Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S.

ZETA STRESS 1

MASS BOOK: CHAPTER 4-1:

MASS ZETA STRESS
Moulden
Anoxia
Spectra
Syndrome

WHAT IS ZETA POTENTIAL?

©DR ANDREW MOULDEN MD, PHD / PROFESSOR FRANK HARTMAN

NOVEMBER 4TH, 2008

Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 2

AUTIS M S pectrum
Spectrum
MAS S IN EVOLUTION
BILATERAL BRAINS TEM Ischemic strokes
IS CHEMIA From vaccines
ACTIVE PHAS E

DTaP Vaccine induced

A Medical Emeregency

No one knows Madison

Is having difuuse hypoxic
strokes at this moment that
are precariously close to
Causing S udden infant
death.
S he will survive..but autism
Is the cost of survival.

FOR MADISON: WHAT UNKIND MAN HAS DONE, MAN KIND WILL UNDUE.
“VACCINES have caused Autism-spectrum, many neurodevelopment disorders, sudden infant
death syndrome, alleged “shaken baby syndrome”, many idiopathic seizure disorders, learning
disabilities, Gardasil adverse reactions and death, Gulf War Syndrome, expressive aphasia,
impaired speech skills, Attention deficit disorders , silent ischemic strokes, blood clots,
idiopathic thrombocytopenia purpura, and much more to many organ systems.” M.A.S.S.
disorders on a MASS scale and cerebral Disconnection syndromes in the M.A.Z.E - MASS
Anoxia Zone Encephalopathy.” Andrew Moulden BA, MA, MD, PhD
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 3

Moulden MASS
Anoxia Anoxia
Spectra Zones
Syndromes Encephalopahies

Hypoxia by inflammation Clinical Relevance Hypoxia by low Zeta

Normal Microcirculation Potentials
Hypoxia by increased
metabolism Hypoxia by MASS response
Moulden
Hypoxia by ischemia
Anoxia MASS
Hypoxia by venous congestion Spectra ANOXIA
Hypoxia by endothelial collapse Syndromes Zones
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 4

BrainGuardMD.com: We have Answers. We have Solutions

WHAT IS ZETA POTENTIAL?

& Autism-Spectrum & neurodevelopmental & neuropsychiatric disorders puzzle

AUTISM PUZZLE PIECE & ONE PHASE OF VACCINE INDUCED MASS

Zeta potential is an abbreviation for electrokinetic potential in colloidal systems. In the colloidal
chemistry literature, it is usually denoted using the Greek letter zeta, hence ζ-potential.

From a theoretical viewpoint, zeta potential is electric potential in the interfacial double layer at
the location of the slipping plane versus a point in the bulk fluid away from the interface. In
other words, zeta potential is the potential difference between the dispersion medium and the
stationary layer of fluid attached to the dispersed particle.

One of the key “slipping planes” inside blood vessels is the smooth glyocalyx layer that lines the
inside surface of all blood vessels. Glycocalyx to blood vessels is like the slime coating on a fish;
the coating creates a slipstream surface in fluid dynamics. In the circulatory system this effect
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 5

allows the fluid medium (serum) and formed blood products (platelets, red & white blood cells)
to slip along the inside surfaces of blood vessel walls smoothly.

Without mechanisms to maintain slipstream surfaces between formed blood products and vessel
walls blood flow would not be laminar. Non-laminar blood flow causes focal areas of blood
clotting. Lowered zeta potential also increases clotting and slows blood flow especially in low
pressure areas like capillaries

Most particles dispersed in an aqueous system will acquire a surface charge, principally either by
ionization of surface groups, or adsorption of charged species. These surface charges alter the
distribution of the surrounding ions, resulting in a layer around the particle that is different to
that of the bulk solution. If the particle moves, under Brownian motion (ie. random movement of
particles suspended in a liquid) this layer moves as part of the particle. The zeta potential is the
potential at the point in this layer where it moves past the bulk solution. This is usually called the
slipping plane. The charge at this plane will be very sensitive to the concentration and type of
ions in solution.

