12-Strand DNA Morphogenetic Engineering Via Holofractal ......12-Strand DNA Morphogenetic Engineering Via Holofractal Morphogenetic Reprogramming of Genetic Information Jere Rivera-Dugenio,

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

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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

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• 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.

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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

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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

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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

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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

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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

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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

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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

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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)

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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.

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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


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


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


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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


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

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• 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


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

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[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.

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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

Documents

12-Strand DNA Morphogenetic Engineering Via Holofractal ......12-Strand DNA Morphogenetic Engineering Via Holofractal Morphogenetic Reprogramming of Genetic Information Jere Rivera-Dugenio,