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.
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:
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.
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.”
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.
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?
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**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 stillno 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.
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.
The Powassan virus is a tick-borne illness transmitted by the same tick that harbors the Lyme disease bacterium. Although it is still considered rare, the number of cases is growing and if contracted the virus can have devastating and long-lasting effects.
“We chose to review the Powassan virus because it only requires 15 min. of tick attachment for transmission, and the sequelae of the neurologic disease are devastating, in addition to a 10% mortality rate.”¹
What is Powassan virus?
The Powassan virus (POW) is a tick-borne flavivirus that is related to other viruses including: dengue, yellow fever, West Nile encephalitis, and tick-borne encephalitis (primarily found in Europe). “Flaviviruses are a group of single stranded RNA viruses that cause severe endemic infection and epidemics on a global scale.”²
In recent years, other viruses transmitted by ticks have been identified including the Heartland virus (phlebovirus) and the Bourbon virus (thogotovirus).
POW is very similar genetically to the deer tick virus and the clinical presentations are identical.
How was it discovered?
Powassan was first discovered in the brain of a young child.
“Powassan virus is named for the Ontario, Canada, town where it was first isolated from the brain of a 5-year-old boy who died of severe encephalitis in 1958,” the authors write.
Where is it?
The second case was reported in New Jersey (1970) and then another in eastern Russia (1978). Although, there have been no reported cases in other countries, the virus has been identified in a growing number of states.
In 2019, 13 U.S. states reported cases: Connecticut, Indiana, Massachusetts, Maine, Minnesota, North Carolina, North Dakota, New Hampshire, New Jersey, New York, Pennsylvania, Rhode Island, and Wisconsin.
Ticks infected with Powassan virus can transmit the disease in only 15 minutes, causing long-lasting neurologic problems in some individuals, in addition to a 10% mortality rate.
How is the virus transmitted?
The Powassan virus is carried and transmitted by Ixodes scapularis ticks, also known as deer ticks or blacklegged ticks. These ticks can also transmit Borrelia burgdorferi, the bacteria which causes Lyme disease.
“Although many flaviviruses have mosquitos as competent vectors, there is no evidence of human POW virus disease transmitted by mosquitos,” the authors point out.
How fast can Powassan virus be transmitted?
Very fast. “Transmission in mice has been shown to occur within 15 min. of I. scapularis attachment,” the authors write.
This rapid transmission occurs because the virus is already present in the salivary glands, compared to other non-viral tick-borne diseases where the pathogen is typically harbored in the tick’s mid-gut.
What is the typical clinical presentation?
“Few people who become infected with the POW virus have clinically significant disease,” the authors write.
However, in some cases, “a Powassan infection can lead to disorientation, headache, neck stiffness, fever up to 40°C, clonus, ocular, and other motor palsies, obtundation and convulsions, and can mimic herpes simplex encephalitis.”
Can Powassan virus be serious?
Yes.
“Approximately 50% of cases result in lasting hemiplegia, memory problems, and muscle wasting,” the authors explain.
“Ten percent of cases are fatal.”
Are there tests for it?
A PCR test is only positive in early stages of a Powassan infection. “IgG by enzyme-linked immunosorbent assay is the mainstay of diagnosis, but confirmation requires specialized testing,” write the authors.
Why are co-infections important?
Treatable tick-borne co-infections may be present. The authors describe a patient with a combination of Powassan encephalitis, Lyme carditis, and Babesia.
Yoon and colleagues described the case of a 17-year-old young man who died waiting for a Powassan virus test.³ He was not treated for a co-infection with Lyme disease. His autopsy showed Borrelia spirochetes, which cause Lyme disease, in his heart and liver. He also had PCR evidence of spirochetes in his brain and lungs.
What is the treatment for a Powassan infection?
There is no treatment for a Powassan virus infection other than supportive care.
Della-Giustina D, Duke C, Goldflam K. Underrecognized Tickborne Illnesses: Borrelia Miyamotoi and Powassan Virus. Wilderness Environ Med. Jun 2021;32(2):240-246. doi:10.1016/j.wem.2021.01.005
Chong HY, Leow CY, Abdul Majeed AB, Leow CH. Flavivirus infection-A review of immunopathogenesis, immunological response, and immunodiagnosis. Virus Res. 2019 Dec;274:197770. doi: 10.1016/j.virusres.2019.197770. Epub 2019 Oct 15. PMID: 31626874.
Yoon EC, Vail E, Kleinman G, et al. Lyme disease: a case report of a 17-year-old male with fatal Lyme carditis. Cardiovasc Pathol. Sep-Oct 2015;24(5):317-21. doi:10.1016/j.carpath.2015.03.003
Lyme borreliosis: a review of data on transmission time after tick attachment: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278789/ The claims that removal of ticks within 24 hours or 48 hours of attachment will effectively prevent LB are not supported by the published data, and the minimum tick attachment time for transmission of LB in humans has never been established.
There are about 5 to 10 percent of infected ticks that have a generalized infection, including salivary glands and saliva at the time of attachment. In such cases, transmission of spirochetes would and does occur immediately at time of attachment.” —Willy Burgdorfer
According to this study by Coppe Labs, right here in Wisconsin, 85% of Powassan infected ticks come from Northern Wisconsin. Another study by Coppe showed that when 95 patients were tested for suspected tick-borne disease, 66% showed evidence of current or prior Lyme infection. Of those patients, 17% had serologic evidence of acute POWV infection, demonstrating that POWV may affect more patients than we know.
