12-Strand DNA Morphogenetic Engineering Via Holofractal Morphogenetic Reprogramming of
Genetic Information
Jere Rivera-Dugenio, Ph.D.
Abstract - Today’s genetics and genomics science is based upon the crude, archaic method of splicing and replacing (ZNF, CRISPR/Cas9, etc.) however this eventually produces the breakdown of the genome. In order to turn on or off a specific gene and prevent the collapse of the genome, one must communicate to the DNA in their natural, organic language of scalar energy. We live in a holo-fractal (holographic-fractal), morphogenetic cosmos therefore it is possible to affect specific genes via transmitting resonant frequencies into the morphogenetic field of the cell utilising the language of our DNA – magnetic, scalar-plasma energy. A chromosome has a magnetic field in between the double-helix known as the major groove, as well as a surrounding morphogenetic field comprised of scalar energy, which contain the holo-fractal, morphogenetic blueprint of that physical chromosome. If a chromosome is carrying a mutation that causes shortened lifespan or disease, then it is possible to reverse that mutated condition by reprogramming new resonant frequencies utilising scalar-plasma energy and low frequencies magnetic sound waves.
Index Terms – genetics, genomics, DNA, morphogenetic, scalar
—————————— ◆ ——————————
Introduction
Atomic, cellular communication between introns
occurs when one cell transmits information and imprints
those instructions onto the receiving intron via the
magnetic vector of a scalar wave. According to Professor
Dr. Konstantin Meyl, the DNA generates a scalar wave
that propagates in the direction of the magnetic field
vector. Hydrogen bonds hold together through Coulomb
forces electrically polarized base pairs in a DNA strand. To
gain access to this polarization, the hydrogen bonds must
be separated, requiring radial outward electric field lines
or, a vortex field. Since the magnetic field vector is
perpendicular to the electric vertical field, a resulting axial
direction to the DNA strand is a logical consequence. The
motion of the vortex field in the direction of the magnetic
field results in a longitudinal wave forming a magnetic
scalar wave. [1]
Morphogenetic Fields
A morphogenetic field is comprised of the primal
substance, units of consciousness energy called the “Source
Particle”, which exist as omni-polar points of static
vibration. Source Particle units are the minutest units of
consciousness energy or the assembling sections of matter
that create the patterns upon which consciousness in all
manifest and un-manifest forms enters materialization.
Source Particle units are omni-polar (holding the
potentiality for all polarities or none) units of vibrating
energy that continuously rotate backward and forward
between a state of bi-polar light radiation (scalar standing
wave) and omni-polar sound vibration.[2]
A scalar wave is a transharmonic
(multidimensional), spherical standing energy array that
radiates out of a static point of sound-light vibration within
the morphogenetic field of the greater cosmic Unified Field
of consciousness (energy). While scalar waves appear to
move from point to point, they are spherical, fixed points of
sound-light that are sequentially threaded together within
the cosmic fabric of the morphogenetic field. The
appearance of the scalar wave movement is created
through the sequential flashing-on (light) and flashing-off
(sound) of scalar wave points that emanate the effect of a
flashing linear series of light bulbs. A prime example is
imagine viewing an electronic billboard in Times Square,
New York City. Although it appears as if the contents of the
electronic billboard are moving, in reality it is the row of a
synchronized series of flashing light bulbs that appears as if
the light moves from one point in the row to another. Scalar
waves embody static points of perpetual fission and fusion
————————————————
• Jere Rivera-Dugenio, Ph.D. received his masters and PhD degree in natural medicine at the International Quantum University for Integrative Medicine, Honolulu, Hawaii, USA. He is currently working on his Genetics and Genomics Certificate Program at Stanford University, USA. PH-+1-775-391-4645. E-mail: [email protected]
Figure 1. Electric ring vortices form a magnetic wave.
950
IJSER © 2020 http://www.ijser.org
IJSER
that radiate from the fabric of morphogenetic fields. [3]
Epigenetic Overlay
The Epigenetic Overlay (EGO) is the biological,
chemical control sheath that covers and controls the DNA
strand function. In the current homo sapien-2 species
(modern human), the epigenetic overlay is mutated due to
the fact it is affected by electromagnetic and cosmic
radiation, which causes the introns to remain inactive.
Stationed within the light-body seed atom located
at the base of thymus gland, there exists the quantum
blueprint that regulate the biorhythms and space-time
relationships of the finite-life, physical atomic body. These
quantum, morphogenetic instructions are biochemically
encrypted as the genetic master instructions within the
DNA/RNA and epigenetic overlay. The epigenetic overlay
must be reprogrammed in order affect the gene code. When
the epigenetic overlay is reprogrammed via perpetual-life
frequencies to its organic, perpetual-life function, the
introns sequentially turn-on and restore the perpetual-life,
biochemical developments intrinsic to the physical-atomic,
finite-life body. [4]
The 12-Sphere Perpetual-Life Fractal Grid
The cosmos is built upon the original 12-Sphere
Perpetual-Life Fractal Grid, which contains the electro-
magnetic, scalar-wave sequencers upon which the 12 DNA
strand blueprints are arranged. Presently, expressed base-
magnetic, 12-sphere Perpetual-life fractal grid spheres 4-7-
10 of the “left body pillar” and the magnetic aspects of
electro-magnetic 12-sphere Perpetual-life fractal grid
center-1 and base-electrical 12-sphere Perpetual-life fractal
grid spheres 2 and 11 on the “central body pillar” are
operating inverted fire-letter sequences.
