• Clarifying Defamation Against Master Peace Zeolites
    Dr. Ariyana Love (ND)
    Defamatory attacks are being waged against Master Peace, a company offering a new and effective zeolite supplement for detox.

    The defamatory content was posted by a woman named “Ria” to a Facebook page called “Ria No Moresilence”. The person running the page is an allopathic practitioner.


    You can see the Facebook page is connected to an online telehealth website called “Long Haulers” which is offering allopathic treatment for vaccine injured and “Covid long haulers”. Ria is a practitioner for Long Haulers.

    The website features Dr. Pierre Kory as the chief Medical Doctor their team is “working in collaboration with”.


    Ria appears to be attacking Master Peace which is a new company offering Clinoptilolite Zeolite infused with Marine Plasma nutrition.

    Ria has claimed that “Master Peace build the graphene oxide filaments".


    Ria goes on to attack the credibility of Master Peace leader, Caroline Mansfield.


    Next, the Long Hauler practitioner further claims that "Master Peace are the building blocks for nanotech and rubbery clots".

    She then references Ana Maria Mihalcea’s article entitled, “Zeolite Use In Nanotechnology Biosensor Applications, Enhancement Of Graphene Quantum Dots Capacity And Increase In Polymer Hydrogel Growth” which reveals a dark underbelly to modern health supplements.


    Ana Maria Mihalcea is not providing her readers with the complete picture of zeolites in her article. She’s using scare tactics to confuse her audience, which serves to deter them from trying more effective natural solutions for detox.

    Zeolites is one of the most effective heavy metal chelator that exist. That is, when this superior natural medicine is pure and unadulterated!

    Zeolites have long been used as a natural treatment to remove heavy radioactive metals from land, water and humans. If you knew that natural zeolites can effectively chelate heavy metals and other toxins, then you might reconsider using Ana Maria’s dangerous pharmaceutical EDTA Acid infusions.

    On the flip side, because natural zeolites are so effective at removing toxic metals from the human body, the market was flooded with contaminated zeolite products leading up to the Covid-19 vaccine democide.

    Already back in 2012, graphene oxide was being attached to the silicalite surface of zeolites, entraping GO nanosheets inside single crystals. In 2015, zeolite nanotechnology was already being tested for drug delivery.

    This patent indicates that aluminum is being mixed into zeolites. Another patent demonstrates that metallic “nanodots” of all kinds can be used in zeolite products.

    But what do these sinister patents have to do with Master Peace zeolites? The answer is absolutely nothing. Master Peace is a natural zeolite supplement that’s sourced from the sea. Master Peace zeolites are volcanic ash harvested from the sea floor bed which is structured and reduced by oxidation to a stabilized nanoparticle size. It’s known as oxygenated clinoptililite. There are no synthetic chemicals used in this process, so essentially, Master Peace is nano minerals, which is not to be confused with harmful nanotechnology.

    A 40-year veteran scientist, Dr. Robert Young, is doing the lab analysis for Master Peace. As the following study shows, the novel oxygenated clinoptilolite efficiently removes aluminum and graphene oxide.



    PLEASE READ: Oxygenated Zeolite (Clinoptilolite) Efficiently Removes Aluminum & Graphene Oxide


    Master Peace zeolites are then infused with sea plasma, which is another essential medicine beneficial for hydration and greater nutrient absorption. It’s a fascinating three-step process worth reading more about.

    So I wonder where Ria the allopathic practitioner got the idea that Master Peace supplement can build graphene oxide filaments and nanotech and promote the growth of rubbery clots? Is Dr. Pierre Kory aware of this defamation? Does Ana Maria have something to do with these false claims, I wonder?

    Listen to Dr. Robert Young on Master Peace and the hexagon via Human Consciousness Support (official channel).

    Follow me on Telegram @drloveariyana.

