Alarming excerpt about medical evidence being hidden from the public (Written by Dave Mihalovic, a Naturopathic Doctor who specializes in vaccine research, cancer prevention and a natural approach to treatment): The only large-scale study ever conducted in the US, at University of California at Los Angeles in 1979, found that one in 875 doses of DTP is followed by convulsions, or an episode of shock or collapse, leading to death in the case of two babies (Pediatrics, 1981; 68: 650-60). As for brain damage, a Swedish study showed a rate of brain damage or death of one in 17,000 children (BMJ, 1967; 4: 320-3). The IOM report concluded that: the triple shot definitely causes anaphylactic shock and extended periods of inconsolable crying or screaming evidence is consistent with a causal relationship between acute encephalitis (inflammation of the brain) and shock and unusual shock-like (hypotonia/hyporesponsive) reactions, causing total collapse (Stratton K, Adverse Events Associated with Childhood Vaccines; Evidence Bearing on Causality, Washington, DC: National Academy Press, 1993). In 1993, The National Childhood Encephalopathy study: a 10-year follow-up reported on the medical, social, behavioural and educational outcomes after serious, acute, neurological illness in early childhood. The analysis found a four-fold increase in the estimated risk of encephalitis from the pertussis vaccine. The analysis showed the risk of encephalitis with the vaccine have been grossly underestimated. Diphtheria and tetanus toxoids and whole-cell pertussis vaccine (DTP) and pediatric diphtheria and tetanus toxoids (DT) are not recommended for individuals 7 years of age or older due to increased adverse reactions. Yet in 1994, a study in the Family Practice Research Journal found that children 7 years of age or older are inadvertently receiving DTP or DT and were unnecessarily experiencing adverse reactions. In another study in the The Journal of the American Medical Association, children vaccinated with pertussis vaccine were six times more likely to develop asthma. In 2004, a study in the British Medical Journal found that the prevalence of asthma and wheezing in non-vaccinated individuals was approximately 50% less at age 69-81 months than children who had 3 or more doses of with the Diptheria and tetanus vaccine. Researchers reported in the OSMA Journal that the pertussis vaccine may cause lasting and permanent brain damage. Physicians are required to warn all responsible parties of vaccine recipients that pertussis vaccine may cause lasting brain damage, but rarely if ever to Physicians inform parents of this fact. In the Journal of Pediatrics researchers found an association observed between the DTP vaccination of preterm infants and a transient increase or recurrence of apnea where they would stop breathing. New England Medical Journal reported in 2001 that the DTP vaccine increases the risk of febrile seizures fivefold on the day of vaccination and that there are significantly elevated risks. According to the Anti-Aging Manual: The Encyclopedia of Natural Health, DTP vaccines may cause Sudden Infant Death Syndrome (SIDS) - 85% in 1 -6 months, same as the 2-4-6-month DTP vaccinations risk; the death rate increases eight times within 3 days of injection; in one study 70% of SIDS deaths occurred within 3 weeks of DTP vaccinations causes reported adverse reactions in 100 per 1000 vaccinations (10%). In a hard hitting editorial in the Indian Journal of Medical Ethics (IJME), Dr. Jacob Puliyel, head of pediatrics at St Stephens Hospital in New Delhi, reports on detailed investigation into the deaths of children in Bhutan, Sri Lanka, India and Vietnam following use of Pentavalent vaccine. This vaccine combines the Diphtheria, Pertussis, Tetanus or DTP vaccine. (See WHO Caught Falsely Stating Pentavalent Vaccine Was Safe After It Was Discontinued In Some Countries Due To Deaths In Children) Several other research citations linking the DTP vaccines to disease have they cause complications in neurological systems, the central nervous system, sudden death, cervical lymphadenitis and convulsions. Former FDA Commissioner David Kessler wrote in the Journal of the American Medical Association that “only about 1% of serious adverse events are reported to the FDA.” This study confirms the systematic under-reporting bias against vaccine adverse reactions. So we could reasonably multiply the incidence in VAERS reports by 100 to get a better handle on the magnitude of the problem. Apparently, no number of VAERS vaccine adverse reaction reports is sufficient to cause the FDA or CDC to raise a red flag or withdraw a vaccine from the market. Sources: iom.edu healthy.net vaccinenewsdaily
Posted on: Sun, 17 Nov 2013 03:49:09 +0000
Trending Topics
Recently Viewed Topics
© 2015