The great Ivermectin deworming hoax

Via The Desert Review

Ivermectin hoax

 Can You Spot the Fake?

“In a normal year, the Kentucky Poison Control Center might receive one call from someone who has taken ivermectin, a drug commonly used to treat parasites in livestock. But amid increasing misinformation about the drug’s ability to both treat and prevent COVID-19, that number has increased to six this year.”

This alarming news was published in Spectrum News – formerly known as Time Warner Cable – on August 24, 2021, and should be a lesson to every American.

https://spectrumnews1.com/ky/louisville/news/2021/08/24/ivermectin-calls-to-kentucky-poison-control-are-up

The lesson is not about Ivermectin being poisonous because it isn’t, but about the pervasiveness of a type of new internet propaganda termed “informational flooding.”

https://dash.harvard.edu/bitstream/handle/1/12274299/Roberts_gsas.harvard_0084L_11469.pdf?sequence=1

In an even more “alarming” report, NPR wrote,

“Minnesota’s Poison Control System is dealing with the same problem. According to the department, only one Ivermectin exposure case [telephone call] was reported in July, but in August, the figure jumped to nine.”

https://www.npr.org/sections/coronavirus-live-updates/2021/09/04/1034217306/ivermectin-overdose-exposure-cases-poison-control-centers

Are you kidding me? Nine telephone calls are enough to make the news? We have 2,213 deaths on August 26 from COVID-19, but these nine telephone calls are enough to make the headlines?

Continue reading “The great Ivermectin deworming hoax”

Follow the Money

Guest Post by Thaisleeze

Something I have seen referenced on several blogs is the claim that alternative treatments such as HCQ and Ivermectin, if shown to be successful, would negate the EUA for Wuflu vaccines which would then have to wait years for full FDA approval. My research found this on a USA dot gov blog;

The COVID-19 vaccines from Pfizer, Moderna and Johnson & Johnson have all received an Emergency Use Authorization (EUA) from the FDA. EUAs may be granted only during a public health emergency and when there are no adequate, approved, and available alternatives.

Approval versus Emergency Use Authorization (EUA): What’s the difference?

Is this the reason that solutions other than vaccines are fought against so bitterly? Profits before health? Hundreds of billions profit over the next 5 years versus life saving solutions via approved, available and patent expired alternatives providing little or no profit for big pharma? Difficult for normal folk to conceive evil to this extent but entirely possible in a world where corporations have captured the FDA, CDC, WHO etc. via the “revolving door” and have the power to dictate to governments.

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FDA reverses itself: rejects COVID antibody test results; insanity reigns

Guest Post by Jon Rappoport

Even a robot programmed to “follow the science” would throw up his hands in despair while reading the latest FDA COVID pronouncement.

After untold numbers of people have been given antibody tests to determine their COVID status, the FDA now states:

Today, the U.S. Food and Drug Administration issued a safety communication informing the public that results from SARS-CoV-2 antibody tests should not be used to evaluate immunity or protection from COVID-19 at any time, and especially after the person received a COVID-19 vaccination.”

Boom.

Continue reading “FDA reverses itself: rejects COVID antibody test results; insanity reigns”