Subject: RE: Tom...nice
meeting you, here's some info right up your alley Date: Wed, 1 May 2002 18:06:01 -0500
Hi Thomas,
Nice to hear from you,
and nice to meet you Monday. Ken and I go to Logan's at least once
every two weeks. Enjoy eating peanuts and throwing the shells on the
floor. As a devoted Georgia peanut farmer, Jimmy Carter would be proud
of Logan's Roadhouses!
This article brings up
a very interesting thing, of how bacteria might have to contend with
cellular disorder and death, etc.
The bacterium itself
is not part of a fixed cellular order such as a human cell in human
tissue is. In the human, healing is actually accomplished by the
cellular regenerative system, not the immune system etc. As you know,
Becker did the best studies available in the West on the cellular
regenerative system. He was nominated for the Nobel Prize more than
once, and I suspect that had Becker had access to higher group symmetry
electrodynamics rather than the standard EM model the biologists use, he
would have totally deciphered the regenerative system.
In protracted work on
the problem, we found that the regenerative system uses pumping due to
their combined scalar potentials on their membranes, etc. to accomplish
very slow time-reversal of the diseased and disordered cells. One can
show that the internal electrodynamic structure of the scalar potential
--- totally ignored in the West though its specified by combining two
Whittaker papers of 1903 and 1904 respectively --- consists of
spacetime-curvature engines. All mass-energy and its structure and
dynamics produces a set of exactly correlated spacetime curvatures and
dynamics (a "vacuum engine" or "spacetime curvature engine" or just
"engine' for short). A slight re-interpretation of Whittaker 1903
decomposition of the scalar potential (Whittaker used two effect waves
in his pair, rather than a causal wave and an effect wave) in accord
with quantum field theory reveals the correlated time-polarized EM wave
and longitudinal EM wave in the basic phase conjugate wavepair in
harmonic set that results. Interestingly, the "mind" aspects are in the
time-polarized EM wave dynamics and internal structuring. The exact
disease pattern of the affected cells, together with the pumped delta
between that malfunctioned engine and the "normal" engine for the cell,
is in both the spatial LW waveset and its associated temporal waveset.
So the deeper aspects of mind have the exact "delta" or departure from
normal of every damaged cell already available there at the cell
itself. All this information is available right inside the scalar
potentials of the cell and its surroundings. Merely increasing the
scalar potential on the cell a little bit, will increase not only
nonlinear optical "pumping" (simply put, squeezing) in 3-space, but will
add "squeezing" in the time domain also. There results a formation of
an exact phase conjugate replica of the exact engine for that cell --
including the exact delta. Squeezing (pumping) in the time domain (by
increasing the scalar potential a bit) thus slowly reduces the damaged
cell and all its parts back toward the normal state, by slowly
decreasing that "delta engine pattern".
That's the way the
human and an animal works.
To recover at all, the
damaged (or threatened) bacterium has to have some semblance of that
same mechanism (that is the universal healing mechanism in all living
things). But that means that its "cellular regeneration system" must
reside in the colony at large, amongst its members. It's a more
primitive state on the development state, so much of the "mind level" is
what Jung would have referred to as the "collective unconscious mind".
Since the mind is totally electromagnetic (just scalar or time-polarized
electromagnetic), it can indeed engineer matter and it also can be
engineered.
I suspect the
"communication" incoming to the cells being exposed to the antibiotic
comes by way of spread of the potentials from the other "normal" cells.
It can spread in any fashion permitted by the media. E.g., in the
Kazhnacheyev experiments, the quartz separated cell cultures still can
transmit the information (at least a harmonic interval is required, and
quartz is open to the IR and UV, and UV is about the first harmonic of
IR if you choose in the range. So even without air connection, the
IR/UV harmonic interval can reconstitute the engines in the targeted
cells. This allowed the induction of essentially any kind of cellular
death or disease between cells, in many thousands of rigorous
experiments.
A modification of that
method in microwave radiation of the U.S. Embassy in Moscow, induced
cellular changes and diseases (responsible for the eventual deaths of
three ambassadors) for several decades. In Johns Hopkins' analyses of
the radiation, the health changes only occurred in personnel who were in
field-free areas. A field free potential is simply a potential that is
stable and not changing; hence its internal structure and its "engine"
is stable and unchanging. That maximizes the effect on the targeted
bodies. Eerily, the actual data of the Johns Hopkins measurements and
correlations falsified their official conclusions from their study, by
simple statistical principles.
But no one did a
higher group symmetry electrodynamics analysis, just using a standard
good electrical engineering analysis, which cannot even model what is
occurring.
