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The subjection of vaccination or immunization is obviously a sensitive one, since a great deal of profit depends on the existence of the paradigm. Fortunately, all paradigms based on deceit eventually fall, aided by the plethora of data which surfaces as a result of the social negativity such paradigms generate. The subject of vaccination is a good example, and we will take the data heretofore presented in volume one and amplify it, based on an overall reassessment which integrates what we have learned since then. Let us start with an examination of the subject of human immunity to disease.
Natural Human Pathotropic Immunity
Natural immunity can be considered the sum total of immunity to disease inherent in biological immune defenses not artificially induced, and is comprised of active immunity, acquired through normal infestation of intestinal and respiratory systems after birth, and passive immunity, generally consisting of antibodies acquired from maternal blood and breast milk.
The human immune system is further characterized as having specific responses, such as the production by the body of specific antibodies to counter specific foreign proteins or antigens, and non-specific responses, which consist of the general systemic response to undesirable substances. Included in the general repertoire of non-specific response is the skin, the mucous membranes of the respiratory and digestive tracts, reflex actions of sneezing and coughing, natural antibodies, complement proteins, interferon, the process of phagocytosis (cells devouring other cells), the effect of fatty acids, inflammatory response, the action of reticulo-endothelial cells, the action of lysozyme and other enzymes, the response of respiratory and intestinal celia, the effect of stomach acid on bacteria, and secretions that contain antibodies themselves, such as secretory immunoglobulin, which assists the process of phagocytosis - an example being the action of white blood cells on pathogenic organisms.
The human body maintains several lines of defense against the invasion of foreign proteins and subsequently produced toxins. The first line of defense is the skin, which is primarily composed of a protein-based material called keratin. The skin also secretes various oils, fatty acids and lactic acids which inhibit the general growth of bacteria, although many body flora that inhabit both the skin and the interior of the body are relatively innocuous, given that the immune system is in a normal condition, and many body processes are assisted by their existence. These organisms that exist in symbiosis with human anatomy are sensitive to antibiotics and synthetic materials administered by current medical practice. Disturbance of the delicate balance can lead to overpopulation of pathogenic organisms. The proliferation of candida albicans caused by administration of commercial antibiotic drugs is an example, as is the diarrhea and bleeding caused by obliteration of intestinal flora by antibiotics. Since the maintenance of internal organisms is an essential part of the human immune response, the death of these organisms weakens the overall immune system capability.
The white cells in the body, the leukocytes, are generally divided into two groups, the granulocytes, which include neutrophils, eosinophils and basophils, and the non-granulated lymphocytes and monocytes. Neutrophils constitute the most prevalent type of granulocyte, and have a nucleus containing a number of lobes. Because of the segmented nature of the nucleus, neutrophils are also called polymorphonuclear leukocytes. They have an interesting property in that they have the ability to form physical barriers against pathogenic organisms. The eosiniphil comprises about 2% of the leukocytes in the bloodstream, and appear to be connected with defense against parasitic infection and allergic response, rather than against microorganisms and toxins. Basophils also have a role to play in allergic response, and contain histamin and heparin. A further form of the leukocyte is the monocyte, which has the capacity to ingest foreign particles and bacteria. The monocyte appears to be active in conditions presented by tuberculosis and fungal infections.
Another natural line of defense is the lymphatic system. Most cellular structures in the body are bathed in lymph, a clear fluid which acts as a general dumping ground for unwanted substances, later filtered out through the liver and kidneys. The lymph moves through a series of ducts and glands by virtue of a specialized series of muscular contractions, many of which are generated during the act of physical exercise. It is the lymphatic system which contains the aforementioned reticulo-endothelial cells which trap and ingest various organisms within the lymph. These cells also form the lining of several important organs, and are also present within the liver and spleen. When a foreign protein structure is located, connective tissue traps the foreign structure and lymphocytes are dispersed to engulf the offending organism. In the circulatory system are macrophages, specialized white blood cells that ingest and disrupt organisms found in the blood. After macrophages perform this action, processed antigens appear on the surface of the macrophages membrane. It is these processed antigens leftover from the destruction of organisms that are sensed by the T-cell lymphocytes, prompting them to send out substances called lymphokines, which in turn alert B-cell lymphocytes to produce an antibody in response to the processed antigen, otherwise taken as a processed foreign protein. Each B-lymphocyte has approximately 100,000 immunoglobulins on its surface.
