COVID-19
The Dystopian Future of Canada Part III: PCR and False Positives

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
Two links below notate testing ‘progress’ in Canada:
Health Canada approves first Canadian-made rapid COVID-19 test | Globalnews.ca
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.
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
COVID-19
Study finds Pfizer COVID vaccine poses 37% greater mortality risk than Moderna

From LifeSiteNews
A study of 1.47 million Florida adults by MIT’s Retsef Levi and Surgeon General Joseph Ladapo finds significantly higher all-cause mortality after Pfizer vaccination compared to Moderna
A new study of 1.47 million Florida adults by MIT’s Retsef Levi and Surgeon General Joseph Ladapo finds significantly higher all-cause, cardiovascular, and COVID-19 mortality after Pfizer vaccination.
The study titled “Twelve-Month All-Cause Mortality after Initial COVID-19 Vaccination with Pfizer-BioNTech or mRNA-1273 among Adults Living in Florida” was just uploaded to the MedRxiv preprint server. This study was headed by MIT Professor Retsef Levi, with Florida Surgeon General Dr. Joseph Ladapo serving as senior author:
Study Overview
- Population: 1,470,100 noninstitutionalized Florida adults (735,050 Pfizer recipients and 735,050 Moderna recipients).
- Intervention: Two doses of either:
- BNT162b2 (Pfizer-BioNTech)
- mRNA-1273 (Moderna)
- Follow-up Duration: 12 months after second dose.
- Comparison: Head-to-head between Pfizer vs. Moderna recipients.
- Main Outcomes:
- All-cause mortality
- Cardiovascular mortality
- COVID-19 mortality
- Non-COVID-19 mortality
All-cause mortality
Pfizer recipients had a significantly higher 12-month all-cause death rate than Moderna recipients — about 37% higher risk.
- Pfizer Risk: 847.2 deaths per 100,000 people
- Moderna Risk: 617.9 deaths per 100,000 people
- Risk Difference:
➔ +229.2 deaths per 100,000 (Pfizer excess) - Risk Ratio (RR):
➔ 1.37 (i.e., 37% higher mortality risk with Pfizer) - Odds Ratio (Adjusted):
➔ 1.384 (95% CI: 1.331–1.439)
Cardiovascular mortality
Pfizer recipients had a 53% higher risk of dying from cardiovascular causes compared to Moderna recipients.
- Pfizer Risk: 248.7 deaths per 100,000 people
- Moderna Risk: 162.4 deaths per 100,000 people
- Risk Difference:
➔ +86.3 deaths per 100,000 (Pfizer excess) - Risk Ratio (RR):
➔ 1.53 (i.e., 53% higher cardiovascular mortality risk) - Odds Ratio (Adjusted):
➔ 1.540 (95% CI: 1.431–1.657)
COVID-19 mortality
Pfizer recipients had nearly double the risk of COVID-19 death compared to Moderna recipients.
- Pfizer Risk: 55.5 deaths per 100,000 people
- Moderna Risk: 29.5 deaths per 100,000 people
- Risk Difference:
➔ +26.0 deaths per 100,000 (Pfizer excess) - Risk Ratio (RR):
➔ 1.88 (i.e., 88% higher COVID-19 mortality risk) - Odds Ratio (Adjusted):
➔ 1.882 (95% CI: 1.596–2.220)
Non-COVID-19 mortality
Pfizer recipients faced a 35% higher risk of dying from non-COVID causes compared to Moderna recipients.
- Pfizer Risk: 791.6 deaths per 100,000 people
- Moderna Risk: 588.4 deaths per 100,000 people
- Risk Difference:
➔ +203.3 deaths per 100,000 (Pfizer excess) - Risk Ratio (RR):
➔ 1.35 (i.e., 35% higher non-COVID mortality risk) - Odds Ratio (Adjusted):
➔ 1.356 (95% CI: 1.303–1.412)
Biological explanations
The findings of this study are surprising, given that Moderna’s mRNA-1273 vaccine contains approximately three times more mRNA (100 µg) than Pfizer’s BNT162b2 vaccine (30 µg). This suggests that the higher mortality observed among Pfizer recipients could potentially be related to higher levels of DNA contamination — an issue that has been consistently reported worldwide:
The paper hypothesizes differences between Pfizer and Moderna may be due to:
- Different lipid nanoparticle compositions
- Differences in manufacturing, biodistribution, or storage conditions
Final conclusion
Florida adults who received Pfizer’s BNT162b2 vaccine had higher 12-month risks of all-cause, cardiovascular, COVID-19, and non-COVID-19 mortality compared to Moderna’s mRNA-1273 vaccine recipients.
Unfortunately, without an unvaccinated group, the study cannot determine the absolute increase in mortality risk attributable to mRNA vaccination itself. However, based on the mountain of existing evidence, it is likely that an unvaccinated cohort would have experienced much lower mortality risks. It’s also important to remember that Moderna mRNA injections are still dangerous.
As the authors conclude:
These findings are suggestive of differential non-specific effects of the BNT162b2 and mRNA-1273 COVID-19 vaccines, and potential concerning adverse effects on all-cause and cardiovascular mortality. They underscore the need to evaluate vaccines using clinical endpoints that extend beyond their targeted diseases.
Epidemiologist and Foundation Administrator, McCullough Foundation
Please consider following both the McCullough Foundation and my personal accounton X (formerly Twitter) for further content.
Reprinted with permission from Focal Points.
COVID-19
Canada’s health department warns COVID vaccine injury payouts to exceed $75 million budget

