Vaccine Ingredients and Vaccine Secrets by Sarah Corriher

There has been much recent concern regarding vaccines given to children and their side effects. Particularly highlighted is the link between early childhood vaccines and autism. What follows will be a list of known ingredients inside vaccines, and their documented side effects. It will aid you in making informed decisions, which is something the industry seems to be against. The corporations involved have attempted to suppress this information for decades. Readers are advised that there are additional chemicals and toxins not mentioned, because we had to base this list upon ingredients that are already public knowledge.

The connection to autism has already been repeatedly established, and there are many other conditions caused by vaccines. Permanent paralysis (Guillain Barré syndrome) is surprisingly common, for example. Vaccines are said to prevent certain diseases. However, the chance of catching these diseases is incredibly remote, and the horrid side effects from vaccines are so common that vaccines overall cause much more harm than good. The chance that a particular vaccine will actually offer protection varies between 35% and 90%, and almost all of them lose effectiveness over time. In some cases, vaccines infect patients with the very diseases that they were meant to offer protection from, because they utilize live viral strains.

"A single vaccine given to a 6 pound infant is the equivalent of giving a 180 lb. adult 30 vaccines in one day."

-- Dr. Boyd Haley

Vaccine Ingredient: Aborted Baby Fetus Tissue and Human Albumin

Did you ever wonder if aborted babies were sold to the pharmaceutical industry? Now you know. From a health perspective, the tissues from another human are foreign tissues, and therefore toxic to the body. One industry-friendly web site matter-of-factly boasted:

"The cells reproduce themselves, so there is no need to abort additional fetuses to sustain the culture supply. Viruses are collected from the diploid cell cultures and then processed further to produce the vaccine itself".

The Liberty Counsel reported:

"You may be surprised to learn that some vaccinations are derived from aborted fetal tissue. Vaccines for chicken pox, Hepatitis-A, and Rubella were produced solely from aborted fetal tissue".

Vaccine Ingredient: Formaldehyde

This ingredient is used in vaccines as a tissue fixative, and preservative. Formaldehyde is oxidized in the human body to become formic acid. Formic acid is the main ingredient of bee and ant venom. Concentrated, it is corrosive and an irritant. While absorbing the oxygen of the body, it may lead to acidosis, nerve, liver and kidney damage. According to the National Research Council, fewer than 20% but perhaps more than 10% of the general population may be susceptible to extreme formaldehyde toxicity, and may violently react to exposure at any level. Formaldehyde is ranked as one of the most hazardous compounds on ecosystems and human health, according to the Environmental Defense Fund. These findings are merely for environmental exposure, and therefore, the dangers are much greater with the formaldehyde included in vaccines, since it is injected directly into the blood. The known effects of environmental formaldehyde exposure are:

Eye, nasal, throat and pulmonary irritation Acute sense of smell due to altered tissue proteins Anaemia Antibodies formation Apathy Blindness Blood in urine Blurred vision Body aches Bronchial spasms Bronchitis Burns nasal and throat Cardiac impairment Palpitations and arrhythmias Central nervous system depression Changes in higher cognitive functions Chemical sensitivity Chest pains and tightness Chronic vaginitis Colds Coma Conjunctivitis Constipation Convulsions Corneal erosion Cough Death Destruction of red blood cells Depression Dermatitis Diarrhea Difficulty concentrating Disorientation Dizziness Ear aches Eczema Emotional upsets Ethmoid polyps Fatigue Fecula bleeding Foetal asphyxiation Flu-like or "common cold" illness Frequent urination with pain Gastritis Astrointestinal inflammation Headaches Haemolytic anaemia Haemolytic haematuria Hoarseness Hyperactive airway disease Hyperactivity Hypomenstrual syndrome Immune system sensitizer Impaired (short) attention span Impaired capacity to attain attention

Inability or difficulty swallowing Inability to recall words and names Inconsistent I.Q. profiles Inflammatory diseases of the reproductive organs Intestinal pain Intrinsic asthma Irritability Jaundice Joint pain Aches and swelling Kidney pain Laryngeal spasm Loss of memory Loss of sense of smell Loss of taste Malaise Menstrual and testicular pain Menstrual irregularities Metallic taste Muscle spasms and cramps Nasal congestions Crusting and mucosa inflammation Nausea Nosebleeds Numbness and tingling of the forearms and finger tips Pale clammy skin Partial laryngeal paralysis Pneumonia Post nasal drip Pulmonary oedema Reduced body temperature Retarded speech pattern Ringing or tingling in the ear Schizophrenic-type symptoms Sensitivity to sound Shock Short term memory loss Shortness of breath Skin lesions Sneezing Sore throat Spacey feeling Speaking difficulty Sterility Swollen glands Tearing Thirst Tracheitis Tracheobronchitis Vertigo Vomiting blood Vomiting Wheezing

Vaccine Ingredient: Mercury

Mercury compounds are used in vaccines as preservatives. The toxicity of mercury has been repeatedly ignored in the area of vaccines by the medical establishment and oversight agencies. Mercury is the second most poisonous element known to mankind (second only to uranium and its derivatives). Brain neurons rapidly and permanently disintegrate in the presence of mercury within 30 minutes of exposure. Mercury is also known to change a body's chromosomes.

The U.S. Government has known about the potential problems of thimerosal (the mercury-containing preservative) for many years. The World Health Organization expressed concerns about it in 1990.

Mercury is a cumulative poison, which means the body has difficulty removing it, and that levels of it in the body will accumulate significantly over time. Large amounts of mercury can accumulate over a lifetime. During a typical day of routine vaccines, infants sometimes receive the same amount of mercury as the absolute maximum set by the World Health Organization for 3 months of adult exposure.

