Tag Archives: Vaccinations

The 7 Most Acidic and Disease Causing Ingredients Used to Make Vaccines including the MMR Vaccine!

Parents have the right to understand what is being put into their child’s body. The production of vaccines uses many acidic dis-ease causing ingredients. Additionally, the components used during the manufacturing process may violate your personal, religious, or ethical beliefs.
Lastly, remember that whatever colorful language is used by the scientific community (using such words as purified), using such substances can come with an enormous cost.
As you read this list, understand cell lines and vaccines are contaminated with the blood of humans and animals. This is often hidden under the term “adventitious agents.”
Acidic Dis-ease Causing Ingredient #1: Cells From Aborted Fetus

Aborted fetal cells, listed on vaccine package inserts as “Human Fetal Diploid Cells.” Two aborted fetal cell lines, WI-38 and MRC-5, have been grown under laboratory conditions since the 1960s.
The cells are used to grow viruses or acidic waste products used which are then collected from the cell cultures and processed further to produce the acidic vaccine itself.
Terms to Investigate: PERC6, MRC5, WI-38, HEK-293
Which Vaccines? Adenovirus vaccine, DTaP vaccine, Hep A vaccine, Hep B vaccine, MMR vaccine, Rabies vaccine, Varicella (Chickenpox) vaccine
Acidic Dis-ease Causing Ingredient #2: Serum From Aborted Calf Fetus Blood
One of the more toxic methods involved in vaccine manufacturing is the collection of fetal bovine serum. The purpose for serum is providing a nutrient broth of acid for bacteria, yeast and/or mold to evolve in cells.
How is the blood collected?
According to the Humane Research Australia website:
“After slaughter and bleeding of the cow at an abattoir, the mother’s uterus containing the calf fetus is removed during the evisceration process (removal of the mother’s internal organs) and transferred to the blood collection room. A needle is then inserted between the fetus’s ribs directly into its heart and the blood is vacuumed into a sterile collection bag. This process is aimed at minimizing the risk of contamination of the serum with micro-organisms from the fetus and its environment. Only fetuses over the age of three months are used otherwise the heart is considered too small to puncture.
Once collected, the blood is allowed to clot at room temperature and the serum separated through a process known as refrigerated centrifugation.” [1]
Terms to Investigate: Fetal Bovine Serum
Which Vaccines? Adenovirus vaccine, MMR vaccine, Rotavirus vaccine, Varicella (Chickenpox) vaccine
Acidic Dis-ease Causing Ingredient #3: Cells From Armyworms
The FDA approved the Flublok vaccine on January 16, 2013.
This new technology is being touted as the wave of the future. It utilizes an insect cell line (expresSF+®) that is derived from cells of the fall armyworm, Spodoptera frugiperda.
The vaccine package insert for Flublok also mentions:
“Each 0.5 mL dose of Flublok may also contain residual amounts of baculovirus and host cell proteins (≤ 28.5 mcg), baculovirus and cellular DNA (≤ 10 ng) …” [2]
Terms to Investigate: insect cell line (expresSF+)
Which Vaccines? Influenza vaccine
Acidic Dis-ease Causing Ingredient #4: Cells From Monkey Kidneys
As mentioned above, monkey kidney tissue is used to support the production of certain viruses or acidic waste products used in vaccine production. There remains a huge controversy over using these cells and their role contaminating the polio vaccine in the 1950s.
The story is best told in the Congressional papers of a courageous scientist, Bernice Eddy. The Executive Reorganization and Government Research of the Committee on Government Operations United States Senate, Ninety-Second Congress, Second Session [1972] states on page 500:
“The next and only serious vaccine crisis that has occurred since the polio episode was the realization in mid-1961 that a monkey virus later shown to cause tumors in hamsters was contaminating both polio and adenovirus vaccines. The virus, known as SV40, was entering the vaccines and, just as in the polio case were surviving the formalin treatment.
There were several states by which the full extent of the SV40 problem became known. First was the discovery in 1959-1960 by a DBS scientist, once again Bernice Eddy, that an unknown agent in the monkey kidney cells used to produce polio and adenovirus vaccines would cause tumors when the cells were injected into hamsters.”
Page 502:
“In 1954 Eddy, as a polio control officer, found live virus in supposedly killed polio vaccine; in 1955 she was relieved of her duties as polio control officer … After her discoveries concerning the SV40 virus, her staff and animal space were reduced and she was demoted from head of a section to head of a unit.”
Page 505:
“ … even when the contaminating virus was found to be oncogenic [cancer causing] in hamsters, the DBS [Division of Biologics Standards] and its expert advisory committee decided to leave existing stocks on the market rather than risk eroding public confidence by a recall.”
“There has been a tendency on the part of certain higher government circles to play down any open discussion of problems associated with vaccines … ” [3]
Terms to Investigate: Vero (monkey kidney) cell culture, SV40, Bernice Eddy
Which Vaccines? DTaP vaccine,  MMR vaccine, Japanese Encephalitis vaccine, Polio vaccine, Rotavirus vaccine, Vaccinia vaccine 
Acidic Dis-ease Causing Ingredient #5: Cells From Dog Kidneys
On November 20, 2012, the FDA approved the seasonal influenza vaccine, Flucelvax, manufactured by Novartis. [4]
This vaccine is mass-produced using the continuous cell line Madin Darby Canine Kidney (MDCK) as vaccine or acid cell substrate. [5]
Terms to Investigate: Madin Darby Canine Kidney (MDCK)
Which Vaccines? Influenza vaccine
Acidic Dis-ease Causing Ingredient #6: Mouse Brain
Viral or Acid vaccines prepared in tissue culture or mouse brain have been used in many Asian countries. According to the CDC website, the inactivated mouse brain-derived JE vaccine used in the United States since 1992 is no longer available. [6]
Of course, with any dis-ease causing vaccine, the adverse reactions are rarely tracked and downplayed by medical authorities. However, the injuries from vaccines can be quite serious. [7, 8]
Terms to Investigate: inactivated mouse brain (IMB), suckling mouse brain (SMB), JE virus (Beijing-1), acute disseminated encephalomyelitis (ADEM)
Which Vaccines? Japanese encephalitis vaccine, Rabies vaccine
Acidic Dis-ease Causing Ingredient #7: Chicken Embryos
Chickens and their embryos have long been used in the production of acidic vaccines.
These methods were popularized in the 1920s and 1930s by Thomas Rivers and others at the Rockefeller Institute for Medical Research. [9]
Terms to Investigate: Chick embryo
Which Vaccines? Influenza vaccine, Rabies vaccine, Yellow fever vaccine
3. Executive Reorganization and Government Research of the Committee on Government Operations United States Senate, Ninety-Second Congress, Second Session. Page 499-505. April 20,21; and May 3,4, 1972.

A Second Thought About Viruses, Vaccines and the HIV, HPV, HEP C, Measles, Mumps, SARS, Hantavirus and Ebola Hypothesis

