Using Quantum Medicine to Unravel Stressors That Provoke Carcinogenesis

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Using Quantum Medicine to Unravel Stressors That Provoke

Carcinogenesis

By Stephen Linsteadt, NHD. and Jorge Llamas, M.D.

 

Quantum physics when applied to the study of biological processes is

known as biophysics. Biophysics studies the living cell as a whole

system with electrical fields that interrelate and penetrate the

entire organism.1 Carcinogenesis occurs when healthy bioelectrical

fields are transformed. Quantum Medicine applies quantum physics

theories to unravel the stressors that cause disruptions within

bioelectrical fields.

Quantum Physics and Biological Processes

Subatomic particles, photons, protons, and electrons, etc., have the

dual characteristic of existing as both particles and wave forms.

Subatomic particles vibrate at different rates or frequencies based

in part on changes in temperature and thermodynamics. In their wave

form state, quantum particles emit a frequency vibration that

extends indefinitely. In this state, subatomic particles are present

in all space in what is known as superposition. In the superposition

state, they are also in contact with every other subatomic particle

in the universe. This interconnection provides a superhighway of

information transfer between all of the building blocks of our

universe, including our own body.

This interconnected web of energy acts like a holographic plate from

which our physical body takes shape. Our cells are also connected to

this sea of subatomic energy. It is known that cells receive, store,

and emit quantum packets of light - photons (Popp). From a

biological standpoint the term " bio-photon " is more appropriate.

Electrons also absorb and emit photons, which is why the electron

rich DNA is a storage house for biophotons.2 It is now thought that

the unique vibratory rate of each biophoton is what activates

specific gene sequencing through what is known as resonance.

Resonance is the vibration that is specific to the frequency

oscillations generated by all kinetic forms of energy. A struck

guitar string, for example, will resonate at a specific frequency.

The vibratory energy of that specific frequency will start in motion

a nearby string that is tuned to the same frequency. Resonance,

therefore, is able to communicate and transmit frequency information

from

one guitar string to another. In the same way the vibratory energy

of biophotons are able to induce responses in other biophotons -

within the same cell and without to neighboring cells - in fact,

throughout the entire organism.

The cell acts as the interface between the quantum superposition

state and the particle state. In the superposition wave form state

all of the possibilities of physical manifestation are present. It

is the quantum measuring apparatus of the cell that forces the

collapse of the superposition state into the particle state. DNA,

RNA, ribosomes, and mitochondria are all proton, electron and photon

level apparatuses. 3 Photons have the ability to knock electrons out

of their atomic and molecular orbits. They are able to direct

electrons to where they are needed to run metabolic processes.

Enzymes capture and transfer electrons and protons along a path to

various protein molecules in order to activate each protein's

specific function. In the quantum world, all of the exponential

numbers of amino acid combinations exist simultaneously. It is the

interface at the enzyme level between the quantum realm and the

physical that accounts for how enzymes can single out the exact

targeted

amino acid chain from the infinite possibilities that is needed at

the precise needed moment.

Dr. Stuart Hameroff has suggested that the microtubules of the human

cell, which move in mysterious, rhythmic ways - dissolving and

reappearing, yet structurally active in the contractile mechanism of

the cell membrane - should be considered as bio-resonators. He

points out that their outer layer is translucent and light

refractive, admitting ultraviolet light into the tube. Once inside

the tube, this light (photons) could be resonantly amplified by the

microtubule and be transmitted as an active regulatory factor in all

cellular processes.4

Photons are what make up the electromagnetic field induced by

electron flow through closed circuits. Bjorn Nordenstrum and Robert

O'Becker have both demonstrated that the body possesses closed

bioelectric circuits. The flow of electrons through these circuits

produces an electromagnetic field. Photons are what make up the

electromagnetic radiation of electrons. Just as flowing electrons

produce an electromagnetic field, electromagnetic fields are also

able to induce electron flow through closed circuits. This means

that there is a constant interchange of electrons and photons within

the body where one system has direct influence over the other. The

flow of biophotons and electrons in the body provides the micro-

electric currents that are responsible for all of our biochemical

processes. All metabolic functions involve a flow and transport of

electrons. The orchestration of these energetic processes are

directed by the resonant signaling of biophotons and explains the

many

metabolic processes that occur at lightning speed, well beyond what

can be accounted for by simple chemical interactions.

Bio-resonance provides the mechanism for electron communication and

interaction that is the catalyst for all biochemical processes.

Resonant frequencies travel through the body along cell membranes,

through bi-polar water molecule chains, along protein chains,

through the electrolyte rich connective tissue reaching every nook

and corner of the body. The communication pathways are the critical

junctions in determining the quality of information transfer. Alfred

Pischinger was one of the first scientists to fully study and

explain the importance of the connective tissue, which he referred

to as the " Ground Regulation System, " or " Extracellular Matrix. "

The Ground Regulation System (GRS) connects all cells in the body

through a mesh of high-polymer sugar-protein complexes, mostly

proteoglycans (PGs) and structural glycoproteins like collagen and

elastin (fig. 1). The transfer of nutrients and oxygen from the

arteries to the cell depends on the extracellular fluid. Nerve

supply to the cell is also seen via terminal autonomic axons with

their blind endings in the extracellular matrix. Cellular waste is

carried away from the cell via the extracellular fluid and

transported to capillaries and lymph vessels. This sponge-like

matrix also stores toxins and serves as a buffer to prevent damage

to vital tissues. A heavy onslaught of toxins can be stored in the

matrix and then released at a rate that the detoxification organs

can handle. This reduces the stress on the liver and kidneys as well

as toxin-sensitive tissues such as the thyroid, pancreas, and

nervous system.5

 

Fig. 1

The extracellular matrix is a redox system. The generation of energy

from oxygen through ATP synthesis creates an excess in extracellular

electrons and protons in the form of oxygen and hydroxyl radicals.

The energy released in antioxidative enzymatic processes can be

taken up by the water-sugar polymers of the extracellular matrix.6

The resulting heat is stored and used for the further stimulation of

biological processes and homeostasis is thereby preserved.

The extracellular matrix can be damaged by an overburdening of

toxins from the environment and a lack of supportive nutrients. In

both cases, the primary culprit is free radical oxidation and

chronic inflammation issues. The toxin storage capacity of the

extracellular matrix becomes exhausted and the buffering systems

begin to fail. Toxins become impregnated in the tissue, the organs

become damaged and cellular metabolic processes become altered.

Once the extracellular matrix is compromised, the transmission of

intercellular information is disrupted. Intracellular communication

depends on coherent biophoton resonance reaching target sites

throughout the body. The accumulation of toxins within the

extracellular matrix creates a chaotic interference pattern that

derails biophoton resonance transmission at the level of DNA.

Fortunately, the body uses a multi-channel system for sending

information signals. The body conducts signals through nerve paths,

protein chains of the tissue and through the meridian channels. Just

as the various organs and tissues of the body have their own unique

resonant oscillation pattern, the meridian system has its own unique

frequency signature.

Quantum Level Stressors That Provoke Carcinogenesis

Free electron " radicals " can travel through lead. They easily pierce

through cell membranes and can break off sections of DNA strands.

Prolonged exposure can do great damage to genes, which in turn

derails DNA communication, RNA transcription, enzymatic processes,

as well as mitochondrial respiration mechanisms. The P-53 gene,

which is very sensitive to redox status, can become damaged or

inactivated and fail in its function of signaling the cell to repair

itself or to self-destruct. In short, rogue electrons create rapid

degeneration at the cellular level leading to genetic mutation and

provokes carcinogenesis.

A large number of chemicals and external electromagnetic fields also

have the capability of changing the internal and external

environment of cells and can lead to the polarization of tissue.7

Once a cell becomes genetically damaged its electrical polarity

potential changes significantly. 8 The shift from a high negative

potential to a very low negative potential causes the cell to lose

contact with the overall regulatory system. Cellular signaling via

HCM molecules and biophoton resonance becomes weakened. The cell

become energetically stagnant and biophoton emissions become

chaotic. The cell loses its specific resonance signature and de-

differentiates and becomes neo-plastic. These de-differentiated

cells become embryonic and as such will grow uncontrollably.

Through Dr. Robert O. Becker's work we find the extraordinary

possibility of cellular regeneration. Becker has demonstrated that

salamanders are able to re-grow missing limbs through changes in

polarity at the tissue edge of the missing limb. Becker has further

demonstrated that the presence of tissue cells at the sight of

injury repair are actually from mesenchyme cells that have

transformed into needed tissue cells. This is understandable when

one considers that the body is a hologram, where every cell and

indeed every biophoton contains all the necessary information of the

whole organism. The template for the whole organism lies within the

energetic blueprint. With the right polarity applied to the end of a

severed limb regeneration is possible as molecules and cells follow

the template of the energetic blueprint.

Becker explains the regeneration process by cell dedifferentiation

followed by redifferentiation. Dedifferentiation of cells, for

example, means that a red blood cell can lose its unique function of

being a red blood cell and can redifferentiate or transform itself

into a muscle cell, a nerve cell or a connective tissue cell (fig.

