Strannik Virtual Scanner

Operation Manual

Mimex Montague Healthcare Limited

Mulberry House, 6 Vine Farm Close, Cotgrave, Nottinghamshire, NG12 3TU. UK
Tel : 0044 115 989 9618 / Mobile : 0044 7885 755847
elena.ewing@mmhcl.co.uk
graham.ewing@mmhcl.co.uk

Company Registered in England & Wales No: 8439352

The "Strannik" Complex: Subconscious (Unconscious) Mind

Diagnostics and Correction.
Basic Principles of Clinical Application.
Strannik Operating Manual
Agenda
1. Introduction
2. Installing the Program
3. What is Virtual Scanning technology and how does it work?
4. Diagnostics - Psychological
5. Diagnostics - Physiological
6. Treatment
7. Summary/Conclusions
8. Regulatory Status
9. Payment
Appendix 1: Bibliography
Appendix 2: Additional Books & Training Courses
Appendix 3: Psychological Diagnostics Vocabulary
Appendix 4: Systems and Organs Reported
Appendix 5: Definitions
Appendix 6: Patient Enrollment Information

Appendix 7: patient Treatment Notes

Preface
The Strannik software program was developed by the medical doctor, physicist,
mathematician and medical researcher Dr Igor Gennadyevich Grakov (Technical Director,
Mimex Montague Healthcare Limited) following an initial program of research at the
University of Novosibirsk in the early 1980s which involved investigating the medical
application of industrial lasers. Dr Grakov identified that this use of monochromatic light
could induce a biological response. It was from such beginnings that Strannik technology
was developed (see www.mimex.ru).
This project has continued to be developed. In the late 20th century and into the 21st
century Dr Grakov has been assisted by Dr.Y. Borovleva, a neurologist; and
Dr.Yu.Spassky, computer programmer; although Dr Spassky has now moved on to the
successful extension of his career with other companies. In early 2014 Mimex and
Montague Healthcare merged in order to enable the merged entity to entertain discussions
with potential investors.
The technology has been presented in several versions to date. Please note that further
versions of the technology are likely although none are likely to involve fundamental
changes to the basic algorithms upon which this technology is based. Originally, this
technology comprised several individual programmes e.g. the psychological profile
(Strannik for Business) and the physiological profile (Strannik for Health); although both
involved the exact same test procedure. Both programmes are now incorporated into this
one software programme. This appears to illustrate that our psychology and physiology are
two-sides of the same coin i.e. that pathological change is accompanied by psychological
change e.g. to cognition and behaviour and/or that psychological change is the consequence
of pathological development. A demonstration of this technology can be viewed on
http://www.montaguediagnostics.co.uk/pmwiki.php/Main/Video
Practitioners may not wish to dwell upon the significance of such developments. They may
not be interested in ther psychological aspects of this technology and may wish to dwell
only upon the ability to screen the patients health and/or to correct autonomic dysfunction.
In such cases the practitioners should choose from the agenda the appropriate selections
which are likely to be of interest to them.
Finally, Strannik practitioners should be trained to use this quite complex technology.
MMHL is able to provide training by Skype and email. Practitioners should recognise that
this needs to accompanied by an in-depth training course to be run by MMHL. They should
plan accordingly. In the event of queries related to the installation of the technology or
interpretation of test data please contact Dr Elena Nikolayevna Ewing, Medical Director &
Training Manager (elena.ewing@montaguehealthcare.co.uk).

5th December 2014

Graham Ewing, Chief Executive

Foreword
All aspects of the bodys function, both physiological and psychological, are essentially
biochemical. Strannik Virtual Scanning & Strannik Light Therapy are based upon a unique
understanding of the relationship between sensory input, the brain, the autonomic nervous
system and physiological systems, and how such changes influence cellular and molecular
biology, i.e. of genotype and phenotype. This is significant because the emergence of
pathologies influences color perception.
Alterations to genotype and phenotype influence our health and behavior. Gene profiling,
in particular, has been adapted for use in matching personality profiles e.g. in gene dating,
although this excludes the very considerable influence of phenotype. Accordingly, changes
to Color Perception can be adapted with diagnostic and therapeutic effect in both
Physiology and Psychology.
Virtual Scanning has evolved significantly since Grakovs first prototypes. Different
versions of the technology are available. In addition other versions of the technology can be
developed according to market or client requirements e.g. biofeedback technologies using
light and colour as the feedback modality have been used in the educational market for
many years however these technologies are experiential. None of these competitor
technologies are based upon a fundamental recognition or understanding of a core scientific
principle.
Strannik PPS is a system for the diagnosis and support of the unconscious (subconscious).

Graham Wilfred Ewing

 copyright

1.
Introduction
Strannik is a technology which is used to assess and correct the subconscious (unconscious)
mind which controls the human body. The following present-day knowledge was taken as a
starting point: the subconscious (unconscious) mind ensures psychophysiological
homeostasis however, while interacting with the environment, errors are introduced into the
bodys regulatory mechanism on a daily basis, thereby changing the stability and/or
function of the organs. This deteriorates the quality of proteins which are produced in the
body e.g. diseases, fat accretion and aging ("destabilization" is the generic term for this
complex of problems).
The brain processes sensory input and stores these experiences as memories. Extremes of
sensory input, which we experience as stress, influence the autonomic nervous structures.
We can use colour to influence the function of the autonomic nervous system e.g. red
influences the sympathetic nervous system and raises heart rate whilst green influences the
parasympathetic nervous system and slows heart rate.
Most medical conditions, diseases, drugs and vaccines influence our colour perception.
They influence the stability of the autonomic nervous system. Accordingly changes to
colour perception must be markers for the many and various pathologies which are
characteristic of common medical conditions, and which are caused by diet, diseases,
drugs, vaccines, etc. For example how the occurrence of diabetes is accompanied by
changes to blue-yellow colour perception.
The prevailing healthcare model or paradigm has yet to explain why we remain healthy and
why we develop morbidities. It has yet to explain the influence of nutrition, viruses,
vaccines, and drugs upon the bodys regulated function. Every drug depends upon the
autonomic nervous system for its effect therefore the solution must depend upon
understanding in greater detail how the brain regulates the autonomic nervous system i.e.
how proteins are genetically expressed, how these expressed proteins subsequently react,
how the bioluminescence of such reactions influences the normal spectrum and intensity of
colour perception, and how such physiological changes influence our function.
The Russian researcher I.G.Grakov has mathematically modelled the autonomic nervous
system. It uses measurements of colour perception as the data sets for the model and links
molecular biology, cellular biology, the function of the organs and organ networks (the
physiological or functional systems) to the function of the brain. As outlined earlier,

changes at the molecular level induce changes to colour perception i.e. proteins emit
biophotons of light during the process of reaction with reactive substrates. The intensity
and colour of the light (bioluminescence) emitted can be used as a biochemical marker.
Moreover this emission of light influences colour perception therefore a cognitive test can
be used to provide the data sets for Grakovs mathematical model. The consequence is a
test which can determine or screen for the emergence and progression of pathologies from
the earliest pre-symptomatic origins, to determine the genetic and phenotypic components
for each medical condition, to determine the common pathologies in each organ (5-15
pathologies in circa 30 organs are reported). In addition, the technique is non-invasive,
results are available in circa 20 minutes and the cost of the test is significantly lower than
that of genetic screening or indeed any other form of medical screening or diagnostic test.
Moreover as the model links molecular biology, cellular biology, the function of the organs
and organ networks then so too must it diagnose at these levels, and it does so in Strannik
Virtual Scanning technology i.e. Strannik Virtual Scanning (SVS). Such a model can be
used predictively to illustrate to patients what will happen to them if they continue with
their current unhealthy lifestyle(s). This has immense value because an estimated 90% of
morbidities are considered preventable i.e. they are the consequence of poor lifestyles.
This technology also has therapeutic potential. The recognition of the pathological profile
or health report can be used to determine the precise parameters of a Biofeedback-type light
therapy i.e. Strannik Light Therapy (SLT). The Strannik solution is intended to detect
and correct the destabilization process (autonomic dysfunction) taking into account that the
color ensures over 90% of control by driving and giving direction to physiological
functions.
The background to Strannik technology has been outlined extensively in a series of articles
published by Graham Ewing (see Appendix 1 bibliography). This augments the early
published work by Anokhin, Vysochin, Grakov, and others.

2.
Installing & Running the Program/incl Therapy Module
2.1 Introduction
The software has been redesigned to run on Windows 7 or Windows 8. The recommended
screen resolution is 1280 x 1024 (the height is not less than 1024 pixels).
The white flash drive has all necessary files for installation of Strannik Virtual Scanner
program as well as Strannik Light Therapy. Insert it in your computer. After installation
you may remove this flash drive from your computer.
The black flash drive is the access key (Sentinel HASP Protection System) for you to
access and use Strannik Virtual Scanner. To be able to access Strannik Virtual Scanner
program this key must be inserted into USB port of your computer. Please note: this key
will be automatically activated the moment you access Strannik Virtual Scanner program
first time and it will be automatically switched off after a month (1, 2, 3, 6 months
according to practitioner contract). See section 9 of the Operating Manual.

Installation Problems
Some antivirus programs might block access to installed program - in this case, you must
manually go into the quarantine section and restore the file to unblock access i.e. the
program may not install properly due to other program e.g. Norton anti-virus. Norton antivirus may detect parts of the program as a virus or unwanted program. This is not a
problem with the Strannik program and can usually be overcome. It is a problem of the
operating parameters which have been included in the Norton program. In such cases we
suggest to contact Dr Elena Ewing who will guide you through this process. Guidance
notes will be issued in the future.

2.2 The Installation Process

1. Insert the white flash drive and you will see three files:
Strannik Install.exe;
k-lite_codec_pack_1075_basic.exe;
treatex_eng_setup.exe
2. Launch Strannik Setup file (Strannik Install.exe).
3. Follow the installation instructions.
4. In case of problem with registering VDIAG.AX during installation choose "Ignore".
5. Launch K-Lite Codec setup (k-lite_codec_pack_1075_basic.exe) and follow instructions
to install all necessary video codec for Strannik if necessary.
6. 7 new shortcuts will appear on your desktop:

Strannik EU (it will launch your Strannik Virtual Scanner program);

Strannik 10 (you may delete it);
Activation Module (you may delete it);
Strannik Codec Pack;
Strannik Client import;
Strannik Key Drivers;
Strannik Key update

7. Launch Treatex_eng_setup.exe file to install Therapy module. (This file you will give to
your patients together with individual treatment files (.dat4 files))
8. New shortcut "Correction Module(Ex)" will appear on your desktop.

9. You are ready to start work with Strannik Virtual Scanner program (to enter the program
- insert the black flush drive into USB port).

2.3 Strannik Light Therapy: Installation Instructions for Patient

To install your individual VS Light Therapy on your computer follow the instructions
below:
1.
2.

Go to your flash-drive (or CD-drive) and select "treatex_eng_setup.exe", then

double-click on it to launch treatment program.
If warning message appears - simply select "This program installed correctly".

3.

Now you have new icon/shortcut "Correction module" on your desktop.

4.

Right-click on "Correction Module", left-click "Properties"/"Shortcut"/"Advanced",

then "tick" box "Run as administrator"/"Ok"/"Apply"/"Ok"
Double-click on "Correction Module", say "Yes" for warning message from your
computer security (you will have to do it every time you are starting your treatment
program).
Click "Add patient", new window appears, go to "Look in", bring up drop-down
menu and select location of your flash-drive (or CD-drive), then select your
individual treatment ".dat4" file and "open" it.
Now you will see your name on the left-hand side and list of organs on your righthand side.
Your therapy course is ready to run.

5.

6.

7.
8.
9.

To initiate your therapy click "Start", read the warning message, click "Start" again,
your therapy will run. It will stop itself, according to your individual treatment time.

3.
What is Strannik Technology & how does it work?
The Strannik software technology, which comprises Strannik Virtual Scanning & Strannik
Light Therapy, is split into three or four parts: the test, the processing of the test results and
the provision of the test results (psychological and physiological), the selection of the light
therapy and the provision of the biofeedback type light therapy.

The test is a games-like procedure which requires the patient to study and memorise a
selection of colours in the computer-based test. It requires the practitioner to insert the
patients identifying details, birth date, weight (weighed on a suitably calibrated set of
scales to within +/- 1 kgs) and gender. The patient presses the ENTER key and the test
begins. The task for the patient is to study and memorise the colours of a video which is
shown to the patient for 15 seconds. At the end of this period the colour selection is altered
by the imposition of a colour filter. The task for the patient is to use the mouse to select
colours from the colour palette and to re-establish, to the best of their abilities, the original

colour balance. The test takes typically 2-3 minutes and is repeated abt 4-5 times with
different colour selections.
N.B. Each patient should have been allowed a short period, typically of 5 minutes duration,
to practice before undertaking the test.
Upon completion of the test, the data is processed and the patient is provided with the test
results and/or alternatively with the therapy programme which is provided by the
practitioner via a flash-drive or CD i.e. to be installed on their home computer. Their task is
to watch the computer programme, a selection of flashing lights, for circa 1-2 times each
day.
A selection of demonstration videos (illustrating version 7G) is available on
http://www.montaguediagnostics.co.uk/pmwiki.php/Main/Video
The results of the analysis: of differences between the subjective reality proposed by the
external environment (in this case, by the computer moving image) and the objective
reality created by the observer based upon his/her ability to complete the test i.e. their
emotional and/or physiological state; are used to detect and develop an information map of
the observer's psychosomatic and physiological condition at a point of time which may be
of value regarding the provision of further psychological or physiological care.
The test process and interpretation of test results are summarized in the following series of
figures 1-35. The process is relatively simple although the interpretation of results is more
complex.

Figure 1: Registration: Add Patient

Figure 2: Registration: Add Patient Information then Press Diagnostics

Figure 3: Registration: Press ESCAPE to avoid this information video

Figure 4: Diagnostics: Press Enter

Figure 5: Test Process: Video

Figure 6: Test Video: Filter

Figure 7: Test Video: Recovering the original colour balance

Figure 8: Test Video: Recovering the original colour balance/best effort

Figure 9: To Process Test Results Press the OK Button

Figure 10: Processing Results

Figure 11: Report Completed Successfully

Figure 12 (a): To Visualise Test Results Press View

Figure 12(b):

Figure 13: Initial Display: Brain (Double-click on the Brain Functions graph)

Figure 14: Example Report of Brain Functions

Figure 15: Results: Peripheral Nervous System

Figure 16: Example Report of Pathologies in Each Organ

Figure 17: Report of Cell Morphology (possible markers) in organs

Figure 18 (a): To Select Different Organs

Figure 18 (b): To Select Different Organs

Figure 19: To Evaluate the Prevailing Cell Morphology in Each Organ

Figure 20: To Evaluate the Prevailing Pathologies in Each Organ

Figure 21: To Evaluate the Prevailing Processes in Each Patient

Figure 22: Physiological Significance of the Pathologies

Figure 23 (a): Press Summary to see Most Destabilised System

Figure 23(b): Press on Most Destabilised System to see Most

Dysfunctional Organ(s)

Figure 23 (c): See List of Organs including Most Destabilised Organs

Figure 24 (a): Report of PFS & Systemic Instability

Figure 24 (b): Report of PFS & Systemic Instability: Predictive

Figure 25 (a): Summary Report: Example male

Figure 25 (b): Summary Report: Example female

Figure 26: Report of Systemic Instability

Figure 27: Psychological Report 1: Preference to Action or Information

Figure 28: Psychological Report 2: Communicability

Figure 29: Psychological Report 3: Personality Profile:

rational/emotional

Figure 30: Personality Features

Figure 31: Selecting Therapy: Select Appropriate System & Dose

Figure 32: Selecting Therapy: Therapy Files Processed

4.
Diagnostics
SuperVisual technologies (figures 1-12) based upon personal biological modeling were
used for diagnostic purposes for the first time in the world. This solution allows the
practitioner to show structural changes of patient's organs (see figures 13-26b) in the most
informative 3D graphic format. For the operator's convenience, these 3D graphic films
come with additional tools (markers, descriptions, bar graphs) which contribute to a better
quality of interpretation of the diagnostic results. These will be described in later chapters.

4.1

Analysis of Brain Function (see figure 14)

Those patients who feel comfortable exhibit a total deviation of up to 10 points from zero.
A higher deviation level gives evidence of certain problems.
Normal brain function charts shall be smooth and synchronous.
Saw-toothed curves show that the patient drank alcohol, took drugs or suffered
from psycho-emotional stress on the days before the diagnostic test.

Determine the dominant function of the patient: this function exhibits lower deviation
from zero.
Each age has its own dominant function:
under 15 yrs: perception; 15-30 yrs: imagination; 31-50 yrs: memory (and associative
thinking);over 50 yrs: information processing (decision-making, image application)
For example (see figure 14). The report shows: perception: +3 units; imagination: +17
units; memory: +25 units; and image application: +18 units. The patient has a total
deviation of >10 units in three functions which indicates the presence of a problem. The
dominant function is perception (+3 units), the most deviated is memory (+25 units).

