CASE 01 - Autopsy proven myocarditis death in AUSTRALIA Barrack Heights NSW, AUSTRALIA - Roberto Garin was only 52 when he ‘died suddenly’ on 28 July 2021. The healthy father of two teenagers began feeling ill 48 hours after his first Pfizer shot and dropped dead in front of his terrified wife Kirsti six days later while she was on the phone to paramedics. Garin’s family immediately suspected the vaccine caused his death. Kirsti was told her husband was the first person to die after a Pfizer shot. In fact, 176 deaths following Pfizer jabs had already been reported to the Therapeutic Goods Administration (TGA), starting in the first week of the vaccine rollout. But when Kirsti shared her concerns with filmmaker Alan Hashem, who released the video together with the accounts of other vaccine injuries and deaths, it unleashed a storm. ‘Misinformation researchers’ published by the ABC dismissed Kirsti’s ‘claims her 52-year-old husband died from “sudden onset myocarditis” after receiving the Pfizer vaccine’ because it didn’t ‘square with official data’. Yet that was exactly what forensic pathologist Bernard l’Ons wrote in a brilliant report on his autopsy stating that the deceased’s heart showed a clear transition to severe giant cell myocarditis that could be ‘histologically dated to the time period of the Covid-19 mRNA vaccination’ and it was ‘reasonable to state that the deceased’s previously undiagnosed cardiac sarcoidosis may have transitioned to a fulminating myocarditis as a result of the Pfizer Covid-19 vaccination’ noting that myocarditis had been reported in reactions to the Pfizer vaccine. L’Ons proposed a mechanism by which the vaccine could trigger fatal myocarditis and advised that a possible therapeutic implication was that sarcoid patients be given an echocardiogram to detect whether their heart was affected in which case alternative vaccination types could be considered. All of this was ignored by the TGA which refuses to admit to this day that any death can be attributed to a Pfizer vaccine and was parroted by the ABC. The TGA did admit that as of 22 August it had received ‘235 reports of suspected myocarditis, (inflammation of the heart muscle) and/or pericarditis (inflammation of the membrane around the heart) following vaccination’ with Pfizer but said, ‘These reports reflect the observations of the people reporting them and have not been confirmed as having been caused by the vaccine,’ and that ‘some events may be coincidental and would have happened anyway, regardless of vaccination.’ This is a particularly misleading statement. Four out of five reports to the TGA are submitted not by random ‘people’, but by highly qualified health professionals and in Garin’s case by a forensic pathologist. Why would the TGA dismiss these reports? That’s a question Associate Professor Michael Nissen could perhaps shed light on. He was appointed to the TGA in February 2021, just as the Covid-19 vaccines were rolled out, to lead its Signal Investigation Unit which investigates safety issues that arise with vaccines in adverse reports or are raised by international regulators or the medical literature. Prior to his appointment, Nissen was the Director of Scientific Affairs and Public Health at GSK Vaccines from October 2014 to January 2021, a period during which GSK and Pfizer entered into a joint venture. Nissen worked concurrently in hospital-based medical care and academia. He has led over 40 clinical trials and authored over 200 peer-reviewed publications including vaccine studies. In all these areas pharmaceutical companies are a major source of funding. The TGA is sensitive about managing conflicts of interest for advisory committee members but offers no guidance on its website with regard to staff members although presumably the same principles should, at least in theory, apply. It notes that shares, involvement in clinical trials, employment, contracts, consultancies, grants, sponsorships, board memberships and so on, may give rise to a conflict of interest. Robert Clancy, an Emeritus Professor of Pathology at the University of Newcastle Medical School and a member of the Australian Academy of Science’s Covid-19 Expert Database wrote in Quadrant online last week that ‘the power of the pharmaceutical industry and its pervasive influence at every level of political and medical decision-making’ has been underestimated in shaping the pandemic narrative which has been driven by commercial imperatives to such an extent that it has crushed scientific debate. Clancy recounts that his approach to the College of Pathology (of which he was a Senior Fellow, a foundation Professor of Pathology, and past-Chairman of the College committee for undergraduate pathology education) calling for a national study to determine whether Covid vaccination was responsible for the increase in excess mortality in Australia and elsewhere by developing a protocol for post-mortems ‘to answer what is arguably the most important question facing medicine’ met with a rejection and a suggestion to take it instead to the TGA. Nowadays, dying suddenly has become ominously familiar. According to a new film Died Suddenly available as of this week to stream via Twitter, in the last 18 months, the term ‘Died Suddenly’ has risen to the very top of ‘most searched’ Google terms. The film documents the surge in excess mortality in highly vaccinated countries. Dr. Peter McCullough, internist, cardiologist, epidemiologist, and one of the top five most-published, and most censored, medical researchers in the US, says that sudden death frequently occurs because the heart has been damaged by inflammation caused by Covid vaccines. Papers that Pfizer and the Food and Drug Administration tried to hide for 75 years show that Pfizer knew in 2020 that myocarditis and pericarditis could be caused by its vaccine. And in the Pfizer trial in Argentina, a report on a healthy 36-year old  participant – Augusto German Roux – who developed pericarditis immediately after his second Pfizer jab, mysteriously disappeared from the published trial results. The Australian Technical Advisory Group on Immunisation (ATAGI) and the Cardiac Society of Australia and New Zealand (CSANZ) belatedly published a warning about myocarditis and pericarditis in September this year. It was too late for Garin. Had his doctors known, his life might have been saved. His grieving family have still not received a cent in compensation. But Pfizer has apparently grossed nearly $100 billion from its sales of Covid-19 vaccines and treatments. Rebecca Weisser is an independent journalist. ====== https://open.substack.com/pub/makismd/p/mrna-injury-stories-australian-dad?r=29hg4d&utm_medium=ios

The COVID-19 Vaccine Antigen Is ANTHRAX Dr. Ariyana Love By Dr. Ariyana Love Covid-19 vaccines use self-replicating, programmable nanotechnology and synthetic, modified RNA (modRNA) otherwise known as Spike Protein. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” but what if the Covid-19 vaccine antigen is ANTHRAX? “…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.” Anthrax was developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene” into the highly deadly Bacillus Anthracis bacteria. This means that Cross-Species-Genomics capability was acquired by governments before 1950. A lethal bacterium and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax. Russia’s Anthrax could be treated with antibiotics even several days after exposure, and thus it met the requirements under the Biological Weapons Convention. A bioweapon of choice, Anthony Fauci decided to increase Anthrax lethality and the NIH began genetic attenuation before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more. According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast). Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.” The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks, but we already know that the D.O.D spearheaded this “Covid-19 vaccine” roll-out. Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014, creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously, in 2014 China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study revealed severe side effects. PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in vaccines under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare. In March 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more. Anthrax causes hemorrhaging. So does Ebola and Marburg. Ebola is used in the J&J and Sinovax jabs, while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop the Anthrax from replicating inside the human body after inoculation due to it being antibiotic resistant. The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquito which is part of DARPA’s weaponized insect project called The Sentinels. Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax. Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero SPIKE PROTEIN IS AEROSOLIZED ANTHRAX There are 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.” The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine”. “The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.” The above quote from the Recombinant Anthrax Vaccine patent reveals that the poisonous Anthrax “antigen” is being used to genetically modify the genome of humans (cellular entry into humans). By cleaving to the amino termini, protein kinases 1 and 2 are inactivated. This is accomplished by genetic deletions. The molecular basis of Anthrax “vaccines” includes “spores and DNA plasmids” that are entering human cells. The following quote about the Anthrax “protective antigen” is particularly revealing: “PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).” Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want, including bacteria. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery with contaminated PCR swabs, the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized. This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic. This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality. ALHYDROGEL According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is a DARPA weapon system called Alhydrogel. Hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health. In the Alhydrogel invention, Anthrax was fused together into a nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”. In layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death. Alhydrogel is infused with 750 μg of aluminum, making it magnetic. Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network. Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There are many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system. This Alhydrogel patent demonstrates it’s use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability. This begs the question, where do venereal diseases come from? This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel. “Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA. Both nanoparticles and Anthrax have been used in vaccines for decades already, without the Informed Consent of the public. Alhydrogel was improved and transformed into the Nanoalum adjuvant. Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor. Alhydrogel is also carried in the lipid coating of nanoparticles. The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites. Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector! ANTHRAX SYMPTOMS AND TREATMENT Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and contaminated PCR swabs. Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements (antibiotic resistance). Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans, it’s extremely toxic and will be rejected by our immune system 100% of the time. Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review Pharma wants us to believe that the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a horrific disaster. U.S. Army statistics that were never published, show the Anthrax “vaccine” induces turbo cancers. The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis and Pericarditis? Anthrax also coagulates the blood. “Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.” Read more here and here. Anthrax induces hemorrhaging. So this explains all the excessive bleeding people have experienced over the last 4 years, following Covid-19 inoculation and from aerosolized exposure, otherwise known as the “shedding” phenomenon. This is a result of Inhalation Anthrax. It becomes clear that the newly dubbed “White Lung Syndrome” and the Chinese ‘pneumonia’ outbreak is none other than Inhalation Anthrax. Mycoplasma pneumonia is on the rise, and it’s listed on Pfizer’s internal documentation as a known Adverse Effect of the Covid-19 inoculation. This study reveals that Mycoplasma Pneumonia is aerosolized. WHO also confirms this phenomenon is Mycoplasma Pneumonia. All naturally occurring bacterium have cell walls. Mycoplasmas are spherical to filamentous cells with no cell walls. It’s genetically manipulated in a laboratory by GAIN-of-Function for the purpose of enhancing replication inside the human body, making it more lethal. Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by proinflammatory cytokine signaling and histological lesions in the spleen. Anthrax has already been tested on the public. According to the NIH, Anthrax spores were intentionally released into “some environments” in NYC during 9/11. According to the NIH, the FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI. Heroine users in Europe have been tested with Injection Anthrax. Our skies are sprayed with smart dust and chemicals daily. Our governments have launched an all-out war against their constituents. We are being poisoned in a myriad of ways, so please keep this in mind: “Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by World Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.” TREATMENT If you have been inoculated with Covid-19 or PCR swabbed, and you are suffering from heart pain, unusual bleeding, skin rashes and abrasions, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated”, then you may have been exposed to Inhalation Anthrax. Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. Since October 4th, I have received many reports of a red eye syndrome where the entire eye is blood-red. This makes sense because eye tissue is more sensitive. If you have been exposed to Inhalation Anthrax, you may feel hot and severely flushed, and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning. Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need an effective natural medicine detox protocol. I have been successfully detoxing people from the Covid-19 bioweapons for three years. Since I began treating people presenting with Anthrax poisoning with strong antibacterials, my clients are experiencing quicker detox results. If you would like to schedule a consultation with me, please do so through my online booking system. Please follow me on Telegram @drloveariyana and X @drloveariyana. If you would like to donate to my research, please do so here. UPDATE: My Anthrax article is now fully edited and published on Substack. Please review and SHARE. The Covid-19 Vaccine Antigen Is ANTHRAX Read more: https://open.substack.com/pub/drloveariyana/p/the-covid-19-vaccine-antigen-is-anthrax?r=2juwfo&utm_campaign=post&utm_medium=web&showWelcomeOnShare=true https://donshafi911.blogspot.com/2024/02/the-covid-19-vaccine-antigen-is-anthrax.html

Screening for Silent Spike Toxicity Spike levels build up over time with repeated exposures and eventually the dam breaks. Here's how to detect toxicity before it causes symptoms. Dr. Syed Haider Pet Toxin Safety - Mill Creek Animal Hospital This post will provide a deep dive on tests for spike toxicity, including the best screening tests for those who have no symptoms, but have been exposed. These tests detect specific spike-induced inflammation, clotting, AIDS, turbo cancer, etc, and can help get ahead of disease developing underneath the surface. In a future post I plan to cover the best tests for fine tuning a healing protocol. There are now hundreds if not thousands of physicians treating spike toxicity with varying protocols and degrees of success. In my experience most hesitate to escalate ivermectin enough. At high enough doses it almost always helps (at mygotodoc.com I usually start where others end, at 0.2mg/kg/day and then may gradually escalate as high as 10 times more than that ie 2mg/kg/day in some patients over the course of 5-10 weeks). Most physicians treating spike toxicity also refrain from much or any testing. This makes sense on a budget, and I often come across patients who can’t afford testing and we skip it as well, but if it can be afforded then it can be helpful in fine tuning the protocol and sometimes uncovering key missing ingredients, like nutritional deficiencies, or particularly stubborn micro clotting requiring escalated dosing and varied types of anticoagulants. The other place for testing is in screening of the general population without symptoms, both vaxxed and unvaxxed (though when you really press you often do find new symptoms have sprouted up since the beginning of the pandemic). But even in those who truly have no new symptoms and feel perfectly