The following was taken from a website affiliated with the National Institutes of Health:

"Symptoms of high exposure to this class of mercury based compounds includes: Aphthous, Stomatitis, Satarrhal gingivitis, nausea, liquid stools, pain, liver disorder, injury to the cardiovascular system and hematopoietic system, deafness and ataxia. Death. Headache, paresthesia of the tongue, lips, fingers and toes, other non-specific dysfunctions, metallic taste, slight gastrointestinal disturbances, excessive flatus and diarrhea may occur. Acute poisoning may cause gastrointestinal irritation and renal failure. Early signs of severe poisoning include fine tremors of extended hands, loss of side vision, slight loss of coordination in the eyes, speech, writing and gait, inability to stand or carry out voluntary movements, occasional muscle atrophy and flexure contractures, generalized myoclonic movements, difficulty understanding ordinary speech, irritability and bad temper progressing to mania, stupor, coma, mental retardation in children, skin irritation, blisters and dermatitis. Other symptoms include chorea, athetosis, tremors, convulsions, pain and numbness in the extremities, nephritis, salivation, loosening of the teeth, blue line on the gums, anxiety, mental depression, insomnia, hallucinations and central nervous system effects. Exposure may also cause irritation of the eyes, mucous membranes and upper respiratory tract."

Complete intolerance to thimerosal is known to develop from previous vaccines. The vaccines stimulate the immune system and cause a sensitization. The neurologic toxicity symptoms caused by mercury compounds have a delayed onset after exposure, so few, if any of these symptoms will be noticed at the time of exposure. The mercury of vaccines causes the suspected long-term neurological symptoms like learning disabilities and behavior disorders, which did not exist in previous generations.

Vaccine Ingredient: Antifreeze


Antifreeze (ethylene glycol) is an ingredient of the polio vaccine. It is classified as a "very toxic material". It would take less than a tablespoonful to kill a 20-pound dog with this substance. Pet owners are generally cautious with this dangerous substance, knowing that only a small amount is fatal. For humans, it is directly injected into the blood through vaccinations.

Antifreeze exposure can eventually lead to kidney, liver, blood and central nervous system disorders. It is quite harmful and likely fatal if swallowed. Effects include behavioral disorders, drowsiness, vomiting, diarrhea, visual disturbances, thirst, convulsions, cyanosis, rapid heart rate, depression, cardiopulmonary effects and kidney disorders. It can also lead to liver and blood disorders. It produces reproductive and developmental effects in experimental animals.

Vaccine Ingredient: Aluminum

Aluminum is a suspected carcinogen. It is a cardiovascular (blood) toxicant, neurotoxicant, and respiratory toxicant. It has been implicated as a cause of brain damage, and is a suspected factor in Alzheimer's disease, dementia, convulsions, and comas. It has been placed on at least 2 federal regulatory lists. It is well known in alternative medicine as a toxic and accumulative heavy metal.

Vaccine Ingredient: 2-Phenoxyethanol

This is a suspected carcinogen. It is a developmental and reproductive toxicant. It is also a metabolic poison, which means that it interferes with the metabolism of all cells. This is the primary factor in the formation of cancer cells. It is capable of disabling the immune system's primary response. It also contains phenol (see below for explanation).

Vaccine Ingredient: Phenol

This is a suspected carcinogen, and a cardiovascular and blood toxicant. It is also known as carbolic acid. It is a developmental toxin, gastrointestinal toxin, liver toxin, kidney toxin, neurotoxin, respiratory toxin, skin or sense organ toxin. It has been placed on at least 8 federal regulatory watch lists.

Vaccine Ingredient: Methanol

This is a volatile, flammable, poisonous liquid alcohol. In industry, it is used as a solvent, and an antifreeze compound in fuel. In the body it is metabolized into formaldehyde (described earlier). Whilst it can be found naturally in the pectin that is present in some common fruits, the naturally occurring variant is only in minute quantities, and the organic form is not known to cause any harmful effects.

Vaccine Ingredient: Borax (sodium tetraborate decahydrate)

This was traditionally used as a pesticide and ant killer. It is suspected to be a cardiovascular or blood toxicant, endocrine toxicant, gastrointestinal toxicant, liver toxicant and neurological toxicant. It was found to cause reproductive damage and reduced fertility rates in studies on rats. It is already banned in foods in the United States due to its toxicity; but astonishingly, it is still allowed for direct injection into the blood through vaccines. It is toxic to all cells, and it has a slow excretion rate through the kidneys. Kidney retention and toxicity are the greatest. It has a cascading effect after causing kidney impairment, causing liver degeneration, cerebral edema, and gastroenteritis.

Vaccine Ingredient: Glutaraldehyde

Glutaraldehyde is always toxic, causing severe eye, nose, throat and lung irritations, along with headaches, drowsiness, and dizziness. The effects mirror the chemical warfare agent known as nerve gas. It is poisonous if ingested, and known to cause birth defects in experimental animals. The effects of direct injection into the blood to bypass the process of ingestion are unknown. It is often used to clean medical equipment. In hospital accidents involving environmental exposure, it has been known to cause the following symptoms:

Throat and lung irritation Breathing difficulty Nose irritation, sneezing, and wheezing Nosebleeds Burning eyes and conjunctivitis

Rash-contact and/or allergic dermatitis Discoloring skin (brownish or tan) Hives Headaches Nausea

Vaccine Ingredient: Monosodium Glutamate (MSG)

Monosodium glutamate is a synthetic flavor enhancer. In a 1995 report by the Federation of American Societies for Experimental Biology, two groups of people were defined as intolerant of MSG. This includes those who eat large quantities of MSG and those with "poorly controlled asthma". Our research indicates that anyone can suffer after consuming monosodium glutamate; especially if they are deficient in either taurine or magnesium. In the 1995 report, which was contracted by the F.D.A., there was public admission that MSG yields the following symptoms:

• Burning sensation in the back of the neck, forearms and chest
• Numbness in the back of the neck, radiating to the arms and back
• Tingling, warmth, and weakness in the face, temples, upper back, neck and arms
• Facial pressure or tightness
• Chest pain
• Headache
• Nausea
• Rapid heartbeat
• Bronchospasm (difficulty breathing)
• Drowsiness
• Weakness

Note that this is the short list (the one with side effects that the F.D.A. actually admits) and it does not consider the higher toxicity of direct injection into the blood. The long list, which is 15 times longer, includes heart attacks. Injections of glutamate in laboratory animals have resulted in rapid damage to nerve cells in the brain. MSG is in a special class of chemicals called excitotoxins, which are known to directly attack brain cells. In 1978, MSG was banned from baby foods and other baby products for infants who were less than one year of age, because the American Academy of Pediatrics and the National Academy of Sciences expressed concerns. It is now being used in these products again, in addition to being added to childhood vaccines.

Vaccine Ingredients: Sulfate and phosphate compounds

These can trigger severe allergies in children which may last throughout their lives to permanently impair their immune systems.

