CoVid Test Kits Archives

FDA AUTHORIZATION OF ANY VACCINE: “As long as no serious harms from the vaccines are discovered, they’ll maintain authorization until the pandemic is over. At that point, the pharmaceutical companies will decide if they want to seek FDA approval.”

The Pandemic has been over for a year yet Biden extended the Public Health Emergency for another three months. Is that legal? The last two variants were determined to be as risky as the flu. People presented with a variety of symptoms that seem compatible with any other nominal condition such as the Common Cold –

The CDC and HHS still declare that vaccines are “safe and effective”. Despite the ‘serious harms’ that are essentially ignored – including the harm of – death.

Hospitals have confirmed that 85% of admissions ‘with’ CoVid are among the vaccinated. These infections are labeled ‘Breakthrough’ cases because the vaccine didn’t work. Neither did the boosters which are now recommended every 2 months.

With the PCR Test tabled, the means for testing is largely via home test kits. Abbott’s BinaxNOW is ‘authorized’. The test is based on identifying igG antibodies. Despite the one study being done on this product having been concluded in January 2022 – no results of the study have been published.

IgG antibodies are the most common and reflect viruses, bacteria and fungi. Clinically, igG antibody detection is used for the serologic immunity to hepatitis, measles, mumps, rubella and chickenpox. A positive test result would indicate you have had these diseases and/or CoVid or been vaccinated ~ according to the CDC. It does NOT determine if someone is currently infected.

In other words, the BinaNOW home test does NOT test for CoVid.

The CUE Test is based on molecular diagnostics. “Positive results indicate the presence of viral RNA, but clinical correlation with past medical history and other diagnostic information is necessary to determine infection status.” In fact, other viruses or even a bacterial infection could produce a positive result ~ according to the FDA. They are no more reliable than the PCR test which was finally quashed by Fauci December 2022.

In other words, molecular tests are just as flawed as the PCR.

The CDC is currently claiming that there are over 101 million accumulated cases since the inception of the disease. The ‘case’ counts have been highest among Hispanics, and lowest among Whites and Asians. The percentage of deaths via ‘cases’ is determined to be .99%.

PLAYING WITH NUMERS: By contrast, the ‘death rate’ for flu is NOT based on cases – but on total population. If one were to extrapolate death rates by population for Covid = .3%.

We are awakening to the Reveal. The Reveal is not a gender assignment, it is a manipulation assignment. Despite Scientists coming forward by the thousands, despite the Vax Deaths labeled Sudden Death, despite numerous authorities exposing the clots, cancers, heart disease, lung disease and complete disability of those receiving the Vax, our esteemed Medical authorities choose to ignore DATA.

TWITTER FILES: Musk opined that the Twitter dump implicating at the very least – Fauci – was forthcoming. Yet it is still in edit.

The revelations that the data truths were purposefully quashed would upend the entire health industry in America – much less the world. It does not mean we are without the ability to cure viruses and bacterial infections which have existed for multiple centuries. Cures are well trialed and tested when coming from a millennium of centuries – as opposed to the inane CDC and FDA trials imposed on a spattering of persons without qualifications of: previous diseases, current disease, age, sex, genetics, weight, prescription consumption, lifestyle, diet, air quality, etc… And trialed on a total of a couple hundred approved persons.

We have always had an alternative.

But the Rockefeller Institute was quite oblique in their massive campaign to discredit everything we knew in favor of their Big Pharma business model in 1918. Doctors not toting the line of Rockefeller were harassed, discredited, shamed and branded quackery. EXACTLY what is happening today.

What it does reveal is an interesting cyclical, intellectual, and strategic ploy that is a continuum – as though they haven’t any other weapon… As though they haven’t the capabilities to evolve. As though there is a singular dynamic. As though the entire simulation comes from a – computer.

While the focus continues to be on the vaccines, who, what and where they were manufactured, Test Cases still dominate the News. So who is manufacturing the Test Kits that create these caseloads?

There are five primary sources in the US: Access Bio, Hologic, Abbott, Roche and Quidel.

Access Bio: Has created three tests; 1. MDX RT PCR – for the rapid detection of human coronavirus SARS COV2 viral RNA extracted via nasal aspirate – which claims it will detect all mutations and takes 83 minutes, 2. lgM/lgG a blood test that identifies antibodies in 10 minutes, and 3. The Rapid POC Test which tests for nucleocapsid protein antigen, and must be administered by medical professionals operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.