fine, it seems that it may simply be a matter of time before spike toxicity catches up with them, especially if, like so many people, they can’t detox quickly enough, can’t break up the atypical microclots fast enough, and then are reexposed to a new variant, or a big shedding bolus, and that tips the scales and sends them into outright long haul. People find it hard to believe that they could feel fantastic and yet there could be something brewing inside that is just 1 straw away from breaking their backs. Yet almost everyone was in this very situation even before the pandemic. We all have a health span and a lifespan, and for most in the modern world the overlap between them has been dramatically shrinking for generations, and it has only gained speed with each passing year, and especially the last 3 years since the pandemic hit. Health is wealthqbak - http://asianpin.com/health-is-wealthqbak/ | Funny cartoons jokes, Funny cartoon pictures, Funny cartoons source In plain English, we often gradually become chronically ill and then debilitated starting decades before we finally die. In the worst cases spending the last years of our lives in nursing homes, oblivious to our surroundings and infrequently visiting loved ones. The reason for this is a chronic mismatch between our bodies and our environments - not just lack of exercise and poor diets, but also the chemical soup we find ourselves in, the toxins in the air, water and soil, the lack of fresh air and sunlight throughout the day, the lack of grounding, and too much toxic blue light at night that is soaked up by our eyes and very skin while we lounge in front of our screens, greatly stressing ourselves, while thinking we’re relaxing, followed by restless, unfulfilling sleep. Most of us are drawing down on our health savings accounts - not the tax free HSA - but a metaphorical account that represents our life force. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share Just like a regular bank account, if it isn’t managed properly and wealth is overused, it will eventually get close to zero, by which time we will be liable to illness at the drop of a hat - anything that is too taxing can overdraw the account since what’s flowing into it can’t overcome what’s flowing out. And then some of us become chronically overdrawn, living on credit, and in the toxic embrace of chronic illness because of it, dragging us into the depths, while we struggle vainly to get back above the surface. This is why when you finally realize you have to change your ways to get better, it makes no sense to give up those changes as soon as you break free of illness. You are just above zero, still liable to dipping below the surface again. You need to build up your reserves of health over time and not overdraw your account again. You have to become a good steward of your body and resources. And over time you can get to the point where you’re on solid ground again and can put up with small and large stressors without backsliding. But you should always keep in mind how bad it can get to motivate you to stay on the straight and narrow going forward. To get back to the topic, the spike protein builds up in our bodies over time and causes detectable changes to our immune and vascular systems. There is an immune fingerprint of various cytokine markers, there are the microclots, there are alterations to the red blood cell zeta potential, there are predictable decreases of various micronutrients. There may be early warning signs of AIDS, or cancer or organ dysfunction. Nowadays almost all new patients with Long COVID or Vax injury made it through a few shots, or a few rounds of COVID without getting long haul, but the final infection or shot put them over the edge. If they had come before they got that last shot or infection I could have detected their susceptibility in the lab and we could have worked to correct it. This is the epidemic of Silent Spike Toxicity. And these are the tests we have available to screen for it: The Microclot Test: only available from 1 lab in the US (mail order). Detects abnormal clotting not seen on any other test. The single most specific spike toxicity test. The Comprehensive Spike Screening Panel: includes imaging tests: EKG, CXR, Echo. Blood tests that detect damage to the heart, lungs, liver, kidneys. Checks zeta potential. Can show the immune fingerprint of spike. Detection of AIDS. Typical gut microbiome changes. Advanced cancer screening (blood & whole body MRI), and more. The Masterjohn-Schilling Spike Healing Panel: detects neuroinflammation, free radicals, mitochondrial dysfunction, autoantibodies, reactivated viruses and bacteria, MCAS, specific micronutrients that are depleted by spike toxicity, and more. Masterjohn’s Deep Dive Nutrition Panel goes beyond nutrients depleted by spike toxicity to provide a complete snapshot of functional nutrition and is indispensable for deep healing when half measures don’t work. source A quick note on tests in general: There is no perfect test. Tests are evaluated by their sensitivity and specificities, but we don’t have research on any of these for spike toxicity diseases. Sensitivity is how good a test is at ruling out a diagnosis and specificity is how good it is at ruling in a diagnosis. The best screening tests would be 100% specific - meaning if you have the diagnosis it will be detected 100% of the time, but in order to gain that level of specificity they often have to cast a wide net and give up some sensitivity. What this means practically is that if the diagnosis is present you will test positive, but there will also be some people who don’t have the diagnosis who also test positive. Highly specific tests are usually paired with confirmatory tests that are hopefully highly sensitive. Meaning they can weed out the people who were including in the first round of screening, but don’t actually have the diagnosis in question. In the absence of research into spike toxicity diseases and optimal screening regimens we have to fall back on expert opinion. It seems that the microclot test is likely the best screening test, because those treating spike toxicity have never come across someone with the clinical symptoms of the disease who doesn’t have elevated microclots. Unfortunately microclots can be elevated by other conditions. So a confirmatory test like the incelldx Incellkyne panel might be ordered from the Comprehensive Spike Screening panel, along with other tests we’ll discuss below. If the diagnosis of spike toxicity is made then the Masterjohn-Schilling panel is the best next step for fine tuning the protocol, ensuring that the right micronutrients are topped up and the right treatments are prescribed. If not improving after targeted and sustained treatment, then the Deep Dive Nutrition panel is indicated to uncover rare and unusual nutritional deficits that could be holding you back. Here I’ll cover the primary screening tests: The Microclot Test and the Comprehensive Spike Screening Panel. In a future article I may cover the more expansive and complicated panels that are used primarily in treatment. Share The Microclot Test figure 3 source Typical microclots are usually found in the elderly and those with chronic illnesses like diabetes. Spike induced atypical amyloid fibrin microclots are found in those with spike induced blood toxicity. The difference between typical and atypical are that spike induced microclots are very difficult to break down, so difficult that they often do not break down at all. This explains why the D-dimer isn’t helpful for detecting spike toxicity. D-dimer is always trapped inside of clots. Typical clots are always being broken down on the margins - at the edge of a typical clot there will be breakdown. Sometimes the breakdown happens slower than the growth of the clot, but there is always a battle going on between clot growth and clot destruction which will release D-dimer into the blood stream. Since it is virtually always elevated in the presence of clotting it is a very specific test, and is used as a screening test when a physician suspects a clotting disorder, but isn’t sure. For example if someone shows up with chest pain and it could be a pulled muscle or a pulmonary embolism (clot in the pulmonary veins), a D-dimer is a simple ad very cheap test that can be done to determine if further confirmatory, but more expensive more risky testing should be considered, like a CT Angiogram of the chest. For this reason every doctor going through residency comes to consider a positive D-dimer as indicative of clotting and a negative D-dimer as indicative of