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Dr. Andrew Moulden - Every Vaccine Produces Harm57-87
Blood Circulation
Blood vessels are like one way streets. They are tubular in shape and blood is intended to flow in only one direction. It flows from the heart through large vessels called arteries. The arteries carry oxygen-rich blood that is red in color.
The arteries divide over and over again and become very small.
Eventually they reach the smallest tubes, which are called capillaries. The capillaries are so small that they cannot be seen with the human eye. Even though capillaries account for 95% of the blood vessels in the entire body, they only contain 5% of the circulating blood at any given time.
While the blood is in the capillaries, it gives up oxygen and collects carbon dioxide and other waste products.
There are 600,000 miles of capillaries in the human body.
When the blood comes out of the capillaries it collects in larger vessels called veins. The blood is now blue in color, because it gave up its oxygen
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in the capillaries. The veins merge together to form larger and larger vessels as they carry the blue blood toward the lungs and heart.
When there is a blood clot or other type of blockage in an artery or in a capillary, then the blood stops moving forward in that location. The result is that the cells and tissues in the area that should be receiving oxygen- rich blood begin to suffocate. All cells require a constant flow of fresh blood to stay alive. If the interruption of blood flow and the subsequent lack of oxygen are prolonged, then cells begin to die.
An animation of a typical human red blood cell cycle in the circulatory system. This animation occurs at real time (20 seconds of cycle) and shows the red blood cell deform as it enters capillaries, as well as changing color as it alternates in states of oxygenation along the circulatory system. Source: Wikimedia
Ischemia and Strokes
The technical name for lack of oxygen in a group of cells is called ischemia. When ischemia happens in the brain, it is called a stroke. A stroke is most commonly thought of as happening in the brain, but a stroke can happen in any organ of the body.
A heart attack involves blockage of a blood vessel that supplies oxygen to the heart. Ischemia in the heart is a stroke to the heart. It is a serious life threatening condition.
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Ischemia in the bowel is also a stroke. Strokes can happen in the blood supply to the large intestine or the small intestine. A stroke to the bowel is mesenteric ischemia.
Ischemia can occur in the kidneys, liver, skin, and anywhere in the body. Every part of the human body requires blood flow and a constant supply of oxygen to maintain life. Without oxygen we cannot maintain health and wellness. When the brain is deprived of oxygen even for a few minutes we become unconscious and the brain begins to die after 4 minutes.
Watershed areas of the Brain and Body
Illustration of an embolic stroke, showing a blockage lodged in a blood vessel. Source: Wikimedia.
Watershed areas are very tiny sections of tissue (group of cells) that are only served by a single set of blood vessels (capillaries). In other tissue areas, there may be several blood vessels that supply oxygen-rich red blood directly to the same cells. There also can be collateral blood vessels that move between small areas of tissue. In these tissues with
multiple sources of oxygen-rich blood, there can be a stroke (blockage) to
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one blood vessel, but the section of tissue is not harmed, because oxygen-rich blood can reach the cells through alternative routes.
In the situation of a watershed area, there is only one pipeline of oxygen- rich blood to the area. If the pipeline gets blocked, then there is absolutely no other way for the cells in that area to obtain oxygen. The result is that the cells begin to die unless the blood flow is restored quickly. Eventually, the whole watershed area could die.
Watershed areas may literally have a bend or kink in the capillaries where the blood changes direction and begins its return journey to the heart and lungs. This is seen at the tips of the toes and fingers. It is seen at the tip
of the nose and the tips of the ears. The watershed areas are vulnerable areas. Frostbite is common in each of these watershed areas, because
the blood flow in the capillaries is very sensitive, and it is easy to disturb.
Watershed areas are also present in the brain and in other organs. These are highly sensitive areas. In the brain, watershed areas are often in
areas that control critical processes.
An example of watershed damage in the brain is seen in transcortical motor aphasia, which involves the area of the brain that enables us to produce speech. A person with this type of watershed damage may be able to understand speech, but he will have lost the ability to form speech once there has been brain damage.
We call this type of damage a stroke when we see it in elderly persons.
However this same watershed damage, when it appears in a young child is not called a stroke, but is simply labeled an autism spectrum disorder.
Regardless of whether the person is young or old, transcortical motor aphasia is always caused by a stroke and cellular death in a specific watershed area of the brain.
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Description of Blood
There are many components of human blood. However, to understand Dr. Moulden’s teaching, we only need to have basic knowledge of the most common aspects of blood physiology.
Plasma
The majority of our blood is made up of an electrically charged watery substance called plasma. Various types of cells are suspended in the watery plasma. The blood cells are carried along in the plasma from one part of the body to the next. If there is a high negative electrical charge in the plasma, then the cells that are suspended in the water will repel one another. Blood cells are intended to repel each other and to move freely without touching one another. Blood with a healthy high negative electrical charge will enable cells in the plasma to flow freely without clumping together. The blood cells flow freely because they have a negative electrical charge that enables them to repel one another and stay separate.
Laminar Blood Flow
Freely flowing blood is called laminar flow. Blood that has an inadequate electrical charge will have blood cells that clump and stick together. The
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clumping of blood cells slows down blood flow and results in blood sludging in which laminar flow has been lost.
Red Blood Cells
The most common cells in the blood are red blood cells. During their journey through the body, they carry oxygen to the capillaries and they carry away carbon dioxide. Some of the capillaries are so small that red blood cells must squeeze to pass through them. In the capillaries, red blood cells must pass through the vessels in a single file stream.
White Blood Cells
White blood cells are part of the immune system, which is intended to destroy invading pathogens such as viruses and bacteria. Most white blood cells are much larger than red blood cells, and they can only pass through larger capillaries. White blood cells are approximately twice as large as red blood cells, though they vary in size depending on the cell type. Under normal circumstances, approximately 1% of the cells that are floating in the blood stream are white blood cells. When the body is threatened by foreign substances or pathogens, then large numbers of white blood cells are released into the blood stream.
When a person receives a vaccine, white blood cells are released as part of the immune system response to the injection of foreign material into the body.
If there are too many white blood cells in circulation, then they can block the opening to large numbers of the smallest capillaries, which are not large enough for them to pass through. When this happens, oxygen delivery can be impaired to watershed areas.
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Platelets
Platelets are a third type of cell. They help with clotting when there is damage to tissues, and blood begins to leak out of the blood vessels. Platelets are about one fifth of the size of red blood cells.
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Three Historic Mechanisms that Impair Normal Blood Flow
Historically, Dr. Rudolf Virchow has been given credit for discovering pulmonary embolisms or blood clots, which form in the veins of the leg and pass into the lung where they cause damage. Dr. Virchow’s understanding of blood flow, blood clotting, and damage to blood flow is very critical for understanding human disease.
Dr. Rudolf Carl Virchow. Source: Wikimedia
Virchow’s Triad, as it is now called, is the beginning point for understanding the entire epidemic of neurodevelopmental disorders that
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are the consequence of vaccinations. Dr. Moulden’s work is an extension of this triad.
Virchow's triad - Wikimedia.
Dr. Virchow described three processes that impair the supply of blood to the cells of the body. These processes result in the formation of blood clots and/or blood sludging. Blood clots are blockages in blood vessels, which can be thought of as plugs in a pipe. Blood sludging can be thought of as a problem of coagulation. Blood sludging slows down the flow of
blood, which can also cause cell starvation, because the rate of flow is too low to support healthy cellular respiration.
Dr. Virchow died in 1902 and since that time additional mechanisms of blood clotting and sludging have been discovered. However, the beginning point for understanding blood flow and how it is impaired rests on Virchow’s Triad. Two additional mechanisms that impair blood flow were described by Dr. Hartman and Dr. Moulden. These new mechanisms called Zeta and MASS will be discussed after Virchow’s Triad. Zeta and MASS are the keys to understanding Dr. Moulden’s model of modern illness.
Each of the three factors in Virchow’s Triad increases the tendency to form blood clots. The clots formed may be large or microscopic. If blood clots occupy greater than 75% of the inside diameter of a blood vessel, then oxygen delivery is impaired and the risk for stroke is increased.
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Ischemic stroke is a generic term which connotes oxygen demand exceeding oxygen supply. It can happen ANYWHERE in the body and not just the brain.
1. How Vaccines and Toxins Alter Normal Blood Flow
Alterations in normal blood flow refers to several situations. These include turbulence in blood flow, stasis (low forward blood flow and pooling), blocked flow (clots), and varicose veins. Normal blood flow is called laminar flow.
Dr. Moulden found that laminar blood flow was altered by vaccinations, infectious diseases, toxins, heavy metals, food additives, and drugs to which a person is immunologically hypersensitive.
