Archive for the ‘vaccines’ Category

BREAKING: 86% of PCR-Positive ‘COVID Cases’ Not Real Infections & 1st Peer Reviewed Evidence Shows COVID Shots Based on Faulty Statistics

https://www.thefocalpoints.com/p/breaking-86-of-pcr-positive-covid?

BREAKING: 86% of PCR-Positive “COVID Cases” Were Not Real Infections

New study finds that during the early pandemic period, only 14% of PCR “COVID cases” were real — proving that lockdowns and vaccine mandates were built on a fraudulent testing illusion.

ByNicolas Hulscher, MPH

A bombshell peer-reviewed study out of Germany just dismantled the scientific foundation used to justify lockdowns, social distancing, and vaccine mandates.

Researchers analyzed data from the Akkreditierte Labore in der Medizin (ALM) — a nationwide consortium of authority-accredited medical laboratories that performed roughly 90% of all SARS-CoV-2 PCR tests in Germany between 2020 and 2023.

When researchers compared the ALM’s week-by-week PCR positivity rates with the same labs’ IgG antibody testing data — essentially measuring who truly developed infection-induced immunity — they discovered something staggering:

Only about 14% of those who tested PCR-positive during the early pandemic period (2020–mid-2021) actually developed antibodies — meaning most early “cases” were never real infections.

Even under the most conservative assumptions — correcting for possible overrepresentation of IgG-positive individuals in the sample — the true infection fraction fell to roughly 10%, implying that nearly 90% of PCR positives were false or non-infectious detections, often just residual RNA fragments amplified at CT thresholds of 35–45.


What This Means

  • Mass PCR testing grossly inflated case numbers worldwide. Every nation that used similar CT thresholds likely overcounted “infections” by an order of magnitude.
  • Lockdowns and mandates were built on a false metric. The German “7-day incidence” used to trigger restrictions was statistically meaningless — and identical logic applied in the U.S., U.K., and elsewhere. In America, the entire “15 Days to Slow the Spread” campaign was predicated on the same inflated PCR scam.
  • Authorities suppressed representative serology data. Germany’s RKI and Ministry of Health had access to these ALM antibody results but never disclosed them — despite their policy relevance.
  • Rewriting pandemic history. If only 10–14% of reported PCR “cases” during the first year reflected true infections, then the infection-fatality rate, transmission models, and emergency declarations were all built on sand. By the end of 2020—months before vaccination began—roughly one-quarter of Germany’s population already carried natural antibodies. In other words, while authorities were declaring an uncontrolled crisis, herd-level immunity was already taking shape. By late 2021, nearly the entire population was IgG-positive. The evidence shows that pandemic policy was driven not by infection reality, but by a diagnostic illusion.

PCR technology and testing thresholds were standardized across WHO member states.
That means the same distortion likely occurred everywhere — a systemic diagnostic inflation that may be the single greatest fraud in public health history.

These tactics were likely used to amplify fear in order to boost compliance with lockdowns and experimental gene-based “vaccines.” This was demonstrated by Gao et al, who found that public fear of COVID-19 (PFC) was positively associated with the number of COVID-19 vaccinations at county-level: “as PFC increases from 0 to 300, the predicted vaccination number increases from 10,000 to 230,000.”

This is in line with fraudulent attempts to artificially increase COVID-19 death counts. Basoulis et al found that 45.3% of “COVID-19 deaths” in Greece were not actually due to COVID-19:

BREAKING — Nearly Half of “COVID-19 Deaths” Were Not Due to COVID-19, New Study Finds

BREAKING — Nearly Half of “COVID-19 Deaths” Were Not Due to COVID-19, New Study Finds

In the end, most of the population did encounter the manufactured virus and develop antibodies—but the PCR data that justified global lockdowns, fear, and vaccine mandates were a complete fraud. Accountability is warranted.


https://panagispolykretis.substack.com/p/this-paper-will-shock-the-world-unveiling

This paper will SHOCK the world: Unveiling hidden biases that inflated COVID-19 vaccine effectiveness and safety

How misclassification of early post-vaccination deaths distorts mortality rates and public health assessments

Today, together with Dr. Marco Alessandria, Dr. Giovanni Trambusti, Dr. Giovanni M. Malatesta, and Dr. Alberto Donzelli, we published an crucial peer-reviewed scientific study titled “Classification bias and impact of COVID-19 vaccination on all-cause mortality: the case of the Italian Region Emilia-Romagna [1]. In this study, we provide the first peer-reviewed evidencebased on real-world data, demonstrating how certain statistical methods have led to an overestimation of the effectiveness and safety of COVID-19 vaccines. This paper will shock the world, because it proves that all scientific studies conducted so far that are affected by this bias should be reassessed.

We addressed a critical bias that can substantially distort real-world evaluations of vaccine effectiveness and safety, known as the “case-counting window bias”. This bias, theorized by Fung et al. [2], occurs because individuals are classified as “unvaccinated” during the first 14 days after receiving the vaccine (the period believed necessary for the immune response to develop fully). As a result, any adverse events, including deaths during this time, are incorrectly attributed to the unvaccinated group, artificially inflating its mortality rate, while simultaneously underestimating mortality among vaccinated individuals.

By analyzing detailed daily data on all-cause mortality and vaccine administration in the Emilia-Romagna region (Italy), obtained through a FOIA request by lawyer Lorenzo Melacarne (in accordance with the art. 5, comma 2 of the Italian Legislative Decree No. 33/2013), we found a clear temporal coincidence between vaccination campaigns and spikes in deaths among those incorrectly classified as unvaccinated during this critical window (Figure 1).

Figure 1. The chart illustrates the daily mortality rate per 100,000 individuals (age group 70-79), comparing those vaccinated (represented by the solid red line) with those unvaccinated (shown by the solid green line). Additionally, it shows the cumulative number of vaccinations administered with at least one dose (indicated by the red dotted line) [taken from Alessandria et al., 2025].

Our statistical analysis demonstrated significant differences in mortality between vaccinated and unvaccinated groups, during the critical 14-day post-vaccination window when misclassification occurs. Importantly, these mortality differences cannot be explained solely by COVID-19 deaths, which accounted for only about 9% of all deaths in Italy in 2021. Even after excluding COVID-19-related deaths, the disparity between groups remained significant, indicating systematic misclassification rather than true vaccine benefit. We also observed that the difference diminished with age, likely reflecting the increased comorbidity burden in older individuals that influences overall mortality risk (for more detailed information, please see the article, which is published in open access format and freely available to everyone).

Our findings suggest a harvesting effect, whereby vulnerable individuals succumb shortly after vaccination, but their deaths are wrongly counted among the unvaccinated. This misclassification masks potential serious vaccine-related adverse events occurring shortly post-vaccination, such as severe allergic reactions, cardiovascular events, or autoimmune responses.  (See link for article)

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**Comment**

I will reiterate: it’s all based on a sham.

And to be bloody clear: governments worldwide claim vaccines are safe and effective but can not produce the gold standard double-blind placebo-controlled trials good science relies on as proof.

Go here for this ‘must see’ clip of Del Bigtree stating:

“We’re injecting our kids with aborted fetal DNA, chopped-up organs from 3-month-old babies—76 in one study—admitted by vaccine chief Stanley Plotkin himself.

Monkey kidneys, hamster cells, cancer lines, mercury, formaldehyde… it’s a cauldron of horrors even Shakespeare couldn’t imagine.

And the worst part?

They admit: ‘We never studied this. We don’t know what it does.

This isn’t science—it’s a witch cult.”
  • Dr. Suzanne Humphries who was raked over the coals for even daring to question the ‘vaccine’ religion states:

Vaccination Introduced Animal Infections into Humanity.”  Source

Wakefield also directed the documentary “Protocol 7,” which exposes real-life events of an actively litigated case in the 3rd Circuit Court of Appeals against Merck for fraudulent activity behind the MMR vaccine.   The vaccine fails to protect against measles, destroys natural immunity, and the CDC admits as many as 94% of children who contracted mumps were vaccinated.  Go here for a scientists rebuttal to the Danish MMR vaccine cohort study.