Fr0m LifeSiteNews
A Department of Health memo warns that Canada’s Vaccine Injury Support Program will exceed its $75 million budget due to high demand, with $16 million already paid out.
COVID vaccine injury payments are expected to go over budget, according to a Canadian Department of Health memo.
According to information published April 28 by Blacklock’s Reporter, the Department of Health will exceed their projected payouts for COVID vaccine injuries, despite already spending $16 million on compensating those harmed by the once-mandated experimental shots.
“A total $75 million in funding has been earmarked for the first five years of the program and $9 million on an ongoing basis,” the December memo read. “However the overall cost of the program is dependent on the volume of claims and compensation awarded over time, and that the demand remains at very high levels.”
“The purpose of this funding is to ensure people in Canada who experience a serious and permanent injury as a result of receiving a Health Canada authorized vaccine administered in Canada on or after December 8, 2020 have access to a fair and timely financial support mechanism,” it continued.
Canada’s Vaccine Injury Support Program (VISP) was launched in December 2020 after the Canadian government gave vaccine makers a shield from liability regarding COVID-19 jab-related injuries.
While Parliament originally budgeted $75 million, thousands of Canadians have filed claims after received the so-called “safe and effective” COVID shots. Of the 3,060 claims received to date, only 219 had been approved so far, with payouts totaling over $16 million.
Since the start of the COVID crisis, official data shows that the virus has been listed as the cause of death for less than 20 kids in Canada under age 15. This is out of six million children in the age group.
The COVID jabs approved in Canada have also been associated with severe side effects such as blood clots, rashes, miscarriages, and even heart attacks in young, healthy men.
Additionally, a recent study done by researchers with Canada-based Correlation Research in the Public Interest showed that 17 countries have found a “definite causal link” between peaks in all-cause mortality and the fast rollouts of the COVID shots as well as boosters.
Interestingly, while the Department of Health has spent $16 million on injury payouts, the Liberal government spent $54 million COVID propaganda promoting the vaccine to young Canadians.
The Public Health Agency of Canada especially targeted young Canadians ages 18-24 because they “may play down the seriousness of the situation.”
The campaign took place despite the fact that the Liberal government knew about COVID vaccine injuries, according to a secret memo.
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