Stasis is an alteration in normal blood flow. It describes a condition where blood pools in the blood vessels and clots can form.
A classic example of this happens when a person sits during a plane flight for a long time. When we do this, the vessels to the back of the leg can be blocked off, which prevents normal blood flow up from the legs. A blood clot can form at the location of the compressed blood vessels. Sometimes when people leave the plane at the end of their flight, a clot will break off from the compressed area and will go into the lungs and form a
pulmonary embolism (plug). This type of large blood clot can be life threatening.
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Stasis can occur in large blood vessels such as those in the legs. It can be in medium to large vessels like the carotid arteries that carry blood up the neck to the brain, or it can happen in the capillaries, which are the tiniest of all blood vessels.
Stasis is a normal occurrence in our bodies. It happens during every day of our lives. In fact, it commonly occurs in the smallest blood vessels in every part of the body many times a day.
Since these clots are the result of the body’s normal functioning, the body has the means to remove the impairments so the blood can keep flowing smoothly. Blood clotting is part of the mechanism that the body uses to bring about healing to damaged tissue.
2. Damage to the Inner Layer of Cells in our Blood Vessels
Damage to the inner layer of cells in our blood vessels also causes impaired blood flow. The innermost layer of cells inside of blood vessels is called the vascular endothelium. This thin layer of cells lines all the blood vessels throughout the body.
Under a microscope, we can see that the vascular endothelium consists of tiny cells that are tightly packed together similar to the scales on a fish. They line up side by side and form a complete tube through which the blood flows. The capillary tubes are somewhat flexible, and can stretch as red blood cells pass through them.
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Injuries and/or trauma to the endothelium can be caused by damage to the vessels arising from stress, hypertension, ischemia, toxins, metabolic derailments, and immune system responses to foreign substances that are in the blood, in tissue, or in the blood vessel walls themselves. Vaccines can cause endothelial damage.
When there is an injury to the inside lining of blood vessel walls, we call that endothelial damage or damage to the vascular endothelium. When the vascular endothelium is damaged, this can lead to clotting or coagulation in that area.
3. How Vaccines and Toxins Cause "Sludging" in the Blood
The third way that clots can develop and tissues can become starved for oxygen involves changes in the constitution of the blood. The blood can develop a tendency to clot even when there are no alterations in blood flow, and when there is no endothelial damage to the lining of blood vessels. Blood that has an abnormal tendency to clot means the blood has become hypercoagulable. This means there is too much clotting going on in the blood and in the body.
Many factors can cause the blood to become hypercoagulable. Possible risk factors include: hyperviscosity, deficiency of antithrombin III, deficiency of proteins C & S, kidney and liver impairment, effects of severe trauma, changes in estrogen levels, disseminated cancer, late pregnancy and delivery, race, age, smoking, obesity, diabetes, use of birth control pills in girls, and heavy metal ion exchanges that lower zeta potential in the blood. (Zeta potential will be discussed shortly.)
Another term that Dr. Moulden used to describe hypercoagulable blood is sludging of the blood. Sludging of the blood can be caused by vaccines and various environmental factors. We can decrease blood sludging by reducing our environmental exposure to toxins and by changing our lifestyle.
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Zeta Potential for Health and Wellness
This diagram shows a graph of the potential difference as a function of distance from the surface of a particle suspended in a dispersion medium. Source: Wikimedia
The weakening of zeta potential in the blood also causes strokes. Zeta is an electrical charge that exists around all particles in the blood. The negative electrical fields cause particles, substances, and cells in the blood to repel one another.
As an example, if you take the negative ends of two magnets and try to push them together, they will repel each other. In the same way, if all blood cells have a high negative charge, then they will repel one another and move freely through the blood vessels without touching one another. This independent movement of cells in the blood is a mark of health. When the strong negative electrical charge on blood cells is lost, then the cells start clumping together. This is seen when the electrical charge is very low or neutral. This leads to poor health and disease.
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If an infant is born without having been exposed to the toxins and diseases of this world, then the baby’s blood cells will not stick together, because the normal high negative electrical charge on blood cells will keep them all separated. The cells will move freely as they were designed to move. They move in a suspended state, which is called colloidal suspension.
When there is proper colloidal suspension, blood cells move smoothly through the smallest blood vessels. The blood flow is laminar – it flows without restriction.