Figure 2. 12-Sphere Perpetual-Life Fractal Grid
Figure 3. 12-Strand DNA Blueprint
Figure 4. Distorted 12-Sphere Grid
Subsequently, the magnetic base codes of present-day
human DNA strand blueprints 1-2-3-4-7-10-11 presently
operate in reverse, making DNA strand-interlacing, and
thus interstellar gateway (star-gate) passage via
“Transmutative Transharmonic Accretion” and Perpetual
life potentiality, impossible. [5]
Figure 5. Present-Day Human DNA Distortions
12 Double-Helix DNA Strands and 12 DNA Fire-Letters
951
IJSER © 2020 http://www.ijser.org
IJSER
The original, celestial human DNA blueprint, the
sub-strand DNA matrix, embodies the scalar-grid
blueprints for 12 “double-helix” DNA strands not 12 single
strands as the Anunnaki-influenced, modern university
science will deliberately misinform us to believe.
Anunnaki disinformation teachings instilled in all
levels of the modern educational system endeavor to depict
the “12-strand DNA” as six (6) sets of two (2) strands,
which in truth is a six (6) strand DNA blueprint
configuration. However, twelve (12) sets of two (2) strands
or 12 double-helix strands is the original, authentic 12-
Strand DNA blueprint. [6] Each strand blueprint
encompasses twelve (12) DNA/fire letters that are intended
to chemically transmute into 12 large chromosomes per
strand blueprint, for a total of 144 full chromosomes (12
scaylons = 12 chromosomes per strand x strands).
Figure 6. The Celestial Human DNA-Strand
The 12 natural chromosomes distinctive to each
strand of 12-strand celestial human chemical DNA is built
upon a genetic alphabet of twelve (12), not four (4),
nucleotide base chemicals. Our physical bodies should
contain a total of 36 full chromosomes: 12 for Strand-1, 12
for strand-2 and 12 for strand-3 totaling 36 full
chromosomes. Presently, we as the current homo-sapien-2
species only have 23 chromosomes somehow missing 13
chromosomes.
Figure 7. The DNA/ fire-letter 36-Chromosome Blueprint
Each of the 12 natural chromosomes per strand is
produced by one primary DNA blueprint/fire-letter. The
chemical conversion of the natural chromosome is designed
through the energetic interconnection between the one
magnetic particle base code, the one electrical antiparticle
acceleration code and the 12-minute vector codes that
create the structure of one DNA/ fire-letter in the DNA
blueprint. All of the 12 DNA strand blueprints contains a
set of 12 scaylons/fire-letters, a set of 12 base-acceleration
code pairs (one pair per scaylon) and a set of 144 vector
codes (12 vector codes per scaylon). [7]
Figure 8. The Celestial Human 12-Strand Blueprint
The Mother-Father Genetic Imprint
The 12 magnetic base codes in each strand
materialize from the “mother-line” (mother’s genetic
imprint) and the 12 electrical acceleration codes per strand
arise from the “father-line” (father’s genetic imprint). The
base code-acceleration code pair that creates one scaylon in
the DNA blueprint, through which one natural chemical
952
IJSER © 2020 http://www.ijser.org
IJSER
chromosome will emerge, forms the two (2) sugar
(deoxyribose) phosphate molecule groups that translate
into the two (2) handrails or helix of the chemical DNA
ladder. In its natural condition, one helix would contain the
sugar-phosphate blueprint inherited from the mother-line
genetic code and the other helix would contain the sugar-
phosphate blueprint inherited from the father-line genetic
code, generating a magnetic particle mother-helix and an
electrical anti-particle father-helix, as the handrails of the
chemical DNA ladder.
In the present-day mutated condition, many of the
base codes and acceleration codes that generate the
scaylons have been electromagnetically polarity-reversed,
which confuse the natural mother-father line chemical
interconnections within the sugar-phosphate handrails.
Within the mutated homo sapien-2 chemical DNA, gene
sequences inherited from both the mother and father will
appear in both helix, as a result of polarity-reversed base
codes and acceleration codes within the DNA blueprint.
This portion of the grid mutation creates the primary
sustainable malfunction in the natural function of the
celestial human 12-strand DNA.
A scaylon is a synthesis of infinitesimal, light-
sound, fission-fusion energy units known as a “Source
Particle”. Scaylon encryption codes are sophisticated
collective of scaylons that form a crystalline template of
light spectra, sound frequency & electro-magnetism that is
the morphogenetic field crystal body (the blueprint upon
which mater and density manifest and materialize).
Mutation of the base code and acceleration code pairs in
select scaylons of the DNA blueprint disrupts the natural
function and projected electromagnetic interconnection
between the mother-helix (magnetic-particle) base codes
and the father-helix (electrical-anti-particle) acceleration
codes, and their chemical sugar-phosphate chains, within
every gene and chromosome in the DNA ladder.
Figure 9. Scaylon (Source Particle)
Merkaba: Energy Vortex Spirals
Everything in manifest creation perpetually and
continually expands outward and returns back to Source.
A merkaba is a set of counter-rotating, electromagnetic
energy vortex-spirals, which perpetually expand and
contract the Perpetual supply of renewed energy radiation
out from and back into Source (or into and out of manifest
creation).
Mer = Source Movement
Ka = Source Expression
Ba = Vehicle
Therefore, merkaba literally means the expression
of Source movement. They are the primal cosmic lungs
and circulation systems of First Creation Process, breathing
primal currents from Source via the electric, clockwise
rotating, male merkaba (into) and out of, via the magnetic,
counterclockwise rotating, female merkaba manifestation
with harmonic precision.
Figure 10. Merkaba Spiral and Field
Merkaba fields are the energy engines and
consciousness carriers through which consciousness
circulates between the internal, Perpetual-life 12-sphere
fractal grid scalar blueprint and the five (5) transharmonic
density veil as they circulate into and out of external
manifest creation. The merkaba field also receives its
instructions for energy circulation from the 12-Sphere
Perpetual-life, fractal grid and DNA blueprint.
When the original, celestial human 12-strand
DNA blueprint is operating naturally, each base code-
acceleration code pair forms their own set of counter-
rotating electromagnetic energy vortices or merkaba fields.
