SIDS 

According to Harris Coulter PhD, “Crib death” was so infrequent in the pre-vaccination era that it was not even mentioned in statistics.  It started to climb in the 1950s with the spread of mass vaccinations.  So much so it even acquired a new name-“SIDS,” Sudden Infant Death Syndrome of unknown origin. The medical establishment assures us that SIDS is unrelated to vaccines which begs the question; How do you know its not vaccines if it is of unknown origin? The three primary doses of DPT are given at two, four and six months of age. Eighty-five per cent of SIDS deaths occur from one to six months of age, with the peak incidence from two to four months. Another coincidence?

In a recent study of SIDS, breathing was monitored before and after vaccination. The data clearly showed that vaccination caused an extraordinary increase in episodes where breathing either nearly ceased or stopped completely. This is why it is so important to have our babies sleep on their backs, if you plan on vaccinating. It is easier for them to breath. Another problem associated with breathing is Asthma. Vaccinated children are shown to be five times more likely to become afflicted with this serious respiratory ailment. 

Dr. William Torch of the University of Nevada School of Medicine did a study of 103 children who died of SIDS. He found that more than two-thirds had been vaccinated with DPT prior to death. Of these, 6.5% died within 12 hours; 13 % died within 24 hours; 26% died within 3 days; and 37, 61 and 70 % within 1,2,3 weeks respectively. Anything that happens to a baby after four weeks is considered God-given. The average time it takes for a vaccine to dissipate in the body is 10-12 days. Click here for Dr Buttram's explanation. Even if a baby dies immediately after a vaccination the cause of death will be labeled SIDS. Here is one example in the vaccine adverse reporting system.

The package insert on the DTP vaccine states the following adverse events have occurred: 

This was very clear to the Japanese. They did not administer the DPT until their babies were two years old. They had the lowest infant mortality rate in the world, until about 1981. This is when the Acellular Pertussis Vaccine, a “less toxic” vaccine was made available to them.  In the U.S, the FDA fail to properly regulate the drug industry after the less reactive DTaP vaccine was licensed for babies in 1996 . They refused to recall the more toxic DPT vaccine and so it was injected into American babies for six more years, just like mercury has been injected into babies for six more years after the FDA told the drug companies to get it out of vaccines.

Delay of DPT immunization until 2 years of age in Japan had resulted in a dramatic decline in adverse side effects. In the period of 1970-1974, when DPT vaccination was begun at 3 to 5 months of age, the Japanese national compensation system paid out claims for 57 permanent severe damage vaccine cases, and 37 deaths. During the ensuing six year period 1975-1980, when DPT injections were delayed to 24 months of age, severe reactions from the vaccine were reduced to a total of eight with three deaths. This represents an 85 to 90 percent reduction in severe cases of damage and death." Raymond Obomsawin, M.D.

The DPaT cut adverse reactions in half. It was 14 years before the U.S. finally licensed the less reactive Acellular Pertussis Vaccine and this only in response to continued pressure placed on the system by parents whose children were injured or died after being injected with whole cell Pertussis vaccine DPT. IOM Immunization Safety Review Session

Take a look at this study and be sure to read the last sentence. Study on DPT

Dr. Robert Reisinger

Dr. Robert Reisinger a Veterinary Scientist, has worked more than forty-five years studying this mechanism of death, and SIDS, in various mammalian species including calves, foals, Rhesus Monkeys and human infants. He has found in fact, that death is not sudden at all. He has proven breastfeeding plays a major part in whether or not the baby will thrive. He implicates E.Coli as the main culprit. This bacterium is a protein-loving organism. The protein content of human breast milk is lower than in any other mammal, and breast milk provides a hostile environment for E. Coli. It also contains neutralizing factors as well. The protein content of formula or any other milk supplement has a direct influence on the numbers of E. Coli in the gut of the child or calf. Example: One bottle of formula is enough to change a baby's gut micro flora dramatically, and it takes two weeks of exclusive breast-feeding to return the gut to normal.

