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CANCER AND
THE UNRESOLVED HEALTH ISSUES IN THE BIOLOGICAL
Largely taken from the author’s presentation, "Mechanism for Long-Term Cumulative Biological Effects of EM Radiation," 70th Annual Meeting of the Alabama Academy of Science, University of Alabama at Huntsville, 25 March 1993. by T.E. Bearden
Abstract Both postulates in the conventional EM bioeffects model are in error, as is the classical electromagnetics model (CEM) itself. Major errors in CEM are presented. The QM view is taken that all EM phenomena are caused by the potentials, not the force fields. Using the Whittaker/Ziolkowski (WZ) internal structure of the scalar potential, Bohm’s quantum potential and an engineerable variant of his hidden variable theory emerge. A strong candidate emerges for the internal mechanisms used for mind, thought, long term memory, and deep cellular control by Popp’s master cellular control system. An environmental negative feedback mechanism is stated for long-term, cumulative causative mutation, yielding Sheldrake’s morphogenetic field, which is a species quantum potential.
Utilizing the new EM bioeffects model, Kaznacheyev’s demonstration
that any cellular death or disease can be caused electromagnetically is
explained. A new definition for cancer is advanced, as is a long-term
cumulative mechanism that causes it. The mechanism for
Priore’s demonstrated
cures of terminal tumors in laboratory animals under rigorous scientific
protocols is explained. A solution for the major cumulative mechanism for
biological effects of EM fields and radiation is presented. A
self-targeting mechanism is presented whereby complex WZ EM biwave pumping
of the "cell as a nonlinear phase conjugate mirror material" produces
an exact EM antidote signal for the specific cellular disease. It is argued that
inexpensive, quick, nondebilitating, cures can be developed for most major dread
diseases, including cancer, arteriosclerosis, and AIDS. Priore’s remarkable and
previously unexplained cures of terminal tumors in lab animals are cited as
examples of applying the new model, albeit unwittingly.
The Basic EM Bioeffects Model Is In Error As is well-known, the field of EM fields and radiation effects on biological systems is actually in something of a shambles. In over 40 years of studies and experiments by careful researchers, the results are inconsistent, contradictory, and usually difficult or sometimes impossible to replicate. Attempted replications often give contradictory results, erratically. Researchers cannot rigorously answer even the simplest question, such as,
Causative mechanisms have so far eluded research. Powerful
vested interests fund many of the studies. Consequently a great deal of
controversy exists in the field. Opinions and
positions range from the ’’microwave oven" position that
"if it doesn’t appreciably heat tissue, it doesn’t harm biological
organisms," to the "total fear" position that "any and all nonionizing radiation is harmful; we just don’t know by what mechanism."
Legal actions to limit human EM radiation exposure are increasingly being
initiated by concerned citizens’ groups.
What
has actually been "proven" by the nearly fruitless EM bioeffects
effort to date is that
the fundamental EM
bioeffects model being utilized by the researchers is totally inadequate for the
task intended.
If that is true, then 40 more years of continuing to apply the same
inadequate model isn’t going to make very much additional progress. Further, if
the fundamental model is faulted, then
what is needed is a detailed examination of the model to discover and correct those foundation faults.
In
tackling this model foundations problem, I have performed a systems engineering layout
of the fundamental EM bioeffects model, and stated its two major postulates.
Both postulates turn out to be in error! Immediately one can easily see why
the field is in such a state of confusion. However, no true systems engineer
would stop there. I have also performed a systems engineering layout of precise
corrections for the two postulates, thereby correcting and extending the model
so that it can yield consistent, replicable results and causative mechanisms.
All of this is a rigorous procedure, and straightforward systems engineering
methodology.
However, the results point to profound
changes, which I have been immersed in deeply studying for quite some time. Out
of this approach has emerged something quite fundamental: a strong candidate for the internal mechanisms used for mind, thought,
long
term memory, and the deep cellular control system for all cells of the body.
A mechanism for species adaptation also
emerges that is quite capable of explaining (and yielding)
long-term directed mutation, including the "species jump," where
a species such as a bird emerges in short order (not gradually) from a species
such as a reptile. The known "species jump" has been a deep mystery to
evolution theory, which simply could not explain it. Another thing that has
emerged is a startling new electromagnetic
causative mechanism for cancer, leukemia, etc. At the June 1993
Brain-Mind Symposium in Los Angeles, I will present that exact mechanism.
The mechanism is capable of laboratory test, and validation or falsification. We
will also present an entirely new approach to EM effects on biological
organisms, and present the major new mechanism involved. The new mechanism has
fundamental application to the theory of diseases, and offers potential curative
mechanisms for dread diseases such as cancer, arteriosclerosis, and AIDS. I
explain some of the necessary background in the following paragraphs.
Classical
Electromagnetics
is Seriously Flawed
As
is well-known, there exist severe contradictions between classical electromagnetics (CEM),
general relativity (GR), and quantum mechanics (QM). As
presently constructed the three disciplines cannot be unified, even by Herculean
efforts. Particularly with respect to the primary causative agents for
electromagnetic phenomena, the foundations of QM and of CEM are in profound
disagreement. CEM assumes the forcefields as
primary causes, paying only lip service to the potentials and treating them as
primarily mathematical conveniences. QM, on the
other hand, has long since [since 1959] shown that the force fields are
simply effects
in and on the charged particle system, and are not causes. Instead, QM has
shown that the potentials are the primary causes of all EM phenomena. In charged
particle systems, potentials can interfere and cause observable EM phenomena
such as the Aharonov-Bohm effect in the complete absence of the force fields.
Herein lies the reason for the present
dire straits of EM bioeffects research. We explain further:
CEM
theory was originally formulated by James Clerk Maxwell in terms of quaternions.
Note that quaternion algebra has a much higher topology than either vectors or
tensors, the mathematics in which CEM is presently expressed. None of the
present "Maxwell’s equations" _ universally taught as due to Maxwell _
ever
At
the time Maxwell’s book was published, Heaviside was just teaching himself
calculus and differential equations. Seeing the book, he was electrified by it,
and Maxwell became his undying hero.
Maxwell died not long after, of stomach cancer.
Heaviside believed _ as did almost every scientist at the time _ in the older medieval tradition
that
forces
were
the causes of all physical effects. He had great difficulty with the potentials,
stating that they were
"mystical and
should be murdered from the theory."
We know today in modern quantum field
theory that forces are effects, not primary causes of anything. In fact, it is
the exchange of virtual particles with a mass that generates all forces upon it.