The Merck case was managed to largely avoid public scrutiny, despite its outcome being very much in the public interest. The film script was written years ago but they sat on it waiting for the court case to be resolved.

The case documents were sealed until recently. They are now being unsealed, albeit in a piecemeal manner. Available documents, including complaints, expert opinions, deposition testimony etc can be found here, which shows the actual fraud was much, much worse than what is presented in the film.

CDC scientist William Thompson admitted scientists purposely destroyed data.
“The omitted data suggested that African-American males who received the MMR vaccine before age 36 months were at increased risk for autism.”  Dr. William Thompson
“Decisions were made regarding the findings of the report that the data was collected and I believe that the final study protocol was not followed.”  Dr. William Thompson  Source
Thompson ONLY came forth with this AFTER he was secretly recorded by Dr. Brian Hooker, a father of a vaccine injured child.
Thompson handed over documents about this case to Congressman Bill Posey.
Within the video Posey speaks before Congress about how not only did the authors of the study withheld vital information, they destroyed evidence.  Source

The Pfizer Job

Before reading the following unbelievably detailed analysis that took the author and his team over 3 years to complete, it’s important to note that ‘the powers that be’ aren’t getting the memo. Bill Gates recently had two meetings at the White House with President Trump and not only wants to inject cows and start putting scary additives into their food to supposedly reduce methane, but he’s funding a new micro-needle patch implant that installs both mRNA and quantum-dot markings into the body. Dr. Jessica Rose has broken it all down here.  Suffice it to say that it’s even worse than the mRNA shots.  In Rose’s words:

[It] involves taking the N1-modified mRNA-LNP technology (Pfizer/Moderna idea) to the next level of crazy, in my opinion.

And, Moderna has just unveiled a new mRNA shot called ‘mNEXSPIKE’ which translated in Latin means ‘violent death, or ‘death spear.’  You seriously can’t make this up.

Does anyone else out there get the distinct impression they want us dead?

https://www.arkmedic.info/p/the-pfizer-job?

The Pfizer Job

How Pfizer carried out the biggest pharma trial heist ever – and the regulators swallowed it hook, line and sinker.

Remember this?

“Pfizer’s vaccine is more than 90% effective”.

Headlines repeated around the world and more importantly by the regulators FDA, TGA, EMA and MHRA.

Just to reiterate – this was about COVID infection. No claims on severity, hospitalisation or death were made by Pfizer.

Given that most of the vaccinated population actually “got COVID” – many of them multiple times, that sounds impossible, right?

That’s because it was.

Yet the trial itself showed 95% reduction in the risk of infection and was published in the infamous New England Journal of Medicine (the same journal that published the fraudulent Surgisphere study) on the 10th December 2020.

….we are going to show that the whole study was a sham and that there never was a benefit – at all, never mind “95% reduction in infection.”  (See link for article)

________________

**Comment**

I’m eternally grateful that researchers and doctors are now onto the prolific research fraud that has been taking place.  Of course, this fraud has been going on in Lymeland for over 40 years, but now it’s on display for the entire world to see.  Yet another silver lining that came out of COVID mania.

SUMMARY:

