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An overview of recent changes to some of the documentation from the CDC and the FDA on the COVID tests, the vaccines, as well as a selection of other related news sources.
On June 12, the FDA issued an order to "Stop Using Innova Medical Group SARS-CoV-2 Antigen Rapid Qualitative Test." The reason cited as, "The FDA has significant concerns that the performance of the test has not been adequately established, presenting a risk to health." [Page 1 of Ref 1]
On July 21, CDC update the instructions for the PCR test. Essentially, the PCR test is worthless. Note the following highlights on pages 37 & 38 of reference 2:
Positive and negative predictive values are highly dependent on prevalence. False-negative test results are more likely when prevalence of disease is high. False-positive test results are more likely when prevalence is moderate to low.
Detection of viral RNA may not indicate the presence of infectious virus or that 2019-nCoV is the causative agent for clinical symptoms.
The performance of this test has not been established for monitoring treatment of 2019-nCoV infection.
The performance of this test has not been established for screening of blood or blood products for the presence of 2019-nCoV.
This test cannot rule out diseases caused by other bacterial or viral pathogens.
Further, note the highlight on page 40, reference 2, which for all intents and purposes, states that 2019-nCov has not been isolated and that the reference for detection is at best a guess.
Since no quantified virus isolates of the 2019-nCoV were available for CDC use at the time the test was developed and this study conducted, assays designed for detection of the 2019-nCoV RNA were tested with characterized stocks of in vitro transcribed full length RNA (N gene; GenBank accession: MN908947.2) of known titer (RNA copies/µL) spiked into a diluent consisting of a suspension of human A549 cells and viral transport medium (VTM) to mimic clinical specimen.
On Jul 8, the FDA updated the fact sheet for the Jennsen "vaccine" to include the following side effects, see pages 3 & 4 of reference 3:
Blood Clots with Low Levels of Platelets
Blood clots involving blood vessels in the brain, lungs, abdomen, and legs along with low levels of platelets (blood cells that help your body stop bleeding), have occurred in some people who have received the Janssen COVID-19 Vaccine. In people who developed these blood clots and low levels of platelets, symptoms began approximately one to two-weeks following vaccination. Reporting of these blood clots and low levels of platelets has been highest in females ages 18 through 49 years.
These may not be all the possible side effects of the Janssen COVID-19 Vaccine. Serious and unexpected effects may occur. The Janssen COVID-19 Vaccine is still being studied in clinical trials.
Guillain Barré Syndrome
Guillain Barré syndrome (a neurological disorder in which the body’s immune system damages nerve cells, causing muscle weakness and sometimes paralysis) has occurred in some people who have received the Janssen COVID-19 Vaccine. In most of these people, symptoms began within 42 days following receipt of the Janssen COVID-19 Vaccine.
Last week, on August 12, the FDA updated the fact sheets for both the Moderna and the Pfizer-BIONtech "vaccine" to include the following side effects. There is similar verbiage in each, see highlights within reference 4 and reference 5:
Myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining outside the heart) have occurred in some people who have received the Moderna/Pfizer-BIONtech COVID-19 Vaccine. In most of these people, symptoms began within a few days following receipt of the second dose of the Moderna COVID-19 Vaccine.
These may not be all the possible side effects of the Moderna COVID-19 Vaccine. Serious and unexpected side effects may occur. The Moderna COVID-19 Vaccine is still being studied in clinical trials.
These may not be all the possible side effects of the Pfizer-BioNTech COVID-19 Vaccine. Serious and unexpected side effects may occur. Pfizer-BioNTech COVID-19 Vaccine is still being studied in clinical trials.
In a study from December, Cardozo and Veazey highlight the fact that vaccinees will develop antibody-dependent enhancement (ADE) putting them at higher risk of future infections. [Ref 6]
The elicitation of antibodies, specifically neutralising antibodies, is the goal of nearly every current SARS-CoV-2 vaccine candidate. The prior evidence that vaccine-elicited, antibody-dependent enhancement (ADE) of disease is likely to occur to some degree with COVID-19 vaccines is vertically consistent from controlled SARS studies in primates to clinical observations in SARS and COVID-19. Thus, a finite, non-theoretical risk is evident in the medical literature that vaccine candidates composed of the SARS-CoV-2 viral spike and eliciting anti-SARS-CoV-2 antibodies, be they neutralising or not, place vaccinees at higher risk for more severe COVID-19 disease when they encounter circulating viruses.
Furthermore, the authors stress that, "This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID-19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials."
Note from above that all three "vaccines" are still in clinical trials.
From Catherine Austin Fitts's group, this excellent form present questions for employers to consider wrt the "vaccine." [Ref 7]
Additionally....
In an interview from May, Luc Montagnier, a French virologist and recipient of the 2008 Nobel Prize in Medicine, "referred to the vaccine program for the coronavirus as an “unacceptable mistake.” Mass vaccinations are a “scientific error as well as a medical error,” he said. “The history books will show that, because it is the vaccination that is creating the variants.”"
In a report from August 6, concerning a case in Barnstable County, Massachusetts, "Among the 469 cases in Massachusetts residents, 346 (74%) occurred in persons who were fully vaccinated..."
Even the failing New York Times has had to admit that the vax is not working, and that Israel, with one of the highest vaccination rates on the planet, is facing a surge of infections.
On Friday, August 7th, Dr. Dan Stock, an Indiana Functional Family Medical Physician, specially trained in Immunology and Inflammation Regulation, spoke to the Mt. Vernon School Board, detailing his concerns about masks and other Covid-19 protocols. In his 6:47 presentation listen as he makes his position clear. “We’re doing things that are not useful.” “Everything being recommended by the CDC and the State Board of Health is actually contrary to all the rules of science.” “You cannot make these viruses go away.” “Vaccination changes none of this.”
I strongly encourage you to watch this video.
And the there is this bombshell today from the talking head CDC Director Walensky, who just told the world: "INCREASED risk of SEVERE disease amongst those VACCINATED early.” As Emerald Robison, put it so nicely,
That's game, set and match to the people who warned you about experimental gene therapies with no long term studies done.
Finally, Dr. Janci Lindsey posted this on LinkedIn about two weeks ago:
It’s way past time to wake up folks.
Namaste, thanks for reading, and keep fighting tyranny.
Mark
August 19, 2021
References
1] FDA Safety Communication of June 10, 2021
2] CDC PCR Test Instructions of July 21, 2021
3] Janssen COVID-19 Vaccine Fact Sheet of July 8,2021
4] Moderna COVID-19 Vaccine Fact Sheet of August 12, 2021
5] Pfizer-BioNTECH COVID-19 Vaccine Fact Sheet of August 12, 2021
6] “Informed Consent…,” Cardozo and Veazey, December 4, 2020
7] Form for Employees Whose Employers Are Requiring Covid-19 Injections
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