For the last two years, Coppe Laboratories has dedicated a significant amount of time and resources to dispelling the myth that infection with Powassan virus, a virus transmitted by tick bite, is rare. The Centers for Disease Prevention and Control (CDC) reports only 100 cases of Powassan virus infection in the United States in the last 10 years. Indeed, that statistic gives the illusion that Powassan infection is rare. However, did you know that the only infections reported to CDC are those that are life-threatening, particularly cases causing severe inflammation of the brain like the case reported in LiveScience? Coppe has published three new papers in the last year that clearly show Powassan virus infection is not rare are at all, and until testing for this virus is included as part of tick-borne disease screening panels infections will continue to be underreported. Coppe’s Powassan Guide, which can be downloaded from the website, summarizes the findings from both tick and human Powassan prevalence studies, as well as defining the patient populations that would benefit most from Powassan testing.
The human body treats it like a pathogen and attracts a web or crown of inflammatory proteins to deal with it, which bears an uncanny resemblance to the crown of the coronavirus. The stealth nano particles are coated with the hydrophilic polymer PEG to dodge the immune system. This referenced article also asks if the triangle of injectable/intranasal modified nanoparticle drug delivery, the rapid expansion of 5G, and the insect diet being promoted (see “Insects on the menu” in this Substack) is to enhance the graphene in the body making it a sensor to gather and transmit information.
Reese has exposed how there are different variations of the shots and that several different batch numbers were deployed – some far more deadly than others. An investigation comparing the flu vaccine to the COVID shot reveals that there was a significant association between state political inclination and COVID shot state adverse event reporting, which was confirmed by the CDC.
Carlita Shaw is an Environmental Biologist & Health Freedom Writer/ Author
PCR test rod particles can act like asbestos in the body
The experimental physicist and biomaterial researcher Dr Antonietta Gatti examined various PCR test rods under the microscope and analyzed their ingredients. Antonietta M. Gatti, Ph.D. is also the coordinator of the Italian Institute of Technology’s Project of Nanoecotoxicology, called INESE.
The irritating result: the PCR test swabs are made of hard materials and contain a variety of (nano) particles made of silver, aluminium, titanium, glass fibres etc, many of which are undeclared in the package leaflet. When they enter the mucous membrane, they can cause wounds and inflammation, the scientist said. ENT doctors told 2020News that they are finding more hardened mucous membranes in people who are often tested for SARS-CoV-2. No longer intact mucous membranes can no longer fulfill their task of repelling viruses, bacteria and fungi before they reach the airways, as the pediatrician Eugen Janzen also reports. The germs thus penetrate into the airways without any immune filter.
Particularly problematic in this context: the warm breath moisture under the masks is the ideal breeding ground for germs of all kinds.
(See link for article and amazing microscopy)
_____________________
**Comment**
According to another independent test on PCR swabs in Slovakia, the material they found was Darpa patented hydrogel, lithium, and nylon.
Important excerpt:
”After spawning a mixture of nylon fiber fragments, Darpa Hydrogel remains on the nasal mucosa under the pituitary and pineal gland along with lithium. This mixture immediately reacts with living structures to form crystals that are directionally oriented to the pineal gland, which has its own electromagnetic field. The shape of the crystals determines the type of hydrogel used. The crystals are conductive due to the lithium contained in it. The crystals can receive the signal from the transmitter to the cell and transmit signals from the cell to the transmitter. These are actually nano-antennas.”
Lithium, aluminum, and mercury (widely used in vaccines) are highly toxic to the pineal gland. In low doses lithium blocks it and in higher doses it can completely destroy it.
Important excerpt:
”Darpa Hydrogel and lithium block and destroy the pineal gland and cause the thinking person to become a controllable biorobot. A hydrogel is a carrier of an active substance, its task is to get the substance into the body at a pre-desired place.” – Nutritruth.org
Interestingly, Ivermectin which has been found to be an effective, safe treatment for COVID, dissolves the hydrogel crystals.
Ivermectin is also being used for recovery of post-injection adverse reactions as it binds with the spike protein thereby helping the body to eliminate it.
This cheap treatment has been widelycensored by our corrupt public health ‘officials’.
Corrupt public health does not want you to recover.
Gatti’s research shows the PCR swab destroys our natural mucosa membrane leaving us more susceptible to further viral infection. Additionally, it appears the hydrogel is causing blood clots in the blood vessels.
It is also ironic that getting COVID injections also makes people more susceptible to further viral infection.Efficacy is extremely low. In fact, they are estimated to be less than 1% effective. Further, the injections do not prevent infection or transmission. All gene-based injections can be expected to cause blood clotting, bleeding, and other adverse events, particularly with:
each re-vaccination and each intervening coronavirus exposure. Over time, whether months or years [35], this renders both vaccination and coronaviruses dangerous to young and healthy age groups, for whom without vaccination COVID-19 poses no substantive risk. Source
These injections are driving the virus to mutate into deadlier variants less responsive to vaccination.
..after saying that indeed those who are vaccinated DO get more acute pathogen-creating illness, like CORONAVIRUS, that should make us all wonder if there are any connections here. The acknowledging that patients DO get ill after flu shots from these other viruses (VIRAL INTERFERENCE) is priceless yet disturbing. Basically patients have been made to feel like they were wrong for decades. I am sure deaths too, have been involved but to correctly blame it on the vaccine has been taboo. Mutating bacteria and viruses are possible for sure and vaccines can also be responsible for that. Source
Graphene Oxide Found in masks, PCR Swabs, and COVID injections
Go here to listen to an ozone practitioner explain how graphene cuts the body up from the inside out causing spontaneous microclotting. She shows an example as well.