The electrical acceleration code portion of one (1)
scaylon/fire letter/chromosome generates a minute clock-
wise rotating vortex-spiral of electrical anti-particle energy
and the paralleling magnetic base code generates a minute
953
IJSER © 2020 http://www.ijser.org
IJSER
counter-clock-wise rotating vortex-spiral of magnetic
particle energy within the DNA blueprint. [8]
Angular Rotation of Particle Spin
The angle of the axis upon which sub-atomic
particles rotate is known in quantum morphogenetic
physics as the angular rotation of particle spin. This is
determined by the core rate of the internal fission-fusion
(merkaba field speed and axis angle) with the source
particle units, which form the spherical, standing scalar
energy blueprint of the trans-dimensional frequency fields.
The rate of particle fission, oscillation and merkaba field
spin rate amplifies vertically via the transharmonic scale
generating increasingly less-dense matter. [9]
Perpetual-Life vs. Finite-Life Merkaba Spins
The organic, Perpetual-life merkaba spin ratio of
Transharmonic Density-1 is 33 1/3 clockwise (CW) and 11
2/3 counter-clockwise (CCW). This organic, natural
merkaba spin ratio creates an electromagnetic anti-
particle/particle equilibrium of 33 1/3 parts base-electrical,
anti-particles that is a masculine, expanding energy to 11
2/3 parts base-magnetic particles, which are feminine,
contracting energy. Simply stated, it is 33 1/3 electrical-
oscillations to 11 2/3 magnetic-vibrations per one (1)
merkaba rotation within the Transharmonic Density-1
matter base.
Organic, Perpetual-life merkaba vehicles originate
with the organic 33 1/3: 11 2/3 spin-speed ratio of a single
set of two (2) counter-rotating spiral vortices that develop
energy thrust and spin-speed to greater than light speed via
internal, quantum self-generation. The numerical ratio
relating to organic merkaba vortex spin-speeds over a
period of time measured in increments can be compared to
one rotation per trillionth of a billionth of a nanosecond
(RP-TBN). This follows the mathematics of the Perpetual-
life Source Spiral sequence and expansion formulae.
Figure 11. Perpetual-Life Merkaba 45 Spin Ratio
The inorganic, finite and self-consuming merkaba
spin ratio is 34 counter-clockwise (CCW) and 21 clockwise
(CW) that generate an electromagnetic anti-particle/particle
balance of 34 parts base-magnetic particles (contracting
energy) to 21 parts base-electrical anti-particles (expanding
energy). Simply stated, it is 34 magnetic-vibrations to 21
electrical-oscillations per one (1) merkaba rotation within
the Transharmonic Density-1 matter base
Inorganic, death science merkaba technologies
utilize the inorganic spin-speed ratios of 34: 21 in relation to
two separate same-spin, fixed vortex sets; four vortices
instead of the organic two, placed in counter rotation to one
another quickening and merging to a common spin of fifty-
five (55) when initiated.
Figure 12. Finite-Life Merkaba 55 Spin Ratio
Chemical DNA and The Sub-Strand Blueprint
The base code, magnetic vortex spirals generally
contained in the mother-line, magnetic helix accrete particle
morphogenetic, scalar frequency from Earth’s planetary
morphogenetic grids into the DNA blueprint. The
acceleration code, electrical vortex spirals typically
transmitted in the father-line, electrical helix accrete anti-
particle morphogenetic, scalar frequency into the DNA
blueprint from the paralleling DNA Template of the
physical body’s anti-particle duplicate (in the parallel Earth,
anti-particle universe).
In the middle of the base code-acceleration code pair in
each scaylon/ fire-letter of each strand of the DNA
blueprint, there is a set of 12 smaller vector codes. The 12
vector codes flanked by each base code-acceleration code
pair operate as the receivers, integrators and transmitters of
the particle and anti-particle morphogenetic, scalar
frequency that accrete into the strand blueprint via the base
954
IJSER © 2020 http://www.ijser.org
IJSER
code-acceleration code pair.
When functioning properly, the vector codes accrete
the particle/anti-particle morphogenetic, scalar frequency
until a critical mass is attained. As soon as critical mass of
particle/anti-particle morphogenetic, scalar frequency is
achieved within the vector codes, the 12 vector codes
transmute and convert the morphogenetic, scalar frequency
blueprints of the base code-acceleration code pair into the
chemical array of the sugar-phosphate molecules that
construct the handrails of the chemical DNA ladder.
At critical mass accretion, each vector code DNA
blueprint transforms chemically convert into the nucleotide
bases and nucleotide base pairs that form the chemical
DNA ladder rungs of which the gene and chromosome
sequences of the human genome are composed. When the
12-Strand DNA blueprint was operating correctly, the
recurring set of 12 vector codes essential to each scaylon/
fire-letter in each strand blueprint would generate the 12
nucleotide base chemicals of the natural “Base-12” celestial
human genetic alphabet. If functioning properly, the 12
vector codes are operational, permitting the full spectrum
of 12 sub-frequency spheres from each dimensional sphere
to flow between the base code and acceleration code in each
scaylon/fire-letter.
Chemically speaking, when the DNA blueprint vector
code are unlocked there is a natural channel of
electromagnetic, morphogenetic scalar frequency streaming
within the properly sequenced chemical channels of the
nucleotide base pairs that make up the genes and
chromosomes.
As a result of this projected natural order, one full,
natural chromosome would be comprised of 12 primary
gene/exon sequences, which are the coding DNA sequences
or chemical blueprints that assemble protein and amino
acid. Each are comprised of millions of nucleotide base
pairs, and one equal and paralleling set of 12 primary
intron sequences, which are the non-coding DNA.
