- It is accented that a research procedure is being discussed,
and no recommendation for medical treatment is intended. For medical treatment
of a disease or disorder, the viewer is referred to a licensed medical
practitioner formally licensed to practice medicine, and to procedures
formally approved for such. No research procedure discussed is intended
or recommended for any kind of usage in medical treatment until properly
developed, tested, and approved by proper authorities and by the FDA for
use by properly licensed and qualified medical practitioners.
-
- We all exist in a very complex dense signal environment
these days, with incredible numbers of weak EM signals bombarding us continuously,
from EM sources everywhere. The electric power lines, e.g., act also as
receiving long wire antennas for EM noise all along their routes, bringing
it right along and into the home, where it broadcasts from gaps, switches,
light bulbs, wiring connections, etc.
-
- The highly nonlinear interactions of the dense signals
with each other also result in some conditioning of the "infolded
Whittaker structuring" of EM fields and potentials in the locality.
That conditioning even includes the local vacuum itself (as Golden once
proved rather conclusively). The vacuum after all can be represented as
a tremendously strong scalar EM potential, in which case it is also comprised
of Whittaker bidirectional EM longitudinal wavepair structuring and interactions.
-
- So our local "environment" ---consisting of
an altered local vacuum internal structure and an envelope of very dense
weak EM signals in the normal background --- permeates the entire body
and every cell in it. We published the deep-penetration mechanism some
time ago. As an analogy, consider the body to be a sort of very porous
boat (more like a fishnet) floating in the active ocean lashed with waves,
so that the local environment of clashing and interacting water waves completely
permeates us.
-
- In the Porthole method I originally worked it out, I
only considered the "textbook" perfect EM noise-free environment,
which means an unconditioned vacuum (spacetime) and no deep environmental
conditioning of the "infolded longitudinal EM wave electrodynamics"
inside the signals and frequencies used in the Porthole method. So we
worked out the "pristine laboratory" and "pristine environment"
approach. That is certainly where any researcher must start. However,
to make it truly effective and not variable in its effects on the recipients,
Bedini has now shown that one must also condition the signals and frequencies
used in the Porthole method so that their own internal environment and
internal structuring corresponds to that of the local environment. That
is a very important new discovery by Bedini, and I think it eventually
will revolutionize and change things such as cloning practices. In theory
it should eliminate or materially improve cloning's very low efficiency
demonstrated worldwide by many researchers in many laboratories.
-
- Bedini discovered that one can condition the infolded
dynamics environment inside the signals, waves, pulses, and fields by using
electron tubes in a fairly straightforward manner, but in addition to their
normal textbook operation the tubes must also be deliberately operated
in a very unusual manner derived by Bedini. The second manner of how the
tube is used is completely backwards from anything in present textbooks
and scientific papers. However, it is possible to detect and measure when
one has got it working correctly, and one can see on one's oscilloscope
that it is working correctly. That is the process that Bedini discovered:
"Adjusting and adapting the local inside environment of the EM signals
utilized in the Porthole Process (or any other process applying or involving
EM signals, fields, and radiations in or to the body to produce epigenetic
reprogramming effects). Epigenetic reprogramming is changing the gene
expression factors so that the genetics is reprogrammed back along the
path formerly taken by the cells during their differentiation and development.
The adaptation of the inside environment of the applied EM signals must
exactly correspond to the inside environment of the local spacetime (local
vacuum and local EM environment) to include both its altered inner structuring
inside local EM fields, waves, and signals and its envelope "ordinary
dense signal" environment.
-
- Bedini's discovery also shows that every previous study
done on long-term effects of EM radiation on biological systems is incomplete.
The largest variable in the long-term effects of cloning and other epigenetic
reprogramming trials has been completely bypassed and missed by previous
researchers who used a theoretical EM model which does not even contain
any conditioned internal structuring of its fields, potentials, waves,
and signals. In short, a higher group symmetry electrodynamics must be
used and understood, so that it can also simulate the vacuum's dynamics
and spacetime dynamics infolded inside dense EM signals in the environments.