Determine the deviation for each function:

If the deviation is 25-50 points (any function): there is susceptibility to unmotivated
emotional breakdowns.
If the deviation is > 50 points (any function): there is the susceptibility to neurotic
reactions.
Note: If all three lines on the diagram are parallel for a long interval this is an
indication that the test procedure has been undertaken incorrectly.
Assess the quality of brain function:
Positive function (+) is an excessive function whilst negative (-) function is a
selective function:
Perception:
Excessive perception: the individual needs additional information to understand
different situations.
Selective perception: the individual uses insufficient amount of information in
his/her daily life.
Imagination:

Excessive imagination: the synthetic imagination prevails.

 Selective Imagination: creative imagination prevails, the individual perceives and

transforms information in a very effective way.
Memory & Associative Thinking:

Excessive associative thinking and memory: high ability to memorise.

Selective associative thinking and memory: susceptibility to associative or

combinatory memory.
Strannik Virtual Scanning enables the practitioner to assess brain functions and detect any
deviations of information perception, processing, analysis and information processing rate
from the genetic and individual norms. Any function may be lower or higher than the
norm. Depending on the deviation value, functional changes may cause pathologic
stimulation, excitation, inhibition or paralysis of the electrochemical processes occurred in
the brain. In addition, the scanning detects a dominant function of the brain (this function
exhibits a minimum deviation). The predominance of certain brain functions is typical for
the specific age groups:
(i)
Predominance of Information Perception - under 15 yrs: Perception and
transmission of information.
In general, this function relates to our perception of our world. Sometimes, even so-called
"normal" people fail to appreciate colors, audio tones, tastes, smells and tactile senses.
Most people consider these main channels, which are used for communicating with the
outer world, as the reality. In the past observers believed that the perception of the
environment is a mandatory normality condition, but they failed to define the way it
happened. To perceive the reality at the present time, the individual shall receive it via the
communication channels used in his/her daily life. Only virtual reality enables us to
conduct the quantitative assessment of perceptual defects.
Excessive function shows that the individual always needs redundant information to
perceive different situations. For instance, to understand a poem this individual needs to
repeat it several times. This results in overloaded perceiving system (sense receptors sight, hearing, etc.) and involvement of multiple nerve tracts to transmit the information.
Insufficient function is evidence that regular shortage of information entering the
brain is required for other functions (imagination, memory, etc.). This shortage is
caused by dysfunction, but not actual unavailability of information. In this case, the
individual feels that the amount of data is excessive. Example: to understand something
the individual needs scant information. This results in incomplete and inadequate
conclusions and actions being made or performed by this individual who builds his/her
world on a poor basis i.e. an inadequate base of knowledge.

The individual with predominating perception (without or with low deviation as compared
to other functions) lives in his/her feelings. This is normal for a child, but absolutely
unacceptable for certain occupations.
(ii)

Predominance of Information Processing - 15-30 yrs: Imagination.

Your capabilities exist in your imagination i.e. a workshop of the mind. Imagination is able
to transform the intellectual energy into ideas, concepts and welfare. The function
manifests itself as the synthetic or creative imagination. The synthetic imagination is
used to make new combinations of available concepts, ideas and designs. Creating nothing
new, this function is commonly used for generalizing observations, as well as in education.
Most inventions originate from this function. Using the creative imagination, the
subconscious mind perceives and transforms all general or new ideas and establishes
contact with the subconscious mind of other individuals. Operating automatically, the
creative imagination needs positive emotional stimulus or stress. Great businessmen,
industrialists, financiers, artists, musicians, poets and writers owe their success to the
creative imagination.
When idle, the imagination fades without disappearing. The more the imagination is used,
the more efficient it is.
Excessive function shows that the individual operates redundant images. The image
(matrix, signal) means presentation of any situation in thinking codes. An increase of
function causes overloading of signals thus generating unnecessary redundant matrices
in the brain. Accordingly the imagination function is delayed and inefficient. The
formation of new matrices becomes increasingly difficult and reduces the capability to
produce new thoughts. In this case, people complain of lack of inspiration. The
combination of excessive imagination and diminished perception entails diseases of
sensory systems (hearing and sight).
Insufficient imagination function generates poor images. The individual is unable to
generalize or learn something new. Such people often "think about nothing".
When imagination is dominant it provides advantages to creative workers, but in other
cases, the correction is recommended. For example, the manager involved in the creative
activity neglects his/her direct functions.
(iii)

Predominance of Information Analysis - 31-50 yrs: Memory & Associative

Thought/Information Analysis

This function, of memory and associative thinking, emerged in the past. The ability to
perceive the present is one side of the reality however an inability to face the past is

evidence of misperception of reality. Associations between past events allow us to retrieve

feelings and memories which were previously recorded by the individual. The individual
draws parallels with his/her previous conclusions and problems. Associative comparisons
assist in learning, research activities and daily life.
Excessive function generally causes storage of large amount of unnecessary
information which is not required for the activity of the individual. His/her brain is
overloaded with unnecessary details such as the fragmentary unrelated data. The
retrieval of required data is hindered therefore the individual wastes too much time for
unnecessary data mining and grappling with trifling problems.
Insufficient function of associative thinking and memory reduces the amount of
information stored in the memory bank and results in poor retrieval of this information.
Such people often say they remember nothing. If dominant, this function will perfectly
suit the white-collar worker. On the contrary, the manager will waste much time
recalling similar situations, but not for making decisions.

(iv)
Predominance of Information Processing Rate - over 50 yrs: DecisionMaking/ Image Application
At present, scientists believe that the decision making process is connected by a flexible
information model formed in the control system of the brain. The "model of the required
future" is the highest level of the hierarchical control system. This flexible and dynamic
program enables the organism to deal with unexpected barriers preventing it from moving
along the path outlined by the main program. Correction pulses intended to reconstruct the
behavior plan will not assist in overcoming the above barriers. In this case the organism
relies upon information provided by the sensory organs which gives a signal to alter the
model (program). This results in minor corrections, deep reorganization and acceptance of
a new program. The modified or new program is used for further correction of behavior.
The program changes and correction of behaviour occurs.
Excessive decision making function requires excess amount of nervous connections
which are activated by the brain. The brain transmits repeated signals i.e. the individual
repeats one and the same thing to persuade his/her interlocutor.
Insufficient function involves an insufficient number of connections. The
transmitted signal is incomplete making the decision ineffective.
The manager with dominant decision making function achieves excellent results in his/her
office.
In Summary,

Alterations in the functional ratio result in dominant changes. In this case, old men revert
to a childlike state and young people start thinking as old men or even worse. As the brain
adapts to its environment, the dominant function may change under specific occupational
conditions e.g. blue-collar workers - perception; creative workers - imagination; whitecollar workers - associative thinking; managers - decision making function; the child acting
as a carer to a parent becomes prematurely mentally and physically mature.
Dominant functional changes may be attributed to many other reasons (in most cases) changes in relations between external and internal environment of human life activity. The
predominance of any function does not mean that other functions disappear. On the
contrary, they naturally act providing support to the dominant function.

4.2

Situation (personality), see the Section "Qualities of personality"

A persons psychological profile is influenced by their genetic profile which is considered

to be mostly an inherited property although genetic change occurs in response to infection
by bacteria, viruses and virus-like particles; to weight and age; and also to stress. This is
our genotype. By contrast the influence of the environment i.e. our phenotype, also
influences our behaviour. Both genotype and phenotype are essential components of our
psychological profile. This can be used to determine all aspects of our psychological profile
and hence our predisposition to actions e.g.

As illustrated in figure 27 the data can be used to determine whether someone is

more disposed to gathering information e.g. procrastinator, or who is overwhelmed by the
excess of information; or whether someone is more disposed to action e.g. we would expect
a younger person to be more active than an older person. We would expect action and
information to have similar values in a balanced person.

As illustrated in figure 28, it can also be used to determine essential personality

traits which could be of value in the workplace e.g. can the person work well as a member
of a team, would they make a good teacher, are they good communicators and would they
make a good manager. The numbers should be balanced in order to reflect a balanced
personality. The scale and significance of the test results: the less the number the less is
their imbalance.

Earlier versions of the technology reported in the book Virtual Scanning The
Next Generation of Healthcare Beyond Biomedicine? discussed how the emergence of

pathologies could influence the patients psychological profile and hence their ability to
start, develop and complete a task i.e. the decision-making progress comprises a sequence
of the following stages: intention wish will knowledge imagination
implementation prioritization - ability to act memory experience supervision effectiveness.

Figures 29 & 30 illustrate how this technology is able to define a wide range of
psychological traits. The full list of psychological traits reported is included in Appendix 3.
An earlier version of this technology expressed these psychological traits in positive and
negative terms e.g. (+/rational) joy, abstinence (devotion), patience, righteousness,
community, truthfulness, goodness, creativity, labour and inventiveness; and (-/emotional)
ignorance (obstinacy/stubbornness), sorrow, immoderation, desire, injustice, greed,
mendacity, envy, cunning, anger (resentment), hastiness, and guile (secretiveness).

Using the recognition that a persons behaviour may be influenced by their

genotype and phenotype i.e. that our behaviour is a function of our health; it was possible
in the earlier version of this technology to add one persons results to another i.e.
mathematical data is additive. This was able to determine e.g. (i) whether an interviewee
would fit seamlessly into a new team and/or whether the team would benefit from their
inclusion; (ii) whether someones subsequent behaviour was influencing their ability to
work within a team e.g. whether they were becoming disruptive; (iii) whether an employee
would work effectively under pressure.
It has been considered that the genes determine our psychological profile and our behaviour
yet there are many who consider that these aspects of our function are linked to the levels
of hormones e.g. of oxytocin, vasopressin, etc. Strannik Virtual Scanning illustrates that it
is not the genes which are significant but instead the nature and level of genetic expression
of the proteins (their level) and hormones which is significant i.e. it is not the genes which
are significant but instead what the genes do which is significant and by how much do they
do it (express proteins); and how this is influenced by the many and various environmental
effects/stresses which we experience during our lifetimes.

4.2.1 Interpreting the Data

There are 12 different pages of personality features listed in the psychological report (see
figure 30). Each set of features comprises a dark-blue signal and a red signal. The darkblue signal is the psychological consequence of genotype whilst the red signal is the
psychological consequence of our phenotype. We can express these aspects of personality
in different ways e.g. (i) in terms of our comfort state (genetic) and departure from this
comfort state (phenotype). (ii) Grakov has in earlier versions of the technology used the
terms rational (genotype) and emotional (phenotype). The significance of these signals is
outlined as follows:

(i)

Only dark-blue signals:

This is indicative of a Personality comfort state. Hereditary/genetic processes are present

without manifesting themselves. The innate regulatory mechanism copes with negative
environmental factors.
(ii)

Red signals are increasingly evident:

The Dark-blue signals exceed the Red signals. This is indicative of the failure of
the innate suppressive mechanisms to cope with environmental aggression.

The Red signals exceed the Dark-blue signals. This is indicative of an emergent
problem i.e. of failure of the innate suppressive mechanisms to cope with environmental
aggression. This would be accompanied by signs of abnormal or altered behaviour.

There are only red signals. This is indicative of a periodic pattern problem perhaps
affecting evening and morning diagnostics i.e. an emergent personality disorder arising
from the failure of the innate suppressive mechanism to cope with environmental
aggression. This could be seen as abnormal behavior "in general" e.g. as eccentric,
cantankerous, angry, moody, etc. A persistent personality disorder is associated with the
onset or emergence of disease i.e. the declining biological function of the body to express
proteins or deal with stress.

5.
Interpretation of the Test Results - Physiological.
The diagnostic results for the health of the patient are outlined in the following chapter.
Before proceeding it is essential to provide a definition of the terms which are used in the
test results:
SIGNAL (expressed as red and blue) this is a combination of chemical, physical and
biological processes that work towards the transition of an organ or a system from healthy
condition to a disease.
The following syndromes are general processes which are mainly expressed in different
organs and systems:
DEGENERATIVE PROCESS - the weakening of vital functions of cells and tissues.
CHRONIC FATIGUE the change in physical, chemical and biological characteristics of
tissues, as a result of stress(es), including psycho-emotional stress(es).
NEOPLASM the rise of cells groups of non-malignant or malignant character and also
any formation of new tissue.

FUNCTIONAL CHANGES - the accomplished volume of work by the organ or system, if

it is more or less than required.
ABNORMALITIES OF DEVELOPMENT - individual or genetically conditioned ways of
development and function.
INTOXICATION EFFECT - unhealthy symptoms which are conditioned by the influence
of harmful substances of external or endogenous origin (at present time or in recent past).
POST-STRESS EFFECT - the reaction of the organ or system rising from the influence of
any strong effects and which are accompanied by the reconstruction of the defensive or
recuperative powers of the organ, system and body.
AGE-RELATED CHANGES the tendency to equal biological and calendar age. As a
norm, biological age is less than calendar age, however if the biological age is equal or
greater than calendar age the processes of ageing are accelerated.
ALLERGENIC PROCESS the increased sensitivity of the tissues to any substance.

5.1

Pathological Signals (see Figure 16)

(a) The dark-blue signals are indicative of the status of the internal environment i.e.
they are indicative of genetic and psychological abilities of the organism to resist
the influence of the environment (phenotype). This includes hereditary problems.
An increase of the genotype signal indicates the declining ability of the organism to
express a particular protein.
(b) The red signals are indicative of changes resulting from the influence of the external
environment (phenotype). They arise from failure of homeostasis and are indicative
of acquired pathological processes.
Signals below 7-10 units are considered to be presymptomatic whilst those above 710 units are considered to be symptomatic.
In general a genotype signal below 7 units is considered to be presymptomatic and
of little significance. It is only when the genotype signal increases above 10 units
that it becomes significant.

5.2

Changes of Organ and Cell Morphology (figures 17 & 19)

The morphology of the organs changes in response to our lifetime of experiences i.e. as the
organism ages and also from the influence of hereditary and/or degenerative processes. The

innate compensatory abilities of the organism declines and changes become more stable
and explicit. The chronic state starts to predominate.
The following options (the colours surrounding the organs or as expressed on the pie-chart)
are indicative of changes of cell morphology (presented by markers as indicators of a
morphology state):
(i)

Green marker. Normal state.

(ii)

Red marker. Increased amount of blood vessels per tissue unit. Indicative of
inflammatory processes.

(iii) Violet marker. Decreased amount of blood vessels per tissue unit. Indicative of
sclerotic processes, heart attacks, apoplectic attacks, etc.
(iv) Light-blue marker. Accelerated function. Indicative of processes with functional
changes e.g. dyskinesia, etc; brought to the fore.
(v)

White marker. Delayed function. Indicative of processes with functional changes,

dyskinesia, etc. brought to front.

(vi) Dark-blue marker. Excess number of young cells. Indicative of neoplasia. Take into
account that the balance periodically tips toward young cells in 2-3 organs of each
individual.
(vii) Yellow marker. Excess number of old cells. Indicative of diminished functional and
adaptive abilities of the organ.
Periodic (unstable) morphological changes: if the colour surrounding the organ changes
e.g. from green to blue to green, the morphological changes are periodic or unstable.
Green marker other colour marker (see figure 19) green marker.
Persistent (stable) morphological changes: if the colour surrounding the organ changes
e.g. from green to red, the morphological changes are persistent or stable.
Green marker other colour marker (see figure 19).

5.3 Explanation of the Combination of Coloured Marker Signals:

Press "Control" (Figures 15 & 16)
(i)

Periodic morphologic changes plus only dark-blue signals.

Organ is in a comfort state. Hereditary processes are present without manifesting

themselves. Own suppression mechanisms cope with negative environmental factors.
(ii)

Periodic morphologic changes plus red signals are available.

The dark-blue signals exceed red signals. Indicative of failure of own suppression
mechanisms to cope with environmental aggression.
(iii)

Periodic morphologic changes plus red signals exceed dark-blue signals.

Problem. Morphology remains within physiologic limits. Indicative of failure of own

suppression mechanisms to cope with environmental aggression.
(iv)

Periodic morphologic changes plus only red signals.

Problem. Morphology remains within physiologic limits. Own mechanisms of

environmental aggression suppression are at the breaking point.
(v)

Persistent morphologic changes plus dark-blue signals.

Problem. Changed morphology. Hereditary diseases manifest themselves. Symptom of

abnormal development.
(vi) Persistent morphologic changes plus red signals are available, dark-blue signals
exceed red signals.
Problem. Changed morphology. Indicative of failure of own suppression mechanisms to
cope with environmental aggression. First symptoms of the disease.
(vii) Persistent morphologic changes plus red signals which exceed dark-blue signals.
Disease. Changed morphology. Failure of own suppression mechanisms to cope with
environmental aggression.
(viii) Persistent morphologic changes plus only red signals.
Disease. Changed morphology. Non-functioning own mechanisms of environmental
aggression suppression.