Vaccine Ingredient: Ammonium Sulfate

This is yet another carcinogen. Ammonium sulfate is prepared by mixing ammonia with sulfuric acid. It is used as a chemical fertilizer for alkaline soils to lower the pH of soils. In the body, it stresses the immune system by causing acidosis. Ammonium sulfate is also a liver toxicant, neurotoxicant, and respiratory toxicant.

Vaccine Ingredient: Gentamicin Sulfate

This is a strong antibiotic, which is often used for life-threatening illnesses like pneumonia. The known side effects follow:

Muscle twitching Numbness Seizures Elevated blood pressure Purpura P Pseudotumor cerebri Photosensitivity when used topically Transient irritation Vesicular and maculopapular dermatitis Stinging Bacterial/fungal corneal ulcers. Nonspecific conjunctivitis

Inflammation Angioneurotic edema Urticaria Alopecia Burning Mydriasis Conjunctival paresthesia Conjunctival hyperemia Conjunctival epithelial defects Eyelid itching and swelling Itching

Vaccine Ingredient: Neomycin Sulfate

We can only speculate about what damage this causes when injected directly into the blood of infants. It interferes with vitamin B-6 absorption, which is the cause of a rare form of epilepsy, and mental retardation. Adult patients given neomycin as an antibiotic are typically placed under close clinical observation (e.g. hospitalized) so that intensive care intervention is immediately available. Neurotoxicity has been reported, along with nephrotoxicity, and permanent bilateral auditory ototoxicity. Sometimes vestibular toxicity is present in patients with normal renal function when treated with higher or longer doses than recommended.

Vaccine Ingredient: Tri(n)butylphosphate

This is yet another carcinogen. This is a kidney toxicant, and a neurotoxicant. It is more hazardous than most chemicals in 2 out of 3 ranking systems. It is on at least 1 federal regulatory list.

Vaccine Ingredient: Polymyxin B

This is another antibiotic. Injection of this is generally avoided by doctors (except in the case of vaccines) due to "severe pain at injection sites, particularly in infants and children".
Known side effects:

• Albuminuria
• Cylindruria
• Azotemia
• Facial flushing
• Dizziness progressing to ataxia
• Drowsiness
• Peripheral paresthesias: circumoral and stocking-glove.
• Apnea
• Signs of meningeal irritation with intrathecal administration

Vaccine Ingredient: Polysorbate 20 / 80 Emulsifier

This is a suspected carcinogen. It is a known skin and sense organ toxin. It is verified as a cancer agent in animals.

Vaccine Ingredient: Sorbitol (Sweetener)

Diabetic retinopathy and neuropathy may be related to excess sorbitol in the cells of the eyes and nerves, leading to blindness. This is another suspected carcinogen. Sorbitol is a gastrointestinal and liver toxicant.

Vaccine Ingredient: Polyribosylribitol

This is an experimental artificial sweetener. The experimentation is ongoing in children, without the knowledge or consent of their parents.

Vaccine Ingredient: Beta-Propiolactone

Documented as a verified carcinogen. It is a gastrointestinal and liver toxicant, respiratory toxicant, skin toxicant, and sense organ toxicant. It is more hazardous than most chemicals earning a 3 out of 3 in ranking systems. It appears on at least 5 federal regulatory lists. It is ranked as one of the most hazardous compounds to humans.

Vaccine Ingredient: Amphotericin B

This can cause irreversible kidney damage, and mild liver failure. It has been known to produce severe histamine (allergic) reactions. There are several reports of anemia and cardiac failure. It is used used to treat fungus infections. Other side effects include blood clots, blood defects, kidney problems, nausea and fever. When used on the skin, allergic reactions can occur.

Vaccine Ingredients: Animal Organ Tissue and Animal Blood

Animal cell lines are used to culture the viruses in vaccines, so animal tissues and impurities are included in the formulation that is injected. Animal tissues are unusable and toxic to the body except for when their protein materials are digested to form amino acids through normal food consumption. There is no digestion process for injections. Injections may also contain many types of animal viruses (see the Animal Viruses section). Animals used include monkey (kidney), cow (heart), calf (serum), chicken (embryo and egg), duck (egg), pig (blood), sheep (blood), dog (kidney), horse (blood), rabbit (brain), guinea pig, etc.

Vaccine Ingredient: Large Foreign Proteins

In addition to the animal tissue impurities, there are large proteins that are deliberately included, and used for such purposes as adjuvants (substances that aggravate an immune response using their inherent toxicity). Egg albumin and gelatin (or gelatine, obtained from selected pieces of calf and cattle skins, demineralized cattle bones and pork skin) are in several vaccines. Casein (milk protein) is in the triple antigen (DPT vaccine). When injected, these normally harmless proteins are toxic to the body. Hence the immune system "response". The immune system is intentionally stressed by this invasion to produce an unnatural sensitization to all of the ingredients. The body will become further sensitive to these substances in the future, rather than becoming immune to them. So, the basic premise of vaccinations, which the public has been sold, is false. This explains why bizarre allergies such as lactose intolerance, egg, and nut allergies have suddenly become common in recent history.

Vaccine Ingredient: Latex

Latex is included in the hepatitis B vaccine, which is given routinely to health workers. The high occurrence of latex allergies among nurses is due to their sensitization to latex through the large amount of chemical rubber that is injected into them. These vaccines produce a panicked immune response. The nurses will suffer with this allergy permanently. Such allergic reactions can be life-threatening. The hepatitis B vaccine is now routinely given to newborn babies in many countries, including Australia, and the United States.

Vaccine Ingredient: Animal Viruses


Some of these can be particularly alien to the human body. The most frequently documented and publicized example is the monkey virus SV40. The virus is harmless in monkeys, but it stimulates rare cancers when injected into humans producing brain (tumors), bone (e.g. multiple myeloma), lungs (mesothelioma), and lymphoid tissue (lymphoma). Monkey Virus SV40 has only appeared in people born in the last 20 years (The Journal of Infectious Diseases, Sept. 1999), long after the manufacturer claimed to have "cleaned up" the polio vaccines where it was initially found. Such cases include the late Alexander Horwin, both of whose parents tested negative for SV40. Therefore, recent cases cannot just be blamed on inheritance from parents who received the vaccine. It proves that manufacturers are secretly including the virus again.