Perpetual-Life DNA Sequences and Celestalline
Between each nucleotide base pair that created each
gene is the area known as the hydrogen bond. Here the
hydrogen molecules form a weak link between the
nucleotide bases of each helix and join the two helices
together in the ladder configuration. Normally, there would
be a set of chemical nucleotide base pairs called “Perpetual-
Life DNA Sequences” that could be deactivated and
activated. Presently, these are not functional within the
current homo sapien-2 species.
In the DNA blueprint, the Perpetual-life DNA
sequence is inactive, and its potential suspended within the
vector code blueprints until the DNA blueprint accretes
specific types of transharmonic, frequency spectra, such as
those contained in interstellar gateways (star gates).
Integrating with higher 12TH dimensional sphere (DS-12)
frequency via specific scalar energy techniques (e.g. The
Eckasha Maharic Seal technique), triggers the
electromagnetic polarity in certain vector codes to naturally
reverse, initiating the vector code blueprints to merge, at
which time the Perpetual-life DNA sequence is chemically
activated.
Figure 2. 15-Dimensional Time Sphere
The “Perpetual-Life DNA Sequences” in each
nucleotide base pair of each gene within every chromosome
permits for the particles and anti-particles within the 12
vector codes in each scaylon/ fire-letter to fuse. When the
Perpetual-life DNA sequence activate in one group of 12
corresponding nucleotide base pairs (12 ladder rungs), the
base code and acceleration code within the paralleling
scaylon/ fire-letter unite to form an infinitesimal micro-
merkaba field.
As a result of activating the Perpetual-life DNA
sequence, this micro-merkaba field (a set of interwoven,
counter-rotating electromagnetic field) triggers in the DNA
blueprint scaylon/fire-letter. Subsequently, the Perpetual-
life DNA sequence merges together in fusion into the
hydrogen bonds of the 12 nucleotide base pairs to which it
parallels.
By means of the hydrogen bonds, the 12 nucleotide
base pairs combine to create a new, transient, composite
955
IJSER © 2020 http://www.ijser.org
IJSER
that is a silica-based, chemical-elemental compound, found
only on the concealed, 144+ table of organic elements
known as celestalline. Celestaline is the chemical element of
atomic, cellular transmutation and is an organic, perpetual,
stable element found within perpetual-life systems and
Perpetual-life beings (O2He3WH2). However, it is a
temporary, unstable and short-lived element within this
finite-life system and finite-life beings (H2N3AUO2).
Celestalline first materializes within the areas of the
hydrogen bonds that link the nucleotide bases of each helix
to create the nucleotide base pair ladder rungs, which
assemble the two sugar-phosphate helix into the double
helix configuration. Celestalline is the chemical of quantum
morphogenetic cellular transmutation. It is the natural
chemical by-product that materializes in the chemical DNA
through activation of the Perpetual-life DNA sequences
within the hydrogen bonds, when the particles and anti-
particles in the DNA blueprint vector codes fuse to convert
the base-acceleration code pair of each scaylon/ fire-letter
into an electromagnetic micro-merkaba field. [10]
Quantum Morphogenetic Cellular Transmutation
This is the process of “quantum morphogenetic cellular
transmutation” in which the hydrogen molecules transform
and release the element Celestaline for the intention of
biological, cellular transmutation. When the introns are
activated to a certain level, this grants your DNA the
temporary ability to create celestalline, which opens the
neutron aperture, the nucleus of your atom. Additionally,
re-introducing nitrogen into the water correspondingly
triggers hydrolase conversion.
Celestalline activates the intron DNA sequences (non-
coding “potential DNA” sequences between active exon
sequences in individual genes) in individual genes,
allowing the intron sequences in the smallest gene to
duplicate the exon sequences in next largest gene,
transmuting the smaller gene into a copy of the larger gene.
This process allows the 12-primary exon/gene sequences
and 12 corresponding intron sequences in a single, natural
chromosome to fuse into one long exon-intron/gene
sequence that is the duplicate of the exon-intron/gene
sequences of the next largest chromosome. Exon and
Intron/gene sequences 1-12 of chromosome-1 combine into
one sequence that is the replica of the exon and intron/gene
sequences of chromosome-2, etc.
Interface DNA Sequence and Bonded Chromosome
When the DNA blueprint is functioning correctly, as
soon as the first sector of Perpetual-life DNA is triggered
and the first set of 12 paralleling nucleotide base pairs fuse
to form celestalline within the nucleotide base pair
hydrogen bonds, an extremely quick chain reaction occurs
in the DNA blueprint and chemical DNA.
The exon-intron/gene sequences in chromosome-1
transmute to replicate those in chromosome-2, triggering
chromosome-2 to initiate the same process with
chromosome-3, etc. Once the set of 12 natural chromosomes
relating to one (1) DNA strand blueprint (and one-
dimensional frequency sphere) triggers, a sufficient amount
of celestalline is accreted in the chemical DNA, to trigger
the same process within the next DNA strand blueprint.
Triggered by the production of celestalline from the
chromosomes of the prior DNA-strand, as each segment of
the Perpetual-life DNA activates in each chromosome,
DNA strand blueprint and chemical DNA ladder, a new
kind of chemical DNA sequence called “Interface DNA
Sequence” materializes. When a sufficient amount of
celestalline is produced by activation of the Perpetual-life
DNA sequences in each gene and chromosome of the first 3
DNA strand blueprints, these new sequences of chemical
interface DNA sequences materialize primarily between
each chromosome.
Celestalline production maintains and accelerates in
the DNA and cell nucleus as the interface DNA sequences
progressively connect together and blend the 12 natural
chromosomes from each of the first 3 DNA strand
blueprints. This creates what is called a “bonded
chromosome”, which is a group of 12 specific full
chromosomes bonded together via the activated interface
DNA sequence, to produce one super-chromosome known
as the “bonded chromosome”. [11]
DNA Strand Interlacing and Compound Morphogene
As the 12 previously separate chromosomes from
each of 3 DNA strand blueprints fuse to form 3 bonded
chromosomes (one for each DNA strand blueprint 1-2-3),
the second sequences of interface DNA sequences
materializes between each of the 3 bonded chromosomes
initiating the process called “DNA strand interlacing”.