    Sign up and order Master Peace here



    https://open.substack.com/pub/drloveariyana/p/clarifying-defamation-against-master?r=29hg4d&utm_medium=ios
    Clarifying Defamation Against Master Peace Zeolites Dr. Ariyana Love (ND) Defamatory attacks are being waged against Master Peace, a company offering a new and effective zeolite supplement for detox. The defamatory content was posted by a woman named “Ria” to a Facebook page called “Ria No Moresilence”. The person running the page is an allopathic practitioner. You can see the Facebook page is connected to an online telehealth website called “Long Haulers” which is offering allopathic treatment for vaccine injured and “Covid long haulers”. Ria is a practitioner for Long Haulers. The website features Dr. Pierre Kory as the chief Medical Doctor their team is “working in collaboration with”. Ria appears to be attacking Master Peace which is a new company offering Clinoptilolite Zeolite infused with Marine Plasma nutrition. Ria has claimed that “Master Peace build the graphene oxide filaments". Ria goes on to attack the credibility of Master Peace leader, Caroline Mansfield. Next, the Long Hauler practitioner further claims that "Master Peace are the building blocks for nanotech and rubbery clots". She then references Ana Maria Mihalcea’s article entitled, “Zeolite Use In Nanotechnology Biosensor Applications, Enhancement Of Graphene Quantum Dots Capacity And Increase In Polymer Hydrogel Growth” which reveals a dark underbelly to modern health supplements. Ana Maria Mihalcea is not providing her readers with the complete picture of zeolites in her article. She’s using scare tactics to confuse her audience, which serves to deter them from trying more effective natural solutions for detox. Zeolites is one of the most effective heavy metal chelator that exist. That is, when this superior natural medicine is pure and unadulterated! Zeolites have long been used as a natural treatment to remove heavy radioactive metals from land, water and humans. If you knew that natural zeolites can effectively chelate heavy metals and other toxins, then you might reconsider using Ana Maria’s dangerous pharmaceutical EDTA Acid infusions. On the flip side, because natural zeolites are so effective at removing toxic metals from the human body, the market was flooded with contaminated zeolite products leading up to the Covid-19 vaccine democide. Already back in 2012, graphene oxide was being attached to the silicalite surface of zeolites, entraping GO nanosheets inside single crystals. In 2015, zeolite nanotechnology was already being tested for drug delivery. This patent indicates that aluminum is being mixed into zeolites. Another patent demonstrates that metallic “nanodots” of all kinds can be used in zeolite products. But what do these sinister patents have to do with Master Peace zeolites? The answer is absolutely nothing. Master Peace is a natural zeolite supplement that’s sourced from the sea. Master Peace zeolites are volcanic ash harvested from the sea floor bed which is structured and reduced by oxidation to a stabilized nanoparticle size. It’s known as oxygenated clinoptililite. There are no synthetic chemicals used in this process, so essentially, Master Peace is nano minerals, which is not to be confused with harmful nanotechnology. A 40-year veteran scientist, Dr. Robert Young, is doing the lab analysis for Master Peace. As the following study shows, the novel oxygenated clinoptilolite efficiently removes aluminum and graphene oxide. PLEASE READ: Oxygenated Zeolite (Clinoptilolite) Efficiently Removes Aluminum & Graphene Oxide Master Peace zeolites are then infused with sea plasma, which is another essential medicine beneficial for hydration and greater nutrient absorption. It’s a fascinating three-step process worth reading more about. So I wonder where Ria the allopathic practitioner got the idea that Master Peace supplement can build graphene oxide filaments and nanotech and promote the growth of rubbery clots? Is Dr. Pierre Kory aware of this defamation? Does Ana Maria have something to do with these false claims, I wonder? Listen to Dr. Robert Young on Master Peace and the hexagon via Human Consciousness Support (official channel). Follow me on Telegram @drloveariyana. Sign up and order Master Peace here https://open.substack.com/pub/drloveariyana/p/clarifying-defamation-against-master?r=29hg4d&utm_medium=ios
    OPEN.SUBSTACK.COM
    Clarifying Defamation Against Master Peace Zeolites
    Defamatory attacks are being waged against Master Peace, a company offering a new and effective zeolite supplement for detox. The defamatory content was posted by a woman named “Ria” to a Facebook page called “Ria No Moresilence”. The person running the page is an allopathic practitioner.
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  • Drinking Boiled Tap Water Reduces Human Intake of Nanoplastics and Microplastics
    Ana Maria Mihalcea, MD, PhD

    Morphology and composition of incrustants in different conditions. (a) Scanning electron microscopic (SEM) images of bare-polystyrene (PS, 1 μm, 1 mg L–1) and incrustant coprecipitates formed in tap water at different temperatures (180 mg L–1 of CaCO3, 40 mL, 25–100 oC); (b) SEM images of bare-PS (1 μm, 1 mg L–1) and incrustant coprecipitates in different water hardness upon boiling (60–300 mg L–1 of CaCO3, 100 oC); (c) SEM images of bare-PS and incrustant coprecipitates in different PS concentrations (1 μm, 0–5 mg L–1) upon boiling of tap water (180 mg L–1 of CaCO3, 100 oC); and (d) SEM images and (e) X-ray diffraction patterns of bare-, carboxyl-, and amino-PS and incrustant coprecipitates upon boiling of tap water (1 and 0.1 μm, 1 mg L–1, 180 mg L–1 of CaCO3, 100 oC).