Vaccine Ingredient: Human Viruses

The live viruses found in some vaccines are frequently said to be killed, inactivated, or attenuated. This is a myth. The main method used to inactivate viruses is treatment with formaldehyde. Its effectiveness is limited and temporary. Once the brew is injected into the body, the formaldehyde is broken down: potentially releasing the virus in its original state. It is documented in orthodox medical literature that these "crippled" viruses can revert to their former virulence.

The viruses and bacteria included in vaccines are claimed to be in very small volume. However, these quantities are high enough for the diseases to occur in some people. Most of the diseases that people are vaccinated against no longer occur in the Western world, and only ever result from the vaccines. When they do occur, the vaccine-induced cases are always more severe than normal infections of the same pathogens, and these cases are sometimes fatal. Deaths have been reported in the British medical journal, Lancet, from vaccine-induced yellow fever. A susceptible person may succumb to infection when exposed to only a minute dose, especially when it is injected directly into the blood stream. Likewise, there are other cases in which a healthy person will not succumb, even when exposed to large doses environmentally. It is not the pathogens, but the interaction methods between pathogens and hosts which causes diseases to appear, and determines their severity.

Most disease symptoms are the visible signs of a body's attempts to defend itself against the infection. With disease injections, many important defenses in the digestion path and mucous membranes are bypassed.

Vaccine Ingredient: Mycoplasma

These are microscopic organisms lacking rigid cell walls and they are considered to be the smallest free-moving organisms. Many are pathogenic, and one species is the cause of mycoplasma pneumonia which interestingly, is noted to occur only "in children and young adults", according to Mosby's Medical Dictionary. This is not simply in vaccines by accident. It is deliberately added as an adjuvant (to increase the immune system's allergic response) to the vaccine.

Vaccine Ingredient: Genetically Engineered Yeast

This is in the hepatitis B vaccine. Given the controversy over the ingestion of genetically modified foods, how much more dangerous could the direct injection of them be?

Vaccine Ingredient: Foreign DNA

DNA is used from such organisms as animals, viruses, fungi, and bacteria. It has been documented that injecting foreign DNA can cause it, or a portion of it, to be incorporated into the recipient's DNA. The horrendous long-term multi-generational implications defy the imagination.

Final Thoughts

The human body has never experienced such a direct invasion as this before. We hope that you consider this list, and the side effects of vaccines before giving your child vaccinations. We have strong reasons to believe that overall, the risks of horrible and long-term side effects far outweigh the risks of the diseases that vaccines are supposed to prevent.

Human blood is supposed to be, and traditionally was, remarkably sterile. There were few bacteria or organisms present in the blood stream. With vaccines now being so prevalent, this is no longer the case. Contrary to what we have been told, they weaken the immune system dramatically instead of strengthening it. In the United States, the hepatitis B vaccine is given to a child on the day of his birth, often weakening his immune system for his lifetime. His small body is just becoming accustomed to the germs around him for the first time, and he needs the strong immune system that he was given to remain intact.

Related Articles

The Shaken Baby Syndrome Lie

The Amish Don't Get Autism but They Do Get Bio-Terrorism

How To Cure Autism and The Time Bomb Of Mercury Poisoning

The 14 Studies Disputing A Mercury Link To Autism and Who Really Funded Them

The Inflammatory Topic Of Vaccines During A Health Information War

The Lead Vaccine Developer Comes Clean So She Can "Sleep At Night": Gardasil and Cervarix Don't Work, Are Dangerous, and Weren't Tested

If Vaccines Are Safe, Then Why Did Congress Give Manufacturers Special Legal Immunity? Why Are They Above the Law?

Children's Programming On P.B.S. Is Admitted Propaganda For Vaccine Industry and Is Sponsored by Governmental Money

Chop Shop Hospitals

Unwilling Guinea Pigs: Using Foster Care Children For Forced Drug Experiments

Mandatory Vaccinations: Have A Taste Of Your Own Medicine, Doctor

The Hepatitis B Vaccine Scam

Proof That The Swine Flu Epidemic Was Man Made and Intentional

A Second Thought About Viruses, Vaccines and the HIV AIDS Hypothesis by Dr. Robert Ol Young

The pH Miracle revised and updated by Dr. Robert O. Young

Sick and Tired by Dr. Robert O. Young

More about → Vaccine Ingredients and Vaccine Secrets by Sarah Corriher

Vaccination - A Peek Beneath The Hood by Roman Bystrianyk and Suzanne Humphries, MD

“It is dangerous to let the public behind the scenes. They are easily disillusioned and then they are angry with you, for it was the illusion they loved.”
– W. Somerset Maugham

Medical history books, almost uniformly extol the virtues of vaccination. Upon reading these books, one is left with the impression that during the 1800s and into the 1900s, there were rampant plagues that killed countless scores of people and that, because of vaccines, this is no longer the case. This is certainly what we believed growing up, and most people we talk to have a similar impression. It generally permeates society as an established fact.

It is difficult to underestimate the contribution of immunization to our well-being. It has been estimated that, were it not for childhood vaccinations against diphtheria, pertussis, measles, mumps, smallpox, and rubella, as well as protection afforded by vaccines against tetanus, cholera, yellow fever, polio, influenza, hepatitis B, bacterial pneumonia, and rabies, childhood death rates would probably hover in the range of 20 to 50%. Indeed, in countries where vaccination is not practiced, the death rates among infants and young children remain at that level. [1]

Paul Offit talks in his recent book Deadly Choices—How the Anti-Vaccine Movement Threatens Us All about how the whooping cough vaccine has reduced deaths from that disease from 7,000 to only 30.

Whooping cough (pertussis) is a devastating infection. Before a vaccine was first used in the United States in the 1940s, about three hundred thousand cases of whooping cough caused seven thousand deaths every year, almost all in young children. Now, because of the pertussis vaccine, fewer than thirty children die every year from the disease. But times are changing. [2]

This type of information can even be found in medical journals. A lengthy study on whooping cough and the whooping cough vaccine was published in 1988 in the journal Pediatrics. The first paragraph of the paper states the following:

In the United States, pertussis has been successfully controlled by routine mass immunization of infants and children. In the prevaccine era, there were 115,000 to 270,000 cases of pertussis and 5,000 to 10,000 deaths due to the disease each year. During the last 10 years, there have been 1,200 to 4,000 cases and five to ten deaths per year. [3]

That paragraph set the tone for the rest of the article by indicating that thousands of people died each year from whooping cough, but after the DTP vaccine was introduced, very few died. Anyone who believed this statement would, of course, believe in the benefit of the vaccine.