no clotting. figure 4 source The D-dimer is often elevated during severe acute COVID-19 infection, and during a severe acute injection reaction, but it is not usually elevated in chronic spike toxicity, including chronic long haul and vaccine injured patients. The reason it isn’t elevated is that most people cannot break down the atypical microclots caused by spike protein without some additional help from medications and supplements. Once medications like aspirin (and sometimes prescriptions ones like plavix and eliquis), supplements like nattokinase, serrapeptase, lumbrokinase, bromelain and NAC are started the atypical microclots start to be broken down and D-dimer goes up, which in this case is usually reason for celebration. So the microclot test is the only test in America today that can detect elevated atypical microclots. It’s only available from one lab in the country via mail order (request it from mygotodoc.com), and it helps detect spike toxicity as well as helping track treatment. If initial treatment for microclots with aspirin and supplements doesn’t bring the levels down then we escalate to using higher doses, or add plavix and then later eliquis. And we can also consider plasma donation, or even therapeutic plasmapheresis, if available. DETOX [spike buster] PRE-ORDER NOW: initial stock is limited! Shipping late November 2023. The Comprehensive Spike Screening Panel This set of tests includes an EKG, CXR, Echo. It includes blood tests to screen for daamage to the major organs including the heart, lungs, liver, and kidneys. It checks for zeta potential in the blood, which is affected by spike toxicity. It detects an immune fingerprint of spike. It can detect AIDS. It covers stool testing for the gut microbiome as well as advanced cancer screening (via blood & whole body MRI), and more. Tests Included in the Panel: Spike antibody test: Measures your B cell’s response to the spike protein. In the absence of a direct test for spike protein this helps indirectly detect and track the spike protein levels in your body. Your body produces antibodies in response to the spike protein, and this test measures those antibodies. Generally speaking the more spike protein in your body, the higher the antibody levels. However, what's considered a problematic level varies by individual. The goal is to lower this level as much as possible. The test can also help detect those individuals who might be transmitting the spike protein to others. This is by no means a perfect test, but in the right setting it is helpful as a red flag for further workup, or as a way of monitoring response to therapies over time. Incellkyne Panel from Incelldx - provides an immune fingerprint of spike protein, a combination of elevated cytokine markers that are typically seen in spike protein disease. There are other immune fingerprints they have identified on this same test that indicate non spike Chronic Fatigue Syndrome and Lyme disease. If CCL-5/RANTES and/or VEGF are elevated (VEGF is almost always elevated) then the medication Maraviroc can be helpful. VEGF indicates vascular inflammation and omega-3s, infrared light exposure, and a number of other approaches can be particularly helpful to deal with that. Other inflammatory markers tested are TNF-alpha, IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, GM-CSF, SCD40L, CCL3, CCL-4, and IFN-Gamma. Ivermectin is known to decrease IL-6, which is commonly elevated in Long Haul and Vax injury. Lymphocyte Subset Panel or Cyrex Lymphocyte MAP: The subset panel is the standard test for AIDS and tests for these immune subsets: CD3, CD19,CD20, CD4, CD8, CD56+. The primary pathognomic feature of AIDS would be a CD4 T cell count lower than 200, though there are other red flags such as NK cell activity <10%, or a deficit of T helper cells (CD4+), as well as these others that would only be found on the Cyrex Lymphocyte MAP test: TH1 insufficiency, Increased T-Reg (CD4+ CD25+), deficits of cytotoxic cells (CD8+, CD56+), increased TGF-beta, etc. The Lymphocyte subset panel is cheaper and available at any standard lab and may be covered by insurance, the Cyrex test is more expensive and is a mail order blood test only that has to be paid in cash up front. The Cyrex test can detect 14 different immunotypes and reveal immune under or overactivity, infections, inflammation, autoimmunity, allergies, asthma, hypersentivities and some cancers. It also helps determine what further immune tests can be done to fine tune a healing protocol. Galleri Cancer Screening is an advanced test for 50+ types of common cancers based on a genetic marker found in the blood. It is a good screening test because it is 99.5% specific. This might be a good option for someone with a family or personal history of cancer as it can detect occurance at a the earliest microscopic stage, far before any visual test like an MRI or CT scan would show a mass. If cancer is found ivermectin, fenbendazole, vitamin C, baking soda and many other of label easily available substances are very promising for treatment. Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer? Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer? Cancer rates have skyrocketed in the past century for a number of reasons not least of which is the incredibly large number of toxins spewed into the environment and incorporated into our food supplies. And now with most of humanity exposed to the cancerous spike protein there is likely to be even further acceleration. Those exposed to the fallout from … Read full story Complete Blood Count (CBC) Measures various components and features of the blood, including red blood cells, white blood cells, and platelets. Amongst the white blood cells we can see various abnormalities - they can be high or low, and subsets like basophils, neutrophils and eosinophils might be off. For example a patient started aspirin which is a cornerstone of most treatments of spike toxicity, but in this case raised the eosinophil level and caused some histaminergic symptoms. The symptoms were the same as her usual disease symptoms so initially were written off as a normal fluctuation in symptomatology over time, but in light of the elevated eosinophil level we finally determined that the aspirin was triggering a problem, since that is possible side effect of aspirin. Once off aspirin the symptoms and the eosinophils normalized. Comprehensive Metabolic Panel (CMP) Measures 14 different substances in the blood. It provides information about kidney and liver function, electrolyte levels, and blood sugar. Blood sugar can be high or low in spike toxicity, and that would indicate a pancreatic issue requiring further workup. Liver function often needs to be tracked in those on ivermectin and many other medications. Potassium balances sodium and usually needs to be supplemented in long haul, since most people don’t get enough, especially if blood pressure is rising. Cystatin C is a more specific marker of kidney dysfunction than the creatinine level that is included on the CMP. D-dimer: as mentioned earlier this is a product of the breakdown of clots, it’s often elevated in the acute phase of spike injury or disease, but over time the microclots being inherently difficult to break down stop releasing D-dimer unless the patient is taking a combination of supplements and/or medications to trigger this. Erythrocyte Sedimentation Rate (ESR) Decoding ESR Test: What Your Results Could Reveal About Your Health | Pathkind Labs Blog Measures the rate at which red blood cells settle in a standardized tube over one hour. It is a nonspecific marker of inflammation in the body. It is also an indication of the zeta potential, which is a measure of the normal negative charge on red cells that prevents them from clumping together. Spike protein lowers the normal zeta potential which usually causes ESR to rise. Potassium citrate can help reverse this trend, as can sunlight and grounding. hs-CRP Test (C-Reactive Protein High-Sensitivity) is another non specific marker of inflammation in the body and if found require further workup. It can be elevated in myo-pericarditis. Troponin T is a protein relatively specific to heart muscle cells, leaked into the blood. This is a cardiac biomarker that indicates myocardial injury and along with an EKG is. one of the primary screening tests for a heart attack as well as for myocarditis/pericarditis. Pro BNP (N-terminal pro-brain natriuretic peptide) is produced by the heart in response to strain, particularly heart failure. Electrocardiogram (EKG) EKG: What is it and what does it mean? – JP Stroke Foundation