    ____________________________________________________________________________

    This is a hopeful article explaining the methodology to decontaminate drinking water. This is very important because we do know that all bottled water is contaminated. You can read that study here:

    Study Shows A Quarter Million Nanoparticle Polymers Per Liter In Water Bottles - Same Polymers Found As In Moderna Patent For Covid 19 Shots, Morgellons Filaments, Blood & Rubbery Clots

    The abstract states:

    Tap water nano/microplastics (NMPs) escaping from centralized water treatment systems are of increasing global concern, because they pose potential health risk to humans via water consumption. Drinking boiled water, an ancient tradition in some Asian countries, is supposedly beneficial for human health, as boiling can remove some chemicals and most biological substances. However, it remains unclear whether boiling is effective in removing NMPs in tap water. Herein we present evidence that polystyrene, polyethylene, and polypropylene NMPs can coprecipitate with calcium carbonate (CaCO3) incrustants in tap water upon boiling. Boiling hard water (>120 mg L–1 of CaCO3) can remove at least 80% of polystyrene, polyethylene, and polypropylene NMPs size between 0.1 and 150 μm. Elevated temperatures promote CaCO3 nucleation on NMPs, resulting in the encapsulation and aggregation of NMPs within CaCO3 incrustants. This simple boiling-water strategy can “decontaminate” NMPs from household tap water and has the potential for harmlessly alleviating human intake of NMPs through water consumption.


    Here is the ACS article:

    Drinking Boiled Tap Water Reduces Human Intake of Nanoplastics and Microplastics

    Here is the sciencedaily write up:

    Want fewer microplastics in your tap water? Try boiling it first

    Contamination of water supplies with nano- and microplastics (NMPs), which can be as small as one thousandth of a millimeter in diameter or as large as 5 millimeters, has become increasingly common. The effects of these particles on human health are still under investigation, though current studies suggest that ingesting them could affect the gut microbiome. Some advanced drinking water filtration systems capture NMPs, but simple, inexpensive methods are needed to substantially help reduce human plastic consumption. So, Zhanjun Li, Eddy Zeng and colleagues wanted to see whether boiling could be an effective method to help remove NMPs from both hard and soft tap water.

    The researchers collected samples of hard tap water from Guangzhou, China, and spiked them with different amounts of NMPs. Samples were boiled for five minutes and allowed to cool. Then, the team measured the free-floating plastic content. Boiling hard water, which is rich in minerals, will naturally form a chalky substance known as limescale, or calcium carbonate (CaCO3). Results from these experiments indicated that as the water temperature increased, CaCO3 formed incrustants, or crystalline structures, which encapsulated the plastic particles. Zeng says that over time, these incrustants would build up like typical limescale, at which point they could be scrubbed away to remove the NMPs. He suggests any remaining incrustants floating in the water could be removed by pouring it through a simple filter such as a coffee filter.

    In the tests, the encapsulation effect was more pronounced in harder water -- in a sample containing 300 milligrams of CaCO3 per liter of water, up to 90% of free-floating MNPs were removed after boiling. However, even in soft water samples (less than 60 milligrams CaCO3 per liter), boiling still removed around 25% of NMPs. The researchers say that this work could provide a simple, yet effective, method to reduce NMP consumption.

    From the paper supplemental information

    Results. Boiling hard water can remove most PS, PE, and PP MPs, and PS, PE, and PP MPs precipitation efficiencies were 95 ± 4%, 81 ± 3%, and 90 ± 3%, respectively, at 100 oC. Increasing temperature accelerated the formation of incrustants on spherical, fragmented, and fibrous MP surfaces. MPs continued to be encapsulated by newly formed incrustants (Figure S2) and finally precipitated under gravity, confirming that spherical PS, fragmented PE, and fibrous PP MPs are able to coprecipitate with incrustants in tap water upon boiling. In concluding, the results with NPs in the main text were also applicable to MPs.

    Here are the polymer plastics found in drinking water throughout the world:



    Thank you to Karen Kingston, who brought this article to my attention.