In DNA strand interlacing, the two (2) helix of the
chemical DNA sequences relating to double helix DNA
strand blueprint-1 de-polarize and combine into a transient,
singular, electrical-antiparticle helix called a “compound
956
IJSER © 2020 http://www.ijser.org
IJSER
morphogene”. The term “compound” refers to the passing
of a chemical DNA sequence that emerges from one strand
blueprint into interlacing or bonding with a paralleling
DNA sequence materializing from the strand blueprint,
which is next in sequence within the dimensional scale.
The term “morphogene” refers to the fact that in
this process of DNA strand interlacing, or “strand fusion”,
the DNA sequence being transported appears to untangle
in structure as it depolarizes to form a single, anti-particle
helix. As the DNA sequence de-polarizes and de-manifests
from its original position in the DNA chain, it leaves behind
a transient, morphogenetic imprint or “morphogene” of its
prior structure within the chemical DNA sequence from
which it transferred.
Once materialized, the compound morphogene
(single de-polarized, electrical helix) then
electromagnetically binds to the hydrogen bonds of the
magnetic particle helix of the chemical DNA sequence
relating to the strand-2 blueprint. As the chemical DNA
sequences relating to DNA strand blueprints 1 and 2 fuse,
the same process is set in motion between DNA strand
blueprints 2 and 3, etc.
The Super-Luminal Element Celesma
As celestalline levels continue to increase, a critical
mass of celestalline is produced within the hydrogen bonds
to sufficiently transmit the celestalline chemical blueprint
from the cell nuclei into the cells via messenger RNA as
chemical instructions for production of new, highly
complex amino-acid chains and proteins.
The new protein chemical building blocks produce a
variety of numerous chemical-hormonal “celestalline
carriers”. Due to the chemical-hormonal celestalline
carriers, the celestalline blueprint is transported into the
bloodstream and all of the chemical-hormonal systems of
the brain and body. As the celestalline blueprint enters the
blood and hormonal systems, a rapid sequence of
biochemical modifications occurs within the glands, organs,
nervous system, brain and blood. Momentarily, the
celestalline blueprint produces chemical-elemental
interactions to occur within the nucleus of red blood cells
and within certain fluid and hormonal secretions.
The chemical-elemental interactions between specific
body fluids and the celestaline blueprint in the body cells
initiate the temporary materialization of minute blood
crystals, hormone crystals and transfiguration and
manifestation of fragments of the physical body’s water
molecules into a silica-like, radioactive, crystalline element
called “celesma”. [12] Celesma, or celesmaic crystal, is a
transient super-luminal, transharmonic element. The spin
rate of celesma atoms is much faster than light speed,
rendering the substance super-luminal and it cannot be
chemically cleaved into simpler substances, which qualifies
it as an element. Celesma can only be produced through the
process of internal, nuclear fusion between specific particle
and anti-particle pairs from two separate 3-dimensional
systems, matter density levels or “trans-harmonics” of
matter density, consequently the element celesma is trans-
harmonic.
Morphogenetic Residue & Blood, Hormone and Celesmaic Crystals
The element celesma itself is short-lived in that it
fractures into unsteady, sub-atomic fragments shortly after
its creation during the cellular transmutation process
however, it leaves behind a “morphogenetic residue” after
a biological form has completed its physical transformation
out of transharmonic-1 density. The formation of the
minute blood, hormone and celesmaic crystals within the
body indicates that the quantity of celestaline blueprint
transported by the chemical hormonal “celestaline carriers”
has reached a maximum accretion within the body cells,
through which the processes of inner cellular fusion and
molecular transmutation will begin.
As the celestalline blueprint reaches maximum
accretion within the blood, fluids and hormonal systems,
and a maximum accretion of blood, hormone and celesmaic
crystals form, the atomic structure of the body enters a
phase of transmutation. The infinitesimal, interdimensional
atomic structure of the chemical celestaline is composed of
a set of complex, alternated particle/anti-particle sub-atomic
units that, at different stages of the chemical’s very brief
life, simulate both waves and particles. In both stages, the
molecular units that celestaline is composed have rates of
spin that are greater than the light-speed in this
dimensional sphere making the atomic structure of
celestaline super-luminal. [13]
Considering that celestaline has an atomic
structure that moves faster than the speed of light, the
chemical itself cannot be detected by public sector
technology, however the effects of its existence upon
identified atomic structure can be physically observed
under the appropriate conditions. When an adequate
quantity of the super-luminal, celestaline blueprint is
transported into the internal organ systems of the body via
chemical-hormonal celestaline carriers, the physical, atomic
structure of the body changes.
Due to the super-luminal interaction between the
957
IJSER © 2020 http://www.ijser.org
IJSER
electromagnetism intrinsic to celestaline and the positive
and negative electrical charges characteristic to the protons
(positive charge particles in cell nucleus with neutrons) and
electrons (negative charge particles outside of cell nucleus
corresponding to protons within nucleus) of cells, the
normal behavior of protons and electrons is transformed
upon interface with adequate quantities of celestaline.
Negative to Positive Neutron
The neutrons in the cell nucleus, which usually
exhibit no charge, take on a momentary negative charge
that corresponds to the sound-wave spectrum of the
dimensional sphere above that in which the interface is
taking place. The momentary “negative-neutron” charge is
greater than the collective positive charge of the protons in
the nucleus, which causes the protons to reverse their
charge and transform into electrons within the nucleus of
the cell. These exchanges within the cell nucleus produce
the negatively charged electrons outside of the nucleus to
reverse their charge to positive, becoming protons, which
are drawn into the nucleus via the negative neutrons.