As soon as the electrostatic charge around these particles in the blood drops toward neutral, then the particles start clumping together. This forms clots and concretions of particles. It's hard to move concretions through small pipes that were designed to only allow one red blood cell to pass through at a time.
Examples of a stable and of an unstable colloidal suspension. The continuous phase is a liquid and the dispersed phase consists of solid particles. Source: Wikimedia.
In chemistry and physics we call this electrical charge “valence.” It is the outer electrical charge around particles. From the point of view of human health and wellness, it is extremely important to avoid the blood sludging problem, because it causes serious health problems. It is important for cells in the blood to have more of a negative electrical charge and not a positive charge.
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Blood with High Negative Charge is Desired
Blood with a positive charge leads to clumping and coagulation. Blood with a high negative charge causes dispersion, keeps things apart and prevents clumping and coagulation.
For example, the dust particles that are floating in the air of a room on a bright sunny day are held up in the air and enabled to float by their high negative charge. It is this negative charge that keeps them suspended in the air and keeps them from coming together. The molecules, particles, suspensoids, and cells inside of the blood will act like dust in the air when they have a negative charge.
The red blood cells carry the electrical charge that is life. The red blood cells are the main carrier. The amino acids, protein, trace minerals, metals, and minerals don't go into solution like sugar and water. They are held in suspension as minute colloids (tiny particles) [1], which start at a size of one micron and go down to as small as six angstroms.
(A micron is one millionth of a meter. An angstrom is much smaller than a micron. Six angstroms was the smallest particle size that could be measured in 2009.)
The following chart shows how zeta potential affects the blood and how it affects human health. A high negative charge is associated with laminar blood flow and overall general good health.
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Loss of Negative Charge in Blood Leads to Sludging of the
Blood, Hypoxia and Strokes
When the red blood cells start losing zeta potential they start to form rouleau. This means that the negative electrical charge around them, which had been keeping cells separated from one another, has decreased and the cells are sticking together. The term “rouleau” describes a situation in which red blood cells clump up or stack up like coins. When rouleau is present, smoothly moving laminar blood flow is compromised. The result is sludging of the blood, hypoxia (low oxygen supply) and strokes. These clumps of cells are not able to pass through most capillaries, because they're too big, especially at points where the
blood vessels turn and change directions – especially at a 90 degree turn.
Rouleau is visible under darkfield live blood microscopic examination.
Unfortunately, the US FDA has banned the use of darkfield live blood analysis for diagnostic purposes. This means that they don’t want anyone to do before-and-after comparisons of the blood to see what happens after vaccines are taken.
Damage to Digestive System Leaves the Body in a State of Perpetual
Infection
One of the areas in the body that is hard hit by reduced zeta potential is the gastrointestinal tract. Reduced capillary flow in the digestive system results in damaged digestion, diseased tissue and numerous abnormal digestive syndromes and diseases.
The reduced flow of blood means that white blood cells cannot get to certain areas and eradicate viruses and bacteria that your body needs to destroy, such as measles, mumps, and rubella. The consequence is that the body cannot eliminate these infectious diseases from the digestive tract. This leaves the body in a state of perpetual infection. The body can’t get rid of these infectious diseases, because the impaired blood flow prevents the immune system from reaching the pathogens to destroy them.
If blood flow is blocked to an area, then the white blood cells cannot reach the pathogens that have taken up residence in that area even if the number of white blood cells is elevated.
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Vaccines are the Straw that Breaks the Camel's Back When it Comes to the Destruction of Zeta Potential
Page from a medical manual showing how to administer multiple vaccines in one doctor visit.
Vaccines are the straw that breaks the camel's back when it comes to the destruction of zeta potential. Vaccines contain everything in one package that is needed to reduce zeta potential in the blood and set up conditions in the body where all manner of modern diseases can develop.
Vaccines contain a combination of infectious pathogens, aluminum, mercury, aborted fetal tissue, genetic materials from animals such as monkeys, preservatives, formaldehyde, and numerous other toxic
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substances. The ingredients in vaccines can cause clumping of blood cells, impaired blood flow, ischemia, cell death, and impaired immune system functioning without any other type of exposure.
Vaccines contain everything that is needed to destroy laminar blood flow, cause clotting and sludging of the blood, deprive cells of oxygen, bring about cellular death, cause neurological damage, cause organ system damage, and lead to severe disability and death.