  According to La Leche League, breastfeeding is nature’s vaccine. The resistance to disease that human milk affords cannot be duplicated by any number of vaccines. Breastfed babies are less likely to experience Haemophilus Influence Type B, pneumonia and Meningitis. Large studies have shown that infants who were not breastfed had two to three times greater risk to die from SIDS than breastfed infants.  

Because the natural antibodies are passed on to the baby through the ‘white blood’ or breast milk, the formula or soy formula fed baby has little or no maternal antibodies, no protection of gastrointestinal land respiratory mucosa. The half-life of this maternally acquired antibody through the placenta is twenty days, so at two months old the baby has only 1/8th of the antibodies he was born with, and at three months, has less than 1/16th. The baby is unable to produce his own protective antibodies for several more months. At this exceedingly vulnerable time it is imperative that he not be subjected to undue stress.  His Reticulo Endothelial System, (which plays a major role in detoxification of harmful substances) is at its limit with E.Coli.  He may be literally "up to the nose" in endotoxin (endotoxin is an integral part of the cell wall of E.Coli and other gram-negative bacteria) but still "holding his own.”   When the ill-timed and ill-advised vaccination procedures are inflicted upon the baby, it can be the straw that breaks the camel’s back. 

The impact on the Reticulo-Endothelial System is monstrous.  Over just hours of time, small amounts of bacterial endotoxin, not detoxified by a temporarily dysfunctional Reticulo-Endothelial System, results in removal of blood platelets and fibrinogen from the circulating blood. This pushes the Reticulo-Endothelial System past the point of endurance, endotoxin slips through and out of the liver into the blood stream, injuring platelets.  The result is the release of relatively large amounts of Serotonin from platelets into the blood plasma. Serotonin is one of the brain's major neurotransmitters. It is the biochemicals used by nerve cells to communicate with each other. Serotonin affects the entire body. In the central nervous system, it plays a role in sleep, appetite, memory, learning, temperature regulation, mood, sexual behavior, cardiovascular function, muscle contraction, endocrine regulation, and depression. Some experiments demonstrated the increase of plasma Serotonin almost one hundred fold after vaccination. Serotonin is associated with deep sleep. It stimulates the Vagus Nerve to slow and even stop the heart. If death occurs early in the course of this syndrome, it is due primarily to Serotonin effect.  Thimerosal in the vaccine may also play a role. Take a look at this study: Serotonin

 Endotoxin has a direct effect on cellular respiration. It interferes with metabolism of mitochondria, which are tiny structures found in every cell, which uses a molecular assembly line to convert food into the energy required for cellular functions. Cells derive approximately 70 percent of their daily energy needs from the mitochondria and approximately 20 percent from another process called glycolysis. High-energy tissues such as the nervous system, skeletal muscle and the heart are often compromised when there is a crisis within these cells. Between three and six hours, vascular capillary permeability has become more substantial, and varying amounts of edema and hemorrhage by the passage of blood cells through the unruptured vessel walls into the tissues may be apparent.   After six to eight hours or more, fibrin-platelet clots have formed, and Disseminated Intravascular Coagulation (DIC) is present in lungs, kidneys, and other organs and tissues.  Depending on where the clot settles decides the fate of the cells involved.  For instance if it appears in the eye, blindness may result.  If it settles in the ear, deafness is the outcome. When major organs are involved, Dr. Reisinger describes this whole effect as being SIDS.   The parents of these children are sometimes charged with child abuse. Small hemorrhages in are found in the brain along with clots that might form as the result of a blow to the head.  These parents are not only devastated at the loss of their baby but wrongly accused of hurting the child as well.  The symptoms of “shaken baby syndrome” are the same as what Dr Reisinger describes as endotoxemia.    FYI....vaccines contain endotoxin which is used as an adjuvant.