Figure 3. Negative to Positive Neutron
Simultaneously, celestalline enters its transitory
super-luminal particle phase, causing the negative-neutrons
to reverse their own charge to a positive charge. As these
electrical connections are transpiring in a synchronized
order within each body cell, the protons and electrons of
the cells fuse in a very specific sequence with their
corresponding anti-particles, as their own charge and axis
spin angle and rate reverse to duplicate that of their anti-
particles. When particles and anti-particles merge within
each cell they do not destroy each other, as would be the
case without the presence of celestalline and its inherent
fusion-sequencing directives.
Modulating Cell Signaling and Magnetic Energy
In 2004, a group of scientists at the University of
Bologna, Italy headed by Carlo Ventura, MD, Ph.D.
published a research paper that turned on stem cell
cardiogenesis with extremely low frequency magnetic
fields. [14] In the research, magnetic fields in the 2.4 GHz
Wi-Fi band range were used with a radio electric
asymmetric conveyer (REAC) to modulate the ability of
stem cells to differentiate or even make the adult non-stem
cells behave like stem cells. The REAC technology utilizes
the interaction of two oscillating magnetic fields; the first is
generated by cells or the entire organism, and the second is
a weaker electromagnetic field produced by the REAC
system. A resultant electromagnetic field induces the cells
to respond with endogenous self-generated micro-currents,
likely ensuing from cellular ionic fluxes. These currents
were detected and conveyed back to the cells with a
conveyer probe.
Figure 15. Turning on Stem Cell Cardiogenesis with Low Frequency Magnetic Fields (2004)
In 2019, the scientists tested an advanced, vortex
electromagnetic coil to observe the effects on stem cells and
the results were even more promising than the previous
REAC technology.
Figure 16. Testing Advanced Vortex Electromagnetic Coil on Stem Cells (2019)
958
IJSER © 2020 http://www.ijser.org
IJSER
Holofractal Morphogenetic Cellular Reprogramming
My theory on “Holofractal Morphogenetic Cellular
Reprogramming” proposes that specific scalar-plasma
technologies along with resonant frequencies transmitted
into the introns via scalar, plasma magnetic waves can:
1) reverse the present day electromagnetic polarity-
reversal mutation within the natural mother-father
genetic imprint,
2) reset the merkaba spin of every atom to the
organic, Perpetual-life merkaba spin ratio of
Transharmonic Density-1 is 33 1/3 clockwise (CW)
and 11 2/3 counter-clockwise (CCW),
3) activate celestaline to materialize in the chemical
DNA. The chemical access DNA sequences within
the hydrogen bonds as the particles and anti-
particles in the DNA blueprint vector codes merge,
convert the base/acceleration code pair of each
scaylon into an electromagnetic micro-merkaba
field. Simply stated, celestaline can be
manufactured within the DNA as it materializes
within the hydrogen bonds that connect the DNA
spirals.
The RASHA Scalar-Plasma Technology
The RASHA is the only D.A.R.P.A-inspired, Tesla
Quantum Access Technology available in the public sector. It is
an authentic scalar-plasma-sound system designed to assist
the biological, human organism to achieve stress release and
relaxation in order to reclaim its innate ability to self-heal. This
is achieved via harmonization of the autonomic nervous
system, brain hemisphere synchronization, emotional trauma
release and systematic chakra realignment.
The RASHA combines the brilliant technologies
of Nikola Tesla, Antoine Priorie' and Dr. Royal Rife into one
integrative quantum self-healthcare system. In addition, as per
Prof. Dr. Konstantin Meyl’s published research and
experiments in magnetic scalar waves being the
communication language of the introns (potential DNA), our
RASHA technology transmits vital information via the
magnetic vector of the scalar field to the magnetic, major
groove in between the double helix of our DNA.
The RASHA is controlled by one of the most
advanced scalar and Rife frequency generating
software technology, RASHA Base-12 Frequencies. When
operated and activated via the software, selected frequencies
(transverse waves) are transmitted through the dual scalar
spiral coils that are then pulsed causing excitation of the
proprietary customs gas blend in the plasma gas tube creating
a powerful, magnetic scalar field. Plasma can transform
transverse waves into longitudinal, scalar waves. Additionally,
plasmas can also create phase conjugate waves or time-
reversed waves.
The RASHA was utilized successfully in reducing
stress and prompting relaxation in the following
pathologies including but not limited to: psycho-emotional
trauma, opioid addiction, depression, suicidal tendencies,
anxiety, PTSD, Alzheimer’s Disease, Autism Spectrum
Disorder, stroke, cardiovascular disease, Lyme Disease,
sports-related injuries, stress related to sports-work-daily
life.
Figure 17. The RASHA-20 Series Model
Protocol
The following RASHA protocol was utilized in the
subsequent case studies:
▪ Clients were scanned with the HeartQuest HRV
(Heart Rate Variability) assessment tool on day one
and on the last day.
▪ Clients experienced at least 90 minutes per day for
the following:
▪ Trilateral Binaural Sine Wave (TBSW) (stress
relief, relaxation)
▪ Chakras (ALL, MULTI)
▪ Source Tones
▪ RASHA PRO – DTM, Cardiovascular, etc.
▪ Combined with the RASHA sessions, some clients
integrated nutraceuticals for detoxification purposes.
959
IJSER © 2020 http://www.ijser.org
IJSER
Client sat within three to six feet of the RASHA during each
90-minute session.
Regarding the autism spectrum disorder cases studies, the
ATEC (Autism Treatment Evaluation Checklist) was utilized to
measure treatment effectiveness.