  • One of the main Pfizer hustles was mandating all PCR swabs for the trial be sent to their own lab in New York as part of the case definition.  Which means that Pfizer decided whether a swab was positive or negative – the only test that mattered.
  • We only know this is due to a FOIA by attorney Aaron Siri.  Pfizer and the FDA tried to withhold this intel for 75 years.
  • Another hustle concerns dates.  The cut off for the trial was Nov. 14, 2020.  The VRBPAC meeting was on Dec. 10, 2020, the same day the trial was published.  The VRBPAC assessment document for the Pfizer submission was written on Dec. 7, 2020, just two weeks after the submission – having to assess 44,000 participants.  The approval was made on the basis of 47 days of follow-up for most patients, but was also made in ONE DAY, because of the VRBPAC meeting on Dec. 20, 2020 – with EUA declared on Dec. 11, 2020.  Certainly a miracle.
  • The dates demonstrate that all of this was impossible, which implies it was a pre-agreed approval based upon Pfizer showing data that there were less infections in the ‘vaccinated’ group based on a test they controllednot on clinical symptoms.
  • Evidently, Doran Fink of the FDA presented in the VRBPAC meeting despite having no clinical data and no experience in handling large data sets.  Unblinding in the trial was not allowed to happen until after Nov. 14, 2020, yet somehow Pfizer knew what was in which arm before that date.  Interestingly, Fink was then given a job at Moderna and now is at GSK, demonstrating clearly the revolving door between the FDA and Big Pharma.
  • Even more miraculously Pfizer, the WEF, and mainstream media already knew by the 9th of November that the ‘vaccine’ had ‘worked’ despite the fact the data cut off was Nov. 14.
  • Susan K Wollersheim’s ability to give the statistical presentation for VRBPAC on a 44,000 participant clinical trial is legendary as she has never published a clinical research study7.  
  • There is no way Fink and Wollersheim did the analysis as they don’t have the skill set and they didn’t have the time necessary to do it.
  • The good doctor who authored this article, Dr Ah Kahn Syed, states that it took him and a handful of people with the skillset required 3 years to sift through over 2 MILLION pages of FDA documents to just write this article.
  • Moderna achieved a similar EUA approval only 7 days later due to a similar hustle.
  • The third hustle: they stopped accumulating cases (in the “vaccinated group” only) for a specified time period in order to make the cut.
  • A tactic they probably used, since they solely controlled testing, was to change the Cycle threshold on the machine recording the tests.  A Ct of over 40 will pick up a bunch of false positives and a low Ct of less than 16 will only pick up real cases with a high viral load.  They didn’t know the ‘sweet spot,’ so they had to change Ct as they went along.  The field that should have recorded the Ct on the machine is conveniently missing.
  • Pfizer knew which tests were from the ‘vaccinated’ or the placebo group because they had the blood tests from every person in the study at their lab. Castruita showed in 2023 that even after 4 weeks there was enough circulating RNA (or DNA) from the COVID-19 vaccines to be able to perform genomic sequencing13.  While unlocking the database would create audit flags, they could easily identify who got what without raising audit flags, so they could then adjust the Ct up or down depending upon the number of positive tests they needed.
  • The author proves that if you correct for the fact that, if you’re vaccinated, you have 2.3x less chance of showing N-antibody on a test, the infection rate of the ‘vaccinated’ and of the placebo group is identical.  There was no 95% reduction in infection in the ‘vaccinated’ group at all.  It was a scam.
  • The author also shows from The FDA’s review that there were over 1100 more fevers and over 2000 more reports of chills in the ‘vaccinated’ group.

Sadly, all of this should have been done before ‘Operation Warp-speed,’ but let this be a solid reminder to not take ANYTHING until you are fully convinced it truly works and is safe.  In short, do not believe anything the medical machine for profit says.  Before you take anything they recommend, wait until independent research has been done.

There are probably many, many people who are now living with a lot of regret.

Bacterial ‘Fingerprints’ Found on COVID ‘Vaccine’ DNA Contamination

https://slaynews.com/news/bacterial-fingerprints-found-covid-vaccine-dna-contamination/

Bacterial ‘Fingerprints’ Found on Covid ‘Vaccine’ DNA Contamination

A groundbreaking new analysis has uncovered evidence that Pfizer’s Covid mRNA shots may have contained bacterial DNA fragments with dangerous immune-activating signatures.

The discovery is raising urgent questions about how regulators ever allowed the injections to reach the public.

The findings were revealed in a preprint published by molecular biologist Kevin McKernan.

McKernan used advanced Oxford Nanopore sequencing technology to analyze a Pfizer vaccine lot (FL8095).

His results revealed:

  • Bacterial-style DNA methylation marks (m6A), a fingerprint of contamination from E. coli–derived DNA.
  • Evidence of incomplete linearization, meaning the DNA used to manufacture the shots may not have been fully processed, leaving behind problematic fragments.
  • Signals that the contamination could, in theory, trigger powerful immune responses, potentially leading to harmful side effects.

These findings raise serious questions about the integrity of the health regulatory process during the declared COVID-19 pandemic.  (See link for article)

_______________

**Comment**

Science show such fragments can set off inflammation and cytokine storms.