Graphene Oxide nanoparticles have been found by electron microscopy and spectroscopy, among other techniques to be in the COVID PCR and antigen testing swabs, masks, and injections.
The pictures are quite clear that COVID injections contain graphene oxide and other potentially harmful substances. Since these substances are not disclosed in the manufacturer’s technical data sheets, the researchers are calling for a stop to the injections and for extensive, independent counter-analysis be done on all COVID shots. The nanoparticles found are not biocompatible and can cause thrombotic activity, hemorrhaging, strokes, myocarditis, and can enter the brain.
German doctors have also discovered that the blood of those getting the COVID injections is changing, and a Canadian doctor has discovering microclotting in 65% of his “vaxxed” patient’s blood.
In this important Q & A video, a highly credentialed scientist from a top 10 science testing facility states that recent testing has now confirmed that the highly toxic element graphene is in our precipitation, along with an already long list of toxins including aluminum nanoparticles.Surfactants have also been confirmed in recent precipitation testing. Climate intervention operations are ubiquitously contaminating the entire planet and every breath we take. While the ‘authorities’ blame ‘climate change,’ they in fact are behind the true damage.
This study shows how graphene oxide in rats not only down-regulates glutamatergic synapses but changes synaptic function which is crucial to learning and memory. These changes are implicated in several brain diseases from dementia to anxiety disorders.
In April, Health Canada issued an advisory warning people not to use face masks which contain graphene or biomass graphene. The reason? Graphene in masks could damage your lungs. They recently updated their guidance and essentially state: nothing to see here.
A large consortium funded by the EU is conducting research on graphene as an “anxiety-reversal agent” which affects the brain. They have published an article, “Soothing the symptoms of anxiety with graphene oxide.” They found the following:
graphene oxide inhibits anxiety-related behaviors
injecting it into a specific region of the brain silences neurons responsible for anxious behavior
Investigative journalist Jon Rappoport asks: “What happens when you walk around all day, day after day, breathing in graphene through a mask? What happens to your lungs? To your brain? To your feelings? To the quality of your thoughts?”
Interestingly, the completely and hopelesslycorruptCDC states that “anxiety” is causing adverse reactions to the COVID injections. What better way to alleviate these fears than with continual dosing of graphene oxide?
The flu vaccine contains graphene oxide nanoparticles and the new flu vaccines and the new intranasal COVID vaccines they are preparing also contain huge doses of graphene oxide nanoparticles.
Graphene nanoparticles cause hypercoagulation (thick blood) which in turn causes blood clotting. It also causes a cytokine storm that alters the immune system negatively and lessens glutathione. It is a a superconductor. If exposed you get a metallic taste and eventually a loss of taste and smell. It also explains the magnetic phenomenon(being able to put metal on the injection site and having it stick) after receiving the COVID injection.
We had access to a sealed vial from Pfizer, and by means of a request for services to a university, specifically in my name, it was sent for an analysis of the vial, where we were looking for the material in question: graphene. After some time of investigation by Dr. Pablo Campra Madrid, Doctor in Chemical Sciences, Bachelor in Biological Sciences and member of the University of Almeria, we obtained this preliminary report where we are told that there is indeed solid evidence of graphene oxide in the sample and that it is also the main component of what they wrongly called a vaccine.
In short, graphene oxide behaves exactly like the supposed SARS-CoV-2 of the official version, generating the same symptomatology of severe COVID-19. When installed at the neuronal level, it causes neurodegeneration or, in other words, neurological COVID-19.
So, from here we started to see what possible compounds, drugs and treatments could degrade graphene oxide. And look what we found: N-acetylcysteine (NAC) or glutathione administered degrades it. Because what glutathione does is counteract free radicals and oxidants, all the toxins that can enter the body.
We now fully understand why those treatments worked: because they addressed all the symptoms of the disease supposedly caused by SARS-CoV-2. Given that to date there is no scientific evidence of an actual sequencing and isolation of SARS-CoV-2, we suspect with many credible indications that COVID-19 disease is actually the side effect of the introduction of graphene oxide into the body by different ways.
‘Researchers at Karolinska Institutet, the University of Manchester and Chalmers University of Technology have shown that the human immune system handles graphene oxide in a manner similar to pathogens, possibly leading to safer biomedical applications in the future.’ Source
Dr. José Luis Sevillano proposes a preventive treatment for Panamanian colleagues who at a conference were very interested in treating patients with zinc, glutathione, and N-acetylcysteine (NAC). These antioxidants have been found to help the body detoxify graphene oxide.
The masks being used and currently marketed contain graphene oxide. Not only the ones that were withdrawn at the time, as indicated by the media, the swabs used in both PCR and antigen tests also contain graphene oxide nanoparticles.
The COVID vaccines in all their variants, AstraZeca, Pfizer, Moderna, Sinovac, Janssen, Johnson & Johnson, etc., also contain a considerable dose of graphene oxide nanoparticles. This has been the result of their analysis by electron microscopy and spectroscopy, among other techniques used by various public universities in our country. Source
This article points out the graphene in face masks are nanoscopically thin, hexagonally-arranged flakes of carbon atoms. Current science indicates that if the material is inhaled and gets into the lower lungs, it can lead to an inflammatory response at high enough concentrations. There is also evidence that the jagged edges of graphene particles can harm cells, also leading to damage. The author states he reached a “dead end” in his search for evidence on the release of graphene particles in face masks.