Micrograph of a solidification of metabolic acid
Parasite or Virus?
So-called Ebola Virus or Parasite?
A Second Thought About Viruses, Vaccines and the HIV/AIDS, HEP C, HPV, Polio, Spanish Flu, Hantavirus, SARS, Measles, Mumps,  and Ebola Hypothesis! – Part 1
“In the sciences, people quickly come to regard as their own personal property that which they have learned and had passed on to them at the Universities and Academies.  If, however, someone else now comes along with new ideas to contradict the credo (that has been recited for years and passed on in turn to others) and in fact, even threaten to overturn it, and all passions are raised against this threat and no methods are left untried to suppress it.  People resist it in every way possible: pretending not to have heard about it; speaking disparagingly of it, as if it were not even worth the effort of looking into the matter.  And so a new truth can have a long wait before finally been excepted.”  – Goethe
The first isolation of the virus was achieved in 1892 by Russian that bacteria hunter Dmitri Ivowski, who gathered fluid from disease , tobacco plants.  He passed this liquid through field for fine enough to retain bacteria; yet to Ivowski’s surprise, the bacteria space free filtrate easily made healthy plants sick.  In 1888, a Dutch botanist, Martinus Wilhelm Beijerinck, repeating the experiment, also recognized that there was an invisible cause and named the infectious agent,  “Tobacco mosaic virus.”  In the same year as Beijerinck’s report, two German scientists, purified a liquid containing ‘filterable viruses’ that caused foot and mouth disease in cattle (viruses were at one time called ‘filterable bacteria’, but eventually the term ‘filterable bacteria’ came to apply only to viruses, and was the words ‘filterable bacteria’ were dropped).  Walter Reed followed in 1901 with a filtrate responsible for yellow fever, and soon dozens of other disease causing viruses were found.
In 1935 , another American, Wendell M. Stanley, went back to the beginning and created pure crystals of tobacco mosaic virus from a filtered liquid solution.  He affirmed that these crystals could easily infect plants, and concluded that a virus was not a living organism, since it could be crystallize like salt and yet still remain infectious.  Subsequently, bacteriologists all over the world began filtering for viruses, and a new era of biology was born – Virology.
Historically, medical science has a baseline on the question of whether any virus is alive.  Originally, it was described as non-living, but is currently said to be an extremely complex molecule or extremely simple microorganism, and is usually referred to as a parasite having a cycle of life.  (The term “Killed” is applied to certain viral vaccines, thus implying an official conviction that viruses are alive.)  Commonly composed of either DNA or RNA cores with protein coverings, and having no inherent reproductive ability, viruses depend upon the host for replication.  They must utilize the nucleic acids of living cells.  They infect to reproduce their proteins (i.e., trick the host into producing them), which are then assembled into new viruses like cars on assembly line.  Theoretically, this is their only means of surviving, and infecting new cells or hosts.
Birth of Virology — a Miscarriage?
Underlying the birth of virology was the doctrine of monomorphism — that all microorganisms (herein called microforms) are fixed species, unchangeable; that each pathological type produces (usually), only one specific disease; that microforms never arise endogenously, i.e., have absolute origin within the host; and that blood and tissues are sterile under healthy conditions.  This last point warrants immediate comment.  Theoretically, under ideal health conditions, the blood might be sterile, though it has the inherent potential to develop morbid microforms, as discussed in my book, Sick and Tired.  Long and repeated observation of live blood in the phase contrast, darkfield microscope, however, shows that the blood can contain various microforms and otherwise asymptomatic host, or in a condition defined as normal or healthy in orthodox terms.  The forms are easily visible before other physical symptoms arise. (Since long and repeated observation has correlated their presence with other disease symptoms and their disappearance with the return of health, they serve as indicators of impending outward signs of disease).
Monomorphism was the cornerstone of developments in 20th-century medical research and treatments.  Refusal by the mainstream to examine fairly, much less except, the demonstrated fact of pleomorphism — that viruses and bacteria (and also yeast, fungi and mold) are evolutions from a small indestructible anatomical element, I referred to as the microzyma.  That microforms can rapidly change their form (evolve and “devolve”) in vivo, one becoming another dependant upon conditions in the inner terrain (environment); that blood and tissues are not necessarily sterile; and that there are no specific diseases, but only specific disease conditions — was the foundation of a latter-day “Galileo debate.”  It is so-called because those who wore the “robes” of scientific authority just like today, reprising the religious fanatics who punished the noted astronomer for his truth, would not be swayed from folly when presented with its contrary theory.  These truths began in earnest with Antoine Bechamp in the 19th-century (who also endured the indignation of a fanatical clergy).
In the early third of the 20th-century, the heated debate took place over ‘filterable bacteria’ versus ‘non-filterable’ bacteria.  This was a major battle concerning micromorphology (discussed briefly below). The orthodox view prevailed: bacterial forms were not small enough to pass, or did not have a smaller, earlier stage.  What passed through ‘bacteria proof’ filters was something else, i.e., viruses.  Standard medical textbooks, long made this filtering distinction between bacteria and viruses.  Subsequently, however, the cellular nature of many filterable forms originally thought to be viruses, such as some mycoplasmas, rickettsias, and various other groups, has been established.  In this writer’s opinion, with the victory of the monomorphic view, deeper understanding of infectious ‘disease’ was lost, setting the stage for cancer, degenerative symptoms, HIV. AIDS, Ebola, Hantavirus, Hep C, HPV, etc.
What You See?
A typical bacteria is about 1 micron in size.  Most filterable bacterial forms now called viruses range in size from .3 microns (300 millimicrons) to .01 microns (10 millimicrons) — particularly in the colloidal range  (.1 to .001 micron). Most of the larger viruses are a third to a quarter the size of the average bacteria.  And size is critical because .3 microns is the resolution limit of modern-day light microscopes.  Thus, as viruses were discovered (except for the very large ones, such as mumps), they required an electron microscope to be seen, especially given the the fact that Royal Rife’s microscope technology and career were destroyed by vested interests.  Unfortunately, electron microscopes and the process of chemical staining disorganize or damage all specimens, whereas Rife’s technology allowed life to proceed and thus evolve under its lens. As viruses became visible to advancing technology, the ratification was that the technology revealed, two minds infected with monomorphism, protein structures deemed foreign in the body.
A New Theory
Formulated by Antoine BeChamp in the 19th-century, the microzymian principal is the basis of the new theory about ‘viruses’.  Recently, this principle holds that in all living organisms are biologically indestructible anatomical elements, which BeChamp called microzymas.  They are independently living organized ferments, capable of producing enzymes and capable of evolving into more complex microforms such as bacteria, yeast or mold.  Bechamp’s thesis, is that disease is a condition of ones internal environment (terrain); that disease (and its symptoms) are “born of us and in us.”; and that disease is not produced by an attack of micro entities, but calls forth their endogenous evolution.
My studies and research suggests that the complexes, science calls viruses and retroviruses originate in the cell, as the microzymian as the principal suggests.  However, they are created in response to an alarming acidic situation (condition of disease) for the purpose of genetic repair.  They are repair proteins, evolved from anatomical elements (microzymas), not pathogenic  microorganisms.
It is known that normal cell activity includes genetic repair.  Both enzymes and proteins must be involved.  What is the mechanism?  Viruses are organized around DNA or RNA, not both.  Thus, they are quite probably intended to repair genetic molecules or other structures, and show up with disease symptoms, because the body needs them.  Since viruses require a living cell/host for reproduction, how do we know that the scenario is not set in motion, for a purpose by the cell (i.e., it’s microzymas), rather than being the result of invasion?  Because disease (disturbance of balance in the organism) is so prevalent, especially that which is not yet becoming indicated by common symptoms, repair proteins may be frequently or constantly present.  A toxified cell may easily suffer localized damage to the genome.  Since most observers are not even aware of the microzymian principal, much less understand or even consider it, and since monomorphism stresses invasion, these proteins complexes are regarded as foreign and disease is attributed to them.
Another note of interest is the size of viruses compared to the microzyma.  Viruses are considered to be some of the smallest biological particles and are frequently of colloidal size: e.g., hepatitis A, 27 nanometers (.027 microns); hepatitis B (.042 microns); polio virus (.03 microns); EBV (.042 microns); HIV (.080 to .12 microns); influenza (.08 to .12 microns); mumps (.15 to .30 microns); smallpox (.30 microns); and, according to BeChamp, the microzyma (.0005 microns).
In his book, ‘The Blood and its Third Anatomical Element’, Bechamp states: “the microzyma is at the beginning and at the end of all organization.  It is the fundamental anatomical element whereby the cellules, the tissues, the organs, the whole of the organism are constituted living . . . . in a state of health, the microzymas act harmoniously and our life is, in every meaning of the word, a regular fermentation.  In the condition of disease, the microzymas do not act harmoniously, the fermentation is disturbed, the microzymas have either change their function or are placed in an abnormal situation by some modification of the median.  The virus is either a self-ordered microzymian polymerization, or (less likely), a structure made by microzymas.  It is envelope in protein which is also composed of microzymas, and could well be thought of as an autonomous molecular tool box.
Along with doctors Glen Dettman and Archie Kalokerinos, I wonder, “whether Bechamp’s writing anticipated, in some respects, the discovery of RNA and DNA?”  Could the genetic structure be the construct, thus a tool, of the microzyma?  They quote a personal communication [1974] from a professor Bayev of the former USSR Academy of Sciences, who discusses his work showing the molecular self- restoration from its parts of pure transfer RNA from brewers yeast is possible.
In my own research I have found molecular restoration similar to that described by Bayev.  In my experiment , I used 10-year-old coagulated capillary blood from a woman with cancer.  With one drop of .9% of sodium chloride, the blood was restored to an appearance and level of activity characteristic of freshly drawn sample of blood.  In other words, the anatomical microzymas of the dry blood were restored to activity.  Even the white blood cells became active again.  One might eagerly asked for explanation of the reversal of polymers made during clotting.  It is unclear at this point how this reversal takes place, except to say that what can evolve apparently has the potential to devolve.  It is observable, however.  For example, I have seen, and recorded on video, rod microforms retro-grading without any visible decomposition from 10 microns in length to the vicinity of .1 micron.
This research supports the very important postulates that the cell is not the smallest living biological unit, as promulgated by conventional medical science.  In fact, a smaller biological unit is the imperishable micros I’m a, which is an organized, living been “of a special category without analog,” said BeChamp, who found them ready to become active in chalk deposits at least 11 million years old.
The Pleomorphic Cycle
I suggest a developmental cycle in vivo consisting of three macro stages: [1] a primitive stage comprising the repair proteins complexes; [2] an intermediate, or bacterial, stage including filterable forms such as the cell wall deficient forms described by Lida Mittman, PhD. [in Cell Wall Deficient Forms, Stealth pathogens]; and [3] a culmination stage consisting of yeast and fungal phases, and then mold, the and phase.  The usual course of development would be from microzyma to repair proteins, and then to bacterium, etc.  However, under certain conditions, such as, for example, it is highly likely that the microzymas can skip the primitive stage and become bacteria directly.  Although these transformations are as astounding as that of a larva to a butterfly, what is equally impressive under observation is in the rapidity with which they can take place — in minutes, even seconds, sometimes.  By the same token, when provoked by acidic conditions and the cycle proceeds to yeast, fungus and then mold, it may occur so rapidly that the bacterial stage, if that happens, has no time to be of any significance.
Thus, symptomgenic microforms can originate within the higher organisms without invasion, via a permutation of the endogenous microzymas when the situation calls for such change.  The situation is an imbalance referred to by Bechamp as a “modification of the median.”  Endogenous evolution is evident under the microscope when bacterial, yeast, and fungal forms are seen coming out of the red blood cells, which initially appear normal.
Biological Basis for the Pleomorphic Cycle
There is a common biological basis for the pleomorphic cycle and its increasing complexity of organization: more complex forms evolve inherently upon the death of an organism for the purpose of recycling its anatomical and chemical structures in the carbon cycle.  The process of rapid evolution [which is reversible] is an essential life process, which, beyond the repair stage, is necessary to return a dead organism to the earth.  The second and third stage microforms degenerate the body’s vital substances and tissues via putrefaction [bacteria] and fermentation [yeast and fungus].  Fermentation results in acidic waste products, which further breakdown tissue.  Disease symptoms, then, especially the degenerative type, are NOT produced by viruses, but manifest as chemical decomposition, or attempted recycling via fermentation and acidic toxins, but with ‘host’ survival processes still, operable.  Obviously, certain other factors may play important roles in producing symptoms, such as heavy-metal toxicity, or state of mind, for example.  Some of the body survival methods also produce symptoms commonly called dis-eases.  An example is eczema, and emergency expulsion of acidic toxins via the pores of the skin.
The aforementioned casual [alarming] situation, or modification of the median, is chronic tissue acidification [pH imbalance] and oxygen deprivation in the blood and tissues due to acidic forming foods, adverse lifestyle, emotional stress, and environmental stress.  This is not an oversimplification!  Acidification/hypoxia biochemically signals a dead host to the microzymas, while creating collapsed areas [dead zone’s] of the colloidal system in the intercellular fluid, and it is the primary physiological disease condition at which the symptoms commonly called specific diseases arise.
Thus, we distinguish between this disease condition and its consequent symptoms, which include both the morbidly evolved microzymas and the physiological science commonly thought of as specific diseases.  As they develop, microforms [bacteria, yeast, fungus and mold] are actually scavenging forms of the microzyma, developed when disease in the cell life requires tissue to be broken up.  These upper development forms are the ones easily visible in the blood before physical symptoms arise.  They disappear, [devolve] when the recycling task is complete, once again becoming microzymas of the earth and/or air.
Virus or Toxin/Acid?
Regarding the early period of virus isolation, a question is whether the unseen entities isolated in filtered fluids were accompanied by the waste products [mycotoxins] of fermentation by yeast and/or fungus of cellular elements, such as DNA.  If virus infiltrates are injected into a host to prove virulence, it is almost certain that easily filterable molecular toxins will be introduced as well.  Could Dr. Stanley’s “pure crystals of tobacco mosaic virus” have been crystallized acidic toxins?  If so, they would certainly be highly symptomgenic, as are exotoxins at the intermediate stage of the cycle, for example.  However, it is not proof of anything that you can create illness by poison injection, except proof of that tautological fact.
In my research utilizing darkfield and phase contrast microscopy, it is common to see acid crystallization’s in the blood.  It is normal for the body to use calcium or other mineral salts, and fats as well, to chelate the acidic waste products from the morbid fermentation of body proteins, fats and sugars.  Such crystal deposits are found in cancer tissue as well.  A malignant tumor removed from the breasts of one of my research clients was found to have numerous calcium deposits attached to it.  It is an attempt to render inactive acidic substances that make our inner streams healthy, poison our cells, and coagulated colloidal systems in blood and intercellular fluid.
The term “virus” is the Latin word for poison, and gives us insight into the immediate cause of disease symptoms — poison is: exotoxins and mycotoxins, and a toxin, exotoxins, and toxins from environmental sources, [many of which are primary or secondary mycotoxins.].  Orthodox medicine is well aware that it is bacterial toxins more than the bacteria them self.  [They feed in-house], that caused the symptoms referred to as infectious disease.  Little if any emphasis is placed on this fine, but important distinction.  Always, the germ is emphasized.  There is little too, no awareness [or knowledge that], either, of the same role played by acidic toxins of the culminate microforms of the pleomorphic cycle.  Their action and the body’s response to them are frequently ascribe to viruses, which do not produce toxins because they are the toxin or acid, but are said to wreck havoc by a number of other means.  However, if they participate in symptom at Genesis in a host it is because they are stimulated to evolve into more complex, toxic genetic forms.  Somewhat less likely is the possibility that they cause damage as a result of erroneous construction or function, for one reason or another — missing mineral nutrients leading to alkaline mineral deficiencies, for example.
Misconception Breeds Contempt
In addition to chemical toxicity, however, what is the impact of the fear [emotional toxicity] that the word “virus” brings to mind and heart?  It has been said that fear it is the most deadly of disease conditions.  If the “disease” kills one person, the fear of it may kill 20.  General prejudice concerning the danger of viruses is fundamental biological error based on Louis Pasteur’s germ theory, and is itself a perpetrator of auto-suggested illness.  For example, in Africa doctors attribute some AIDS sickness to “voodoo death” syndrome, the term for illnesses induced psychologically.  According to one nurse, “we had people who were symptomatically AIDS patients.  They were dying of AIDS, but when they were tested and found out they were negative they suddenly rebounded and are now perfectly healthy.”  Ironically, if the germ theory were found on facts, it would be correct to fear viruses, except there would be few, if any, humans living to discuss the issues.  These so-called pathogenic entities are to researchers, medical practitioners and the press what criminals are to detectives — the focus and justification of their existence.
The Encyclopedia Britannica has this to say about bacteria, which relates also to viruses:
“The common idea of bacteria in the minds of most people is that of the hidden and sinister scourge lying in wait for mankind.  This popular conception is born of the fact that attention was first focused upon bacteria through the discovery, some seven years ago, of the relationship of bacteria to disease in man, and that in its infancy, the study of bacteriology was a branch of medical science.  Relatively few people assigned to bacteria, the important position in the world of living things that they rightly occupied, for it is only a few of the bacteria known today that have developed in such a way that they can live in the human body, and for everyone of this kind, there are scores of others which are perfectly harmless and far from being regarded as the enemies of mankind, must be numbered among his best friends.
It is in fact, no exaggeration to say that upon the activities of bacteria.  The very existence of man depends; indeed, without bacteria there could be no other living thing in the world; for every animal and plant owes its existence to the fertility of the soil, and this in turn depends upon the activity of the microorganisms which inhabit the soil in almost inconceivable numbers.  It Is one of the main objects of this article to show how true is this statement; there will be found in it only passing reference to the organisms which produce disease in man and animals — for information on these see Pathology and Immunity.  [Encyclopedia Britannica, 14th ed., Volume 2, page 899].
The general message of the foregoing article applies even more aptly to viruses in the sense that much fear has been bred and cultivated around them, although they never produce disease symptoms, whereas the acid waste products of bacteria, yeast, fungus and mold do.  The writer of the above understands bacteria, with the exceptions that symptomgenic bacteria found in man and animals do not produce disease.  [Only secondary symptoms], that their precursors are endogenous to higher organisms, and they have not “developed in such a way that they can live in the human body.”  If anything, the reverse is true.  According to one theory of microbiology, microforms have colonized over eons to become higher organisms.  In one sense, then, the human body has developed as a specialized environment for them.
An important dimension of the bacterial dependence of higher life forms is the floral population in the human digestive tract.  Literally, these “foreign species” keep us alive.  Most bacteria have the same underlying function, whether found in the soil, sewage, in the human digestive tract, or elsewhere in nature: they are an essential part of the life processes of hire organisms.  They will not or cannot attack healthy cells or tissues, but certain ones will recycle sick or dead tissue in much the same way insect pests are drawn to weaker plants.  As Bechamp said, “nothing is the prey of death; all things are the prey of life.”
Following in the wake of misconceptions arising from the fundamental biological error known as the germ theory of disease, defying infiltrates of disease tissue as a newly discovered infectious microforms was the birth of a major corollary error in bio science.
Viral Behavior Reconsidered
Listed below are ways of viruses are said to disrupt or destroy host cells.  According to orthodox medical science and the germ theory advocates.  Following each in its italics is a different interpretation following from microzymian principle:
1.  Viral proteins insert into the host cells , plasma membrane and directly damage its integrity , to promote cell fusion [HIV, measles, and herpes viruses.].
Proteins are attempting to repair membrane damage, or enter cells to repair other proteins.  There is the question as to whether viruses on cell walls are coming or going.  In both cases, it would be a matter of whether or not a cell has been disturbed by excess fermentation and acidity.  But in the former case, the cell would be dysfunctional before attachment occurs, thus requiring the repair complex.  Another possibility, perhaps remote, is that dysfunctional receptors on cells are in need of repair, or they are covered by these complexes to inactivate malfunction of the cells.  Positive electrical charges in a compromised acidic terrain, primarily on acidic molecules from fermentation’s, discharge cell membranes and act as mortar to stick cells together causing rouleau and clotting.
2.  Viruses inhibit a host cell DNA, RNA, or protein synthesis.  For example, polio virus inactivates cap-binding protein, which is essential for protein synthesis, directed by capped host cell mRNA’s, while allowing protein synthesis from uncapped polio virus in mRNA’s.
Protein inactivation is probably being done by fermentation or by acidic toxins from fermentation, while “poliovirus” is produced in the cell to reverse the damage.
3.  Viruses replicate efficiently and lyse host cells, e.g., liver cells by yellow fever, and neurons by poliovirus.
Highly unlikely.  The lysing is more likely caused by acidic mycotoxicosis, or by free radicals released in response to mycotoxic stress, or from other sources [I lysine radiation, for example].  Repair particles are residual after cell wall disruption.
4.  Slow-virus infections [e.g., sub acute sclerosing panencephalitis caused by the measles virus] culminate in severe progressive disease is after a long latency period.
How is this demonstrated?  Perhaps “latency” is a period of unsuccessful or attempted repair that eventually falters.  Symptomology naturally appears in the weakest parts of the body.  Excess acidity is always a systemic problem that localizes, just as cancer is a systemic acidic condition that localizes, even though it its symtogenic influence may later spread.
5.  Viral antigen proteins on the surface of the host cells are recognized by the immune system, and the host lymphocytes attack, the virus infected cells [e.g., liver cells infected with hepatitis B].
Liver cells are damaged beyond repair by exotoxins and mycotoxicosis, and the immune system, our elaborate janitorial service, is cleaning out the garbage.  Perhaps the repair protein antigen is expressed to signal any in response [because the cell is beyond repair], which is one explanation for why there are antibodies to these proteins.
6.  Viruses damage cells involved in the host anti-microbial defense, leading to secondary infections.
The function of immune cells are damaged by bacterial or fungal waste products/acidic and/or overworked by toxic acidic overload, preventing proper cleanup and elimination of disharmonious, symptomgenic elements.
7.  Viral killing the one cell type causes the death of other cells that depend on them, e.g., degeneration of muscle cells enervated by the attack of poliovirus on motor neurons.
Once again, a misinterpretation and lack of understanding that is not viral microforms that damage neurons.  Acidic toxins from bacteria, yeast, fungus and mold — as well as the ferments of glucose, uric acid from proteins, hormones and acetic acids from fats — produce, or influence the body to produce, dis-ease  or inflammatory symptoms.  Not recognizing “virus,” for what it is, observers attribute dis-ease or disease to it.
8.  Host cell responses to viruses include metabolic derangement and transformations resulting in neoplastic changes.
Metabolic derangement has occurred prior to the appearance of repair proteins, due to toxic overload in the cell.  It is more likely that the proteins attempt to prevent cell transformation, and that cancerous development is cell conversion from primarily oxidative to wholly fermentation of metabolism, mediated by yeast, fungus and mold.
9.  According to orthodox theory, viruses enter a host cell and replicate at the host’s expense.  Replication is accomplished using enzymes, which are distinct for each virus family.  For example, RNA polymerase is used by negative stranded RNA viruses degenerates positive stranded mRNA, or as reverse transcriptase is used by retroviruses to generate DNA from their RNA template and to integrate that DNA into the host genome.
It is normal for repair proteins to generate enzymes or acidic waste products as they do their work of repair.
10.  one reason suggested for viral tropism [the tendency to infect some cells, but not others] is the presence or absence of host cell receptors that allow the virus to attach.  It is said, for example, that HIV binds to the proteins [CD4] involved with antigen presentation on a helper.  The lymphocytes, that Epstein-Barr virus binds to the complement receptor [CD2] on macrophages, that rabies virus binds to the acetylcholine receptor on neurons, and that rhino viruses bind to the adhesion proteins [ICAM-1] on mucosal cells.
See answer to number 1 above.
Theoretically, once attach, the entire virion, or a portion containing the genome and essential polymerases, penetrates into the cell saddle plasma in one of three ways: [one] translocation of the entire virus across the plasma membrane; [two] receptor mediated endocytosis of the virus and fusion with endosomal membranes; or , [three] fusion of the viral envelope with the cell membrane.  Theory suggests that within the cell the virus uncoats, separating its genome from its structional components and losing its infectivity before replication.  In either the nucleus or the cytoplasma, newly synthesize viral genomes and capsid proteins are assembled into progeny virions, which may then bud to the plasma membrane.  Unencapsulated viruses may be released also, directly through the membrane.
It is interesting, however, that viruses can somehow choose the “infection.”  To be aborted, latent or persistent, meaning respectively: [one] viral infections with incomplete replication cycles; [two] persisting in the cryptic state, like herpes zoster within a dorsal root ganglion, which suddenly becomes active to produce shingles; [three continuously synthesized virions, with or without altered cell function [e.g., hepatitis B].  These three ideas, especially latency, have arisen as feeble excuses for the untenable virus theory.
11.  In order for viruses to reproduce, they must complete the following four steps:
a] Adsorption and penetration of the cell.  The viral particle binds to the host cell membrane.  This is unusually a specific interaction in which a viral encoded protein on the capsid or a glycoprotein embedded in the virion envelope binds to a host cell membrane receptor and is then internalized.  This internalization occurs by endocytosis or by fusion of the virion envelope with the host cell membrane.
This is the mechanism whereby the viral particle enters the cell for the purposes of carrying out repairs to the damaged DNA or RNA.
b) Uncoating of the virus, so that the nucleic acid can be released from the capsid into the nucleus or cytoplasm.
Repair work may require uncoating.  An uncoated “virus” in the saddle plasma, may have, from the nucleus and not yet have a code, as in the case of hepatitis B , according to medical science.  A coat is then created to protect the nucleic acid, to make a communicative or response to protein complex, or to allow exiting the cell for remote function or for neutralization and recycling by the immune system.
c) Synthesis and assembly of viral products, as well as in addition of the host cell’s own DNA, RNA and protein synthesis.
Protein complex is produced in response to an alarming acidic situation — fermentation and mycotoxic stress — are capable of self-reported replication.  As suggested by Bechamp, the microzyma is specific for each organ, therefore specific repair proteins will be needed for specific cells that make a specific organ that are being disturbed by dietary and/or metabolic acidic waste products.  There is the question of why the great numbers in some cases.  One possibility is simply over reaction; for example, fever can be extreme.  Why?  To remove dietary, metabolic acids or acids from bacteria, yeast, fungus and/or mold.
d) And finally, release of virions from the host cell either by budding or lysis.
[1] Complexes leave the cell for remote function or to be neutralize; [2] repairs have failed, and complexes are released prior to or during the breakdown of the cell by acidic toxins or the immune system.
Further Considerations
Virologists referred to certain microforms as passenger viruses, which are present in asymptomatic situations, riding on their host genetic molecule like a passenger.  To the conventional mind searching for new diseases or for viral cause of unexplained ones, they are most interesting, because the status virologist in the scientific community depends upon the pathogenic potential of the viruses they study.  Due to their location, passenger viruses are thought to have much disease potential, thus their true function goes unnoticed.  These colloidal passengers are the silent majority of animal and human intranuclear proteins essential for genetic repair.
Kalokerinos and Dettman quote Dr. Fred Klenner regarding the changeability of viruses, “I am of the opinion that virus units have the potential of going from one type to another by altering their protein coat.  We see chickenpox at Thanksgiving, mumps at Christmas, read measles in the spring, and polio and Coxsackie in the summer.”  Seasonal appearance of different forms may be mediated by variations of imbalance in the biological terrain or nutritive median due to the fermentation of dietary excesses such as sugar and animal proteins that accompany holidays and seasons, calling for different repair proteins.  For example, outbreaks of polio have been associated with sugar consumption in summer.  Various psychoemotional stresses correspond to the seasons as well.”
Supporting the general idea of dietary culpability is a statement published by the great English physician, Sir Robert McCarrison in 1936: “obsessed with the invisible microbe, virus, protozoa as all-important excite tens of disease, subservient to lavatory methods of diagnosis, hidebound by our system of nomenclature, we have to forget the most fundamental of all rules for the physician, but the right kind of food [nutrition] is the most important single factor in the promotion of health and the rhonchi to food.  The most important single factor in the promotion of disease.”
Six years before BeChamp identified the microzyma as a ferment and, with his devoted associate, Professor Estor, began a 13 year odyssey of research into its nature. Florence Nightingale published a statement about the germ theory,  In ‘Notes on Nursing’, first addition, 1860, she said of infection:
“Diseases are not individuals arranged in classes, like cats and dogs, but conditions growing out of one another.
Is it not living in a continual mistake to look upon diseases, as we do now, as separate entities, which must exist, like cats and dogs, instead of looking upon them as conditions, like a dirty and a clean condition, and just as much under our own control; or rather, as the reactions of kindly nature against the conditions in which we have placed ourselves?
I was brought out . . . . distinctly to believe that smallpox, for instance, was a thing of which there was once a first specimen in the world, which went on propagating itself in a perpetual chain of dissent, just as much as that there was a first dog, [or a first pair of dogs], and that smallpox would not begin itself anymore than a new dog would begin without there having been a parent dog.
Since then, I have seen it with my eyes and smelt it with my nose smallpox growing up in the first specimens, ear in close rooms or in overcrowded wards, where it could not by any possibility have been ‘caught’,  but must have begun.  Nay, more, I have seen diseases begin, grow up, and pass into one another . . . . I have seen, for instance, with a little overcrowding, continued fever grow up; and with a little more, typhoid fever; and when little more, typhus, and all in the same ward or hut.
Would it not be far better, truer, and more practical, if we looked upon disease in this light?  For diseases, as all experience shows, are adjectives, not noun- substantives.”
That is, symptoms [called diseases] are described first of the situation.
I find legitimate BeChamp’s conclusion that what are called germs of the air are fundamentally microzyma’s of beings, which are being consumed by the recycling process, i.e., some kind of vegetative digestion — putrefaction or fermentation.  In short, there are no pre-existing disease germ species.  The principals of microbial medicine constitute a fundamental biological ERROR!!!!!!  As BeChamp said, “the microbial doctrine is the greatest scientific silliness of this age.”  This is not to say there is no transmission, only that invasion is not necessary for symptogenesis, nor is it the primary mechanism for illness.  It is to say that for transmission to take place, susceptibility in the form of a compromised terrain must pre-exist in the receiver, who was then likely to be ill anyway.  With the exception of the immune component in the mucosal barrier, primary host “resistance” is a function of terrain condition rather than immunity per se.
Phantom Viruses
Hepatitis can be a painful symptom that has yielded profitable virus hunting opportunities in recent years.  Although there are several categories of this disorder, three main varieties of what is called “acute viral hepatitis” exist: Type A [formally, ‘Infectious hepatitis’], Type B [formally ‘Serum hepatitis’], and hepatitis Type C (formally ‘non A, non-B’].  The corresponding viruses are HIV, HBV, and the non-A, non-B ‘group’, now called C. Type A is said to be caused by an RNA virus, spread primarily by fecal contamination of water and food, with blood and secretions also possibly being infectious [but it is due to the acidic toxins associated with unsanitary conditions].  Hepatitis B, discovered in the sixties, is said to be caused by a DNA virus, which replicates in the hepatocyte nucleus and receives its surface coat in the cytoplasma.  It is said to be transmitted by transfused blood or blood products, or via common use of needles by intravenous drug users [but it is due primarily to over-acidification from the drugs, especially heroine.  The exchange of body fluids into the blood, whether by sterilize needles, abusive sexual activity, eccentric sexual activity, etc. can also play a role overtime, because of repeated immune stress caused by foreign proteins].  Third World babies with poor nutrition and unsanitary conditions around the time of birth are also susceptible.
The third type of hepatitis, discovered in the seventies, is found among drug users and alcoholics, and accounts for 80 to 90% of hepatitis caused by blood transfusion.  It is thus akin to B type and was at first thought by scientists to be hepatitis B until thorough testing a subject revealed no virus B nor A, for that matter.  It was thus called “non-A, non-B” hepatitis and thought to be at least two viruses and perhaps more.
In 1987 scientists believed they found a single virus causing the third type, what is known today as the hepatitis C virus.  However, what they identified was an antibody, they associated with a virus.  Now, just as with HIV, they could test patients for antibodies against an elusive or invisible phantom virus.  With this new observation, however, new paradoxes confronted the viral hypothesis.  Huge numbers of people testing positive for the Phantom C virus never developed any symptoms.  Hepatitis C is truly the result of an over-acidification or toxification of the largest filter organ in the body by such substances as lactic acid, acetylaldehyde and ethanol alcohol — not the disease of a pathological phantom virus.  It is interesting to note also that all these hepatitis viruses have incubation periods of two to 25 weeks, violating Farr’s law, [see below], yet are not classified as slow viruses.  Also, the point at which a “natural invasion” takes place, as opposed to a highly artificial in objective one, and thus, how true incubation periods are determined, is another interesting question.  Bottom-line there is no Hepatitis C virus.
A recent example of unwarranted panic in American bio medicine was the eminent hantavirus of 1994.  Presumably, it had jumped species, from mouse to man [the American Navajo Indians].  However, after supposedly killing a number of people, this phantom virus apparently made peace with the Indians and retired to its mouse reservoir.  The virus failed to materialize.  A front-page article in the San Francisco Chronicle reported that CDC “epidemiologist across the nation are carefully monitoring the deer mouse population and the level of virus within it.”  But all that was left to discover of the former.  “Navajo flu” by the CDC epidemiologist [shown in their space suits] were healthy mice in the mountains.  The Navajo flu is nothing new to the Native Americans and is most likely tied to sanitation, nutrition and lifestyle.
In May 1995 , the CDC announced the new, threatening Ebola virus.  The deadly killer virus was expected to leave its hidden reservoir in the rain forest of Africa to claim Europe and the United States.  An article in Time magazine was peppered with men in space suits and color electron micrographs of the virus  [even though electron microscopes cannot take color pictures and the pictures were of parasites].  A CDC virologist suggested the virus could leave the rain forest a if “we get a virus that is both deadly to man and transmitted in the air.”  We are thus asked to fear the false image of virus somehow being launched into the air, perhaps by injection from a host, and then floating on a killer breeze to other lands.  A more imaginable scenario was suggested by European epidemiologist who heads the United Nations AIDS program.  Echoing the the CDC’s alarm, he stated, “it’s theoretically feasible.  Then infected person from Kuwait could go to Tunisia, get on a plane to New York, fall ill, and present transmission risk there.”  But within a month, the virus had disappeared in Africa, and not a single Ebola case was reported in the United States or Europe.
The World Health Organization announced on December 19, 1995 that the Ebola virus epidemic that killed 245 people in West Africa was over.  All tests on any remaining suspected cases were negative.  A somewhat unsettling revelation was that every Ebola outbreak in Africa, “is associated to have spread to public hospitals.”  As it turned out, it was associated with reused hypodermic needles in these hospitals.  Just like hantavirus, Ebola vanished, never to be heard from again, until NOW!  Most interesting is that this so-called epidemic, as epidemics will, stopped without vaccines or other drugs.  Consider the impact such stories have made upon our minds and on the way we view and understand germs.  What’s next in the virodrama, the Andromeda strain?  NO!  Here we go again with the same old phantom viral story!
There is one insidious possibility that must be mentioned in passing.  Some mysterious outbreaks of the past have shown years later to have been man-made.  In some cases, government agency have used the public to test releases of organisms and weak biochemical acidic toxins in order to verify, through medical reports, expectations of bio-warfare activity.  These incidents and the whole story of such behavior is well documented in the book, all higher forms of killing by Robert Harris and Jeremy Paxman [Hill and Wang, 1982].  In this scenario, the cause of such an incident would be constructed officially, or left as a mystery, in order to draw attention away from the truth.
  1. To read Part 2 and Part 3 and for all references for this article read Sick and Tired by Dr. Robert O. Young – http://www.phoreveryoung.com, http://www.phmiracle.com or http://www.phmiraclebooks.com