    https://anamihalceamdphd.substack.com/p/drinking-boiled-tap-water-reduces

    https://telegra.ph/Drinking-Boiled-Tap-Water-Reduces-Human-Intake-of-Nanoplastics-and-Microplastics-04-02
    Drinking Boiled Tap Water Reduces Human Intake of Nanoplastics and Microplastics Ana Maria Mihalcea, MD, PhD Morphology and composition of incrustants in different conditions. (a) Scanning electron microscopic (SEM) images of bare-polystyrene (PS, 1 μm, 1 mg L–1) and incrustant coprecipitates formed in tap water at different temperatures (180 mg L–1 of CaCO3, 40 mL, 25–100 oC); (b) SEM images of bare-PS (1 μm, 1 mg L–1) and incrustant coprecipitates in different water hardness upon boiling (60–300 mg L–1 of CaCO3, 100 oC); (c) SEM images of bare-PS and incrustant coprecipitates in different PS concentrations (1 μm, 0–5 mg L–1) upon boiling of tap water (180 mg L–1 of CaCO3, 100 oC); and (d) SEM images and (e) X-ray diffraction patterns of bare-, carboxyl-, and amino-PS and incrustant coprecipitates upon boiling of tap water (1 and 0.1 μm, 1 mg L–1, 180 mg L–1 of CaCO3, 100 oC). ____________________________________________________________________________ This is a hopeful article explaining the methodology to decontaminate drinking water. This is very important because we do know that all bottled water is contaminated. You can read that study here: Study Shows A Quarter Million Nanoparticle Polymers Per Liter In Water Bottles - Same Polymers Found As In Moderna Patent For Covid 19 Shots, Morgellons Filaments, Blood & Rubbery Clots The abstract states: Tap water nano/microplastics (NMPs) escaping from centralized water treatment systems are of increasing global concern, because they pose potential health risk to humans via water consumption. Drinking boiled water, an ancient tradition in some Asian countries, is supposedly beneficial for human health, as boiling can remove some chemicals and most biological substances. However, it remains unclear whether boiling is effective in removing NMPs in tap water. Herein we present evidence that polystyrene, polyethylene, and polypropylene NMPs can coprecipitate with calcium carbonate (CaCO3) incrustants in tap water upon boiling. Boiling hard water (>120 mg L–1 of CaCO3) can remove at least 80% of polystyrene, polyethylene, and polypropylene NMPs size between 0.1 and 150 μm. Elevated temperatures promote CaCO3 nucleation on NMPs, resulting in the encapsulation and aggregation of NMPs within CaCO3 incrustants. This simple boiling-water strategy can “decontaminate” NMPs from household tap water and has the potential for harmlessly alleviating human intake of NMPs through water consumption. Here is the ACS article: Drinking Boiled Tap Water Reduces Human Intake of Nanoplastics and Microplastics Here is the sciencedaily write up: Want fewer microplastics in your tap water? Try boiling it first Contamination of water supplies with nano- and microplastics (NMPs), which can be as small as one thousandth of a millimeter in diameter or as large as 5 millimeters, has become increasingly common. The effects of these particles on human health are still under investigation, though current studies suggest that ingesting them could affect the gut microbiome. Some advanced drinking water filtration systems capture NMPs, but simple, inexpensive methods are needed to substantially help reduce human plastic consumption. So, Zhanjun Li, Eddy Zeng and colleagues wanted to see whether boiling could be an effective method to help remove NMPs from both hard and soft tap water. The researchers collected samples of hard tap water from Guangzhou, China, and spiked them with different amounts of NMPs. Samples were boiled for five minutes and allowed to cool. Then, the team measured the free-floating plastic content. Boiling hard water, which is rich in minerals, will naturally form a chalky substance known as limescale, or calcium carbonate (CaCO3). Results from these experiments indicated that as the water temperature increased, CaCO3 formed incrustants, or crystalline structures, which encapsulated the plastic particles. Zeng says that over time, these incrustants would build up like typical limescale, at which point they could be scrubbed away to remove the NMPs. He suggests any remaining incrustants floating in the water could be removed by pouring it through a simple filter such as a coffee filter. In the tests, the encapsulation effect was more pronounced in harder water -- in a sample containing 300 milligrams of CaCO3 per liter of water, up to 90% of free-floating MNPs were removed after boiling. However, even in soft water samples (less than 60 milligrams CaCO3 per liter), boiling still removed around 25% of NMPs. The researchers say that this work could provide a simple, yet effective, method to reduce NMP consumption. From the paper supplemental information Results. Boiling hard water can remove most PS, PE, and PP MPs, and PS, PE, and PP MPs precipitation efficiencies were 95 ± 4%, 81 ± 3%, and 90 ± 3%, respectively, at 100 oC. Increasing temperature accelerated the formation of incrustants on spherical, fragmented, and fibrous MP surfaces. MPs continued to be encapsulated by newly formed incrustants (Figure S2) and finally precipitated under gravity, confirming that spherical PS, fragmented PE, and fibrous PP MPs are able to coprecipitate with incrustants in tap water upon boiling. In concluding, the results with NPs in the main text were also applicable to MPs. Here are the polymer plastics found in drinking water throughout the world: Thank you to Karen Kingston, who brought this article to my attention. https://anamihalceamdphd.substack.com/p/drinking-boiled-tap-water-reduces https://telegra.ph/Drinking-Boiled-Tap-Water-Reduces-Human-Intake-of-Nanoplastics-and-Microplastics-04-02
    ANAMIHALCEAMDPHD.SUBSTACK.COM
    Drinking Boiled Tap Water Reduces Human Intake of Nanoplastics and Microplastics
    Morphology and composition of incrustants in different conditions. (a) Scanning electron microscopic (SEM) images of bare-polystyrene (PS, 1 μm, 1 mg L–1) and incrustant coprecipitates formed in tap water at different temperatures (180 mg L–1 of CaCO3, 40 mL, 25–100 oC); (b) SEM images of bare-PS (1 μm, 1 mg L–1) and incrustant coprecipitates in different water hardness upon boiling (60–300 mg L–1 of CaCO3, 100 oC); (c) SEM images of bare-PS and incrustant coprecipitates in different PS concentrations (1 μm, 0–5 mg L–1) upon boiling of tap water (180 mg L–1 of CaCO3, 100 oC); and (d) SEM images and (e) X-ray diffraction patterns of bare-, carboxyl-, and amino-PS and incrustant coprecipitates upon boiling of tap water (1 and 0.1 μm, 1 mg L–1, 180 mg L–1 of CaCO3, 100 oC).
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  • 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
    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
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  • Environmental Filaments UV Light Fluorescence Darkfield Microscopy
    Ana Maria Mihalcea, MD, PhD