The problem with these statements is that they are not supported by the evidence. When we look at the actual data, we see that although many people did die from whooping cough in the early part of the 1900s, by the time the vaccine had been introduced the death rate in the United States had declined by more than 90 percent. Using the source that was referenced to make the statement in the Pediatrics paper, we see that the decline in deaths from the peak was approximately 92 percent before the introduction of the DTP vaccine. [4]

The article in the journal Pediatrics is quite damaging because it would have been read primarily by doctors, leaving many with the impression that vaccines were completely responsible for the decline in deaths. The actual number of deaths by the time of the introduction of the DTP vaccine was approximately 1,200—not the 5,000 to 10,000 often cited. Again, this faulty thinking that vaccines were responsible for the lion’s share of mortality decline is pervasive in all corners of society.

An additional important point to notice is that when looking at the graph you can clearly see that each year the trend was that of a decrease in deaths from whooping cough. At the point the vaccine was introduced there was no apparent effect in the downward trend.

Another data set from England starting at the beginning of the 20th century shows the lack of impact of the vaccines even more dramatically. Here you can see that the death rate had fallen by over 98% before the national use of the DTP vaccine in the 1950s.

England began keeping statistics in 1838, which was 62 years before official U.S. statistics were gathered. Looking at this data, we can see that the death rate from infectious diseases was high during the 1800s and declined from the mid-1800s to the mid-1900s to almost zero. Looking at the whooping coughs death from England, deaths had decreased by more than 99 percent before any vaccine.

In the case of measles, the death rate had declined by almost 100 percent.

Analysis of the data shows this often-repeated mantra that vaccines were key in the decline of infectious disease deaths is a fallacy. Deaths had decreased by massive amounts before vaccinations. In the case of scarlet fever and other infectious diseases, deaths declined to near zero without any widespread vaccination.

Unfortunately, this erroneous belief has led people to trust in vaccination as the sole way to handle infectious diseases when there were clearly other factors that caused mortality to decline. Those factors were improved hygiene, sanitation, nutrition, labor laws, electricity, chlorination, refrigeration, pasteurization, and many other facets that we now generally take for granted as part of modern life. Very little of the improvement in the death rate had anything to do with medicine. A 1977 report estimated that, at best, approximately 3 percent of the mortality decline from infectious disease could be attributed to modern medical care.

In general, medical measures (both chemotherapeutic and prophylactic) appear to have contributed little to the overall decline in mortality in the United States since about 1900—having in many instances been introduced several decades after a marked decline had already set in and having no detectable influence in most instances. More specifically, with reference to those five conditions (influenza, pneumonia, diphtheria, whooping cough, and poliomyelitis) for which the decline in mortality appears substantial after the point of intervention—and on the unlikely assumption that all of this decline is attributable to the intervention . . . it is estimated that at most 3.5 percent of the total decline in mortality since 1900 could be ascribed to medical measures introduced for the diseases considered here. [5]

The emphasis today on more and more vaccines, is in part built on this ingrained thinking. The fact that deaths from infectious diseases declined so greatly before vaccines and antibiotics, is ignored. This lapse in study has created a situation where we could have learned a better way to manage all infections in a more comprehensive way. Yet, to this day, despite such a phenomenal transformation, we have failed to learn the lessons of this history. The solutions that led to a 99 percent decline in death has been ignored, with the entire emphasis on the final 1 percent, which would have occurred anyway even without a vaccine.

However, in some corners, there is recognition that vaccines were not what caused the major decline in infectious disease mortality. They often erroneously point to antibiotics and improved medical care and grudgingly give some credit to sanitation and other factors. There is little curiosity as to how all these factors worked and how they still apply today. The shift on emphasis is now on the incidence of disease after vaccination with a decreased emphasis on mortality. The thinking goes that, by wiping out the disease with vaccines, there is no risk of death. This appears to be a reasonable approach. How well has it worked?

Let’s take whooping cough as an example. In 1979 Sweden withdrew use of the DTP vaccine on the basis that it was not effective and possibly unsafe. The fear, of course, would be that with lower vaccination rates, the death rate would increase. So what happened in this case?

A 1995 letter from Victoria Romanus at the Swedish Institute of Infectious Disease Control indicated that deaths from whooping cough remained near zero. Sweden’s population was 8,294,000 in 1979 and 8,831,000 by 1995. From 1981 to 1993, eight children were recorded as dying, with the cause of death listed as pertussis. This averaged to be about 0.6 children per year possibly dying from whooping cough. These numbers show that the odds of dying from pertussis in Sweden were about 1 in 13,000,000 even when there was no national vaccination program. [6]

In another case, DTP vaccination coverage in England dropped from about 78 percent to 30 or 40 percent because of concerns over safety. The assumption was that there would be an increase in deaths due to the decreased coverage. The years from 1976 to 1980 were the ones when vaccination rates were at their lowest. Using official statistics, the number of deaths in those years totaled 35. The deaths from the previous five years (1971 to 1975), while vaccination rates were higher, totaled 55, or about 1.5 times greater than when vaccination rates were lower. [7] This was directly opposite what is generally believed should have happened.

And have whooping cough rates really been controlled? The sad truth is that whooping cough never really went away and is endemic. Huge numbers of people still cough from Bordetella pertussis, the bacteria involved in whooping cough. Because of waning vaccine- immunity, up to one-third of persistent coughs are whooping cough.

Although pertussis traditionally has been considered a disease of childhood, it was well-documented in adults nearly a century ago and is currently recognized as an important cause of respiratory disease in adolescents and adults, including the elderly. Because of waning immunity, adult and adolescent pertussis can occur even when there is a history of full immunization or natural disease . . . Studies from Canada, Denmark, Germany, France, and the United States indicate that between 12 and 32% of adults and adolescents with a coughing illness for at least 1 week are infected with Bordetella pertussis. [8]

Let’s focus on another infectious disease—measles. Keep in mind that by 1963, almost no one died from measles. During this year, the whole of New England had only five deaths (Maine: 1, New Hampshire: 0, Vermont: 3, Massachusetts: 0, Rhode Island: 1, Connecticut: 0) that were attributed to measles. [9] Deaths from asthma were actually 56 times greater than from measles during that year.

