Mandating hpv vaccination arguments
Natural News has also learned that HPV vaccines have been proven to be flatly worthless in clearing the HPV virus from women who have already been exposed to HPV (which includes most sexually active women), calling into question the scientific justification of mandatory “vaccinate everyone” policies.Furthermore, this story reveals evidence that the vaccine currently being administered for HPV — Gardasil — may increase the risk of precancerous cervical lesions by an alarming 44.6 percent in some women.Hi Fi DNA Tech has been trying to get its HPV detection device downgraded to a Class II device based on the following arguments: • For more than 20 years, the FDA had regulated the HPV test as a “test for cervical cancer.” • But since at least 2003, the FDA has changed its position on the relationship between Human Papilloma Virus and cervical cancer, stating that the HPV strain is “not associated with cervical cancer.” • Accordingly, Hi Fi DNA Tech is arguing that the HPV test it has developed — a shift that makes the test far more reliable in its primary purpose.In other words, the test is merely detecting the presence of a virus, not making a diagnosis of a disease (which would be a much higher standard to meet).
In other words, since 2003 the scientific staff of the FDA no longer considers HPV infection to be a high-risk disease when writing educational materials for the general public whereas the regulatory arm of the agency is still bound by the old classification scheme that had placed HPV test as a test to stratify risk for cervical cancer in regulating the industry.In order for such a device to be marketed to the public, it must be downgraded to Class II status, which is considered a “special controls” status.Class II devices are, “…those devices for which the general controls by themselves are insufficient to provide reasonable assurance of safety and effectiveness, but for which there is sufficient information to establish special controls to provide such assurance, including performance standards, postmarket surveillance, patient registries, development and dissemination of guidelines, recommendations, and any other appropriate actions the agency deems necessary.” In other words, a Class II device may or may not actually be safe, but the FDA considers is safe enough to release to the public.• Why mandatory HPV vaccination policies may cause great harm to young girls.• Why HPV infections are self-limiting and pose no real danger in healthy women • Little-known FDA documents that reveal astounding facts about Gardasil • How Big Pharma promoted its Gardasil vaccine using disease mongering and fear mongering Click the NEXT button below to continue reading…
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To understand why this is a big deal, you have to understand the differences between “Class II” and “Class III” virology testing devices.