He states lack of findings are a red flag because small quantities of this material have the potential to cause a lot of harm – 5-10 um in diameter could potentially be a health hazard.
The irony here is that hundreds of millions of dollars have been poured into studying the risks of engineered nanomaterials over the past couple of decades. Yet when it comes to real-world products and real-world risks, no-one seems to be asking the questions that count, or providing answers! – Andrew Maynard
It doesn’t take a brain surgeon to see the potential problem here so poignantly pointed out by free-lance investigative journalist Jon Rappoport:
Step one: breathe in nanoparticles of graphene
Step two: develop a so-called major COVID symptom—lung infection
In an interview with Dr. Mylo Canderian, Ph.D., developer of the graphene oxidepatent as a Hematological Bioweapon in 2015, states those “vaccinated” with the COVID shots will all die within a maximum window of 10 years.
The “vaccinated” having a 20% graphene oxide deterioration in their blood, barring any other input criteria, live for 8 years (10 years less 20%).
Those with 70% graphene oxide deterioration will not live more than 3 years (10 years less 70%).
When asked about what effect boosters have, Mylo replied it can all be determined through blood testing. The more shots and boosters get the worse their blood will look under the microscope and the “quicker they will turn to fertilizer.”
Graphene oxide and 5G were the main sources of attraction at the Mobile World congress. Bill Gates’ Microsoft patent made on March 26, 2020 for a “body Activity Data” apparatus #WO2020060606, which is described as a “Cryptocurrency System Using Body Activity Data,” senses body activity of the user.
“Human body activity associated with a task provided to a user(1) may be used in a mining process of a cryptocurrency system. A server may provide a task to a device of a user which is communicatively coupled to the server(2). A sensor communicatively coupled to or comprised in the device(3) of the user may sense body activity of the user. Body activity data may be generated based on the sensed body activity of the user. The cryptocurrency system communicatively coupled to the device of the user may verify if the body activity data satisfies one or more conditions set by the cryptocurrency system(4), and award cryptocurrency to the user whose body activity data is verified.”(5) https://operation-nation.com/bill-gates-microsoft-file-patent-for-dystopian-body-activity-data-implants/
These ‘digital certificates’ are human-implantable ‘QUANTUM-DOT TATTOOS’ that researchers at MIT and Rice University are working on as a way to hold vaccination records. It was last year in December when scientists from the two universities revealed that they were working on these quantum-dot tattoos after Bill Gates approached them about solving the problem of identifying those who have not been vaccinated.
Quote by Gates to the Financial Times:
“YOU DON’T HAVE A CHOICE. NORMALCY ONLY RETURNS WHEN WE’VE VACCINATED THE ENTIRE GLOBAL POPULATION.”
Now, Tyson Gabriel, an industrial hygienist, safety engineer, and risk manager who trains doctors and has 20 years of experience implementing exposure prevention plans in industry, and is lead researcher for his team, has examined each mask study on the CDC’s website. Also see these reports.
Our corrupt health ‘authorities’ also never mention the negative impacts of masks.
Researchers from Germany similarly questioned whether a mask that covers your nose and mouth is “free from undesirable side effects” and potential hazards in everyday use. It turns out they pose significant adverse effects and pathophysiological changes, including the following, which often occur in combination:
Increase in dead space volume
Increase in breathing resistance
Increase in blood carbon dioxide
Decrease in blood oxygen saturation
Increase in heart rate
Decrease in cardiopulmonary capacity
Feeling of exhaustion
Increase in respiratory rate
Difficulty breathing and shortness of breath
Headache
Dizziness
Feeling of dampness and heat
Drowsiness
Decrease in empathy perception
Impaired skin barrier function with acne, itching and skin lesions
Boiling Point: The Lyme + Fibromyalgia + Chronic Fatigue Connection
by Dr. Bill Rawls
Updated 6/11/21
The misery of chronic illness is very real. But if you’re the one who’s suffering, you know that those around you typically can’t see it or understand it — not family, friends, or even medical providers.
They don’t know what it’s like:
…to push through oppressive fatigue day after day.
…to be tired beyond exhaustion but unable to sleep.
…to ache all over so badly that all you want to do is curl up in a ball inside a dark closet.
…to feel like you have the flu every day of your life but still have to go to work.
…to be isolated, both socially and professionally.
…to have bizarre symptoms that no one can put a finger on.
…to be told that all your lab tests are normal, even though something is obviously wrong.
…to become dependent on symptom-suppressing drugs prescribed by well-meaning doctors who didn’t know enough to know better.
I can relate better than most doctors because I’ve lived it. I am part of a growing epidemic of people suffering from chronic ailments that the modern medical system is at a loss to help.
An unexpected twist during my late 40s changed my life and career path forever. Unrelenting stress from a too-busy medical practice combined with an entanglement of unpredicted life stressors plunged me into chronic misery that took me 10 years to escape.
For one, they carry a stigma. Many Americans believe fibromyalgia and chronic fatigue are made-up excuses for getting out of work and other life obligations. This would help explain why people with fibromyalgia suffer for nearly a year on average before seeking treatment.
What’s worse, both of these conditions are considered disorders and not true diseases. Why is that significant? Because a disease is considered treatable, whereas a disorder is a label given to a collection of symptoms for which there is no known cause or treatment.
Doctors prefer treating illnesses that are easy to define and have known solutions. If you have something that’s difficult to define and has no known treatment, they don’t want to mess with it. I admit, I know the feeling: I’ve been confronted with patients who have a long list of seemingly unrelated symptoms, and when no tests pointed to a specific diagnosis, it was frustrating.