Non-invasive medical test that records the heart's electrical activity. Can be used to diagnose myocarditis/pericarditis, heart attack, and various rhythm abnormalities like atrial fibrillation, SVTs and more that can raise the risk of sudden cardiac arrest, such as that seen in some athletes who have been vaxxed. Echocardiogram (ECHO) Provides valuable information about the heart's structure, function, and blood flow and is an important test for helping visualize the inflammatory changes of myocarditis-pericarditis, such as fluid leaking into the sack around the heart. Chest X-ray source Non-invasive imaging test that uses X-rays to visualize the structures and organs within the chest, including the lungs, heart, ribs, diaphragm, and large arteries. Anyone with shortness of breath should have a Chest Xray as a first screening test looking for pneumonia, inflammation, scarring, nodules/cancer, etc. Whole Body MRI The Latest Quantified Self Trend: Whole-Body MRI Another imaging modality that can turn up hidden cancers and a whole host of other abnormalities and might be ordered for someone where the Galleri test was negative but there was still some suspicion present (here is always the risk of over diagnosis with imaging tests like this, which can lead to otherwise unnecessary stress and procedures that can themselves cause harm). Microbiome testing: Microbiomix Metagenomic Sequencing of Stool by Genova or Sabine Hazan’s Whole Genome Deep Sequencing by Progenabiome. Spike toxicity leads to depletion of beneficial gut bacterials species such as Bifidobacterium pseudocatenulatum, Faecalibacterium prausnitzii, Roseburia inulinivorans, and Roseburia hominis all of which are associated with long COVID complications. Presence of 'unfriendly' bacterial species is linked to poor performance on the 6-minute walk test among long COVID patients. Microbiomix is cheaper because it uses a less thorough sequencing technique, but can show some changes found due to spike toxicity. Sabine Hazan’s test is better if budgeting allows, both because it does a whole genome sequencing, but also because it benefits from her proprietary and private knowledge base (essentially studies and findings that have not yet been published). There are some supplements that can help correct deficits, and in stubborn cases a stool transplant can be transformative, though this is somewhat difficult to get done as it usually requires travel. And that’s a wrap! Next time We’ll look at the Masterjohn-Schilling panel which is our go to for optimizing treatment of long haul/vax injury and perhaps the Comprehensive Nutrition panel, which is important for anyone who has a chronic illness resistant to treatment, including long haul syndromes. https://blog.mygotodoc.com/p/screening-for-silent-spike-toxicity https://telegra.ph/Screening-for-Silent-Spike-Toxicity-01-07

Japan's CBC News, January 19, 2024. Highlights-------------------------- There have been 36,714 reports of suspected adverse reactions after vaccination. This number exceeds 36,714. Among these, there are 2,122 reports of suspected deaths after vaccination. - A 9-year-old boy. The disease name or disability name is Nephrotic Syndrome, - This is a boy who received vaccinations at the age of 17 and 18. It means he received two doses. Encephalitis (Brain Inflammation), convulsion assistance. - A 17-year-old girl. Glandular pain syndrome. - And the boy who received shots at the ages of 15 and 16 has peripheral nerve damage and weakness. - A boy at the ages of 15 and 18, acute myocarditis and acute pericarditis. -And here is a 10-year-old girl. Alopecia areata onset. -A 15-year-old girl. Headache, abdominal pain, diarrhea, fatigue, loss of appetite, numbness in both hands and feet, and hypersensitivity to auditory stimuli. ETC ETC Children under 10 and teenagers are suffering from these symptoms.

Unvaxed will not get myocarditis. Israeli study of 190,000 unvaccinated people came out late 2022 proving that covid infection doesn't cause myocarditis or pericarditis. Significant result because authorities claimed covid infection was riskier than vaccine! https://x.com/_Pav__/status/1748569170781073531?s=20

🚨🚨🚨Japan's CBC News, January 19, 2024. Look at all the teenagers with suspected post vaccination serious adverse events in Japan!! Highlights-------------------------- There have been 36,714 reports of suspected adverse reactions after vaccination. This number exceeds 36,714. Among these, there are 2,122 reports of suspected deaths after vaccination. Among these, there are only 2 cases where causation cannot be denied. Most of them are "unassessable". The reason for being unassessable, according to the Ministry of Health, Labor and Welfare, is insufficient information. How many cases of compensation have been accepted for the new coronavirus vaccine? The number is 9,910. However, applying for the relief system requires a tremendous amount of documentation. For some people, they need to gather more than 1,000 documents. Gathering over 1,000 documents while unwell is truly challenging and has a high hurdle. Therefore, many people have not even applied. - A 9-year-old boy. The disease name or disability name is Nephrotic Syndrome, Both anal cancer, and central cancer with stone-colored pigmentation. Nephrotic Syndrome is a condition where a lot of protein is excreted in the urine. The protein in the blood may decrease. There can also be swelling in the body. In some cases, this can lead to kidney failure or thrombosis. Thrombosis can potentially cause heart attacks or strokes. And anal cancer is a condition where the pressure in both eyes rapidly increases, resulting in symptoms such as eye pain, nausea, and headaches. - This is a boy who received vaccinations at the age of 17 and 18. It means he received two doses. Encephalitis (Brain Inflammation), convulsion assistance. Encephalitis can cause fever, headache, and seizures after vaccination. Convulsion assistance involves losing consciousness and experiencing seizures. - A 17-year-old girl. Glandular pain syndrome. The pain from glandular pain syndrome has worsened. - And the boy who received shots at the ages of 15 and 16 has peripheral nerve damage and weakness. Also, dysesthesia, numbness in both hands and feet, and head. Now, this is quite noteworthy. - A boy at the ages of 15 and 18, acute myocarditis and acute pericarditis. Teenage boys, young men in their early twenties are said to be prone to myocarditis and pericarditis. This boy is experiencing symptoms of both myocarditis and pericarditis. -And here is a 10-year-old girl. Alopecia areata onset. So, maybe she had alopecia areata originally. However, the symptoms reappeared after vaccination. Let's take a look at the next page. This is a single case. -A 15-year-old girl. Headache, abdominal pain, diarrhea, fatigue, loss of appetite, numbness in both hands and feet, and hypersensitivity to auditory stimuli. The symptoms are diverse. This is also a characteristic example of post-vaccination effects. Now, here is another case. -A 17-year-old girl. Bilateral leg weakness and continued weakness in the entire body. -A 15-year-old girl. Fever, fatigue, joint pain, pain in both legs, numbness, walking difficulties, and continued depressive state. Among the people I interviewed, some have even experienced a deterioration in their mental state. And this is the last page. -A 14-year-old girl. Headache, visual impairment. -And an 18-year-old male. This is related to vasospastic angina. Temporary strong contractions caused by spasms in the coronary arteries. And poor blood flow to the heart muscle. Due to spasms and constriction of blood vessels, blood flow is impaired, leading to angina. Children under 10 and teenagers are suffering from these symptoms. --------------------------- H/T:@You3_JP https://x.com/_aussie17/status/1748559029620846597?s=46&t=BnqCjhlm68VHjRNptPlFjA