So far, the clot shot contains:

ACTION: Retract Deplorable Lyme Disease CME Which Ignores Persistent Bb Part 2

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/34014349?cs_tk=A8-

Medscape Now! Interprofessional Care of Post-Treatment Lyme Disease Syndrome (Part2)

Carl Tuttle
Hudson, NH, United States
Oct 28, 2025

Follow-up email to Adrian Duncan, Group Vice President, Global Head of Education & Medical Affairs at WebMD.

First email can be found here.

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “aduncan@webmd.net” <aduncan@webmd.net>
Cc: “cme@medscape.net” <cme@medscape.net>, “caitlin@medlitera.com” <caitlin@medlitera.com>, “naseem@medlitera.com” <naseem@medlitera.com>, “michelle@medlitera.com” <michelle@medlitera.com>
Date: 10/28/2025 9:28 AM EDT
Subject: Re: Medscape Now! Understanding the Latest Evidence and Best Practices for Interprofessional Care of Post-Treatment Lyme Disease Syndrome

Dear Mr. Duncan,

In 2016 Dr. Paul Auwaerter, past president of the Infectious Diseases Society of America coauthored a study revealing the persister form of Borrelia burgdorferi resistant to antibiotics.

Here is a timeline of events:

2015

Standard antibiotic treatment for Lyme disease does not kill persistent Borrelia bacteria.
http://droopyyoupi.blogspot.com/2015/08/standart-antibiotic-treatment-for-lyme.html

Excerpt:

What has tuberculosis and Borrelia burgdorferi in common? In the late stage of the disease occurs persistent (tolerant) bacteria, which essentially means that the bacteria lasts and lasts and lasts. They protect themselves against antibiotics and are difficult to treat.

Both Borrelia burgdorferi and tuberculosis is relatively easy to cure in the early stages, even with the use of one antibiotic. In the late stage it is impossible to cure the disease with the same type of treatment in the acute phase, said Dr. Ying Zhang when he visited the year NorVect conference.

-Dr. Ying Zhang is a professor at the Department of Molecular Microbiology and Immunology at the Johns Hopkins Bloomberg School of Public Health

Two days after NorVect conference, published Dr. Ying Zhang’s latest research Identification of new compounds with high activity against stationary phase Borrelia burgdorferi from the NCI compound collection.

2016

A Drug Combination Screen Identifies Drugs Active against Amoxicillin-Induced Round Bodies of In Vitro Borrelia burgdorferi Persisters from an FDA Drug Library
Jie Feng 1, Wanliang Shi 1, Shuo Zhang 1, David Sullivan 1, Paul G Auwaerter 2, Ying Zhang 1
https://pubmed.ncbi.nlm.nih.gov/27242757/

Abstract

Under experimental stress conditions such as starvation or antibiotic exposure, Borrelia burgdorferi can develop round body forms, which are a type of persister bacteria that appear resistant in vitro to customary first-line antibiotics for Lyme disease. To identify more effective drugs with activity against the round body form of B. burgdorferi, we established a round body persister model induced by exposure to amoxicillin (50 μg/ml) and then screened the Food and Drug Administration drug library consisting of 1581 drug compounds and also 22 drug combinations using the SYBR Green I/propidium iodide viability assay. We identified 23 drug candidates that have higher activity against the round bodies of B. burgdorferi than either amoxicillin or doxycycline.

2022

Nitroxoline Drug Combinations Are More Active Than Lyme Antibiotic Combination and Can Eradicate Stationary-Phase Borrelia burgdorferi
Alvarez-Manzo, Hector S.1; Zhang, Yumin1; Zhang, Ying2,✉
https://journals.lww.com/imd/fulltext/2022/09000/nitroxoline_drug_combinations_are_more_active_than.7.aspx

Abstract

Lyme disease (LD), caused by Borrelia burgdorferi, is the most common vector-borne disease in the United States and Europe. Despite the standard 2–4 weeks’ antibiotic treatment, approximately 10%–20% of patients will develop post treatment LD syndrome, a condition that is poorly understood. One of the probable causes is thought to be the presence of B. burgdorferi persister forms that are not effectively killed by the current LD antibiotics. In this study, we evaluated nitroxoline, an antibiotic used to treat urinary tract infections, for its activity against a stationary-phase culture enriched with persister forms of B. burgdorferi. Nitroxoline was found to be more active than doxycycline and equally active as cefuroxime (standard LD antibiotics) against B. burgdorferi. Importantly, the nitroxoline two-drug combinations nitroxoline + cefuroxime and nitroxoline + clarithromycin, as well as the nitroxoline three-drug combination nitroxoline + cefuroxime + clarithromycin, were as effective as the persister drug daptomycin-based positive control three-drug combination cefuroxime + doxycycline + daptomycin, completely eradicating stationary-phase B. burgdorferi in the drug-exposure experiments and preventing regrowth in the subculture study. Future studies should evaluate these promising drug combinations in a persistent LD mouse model.
 
Mr. Duncan…. This is the missing research that should have been conducted early in the discovery phase of the disease but as we now know, all the eggs were put into the vaccine basket while a campaign was orchestrated to discredit the sick and disabled patient population along with the courageous clinicians attempting to help these patients. What has been deceitfully established here in the US is wreaking havoc globally. Example: Lyme disease: Australians ‘being treated worse than a dog riddled with mange’, Senator John Madigan says
https://www.abc.net.au/news/2016-01-11/lyme-disease-treatment-in-australia-criticised-by-john-madigan/7080708

This research is being suppressed as the disabled Lyme patient population around the globe remain sick indefinitely. (Three decades and counting)

Carl Tuttle

______________

**Comment**

We should all be eternally grateful for Lyme patient and advocate Carl Tuttle who is like a dog with a bone when it comes to relentlessly fighting for patients.  His letter makes numerous salient points completely ignored by the medical machine which runs on ‘consensus’ based medicine auto-pilot, where doctors are nothing more than automatons and where AI is more likely to diagnose patients than doctors.

In part one he calls on patients to write letters to Adrian Duncan of Medscape/WebMD.  The medical machine needs to hear from people who live this experience.  For ideas, feel free to read the letter I wrote back in 2020 to the TBDWG which I adapted for the Medscape letter. Use your own experience and ask him to retract this harmful CME course for doctors which only entrenches the false narrative of Lyme/MSIDS.

Pandemic Politics: Fear as a Blueprint for Global Control

http://

Oct. 26, 2025

**Comment**

Thankfully, there is a global awakening to the tyranny we are living through.

Those of us who have lived in Lymeland very long have learned that there is a parallel universe where mythology abounds and tyrants rule. This universe was exposed recently to those with open eyes and ears due to COVID.  The resemblance to Lymeland was uncannily similar.

It simply doesn’t matter that those who are ill with Lyme/MSIDS suffer with ongoing symptoms, the system tells them they are either imagining it or making it all up.  The parallel universe is ruled by ‘consensus‘ based medicine where a group decides what is true or not true and then teaches doctors their decision, demands complete obedience, which omits case studies, global research, and anything that defies the consensus narrative. Then insurance companies smugly hide behind these edicts given from above so patients are forced to pay out of pocket for any true help they receive.

Further, ‘the powers that be’ are actually behind the manipulation of these pathogens in a lab to make them stronger and more infectious. No wonder they don’t want to come clean.  They have a lot to answer for. Remember the Tuskagee experiment?  Author Dr. Colin Ross obtained FOIA documents for this unethical government experimentation and noted that:

“The Tuskeegee Syphilis Study was eventually shut down in 1972 because of the efforts of an investigative journalist. There is no evidence to suggest that the government or the medical profession had any intention of closing the study as of 1972.”

There’s many other experiments as well.

So denying it all is a perfect win.

For them.

In the video, Dr. Wodarg (pulmonologist and epidemiologist) speaks about how a false COVID ‘pandemic’ has been used for control.  But COVID wasn’t his first rodeo.  In the past he declared  H1N1 a “false pandemic” and “one of the greatest medicine scandals of the century.” (Forbes, February 10, 2010).  He is a modern day hero in my book.