Then, I became the patient — I could almost sense my doctors roll their eyes the minute I came through the door.
To be honest, I didn’t completely fit the strict criteria for either fibromyalgia or ME/CFS — I had more muscular pain than you’re supposed to have for chronic fatigue, but I also didn’t have all the specific trigger points of fibromyalgia. I now know that’s the norm. Studies have shown that greater than 70% of people given the label of fibromyalgia don’t fit the strict criteria for the diagnosis, and similar for ME/CFS.
Diagnosis Break Down
The concept of “diagnosis” is artificial by nature — it’s simply a way to categorize an illness to define a treatment plan. It works well for acute illnesses, such as a broken leg, acute appendicitis, heart attack, stroke, acute pneumonia, or kidney stones, where the cause is well defined, and interventions exist specifically to address it.
However, the concept of diagnosis is often less functional when applied to chronic illnesses. The signs and symptoms of many chronic illnesses overlap, and the underlying causes are not straightforward. All too often, patients are left endlessly searching for the “right” diagnosis or end up with a diagnosis like fibromyalgia or ME/CFS.
Unfortunately, for most chronic illnesses, medical therapies are designed to artificially block symptoms or the progression of the condition. Patients end up in a state of managed illness and never get well. This is true not only for fibromyalgia and chronic fatigue but also for a range of other chronic illnesses, including autoimmune diseases, chronic Lyme disease, multiple sclerosis, Parkinson’s disease, and ALS.
Dissatisfied with symptom management alone, I decided to aggressively pursue healing. Along the way, I discovered I was carrying the bacteria associated with Lyme disease, Borrelia burgdorferi. At first, I was relieved. Finally, a “real” diagnosis! But after several rounds of antibiotics left me sicker than when I started, my presumptive diagnosis of Lyme disease generated more questions than answers. If I had Lyme, why didn’t antibiotics help?
The reason: Once the bacteria are buried deeply in tissues, testing is often inaccurate, and the bacteria are extremely resistant to antibiotic therapy. What’s more, there are many other bacteria that can cause Lyme disease-like symptoms, equally as resistant to antibiotics. And like me, many patients diagnosed with fibromyalgia and ME/CFS often end up finding out they are carrying the bacteria associated with Lyme disease.
After antibiotics failed and otherwise getting nowhere with the medical system, I decided to take things into my own hands. Somehow I knew that I was destined to figure this thing out — and if I was successful, I could help others who were suffering like I was.
But first, I had to rethink the concept of chronic illness as I was taught in medical school. Instead of studying how to label and inhibit disease (mostly with drugs), I was searching for answers as to why chronic illness happens in the first place. Deep down, I felt that chronic Lyme disease, fibromyalgia, and ME/CFS were somehow related, and these and many other chronic illnesses shared common root causes.
It wasn’t an overnight revelation; it took years of intense research and deep introspection. My search began with an extensive review of human biochemistry, physiology, and pathology.
“Many patients diagnosed with fibromyalgia and ME/CFS often end up finding out they are carrying the bacteria associated with Lyme disease.”My conclusion?
Wellness boils down to one thing: the health of the cells of your body.
Healthy Cells Equal a Healthy Body
The human body is a complex collection of living cells. When all the cells in the body are healthy and working in unison, you feel well. Symptoms occur when cells are stressed. Sometimes the symptom points to the source of stress: for example, joint pain indicates that cells in the joints have been taxed or injured. Symptoms like fatigue, however, suggest that cells throughout the body are overburdened, and communications that unify cellular functions have been compromised.
Fortunately, cells can recover from being stressed; it’s what healing is all about. Cells can repair internal damage, and even when they’re injured beyond repair, other cells in the body can divide to make replacements (some cells do this better than others: skin cells have the highest potential in the body to regenerate and nerve cells have the lowest potential). That is, if the stress resolves or is relieved.
Chronic illness occurs when stress never resolves, and our cells don’t get a chance to recover from being overworked. There are many different chronic illnesses because different cells in the body can become chronically stressed in different ways.
The immune system plays an enormous role in the healing process. It’s responsible for removing old and abnormal cells, cleaning up cellular debris and dead microbes, clearing foreign substances from the bloodstream, and purging toxins from the body. During chronic illness, cellular turnover is increased to the point that the immune system becomes overtaxed. When the immune system can’t do its job, all cells in the body suffer.
It becomes a vicious cycle that increases cellular stress throughout the body and intensifies the process of chronic illness.
So, What Stresses Cells?
The factors that stress or threaten cells are intimately tied to the fact that we must interact with the surrounding environment to survive. The nutrients, water, and oxygen that cells need to thrive must come from outside the body. This mandatory interaction with the outside environment poses a variety of different risks to cells of the body.
All totaled, there are five categories of factors that can stress cells of the body and lead to chronic illness.
5 Cellular Stress Factors
#1 Unnatural diet: To function properly, cells require carbohydrates and fats to generate energy, amino acids to make proteins, and a wide spectrum of nutrients, including vitamins and minerals, all of which must be extracted from food by the intestinal tract. Though humans can tolerate a wide variety of foods, if the right balance of nutrients isn’t present, then cells suffer. It’s not just deficiencies of nutrients that cause problems; the gross excess of carbohydrates and refined fats that have become signatures of the modern diet is extremely damaging to cells.
The type of food you eat also influences how well the digestive system works; the intestinal tract requires dietary fiber and a healthy balance of bacteria to function properly. Carb-loaded processed food causes overgrowth of bacteria, which compromises the intestine’s protective barrier. This allows foreign proteins and bacteria to leak across the gut-blood barrier, which sends the immune system into overdrive, causing fatigue, brain fog, flu-like symptoms, and other symptoms.