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Aluminum Destroys Negative Zeta Potential
Vaccines and environmental contamination expose people to aluminum. The accumulation of aluminum in the body has a strong harmful effect on zeta potential. Aluminum accumulates in the body and tends to reduce zeta potential as we age. 4 parts per million of aluminum in human blood can cause blood to coagulate. [3]
Thus, vaccination of the elderly, or those with hypercoagulable states, may reduce zeta potential to the tipping point where even an emotional upset can trigger a microvascular clot in the brain (stroke) – or a heart attack.
The next chapter will provide additional information about the harmful effects of aluminum in the context of Moulden Anoxia Spectrum Syndrome.
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Conclusion: Vaccines Reduce Negative Zeta Potential
Zeta potential can be used as an indicator of health. High negative zeta in the range of -100 millivolts to -60 millivolts is associated with strong colloidal suspensions. Blood cells and other colloidal particles are widely separated and do not clump together. This provides for laminar blood
flow, in which there is reduced likelihood of blood sludging and blood clotting. Sludging and clotting can be caused by other factors, but when
negative zeta is high, then one major factor for sludging and clotting is
greatly reduced and overall health will be high.
When vaccines are given or when other environmental toxins are brought into the body, then negative zeta falls. Repeated exposure to vaccines and environmental toxins will over time push down negative zeta toward the positive range. If the zeta falls to the range of -30 millivolts to -15 millivolts, then the cells and particles in blood start coming close to one another. If the zeta is in the range of -15 millivolts to -10 millivolts, then blood clumping and sludging is already occurring.
If a vaccine is taken at this point, then it has the potential of driving down zeta toward neutral, where intense blood sludging is possible. This can lead to microvascular strokes and anoxia in which certain watershed areas of the body can become starved for oxygen.
Each time a vaccine is taken, it reduces negative zeta potential. Since good health is associated with a relatively wide range of negative zeta, a single dose of vaccine may not produce immediate or noticeable harm, as long as negative zeta remains in the high range. But aluminum collects in the body and is not easily excreted, which means that aluminum from vaccines continues to push down zeta toward the point where harm can occur.
Vaccine damage is not predictable. Many factors determine the impact on zeta and the severity of damage that will be caused by taking vaccines. We do not have a formula to estimate how much damage to zeta will be produced by a single dose of vaccine. We know that the aluminum in vaccines is a powerful agent, which draws down zeta toward neutral.
In the next chapter I will discuss the second key to understanding how vaccine damage occurs. It will discuss Moulden Anoxia Spectrum Syndromes (MASS), and explain how Zeta and MASS work together to bring about illness. Finally, the last chapter will discuss the system of
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noninvasive methods that can be used by anyone to identify when vaccine damage has occurred.
Comment on this chapter at VaccineImpact.com
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Chapter 4 – Dr. Moulden’s New Medical Discovery: Moulden Anoxia Spectrum Syndromes (MASS)
Dr. Andrew Moulden tried to explain the mechanisms that were causing damage to people who were taking vaccines. He made a strong case to prove that numerous modern neurodevelopmental illnesses are the result of microvascular damage and impaired blood flow. The ministrokes that result from vaccine use and exposure to toxins in the environment and food cause the same type of reactions in the body, and cause a wide range of illnesses.
He dared to say that the germ theory of disease and genetic models could not explain the causes of the epidemic rise in modern diseases such as autism spectrum disorder; Alzheimer’s disease; learning disabilities; attention deficit and hyperactivity disorders; chronic fatigue; fibromyalgia; Gulf War Syndrome; sudden death in infants, teens and adults; Parkinson's disease; and various other conditions of nerve palsy and paralysis that we see all around us.
He rightly understood that we are now living in an age when multiple factors combine to create conditions in which modern neurodevelopmental diseases can occur. It is not just the vaccines and the toxins in our environment and food that challenge healthy normal human functioning, but it is also the condition of the body itself -- especially the nutritional status and gut flora, which determines whether the reaction to vaccines and environmental toxins will be minimal, moderate, or severe.
Zeta potential was shown by Dr Moulden to be an important factor in determining whether vaccines and other toxins will produce severe health reactions.
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Moving Beyond the Germ Theory of Illness
The germ theory of disease tries to explain that diseases are caused by germs. It tries to isolate and condense everything down to a single chain of events that lead to a disease. Exposure to pathogen “A” causes disease “B”, with symptom “C”, which can be treated with pharmaceutical
drug “D” or prevented with vaccine “E.” This might work in a test tube or in an isolated laboratory setting full of mice or rats, but in the real world in
which we now live, it fails to identify realistic levels of possible harm or to
give us cures for common illnesses.