As is well-known to foundations physicists today, "force" does not
exist without the mass present to be acted upon, and without the action of a
potential gradient upon the mass. We know that there are no force fields in the
vacuum, and hence potential gradients in the vacuum are not forces, even though
they are commonly assumed to be. CEM has not been corrected for these glaring
defects: it prescribes force fields in the vacuum, and it prescribes that
potential gradients are forces, even in the absence of any mass for the
gradients to act upon.
Heaviside
also abhorred the quaternion theory. The coupling of a scalar component with
three directional components was, in his view, "mixing apples and
oranges." He knew that engineers would never master Maxwell’s use of
quaternion mathematics because of its difficulty. Consequently, Heaviside simply
chopped off the scalar component of the quaternion and discarded it, then
formulated this new "truncated to a vector" version as a much simpler
mathematics, albeit of decreased
topology. What he unknowingly threw away was
the ability of the quaternion theory to capture an internal
deterministic, vectorial EM structure of the scalar potential. [It turns out that he also discarded the unification of EM and gravitation by throwing out the scalar component, but
that is outside the scope of my presentation.] Years later as a lonely
recluse in a small upstairs apartment, Heaviside turned back to quaternions to
work on a theory of gravitation, according to papers found hidden beneath the
floor of his study many years after his
death.
Learned
journals of the day would not accept Heaviside’s papers for publication, because
of the assumed "brutality" of his mathematical methods. So Heaviside
began publishing very practical papers in a technical magazine, for the time
roughly equivalent to Scientific American today. These practical papers gave transmission line theory,
transformer theory, etc. _ things very useful to the early would-be
"engineers" who were struggling with installing telegraph lines,
undersea telegraph cables, etc. The vector mathematics utilized by Heaviside was
much easier to understand and apply, and his work was eminently practical.
Consequently it was eagerly seized upon and applied. The result was that
Heaviside’s EM model became the ipso facto CEM standard. Note that, at the time,
only about 30 or so scientists in the world were truly "learned" in EM
- either from the vector standpoint or from the quaternion standpoint. Further,
not much practical work was being done
by the few quaternion practitioners. A short "debate" over whether EM should use Maxwell’s quaternion model or the Heaviside/Gibbs vector model occurred prior to the turn of the century, mostly in the journal Nature. It never involved over a handful of scientists, and it wasn’t much of a debate. The vectorists simply threw out the quaternion EM theory and adopted the vector theory of Heaviside and Gibbs. Note that this represented a substantial curtailment of Maxwell’s actual theory. In other words, you can actually do a lot more in and with EM fields and circuits than what now appears in "modern" EM theory, and "modern" EM analysis won’t even show it. Barrett’s Oscillator-Shuttle-Circuit analysis of Tesla’s actual patented circuits shows this clearly and resoundingly. Also, living systems utilize the discarded subset of EM for their most vital control functions, and the present theory and methodology will not detect or "see " this. Thus this curtailment alone has resulted in the profound crippling of the conventional EM bioeffects model and efforts to apply it.
The Present CEM is a Flawed
Subset of Nature’s
Electromagnetics
So we have several serious things that are quite wrong with
current CEM theory.
First, the theory (and its practice) are artificially
limited
to only a subset of the real EM that can be achieved and utilized. The present
CEM unwittingly excludes the very type of EM utilized by living systems for
their deepest control functions. It also excludes electrogravitation.
Second, Maxwell’s theory was actually based upon the assumption of a mechanical
(material) ether, which meant that he could logically assign material forces to the
"vacuum" or "ether fluid." Heaviside’s translation (and
curtailment) to vectors did not charge this "material ether" and
"force field in vacuum" assumption.
However,
in 1887 the Michelson-Morley experiment resoundingly destroyed the notion
that the ether is material. If the ether
were truly a thin material fluid, then forces and EM force fields would
indeed exist in it. Since the ether is not material and forces exist only in,
on, and of matter, no E-field or B-field exists in the nonmaterial
vacuum; none ever has, and none ever will. In his three volumes of physics,
Feynman pointed out that only the
potential
for the EM force fields exists in
the vacuum; the only thing that exists in vacuum is
potentials,
after all! The vacuum is just a fantastic collection of interfering
potentials and potential gradients. Rigorously, the E- and B-fields
we detect with our instruments
exist
only in the electron gas in the probes we utilize.
This is well-known to a few foundations
physicists, but the CEM model has never been corrected for these foundations
errors.
Note that the loss of the material ether also falsifies
one of the three key assumptions in modern potential theory: the notion that the
gradient of the potential comprises a force field. We know today that the CEM
equation E = -Ñf, is actually incorrect
for
the vacuum.
It
is correctly
measured;
since that is exactly what is detected when the vacuum
Ñf potential
gradient couples to the free electrons in our detecting/measuring instruments.
What we detect as E, however, is actually
[(Ñf ·
(e-)], or the potential
gradient coupled to the electrons, including their masses. Specifically, we do
not detect the nonmaterial (VO that actually exists in the vacuum. We detect
electron wiggles in the free electron gas in the conductors of our instruments;
we do not detect "vacuum wiggles" per se. Neither Maxwell’s quaternion EM equations nor Heaviside’s vector EM equations include electron spin effects, but actually model electricity as a "thin fluid." Hence the EM equations of either model are fluid dynamic equations. Specifically, the measured transverse EM waves exist in the electron gas of our detectors; any detector detects only its own internal change, not the external agent that interacted and caused that internal change. White the "signal" races down the conductors in our probes and sensors at essentially the speed of light, the "free" electrons in the electron gas in those conductors are longitudinally restrained. The electrons must essentially move laterally from their initial distribution inside the conductor to its skin, then "slip" slightly down the wire on the skin at only the electron drift velocity, which is a fraction of a centimeter per second. The spinning electrons in the electron gas, being longitudinally restrained, act as gyroscopes. When disturbed by an interacting force, they precess. It follows that the lateral motion of the electrons inside the conductors of our detectors is just this "electron precession." It also follows that the direction of the disturbing force must be at right angles to the electrons’ measured transverse precession movement. Rigorously, EM waves in the vacuum thus are longitudinal, not transverse. We measure transverse waves in our detectors and instruments because we are detecting and measuring the electron precession waves in the free electron gas in the conductors of those instruments. But as Tesla pointed out, there are no Hertz waves in the vacuum; instead, EM waves in the vacuum are longitudinal "sound" waves, or waves of rarefaction and compression of the medium. From modern QM we also know what the medium is: it is a flux of virtual particles. Again, as can be seen, the CEM model is seriously in error in its representation of EM waves in the vacuum.