The EM model used by present biological researchers erroneously assumes
a perfectly flat spacetime, no active vacuum, no spacetime curvature dynamics
engendered on the biology by the EM, and no active vacuum dynamics engendered
on the biology by the EM.
-
- So thanks to Bedini's important discovery, we now understand
what the "missing ingredient" in Rife's work (completely unknown
to Rife himself) and in Prior's work (again, completely unknown to Prior
and all of the scientists who worked with him). It also is a missing ingredient
in the "pristine" Porthole Concept I originally produced. Any
application is "pristine" if it does not include Bedini's environmental
adaptive and fitting process. One must think backwards! In this case,
a pristine signal (with unstructured inner environment) actually transports
a very noisy "infolded EM difference and jamming" into the targeted
cells. Those cells do not have a pristine infolded EM environment, but
have a specific one.
-
- As shown in a paper by Evans et al., interference (scalar
interferometry) between two such infolded environments does produce spurious
outfolded (normal) EM signals in the zone of interference, resulting in
electromagnetically jamming the cellular reprogramming process that is
implemented. For proper results and to avoid this jamming, the application
must not be pristine but must be environmentally fitted to the specific
environment of the targeted cells. We are very happy to point that out
as real progress! We have congratulated Bedini on what we believe is a
truly important discovery, which will eventually affect many elements of
biology and medicine in presently unsuspected manner and degree.
-
- Once the "causative" textbook signals are "force-fitted"
rather strongly to the local vacuum environment's internal structuring
and to the local complex dense weak signals EM environment, then the Porthole
Concept will work as intended, as will a plasma tube concept such as Prior's,
etc. and a tube concept such as Rife's. All these experimenters used tubes,
because transistors were either non-existent or not really too much in
vogue when most of their formative work was done. What no one previously
has known or recognized is Bedini's rather startling new way of using a
tube in a manner completely unheard of. With the Bedini method, the tube
will change the internal structuring of its processed signals, waves,
fields, pulses, etc. so that they have a "internal infolded EM environment"
rather perfectly matching --- and perfectly phased to --- the complete
local EM environment, including both the environment's envelope transverse
EM waves and internal infolded longitudinal EM waves.
-
- As Whittaker showed in 1904, all EM fields, potentials,
waves, etc. are comprised of differential functions imposed upon two scalar
potentials. In 1903 he had already shown that a scalar potential decomposes
into a harmonic series of bidirectional longitudinal EM wavepairs, where
each wavepair is a phase conjugate pair. By combining the two Whittaker
decompositions, then the dynamics of any EM signal environment whatsoever
is comprised of the dynamics of differential functions imposed upon two
harmonic sets of bidirectional EM longitudinal wavepairs.
-
- Previously we slightly modified Whittaker's 1903 decomposition
to agree with quantum field theory. In that theory, there are four polarizations
of a photon, which are x, y, z, and t polarized. Polarization in x or
y gives the familiar transverse photon. Polarization along the line of
propagation, z, gives a longitudinal photon, where the EM energy is oscillating
to and fro along the line of travel. Polarization on the 4th Minkowski
axis, for the time-polarized or scalar photon, means that the EM energy
is oscillating on the time axis, where time can be taken as spatial EM
energy compressed by the factor c-squared. Hence time has the same energy
density as mass. In quantum field theory, neither the longitudinal photon
nor the scalar photon is individually observable. However, in the presence
of charge, the combination of the scalar photon and the longitudinal photon
gives the instantaneous scalar potential. To be consistent, Whittaker's
bidirectional longitudinal EM wavepair must be interpreted as a paired
scalar wave and longitudinal wave. After all, a scalar (time-polarized)
EM wave is indeed a longitudinal wave, but on the 4th axis rather than
in 3-space along the z axis.
-
- With Bedini's signal environment conditioning, one then
should get essentially flawless cellular time-reversal (physics terminology)
--- which is epigenetic reprogramming, in biological terms --- when applying
the Porthole Concept . Let me also try to put it into conventional biology
terms for biologists.
-
- What is necessary is to temporarily move the cells back
(reprogram the cellular genetics expression) toward what is called totipotency
--- a nascent state the newly fertilized egg in the early embryo achieves.