    Image: Environmental filaments collected in regular light and under UV light

    I was visited by Dr. Justin Coy, a former Defense Department Contractor who has been following and validating my research. He brought me an environmental filament sample and a UV flashlight - 365nm. In this post, I am documenting the darkfield microscopy of these filaments and experiments with UV light. He was suspecting Luciferase to be present in the filaments and asked me to take a look. From my research there are metal nanoparticles in the filaments and they can cause fluorescence. Luciferase is used in in molecular biology that uses the luciferase enzyme and a substrate (such as luciferin) to study gene regulation at the level of transcription. I do not think that is the mechanism of the fluorescence of the polymers as other mechanisms using metals have been described in the literature and since Clifford Carnicoms analysis showed huge amounts of metals in the filaments that could be plausible.

    There have been developments of bright orange proteins fused with Luciferase in biological systems - this remains a question for further research and discovery.

    Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals

    We know that embedded Quantum Dot technology can make filaments emit different light and filaments found in the blood have been shown to have bifringence. We also know that UV light can be used as an energy source by nano sensors which can embed themselves in the self assembly polymers. Karl C has done some remarkable microscopy research showing this unusual light emission which I posted here: Extraordinary Microscopy Of Self Assembly Nanotechnology - A Request For Funding Help For Karl C


    Here are different images of the filaments analyzed by me observing how they change with normal light and then UV light:


    Image: Darkfield Microscopy: UV light off left, UV light on right


    Image above: normal light


    Image: UV light

    I then wanted to see if different aspects of the filament react differently to UV light, and they appear to. Some areas are more luminescent then others.


    Image: UV light on, both pictures.

    Below you can see a closer view of the filament under UV light, and there being very specific region that react to the UV light more:


    Off the orange appearing filament a white one came forth. Magnification of 2000x on the right shows a central cavitation of the filament


    Below you can see the orange environmental filament compared to a "self assembly nanotechnology hydrogel” filament from shedding in C19 unvaccinated blood with many visible Quantum Dot like structures seen embedded. The filament composition look the same except the colors differ.


    Here are different areas of the filament that have enormous glow under UV light, magnification 2000x:


    Here is an area of the filament with UV light:


    Same without UV light:


    Here are some research articles on fluorescent polymers:

    New 'smart' polymer glows brighter when stretched

    Spider fossils glow under UV light, a clue to their remarkable preservation

    Plastics shine bright to warn of invisible cracks Damage to polymers ruptures microcapsules, releasing fluorescent molecules

    I have been speaking about spider silk which is a polyamide protein and recently did microscopy on an environmental filament found:

    Spider Silk Polymer Sprayed Via Geoengineering Operations From California - Darkfield Microscopy Analysis

    This article explains that if metals are introduced the the nanofibers, florescence can be achieved:

    Optical fluorescent spider silk electrospun nanofibers with embedded cerium oxide nanoparticles

    The work demonstrates an electrospun nanocomposite of recombinant spider silk protein (rSSp) nanofibers with embedded cerium oxide (ceria) nanoparticles. RSSP (MaSp1) has been produced, extracted from goat milk, and fabricated into nanofibers using an electrospinning process. The resulting electrospun nanofibers have a mean diameter of ∼50 nm. Furthermore, ceria nanoparticles of mean diameter 10 nm were added in the spinning dope to be embedded within the generated nanofibers. These nanoparticles show certain optical activity due to optical trivaliant cerium ions, associated with formed oxygen vacancies. The formed nanocomposite shows promising mechanical properties such as the Young's modulus, elasticity (or elongation at break), and toughness. In addition, the electrospun mat becomes fluorescent with 520-nm emission upon exposure to UV light, due to excitation of the optically active ceria nanoparticles. Also, the formed nanocomposite shows a decay of its electric resistance over time upon exposure to cyclic loads at different humidity conditions. The synthesized nanocomposite can be utilized in different biomedical, textile, and sensing applications.

