Prior to 2017, neither HHS nor WHO performed the kind of study necessary to ascertain whether the DTP vaccine was actually yielding the beneficial health outcomes about which Gates frequently boasts. That year, the Danish government and the Scandinavian vaccine behemoths, Statens Serum Institut19 and Novo Nordisk, commissioned prominent Scandinavian scientists S?ren Mogensen and Peter Aaby— both vocal champions of the Africa vaccine program—to lead an illustrious team of international researchers to examine all-cause mortalities after the DTP inoculations.
That massive study put the lie to Gates’s mantric incantation that his investment in the DTP vaccine has saved millions of lives. In June 2017, the team published a peer-reviewed study in EBioMedicine, a high-gravitas journal in Elsevier’s publishing house armada. The article parsed data from a so-called “natural experiment” in Guinea Bissau, where half the children in certain age groups were vaccinated and the other half were not. The division was randomized.
That 2017 study (Mogensen et al., 2017)20 shows that, following their DTP immunization at three months, vaccinated girls had tenfold higher mortality than unvaccinated children. The girls were dying of a wide range of diseases—pneumonia, anemia, malaria, dysentery—and for two decades no one noticed that the dying children were predominantly those who received the vaccine. The DTP vaccine—while protecting children against diphtheria, tetanus, and pertussis—had ruined their immune systems, making them vulnerable to a wide range of deadly nontarget infections. Mogensen’s team arrived at that conclusion, as had the 1977 Lancet study researchers exactly forty years earlier: “DTP vaccine may kill more children from other causes than it saves from diphtheria, tetanus or pertussis.”21
In other words, Gates’s DTP vaccine—instead of saving 10 million lives, as he claims22—may have unnecessarily killed millions of African girls. At least seven other studies have confirmed DTP’s association with high mortality in vaccinated girls compared to unvaccinated.23 The idealistic Americans who donated to Gates’s African vaccine project—believing they were saving African babies—were actually funding a continent-wide female genocide.24
After completing the study and verifying its shocking results, Peter Aaby—a virtual deity among African vaccine researchers—made an impassioned, and remorseful, plea to the WHO to reconsider the DTP vaccine. “I guess most of you think that we know what our vaccines are doing,” he said. “We don’t.”25
Gates, WHO, and GAVI ignored Aaby’s appeal and redoubled their efforts to expand DTP vaccinations and to shore up support for the girl-killing jab. The Lancet published a commentary by Gates Foundation plenipotentiary Chris Elias, Dr. Anthony Fauci, and three apparatchiks from lesser Gates-funded consortia, WHO’s Margaret Chan, UNICEF’s Director Anthony Lake, and Seth Berkley of GAVI, who portray their deadly African DTP program as a public health triumph. These charlatans proclaimed DTP as one of the “bright spots” in global well-being and gasconaded that “more children are being immunized worldwide than ever before with the highest level of routine coverage in history (as measured by coverage of three doses of the diphtheria-tetanus-pertussis (DTP)-containing vaccine).”26 That project also involved reputationally demoting Aaby with a defamation campaign.
A subsequent expert review by the founder of the Cochrane Collaborative, Peter G?tzsche, condemned the WHO’s attempt to downplay the risks of DTP vaccine. The WHO, he observed, had been dismissive of studies finding detrimental nonspecific effects for the DTP vaccine while accepting studies finding beneficial nonspecific effects for the measles vaccine. The WHO is “inconsistent and biased toward positive effects of vaccines. When a result pleases the WHO, it can be accepted, but not when a result does not please the WHO.”27 G?tzsche found the studies by Mogensen and Aaby “superior in every respect to the Gates-generated Lancet study.”
Gates and his WHO vassals continue to bully African nations into taking their lethal DTP vaccines by threatening to withdraw financial aid to their health departments and HIV programs if the government fails to achieve national uptake targets (90 percent).
Mercury Rising
Many vaccines shipped to underdeveloped countries—including the hepatitis B, haemophilus influenzae type B, and DTP inoculations—contain bolus doses of the mercury-based preservative and adjuvant thimerosal.28
The immunity provisions of the 1986 Vaccine Act gave a blank check to US pharmaceutical companies to promote the most shoddily tested vaccines without consequences or cost. Pharma responded with a gold rush to add new lucrative vaccines to the schedule, and by 1991, mercury exposures to US children from the vaccine preservative thimerosal had more than doubled.29 Parents, physicians, and researchers blamed a subsequent explosion of neurological and autoimmune disease on thimerosal.
Alarmed at the exploding epidemics of neurodevelopmental, allergic, and autoimmune diseases in children that began in 1986, CDC commenced in 1999 an in-house study of the vast repository of health and vaccination data from the ten largest HMOs stored in the Vaccine Safety Datalink (VSD). A specially assembled CDC research team led by Belgian epidemiologist Thomas Verstraeten compared health outcomes in hundreds of thousands of vaccinated versus unvaccinated children. The raw data from CDC’s 1999 Verstraeten study showed that children who took thimerosal-containing hepatitis B vaccines in their first thirty days suffered an astonishing 1,135 percent higher rate of autism than children who did not.30 Verstraeten also documented a grim inventory of other neurological injuries including ADD/ADHD, speech and language delays, tics, and sleep disorders in children exposed to thimerosal. Verstraeten reported that these shocking signals prompted him to review, for the first time, the published medical literature, where he confirmed the alarming toxicity of mercury (thimerosal) to cause these injuries was biologically plausible.
Overwhelming science—over 450 studies—by then attested to thimerosal’s devastating toxicity.31 Because testosterone amplifies the neurotoxicity of the mercury molecule, boys disproportionately suffered reduced IQ and a range of developmental disorders—ADD, ADHD, speech delay, tics, Tourette’s syndrome, narcolepsy, ASD, and autism following exposure to ethylmercury in thimerosal. Numerous studies link thimerosal to miscarriage and Sudden Infant Death. There is simply no study ever published that demonstrates thimerosal’s safety.