Screening for Silent Spike Toxicity Spike levels build up over time with repeated exposures and eventually the dam breaks. Here's how to detect toxicity before it causes symptoms. Dr. Syed Haider Pet Toxin Safety - Mill Creek Animal Hospital This post will provide a deep dive on tests for spike toxicity, including the best screening tests for those who have no symptoms, but have been exposed. These tests detect specific spike-induced inflammation, clotting, AIDS, turbo cancer, etc, and can help get ahead of disease developing underneath the surface. In a future post I plan to cover the best tests for fine tuning a healing protocol. There are now hundreds if not thousands of physicians treating spike toxicity with varying protocols and degrees of success. In my experience most hesitate to escalate ivermectin enough. At high enough doses it almost always helps (at mygotodoc.com I usually start where others end, at 0.2mg/kg/day and then may gradually escalate as high as 10 times more than that ie 2mg/kg/day in some patients over the course of 5-10 weeks). Most physicians treating spike toxicity also refrain from much or any testing. This makes sense on a budget, and I often come across patients who can’t afford testing and we skip it as well, but if it can be afforded then it can be helpful in fine tuning the protocol and sometimes uncovering key missing ingredients, like nutritional deficiencies, or particularly stubborn micro clotting requiring escalated dosing and varied types of anticoagulants. The other place for testing is in screening of the general population without symptoms, both vaxxed and unvaxxed (though when you really press you often do find new symptoms have sprouted up since the beginning of the pandemic). But even in those who truly have no new symptoms and feel perfectly fine, it seems that it may simply be a matter of time before spike toxicity catches up with them, especially if, like so many people, they can’t detox quickly enough, can’t break up the atypical microclots fast enough, and then are reexposed to a new variant, or a big shedding bolus, and that tips the scales and sends them into outright long haul. People find it hard to believe that they could feel fantastic and yet there could be something brewing inside that is just 1 straw away from breaking their backs. Yet almost everyone was in this very situation even before the pandemic. We all have a health span and a lifespan, and for most in the modern world the overlap between them has been dramatically shrinking for generations, and it has only gained speed with each passing year, and especially the last 3 years since the pandemic hit. Health is wealthqbak - http://asianpin.com/health-is-wealthqbak/ | Funny cartoons jokes, Funny cartoon pictures, Funny cartoons source In plain English, we often gradually become chronically ill and then debilitated starting decades before we finally die. In the worst cases spending the last years of our lives in nursing homes, oblivious to our surroundings and infrequently visiting loved ones. The reason for this is a chronic mismatch between our bodies and our environments - not just lack of exercise and poor diets, but also the chemical soup we find ourselves in, the toxins in the air, water and soil, the lack of fresh air and sunlight throughout the day, the lack of grounding, and too much toxic blue light at night that is soaked up by our eyes and very skin while we lounge in front of our screens, greatly stressing ourselves, while thinking we’re relaxing, followed by restless, unfulfilling sleep. Most of us are drawing down on our health savings accounts - not the tax free HSA - but a metaphorical account that represents our life force. Thank you for reading Dr. Syed Haider. This post is public so feel free to share it. Share Just like a regular bank account, if it isn’t managed properly and wealth is overused, it will eventually get close to zero, by which time we will be liable to illness at the drop of a hat - anything that is too taxing can overdraw the account since what’s flowing into it can’t overcome what’s flowing out. And then some of us become chronically overdrawn, living on credit, and in the toxic embrace of chronic illness because of it, dragging us into the depths, while we struggle vainly to get back above the surface. This is why when you finally realize you have to change your ways to get better, it makes no sense to give up those changes as soon as you break free of illness. You are just above zero, still liable to dipping below the surface again. You need to build up your reserves of health over time and not overdraw your account again. You have to become a good steward of your body and resources. And over time you can get to the point where you’re on solid ground again and can put up with small and large stressors without backsliding. But you should always keep in mind how bad it can get to motivate you to stay on the straight and narrow going forward. To get back to the topic, the spike protein builds up in our bodies over time and causes detectable changes to our immune and vascular systems. There is an immune fingerprint of various cytokine markers, there are the microclots, there are alterations to the red blood cell zeta potential, there are predictable decreases of various micronutrients. There may be early warning signs of AIDS, or cancer or organ dysfunction. Nowadays almost all new patients with Long COVID or Vax injury made it through a few shots, or a few rounds of COVID without getting long haul, but the final infection or shot put them over the edge. If they had come before they got that last shot or infection I could have detected their susceptibility in the lab and we could have worked to correct it. This is the epidemic of Silent Spike Toxicity. And these are the tests we have available to screen for it: The Microclot Test: only available from 1 lab in the US (mail order). Detects abnormal clotting not seen on any other test. The single most specific spike toxicity test. The Comprehensive Spike Screening Panel: includes imaging tests: EKG, CXR, Echo. Blood tests that detect damage to the heart, lungs, liver, kidneys. Checks zeta potential. Can show the immune fingerprint of spike. Detection of AIDS. Typical gut microbiome changes. Advanced cancer screening (blood & whole body MRI), and more. The Masterjohn-Schilling Spike Healing Panel: detects neuroinflammation, free radicals, mitochondrial dysfunction, autoantibodies, reactivated viruses and bacteria, MCAS, specific micronutrients that are depleted by spike toxicity, and more. Masterjohn’s Deep Dive Nutrition Panel goes beyond nutrients depleted by spike toxicity to provide a complete snapshot of functional nutrition and is indispensable for deep healing when half measures don’t work. source A quick note on tests in general: There is no perfect test. Tests are evaluated by their sensitivity and specificities, but we don’t have research on any of these for spike toxicity diseases. Sensitivity is how good a test is at ruling out a diagnosis and specificity is how good it is at ruling in a diagnosis. The best screening tests would be 100% specific - meaning if you have the diagnosis it will be detected 100% of the time, but in order to gain that level of specificity they often have to cast a wide net and give up some sensitivity. What this means practically is that if the diagnosis is present you will test positive, but there will also be some people who don’t have the diagnosis who also test positive. Highly specific tests are usually paired with confirmatory tests that are hopefully highly sensitive. Meaning they can weed out the people who were including in the first round of screening, but don’t actually have the diagnosis in question. In the absence of research into spike toxicity diseases and optimal screening regimens we have to fall back on expert opinion. It seems that the microclot test is likely the best screening test, because those treating spike toxicity have never come across someone with the clinical symptoms of the disease who doesn’t have elevated microclots. Unfortunately microclots can be elevated by other conditions. So a confirmatory test like the incelldx Incellkyne panel might be ordered from the Comprehensive Spike Screening panel, along with other tests we’ll discuss below. If the diagnosis of spike toxicity is made then the Masterjohn-Schilling panel is the best next step for fine tuning the protocol, ensuring that the right micronutrients are topped up and the right treatments are prescribed. If not improving after targeted and sustained treatment, then the Deep Dive Nutrition panel is indicated to uncover rare and unusual nutritional deficits that could be holding you back. Here I’ll cover the primary screening tests: The Microclot Test and the Comprehensive Spike Screening Panel. In a future article I may cover the more expansive and complicated panels that are used primarily in treatment. Share The Microclot Test figure 3 source Typical microclots are usually found in the elderly and those with chronic illnesses like diabetes. Spike induced atypical amyloid fibrin microclots are found in those with spike induced blood toxicity. The difference between typical and atypical are that spike induced microclots are very difficult to break down, so difficult that they