We
will not pursue this further; it is well-known to a few physicists in
foundations work (but not to most electrical engineers and electrical
physicists!) that classical EM theory is seriously flawed, and that it should be
upgraded to correct those flaws. As is well-known in QM since 1959, it is
the potentials
that are the actual causes of all EM phenomena, and the potentials can
interfere to cause real EM effects in charged particle systems, even in the
absence of the force fields. The Aharonov-Bohm effect is an example, as
are several other derivative effects well-established in the literature. What
has been ignored even in QM, however, is the organized
internal structure of the potential, even though the original (vector)
discovery by Stoney occurred in 1897 and was extended by Whittaker in 1903.
This
internal structure of the scalar potential had been implicitly present in
Maxwell’s 1873 quaternion theory, as an integral part of the scalar component of
the quaternion resultant of the interaction
between two or more quaternions. In quaternions, a scalar entity may be
regarded as a special quaternion entity whose translation has been reduced to
zero. A vector entity may be regarded as a special quaternion entity all aspects
of which are translating, and no nontranslating aspect is present. Thus the
scalar quaternion entity may be totally composed of vector components, so long
as they sum or multiply to a zero translation resultant but possess a finite
nontranslating magnitude.
The Scalar Potential Has an Internal Bidirectional Wave-Pair
Structure
In
a profound but ignored 1903 paper of enormous consequences,
E.T. Whittaker (below
right image)
decomposed the scalar EM potential into a harmonic set of bidirectional wave
pairs, extending the original 1897 work of Stoney. Each wave pair consists of
E.g.,
you can alter the internal structure of the Schroedinger potential, and place
deterministic biwave "hidden variables" inside. You can then
"engineer" these hidden variables - and consequently the Schroedinger
potential - by external means. In other words, you can even accomplish at least limited engineering of quantum change itself. This of
course reduces the Gibbs statistics (which assumes a totally random quantum
change) to a special case, and provides a more general case of chaotic quantum
change, which is still statistical but may contain hidden order. Note that this
statement is experimentally testable. It also resolves the greatest problem in
quantum mechanics today: the problem of the missing chaos (hidden order).
In
1989 Ignatovich placed a paper in the
American
Journal of
Physics
pointing out a similar internal biwave structure of the Schroedinger
potential, but none of our scientists seems to have realized the profound
implications. If we apply these proven
mathematical extensions of electromagnetics,
we are now
dealing
with a higher topology hidden variable theory, along the lines shown by Bohm,
but one that is engineerable on the lab bench.
Ziolkowski’s
Extension
Allows Hyperspatial Communication
In
1985, a brilliant EM scientist named Ziolkowski independently rediscovered
Whittaker’s internal biwave harmonic decomposition of the scalar potential. He
also extended the "internal structure" theory, to encompass not only
the sum set but also the product set. Since the product of waves represents
modulation, Ziolkowski’s brilliant work provides the setting for direct information communication capability in the internal
structuring of the scalar EM potential.
Further,
this internal channel is in the virtual state, so one is accomplishing virtual
state engineering, in the sense of the vacuum engineering posed by Nobelian Lee.
If one uses a 4space Minkowski model, the Whittaker/Ziolkowski channel
information may be viewed as
subspace
communications.
If one utilizes an n-space Kaluza-Klein model, where n is greater
than 4, then the Whittaker/Ziolkowski channel information may be viewed as
hyperspace
communications.
Living
systems already use this inner EM channel.
Living Systems Use the Internal Channel Communication
It
turns out that living systems utilize precisely the Whittaker/Ziolkowski (W/Z)
mechanism for their deepest functions and control systems _ including mind,
thought, long-term memory, and the master cellular control system (MCCS)
discovered by Dr. Popp of Germany. What we are stating is that, for the very first
time, we now know where and how the
mind’s
"deepest
software" is, its fundamental mechanism, and how to go about programming it
directly.
However,
we first must develop new measurement instruments.
Unfortunately,
present EM instruments are almost all only "electron-wiggle"
detectors; they detect only the
translation
of electrons. A gradient
in
the potential will couple to electrons and translate them. The
gradient-free
potential does not translate electrons, and it is the internal biwave
W/Z structure of that gradient-free potential that we need to measure.
Presently no known instrumentation will do that.
However,
if two different scalar potentials are interfered [Whittaker 1904], their
interference reproduces potential gradients [normal "force field" EM],
which
do couple to electrons and translate them.
In
fact, potential gradients (which in CEM are erroneously called "force fields")
were already shown by Whittaker to be entirely due to the interferometry of two
scalar potentials. So new "scalar interferometry" instruments must be
developed to "outfold" the internal contents of the scalar potential
as gradients, and then utilize normal instrumentation to measure those
interference gradients and calculate the potential’s internal structuring. One
form for the detector is the use of a standard potential (with a known internal biwave structure) inside a Faraday-shielded chamber, so that the test
gradient-free potential (which penetrates such a cage) interferes with the
standard potential inside the cage to produce gradients therein. A
probe
in the interference zone detects the gradients as electron translations, which
are conducted externally to amplifiers, meters, spectrum analyzers, computer
programs, etc. The end result is the determination of the internal WZ structure
of the test potential. Other detector types are possible; this is just a
"straightforward" type.
Thoughts, Mind, Memory, and Cellular Control Are Measurable
What
we are saying is that, by developing the proper instrumentation, it is possible
to directly detect and examine thoughts, memory, and deep control system
functioning of the biological organism, including the deep internalistics of its
personal quantum potential. We are speaking of the pending emergence of an
experimental science, not just a speculation.
However,
we are dealing now with a form of "hidden variable" theory, but one
that is engineerable and testable. So we will become directly involved with
Bohm’s
quantum potential,
both experimentally and theoretically. A
quantum
potential can connect widely separated systems by instantaneous effects, as if
the systems were not separated but were located together as a single system.
Further, the quantum potential does not have a single localized source.
Suffice it to say that in 1991 I published the discovery of how a quantum
potential is actually created. If one utilizes the proven
"self-targeting" or iterative phase conjugate shooting mechanism
from the Strategic Defense Initiative, and applies it to the WZ waves internal
to the scalar EM potentials from two separated charges, then in a dense signal
environment the selftargeting interaction may be initiated, so that the
separate potentials merge into a single
nonlocalized
or "spread-out" potential consisting of laser-like beams
between the charged particles comprising the separated systems involved. In that
case, part or all of any EM change in one system is immediately experienced in
the other systems participating in the effect. The communication is superluminal.