But did incidence decline as vaccine proponents emphasize? There are some graphs you can find on the Internet that claim there was little decrease in incidence. The graph I have seen that shows this only has a few data points and a line between two distant points in time. This graph is of poor quality and draws an incorrect conclusion. Looking at more comprehensive incidence data, we can see a drop in incidence in 1963 at the introduction of the measles vaccine.

Measles incidence did apparently dramatically drop after 1963. But can this drop be completely attributed to the success of the measles vaccine? The early measles vaccine that contained “killed” virus was an aluminum-precipitated vaccine produced from formaldehyde-inactivated monkey kidney cell cultures. A study from 1967 revealed that the vaccine could cause pneumonia as well as encephalopathy (inflammation of the brain).

Pneumonia is a consistent and prominent finding. Fever is severe and persistent and the degree of headache, when present, suggests a central nervous system involvement. Indeed one patient in our series who was examined by EEG, evidence of disturbed electrical activity of the brain was found, suggestive of encephalopathy . . . These untoward results of inactivated measles virus immunization was unanticipated. The fact that they have occurred should impose a restriction on the use of inactivated measles virus vaccine. We now recommend that inactivated measles virus vaccine should no longer be administered. [10]

The killed vaccines were quickly abandoned. [11] But there were also significant issues with the live vaccines, which were not highly attenuated and produced a “modified measles” rash in about half of those injected—essentially equivalent to a case of measles. Forty-eight percent of people had rash, and 83 percent had fevers up to 106°F post-injection.

So how did measles incidence drop so dramatically after the 1963 vaccine? In part, it had to do with a definition. If you had a high fever and you had a vaccine, of course you didn’t have measles even if you were sicker than you would have been if you contracted measles naturally.

Back in the 1960s, it was expected that a single shot would protect you for life without serious effects, which would later turn out not to be true.

The United State Public Health Service licensed a new, refined, live-measles vaccine. Although several live vaccines have been licensed since 1963—all of them one-shot treatments that give life immunity without serious side-effects—the new one is considered by epidemiologists as “the best so far in minimizing the side-effects.” [12]

Claims were even made in the 1960s that only a certain number of children needed to be vaccinated in order to wipe out measles.

Measles, the “harmless” childhood disease that can kill, will be nearly eradicated from most areas of the country a year from now, officials of the United States Public Health Service predict . . . Although there are still more than 12 million susceptible children, vaccination of the “right” two million to four million youngsters could wipe out the disease, according to Dr. Robert J. Warren of the Communicable Disease Center in Atlanta. [13]

More than a decade later, the objective of measles elimination was still not achieved. There were repeat epidemics that happened throughout the United States.

By 1989 the new theory on failure to eradicate was that the earlier vaccines were not as effective as originally believed. Some of the first vaccines mass produced in 1963 contained a killed virus. In 1989 Dr. Feigin of Texas Children’s Hospital stated that he believed the 1963 vaccine was “not widely effective” and that the 1967 vaccine was unsta¬ble and lost its “effectiveness” if not properly refrigerated. It was not until 1980 that a stable live measles vaccine became available. [14]

In the same year, after three types of measles vaccines had failed to produce eradication or even predictable herd immunity, vaccine scientists changed course from one shot and stated that, in using the new live vaccine, two doses would be required for reliable protection. They also recommended that everyone under the age of 32 be revaccinated because the old vaccines they received were inadequate. The single shot once promised to provide lifelong immunity against measles in the 1960s was never produced.

And was the measles incidence declining before 1963 anyway? Looking at the measles incidence data, the trend line shows that incidence was on the decline.

In fact, if that trend line held, measles incidence would have hit zero by around the year 2000. This is actually the year when the CDC declared measles had been eliminated from the United States.

So were all these vaccines worth the cost, effort, and adverse reactions to tackle what was by 1963 considered a mild childhood illness?

When we hear about vaccines, we are often told a simple story of how they stimulate antibodies. The theory goes that the stimulation of antibodies creates a memory of a disease so the next time you encounter it, your body will quickly defeat the enemy. It’s a nice, simple, and easy-to-remember story.

Believing you understand the immune system because you hear the words “antibodies” and “protection” mentioned together is like thinking you know how a car really works because you see it has wheels. The immune system is a highly complex, still-poorly understood entity, composed of many different cell lines, each producing different chemicals that are released into the blood. These chemicals are used by the body and are affected by age, stress, nutritional status, environment, and a whole host of factors that are barely understood.

“. . . the immune system remains a black box,” says Garry Fathman, MD, a professor of immunology and rheumatology and associate director of the Institute for Immunology, Transplantation and Infection . . . “It’s staggeringly complex, comprising at least 15 different interacting cell types that spew dozens of different molecules into the blood to communicate with one another and to do battle. Within each of those cells sit tens of thousands of genes whose activity can be altered by age, exercise, infection, vaccination status, diet, stress, you name it. . . . That’s an awful lot of moving parts. And we don’t really know what the vast majority of them do, or should be doing . . . [15]

The immune system is traditionally divided into the humoral immune system that is involved with antibodies and the cellular immune system that does not involve antibodies but entails the activation of various cells such as natural killer cells. What we do know is that, contrary to popular belief, antibodies are not necessary when it comes to full measles recovery.

. . . children with antibody deficiency syndromes have quite unremarkable attacks of measles with the characteristic rash and normal recovery. Furthermore, they are not unduly prone to reinfection. It therefore seems that serum antibody, at any rate in any quantity, is not required for the production of the measles rash; nor for the normal recovery from the disease; nor to prevent reinfection. [16]

Children with a deficit in antibody production, called agamma-globulinemia, recover from measles just as well as normal antibody producers, and this has been known since the late 1960s when vaccines were being developed and advanced. But antibody response is really the only thing that is talked about and promoted when it comes to vaccines. Because this knowledge disturbed the simplistic antibody-protection paradigm, it was considered a “disconcerting” discovery in this 1968 medical paper.