often do not break down at all. This explains why the D-dimer isn’t helpful for detecting spike toxicity. D-dimer is always trapped inside of clots. Typical clots are always being broken down on the margins - at the edge of a typical clot there will be breakdown. Sometimes the breakdown happens slower than the growth of the clot, but there is always a battle going on between clot growth and clot destruction which will release D-dimer into the blood stream. Since it is virtually always elevated in the presence of clotting it is a very specific test, and is used as a screening test when a physician suspects a clotting disorder, but isn’t sure. For example if someone shows up with chest pain and it could be a pulled muscle or a pulmonary embolism (clot in the pulmonary veins), a D-dimer is a simple ad very cheap test that can be done to determine if further confirmatory, but more expensive more risky testing should be considered, like a CT Angiogram of the chest. For this reason every doctor going through residency comes to consider a positive D-dimer as indicative of clotting and a negative D-dimer as indicative of no clotting. figure 4 source The D-dimer is often elevated during severe acute COVID-19 infection, and during a severe acute injection reaction, but it is not usually elevated in chronic spike toxicity, including chronic long haul and vaccine injured patients. The reason it isn’t elevated is that most people cannot break down the atypical microclots caused by spike protein without some additional help from medications and supplements. Once medications like aspirin (and sometimes prescriptions ones like plavix and eliquis), supplements like nattokinase, serrapeptase, lumbrokinase, bromelain and NAC are started the atypical microclots start to be broken down and D-dimer goes up, which in this case is usually reason for celebration. So the microclot test is the only test in America today that can detect elevated atypical microclots. It’s only available from one lab in the country via mail order (request it from mygotodoc.com), and it helps detect spike toxicity as well as helping track treatment. If initial treatment for microclots with aspirin and supplements doesn’t bring the levels down then we escalate to using higher doses, or add plavix and then later eliquis. And we can also consider plasma donation, or even therapeutic plasmapheresis, if available. DETOX [spike buster] PRE-ORDER NOW: initial stock is limited! Shipping late November 2023. The Comprehensive Spike Screening Panel This set of tests includes an EKG, CXR, Echo. It includes blood tests to screen for daamage to the major organs including the heart, lungs, liver, and kidneys. It checks for zeta potential in the blood, which is affected by spike toxicity. It detects an immune fingerprint of spike. It can detect AIDS. It covers stool testing for the gut microbiome as well as advanced cancer screening (via blood & whole body MRI), and more. Tests Included in the Panel: Spike antibody test: Measures your B cell’s response to the spike protein. In the absence of a direct test for spike protein this helps indirectly detect and track the spike protein levels in your body. Your body produces antibodies in response to the spike protein, and this test measures those antibodies. Generally speaking the more spike protein in your body, the higher the antibody levels. However, what's considered a problematic level varies by individual. The goal is to lower this level as much as possible. The test can also help detect those individuals who might be transmitting the spike protein to others. This is by no means a perfect test, but in the right setting it is helpful as a red flag for further workup, or as a way of monitoring response to therapies over time. Incellkyne Panel from Incelldx - provides an immune fingerprint of spike protein, a combination of elevated cytokine markers that are typically seen in spike protein disease. There are other immune fingerprints they have identified on this same test that indicate non spike Chronic Fatigue Syndrome and Lyme disease. If CCL-5/RANTES and/or VEGF are elevated (VEGF is almost always elevated) then the medication Maraviroc can be helpful. VEGF indicates vascular inflammation and omega-3s, infrared light exposure, and a number of other approaches can be particularly helpful to deal with that. Other inflammatory markers tested are TNF-alpha, IL-2, IL-4, IL-6, IL-8, IL-10, IL-13, GM-CSF, SCD40L, CCL3, CCL-4, and IFN-Gamma. Ivermectin is known to decrease IL-6, which is commonly elevated in Long Haul and Vax injury. Lymphocyte Subset Panel or Cyrex Lymphocyte MAP: The subset panel is the standard test for AIDS and tests for these immune subsets: CD3, CD19,CD20, CD4, CD8, CD56+. The primary pathognomic feature of AIDS would be a CD4 T cell count lower than 200, though there are other red flags such as NK cell activity <10%, or a deficit of T helper cells (CD4+), as well as these others that would only be found on the Cyrex Lymphocyte MAP test: TH1 insufficiency, Increased T-Reg (CD4+ CD25+), deficits of cytotoxic cells (CD8+, CD56+), increased TGF-beta, etc. The Lymphocyte subset panel is cheaper and available at any standard lab and may be covered by insurance, the Cyrex test is more expensive and is a mail order blood test only that has to be paid in cash up front. The Cyrex test can detect 14 different immunotypes and reveal immune under or overactivity, infections, inflammation, autoimmunity, allergies, asthma, hypersentivities and some cancers. It also helps determine what further immune tests can be done to fine tune a healing protocol. Galleri Cancer Screening is an advanced test for 50+ types of common cancers based on a genetic marker found in the blood. It is a good screening test because it is 99.5% specific. This might be a good option for someone with a family or personal history of cancer as it can detect occurance at a the earliest microscopic stage, far before any visual test like an MRI or CT scan would show a mass. If cancer is found ivermectin, fenbendazole, vitamin C, baking soda and many other of label easily available substances are very promising for treatment. Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer? Can 2 Cheap Meds, 1 Vitamin & Baking Soda Kill Any Cancer? Cancer rates have skyrocketed in the past century for a number of reasons not least of which is the incredibly large number of toxins spewed into the environment and incorporated into our food supplies. And now with most of humanity exposed to the cancerous spike protein there is likely to be even further acceleration. Those exposed to the fallout from … Read full story Complete Blood Count (CBC) Measures various components and features of the blood, including red blood cells, white blood cells, and platelets. Amongst the white blood cells we can see various abnormalities - they can be high or low, and subsets like basophils, neutrophils and eosinophils might be off. For example a patient started aspirin which is a cornerstone of most treatments of spike toxicity, but in this case raised the eosinophil level and caused some histaminergic symptoms. The symptoms were the same as her usual disease symptoms so initially were written off as a normal fluctuation in symptomatology over time, but in light of the elevated eosinophil level we finally determined that the aspirin was triggering a problem, since that is possible side effect of aspirin. Once off aspirin the symptoms and the eosinophils normalized. Comprehensive Metabolic Panel (CMP) Measures 14 different substances in the blood. It provides information about kidney and liver function, electrolyte levels, and blood sugar. Blood sugar can be high or low in spike toxicity, and that would indicate a pancreatic issue requiring further workup. Liver function often needs to be tracked in those on ivermectin and many other medications. Potassium balances sodium and usually needs to be supplemented in long haul, since most people don’t get enough, especially if blood pressure is rising. Cystatin C is a more specific marker of kidney dysfunction than the creatinine level that is included on the CMP. D-dimer: as mentioned earlier this is a product of the breakdown of clots, it’s often elevated in the acute phase of spike injury or disease, but over time the microclots being inherently difficult to break down stop releasing D-dimer unless the patient is taking a combination of supplements and/or medications to trigger this. Erythrocyte Sedimentation Rate (ESR) Decoding ESR Test: What Your Results Could Reveal About Your Health | Pathkind Labs Blog Measures the