The limitation to luminal velocity applies only to the "surface
gradient" of a potential, not necessarily to the bidirectional waves in its
WZ internal structure. Those internal waves are in either hyperspace or
subspace, depending upon whether one models the situation in more than four
dimensions or in only four.
The
point is, the quantum potential also has a
W/Z internal
structure.
And
that structure can be deliberately created and engineered by external means.
Action at a distance is not only possible but engineerable.
Living Systems and Quantum Potentials
It
turns out that the living organism utilizes a quantum potential _ a
special
scalar potential connecting
all its internal atomic nuclei _ for its volition, deep control, and mind
and thought processes and operations. This can even be taken as a flat
definition of a living system. A living system utilizes internal WZ structuring
of this scalar potential connecting all the atoms (nuclei) of its body mass, for
its deepest control processes. Any system not having or doing this is not a
living system. This also resolves the age-old philosophical question of
how mental intent cm cause physical
response, but that is beyond the scope of my presentation. It also explains why
viruses can be precipitated out of solution as a crystal, and the crystal stored
for decades. Then when the crystal is redissolved, the individual viruses
separate and resume their "living" state. Suspended animation of the
viruses results when their physical matter and its quantum potential remain
intact, and the stored WZ structures in the quantum potentials on the atomic
nuclei of that matter remain the same.
It
further turns out that the species itself has a much weaker (at a deeper level
topologically) quantum potential connecting all its members (all the atomic
nuclei in their bodies). This corresponds to Sheldrake’s morphogenetic field _
that field is just a species quantum
potential. Jung’s collective unconscious, e.g., can be directly expressed in
this model scientifically and testably _ but again that is beyond the scope of
this presentation.
Newton’s Third Law Requires Forces to Occur in Oppositive Pairs
Newton’s
third law is a sleeping tiger, with surprising implications when awakened and
explored. For example, it rigorously requires that forces (including EM forces)
must occur in oppositive pairs. This alone falsifies the CEM notion that oscillating "singular-force" electric and magnetic waves appear in either a material ether or
physical matter. At least two waves must exist, the wave and its oppositive or antiwave.
Further, the wave and antiwave must be intimately coupled. Heretofore the antiwave has simply been ignored, or when anyone pointed out that it was present
in our detectors, it was just considered to be "Newton’s third law reaction
wave." "Newton’s third law" was just mysteriously invoked, as if
it had no causative mechanism. Yet in quantum field theory the cause of all
forces is the absorption or emission of virtual particles. The cause of all mechanical and electromagnetic
forces is the absorption or emission of virtual photons. So Newton’s third law for mechanical and electromagnetic
reactions must also be due to the exchange of virtual photons. In other words,
there was an extra half of the "something" in the vacuum that
interacted with our detectors and gave us the "free electron gas’s
transverse precession waves. That "extra half’ was exactly equal and
opposite, and interacted in the atomic nuclei of the conductors and the mass of
the instrument to give a set of physical Newtonian recoils. That half is equal
and opposite to the half we actually recognized. The point is, equal and
opposite forces actually interacted with our instrument. Thus a stress wave
interacted with it, not a unitary oscillating wave.
What
occurs in vacuum must be a stress wave, not a unitary force field wave. In
short, as stated (but not elaborated) by Feynman, it is a potential
wave, or an oscillation in the potential gradients and magnitudes, not the
force fields. Since in modern theory force is an effect and not a cause, we interpret and extend Newton’s third law
to state that the causes of all forces
must occur in oppositive pairs also. Thus the cause of an EM force field must be
the interaction of two scalar potentials - just as Whittaker’s 1904 paper
proves.
In
quantum field theory any mechanical or EM force is caused on a mass by
absorption and emission of virtual photons. Accordingly, let us examine the
smallest possible EM or mechanical "force" _ that one caused by the
absorption of a single virtual photon. Newton’s third law requires that two
photons (the causes) must occur, not one. Further, in all cases, the one must be
the exact antiparallel to the other. The only thing always meeting that
condition for a photon is its exact antiphoton _ its time-reversed,
phase conjugate replica twin. But a phase conjugate replica photon must also superpose spatially with its parent photon
_ that’s what phase conjugate replicas normally do, according to the distortion correction theorem of nonlinear
phase conjugate optics. Thus instead of the conventional "single
photon" interaction, the actual vacuum entity engaged in the interaction
with an atom is a coupled
photon/antiphoton pair. A coupled photon/antiphoton pair has spin-2,
hence is a graviton.
Gravitons and Graviton Interaction
So
arguably "photon interaction" has been graviton
interaction all along. In the interaction with an atom, the graviton splits
into a photon and an antiphoton. The photon usually interacts with the electron
shells, being absorbed by an electron to raise its energy level, then
re-emitted and scattered outward
from the atom. This absorption and scattering of photons _ containing
their components of energy and time _ from the electron shells of the atom
creates movement of the atom through external observer time. The photon
interaction between a mass and its environment creates the forward flow of time
for that atom and its seemingly entropic external (photon interaction created)
universe.
The
antiphoton half of the graviton is time-reversed, which we see as spatially
reversed. Consequently we see it move in the opposite direction to its externally-directed
photon twin. So the antiphoton focuses inward and interacts with the atomic
nucleus, providing the Newtonian third law recoil of the atom. The blithe
assumption of an "automatic" third law reaction force has always
concealed the fact that the so-called photon interaction is actually a graviton interaction. Further, the positive charge of the atomic
nucleus is due to the time reversal interactions of antiphotons with the
nucleons, which reverses the charge from that of the negatively charged
electrons in the atom’s electron shells.
Proof: Excising the Antiphoton Violates Newton’s Third
Law
This
graviton interaction hypothesis is testable. Note that, if the hypothesis is
correct, then when an atom or mass emits antiphotons or antiwaves (phase
conjugate photons or phase conjugate replica waves), it means that the
inward-burrowing antiphotons have been "tricked" into coming out
of the atom instead, so they can comprise the time-reversed wave. If they
come outward instead of going inward when they split from the parent gravitons,
they do not interact with the nuclei to cause their recoil. In that case, there
would be no recoil. And indeed, so it is.
In a phase conjugate mirror material, the mirror does not recoil when it emits a
phase conjugate replica wave, even a powerful one due to powerful pumping. This
is not true when the mirror material emits a pseudo-conjugate wave. A
pseudo-conjugate mirror, e.g., emits an ordinary
’’time-forward" wave with a distorted wave front, so that it will
"retroreflect" in a manner similar to the phase conjugate replica wave.
However, the pseudo-conjugate wave is not a true time-reversed wave.
