Dr. Lee’s pathology report indicates that Gardasil® material was lodging in tissue and may have been causing health problems. The fact that Gardasil® DNA fragments were suspended in post-mortem blood—and six months post vaccination—indicates there is pathology that HPV vaccine makers did not warn about on the vaccine package inserts as a contradiction. How serious a problem is that for vaccine makers?
In my opinion, it poses a quite serious problem for two reasons. First, the manufacturer went to great lengths to remove all residual HPV DNA from the vaccine, including using a patented process to remove it from the vaccine. They assured regulatory agencies worldwide that there was no ‘viral DNA’ in the vaccine in order to obtain approval for marketing their product. Any way you slice it, HPV DNA is viral DNA – it need not be the complete virus to be viral DNA.
After we reported the presence of HPV DNA in Gardasil® to the FDA, FDA declared without presenting any supportive data that rDNA fragments are an acceptable excipient. The fact is the FDA does not know the physical condition of the HPV DNA or plasmid DNA in the vaccine. The physical condition of naked foreign DNA determines the fate of these DNA fragments and their pathophysiological effects in the human body.
Up to now, the vaccine industry always knew “The FDA specifically requires vaccine developers to show that VLPs [virus-like particles] do not encapsidate “specific” nucleic acid sequences from the expression system, and especially those encoding VLPs components.” (Valley-Omar’s paper)
Second, had Jasmine had wild (natural) HPV in her blood, it would not have lasted very long as the macrophages would have degraded it within a couple of days. Therefore, according to Dr. Lee: “The finding of these foreign DNA fragments in the post-mortem samples six months after vaccination indicates that some of the residual DNA fragments from the viral gene or plasmid injected with Gardasil® have been protected from degradation in the form of DNA-aluminum complexes in the macrophages; or via integration into the human genome. Undegraded viral and plasmid DNA fragments are known to activate macrophages, causing them to release tumor necrosis factor, a myocardial depressant which can induce lethal shock in animals and humans.”
Norma, could that tumor necrosis factor include cancer? Are there other ‘unknowns’?
TNF [tumor necrosis factor] is but one possible byproduct of macrophage activation. To the best of my knowledge, it only affects the heart. Other cytokines also could theoretically be produced as a result of macrophage activation causing other problems – no one knows. Study in this area is relatively new.
No one knows the potential consequences of these foreign DNA fragments remaining in the human body. Can they cause cancer? Can they cause autoimmune disorders? Can they cause birth defects? Can they cause death? No one knows – that is a HUGE problem, in my opinion.
Do you think AAHS [amorphous aluminum hydroxyphosphate sulfate] in Gardasil® can be the primary contributing factor to so many deaths and adverse reactions in young girls who were vaccinated with Gardasil® ? Please elaborate.
Personally, having looked at the results of the clinical trials where the vaccine was tested against the AAHS as a control, I believe it is a strong possibility that AAHS is a contributing factor. The reason being the adverse events during the trials were somewhat evenly distributed between the two groups. Unfortunately, over 70% of all trial participants experienced a ‘new medical condition’ during the trials – which, by the way, is the CDC’s definition of an adverse event.
Folks this is about as serious as it gets IMO. Please take the time to understand this issue as the future of "vaccination" is genetic modification. Please note the reflexive totally unscientific action by our "protector" the FDA to attempt to cover up this horrible mess without even physical examination. These are not people you want to trust your children's life to IMO.