ZETA POTENTIAL ALTERATIONS IN FLUID DYNAMICS: MASS & MAZE

Vaccine adjuvant, ischemia, endothelial damage, and non-specific immune hyper stimulation are
some of the factors that can alter zeta potential in mammalian circulatory fluid dynamics. These
and other factors, individually and collectively, impair blood flow through microcirculatory
capillary units at the transition zone between arterial and venous circulatory systems.

M.A.S.S. (Moulden Anoxia Spectra Syndromes) is the specific microbiological processes and
phases by which blood flow through microcirculation units in the brain and body is impaired
from vaccines, infectious diseases, antigens, toxins, and heavy metals.

MASS is the cause of Autism-spectrum disorders and many other health problems. M.A.Z.E.
(MASS Anoxia Zone Encephalopathies) is the main category within which a multitude of brain
and behavioral disorders emerge that is caused by MASS. The common denominator across all
MASS brain and behavior disorders is MASS impairment of tissue oxygenation (ischemia) of
which lowered Zeta potential is invariably a component process that acts as a trigger or an
emergent property of MASS physiology from non-specific immune hyper stimulation.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 6

MASS has multiple triggers, however, the mechanism to disease and disorders is the same
irrespective of the trigger. It is for this reason that we are now in the favorable position of
knowing what to do in order to maximize health & wellness across broad categories of disease
and chronic illness – including vaccine induced autism-spectrum.

Zeta Potential, Blood vessel, Blood flow & MASS Disorders: Schematic representation of Zeta
potential & a blood vessel lumen. Note that even capillary blood vessels have their own, tiny,
blood vessels called the vasa vasorum. If blood flow is impeded, then blood vessels of blood
vessels are the first to be rendered hypoxic. Blood flow is governed by non-Newtonian fluid
dynamics which represents any fluid with flow properties that are not described by a single
constant value of viscosity. In a non-Newtonian fluid, the relation between the shear stress and
the strain rate is nonlinear, and can even be time-dependent. Therefore a constant coefficient of
viscosity can not be defined. MASS Disorders, and many pathological states as it turns out, has a
common origin in non-Newtonian fluid mechanics. Blood flow, at the microscopic level, is
crucial to health and wellness, for all organ systems, and all diseases.

Rheology is the study of the flow of matter including liquids, soft solids, and solids under
conditions in which they flow rather than deform elastically. Materials flow when subjected to a
stress which is a force per area. Rheology is concerned with forces, stresses, and with extending
the "classical" disciplines of elasticity and (Newtonian) fluid mechanics to materials whose
mechanical behavior cannot be described with the classical theories.

Since Isaac Newton originated the concept of viscosity, the study of variable viscosity liquids,
such as blood and bodily fluids, is also often called Non-Newtonian fluid mechanics

One part of the answer to the cause of vaccine-Autism-neurodevelopment disorders is to be

found in rheology and Non-Newtonian fluid dynamics at the microcirculation unit.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 7

High ZETA

LOW ZETA

LOW ZETA POTENTIAL CAUSES INTRAVASCULAR COAGLATION

Zeta potential is one of the main forces that mediate inter particle interactions. Particles with a
high zeta potential of the same charge sign, either positive or negative, will repel each other.
Conventionally a high zeta potential can be high in a positive or negative sense, i.e. <-30mV and
>+30mV would both be considered as high zeta potentials. For molecules and particles that are
small enough, and of low enough density to remain in suspension, a high zeta potential will
confer stability, i.e. the solution or dispersion will resist aggregation.

Intense microbial action (infection) or microbial agents cause a reduction in zeta potential which
changes blood to "sludge." The administration of more than one vaccine at a time multiplies this
effect thereby increasing the amount of intravascular coagulation and bloodclots.

The use of aluminum salts to stabilize vaccines exacerbates the clotting effect by a multiple of
6000 times. (See explanation below)

Infection whether by vaccine or other disease agents lowers zeta potential causing clots. This is a
component sub-process of MASS – Moulden Anoxia Spectra Syndromes.

In a person with high zeta potential of the blood, immunogenic challenge may cause only local
reduction and aggravation. In other cases, it can result in micro capillary clotting destroying and
impairing organ function in clinically apparent and silent ways.

Zeta potential changes, as a part of MASS brain and behavioral disorders accounts for the wide
range of neuropsychiatric, neuromotor, neurocognitive, neurodevelopment, and neurosensory
disorders as well as other organ pathological states since the site and degree of the micro
vascular clotting cascade is unpredictable. The effect may start out as only an adhesion and
through further reduction of zeta potential may change to a clot or hemorrhage.