#2 Toxic environment: Though toxic substances have always been present in the earth’s atmosphere, our modern environment has become inundated with unnatural chemicals that are toxic to all lifeforms. Toxic substances in water, food, and air, or those that come in contact with skin, have the potential to disrupt biological processes of cells directly or impede communications (hormones, neurotransmitters), which interferes with all cells in the body.
Beyond toxic chemicals, the modern sea of artificial radiation generated by cell phones, computers, microwave transmission towers, and hundreds of other sources can disrupt cellular functions.
#3 Chronic mental stress: The complexities of 21st-century life cause a certain level of pervasive, low-grade tension. Continually remaining in high-alert mode hampers all communication systems in the body. Eventually, the body and cells begin to break down. Chronic stress also disrupts normal sleep — a necessity if cells are to have downtime to recover from being stressed. Normal health is not possible without adequate sleep.
#4 Sedentary lifestyle: Until about 100 years ago, physical stress would have been characterized by excessive physical labor. Today, the opposite is true. Modern life, however, requires little in the way of physical effort. Increased blood flow associated with physical activity flushes debris and metabolic waste that has collected around cells. It’s such an integral part of cellular health that being sedentary is extremely detrimental. Without regular movement, everything in the body stagnates, toxic substances accumulate, muscles turn to mush, arteries become clogged, and cell loss is increased.
#5 Microbes: We share our bodies with trillions of microorganisms known as the microbiome; by numbers alone, they outnumber our cells 10:1. The list includes 20-40 thousand different species of bacteria but also protozoa, fungi, multicellular parasites, and an untold number of different viruses. Though we have a mutually beneficial relationship with most of our microbes, some aren’t so friendly. Beyond that, foreign microbes from the outside are constantly trying to get inside the body.
They all want food — the carbohydrates, fats, proteins, vitamins, and minerals that make up our cells provide everything that microbes need to make more microbes. Therefore, infection is simply microbes trying to get inside your body to consume your cells.
Microbes: A Key to Chronic Illness
The vast majority of microbes that inhabit the body are confined to the gut, skin, and body openings. Technically, however, these microbes are outside the tissues of the body. Because all microbes have the potential to consume our cells, the body maintains barriers to keep them out. The primary barriers include:
Skin
Mucous membranes lining the mouth and nasal passages
Bronchial passageways in the lungs
Linings of the stomach and intestinal tract
In other words, even though our microbes are part of us, they are kept apart from the cells that make up our tissues because of the potential to do us harm. Of course, certain microbes have a higher potential to cause harm than others.
The microbes with the lowest potential for harm are defined as normal flora. Normal flora are microbes that your immune system knows better than any others — it’s a relationship that has been honed over millions of years. Because the immune system is able to keep these microbes completely in check, the partnership is mutually beneficial.
We depend on our normal flora to keep other, more aggressive microbes in the gut and on the skin suppressed. Intestinal and skin diseases result when the balance of normal flora is disrupted by poor diet, chronic stress, or antibiotic therapy.
Because the barriers of the body aren’t nearly as secure as you might hope, you rely on your immune system to protect your cells from pathogens that get through. Without protection from the immune system, your cells are defenseless.
Studies over the past decade, however, have shown that microbes regularly trickle across barriers. This means the immune system must constantly stay on guard to protect cells. Beyond that, microbes from the outside are constantly trying to cross barriers to get inside the body.
Case in point: Every time you get bitten by a tick, mosquito, or flea, are nipped or scratched by a dog or cat, scrape or cut your skin, put your fingers in your mouth or your nose, hug or kiss another person, have sex, use a public toilet just after someone else has been there, take a breath just after someone sneezes, swim in a natural pond, lake, or river, or consume any food or beverage — foreign microbes enter your body.
A microbe that can do us harm is called a pathogen. The potential of a pathogen to do harm is more about the relationship our immune system has with a particular microbe than the microbe itself.
Of course, there are varying degrees of pathogens; some are more threatening than others. A microbe like the Ebola virus is so dangerous because humans have rarely been exposed to it. Therefore, we don’t have built-in immunity to it. When Ebola crosses barriers into tissues, it’s able to ravage cells of the body.
Fortunately, most of the foreign microbes you will be exposed to during your lifetime are low-grade pathogens. They are well known to your immune system, and, if your immune system is healthy, they have a low potential to cause you harm.
But if your immune system becomes compromised, low-grade pathogens can also be problematic to you. Certain microbes have adopted stealth as a primary strategy for evading immune functions. First, they enter your bloodstream. Then, they hitch a ride inside white blood cells to all tissues throughout the body — muscles, joints, heart, organs, intestines, and even the brain and nervous system. Termed intracellular microbes, they’ve adopted the ability to live inside cells by cannibalizing them for nutrients to survive and make new microbes. When that cell is used up, they emerge to infect other cells.
Beyond borrelia, there are many known microbes that fit the description of being intracellular, and many more yet to be discovered. Mycoplasma, bartonella, chlamydia, and babesia are a few well-known examples, and coinfections with these microbes are common in people with Lyme, fibromyalgia, chronic fatigue, and other chronic illnesses.
Despite intracellular microbes’ manipulative ways, your immune system is well versed in all of their tricks. It evolved over millions of years from repetitive exposure to many thousands of microbes, and each encounter was recorded in your genes for future reference. The better your immune system “knows” a microbe, the better it is able to slow its growth rate and maintain ultra-low concentrations in tissues.