CASE STUDIES
Client sat within three to six feet of the RASHA
during each 90-minute session
Case #1: 24-yr, Male, bi-polar, depression, suicidal, insomnia
Figure 18. The RASHA-20 Series Model
Results: The entire RASHA Protocol lasted twelve (12) weeks
and comprised of a total of fourteen (14) ninety-minute
RASHA sessions. At the end of the first week, the client’s
medication was titrated down by fifty percent (50%). By the
end of the twelve weeks, the client was completely taken off
his medication as per his physician’s orders.
Case #2: 23-yr, Male, opioid addiction, depression, suicidal
Figure 19. The RASHA-20 Series Model
Results: The entire RASHA Protocol lasted twelve (12) weeks
and comprised of a total of twenty five (25) ninety-minute
RASHA sessions. At the end of the first week, the client only
experienced one 24-hour withdrawal phase. By the end of the
fourth week, the client was free from suicidal thoughts and
depression.
Case #3: 79-yr, Female, diabetes mellitus Type-2, Aortic
Valve stenosis
Figure 20. The RASHA-20 Series Model
960
IJSER © 2020 http://www.ijser.org
IJSER
Figure 21. The RASHA-20 Series Model
Results: The entire RASHA Protocol lasted eight (8) weeks and
comprised of a total of forty (40) ninety-minute RASHA
sessions. At the end of the two months, the client lowered
stress index, balanced the autonomic nervous system,
increased vital force, lowered actual versus biological age by
fourteen (14) years and finally, increased peak performance
condition by twenty-four (24%) percent.
Case #4: 5-yrs, Male, Autism Spectrum Disorder
Diagnosis/Symptoms:
• ABA, Speech, OT, PT
• Age: 4, Biomedical approach with little to no
progress
• Does not attend school
• Main challenges
• Non-verbal
• Compromised immune system
• Aggression
• Self-Injurious behaviors
• Constant tantrums
• First introduced to scalar wave therapies at 4
years of age
• Utilized the ATEC to monitor progress over
the time
Figure 22. The RASHA-20 Series Model
Results:
• Dropped 54 ATEC points since beginning the
RASHA protocol
• Increase in level of awareness
• Potty trained
• Decrease in aggression and tantrum behaviors
• Emerging social referencing
• Initiating engagement with parents
• Maintains eye contact during
interaction
• Increase in speech and language
skills
• Increase in facial expression and affect, as well as
intonation while speaking
• Overall increase in immune system health
• Frequency, severity and duration of illness
has decreased drastically
• No longer needs regular use of inhaler or
nebulizer
• Normalized sleep patterns
• Weight gain
• Regular bowel movements
• Emerging interest and engagement in peer
interaction.
• Was able to attend school in Fall of that year
Case #5: 7-yr, Male, Autism Spectrum Disorder
Diagnosis/Symptoms:
• Series of high fevers (103 - 104 degrees) off and on for
approximately 4 weeks at 16 months of age due to
unknown illness (lost vocalizations, eye contact)
• Began Speech, OT, PT and Early Intervention at the
18 months of age
• Began intensive 35hr/wk. ABA program at 2 years of
age
961
IJSER © 2020 http://www.ijser.org
IJSER
• Formally received Autism diagnosis at 3 years of age
• Main health challenges
• Compromised immune system (~3/yr. avg
hospitalizations)
• Asthma
• Constipation
• Poor weight gain
• Irregular sleep patterns (including night
terrors)
• First introduced to scalar wave therapies at 3 years, 9
months of age
• Utilized the ATEC to monitor progress over the time
Figure 23. The RASHA-20 Series Model
Results:
• Dropped 154 ATEC points over the span of four
years.
• According to ATEC, the child is no longer considered
on the autism spectrum.
CONCLUSION
In order to reverse mutate the finite-life, DNA
mutation encryption within our current homo sapien-2
species gene code and reclaim our innate ability to achieve
“Holofractal Morphogenetic Cellular Reprogramming”, we
must reprogram our epigenetic overlay with the perpetual-
life merkaba spin encryption. This is achieved via scalar,
plasma, magnetic sound frequencies containing the 33 1/3
(CW or right), and 11 2/3 (CCW or left) counter-rotating
spin ratio as this creates an electromagnetic force field for
self-healing. This conclusion has been verified with 100%
efficacy in the five (5) different case research studies that
was performed and observed for this research study.
REFERENCES
[1] K. Meyl (2011b) DNA—reading and writing by scalar waves. 2nd World DNA Day—China, 2011, Track 2.7, conf. proc., p.101
[2] J. J. Rivera-Dugenio, “The Language of our DNA”, International Journal of Scientific & Engineering Research, Volume 10, Issue 4, April 2019 Edition.
ISSN 2229-5518
{3] J. Rivera-Dugenio, “The Evolution of Consciousness to Matter”, International Journal of Scientific & Engineering Research, Volume 10, Issue 1,
January 2019 Edition. ISSN 2229-5518
[4] A. Dean, “Twelve Tribes Classes - Introduction to the 12 Tribes of Aquafereion”, Phoenix, Arizona. 2008
[5], [6]. [7], [8] J. Rivera-Dugenio, “The Planetary Grid-Chemical DNA Mutation, Merkaba Reversal, and Cellular Transmutation”, International Journal
of Scientific & Engineering Research Volume 10, Issue 6, June-2019 500 ISSN 2229-5518
[9] A. Dean, “Voyagers II Secrets of Amenti”, ISBN-13: 978-1893183254. Granite Publishing (2002)
[10], [11], [12],[13] J. Rivera-Dugenio, “The Solar Synthesis-Deuterium Depletion-Hydrolase Transfiguration Principle”, International Journal of Scientific
& Engineering Research Volume 10, Issue 3, March-2019 500 ISSN 2229-5518
962
IJSER © 2020 http://www.ijser.org
IJSER
[14]. Ventura C, Maioli M, Asara Y, Santoni D, Mesirca P, Remondini D, Bersani F. “Turning on stem cell Cardiogenesis with extremely low frequency
magnetic fields”, FASEB J. 2005 Jan;19(1):155-7. Epub 2004 Oct 26.
