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The Dystopian Future of Canada Part III: PCR and False Positives

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12 minute read

Canada, like the whole world, has seemingly descended into chaos.

At the core of lockdowns across most our country and measures ranging from military implementation to Alberta’s light touch with growing positive test numbers (identified as cases) seemingly out of control is a potentially faulty test methodology.

Recently, a family member tested positive for Covid 19 and as a result, we had the opportunity to examine the test result from the Calgary lab.  However, it was not until we read past the test result that questions started to surface.

As you can see, the specimen type is identified, nasal swab.

The method of testing is identified as NAT or PCR and ‘was performed using primers and probes targeting the E (envelope protein) gene of the SARS-CoV-2 virus DEVELOPED AT ProvLab.’  ProvLab is the Alberta Government testing lab with multiple sites for sample testing.

I was aware that the blue non-surgical masks people use across the world note on the box that they do not stop viruses or virus based infections, a fact which renders them largely useless for Covid prevention but I was not prepared for the disclaimer printed on the bottom of the test which reads:

“This method was validated at ProvLab.  IT HAS NOT BEEN CLEARED OR APPROVED BY THE US FDA OR HEALTH CANADA AND RESULTS SHOULD BE INTERPRETED IN A CLINICAL CONTEXT.”

If this NAT/PCR test has NOT been approved by Health Canada OR the US FDA, then why is Alberta using it and how can we trust the results?  According to the Health Canada website, “unauthorized tests may not produce accurate results, leading to potential misdiagnosis,” which could have dire consequences.

Checking into Health Canada, two facts can easily be found.  Firstly, there are 102 Covid tests ‘under review’ at present, one of which may be this test executed by ProvLab of Calgary.  The tests fall under three broad categories, Antigen, PCR and Serology with rapid and regular kits available to test for Covid 19, SARS and Influenza.

List of testing devices for COVID-19: applications under evaluation – Canada.ca

https://www.canada.ca/en/health-canada/services/drugs-health-products/covid19-industry/medical-devices/authorized/list.html

Two links below notate testing ‘progress’ in Canada:

Health Canada approves first Canadian-made rapid COVID-19 test | Globalnews.ca

Sask. working to identify best version of antibody test that could measure public COVID-19 immunity | CBC News

Potential patients who test positive may not be testing FOR Covid, but rather one of the family of Corona Viruses.  Your mother, father, brother, sister or child could have a regular cold and have the luxury of 2 weeks in lockdown.  There have been circumstances of individuals receiving the influenza vaccine testing positive FOR covid shortly thereafter.

And, a second and third verification from British Columbia and the FDA is below:

 

With a little research by a government friend, I was able to find the following out about the test and results directly from the Health Ministers Office.

“Alberta does not use a commercial test kit for the lab-based reverse transcriptase (RT) polymerase chain reaction (PCR) assay used for diagnostic testing for the SARS-CoV-2 virus. Alberta’s COVID-19 test was developed and validated at Alberta Precision Laboratories (APL) and the test was further validated by the National Microbiology Lab.

All PCR testing involves amplification cycles. The PCR test used in Alberta has been confirmed to be highly specific for SARS-CoV-2. It does not react to other viruses and it cannot amplify a negative sample into a positive.

Alberta is currently evaluation a rapid antigen test, the Abbott PanBio test, for use in Alberta and this test is being used in a limited number of real-world settings. It is important to note that these rapid POC testing technologies are not as sensitive and are limited in their testing capacity when compared with the existing diagnostic test currently used in the province. Due to their limitations, rapid POC tests cannot replace all existing testing and public health measures, and instead will be used to augment current testing program. The Government of Alberta, in partnership with Alberta Health Services, is committed to monitoring evolving testing evidence and technology to improve our testing approach.”

