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This video discusses the PCR test used for COVID-19 and raises concerns about its accuracy and potential misuse. It explains that the test amplifies a small amount of DNA to detect the virus, but if amplified too much, it can result in false positives. The inventor of the PCR test, Kary Mullis, stated that it was not meant for diagnosing viruses. The video suggests that the high cycle thresholds used in testing lead to inflated case numbers and a false sense of a pandemic. It also mentions the potential dangers of the test, such as the use of sterilizing solutions and the possibility of containing the vaccine. The video encourages critical thinking and research to understand the true nature of the situation.

Vaccines must be carefully studied to ensure they do not worsen infections. Past vaccines, like the respiratory syncytial virus vaccine for children, have unexpectedly made things worse. Similarly, an HIV vaccine increased infection risk in some cases. It's crucial to conduct thorough studies in high-risk populations to understand how vaccines truly impact infections before widespread use.

What kind of work are you doing now? I work for Eurofins in various clinical trial settings. I don't believe you know how to read and interpret the tests. What tests? Let's discuss PCR validation. How do you validate a PCR? What’s the sensitivity of a test? It’s how well the test can detect low amounts of material. Sensitivity is the percent chance that an infected person tests positive. That’s a good way to put it. Now, specificity? It’s how accurate the test is in detecting what it’s supposed to detect, not something else. What you’re hoping to detect?

The PCR test, commonly used for COVID-19, involves a nasal swab. According to Kary Mullis, the Nobel Prize-winning scientist who created the test, it can detect almost anything if amplified enough. However, Mullis himself stated that the PCR test should not be used to diagnose diseases, as it only detects fragments of illness. Many laboratories worldwide run the test at high amplification levels, leading to a high rate of false positives. Even Anthony Fauci acknowledged that results beyond 33 cycles are likely not infectious material. The New York Times reported that 90% of PCR tests were not indicative of active illness. Lowering the amplification cycles resulted in significant reductions in case numbers. In the past, PCR tests have caused false positives, such as in a whooping cough pseudoepidemic. Some criticize Fauci for misleading the public.

The widely used PCR tests for COVID-19 are too sensitive, meaning they can detect not only live virus but also dead virus and other materials. The problem is that the results sent to doctors and patients don't specify whether the virus is live or dead. Recent data from Massachusetts, New York, and Nevada showed that 90% of positive cases carried very little virus. If this trend applies nationwide, only a small fraction of positive cases would actually need to isolate and undergo contact tracing. To prevent unnecessary disruptions, it's important to test in a smarter way, focusing on the contagiousness of individuals. This approach would help schools reopen faster and make more sense overall.

A Chinese study published in Nature conducted 10 million PCR tests in Wuhan and found that out of the 300 asymptomatic cases, none produced a live virus in the lab setting. This suggests that high cycling of PCR was generating false positives. PCR detects nucleic acid, not disease, and is typically followed up with confirmatory tests. The study did not confirm the presence of infectious viral particles through culture-based methods. False positives occur when healthy individuals with residual viral DNA are magnified due to high cycling. PCR can detect viral RNA long after the disappearance of the infectious virus.

The PCR test, used to determine COVID-19 cases, amplifies RNA fragments to detect the virus. However, the high amplification can also detect traces of dead virus or remnants from other coronaviruses. Scientists recommend not testing over 30 cycle thresholds to avoid false positives. When labs reduced the cycles, case numbers significantly decreased. False positives can occur almost half the time, especially in populations with low COVID-19 prevalence. In the past, PCR tests have caused false epidemics. The test requires skilled technicians and careful handling, but it is currently being conducted on a large scale with hastily trained personnel. Therefore, it is important to question the accuracy of reported case numbers.

Testing could have been increased rapidly in countries like Taiwan, New Zealand, and Australia, which effectively avoided the epidemic. These countries learned from their past experiences and were better prepared, enabling them to act swiftly. It is crucial that we learn from this and be ready for the next outbreak, as it will undoubtedly receive significant attention.

Dr. Kary Mullis, the inventor of the PCR test, explained that the test can find almost anything in anyone if done well. However, using it to claim meaning or diagnose a virus is a misuse. The official protocol for COVID-19 PCR testing has led to false positives, labeling asymptomatic individuals as infected. 30 years ago, Dr. Anthony Fauci pushed for higher doses of the drug AZT for AIDS patients, despite lacking evidence. Mullis discovered there was no proof of HIV causing AIDS. He questioned the CDC's profit motives and the involvement of high-level officials. Mullis wanted to expose Fauci and Gallo but faced little attention. He passed away in 2019, just before the emergence of COVID-19, leaving many questioning the timing.

We need to be sure that being vaccinated prevents both contracting and transmitting the disease before implementing a vaccine passport. Allowing vaccinated individuals to access certain places based on proof of vaccination makes sense, but only if we are certain that being vaccinated prevents disease transmission.