Mississippi Has America’s Top Vaccine Rate and the World’s Highest Infant Mortality!


Health Impact News Editor

Lindey Magee of Mississippi Parents for Vaccine Rights recently commented on an article published in Mississippi’s Clarion Ledger on their front page:


Mississippi has the highest rate of childhood vaccination because it is one of only two states in the U.S. that does not allow parents a choice regarding vaccines, as a requirement for attending school. Only a medical doctor can provide an exemption, as religious and philosophical exemptions are not allowed.

The Clarion Ledger was obviously proud of their vaccination rates, and many around the country want to follow their model and remove vaccine choice from parents and families.

However, does not think Mississippi should be so proud of their vaccination rates, given the fact that Mississippi ranks last in the U.S. with the highest infant mortality rates, and very low scores in other key health figures for children:

To be clear, ranking as the most highly vaccinated state is NOT something to be proud of.

More educated states are seeing more and more parents opt out of some of the 49 doses of vaccines administered to our children before kindergarten. Ranking first in vaccination compliance only indicates that Mississippi families are being exploited for its reputation of ignorance and lack of education.It is an embarrassment, not a badge of honor.

As citizens of this state, it is time we take notice of our state’s archaic vaccine law. As it is now, the state of Mississippi requires children first be vaccine-injured before a parent can begin the uphill, long battle to secure said injured child from further damage. That is barbaric! Meanwhile, forty-eight other healthier states provide religious and/or philosophical vaccine waivers.

While we have the highest vaccination rates, Mississippi also has the highest infant mortality rate in the U.S. Keep in mind that the U.S. is the most highly vaccinated country in the world; now consider that as a nation, our infant mortality rate falls below 27 other wealthy countries-some of which do not even mandate vaccines at all! Mississippi has the most highly vaccinated pediatric population IN THE WORLD.Why then are we the LEAST healthy? Yes, poverty and crap food, etc. plays a part, but too many vaccines too soon cannot be ignored.

I implore those who buy into this “vaccines must be mandated” notion that uses seriously dangerous diseases like polio and smallpox to sell 30+ doses of vaccines to all babies by six months to reexamine the topic. I was born in 1979 and received 10 doses of vaccines by high school. Where will it end? Mandated medicine is a slippery slope and is affecting a generation of over-vaccinated children! (Source.)


– See more at: http://healthimpactnews.com/2014/mississippi-first-in-infant-vaccination-rates-last-in-infant-mortalities/#sthash.wGjoSATU.r23cDxx8.dpuf

The United States is Number 1 in the World for Vaccinations and Infant Mortality1


Do Vaccines Violate Our Christian Faith? by Courtney Charles

The Worst Cover-Up In The History Of The World! Vaccinations Are Monkey Business!

The following newsletter on the history of virology,
bacteriology, mycology and vaccination is extremely
long but important for the world to know the truth.
May I suggest before reading further to please
watch the following YouTube video entitled,
“The Worst Cover-up in the History of the Military.”
And finally, please share this information with
everyone you know.http://www.youtube.com/watch?v=Xj7AN4fRe6sThe story of marine David Fey reads like a crime
novel and is typical of all the cases I am
personally aware of. It is shocking and sad to
think that our soldiers pledging their lives to
defend the United States are being used as guinea
pigs for unknown vaccinations. It is nothing new
because it has been going on for 100’s of years.Let’s start with a few quotes:

“The most dangerous man to any government is the man who is able to think things out… without regard to the prevailing superstitions and taboos. Almost inevitably he comes to the conclusion that the government he lives under is dishonest, insane, intolerable.”

– H L Mencken

“No country and no people can be free and ignorant at the same time.”

– Thomas Jefferson

“The only safe vaccine is the one that is never used.”

– James Shannon
Former National Institutes of Health (NIH) Director

“I haven’t got a flu shot and I don’t intend to.”
– George W. Bush 2004 Presidential Candidate

“Vaccinations only prove that you can inject someone
with highly acidic toxic poisonous chemicals and that person
hopefully surviving the debilitating side effects, such as multiple
sclerosis, lesions on the brain, paralysis, breakdown of the red
and white blood cells, ulcerations of the liver, lung, kidney, pancreas,
stomach and bowels, seizures and death. Vaccinations provide
zero immunity. True immunity that leads to health and fitness
can only be achieved by making healthy lifestyle and dietary choices.”

– Dr. Robert O. Young
The pH Miracle Living Center

The following is a history of virology, bacteriology, mycology and vaccination that has lead to many of the out-breaks and/or epidemics from the Spanish Flu Epidemic to Polio to HIV/AIDS to the Gulf War Syndrome and now to our latest epidemics of prostate and breast cancer, diabetes, obesity and the rise of autism in children.

Dr. Young has stated that the use of vaccinations, antibiotics and anti-fungals will only poison the body leading to the one sickness and one disease – latent tissue acidosis and then death.

All vaccinations, antibiotics and anti-fungals are the acids of morbid fermentation of plant, animal and human matter and when ingested or injected can only prove that you can poison the body and hopefully live through it.

The day will soon come when scientists will proclaim that the use of vaccinations, antibiotics and anti-fungals are harmful to the human body and should not be used under ANY circumstances.

