Thanks for the link, Dr. Sutherland: a fascinating web site, albeit, one way over my head. Why are all the cool books written in German?!

Thank goodness for people like you who translate bits of these ideas into usable concepts for the layperson.

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The only effect I noticed from running the nanobacteria frequencies at the scalar octave (via the f155 and the ABPA) was a thickened tongue coat that evening. In chinese medicine this is interpreted as "dampness" or "phlegm", which could reflect some sort of waste accumulation or die off. The tongue coat has returned to normal this morning (I drank a good bit of ozonated water, thinking this might help clear things up)

Here is my modification of your program:

repeat 16
dwell 60
duty 50
pulse 64 75
43644.3 #mercury release
4202.30 #DNA database
converge 12 1
127724
converge 1.5 .05 #dropped down for the smaller freqs.
#previously: converge 30 1
137692.91 #scalar octave of 2765636 (divide by e^3)
176024.47 #3535546
181506.08 #3645647
172614.5 #3467055
172623.47 #3467235
converge .25 .05 #5 1
172628.2 #3467330
172631.18 #3467390
172656.57 #3467900
172661.55 #3468000
converge .5 .05 #10 1
172632.43 #3467415
converge 2 .05 #40 1
172640.39 #3467575
172662.55 #3468020
converge 33 1
763545
666767
665386
634671
563124
554365
296214
264224
247458
187613
141346
134443
converge 4 0.1
1902 317 #CAFL list freqs that work
end repeat


My setup was not perfect. My photo for the ABPA was taken by a friend on his 7.1 megapixel camera and then he printed it on a very nice printer with photo quality paper (I do not know the dpi, but it is a brand new printer). However, I must assume that his camera translated the picture to a jpg (he plugs the memory card directly into the printer and I could not review the file on my pc) which maybe resulted in information loss. And then the picture itself would not fit in the ABPA well so I have it folded in half.

I am curious about the frequency running on channel B: 64hz with a 75% duty cycle. Is there a working theory behind this or was it established via the aurameter?

You had mentioned using a carrier frequency of the actual pathogen...this implies that channel B, in this case the 64hz wave, is what is modulating the carrier, channel A (which runs the actual pathogenic numbers).

I feel like I need some kind of working-theory FAQ to help explain general ideas underneath this stuff. In trying to experiment or modify my program for testing purposes, I feel I really dont benefit from people's experience out there because I miss the point behind what is being done...[the purpose and selection of the channel B frequency, for example].

Thank goodness for this forum!

dave