By  The Defender Staff

Using vaccine “shortages” as an excuse, the U.S. Food and Drug Administration arranged a liability shield for the Jynneos monkeypox vaccine by issuing a new Emergency Use Authorization for “fractional doses” using a different mode of administration, and allowing the vaccine’s use in “high risk” children under age 18.


Just like the coronavirus Event 201, the reported monkeypox outbreak was prefigured by a “tabletop simulation” one year prior and by “suspiciously” timed, before-the-fact clinical trials of monkeypox treatments and vaccines.

With the “outbreak” thus positioned in the headlines, what happened next?

  • After allowing suspense to build for a couple of months but with fewer than a dozen deaths worldwide, the World Health Organization (WHO) head Tedros Adhanom Ghebreyesus in late July “side-stepped” his own advisors to pronounce monkeypox a “public health emergency of international concern,” the WHO’s first such