In the words of Thomas Edison, ‘The Doctor of the Future will give no medicine, but will involve the patient in the proper use of food, fresh air, and exercise.’

The future that Thomas Edison speaks is here and now! Read on to understand and to see the course we have been walking for the last several centuries and how things must change before it is to late.


1798 General vaccine programs against cowpox instituted in the US.

1801 First widespread experimentation with vaccines begins.

1802 The British government gives Edward Jenner £10,000 for continued experimentation with ‘smallpox vaccine.’ The paradigm that vaccines provide ‘lifetime immunity’ is abandoned, and the concept of ‘re-vaccination’ is sanctioned.

1822 The British government advances Edward Jenner another £20,000 for ‘smallpox vaccine’ experimentation. Jenner suppresses reports which indicate his concept is causing more death than saving lives.

1844 Fredrich Loeffler isolated the diphtheria bacillus from the throats of patients.

1881 Sternberg in his own lab isolated the pneumococcus

1882 Robert Koch isolates the tubercle bacillus

1883 Robert Koch isolates the cholera bacillus.

1883 Max Von Pettenkofer suggested that Koch’s bacteria were only one of the many factors in the causation of cholera. He prepared test tubes thick with lethal cholera bacteria and he and several of his students drank them down with no side affects.

1888 Bacteriological Institute opens in Paris for experimentation with animals and production of vaccines and sera. Other institutes open around the world modeled after the Paris Institute.

1888 Bacteriological Institute in Odessa, Russia tries its hand at a vaccine for anthrax. Over 4500 sheep are vaccinated; 3,700 of them die from the vaccination.

1909 New York Press, January 26, 1909 publishes a report by W.B. Clark which states, ‘cancer was practically unknown until cowpox vaccination began to be introduced. I have seen 200 cases of cancer, and I never saw a case of cancer in an un-vaccinated person.’ Scientific evidence begins to mount that where human lymph is employed in a vaccine, syphilis, leprosy and TB soon follow. Where calf lymph is employed in the creation of a vaccine, TB and cancer soon follow. (Cancer and Vaccination by Esculapius).

1911 The head of French Public Health for the French Army said that germs alone were ‘powerless to create an epidemic.’

1912 First whooping cough (Pertussis) vaccine created by two French bacteriologists, Jules Bordet and Octave Gengou, who wanted to use it in Tunisia. After they grew Pertussis bacteria in large pots, they killed it with heat, mixed it with formaldehyde (used to embalm bodies) and injected it into children.

“Vaccinations, Not a Virus, Is Responsible for Spanish Flu – 1918”

– Dr. Robert O. Young
The pH Miracle Living Center

1933 a British science team to identify the first filterable bacteria in man, yet propaganda says that the virus of Spanish flu killed millions of civilians and soldiers during the pandemic from 1918 to 1920.

Many would have us believe that all those American soldiers who died from non-combatant causes died from Spanish flu. However, U.S. Army records show that seven men died after being vaccinated.

A report from U.S. Secretary of War Henry L Stimson, the deaths were not only verified but also there had been 63 deaths and 28,585 cases of hepatitis reported as a direct result of yellow fever vaccination during only six months of the war. Plus, the yellow fever vaccination was only one of the 14 to 25 shots given to recruits.

1911 vaccinations became a requirement in the U.S. Army. Cases of typhoid and vaccinial diseases increased rapidly, according to Army records.

1917 The death rate from typhoid reached the highest point in the history of the U.S. Army after America entered the war.

In 1917, 19,608 men were admitted into army hospitals due to anti typhoid inoculation and vaccinia, according to a report of the Surgeon-General of the U.S. Army; and this doesn’t take into account others whose symptoms were attributed to other causes. The army doctors knew all these cases of disease and death were due to vaccination and were honest enough to admit it in their medical reports. Army doctors tried to suppress the symptoms of typhoid with a stronger vaccine, however it caused a worse form of typhoid, paratyphoid. They then concocted an even stronger vaccine to suppress the previous one and created an even worse disease–Spanish flu.

After the war, this was one of the vaccines used to protect a panic-stricken world from the soldiers returning from WWI battle fronts infected with dangerous diseases.

The rest is history.

1918 Great influenza epidemic attributed to widespread use of vaccines that killed up to 100 million people.

1921 BCG tuberculosis vaccine developed.

1922 A study by Samuel Torrey Orton connects emotional disturbance with neurological problems. This insight was lost after World War II when psychology, psychiatry and psychoanalysis became popular, breaking the connection. The emotional disturbances caused by vaccines then became financial fodder for the new psych-industries. With the causes suppressed, a new industry was born.

1925 Danish researcher Thorvald Madsen tries a modified Pertussis vaccine during an epidemic in the Faroc Islands. It did not prevent Pertussis. (See 1933).

1925 General vaccine programs against tuberculosis began in the United States.

1927 British government appoints a committee to inquire into ‘vaccine lymph’, as it is noticed that the ‘glycerinated calf lymph’ used in vaccinations causes deaths from ‘sleepy sickness’. Two London professors bring notice of the problem to the government in 1922. It takes 5 years before the government responds.

April, 1930 Eli Lilly, makers of thimerisol, inject the product into 22 people with meningitis who all die. Lilly publishes the “study”, claiming that thimerisol, 50% mercury by weight, is safe.

1930 Max Theiler develops a yellow fever vaccine.

1931 Roosevelt endorses polio ‘immune serum’, precursor to vaccines in 1950’s.

1932 Diptheria vaccines injure 171 and kill 1 in Charolles, France.

1933 Danish researcher Thorvald Madsen discovers the Pertussis vaccines ability to kill infants without warning (SID). He reports that two babies vaccinated immediately after birth died in a few minutes.

1933 American researchers report that children react to Pertussis vaccine with fever, convulsions and collapse.

1936 Pertussis vaccine introduced in the United States. Autism begins to appear in children shortly thereafter.

1936 Diptheria vaccine injures 75 in France.

1943 American vaccine researcher Pearl Kendrick reports that adding a metallic salt seemed to heighten the capacity of the Pertussis vaccine to produce anti-bodies. (Metal salt is an ‘adjuvant’ in this way). Some metallic salts used are those of aluminum (alum). Pearl Kendrick is the researcher that urged that Pertussis vaccine be combined with Diptheria vaccine. Later the Tetanus vaccine was added, producing the nefarious DPT Vaccine.

1943 General vaccine program against influenza begins in the US.

1944 Health Practitioners Journal, June 1944, reports Dr. S.S. Goldwater, the New York Commissioner of Hospitals states ‘as a result of the drugs, vaccines and other suppressive treatments used to check diseases, chronic diseases are growing at such a rate that America may become a nation of invalids.’

1945 Japan surrenders twice, followed by US bombing of Hiroshima/Nagasaki and a third and final surrender. The Allies mandate compulsory vaccination in Japan. The first cases of autism follow pertussis vaccine introduction.

1946 US Government Pertussis vaccine expert Margaret Pittman and FDA’s Charles Kendrick decide to test Pertussis vaccine by injecting it into the brains of mice and see how many survive.

1946 Werne and Garrow describe the deaths of identical twins within 24 hours of their second Pertussis shot.

1947 Matthew Brody at the Brooklyn Hospital gives detailed descriptions of two cases of brain damage leading to death in children receiving Pertussis shots.

1947 Charles Posner of the Harvard Medical School Department of Neurology writes, ‘almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system. The common denominator consists of vasculopathy that is often associated with demyelination.’ (demyelination is the stripping of the insulation away from the nerves).

1947 The British Medical Research Council begins testing 50,000 children in Britain with the Pertussis vaccine. All children tested are more than 14 months old (not newborns). Eight infants had convulsions within 72 hours of the shot, 34 had convulsions within 28 days of the shot. British doctors denied a connection between the vaccine and the convulsions, declaring the tests a success and began administering it to all British children.

Despite the fact that none of the tests were conducted on children under 14 months old (newborns & babies), the United States holds the tests in evidence that the vaccine is safe for newborns as young as 6 weeks of age. The testing would continue until 1957.

1948 Randolph K. Byers and Frederick C. Moll of the Harvard Medical School publish an article describing children who had suffered brain damage after receiving Pertussis vaccine. The findings provided the first clear evidence that the vaccine caused the serious neurological complications in children.

1948 Randolph Byes and Frederick Moll of Harvard Medical School validate that severe neurological disorders follow the administration of DPT vaccine. The research was performed at Children’s Hospital in Boston and published in Pediatrics magazine. Nothing was done by physicians to halt the use of DPT vaccine.

1948 A study on Pertussis vaccine reaction is done by Randolph K. Byers and Frederick C. Moll of the Harvard Medical School. They examine 15 children who had reacted violently within 72 hours of a Pertussis vaccination. All the children were normal before the shot. None had ever had a convulsion before. One of the children became blind, deaf, spastic and helpless after being given the Pertussis shot. Out of the 15 children, 2 died and 9 suffered from damage to their nervous system. Physicians were displeased by these results.

1948 England bans smallpox vaccine.

1948 North Carolina polio cases number 2,498. See 1949.

1948 Louis Sauer makes an interesting observation at an AMA meeting where Pertussis vaccination was discussed. Louis Sauer points out that ‘the neurological damage caused by Pertussis vaccine is the same as the damage caused by Pertussis (whooping cough–Which is logical, because they use the bacteria in the vaccine). According to Sauer, ‘a customary prophylactic dose of Pertussis vaccine seems to illicit a chain of nervous system reactions and in some cases irreversible pathological changes in the brain. These findings resemble those encountered in cases of severe whooping cough (Pertussis).’ In other words, the vaccine is causing the disease condition.

1949 US Public Health Service Division of Biologics Standards establish a national potency test for Pertussis vaccine, and modify it in 1953 to establish potency limits. Despite this, the Pertussis vaccine that is pronounced ‘safe’ still causes minimal brain damage (MBD) in humans.

1951 Theiler wins Nobel for work on yellow fever vaccine.

1952 Formulation of the polio vaccine begins. Tens of millions of doses of polio vaccines produced from virus grown in monkey cells infected with SV-40 (Simian Virus #40). Scientists ‘perform experiments in laboratories to determine the correct doses of antigen and supplementary chemicals to use in the polio
vaccine. (Ironically, since the scientific premise of vaccination is faulty, a ‘correct dose of antigen and chemicals’ does not exist).

1953 At the University of Zurich, Dr. S.Kong of the Pediatric Clinic compiles a list of 82 cases of Pertussis vaccine damage from world literature.

1953 The Swedish conduct a study on the Pertussis vaccine. Anna L. Annell, a Swedish researcher, writes a major work on Pertussis which indicates that ‘pertussis vaccine may be associated with the most varying kinds of cerebral complications which may be cortical, subcortical or peripheral.’

Encephalitis after vaccination is known to produce the same range of disabilities and impairment. Annel also wrote, ‘during the past few decades certain of the epidemic children’s disease, measles in particular, have shown an increased tendency to attack the central nervous system. After the 1920’s a large number of cases involving CNS damage were reported.

1954 Salk vaccine begins to be given to school children in Philadelphia.

1954 Parke-Davis pharmaceutical company combines the DPT shot with Polio vaccine. The new combination of four vaccines is called Quadrigen. (See 1959).

1954 Reward of $30,000 offered to anyone who proves polio vaccine not a fraud. Not one person was able to claim the reward.

1954 Mrs. Oveta Culp Hobby, Secretary of Health, Education and Welfare, allows a press photo to be taken during a ceremony declaring Salk vaccine safe.

1954 Polio rate caused by the vaccine accelerates ten-fold in Massachusetts.

1954 Eli Lilly company begins renovation of a five-story building in Indianapolis in July 1954 for the production of Salk vaccine. It is in full production by October of

1954. Wyeth, Parke-Davis and others follow suit.

1954 A study on ‘neurologic sequelae of prophylactic innoculation’ summarized state-of-the-art knowledge in noting that the common factor in the pathology of encephalitis from vaccination is ‘anaphlactic hypersensitivity’.

1955 Georgia State public health officers meet in Atlanta (May 1955) to discuss what was going wrong with the Salk vaccine program. A U.S. Public Health scientist at the meeting told the group that ‘he was not permitted to disclose what had happened because it would jeopardize the investment of the pharmaceutical firms in the vaccine program.’

1955 Measles death rate has naturally declined, without vaccines, to .03 per 100,000 by 1955.

1955 At the University of Illinois School of Medicine, Department of Neurology, Niels Low shows that the EEG of infants is sometimes altered by a DPT shot,concluding that significant cerebral reactions and neurological changes occur.

1955 American Cancer Society advertising circular states ‘cancer will strike one of every four persons now living. More children from 3 to 15 years of age die of cancer than from any other disease.’ (50 years before, cancer was unheard of in children). According to the ACS, they are predicting 6.4 million deaths from cancer, compared with 128,000 in 1933–an increase of 6.2 million cases in 22 years. Vaccination, pesticide use and chemical pollution are the main factors that have increased since 1933.

1955 Despite the sky rocketing cases of vaccine-induced polio, the AMA, NFIP and USPHS claim a reduction of 40-50%.

1955 Idaho brings its Salk vaccination program to a halt on July 1, 1955.

Utah does the same on July 12, 1955.

1955 Boston Herald newspaper reports on April 18, 1955, features an article entitled ‘Drug Companies Expecting Big Profit on Salk Vaccine’, which stated. ‘A spokesman for Parke-Davis, which made 50% of the Salk vaccine, said ‘now that it has been declared safe, we can get back the millions we invested in the development of the Salk vaccine and make a profit out of it. Our company will made over $10 million on Salk vaccine in 1955.’

1955 Rhodes and Company, Wall Street brokers specializing in drug securities, estimate that the gross revenue of the six vaccine houses licensed to produce and sell Salk vaccine would be about $60 million, with profits of $20 million.

1955 The CIA conducts a biological warfare experiment in the Tampa Bay area in Florida with agents withdrawn from an Army CBW center. A sharp rise in whooping cough (Pertussis) cases occurs, including 12 deaths, following the test.

1955 Washington Bureau of the Detroit Free Press reports, on June 3, 1955, that ‘The USPHS reported that more children who received Salk shots made by the Wyeth Labs suffered polio more than could normally be expected;’

1955 AMA Conference in Atlantic City, New Jersey. Article by James C. Spaulding who covered the conference was published in the AMA Journal, June 19,

1955, ‘A policy of secrecy and deception has been followed by the National Foundation for Infantile Paralysis and the US Public Health Service in the polio vaccine programs. The nation’s physicians were prevented from learning vital information about the trouble with Salk vaccine. The US Public Health Service had an advisory group made up almost entirely of scientists who were receiving money from the National Foundation of Infantile Paralysis, which was exerting pressure to go ahead with the program even after Salk vaccine was found to be dangerous.’ Spaulding further said, ‘the Infantile Paralysis Foundation kept secret the fact that live virus was detected in four out of six supposedly ‘finished and safe’ lots of vaccine.’

1955 Salk Polio Vaccine again used in the US. Cases of polio skyrocket again in the United States.

1955 Reported that doctors on the staff of the National Institutes for Health are avoiding vaccination of their children with the Salk vaccine, and that after experimenting with 1200 monkeys, they declared the Salk vaccine worthless as a preventative and a danger to take.

1955 First vaccinated generation become adolescents.

1955 Massachusetts reports 642% increase in polio since vaccinations began in 1954 with vaccination of 130,000 children. In response, the National Foundation for Infantile Paralysis states that the increase in cases was due to the fact that ‘no children were vaccinated there.’

1955 Massachusetts bans the sale of Salk vaccine.’

1955 Dr. Graham W. Wilson, director of Britain’s Public Health Laboratory Service, who knew about the NIH Salk vaccine trials, says ‘I do not see how any vaccine prepared by Salk’s method can be guaranteed safe.’

1955 US Surgeon General Scheele admits in a closed session of the AMA that ‘Salk polio vaccine is hard to make and no batch can be proven safe before given to children’. Despite this fact, the public is told that the vaccine is safe. The government announces that it has the intention to vaccinate 57 million people before August 1955.

1955 Surgeon General Scheele (who never practiced medicine a day in his life!) goes on public radio saying ‘I have complete confidence in the Salk vaccine. I urge doctors to continue vaccinations.’

1956 Seventeen states in the United States reject their government-supplied Salk polio vaccine.

1956 US government appropriates $53.6 million to ‘aid states in providing free vaccine to people under 20 years of age’.

1956 Idaho health director Peterson states that polio only struck vaccinated children in areas where there had been no cases of polio since the preceding autumn. In 90% of the cases, the paralysis occurred in the arm in which the vaccine had been injected.

1956 American Public Health Service announces 168 cases of polio and 6 deaths among those vaccinated. Censorship is then imposed on the reporting of reactions to Salk vaccine.

1956 Oral polio vaccine developed further by Sabin.

1956 The US Public Health Service and the National Foundation for Infantile Paralysis (Rockefeller) put on a drive to ‘sell’ Salk polio vaccine to the public.

1957 Governor Knight of California asks the legislature for $3 million in order to insure vaccination for all those under 40 years old with Salk polio vaccine. The newspapers report that corporate profits from the Salk vaccine will be in excess of $5 billion. (Feb 6, 1957). Governor Knight notes there are 4 million Californians under 40 and signs the bill.

1957 Pertussis vaccination programs exist in all industrialized nations, with the US leading the way. The vaccine is promoted as ‘risk free’.

1957 Scientists isolate a series of Simian (monkey) viruses and discover that these same viruses contaminate polio vaccines. SV-40 found in both Sabin and Salk polio vaccines. (made since early ’50s), Information not made public. The same vaccines continued to be used until the early 1960’s.

1958 World literature now contains 107 cases of severe reaction to Pertussis vaccine (93 of those cases were in the US). At the Fountain Hospital in London, Dr. J.M. Berg analyzed the 107 cases and found that 31 of them showed signs of permanent brain damage. Berg calls attention to the danger of mental retardation as an effect of the Pertussis vaccine and emphasizes that ‘any suggestion of a neurological reaction to a Pertussis vaccination should be an absolute contraindication to further inoculation.’ The United States medical establishment ignores and suppresses the data. American physicians maintain that the damage caused is small compared to ‘lack of ‘serious’ reactions in children vaccinated.’ No data has ever been found to justify a basis for this conclusion.

1958 Verdict of $147,000 rendered against Cutter Laboratories in California for the crippling of two children with the Salk polio vaccine. Cutter Labs was the only vaccine manufacturer not part of the Rockefeller Trust.

1959 The United States never conducts its own clinical trials on Pertussis vaccine, but instead relies (as it still does today) on data collected by Britain’s Medical Research Council in clinical trials in England in the 1950’s for ‘proof of vaccine safety and effectiveness in newborns and children.’ Interestingly, Britain’s trials on 50,000 British children were performed on children more than 14 months old. None of the children were newborns.

1959 National Institutes of Health (NIH) approves licensing of Quadrigen vaccine for children, containing Pertussis, Diptheria, Tetanus and Polio vaccines. The new combination vaccine was found to be highly reactive and was withdrawn from the market in 1968 after parents started filing lawsuits against Parke- Davis for vaccine damaged children.

1959 Pertussis vaccine found to have allergenic effect on animals.

1960 British Medical Journal publishes an article by Swedish vaccine researcher Justus Strom, who stated that the neurological complications from the disease Pertussis are less than that in the Pertussis vaccine. Strom also pointed out that ‘whooping cough (Pertussis) had changed and had become a milder disease, making it questionable whether universal vaccination against it is justified.’

1960 General vaccination program for measles begins in the United States.

1960 It is estimated in 1960 that over 1,000,000 children have vaccine-caused disabilities, including learning difficulties and school behavioral problems, behavioral disturbances, allergies, speech difficulties, visual problems, and problems in adjustment and coping.

1961 A senior school medical officer in Northern England, J.M. Hooper, finds that parents are beginning to refuse to bring children for a Pertussis booster shot, based on earlier violent reaction to the ‘vaccination.’ Children were suffering from collapse, vomiting, and uncontrollable screaming. No one paid attention to these warnings.

1961 Sabin polio vaccine immunization campaign.

1963 American researcher John F. Enders creates a measles vaccine. Mass inoculations begin.

1963 Children vaccinated with killed measles vaccine between 1963 and 1967 develop Atypical Measles Syndrome (AMS). Studies suggest the children’s response to the ‘wild’ measles virus is ‘altered’ and that the severity and persistence of symptoms suggests encephalopathy (brain damage.) See 1967.

1964 Reward of $30,000 offered to prove polio vaccine was not fraud. No takers.

1965 US Government’s leading Pertussis vaccine specialist, Margaret Pittman, (until 1971) states, ‘Bordetella Pertussis is unique among infectious bacteria in its marked ability to modify biological processes.’

1965 Congress passes the Immunization Assistance Act. More states made their vaccination programs mandatory/obligatory.

1967 The FDA stops the use of an experimental cancer vaccine which was producing significant results. Developed by James Rand and Eernest Ayre, a recognized cancer specialist. The Rand vaccine produced significant improvement in terminal patients in over 30% of patients. It cured tumors and breast cancer in four to six months, without radiation, surgery or chemotherapy. The FDA Commissioner was James L. Goddard, the same man who persecuted the use of DMSO. Goddard used the DMSO issue in 1966 in an attempt to foster a medical dictatorship in the US in collusion with the medical and pharmaceutical industries, and remove viable treatments from public access.

1967 At the Bland-Sutton Institute of Middlesex Hospital in London, George Dick writes, ‘it has been long known that increasing the number of Pertussis bacteria per dose of vaccine increases the frequency of reactions. It would be surprising if decreasing the size of the infants receiving a particular vaccine did not also increase the reactions.’ A violation of a standard axiom in medicine, which matches the size and weight to an amount of substance. (Why are newborns getting the same dosage as an adult?).

1967 Dr. Vicent Fulginiti, M.D., former chairman of the American Academy of Pediatrics Committee on Infectious Diseases, asserts that inactivated measles vaccine should no longer be administered. See 1963.

1967 Killed measles vaccine is discontinued in the United States.

1967 General vaccination program for Mumps begins in the United States.

1967 Science magazine (10/20/67) features article on Joshua Lederberg of the Department of Genetics, Stanford University School of Medicine. Lederberg notifies the scientific world that ‘live viruses (as in vaccines) are genetic messages used for the purpose of programming human cells’ and ‘we already practice biological engineering on a rather large scale by use of live viruses in mass immunization campaigns’

1970 Due to the increasingly mild nature of whooping cough (Pertussis), infant deaths cease from naturally acquired Pertussis in Sweden. Deaths associated with vaccine continue. Sweden stops Pertussis vaccination in 1970.

1970 A study by Pittman reveals Pertussis vaccine can induce hypoglycemia due to increased production of insulin. (Ref: DPT shots). Study is corroborated in 1978 by Hannick and Cohen and by Hennessen and Quast in West Germany. Result: Pertussis and DPT vaccines can cause diabetes.

1972 British Journal of Psychiatry #120 reveals that ‘psychotic disorders may be caused by viral infections.’ (Ref: viruses induced by vaccines).

1972 WHO begins its “Special Programme” in human reproduction with programs for both male fertility control through vaccines and female fertility control.

1972 the World Health Organization (WHO) Bulletin No.47 refers to creation of an immune virus and suggests that a useful way to study the effects would be “to put it into a vaccination program and observe the results.” It is theorized that WHO used the smallpox vaccination program in Central Africa for this study, since the spread of HIV infection coincides precisely with the most intense and recent smallpox vaccination campaigns. Information on the Central African countries most infected with HIV precisely matches WHO figures indicating the number of people vaccinated in these areas. The virus requested would selectively destroy the T-cell system. (1972 Federation Proceedings of WHO).

1973 The field of genetic engineering is opened by advances in scientific research, making way for creation of recombinant micro-organisms and new viral structures in the laboratory. The U.S. military applies the technology to its chemical and biological weapons program, claiming overtly that such work is ‘to develop defensive vaccines’.

1974 British researcher George Disk estimates that there are 80 cases of severe neurological complications from Pertussis vaccine annually. Over 33% of these children died and another 33% were left with brain damage. Dick maintains he is not convinced that the community benefit from the vaccine outweighs the damage.

1974 The Association of Parents of Vaccine Damaged Children is formed in Britain, & pressures the government to study adverse reactions to Pertussis vaccine.

1974 Henry Kissenger writes a classified “National Security Study Memorandium 2000: Implications of worldwide population growth for U.S. security and overseas interest (NSSM 200)” which identifies India, Bangladesh, Pakistan, Nigeria, Mexico, Indonesia, Brazil, the Philippines, thailand, Egypt, Turkey, Ethiopia and Columbia as targets for initial population reduction. The Philippine Supreme Court found that 3 million Philippians between 12 and 45 years of age were given this vaccine. Native American Woman and Black women in the US received this vaccine. Sterility rates in Native American Women in the US is over 35%. Sterility rates in Black Women in the US is over 25%.

1975 Federal Drug Administration Bureau of Biologics concludes that Diphtheria toxoid (vaccine) is ‘not as effective an immunizing agent as might be anticipated.’ They admit that Diphtheria may occur in vaccinated people, and note that ‘the permanence of immunity induced by the toxoid is open to question.’

1975 Japan stops using Pertussis vaccine following publicity about vaccine-related deaths.

1976 FDA Pertussis vaccine specialist Charles Manclark comments ‘Pertussis vaccine is one of the most troublesome products to produce and assay. It has one of the highest failure rates of all products submitted to the Bureau of Biologics for testing and release. Approximately 15-20% of all lots which pass manufacturer tests fail to pass the tests of the Bureau.’

1976 According to a letter from the British Association for Parents of Vaccine Damaged Children, published in the British Medical Journal of February 1976, ‘two years ago we started to collect details from parents of serious reactions suffered by their children to immunizations of all kinds. In 65% of the cases referred to us, reactions followed ‘triple’ vaccinations. The children in this group total 182 to date. All are severely brain damaged, some are paralyzed, and 5 have died during the past 18 months. Approximately 60% of reactions (major convulsions, collapse, screaming) happened within 3 days and all within 12 days.

1976 Dr. Jonas Salk, creator of the polio vaccine, says that analysis indicates that the live virus vaccine in use since the 1960’s is the principle, if not sole cause of all polio cases since 1961.

1976 More than 500 people receiving flu vaccinations become paralyzed with Guilain-Barre Syndrome.

December 1976 No epidemic of Swine flu surfaces despite rapid approval and response to perceived threat following 1 death of a solder at Ft. Dix, NJ. Swine Flu inoculation program shut down after risk of death and polio like syndrome from the vaccination is found to be almost 12 times greater in vaccinated than un-vaccinated people. 5% of people afflicted die, 10% are crippled or maimed for life.


1977 A Blue Ribbon Panel is convened to investigate the reason for the drop in the general IQ of the United States. Seventy-nine theories were advanced, but none of them satisfactorily explained the drop in mental capacity of the US population. The idea that vaccines could be part of the problem was not brought up. Y.L. Warten, 1977. (The Prussian education system is also part of the problem, for those volkschuelen).

1977 The British government is pressured by the publicity following the new data about Pertussis and DPT vaccinations.

1977 The University of Glasgow in Scotland, Department of Community Medicine, Dr. Gordon Stuart, publishes a study analyzing 160 cases of adverse reaction and neurotoxicity following DPT vaccination. In 65 of those cases, reactions to DPT shots included convulsions, hyperactivity and severe mental defect. In a stern statement, Stuart says, ‘it seems likely that most adverse reactions are unreported and/or overlooked.’

1977 The British government conducts the National Childhood Encephalopathy Study (NCES) which tests the connection between vaccinations and neurological disease.

1977 (Mar) Jonas and Darrell Salk warn live virus vaccines produce same disease.

1978 According to Charlotte Parker of the University of Texas Department of Microbiology, the nature of the organism Bordetella Pertussis means that different lots of vaccine made from the same strains sometimes show different properties.

1978 In the United States, the FDA finances and conducts a study at UCLA from January 1, 1978 to December 15, 1979 called ‘Pertussis Vaccine Project: Rates, Nature and Etiology of Adverse Reactions Associated with DPT Vaccine’. The results of the study were published in Pediatrics in November.

1978 In England, Griffith studies pertussis vaccine reactions in children, noting a case in which a boy experiences brain damage 3 days after vaccination and dies 27 days later due to injection of triple vaccine.

1981 The unpublished contractors ‘Final Report’ was submitted to the FDA on March 18, 1980 (a year earlier) and contained revealing data. The study found a higher incidence of adverse reactions to the DPT shot than any previously reported in literature. After the study had run nine months, the FDA convened a Pertussis Symposium, at which it was revealed that ‘the most striking finding in this preliminary analysis is the high frequency of persistent crying, episodes of convulsions and collapse following DPT immunization.’ Because of these findings, the study was curtailed from the planned examination of 50,000 vaccinations to only 17,000. The UCLA FDA study also found that systemic reactions in the central nervous system were present in 50% of the vaccinations. Because of this potentially damaging information, the FDA placed an arbitrary time limit of 48 hours within which reactions had to occur, despite ongoing data which indicates that serious reactions occur after that time limit, in order to limit the statistical data and conceal the extent of the problem from the population. (See 1981).

1985 WHO Vaccines for smallpox and tetanus are laced with female reproductive hormones to induce permanent sterility to “eliminate 150 million excess Sub-Saharan Africans” according to WHO documents.

May 1987 the Times of London reported on its front page that smallpox vaccine administered by the World Health organization had triggered HIV/AIDS. 100 Million vaccinated Africans are at risk. Areas with highest vaccination rate show highest HIV/AIDS rates. Robert Gallo, discoverer of the HIV/AIDS virus, defends those figures and says, “AIDS researchers will keep their mouths shut because they are paid to do so.”

In 1988, an FDA-sponsored follow-up study of the ’18’ children with neurological reactions concluded ‘no significant neurological impairment.’

A 1988 re-examination of those same children by an independent researcher, pediatric neurologist Ronald Gabriel, not associated with the FDA, proved that the FDA lied–only 4 of the 18 were normal. The results were presented at a May 1980 meeting of the Institute of Medicine. Results indicate that encephalopathy is followed by subtle learning, behavioral and neurological problems. (Note: See the book Vaccination, Social Violence and Criminality: the Medical Assault on the American Brain, by Harris Coulter,1990. The FDA is continuously involved in criminal conspiracy and racketeering along with pharmaceutical and chemical companies in the United States.)

1978 Trials of Hepatitis B vaccine in New York City on non-monogamous males between 20 and 40 years old. Homosexuals receive a different vaccine.

1979 Two pediatricians in California report brain swelling associated with DPT vaccine administration.

1979 New rubella vaccine introduced. See 1988.

1979 The US Food and Drug Administration (FDA) funds a study which represents the first significant ‘attempt’ to evaluate reactions to the DPT shot. The study is conducted at the University of California (UCLA) and was published in Pediatrics in

1981. After studying 16,000 DPT and DT vaccination cases, they concluded that the Pertussis (P) element of the DPT shot was the element causing reactions. They also found that the incidence of all DPT reactions was much higher in the population than had been suspected or reported in the scientific literature. Despite these results, even in 1994 physicians promote Pertussis vaccine with confidence, pay little attention to identification of high risk children, and do not carefully observe contraindications. Parents are legally required to vaccinate their children with Pertussis before entering them in school. (See 1982)
1980 Estimated 2 million American children with vaccine-caused disabilities.

1981 At the headquarters of the Occupational Safety and Health Administration (OSHA), the director of the OSHA office of carcinogenic identification, Dr. Peter Infante, pointed out that a Current Intelligence Bulletin (CIB) on formaldehyde was ‘an important document assessing formaldehyde’s cancer causing potential’. The top bureaucracy at OSHA were embarrassed at the release of the truth, and tried to dismiss Infante. On July 27th, Infante writes Dr. John Higginson, director of the International Agency for Research on Cancer (IARC), disagreeing with the IARC decision to conceal the carcinogenic nature of the substance. Formaldehyde is a common component of vaccines.

