This devastating article exposes just how pernicious and genocidal TPTB are when it comes to imposes unconscionable medical tyranny on the population.

by axolotl_peyotl

Vaccines appear to be at the heart of this genocide, as their connection to the military industrial complex is palpable.

“Polio” was merely reclassified in the 50’s to mask the fact that the vaccine was increasing polio outbreaks.

To hide this horrific disaster of a vaccine campaign, “polio” was reclassified as a number of other conditions, so on paper it appears that the vaccine was reducing polio cases, when in fact the opposite was true (they were just not calling them “polio”).

via activistpost:

Poliomyelitis and Acute Flaccid Myelitis are the same. “Infantile Paralysis” was also poliomyelitis or polio for short.

AFM has developed from a minor variation in the Salk Type-1 (Mahoney) strain of vaccine virus that has been renamed as EV-D68 and appears following the switch to Medium 199 in Ipol, the Sanofi-Pasteur vaccine now used exclusively in the U.S.

Medium 199 (M-199) is a synthetic trypsin apparently used to provide enhanced potency IPV. Trypsin traditionally was required in the final stage of polio vaccine production to enable polio virus infection of the monkey kidney cells.

Curiously it also happened to be the solution injected into the Placebo group during the Francis Field Trial. The Placebo group acquired polio from the Salk vaccine being tested at twice the rate of the Recipients injected with Salk IPV and matched the reported incidences of polio victims who acquired polio from recipients of Salk vaccine in “The Cutter Incident.”

Trypsin is also used in proteomics to cleave protein sequences for proteomic analyses.

When placed in the final vaccine injection, it may break down cells and cleave sequences of the injected viruses simultaneously. This would theoretically enhance potency but also provide an infectious path for variants of the injected viruses.

Paraphrasing Albert Sabin’s comment on Salk’s injected vaccine, you can’t get an antibody response without a live virus in the vaccine. M-199 is designed to enhance that response; AFM is the result.

Keep in mind here that Salk and Sabin both were under the direct control of the military, which financed the development of the polio and measles vaccines through the infectious disease laboratory at Boston Children’s Hospital.

Nobel Laureates John Enders, Fredrick Robbins and Thomas Weller, who developed the trypsinization technique that made mass production of polio vaccine possible and gained them the 1954 Nobel Prize, were also under direct control of the military, which financed their projects.

According to CDC’s Alexander Langmuir, Salk believed you could actually inject live polio viruses into people and they would acquire polio only rarely if the injected live virus accessed a peripheral nerve but would never cause systemic infection that could spread to those in contact with the vaccine recipient. (June 30, 1955 Assessment of Poliomyelitis Vaccine by Langmuir)

That was Langmuir’s assessment in June 1955 after the Cutter Incident that arose immediately after licensure of Salk IPV following the Francis Field Trial.

Soon after Cutter in the summer of 1955 a Parke-Davis Salk vaccine caused polio (aka Acute Flaccid Myelitis) in over 4000 in Massachusetts and several thousand in other states. Keep in mind that most cases arose in contacts of the vaccine recipients at double the rate of polio in the actual vaccine recipient.

CDC never admitted to those epidemics, safety of the vaccine was concocted by Langmuir’s “epidemiological analyses” on behalf of his military overseer. These outbreaks of AFM appear as another minor glitch in a fundamentally flawed immunization program in which the Francis Field Trial is considered the “Gold Standard.”

Back in 2011, the country of India had a similar occurrence when 47,500 children were stricken by a polio-like paralysis, which occurred during/after the Bill and Melinda Gates Foundation polio vaccination campaign to India, a country where polio previously had been declared eradicated.

Interestingly, Jeff Almond proved in 1988 that the Type-3 strain of the live polio vaccine reverted to wild polio potency within two days of administration. These cases would be defined as caused by the vaccine under the Vaccine Injury Table.

Thus one can conclude, based on the experience in India, that the term Acute Flaccid Myelitis (AFM) is a deceptive moniker for the traditional diagnosis of Vaccine Acquired Paralytic Poliomyelitis (VAPP).

 

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