Craig Stellpflug - Natural News - May 16, 2012
There is only one kind of immunity and that is natural immunity which is achieved by battling the infectious diseases itself.
Vaccination is merely the artificial triggering of temporary responses to manmade pathogens. Vaccines are both harmful and dangerous and are leading to generations of humans with no natural defenses to disease.
Vaccines do not provide long-term immunity; only temporary at best. In vaccines, an antigen is injected into the body to produce a reaction and the immune system responds in the form of antibodies, but antibody presence does not confer immunity. People still catch the diseases that they are vaccinated against. Vaccines actually skip the normal immune responses to activate killer cells which can trigger an overproduction of cytokines in response to the toxic vaccine adjuvants and can damage tissues and organs and even stop the heart and block air pathways.
Vaccines should never be called immunizations because that is a misnomer. Immunity and vaccinations are two different subjects altogether. In fact, breast milk is so potent with immune energizing effects in the infant that researchers at the CDC recommend women withhold breastfeeding their children in order to boost the “effectiveness” of childhood vaccines. The paper claims that women should stop breastfeeding long enough for the man-made poison to work on artificial/temporary “immunity.”
There is no such thing as a “side effect”
After-effects of vaccines are only followed for a very short time. Effects that are not seen for 30 years will not even be associated with the vaccine. Immunizations are contributing to the lowering of immunity along with the spread of auto-immune diseases such as arthritis and even AIDS throughout the world. Research clearly shows that aluminum mixed into vaccines carries a risk for autoimmunity, long-term brain inflammation, and subsequent neurological complications and may have profound and widespread adverse health complications. Many vaccines contain both aluminum and trace amounts of mercury. When you mix these 2 metals together it causes Extreme Synergistic Toxicity.
As vaccinated disease rates go down (but not necessarily as a result of toxic vaccinations), the rate of chronic disease goes up in lock-step. Vaccines, as they are commonly given, destroy the natural immunity process and accelerate the auto-immune disease process.
Deaths from measles in 1900 were 13 per 100,000 people. In 1948: less than one. Measles vaccines introduced in 1963 but took full credit for what they never did – eliminate measles. Japanese health authorities realized that early inoculations were causing crib deaths so they postponed them until the 24th month and SIDS virtually disappeared along with whooping cough (pertussis) during the first two years of babies’ lives. Instead of preventing whooping cough the DPT promotes it as well as SIDS. Reuters recently reports that according to the CDC, the number of pertussis cases is growing – in
the fully vaccinated population!
The recent Bachmair vaccine study reveals that the allergy rate in vaccinated children is more than double the rate in unvaccinated ones. Vaccinated children are also nearly eight times more prone to develop asthma or chronic bronchitis than unvaccinated. Furthermore, vaccinated kiddos suffer from more neurodermatitis, herpes, otitis media, hay fever, hyperactivity, scoliosis, epilepsy and seizures, migraine headaches, thyroid disease, and SIDS than unvaccinated children. Vaccinated kids historically also have more measles than unvaccinated kids.
Doctor after doctor will tell you that vaccinations have reduced the incidence of many infectious diseases but they have no real proof. In fact, all the epidemical evidence shows that disease rates rise after vaccines – in the vaccinated population. Should we trust them just on their word? Make an informed decision about you and your child’s health.
Sources for this article include:
Tomljenovic L and Shaw CA. Aluminum vaccine adjuvants: Are they Safe? Current Medicinal Chemistry. 2011; 18: 2630-2637.
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