    We do know that these polymers are used for transhumanist surveillance and synthetic biology. Here they used spider silk as an inspiration. Note how they describe that these polymers can wrap around nerves, muscles and hearts and be the next generation tissue electronic interface:

    Polymer films inspired by spider silk connect biological tissues and electronic devices

    Linking biological tissues with electronic devices is challenging owing to the softness of tissues and their arbitrary shapes and sizes. An innovative water-responsive, supercontractile polymer film, inspired by spider silk, allows the construction of soft, stretchable and shape-adaptive tissue–electronic interfaces.

    We designed water-responsive supercontractile polymer films composed of poly(ethylene oxide) and poly(ethylene glycol)-α-cyclodextrin inclusion complex, which are initially dry, flexible and stable under ambient conditions, contract by more than 50% of their original length within seconds (about 30% per second) after wetting and become soft (about 100 kPa) and stretchable (around 600%) hydrogel thin films thereafter. This supercontraction is attributed to the aligned microporous hierarchical structures of the films, which also facilitate electronic integration. We used this film to fabricate shape-adaptive electrode arrays that simplify the implantation procedure through supercontraction and conformally wrap around nerves, muscles and hearts of different sizes when wetted for in vivo nerve stimulation and electrophysiological signal recording. This study demonstrates that this water-responsive material can play an important part in shaping the next-generation tissue–electronics interfaces as well as broadening the biomedical application of shape-adaptive materials.

    Here is video of the microscopy UV light on in both videos:

    UV light on playing with the focus:

    I took a blood sample and applied the UV light to see what happens to the micro robots. As in my experiments with the 450nm cold laser, the robots are quite happy and seem to absorb the extra energy - if you look at the robot its light emission intensifies, and that is consistent with the WBAN article I just posted that light is an energy source for the biosensors. Energy Harvesting From The Human Body By Wireless Body Area Network - A Cause For The Electrical Conductivity Loss in Human Blood?