1981 Britain conducts the National Childhood Encephalopathy Study, and finds that there exists a significant correlation between serious neurological illness and Pertussis vaccination occurring within 7 days of the shot. In the US, the FDA limits statistical data to 48 hours in order to conceal damaging data and eliminate data on deaths and damage occurring after that period of time.

1981 Japan begins use of a new childhood Pertussis vaccine, recommended to be given as 4th and 5th dose. US vaccine used for 1st,2nd,3rd doses. 1981 In Britain, Dr. D.L. Miller reports to the NCES on an analysis of the first 1,000 cases of neurological illness. He reported ‘a significant association was shown between serious neurological illness and Pertussis (also DPT) vaccine.’

1981 New England Journal of Medicine (11/26/81) publishes a study showing that tetanus vaccines cause T-cell ratios to drop below normal, with the greatest decrease after two weeks. The altered ratios were found to be similar to those found in AIDS victims.

1982 A reporter at WRC-TV in Washington, DC breaks a story on Pertussis vaccine reactions in the documentary ‘DPT: Vaccine Roulette’, which generally informs the American public that their children are at risk from Pertussis vaccinations. (See 1988)

1982 Homosexuals in Chicago, St. Louis, Denver, Los Angeles and San Francisco get Hepatitis B vaccine.

1983 Bellman, Ross and Miller publish a study of 269 cases of infantile spasms which returns to the establishment position that ‘DPT vaccines do not cause infantile spasms, but may trigger their onset in those children in whom the disorder is ‘destined to develop’. (Note: Using this logic, if one can)

1983 Stanford University Study on Pertussis Vaccine. Lawrence Steinman and colleagues at Stanford University School of Medicine perform a study which reveals that children with allergies may overreact to Pertussis vaccine.

1984 – The 1984 Connaught Laboratory package insert for DPT vaccine cites a 1978 Scandinavian study linking the vaccine to the development of hemolytic anemia and warns that this is a contraindication. By 1991, they would remove this warning from their package inserts in order to conceal this data. This kind of anemia is typified by weakness and periodic loss of consciousness.

1984 A complaint was filed by a group of US physicians with the UN Center for Human Rights in Geneva, entitled ‘A Complaint Against Medical Tyranny As Practiced in the United States of America: American Medical Genocide’; the existence of the report was suppressed by the Bush Administration and the media. Reprinted in The Leading Edge in Oct/Nov 1994.

1984 Shaywitz Study at Yale Medical School Pediatrics revealed that ‘minimal brain damage is perhaps the most common and time-consuming problem in current pediatric practice.’

1984 Wyeth Laboratories package insert for DPT vaccine states, ‘The occurrence of Sudden Infant Death Syndrome (SIDS) has been reported following administration of DTP vaccine’ and that ‘approximately 85% of SIDS cases occur in the period 1 through 6 months of age, with the peak incidence at age 2 to 4 months.’

Two years later in 1986, the Wyeth insert stated, ‘SIDS has occurred in infants following administration of DPT’ but went on to state that ‘one study showed that there was no causal connection’. (Note: One wonders who paid for and did that specific study.)

1984 CDC acknowledges that 60% of those receiving hepatitis vaccine are HIV +.

1985 Tests developed to detect simian viruses in vaccines.

1985 The Assistant Secretary of Health, Edward Brandt, Jr., M.D, testifies before a Senate Committee, ‘every year 35,000 children suffer neurological complications because of DPT vaccine.’ (May 3, 1985).

1985 Hemophilus Influenza type B (HIB) vaccine approved for general use in US. The HIB vaccine is often referred to as the ‘meningitis’ vaccine, but meningitis has several causes.

1986 150 lawsuits pending against DPT vaccine makers.

1986 National Childhood Vaccine Injury Act. Administered by the US Claims Court in Washington, DC, which does recognize an association between the DPT shot and infantile spasms. The court awarded $2 million to a body in 1989 relative to a reaction to DPT vaccine.

1986 National Health Survey finds that between 1969 and 1981, the prevalence of ‘activity-limiting chronic conditions’ in children increased by 44%, from 2.9 million children to 3.8 million children. Almost all of the increase happened between 1969 and 1975. Most of these conditions are readily associated with post-encephalitic syndrome. Childhood respiratory disease during this period increased 47%, childhood asthma increased 65% (with deaths from asthma increasing), mental and nervous system disorders increased 80%, personality and other non-psychotic disorders (behavior disorders, drug abuse and hyperactivity) increased 300%, diseases of the eyes and ears (especially otitis media) rose 120%, and cases of hearing loss in the ears rose 129%. All of these increases were identical in both high and low income groups. For the same period of time, levels of disease not associated with vaccine damage remained unchanged.

1986 Connaught Laboratory, manufacturer of DPT vaccine, changes the product info sheet to warn against ‘allergies’ and ‘anaphylactic sensitivity’.

1986 Connaught Laboratories package insert for their DPT vaccine reads ‘some data suggests that fever is more likely to happen in those who have had local reactions, and that local reactions are more likely to occur with increasing numbers of doses of DPT.’

1987 Centers for Disease Control (CDC) releases a study indicating that the Hib vaccine shows an efficacy (effectiveness) rate of 41%. Children were found to be 5 times more likely to contract the disease than those not vaccinated.

1987 66 Japanese victims of Pertussis vaccine receive huge damage awards from the Japanese government.

1988 Lederle Laboratories package insert for DPT vaccine reads ‘Pertussis vaccine has been associated with a greater proportion of adverse reactions than many other childhood vaccinations. Local reactions are common after administration of DTP, occurring in 35-50% of recipients. Febrile [feverish] reactions are more likely to occur in those who have experienced such responses after prior doses.’

1988 Two scientific studies find that new rubella vaccine introduced in 1979 was found to be the cause of Chronic Fatigue Syndrome (Epstein-Barr virus), an immune disorder first reported in 1982.

1988 Robert S. Mendelsohn M.D, publishes material indicating that Dr. John Seal of the National Institute of Allergy and Infectious Disease believes that ‘any and all flu vaccines are capable of causing Guillain-Barre.’

1988 New ‘conjugated’ [joined together] Hib vaccine approved for use in children at least 18 months old in the United States. Hib = Hemophilus Influenza Type B.

July, 1989 after years of denial, a scientific paper demonstrates conclusively that WHO tetanus vaccines used in the Philippines contained female reproductive hormones, inducing permanent sterility without consent or knowledge of the women treated.
Tetanus toxoid is linked to the human reproductive hormone to overcome immunological tolerance to the hormone and prod the body of the woman into producing antibodies to her own reproductive hormones.

1990 Health Consciousness magazine features article entitled ‘Live Virus Vaccines and Genetic Mutation’ by H.E.Buttram, M.D, in which it is determined that ‘the physical invasion of the human body by foreign genetic material may have the immediate effect of permanently weakening the immune system, setting in motion a new era of autoimmune diseases.’

1990 The US Public Health Service Immunization Practices Advisory Committee (ACIP) and the American Academy of Pediatrics considers high-pitched screaming after a Pertussis (DPT) vaccination an absolute contraindication to further Pertussis vaccine.

1990 Pediatric neurologist Dr. John H. Menkes, professor emeritus at UCLA, reports on 46 children experiencing neurological adverse reaction within 72 hours of a DPT shot. Over 87% of the children reacted with a seizure, 2 children died and most surviving children became retarded, with 72% having uncontrollable seizure disorders. Menkes conclude, ‘Pertussis vaccine encephalopathy (brain damage) is not a myth but rather a serious complication of immunization.’

1990 U.S. Claims Court, as of October 31, 1990, indicates that ‘several thousand claims for compensation from injuries or death caused by vaccines have already been filed.’ National Vaccine Information Center.

1990 Estimated 3 million in US with vaccine-caused disabilities.

1990 In December of 1990, a federal regulation was adopted permitting the FDA to circumvent US and International laws forbidding medical experimentation on unwilling subjects. This regulation permits the FDA to inject American military with unapproved experimental drugs or vaccines without informed consent. The FDA merely needs to deem it ‘not feasible’ to obtain the soldiers permission. See Health Letter, Washington, DC. Public Citizens Health Research Group ‘400,000 Human Guinea Pigs in the Persian Gulf’, Feb 12, 1991. See 1991 Gulf War Entry.

June 1990, Court case reveals that babies in Los Angeles were used as human guinea pigs with a experimental measles vaccine called Edmonston Zagreb high titer measles vaccine (E-Z ). From 1989-1991, Kaiser Permanente and LA County Dep’t of Health and CDC injected 700+ “mostly minority” babies with unlicensed experimental vaccines with fraudulently-obtained parental consent. E-Z is closely associated with increased death rate in infant girls in Sendgal, Guneau Bisseau, and Haiti before their second birthday. Most of the families are not aware to date that their child was used as a human guinea pig.

1991 Operation Desert Storm. Bush stops war after 100 hours at preserve Iraq as a threat. American troops are given experimental vaccines against biological agents. Within months thousands of troops sicken with the acids that cause cancer. Disease deemed ‘Gulf War Syndrome’. Government denies responsibility. Over 8,000 troops were vaccinated with Botulism, over 150,000 troops were given anthrax vaccine, and all 500,000 troops were given Pyristigimine, an experimental nerve agent. All drugs were experimental.

1991 New York Times, Mar 17th, 1991 ‘US Vaccine Plan Uses Welfare Offices’ indicates the Federal government has considered denying welfare and nutritional benefits to families who refuse vaccinations.

1991 The US Public Health Service Advisory Committee on Immunization Practices (ACIP) drafts new guidelines which eliminate most contraindications to Pertussis vaccine. Essentially, this results in a denial or cover-up of most reactions on the grounds that ‘there is no proof the vaccine causes brain ‘ They base their position on several studies financed by vaccine manufacturers conducted in the late 1980’s by vaccine policymakers such as Dr. James Cherry and Dr. Edward Mortimer, who sit on the ACIP Committee and are also paid consultants to US Pertussis vaccine manufacturers, resulting in biased and flawed studies in order to prove ‘no cause and effect’ between the Pertussis vaccine and permanent brain damage. US vaccine policymakers are the CDC and the American Academy of Pediatrics. All this, despite decades of experience indicating the opposite conclusion. (Note: This policy constitutes criminal neglect, racketeering and conspiracy!).

1991 The ‘conjugated’ Hib vaccine introduced in 1988 is extended for use in infants as young as two months. It becomes mandated in 44 states in the US.
–The Olympian, Nov 23, 1994. Pertussis also can cause Sudden Infant Death.

1991 The CDC begins the process of mandating Hepatitis B vaccinations for all infants in the United States. Many infants receive multiple doses from birth.

1992 Lancet, Journal of the British Medical Association, reports (3/7/92) that the oral polio vaccine used in the mid 1970’s to treat recurrent herpes was contaminated with a number of potentially dangerous retroviruses, and may have seeded HIV among Americans’.

1992 Article in the Washington Post, Nov 2, ‘On Vaccinating Safely’ and Dec 14th press release by the National Vaccine Information Center indicate release by the FDA of a report acknowledging more than 17,000 adverse events– including more than 350 deaths–following vaccination, all in a 20 month period ending July 31,

1992. Reported events number far less than actual events, so number is actually larger, perhaps 170,000 or more. 1992 From 1988 to 1992, over $249 million has already been awarded due to hundreds of deaths and injuries caused by mandated vaccines. Thousands of cases are still pending. The permanent injuries from vaccines include, but are not limited to, learning disabilities, seizure disorders, mental retardation, and paralysis. Many of the awards for pertussis vaccine deaths were initially (and wrongfully) misclassified as Sudden Death Syndrome (SIDS).

1992 Centers for Disease Control (CDC) reports that 87% of all cases of polio in the United States between 1973 and 1983 were caused by the vaccine. The CDC also said that every case from 1980 to 1989 was caused by vaccine.

March 19, 1992, Dr. David Heymann, head of the office of research for the World Health Organization’s Global Programme on AIDS, and Harvard pathology professor William Haseltine refuse to discuss the possibility of AIDS transmission via vaccines. Dr. Heymann states in a phone interview from Geneva, “The origin of the AIDS virus is of no importance to science today. Any speculation on how it arose is of no importance.” Haseltine is even more adamant. “It’s distracting, it’s nonproductive, it’s confusing to the public, and I think it’s grossly misleading in terms of getting to the solution of the problem. It’s over, it’s done with, it’s very, very, very unlikely it happened that way, and it’s another nonsense article. It’s the worst kind of reporting as far as I’m concerned.”

1993 Clinton administration announces plans for a National Childhood Vaccination Program. 103rd Congress introduces S732,S733,HR1460, legislation that would attempt to vaccine all children in the United States, while severely limiting exemptions parents could claim. The bills also seek to set up a national vaccine registry to track down parents who resist.

1993 Seattle Times reports that all polio in the US is caused by vaccines. (6/10/93).

1993 The US Army directs Walter Reed Army Institute of Research to sign an agreement with MicroGeneSys in Meridan, Connecticut for a ‘large scale clinical evaluation’ of an AIDS vaccine designed to block destruction of the immune system. The VaxSyn vaccine uses a genetically engineered protein that matches a protein called (gp160) that covers the surface of the HIV virus. (Note: That the HIV virus is harmless and does not ’cause AIDS’ is known, illustrating that the military is in on the AIDS scam). See Duesberg material.

1993 WHO committees more than $356 million on “reproductive health” research. Funding for abortificant (abortion producing) vaccine comes from many sources.

1. $90+ million contributed by Sweden
2. $52+ million contributed by Great Britain
3. $41 million contributed by Norway
4. $27 million contributed by Denmark
5. $12 million contributed by Germany
6. $5.7 million contributed by US
7. $61 million contributed by UNFPA
8. $15.5 million contributed by World Bank
9. $2.5 million contributed by Rockefeller Foundation
10. $1+ million contributed by Ford Foundation
11. $716.5 thousand contributed by IDRC (International Research and Development Centre of Canada)

1994 Researchers at the Gladstone Institute of Virology and Immunology use genetic engineering to alter a Polio virus (Sabin type) to allow it to carry two key genes from the HIV virus, plus proteins from both cholera bacteria and influenza virus, in a misguided attempt to create an ‘AIDS vaccine’ by induction of immune reaction to foreign proteins. (San Francisco Chronicle 9/2/94)

1994 Sweden reports the testing of a ‘new safer Pertussis vaccine’ to combat whooping cough (what is now a relatively mild disease). According to an article in The Olympian, Olympia, Washington, it ‘could be available in the United States, according to federal health officials.’ According to the article ‘the vaccine could mean the end of rare, severe side effects associated with the Pertussis/whooping cough vaccine.’ (Note: On the contrary, the evidence proves the Pertussis organism found in Pertussis ‘vaccine’, whether bred in live tissue (‘live’ virus) or dead tissue (‘killed virus’), causes brain damage and other pathology in humans).

1889 Protégé’s of Louis Pasteur, Emile Rouz & Alexandre Yersin grew a broth thick with diphtheria bacteria and used compressed air to force the broth through a filter of unglazed porcelain.

NO bacteria or solids could pass through the porcelain – only liquid.

They then sterilized the liquid.

They took the sterilized liquid of diphtheria toxin and injected into animals.

The liquid killed the animals not the bacteria!

According to Dr. Young, this early scientific test showed that a liquid toxic acid kills, not a bacteria or fungi. The major contributors to an acidic body that leads to irritation, inflammation, induration, ulceration and degeneration are as follows:

1) Nitric, sulphuric, phosphoric and uric acids from animal proteins including eggs.

2) Lactic acids from dairy products.

3) All sugars including herbal sugars which are all acids including glucose and ethanol alcohol.

4) Vinegar which is diluted acetylaldehyde an acid that destroys brain cells.

5) All mushrooms and algae which break down dead bodies.

6) Peanuts and corn which produce exotoxins and mycotoxins.

7) All fermented foods including soy sauce.

8) Antibiotics which are mycotoxins.

9) Anti-fungals which are stronger mycotoxins.

