this will make you ill... how vaccines are made.

A study in New Zealand reports that of 1,265 children born in 1977, 23 received no childhood vaccinations and none suffered childhood asthma. Among the 1,242 who got polio and DPT shots, 23% later had episodes of asthma, 23% had asthma consultations and 30% had consultations for other allergic illness.



How Vaccines Are Made?


Vaccine production is a disgusting procedure. To begin, one must first acquire the disease germ – a toxic bacterium or a live virus. To make a “live” vaccine, the live virus must be attenuated, or weakened for human use. This is accomplished by serial passage – passing the virus through animal tissue several times to reduce its potency. For example, measles virus is passed through chick embryos, polio virus through monkey kidneys, and the rubella virus through human diploid cells – the dissected organs of an aborted fetus! “Killed” vaccines are “inactivated” through heat, radiation, or chemicals. But obtaining materials from these sources is expensive and in terms of enormous numbers of vaccines made, monkeys and so on would soon be extinct. So lab technicians have devised a way of continuous cloning to repeat these cells endlessly. One could say they are therefore cancerous cells. But these cloned cells are thought to be safe until about the 38th usage, when they are supposed to be destroyed, as they then become potentially carcinogenic. We have no guarantee that they are always destroyed at the

38th stage or that it is at the 32nd stage they become cancerous and not the 38th stage. In addition growth factor must be used. Whooping cough uses the mucus of infected children. Typhoid the excrement of victims. Rubella is grown on aborted fetuses. The old Hep B vaccine was derived from human blood, specifically the blood of homosexual men who have had hepatitis.(this vaccine was replaced by a genetically engineered version which is grown on yeast cells, however the older version was never withdrawn until they used all of it up).



The weakened germ must then be strengthened with adjuvants (antibody boosters) and stabilizers. This is done by adding drugs, antibiotics, and toxic disinfectants to the concoction: neomycin, streptomycin, sodium chloride, sodium hydroxide, aluminum hydroxide, aluminum hydrochloride, sorbitol, hydrolized gelatin, formaldehyde, and thimerosal (a mercury derivative).



Aluminum, formaldehyde, and mercury are extremely toxic substances with a long history of documented hazardous effects. Studies confirm again and again that microscopic doses of these substances can lead to cancer, neurological damage, and death. Yet, each of them may be found in childhood vaccines.



In addition to the deliberately planned additives, unanticipated matter may contaminate the shots. For example, during serial passage of the virus through animal cells, animal RNA and DNA – foreign genetic material – is transferred from one host to another. Because this biological matter is injected directly into the body, researchers say it can change our genetic makeup.



What happens next, once this foul concoction – live viruses, bacteria, toxic substances, and diseased animal matter – is created? This witch’s brew is forced into the healthy child.

Vaccine complications:



It took 85 years for humanity to link the observed side effects, including death, to the smallpox vaccine. The general public is essentially unaware of the true number of people who have been permanently damaged or killed by vaccines. In fact, most parents would be surprised to learn that the government has a computer database filled with several thousand names of disabled and dead babies, children who were healthy and alive just prior to receiving the vaccines.



If we want to know infant deaths in relation to vaccinations we have to look at overall – countrywide statistics. For E.g.: -



1. When Japan stopped injecting infants with DPT and moved up the age of vaccination to two years cot deaths (SIDS) virtually disappeared in Japan.

There was also a decline in spinal meningitis. Japan then went on to have the lowest

infant mortality in the world.

2. Sweden dropped Pertussis vaccines in 1979 and the infant mortality rate dropped.

3. Italy does not use the DPT vaccine.

4. Similarly when the Australian government made DPT vaccines a voluntary choice, the incidence of SIDS dropped by 50%. (The same in the U.K)

5. On the contrary in the US there are nearly 10 000 baby deaths every year from SIDS where vaccines are given.

6. New Zealand has the highest rate of SIDS in the world, 2 per 1000 live births. DPH3 is given at 6/5 and 12 weeks after birth – deaths cluster around 8-16/52 mark.



In 1974 Dr Robert Risenger showed that one of the reasons breastfed babies fared better is that there is far less Ecoli in their gut and that it is this bacteria in their gut, in combination with DPT vaccines which causes endotoxic shock, heart and breathing difficulties. He has been ignored.



In 1994 the US Institute of Medicine, looking at up to 10 000 cases of SIDS per year in the US, admitted that the evidence is consistent for a causal relation between DPT vaccine and acute encephalopathy, encephalitis or encephalomyelitis.

This was reported in JAMA. In fact it has also been demonstrated in lab animals.



Dr Archie Kalokennos of Australia noted that often vaccinations carried out in the Aboriginal community, up to 50% of the children went into endotoxic shock and died. He was able to rescue a few – near deaths by giving large doses of Vitamin C (a detoxifier) IM or IV.

He realized that these poor infants were so malnourished that they could not cope with the impact of the vaccination.

So before the vaccinations he built them up with Vitamins especially vitamin C and most survived the vaccines. Despite this the medical world refuse to take heed.