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ISIS Digital Remedy Library - Testing and Validation

The initial testing included an oscilloscope, a frequency generator, a 5 Khz ocscillator, and a 10 Khz oscillator.

Frequencies were output from the frequency generator directly to the oscilloscope and the signals were studied. Then a wire was run from the frequency generator into the Capture Chamber and the same frequencies were studied on the oscilloscope. This time the frequencies were coming from the chamber and although there was a little more distortion, the exact same frequencies were clearly being sent from the Capture Chamber to the oscilloscope. This verified that the chamber itself was working correctly.

A 5Khz oscillator was then placed into the chamber and the oscilloscope was used to verify that the chamber was sending a 5Khz signal. The test was repeated using a 10 Khz oscillator. Both tests verified the functioning of the chamber.

All the above tests were then repeated, but rather than connecting the chamber output to a scope, the output was sent to a Digital/Analog converter (using a high-end sound card) into a computer. WaveLab software was used to capture the signals from the chamber and view them as a 3D frequency analysis waveform.

In each case, the known frequency in the chamber was easily seen on the 3D frequency analysis graph. Here is an example of a 3D frequency analysis graph that illustrates what the captured waveform looked like with the lid of the capture chamber open:

Notice the spike (in blue). This is at 60 Hz. This spike occured because the chamber lid was open at the time. Because the lid was open the signal recorded included the 60Hz from the lighting present in the room. This also confirmed that the capture chamber was functioning correctly.

Once the capture chamber and process was deemed to be working correctly empirical testing began.

A variety of different substances were digitally captured in the above manner. Homeopathic remedies, supplements, herbs, foods, etc. were all digitally recorded.

For each test substance an Electro-Acupuncture Device was used to measure a volunteer’s response to the actual substance which was in turn compared to the volunteer's response using the captured sound file of the substance when played back to the volunteer.

In every test
we saw an identical response between the actual substance and the corresponding digitised sound of the substance when played to the volunteer.

This testing verfied that the digitised substances provoked the same reaction as the original substance using the EAV device.

The digital remedies provided within ISIS have been used in practice on thousands of patients.