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
From the Daily Caller News Foundation
By Emily Kopp
The letter, exclusively shared with the Daily Caller News Foundation, seeks more details about those deaths and the passive U.S. vaccine safety surveillance system and complacent Food and Drug Administration (FDA) bureaucracy under the Biden administration that delayed their reporting for years.
“Nobody wanted to admit that these things were causing death. This is absolutely a case of willful ignorance,” Johnson said in an interview with the DCNF.
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The letter requests from the Department of Health and Human Services (HHS) “all records referring or relating to the review of the 96 reports of death following a COVID-19 vaccine … including but not limited to, any memorandum or report created following that review and the data underlying the reports.”
“I am grateful that we now have individuals at our federal health agencies who care about vaccine safety and efficacy. I am, however, disappointed that despite having subpoenaed HHS for the type of data and information described in Dr. Prasad’s memo, it does not appear to have been provided to my office,” the letter reads.
HHS did not immediately respond to a request for comment.
“This is a profound revelation. For the first time, the US FDA will acknowledge that COVID-19 vaccines have killed American children. Healthy young children who faced tremendously low risk of death were coerced, at the behest of the Biden administration, via school and work mandates, to receive a vaccine that could result in death. In many cases, such mandates were harmful. It is difficult to read cases where kids aged 7 to 16 may be dead as a result of covid vaccines,” Prasad wrote. “There is no doubt that without this FDA commissioner [Marty Makary], we would not have performed this investigation and identified this safety concern. This fact also demands serious introspection and reform.”
“One reason I’m writing this letter is that this memo needs much greater attention. This should be a blockbuster,” the Wisconsin senator told the DCNF.
Johnson, who has investigated the issue of COVID vaccine-linked adverse events since June 2021, also seeks more clarity about why FDA only examined a fraction of total reports to the Vaccine Adverse Event Reporting System (VAERS). He noted that the 96 deaths scrutinized by FDA staff in its investigation represents a sliver of the raw VAERS reports of 9,299 deaths worldwide within two days of vaccination.
Distinguishing which VAERS reports indicate genuine fatal side effects and which represent mere coincidences requires autopsy reports, which regulators and physicians often do not request because of a ideological reluctance to acknowledge that vaccines can carry risks, Johnson told the DCNF. Johnson said he has spoken to families who suspected a vaccine injury but struggled to obtain autopsies.
“With some of these officials at federal health agencies and within the medical establishment, vaccines are religion. The do not want to muddy the water with facts,” he said.
Johnson’s letter notes that Prasad acknowledged a culture at FDA “where vaccines are exculpated rather than indicted in cases of ambiguity,” and that the true number of deaths is likely higher.
Johnson has as chair of the Senate Permanent Subcommittee on Investigations investigated the Biden administration’s headlong expansion of COVID vaccines and booster shots to healthy young adults and children.
His committee uncovered internal federal documents showing the Centers for Disease Control and Prevention never updated its vaccine surveillance tool “V-Safe” to include cardiac symptoms, despite naming myocarditis as a potential adverse event by October 2020, per a May report. The investigation also found that top officials at FDA obstructed a warning to pediatricians and other providers about the risk of myocarditis after the May 2021 authorization of the Pfizer vaccine for 12 to 15-year-olds, months after Israeli health officials first detected the safety signal in February 2021.
Johnson’s letter highlights missing safety studies that the drugmakers never conducted.
Under the Biden administration, the FDA waived the responsibility of the drugmakers to conduct post-market studies that they had pledged to regulators, scientific advisors on the FDA Vaccines and Related Products Advisory Committee, and the public that they would complete. These uncompleted studies include promised research into subclinical myocarditis, undocumented rates of heart inflammation without obvious symptoms, Prasad’s memo states.
Johnson’s letter reveals the committee has not received any records from HHS about the liability shield for COVID-19 vaccines.
A public health media personality reported on Dec. 11 that FDA staff had downgraded the certainty with which it can attribute some the deaths to the vaccine in the weeks since Prasad received their top line results — echoing prior leaks from career officials aimed at undermining FDA’s new bosses.
Center for Drug Evaluation and Research Acting Director Tracy Beth Hoeg first concluded in a separate analysis that there were in fact deaths in children in the summer, but career staff leaked the results to reporters who “portrayed the incident as Dr. Hoeg attempting to create a false fear regarding vaccines” soon after, per Prasad’s memo.
Johnson’s letter seeks documentation of Hoeg’s meeting, including “a list of all attendees.”
From the Daily Caller News Foundation
China is escalating its legal fight with Missouri after the state secured a massive court victory earlier this year over Beijing’s role in the COVID-19 pandemic, according to the state attorney general’s office.
Missouri Attorney General Catherine Hanaway announced Tuesday that the People’s Government of Wuhan Municipality, the Chinese Academy of Sciences and the Wuhan Institute of Virology have filed a $50 billion lawsuit against the state, claiming Missouri poses an “economic and reputational threat” to the People’s Republic of China (PRC). The suit comes as Missouri moves to seize Chinese-owned assets to collect on a historic federal court judgment the state won in March.
Missouri first sued China in 2020, seeking $25 billion in damages “for causing and exacerbating the COVID-19 pandemic” and for hoarding critical medical supplies while the virus spread, according to the state attorney general’s office. China and several affiliated entities were ordered to pay Missouri roughly $24.49 billion, plus post-judgment interest. Senior U.S. District Judge Stephen Limbaugh ruled that China and the other defendants “failed to appear or otherwise answer after being properly served,” resulting in the default judgment.
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Missouri maintained that China was attempting to shield itself from legal consequences by relying on proxy organizations to speak on its behalf — an accusation Beijing now disputes in its own lawsuit against the state.
In its lawsuit, China alleges that Missouri’s actions have had “negative effects on the soft power” of Wuhan and have “belittled the social evaluation” as well as adversely affected the “productivity and commercialization of scientific and technological achievements” of the Chinese Academy of Sciences and the Wuhan Institute of Virology. The filing further alleges that Missouri’s “vexatious litigation” has “defamed Plaintiffs’ reputation, resulting in huge economic losses of the Plaintiffs, and deeply endangering sovereignty, security and development interests of China.”
The suit names the state of Missouri, Republican Missouri Sen. Eric Schmitt and the former Missouri Attorney General Andrew Bailey as the defendants.
China’s lawsuit demands the defendants “issue public apologies on New York Times, CNN, Wall Street Journal, Washington Post, YouTube and other American media or internet platforms, and People’s Daily, Xinhuanet and other Chinese media or internet platforms.”
Hanaway rejected the demand and said the state remains focused on enforcing the federal judgment.
“I find it extremely telling that the Chinese blame our great state for ‘belittling the social evaluation’ of The Wuhan Institute of Virology. This lawsuit is a stalling tactic and tells me that we have been on the right side of this issue all along,” Hanaway said in a statement. “We stand undeterred in our mission to collect on our $24 billion judgment that was lawfully handed down in federal court.”
Schmitt described China’s suit as “frivolous lawfare, attempting to absolve themselves of all wrongdoing in the early days of the pandemic.”
“This is their way of distracting from what the world already knows, China has blood on its hands. China lied about the origins of COVID virus, they tried to cover it up, and they upended the world by creating a global pandemic that resulted in immense human loss,” Schmitt added.
Missouri, Hanaway said, is continuing efforts to obtain certification that would allow the state to seize Chinese-owned assets, including real estate, financial interests, and other holdings tied to the defendants.
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