963
IJSER © 2020 http://www.ijser.org
IJSER
12-Strand DNA Morphogenetic Engineering Via Holofractal Morphogenetic Reprogramming of Genetic InformationJere Rivera-Dugenio, Ph.D.Index Terms – genetics, genomics, DNA, morphogenetic, scalarIntroductionMorphogenetic FieldsA scalar wave is a transharmonic (multidimensional), spherical standing energy array that radiates out of a static point of sound-light vibration within the morphogenetic field of the greater cosmic Unified Field of consciousness (energy). While scala...Epigenetic OverlayThe Epigenetic Overlay (EGO) is the biological, chemical control sheath that covers and controls the DNA strand function. In the current homo sapien-2 species (modern human), the epigenetic overlay is mutated due to the fact it is affected by electrom...Stationed within the light-body seed atom located at the base of thymus gland, there exists the quantum blueprint that regulate the biorhythms and space-time relationships of the finite-life, physical atomic body. These quantum, morphogenetic instruct...The 12-Sphere Perpetual-Life Fractal GridThe original, celestial human DNA blueprint, the sub-strand DNA matrix, embodies the scalar-grid blueprints for 12 “double-helix” DNA strands not 12 single strands as the Anunnaki-influenced, modern university science will deliberately misinform us to...The Mother-Father Genetic ImprintAngular Rotation of Particle SpinThe angle of the axis upon which sub-atomic particles rotate is known in quantum morphogenetic physics as the angular rotation of particle spin. This is determined by the core rate of the internal fission-fusion (merkaba field speed and axis angle) wi...Perpetual-Life vs. Finite-Life Merkaba SpinsChemical DNA and The Sub-Strand BlueprintPerpetual-Life DNA Sequences and CelestallineQuantum Morphogenetic Cellular TransmutationThe Super-Luminal Element CelesmaModulating Cell Signaling and Magnetic EnergyHolofractal Morphogenetic Cellular ReprogrammingThe following RASHA protocol was utilized in the subsequent case studies: Clients were scanned with the HeartQuest HRV (Heart Rate Variability) assessment tool on day one and on the last day. Clients experienced at least 90 minutes per day for the following: Trilateral Binaural Sine Wave (TBSW) (stress relief, relaxation) Chakras (ALL, MULTI) Source Tones RASHA PRO – DTM, Cardiovascular, etc. Combined with the RASHA sessions, some clients integrated nutraceuticals for detoxification purposes.Client sat within three to six feet of the RASHA during each 90-minute session.Regarding the autism spectrum disorder cases studies, the ATEC (Autism Treatment Evaluation Checklist) was utilized to measure treatment effectiveness.Client sat within three to six feet of the RASHA during each 90-minute sessionCase #1: 24-yr, Male, bi-polar, depression, suicidal, insomniaResults: The entire RASHA Protocol lasted twelve (12) weeks and comprised of a total of fourteen (14) ninety-minute RASHA sessions. At the end of the first week, the client’s medication was titrated down by fifty percent (50%). By the end of the twelv...Case #2: 23-yr, Male, opioid addiction, depression, suicidalResults: The entire RASHA Protocol lasted twelve (12) weeks and comprised of a total of twenty five (25) ninety-minute RASHA sessions. At the end of the first week, the client only experienced one 24-hour withdrawal phase. By the end of the fourth wee...Case #3: 79-yr, Female, diabetes mellitus Type-2, Aortic Valve stenosisResults: The entire RASHA Protocol lasted eight (8) weeks and comprised of a total of forty (40) ninety-minute RASHA sessions. At the end of the two months, the client lowered stress index, balanced the autonomic nervous system, increased vital force,...Case #4: 5-yrs, Male, Autism Spectrum DisorderDiagnosis/Symptoms:• ABA, Speech, OT, PT• Age: 4, Biomedical approach with little to no progress• Does not attend school• Main challenges• Non-verbal• Compromised immune system• Aggression• Self-Injurious behaviors• Constant tantrums• First introduced to scalar wave therapies at 4 years of age• Utilized the ATEC to monitor progress over the timeResults:• Dropped 54 ATEC points since beginning the RASHA protocol• Increase in level of awareness• Potty trained• Decrease in aggression and tantrum behaviors• Emerging social referencing• Initiating engagement with parents• Maintains eye contact during interaction• Increase in speech and language skills• Increase in facial expression and affect, as well as intonation while speaking• Overall increase in immune system health• Frequency, severity and duration of illness has decreased drastically• No longer needs regular use of inhaler or nebulizer• Normalized sleep patterns• Weight gain• Regular bowel movements• Emerging interest and engagement in peer interaction.• Was able to attend school in Fall of that yearCase #5: 7-yr, Male, Autism Spectrum DisorderDiagnosis/Symptoms:• Series of high fevers (103 - 104 degrees) off and on for approximately 4 weeks at 16 months of age due to unknown illness (lost vocalizations, eye contact)• Began Speech, OT, PT and Early Intervention at the 18 months of age• Began intensive 35hr/wk. ABA program at 2 years of age• Formally received Autism diagnosis at 3 years of age• Main health challenges• Compromised immune system (~3/yr. avg hospitalizations)• Asthma• Constipation• Poor weight gain• Irregular sleep patterns (including night terrors)• First introduced to scalar wave therapies at 3 years, 9 months of age• Utilized the ATEC to monitor progress over the timeResults: Dropped 154 ATEC points over the span of four years. According to ATEC, the child is no longer considered on the autism spectrum.CONCLUSIONREFERENCES