Notice I didn’t say the microbes are eradicated. They are very good at persisting. A much more common outcome is a stalemate in which the stealth microbes are marginalized, and their potential for harm is minimized (their natural aggressiveness is kept in check). But they can stay alive and dormant deep in tissues for a lifetime without you ever knowing they are there.
Though science is just starting to understand the role that stealth microbes and other opportunistic pathogens play in the microbiome, one fact is quite clear: Everyone, even the healthiest of us, harbors a variety of intracellular microbes that are low-grade pathogens. As long as your immune system is healthy, you’ll never hear from them.
But cells overwhelmed by poor nutrition, toxic environment, chronic mental stress, and sedentary lifestyle become more vulnerable to invasion by intracellular pathogens. Increased cellular turnover and increased microbe activity overtaxes the immune system. At a certain point, a threshold is crossed, such that symptoms occur.
Impaired immune function allows the microbiome to shift off balance and pathogens in your tissues and gut to flourish. It’s not just one microbe that becomes activated, but all the questionable suspects — stealth microbes that have been dormant in tissues, pathogens in the gut and on the skin, and viruses in tissues such as Epstein-Barr virus(EBV) and cytomegalovirus (CMV), setting the stage for chronic illness. The associated symptoms result from the immune system’s reaction to the microbes and the damage the microbes inflict upon the cells directly.
When Symptoms Boil Up
You can think of it as a pot of water on the stove that starts out over a low simmer. As the simmer increases, minor discomforts start showing up — general body aches and joint stiffness; bloating, gas, and digestive issues; lack of energy; and simply not feeling well. Often, these kinds of changes become accepted as part of aging or life in general.
It’s not until the pot is fully boiling over that things become noticeably uncomfortable. Sometimes it’s a specific event that causes the pot to bubble over — severe emotional stress, an accident or trauma, an acute viral illness, or even a tick bite. But most often, it’s a perfect storm of cellular stress factors accumulating over time until a tipping point is reached.
At that point, the immune system can no longer keep a lid on things, and life becomes miserable. I refer to this as Chronic Immune Dysfunction.
What Chronic Immune Dysfunction Looks Like
Typical Chronic Immune Dysfunction (CID) symptoms include fatigue, decreased stamina, stress intolerance, feeling flu-like, muscle pain, joint pain, and sleep disturbances. Also common are temperature fluctuations, digestive dysfunction, mood changes, brain fog, skin rashes, a range of neurologic symptoms, and allergic-type reactions.
If you hadn’t already guessed, the default diagnosis for this morass of symptoms is fibromyalgia, when pain is the primary symptom. Or, if fatigue predominates, it’s labeled myalgic encephalomyelitis/chronic fatigue syndrome. Both are conditions, not diseases, and thus, are considered to have no known cause or treatment by the conventional medical community.
If a patient presenting with CID symptoms has any history of tick exposure, some providers may consider the possibility of Lyme disease. On the surface, this might seem like a much more attractive diagnosis than fibromyalgia or chronic fatigue because it has a recognized cause (infection with a microbe), which implies a condition is treatable with antibiotics.
Unfortunately, this only applies to acute Lyme infection. Chronic Lyme disease is actually another consequence of CID, in which immune reaction is dysfunctional, and the entire microbiome is disrupted. Concentrations of borrelia are low and embedded deep in tissues where antibiotics can’t reach them. As a result, treating chronic Lyme isn’t much different from treating fibromyalgia or ME/CFS.
When you consider the cause of all three of these chronic illnesses, the concept of diagnosis becomes practically irrelevant. Instead of being entirely separate illnesses, they are all very likely just different variations of the pot boiling over.
Indeed, all chronic illnesses — fibromyalgia, ME/CFS, chronic Lyme disease, and even more definitive diagnoses such as Parkinson’s disease, multiple sclerosis, ALS, and autoimmune diseases — share an association with Chronic Immune Dysfunction.
What types of illness you end up with during your life is dependent on three factors:
Genetics: Your genes define your risk of different illnesses, but not whether you will actually get those illnesses.
How cellular stress factors come together to disrupt immune system functions.
Which intracellular microbes you pick up through life. Because intracellular microbes have a preference for certain cells of the body, the various combinations of these microbes give rise to different chronic illnesses. In other words, when it comes to defining the spectrum of chronic illnesses, microbes are the wild card.
When chronic illness is considered as a “pot boiling over” problem, the best solutions are directed toward decreasing cellular stress factors to restore normal immune system functions and balance in the microbiome, instead of treating symptoms alone. Take this route, and wellness becomes a reachable endpoint, as opposed to living in a chronic state of managed illness. Here’s how to get from here to there.
Real Solutions for Chronic Immune Dysfunction
I divide options for overcoming illnesses associated with Chronic Immune Dysfunction and stealth microbes into two categories: Heroic Therapies and Restorative Therapies.
A third category of solutions, Symptomatic Therapies, is best reserved for acute relief. Specifically directed at controlling symptoms, Symptomatic Therapies come mostly in the form of prescription drugs and contribute only minimally to healing and wellness.
Heroic Therapies
Heroic Therapies have significant limitations. They include single-agent chemical warfare (antibiotics), oxidative therapies (ozone, hyperbaric oxygen), rife machines, and any other therapies directed specifically at killing pathogens. But stealth microbes hide in protected niches in the body, occur in low concentrations, and typically grow very slowly, so they are extremely hard to eradicate with antibiotics.