Some tissue areas have high affinity for certain toxins (e.g. the substantia nigra and MPP+ and
certain pesticides in Parkinson’s disease). In these instances, the tissue regions with affinity for a
particular toxin or particulate matter, becomes a regional discrete area that is preferentially
affected by low zeta and MASS.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 8

LOW ZETA, VACCINES, MASS & ALLEGED “SHAKEN BABY SYSNDROME”

The hemorrhagic transformation from vaccine induced micro vascular ischemia, has been
responsible for many wrongful criminal convictions of alleged “child abuse: under the diagnosis
of “shaken baby syndrome.”

Doctor’s rely on retinal hemorrhages and bleeding within the brain (intra-cerebral hemorrhage)
specific hallmarks of “shaken baby syndrome.” Unfortunately, these “hallmarks” are also
cardinal features of vaccine induced MASS and MAZE – MASS Anoxic Zone Encephalopathies,
of which sudden infant death is a variant.

Since MAZE is a process that deprives tissues of oxygen, this can precipitate seizures in the
infant that can occur during sleep. Since the infants long bines are not yet calcified, the tonic-
clonic phase of seizures can precipitate fractures and fracture lines along bones that generally
imply child abuse. If the parent brings their child to an emergency department and x-rays are
done, the physician may find multiple fractures, of different stages of healing that imply abuse
when in fact the forensic features actually reflect adversity from vaccination and/or infectious
disease.

This is not to say that no one is guilty of child abuse. It simply points out that the features
Doctors, police, and courts rely upon to convict an individual of child abuse are not necessarily
pathognomonnic (specific features of) a singular explanation for the infants clinical and
pathological findings in exam. MASS and low Zeta can achieve the same effect as shaken baby.
Criminal cases may not be criminal at all as the actus reus (physical act) and mens rea (mental
intent) was never formed for MASS MAZE pathologies.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 9

VACCINE ADJUVANT, ALUMINUM, & NEUROCOGNITIVE IMPAIRMENT

Eliminating aluminum salts and monitoring of the blood vessels of the white of the eyes for
intravascular coagulation would greatly reduce risks of vaccinations. However due to
environment and aluminum accumulations, zeta potential tends to reduce with age. Thus,
vaccination of the elderly, or those with hypercoagulable states, may reduce zeta potential close
to the phase change point so that even an emotional upset can trigger a micro vascular clot – or
heart attack for that matter.

We now have 1 adult in 13 over the age of 65 diagnosed with dementia of the Alzheimer type.
One person in three over the age of 85 is diagnosed with Alzheimer-type dementia. Aluminum, a
vaccine adjuvant, is at the core of the pathological plaques and tangle in the human brain of
Alzheimer’s type dementia patients. Aluminum salts are non-specific immune system accelerants
used in all vaccines. Upwards of twenty percent of all Alzheimer deaths show micro vascular
lesions in the brain in addition to the classic “plaque and tangle” microscopic features seen post-
mortem. Notably, these micro vascular ischemic area (micro strokes) unfolded in clinically silent
ways during life. This situation is not any different from Autism-spectrum, Parkinson disease,
specific learning disabilities, attention deficit disorders, Gardasil deaths, Gulf War Syndrome,
schizophrenia, and other morbid pathological states.

The MASS intravascular clotting process and tissue healing process is happening in most if not
all vaccine acquired neurodevelopment disorders, albeit in temporally compressed, discrete
episodes. The damages, like Alzheimer’s disease, are cumulative albeit not necessarily
progressive.

Even skin reactions can occur immediately and continue for seven or eight years or may not
appear until one to six years later. This happens in all mammals from vaccines. There are over
7000 references to aluminum toxicity. Some key ones including this can be found at :

http://www.luminet.net/~wenonah/hydro/al.htm

Subcutaneous nodules in patients hyposensitized with aluminum-containing allergen extracts.

Garcia-Patos V. – Pujol R.M. – Alomar A. – Cistero A. – Curell R. – Fernandez-Figueras M.T. – de

Moragas J.M.