Antibodies produced by the B-cells are sometimes called immunoglobulins, designated by the symbol Ig, and are released as the B-cell is stimulated by the presence of foreign antigens to transform into a plasma cell which manufactures the specific antibody required for the foreign antigen. There are generally five types of immunoglobulins. The first antibody, IgM, reproduced in response to a foreign antigen is a large molecule found typically in the blood which stimulates the process of phagocytosis. The process of passive immunity involving maternal blood given to the fetus involves the antibody IgG, which is responsible for activating the macrophages. It can directly destroy many antigens on contact, and is the most abundant immunoglobulin in the body. Membranes in the respiratory tract, urinary tract and intestines produce IgA, which is produced directly at the site of an attack on a membrane by a foreign antigen. When the human body is experiencing an allergic reaction, IgE is released. The last immunoglobin identified, IgD, is not well understood, and is found in minimal quantities in the blood, as well as on the surface of B-cell lymphocyte membranes.
Another line of defense involves complements, substances manufactured in the linings of the intestines, the liver, spleen and microphages. The main substance is known as properdin, and its function is the neutralization of viruses and bacteria.
The reticulo-endothelial cells mentioned earlier comprise another line of defense known as the reticulo-endothelial system, and produce specific sunstances involved in phsiological defense, primarily proteases, which play a role in detoxification of harmful substances.
In addition to the immunological defense system mentioned above, the body maintains a chemical defense system. The blood itself, by virtue of its chemistry, is to a great degree bacteriostatic and virucidal, but this depends very heavily on correct nutrition which produces optimum levels of vitamin C and vitamin B6 (pyridoxine), in addition to other substances. In fact, the optimum response of the immune system is said to depend heavily upon adequate levels of vitamin B6. The very fact that most vitamins are removed from processed foods and replaced with synthetic vitamins made from petroleum ought to tell you that processed foods have a significant role to play in immune system depression, and that it is being done knowlingly. The level of vitamin C in the blood can make the vital difference in human response to toxic vaccines, especially in infants, who often go into immunological shock. Alcohol and tobacco use, besides the obvious toxic consequences, reduce the level of vitamin C in the bloodstream, and are heavily promoted.
Vitamin C in the bloodstream also plays a role in detoxification of heavy metals such as lead. It is estimated that the average individual in todays society requires vitamin C supplementation of 400-600 milligrams daily. For additional data on the impact of human diet on disease, refer to that chapter.
During the early 1950s there was an unusual chain of events relative to the health status of Aborigines in Australia. A New South Wales doctor by the name of Archie Kalokerinos spent seventeen years in the outback, and was appalled by the death rate in Aborigines from all kinds of bacterial and viral infections. In analyzing their diet, which consisted primarily of sugar, bread, and sausage, he made the determination that they were deficient in Vitamin C. Since they did not "show normal signs of Vitamin C deficiency (scurvy)" other doctors, displayed their immense lack of intelligence, declared that a Vitamin C deficiency was not indicated, ignoring entirely the diet of the people. Kalokerinos concluded that the death rates of Aborigines could be cut in half by allowing them various supplementary vitamins. Subsequent blood analysis by the skeptic doctors proved the deficiency in Vitamin C.
In 1970, the Australian government stepped up their vaccination programs, and the results proved disastrous for the children. The infant death rate in the Northern Territory doubled within one year. By 1971, the death rate in some areas was approaching 50 percent. Kolokerinos concluded that the malnourishment of the children contributed to an even weaker immune system; when a vaccination was given, the result was fatal. Investigation into the apparent and purposeful decimation of the Aborigine people during this period, by what was essentially an exercise in bacteriological warfare against a specific group of people, provided information that the government's vaccine program purposely excluded any medical examination before vaccines were given, any case history of the Aborigine, and no checking of any dietary deficiencies. Subsequent deaths were from acute Vitamin C deficiency precipitated by the vaccination. If some infants survived the first vaccination, they would be lined up within another 30 days for another one. The Australian government denied that any relationship existed between the injections and the subsequent death of children. Because of this incident, it was discovered that high doses of Vitamin C reversed toxic and deadly effects of experimental injections.
The Concept of Vaccination and Synthetic Immunity
Vaccine: "a preparation containing protein antigens and toxins, commonly bacteria, viruses and chemicals, used with the intent of inducing artificial immunity against a specific disease, mimicking the process of naturally occurring infections by artificial means, producing infection and production of antibodies, commonly with physiological side effects, with the aim of preventing full-blown clinical disease of the type that would be theoretically contracted without injection of the vaccine, provided that living standards, hygiene, acquired immunity, maternal care and natural immunity partially or completely fail in order to allow the disease to occur."
The composite definition above is not one you will find in a medical journal, but is one assembled from a functional analysis of the conceptual paradigm of vaccination. Websters Medical Dictionary simply defines a vaccine as: "matter or a preparation containing the virus of cowpox in a form used for vaccination, or a preparation of killed microorganisms, living attenuated organisms, or living fully virulent organisms that is administered to produce or artificially increase immunity to a particular disease." Vaccination itself , according to Webster's, is defined as "the introduction into man or domestic animals of microorganisms, active or latent viruses or bacteria, that have previously been treated to make them harmless for the purpose of inducing the development of immunity to a particular disease."
Within the paradigm of vaccination, active immunity is achieved from the physiological reaction to the foreign antigens in the vaccine, and passive immunity is defined as that achieved with the injection of immune serum containing human or animal antibodies. Compare the concepts of artificial active and passive immunity in the vaccination paradigm with those given for natural immunity earlier in this chapter. The use of injected toxic vaccines by-passes the natural defense systems of the body and exposes the individual to more risks than benefits - at least this is the overall consensus by qualified experts. If you ask any doctor the question of whether the idea of immunity by vaccine is the same as immunity by disease, they will answer "of course"; the actual facts indicate otherwise. Another way of asking the question is "is the 'immunity' gained by injection the same as 'normal' or "pathotropic" immunity?"
Vaccination as a procedure is based on several medical assumptions, all of which constitute a mind-set and belief system that not only fails to address known scientific knowledge, but one that forms the basis, on upper levels, for deliberate suppression of that knowledge and maintenance of a medical orthodoxy that insures its own continuance by promotion of disease conditions in the human community. These "medical assumptions" are: (1) a belief that disease agents are the only or primary cause of certain conditions, (2) a belief that the body can build a defense mechanism against such agents and prevent clinical illness with a lack of adverse consequences, and (3) a belief that this can be arbitrarily achieved by the administration of a certain form of the disease agent.
Classification of Vaccines
Vaccines are generally divided into two main groups, those made from bacteria and those made from viruses. Furthermore, vaccines contain either killed or live bacteria or viruses. Within the paradigm, those vaccines using live organisms must be weakened or attenuated, "so as not to cause disease in the recipient." There are several ways that viruses or bacteria are commercially attenuated. The most frequent procedure is by the method of serial passage, which is to pass the organism through animal cell cultures a number of times. Vaccines incorporating viruses may be passed through animal cells literally hundreds of times before it is declared to be attenuated. The type of animal cell that a virus is passed through depends on the type of virus. The measles virus, for example, is passed through successive groups of chicken embryo cells, polio viruses are passed through monkey kidney cells, rubella virus is passed through duck or rabbit cells, and yellow fever is passed through rodent cells or chicken embryo cells. Live vaccines have the capability of reproducing in the host human. The impact of injection of foreign animal protein complexes into humans will be discussed in detail later.
