Every
Vaccine Elicits an Immune Response that Triggers Impaired Blood Flow in
the Brain, Causing Ischemic Strokes, Resulting in Debilitations from
Autism to SIDS
Dr Andrew Moulden MD, PhD – http://www.scribd.com/doc/11564520/Ch-4-Mass-Zeta-Stress
“Vaccines have caused
Autism-spectrum, many neuro-development 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, PhD
What is Zeta Potential?
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
[“Z”], hence-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, 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
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.
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 [expressed as Voltage]
can be high in a positive or negative sense, i.e. <-30mV and
>+30mV [less than minus 30 millivolts and greater than plus 30 millivolts]
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 [clumping]. 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 blood clots.
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, but also 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 microvascular 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.
Alleged Shaken Baby Syndrome
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 infant’s long bines [skull suture
lines] 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 which
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 infant’s clinical and pathological findings
in exammination. 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.
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.scribd.com/doc/11564520/Ch-4-Mass-Zeta-Stress
Zeta Potential meets MASS (Moulden Anoxia Spectra Syndromes)
Immumological 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 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.
Global Vaccinations – 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:
Congenital Rubella and Intravascular Coagulation
The autopsy reports of nine
toddlers aged 13 hours to 11 ½ months are presented below. These are
congenital rubella (German Measles) cases 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.
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 – not 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 [found in
vaccines] (DTaP, Gardasil Anthrax, Hepatitis A/B, MMR, influenza, etc..)
are creating the same lesions across the [person’s] life span 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.
1) Microscopic intravascular
coagulation, 2) anoxic states, 3) MASS, and 4) 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 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 “bug’s” ability to elicit an intense non-specific immune
response. Since this non-specific immune response is the same cause of
morbidity across all pathogens, then prevention of morbidity is best
suited by targeting the non-specific immune response directly – on an
as-needed basis.
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:
- 1 child in 6 with specific learning disabilities.
- 1 child in 87 [today 1 in 50] with Autism (it used to be 1 in 10,000)
- 1 child in 9 with Asthma
- 15% of children with Attention Deficit Disorders [ADD]
- 1-2% incidence of Sudden Infant Death Syndrome [SIDS]
- 1 in 4 Gulf War vets (250,000 of 800,00 vaccinated) to suffer from Gulf War Syndrome, with 42,00 deaths (and rising).
- 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. [Now over 140 VAERS reported deaths, with a
known 1 to 10% reporting factor].
- Allegations, charges & convictions [of innocent parents] for shaken baby syndrome that are vaccine damages.
Dr. Hans Selye’s 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 Dr. 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: 1) a set of responses
which he called the general adaptation syndrome [GAS], and 2) the
development of a pathological state from ongoing, unrelieved stress. The
“stress” in Selye’s model, summated over the course of a lifetime,
causes 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 [no longer online] 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 Syndrome to Autism, to learning
disabilities, to Gardasil adversity, to Tourettes syndrome, to Chronic
Fatigue, to Gulf War syndrome, to Dementia, to gastrointestinal
pathology, to death. This is MASS in medical physiology. This is
“Stress” in Selye’s terminology. This is vaccine induced
autism-spectrum. 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 [low oxygen].
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 within the body.
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.
We have been inducing immune
tolerance in many of us by virtue of multiple, repeat vaccinations laced
with adjuvant. Each of these activities A) increases the non-specific
immune system response, B) lowers zeta potentials, and C) 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 hyperstimulated
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” that 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.
The Take Home Message
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
Source: http://www.scribd.com/doc/11564520/Ch-4-Mass-Zeta-Stress
Related
Vaccination toxicity: The Zeta phase of MASS and “blood sludging”
Iindex of articles
http://www.vacfacts.info/vaccination-toxicity-the-zeta-phase-of-mass-and-ldquoblood-sludgingrdquo.html
Shaken Babies by Dr. Archie Kalokerinos, MD
http://www.whale.to/a/kalokerinos_sbs.html
Brainwashed Police Prosecute Parents to Protect Vaccines | Vactruth.com
http://vactruth.com/2012/11/08/brainwashed-police-ignore-vaccine-injuries/
How the Medical Profession Covered Up Vaccine Injuries and Called it ‘Child Abuse’ | Vactruth.com
http://vactruth.com/2012/02/14/medical-cover-up-child-abuse/
Index-Articles
http://www.vaclib.org/basic/sbsindex.htm
[PDF] Mohammed Ali Al-Bayati, PhD, DABT, DABVT – Vacinfo.Org
www.vacinfo.org/Man117_129.pdf
Dr. Mohammad Ali Al-Bayati, PhD, DABT, DABVT Toxicologist & Pathologist
http://www.toxi-health.com/falseaccusationsofsbs.html
Shaken Baby Syndrome or Vaccine-Induced Encephalitis?
Harold E. Buttram, MD
http://www.jpands.org/hacienda/buttram.html
http://www.profitableharm.com/Harold%20E.%20Buttram.html
Shaken Baby Syndrome or Vaccine-Induced Encephalomyelitis?
The Story of Baby Alan
http://www.freeyurko.bizland.com/storyofbabyalan.html
Shaken Baby Syndrome Diagnosis On Shaky Ground
Viera Scheibner, PhD
[PDF]www.medicalveritas.com/R0014.pdf
Are mothers natural protectors or baby killers? Shaken Baby Syndrome and vaccines
http://vactruth.com/2010/01/26/are-mothers-natural-protectors-or-baby-killers-shaken-baby-syndrome-and-vaccines/
The Stepchildren of Modern Medicine, as Applied to Shaken Baby Syndrome (SBS)/Non-accidental Injury (NAI)
http://www.vaccinationcouncil.org/2010/07/21/the-stepchildren-of-modern-medicine-as-app
lied-to-shaken-baby-syndrome-sbsnon-accidental-injury-nai/
This content was previously posted on FROT, April 16, 2016