From: Arch Dermatol (1995 Dec) 131(12):1421-4

Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 10

These lesions have been mainly attributed to a hypersensitivity reaction to aluminum

hydroxide, which is used as an absorbing agent in many vaccines and hyposensitization
preparations. Patch tests with standard antigens and aluminum compounds and
histopathologic and ultrastructural studies were performed on 10 patients with persistent
subcutaneous nodules on the upper part of their arms after injection of aluminum-
adsorbed dust and/or pollen extracts. The nodules appeared 1 month to 6.5 years after
injections.

PEACHES

The case of Peaches is below. This highlights that MASS/ZETA is also an ischemic
vaccine problem for our companion pets and the problems are not solely at the injection
site.

“This same process

Damages all small
Blood vessels in
The body/brain
& causes autism
From any vaccination.
Dr. Andrew Moulden MD, PhD

Moulden
Anoxia
Spectra
Syndromes

“The mechanism is now known”

Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 11

ZETA POTENTIAL MEETS VACCINE MASS – MOULDEN ANOXIA SPECTRA SYNDROMES -

& IMMUNOLOGICAL TOLERANCE LOST & FOUND

The introduction of any bacteria or bacterial filtrates alive or dead (vaccine) causes a reaction of
the body that results in blood clots from intense microbial action reducing zeta potential. These
clots may be small adhesions that attach to the blood vessels or organs impairing their function
or complete obstructions resulting in organ death. They are particularly common in kidney, lung,
liver and brain.

This intravascular (within blood vessels) coagulation (clotting) is readily apparent in an

examination of the blood vessels in the sclera (whites) of the eyes from vaccines or other
infections.

Microorganisms take days to weeks to months to demonstrate their full effect on a system. This
is known as the Sarannelli/ Schwartzman phenomena. There are several hundred references to its
occurrence in the National Library of Medicine. It is called “phenomena” because the cause has
not been understood.

It is precisely this missing medical physiology “pheneomena” that has been discovered and
elucidated by MASS – Moulden Anoxia Spectra Syndromes. MASS, as it turns out, in
physiology and process, IS the cause of acquired mammalian disease states - all of them!

MASS “phenomena” has now been elucidated right down to the microbiological processes,
phases, and stages that are latently activated to cause mammalian disease , vaccine adversity, and
autism-spectrum. Remarkably, solving the medical mystery behind vaccine induced
neurodevelopment disorders has resulted in the solution for much human disease, in cause,
prevention, and now on the horizon is the means to effect targeted cures. This includes many
ailments, some cancers. Alzheimer’s disease, schizophrenia, and much more.

Zeta potential is one of several physiological phases of MASS (and human disease). MASS can
be immunologically triggered in the absence of lowered Zeta potentials. However, irrespective of
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 12

which MASS phase comes first, lowered Zeta potential eventually emerges even if only at the
microcirculation units in the body. The end result is clotting within the micro blood vessels and
impaired oxygen delivery to cells and tissue. This is hypoxia (low oxygen), anoxia (no oxygen)
and ischemia (low oxygen from low blood flow) and stroke (oxygen demand exceeding oxygen
supply). This is human disease, chronic illness, disorders, death, vaccine induced autism-
spectrum, sudden infant death syndrome, and multi-organ disease and functional impairments.
MASS is like a “one-stop-shop” to health, wellness, and morbidity.

CONGENITAL RUBELLA & INTRAVASCULAR COAGULATION – CASES IN POINT

The autopsy reports of nine toddlers aged 13 hours to 11 ½ months are presented below. These
are congenital rubella (German Measles) cases are from 1964. The autopsy table demonstrates
clearly that the intravascular coagulation effect from these “pathogens” cuts across all organ
systems. The effects can take several months to manifest. This is intravascular clotting cascades
at work. This is Zeta potential in action. This is the means by which virulent pathogens have
harmed, paralyzed, and killed in the pre-vaccine era. This is the means that these same
pathogens, whether they are killed or attenuated, are causing the same problems, albeit in an
attenuated form, now that we are injecting them with mass vaccination programs.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 13

General Autopsy Findings (above): Diffuse Vascular Damages – All organ systems affected
These were clinically silent vascular ischemic lesions including the ischemic lesions to the brain.
Many of these children were developmentally impaired and autistic (Autism in children with
congenital rubella. Stella Chess. Journal of Autism and Childhood Schizophrenia 1971 Jan-
Mar;1(1):33-47).