10) All vaccinations are full of exotoxins and mycotoxins.

1994 Dr. Robert O. Young discovers the pH factor in triggering biological transformation of the red blood cells into bacteria and yeast.

1994 Dr. Robert O. Young discovers that there is only one sickness and one disease and that is the over-acidification of the blood and tissues due to an inverted way of living eating and thinking.

1994 to the present the increase of Autism is at epidemic proportions – 1 in 90 boys and 1 in 150 girls are affected. Dr. Young has suggested that this is a result of congestion of the bowels from eating animal proteins and dairy as well as vaccinations and antibiotics that destroys the root system or intestinal villi of the small intestine – the focal point where new blood is produced.

1994 to the present the increase of breast cancers is now 1 in 3 and the increase of prostate cancers in men is now 1 in 2. Dr. Young has suggested that this is a result of antibiotic and anti-fungal use, vaccination and an acidic lifestyle and diet.

March 1997 zero confirmed “H5N1” human cases exist anywhere in the word. The U.S. Armed Forces Institute of Pathology, Ft. Detrick, Rockville, Maryland, the US research center for biological weaponry, commissions Dr. Jeffery Taubenberger to lead a research team to ISOLATE the 1918 Flu Virus’ genetic code, the most lethal pathogen in history.

Aug. 24, 1997 Brevig, Alaska. Research Team member Johan Hultin sends well-preserved 1918 flu virus specimens (from a frozen body killed by the 1918 flu) to Dr. Taubenberger’s lab in Maryland.
Days later, Taubenberger detects the genetic fragments for which he has been searching. The 1918 virus’ RNA-based gene fragments are analyzed by computer sequencing in order to reveal its complete genetic code. Even with a super-computer, this code sequencing will take years to complete.

April 2000 Observer Newspaper rerports Glaxo, Pfizer, Squibb and Genentec experimented on children at Incarnation Children’s Center, NY. Incarnation Children’s Center is run by Columbia University which was paid to experiment on children, mostly wards of the state minority children. Babies as young as 6 months were injected with double doses of experimental measles vaccine.
Children as young as 4 were given multi-drug cocktails. More than 100 orphans and babies were used in 36 experiments.

November 28, 2002, a rider tacked onto the end of the Homeland Security Bill confers immunity from liability prosecution on Eli Lilly and other manufacturers of vaccines.

October, 2003 Taubenberger’s team finally deciphers the deadly 1918 flu virus’ entire genetic code – completing a 6 year project. Taubenberger’s colleague, R.G. Webster, publishes article in American Scientist Magazine declaring: “The world is teetering on the edge of a flu pandemic that could kill a large fraction of the human population”.

October, 2004 Dmtry Lvov, head of the Russian Virology Institute declares that up to one billion people around the world could die during the next pandemic.

June, 2005 at Mount Sinai School of Medicine in New York (alleged to be Rockefeller controlled), Taubenberger,Peter Palese and Adolfo Garcia-Sastro create plasmids, or DNA rings, from the 1918 killer virus, permanently “stabilizing” its genetic material for use as a biological weapon. This is the final step in revitalizing the deadly pathogen but the press is told tit will only to be used as a “vaccination tool” – even though the disease is currently non-existent.

August, 2005 Taugenberger’s team inserts plasmids into human kidney cells which then transfers human DNA into the virus making it “human specific.” The 1918 virus, responsible for the death of millions around the world is now ready for use by humans

Sept. 9, 2005 the UN in New York City issues a world-wide press release introducing David Nabarro as the “UN System Senior Coordinator for Avian, Human Influenza”.

Sept. 29, 2005 Nabarro issues an “Official U.N. Warning” that “an outbreak of ‘avian influenza’ would kill between 5 million and 150 million people on each continent.”

Oct. 2005 Pres. Bush’s newly appointed secretary of Health and Human Services (HHS, the parent organization of both the CDC and the FDA), former Utah Governor Mike O. Leavitt, intensifies multi-billion Pandemic Bird Flu preparations.

Dec. 2005 Bush solicits Congress for $7.1 Billion to fund “preparations” — $3.3 billion is immediately allocated to Leavitt’s HHS.

January 24, 2006 the Department of Homeland Security awards KBR, a Halliburton subsidiary, a $385 million contract for US detention centers.

Jan. 2006 Leavitt launches website – http://www.pandemicflu.gov – on which he says: “Let me be clear. It is only a matter of time before we discover H5N1 in America. The migration patterns of the wild fowl that carry the virus makes it appearance here almost inevitable!” China hosts the “International Pledging Conference on Avian and Human Influenza” in Beijing and is promised massive sums of money from the west — Leavitt alone commits $334 million in funds to aid China’s research into “vaccine development.” Leavitt has a long history of fostering Chinese trade activities as Utah’s Governor.

March 2006 breaking new ground, Leavitt’s HHS allocates funds to a private television network to produce a “made-for-TV” movie about the “bird flu.” Leavitt jokes that he wants “the handsomest actor” to play his character. Leavitt declares on HHS website (exactly as John D. Rockefeller declared in 1916): “The best defense against influenza is VACCINATION.” Leavitt further declares: “The current U.S. capacity for manufacturing egg-based vaccines is not sufficient to supply our entire population. HHS is supporting research into [human kidney] cell-based vaccine manufacture of producing vaccine domestically.

April, 2006 HHS announces a $97 million contract for the development of cell-based flu vaccine. Leavitt declares: “The FDA can use its Emergency Use Authorization authority to permit the use of unapproved products if there’s a reasonable belief the products may be effective.” 32 states pass laws which make resisting inoculation once ordered by the governor a felony.
These laws join Patriot Act I, II, BARDA, BIOSHIELD I, II in making drug treatment and inoculation mandatory once a Pandemic is called. Unlimited quarantine without review is mandated under these laws for those who resist inoculation under Pandemic conditions. Fully staffed, empty detention centers exist all over North America. The largest, in Alaska, is rumored to have a 2.5 million person capacity.

December, 2006 New York Times reports Gulf War Syndrome positively linked to vaccination of Veterans. More than 100,000 vets contracted the syndrome during the 1991 Desert Storm Operation. More than 20,000 vets have died to date from this syndrome believed to be triggered by squalene, a vaccine “adjuvant.” All modern vaccines contain squalene.

April 17, 2007 The Food and Drug Adminstration (FDA) branch of HHS utilizes its Emergency Use Authorization authority and awards a license to produce H5N1 “Bird Flu” vaccines to Sanofi-Pasteur.
FDA Bird Flu approval letter states: “We have approved your Biologics License Application (BLA) for Influenza Virus Vaccine, H5N1, effective this date. You are hereby authorized to introduce or deliver for introduction into interstate commerce, Influenza Virus Vaccine, H5N1, under your existing Department of Health and Human Services U.S. License No. 1725; however, we acknowledge your statement provided in your submission of April 5, 2007, that Sanofi Pasteur Inc. does not intend to license this product for commercial distribution, since it was produced under contract to the U.S. Department of Health and Human Services as part of national pandemic preparedness initiatives. Influenza Virus Vaccine, H5N1, is indicated for active immunization of persons 18 through 64 years of age at increased risk of exposure to the H5N1 influenza virus subtype contained in the vaccine.” Among the required post-market studies on this untested vaccine are;

1. Protocol submission: Study DMID 04-077: “A randomized, double-blinded, phase I/II, study of the safety, reactogenicity, and immunogenicity of intramuscular inactivated influenza A/H5N1 vaccine in healthy children aged 2 years through 9 years.”

2. Final study report submission: September 30, 2008.Study DMID 04-076: “A randomized double-blinded, placebo-controlled, phase I/II, dose-ranging study of the safety, reactogenicity, and immunogenicity of intramuscular inactivated influenza A/H5N1 vaccine in healthy elderly adults.”

3. Study DMID 05-0043: “Re-vaccination of healthy subjects with intramuscular inactivated subunit influenza A/Vietnam/1203/2004 (H5N1) vaccine representing a drifted variant.

4. “Study DMID 05-0090: “Evaluation of a booster dose of A/Vietnam/1203/04 (H5N1) vaccine administered at 6 months to healthy adult subjects after a two dose schedule at 0 and 1 month.”

5. Study DMID 05-0129: “Open label evaluation of H5N1 vaccine at vaccine manufacturing facilities.”

6. Study DMID 05-0130: “A single center, open label, phase I/II study of the safety and immunogenicity of two 90 µg doses of intramuscular inactivated influenza A/H5N1 vaccine in healthy adult subjects.”

Nov. 26, 2007: Leavitt’s HHS orders 100 million H5N1 “vaccines [doses]” from Sanofi-Pasteur. Expected delivery date, August, 2008. Sanofi-Pasteur issues a press release announcing their lucrative HHS contract (100 million vaccines @ $15 USD each) and declares that the cell-based vaccine will be mass produced in the company’s CHINA facility – then shipped to Stillwater, PA for hypodermic syringe-friendly packaging. Approval and contract have all been consummated in the absence of official human testing.

Jan. 2008 covert ‘human trials’ of Sanofi-Pasteur H5N1 vaccine is conducted on 350 homeless vagrants in Poland. According to London Telegraph:

and Examiner articles, this results in 21 “instant” deaths and over 200 severely incapacitated or hospitalized.” Development and sales of H5N1 vaccine continues.

February 14, 2008 U.S. Air Force Gen. Gene Renuart, commander of North American Aerospace Defense Command and U.S. Northern Command, and Canadian Air Force Lt.-Gen. Marc Dumais, commander of Canada Command, sign a Civil Assistance Plan that allows the military from one nation to support the armed forces of the other nation during a civil emergency. “Our commands were created by our respective governments to respond to the defense and security challenges of the twenty-first century, and we both realize that these and other challenges are best met through cooperation between friends…. The plan facilitates the military-to-military support of civil authorities once government authorities have agreed on an appropriate response.” Avian Flu response is a part of NorthCom’s mission, and according to Gen. Stubblebine’s analysis, appears to be the primary element in its mission:


March 2008 Haruna Kaita, a pharmaceutical scientists and head of a Nigerian University analyzed the latest WHO vaccine in Indian labs. Sterility agents were among the contaminants found in the samples. According to the local population of the Akha, a Thai hill tribe, pregnant women are forced to receive the vaccine in order to get ID cards for their children. Violent still births and miscarriages result.

June 17, 2008 Dr. David Nabarro, UN Influenza Coordinator, welcomes a donation of 60 million doses of H5N1 Avian Flu vaccine by Sanofi-Pasteur. This adds to the stockpile of a previous donation of 30 million doses by GlaxoSmithKline Dr. Nabarro said that good progress had been made but Avian Flu could still kill as many of 150 million people. Avian Flu still entrenched in Viet Nam, Bangladesh, India, Egypt and India [sic] says Dr. Nabarro. Outbreaks recorded in 60 more countries according to US Influenza Coordinator. But the people who make vaccines are ethical and look out for our best interests don’t they? The cold, hard fact is that vaccine makers are neither ethical nor concerned with health and longevity of their recipients.

1994 – 1999 –  A study contacted by Dr. Laure Hewitson at the University of Pittsburgh showed that the  MMR vaccine given to children and several thimerosal mercury containing vaccines injected into children causes Autism.

Monkeys Get Autism-like Reactions to MMR & Other Vaccines In University of Pittsburgh Vaccine Study
Apr 29th, 2012  by 

Someone did perform safety studies the U.S. Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA) should have mandated be performed and vetted BEFORE numerous vaccines were released into the public sector for mass vaccinations.
Lead investigator Laura Hewitson, PhD, probably dropped a bombshell when she and her colleagues completed a macaque monkey (primates) study of the very same vaccines given to children during 1994-1999, i.e., the Measles-Mumps-Rubella (MMR) vaccine and several Thimerosal mercury-containing vaccines injected into children during that time frame when the autism spectrum disorder skyrocketed.
The results of that pilot study were published as a Research Paper in Acta Neurobiological Experimentals in 2010 and titled “Influence of pediatric vaccines on amydgala growth and opioid ligand binding in rhesus macaque infants: A pilot study.” [1] Even though there was alleged controversy revolving around Hewitson’s monkey studies, e.g., charges of conflicts of interest since she filed a claim with the vaccine court on behalf of her child, [2] the information generated needs to be revisited and duplicate studies need to be undertaken. Why haven’t they?  Is there too much influence from vaccine makers not to do them? Parents need to make demands on the U.S. Congress to require such safety studies on monkeys be duplicated immediately, plus suspend all mandates on vaccinations until the study results are in.  Did Dr Hewitson become another professional persona non-gratabecause she may have been on the right track?
Congress needs to consider seriously the Hewitson, et al. report that stated:
“Vaccine-exposed and saline-injected control infants [monkeys] underwent MRI and PET imaging at approximately 4 and 6 months of age, representing two specific timeframes within the vaccination schedule. …
 “These results suggest that maturational changes in amygdala volume and the binding capacity of [11C]DPN in the amygdala was significantly altered in infant macaques receiving the vaccine schedule.”[1]
That alone should be the explicit reason for duplicating the monkey study with independent non-pharmaceutical industry conflict of interest scientists. 
In this author’s opinion, no one has bigger conflicts of interest in study outcomes than the pharmaceutical makers who routinely perform them.  Those are the very studies that should be subject to the same criticism as Dr Hewitson’s.  Why aren’t they?  Good question?
For those keeping track data, ASD went from 1 in 5,000 in the 1990s to the recently acknowledged [March 2012] figures of 1 in 88 along with 1 in 6 children in the USA having developmental disabilities.  These stats were generated for data in the years 2006 to 2008. [3] There’s a 4 to 6 year lag time.  Could ASD be 1 in 50 by now at the rate it is escalating?, especially since there’s a heavier push on mandates for vaccinations.
According to the Hewitson, et al. research study, biological changes and altered behaviors did occur in vaccinated monkeys, which resembled and were similar to those observed in ASD diagnosed children.  However, there were no such symptoms showing or present in unvaccinated monkeys.  Don’t you just gotta love those little monkeys! Guess what else the ASD monkeys came up with, and Dr Wakefield is gonna like this one: Gastrointestinal problems manifested in vaccinated macaques such as “many significant differences in the GI tissue gene expression profiles between vaccinated and unvaccinated animals.” [3] It’s been a deeply debated topic within medicine that vaccinated children who contract ASD also have GI tract issues.  Personally, I gotta wonder how theBritish Medical Journal is going to deal with encrusted dried egg on its face when duplicate studies confirm the Hewitson monkey results.  Perhaps the infamous BMJ retraction of the Wakefield article and Doctor’s professional evisceration, commonly referred to as the “Wakefield Syndrome,” euphemistically speaking is medicine protecting its vested interests.
Those little monkeys, however, came up with some other significant information that led former National Institutes of Health director Dr Bernadine Healy to voice some bon mots like:
“I think public health officials have been too quick to dismiss the hypothesis as ‘irrational,’ without sufficient studies of causation…without studying the population that got sick.”
“I have not seen major studies that focus on 300 kids who got autistic symptoms within a period of a few weeks of the vaccines.” [4]
Perhaps the most on-point quote regarding the monkey study came from Scott Bono, the National Autism Association chairman, i.e., something those who are accused of being against vaccinations have been questioning and demanding:
 “To date, the CDC has conducted no safety testing on the possible harmful effects of simultaneously administering multiple vaccines to infants, and has steadfastly refused to state a preference for mercury-free vaccines to be given to children and pregnant women.  It’s time for HHS and Congress to step in and take vaccine safety away from the CDC.”  [4]
This author’s retort to Mr. Bono’s remark is that vaccine safety should be taken away from the Food and Drug Administration too!  I’d like to remind readers that Congress is more at fault than anyone in this vaccine debacle. Congress has oversight and it has dropped the ball big time, probably due to all the lobbyists from Big Pharma who prowl the halls of Congress with deep pockets and nice expensive luncheon dates. 
One of the issues I feel Congress has been remiss about is that it has not demanded safety studies and interaction of multiple vaccines studies BEFORE being placed into the marketplace.  According to common and accepted knowledge, no such safety research or studies have been done on the current childhood vaccination regimen, except until the Hewitson ‘monkey business’ that was funded by independent, private money, for which everyone, I think, should be eternally grateful. However, the study had to be shot down since it was not favorable to vaccine makers.  Why isn’t someone else duplicating the monkey studies?  Are they afraid of becoming another victim of science?  Why, when isn’t that what medical science should be all about: investigating problems and theories, publishing results, and interacting with other sciences, NOT excommunication as if they were breaking some religious dogma.  Or, do they, in some vested interests minds?