5.4

Assessment of Homeostasis and State of Functional Systems

(Figures 23 (a-c))

The functional systems are involved in homeostasis. The top box lists the physiological
systems.
Highlight one of the physiological functional systems. This will be accompanied by a list
(below on the lhs) of the organs which constitute the highlighted physiological functional
system. (In figure 23(a) highlighted physiological functional system is the system which
sustains optimal cell content of the blood). The organs contained in this particular
physiological functional system are: brain, pituitary gland, adrenal gland, blood and
peripheral blood vessels, musculoskeletal system, and spleen.
To see the most destabilized physiological functional system press SUMMARY in figure
23(a) e.g. maintains optimal sleeping pattern in figure 23(b & c); then select an organ
which has a dominant role in changes of destabilizing functional system in "Summary" e.g.
as highlighted in figure 23: EAR: 61 units. Strannik defines the origin of the changes
(hereditary or acquired) and shows the stability (recurrence) of the changes.
The operator may look through a list of functional systems via "Summary". Strannik shows
the role of each system in homeostasis changes. If necessary, the operator may display the
content and function of each system.

5.5

Assessment of Physiological Systems and Internal Organs

(See Figures 21 & 26)

Strannik Virtual Scanning enables the practitioner to assess the state of each physiological
system. The most destabilized physiological system is indicated in figure 26. Each system
is defined according to the morphology which is defined in each pie chart or set of bar
graphs.

5.5.1 The Assessment of Each Organ

To assess each organ examine each organ one by one; define the nature (hereditary or
acquired) and patterns of the complexes (see the description under the bar graph or by
mousing over a colour bar or arrow).
Assess the morphology condition. Take into account organs with "non-recurrent"
morphology. Show the changes in organ function (see comments under a film frame).

5.5.2 Reported Psycho-Oncological Risks (See figures 21, 25 a & b)

The scales outlined in table 21, 25 (a) and 25(b) are indicative of the onset of psychooncological risk.
(a)

Indications of Hayflick limit violation;

(b)

Indications of altered or increased levels of new cells;

(c)

Indications of increased levels of enzymes which have damaging effect upon

connective tissues and vessels;
Indications of altered tissue innervation.

(d)

The presence of red signals on each of the above four scales and nonconformity of age
criteria (when the biological age exceeds the calendar age) is indicative of greater psychooncological risk. The summary report (figures 25 a & b) highlights the areas of greatest
psycho-oncological risk. If the results denote:
Present the instead of Absent,

(e.g. of hormonal neoplasm growth stimulation)

Does not maintain instead of Maintains (e.g. neoplasm growth inhibition)

High level instead of Low level (e.g. psychosomatic signal level)
the results are significant and should be worthy of further investigations by an oncologist.

5.5.3 Determination of the Degree of Morphological Changes which are

Related to the Age of the Patient (See figure 21)
The number of organs with persistent morphologic changes, which exceed the allowable
age limits, gives evidence of increased biological age.
Such people believe that in general they are healthy.
Under 20 yrs.

Periodic morphologic changes accompanied by dark-blue signals.

Under 30 yrs.

Periodic morphologic changes accompanied by infrequent red

signals. At a level which is less than 5 points. These signals are
always less than the dark-blue signals.

Under 40 yrs.

8-10 organs with persistent morphologic changes.

Under 50 yrs.

7-13 organs with persistent morphologic changes.

Over 50 yrs.

11-19 organs with persistent morphologic changes.

Under 70 yrs.

15-25 organs with persistent morphologic changes.

Over 70 yrs.

21-29 organs with persistent morphologic changes.

5.5.4 Detection and Assessment of Pathological Functional System

(See figures 24 a & 24b)

A Pathological Functional System is a non-typical psychophysical system causing and
maintaining the development of morbidity, discomfort and diseases of this patient. A stable
pathological functional system is often noted as a chronic pathology. It exists when organs
in the body do not function as part of the normal physiological systems but instead as part
of alternative yet stable pathological systems. Such a philosophy has been widely
researched by Russian researchers. The existence of stable pathological functional systems
often suppresses the normal processes of recovery.
The data delivered by the Strannik system shall be interpreted by a qualified and suitably
trained practitioner.

5.5.5 Quality Control

This section enables the practitioner to include in the SVS health report the results obtained
from contemporary diagnostic tests and to verify and/or otherwise validate the SVS test
results.

Diagnostics quality control "Control" key (figures 15 & 16)

This is intended to control the diagnostics quality, comes with the self-learning system
ensuring automated adjustment of the diagnostic modules in the most efficient mode.
Use the quality control block to check unsatisfactory test results. Remove faulty diagnoses
in the correspondent cabinets stating the criteria for questioning the work of the system
from the following list:
clinical data; laboratory; biopsy; X-ray analysis; ultrasound investigation; computerized
tomography; nuclear magnetic resonance; endoscopy; surgical data; postmortem
examination data.
The diagnostic modules will be adjusted based upon the analysis of the above data. The
operator of the system e.g. the doctor/practitioner shall be fully liable for the quality and
significance of the input data.
If you made such a mistake, reinstall the program by booting from the original installation
source.

Report (for the patient).

The report contains bar graphs only. In general, bar graphs are sufficient because the
patient has been already consulted by the doctor over his/her health status.

6.
Treatment (Colour Correction/Strannik Light Therapy)
6.1 Correction Process Overview
Strannik Light Therapy (SLT) is used for correction. By giving an exact treatment mode
within the space-time and spectrum range, the SLT technology provides new opportunities
for interaction between visible light range and living tissue. This interaction has a positive
effect on the biological tissue. SLT enables the practitioner and patient to carry out highly
selective photo-processing with accurate localization, individual dosing and absolute
sterility. Due to its high efficiency, SLT could be the first stage of treatment of any disease
(discomfort), along with further involvement of other methods, if necessary.

6.2 Strannik Light Therapy: Operation & Effects

SLT is a set of electromagnetic waves which are precisely calculated for each patient. It
displays variable colours and/or shadres of colour on the computer in order to configure an
adequate reaction of the body to the objective reality i.e. to stimulate a biological response..
It is a highly accurate method for color therapy of the subconscious (unconscious) mind . It
involves a complex calculation which is intended to determine the patient's personal

biomathematical model and a required course of colour therapy which is based on the
patients unique and personal diagnostic results. There are over 16,000, 000 colour shades.
In practice, the light therapy has the following effect on the human body: light photon with
preset parameters -> eye -> neuron -> control signal to the preset organ. The colour
parameters are calculated in the reverse order. The precise characteristics of the control
signal depends on pathological problems which are detected at the diagnostic stage. In
addition to colours, SLT calculates the pulsation frequency (pulsating color set) and
duration (dose) for each patient.
Any computer may be used to conduct the correction. In this case, a small program shall be
installed on the patient's computer. After the diagnostic test, the patient is given a digital
computer file containing his/her correction course. To start the correction course, the
patient shall integrate this file into the correction program. The correction course is unique
for each patient.
It is recommended that the patient apply the therapy twice daily e.g. in the morning and
evening. It would be even better, if one of the daily applications of the therapy is done at
the time of day the diagnostic test was taken. An ideal time for therapy: just after the test.
To check things, take two tests, one in the morning and one in the evening, when the person
is tired.
SLT is the most promising correction method intended to recover regulatory abilities of the
organism. In addition to required local effects, this correction technology appears to
produce the following general effects:
Increased number of lymphocytes and red blood cells.
Increased maximum oxygen consumption and improved oxygen supply to the
heart.
Accelerated ptyalin activity and increased secretion of digestive juices.
Increased enzyme content in the pancreatin, normalized absorption of fatty acids in
the intestine and improved motor function of the large intestine.
Increased content of blood thyroxin and pancreatic beta cells.
Increased content of male reproductive hormones/Increased female estrogen
secretion.
Increased levels of immune function
Improved hearing, sight and sense of smell.

 Improved skin plasticity.

Inhibition of osteoporosis.
Improved perception, concentration, memory and emotional stability.
Normalized metabolism and, as consequence, increased formation of internal water
due to active fat oxidation with typical increased daily discharge of fluid from the
body.
Inhibited biologic aging processes (decreased number of aging signs - grey hair,
hair growth in unusual places and senile skin pigmentation).
Improved sleep

6.3 Calculation of the Correct Dosage.

The general success of the treatment is rooted in correct calculation of the individual
correction dosage. There is a range of reasons for calculating the individual dose:
1. We work with photoregulation systems which are characterized by high
photosensitivity.
2. A trigger effect involves a narrow frequency range and duration of correction i.e.
sensitivity peaks. (Trigger effect: the organism is activated to the required state in
discrete steps following the application of the signal).
3. All other conditions being equal, the effect depends on the correction session duration
(dose per session) and total number of sessions (dose per course).
4. The degree of photosensitivity depends on the age and sex. In particular, women need
higher correction dose per session and course to reach the peak than men.
5. Colour correction is the absorption of low energy of visible light quanta resulting in a
photochemical reaction involving activated molecules and, at a later stage, neurons with
further development of associated neurochemical reactions.

6. Sensitivity peaks differ in number (portion) of neurons involved in the above reactions,
rather than in degree of effect manifestation for certain neurons. Different peaks are
characterized by different degree of manifestation of the required reaction.
The color correction dosage directly depends on the results of diagnostics performed by the
patient. In fact, the dose level gives an indirect evidence of the adequate response of the
subconscious (unconscious) mind to the external action, i.e. the lower percentage the color
correction is, the more adequate response is delivered by the brain to the environment and
thus the more stable the body functions (homeostasis is ensured).

6.3.1 Guidance Notes

However, sometimes the diagnostic results may be wrong thus increasing the correction
dose. This dose is false. In general, the dose of patients with express pathologic changes
exceeds 150 percent. An Acceptable dose is 40-150%. See figure 31: Adjust Therapy
Doseage.
If the size of the correction file exceeds 20KB, the test must be repeated, the file is not
valid for therapy. A persistently high therapy dose in combination with expressed therapy
intolerance shows inadequate response of the brain to the environment.
For Color Correction Dose which exceeds 100 percent: explain to the patient what he/she
has to repeat once again the diagnostic procedure. If the repeated diagnostics shows the
dose exceeding 100 percent again, assign this dose and explain that the treatment session
may take 40-60 minutes. In case of express intolerance of the dose exceeding 100 percent
(the patient is unable to sustain the session duration: he/she feels anger, irritation or exhibits
hysteric reaction, etc.) repeat the diagnostic procedure. Recalculate the therapy block or
course for 75 percent despite of recommended previous dose.

6.4 Available Colour Correction Modules (figures 31-33)

The following therapy modules may be selected:
Optimal blood composition.
Optimal circulating blood volume .
Optimal pH level.
Optimal osmotic pressure.
Optimal blood glucose level.
Optimal blood pressure.

Optimal respiratory levels.

Optimal digestion levels.
Optimal body temperature.
Optimal extraction levels.
Optimal sexual functions.
Optimal locomotion, communications and manipulation.
Optimal sleep pattern.
Excess weight.
Biologic aging.
Natural potency recovery.
Physical destructive factors - control.
Chemical destructive factors - control.
Biologic destructive factors - control.
Psycho-emotional destructive factors - control.
Single-organ therapy.
Wave therapy.
Recommend the therapy and prescribe color treatment of the pathologic functional system.
Proceed as necessary. In general, no additional chemical medicines are required for
Strannik color therapy. If accompanied with medicines, decrease the dose and increase
dosing interval. (The effect of "color therapy influences medicinal dose").

6.5 Advisory Notes for the Patient

6.5.1 Precautions
This treatment is specific to your own medical condition. UNDER NO
CIRCUMSTANCES SHOULD ANYONE ELSE USE YOUR COURSE OF
TREATMENT. Do not allow anyone else to sit in the same room as you in a position
where he or she is aware of the flashing colours whilst you undergo each treatment session.
Do not allow anyone to sit in front of your computer during any part, however small, of any
treatment session.
Do not reload the treatment disc onto another computer and re-commence the treatment
from the beginning. If for any reason you need to transfer the treatment to a different
computer, see our instructions.
Please ensure that you keep your treatment log (supplied with your treatment disc) up to
date. We are unable to verify the completeness of your treatment if the log is incomplete.

You will find the log of great value if you need to switch from one computer to another
between treatment sessions. Before you begin using the treatment, please ensure that your
computer has the minimum specification set out later in this manual.

6.5.2 What you can Expect/Symptoms

It is possible that you will feel worse after the first few sessions in one or more modules.
This is normal, and will pass after two or three more sessions. Do not stop your treatment.
The initial modules of the treatment course are of vital importance but may not produce any
noticeable effect on your condition. Do not let this put you off the treatment is a carefully
programmed course running for several weeks or months and you should not expect to feel
any different after the initial modules. Please persist with the treatment.
Contact: If you have any concerns about any aspect of your treatment, please do not
hesitate to contact your practitioner

6.5.3 Undergoing Treatment

Preparation
Once a session starts, it SHOULD NOT BE INTERRUPTED. It is therefore important that
you prepare yourself properly before commencing. Ensure that you are not likely to be
disturbed or called away from the computer e.g.

Switch off all telephones or switch on the answerphone.

If you are alone at home, consider putting a sign outside your front door saying
Do not disturb or be prepared to ignore anyone who calls.

By all means have a soft drink or a hot drink but do not drink alcohol in the 24 hours before
or during a treatment. Do not undergo treatment if you are tired, under the influence of
alcohol or any drugs or medicines that cause drowsiness, sleepiness, or any form of
hallucination.
Ambience

The room should be dimmed and quiet. Soft, calming music played at low volume is ideal.
But any music will be of benefit if it helps you to watch the computer screen.
Seating position
Sit directly in front of the computer screen as you would for normal computer use (as
recommended in your computer user documentation). Look at the screen throughout each
session. Try to avoid looking away from the computer for any length of time. You can
glance slightly to the side, top or bottom of the computer it is not strictly necessary to
stare continually into the screen.
Frequency
You must undergo a treatment session at least once every 24 hours (if not recommended
otherwise). If you miss a session for any reason any day, run the session as soon as possible
after it has been missed and then return to your 24-hour cycle. If you miss the treatment for
any more than seven days running, then please call the practitioner who provided your
treatment disc for advice. If you miss the treatment for several days, and you then re-start
the treatment for up to five sessions, and then find that you miss the treatment for any more
than 48 hours, please call the practitioner who provided your treatment disc for advice. It is
possible to catch up by running a session in the morning and one in the afternoon. You
should leave at least 2 hours between each session as a minimum (if not recommended
otherwise).
THE BEST RESULTS WILL BE OBTAINED IF THE FULL TREATMENT IS
CARRIED OUT ON A CONSISTENT BASIS ONCE OR TWICE EVERY 24 HOURS.
Duration of the Therapy Sessions
Sessions are of varying length from 15 to 35 minutes, typically 20 minutes. The full course
of treatment is broken down into a number of modules. The various modules applicable to
your treatment are shown in the right hand box/column of the 'Correction Module' front
screen. Each module comprises a number of treatment sessions. To find out how many
sessions are included in your full treatment, highlight each module in turn on the right hand
screen. As you move into a new module, the box at the bottom left of the 'Correction
Module' front screen will tell you how many sessions are included in that module. The
colours and/or the colour sequence appearing in each module might be different however
the sessions within a particular module are usually similar in content, and of the same
length. The only way you can find out how long each session will take is to undergo the

first session in each module and check the time yourself. It is not possible to skip modules.
Sessions can be skipped by pressing the esc key as soon as they have started, or by simply
not watching the screen. This will of course negate the effectiveness of the treatment!
Running a treatment session on your computer
When undertaking the therapy start the treatment module at the brain and complete the
brain module before proceeding to another organ module. Complete each module in turn.
IF YOU START A TREATMENT SESSION WITH ANOTHER PROGRAM RUNNING
WHICH CAUSES A CONFLICT WITH THE TREATMENT, THE TREATMENT
SESSION MAY FREEZE PART WAY THROUGH.
You should see a 'Correction Module' icon on your desktop. Double click this and the
treatment program will load. Follow the screen prompts.
If the system should freeze quit the programme. Pressing the ESC key will work on some
computers. You will be asked if the session should be treated as complete. If you think the
session is almost complete, based on the length of time it was running, click YES. But if
the session is probably 50% or less complete, click NO. You will then be able to re-run the
session.
If you cannot exit by pressing the ESC key, press the CTR-ALT-DEL keys at the same
time. This will enable you to quit the program instead.
If you have quit the treatment using CTR-ALT-DEL, the program will not recognise the
session as complete. As above, if you think the session was almost complete there is no
need to re-run it completely. To advance the session counter, re-start the session, exit
immediately by pressing the ESC key and when asked, should I count the session as
complete click YES.
Before you re-start any session which you have had to end part way through, REMEMBER
to close down any open program which may have caused the treatment session to freeze.
If your treatment session does not load, simply press ctrl-alt-del and when the Close
Program dialogue box appears click end task. This should restore your desktop. Double
click the treatment icon again this time the program should run perfectly.
What if a session is missed?