2). It is the biophoton-field of energy that provides the vibratory

frequency that distinguishes one type of cell from another.

Dedifferentiation and redifferentiation are cellular responses to

changes in biophoton-field resonant patterns on the molecular level.

 

Fig. 2 - The Body Electric, Becker

Kikuo Chishima, Professor of the Nagoya Commercial University,

Japan, found that under pathological conditions erythrocytes show

transitions into cancer cells, neoplasmic cells, all kinds of

cellular elements in inflammatory regions, even into pus, and into

the tissue elements of regeneration or wound healing.9 According to

Chishima, erythrocytes generally show no signs of differentiating

into other kinds of cells while they are circulating in living blood

vessels, but when they are physiologically, or pathologically

extravasated into interstitial spaces of living tissue where the

circulation of blood is stagnated or stopped, they begin to

differentiate into other kinds of cells according to their

environment or local vibratory resonance.

This is the Impregnation Phase according to Dr. Hans-Heinrich

Reckeweg's homotoxicology model. Degeneration quickly follows as

stagnation causes oxygen depravation and the cell's oxygen dependent

metabolism mutates into one of anaerobic glucose dependent energy

production (glycolysis) . Alterations in cellular enzymes and

genetic damage is the beginning of the Neoplasm Stage according to

Reckeweg. It is here, at the level of the ECM, where toxin induced

stagnation causes normal cells to loose their specific biophoton

resonance and dedifferentiate into embryonic cells. These embryonic

cells have no specific frequency oscillation that provides them with

functional instructions. Their membranes don't line up in the

normal, specific ways, and they form a jumbled mass instead of

useful architecture. 10

The ability of some animals to regenerate missing limbs is dependent

upon the amount of negatively charged electrons they are able to

produce at the site of injury. The accumulation of negative charge

at a particular location requires that there is a flow of current,

which implies the presence of a closed electrical circuit. All

electrical currents generate a magnetic field around themselves,

which convey information in its fluctuations. Electromagnetic

radiation is made up of photons. Photons, or rather biophotons, are

able to induce a current that sets electrons in motion. If it is a

lack of biophoton communication that provokes carcinogenesis, then

the ability to accumulate biophotons at the site of malignancy can

be the key to reversing the process. In " The Body Electric, " Becker

points out that those animals that regenerate best are least

susceptible to cancer. He cites studies by G. Andres and M. Rose

that proved that these internal cellular regeneration guidance

systems could also control cancer. The key to regeneration lies in

the organisms ability to quickly generate negative electrical

potential at the site of injury (fig. 3).

 

 

Fig. 3 - The Body Electric, Becker Cancer cells have a very low

potential of -10 mV, compared to normal cells (fig. 4).

 

Fig. 4 - Membrane Potential in mV (Data from Bingelli and Weinstein

1986)

At this level cancer cells are electrobiologically inert. Dr. Becker

hypothesises that cancer cells are stuck in a state of incomplete

dedifferentiation and the application of small negative currents

causes a complete dedifferentiation to occur. Once the cells are

completely dedifferentiated normal processes in the body turn them

into healthy mature cells.11 The application of low levels of DC

current into low energy cancer cells has been demonstrated by both

Dr. Rudolph Pekar and Dr. Bjorn Nordenstrom to cause

redifferentiation of human cancer cells into normal cells.

When the brain reacts to any stimulus, it produces a wave of

electrical activity.12 Mental processes can influence electrical

properties as seen in polarity reversal in hypnosis and anesthesia.

Every mental command, every thought, every feeling, conducts

bioelectrical pulses to every cell in the body.

Stress and Negative Emotions

Stress and negative emotions can cause an acute stimulation of the

sympathetic nervous system leading to a cascade of hormonal

responses that can also effect changes in cellular polarity.

Clinical experience reveals the presence of an unresolved emotional

issue behind the majority of cancer cases. In addition to employing

Quantum Medicine protocols to the determination of the stressors

that provoke carcinogenesis, the presence of unresolved emotional

traumas and subconscious self-sabotaging patterns must also be

identified.

Chloe Faith Wordsworth developed a system called Holographic

Repatterning, that utilizes bio-kinesiology to access and release

emotional trauma patterns in the body. Holographic Repatterning is a

very effective method for quickly identifying emotional and

psychological stressors.13 The way we react to an event is recorded

in our molecular matrix. If each cell contains all of the

information for the whole organism, then our experiences, good or

bad, are also recorded on a cellular level. Those experiences that

we perceived as life threatening, where we were not able to resolve

the conflict or dissipate the energy of it, may continue to resonate

within the memory banks of the crystalline and water molecule

matrix. The matrix memory can alter our behavior or our belief about

ourselves as a result of the earlier, traumatic experience. These

feelings all have a resonant frequency signature that continue to

vibrate throughout our being. This energetic disturbance can upset

neurohormonal pathways in our body, constrict the energetic flow to

cells and upset DNA signaling.