Consequently, the mirror will
recoil
when it emits the pseudoconjugate wave, because the antiphotons from the
graviton interaction still penetrate to the
nucleus
and interact there, while the time-forward photons constitute the
pseudo-conjugate wave actually
emitted. This is experimentally verifiable. Among other things, it
establishes that there exist differences between the photon and the antiphoton.
Looking
at the photon aspects of this, one realizes that one must be very careful in
applying the conventional assumption that the photon and the antiphoton are
identically the same. Actually they are not the same "internally." The
photon can be thought of as carrying or consisting of (+ΛE)(+Λt), while the antiphoton can be thought of as carrying or consisting of (-ΛE)(-Λt). Thus both have positive spin, but differ in their
internal components. The lack of recoil in a phase conjugate mirror that emits a
true time-reversed replica wave is already in the literature, though
derived by statistical quantum mechanical arguments. It has also been pointed
out by other physicists that all measurement/detection
is actually binary, but that the "internal energy" half is almost
always ignored [it’s just considered to be "Newton’s law",
automatically revoked, and swept away in that euphemism.].
Graviton Lattice
Structure
of the
Scalar
Potential
When
we examine the WZ structure of a scalar potential, in each biwave the wave and
antiwave are phase conjugates. It follows that the photons in the wave and the
antiphotons in the antiwave are phase conjugates also. This means that, as the
two waves flow through each other spatially, photon/antiphoton pairs continually
couple and uncouple. Hence gravitons continually couple and uncouple. Further,
since the wave pair frequencies are phaselocked between pairs, the scalar potential is a phaselocked lattice of statistical
(continually forming and
unforming) gravitons.
Let
us now consider the interactions of an organism with environmental photons as
the interactions of the organism with environmental
gravitons,
and specifically
with graviton lattices.
Cumulative Buildup in the Quantum Potential of the Antisignal
If
the
photon half (of the graviton interactions)
in
the electron shells of the living body are considered as environment
signals/interactions, then precise
antisignals
or
anti-interactions, constituting perfect negative feedback from all of an
organism’s physical environmental experiences, are experienced in the organism’s
atomic nuclei. Note that there they have partially affected the internal
structuring of the quantum potentials _ both the personal quantum potential and
the species quantum potential. The point is,
cumulative
negative feedbacks (exact phase conjugates) for all the environmental
experiences and stresses an organism experiences,
build
in both the personal QP and the species QP of that organism.
A part of the entire species’ cumulation of species-common
antisignals also exists deep in the quantum potential of the living biological
system.
So
for any protracted stress experienced by the organism, in its personal QP a
coherent cumulative negative countermeasure feedback _ one which by its
time-reversed nature would reduce that stress _ continually builds. The
phase conjugates of the "well-rounded" or highly varying
stresses of multiple types will tend to mostly balance or "zero out."
However, a sustained stress of one kind will result in coherent cumulation and
increase in the "signal-tonoise ratio" of the amplitude of the
antisignal for that particular stress, compared to the amplitude of the average
of all the antisignals experienced. This is similar to the case where, in a sea
of radar noise, a coherent radar signal were continually present and integrating
coherently. Continual coherent integration, of course, results in continual
increase of the signal-to-noise ratio for the coherent signal, and
eventually it emerges from the "sea of noise" as a discernible [in
this case, observable and physical] antisignal.
This
"cumulative kindling of antisignals" occurs in both the personal QP
and the species QP; however, the species QP is many, many orders of magnitude
less than the personal QP. Hence much greater time is required for
"kindling" of species changes (evolution) than for kindling individual
countering adaptations.
Exercising
to get in shape is a simple example of physically stressing the body cells so
that the high-level feedback mechanism in the MCCS will kindle appropriate
antisignals and order the cells to adjust their functioning in a fashion such
that the level of performance being called for can be
accomplished more easily, thus reducing the stress level. The adaptive
mechanism ordering the adjustment of the body cells is the coherent negative
feedback in the personal QP, created from the stress signals from the sustained
"workout" exercises. This is a fairly rapid, "high-level"
mechanism; many other much slower (and some much faster) feedback reaction mechanisms
also exist.
Hypoxia As a Result of
Interference
With Hydrogen Bonding to Hemoglobin
We
now point out the recently discovered water H-bonding effect on the
hemoglobin in the blood, where the H-bonding activity increases the
ability of the hemoglobin to carry oxygen. Some 60 or 70 water molecules
surround the hemoglobin molecule, engaging in extensive Hbonding interactions
with it, which substantially increases the hemoglobin’s purely chemical ability
to bind and transport oxygen. Importantly, contamination of this water in the
blood fluid drastically affects this H-bonding benefit, and reduces the
hemoglobin’s ability to carry the extra oxygen. Thus contamination of the
internal blood fluid by chemicals, agricultural pesticides, smoke,
etc. directly
and dramatically lower the oxygen availability to the body’s cells,
resulting in a continuing "oxygen hungry" state (hypoxia) in most of
the body’s cells.
It also is now known that
H-bond structuring of water is highly dynamic
and constantly adaptable, and it possesses a high degree of internal order. A
conglomerate of H-bond structures in an area or a volume can be considered
an H-bond potential, since the
gradient oppositions sum to produce stress potentials. Thus in the
H-bonding fluid surrounding the hemoglobin molecule, there exists an
H-bond scalar potential, and by Whittaker/Ziolkowski (W/Z) decomposition
it has a multi-wave structure. Any and all contamination of the fluid _
including by electromagnetic fields and signals, chemicals, etc. _ alters the
H-bonding structuring and hence the internal W/Z structure of the
H-bond potential.
The end result
of adulteration
of the H-bonding structure
of the blood fluid is a condition
of hypoxia
induced in the cells of the body due to reduced oxygen transport by the
hemoglobin
of the red blood cells.
Any single EM signal is the result of the interference of two scalar EM potentials, as shown by Whittaker. It is the result of the interference of the internal EM wave structures of those scalar EM potentials. Multi-signal EM radiation must be regarded as interference of multiple pairs of scalar potentials. These interfering potentials penetrate to the atomic nucleus in the body, and thus interact with the internal personal quantum potential utilized by the body in its deep cellular control. Also this multi-signal EM radiation, no matter how weak, directly interacts with the Hbonding structure of the H-bonding blood fluid. Even single-signal EM radiation still forms oppositive pairings with the weak fields already existing in the body, thus also forming W/Z structured potentials. From the interferences in the body of multiple such potentials and their internal structures, there also are created gradient (force field) interactions upon the blood cells and the hemoglobin. In short, low-level background EM radiation can also interact with the Hbonding of the hemoglobin to seriously lower its oxygen transport capability, just as any other contaminant. The denser the external environment, the greater is the interferometry and the interference with the hydrogen-bonding augmentation of oxygen transport. It follows that, when thrust into a truly dense signal environment, some exposed individuals may receive a "cumulative H-bonding interference dosage" that, when added to their existing prior dosage, is sufficient to result in physical symptoms "ordered" into the cells by the antisignals kindled in their quantum potentials. In the recent Gulf War, many Americans were suddenly thrust into one of the densest EM signals environment in history.