If you simply do not run a session in any particular day, run it as soon as possible
afterwards see above. If you start a session and have to move away from the computer but
you let the session run its course, you cannot return to it and you have therefore missed a
session. This will reduce the benefits of the treatment program. Thus if you do have to
move away from the computer, press the ESC key to escape the session without letting it
run its course. See above.
Is it possible to exit a treatment module once it starts running?
Yes by pressing the ESC key (see above) however, this is not recommended. You should
try to start a session at a time when you have every chance of completing it.
If black lines appear between colour flashes on your monitor
The reason for this may be due to the computers ability to display the required brightness
of colour, which in turn depends on the capability of its Graphics card. This line actually is
the part of the screen, which is not filled with colour fast enough. In other words the dose
you are receiving is a little bit less than necessary. This is not significant the percentage
of dose reduction, even on computers with a very slow Graphics card is no more than 0.5%.
Your Treatment Log
On your treatment disc or flash drive you will find a treatment log upon which you should
record details of all sessions as you complete them. Alternatively if a treatment log has not
been provided you should keep your own log of therapy sessions in which you detail any
notable occurrences and/or changes to your health.
You may wish to print out this log and keep a manual version. Please ensure that at least
one of these logs is kept up to date. Bring the completed log with you every time you visit
the clinic. This is important to us. If you have not improved as a result of your treatment we
will want to honour our commitment under our guarantee. And we will also want to try to
find out why you have not found any benefit from our system. We need to be sure that the
treatment has been undertaken fully and properly. The following processes help us to
ensure that the treatments have been properly run:

Some treatment programs carry a numerical code, which appears on screen for
about 3 seconds at the end of sessions during the whole course of treatment. If you
see this number in any of your sessions, follow the screen prompts. You will not be
able to leave the program until you have worked through the prompts.

The computer automatically writes back to the treatment file the date when each
session is fully run.

If a log sheet is not provided, please keep a note of each treatment session: date, time and
anything interesting.
When the treatment is complete
Please contact the Strannik practitioner to arrange the follow assessment to check your
condition. When you visit the clinic please ensure that you bring your treatment log with
you for our records (unless you have forwarded this to us already by e-mail).

6.6 Limitations of the Technology

Strannik Virtual Scanning is unable to distinguish between a normal organ and an artificial
organ or if an organ has been surgically removed. In addition, it cannot determine
pathologies of the eyes, tonsils/throat, and appendix. It should not be used to diagnose the
health of a pregnant woman.
Care should be taken when testing patients who are very young or very old. It is necessary
to ensure that that are suitably trained or cognitively able to do the test.
Strannik Light Therapy cannot reverse the irreversible i.e. it treats autonomic dysfunction.
It is able to correct the bodys dysfunction but it cannot reverse physiological damage or
the influence of inherited genetic conditions.
Care should be taken when treating patients with epilepsy. It is recommended that patients
who have epilepsy who undertake therapy should be supported by medical staff.
The Strannik Virtual Scanning test is dependent upon the patient being adequately coached
to do the test. Unfortunately there will be patients who, for whatever reason, do not do the
test as instructed. This may lead to erroneous results. It is an unpalatable fact that there will
be those e.g. patients, sceptics, competitors, etc; who may wish to disprove the validity of
this technology. Accordingly the practitioner should at all times monitor how each patient
conducts the test. This may be noted in their tests results. In order to deal with such
situations the practitioner should consider whether the patient has done the test to their
satisfaction and whether test results make sense e.g.
(i)

a visual check of how the patient is doing the test;

(ii)

whether the selected therapy is significantly greater than 100% which could indicate
abnormal brain function;

(iii)

whether the results look normal e.g. (a) if there was an organ with a sequence of
pathological results which give zero indication, (b) whether there was an organ or
sequence of organs in which the results reported only blue/genotype signals, (c)
whether the patient is exhibiting signs of cognitive dysfunction. In the latter case it
may be useful not to rely upon the results obtained but to give the patient Strannik
Light Therapy and invite them to be retested in several weeks.

Contra-indications
It is advised that Strannik Light Therapy should not be used concurrently with other
complementary therapies, in particular techniques which are based upon stimulating
function of the acupuncture meridians. This includes acupuncture, electroacupuncture (the
Voll system), photopuncture, etc. Different complementary therapies have different modes
of action which do not necessarily have a complementary function. Some are based upon
the feed-forward of information from the brain to the organs whilst others are based upon a
feed-back mechanism which involves the flow of information from the periphery to the
brain. Accordingly, it is recommended that practitioners remain vigilant of such
possibilities and that they record and/or report significant side-effects to their local health
authorities.

7.
Conclusions
Apart from the various conclusions which have been reported in MMHL bibliography (see
appendix 1), this programme of research enables the practitioner to make a number of
scientifically significant conclusions e.g.
1.
2.

3.
4.
5.

The subconscious mind accumulates and stores information on cells, tissues, internals
and systems represented in the form of matrices (image signals).
This information always reflects both problems of the specific organ and its
connections with other organs, tissues, systems, organism, internal and external
environment.
The subconscious mind always has information on any changes in the body
represented in different relations of matrices.
The subconscious mind controls the functions of the human body bringing its organs,
systems and tissues in line with the available information.
The Strannik system allows to obtain information at any level of subconscious
function, change this information and to exercise positive impact on the state of
organs, systems, tissues and organism.

6.

User-friendly and absolutely safe Strannik Virtual Scanning system always takes into
account the superfine individual peculiarities of each patient.

8.
Regulatory Status
Strannik is a cutting-edge, non-invasive, cognitive technology which is based upon an
unprecedented level of understanding of the relationship between sensory input, brain
function and the autonomic nervous system. It is designed for quick, extended and accurate
assessment of the state of the unconscious mind thus providing new and effective
therapeutic opportunities with unprecedented selective intervention.
This technology was approved by USSR Academy of Medical Sciences. The Strannik
technology (called abroad "Strannik Virtual Scanner Software") is based upon law of
biologic response to the wave impact (Proceedings of the meeting of the Presidium of
Siberian Department of USSR Academy of Medical Sciences (Minutes No. 11 dated
December 04, 1985)).
This technology was approved by the RF Ministry of Health. Strannik meets all medical
parameters and requirements of the specifications (Minutes No. 27-11/02-6, expert check
of software and data bases of the RF Ministry of Health). Strannik was ranked No.1 health-

improving technology (Industry Program of the RF Ministry of Health "Health protection

and improvement for 2003-2010").
Strannik meets the following national standards: GOST 28195-89 (Table 1, sub-clause
2.3.3), GOST R ISO/MEC TO 9294-93 (sub-clause 7.2.2), GOST R ISO/MEC 9126-93
(Appendix A, sub-clauses .2.1, .2.3), GOST R ISO 9127-94 (sub-clause 6.3-6.5), GOST
34.602-89, GOST 19.208-78, GOST 19.502-78 (Sections 6-7). Test certificate No. 1/2002
dated January 14, 2002 (OKP code: 50 8000) GOST R certification system.
Efficiency of psychological applications. Approved by the RF State Physical Culture and
Sports Committee. R&D Report of St. Petersburg State Scientific Research Institute of
Sports and Health-Improving Technologies named after P.F Lesgaft dated August 15, 2002
Copyright: RF Certificate of official registration of program No. 980696.
Strannik is a software designed for delivery of psychological services exempt of licensing
and special use permits. Article 12, Federal Law No. 99-FZ "On Licensing of Particular
Activities" dated May 04, 2011.
In Europe, the definition of a medical device has been altered. This change has been
brought about by the development of APPs which are intended to run on a mobile platform
such as an iPhone. The revised definition considers that a medical device is a device, and
hence subject to the Medical Devices Directive, if the reported results are used to prescribe
a drug or a therapy. If the technology is used to provide a patient with a health report which
can assist them to manage their health it is now considered that this is outwith the scope of
the prevailing directive. Accordingly, Strannik Virtual Scanning is now considered to be an
APP. In effect if the technology is used in a non-clinical environment it remains outwith the
scope of the directive. If it is used in a clinical environment and is intended to determine
the drug to be prescribed and/or the dose to be prescribed it becomes subject to the
prevailing directive i.e. as a self-certifiable device/type 1 medical device. The legal status
of this technology appears now to be similar to that of the US market.
In apparent contradiction there is the Medical Device Directive which states:
Software that has a medical purpose could be a medical device. A medical device is defined in the medical
device Directive (MDD) as:
software intended by the manufacturer to be used for human beings for the purpose of:

diagnosis, prevention, monitoring, treatment or alleviation of disease,

diagnosis, monitoring, treatment, alleviation of or compensation for an injury or handicap,
investigation, replacement or modification of the anatomy or of a physiological process,
control of conception.

Accordingly, MMHL advise any medical practitioners who wish to introduce SVS into
their practice that they should independently ascertain the regulatory requirements for this
technology in their markets i.e. before placing the technology on the market.
Nevertheless Strannik Light Therapy remains subject to the provisions of the Medical
Devices Directive i.e. as a type 2a Device. It may not be placed on the market until a
technical dossier has been compiled which includes the results of clinical studies however
this does not preclude the demonstration of the technology, gathering data, and/or
undertaking proof of concept studies and clinical studies.
http://www.mhra.gov.uk/Howweregulate/Devices/Software/index.htm
http://www.gsma.com/connectedliving/wpcontent/uploads/2012/03/gsmaunderstandingmedicaldeviceregulationformhealthreport1.pdf

9.
Paying for Tests
The flash-drive has been organized to allow the practitioner to purchase a monthly
allocation of tests or alternatively a set number of tests which must be used within a
specific period of time.
Contact MMHL if you wish to place a longer contract e.g. to cover 3 months, 6 months or
12 months. This will enable you to receive lower test costs.
The current payment schedule is as follows:
10 tests: 295
20 tests: 395
30 tests: 495
>30 tests:

(29.50/test)
(19.75/test)
(16.50/test)
15.00/test

For large-volume end-users, and to discuss volume discounts, please contact Graham
Ewing.
Payment to: HSBC Bank, 1 Leeming Street, Mansfield, Nottinghamshire
Bank Sort Code: 40-32-01 Bank Account No: ..
You will be issued with a payment form before the expiry of your key to enable you to
order your tests for the next calendar period/number of tests. Please place orders at least
one week before expiry of your flash-drive to enable MMHL to organize the smooth
transition from one period to the next.
Please note that MMHL plans to issue a revised version of the Strannik program which will
enable the practitioner to pay on-line. This will be issued and sent to you free of charge. If
you do not make the payment your key will be disconnected.
Please contact Kim Wallis if you are experiencing any difficulties.

G.Ewing

9th December 2014

Appendix 1
Peer-reviewed Publications, Abstracts and Presentations
Ewing GW. A Framework for a Mathematical Model of the Autonomic Nervous System and Physiological
Systems submitted to Journal of Computer Science & Systems Biology on 28th October 2014.
Ewing GW. Healthcare or Wealthcare? Innovation Leaders Conference, Clare College, Cambridge
University 27th/28th February 2014.
Ewing GW. Grakov IG. A Further Review of the Genetic and Phenotypic Nature of Diabetes Mellitus. Case
Reports in Clinical Medicine 2013;2(9):538-553. http://dx.doi.org/10.4236/crcm.2013.29140
Ewing GW. The Biology of Systems or the Systems of Biology: Looking at Diabetes from the Systemic
Perspective. Presented at 2nd World Neuroscience Online Conference, 20th June 2013.
Ewing GW. Virtual Scanning: a New Medical Paradigm? Journal of Computer Science and Systems Biology
2013;6:93-98. http://www.omicsonline.org/0974-7230/JCSB-06-093.php?aid=12357
Ewing GW. The Biology of Systems or the Systems of Biology: Looking at Diabetes from the Systemic
Perspective. International Journal of Systems Biology 2013;4(1):45-56.
http://bioinfopublication.org/jouarchive.php?opt=&jouid=BPJ0000252
http://bioinfopublication.org/jouarticles.php?opt=&jouid=BPJ0000252&my=05-2013&vol=4&iss=1

Ewing GW. Educational Dysfunction: A Systemic Perspective upon the Biological Basis of Learning.
Published in Education Today, the quarterly journal of the College of Teachers, 21 st June 2013.
Ewing GW. The successful treatment of Dysarthria using Biofeedback: a case study. Accepted for publication
in Biogenic Amines 2013.
Ewing GW. A Comparison of the Diagnostic Scope of Biomarker techniques, Genetic Screening and Virtual
Scanning. Immunology, Endocrine & Metabolic Agents in Medicinal Chemistry 2013; 13(1):35-45(11).
Ewing GW. What are the Mechanisms which Regulate the Bodys Function and, in particular, which Regulate
Blood Glucose? Presented to Ottawa 2012 International Symposium on Biochemistry & Biophysics, Canada,
24th-25th October, 2012.
Ewing GW. How Colour Perception and the Autonomic Nervous System influences the Stability of the
Physiological Systems: the application of Higher-level Mathematics and Pattern Recognition. 1st World
Neuroscience Online Conference, 14th June 2012.
Ewing GW. Blood Glucose is Neurally Regulated: the significance. Minerva Endocrinologica 2012 Supp1;
4:62-65. Presented at 7th WCPD in Madrid, 12-13th November 2012.
Ewing GW. Book Chapter, Complementary Therapies for the Contemporary Healthcare pub InTech,
September 2012. Cognitive, top-down, Systems Biology: Virtual Scanning ISBN 978-953-51-0801-6
Ewing GW. International Light Association (October 2012, Berlin), Virtual Scanning workshop (3hrs)
Ewing GW, Grakov IG. Fashion or Science? How can orthodox biomedicine explain the bodys function and
regulation? N.Am.J.Med.Sci. 2012;4(2):57-61.
Ewing GW. Further Developments in Systems Biology: Virtual Scanning. Metabolomics & Systems Biology
2012 (20-22 February 2012 San Francisco) published in: Proceedings of International Conference and
Exhibition on Metabolomics & Systems Biology April 2012 (Ewing GW (2012) Further Developments in
Systems Biology. Metabolomics 2012; S1:001. doi:10.4172/2153-0769.S1-001)
Ewing GW. Invited keynote speaker: 80th Annual Conference on Light and Vision (May 2012 Colorado
Springs).
Ewing GW. The Regulation of pH is a Physiological System. Increased Acidity alters Protein Conformation
and Cell Morphology and is a Significant Factor in the onset of Diabetes and other common pathologies. The
Open Systems Biology Journal 2012;5:1-12.
Ewing GW. The Application of Computer-based technologies in Medical Diagnosis: how this leads to a
greater understanding of the processes which the body employs to regulate its function and which influence
education and learning. Practical demonstration delivered at the. Interactive Technologies and Games 2011
(Nottingham, October 23-25, 2011).
Ewing GW. The Influence of the Autonomic Nervous System upon Learning Ability including a
demonstration of Virtual Scanning light therapy. Practical Paper delivered at the First European Conference
on Learning Disabilities (September 9-10, 2011) in Zrich/Switzerland.