    https://anamihalceamdphd.substack.com/p/environmental-filaments-uv-light?utm_medium=ios
    Environmental Filaments UV Light Fluorescence Darkfield Microscopy Ana Maria Mihalcea, MD, PhD Image: Environmental filaments collected in regular light and under UV light I was visited by Dr. Justin Coy, a former Defense Department Contractor who has been following and validating my research. He brought me an environmental filament sample and a UV flashlight - 365nm. In this post, I am documenting the darkfield microscopy of these filaments and experiments with UV light. He was suspecting Luciferase to be present in the filaments and asked me to take a look. From my research there are metal nanoparticles in the filaments and they can cause fluorescence. Luciferase is used in in molecular biology that uses the luciferase enzyme and a substrate (such as luciferin) to study gene regulation at the level of transcription. I do not think that is the mechanism of the fluorescence of the polymers as other mechanisms using metals have been described in the literature and since Clifford Carnicoms analysis showed huge amounts of metals in the filaments that could be plausible. There have been developments of bright orange proteins fused with Luciferase in biological systems - this remains a question for further research and discovery. Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals We know that embedded Quantum Dot technology can make filaments emit different light and filaments found in the blood have been shown to have bifringence. We also know that UV light can be used as an energy source by nano sensors which can embed themselves in the self assembly polymers. Karl C has done some remarkable microscopy research showing this unusual light emission which I posted here: Extraordinary Microscopy Of Self Assembly Nanotechnology - A Request For Funding Help For Karl C Here are different images of the filaments analyzed by me observing how they change with normal light and then UV light: Image: Darkfield Microscopy: UV light off left, UV light on right Image above: normal light Image: UV light I then wanted to see if different aspects of the filament react differently to UV light, and they appear to. Some areas are more luminescent then others. Image: UV light on, both pictures. Below you can see a closer view of the filament under UV light, and there being very specific region that react to the UV light more: Off the orange appearing filament a white one came forth. Magnification of 2000x on the right shows a central cavitation of the filament Below you can see the orange environmental filament compared to a "self assembly nanotechnology hydrogel” filament from shedding in C19 unvaccinated blood with many visible Quantum Dot like structures seen embedded. The filament composition look the same except the colors differ. Here are different areas of the filament that have enormous glow under UV light, magnification 2000x: Here is an area of the filament with UV light: Same without UV light: Here are some research articles on fluorescent polymers: New 'smart' polymer glows brighter when stretched Spider fossils glow under UV light, a clue to their remarkable preservation Plastics shine bright to warn of invisible cracks Damage to polymers ruptures microcapsules, releasing fluorescent molecules I have been speaking about spider silk which is a polyamide protein and recently did microscopy on an environmental filament found: Spider Silk Polymer Sprayed Via Geoengineering Operations From California - Darkfield Microscopy Analysis This article explains that if metals are introduced the the nanofibers, florescence can be achieved: Optical fluorescent spider silk electrospun nanofibers with embedded cerium oxide nanoparticles The work demonstrates an electrospun nanocomposite of recombinant spider silk protein (rSSp) nanofibers with embedded cerium oxide (ceria) nanoparticles. RSSP (MaSp1) has been produced, extracted from goat milk, and fabricated into nanofibers using an electrospinning process. The resulting electrospun nanofibers have a mean diameter of ∼50 nm. Furthermore, ceria nanoparticles of mean diameter 10 nm were added in the spinning dope to be embedded within the generated nanofibers. These nanoparticles show certain optical activity due to optical trivaliant cerium ions, associated with formed oxygen vacancies. The formed nanocomposite shows promising mechanical properties such as the Young's modulus, elasticity (or elongation at break), and toughness. In addition, the electrospun mat becomes fluorescent with 520-nm emission upon exposure to UV light, due to excitation of the optically active ceria nanoparticles. Also, the formed nanocomposite shows a decay of its electric resistance over time upon exposure to cyclic loads at different humidity conditions. The synthesized nanocomposite can be utilized in different biomedical, textile, and sensing applications. We do know that these polymers are used for transhumanist surveillance and synthetic biology. Here they used spider silk as an inspiration. Note how they describe that these polymers can wrap around nerves, muscles and hearts and be the next generation tissue electronic interface: Polymer films inspired by spider silk connect biological tissues and electronic devices Linking biological tissues with electronic devices is challenging owing to the softness of tissues and their arbitrary shapes and sizes. An innovative water-responsive, supercontractile polymer film, inspired by spider silk, allows the construction of soft, stretchable and shape-adaptive tissue–electronic interfaces. We designed water-responsive supercontractile polymer films composed of poly(ethylene oxide) and poly(ethylene glycol)-α-cyclodextrin inclusion complex, which are initially dry, flexible and stable under ambient conditions, contract by more than 50% of their original length within seconds (about 30% per second) after wetting and become soft (about 100 kPa) and stretchable (around 600%) hydrogel thin films thereafter. This supercontraction is attributed to the aligned microporous hierarchical structures of the films, which also facilitate electronic integration. We used this film to fabricate shape-adaptive electrode arrays that simplify the implantation procedure through supercontraction and conformally wrap around nerves, muscles and hearts of different sizes when wetted for in vivo nerve stimulation and electrophysiological signal recording. This study demonstrates that this water-responsive material can play an important part in shaping the next-generation tissue–electronics interfaces as well as broadening the biomedical application of shape-adaptive materials. Here is video of the microscopy UV light on in both videos: UV light on playing with the focus: I took a blood sample and applied the UV light to see what happens to the micro robots. As in my experiments with the 450nm cold laser, the robots are quite happy and seem to absorb the extra energy - if you look at the robot its light emission intensifies, and that is consistent with the WBAN article I just posted that light is an energy source for the biosensors. Energy Harvesting From The Human Body By Wireless Body Area Network - A Cause For The Electrical Conductivity Loss in Human Blood? https://anamihalceamdphd.substack.com/p/environmental-filaments-uv-light?utm_medium=ios
    ANAMIHALCEAMDPHD.SUBSTACK.COM
    Environmental Filaments UV Light Fluorescence Darkfield Microscopy
    Image: Environmental filaments collected in regular light and under UV light I was visited by Dr. Justin Coy, a former Defense Department Contractor who has been following and validating my research. He brought me an environmental filament sample and a UV flashlight - 365nm. In this post, I am documenting the darkfield microscopy of these filaments and experiments with UV light. He was suspecting Luciferase to be present in the filaments and asked me to take a look. From my research there are metal nanoparticles in the filaments and they can cause fluorescence. Luciferase is used in in molecular biology that uses the
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  • Rubbery Clot Development Observations In C19 Unvaccinated Blood With Different Anti Oxidant Compounds - Comparison with Clifford Carnicoms CDB/Morgellons Historical Culture Work
    Ana Maria Mihalcea, MD, PhD

    Image: C19 unvaccinated blood from 2 different individuals. First 4 syringes contain Alpha lipoic Acid, Glutathione, Plaquex and Control sample. Second Set contain Methylene Blue and Glutathione and a Control Sample.

    I had previously posted experiments with C19 unvaccinated blood and different compounds that could inhibit the production of the rubbery clot material that Clifford Carnicom and I have shown to be Cross Domain Bacteria ( CDB) or Morgellon’s like - a polymerized protein that creates the rubbery clots. My most successful clot inhibition was with EDTA and Vitamin C. I have written multiple substacks regarding this research of the rubbery clot formation:

    Rubbery Clot Development In C19 Unvaccinated Individual With Previous Deep Vein Thrombosis and Massive Pulmonary Emboli - While On Eliquis, Nattokinase, Lumbrokinase and Serreptase

    Correlation Of Severity Of Live Blood Contamination Seen On Darkfield Microscopy With Visible Clotting In C19 Unvaccinated Individual

    C19 Unvaccinated Have Same Blood Clotting Problem As C19 Vaccinated - EDTA And Vitamin C Prevents Blood Clotting In C19 Unvaccinated

    What Happens To A Human When There Is More Hydrogel, Nanotechnology And Synthetic Biology Then Blood? And A HAARP Warning BY Cathy O'Brien From 1990's - Is 4Hz Accelerating This Process?