Shortly after returning from that ultrashort conflict, many of these exposed
veterans have experienced delayed health changes presently known as "Gulf
War Syndrome." While the military has attempted to portray this syndrome as
"stress-induced" emotional’ trauma, most of these veterans when
tested are found to be emotionally stable. Further, there was much less combat
stress on our troops in the Gulf war than in WWII, the Korean War, or the Viet
Nam War, as shown by less than 200 combat deaths! Essentially the war was almost
a "shooting gallery," and so combat stress is simply not viable as a
proposed causative agent for the Gulf War Syndrome.
Chemical, Mechanical, and Electrical Interactions are Electromagnetic
Anyway
Indeed,
chemistry is largely due to electric charge and charge distribution anyway. So
if we view the physical contaminants in the blood view chemically,
they are caused by electromagnetic means at root basis. Thus even the
"chemical" contaminants interact electrically and via potential
(multiwave) interferometry with the H-bonding potential. Further, in
quantum field theory, all mechanical forces are due to the exchange of virtual
photons, and hence also are electromagnetic
at their very basis. The bottom line is that all chemical, mechanical, and electrical
interactions are in fact electromagnetically caused. Further, since both the
internal and external structures of the potential are engineerable, the
mechanical and electrical forces on the mass particles _ and the virtual photon
exchanges causing these forces _ are directly engineerable.
All
of these chemical, mechanical, and electrical interactions in the cells can be
affected
and even engineered electrically. This is true from the atomic nucleus, to
molecules, to material lattices, to human cells, to tissues, and even to the
mind and long-term storage templates (internal
WZ structured
forms
in the QP) in the biological organism.
As
cam be seen there are many other weaker, direct interactions of
"force-field" radiation; however, here we are interested in the
interaction of that radiation with the inner structure of the H-bond potential’.,
to reduce the oxygen transport capability of the hemoglobin.
In
any case, the total sustained interaction of chemical and physical contaminants
and EM fields
and radiation can result in a sustained oxygen-deprivation (hypoxia)
condition for the body cells, even to a dramatic degree.
Further, by
graviton interaction, a sustained,
cumulated set of antisignals is also automatically generated in the personal
quantum potential as a set of negative feedback signals to take corrective
actions to alleviate the oxygen depletion condition. Note that the
cumulating antisignal condition is general and affects the immune system and its
cells as well.
The Example of Smoking
Obviously the tars, particles, and nicotine of the smoke inhaled by the smoker dramatically contaminate the fluid in the smoker’s lungs, in the very place where the hemoglobin of the red cells is taking on oxygen. Drastic interference with the H-bond stimulus of the hemoglobin occurs. The result is an immediate and dramatic reduction of the oxygen-transport capability of all the hemoglobin in the red cells as they pass through the contaminated lungs and are exposed to fluid contamination. An immediate oxygen-deprivation condition thus is created in the body.
Due to the magnitude of the stressing
signal, the major portion of the antisignal is also of substantial magnitude _
hence immediate counteraction orders accumulate in the personal QP, specifically
in Popp’s master cellular control system. So very rapidly the body has negative
feedback countersignals from the central cellular control system, ordering the
body to take actions to reduce the cellular need for oxygen. The metabolism is
lowered, the body relaxes, and the appetite is suppressed; all counters to the
cells’ hypoxia condition by lowering the cellular requirement for oxygen.
In
spite of heroic "high level antisignal" physical cellular
compensations to reduce the use of oxygen, however, the condition of cellular
oxygen shortage may still continue, in the case of the smoker or substantial
environmental contaminants such as secondary smoke. So in addition to the prompt
countersignals, additional much-weaker countersignals are also slowly
accumulating in the personal quantum potential’s central cellular control
system.
Cumulative,
Deep, Long-Term Countering Signals
We
now need one additional bit of information. In addition to its personal quantum
potential, a biological organism also is connected to a species quantum
potential joining all the members of its species. This is a much weaker quantum
potential; nonetheless, potentials superpose, so one small "part" of
the personal quantum potential is actually the species quantum potential _ in
other words,
Sheldrake’s morphogenetic field. Deep within its own personal
quantum potential the living system also
possesses all the cumulatively ordered steps (species antisignals that were
implemented) of its species evolution. With very
long
coherent cumulation, countersignals can be stimulated in the individual
bio-organism’s quantum potential _ and in its deep cellular control _ that
are counters to the original signals that ordered directed mutation and
the primeval evolution of the constituent cells themselves.
In
a sustained cellular hypoxia stress environment, the "do whatever is
necessary to reduce oxygen usage" countersignals will continue to cumulate
from successively deeper levels in the QP over an appreciable time. These
continue to slowly "kindle" after the "first high-level
antisignal actions" that cumulated past the "noise" (quantum)
threshold reached their limits of physical reactions and are still insufficient
to resolve the problem. As the hypoxia stress in the cells continues, then much
weaker but coherent countersignals that trigger deeper cellular adaptation
actions eventually have time to cumulate past the quantum threshold to the observable
state. These long-term cumulated antisignals come from much deeper, even
from the species quantum potential itself.
These
cumulating deep countersignals are phase conjugates _ reversals,
or dedifferentiation commands _ of the previous directed mutation signals that
ordered evolutionary changes in their predecessor cells in the far distant past.
These long-term antisignals thus
contain a signal to reverse the original cumulative countersignals in the
cellular species potential that caused the cells
early ancestral anaerobic cells on
earth to change (differentiate) into largely aerobic cells, after the earth’s
atmosphere acquired significant amounts of oxygen. In short, a deep signal is
slowly cumulating that, when it emerges, will order the dedifferentiation of the
affected cell back down the evolutionary road toward the anaerobe.
The first
steps are reductions of centralized cellular control, including growth control.