The speaker discusses the issue of cycle thresholds in PCR testing. They explain that the original protocol used a cycle threshold of 45, which amplifies the results by 10. This means that even unlikely findings, such as particles from Mars, could be detected. The speaker suggests that by using a high cycle threshold, it is possible to create a pandemic by testing healthy individuals and spreading the myth of asymptomatic spread. This is how cases are created, according to the speaker.

It is important to prioritize PCR tests, but our capacity is not sufficient. Vienna can conduct more PCR tests in a day than all the labs in Germany combined. We lack equipment and personnel, and the German healthcare policy prioritizes the number of tests per person less than Vienna. Currently, rapid tests are essential, but their quality varies, especially regarding the Omicron variant. Authorities, including politicians, should ensure that high-quality rapid tests are used in testing centers, schools, and care homes. We pay a lot for these tests, and we rely on them. However, even the best rapid test is useless if not administered properly. Some test centers have questionable methods, and authorities need to increase supervision.

Do you have an open mind? Consider that we live in a toxic world, where our cells respond to poisons by packaging and releasing damaged genetic material, called exosomes. This contrasts with the established theory of viruses, which are seen as non-living entities that can cause illness. The coronavirus emerged when a respiratory illness was linked to a new RNA fragment found in patients. Testing methods, like PCR, amplify genetic material, but their arbitrary cutoff points can lead to misleading results. Cases like the Diamond Princess cruise ship show conflicting test results among close contacts, challenging the infectious virus theory. Many who test positive remain asymptomatic, and some fluctuate between positive and negative results. This raises questions about the reliability of PCR tests and whether exosomes could be misidentified as viruses. Ultimately, how confident are you in these tests? Would you choose to be tested?

There have been reports of patients shedding viral RNA for weeks, but it doesn't seem to be infectious. The question is whether we can use a cutoff of viral load determined by PCR to determine if a patient is no longer infectious. If the cycle threshold is 35 or more, the chances of it being replication competent are very low. It's frustrating for both patients and physicians when the PCR results show a high cycle threshold, like 37, because it's unlikely to culture virus from that. So if someone has a cycle threshold of 37, 38, or even 36, it's just dead nucleotides.

The speaker asks if a PCR test can be used to determine if a patient is no longer infectious. The other speaker explains that if the cycle threshold is 35 or higher, the chances of the virus being able to replicate are very low. They mention that it is frustrating for both patients and physicians when the cycle threshold is high, but it is unlikely to culture the virus. They conclude that if the cycle threshold is 37, 38, or even 36, it is just dead nucleotides.

We should be testing every cow weekly using pool PCR to detect asymptomatic infections. America's innovation allows for breakthroughs like pool testing dairy workers. Undetected cases in humans exist because we only track symptomatic individuals, leading to the spread of the virus. Switching to definitive laboratory testing is crucial to identify asymptomatic or mild cases that go unnoticed.

The speakers discuss the misuse of PCR in estimating viral RNA. They explain that PCR can detect almost anything in the body, making it easy to find even rare viruses like HIV. However, they argue that testing for HIV specifically is unnecessary because individuals with HIV are likely to have other viruses as well. They emphasize that PCR is a quantitative tool that provides measurable information, but it does not determine sickness or the potential harm of a virus. The speakers also mention that PCR cannot differentiate between virus particles and active live viruses. Overall, they highlight the limitations and misinterpretations of PCR testing.

The speaker asks if a PCR test can be used to determine if a patient is no longer infectious. They mention that if the cycle threshold is 35 or higher, the chances of the virus being contagious are very low. They also mention that even if a patient has a cycle threshold of 37 or higher, it is unlikely that the virus can be cultured. Therefore, they conclude that a cycle threshold of 37 or higher indicates that the virus is no longer viable.

PCR is a process that can amplify molecules in the body, making it possible to find almost anything in anyone. However, this doesn't necessarily mean that the presence of a molecule indicates illness or harm. The measurement for HIV, for example, is not exact and is based on invisible factors. PCR itself is just a method to create more of something. It doesn't determine sickness or potential harm.

Certain people may be segregated based on a biomarker, preventing them from returning to normal life. This raises the question of whether we would accept such inequity. Personally, I believe it is preferable to the current situation. If we can allow 10 or 20% of individuals with proven immunity, determined by lab results, to resume normal activities, it would be beneficial for everyone.

The PCR test, used to detect the presence of the SARS CoV-2 virus, has come under scrutiny for its reliability and potential for false positives. The test amplifies RNA fragments to identify the virus, but it can also detect traces of dead virus or remnants from other coronaviruses. Testing at high cycle thresholds can result in false positives, especially in populations with low COVID-19 prevalence. Scientists recommend not testing over 30 cycle thresholds to reduce false positives. Lowering the cycle thresholds has led to significant reductions in reported cases. The misuse and misinterpretation of the PCR test has contributed to inflated case numbers and unnecessary panic.

