Internal CDC records prove that Lilly made the Cutter Vaccine. Lilly and Parke-Davis were the only manufacturers (the two actually only “inactivated” and mixed polio batches made in Canada) for the Francis Field Trial.
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. What are your comments about any similarities in India and what’s going on here in the U.S. now?
[WK] 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. Here is the link to the 12-page HHS/HRSA 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).
In all the years I’ve been researching vaccine data, I often have read of the sordid experiments Salk and others performed on orphaned and disabled children housed in the orphanage facility in Hamburg, Pennsylvania, in the 1940s and ‘50s. That’s the experimental lab venue where those early polio vaccine researchers performed “carte blanche” polio and other vaccines experiments and trials on innocent children. Any comments from your perspective about that, Walter?
[WK] Salk performed such human experimentation under orders from military. Ypsilanti Hospital paled in comparison to the Tuskegee Syphilis Study, the Guatemalan Experiments (which continue to this day), and the Francis Field Trial that justified the use of Salk vaccine.
All were under control of the military with funding from the Rockefeller Foundation. In the Francis Field Trial, Salk defined every case of polio in recipients of the experimental vaccine as caused by wild polio, not from his injection of live polio viruses into them. CDC now touts the Francis Field Trial as the Gold Standard of vaccine field trials.
The Francis Field Trial was the greatest medical fraud in history, I’d say.
The continued use of that bogus modeling can only continue as long as the FDA is allowed to prohibit the use of technology that can diagnose vaccine reactions. An advanced microbial detection array technology with the capability of predicting vaccine reactions has been available to diagnose and even predict vaccine reactions following immunizations for about the last ten years.
[Readers, the reference is to the interview discussing the LLMDA – Lawrence Livermore Microbial Detection Array in the Aug. 4, 2012 Interview link above, per Attorney Kyle.]
What do you know about a process of cell dissociation using trypsin, a proteolytic enzyme that breaks down proteins?
[WK] Trypsin was the chemical that garnered the Nobel Prize for Enders, Robbins and Weller in 1954. Without trypsin wild polio could only infect neural cells (hence Salk’s assumption that injection of live polio viruses could only rarely cause polio if it accessed peripheral nerve cells and worked its way back into the spinal cord). Enders used trypsin to enable polio viruses to infect foreskin tissue from Boston Children’s Hospital. Trypsin changed the nature of the cell’s resistance to infection as well as the nature of the virus.
Trypsin is used to “activate” viruses and enable infection of cells and is widely used in the field of proteomics to cleave protein sequences for Mass Spectrometry analyses.
Salk was wrong and lied about it when testifying before Kennedy at a hearing that preceded the construction of the Vaccine Injury Table, “No cases of polio in 450 million doses of IPV.” Kennedy had to know Salk was lying after the Boston epidemic in 1955 and the Massachusetts Medical Society withdrew their recommendation of immunization with Salk vaccine.
Wasn’t that process used in the Rockefeller Foundation Type1 polio virus Salk vaccine that required trypsinization?
[WK] Trypsin is a pancreatic extract from pigs or cows that is used in digestion. In polio vaccine production it was used historically in three stages..
For classical polio vaccine production using individual monkeys, trypsin is used in three distinct stages:
First Stage a live monkey would be infused with trypsin to dissolve the binding materials inside its kidneys and allow the cells to flow out into a flask.
Second Stage when the cells were grown out in Modified Eagle medium, trypsin was used to dissolve any binding materials and allow the cells to grow in a smooth monolayer.
Third Stage in the final stage, after a monolayer of cells are grown out, trypsin is added to allow the polio viruses to infect the cells by modification of the cell membrane and potentially the vaccine strain virus also.
75-85% of the porcine trypsin used in vaccine production in the EU and US is contaminated with circoviruses that replicate in a way reminiscent of auto-immune disease outbreaks. Trypsin also allows any other monkey viruses present in the kidney cells to access them like polio viruses, SV-40, for example in Salk IPV of the 1950s. Simian Immunodeficiency Viruses, Epstein Barr Virus, Cytomegaloviruses and Simian Agent 8 (HSV-1 & 2, genital herpes) were just a few of the 20+ other viruses carried by the monkeys used in Sabin vaccine production that used all three stages of trypsin.
Julius Youngner, Salk’s assistant, discovered trypsin allowed polio to infect monkey kidney cells, a plentiful source for massive vaccine production.
Salk made the assumption, based on this history, that injections containing live polio viruses would not cause systemic infections (flu, fevers, excretion in the stool), and rarely cause paralysis if the injected virus accessed a nerve cell and moved backwards into the spinal cord (retrograde atonal transport).
But trypsin changed the nature of injected viruses, and according to Langmuir, caused multiple systemic infections per his June 30, 1955 Memo entitled “Poliomyelitis Vaccine Assessment.” That appears poignant to today’s AFM outbreak where synthetic trypsin (Medium 199) is injected with the vaccine viruses.
Did trypsinization cause retrograde axonal transport that leads to injection limb paralysis, which was similar to the Salk outbreaks in California and Boston? What can you tell us about any victims of those outbreaks?
Historically, Salk expected retrograde atonal transport would result if a live injected virus accessed a nerve and made its way back to the spinal cord, which would result in injection limb or opposite injected limb paralysis as the first sign of poliomyelitis. Note that paralytic polio caused by wild virus was systemic and classically began in one of the lower legs, then the other and moved up the body, thus it was diagnosed as asymmetric, ascending flaccid paralysis.
It is important to emphasize that most of the victims were family members, or classmates, of the recipient of the vaccine who might never be paralyzed but the recipient’s systemic infections could paralyze people in close personal contact with them. The Vaccine Injury Table recognizes the phenomenon.
Most of the victims of the polio virus in Salk Vaccine (which was also contaminated with SV-40) were contacts of the recipient. These victims’ paralysis arose from the systemic infection of the recipient – not retrograde axonal transport that involved either the injection itself or spread from the recipients to simultaneously M-199 injected Placebos in the Francis Field Trial.
Fathers acquired polio from Salk vaccine in the Boston epidemic at a higher rate than Mothers of injected children – a unique anomaly that is consistent with the first case of AFM in the 29-year-old father of an immunized child.
BOSTON – Summer of 1955 – after “The Cutter Incident.”
The Parke Davis (Lot 1018) rework in Boston and Wisconsin involved over 7000 cases of poliomyelitis. Over 400,000 cases may have occurred in Massachusetts alone, including the non-paralytic events. All BOSTON Hospitals shut down non-emergency services to care for victims of the Salk vaccine.
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