In
other words, under sustained cellular hypoxia a countermeasures signal to the
cells, ordering them to dedifferentiate back toward the anaerobic state, is
slowly building in the personal quantum potential from a much weaker, lower level
"under the common countersignals noise level" all the while. If significant
oxygen-deprivation continues for a sufficiently long time, this deep
countersignal eventually emerges in Popp’s MCCS system in the personal QP, ordering the affected cells to dedifferentiate back toward their
anaerobic state. The first step back is to break away from centralized
control by the higher organism _ which results in individual "tumerous"
or "uncontrolled" cells. From sustained cellular hypoxia there exists a slowly increasing
precancerous state, even years before the outbreak of physical cancer. This
precancerous state has great influence upon the "single cells" of the
organism, which includes the cells of the immune system. Thus the precancerous
state is characterized by increasing errors in, and slow weakening of, the
immune system. Arthritis and similar debilitating immune system disorders appear
to be largely the result of this "precancerous" long-term
cumulation.
Note
that the most stressed cells in the body automatically provided
the greatest magnitude of "negative feedback input." Notice also
that the feedback is a phase conjugate replica; it therefore
"backtracks" its initiating stress input signal. In short, the degree
of feedback antisignal received by a cell or group of cells varies according to
the degree of stress they experienced. Thus those cells sustaining the longest
and greatest stress get this drastic dedifferentiation countersignal first.
E.g., this accounts for the (usual) localization of the resultant tumor in the
lungs of a smoker, at least initially. It also accounts for the
stress-damage mechanism for such disorders as arthritis.
A
New Definition of Cancer
In
the new model being advanced,
cancer and
leukemia are
centrally-commanded.
final, desperate.
"first-step
dedifferentiation"
adaptive
attempts
by
the stressed. affected cells
experiencing
sustained oxygen
shortage
(hypoxia)
to reverse their cellular evolution and return to the anaerobic stage
of their distant
ancestry.
The
cause of cancer and leukemia - and indeed of all diseases - is electromagnetic
in nature, and it can be straightforwardly treated and cured electromagnetically,
if one utilizes the extended W/Z aspects of the higher topology EM actually
written by James Clerk Maxwell. This statement is based on experimental proof;
it is not conjecture. We discuss that proof below. As we saw, in general the strength of the cumulating countersignal inversely depends on the distance in the body of the affected cells from the source of greatest contaminant stimulation. As the deeper "dedifferentiation" countersignal reaches the quantum threshold in the most affected area, a small group of localized cells located there take the first step back along the "singleanaerobe to single aerobe to multiple aerobe" evolutionary chain. That first dedifferentiation step breaks the cells away from centralized control of the MCCS in the personal quantum potential. Those dedifferentiated cells become independent cells or a small independent cellgroupings. They constitute a tumor, or leukemia if occurring in the blood cells. They simply are no longer under the control of the body’s MCCS in the personal quantum potential, even though the body’s logistical services (nutrients, oxygen, etc.) continue to be furnished to them.
At
this point the
tumor
becomes an independent
cellular organism, living in an environment where its body host continues to
furnish its food and oxygen, and
its host’s immune system cells do not recognize the altered cells as foreigners
to be attacked
and destroyed.
Consequently there is no "large organism"
central control of the tumor’s growth, and the tumor cells divide and multiply
apace. This loss of centralized growth control and the resulting unchecked
cellular division and replication is in fact recognized by scientists as the
major distinguishing characteristic of cancer and leukemia. With central control
lost, groups of cancer cells or individual cancer cells may break away and
travel to other locations in the body via body circulation systems. This results
in metastasis, the spread of the cancer to other sites in the body, where they
continue to be recognized as "self" by the immune system cells and continue
to be supplied with oxygen and nutrients for continued growth.
The Tumor Has Become a Parasite Organization
Think of it this way: In a living body, each cell is already a single, independent, living creature all its own. It even has its own small "personal quantum potential" - we have argued that that is an a priori condition of being alive. However, each cell in a multicellular organism normally is under a centralized electromagnetic control system (which functions in the organism’s higherlevel personal quantum potential), so that the organism lives and functions as an overall higherlevel unit. If a cell (or group of cells) has separated from this centralized EM control, but is still living and functioning, then obviously the cell is no longer under the whole organism’s MCCS and personal quantum potential.
However, it still possesses its
own control system, and its own personal QP. If the breakaway is by a small group of cells, then they are loosely
under a "small group" quantum potential and MCCS as well. That is,
they have gone from "large-scale central control" to a
"much lower" level of centralized cellular control, accounting for the
"tumor as an individual multicellular entity." Nourished by the host
body, the new parasitic organism _ the tumor _ grows at an unchecked rate.
Again, we argue that
the problem is
electromagnetic in nature, and it can be
"fixed" electromagnetically.
The Cumulative Pre-Cancer State
With
this picture of the long-term cumulative causative mechanism for cancer
and leukemia, a far better picture of the pre-cancer state has emerged.
The pre-cancer state is a hidden EM change of state comprised of a cellular
dedifferentiation order, back down the species’ cellular evolution trail,
and the magnitude of that change of state is slowly increasing inside the
organism’s quantum potential. The eventual observable cancer is an actual
cellular dedifferentiation due to the localized breaching of the quantum
threshold by this cumulating hidden EM dedifferentiation order to move away from
centralized control and back toward the anaerobic cellular state.
Becker’s
Profound Experiments
It has already been experimentally shown that very minute amounts of direct electrical currents, e.g., can cause cellular dedifferentiation and redifferentiation. In breathtaking work of Nobelian quality, Becker has proven that even picoamperes of localized electrical current are sufficient to cause cellular dedifferentiation and redifferentiation, even repetitively. Incredibly, he proved that this was true for red blood cells, which first dedifferentiated to more primitive cells, the redifferentiated to precursors of cartilage cells, then redifferentiated to bone cells in a "bone fracture" area and healed the bone fracture. Since picoamperes can be generated by the cumulative countersignal mechanism (via Whittaker scalar interferometry), directly affecting the MCCS and the cells as well, then the connection between scalar potentials/potential interferometry and dedifferentiation mechanisms assumed to be involved in cancer and leukemia essentially follows from interpretation of Becker’s pioneering work.
To further strengthen the
assumption, Hsue has recently (1993) shown that a DC voltage is in fact
equivalent to two bidirectional EM traveling waves - which directly indicates a WZ type implication in Becker’s profound work itself. Thus
Becker actually
utilized a hidden, bidirectional WZ wave structure inside the voltage gradient
between his electrodes in his DC current dedifferentiation and redifferentiation
of blood cells. He conclusively demonstrated that cellular dedifferentiation and
redifferentiation _ both of them genetic changes
_ can in fact be caused by such an internal biwave EM structure of a steady,
persistent scalar potential gradient. Further, he demonstrated that
these
El~-induced cellular genetic changes can be self-targeted toward
reversal of the
specific
damage condition, even though several successive genetic changes may be
necessary m reach the ultimate cellular genetic form required for healing.