In fact, keeping stealth microbes at bay is just about impossible without restoring normal immune function. When people do get better with heroic therapies, it’s only because microbes are suppressed enough to allow rebound of immune function to get a handle on things, not because the heroic therapy eradicated the microbes completely. And sometimes, heroic therapies can suppress immune function further and actually make the person more ill.
Ultimately, where you want to be is with a healthy immune system keeping all stealth microbes well marginalized, so harm is minimized and you can enjoy a normal, vibrant life. Restorative Therapies are the best way to get you there. They focus on minimizing Cellular Stress Factors to optimize immune function and restore homeostasis (natural balance in hormone and healing systems in the body), as well as killing or suppressing microbes.
Restorative Therapies
With Restorative Therapies, the ability of the body to heal itself is restored, along with the ability of the immune system to control any threatening microbes in the margins. This approach takes time and patience, but because it has such low potential for harm, it can be followed for a lifetime.
A comprehensive restorative program includes the following essential components:
Balance your microbiome with herbal therapy. Take synergistic herbal therapy to suppress microbes, promote microbiome balance, and help counter the other cellular stress factors.
Herbal therapy is the cornerstone of any restorative approach. Over millions of years of evolution, plants have developed an impressive array of phytochemicals that offer very sophisticated biochemical solutions to the same stress factors that threaten our health, including every variety of microbe, free radicals, toxins, radiation, physical stress, and maybe even emotional stress.
Medicinal herbs are plants that mesh particularly well with human biochemistry. Evidence supporting herbal therapy includes historical information from traditional use by every culture on earth, population studies of current use, lab-based studies, animal studies, and human studies. All totaled, we know more about medicinal herbs than any other therapy currently available, including all drugs.
Here are just some of the benefits of natural herbal therapy for overcoming all sorts of chronic illness:
Balances the microbiome by suppressing intracellular microbes and supporting normal flora
Supports normal immune function
Reduces immune messengers stimulated by stealth microbes that cause inflammation
Restores homeostasis (balances hormones and supports healing systems in the body)
Nourish your body. A healthy diet for immune system support should focus on whole foods, ample vegetables that are rich in phytochemicals (beneficial plant chemicals that support your body’s systems and functions), and healthy fats. Keep processed foods, grain-fed meats, excess carbohydrates, and unhealthy fats to a minimum, and fill at least 50% of your plate with veggies.
Purify your environment. Reduce your exposure to environmental toxins whenever you can. Opt for organic foods when feasible, filter your water and air, and choose non-toxic cleaning supplies and beauty products.
Calm your mind. Adopt some daily stress reduction and management techniques such as practicing meditation, doing yoga, walking outdoors, or even napping.
Activate your body. Doing gentle, restorative exercise every day helps keep the body moving and counters the modern-day pitfall of being too sedentary.
The Bottom Line
Natural herbal therapy combined with the other Restorative Therapies — healthy diet, detox, stress management, and regular exercise — is the best countermeasure for the cellular stress factors that impair immune function and make us vulnerable to chronic illness. It wasn’t until I embraced them that I was able to begin crawling out of the deep dark well of chronic illness.
Since then, I’ve used everything I learned on my journey back to health to create a holistic and herbal protocol that simplifies the process of reversing Chronic Immune Dysfunction. I also chronicled the exact steps I took to recover in my book, Unlocking Lyme.
I hope these resources can serve as a guiding light to those who need them. But none of it works unless you remember this: Your body is naturally powerful. It possesses the inherent ability to overcome chronic illness and fend off future illness. Clear the path of obstacles, and you will empower your body to find its own way to optimal wellness.
Dr. Rawls is a physician who overcame Lyme disease through natural herbal therapy. You can learn more about Lyme disease in Dr. Rawls’ new best selling book, Unlocking Lyme.
You can also learn about Dr. Rawls’ personal journey in overcoming Lyme disease and fibromyalgia in his popular blog post, My Chronic Lyme Journey.
REFERENCES
1. Potgieter M, Bester J, Kell DB, Pretorius E. The dormant blood microbiome in chronic, inflammatory diseases. FEMS Microbiol Rev. 2015;39(4):567-591. doi: 10.1093/femsre/fuv013
2. Walitt B, Katz RS, Bergman MJ, Wolfe F. Three-Quarters of Persons in the US Population Reporting a Clinical Diagnosis of Fibromyalgia Do Not Satisfy Fibromyalgia Criteria: The 2012 National Health Interview Survey. PLoS One. 2016;11(6):e0157235. Published 2016 Jun 9. doi: 10.1371/journal.pone.0157235
Donor 1 ▪ Borrelia was detected by nPCR, FISH and protein was detected by immunohistology in biopsied thoracic artery tissue. It was not detected in the other cardiac tissues. ▪ Borrelia burgdorferi DNA present only at low abundance in connective tissue ▪ These results validate the clinical diagnosis of Lyme disease in this individual, US serology and tick exposure ▪ Limited detection is consistent with aggressive treatment, although Borrelia DNA was detected. Viability cannot be assessed by these methods. ▪ Round body more common than long/spriocheatal forms ▪ The individual is still well, active and healthy
Donor 2 ▪ Abundant Borrelia was detected by FISH in the pericardium ▪ Other tissues still to be tested ▪ These results are consistent with tick exposure and US WB but not Canadian serology ▪ Round body more common than long/spriocheatal forms ▪ Involvement of Borrelia infection in donor 2’s heart failure is an important question for the family and for all individuals living in endemic areas
Significance
➢ This study demonstrates that Borrelia DNA can be detected in human tissues using molecular methods