Of course, germs are involved in some illnesses, but Dr. Moulden found that germs are not necessarily the direct cause of illness, rather they cause a reaction in the body, which causes illness. It is this reaction that was at the center of Dr. Moulden’s model of illness. Pathogens can sometimes establish themselves in areas where there is on-going microvascular damage and ischemia, because this damage is preventing white blood cells from reaching the pathogens. Infections get established because of a weakness in the body -- the existence of an area that the immune system cannot effectively reach.
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Research by Pharmaceutical Companies does not Evaluate
Interactions with Thousands of Toxins in the Environment
Dr. Moulden explained that the thousands of chemicals in our water, air, and food, are limiting the value of experiments that test for the safety of individual substances. Research studies conducted by pharmaceutical companies and chemical companies, used to gain approval of new drugs and chemical compounds, do not evaluate the interactions of their new products with the thousands of toxins that are already in the environment and in factory manufactured food. They just try to show the potential safety of their new patent, as if animals and people were not being exposed to other toxic substances. Thus, their experiments do not detect harmful effects as they occur in real life.
Dr. Moulden was quick to point out that the pharmaceutical industry does not identify harmful reactions to their products, because they aren’t attempting to measure the factors that are clear indications of damage. If you don’t know what to look for, then you don’t have to worry about finding evidence of harm. If you use research methods that were designed to show statistical safety for groups of animals or people, then you will not find the real harm that is experienced by individual subjects.
Researchers do double blind control group experiments. They do not evaluate the potential harm or effectiveness of the new product within the context of other vaccines and thousands of other chemicals to which people are already being exposed. They also do not use a “within
subjects design” to measure health and symptoms before and after giving vaccines for each person tested. They make a serious error when they
assume that if a new product doesn’t produce harm when it is tested in
isolation that it will not produce harm when it is used along with other toxins.
Simply put, scientists do not have the capability to simultaneously analyze the interaction of thousands of toxic chemicals, drugs, and vaccines. Thus they conduct unrealistic experiments, which are incapable of identifying
the actual harm that comes from the combination of drugs, vaccines, pesticides, and other chemicals that people are exposed to every day.
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Modern Drug Development only Focuses on Genetics
Drug companies and chemical companies are now turning to genetic abnormalities to explain why people get sick. They want us to believe that it is not their toxic products that are harming people, rather, it is our genetic make-up, which is the problem. Their products are not the problem, we are the problem.
Dr. Moulden did not accept genetics as the cause of modern neurodevelopmental diseases. He also did not accept germs as being the cause of these illnesses. His work clearly showed that it was the introduction of foreign substances into the human body through vaccines and other environmental chemicals, which were causing the exponential growth in modern diseases since the middle of the twentieth century.
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Zeta Potential: Electrical Charge in the Blood
Diagram of zeta potential in dispersion. Source: Wikimedia.
In the previous chapter I discussed zeta potential and how the electrical charge in the blood needs to be strongly negative to avoid the clumping together of blood cells. We saw that when zeta falls toward neutral, blood cells no longer repel each other and will start sticking together. This creates a situation in which the blood flow becomes sluggish.
Blood sludging slows down the flow of blood through capillaries and may completely block blood flow. When this happens, oxygen is no longer available to watershed areas that are served by a single network of capillaries. The result is ministrokes, which can occur anywhere in the body. Sometimes these strokes resolve themselves in a day or so; at other times the damage is permanent.
Vaccines, environmental chemicals, and various food additives used in commercially produced food all have the ability to reduce zeta potential to the point where blood sludging and ministrokes can occur. These ministrokes are the cause of modern neurodevelopmental illnesses and syndromes.
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Low negative zeta levels in blood, however, are not the only cause of microvascular blockage and ministrokes. We must also consider Moulden Anoxia Spectrum Syndromes (MASS), which was the heart of Dr. Moulden’s model of illness.
Listen to Dr. Moulden in his own words give evidence to the mechanisms that cause vaccine damage in “Tolerance Lost.” See the evidence of vaccine damage in the faces of children. Link here.
Listen to a presentation from Dr. Moulden that summarizes key principles of his Research. Link here.
