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A Warrior Calls-Christopher James Proves in Court that No Virus Has Ever Been Properly Isolated. Not Just Covid-19, But All Viruses. Legal Evidence Documents Prove It. Conspiracy Fact. Boom...

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THIS IS ONE OF THE BIGGEST BOMBSHELLS IN MEDICAL/SCIENTIFIC/LAW IN HISTORY

He Has Proven in Court, That Not Only Have They Not Isolated and Proven the Existence of Covid-19 Sars Cov2-

THEY HAVE NEVER PROPERLY ISOLATED  A-N-Y  VIRUS

And he has Proven It in Court. See Actual Documents Used In Court below

Christopher James is a One-Man Army of Common Law, and is Fighting a Truly Heroic War. AND HE IS WINNING

He has Proven He Can Win Against the Plandemic Lies in Court
 


CHRISTOPHER JAMES: HOW TO STOP THE VACCINE INSANITY  9-30-2021
A Warrior Calls Archive. See First File In Documents Folder:

A Warrior Calls Archive. See First File In Documents Folder:
 

Christopher James- A Warrior Calls:  COMMON LAW SERVED ON THE HIGH COURT
 

SGTReport:  KNOWLEDGE, HONOR & COURAGE IS THE LIGHT — A WARRIOR CALLS

NOT ONLY IS THIS MEDICAL TEST TRIAL MEANINGLESS-

ALL OF THE VIRUS-RELATED VACCINE TRIALS HAVE BEEN PROVEN MEANINGLESS

OK, The New Oral Vaccine by Merck is an Anti-Viral. That is Great. It Sure as Hell beats Any mRNA Poison Vax.

BUT WTF??? Ivermectine and Hydroxy-Chloroquine are long Approved, Proven Safe and Very Effective in Preventing or Curing all forms of Covid.  AND IT IS VERY CHEAP

(THEY HAD A CURE FOR THE COMMON COLD AND FLU ALL ALONG) BUT KEPT IT HIDDEN

 


Clinical trial produces effective oral antiviral to combat COVID-19

First COVID-19 pill succeeds in clinical trial, seeking emergency use authorization immediately
“With these compelling results, we are optimistic that molnupiravir can become an important medicine as part of the global effort to fight the pandemic,” said the president of Merck.
By Jenna Romaine | Oct. 1, 2021

First COVID-19 pill succeeds in clinical trial, seeking emergency use authorization immediately

Merck and Ridgeback’s Investigational Oral Antiviral Molnupiravir Reduced the Risk of Hospitalization or Death by Approximately 50 Percent Compared to Placebo for Patients with Mild or Moderate COVID-19 in Positive Interim Analysis of Phase 3 Study

Eligibility criteria required that all patients had laboratory-confirmed mild-to-moderate COVID-19, with symptom onset within 5 days of study randomization. All patients were required to have at least one risk factor associated with poor disease outcome at study entry. Molnupiravir reduced the risk of hospitalization and/or death across all key subgroups; efficacy was not affected by timing of symptom onset or underlying risk factor. Additionally, based on the participants with available viral sequencing data (approximately 40% of participants), molnupiravir demonstrated consistent efficacy across viral variants Gamma, Delta, and Mu.

New Merck Pill Vaccine Medical Trial Study is Based Upon False Science, Yet Emergency Use Authorization is Being Fast Tracked

New Merck Pill Vaccine Medical Trial Study is Based Upon False Science, Yet Emergency Use Authorization is Being Fast Tracked

The Big-Pharma Snake Oil Salesman Need To Be Exposed for Scientific Medical Fraud.

A Warrior Calls- Christopher James has Already Proven in Court that Big-Pharma HAS NO PROOF, AND CAN NOT PROVIDE ANY EVIDENCE FOR THE BASIS OF THEIR CLAIMS

IT IS IMPOSSIBLE TO GET OVER THE FIRST HURDLE- AND RETAIN ANY CREDIBILITY
(No Matter What Lies They Tell You)

The Covid-19 Sars Cov 2- HAS NEVER BEEN ISOLATED.  They Cannot Provide an Actual Real Sample of the Virus.
The Entire Basis of the Virus is from Genetic Samples of those Believed to be Infected with Covid-19.  Just Because the Chinese Patients were Sick, DOES NOT PROVE THEY HAD COVID-19. 

And the Official PCR Test Method DOES NOT EVEN LOOK FOR A VIRUS.  It Looks for the Same Genetic Markers that were Found in the So Called Covid-19 Infected Patients in China.

The Additional Problem is, These Genetic Markers are also Naturally Occurring in Humans. And other Animals. This is very likely the Cause of a Vast Number of False Positive Test Results. 

(This is Another Reason to Question the Validity of Any Test Results)

This is why a Goat or a Fruit Can Test Positive for Covid-19.

WITHOUT HAVING AN ACTUAL VIRUS TO COMPARE- ANY TEST IS MEANINGLESS

This also Means they Can’t Prove a Delta Variant or Any Variant Even Exists.
(You Can Not Have a Variant of Something Never Proven to Exist)

So, the Entire Basis of this Study IS MEANINGLESS if the PCR was used. Especially if the PCR Tests went over 30 Cycles. They Conveniently Omitted any Specifics Disclosure of Test Method Details.

Also, if other Test Methods were used such as Antibody Tests-
THEY STILL DO NOT DISTINGUISH BETWEEN COVID-19 OR THE FLU OR THE COMMON COLD
And We All Have These Antibodies.

This will all be a Laughable Joke is it was not a Serious Matter. BUT THIS IS DEADLY SERIOUS
Patients have Not Only Been Lied to and Swindled Out of Hundreds of Trillions of Dollars-

THE EXTENT OF DEATH, SUFFERING AND MISERY IS INCALCULABLE
Take a look how they Perpetuate this Medical Fraud and Criminal Malpractice:

Efficacy and Safety of Molnupiravir (MK-4482) in Non-Hospitalized Adult Participants With COVID-19 (MK-4482-002)

Efficacy and Safety of Molnupiravir (MK-4482) in Non-Hospitalized Adult Participants With COVID-19 (MK-4482-002)
 

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
(The U.S. Government never does an Independent Study to Confirm Results)

Inclusion Criteria:
Has documentation of laboratory confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection with sample collection ≤5 days prior to the day of randomization.

PCR is the preferred method; however, with evolving approaches to laboratory confirmation of SARS-CoV-2 infection, other molecular or antigen tests that detect viral ribonucleic acid (RNA) or protein are allowed if authorized for use in the country. Serological tests that detect host antibodies generated in response to recent or prior infection are not allowed.

Had initial onset of signs/symptoms attributable to COVID-19 for ≤5 days prior to the day of randomization and at least 1 of the following sign/symptoms attributable to COVID-19 on the day of randomization.

Has mild or moderate COVID-19.  Has at least 1 characteristic or underlying medical condition associated with an increased risk of severe illness from COVID-19.

DO YOU UNDERSTAND THAT ANYONE WITH A REASONABLY COMPTENT LAWER CAN WIN ANY COVID RELATED COURT CASE WITH THESE SIMPLE FACTS???

GO TO WAR MY FRIENDS. AND TAKE NO PRISONERS

@OratorBlog   10-3-2021

 

 

 

 

 

 



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