The biological term for this is epigenetic reprogramming --- resetting
the gene-expression programs of specialized cells, in a similar way to
how sperm and egg combine and change to form embryonic cells that are undifferentiated.
-
- In physics terms, that is a "time reversal"
of the cell back over its previous cellular differentiation pathway, back
down what is called the Waddington cell lineage path in biology. Waddington
compared the "forward differentiation" of cells to a ball rolling
down a sloping set of branching valleys, one must seek to "dedifferentiate"
the cells by moving them precisely back up the path previously taken downward,
in Waddington's analogy. Becker already showed that red blood cells, for
example, can be dedifferentiated and then redifferentiated by applying
scalar potentials (or other signals) to otherwise intractable bone fractures.
So the part played by the potential (involving scalar and longitudinal
photons) in differentiation and redifferentiation has been experimentally
demonstrated for some time, at least in overall terms.
-
- Any EM noise introduced into the cellular dedifferentiation
or "gene-expression resetting" procedure's electrodynamics is
obviously a corruption of the procedure, whether in a healing attempt by
the body (cellular regeneration) or a cloning attempt. Such corruption
in the actual EM control signals involved, will result in corrupting the
end result achieved. At base level, all cellular EM signals, waves, fields,
and pulses are comprised of paired couplets of a scalar EM wave and a longitudinal
EM wave (scalar photons and longitudinal photons) comprising each couplet.
Hence any corruption of any of this internal longitudinal EM wave structure
inside the cloning or healing process is a noise jamming process at the
most fundamental biocontrol and biodynamics level.
-
- The dedifferentiation or time reversal of the cell back
along its exact Waddington lineage path is part of the requirement, in
biological terms. The other part involves transdifferentiation, where one
attempts to just "jump" the cells (Waddington's ball) from one
erroneously branched valley it previously took, over the intervening mountainside
to the adjacent "correct" or "normal" valley. For
the layman, "transdifferentiation" roughly means "jumping
across the intervening gap between two adjacent Waddington valleys (cell
paths) the cell took as it developed. The Porthole Concept is designed
to continuously "eliminate the delta" between the Waddington
valley a diseased or disordered cell is actually in, and the adjacent Waddington
valley it would be in if it were a normal cell. In that way, the Porthole
Concept also strongly focused on transdifferentiation as well as de-differentiation.
-
- As an example, something like cancer is a deviation from
the proper cell lineage (Waddington differentiation valley) to a side-valley
that is off-course from the "healthy, normal" Waddington lineage.
-
- All of that is familiar to the biologist in those terms,
particularly those working in cloning, which does require efficiently resetting
the gene-expression programs, essentially back to totipotency. In cloning,
one introduces somatic nuclei into eggs, for example, and these nuclei
introduced into the eggs must undergo epigenetic reprogramming along with
the egg, to thus approximate closely the totipotency state of the usual
sperm and egg fertilization and early embryonic cell.
-
- The thing that makes such epigenetic reprogramming possible
is that the differences in gene expression are fairly well known to occur
without DNA sequence change. Gordon in fact did the pioneering experiments
which showed that the DNA sequence did not change. Successful cloning
itself is such a demonstration.
-
- However, the efficiency of cloning is well-known to be
low worldwide. We believe that Bedini has now uncovered either the total
reason or the major reason for that low efficiency. Heretofore no biological
researcher considering EM effects in cells has considered the higher group
symmetry EM effects that occur and are involved in both the infolded and
outfolded cellular EM environments, whether one is speaking of differentiation,
dedifferentiation, epigenetic reprogramming, or cloning. The internalized
longitudinal EM wave dynamics inside all fields, potentials, signals, pulses,
etc. has been completely ignored. Normal egg fertilization by sperm usually
occurs under conditions between two mating bodies where both bodies --
to include both the egg and the sperm --- are already thoroughly conditioned
to both the envelope "dense EM signal" environment and the infolded
longitudinal EM wave dynamics environment inside all the biological EM
signals that the biologists study.
-
- So a major variable in present cloning experiments has
been ignored. It has also been ignored unwittingly by researchers experimenting
with environmental EM bioeffects and with the possible use of EM signals
in healing processes. We suspect it eventually may prove to be a factor
in the progressive development of disease agents into resistant strains,
that occurs in our hospitals and treatment facilities.
-
- The Porthole Concept is intended to be a research method
for deliberately using the highly nonlinear characteristics of the cell
and all its parts, to electromagnetically recondition the internal infolded
EM environment of the cells as well as the internal infolded environment
of the cells' own ordinary EM signals, potentials, and fields. In short,
the Porthole Concept is a research process for epigenetic reprogramming,
as well as transdifferentiation controlled by the exact difference between
the Waddington valley previously taken (cell lineage actually followed
to develop the disease or disorder) and the normal disease-free and disorder-free
Waddington valley that ideally should have been taken.
-
- Now Bedini has added a major improvement to the "pristine"
Porthole process and to many other processes, by showing the importance
of first "fitting" the external signals used in the Porthole
concept so that their inner EM dynamics content precisely matches the local
environment's inner EM dynamics. Otherwise, one is adding signals which
externally appear to be "pure signals", but which internally
contain a great deal of "infolded inner EM noise" with respect
to the local inner EM environment of the targeted cells.
-
- So Bedini may well have found why present cloning is
so inefficient and difficult. The cloning procedures followed by the biologists
have been unwittingly applying a great deal of infolded inner noise to
the infolded internal EM environment of the egg cells, etc. The scalar
interferometry between the input signals "environmental inner electrodynamics"
and the receiving cell's "environmental inner electrodynamics"
generates overt EM jamming signals that jam, distort, and alter the intended
epigenetic reprogramming. In essence, researchers have not been considering
all the major variables that condition and affect epigenetic reprogramming
and transdifferentiation; specifically, they have not considered infolded
EM environment mismatch between the somatic nucleus and the egg cell, and
the resulting interferometry due to two differing infolded electromagnetic
environments. And so the results of cloning experiments worldwide do indicate
that something major is wrong, and that one or more major variables profoundly
affecting the success or failure of the cloning process is missing from
the present biology literature entirely.
-
- At any rate, we are very happy to point out the necessity
to adapt the Porthole Process to the local environments as stated, using
Bedini's newly discovered method of "local Waddington valley environment
matching" both in the inner EM environment and the outer EM environment.
In that manner, the cellular reversal (epigenetic reprogramming"
can be made true to the real Waddington valley or cell lineage that was
actually followed.
-
- The main point is Bedini's EM extension to Waddington's
fundamental work: Not only are there Waddington valleys to be considered,
but one must also consider and adapt the experiments to the exact cellular
EM environment --- both infolded and outfolded --- existing in all these
valleys when the differentiation cell route (valleys) were previously taken.
So one must consider both the Waddington valley and its infolded EM environment.
Epigenetic reprogramming and transdifferentiation --- by whatever means
it is to be obtained --- must be extended to add Bedini's EM environmental
conditioning so that the exact Waddington valleys and environments previously
taken by the cell are the valleys and environments now retraced back toward
totipotency. The key addition is the phrase "valleys and environments"
that replaces the former "valleys".
-
- The reader will carefully note that we have not revealed
the actual mechanism and process that Bedini uses in his startling new
method of using tubes. Instead, we have released only the overall description
of how the process works in general. No specifics have been released,
so we have not altered the proprietary intellectual property rights John
possesses because of his very important discovery.
-
- References:
-
- 1. T. E. Bearden (et al.???). TBD. Should reference
the PPA that is to be placed on the website. 2. E. T. Whittaker, "On
the Partial Differential Equations of Mathematical Physics," Mathematische
Annalen, Vol. 57, 1903, p. 333-355. 3. E. T. Whittaker, "On an Expression
of the Electromagnetic Field Due to Electrons by Means of Two Scalar Potential
Functions," Proc. Lond. Math. Soc., Series 2, Vol. 1, 1904, p. 367-372.
