Take Another Swig

Who knew that taking the experimental chemical goo clot shot also allowed one to practice their faith in the cult of the cornholio. Believe in all they say without seeing any long term studies on their poison. Believing without seeing…can we get an amen?

Sadly now, some who trusted the high end talent from Hell to fight off a virus with a 99% recovery rate with an injection of the likes of battery acid, will have to enlist the eyes of others for seeing….on a permanent basis:

Many People Fully Vaccinated for Covid Are Now Going Blind – via globalresearch.ca

Wait…wuuuut!  Was that listed as a side effect?  Come on, shitposting writer, true believers don’t believe in side effects other than the ones they might experience upon hearing the truth. When that happens….clear the path to the shitter.

The latest data out of the United Kingdom suggests that a growing number of fully jabbed people are losing their eyesight. The Medicines and Healthcare products Regulatory Agency (MHRA) Yellow Card system currently shows 163 cases of total blindness among people who got jabbed with the Pfizer-BioNTech needle, along with an additional six cases of central vision loss and four cases of sudden visual loss.

Twenty-one people also reportedly now suffer from “blindness transient” specifically caused by the Pfizer injection. This adverse reaction involves visual disturbance or loss of sight in one eye for a few seconds or even minutes at a time.

Another 20 people beyond that are reported to have suffered from a reaction called “unilateral blindness,” which is when a person got blind or blurred vision in just one eye.

“In total, there have been 8,016 eye disorders reported as adverse reactions to the Pfizer jab as of 6th April 2022,” reported the Daily Exposé.

Meanwhile, it’s just not the jabs that can bring on Father Time’s dirt nap, Big Pharma has a whole lotta of other fuckery at their disposal to ensure you too might suffer from the crap they produce that you pay for.

Children’s Health Defense demands FDA withdraw its approval of Remdesivir for infants and children, citing 72% adverse events rate

WASHINGTON, D.C. (Children’s Health Defense) – The U.S. Food and Drug Administration (FDA) announced on April 25 its approval of remdesivir (Veklury), an antiviral treatment for COVID in infants 28 days and older who weigh at least 7 pounds and are either hospitalized with a positive COVID test or have mild to moderate COVID and are at “high risk” for progression to severe disease or death. The approval came despite a lack of short- and long-term data to support that remdesivir is effective or safe for young children.

Remdesivir, developed by Gilead Sciences, is known to be highly toxic in adults. A study published in the New England Journal of Medicine found “serious adverse events were reported in 131 of the 532 patients who received remdesivir (24.6%).”

According to an FDA press release, its decision to approve the therapy is supported by a clinical study conducted on infants four weeks and older weighing a minimum of 6.6 pounds. However, the study won’t be completed until February 2023. Gilead Sciences issued its own press release the same day regarding the study and provided the following details on what the study has found so far:

  • A total of 53 hospitalized pediatric patients were enrolled in the clinical study
  • 72% suffered adverse events
  • 21% suffered serious adverse events determined to be unrelated to the drug
  • Three children died from either underlying conditions or COVID-19

Will you hear of any of this from the corporate media?  Naw! Too much other propaganda to peddle.

Is keeping information from the public considered misinformation?  Probably…fits in with the present state of the vaudeville.


“All the good music has already been written by people with wigs and stuff.” ― Frank Zappa


Tonight’s musical offering:

Mozart: Serenade No 10 for Winds ‘Gran Partita’, III. Adagio | London Symphony Orchestra Wind Ensemble

Photo by Lena Balk on Unsplash

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