These congenital rubella syndrome children exhibit the same hard neurological measures of
ischemic brain injuries using our BrainGuardMD.com imaging protocols as do contemporary
autistic children post vaccination as a function of any vaccine – nit just MMR.. Remarkably, we
now show that these neurovascular lesions are emerging within hours and days of vaccination
and the lesion are identical to those seem in the pre-vaccine era – all pathogens (DTaP, Gardasil
Anthrax, Hepatitis A/B, MMR, influenza, etc..) are creating the same lesions across the lifespan
and across all emergent medical diagnoses.. This is a generic non-specific response to any
immune challenge and not a particular “germ.” This means no vaccination is safe as currently
constituted.

Microscopic intravascular coagulation, anoxic states, MASS, and low Zeta Potential is the cause
of acquired disease in response to anything foreign entering the human body under conditions of
immune hyper stimulation. Foreign substances that sequester in tissue lines and cannot be readily
removed by cannot normal immunological means, becomes a focal point for on-going non-
specific immune assault to the area. This is a factor in diseases wherein tissue is slowly lost in
focal areas such as insulin dependent diabetes mellitus, Parkinson’s disease, and Alzheimer’s
type dementia.

When all vaccines and infectious diseases create the same pathological symptoms in all people,
then it is NOT the pathogen that is causing the disease. Rather, disease is emerging as a generic
response to non-specific immunological challenge. Accordingly, vaccines do nothing to address
the cause of disease or morbidity from infectious diseases. Vaccines simply weaken any
particular “bugs” ability to elicit an intense non-specific immune response. Since this non-
specific immune response is the same cause of morbidity across al pathogens, then prevention of
morbidity is best suited by targeting the non-specific immune response directly – on an as-
needed basis.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 14
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 15

6th nerve ischemic strokes

Moulden
Anoxia
Spectra
Syndromes
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 16

© Dr Andrew Moulden MD, PhD © Dr Andrew Moulden MD, PhD

Right 6th nerve Left 6th nerve

www.BrainGuardMD.com
1-705-498-6284 for solutions

Moulden
Anoxia
Spectra
Syndromes MADISON
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 17
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 18

THIS IS SUDDEN INFANT DEATH FROM VACCINES AND MASS

Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 19

THIS IS HOW VACCINES CAUSE SUDDEN INFANT DEATH SYNDROME & VACCINE DEATH

GLOBAL VACCINATIONS: WHAT’S IN A VACCINE?

Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 20

COGITO ERRATUM SUM PROFIT

Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 21
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 22
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 23

GLOBAL VACCINATIONS: A $$ PROFITABLE $$ COCKTAIL FOR WHO?

Making matters worse, every foreign substance, dead or alive, added to the vaccines, including
aluminum additives, mercury preservatives, formaldehyde, human and animal cells, and
contaminants, each triggers a MASS response in their own right. It is the magnitude of MASS
that determines disease. MASS is additive, summative, and has immunological memory. The
magnitude of the MASS response is more a function of the net immunogenic load at a given
point in time rather than the specific “pathogen” one is injected with.

Considering the record profits that have been made selling vaccines to the world, one should
think that society should hold accountable and responsible, financially, all who have profited
from vaccines – including the physicians who have administered them. These funds must be
directed to victims (we are all victims), recovery efforts, and solutions that are metered by
parents and the public not by corporations, politicians, governmental bodies and officials.
The damages, globally, are astounding:
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 24

MASS Ischemia: Autism-spectrum and learning disabilities are along the same continuum of
range and breadth of brain injury from the same vaccine triggered MASS pathophysiological
cascade and all vaccines. This is why universal one-size fits all vaccines, as currently constituted,
have caused an epidemic of neurodevelopment disorders that includes:
Moulden
Anoxia
Spectra
Syndromes

1. 1 child in 6 with specific learning disabilities.

2. 1 child in 87 with autism (it used to be 1 in 10,000)

3. 1 child in 9 with Asthma

4. 15% of children with attention deficit disorders

5. 1-2% incidence of sudden infant death syndrome

6. 1 in 4 Gulf War vets (250,000 of 800,00 vaccinated) to suffer from Gulf War Syndrome,
with 42,00 deaths (and rising).

7. 10,000 plus Gardasil adverse reactions and over 21 deaths, including blood clots and
strokes. MASS is the same mechanism by which Merck’s Vioxx caused strokes.

8. Allegations, charges & convictions for shaken baby syndrome that are vaccine damages..
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 25

Dr Hans Selye
(1907-1982) “Stress” = MASS

GAS – GENERAL ADAPTATION SYNDROME “STRESS” IS MASS:

ZETA POTENTIAL IS A PART OF MASS

The micro vascular and tissue bed damages caused by MASS responses are cumulative. MASS
is the physiological process behind vaccine morbidities and Canadian endocrinologist Hans
Selye’s “Stress” model of human disease.

Dr. Hans Selye was a Canadian endocrinologist who did research on the hypothetical non-
specific response of the organism to stressors. Selye conceptualized the physiology of “stress” as
having two components: a set of responses which he called the general adaptation syndrome,
and the development of a pathological state from ongoing, unrelieved stress. The “stress”, in
Selye’s model, summated over the course of a lifetime and caused diseases at the organ and
systems level.

Dr. Selye’ is initial inspiration for General Adaptation Syndrome (GAS, a theory of stress) came
from an endocrinological experiment in which he injected mice with extracts of various organs.
He at first believed he had discovered a new hormone, but was proved wrong when every
irritating substance he injected produced the same symptoms (swelling of the adrenal cortex,
atrophy of the thymus, gastric and duodenal ulcers). This, paired with his observation that people
with different diseases exhibit similar symptoms, led to his description of the effects of "noxious
agents" as he at first called it. He later coined the term "stress.”

Dr. Selye’s “Stress & G.A.S.” is actually “M.A.S.S.” in human physiology, including vaccine
induced autism-spectrum disorders and all other chronic ailments that emerge from foreign
agents entering the mammalian body and bloodstream.

Remarkably, our www.BrainGuardMD.com non-invasive, indirect neurovascular functional

brain imaging protocols, constrained to clinical neurology and neuroanatomy, shows the exact
same “stress” disease pattern as recorded by Dr. Selye. Irrespective of the vaccine strain,
infectious disease source, pathogenic determinant, or emergent morbid sate, the neurological
(neurovascular) damages are the same for everyone from sudden infant death to autism to
learning disabilities to Gardasil adversity to Tourettes syndrome to Chronic Fatique to Gulf War
syndrome to dementia to gatsointestinal pathology to death. This is MASS in medical
physiology. This is “Stress” in Selye’s terminology. This is vaccine induced autism-spectrum.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 26

This is human disease. This is a generic response to any foreign substances entering or injected
into mammalian tissue, bloodstream, physiology and anatomy.

Inducing Tolerance

The only reason the congenital form of rubella is harmful is because infection within the first
trimester of gestation places the immune system in a state of immune tolerance.

Immune tolerance causes a disproportionate increase in the non-specific immune response as the
antibody-mediated arm of the immune system, specific to key antigens (germ specific proteins
that identify the pathogen as foreign) are “turned off or deleted”. This means antibodies, much
like bullets, can be present, but they are duds – they will never “fire”. It is for this reason that
some researchers (e.g. A. Wakefield et al., 1997, The Lancet) have occasionally found vaccine
strain measles in the guts of autistic children. The immune system has been partially paralyzed in
its ability to eradicate the germ. However, it is not the germ that is causing morbidity. It is the
hyperactive non-specific, white blood cell response to the germ which is causing disease and
organ specific functional derailments and distress.

Immune tolerance is an adaptive immune response by the body in an attempt to curtail the
emergence of autoimmunity. Immune tolerance, once induced, becomes a trigger for cellular,
tissue, micro vascular, and organ specific collateral damages via hypoxia.

The damages/disease/disorders that emerge are a function of the hyper stimulated white blood
cell response. This is “friendly fire” and collateral damages from the act of microscopic war
within the body. All vaccines wage war. All repeat vaccines have the propensity to induce
tolerance. All vaccines induce a white blood cell response. This non-specific response and latent
tissue damage increases in magnitude and breadth with each subsequent vaccination, albeit in
clinically imperceptible ways. This is the MASS response in physiology. It is causing death,
disability, chronic illnesses, disorders, hypoxia, genetic derailments in cells from transcription
errors under hypoxic states, and likely many cancers.