Ewing GW, Parvez SH. The influence of Pathologies and EEG frequencies upon sense perception and
coordination in Developmental Dyslexia. A Unified Theory of Developmental Dyslexia. N.Am.J.Med.Sci.
2012;4(3):109-116.
Ewing GW, Parvez SH, Grakov IG. Further Observations on Visual Perception: the influence of pathologies
upon the absorption of light and emission of bioluminescence. The Open Systems Biology Journal 2011;4:17.
Ewing GW, Parvez SH. The Multi-systemic Nature of Diabetes Mellitus: genotype or phenotype?
N.Am.J.Med.Sci 2010;2(10):444-456.http://www.najms.org/old/NAJMS-2010-issue-10.html
Ewing GW. Mathematical Modeling the Neuroregulation of Blood Pressure using a Cognitive Top-down
Approach. N.Am.J.Med.Sci.2010;2(8):341-352.http://www.najms.org/NAJMS-2010-Vol-2-No-8-341396.html
Ewing GW, Parvez SH. Mathematical Modeling the Systemic Regulation of Blood Glucose: a top-down
Systems Biology Approach. NeuroEndocrine Letters 2011;32(4):371-9
Ewing GW. The Multi-Systemic Nature of Diabetes Mellitus. Presented at 6th World Congress on Prevention
of Diabetes and its Complications 2010, Dresden held 8-11th April 2010.
http://www.wcpd2010.com/programme_web/saturday/plenary4/poster/poster12/pdf/abstract_172.pdf
Ewing GW. There is a need for an Alternative or Modified Medical Paradigm involving an understanding of
the nature and significance of the Physiological Systems. N.Am.J.Med.Sci. 2010;2(6):1-6.
http://www.najms.org/resources/PDF+246251+There+is+a+need+for+an+alternative+or+modified+medical+paradigm+incorporating+an+understandin
g+of+the+nature+and+significance+of+the+physiological+systems.pdf
Nwose EN, Richards RS. Management of Stress and Stress-related Disease: Emerging computer-based
technologies and the rationale for clinical laboratory assessment. N.Am.J.Med.Sci. 2009;1(6):288-294.
Ewing GW, Parvez SH. The Dynamic Relationship between Cognition, the Physiological Systems, and
Cellular and Molecular Biochemistry: a Systems-based Perspective on the Processes of Pathology. Act. Nerv.
Super. Rediviva 2010; 52(1):29-36.
Ewing GW. A Theoretical Framework for Photosensitivity: Evidence of Systemic Regulation. Journal of
Computer Science and System Biology 2009;2(6):287-297.
http://www.omicsonline.com/ArchiveJCSB/2009/December/03/JCSB2.287.php
Nwose EU, Ewing GW. Computer diagnosis in cardiology: oxidative stress hypothesis. N.Am.J.Med.Sci.
2009;1(5):220-5.
http://www.najms.org/resources/PDF+220225+Computer+diagnosis+in+cardiology+oxidative+stress+hypothesis.pdf
Ewing GW, Ewing EN. Computer Diagnosis in Cardiology. N.Am.J.Med.Sci. 2009;1:152-159.
http://www.najms.org/resources/PDF+152-159+Computer+diagnosis+in+cardiology.pdf
Ewing GW, Ewing EN, Parvez SH. Developmental Dyslexia: the link with the Autonomic Nervous System
and the Physiological Systems. Biogenic Amines 2009;23(3):115-190. http://node.nel.edu/?node_id=10508
Ewing GW. What is regressive autism and why does it occur? Is it the consequence of multi-systemic
dysfunction affecting the elimination of heavy metals and the ability to regulate neural temperature?
N.Am.J.Med.Sci. 2009;1(2):28-47. http://www.najms.org/NAJMS2009No228-95.html

Ewing GW. Does an improved understanding of the nature and structure of the Physiological Systems lead to
a better understanding of the therapeutic scope of Complementary & Conventional Medicine? Journal of
Computer Science and Systems Biology 2009;2(3):174-179.
http://www.omicsonline.com/ArchiveJCSB/2009/June/01/JCSB2.174.pdf
Ewing GW, Nwose EU, Ewing EN. Obstructive Sleep Apnea Management with Interactive Computer
Technology and Nutrition: Two Case Reports. Journal of Alternative and Complementary Medicine
2009;15(12):1379-1381
http://www.ncbi.nlm.nih.gov/pubmed/19954336?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPane
l.Pubmed_RVDocSum&ordinalpos=1
Nwose EU, Ewing GW, Ewing EN. Migraine can be managed with Virtual Scanning: case report. The Open
Complementary Medicine Journal 2009;1:16-18. http://bentham.org/open/toaltmedj/openaccess2.htm
Ewing GW, Ewing EN. Cognition, the Autonomic Nervous System and the Physiological Systems. Biogenic
Amines 2008;22(3):140-163. http://node.nel.edu/?node_id=8155
Ewing GW, Ewing EN, Nwose EU. Virtual Scanning technology the relationship to oxidative stress and
applicability to diabetes management. Biogenic Amines 2008;22( 4-5):195-207.
http://node.nel.edu/?node_id=8718
Ewing GW, Ewing EN. NeuroRegulation of the Physiological Systems by the Autonomic Nervous System
their relationship to Insulin Resistance and Metabolic Syndrome. Biogenic Amines 2008;22(4-5):208-239.
http://node.nel.edu/?node_id=8712
Ewing GW, Parvez SH. Systemic Regulation of Metabolic Function. Biogenic Amines 2008;22(6):279-294.
http://node.nel.edu/?node_id=8740
Ewing GW, Ewing EN, Parvez SH. The Multi-systemic Origins of Migraine. Biogenic Amines 2009;23(1):152. http://node.nel.edu/?node_id=10468
Ewing GW. ICHM August 2008, published in the conference proceedings: The relationship between the
autonomic nervous system, the physiological systems and their significance to complementary medicine'
(including a demonstration of Virtual Scanning).
Ewing GW, Ewing EN. Virtual Scanning a new generation of medical technology beyond biomedicine?
ISBN 978-0-9556213-0-7 pub Montague Healthcare books.
Hankey A, Ewing EN. New Light on Chromotherapy: Grakov's Virtual Scanning System of Medical
Assessment and Treatment. eCAM 2007;4(2):139-144.
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1876617
Ewing GW, Ewing EN, Hankey A. Virtual Scanning - Medical Assessment and Treatment. Journal of
Alternative and Complementary Medicine 2007;13(2):271286.http://www.liebertonline.com/toc/acm/13/2?cookieSet=1
Grakov IG. Strannik Diagnostic and Treatment System: a Virtual Scanner for the Health Service. Minutes of
Meeting No. 11 of the Praesidium of the Siberian of the Academy of Medical Sciences of the USSR (AMN)
held in Novosibirsk 4 December 1985.

Vysochin Yu et al, 2001. Methodology and Technology of Invigoration of Different Population Orders. In:
Consolidated 5 year Research Plan of Physical Training, Sports and Tourism State Committee of the Russian
Federation. 2000. English translation available at:
http://www.montaguehealthcare.co.uk/files/Vysochin/Vysochin.pdf

Appendix 2
Additional Books
Ewing GW, Ewing EN. Virtual Scanning a new generation of medical technology beyond biomedicine?
ISBN 978-0-9556213-0-7 pub Montague Healthcare books.
Ewing GW. The Great Medical Controversy of our Time: Why Vaccines MUST be Implicated in the
Occurrence of Regressive Autism. ISBN 978-0-9556213-1-4 pub Montague Healthcare Books.

Training Courses

Available from MMHL upon request.

Appendix 3
Psychological Diagnostics Vocabulary
Perception (Information Reception) is a mental cognitive process implying the integral
reflection of objects, subjects and events having a direct effect on individual's sense organs
in individual's mind, but not the sensation-like partial reflection.
Imagination (Information Processing) is a mental cognitive process resulting in creation
of new images and ideas, programming of situations and possible scenarios basing upon
individual's ideas, knowledge and experience or sometimes without the required knowledge
in this field.
Memory (Image Formation) is a mental cognitive process involving memorization,
storage and further retrieval of what the individual did, felt or perceived in the conscious
mind or during any activity.
Decision Making (Image Use) is a system of interconnected reflex and conscious
(physical and mental) actions representing the capability to make own responsible decisions
and act in an active and purposeful way in order to implement these decisions in different
situations.

Definition of Selected Personality Features:

Ambition is a feeling, one of the forms of manifestation of personality orientation

characterized by the achievement drive. In some cases, the individual may be unaware of
all reasons of this drive.
Self-confidence is the self-belief, cumulative self-concepts of the individual associated
with assessment of these concepts.
Decisiveness is a quality of the personality, character trait manifested in capability to make
own responsible decisions and act in an active and purposeful way in order to implement
these decisions in different situations.
Apathy is a mental state caused by nervous exhaustion of the organism and manifested in
loss of interest, indifference to the environment and low mental activity level. Apathy may
originate from the sustained physical and mental overload and from the severe stress or
frustration factors (accident, catastrophe).
Determination is a form of mental reflection of the reality allowing the individual to
overcome obstacles, reach subjective goals, control his/her actions and psychological
processes and to achieve to his/her capacity for volition regulation.
Realism is objective and subjective reflection of the world by the individual. Realism is a
mental and conscious phenomenon. Derealization is inadequate reflection of the
environment.
Ethics is an individual persistent form of individual's communication behavior manifested
in any interaction with others. Internal taboos and permissions of the Ego.
Logic is a rational cognitive activity of the personality associated with the use of concepts,
categories, logic constructions and generalization to create new images, ideas and
conclusions. Making conceptual connections in the available material. Main logic forms:
concept, estimation and conclusion.
Envy is a mental experience accompanied by negative emotions and entailed by activation
of the drive when somebody's real or imaginary advantages are seen as a threat to Ego
value.
Self-motivation is a suggestion process directed by the individual toward him/herself for
autoregulation and self-education; personality's self-organization method involving
conscious use of the second signal-system to have an effect on mental and even
physiological body processes.
Adaptability is the available information about the environment and individual's inward
fixed in his/her conscious and unconscious mind. Capabilities allowing to adapt in a prompt
and effective way.
Special knowledge are capabilities and prospects of individual's survival under extreme or
altered reality situations. It is important to transfer the knowledge into the structure of the
current activity.
Creativity is a mental cognitive process resulting in creation of new images and ideas,
programming of situations and possible scenarios basing upon individual's ideas,
knowledge and experience or sometimes without the required knowledge in this field.

Planning is the prediction of scenarios for further conscious planning of practicable

actions. Analysis of the past scenarios and present situation and setting of workable
objectives for the future.
Persistence is a volition quality of the personality manifested in decisive and purposeful
actions for achieving intended objectives and for overcoming difficulties and obstacles.
Inexpedient and senseless persistence transforms into stubbornness.
Sexualism (Libido, Appeal, Lech, Passion, Appetite) is a mental energy based upon the
sexual need which transforms into different types of mental activity in the unconscious
mind (mainly into mental energy concealed in the unconscious mind).
Intellect (Cognition, Understanding, Mind) is a relatively stable structure of capabilities
based both upon conscious and unconscious processes used for processing and conscious
evaluation of heterogeneous information.
Fear is a mental state associated with express manifestation of asthenic feelings (agitation,
anxiety and other feelings) in case of any threat to biological or social being of the
individual and oriented toward the source of the real or imaginary danger.
Fear of Illness is diseased state of personality's mind involving baseless fears of his/her
health and life.
Fear of Death is a tension between consciousness of death and eternal life wish.
Fear of Old Age is a psychological traumatic factor of fear of expected changes in life.
Fear of the future.
Frustration is an impediment to the objective entailing the anxiety.
Fear of Poverty is a fear of shortage of resources required for individual's normal life
activity or belonging to a social group.
Fear of Criticism is the dependence on the society's opinion. Hypersensitivity to
evaluation of his/her personality, abilities, qualities and place among other people.
Arrogance is the hyperbolic self-esteem. Groundless snobbery.
Hostility is a negative attitude to others, striving for violence toward them. Form of stress
relieving.
Indignation is a response to mismatch of the reality and individual's ideas and
requirements; complaints.
Anger (Rage) is the internal state of accumulated aggression which may be directed
against the individual him/herself.
Readiness to Argue is the readiness to settle the internal and external conflict and to
change the situation.
Interest in others is the need to establish, maintain and strengthen position relations with
other people; enriching each other through common interests.
Indifference is lowering of mental activity level and interest in the outworld.
Strength (Vigour) is the fulfillment of individual's potential, talent, capabilities and
opportunities, coordination of efforts and autoregulation.

Initiative is a personality's activity driven by motivations. Motives may include instincts

and inclinations.
Enterprise is a practical activity focused on achievement of profit-making goals (business,
production launching).
Sensitivity is a special form of mental reflection of the outworld, personality's attitude to
the environment manifested in social induced feelings activating (sthenic) or inhibiting
(asthenic) the activity.
Practicality is a material, sensory substantive and purposeful activity of the individual
implying transformation of natural and social objects considered as a basis for human
society development.
Inclination to analyse is a thinking peculiarity manifested in the use of logical
constructions, concepts, categories and generalization.
Sensibility (Insight) is a sphere of individual mind with obscure and intuitive reflection of
the reality (often at the premonition level). Sudden logical understanding of the essence of
phenomena, situations and problem solutions.
Efficiency (Pragmatism) is an efficient interaction of the personality with the environment
taking into account personal interests.
Sociability is a trait of the personality showing his/her need and ability to communicate,
contact and achieve mutual understanding with other people.
Communicability is an ability of the individual to establish and maintain positive
emotional, friendly and intimate relations with others.
Business-like Character is a practical and theoretical activity involving motivated
achievement of the preset goal for cognizing or transforming objects.
Respect for others is a capacity for compassion, decency, finesse, tolerance and empathy.
Decency is a moral behavior based upon social order morality.
Consistency is an existing dynamic stereotype, mode of behavior which may have force of
the drive in the specific situation. Includes worldview and personal ideas.
Trust is an internal sympathy, positive emotional perception of other individual.
Stability is a combination of social, physical and psychological conditions under which the
personality exists. Subjective and objective feeling of protection and love.
Fidelity (Loyalty) is an existing dynamic stereotype, mode of behavior in the specific
situation having force of the drive.
Fantasy is a theoretical thinking based upon creation of images and actions which do not
exist at present. The product of imagination revealing intimate and often unreal or
impossible ambitions or dreams of sublimated nature.
Social Consciousness includes: philosophical, political, economical, moral, esthetic, legal
and religious conscience of the personality within the spiritual life of the society.
Negativity (Dishonesty) is a trait of the personality manifested in the social protection of
the Ego through conscious perversion of the state of things and desire to provide false

information on the actual state of affairs. The genuine understanding of dishonesty motives
and causes is required for evaluating its specific manifestations.
Vengefulness (Rancour) are emotional actions or thoughts manifested in hostility or
negative feelings against others.
Strive for Power
Over-estimation (Greed) is a social and biological induced trait of the personality which
preconfigures the behavior in social and natural environment.
Vulgarity is a quality of the personality resulted in negative self-perception; ability to
make a negative impression by the appearance, manners and behavior.
Aggressivity (Spite) is a process, aggressive state of the personality emerging as a
response to any impact.
Gluttony is a normal or excess physiological and psychological need in food.
Realisation (Prodigality) is an inadequate estimation of personality's capabilities
mismatching the objective condition of the individual.
Racial Prejudices (acquired uncritically without a moment's thought) are attitudes
manifested in the form of superstition and prejudice hindering adequate perception of any
nationality.
Indecency is a social and biological induced quality of the personality. Sexual perversions
existing under conditions hindering satisfaction of the sexual needs shall be transferred,
transformed or sublimated to other types of energy (sports, active professional activity,
etc.).
Pride is a concept of the individual him/herself and his/her qualities associated with a high
estimate thereof.
Bravery (Courage) is a quality of the personality manifested in fearlessness and
hyperactivity in dangerous situations; ability to jeopardize life to achieve the goal.
Covetousness

Appendix 4:
Systems and Organs Reported
TABLE 1: REGULATORY SYSTEMS (named for the physiological
factors for which they maintain
optimal functional levels)
(1) Blood Cell Content

(8) Digestion

(2) Circulating Blood Volume

(3) pH Level

(9) Body temperature

(4) Osmotic Pressure in the Body

(10) Excretion

(5) Blood glucose

(11) Sexual Function

(6) Blood pressure

(12) Bodily Posture

(7) Breathing Level

(13) Sleeping Patterns

(14) Locomotion, Communication and

Manipulation

TABLE 2: ORGANS
(1) Brain
(2) Spinal Cord
(3) Peripheral Nervous System
(4) Ear
(5) Nose
(6) Pituitary
(7) Thyroid
(8) Adrenals
(9) Liver
(10) Gall Bladder
(11) Pancreas
(12) Heart
(13) Blood and Peripheral Blood Vessels
(14) Spleen
(15) Lungs and Bronchi
(16) Skin
(17) Oesophagus
(18) Stomach
(19) Duodenum
(20) Small Intestine
(21) Colon
(22) Kidneys
(23) Urinary Bladder
(24/25) Penis / Uterus
(26/27) Testicles / Ovaries
(28/29) Prostate / Mammary Glands

(30) Muscular Skeletal System

TABLE 3: ORGANS in EACH REGULATORY SYSTEM

That sustains optimal cell content of blood
Organs and Functional Systems monitored:
Brain
Pituitary gland
Thyroid Gland
Adrenal Glands
Blood and Peripheral blood vessels
Spleen
Skeletal & Muscular system
Description: cell content of blood is an irregular characteristic. Change in number of
erythrocytes affects metabolism quicker than anything else. Role of leukocytes becomes
very important during inflammatory processes and in immune processes. Trombocytes
play substantial role in early processes of blood clotting. Forming elements that,
together with plasma, constitute a special type of tissue/blood/function in close
interaction based upon the principle of multi-link regulation.
That provides optimal volume of circulating blood
Organs and Functional Systems monitored:
Brain
Pituitary gland
Adrenal Glands
Heart
Blood and Peripheral Blood Vessels

Thyroid Gland
Kidneys

Description: human body contains 6-8% by weight of blood (4-6 litres). The quantity
of blood in the organism is a quite stable and precisely regulated characteristic. The
higher the metabolic rate the higher the organisms requirement for oxygen and the
greater the volume of blood. Normally, not all blood circulates through vessels
continuously - part of it is retained within reserves in the liver (circa 20%), spleen(circa
16%), skin (circa 10%). The volume of blood is closely connected to the level of blood
pressure and the level of the osmotic pressure in the organism
That sustains optimal pH level
Organs and Functional Systems monitored:
Brain
Pituitary gland
Adrenal Glands
Liver
Blood and Peripheral Blood Vessels
Skin
Stomach
Small Intestine
Large Intestine