One of the most disconcerting discoveries in clinical medicine was the finding that children with congenital agamma-globulinaemia, who could make no antibody and had only insignificant traces of immunoglobulin in circulation, contracted measles in normal fashion, showed the usual sequence of symptoms and signs, and were subsequently immune. [17]

How does nutrition play a role in disease? Discovered in the 1920s, vitamin A was dubbed the “anti-infective” vitamin. It alone has a tremendous impact on measles deaths. During the 1990s, mortality reductions of 60 to 90 percent were measured in poor countries using vitamin A in hospitalized measles cases.

Combined analyses showed that massive doses of vitamin A given to patients hospitalized with measles were associated with an approximately 60% reduction in the risk of death overall, and with an approximate 90% reduction among infants . . . Administration of vitamin A to children who developed pneumonia before or during hospital stay reduced mortality by about 70% compared with control children. [18]

Availability of vitamin C-rich fruits and vegetables was another factor in disease morbidity and mortality reduction. There were improving trends in overall nutrition, as seen by a parallel in the decline in deaths from measles and the vitamin C deficiency disease, scurvy. Experiments done in the 1940s showed that vitamin C was effective against measles, especially when used in higher doses.

During an epidemic [of measles] vitamin C was used prophylactically and all those who received as much as 1000 mg. every six hours, by vein or muscle, were protected from the virus. Given by mouth, 1000 mg. in fruit juice every two hours was not protective unless it was given around the clock. It was further found that 1000 mg. by mouth, four to six times each day, would modify the attack; with the appearance of Koplik’s spots and fever, if the administration was increased to 12 doses each 24 hours, all signs and symptoms would disappear in 48 hours. [19]

In the early 1900s, other treatments were being successfully used to treat measles. In 1919 Dr. Drummond commented that cinnamon oil was an effective prophylactic against measles or that it made measles milder.

It has been my practice, when I meet with a case of measles in a family, to prescribe a course of cinnamon for all unprotected members of the family. In the majority of cases the person so treated [with cinnamon] escaped the disease [measles] altogether, or else had it in very mild form. [20]

Nutrition and other factors have a big impact on measles, so why aren’t we talking about them at all? Because the emphasis is always on a single, highly lucrative medical procedure—vaccination. This sole paradigm has swept virtually all other strategies to the wayside.
Another key factor to consider is that measles vaccine does not create lifelong immunity, whereas natural infection with measles does. The only way to remain immune with artificial immunity via vaccines is to be vaccinated several times during a lifetime. We have not yet seen how the vaccine will play out over several generations of exclusively vaccinated people. Epidemics are likely to become more common in the future.

A 2009 study published in Proceedings of the Royal Society investigated what could happen with waning measles vaccine immunity even with high vaccine coverage among children. They predicted that, after a long disease-free period in the population, the introduction of infection will lead to far larger epidemics than predicted by standard models.

We can foresee that vaccination will have two conflicting effects . . . it will reduce the number of newborn susceptibles and hence should have some of the usual associated public-health benefits reducing the number of cases in young children. However, this reduction in cases will lead to a reduction in boosting and therefore a greater susceptibility to infection in older age classes . . . When immunity wanes, vaccination has a far more limited impact on the average number of cases. While this observation has clear public-health implications, the dynamic consequences of the interaction between vaccination, waning immunity and boosting are far more striking. For high levels of vaccination (greater than 80%) and moderate levels of waning immunity (greater than 30 years), large-scale epidemic cycles can be induced. [21]

A 1984 study [22] reported that by 2050, the proportion of measles susceptibles may be greater than in the pre-vaccine era. So have we created a ticking time bomb with waning immunity? Will there actually be bigger measles epidemics in the future? If there are, the response will probably be to blame the unvaccinated, which has in fact been done for over 100 years, and then to enforce more vaccinations upon different age groups.

Because of the zealous pro-vaccine bias that permeates society, the true forces that drove the major decline in deaths from infectious diseases are not acknowledged. At most, there is a slight admission that “sanitation” has some effect, but better medical care and antibiotics are still given the credit.

Groups of individuals who have anointed themselves as “skeptics” seek to derail anything that questions vaccination. The definition of skeptic used to be “one who instinctively or habitually doubts, questions, or disagrees with assertions or generally accepted conclusions,” but this definition in its modern usage has been hijacked and transformed to someone that essentially blindly supports any orthodox position as gospel. These people will continue on their crusade of supporting vaccines at all costs and to assail anything that might question their myopic view. If those people had a desire to learn the truth, perhaps they would peek beneath the hood of infectious diseases and vaccines, and learn a little more. Imagine what could be in the trunk!

Suzanne Humphries and Roman Bystrianyk are authors of Dissolving Illusions: Disease, Vaccines and the Forgotten History available on amazon.

Bibliography:

