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Re: The godzilla formula

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Bob, your formula gives me the idea again, that electrodes connected to

multiple sites will be ideal for treating microbes. I'm thinking all the

major arteries, and liver in my case, given the juice for for as long as

is feasible each day.

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ANy one know of anything or any one that has used the Godzilla for

Myelodysplastic Syndrome (secondary)?

Please let me know

Dan

bobluhrs@... wrote:

>I = (C x T)P

>

>Inactivation equals the quantity current times time to the Path

>power.  Where current is a range from .1mA - 1.0mA depends on the

>individual, time is just time spent with it connected and running on

>the body, and Path is the location of the microbe in the circuit.

>The microbe is Part of the circuit, and if it moves out of the

>circuit path, the effect is lost.  The closer it gets to being right

>in the path of the current the effect goes up exponentially.

>

>Here's sample of what it looks like in practice.

>

>EXAMPLE #1, MICROBE EXACTLY BEWTEEN ELECTRODES

>HIV Inactivation 94% = (7.7 microamps in one sq mm electrode surface

>area x 3 minutes time of application) raised to the first power

>(unity).

>

>EXAMPLE #2, MICROBE MISALIGNED BY 20 DEGREES OFF CENTER OF LINE

>BETWEEN ELECTRODES

>HIV Inactivation 10% = (7.7 microamps in one sq mm electrode surface

>area x 3 minutes) raised to 1/3 power since in this case the

>microbes only get a small fraction of the current.

>

>This is perhaps the best way to express it.

>

>The greatest loss occurs when you move the electrodes into the wrong

>positions, not when you lower the power, or cut the time.  That is

>what this equation hopes to show us.  It's just a SWAG.  (Silly wild-

>ass guess), but I think it will prove to be remarkably accurate.

>

>bG

>

>

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well..in practical terms a nightime head to toe approach while

sleeping, possibly with a mild current especially targetting the

liver, with a full body circuit from toes to top of head makes

sense. Milder current for whole body a bit harder on the liver. ??

bob

> Bob, your formula gives me the idea again, that electrodes

connected to

> multiple sites will be ideal for treating microbes. I'm thinking

all the

> major arteries, and liver in my case, given the juice for for as

long as

> is feasible each day.

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I think most of these questions are what we are researching, Randy.

They're all good questions, too. I'm sure you will find it out

faster than anybody, since you have the curiosity to discover.

The goals with HIV, other than 100 % riddance of it, might be

summarized as follows:

1. reduce to sub-clinical levels indefinitely with minimal amount of

trouble.

2. limit the virus to one or two innocuous places in the body where

it lives but causes no issues. this is similar to shingles,

everyone who had chicken pox has shingles potentially, but may never

experience it. The virus lives in the vertebrae and never comes out.

3. repeatedly reduce the virus to where it runs out of steam and its

mutations slow down or cease, at which point, it is truly gone.

4. reduce the virus in the bloodstream to where the body has enough

defenses to fight off the usual opportunistic infections and limit

the spread of AIDS. Limiting HIV to HIV. This only requires a 2%

reduction in the bloodstream, and is undoubtedly what Beck was

doing.

5. keep the virus low enough that strains living in blood are not

created. HIV strains that do not infect the bloodstream are usually

less harmful than the ones which inhabit other areas.

100% riddance may be possible, but probably would only be verifiable

on autopsy, where linings of the intestines could be examined for

the virus.

Short of that, a complete negative blood test would show the virus

did not produce strains that could live in blood.

bG

> > Bob, your formula gives me the idea again, that electrodes

> connected to

> > multiple sites will be ideal for treating microbes. I'm thinking

> all the

> > major arteries, and liver in my case, given the juice for for as

> long as

> > is feasible each day.

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