Vaccines designated as "killed vaccines" are those containing viruses or bacteria that are "inactivated" by the use of radiation, heat or chemicals, resulting in altered whole cells or viruses, split or fragmented cells or viruses, all chemically extracted, synthetic molecular structures, or what are known as toxoids. The physiological response to a killed vaccine is the production of antibodies that continue to circulate throughout the body. A great number of situations have arisen in which supposedly killed vaccines still contain live components. This happened in 1955 with the administration of Salk polio vaccine that produced a number of cases of paralytic polio. The preparation contained formalin, a carcinogenic germicide that was thought to have inactivated the virus. Obviously, it did not work. Let us not forget that all vaccines are experimental in nature.
Viruses themselves are non-living pieces of nucleic acid surrounded by a coat of protein. When a virus enters a cell, it makes use of cellular enzymes and duplicates itself. They can be active or assume a latent, passive infective condition within the cell, waiting for the right conditions to activate. Viruses can remain undetected and latent for years within the body, only to suddenly manifest themselves explosively. Viruses can infect plants and animals, as well as bacteria. Duplication of the virus within a cellular structure often results in the death of the host cell, and viral particles are released through broken cell membranes and infect other cells. Viruses also have the capability to combine with the genetic material in the host cell chromosomes without killing the host cell. The nucleic acids RNA and DNA are spiral-shaped protein chains that express heredity codes transferred genetically and direct the formation of various protein substances. Nucleic acids contain individual packets of information which are species-specific.
The "D" in DNA and the "R" in RNA have characteristics which are dependent on the kind of sugar molecule associated with it. DNA exists predominantly in the nucleus, but is also represented in the cytoplasm and in the mitochondria. RNA is also present in the cytoplasm. When viral RNA or DNA combines with the genetic material in the cell itself, the viral genetic material can become part of the host cell genetic code, altering the genetic structure of the cell. When the altered cell duplicates, the encoded viral genetic material may affect cellular processes in such a way as to produce abnormal cells, which sometimes become malignant or cancerous.
Another designation applying to viruses is the slow virus, characterized by extremely long periods of latency and very often fatal. Creutzfeld-Jacob disease, characterized by dementia and motor convulsive disorders, is an example of a well-known slow virus, as is Kuru, a virus that plagued a cannibalistic tribe in New Guinea. Since viral particles blend easily with cellular genetic material, it is quite likely that generations of vaccination is a co-factor contributing to the general decline in the immune system of the general population.
It is interesting to note that the oxymoronic World Health Organization in Geneva has a program called "Health for All by the Year 2000" that "demands a significant increase in the production of viral vaccines and other biologically active substances without a reduction in potency." Furthermore, they have decided to develop cell line seed banks for use in vaccines for baby hamster kidney cells and African green monkey kidney cells known to contain simian virus 40 (SV-40).
Natural vs Invasive Viral Entry Processes
Normally, the natural portal of entry of a virus into the body appears to be when it lands on a mucous membrane lining, which itself possesses certain types of defense mechanisms. The actual immunity conveyed by these membranes is due to the local production and release of IgA, which is a membrane or glandular anti-body, and it is more abundant in those tissues than in blood. The apparent action is that the IgA coats or wraps a virus, thereby neutralizing it. The process of injection, on the other hand, permits a viral entry through a route that is different than the natural portals, decreasing the appropriate antibody response and bypassing the body's first line of defense. This is common knowledge, which makes the deliberate use and intent to use injection processes an even more dubious approach; it can result in nothing but an increase in the general ill health of the population, which of course guarantees a line of income for quite some time, due to the long-term effects incurred. This is another case of criminal activity, knowledge of which is kept from the general public.