4. Wolf Reik and Wendy Dean, "Back to the Beginning," Nature,
Vol. 420, 14 Nov. 2002, p. 127. 5. W. Reik, W. Dean, and J. Walter, "Epigenetic
Reprogramming in Mammalian Development," Science, vol. 293, 2001,
p. 1089-1093. 6. H. M. Blau, "A twist of fate," Nature, Vol.
419, 3 Oct. 2002, p. 437. 7. C. H. Waddington, Organisers and Genes, Cambridge
University Press, Cambridge, 1940. 8. J. B. Gordon and V. Uehlinger, "
'Fertile' intestine nuclei," Nature, Vol. 210, 1966, p. 1240-1241.
9. Antoine Prior, Antoine, "Method of producing radiations for penetrating
living cells," U.S. Patent No. 3,280,816, Oct. 25, 1966. 10. Antoine
Prior, "Apparatus for producing radiations penetrating living cells,"
U.S. Patent No. 3,368,155, Feb. 6, 1968. 11. Antoine Prior, "Procede
et dispositif de production de rayonnements utilisables notamment pour
le traitement de cellules vivantes," [Procedure and Assemblage for
Production of Radiation Especially Serviceable for the Treatment of Living
Cells], Republique Francais Brevet d'Invention P.V. No. 899.414, No. 1,342,772,
Oct. 7, 1963. 11. R. Courrier, "Expos par M. le Professeur R. Courrier,
Secretaire Perpetuel de L'Academie des Sciences fait au cours d'une reunion
a L'Institut sur les effets de la Machine de M. A. Prior le 26 Avril 1977,"
[Presentation by Professeur R. Courrier, Perpetual Secretary of the Academy
of Sciences, made at the meeting of the Academy on the effects of the machine
of M. A. Prior.] 13. A. Prior, Gurison de la Trypanosomiase Exprimentale
Aigu et Chronique par L'action Combine de Champs Magntiques et D'Ondes
Electromagntiques Moduls. [Healing of intense and chronic experimental
trypanosomiasis by the combined action of magnetic fields and modulated
electromagnetic waves], thesis submitted in candidacy for the doctoral
degree, 1973. Prior's doctoral thesis (which was rejected when the project
was suppressed). 14. D. Solter, "Mammalian cloning: advances and
limitations," Nat. Rev. Gen., Vol. 1(3), 2000, p. 199-207. 15. F.
Mandl and G. Shaw, Quantum Field Theory, Wiley, 1984, Revised Edition 1993,
under the heading "5.2 Covariant Quantization" and "5.3
The Photon Propagator" in Chapter 5. 16. Richard W. Ziolkowski,
"Exact Solutions of the Wave Equation With Complex Source Locations,"
Journal of Mathematical Physics, 26(4), April 1985, p. 861-863. 17. I.M.
Besieris, A.M. Shaarawi, and R. W. Ziolkowski, "A bidirectional travelling
plane wave representation of exact solutions of the scalar wave equation,"
Journal of Mathematical Physics, 30(6), 1989, p. 1254-1269. 18. Rod Donnelly
and Richard Ziolkowski, "A method for constructing solutions of homogeneous
partial differential equations: localized waves," Proceedings of the
Royal Society of London A., Vol. 437, 1992, p. 673-692. 19. R. O. Becker
and David G. Murray, "The electrical control system regulating fracture
healing in amphibians," Clinical Orthopaedics and Related Research,
No. 73, Nov.-Dec. 1970, p. 169-198. 20. R. O. Becker and David G. Murray,
"A method for producing cellular dedifferentiation by means of very
small electrical currents," Transactions, New York Academy of Sciences,
29(5), Mar. 1967, p. 606-615. 21. R. O. Becker, Carlton F. Hazlewood,
Abraham R. Liboff, and Jan Walleczek, Electromagnetic Applications In Medicine,"
NIH-OAM Electromagnetics Panel Report, Jan. 15, 1993. 22. M. W. Evans
et al., "On Whittaker's Representation of the Electromagnetic Entity
in Vacuo, Part V: The Production of Transverse Fields and Energy by Scalar
Interferometry," Journal of New Energy, 4(3), Special Issue, Winter
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