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Moulden Anoxia Spectrum Syndromes (MASS) - A New
Medical Discovery Developed by Dr. Moulden
MASS (Moulden Anoxia Spectrum Syndromes) is a new medical discovery developed by Dr. Moulden. It shows that there are situations in which blood clotting and sludging does not follow the three classic clotting pathways described in Virchow’s Triad. MASS is closely linked to zeta potential. It is common for MASS and weakened zeta potential to occur together; but they are two distinct processes.
The MASS reaction is technically called excessive non-specific immune hyperstimulation. It is marked by an unusually high level of white blood cells in the blood, which causes blood sludging and blood clotting at the microvascular level of the capillaries. The consequence is ministrokes, which damage normal neurological and organ functioning. Even though weak negative zeta and MASS both cause microvascular circulation problems and ministrokes, the mechanisms are very different.
Excessive non-specific immune hyperstimulation causes large numbers of white blood cells to be released into the blood stream. This contributes to blood sludging and clotting, because white blood cells are twice as large as red blood cells, and they cannot pass through the smallest capillaries. The result is that the excess white blood cells plug up watershed areas in capillary beds.
The presence of large numbers of white blood cells at the openings of capillaries prevents red blood cells from passing into the capillaries. They clog up the entry points for the smallest capillaries and cause ischemia.
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When there is endothelial damage to the inner lining of blood vessels, then the white blood cells tend to cling to the walls of blood vessels and roll along the walls of the blood vessels instead of freely flowing along with the plasma. This reduces laminar blood flow in the smaller blood vessels and adds to the sludging problem.
When there is a normal level of white blood cells, there will still be occasional blockages during the typical day. However the body is able to deal with these and prevent harm. When the number of white blood cells is elevated, then the number of capillary blockages will be increased.
In situations of vascular inflammation, which is also part of the MASS reaction, some capillaries will functionally be closed off. The inner area of the capillaries becomes so occluded that not even red blood cells can pass through them, which starves the cells in that area of oxygen.
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MASS Response does not Follow Classic Steps in Blood
Clotting
The MASS response does not follow classic steps in the clotting cascade. The damage caused by MASS is transient, recurrent, and cumulative. MASS responses vary greatly from person to person, and MASS responses can be quite different in the same person at different points in time. The MASS process is recurrent and clinically silent until major damage begins to appear.
MASS causes hypoxia (low oxygen), anoxia (no oxygen), ischemia (low oxygen from low blood flow), and stroke (oxygen demand exceeding oxygen supply). These types of reactions cause human disease, chronic illness, disorders, death, vaccine induced autism-spectrum disorders, sudden infant death syndrome, and multi-organ disease and functional impairments. MASS is an overarching principle that stretches across numerous modern diseases compromising human health and wellness, and contributing to morbidity and mortality.
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What Causes MASS Reaction?
Defining the words Anoxia, Spectrum, and Syndromes that are in the acronym M.A.S.S will help describe the process.
Anoxia
Anoxia is a condition in which the supply of oxygen to a group of cells or to an organ is absent. Anoxia is the result of restricted blood flow. When the blood flow is very sluggish, the flow can easily be stopped altogether or may even reverse its direction. In this situation, oxygen cannot be delivered to cells and they begin to die. They literally suffocate to death.
Dying or dead cells in specific cranial nerve pathways can be observed in the human face, because damage to these nerves produces muscular palsy, which alters the expression and impairs the movement of the eyes, eyelids, and mouth.
Syndrome
A syndrome is different from a disease, because it implies multiple causes and multiple symptoms. We tend to think of learning disabilities, autism, Alzheimer’s, irritable bowel disease, Crohn’s disease, colitis, food
allergies, shaken baby syndrome, sudden infant death, idiopathic seizure disorders, Gulf War syndrome, Gardasil adverse reactions, schizophrenia, Tourette’s syndrome, chronic fatigue syndrome, fibromyalgia, expressive aphasia, impaired speech skills, attention deficit disorders, silent ischemic strokes, blood clots, idiopathic thrombocytopenia purpura, Parkinson's disease, and other modern neurodevelopment disorders as being individual diseases that must have individual causes.
However, if we step out of the box of conventional germ theory, where every disease has one cause, then it is possible to begin seeing illness and the recovery from illness in a very different way. Doctor Moulden brought the above modern conditions together under the term MASS, because he could see that there were common mechanisms at work in all of them.
Spectrum
Spectrum indicates that we are talking about a syndrome that ranges in severity or intensity. The symptoms of the syndrome can range from mild
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