rate at which red blood cells settle in a standardized tube over one hour. It is a nonspecific marker of inflammation in the body. It is also an indication of the zeta potential, which is a measure of the normal negative charge on red cells that prevents them from clumping together. Spike protein lowers the normal zeta potential which usually causes ESR to rise. Potassium citrate can help reverse this trend, as can sunlight and grounding. hs-CRP Test (C-Reactive Protein High-Sensitivity) is another non specific marker of inflammation in the body and if found require further workup. It can be elevated in myo-pericarditis. Troponin T is a protein relatively specific to heart muscle cells, leaked into the blood. This is a cardiac biomarker that indicates myocardial injury and along with an EKG is. one of the primary screening tests for a heart attack as well as for myocarditis/pericarditis. Pro BNP (N-terminal pro-brain natriuretic peptide) is produced by the heart in response to strain, particularly heart failure. Electrocardiogram (EKG) EKG: What is it and what does it mean? – JP Stroke Foundation Non-invasive medical test that records the heart's electrical activity. Can be used to diagnose myocarditis/pericarditis, heart attack, and various rhythm abnormalities like atrial fibrillation, SVTs and more that can raise the risk of sudden cardiac arrest, such as that seen in some athletes who have been vaxxed. Echocardiogram (ECHO) Provides valuable information about the heart's structure, function, and blood flow and is an important test for helping visualize the inflammatory changes of myocarditis-pericarditis, such as fluid leaking into the sack around the heart. Chest X-ray source Non-invasive imaging test that uses X-rays to visualize the structures and organs within the chest, including the lungs, heart, ribs, diaphragm, and large arteries. Anyone with shortness of breath should have a Chest Xray as a first screening test looking for pneumonia, inflammation, scarring, nodules/cancer, etc. Whole Body MRI The Latest Quantified Self Trend: Whole-Body MRI Another imaging modality that can turn up hidden cancers and a whole host of other abnormalities and might be ordered for someone where the Galleri test was negative but there was still some suspicion present (here is always the risk of over diagnosis with imaging tests like this, which can lead to otherwise unnecessary stress and procedures that can themselves cause harm). Microbiome testing: Microbiomix Metagenomic Sequencing of Stool by Genova or Sabine Hazan’s Whole Genome Deep Sequencing by Progenabiome. Spike toxicity leads to depletion of beneficial gut bacterials species such as Bifidobacterium pseudocatenulatum, Faecalibacterium prausnitzii, Roseburia inulinivorans, and Roseburia hominis all of which are associated with long COVID complications. Presence of 'unfriendly' bacterial species is linked to poor performance on the 6-minute walk test among long COVID patients. Microbiomix is cheaper because it uses a less thorough sequencing technique, but can show some changes found due to spike toxicity. Sabine Hazan’s test is better if budgeting allows, both because it does a whole genome sequencing, but also because it benefits from her proprietary and private knowledge base (essentially studies and findings that have not yet been published). There are some supplements that can help correct deficits, and in stubborn cases a stool transplant can be transformative, though this is somewhat difficult to get done as it usually requires travel. And that’s a wrap! Next time We’ll look at the Masterjohn-Schilling panel which is our go to for optimizing treatment of long haul/vax injury and perhaps the Comprehensive Nutrition panel, which is important for anyone who has a chronic illness resistant to treatment, including long haul syndromes. https://blog.mygotodoc.com/p/screening-for-silent-spike-toxicity?utm_campaign=post&utm_medium=web https://donshafi911.blogspot.com/2024/01/screening-for-silent-spike-toxicity.html

Spike Protein Syndrome STILL in FULL EFFECT 2 years later – yet most of the injected masses have no clue what’s happening to them – NaturalNews.com Not one single person injected with the Wuhan coronavirus (COVID-19) vaccine can figure out what is happening to their body, brain, and overall functioning, and neither can their doctors. Millions of protein prions created by mRNA "technology" have invaded their vascular system, their cleansing organs, their reproductive organs, and their brains, and the symptoms of Spike Protein Syndrome (SPS) range from minor and recurring to massive deadly, including sudden "unexplainable" death. Medical doctors cannot DARE mention it, if they can even get their own heads around it, as the medical industrial complex tells them what to do, when to do it, how to do it, and to do nothing else. This involves billions of dollars daily in diagnostic testing, blood work, more vaccines and deadly prescription drugs (that still only address the symptoms, never the root cause). Yes, SPS, Spike Protein Syndrome, is sweeping the nation and the world like a pandemic, and the injected sheeple and their doctors are all like ostriches with their heads buried in the sand. Welcome to the gain of function plandemic, with 270 million Americans involved in the biggest medical experiment of our age. Over 270 million Americans are guinea pigs in Big Pharma's ultimate "inside job" New studies reveal more than HALF of all COVID-19 vaxxed sheeple feel sick up to at least a whole year later, and their quality of life has significantly declined due directly to the Wuhan virus stabs. Follow the bouncing ball. COVID-19 vaccine recipients are suffering needlessly from health complications from spike proteins and graphene nanoparticles being created relentlessly by their mRNA-reprogrammed cells, and this clogs and clots their vascular system, straining the heart. Plus, the virus-mimicking protein prions invade their cleansing organs and their brain, sending the immune system into shock, telling it to ATTACK those vital organs to kill the parasites (but the parasites are now created by their own body, every minute, every hour, every day, possibly forever. Yes, a study published at ScienceDirect just this month examined PCVS (post COVID vaccine syndrome) to assess these people's quality of life, and the news was grim, to say the least. It gets worse. The quality of life of those suffering from post-COVID-vax-syndrome got WORSE after twelve months. Those who were ignorant enough to take the COVID booster shots that Gain-of-Function-Fauci highly recommended had far higher PCVS than everyone else. It gets spooky too. PCVS debilitating health conditions are very similar to long-term COVID. Could it be the peptides from the snake venom? That would explain all the miscarriages of pregnant women who got jabbed, and people experiencing hallucinations and major organ failure. Time for all the naysayers to check the VenomTech website for more information about medicine made from deadly venoms, including these so-called COVID "vaccinations" that aren't really vaccines at all. Many perfectly healthy people are rushing to the hospital with sharp shooting pains in their brain that nobody can explain, including their doctors, who all seem even more confused after exhaustive and expensive diagnostic testing. Others suffer swelling of the heart muscle, and sudden "rare" blood clots that aren't even made of blood (just white rubbery stuff with heavy metals in it -- hence the nanoparticles chelating). Many others suffer from relentless lethargy, having no energy or motivation to even keep living their lives (lives that they enjoyed before they got the COVID jabs). It's important to note that no financial or interpersonal conflicts have affected the study results, and that is one reason you won't see this vital information published via mainstream media, including being searchable via Google. Still, the National Library of Medicine analyzed over 80 articles confirming cardiovascular complications in over 17,000 people who got stuck with the mRNA prion-creating jab, and that includes nearly 300 of those folks dying from it. Bookmark Vaccines.news to your favorite independent websites for updates on experimental gene therapy injections that lead directly to vascular clots, hypertension, myocarditis, pericarditis, heart attacks, strokes, PCVS, SPS and Long-Vax-Syndrome. Sources for this article include: Pandemic.news ScienceDirect.com TheEpochTimes.com NaturalNews.com https://www.naturalnews.com/2023-12-04-spike-protein-syndrome-still-in-full-effect.html