1. Irwin W. Sherman, Twelve Diseases That Changed Our World, 2007, p. 66.
2. Paul A. Offit, MD, Deadly Choices—How the Anti-Vaccine Movement Threatens Us All, 2011, p. xii.
3. James D. Cherry, MD MSc; Philip A. Brunell, MD; Gerald S. Golden, MD; and David T. Karzon, MD, “Report on the Task Force on Pertussis and Pertussis Immunization—1988,” Pediatrics, June 1988, vol. 81, no. 6, Part 2, p. 939.
4. Historical Statistics of the United States Colonial Times to 1970 Part 1, Bureau of the Census, 1975, pp. 77.
5. John B. McKinlay and Sonja M. McKinlay, “The Questionable Contribution of Medical Measures to the Decline of Mortality in the United States in the Twentieth Century,” The Milbank Memorial Fund Quarterly, Health and Society, vol. 55, no. 3, summer 1977, p. 425.
6. Letter from Victoria Romanus, MD, PhD, Department of Epidemiology Swedish Institute of Infectious Disease Control, Stockholm Sweden, August 25, 1995.
7. Record of Mortality in England and Wales for 95 Years as Provided by the Office of National Statistics, 1997; Health Protection Agency Table: Notification of Deaths, England and Wales, 1970–2008.
8. Edward Rothstein, MD, and Kathryn Edwards, MD, “Health Burden of Pertussis in Adolescents and Adults,” Pediatric Infectious Disease Journal, vol. 24, no. 5, May 2005, p. S44.
9. Vital Statistics of the United States 1963, Vol. II—Mortality, Part A, pp. 1–18, 1–19, 1–21.
10. Vincent A. Fulginiti, MD; Jerry J. Eller, MD; Allan W. Downie, MD; and C. Henry Kempe, MD, “Altered Reactivity to Measles Virus: Atypical Measles in Children Previously Immunized with Inactivated Measles Virus Vaccines,” Journal of the American Medical Association, vol. 202, no. 12, December 18, 1967, p. 1080.
11. “Measles Vaccine Effective in Test—Injections with Live Virus Protect 100 Per Cent of Children in Epidemics,” New York Times, September 14, 1961.
12. “Thaler to Hold State Senate Hearing to Find Fastest Way to Expedite Plan,” New York Times, February 24, 1965.
13. Jane E. Brody, “Measles Will Be Nearly Ended by ’67, U.S. Health Aides Say,” New York Times, May 24, 1966.
14. Lisa Belkin, “Measles, Not Yet a Thing of the Past, Reveals the Limits of an Old Vaccine,” New York Times, February 25, 1989.
15. B. Goldman, “The Bodyguard: Tapping the Immune System’s Secrets,” Stanford Medicine, summer 2011.
16. P. J. Lachmann, “Immunopathology of Measles,” Proceedings Royal Society of Medicine, vol. 67, November 1974, p. 1120.
17. “Measles as an Index of Immunological Function,” The Lancet, September 14, 1968, p. 611.
18. Wafaie W. Fawzi, MD; Thomas C. Chalmers, MD; M. Guillermo Herrera, MD; and Frederick Mosteller, PhD, “Vitamin A Supplementation and Child Mortality: A Meta-Analysis,” Journal of the American Medical Association, February 17, 1993, p. 901.
19. Fred R. Klenner, MD, “The Treatment of Poliomyelitis and Other Virus Diseases with Vitamin C,” Southern Medicine & Surgery, July 1949.
20. “Cinnamon as a Preventive of Measles,” American Druggist Pharmaceutical Record, New York, November 1919, p. 47.
21.J. M. Heffernan and M. J. Keeling, “Implications of Vaccination and Waning Immunity,” Proceedings of the Royal Society B, vol. 276, 2009.
22. D. L. Levy, “The Future of Measles in Highly Immunized Populations: A Modeling Approach,” American Journal of Epidemiology, vol. 120, no. 1, July 1984, pp. 39–48.

- See more at: http://www.vaccinationcouncil.org/2013/11/12/vaccines-a-peek-beneath-the-hood-by-roman-bystrianyk-and-suzanne-humphries-md/?utm_source=feedburner&utm_medium=email&utm_campaign=Feed%3A+vaccinationcouncil+%28International+Medical+Council+on+Vaccination%29#sthash.USPFGy4x.BoGo2vJE.dpuf

More about → Vaccination - A Peek Beneath The Hood by Roman Bystrianyk and Suzanne Humphries, MD

Vaccinations - The Worst Cover-Up In The History of the World!

A History of Vaccines and Their Acidic Affects on Human Life!

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=Xj7AN4fRe6s

The 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
www.phmiracleliving.com

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.

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.

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
www.phmiracleliving.com

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.

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.

1976 - 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.

http://www.haverford.edu/biology/edwards/disease/viral_essays/warnervirus.htm

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.

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.

1980 Estimated 2 million American children with vaccine-caused disabilities.

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)

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.

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).

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 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.

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.

1987 - May 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.)

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.

1989. July, 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.

1990, June, 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.

1992, March 19, 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).

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.

1997, August 24, 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.

2000, April, 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.

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

2003, October, 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".

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

2005, June, 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.

2005, August, 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

2005, September 9, 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".

2005, September 29, 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."

2005, October, 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.

2005, December, Bush solicits Congress for $7.1 Billion to fund "preparations" --- $3.3 billion is immediately allocated to Leavitt's HHS.

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

2006, January, Leavitt launches website - 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.

2006, March, 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.

2006, April, 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.

2007, April 17, 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."

2007, November 26, 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.

2008, January, covert 'human trials' of Sanofi-Pasteur H5N1 vaccine is conducted on 350 homeless vagrants in Poland. According to London Telegraph:
(http://www.telegraph.co.uk/news/worldnews/europe/poland/2235676/Homeless-people-die-after-bird-flu-vaccine-trial-in-Poland.html) and Examiner articles, this results in 21 "instant" deaths and over 200 severely incapacitated or hospitalized." Development and sales of H5N1 vaccine continues.

2008, February 14, 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:

http://www.northcom.mil/Avian%20Flu/index.html

2008, March, 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.

2008, June 17, 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.

2012, April, 29, A study contacted by Dr. Laure Hewitson at the University of Pittsburgh from 1994 to 1999 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 Catherine J. Frompovich

• 45.9K
• 18
  inShare

A University of Pittsburgh study showed vaccines altered the behavior in monkeys.

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?

2012 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?

2012, April, 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.

References:

[1] http://www.ane.pl/pdf/7020.pdf

[2] http://leftbrainrightbrain.co.uk/2010/07/laura-hewitson-has-left-the-university-of-pittsburgh/

[3] http://www.cdc.gov/ncbddd/autism/data.html

[4] http://www.vaccineriskawareness.com/Infant-Vaccines-Produce-Autism-Symptoms-In-Primates

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?

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.

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:

www.phmiracleliving.com

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...

Not part of our healing alkaline community?
Visit our website at:

www.phmiracleliving.com

To learn more about the science of Dr. Robert and Shelley Young go to:

www.articlesofhealth.blogspot.com

'Miracles happen not in opposition to nature, but in opposition to what we know of nature.' St. Augustine

'Any sufficiently advanced technology is indistinguishable from magic' ....Arthur C. Clarke

'There are only two ways to live your life. One, is as though there are no miracles. The other is as though everything is a miracle.' Albert Einstein

pH Miracle Living Center
16390 Dia Del Sol
Valley Center, California 92082 US

© Copyright 2012 - Dr. Robert O. Young
All rights are reserved. Content may be reproduced, downloaded, disseminated,
or transferred, for single use, or by nonprofit organizations for educational
purposes, if correct attribution is made to Dr. Robert O. Young.

Connect with us on Facebook and MySpace:
Dr. Robert O. Young:
http://www.facebook.com/profile.php?id=1279807836
http://myspace.com/drrobertoyoung
Shelley Young:
http://www.facebook.com/profile.php?id=691213155

More about → Vaccinations - The Worst Cover-Up In The History of the World!