The area of the body that has been energetically weakened by an

emotional experience or is harboring the resonance of a negative

emotion is often the same area found to be energetically stagnant,

prone to toxin accumulation, and the site of malignancy.

Animals functioning primarily from the reptilian brain response to

trauma are able to reset their sympathetic nervous systems almost

immediately. Higher mammals with developed limbic processing respond

to stress or trauma with an integrated social response. They tend to

travel in groups and will alert and protect each other. They also

resolve the fight, flight or freeze response within a short period

of time.

Humans containing the cerebral cortex impose logic into the alarm

response. Instead of reacting instinctually to a stressful or

threatening situation we stop to ponder the age old question, " why

me? " We are the only species that relives the situation in our minds

over and over again (fig. 5).14

 

Fig. 5

Replaying the unresolved emotional conflict over and over in our

minds generates an outflow of frequency vibrations throughout our

body. Various organs are sensitive to specific emotional vibrations

and will " resonate " in response to these thoughts. For example, when

thoughts of anger are dominant it is the liver that becomes over

activated and loses coherence. Strangely enough, it is not always

the liver that displays the symptoms of this stress. Through the

Chinese system of the Five Elements it can be seen that the stress

to the liver, which is within the Wood Element, places an energetic

stress on the Fire Element. Stress to the Fire Element may show up

symptomatically as gastrointestinal complaints (fig. 6).

This points to the need for careful evaluation of the symptoms and

their underlying causes. Without addressing the underlying

unresolved issue of anger from the example above any therapeutic

work done around the gastrointestinal complaints will only provide

short-term relief at best.

Quantum Medicine protocols that include techniques for identifying

and resolving these underlying emotional stressors provides a true

body-mind healing system.

 

Fig. 6

Unraveling the Stressors Behind Carcinogenesis

Clinical experience reveals several primary stressors that provoke

carcinogenesis:

Lousy Diet

Stress and Emotional Upsets

Pathogenic Load

Environmental Toxins

Geopathic Stress and Radiation Exposure

 

These factors all contribute to a loss of coherent biophoton

communication. A lousy diet in no way diminishes the horrific

problems we are facing from environmental toxins and exposure to low

level environmental frequencies (ELF), both natural and man-made.

Toxins hinder the unrestricted flow of energy through the ECM and

introduces wrong electromagnetic oscillations leading to genetic

instability. 15 Exposure to these substances puts a great deal of

stress on the body's elimination processes. Detoxification pathways

are the body's first line of defense against the onslaught of toxins

from the environment, including what we put into our mouths. From

this standpoint it makes sense to ensure that we are eating a diet

rich in nutrients needed for the proper functioning of elimination

processes and one that contains as few toxins as possible.

The stressors that provoke carcinogenesis is more a question of what

is missing rather than what we have. From the standpoint of the

Quantum Medicine model it is the precursor nutrients that are not

available that derail the body's ability to de-toxify itself. The

ability to detoxify is key to maintaining homeostasis within the

ECM. Homeostasis within the ECM is the key to proper biophoton

communication and the efficient functioning of the body's self-

regulating mechanisms.

If carcinogenesis is viewed as resulting from the damage done to DNA

and cellular metabolism by free radical species, then the stressors

that provoke carcinogenesis must be viewed as the contributing

factors behind the lack of antioxidant protection.

Once carcinogenesis becomes diagnosable, significant genetic damage

has already been done. A full blown antioxidant therapy program will

certainly help to prevent further genetic damage, but it will not

necessarily reverse active cancer. The key lies in determining what

protective mechanisms failed and why.

In The Quantum Medicine Professional' s Guide there are listed 5

pathways to degeneration based on a modification of Dr. Helmut

Schimmel's basic pathogenetic patterns. The pathogenic patterns

start with the duodenum (fig. 7).

 

Fig. 7

Irritation to the duodenum begins with an imbalance in pH (fig. 8).