If a PCR test has a cycle threshold (CT) of 35 or higher, the chances of it being replication competent are very low. So, if someone's PCR test has a CT of 37 or higher, it's unlikely that the virus can be cultured from it. In fact, even a CT of 36 may indicate that it's just dead nucleotides.

Dr. Andreas Sönnigsen appears on Klar TV to discuss the Masern (measles) vaccination and the recent ARD/Tagesschau coverage. He presents his professional background: born and raised in Germany, studied medicine in the USA and Munich, practiced as a general internist from 1997 to 2012, and held professorships at Paracelsus University Salzburg, University of Witten/Herdecke, and Medical University of Vienna. He received the David Sackett Award for evidence-based medicine in 2013 and led the German Network for Evidence-Based Medicine from 2019 to 2021. He has authored works on scientific competence in medicine and on the Corona crisis, and has published over 100 international papers. He has long criticized conflicts of interest that he believes lead to an overly positive portrayal of medical interventions, a critique he says intensified during the Corona era, costing him his Vienna professorship and his chair at the German Network for Evidence-Based Medicine. He remains active post-Corona, including critical views on the measles vaccination mandate, including a talk at a press symposium on the Masernschutzgesetz. His conclusion on the question “does vaccination harm?” is that the benefit–risk ratio from the perspective of an individual child is definitively negative. In the Panorama segment from February 26, 2026, Sönnigsen is asked how he became part of a balanced-for-and-against discussion about the measles vaccination mandate. He explains he was contacted by a Norddeutscher Rundfunk journalist seeking balance and agreed to participate to stimulate discourse. He clarifies he is not an anti-vaxxer but a proponent of evidence-based medicine and argues that each vaccination, including the measles vaccine, should be evaluated for pros and cons, study quality, the epidemic situation, justification, effectiveness, and side effects, and that this discourse must be conducted. Sönnigsen contends that the show was not balanced. He discusses the dangers of measles, acknowledging it is not harmless, but argues that in the US, where measles became a notifiable disease in 1912, mortality declined to near zero by the early 1960s, and that the later impact of vaccination showed no further drop in mortality, suggesting in his view that vaccination did not drive the reduction. He asserts that in Germany, comparing mortality from the 1950s/60s to today is inappropriate due to postwar differences in healthcare and hygiene. He claims current German annual measles case numbers are about 330 per year nationwide (over 80 million population), and argues that herd immunity is largely due to people who had natural measles, with about 50% of the population having natural immunity from those born before 1973. He asserts real vaccine effectiveness is 80–85% rather than the commonly cited 98%, citing observational studies and a Cochrane review, and argues the 98% figure is incorrect. He explains that seroconversion rates after vaccination are lower than after natural infection, and that the metric should be real vaccine effectiveness rather than seroconversion rates. Turning to vaccine safety, Sönnigsen counters Panorama’s claim that there are few and minor vaccine adverse events. He states approximately 100–150 severe vaccine adverse events are reported to the Paul-Ehrlich-Institut each year (2001–2012 analysis). He notes that about half of these have a possible or probable causal link to vaccination, and that there is underreporting by roughly a factor of 10–20. He references the Henry Ford study suggesting vaccinated children have a higher risk of chronic illness (about 60% with at least one chronic condition vs. 18% among unvaccinated), arguing vaccines’ adverse effects are not rare. He calculates that with about 1.2 million annual vaccinations and about 1,200 serious adverse events (assuming 5–10% causal and 10–20x underreporting), roughly one in every thousand children could be affected by a vaccine injury, a figure he uses to argue that the individual risk is high relative to the immediate benefit in a German epidemiological context where measles is rare in ordinary times. Sönnigsen insists the measles vaccine’s benefits for an average healthy child in Germany are negative in the current epidemiological situation, argues for a “relative contraindication” to vaccination, and emphasizes that parental autonomy should determine whether to vaccinate. He attributes the push for vaccination mandates to government coercion and argues that mandates could backfire, increasing resistance. He also contends that measles cannot be eradicated globally through a German vaccination mandate, given worldwide reservoirs and migration, and notes that the Masernimpfpflicht (measles mandate) comes from 2019 (Spahn’s Masernschutzgesetz) rather than being a universal solution. The interview closes with the assertion that people should form their own, balanced view, and that the state should not dominate medical decisions.

PCR is not misused, but its interpretation can be. PCR can find almost anything in anybody by amplifying a single molecule. Testing for HIV and claiming it has special meaning is the problem, because someone with HIV likely has other viruses. PCR is quantitative and makes minuscule amounts measurable, but this can lead to misinterpretations. HIV measurements are not exact. HIV tests are based on invisible things and inferred results. PCR makes a lot of something out of something, but it doesn't indicate sickness or harm. Even if you believe in HIV, PCR can't differentiate between virus particles or active live virus.