Current Vaccine Safety Activism in Congress

Now here is something every VacTruth reader should consider seriously: Supporting Congressman Dan Burton’s (R-5-IN) request to the House Committee on Oversight and Government Reform Chairman Darrell Issa to hold hearings on the Vaccination Injury Compensation Program. Back on January 12, 2011, this writer filed a Whistleblower’s Complaint on Vaccines with Chairman Issa and has yet to receive an acknowledgement of that filing. 
Isn’t about time to revisit, update, and do more extensive research into the Autism Spectrum Disorder pandemicthat is spreading globally?
April 24, 2012 Congressman Burton posted a letter to The Hill’s Congress Blog titled, “It is time to re-engage on the autism epidemic.”  He also wants to pass legislation to force the President to address the ASD epidemic and its impact on Americans.  Burton is committed to helping millions of children, adults, and families afflicted with ASD. We need to support Congressman Burton ASAP and here’s how:
  1. Contact the Canary Party to support their Facebook pages to hold Congressional hearings and a White House Conference on Autism.  Contact News@CanaryParty.org.
  2. Contact Congressman Darrell Issa at the Oversight and Government Reform Committee at 2157 Rayburn House Office Bldg., Washington, DC 20515 or preferably telephone your request for Autism Investigation Hearings to 202-225-5074.
For those who want to know about this information, the National Autism Association (www.nationalautism.org) will be holding a rally for toxin-free immunizations in Washington, DC on June 4, 2012, titled “Green Our Vaccines,” which this author thinks is an oxymoron.  How can you green vaccines when every ingredient is toxic?  Just check out the CDC’s PinkBook Vaccine Excipient & Media Summary athttp://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf.
Before I leave this article, I would like VacTruth readers to know that my colleague who also writes for VacTruth, Laraine C Abbey, RN (retired) and I co-edited a 150 page monograph in January 2011 titled Vaccines & Vaccinations: The Need for Congressional Investigation, which you can read in full on VacTruth athttp://vactruth.com/vaccines-vaccinations-the-need-for-congressional-investigation/.
Apparently others have read it and agree.
Congressman Burton, Nurse Abbey and I congratulate you on taking the stand you have, and we offer you our resources in obtaining a Congressional investigation.
President Obama, Nurse Abbey and I respectfully request a White House conference on Autism, and we offer you our resources to effectuate a non-biased conference.
VacTruth readers, I charge you with spreading this information and article as far and wide as you possibly can so that we can get an investigation that ought to be open, not biased, and the scientific facts—nothing but the facts, like those the monkeys finally had to prove.  It was not monkey business; it’s the real deal.
Remember: vaccination remains an un-insurable risk: no parent, physician or pharmaceutical company can buy insurance against vaccine induced harm. The insurance industry refuses to accept the risk. That’s why Congress created the Vaccine Injury Compensation Program that is funded by a special tax added to the cost of each vaccine shot: we pay to protect pharmaceutical company profits.

Vaccines can be used for a great deal more than just for what it says on the label. After all, faced with a syringe of fluid, who is to say exactly what is in there and what the intended, or unintended outcomes of being injected will be?

Shielded by the FDA, vaccine (and drug) manufacturers are immune from prosecution for wrong doing and continue to do wrong with horrifying impunity.

For more information on viruses, bacteria, yeast and vaccines read Sick and Tired, Reclaim Your Inner Terrain, or A Second Thought About Viruses, Vaccines and the HIV AIDS Hypothesis, both by Dr. Robert O. Young.

I would also recommend reading Antione BeChamp’s books, The Blood The Third Anatomical Element and The Origin of Organic Beings.

You can find these books at:


As someone that looks to improve their health we are pleased to offer you this free audio, an excerpt of a powerful two hour interview with Dr Robert O. Young and Anthony Robbins. (it is free to listen!)

Click here to listen: http://www.1shoppingcart.com/app/?Clk=1870270

I trust you’ll enjoy this…

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Mandatory Vaccines in Australia but NOT for the Politicians!


Education NOT Vaccination!  Health Care NOT Sick Care!

Wonder if the same is true for the Legislators’ children and grandchildren in the U.S., as they vote to take away your right to choose?

1) https://jonrappoport.wordpress.com/2015/04/26/australia-everyone-must-get-vaccinated-except-the-prime-ministers-daughters/

What is happening in California – mandatory vaccinations for ALL children!


THE GREATER GOOD MOVIE — It’s time to Think Again About Vaccines!

This documentary tells the rarely heard stories of three families adversely impacted by vaccination. This important perspective on the issue of vaccine safety has been left out of the mainstream media debate for too long. These courageous families show us that it is time to Think Again:

Think Again about the many more studies that are necessary to be certain that children are protected

Think Again about protecting the rights of families to choose a vaccination plan that works for their family’s unique medical situation

Think Again about how to make sure vaccines are tested properly

THE GREATER GOOD is inspiring parents nationwide to learn more about the issue, and to foster an informed, balanced conversation with their doctors, schools and communities.

Before ANY Vaccination Have Your Doctor Sign This Form!!!!!! Physician’s Warranty of Vaccine Safety!

Senior Medical - Vaccination


(Physician’s name, degree)_______________, _____ am a physician licensed to practice medicine in the State/Province of _________. My State/Provincial license number is ___________ , and my DEA number is ____________. My medical specialty is _______________I have a thorough understanding of the risks and benefits of all the medications that I prescribe for or administer to my patients. In the case of (Patient’s name) ______________ , age _____ , whom I have examined, I find that certain risk factors exist that justify the recommended vaccinations. The following is a list of said risk factors and the vaccinations that will protect against them:
Risk Factor __________________________
Vaccination __________________________
Risk Factor __________________________
Vaccination __________________________
Risk Factor __________________________
Vaccination __________________________I am aware that vaccines may contain many of the following chemicals, excipients, preservatives and fillers:* aluminum hydroxide
* aluminum phosphate
* ammonium sulfate
* amphotericin B
* animal tissues: pig blood, horse blood, rabbit brain,
* arginine hydrochloride
* dog kidney, monkey kidney,
* dibasic potassium phosphate
* chick embryo, chicken egg, duck egg
* calf (bovine) serum
* betapropiolactone
* fetal bovine serum
* formaldehyde
* formalin
* gelatin
* gentamicin sulfate
* glycerol
* human diploid cells (originating from human aborted fetal tissue)
* hydrocortisone
* hydrolized gelatin
* mercury thimerosol (thimerosal, Merthiolate(r))
* monosodium glutamate (MSG)
* monobasic potassium phosphate
* neomycin
* neomycin sulfate
* nonylphenol ethoxylate
* octylphenol ethoxylate
* octoxynol 10
* phenol red indicator
* phenoxyethanol (antifreeze)
* potassium chloride
* potassium diphosphate
* potassium monophosphate
* polymyxin B
* polysorbate 20
* polysorbate 80
* porcine (pig) pancreatic hydrolysate of casein
* residual MRC5 proteins
* sodium deoxycholate
* sorbitol
* thimerosal
* tri(n)butylphosphate,
* VERO cells, a continuous line of monkey kidney cells, and
* washed sheep red bloodand, hereby, warrant that these ingredients are safe for injection into the body of my patient. I have researched reports to the contrary, such as reports that mercury thimerosal causes severe neurological and immunological damage, and find that they are not credible.

I am aware that some vaccines have been found to have been contaminated with Simian Virus 40 (SV 40) and that SV 40 is causally linked by some researchers to non-Hodgkin’s lymphoma and mesotheliomas in humans as well as in experimental animals. I hereby warrant that the vaccines I employ in my practice do not contain SV 40 or any other live viruses. (Alternately, I hereby warrant that said SV-40 virus or other viruses pose no substantive risk to my patient.)

I hereby warrant that the vaccines I am recommending for the care of (Patient’s name) _______________ do not contain any tissue from aborted human babies (also known as “fetuses”).

In order to protect my patient’s well being, I have taken the following steps to guarantee that the vaccines I will use will contain no damaging contaminants.

STEPS TAKEN: _________________________

I have personally investigated the reports made to the VAERS (Vaccine Adverse Event Reporting System) and state that it is my professional opinion that the vaccines I am recommending are safe for administration to a child under the age of 5 years.

The basis for my opinion are itemized on Exhibit A, attached hereto, — “Physician’s Bases for Professional Opinion of Vaccine Safety.” (Please itemize each recommended vaccine separately along with the basis for arriving at the conclusion that the vaccine is safe for administration to a child under the age of 5 years.)

The professional journal articles I have relied upon in the issuance of this Physician’s Warranty of Vaccine Safety are itemized on Exhibit B , attached hereto, — “Scientific Articles in Support of Physician’s Warranty of Vaccine Safety.”

The professional journal articles that I have read which contain opinions adverse to my opinion are itemized on Exhibit C , attached hereto, — “Scientific Articles Contrary to Physician’s Opinion of Vaccine Safety”

The reasons for my determining that the articles in Exhibit C were invalid are delineated in Attachment D , attached hereto, — “Physician’s Reasons for Determining the Invalidity of Adverse Scientific Opinions.”

Hepatitis B

I understand that 60 percent of patients who are vaccinated for Hepatitis B will lose detectable antibodies to Hepatitis B within 12 years. I understand that in 1996 only 54 cases of Hepatitis B were reported to the CDC in the 0-1 year age group. I understand that in the VAERS, there were 1,080 total reports of adverse reactions from Hepatitis B vaccine in 1996 in the 0-1 year age group, with 47 deaths reported.

I understand that 50 percent of patients who contract Hepatitis B develop no symptoms after exposure. I understand that 30 percent will develop only flu-like symptoms and will have lifetime immunity. I understand that 20 percent will develop the symptoms of the disease, but that 95 percent will fully recover and have lifetime immunity.

I understand that 5 percent of the patients who are exposed to Hepatitis B will become chronic carriers of the disease. I understand that 75 percent of the chronic carriers will live with an asymptomatic infection and that only 25 percent of the chronic carriers will develop chronic liver disease or liver cancer, 10-30 years after the acute infection. The following scientific studies have been performed to demonstrate the safety of the Hepatitis B vaccine in children under the age of 5 years.
____________________________________ _____________________________________

In addition to the recommended vaccinations as protections against the above cited risk factors, I have recommended other non-vaccine measures to protect the health of my patient and have enumerated said non-vaccine measures on Exhibit D , attached hereto, “Non-vaccine Measures to Protect Against Risk Factors” I am issuing this Physician’s Warranty of Vaccine Safety in my professional capacity as the attending physician to (Patient’s name) ________________________________. Regardless of the legal entity under which I normally practice medicine, I am issuing this statement in both my business and individual capacities and hereby waive any statutory, Common Law, Constitutional, UCC, international treaty, and any other legal immunities from liability lawsuits in the instant case. I issue this document of my own free will after consultation with competent legal counsel whose name is _____________________________, an attorney admitted to the Bar in the State of __________________ .
_________________________ (Name of Attending Physician)
______________________ L.S. (Signature of Attending Physician)
Signed on this _______ day of ______________ A.D. ________
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How Many Deaths Due To Measles In The Last 10 Years – NOW The TRUTH – NONE!!!!!!!!!!!!!!!!


Brian Shilhavy

With the measles and measles vaccine debate reaching a near frenzy on the Internet, it is always nice to throw some cold hard facts on the firestorm currently raging in the measles debate.

So here are some easily verifiable facts regarding deaths associated with measles in the United States for the past 10 years, and deaths associated with measles vaccines during the same 10 year period.

First, the Centers for Disease Control and Prevention (CDC) keeps a weekly tally of disease outbreaks, including deaths. According to a statement made by Dr. Anne Schuchat, the director of CDC’s National Center for Immunization and Respiratory Diseases, in an Associated Press story picked up by Fox News on April 25, 2014:

There have been no measles deaths reported in the U.S. since 2003

The weekly CDC Morbidity and Mortality Weekly Reports (MMWR) since that date have not revealed any measles deaths either.

And while health authorities are blaming measles outbreaks in recent years on unvaccinated children, when you mention the fact that nobody is dying from measles in the U.S., they are quick to turn around and claim vaccines have eliminated measles deaths (even though they cannot eliminate the disease itself apparently.)

Besides the obvious contradiction in reasoning with such a claim, the historical evidence just does not support it either:

Death by Measles Vaccines


What about deaths associated with the measles vaccine during the same time period?

The U.S. Government keeps a database of reports called The Vaccine Adverse Event Reporting System (VAERS). The database is available to the public, and there is a search portal the public can use at Medalerts.org.

We ran a search for a ten year period for deaths reported with measles vaccines, including a few that are no longer in production. The search result contained 108 deaths over this period, associated with four different measles vaccines sold in the United States during the past 10 years.


Today, one can only purchase a measles vaccine in combination with the mumps and rubella vaccines (MMR Vaccine).

When searching for just the MMR vaccine during the past 10 years, 96 deaths were reported:


Anyone with a computer and Internet access can search this database by visiting MedAlerts.org.

This database reflects only deaths that were reported during the time frame, and therefore probably reflects a much lower number than actual deaths, since most doctors and health authorities believe vaccines are safe, and would not normally attribute a death to a vaccine and actually report it.

The U.S. Government Settlements on Measles Vaccine Injuries

The other place to find facts regarding injuries and deaths due to the measles vaccine is to look at U.S. Government settlements for MMR vaccine injuries and deaths. The U.S. public is largely unaware that manufacturers of vaccines have been given legal immunity from being prosecuted in civil court for vaccine injuries and deaths, since 1986. If someone is injured or killed by a vaccine, they have to sue the U.S. Government in a special “vaccine court.”

The Department of Justice issues quarterly reports on claims and settlements, and one can search for specific vaccines settlements  at the United States Federal Courts website.

As search here for “measles” returns a result of 111 claims settled for the MMR vaccine since 2004. Some of them are for settlements due to deaths related to the MMR vaccine, as determined by the judge.


We did not click on and read each decision to find out how many resulted in deaths, but if we get a few reports from others who are willing to do so, and the numbers match, we will update this story with the actual death figure.

It takes many years to win a case in this vaccine court, so this probably represents only a tiny fraction of actual injuries and deaths due to the MMR vaccine.

Conclusion: Measles Vaccine Enthusiasm based Largely on Fear and Beliefs

We fully realize that those who believe in the value of vaccines will probably not be persuaded by these facts, which anyone with a computer and Internet access can verify from U.S. Government sources.

Having now published a few stories on the measles issue, and having received many hundreds of comments, it has become very clear to me that those who have strong opinions on the measles vaccine are based more on fear and beliefs, than on facts or science. Any attempt by these vaccine proponents to force their beliefs on the rest of the U.S. public should be vigorously opposed.

See Also:

Dr. Rowen: Measles Spread by those Vaccinated

The Truth About Measles the Mainstream Media is Suppressing

Arizona Cardiologist Responds to Critics Regarding Measles and Vaccines

UCLA Medical Center Pediatrician: Let Parents Choose on Measles Vaccine

CDC Admits Flu Vaccine Does Not Work!

NEW YORK - MAY 29:  U.S. sailors march in the Little Neck/Dougla

Health Impact News Editor Comments

Need proof that the seasonal flu vaccine is not effective? Look no further than the CDC’s own publication admitting the fact: Influenza Outbreak in a Vaccinated Population.

Earlier this year (2014) the CDC published a report documenting an influenza outbreak which occurred among fully vaccinated navy personnel aboard the USS Ardent, a U.S. Navy minesweeper moored in San Diego, California while conducting training.

Continue reading CDC Admits Flu Vaccine Does Not Work!