Thyroid Gland
Pancreas
Lungs and Bronchi
Duodenum
Kidneys

Description: Most important part in chemical characteristics of internal

environment/medium of the body belongs to basic acidic condition of the blood.
Activeness of ferments/enzymes, intensity of reducing-oxidising reactions, processes of
breaking and synthesis of proteins, oxidising of carbohydrates and lipids, sensitivity of
cell receptors to mediators and hormones, ability to penetrate membranes, chemical
characteristics of colloid systems of cells and inter-cellular structures depend upon the
relation of concentration of hydrogen and hydroxyl ions in blood.
That Determines the Optimal Level of Osmotic Pressure in the Body
Organs and Functional Systems monitored:
Brain
Pituitary gland
Thyroid Gland
Adrenal Glands
Blood and Peripheral Blood Vessels
Spleen
Lungs and Bronchi
Skin
Oesophagus
Stomach
Duodenum
Small Intestine
Large Intestine
Kidneys

Description: Osmotic pressure has one of the leading roles amongst varying
characteristics of internal medium. Osmotic pressure is one of comparatively rigid
constants of the bodys internal medium. Ability of the body to keep the osmotic
pressure provides the normal flow of metabolic processes in tissues. Osmotic pressure
always stays on a relatively stable optimal metabolic level which for mammals is
7.3atm.
That sustains optimal quantity of glucose in blood
Organs and Functional Systems monitored:
Brain
Pituitary gland
Adrenal Glands
Liver
Blood and peripheral blood vessels Small Intestine

Thyroid Gland
Pancreas
Kidneys

Description: Carbohydrates play a leading role in energy exchange. The activity of all
organs depends upon the content of the carbohydrates in the blood which is supplied.
The daily norm of carbohydrates depends upon the physical activity of the organism.
The average norm is 500 gm/day. The lack of incoming carbohydrates can be
substituted by fatty acids. Local reserves of carbohydrates are different in different
tissues. The speed of metabolic processes in organs and their functions are determined
by the concentration of glucose in blood.
That sustains optimal level of blood pressure
Organs and Functional Systems monitored:
Brain
Pituitary gland
Adrenal Glands
Liver
Blood and Peripheral Blood Vessels

Thyroid Gland
Heart
Spleen

Description: Metabolic processes can take place on the optimal levels only if there is
optimal blood pressure in the capillaries of tissues. This characteristic is flexible and is
the result of constant adjustment of the body to changing conditions of the environment.
It changes when there is a need of redistribution of liquid, salts, nutrients. It is important
that this characteristic returns to the starting levels and is supported within certain
physiological boundaries.
That sustains optimal breathing levels
Organs and Functional Systems monitored:
Brain
Pituitary Gland
Thyroid Gland
Adrenal Glands
Nose
Lungs and Bronchi
Heart
Blood and Peripheral Blood Vessels
Skin
Small Intestine
Kidneys
Description: Exchange of gases between the atmosphere and cells is called breathing.
Body activity is accompanied by constant consumption of oxygen and production of
carbon dioxide in tissues. During inhalation atmospheric air fills up lungs. The blood
supplied to lungs saturates with oxygen and surplus carbon dioxide is removed with
exhaled air. Refreshment of air in lungs allows the organism to sustain breathing
homeostasis relatively constant gas consumption in blood and tissues on an optimal
level. Stabilisation of oxygen carbon dioxide balance in the body and refill of gas
requirement is the main task.

That sustains optimal digestion levels

Organs and Functional Systems monitored:
Brain
Pituitary Gland
Thyroid Gland
Adrenal Glands
Liver
Gall Bladder
Pancreas
Blood and Peripheral Blood Vessels
Oesophagus
Stomach
Duodenum
Small Intestine
Large Intestine
Description: Definition of the normal metabolism when there are no nutrients supplied
from the outside. Definition of food requirement. Processing of food and extraction of
substances that are able to be absorbed by the intestinal wall amino acids, fatty acids,
monosugars, etc. Supply of nutrients to the blood flow. Removal of poisonous and
unprocessed substances. As a result, the balance between the supply of nutrients to the
blood and their constant use in the organism is sustained.
That sustains optimal body temperature
Organs and Functional Systems monitored:
Brain
Pituitary Gland
Thyroid Gland
Adrenal Glands
Blood and Peripheral Blood Vessels
Lungs and Bronchi
Skin
Kidneys
Description: The body constantly uses certain amounts of energy to support processes of
life activity. Oxidising processes are the most important sources of energy. During
oxidation, potential energy of cellular substances is transformed into various types of
kinetic energy: mechanical, chemical, electrical and heat. Temperature of the body is
sustained at a constant level independent of the temperature of the environment. The
temperature of the internal organs is sustained at 36-37C level. This temperature is the
optimal one for the functioning of most enzymes and influences the speed of
fermentation reactions.
That sustains optimal extraction level
Organs and Functional Systems monitored:
Brain
Pituitary Gland
Thyroid Gland
Adrenal Glands
Blood and Peripheral Blood Vessels
Peripheral Nervous System
Kidneys
Urinary Bladder
Skin
Lungs and Bronchi
Small Intestine
Description: The main target of this system is sustaining normal balance of electrolytes
and extraction from the organism the waste products which are urea, uric acid,
creatinine, indican, urabilin, etc. Significant increases of concentration of these products
is the result of various disorders in the processes of life activity. Actually any
physiologically active substance which increases within the tissues could become
harmful and normal life activity could be restored only after extraction of the excesses
of these substances.
That sustains optimal sexual functions
Organs and Functional Systems monitored:
Brain
Pituitary Gland
Thyroid Gland
Adrenal Glands
Blood and Peripheral Blood Vessels
Ovaries
Testicles
Womb and Appendages
Prostate Gland
Penis
Mammary Glands

Description: Sexual functions include - ripening and differentiation of sexual cells,

formation of sexual motivation, sexual behaviour, process of conception, raising
children; with women this also includes pregnancy, delivery and lactation.
That sustains optimal position of body in the environment
Organs and Functional Systems monitored:
Brain
Spinal Cord
Pituitary Gland
Thyroid Gland
Blood and Peripheral Blood Vessels

Peripheral Nervous System

Adrenal Glands
Skeletal and Muscular System

Description: Life is accompanied by constant change of different forms of movement.

Movements carry a number of active functions: locomotion (e.g. walking, running,
swimming), manipulation (activity with subjects), and communication (writing, speech,
gesticulation, mimicry).
That sustains optimal sleeping pattern
Organs and Functional Systems monitored:
Brain
Pituitary Gland
Peripheral Nervous System
Ear and Nose

Spinal Chord

Description: Sleeping is the second (after being awake) state of active life. Accounting
for the information which is absorbed during the day; preparation of the controlling
programme for the next day; check-up of the condition of organs and tissues; correction
of controlling signals.

TABLE 4: PATHOLOGIES REPORTED FOR EACH ORGAN

1. BRAIN (18)
Allergic Process, Age-related Changes, Intoxication Effects, Epilepsy, Neoplasm,
Chronic Fatigue, Degenerative Process, Migraine, Functional Changes, Abnormalities
of Development, Encephalitis, Vertebral Artery Syndrome, Arachnoiditis,
Encephalopathy, Post-stress Effects, Impairment of Cerebral Circulation, Tissue
Growth, Consequences of Brain Traumas
2. SPINAL CORD (13)
Mielitis, Chronic Fatigue, Allergic Process, Spinal Arachnoiditis, Degenerative Process,
Neoplasm, Impairment of Spinal Circulation, Functional Changes, Abnormalities of
Development, Age-related Changes, Intoxication Effects, Post-stress Effects, Tissue
Growth
3. PERIPHERAL NERVOUS SYSTEM (15)
Allergic Process, Neuritis, Chronic Fatigue, Ganglioradiculitis, Polyneuropathy,
Hereditary Degenerative Process, Intoxication Effects, Age-related Changes,
Radiculitis,
Degenerative Process, Neoplasm, Functional Changes, Abnormalities of Development,
Post-stress Effects, Tissue Growth
4. EAR (15)
Intoxication Effects, Abnormalities of Development, Otogenous Labyrynthitis,
Degenerative Process, Cochlear Neuritis, Chronic Otitis, Age-related Changes.
Functional Changes, Chronic Fatigue, Allergic Process, Inflammation of External Ear,
Inflammation of Middle Ear, Neoplasm, Post-stress Effects, Tissue Growth
5. NOSE (13)
Chronic Fatigue, Intoxication Effects, Degenerative Process, Maxillary Sinusitis, Agerelated Changes, Abnormalities of Development, Rhinitis, Functional Changes,
Frontitis, Neoplasm, Post-stress Effects, Allergic Process, Tissue Growth
6. PITUITARY GLAND (10)
Intoxication Effects, Allergic Process, Age-related Changes, Degenerative Process,
Tissue Growth, Functional Changes, Abnormalities of Development, Neoplasm,
Chronic Fatigue, Post-stress Effects
7. THYROID GLAND (13)
Hypoparathyrosis, Allergic Process, Intoxication Effects, Thyroiditis, Chronic Fatigue,
Abnormalities of Development, Functional Changes, Hypothyrosis, Degenerative
Process, Neoplasm, Age-related Changes, Tissue Growth, Post-stress Effects
8. ADRENAL GLAND (13)
Insufficiency of Adrenal Cortex, Intoxication Effects, Degenerative Process, Crohn's
Syndrome, Chronic Fatigue, Tissue Growth, Cushings Syndrome, Age-related Changes,
Functional Changes, Abnormalities of Development, Allergic Process, Neoplasm, Poststress Effects (8) Adrenals (9) Liver (10) Gall Bladder
9. LIVER (14)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Portal Hypertension, Liver Insufficiency,
Cirrhosis, Hepatitis

10. GALL BLADDER (14)

Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Cholecystitis, Cholelithiasis, Cholangitis,
Dyskinesia of Biliary Ducts & Gall Bladder
11. PANCREAS (13)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Sclerotic Pancreatitis, Pancreatitis, Pathology of
Islands of Langerhans
12. HEART (19)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Myocarditis, Cardiosclerosis, Ischaemic Heart
Disease, Cardiac Insufficiency, Cardiac Myopathy, Angina Pectoris, Cardiac Infarction,
Myocardial Dystrophy, Impairment of Rhythm and Conduction
13. BLOOD & PERIPHERAL BLOOD VESSELS (17)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Haemorrhagic Diathesis, Anaemia, Haemorrhagic
Vasculitis, Leukopenia, Idiopathic Hypotension, Hypertonia, Phlebitis and
Thrombophlebitis
14. SPLEEN (13)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Hyposplenism, Hypersplenism, Splenomegaly
15. LUNGS & BRONCHI (16)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Chronic Breathing Insufficiency, Pleurisy,
Pneumonia, Bronchitis, Bronchal Asthma, Bronchiectatic Disease
16. SKIN (18)
Degenerative Process, Abnormalities of Development, Neoplasm & Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes.
Chronic Fatigue, Post-stress Effects, Urticaria, Psoriasis, Herpes, Erythema, Eczema,
Dermatitis, Lichen Planus, Neurodermatitis, Dermatomyositis
17. OESOPHAGUS (13)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Diverticulum, Neurosis of Oesophagus,
Oesophagitis
18. STOMACH (12)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Ulcerative Disease, Gastritis
19. DUODENUM (12)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,

Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,

Chronic Fatigue, Post-stress Effects, Dyskinesia, Duodenitis, Ulcerative Disease
20. SMALL INTESTINE (12)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Dyskinesia, Enteritis, Diverticulum
21. LARGE INTESTINE(12)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,,
Chronic Fatigue, Post-stress Effects, Diverticulum, Colitis, Proctitis, Haemorrhoids,
Sigmoiditis
22. KIDNEYS (14)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Renal Insufficiency, Pyelonephritis, Urolithiasis,
Glomerulonephritis
23. URINARY BLADDER (14)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Urethral Infections, Urinary Bladder Polyposis,
Urolithiasis, Cystitis
24. PENIS (10)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects
25. UTERUS (15)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Kraurosis, Uterine Myoma, Salpingitis, Cervical
Erosion, Endometritis
26. TESTICLES (10)
Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects
27. OVARIES (11)
Tissue Growth, Chronic Fatigue, Ovarian Cyst, Neoplasm, Functional Changes,
Degenerative Process, Age-related Changes, Allergic Process, Intoxication Effects,
Abnormalities of Development, Post-stress Effects
28. PROSTATE GLAND (12)
Functional Changes, Chronic Fatigue, Age-related Changes, Intoxication Effects,
Degenerative Process, Allergic Process, Calculous Prostatitis, Prostatitis, Neoplasm,
Abnormalities of Development, Post-stress Effects, Tissue Growth
29. MAMMARY GLANDS (12)
Age-related Changes, Tissue Growth, Degenerative Process, Mammary Gland Cyst,
Intoxication Effects, Chronic Fatigue, Abnormalities of Development, Mastitis,
Functional Changes, Mastopathy, Neoplasm, Allergic Process, Post-stress Effects

30. MUSCULAR SKELETAL SYSTEM (17)

Degenerative Process, Abnormalities of Development, Neoplasm, Tissue Growth,
Intoxication Effects, Functional Changes, Allergic Process, Age-related Changes,
Chronic Fatigue, Post-stress Effects, Arthrosis. Polyarthritis, Arthritis, Osteochondrosis,
Osteoporosis, Radiculitis, Myositis.

Table 5: Connections ORGANS-COMPLEX-PATTERN

The following table will assist the practitioner to recognise the specific pathological and
morphological indications which are likely to develop in each organ.

ORGANS
Brain

COMPLEX
(pathological condition)

PATTERN
(morphological situation)

Encephalitis

Increased circulation(inflammation)
Cell function slow

Abnormalities of development

Lack of Blood circulation

Low function or high function of cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Arachnoiditis

Increased circulation(inflammation)
Cell function slow

Functional changes

Low or high function of cells

Cerebrovascular Disorder

Increased circulation(inflammation)
Lack of Blood circulation (sclerosis
and or infarction)

Intoxication effects

Low or high function of the cells

Chronic fatigue

Increased circulation(inflammation)
Low function of cells

Encephalopathy

Lack of blood circulation

Slow cell function

Allergic process

Lack of Blood circulation (sclerosis

and or infarction)
Cell function slow
Old cells

Consequences of Brain trauma

Increased circulation(inflammation)
High function of the cells

Epilepsy

Lack of Blood circulation

Low function of the cells

Vertebro-basilar artery
syndrome

Increased circulation(inflammation)
High function of the cells

Migraine

Lack of Blood circulation

Low function of the cells
Increased circulation(inflammation)
or
Lack of Blood circulation

Neoplasm

Low or high function of the cells

Increased circulation
high function of the cells
Young cells

Spinal
Cord

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of cells

Myelitis

Increased circulation(inflammation)
Low function of cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Disorder of Spinal circulation

Lack of Blood circulation

Function of the cells low

Spinal Arachnoiditis

Increased circulation(inflammation)
Low or high function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of cells

Abnormalities of development

Lack of Blood circulation

Low function or high function of cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Functional changes

Low or high function of cells

Peripheral Neuritis
Nervous
System
Osteochondropathy with
Neurological effects

Increased circulation(inflammation)
Low function of cells
Lack of Blood circulation
Function of the cells low
Old cells

Ganglioradiculitis

Increased circulation(inflammation)
Low function of the cells

Polyneuropathy

Lack of Blood circulation

Function of the cells low
Old Cells

Radiculitis

Increased circulation(inflammation)
Low function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of cells

Abnormalities of development

Low Circulation
Low function or high function of cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Functional changes

Low or high function of cells

Ear

Thyroid
Gland

External Otitis

Increased circulation(inflammation)
Low function of cells

Medium Otitis

Increased circulation(inflammation)
Low function of cells

Cochlear Neuritis

Increased circulation(inflammation)
Low function of cells

Otogenic Labyrinthis

Increased circulation(inflammation)
Low function of cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

HyperThyroidism

Increased circulation(inflammation)
High function of cells

HypoThyroidism

Lack of Blood circulation

Low function of the cells

Thyroidtoxicosis

Increased circulation(inflammation)
High function of the cells

HyperParathyroidism

Lack of Blood circulation

Function of the cells low

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Adrenal
Glands

Abnormalities of development

Lack of Blood circulation

Low function or high function of
cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Functional changes

Low or high function of cells

Insufficiency

Lack of Blood circulation

Low function of the cells

Cushing Syndrome

Increased circulation(inflammation)
High function of the cells
Old Cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells
Lack of Blood circulation

Abnormalities of development

Heart

Ischaemic Heart Disease

Lack of Blood circulation(infraction,

sclerosis)
Low or High function of the cells

Angina Pectoris

Lack of Blood circulation(infraction,

sclerosis)
Low or High function of the cells

Myocardial Infraction

Lack of Blood circulation(infraction,

sclerosis)
Low or High function of the cells

Cardio Sclerosis

Lack of Blood circulation(infraction,

sclerosis)
Low or High function of the cells

Myocardial-dystrophy

Lack of Blood circulation(infraction,

sclerosis)
Low or High function of the cells

Myocarditis

Increased circulation(inflammation)
Low function of the cells

Cardiac Insufficiency

Lack of Blood circulation

Function of the cells low

Cardio-Myopathy

Lack of Blood circulation

Function of the cells low
Old Cells

Abnormalities of Cardiac
Rhythm and conduction

Lack of Blood circulation

High or Low Function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Age Related Changes

