The following is an excerpt from a January 5 AFP report headlined “BREAKING: DOD CONTROLLED COVID ‘VACCINES’ FROM THE START UNDER NATIONAL SECURITY PROGRAM – LIED THE ENTIRE TIME – Were NEVER ‘Safe and Effective’”.
To ensure that the Pharma is free to conduct the fake clinical trials without financial risk, the contracts include the removal of all liability for the manufacturers and any contractors along the supply and distribution chain under the 2005 PREP Act and related federal legislation.
Why is no action by regulators or courts? According to Latypova and Watt, a combination of recently passed legislation and executive orders make it LEGAL to LIE! The HHS Secretary is accountable to no one if the Health National Emergency continues to be extended by Congress every three months.
A significant information operation was set in motion the minute COVID-19 hit. The U.S. government, the intelligence community, the media, and Big Tech colluded to orchestrate and implement an intense pressure campaign designed to get the vaccine legally designated under the Emergency Use Authorization Act while vilifying dissenting doctors, critics, and viable alternative treatments. This designation allowed for speedy manufacturing devoid of the standard safety and public health protocols.
For a vaccine to receive designation under the EUA, there can be no other known treatments or cures. Therefore, many proven treatments such as ivermectin and hydroxychloroquine were blacklisted in the media and dismissed as “horse dewormers” when these cheap, readily available drugs were in the past heralded for their effectiveness.
Eminent COVID-treating doctors such as Peter M. McCullough and Pierre Kory have faced unprecedented attacks on their medical credentials.
Read the report: