Archive for the ‘Viruses’ Category

CDC Quietly Withdraws EUA for COVID PCR Test – It Can’t Distinguish Between COVID & the Flu

https://healthimpactnews.com/2021/cdc-to-withdraw-emergency-use-authorization-for-rt-pcr-test-because-it-cannot-distinguish-between-sars-cov-2-and-the-flu/

CDC to Withdraw Emergency Use Authorization for RT PCR Test Because It Cannot Distinguish Between SARS-CoV-2 and the Flu

by Brian Shilhavy, July 25, 2021
Editor, Health Impact News

The CDC quietly announced last week that it was withdrawing its request to the FDA for Emergency Use Authorization (EUA) of the 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2.

Most of the public is probably unaware that similar to the current COVID-19 injections that are not yet approved by the FDA, but only given Emergency Use Authorization, so too the hundreds of diagnostic tests that supposedly detect COVID-19 are also NOT approved by the FDA, but only authorized via an EUA.

What is the reason the CDC is withdrawing its EUA request for the Real-Time RT-PCR Diagnostic Panel?

In preparation for this change, CDC recommends clinical laboratories and testing sites that have been using the CDC 2019-nCoV RT-PCR assay select and begin their transition to another FDA-authorized COVID-19 test.

CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. (Source.)

Caitlin McFall, writing for Fox News, is the only one in the corporate media I could find that even reported this, and the few reports I found in the Alternative media so far have been mostly inaccurate.

McFall reports:

The Centers for Disease Control and Prevention (CDC) urged labs this week to stock clinics with kits that can test for both the coronavirus and the flu as the “influenza season” draws near.

The CDC said Wednesday it will withdrawal its request for the “Emergency Use Authorization” of real-time diagnostic testing kits, which were used starting in February 2020 to detect signs of the coronavirus, by the end of the year.

“CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives,” the agency said.

The U.S. has reported more than 34.4 million cases of the coronavirus since the pandemic began in 2020 and more than 610,000 deaths.

But while cases of COVID-19 soared nationwide, hospitalizations and deaths caused by influenza dropped.

According to data released by the CDC earlier this month, influenza mortality rates were significantly lower throughout 2020 than previous years.

There were 646 deaths relating to the flu among adults reported in 2020, whereas in 2019 the CDC estimated that between 24,000 and 62,000 people died from influenza-related illnesses.

The CDC urged laboratories to “save both time and resources” by introducing kits that can determine and distinguish a positive test for the coronavirus and flu. (Source.)

So there you have it.

The CDC just basically admitted that many of the COVID-19 cases this past year could not be distinguished from “flu cases.” No wonder flu cases decreased to zero in so many places. See:
Health Officials Admit that Only Those Vaccinated for the Flu are Getting the Flu This Year

The ending of the EUA for the Real-Time RT-PCR Diagnostic Panel will not happen until the end of the year, December 31, 2021, and the CDC recommends that laboratories start transitioning to other types of COVID-19 diagnostic tests that have been given an EUA by the FDA here.

At the time of publication of this article, the FDA has issued 251 EUAs for COVID-19 diagnostic tests since April 1, 2020. The vast majority of them are for the RT-PCR tests, including about 20 that were just issued EUAs since the beginning of this month, July, 2021.

The cash cow for these tests and the hundreds of companies that got rich selling them will now have to move on to the next phase to be able to cash in.

Diagnostic Testing Fraud: Controlling the Masses and Medical Kidnapping

We have been covering the corruption in the medical diagnostic testing field for the better part of a decade now, and we exposed it early on in the COVID-19 Plandemic last year as well.

Here are some of our previous articles from last year exposing the fraud of COVID-19 diagnostic testing.

When we started MedicalKidnap.com back in 2014, we learned that fraudulent diagnostic testing was a common way for doctors and hospitals to order children be removed from their homes.

Often they create false drug test positive results to remove children from their parents.

Alabama Lab Owner Arrested for Falsifying Results of Drug Tests Used to Medically Kidnap Children

The worst offender, by far, in medically kidnapping children by use of a medical diagnostic test, is within the field of radiology and finding “proof” of child abuse simply by looking at x-rays.

This whole field has developed a recent new class of pediatricians “certified” as “Child Abuse Pediatricians,” and the lucrative jobs of these doctors depend on them finding abused children and putting them into the lucrative child trafficking network known as “foster care.”

We have actually published an eBook on this topic, or you can look up individual cases on our MedicaKidnap.com website to learn how this evil system works.

When it comes to diagnosing “influenza,” we have exposed the fraud there as well, as pre-COVID-19 the CDC simply used estimates of cases of the flu, since they cannot verify actual numbers each year by diagnostic testing.

Annual Flu Deaths Scam Unwittingly Exposed and Replaced by the COVID Deaths Scam

So COVID-19 allowed them to just further exploit the fraud of diagnostic testing to create fear and panic, and achieve their goals of enslaving the public and rolling out their experimental mRNA injections.

With this latest announcement by the CDC that they are now going to retire the RT-PCR Diagnostic tests and replace them with other tests that can now test both COVID and influenza, it is pretty easy to see what their game plan is for later this year.

Just about everyone in the U.S. will be able to be tested “positive” for something by this Fall when the flu season starts.

This will be the “Hegelian principle” implementation for 2021. The government creates the problem, and then they create the solution, which we know now is more “vaccines” for everything in life that ails us, and try to punish those who don’t want to play their game.

I’m ready. Are you?

___________________

**Comment**

The CDC often quietly updates its website with inconvenient truth, when it works in their favor.  With COVID, this new information will make it possible for them to now jack the numbers of flu cases since they literally quit counting them making everything COVID.  I’m sure this will also be used to push the flu vaccine, which has never been effective, doesn’t prevent transmission, and actually increases your risk of contracting non-flu respiratory illness by 65%.

But there’s even something more diabolical going on here.

According to Jon Rappoport, the CDC/FDA is essentially confessing that they didn’t have a “virus” to begin with when they concocted the test using contrived samples of the virus. In short, they invented synthetic gene sequences and stated these sequences HAD TO BE close to the sequence of SARS-CoV-2. There is still no proof there is something called SARS-CoV-2. This article shows that the sequence used in PCR testing is present in ALL human DNA which equates C8 as a foreign hostile material and indeed the coronavirus – Covid19 – itself.

Each of the 59 different PCR tests for SARS-CoV-2 told different lies and concocted different fabrications about the genetic makeup of the virus—the virus we didn’t have. Obviously, then, these tests would give unreliable results.

BUT, don’t worry, be happy, because NOW, the CDC and the FDA say, they really do have actual virus samples of SARS-CoV-2 from patients; they have better targets for the PCR test, and labs should start gearing up for the new and improved tests.
In other words, they were lying THEN, but they’re not lying NOW. They were “contriving,” but now they’re telling the truth.

Rappoport states virology’s version of “we isolated the virus” to mean they created a soup in the lab containing monkey cells, toxic chemicals, drugs and random genetic material.  Researchers than assume that cells die due to a bit of mucus from a patient they dropped in the soup, therefore the virus must be the killer agent in the mucus – when it very well could be any of the components within the contrived soup.

The “new and improved” tests are nothing more than a money-maker for our corrupt public health ‘authorities’, who own patents on virtually every aspect surrounding COVID, including the spike protein.
They will now continue spinning their narrative utilizing these phoney tests.

Regarding Lyme/MSIDS, the CDC quietly updated their website from previously insisting Lyme can’t be spread congenitally to now admitting it’s possible, but rare.  But, as Lyme advocate Carl Tuttle points out: How can it be rare when nobody’s counting? The timing is impeccable.  Whenever there is a Lyme vaccine in the pipeline, the CDC finally admits how devastating and prolific tick-borne illness is.  I stand firmly with Tuttle that No Lyme vaccine should be considered until persistent infection is recognized.  But this will never happen because if they admit to persistent infection, they are also admitting that a vaccine would be ineffective against it.

The CDC often makes bold proclamations without a shred of evidence.  

For more on the PCR scam:

This completely bogus test has caused irreparable harm.  It’s been used to falsely elevate cases, then used to make the COVID injections appear to be working (by lowering the cycle threshold).  It has been used to make it appear that fully “vaccinated” people aren’t contracting or dying from COVID (called “break-through” cases) when many are, as well as to quarantine people, keep them from working, and causing unsubstantiated fear in the public.

This is not new.  Lyme/MSIDS patients have also been in a war due to faulty, arbitrary testing  that’s been rigged for a pre-determined outcome.

NIH Developed Stabilized Spike Protein in 2019 – Before Identification of SARS-CoV-2

https://www.nature.com/articles/s41587-021-00912-9

A network analysis of COVID-19 mRNA vaccine patents

A preliminary network analysis highlights the complex intellectual property landscape behind mRNA-based COVID-19 vaccines.

The COVID-19 pandemic has had a substantial impact on global health and highlighted the importance of international cooperation to effectively combat SARS-CoV-2. Since the discovery and publication of the virus’s genome in January 2020, scientists have rushed to develop vaccines, therapeutics and diagnostics on an unprecedented timescale. To date there are 80 vaccines in clinical trials and 70 more in clinical development, setting the stage for some of the fastest vaccine development and testing in modern history1. The vaccine technology platforms used by the most promising vaccine candidates range from viral vector–based and protein-based technologies to mRNA and lipid nanoparticle technology. Despite these impressive scientific achievements, barriers such as the vaccine cold chain and multiple forms of intellectual property (IP) protection stand in the way of equitable access and fair allocation.

Webs of intellectual property claims underpin the marketing of many vaccines. For example, the underlying technology used to develop a vaccine can be protected by patents, while manufacturing methods and techniques (know-how) can be protected by trade secrets.  (See link for article)

___________________

**Comment**

This important paper looks at patent applications and intellectual property claims. What is important to note is the revelation that our very own National Institutes of Health (NIH) developed the stabilized version of the spike protein used in COVID injections all the way back in 2019 – before the identification of SARS-CoV-2. 

The NIH has four other patent applications on a novel coronavirus vaccine. They have been studying mRNA for decades and the NIH patents are connected to more than a dozen vaccine developers. Please remember, the CDC is a vaccine manufacturer, owning over 50 vaccine patents, purchases and sells $4.1 billion in vaccines annually, and is not a neutral government agency. CDC scientists have exposed a long litany of agency corruption.

Also, important to understand is Youtube’s parent company Google has direct investment in the AstraZeneca/Oxford COVID “vaccine.” This is why YouTube censors anything that threatens the rollout and future profits of COVID-19 gene modification therapies.  Further:

  • Google is also partnered directly with the U.S. military, which is increasingly working on a transhumanist agenda
  • DARPA is heavily invested in transhumanist technologies for the use in soldiers, including brain-machine interfaces and other even more extreme ideas. They recently teamed up with the Wellcome Trust to create something called “Wellcome Leap,” a movement to usher in transhumanism
  • Investors are excited because the COVID-19 shot will most likely become an annual “vaccine” that is updated each season much like the seasonal flu vaccine  (which isn’t effective or safe)

I know that it feels daily as if we are stuck in a SyFy novel, but the truth is often stranger than fiction.  The reason they can get away with pushing gene therapy is by giving them the label of “vaccines,” to obtain Emergency Use Authorization (EUA).  Without this, slight of hand, the injections would be forced to go through lengthy safety testing, which has all been bypassed.  Please also see:   https://madisonarealymesupportgroup.com/2021/07/09/covid-vaccine-invented-before-covid-whats-going-on/

Dr. Wolfgang Wodarg, German physician and epidemiologist, wonders whether the drug industry may simply be using the EUA to learn more about how the mRNA technology actually works, using the public as guinea pigs.  He points out that some injections have been found to be nothing but saline, which suggests some people are actually getting a placebo injection, even though they’re being told they’re getting the real thing and they’ve not signed up for a formal trial.

Are “undercover” studies being performed that we’ve not been told about? There are many unanswered questions about what’s really going on with this COVID “vaccine” rollout. 

In the case of the U.S., the main manufacturer, not just for the Johnson & Johnson vaccine, [but also] a few others, is that same company, Emergent BioSolutions, which has an awful track record. The Pentagon lost a lawsuit in 2004 where they were accused of using U.S. military personnel as lab rats in an experimental off-label use of that particular anthrax vaccine they were producing …

Wodarg is very concerned that COVID-19 “vaccine” makers may be experimenting with various amounts of lipid nanoparticles, which could help explain some of the acutely lethal effects, and perhaps even the transfer phenomenon that appears to be occurring between vaccinated individuals and unvaccinated ones.

Of course, we don’t know if secret comparison trials are being done without our knowledge. What we do know is that Moderna has been working on mRNA vaccine technology for many years, and had been unable to solve the nanolipid toxicity problem. When the dosage was too low, the mRNA didn’t stick around long enough for the drug to work, and when too high, it became toxic.

Despite years of work, they were never able to determine an effective nontoxic dose of mRNA in nanolipid. At least they never announced success. Now we’re supposed to take their word that they got it all figured out in less than a year? No, most likely, they never did figure it out and are using the cover of the pandemic to release an untested vaccine on the public under the guise of emergency use authorization.

Effective nontoxic dosing is probably what the public COVID vaccination campaign is going to help them determine, so that knowledge can then be applied to other gene modification drugs and vaccines. It’s convenient in the extreme, seeing how they are not accountable for any of the damage and death their products are causing, and their unremunerated human test subjects now number in the billions.

As noted b Dr. Reiner Fuellmich, German attorney and co-founder of the German Corona Extra-Parliamentary Inquiry Committee, it appears we’re observing “the coming out of a very long-running strategy” to reduce the population and alter those who are left.  Source

In this powerful paper, posted all the way back in Sept. 2020, Dr. James Fetzer follows the long chronology which clearly demonstrates this ‘pandemic’ has been planned all along.  

It is my firm belief that the latest crack-down on those revealing this pertinent information has to do with the fact they are effectively getting to the root of the matter and need to be squashed.

  • In an unprecedented move of tyrannical proportions, the current regime is singling out 12 individuals for “killing people” due to simply giving information to base informed consent upon.
  • Public health ‘officials’ are wrongly pinning COVID cases upon the unvaccinated, despite testimony of true vaccine experts who state mass vaccination campaigns drive viral mutations, and the fact there are thousands of “break-through” cases – some of which end in death. There is also the data that shows the most “vaccinated” countries are the ones experiencing surges in cases, while the least-vaccinated countries are not. As of July, 5,492 fully “vaccinated” people have been hospitalized and over 1,000 have died.  Source  But this has been seriously understated as the CDC is lowering the PCR cycle threshold only for those getting the injections to downplay the fact many “fully vaccinated” are contracting COVID.
  • These officials also have issued an advisory telling Big Tech to to impose consequences (censoring 1st amendment free speech) on anyone defying the top-down accepted narrative.
  • This article states Facebook now says medical studies published in peer-reviewed journals are FAKE NEWS if they conclude things it disagrees with. 
  • And to continue their efforts to convince everyone to take their lucrative jab, they are now working with SMS carriers to dispel “misinformation” not just on social media, but in your private text messages, yet state they are “keeping politics out of the effort,” while they continue to deny life-saving treatments to suffering patients, deny the fact natural immunity to COVID may last years if not decades, and that previous infection may cut risk of reinfection by 84%.
Welcome to the new normal, where public health ‘officials’ censor experts trying to help patients.

As stated by Dr. McCullough, “All roads lead to the vaccine.”

For Lyme/MSIDS patients, this fact is nothing new.

COVID-19 Vaccine Associated Parkinson’s Disease

https://scivisionpub.com/pdfs/covid19-vaccine-associated-parkinsons-disease-a-prion-disease-signal-in-the-uk-yellow-card-adverse-event-database-1746.pdf

COVID-19 Vaccine Associated Parkinson’s Disease, A Prion Disease Signal in the UK Yellow Card Adverse Event Database

Citation: Classen JB. COVID-19 Vaccine Associated Parkinson’s Disease, A Prion Disease Signal in the UK Yellow Card Adverse Event Database. J Med – Clin Res & Rev. 2021; 5(7): 1-6.

* Correspondence: J. Bart Classen, MD, Classen Immunotherapies, Inc, 3637 Rockdale Road, Manchester, MD 21102, Tel: 410-377-8526. Received: 25 June 2021; Accepted: 18 July 2021

ABSTRACT

Many have argued that SARS-CoV-2 spike protein and its mRNA sequence, found in all COVID-19 vaccines, are priongenic. The UK’s Yellow Card database of COVID-19 vaccine adverse event reports was evaluated for signals consistent with a pending epidemic of COVID vaccine induced prion disease. Adverse event reaction rates from AstraZeneca’s vaccine were compared to adverse event rates for Pfizer’s COVID vaccines. The vaccines employ different technologies allowing for potential differences in adverse event rates but allowing each to serve as a control group for the other. The analysis showed a highly statistically significant and clinically relevant (2.6-fold) increase in Parkinson’s disease, a prion disease, in the AstraZeneca adverse reaction reports compared to the Pfizer vaccine adverse reaction reports (p= 0.000024). These results are consistent with monkey toxicity studies showing infection with SARS-CoV-2 results in Lewy Body formation.

The findings suggest that regulatory approval, even under an emergency use authorization, for COVID vaccines was premature and that widespread use should be halted until full long term safety studies evaluating prion toxicity has been complete. Alternative vaccines like the Measles Mumps Rubella (MMR) vaccine should be explored for those desiring immunization against COVID-19.

___________________

**Comment**

This is paper #2 from Classen, an immunologist and former NIH contract scientist, showing COVID injections to be extremely dangerous as they can cause prion disease. In his current paper he utilizes 6-months of UK adverse event data on AstraZeneca (uses GM adenoviruses) and Pfizer injections (uses lipid-encapsulated synthetic mRNA), whose goal is to stimulate the spike protein and antibodies, which show clear signs of causing symptoms of neurodegenerative disorders such as Parkinson’s, Alzheimer’s ALS, and others.  

The study showed nervous disorders, tremors, and sleep disturbances, after the COVID injections – all of which are symptoms of prion disease.  

Classen is concerned because the reporting system is set up to report acute events, not neurodegenerative issues, which can be non-specific or overlap with other conditions, which could occur years or decades later.  Due to this, findings could be exponentially higher.

Paper #1 which analyzed the Pfizer injection is here and points out many important details to consider, including an important excerpt from the summary:

Many have raised the warning that the current epidemic of COVID-19 is actually the result of an bioweapons attack released in part by individuals in the United States government [10,11]. Such a theory is not far fetched given that the 2001 anthrax attack in the US originated at Fort Detrick, a US army bioweapon facility. Because the FBI’s anthrax investigation was closed against the advice of the lead FBI agent in the case, there are likely conspirators still working in the US government. In such a scenario the primary focus of stopping a bioweapons attack must be to apprehend the conspirators or the attacks will never cease. Approving a vaccine, utilizing novel RNA technology without extensive testing is extremely dangerous. The vaccine could be a bioweapon and even more dangerous than the original infection.

Important excerpt:

This analysis should serve as an urgent warning to those mindlessly following advice of politicians and public health officials regarding COVID immunization. Both groups have had a dismal record of protecting the health of the public. US public health officials ran the infamous Tuskegee syphilis study allowing people of color to die from syphilis because the public health officials refused to inform the patients, they had syphilis and that a treatment existed. There have been numerous less well-known experiments on prisoners and other vulnerable populations in North America. The infamous Nazi physician Josef Mengele was a public health doctor.…

5 doctors state the injections are bioweapons & what you can do about it. The injections are NOT “vaccines” but cause YOU to manufacture spike proteins – perhaps indefinitely – the very thing causing illness. Those getting the injections are possibly transmitting this spike protein to those foregoing the injections.  

 

Dr. Stephanie Seneff – Risk of Prion Disease video

(Approx. 3 Min)

Unintended Consequences of COVID Mitigation Efforts – ‘Antimicrobial Resistance’

https://articles.mercola.com/sites/articles/archive/2021/07/21/covid-19-antibiotics-overuse

Surprising Ways COVID-19 Will Destroy Your Immune System

Analysis by Dr. Joseph MercolaFact Checked
covid 19 antibiotics overuse

STORY AT-A-GLANCE

  • The overuse of antibiotics, biocides and disinfectants to fight COVID-19 may “raise disastrous effects” for antimicrobial resistance (AMR)
  • The COVID-19 pandemic has accelerated the spread of AMR, as the majority of patients are treated with antibiotics, despite most not having a bacterial co-infection
  • The excessive and liberal use of antimicrobial products like household and industrial disinfectants, hand sanitizers and other cleaners is raising the risk of AMR in the environment
  • Your mitochondria, which play a role in antibacterial and antiviral immune responses, are an off-site target of certain antibiotics, thus antibiotic therapy may in turn may weaken your immune response
  • With proper “training” at regular intervals denied by COVID lockdowns, your immune system can overreact when triggered by ordinarily harmless substances, leading to allergies and inflammation

Antimicrobial resistance (AMR) has been declared one of the top 10 global public health threats to humanity,1 and it didn’t disappear once the COVID-19 pandemic appeared. Instead, it’s gotten worse, as infection control measures and hand hygiene using antimicrobial gels have become ubiquitous.

AMR causes about 700,000 deaths globally every year, but researchers estimated in mid-2020 that an additional 130,000 AMR deaths would occur in 2020 due to the COVID-19 pandemic.2 

The number of AMR deaths will likely surpass the number of COVID-19 deaths by at least threefold — annually — by 2050,3 with some estimates suggesting AMR deaths may reach as high as 10 million deaths per year.4

Prior to the pandemic, antimicrobial stewardship programs5 had been set up worldwide to help stop the inappropriate use of antimicrobials in hospitals, long-term care facilities and other settings, but a review by scientists with Shahid Beheshti University of Medical Sciences in Iran, published in Frontiers in Microbiology, predicts that an overuse of antibiotics, biocides and disinfectants to fight COVID-19 may “raise disastrous effects.”6 Further, the overuse of antibiotics may also be directly harming immune response.

Antibiotics Given to COVID-19 Patients ‘Just in Case’

Now remember that COVID-19 is caused by the SARS-CoV-2 virus, which means antibiotics are useless against it. Despite this, antibiotics have been used prophylactically throughout the pandemic for COVID-19 patients, typically using the logic that it could prevent bacterial co-infections.

However, the rate of secondary bacterial co-infections has generally been low, while the use of antibiotics has remained high. This isn’t a case of antibiotics being used strategically for patients who develop bacterial infections, but rather using them “just in case.”7 In a study of 38 Michigan hospitals, 56.6% of patients with COVID-19 were given antibiotics early in their stay, but only 3.5% of them turned out to have a bacterial infection.8

“For every patient who eventually tested positive for both SARS-Cov2 and a co-occurring bacterial infection that was present on their arrival, 20 other patients received antibiotics but turned out not to need them,” Dr. Valerie Vaughn, the study’s lead author, said.9 Other studies have revealed similar signs of rampant antibiotic overuse.

In a study of 99 COVID-19 patients in Wuhan, China, 71% received antibiotic treatment, but only 1% had bacterial co-infections.10 Overall, it’s estimated that 1% to 10% of patients with COVID-19 contract a bacterial co-infection,11 yet antibiotics remained a mainstay of treatment for the majority of cases.

Antibiotics Considered ‘Routine’ Part of COVID-19 Treatment

Despite decades of efforts to reduce the unnecessary use of antibiotics, one of the largest studies of antibiotic use in hospitalized COVID-19 patients revealed that such drugs are being used indiscriminately and inappropriately for COVID-19. More than half (52%) of the approximately 5,000 patients included in the study received antibiotics, and in 36% of cases, more than one antibiotic was given.12

Most of the time, in 96% of cases, the antibiotics were given before a bacterial infection was confirmed, either at admission or within the first 48 hours of hospitalization. As it turned out, only 20% ended up actually having a suspected or confirmed bacterial infection for which the antibiotics would be indicated. The rest received them unnecessarily. The Frontiers in Microbiology researchers explained:13

“It is noteworthy to be highlighted that the inappropriate use of antibiotics could considerably and silently lead to AMR development during this global outbreak. Unfortunately, recent studies reveal that, in several countries, common and extensive use of antibiotic treatment for COVID-19 hospitalized patients is considered as a part of the routine treatment package.”

Even the World Health Organization made it clear that countries were at risk of the accelerated spread of AMR due to the COVID-19 pandemic. They cited data showing antibiotic use increased throughout the pandemic. About 79% to 96% of people who reported taking antibiotics didn’t have COVID-19 but were taking them in the hopes of preventing infection, even though antibiotics don’t work against viral infections.14

Antimicrobial Overuse Could Damage Immunity

Antibiotics can cause a number of serious adverse effects, a little-known one being damage to your mitochondria, which are genetically closely linked to bacteria.15 Your mitochondria are responsible for most of your cellular energy production and also play a role in antibacterial and antiviral immune responses — and they’re an off-site target of certain antibiotics,16 which are known to inhibit mitochondrial activity, DNA synthesis and biogenesis.

“Thus, antibiotic therapy could be an important and not well appreciated cause of mitochondrial dysfunction. This in turn may weaken your immune response against the COVID-19 infection,” according to the featured review.17 In April 2020, scientists called for “urgent thinking out of the box” when it comes to antibiotics against COVID-19, as they noted:18

“ … mitochondria are vulnerable to antibacterial treatments, interrupting their physiology. Inhibition of these processes by antibiotics might render the immune system less capable of fighting acute COVID-19 viral infections.”

Concerning Overuse of Biocides and Disinfectants

The COVID-19 pandemic is poised to send antimicrobial-resistant disease sky high, as along with antibiotics overuse came the excessive and liberal use of antimicrobial products like household and industrial disinfectants, hand sanitizers and other cleaners.

The ramifications are immense and only beginning to be understood. There are potential adverse effects to human health from inhaling disinfectants, as such chemicals are known to accumulate in the lungs, liver, kidneys, stomach, brain and blood.19 Exposures were certainly elevated during the pandemic for many people, who were exposed to disinfectants by inhalation and oral routes, as well as via the skin and eyes.

There are also significant environmental concerns due to the “unusual release and dissemination of higher concentrations of biocide-based products into the surface and underground waters and also wastewater treatment systems” during the pandemic.20 When disinfectants and biocides enter the environment, they can wipe out beneficial bacterial species that are keeping drug-resistant microorganisms in check.

“[I]f the biocide concentrations reach the sub-minimum inhibitory concentration (sub-MIC), this event may augment the selective pressure, boost the horizontal gene transfer (HGT), and drive the evolution of AMR,” scientists warn.21

A team from the University of Plymouth in England also conducted a risk assessment to determine the potential environmental impact of prescribing COVID-19 patients antibiotics, which revealed, “The data for amoxicillin indicate a potential environmental concern for selection of AMR … ”22 The team urged such assessments be carried out in the future to keep tabs on the potentially disastrous effects of pandemic prescribing habits on AMR.23

Gut Microbiome Influences Immune Response to COVID

Antibiotics disturb your gut microbiome, which has far-reaching effects on your overall health, including your immune system’s ability to fight COVID-19 — marking yet another way that indiscriminate antibiotics usage is counterproductive.

When researchers with The Chinese University of Hong Kong analyzed gut microbiome compositions from 100 patients with COVID-19, they found gut commensals known to modulate the immune system were low compared to people without the infection.24 The makeup of patients’ gut bacteria — including both the volume and variety — affected the severity of COVID-19 infection as well as the immune response.25

Imbalanced gut microbiome could also contribute to the inflammatory symptoms associated with “long COVID,” in which symptoms persist for months after infection. According to the study:26

“In light of reports that a subset of recovered patients with COVID-19 experience persistent symptoms such as fatigue, dyspnea and joint pains, some over 80 days after initial onset of symptoms, we posit that the dysbiotic gut microbiome could contribute to immune-related health problems post-COVID-19.”

In the study, 50% to 75% of patients received antibiotics, while less than 7% had bacterial infections. While the researchers found no difference in outcomes with or without antibiotics, the drugs were not linked to improved patient outcome and, they noted, “it is still possible that a higher prevalence of antibiotic administration in severe and critical patients could worsen inflammation.”27

Isolation Disturbs Your Immune Response

Of all the negative effects of social isolation endured during the pandemic, those experienced by your immune system may be the last that come to mind, despite being among the most significant for your future health. What does staying home have to do with your immune system?

It alters your 24-hour light/dark cycle, on which your body is built to respond. With more time spent indoors, you have less sunlight exposure and less opportunity to produce vitamin D, which activates macrophages in your lungs that act as a first line defense against respiratory infections, among other immune activities.28

It’s true that taking vitamin D supplements can somewhat compensate for this, provided your levels are optimized, but other ill effects of lockdown are less easily remedied. Take exercise, another crucial component of a well-oiled immune response, that can reduce stress levels and diseases like heart disease and Type 2 diabetes, which are linked to worsened outcomes from COVID-19.

But even beyond that, staying indoors means you lose out on regular exposures to the natural world, which come with their own set of immune benefits. Trees release phytoncides, which people inhale and are known to alter natural killer cells.29 This is why, in Japan, shinrin-yoku, or forest bathing, is said to enhance immune function30 — but it’s difficult to spend much time immersed in the forest if you’re locked down at home.

The other factor that cannot be ignored is the lack of exposure to everyday dirt and germs that is missed when people stay home, socially distanced and sanitized. “Our immune system needs a job,” Dr. Meg Lemon, a Denver dermatologist, told The New York Times. “We evolved over millions of years to have our immune systems under constant assault. Now they don’t have anything to do.”31

What is perhaps most disturbing is that this comment was made in March 2019 — prior to the pandemic. Now, it’s exponentially worse, and your immune system is likely missing out on interactions with bacteria and other microorganisms that teach it, train it how to respond and keep it primed throughout your life.

Without proper “training” at regular intervals, your immune system can overreact when triggered by ordinarily harmless substances, leading to allergies and inflammation. Might a generation of children, kept isolated and masked, have immune repercussions when exposed to ordinarily routine childhood viruses post-pandemic?

Already, cases of respiratory syncytial virus (RSV), which normally circulates in the winter, have popped up in the summer months, suggesting possibly increased immunological susceptibility.32

New Antibiotics Are Unlikely to Save Us

There are 43 antibiotics in clinical development, but none of them shows much promise for solving rapidly rising AMR, as innovation is stagnant — most “new” antibiotics brought to the market are variations of drug classes that have been around since the 1980s. Further, according to WHO’s annual Antibacterial Pipeline Report, antibiotics currently in development are insufficient to tackle AMR:33

“The 2020 report reveals a near static pipeline with only few antibiotics being approved by regulatory agencies in recent years. Most of these agents in development offer limited clinical benefit over existing treatments, with 82% of the recently approved antibiotics being derivatives of existing antibiotic classes with well-established drug-resistance. Therefore, rapid emergence of drug-resistance to these new agents is expected.”