In the bacteria case
here, the molecules and ions in the air that have contacted the healthy
cells and are "coming from them" to the bacteria facing the antibiotics,
have "shared" potential substructures with the normal cells upon
exposure. Two potentials superpose; that is the first law of
potentials. That means their internal structures (their engines) also
superpose, and each engine from one potential also "diffuses" into the
other potential.
Voila! Now when those
molecules and ions etc. reach the bacteria facing the antibiotics, there
is a constant exchange with those bacteria of the diffusing "normal
engines" taken on by diffusion from the normal cells.
Each affected
bacterium now has its own little "engines" which have been contaminated
by the "diffusing potential engines" of the antibiotics (the compounds
have potentials and engines also). If no additional normal engines are
received by diffusion, the little bacterium's own "normal engine" is
contaminated by the steadily diffusing engines from the antibiotics.
Hence it steadily worsens, and dies.
On the other hand, if
the affected bacterium is also receiving a continuing influx of "normal
engines" from that entering environmental molecules and air and ions,
its rate of "engine contamination" is dramatically lowered, because it
also gets now a continuous "injection" of "normal engines".
The result can be that
the bacterium gets enough "normal engine" flow rate to stabilize and not
die. It's continued pumping then will cause actual genetic changes (not
too different from what Becker's red cells showed in some of his
experiments with bone fractures having potentials placed across them).
The red cells dedifferentiated back to an earlier state (in physics
terms, time-reversed back to a previous state), then redifferentiated
forward to the type of cells that make cartilage, then further
redifferentiated even further into the type of cells that make bone,
with these cells being deposited in the fracture and healing it.
The "delta engine"
representing the disorder, poisoning, or damage --- when amplified and
phase conjugated (time reversed by pumping to produce an amplified phase
conjugate replica), is thus steadily eliminated. All the elements of
the cell or bacterium are available to this pumping, so that "decay" to
erase the delta can occur genetically as well as chemically,
electrically, mechanically, etc. The forces at the levels required for
all these are produced and produced exactly.
The result is that the
bacterium adapts -- or some of them do -- to the specific antibiotic.
That means it acquires resistance to that specific antibiotic. In
controlled lab conditions and experiments, this adaptation ought to be
engendered much sooner and easier than when being engendered in the
great world where --- e.g. --- such antibiotic resistance is slowly
acquired due to, say, feeding that antibiotic to cattle in their feed (a
common practice). Same mechanism involved, but in the cattle case there
is no laboratory control of the variables nor is there deliberate
optimization. In the lab, these conditions can be deliberately produced
and controlled.
Anyway, something like
that is what is going on. The real problem is that the
electrodynamicists and physicists --- for some inexplicable reason --
have continued to ignore the inner longitudinal EM wave electrodynamics
inside all EM potentials, fields, and waves. That "inner"
electrodynamics in fact controls and "makes" the outer stuff anyway.
The direct engineering
of much of reality -- from the quarks inside the nucleus to the DNA of
those bacteria -- is directly engineerable using the internal paired
scalar/longitudinal wave electrodynamics first shown by Whittaker in
1903, if we slightly reinterpret Whittaker's work along the lines shown
in quantum field theory where the photon pair consisting of the scalar
photon and the longitudinal photon are indeed observable as the
instantaneous scalar potential. Nearly a century after Whittaker's
decomposition, our scientists continue to blithely ignore it. Whittaker
showed the linear superposition of the internal waves in his
decomposition; Ziolkowski a couple decades or so ago also showed the
products of the waves in similar decomposition, which means modulation
and information, not just mixing, and not noise. Unfortunately our
biologists and physicists continue to ignore a far more fundamental and
powerful electrodynamics (and unified field theory physics) than what
they teach in universities.
Priori succeeded in
laboriously amplifying the pumping and therefore the formation and use
of an exact "antiengine" to precisely reverse cellular disease --- all
without realizing the nature of what he was doing. My own small
contribution has been to show that one does not have to make the
longitudinal EM waves externally, but can use the regular EM waves to
cause the body to make the transduction for you. In this way, very
small and rapid treatment devices effective against mass casualties (in
the millions) could be built and used, saving millions of American lives
in the coming anthrax, smallpox, and camelpox strikes on one or more
American cities, or use of a dirty nuclear device, etc. We strongly
proposed that to the DoD in 1998, and to the USAF, NIH, CDC, etc.
Sadly, they did not
even know what we were talking about. Prior to 9/11/01, even in the
government they were not really taking the terrorist threat very
seriously.
And we still do not
have a proper mass treatment system that will save those millions of
Americans who are going to die. We also are not going to try to develop
one, unfortunately.
As the French say, the
more things change, the more they are the same.
Best wishes,
Tom Bearden
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