The National Microbiology Lab is Canada’s Level Four lab which signifies that they are able to safely test and respond to the world’s most dangerous infectious diseases such as the Ebola virus, toxigenic e-coli and also highly pathogenic influenzas.  They were briefly mentioned in a 2019 ouster/defection of Chinese scientists including Xiangguo Qiu who was escorted out of the Winnipeg lab in July for a possible “policy breach.”  Qiuu was invited to go to the Wuhan National Biosafety Laboratory of the Chinese Academy of Sciences twice a year for two years, for up to two weeks each time from 2017 to 2019. It has been suggested that this may be the source of the Wuhan Virus (Covid 2019).

Globally, PCR testing is considered to be the ‘gold standard,’ with high accuracy dependant on the sampling methodology.  Yet the CDC has noted that false negatives are more prevalent than false positives.  We must also consider the publicized case of Elon Musk who tested 4 times, 2 negative and 2 positive and the 50 % false results.  Other studies have posited that accuracy may be as low as 10% or as high as 90%, with 20% being more common with 34 cycles for the test.

According to a British Columbia Centre for Disease Control report AND a FDA report, their evidence does not support the ‘gold standard,’ but rather that “The CT scan is not a gold standard for diagnosis of Covid 19 and scan cannot differentiate amongst the many microbiological causes of pneumonia.”  (https://www.fda.gov/media/134922/download)

However, there is one salient point that detection of Covid 19 is dependant upon a purified sample from a patient that is not mixed with monkey or bovine material.  To date, no pure samples are available and upon questioning of 34 jurisdictions (Canada, New Zealand, Australia, Scotland, the United Kingdom, United States (CDC) and others as shared on:

Health Canada has no record of “COVID-19 virus” isolation – Fluoride Free Peel

So, the question can be asked again, if the CDC does not have a pure sample and Health Canada does not have a pure sample, how can tests and vaccinations be produced?  It has been noted widely that it took decades for Polio, the Influenza and other vaccines to be produced, yet we have hundreds of potential miracle cures for Covid 19 in less than a year?  You have to wonder what kind of research and testing has been done?  Is it possible that this really is a manmade virus (that is patented by the CDC) therefore a vaccine can be produced as the model IS known?

One potential answer given for the rapid development of vaccines is the similarity of Covid 19 to SARS and MERS.  Promising research has indicated the presence of an E gene (Protein) that accompanies the virus which seems to accelerate its spread or to act as a retardant and which may be the key to halting its reach.

SARS-CoV-2 E protein is a potential ion channel that can be inhibited by Gliclazide and Memantine – ScienceDirect

 

However, as noted, how long does good testing and development take that does not endanger human lives with potentially fatal unintended consequences?

There is another big story that has not been reported in Western media.  In early November, the Portuguese courts have ruled that the PCR process is not a reliable test for Sars-Cov-2, and therefore any enforced quarantine based on those test results is unlawful and a violation of constitutional rights.

In addition, during their decision they cited a European study that showed that if more than 35 cycles are used in the test that the probability of actually detecting ‘real’  Covid 19 is 3 % and  a 97 % probability for a false positive detection.

Portuguese Court Rules PCR Tests “Unreliable” & Quarantines “Unlawful”

The big question is, if  we believe that a vaccine can help the world in the fight against Covid 19 in so quick a time and that desperate measures are justified in this fight against this unseen (and potentially imaginary) enemy then we are ripe for the Great Reset which has come into public knowledge this year under the guise of medical emergence, a fact which Justin Trudeau himself has made reference to at the UN in September!

If we hearken back to basic science and believe that vaccines cannot stop virus infections but rather good nutrition and healthy immune systems lead to efficient patient recoveries, then the citizens of the world will be able to counter the biological war that is in our borders.

To end off the thread on which this discussion started, on November 27, 2020 my family received a letter from my mothers’ retirement home (Revera) that calm states the following:

November 27, 2020

Dear Resident/Family Member at Aspen Ridge

I am writing to you to confirm that we have had no other residents at Aspen Ridge test

positive for COVID-19. With that being said, we have taken many residents off isolation today

due to a clerical error from AHS that resulted in a false positive reporting.

 

With that teaser, look for part II of Positive Corona Virus Diagnosis Errors…

 

Please feel free to read the first part of this series

 

The Dystopian Future of Canada, Part 2-Corona Virus Testing Cause or Curse? – Todayville

 

 

 

 

 

 

 

 

Tim Lasiuta is a Red Deer writer, entrepreneur and communicator. He has interests in history and the future for our country.

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COVID-19

FDA requires new warning on mRNA COVID shots due to heart damage in young men

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From LifeSiteNews

By Doug Mainwaring

Pfizer and Moderna’s mRNA COVID shots must now include warnings that they cause ‘extremely high risk’ of heart inflammation and irreversible damage in males up to age 24.

The Trump administration’s Food and Drug Administration (FDA) announced it will now require updated safety warnings on mRNA COVID-19 shots to include the “extremely high risk” of myocarditis/pericarditis and the likelihood of  long-term, irreversible heart damage for teen boys and young men up to age 24.

The required safety updates apply to Comirnaty, the mRNA COVID shot manufactured by Pfizer Inc., and Spikevax, the mRNA COVID shot manufactured ModernaTX, Inc.

According to a press release, the FDA now requires each of those manufacturers to update the warning about the risks of myocarditis and pericarditis to include information about:

  1. the estimated unadjusted incidence of myocarditis and/or pericarditis following administration of the 2023-2024 Formula of mRNA COVID-19 shots and
  2. the results of a study that collected information on cardiac magnetic resonance imaging (cardiac MRI) in people who developed myocarditis after receiving an mRNA COVID-19 injection.

The FDA has also required the manufacturers to describe the new safety information in the adverse reactions section of the prescribing information and in the information for recipients and caregivers.

Additionally, the fact sheets for healthcare providers and for recipients and caregivers for Moderna COVID-19 shot and Pfizer-BioNTech COVID-19 shot, which are authorized for emergency use in individuals 6 months through 11 years of age, have also been updated to include the new safety information in alignment with the Comirnaty and Spikevax prescribing information and information for recipients and caregivers.

In a video published on social media, Dr. Vinay Prasad, director of the Center for Biologics Evaluation & Research Chief Medical and Scientific Officer, explained the alarming reasons for the warning updates.

While heart problems arose in approximately 8 out of 1 million persons ages 6 months to 64 years following reception of the cited shots, that number more than triples to 27 per million for males ages 12 to 24.

Prasad noted that multiple studies have arrived at similar findings.

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COVID-19

Court compels RCMP and TD Bank to hand over records related to freezing of peaceful protestor’s bank accounts

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Justice Centre for Constitutional Freedoms

The Justice Centre for Constitutional Freedoms announces that a judge of the Ontario Court of Justice has ordered the RCMP and TD Bank to produce records relating to the freezing of Mr. Evan Blackman’s bank accounts during the 2022 Freedom Convoy protest.

Mr. Blackman was arrested in downtown Ottawa on February 18, 2022, during the federal government’s unprecedented use of the Emergencies Act. He was charged with mischief and obstruction, but he was acquitted of these charges at trial in October 2023. 

However, the Crown appealed Mr. Blackman’s acquittal in 2024, and a new trial is scheduled to begin on August 14, 2025. 

Mr. Blackman is seeking the records concerning the freezing of his bank accounts to support an application under the Charter at his upcoming retrial.

His lawyers plan to argue that the freezing of his bank accounts was a serious violation of his rights, and are asking the court to stay the case accordingly.

“The freezing of Mr. Blackman’s bank accounts was an extreme overreach on the part of the police and the federal government,” says constitutional lawyer Chris Fleury.

“These records will hopefully reveal exactly how and why Mr. Blackman’s accounts were frozen,” he says.

Mr. Blackman agreed, saying, “I’m delighted that we will finally get records that may reveal why my bank accounts were frozen.” 

This ruling marks a significant step in what is believed to be the first criminal case in Canada involving a proposed Charter application based on the freezing of personal bank accounts under the Emergencies Act. 

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