Also at issue, hospital reimbursement systems discourage the use of expensive new antibiotics, because they are only reimbursed up to a point. This means patients may be given older drugs that won’t work as well to protect the hospital from financial losses.

Legislation to reform this — the Developing an Innovative Strategy for Antimicrobial Resistant Microorganisms Act — has been introduced to help open up the use of new targeted antibiotics for superbug infections.34 Preserving the efficacy of existing antibiotics is also important, and agricultural antibiotics overuse cannot be ignored in this equation.

Worldwide, most antibiotics are used not for human illness or companion pets, but for livestock.35 Writing in the International Journal of Antimicrobial Agents, researchers stated, “the ongoing pandemic is stretching the limits of optimal antibiotic stewardship”36 and called for an end to unnecessary use of antimicrobial agents.37

So, be sure you always avoid antibiotics unless they are absolutely necessary. Additionally, choosing organic foods, including grass fed meats and dairy products, can help you avoid exposure to antibiotic residues in the food supply, while also supporting food growers who are not contributing to AMR.

You’ll also want to be careful in your use of disinfectants and sanitizers, using them sparingly and only when truly necessary, which — if you’re outside of a hospital — will be hardly at all.

+ Sources and References
 
Unfortunately what isn’t mentioned is that one of the greatest causes of antibiotic resistance is due to agriculture.
 
While we must certainly be careful in their usage in humans, clinicians were stabbing in the dark in the beginning of COVID to try to determine what would save lives.  Since that time, effective treatments that aren’t antibiotics have been found, but continue to be highly censored by our corrupt public health ‘authorities’, mainstream medicine, and the media, who are nothing more than puppets with severe conflicts of interest.  ‘Authorities’ are even banning natural substances in their efforts to make everyone get the jab.
 
The over usage of extremely toxic chemicals in effort to eradicate germs is truly causing untold damage.  I saw a picture recently of a child who developed horrible rashes on his legs after merely sitting in a grocery cart that had been sprayed and swabbed with these toxic cleaners.  This is new, prevalent, and must stop. 
These cleaners are far worse than a “virus” that has over a 99% survival rate, as well as effective treatments.
The effects of these cleaners will only be determined in time; however, the effects will most probably be pinned on COVID – like everything else.

Go here to listen to James Lyons-Weiler on the toxicity of QUATS.

Attorney Files Lawsuit Against CDC Based on “Sworn Declaration” From Whistleblower Claiming 45,000 Deaths Reported To VAERS – All Within 3 Days of COVID-19 Shots

https://healthimpactnews.com/2021/attorney-files-lawsuit-against-cdc-based-on-sworn-declaration-from-whistleblower-claiming-45000-deaths-are-reported-to-vaers-all-within-3-days-of-covid-19-shots/

Attorney Files Lawsuit Against CDC Based on “Sworn Declaration” from Whistleblower Claiming 45,000 Deaths are Reported to VAERS – All Within 3 Days of COVID-19 Shots

by Brian Shilhavy
Editor, Health Impact News

July 19, 2021

Ohio-based Attorney Thomas Renz was one of several speakers this past weekend at a conference in Anaheim, California, where he announced that with the help of America’s Frontline Doctors, he was filing a federal lawsuit in Alabama based on a “sworn declaration, under threat of perjury,” from an alleged whistleblower who claims to have inside knowledge of a cover-up of reported deaths filed with the Vaccine Adverse Event Reporting System (VAERS), which is operated by the CDC.

This whistleblower has allegedly claimed, under oath, that there are at least 45,000 reported deaths that have occurred within 3 days of receiving a COVID-19 “vaccine.” Renz states that this report of 45,000 deaths is just from “one system” that reports to VAERS.

This would be significantly greater than what the CDC is currently reporting, which is 10,991 deaths, and many of those are beyond 3 days following the shots. See:  CENSORED: CDC Records Almost 12,000 DEATHS in 7 Months Following COVID-19 Injections

Renz also states that he believes Google, Facebook, and Twitter are “complicit with causing death” due to their censorship, and he stated “I cannot wait to sue you, over and over again.”  (See link for article)

Here is the 10 minute clip of Attorney Thomas Renz’s announcement and discussion of the lawsuit and CDC whistleblower.

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“You see it in each country, it’s the same: the curve of vaccination is followed by the curve of deaths.  I’m following this closely and I a doing experiments at the Institute with patients who became sick with Corona after being vaccinated. Luc Montagnier, French virologist