Unfortunately, taking out the antibody response to a pathogen is equivalent to side-lining the
cavalry on a battlefield – the soldiers on the ground must pick up the slack and increase their
efforts and numbers in order to successfully wage war. It is the magnitude of the white blood cell
“ground soldier” response that is harmful and not the pathogens in and of themselves.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 27

We have been inducing immune tolerance in many of us by virtue of multiple, repeat

vaccinations laced with adjuvant. Each of these activities increases the non-specific immune
system, response, lowers zeta potentials, and causes microscopic to macroscopic intravascular
coagulation as a part of the normal healing process in mammalian tissue. It is this healing phase
of tissue repair, when hyper stimulated, that is causing disease – from virulent organisms to
inorganic particles to high frequency, high dosing, one size fits all attenuated multi-vaccines.

Neutrophils, aluminum adjuvant, and dementia of the Alzheimer’s type

The body makes upwards of ten trillion white blood cell “neutrophil” soldiers/daily under
conditions of “war.” Neutrophils have a lifespan of only six hours. They are “born to die.”

In battle, the white blood cells can cause considerable collateral damages especially if hyper
stimulated or induced to wage war over with multiple “battalions” over a protracted period of
time.

Vaccine adjuvant like aluminum increase the number of “battalions” and extends “the war” for
several months to years. The aluminum adjuvant, like any foreign substance in any tissue, once
sequestered in the brain, causes slow neurodegeneration and dementia of the Alzheimer type.

Dementia emerges as the collateral damage from an un-ending “war” is waged between the white
blood cells and their foe – in this case, a heavy metal for which the white blood cells lack the
arsenal to destroy – although they try. It is the enzymatic warfare that slowly erodes brain tissue
via hypoxia, vascular and tissue damages.

Death occurs by tissue specific hypoxic strangulation. This is MASS. This is largely a vascular
and non-Newtonian fluid dynamics problem as a function of non-specific immune warfare to a
foreign substance that the body cannot eradicate.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 28

www.BrainGuardMD.com

THE TAKE HOME MESSAGE PART 4-1

The important point is this: it is not any specific “germ” that is causing such wide-spread
vascular damages throughout the body; it is the body’s non-specific immune response to ANY
foreign substance entering the body (re: M.A.S.S. Disorders).

MASS is a generic sequence of microbiological steps involved in tissue repair and healing.

The MASS response is a common response across ALL pathogens and all foreign entities
entering the body.

It is the magnitude, chronicity, and frequency of the non-specific (white blood cell) immune
response that is causing tissue damage, disease, and organ impairments and not the pathogens in
and of themselves.

The damages MASS cause are cumulative when MASS is activated systemically.

Multiple organ systems are harmed by MASS, by ischemia, in clinically imperceptible ways.

One-size fits-all, high frequency, repeat dosing, multi-vaccines, laced with a multitude of
contaminants and immune accelerants, are causing a multitude of non-descript chronic ailments,
of which autism-spectrum and the global epidemic of neurodevelopment disorders is but one
category of vaccine induced pathology.

The magnitude of the white blood cell response is a function of the virulence of the pathogen.
We need not be vaccinating for every virulent organism on the planet, we need to be addressing
the common cause of pathology across all of them – this is our body’s non-specific immune
response which is the main cause of disease, disability, and morbidity for all.

There are avenues for dealing with ALL infectious diseases now, in medical physiology, directed
at the cause of disease (MASS) rather than individual vaccinations for every bug conceivable
that an individual might someday acquire.
Dr Andrew Moulden MD, PhD © MASS BOOK Chapt.4-1: M.A.S.S. ZETA STRESS 29

Moulden
Anoxia
Spectra
Syndromes

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Dr Andrew Moulden

Dr Andrew Moulden BA, MA, MD, PhD

CNAPS Medical Devices Inc.
122-250 The East Mall, #1601
Etobicoke, Ontario, Canada
M9B 6L3
1-705-498-6284
info@AMassNetwork.com

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