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You are here: Home / Science Supporting Vaccine Risk / Death

Death

  • Autoimmune Tissue Scurvy Misdiagnosed as Child Abuse Some doctors are unaware of the pathophysiological processes of autoimmunity, haemostasis and osteogenesis and are misdiagnosing vaccine induced Tissue Scurvy, absence of Vitamin C within the cell, as Non-accidental Injury.
  • Comparison of VAERS fetal-loss reports during three consecutive influenza seasons: was there a synergistic fetal toxicity associated with the two-vaccine 2009/2010 season? it is biologically plausible that during the two-vaccine 2009/2010 influenza season, when pregnant women were administered two Thimerosal-containing influenza vaccines each delivering 50 mcg of Thimerosal (or 25 mcg of mercury per dose), the fetus’ mercury dose exceeded the EPAs reference dose (0.1 mcg of mercury/kg/day). This overexposure could be a significant contributing factor to some of the reported SABs [spontaneous abortions] and SBs [stillbirths]. Moreover, the mercury in injected Thimerosal-containing vaccine doses has been found to preferentially bioaccumulate in the fetal tissues….depending upon the gestational age, the safety level of mercury (as specified by the EPA’s reference dose) may be exceeded by several thousand fold for an early developing fetus during the first trimester. And, a synergistic fetal toxicity likely resulted from the administration of both the pandemic (A-H1N1) and seasonal influenza vaccines during the 2009/2010 season.
  • Maternal transfer of mercury to the developing embryo/fetus: is there a safe level? Current Hg exposure advisories do not appear to account for (or offer protection of) developing embryos and fetuses which are exposed to Hg via maternal (placental) transfer. Data presented suggest that fetal Hg exposure is intolerably high even under conservative scenarios of maternal exposure and placental transfer. Critical perusal of the data demonstrates that available Hg crossing the placenta throughout the entire gestation period following a single fish consumption event ranges between 6 and 6,000,000 times higher than the USEPA RfD [US Environmental Protection Agency reference dose] maximum recommended daily exposure for MeHg, even under conservative exposure and placental transfer scenarios. The equavalent fetal Hg exposure following a single SEMT-preserved [Thimerosal-preserved] maternal influenza vaccination ranges between 1 and 1,000,000 times higher than the USEPA RfD maximum. There is, therefore, no safe level of maternal transfer of Hg to a developing human embryo/fetus.
  • Fatal varicella due to the vaccine-strain varicella-zoster virus We describe a death in a 15-mo old girl who developed a varicella-like rash 20 d after varicella vaccination that lasted for 2 mo despite acyclovir treatment. The rash was confirmed to be due to vaccine-strain varicella-zoster virus (VZV). … The patient developed severe respiratory complications that worsened with each new crop of varicella lesions; vaccine-strain VZV was detected in the bronchial lavage specimen. Sepsis and multi-organ failure led to death.
  • Prolonged measles virus shedding in human immunodeficiency virus-infected children, detected by reverse transcriptase-polymerase chain reaction Prolonged measles virus shedding did not correlate with levels of measles virus-specific antibody. HIV-infected children with measles may have a prolonged infectious period that potentially enhances measles virus transmission and hinders measles control. … Although not statistically significant, boys were more likely to have prolonged measles virus shedding than girls. Other investigators have observed differences between boys and girls in relation to clinical and immunologic responses to measles and measles vaccine. Increased mortality in girls was observed after administration of high-titer measles vaccine. [Emphasis ours.]

(Also see the HPV Vaccine section of Vaccination with Specific Vaccines and the Vaccine Failure section of Vaccine Failure and Ability to Transmit Disease.)

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