Normal Processes of Viral Penetration
Respiratory viruses enter through the surface cells of the respiratory tract. Unless the individual has a strong pathotropic (surface membrane) immunity, which is usually not long lived, invasion will occur. Higher amounts of internal protection from the defensive abilities of the membrane may be offered if high amounts of circulating IgG is present in the blood. Next, the virus may enter through the lymphatic glands in the digestive tract. The tonsils are major guardians in this area. Presumably, this is why medical edict required their removal, as an "organ with no apparent function", for so many years in this society. In the case of vaccine and smallpox virus, cell-to-cell transmission of the viral particles occurs - this cause progressive death of the tissues involved (necrosis) which is then unaffected by the presence of anti-bodies but apparently arrested by sensitized immune lymphocytes. Presumably, this is achieved by a graft-type rejection of the infected cells whereby virus synthesis is interrupted and already-formed viruses are neutralized by anti-bodies.
Other mucous membrane penetration is through micro-lesions created during anal intercourse, inoculation into the womb by intercourse during the menstrual period, direct injection into the blood stream, through micro-lesions in the gum tissue in the mouth caused by the use of tooth-brushes and dental floss, and ingestion of fragments (bone, etc.) within food, which injure the intestinal lining.
Abnormal Viral Penetration By Injection
Viruses directly injected into the blood stream below the skin level avoids the proper immunogobulins and the naturally occurring oleic acid mantle, and are neutralized or blocked by circulating antibodies. We are talking about viruses that are not the result of genetic engineering. The body produced only one type, IgA, as the first line of defense, and this is against arthropod or insect-borne viruses which are carried by blood-sucking and stinging vectors injected directly into the blood or lymph. In other words, nature provides appropriate protection against predatory viruses as long as they attack through their natural routes. The problem comes in when viruses normally meant to run this gambit are injected, as when commercial immunizations are administered intramuscularly or subcutaneously.
One of the primary vaccines made from bacteria is the diphtheria vaccine. Horses are injected with diphtheria bacteria and then bled, producing antiserum. Another preparation using diphtheria bacteria is called toxin-antitoxin mixture, combining both the toxic components and the antidote in one preparation, and a number of serious reactions prompted the development of a diphtheria vaccine prepared from toxoids, which are toxins theoretically rendered non-poisonous by combining it with a chemical agent. Diphtheria toxoids came into existence in the 1920's, using carcinogenic formaldehyde (used to emblam bodies) as the chemical agent in the vaccine.
The DPT vaccine, which we will discuss later, combines the toxoids of diphtheria and tetanus with the whole cells of pertussis bacteria to form a single vaccine which has proven to be quite lethal to humans, especially infants with immature immune systems and unmyelinated nerves, and has resulted in death, encephalitic paralysis and brain damage. DPT vaccine is produced by taking tetanus bacteria and adding it to a broth of dextrose, beef heart infusion, salt and casein. Diphtheria bacteria are added to a similar broth. After the poisonous toxins are produced in each of the vats, the broth is filtered and carcinogenic formalin is added in an futile attempt to attenuate the toxoids. Poisonous methanol alcohol is then added to precipitate the toxoid, which is dried to a powder and mixed with glycerine. Pertussis bacteria are chemically killed by adding a poisonous mercury-based chemical called thimerosal, and aluminum hydroxide or potassium sulfate is added. The result is called DPT vaccine, which is injected into human children after testing on mice to determine the strength at which 50% of a test lot of mice survive. The result will be discussed later in detail, but the neurological disorders produced by such activity are part of the puzzle of why crime is so rampant in our society today. This fact is discussed in another chapter which illustrates that despite the fact they have known vaccines produce minimum brain damage since 1926, and they have known that this MBD produces aberrant behavior leading to criminal activity, they ignore that fact and do it anyway. Hegelian production of social aberration to justifiy greater social control. Simple.