Post-Stress effects

Abnormalities of development

Lack of Blood circulation

Low function of the cells
Old cells
Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells
Lack of Blood circulation

Blood and
Peripheral
Blood
Vessels

Anemia

Lack of Blood circulation

Low function of the cells
Young Cells

Leukopenia

Lack of Blood circulation

Low function of the cells
Young or old Cells

Abnormalities of
development

Lack of Blood circulation

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Hemorrhagic Diathesis

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Increased circulation(inflammation)
Or Lack of Blood circulation
(infraction, sclerosis)
Low or High function of the cells
Young or old Cells
Increased circulation(inflammation)
Low function of the cells

Hemorrhagic Vasculitis

Phlebitis and
thrombophlebitis

Increased circulation(inflammation)
Low function of the cells
Lack of Blood circulation
Low function of the cells
Increased circulation(inflammation)
High function of the cells

Idiopathic hypotension

Hypertension

Lack of Blood circulation

Function of the cells low
Old Cells
Increased circulation(inflammation)
High function of the cells

Degenerative process

Allergic process

Spleen

Nose

Splenomegaly

Increased circulation(inflammation)
Low function of the cells
Young or old Cells

Hypersplenism

Increased circulation(inflammation)
Low function of the cells
Young or old Cells

Hyposplenism

Lack of Blood circulation (infraction,

sclerosis)
Low function of the cells
Young or old Cells

Chronic Congestive
Splenomegaly

Increased circulation(inflammation)
Low function of the cells
Young or old Cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of
development

Lack of Blood circulation

Rhinitis

Increased circulation(inflammation)
Low function of cells

Frontitis

Increased circulation(inflammation)
Low function of cells

Maxillary Sinusitis

Increased circulation(inflammation)
Low function of cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Lungs and
Bronchi

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of
development

Lack of Blood circulation

Bronchitis

Increased circulation(inflammation)
Low function of the cells

Bronchiectatic Disease

Lack of Blood circulation

Low function of the cells
Old Cells

Bronchial Asthma

Increased circulation(inflammation)
High function of the cells

Pneumonia

Increased circulation(inflammation)
Low function of the cells

Pleuritis

Increased circulation(inflammation)
Low function of the cells

Myocarditis

Increased circulation(inflammation)
Low function of the cells

Chronic Respiratory
insufficiency

Lack of Blood circulation

Low or High function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Oesophagus

Stomach

Duodenum

Diverticulas

Lack of Blood circulation

Low function of the cells
Old Cells

Oesophagitis

Increased circulation(inflammation)
Low function of the cells

Neurosis of Oesophagus

Lack of Blood circulation

High function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Gastritis

Increased circulation(inflammation)
Low function of the cells

Ulcerative disease

Lack of Blood circulation

Function of the cells low
Young or Old Cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of
development

Lack of Blood circulation

Duodenitis

Increased circulation (inflammation)

High function of the cells

Ulcerative disease

Lack of Blood circulation

Function of the cells low

Young or Old Cells

Small
Intestine

Large
Intestine

Dyskinesia

Low or High function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Enteritis

Increased circulation(inflammation)
High function of the cells

Diverticula

Lack of Blood circulation

Function of the cells low
Old Cells

Dyskinesia

Low or High function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of
development

Lack of Blood circulation

Colitis

Increased circulation(inflammation)
High or low function of the cells

Diverticula

Lack of Blood circulation

Function of the cells low
Old Cells

Sigmoiditis

Increased circulation(inflammation)
High or low function of the cells

Haemorrhoids

Increased circulation(inflammation)
Low function of the cells
Old Cells

Functional Changes

High or low function of the cells

Proctatis

Increased circulation(inflammation)
Low function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of
development

Lack of Blood circulation

Liver

Gall
Bladder

Hepatitis

Increased circulation(inflammation)
Low function of the cells

Cirrhosis

Lack of Blood circulation

(infraction, sclerosis)
Low function of the cells
Old Cells

Portal hypertension

Increased circulation(inflammation)
Low function of the cells

Bilirubin Matabolism
Disorder

Low or High function of the cells

Young or old Cells

Hepatic Insufficiency

Increased circulation(inflammation)
or Lack of Blood circulation
Low function of the cells
Old Cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Cholecystitis

Increased circulation(inflammation)
Low function of the cells

Cholangitis

Increased circulation(inflammation)
Low or High function of the cells

Biliary tract Dyskinesia

Low or High function of the cells

Cholelithiasis

Function of the cells low

Old Cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

Pancreas

Pancreatitis

Increased circulation(inflammation)
Low function of the cells

Sclerotic Pancreatitis

Lack of Blood circulation

Function of the cells low
Old Cells

Pathology of Islets of
Langerhans

Low or High function of the cells

Young or Old Cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

Kidneys

Glomerulonephritis

Increased circulation(inflammation)
Low function of the cells

Pyelonephritis

Increased circulation(inflammation)
Low function of the cells

Reno-vascular impairment

Lack of Blood circulation

Low function of the cells

Renal insufficiency

Lack of Blood circulation

Low function of the cells
Old Cells

Urolithiasis

Low function of the cells

Old Cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

Urinary
Bladder

Urolithiasis

Low function of the cells

Old Cells

Cystitis

Increased circulation(inflammation)
Low or High function of the cells

Polyposis

Increased circulation(inflammation)
Low or High function of the cells
Young Cells

Urogenital Infections

Increased circulation(inflammation)
High function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

MusculoSkeletal
System

Arthrosis

Lack of Blood circulation

Function of the cells low
Old cells

Osteochondropathy

Lack of Blood circulation

Low Function of the cells
Old cells

Arthritis

Increased circulation(inflammation)
Low function of the cells

Polyarthritis

Increased circulation(inflammation)
Low function of the cells

Radiculitis

Increased circulation(inflammation)
Low function of the cells

Myositis

Increased circulation(inflammation)
Low function of the cells

Osteoporosis

Lack of Blood circulation

Function of the cells low
Old cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

Skin

Dermatomyositis

Increased circulation(inflammation)
Low function of the cells

Lichen Planus

Increased circulation(inflammation)
Low function of the cells
Young or Old cells

Psoriasis

Increased circulation(inflammation)
Low function of the cells
Young or Old cells

Neurodermatitis

Increased circulation(inflammation)
Low function of the cells

Urticaria

Increased circulation(inflammation)
High function of the cells

Eczema

Increased circulation (inflammation)

High function of the cells
Young cells

Dermatitis

Increased circulation(inflammation)
Low function of the cells

Erythema

Increased circulation(inflammation)
High function of the cells

Herpes

Increased circulation(inflammation)
High function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

Prostate
Gland

Prostatitis

Increased circulation(inflammation)
Low function of the cells

Calculous Prostatitis

Lack of Blood circulation

Low Function of the cells

Sclerosis Prostatitis

Lack of Blood circulation

Low Function of the cells
Old Cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

Mammary
Glands

Mastopathy

Increased circulation(inflammation)
High function of the cells

Mammary Gland Cyst

Lack of Blood circulation

High Function of the cells

Mastitis

Increased circulation(inflammation)
High function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

Ovaries
Cyst

Lack of Blood circulation

Low Function of the cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

Uterus and Adnexitis

Appendages

Increased circulation(inflammation)
Low function of the cells

Cervical Erosion

Increased circulation(inflammation)
Young or Old Cells

Endometritis

Increased circulation(inflammation)
Low function of the cells

Salpingitis

Increased circulation(inflammation)
Low function of the cells

Kraurosis Vulvae

Increased circulation(inflammation)
High function of the cells
Young Cells

Uterine myoma

Lack of Blood circulation

Low Function of the cells
Young Cells

Degenerative process

Lack of Blood circulation

Function of the cells low
Old Cells

Allergic process

Increased circulation(inflammation)
High function of the cells

Neoplasm

Increased circulation
High function of the cells
Young cells

Age Related Changes

Lack of Blood circulation

Low function of the cells
Old cells

Post-Stress effects

Increased circulation(inflammation)
Lack of Blood circulation
Low function or high function of
cells

Abnormalities of development Lack of Blood circulation

Appendix 5: Definitions
The following background, definitions and/or text are included to assist the practitioner to
better understand the terminology used in
Hayflick Limit Theory
In 1962 two cell biologists, Dr. Hayflick and Dr. Moorehead, made one of the greatest
contributions to the history of cellular biology by demonstrating the senescence of
cultured human cells. Hayflick theorized that the aging process was controlled by a
biological clock contained within each living cell. The 1961 studies concluded that
human fibroblast cells (lung, skin, muscle, heart) have a limited life span. They divided
approximately 50 times over a period of years and then suddenly stopped. Nutrition
seemed to have an effect on the rate of cell division: overfed cells made up to 50
divisions in a year, while underfed cells took up to three times as long as normal cells to
make divisions. Alterations and degenerations occurred within some cells before they
reached their growth limit. The most evident changes took place in the cell organelles,
membranes and genetic material. This improper functioning of cells and loss of cells in
organs and tissues may be responsible for the effects of aging.
Limited Number of Cell Divisions Theory
The number of cell divisions id directly affected by the accumulations of the cell's waste
products. The more wastes we are accumulate over time the faster cells degenerate.
Although an ordinary chicken does not live anywhere near 20 years, French surgeon Dr.
Alexis Carrel was able to keep pieces of a chicken heart alive in a saline solution which
contained minerals in the same proportion as chicken blood for 28 years. He believed
that he had achieved this by disposing off the waste products daily. Although Carrel's
theory was eventually overturned by Dr. Leonard Hayflick when it was found that fresh
cells had been inadvertently added to the cultures making the chicken cells seem
"immortal," the experiment helped explain why cells from older people with more waste
divided fewer times than cells from embryos which divided the most.
Waste Accumulation Theory
In the course of their life spans cells produce more waste than they can properly
eliminate. This waste can include various toxins which when accumulated to a certain
level, can interfere with normal cell function, ultimately killing the cell.
Evidence supporting this theory is the presence of a waste product called lipofuscin
leading to age pigment. The cells most commonly found to contain lipofuscin are nerve
and heart muscle cells, both critical to life. Lipofuscin is formed by a complex reaction
that binds fat in the cells to proteins. This waste accumulates in the cells as small
granules and increases in size as a person ages. Because lipofuscin builds up over time,
it has been described as "the ashes of our dwindling metabolic fires"
The Free Radical Theory
This exciting development in anti-aging research was first introduced by R. Gerschman
in 1954, but was developed by Dr. Denham Harman of the University of Nebraska,
College of Medicine. "Free radical" is a term used to describe any molecule that differs

from conventional molecules in that it possesses a free electron, a property that makes
it react with other molecules in highly volatile and destructive ways.
In a conventional molecule the electrical charge is balanced. Electrons come in pairs so
that their electrical energies cancel each other out. Atoms that are missing electrons
combine with atoms that have extra electrons, creating a stable molecule with evenly
paired electrons and a neutral electrical charge.
The free radical on the other hand has an extra negative charge. This unbalanced
electrical energy tends to make the free radical attach itself to other molecules as it tries
to steal a matching electron to attain electrical equilibrium. Some scientist speak of
these free radicals as "promiscuous," breaking up the happy marriages of paired
electrons in neighboring molecules in order to steal an electron "partner" for
themselves. In doing so they create free radicals and extensive bodily damage.
Free-radical activity within the body is not only or even primarily negative. Without
free-radical activity, that is without biochemical electricity, we would not be able to
produce energy, maintain immunity, transmit nerve impulses, synthesize hormones or
even contract our muscles. The body's electricity enables us to perform these functions
and that electricity comes from the unbalanced electron activity of free radicals.
But free radicals also attack the structure of our cell membranes, creating metabolic
waste products, including substances known as lipofuscins. An excess of lipofuscins in
the body is shown as a darkening of the skin in certain areas, so-called "aging spots."
Lipofuscins in turn interfere with the cells ability to repair and reproduce themselves.
They disturb DNA and RNA synthesis, interfere with synthesis of protein, lower our
energy levels, prevent the body from building muscle mass and destroy cellular
enzymes, which are needed for vital chemical processes.
This type of free-radical damage begins at birth and continue until we die. In our youth
its effects are relatively minor since the body has extensive repair and replacement
mechanisms that in healthy young people function to keep cells and organs in working
order. With age however the accumulated effects of free-radical damage begin to take
their toll. Free-radical disruption of cell metabolism is part of what ages our cells; it
may also create mutant cells leading ultimately to cancer and death.
Free radicals attack collagen and elastin, the substances that keep our skin moist,
smooth, flexible and elastic. These vital tissues fray and break under the assaults of free
radicals, a process particularly noticeable in the face, where folds of skin and deep-cut
wrinkles are testaments to the long-term effect of free-radical damage.
Another way of looking at free-radical changes is to think of its as oxidation, the
process of adding oxygen to a substance. Another word for oxidation is rust and in a
sense our aging process is analogous to the rusting away of a once-intact piece of
metal. Because forms of oxygen itself are free radicals, our very breathing and our
otherwise healthy aerobic exercise generate free radicals that help along the aging
process.
Substances that prevent the harmful effects of oxidation are known as antioxidants.
Natural antioxidants include vitamin C, vitamin E and beta carotene, the substance that
our body uses to produce vitamin A. Specialists in anti-aging medicine prescribe a host
of natural and manufactured antioxidants to help combat the effects of aging.
Another substance that combats free-radical damage is known as a free-radical
scavenger. Free-radical scavengers actually seek out free radicals and harmlessly bind

them before they can attach themselves to other molecules and/or cause cross-linking.
As we'll see in subsequent chapters many vitamins and minerals and other substances
fight aging by acting as free-radical scavengers.
The Genetic Control Theory
This planned-obsolescence theory focuses on the genetic programming encoded
within our DNA. We are born with a unique genetic code, a predetermined tendency
to certain types of physical and mental functioning, and that genetic inheritance has a
great deal to say about how quickly we age and how long we live. To use a macabre
analogy it's as though each of us comes into the world as a machine that is
preprogrammed to self-destruct. Each of us has a biological clock ticking away set to
go off at a particular time, give or take a few years. When that clock goes off it signals
our bodies first to age and then to die.
However, as with all aspects of our genetic inheritance the timing on this genetic
clock is subject to enormous variation, depending on what happens to us as we grow
up and on how we actually live (the old "nature versus nurture" debate).
Anti-aging medicine addresses this issue by augmenting the basic building blocks of
DNA within each of our cells, preventing damage to and increasing repair of DNA. In
this way we believe anti-aging treatment can help us escape our genetic destinies, at
least to some extent.
The Neuroendocrine Theory
This theory developed by Vladimir Dilman, Ph.D., elaborates on the wear and tear
theory by focusing on the neuroendocrine system, the complicated network of
biochemicals that governs the release of our hormones and other vital bodily elements.
When we are young, our hormones work together to regulate many bodily functions,
including our responses to heat and cold, our life experiences and our sexual activity.
Different organs release various hormones all under the governance of the
hypothalamus, a walnut-sized gland located within the brain.
The hypothalamus sets off various chain reactions whereby an organ releases a
hormone which in turn stimulates the release of another hormone, which in turn
stimulates yet another bodily response. The hypothalamus responds to the body's
hormone levels as its guide to regulating hormonal activity.
When we're young hormone levels tend to be high, accounting for among other things,
menstruation in women and high libido in both sexes. As we age the body produces
lower levels of hormones which can have disastrous effects on our functioning. The
growth hormones that help us form muscle mass, hGH, testosterone and thyroid, for
example, drop dramatically as we age so that even if an elderly person has not gained
weight, he or she has undoubtedly increased the ratio of fat-to-muscle.
Hormones are vital for repairing and regulating our bodily functions, and when aging
causes a drop in hormone production, it causes a decline in our body's ability to repair
and regulate itself as well. Moreover hormone production is highly interactive. The
drop in production of any one hormone is likely to have a feedback effect on the
whole mechanism, signaling other organs to release lower levels of other hormones
which will cause other body parts to release lower levels of yet other hormones. Thus
hormone replacement therapy, a frequent component of any anti-aging treatment,
helps to reset the body's hormonal clock and so can reverse or delay the effects of
aging. If our hormones are being produced at youthful levels in a very real sense the

cells of our bodies are stimulated to be metabolically active and thus we stay young.
The "Wear and Tear" Theory
Dr. August Weismann, a German biologist, first introduced this theory in 1882. He
believed that the body and its cells were damaged by overuse and abuse. The organs,
liver, stomach, kidneys, skin and so on are worn down by toxins in our diet and in the
environment; by the excessive consumption of fat, sugar, caffeine, alcohol and
nicotine; by the ultra-violet rays of the sun and by the many other physical and
emotional stresses to which we subject our bodies. Wear and tear is not confined to our
organs, however; it also takes place on the cellular level.
Of course even if you've never touched a cigarette or had a glass of wine, stayed out of
the sun and eaten only natural foods, simply using the organs that nature endowed you
is going to wear them out. Abuse will only wear them out more quickly. Likewise as
the body ages our very cells feel the effect, no matter how healthy our life style.
When we are young the body's own maintenance and repair systems keep
compensating for the effects of both normal and excessive wear and tear. (That's why
young people can more easily get away with a night of heavy drinking or a binge of
pizza or sweets.) With age the body loses its ability to repair damage caused by diet,
environmental toxins, bacteria or a virus. Thus many elderly people die of diseases that
they could have resisted when they were younger.
By the same token nutritional supplements and other treatments covered in this book
can help reverse the aging process by stimulating the body's own ability to repair and
maintain its organs and cells.