A diet high in junk food and low in fresh produce is guaranteed to

deplete the body's reserves of alkaline buffering minerals. This in

turn acts to lower the stomach's production of hydrochloric acid,

which is needed for proper digestion and is an important first line

of defense for invading pathogens. A resulting infection or

irritation of the duodenum results in blockages of the liver

detoxification functions, lymphatic congestion and poor functioning

of the pancreas. The reduction of bile salts due to depleted mineral

reserves affects fat metabolism. Poor fat metabolism and reduced

pancreatic enzymes leads to partly digested food entering the

digestive tract, which ferments and putrefies resulting in

dysbiosis, constipation, and accumulating toxins being reabsorbed

into the liver and into the blood stream.

Acidosis induced dysbiosis can cause intestinal bacteria to become

hostile, which puts a strain on the immune system. Intestinal

irritation and dysbiosis causes the immune system release of nitric

oxide, which is in itself a free radical species. Byproducts of

cytochrome P450 are also free radical species and can do more damage

than the original toxins themselves if not neutralized by phase II

conjugation processes. When duodenitis blocks the biliary ducts and

the liver is unable to adequately remove toxins they become impacted

in the ECM and lymphatic system. The resulting reactive oxygen

species can damage the liver, the endocrine, immune and nervous

systems.

The GALT immune response to foreign substances entering the

intestines is predominately one of pro-inflammatory reactions in the

mucosa causing chronic activation of the TH2 lymphocyte subsets.

This results in the suppression of the TH1 subsets, which are

responsible for immune responses against intracellular microbes, NK

cell activation, and apoptosis of infected or mutant cells and

tumors. In short, intestinal toxicity is a double-edged sword

causing the release of free radical species on one hand and

suppressing the carcinogenic immune response on the other.

Pancreatic tissue and thyroid cells are particularly susceptible to

damage caused by toxins. Toxins in the pancreas can result in the

dysregulation of insulin, which can affect the basal metabolic rate

and other hormone functions. Impaired liver detoxification pathways

can result in the inability of the liver to convert T4 to T3. An

insufficiency in T3 can impair mitochondrial production of cellular

fuel (ATP). Optimal mitochondrial functioning is critical to

supplying the energy that drives all metabolic processes. Inadequate

mitochondrial output will seriously impair liver phase I and phase

II metabolic detoxification processes. Unconjugated toxins from the

liver become impregnated in the skin, fatty tissue, and the

connective tissue (ECM) and results in cellular degeneration,

mutation, and neoplasia:

 

Fig. 8 - Dr. Stephen Linsteadt, N.H.D. © 2002

Key Steps to Identifying Stressors

Systematic measurements of conductance at specific meridian points

provides a window into the ECM (fig. 9). The ability of low

electromagnetic charges to travel unimpeded along a meridian pathway

provides a measure of the status of the electrolyte rich

extracellular fluid. Low conductive measurements are generally

associated with degeneration of the associated meridian organ or

regulatory blockages within the ECM itself or both.

 

Fig. 9

Resonance generators can be added to the circuit in order to provide

a frequency oscillation that will act as a stimulant to the organ or

system involved in dysregulation. The electromagnetic oscillation,

when in resonance with the particular bioresonance frequencies of

the organism, will induce an influx of energy to the specific

resonance matched organ or system. When a resonance match is

achieved, the increase in regulative potentiating energy will

immediately register as increased conductance along the organ

specific meridian channel.

Inverse resonance oscillations have the effect of canceling out

disturbing energy fields within the ECM and along the specific organ

related meridian channel. A particular toxin or pathogen can be

placed into the circuit of a resonance oscillator and when the

inverted resonance frequency energizes the tested meridian it is a

good indication that the tested substance is one of the culprits

causing dysregulation within the ECM.

Different orthomolecular substances can be placed in the circuit and

provide diagnostic information concerning what is needed in the

system to bring about harmonization. For example, a low conductance

value along the acupuncture point related to metabolism may

normalize when the coenzyme form of the B vitamins are added to the

circuit. If other mitochondrial resuscitating nutrients such as

CoQ10, reduced glutathione and alph-lipoic acid are added to the

circuit and the conductance increases to the normal value, one can

be sure that there is a problem in mitochondrial metabolism.

Once mitochondrial metabolism is resuscitated, the detoxification

pathways of the liver can be tested in the same fashion. Once

specific nutritive deficiencies are found it is important to also

test for the precursor nutrients required for the proper synthesis

of these pathways (fig. 10 and 11).

 

Liver Detoxification Pathway Phase I

Cytochrome P450

 

Fig. 10

Liver Detoxification Pathway Phase II

 

Fig. 11

In a systematic approach one can determine the overall functioning

of the ECM and determine what toxins, heavy metals, pathogens and/or

missing precursor nutrients are contributing factors to the causal

chain of carcinogenesis.