Access Bio’s headquarters is in New Jersey and it works in affiliation with the Bill & Melinda Gates Foundation, the Global Good Fund, UNICEF, WHO, and Doctors Without Borders. Its specialty is the testing for Malaria. AH – surprise! In 2017 they brought an asymptomatic malaria test to market. Because it is important to determine if someone needs a vaccine even though they have absolutely no verifiable symptoms of disease…

The Global Good Fund partners include the Smithfield Foundation (as in Smithfield sold to China), The John Maxwell Company, GCH Partners, Global Partnership for Social Accountability, and Johnson & Johnson, among others.

The Global Partnership for Social Accountability (GPSA) has a large swathe of investors including; Scytl, National Democratic Institute, Ford Foundation, Open Government Partnership and the Open Society Foundations. It’s steering committee consists of donor members including, Jonas Rolett who is special advisor to the Chairman, George Soros from the Open Society. Well Dang Nabbit!

Gregory Mark Hill is the Managing Partner of GCH Partners. Hill serves as the China liaison having spent many years in various company capacities in Beijing including: V2V Ventures of Tsinghua Venture Capital, which is owned by the CCP. As in Communist China.

So we have a manufacturer of CoVid test kits used in the US and UK which are funded by Bill & Melinda Gates in partnership with various organizations that include Soros, China – CCP, Scytl, a voting tabulation company that has been charged with manipulating the US Presidential Election, and the National Democratic Institute which is funded by the Orange Revolution cult, National Endowment for Democracy!

I think I’ll pass on those test kits!

Another company; Hologic was given permission by the FDA for emergency use of CoVid 19 test kits. In November 2020, Hologic won a $119 million contract from the U.S. Department of Health and Human Services and the Department of Defense to help expand production facilities in three states, Wisconsin, Maine and California, with the goal to provide 13 million COVID tests per month by January 2022. 2022????

The obvious question would be why would we need tests in 2022?

They offer two different tests both of which are built to detect RNA and are ‘so sensitive’ they can detect SARS in asymptomatic as well as symptomatic individuals. According to their package insert, they make this unusual statement: “Positive results do not rule out bacterial infection or co-infection with other viruses.” In addition, a negative result does not mean you are truly negative.

While the tests have been cleared by the FDA under emergency use, they have not been approved. The insert, which is 34 pages, defines the proper means, use, and requirement that a health professional certified in providing these tests must be utilized.

And then there is this nugget: Hologic Global Access Initiative is a global partnership with the Clinton Health Initiative and MedAccess backed by the UK Government to provide low cost HIV testing for Africa.

Would you touch a Clinton CoVid test?

QUIDEL: The insert for the Quidel CoVid test makes an interesting acknowledgement: There are no ‘approved’ tests by the FDA. These tests are simply ‘available’ under emergency use.

Roche makes the statement that their CoVid test actually makes an assay of the entire subgenus family which would include ALL Coronaviruses – meaning a positive result could indicate you have antibodies for SARS, MERS, or a Cold.

All these tests are based on a best-guess-estimate of science that would seem to have not been ‘approved’ by any government organization or tested by any independent organization under a large sample of volunteers. Yet, that would encapsulate every single CoVid Test manufactured everywhere…

There are two basic forms of tests: Molecular and Antigen.

Molecular diagnostics are individually dependent upon a person’s genomes via strands of DNA. Assays are simply markers used to detect ‘the flu’ and have not been thoroughly studied and researched in specific types of ‘flu’, therefore their reliability is nonspecific.

According to the CDC, Antigen tests are commonly used in the diagnosis of “respiratory pathogens, including influenza viruses and respiratory syncytial virus”. Antigen tests are best used when the viral load is at its height and it is already known the patient has been exposed, or if the patient has already had the virus and antibodies are still active.

Therefore, a physician’s determination is not just based on the test result, but on external theory. For example: if a patient has already been exposed to a virus and is having symptoms, the antigen test could confirm the external evaluation.

While the CDC claims that antigen tests must comply with Clinical Laboratory Improvement Amendments (CLIA) regulations. Those regulations have been ‘waived’ for ALL CoVid testing.

We have essentially handed our livelihoods to Big Pharma – sometimes in collaboration with the same organizations that produce the vaccines for the disease they are testing whether it be Malaria, HIV or Flu; ie Bill Gates.

If manufacturers are being told to ramp up testing for future development years in advance, that would indicate they anticipate the vaccine will either be worthless, or become a commonly required jab, not unlike H1N1 which has been whirled into the witches brew as an annual flu shot for 8+ years.

TESTING is virtually meaningless in the True Scientific genre of philosophy and medicine. It negates the individual DNA/RNA and supercedes it with a global version that is simply NOT possible. That would be like saying our genes are all the same – our immunity is all the same – our DNA is all the same. In which case, sampling a person’s DNA to determine if they were responsible for a particular crime – would encapsulate every person on the planet! AH!