Pre-Cancer State and Prognosis For Treatment Effectiveness
To
summarize, whenever a cancer or leukemia detectably exists, regardless of the
cancer site, a pre-cancer state also exists in the remainder of the body,
and the immune system is affected generally. Further, this pre-cancer
state pre-existed the actual emergence of the tumor itself. The new EM
bioeffects model also sheds light on the probable effectiveness of conventional
treatment, and probability for a ’’cure" that lasts for the rest of the
patient’s life.
If
the cumulative countersignal slowly kindling in the remaining pre-cancer
state is sufficiently below the quantum threshold, then conventional treatment
of the cancer - such as excision - can eliminate the tumor, and no other tumors
may then develop before the normal physical death
of the body,
even though slow increase of the pre-cancer state
continues. In other words, in that case the cumulative antisignals in the
pre-cancer state locations other than the original cancer site never reach
the quantum threshold prior to the natural death of the patient. On the other
hand, if the cumulating antisignals in the pre-cancer state generally are
very close to the quantum threshold, then recurrence of the tumor is highly
likely. In the first case the curative prognosis is excellent; in the second
case it is poor. Also, we point out that many present treatments (such as nuclear radiation) themselves cause significant stress on the body and its cells and further deterioration of the immune system. They also generate an additional "antisignals" level in the personal quantum potential, resulting in an actual increase in the level of the pre-cancer state in the organism. If the combination of the pre-cancer state at time of treatment, plus the increase in the pre-cancer state due to treatment, is sufficient to breach the quantum level, then that treatment will prove to be of little or no avail to the patient.
The tumorous condition will
recur, and sometimes massively (the tumor metastasizes), regardless of whether
further treatment is given or not. In that case the patient will die, unless
somehow the pre-cancer state is lowered, the tumor cells are reverted back
to centralized cellular control, and the immune system is restored to effective
functioning so that excess cells are eliminated. Presently there is no
conventional treatment that is capable of accomplishing the three requirements
for a desperately
ill
patient’s
recovery from the "terminal" cancer condition.
Seeking the Complete Cancer Cure
From
the new EM definition of cancer and leukemia and the new cumulative causative
mechanism, one can see just how severely limited are the present medical weapons
against this dread disease. It follows that,
if
the cause is totally electromagnetic, then a totally effective treatment can
only be sought as an electromagnetic therapy. Since the EM cause is in an
extended EM domain, then axiomatically a totally effective treatment can only be
sought in the same extended EM domain.
The
complete cure for cancer and leukemia, of course, would be to completely
neutralize or "zero-out" the patient’s cumulative
Whittaker/Ziolkowski countersignal buildup in the MCCS/personal QP. This can be
done prior to the cumulation reaching
the overt physical disease stage, or after
it has already reached that stage. It can readily be done
electromagnetically, using the multi-biwave tailored EM and
self-targeting to provide an exact counter-countersignal (or
antidote signal) to the cumulation signal itself.
This
is a scientific
fact and it has been rigorously proven, although the methodology could not
heretofore be technically explained and understood.
Priore’s Cure of Terminal Tumors and Other Diseases Such a total cancer-curative procedure was repeatedly demonstrated in live animal experiments in the late 1960s and early 1970s by Antoine Priore in France, under rigorous scientific protocols and supervision by eminent French scientists [such as Robert Courrier, head of the Biology Section of the French Academy of Science, and Secretaire Perpetuel of the Academy at the time]. The advantage of the Priore type approach was that it rapidly reversed the dedifferentiation away from centralized control of the affected (tumor) cells. The tumorous cells simply redifferentiated back to normal cells under centralized control of the MCCS/personal QP. (If too numerous because of the tumor’s growth prior to its redifferentiation, normal body mechanisms absorb and dispose of the excess cells). Further, such treatment removed all the pre-cancerous state from the rest of the body, preventing recurrence or spread of the tumor. It is the only "total cure" for cancer, including the cumulated pre-cancer state, that has ever been scientifically demonstrated. And lastly, it accomplished these results without severe trauma to the body or further trauma to the immune system. Indeed, the exact opposite was the case.
Working with Priore, the eminent French scientist
Pautrizel showed that the Priore
treatment restored and stimulated
the immune system back to its robust normal functioning, as would be
predicted by the present model we are proposing.
Scientists at the Time Did Not
Have
the Necessary Knowledge for Understanding
It is a great tragedy that the active mechanism of the
Priore device was not
understood - even by Priore himself and even by very knowledgeable physicists
assigned to the program to try to ascertain the machine’s mechanism. The phase
conjugate or "time-reversed" EM wave was unknown until it was
discovered in the open Soviet literature in 1972. Almost all of our knowledge of
such waves dates from that time. In the same year, two Soviet scientists briefed
American scientists at Lawrence Livermore National Laboratory on optical
phase conjugation. Thereafter, some American scientists began intense work
on optical phase conjugation.
However,
the time-reversed wave is a solution to the wave equation and applies to
all kinds of waves, not just EM. Phase conjugation of sound waves, e.g., is
readily accomplished. The time-reversed wave solution actually appeared in
the scientific literature in 1898 in a paper by Barus, who pointed out that this
strange solution "made the wave run backward." But at the time the
Priore program’s funding was withdrawn by the French government about
1974-75, little or no understanding of the time-reversed EM wave
existed as yet in the West, and of course the Whittaker work had always been
ignored and was unknown also.
Literally,
with the technical tools available to them at the time, the French physicists,
biologists, and oncologists had no chance at all
of fathoming
the causative mechanism in the Priore experiments.
Nature of the Priore Treatment
Briefly, Priore mixed some 17 frequencies in a rotating plasma in a giant tube. We know today that one function of the kind of plasma he used is to produce a phase conjugate replica wave, for an input wave. Thus Priore unknowingly achieved coupled wave/antiwave pairs in his device. The output of the plasma tube was then coupled to (modu |
a
wave and its phase conjugate replica (its "anti-wave" or
"time-reversed twin".). Thus the scalar potential has a rich
internal biwave structure. [Further, one can make
a scalar potential by simply assembling the necessary multiple waves, and
one can alter the internal structure of the potential at will by altering the
waves utilized in the assembly process.] In 1904 Whittaker published a
formidable second paper, showing that all of CEM could readily be replaced by
scalar potential
(hidden mult