-400 scan, 420-470 scan HZ at 100 gauss minimum. About seven treatments are required, exposing each infected area of the body for about 3 minutes per treatment.
Though all frequency devices are imparting electromagnetic frequency waves (whether sine, square, whatever), what I get from some Gary Wade writings is, it appears the coil device, with its pulsed magnetic field, uniquely creates an electronic field at right angles to the magnetic field. So you have magnetic field at a frequency and a generated electronic field and, it appears, the creation of broad-band ultrasound which goes throughout the body (via body fluids). With this being the case, the hi-powered application of pulsed magnetic signal (in addition to the critical MORs), creates a "side-effect" of electronic field also capable of creating mortal oscillations.
The relationship is proportional too - if the magnetic field strength is increased by a factor of 100, the crossed electronic is also increased by a factor of 100.
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