Appendix 6.
The following text is used as an example of how the practitioner should liase with their
patients and prepare them for their SVS consultation and test. Please feel free to adapt these
texts as you feel is necessary.

Mimex Montague Healthcare Limited, Mulberry House, 6 Vine Farm Close, Cotgrave,
Nottinghamshire NG12 3TU
Tel: 0044-(0)115-9899618/9890304/fax 989 9826/mob: 07885 755847
E-mail: enquiries@montague-diagnostics.co.uk; elena.ewing@montaguediagnostics.co.uk; graham.ewing@montague-diagnostics.co.uk
Dear Sir/Madam
Thank you for arranging a consultation with Montague Healthcare.
Your assessment will take place at: Mulberry House, 6 Vine Farm Close, Cotgrave,
Nottinghamshire, NG12 3TU. Our premises are located in the centre of Cotgrave within 200
metres from the large prominent All Saints church which is a significant landmark. Vine
Farm Close is more or less opposite The Manvers Arms which is next to the church.
Cotgrave can easily be reached from the A46 and A52 trunk roads which cross
Nottinghamshire. For directions refer to www.multimap.co.uk
Please arrive 10-15 minutes before the time of your appointment. Please do not drink any
alcohol, caffeine (tea and/or coffee) or take any drugs or medicines (other than any necessary
prescribed drugs or medicines) in the 24 hours prior to the consultation. Pharmaceutical
medications can in some cases mask some of the test results (e.g. if you take insulin this will
mask any indications of diabetes). Please note that we cannot provide an accurate assessment
for pregnant women and people suffering certain psychiatric problems. Accordingly if you are
pregnant or have psychiatric problems please let us know immediately. In addition, we require
parental consent for any person under 17 at the date of his or her first consultation.
Cancellations with less than 2 full working days notice must be paid for in full.
Payment for the consultation will be required during your visit please bring cash or your
chequebook, cheque guarantee card and/or proof of identity with you. We are not yet able to
accept payment by credit card.

Personal information (Please print in legible block capitals)

Please complete this form and hand it in to reception when you arrive at the clinic. The
information has to be processed before your test can begin. If the form is complete it helps us
to avoid delays.
First name ______________________________
Middle name(s) __________________________
Last name ______________________________
Date of Birth ____________________________
Gender: male or female (please underline)
Weight (kgs) _______

Height _______

Address (inc. postcode) __________________________________________________

_______________________________________________________________________

Telephone: Home ________________________

Work _______________________

Mobile __________________________

E-mail: ______________________________________________________________

Acceptance for a Virtual Scanning Health assessment

PATIENT NAME (Mr/Mrs/Miss/Ms) __________________________________________
PATIENT REFERENCE (office use only) ______________________________________

You are to undergo a consultation which involves a Virtual Scanning assessment. The
assessment is safe, completely non-invasive and requires you to interpret colours on a
computer screen for 15-20 minutes. The results of this test will be assessed by our practitioner
who will process the results through the sophisticated computer programme. This enables the
practitioner to select the appropriate light therapy for your condition.
There will be no unauthorised disclosure of your information to any external party. This
authorization is required by the Data Protection Act and Montague Healthcare accepts to be
bound by same. Mimex Montague Healthcare Limited may wish to use patient data to
demonstrate the accuracy and effectiveness of the system to academics/scientists, medical
specialists and regulatory bodies. Any data which may be used for demonstration purposes
would be sanitised to eliminate any names or identifying marks which could enable any
external party to identify the origin of the data.
Montague Healthcare will not accept responsibility for any action taken as a direct and sole
result of the assessment OR of the therapy. The therapy program comprises a series of
selected colours of varying intensity, frequency and tint. This therapy will be explained to you
during your visit.
Signed to confirm the information I have provided is accurate and to confirm my
understanding and agreement to the above.
Signed ___________________________

Dated ________________________

Please print name ________________________________________________________

If you are signing on behalf of a minor (aged under 17), please state your relationship with the
patient __________________________________________________________

Back pain, slipped disc, rheumatism,

arthritis or other muscle or spinal
problem

Any disorder of the kidneys or

bladder, urinary problems, or
diabetes

Stress, depression, anxiety, chronic

fatigue, mental breakdown or
psychiatric disorder

Asthma, bronchitis, or any

disorder of the lungs

Tumour, growth cyst or lump

Any defect or disease of the

eyes or ears

High blood pressure, palpitations,

chest pain, any heart or circulation
problem

Any gynaecological problems

Recurring indigestion, liver or

pancreas disease, ulcer, colitis or other
bowel problem

HIV/AIDS, Hepatitis B or C,
or any sexually transmitted
disease

Fits, blackouts, migraine, multiple

sclerosis, or any disease of the
nervous system

Any other recurring illness,

any long term injury or any
surgical operation incl.
removal or replacement of
organs

We/Mimex Montague Healthcare Limited are accumulating data which we can use to
demonstrate that this excellent world-leading medical screening technology does indeed do
what the originating company claims. Accordingly, it may be useful to know about your
previous medical history for comparison purposes. We request that you complete the
following questionnaire by placing a tick in the column to the right of the description if you
suffer from or have suffered from any problem described below.
For any items ticked above, please provide any relevant information below. Use the back of
this page if any further space is required. Please use block capitals. Or type the details on
another sheet.

Problem

Approx
Date
started

If
recovered
approx
date

Comments

Which drugs have you been

prescribed by your doctor, now
and in the recent past?

Please advise if you smoke

Please advise if you are

undertaking any other therapies
Please advise if you have a
family pet (a cat, dog, etc.)
We suggest that you do not disclose this information to Mimex Montague Healthcare prior to
the assessment so that you can make a comparison of the effectiveness of Strannik Virtual
Scanning with the results obtained from contemporary diagnostic tests.

Acceptance for Virtual Scanning Light Therapy

PATIENT NAME (Mr/Mrs/Miss/Ms)

_________________________________________
PATIENT REFERENCE (office use only)
______________________________________
I understand and agree that:
It is envisaged that the course of therapy will involve this first consultation and a
number of repeat re-assessments over a period of typically 4-6 months. The therapy
course comprises a number of modules and each module comprises typically 6 sessions.
I will make every effort to undergo each therapy session 1-2 times every 24 hours;
The therapy involves sitting in front of a computer screen (circa 0.5m from the screen),
usually on my home PC, watching a display of flashing colours for typically 15 20
minutes per session, but more problematic conditions may require longer sessions;
I will read the instructions supplied with the therapy disc before I commence my
treatment and will follow the guidance in the instructions;
I will use a computer that meets the minimum specification set out in the manual;
I will maintain the log provided to me of each therapy session undertaken.
Signed to confirm my understanding and agreement to the above and my consent to
undergo the treatment course.

Signed ___________________________

Dated ________________________

Please print name ________________________________________________________

If you are signing on behalf of a minor (aged under 17), please state your relationship
with the patient
__________________________________________________________
Note:
Montague Healthcare recommends that patients should not undertake any courses of
acupuncture, electro-acupuncture, treatment by Scenar, or treatment by any
technologies which act upon the meridians during the course of Strannik Light
Therapy. In the event that a patient undertakes another therapy coincidently with
Strannik Light Therapy Mimex Montague Healthcare Limited will not accept any
responsibility for any side-effects.

Terms & Conditions of Business

Montague Healthcare provides Strannik Virtual Scanner Assessments and Strannik
Light Therapy.
Elena Nikolayevna Ewing, Medical Director of Montague Healthcare, is qualified in
medicine in Russia (with significant experience in ophthalmology (as an ophthalmic
surgeon), dermatology and venereology) although in the UK she is qualified to practice
only as a Complementary Health Therapist (Colour Therapy). For several years Elena
appeared on Ural TV and Ural radio as a medical expert answering medical queries.
Anyone experiencing an adverse medical occurrence as a result of Virtual Scanner Light
Therapy should notify Elena Ewing of Montague Healthcare immediately. The
information should be recorded by the patient and notified to Montague Healthcare
who, if significant or necessary, will report the occurrence to the relevant authorities. In
the event of an adverse event we recommend that the patient should contact their GP or
an appropriate medical authority.
Graham Ewing, Commercial Director

Accommodation
Various levels of accommodation are available within the locality and we will be
pleased to assist patients, practitioners to book accommodation. We recommend:

Travel
For UK travellers please refer to our postcode NG12 3TU and/or use
www.multimap.com to gain travel instructions. For travelers from the south we
recommend to use the M1 motorway, junction 21a signposted to Newark, travel north
until the end of the dual carriageway, follow the A46 single carriageway for three miles
until signposted Cotgrave.
For international travellers we recommend flying to Nottingham East Midlands airport.
We will, in some cases and by prior agreement, arrange collection from the airport or
from Nottingham Railway Station.
For travelers from the north we recommend taking the A1 to Newark, the A46 to and
beyond Bingham. After Bingham, cross the A52, continuing on the A46 for a further 23 miles to the first set of traffic lights. Turn right, after 800 metres turn left. We are
located in Vine Farm Close which is the 5th turn on the right (approximately 100 metres
beyond the Sainsbury supermarket.

Appendix 7:
Advisory Notes to be provided to the Patient
Precautions
This course of Strannik Light Therapy is specifically designed for your own medical condition. UNDER
NO CIRCUMSTANCES SHOULD ANYONE ELSE USE YOUR COURSE OF TREATMENT. Do not
allow anyone else to sit in the same room as you in a position where he or she is aware of the flashing
colours whilst you undergo each treatment session. Do not allow anyone to sit in front of your computer
during any part, however small, of any treatment session.
Do not reload the treatment disc onto another computer and re-commence the treatment from the
beginning. If for any reason you need to transfer the treatment to a different computer, see our
instructions.
Please ensure that you keep a record of your treatment i.e. date and me of the therapy session and
anything which you feel is useful to record. We are unable to verify the completeness of your treatment if
the log is incomplete. You may find this log to be of value if you need to switch from one computer to
another between treatment sessions.
Contra-indications.
Please do not undertake any other forms of therapy during this course of therapy. We specifically advise
to avoid any forms of treatment involving acupuncture (including TENS type devices) or any other forms
of treatment involving stimulation of the acupuncture meridians.
What you can Expect/Symptoms
In some cases some patients may feel slightly worse after the first few sessions in one or more modules.
This is normal, and will pass after two or three more sessions. Do not stop your treatment. The initial
modules of the treatment course are of vital importance but may not produce any noticeable effect on
your condition. Do not let this put you off the treatment is a carefully programmed course running for
several weeks or months and you should not expect to feel any different after the initial modules. Please
persist with the treatment.
Contact: If you have any concerns about any aspect of your treatment, please do not hesitate to contact
your practitioner.
Undergoing Treatment
Preparation
Once a session starts, it SHOULD NOT BE INTERRUPTED. It is therefore important that you prepare
yourself properly before commencing. Ensure that you are not likely to be disturbed or called away from
the computer e.g.
*

Switch off all telephones or switch on the answerphone.

If you are alone at home, consider putting a sign outside your front door saying Do not disturb
or be prepared to ignore anyone who calls.

By all means have a soft drink or a hot drink but do not drink alcohol in the 12 hours before or during a
treatment. Do not undergo treatment if you are tired, under the influence of alcohol or any drugs or
medicines that cause drowsiness, sleepiness, or any form of hallucination.
Ambience
The room should be dimmed and quiet. Soft, calming music played at low volume is ideal. But any music
will be of benefit if it helps you to watch the computer screen.
Seating position
Sit directly in front of the computer screen as you would for normal computer use (as recommended in
your computer user documentation). Look at the screen throughout each session. Try to avoid looking
away from the computer for any length of time. You can glance slightly to the side, top or bottom of the
computer it is not strictly necessary to stare continually into the screen.
Frequency
You must undergo a treatment session at least once every 24 hours (if not recommended otherwise), and
preferably twice per day (once in the morning and once in the early evening). If you miss a session for
any reason any day, run the session as soon as possible after it has been missed and then return to your
24-hour cycle. If you miss the treatment for any more than seven days running, then please call your
practitioner who provided your treatment for advice. If you miss the treatment for several days, and you
then re-start the treatment for up to five sessions, and then find that you miss the treatment for any more
than 48 hours, please call the practitioner who provided your treatment disc for advice. It is possible to
catch up by running a session in the morning and one in the afternoon. You should leave at least 2 hours
between each session as a minimum (if not recommended otherwise).
THE BEST RESULTS WILL BE OBTAINED IF THE FULL TREATMENT IS CARRIED OUT ON A
CONSISTENT BASIS ONCE OR TWICE EVERY 24 HOURS.
Duration of the Therapy Sessions
Sessions are of varying length from 15 to 35 minutes, typically 20 minutes. The full course of treatment is
broken down into a number of modules. The various modules applicable to your treatment are shown in
the right hand box/column of the 'Correction Module' front screen. Each module comprises a number of
treatment sessions.
The colours and/or the colour sequence appearing in each module might be different however the sessions
within a particular module are usually similar in content, and of the same length. The only way you can
find out how long each session will take is to undergo the first session in each module and check the time
yourself. It is not possible to skip modules. Sessions can be skipped by pressing the esc key as soon as
they have started, or by simply not watching the screen. This will of course negate the effectiveness of the
treatment!
Running a treatment session on your computer
When undertaking the therapy start the treatment module at the brain and complete the brain module
before proceeding to another organ module. Complete each module in turn.

You should see a 'Correction Module' icon on your desktop. Double click this and the treatment program
will load. Follow the screen prompts.
If the system should freeze quit the programme. Pressing the ESC key will work on some computers. You
will be asked if the session should be treated as complete. If you think the session is almost complete,
based on the length of time it was running, click YES. But if the session is probably 50% or less
complete, click NO. You will then be able to re-run the session.
If you cannot exit by pressing the ESC key, press the CTR-ALT-DEL keys at the same time. This will
enable you to quit the program instead.
If you have quit the treatment using CTR-ALT-DEL, the program will not recognise the session as
complete. As above, if you think the session was almost complete there is no need to re-run it completely.
To advance the session counter, re-start the session, exit immediately by pressing the ESC key and when
asked, should I count the session as complete click YES.
Before you re-start any session which you have had to end part way through, REMEMBER to close down
any open program which may have caused the treatment session to freeze.
If your treatment session does not load, simply press ctrl-alt-del and when the Close Program dialogue
box appears click end task. This should restore your desktop. Double click the treatment icon again
this time the program should run perfectly.
What if a session is missed?
If you simply do not run a session in any particular day, run it as soon as possible afterwards see above.
If you start a session and have to move away from the computer but you let the session run its course, you
cannot return to it and you have therefore missed a session. This will reduce the benefits of the treatment
program. Thus if you do have to move away from the computer, press the ESC key to escape the session
without letting it run its course. See above.
Is it possible to exit a treatment module once it starts running?
Yes by pressing the ESC key (see above) however, this is not recommended. You should try to start a
session at a time when you have every chance of completing it.
If black lines appear between colour flashes on your monitor
The reason for this may be due to the computers ability to display the required brightness of colour,
which in turn depends on the capability of its Graphics card. This line actually is the part of the screen,
which is not filled with colour fast enough. In other words the dose you are receiving is a little bit less
than necessary. This is not significant the percentage of dose reduction, even on computers with a very
slow Graphics card is no more than 0.5%.
Your Treatment Log
On your treatment disc you will find a treatment log upon which you should record details of all sessions
as you complete them. You may wish to print out this log and keep a manual version. Please ensure that
at least one of these logs is kept up to date. Bring the completed log with you every time you visit the
clinic. This is important to us. If you have not improved as a result of your treatment we will want to
honour our commitment under our guarantee. And we will also want to try to find out why you have not

found any benefit from our system. We need to be sure that the treatment has been undertaken fully and
properly. The following processes help us to ensure that the treatments have been properly run:
* Some treatment programs carry a numerical code, which appears on screen for about 3 seconds at
the end of sessions during the whole course of treatment. If you see this number in any of your
sessions, follow the screen prompts. You will not be able to leave the program until you have
worked through the prompts.
* The computer automatically writes back to the treatment file the date when each session is fully
run.
If a log sheet is not provided, please keep a note of each treatment session: date, time and anything
interesting.
When the treatment is complete
Please contact the Strannik practitioner to arrange the follow assessment to check your condition. When
you visit the clinic please ensure that you bring your treatment log with you for our records (unless you
have forwarded this to us already by e-mail).

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