    Blood Clot Analysis From Living & Deceased Individuals Shows Consistent Findings: A Rubber Like Polymerized Protein - Microscopy Shows Filaments. Part 1 of 3 - Dr. Ana Mihalcea With Clifford Carnicom

    Blood Clot Analysis From Living And Deceased Individuals Near Infrared Spectroscopy Shows Multiple Hydrogel Polymer Components - Part 2 of 3 - Dr. Ana Mihalcea With Clifford Carnicom

    Blood Clot Analysis From Living And Deceased Individuals - Preliminary Chemical Solubility Testing - Part 3 of 3 - Dr. Ana Mihalcea With Clifford Carnicom

    The original research by Clifford Carnicom has similar results. Vitamin C had a very strong inhibition of replication of the CDB/ Morgellons which we have correlated to the rubbery clot development in the studies outlined above. NAC was also effective with Glutathione having some effects compared to no treatment but being less effective than the other two. Here are Cliffords historical articles:

    Growth Inhibition Achieved - Original article on Vitamin C, NAC, Glutathione testing

    Morgellons : A Working Hypothesis – PART III POTENTIAL MITIGATING STRATEGIES (RESEARCH BASED)


    Image: CDB cultures and inhibitory effects of Vitamin C, NAC, Glutathione by Carnicom Institute

    In the first image above, I show blood drawn from two C19 unvaccinated individuals mixed with different compounds - ages 40’s and 50’s. The blood was left to sit overnight before the syringes were examined. Both patients have been on detoxification strategies. This is the first set of C19 unvaccinated control blood, a rubbery clot clearly developed. I want to reiterate how abnormal this is and absolutely catastrophic for the human species. If you count medical school, I have been in the medical field now for 30 years. I have never ever seen blood turn into rubber until this past year, when I started looking at this nanotechnology and synthetic biology phenomenon - after the C19 bioweapon roll out. I was just part of a court hearing and will be part of the upcoming trial as a witness. Is there someone that comprehends the catastrophic nature of this single finding in clinical practice? Someone who can look at this and via sheer logic understand the ramifications of what this means - that unvaccinated people are developing the same rubbery clots as the C19 injected due to shedding?


    Image - courtesy Karen Kingston, FDA guidance on shedding

    Still, most people ignore these findings and think they are safe, even though more and more people, including the unvaccinated are developing turbo cancers and are dying suddenly. I believe the reason for this development can be found in the blood, and if not mitigated or ignored, can have detrimental health effects.


    Image: C19 Unvaccinated blood control shows yellow rubbery hydrogel development

    In the video below you see the sample of 30 ml of C19 unvaccinated blood mixed with 1 cc Glutathione 200mg/ml concentration:

    Here is Methylene Blue, a molecule used for anti aging purposes, a precursor for Hydroxychloroquine. I use Methylene Blue a lot due to its ability as a direct electron donor bypassing mitochondrial dysfunction and its capacity to increase oxygen delivery between 30-70 %. You can see that the hydrogel development was inhibited, while the blood clot part was still rubbery. Normally you should be able to break apart a clot with your hands and I am not able to do anything to this rubber.

    This is C19 unvaccinated blood from a second person - this time mixed with Alpha Lipoic Acid 1 ml - Concentration 200mg/ ml. No inhibition of hydrogel seen.

    Here is it mixed with Plaquex, a patented form of Phosphatidylcholine that reverses Atherosclerosis. While these molecules do not inhibit growth after blood is drawn, I still highly recommend them for other functions. Plaquex has been shown to work amazing in reversing oxidative stress affecting the cell membranes of red blood cells and appears to make them more resistant to the assault of the CBD/ microbots. I have shown this in previous live blood analysis.

    This is the control sample without anything in it except C19 unvaccinated blood. Huge hydrogel rubbery clot developed that sticks to the syringe.

    I tested Glutathione again, this is actually my third time and it does not inhibit the hydrogel/ CDB growth.

    Summary:

    I am still exploring mitigation strategies and test molecules that I have been using already for my detoxification protocol to help support the body. In my clinic, I have seen that oral supplements must be supported with iv therapy - if you take supplements my mouth only, even EDTA - it is simply not enough anymore. A maintenance with oral EDTA/ Minerals and regular IV therapy at this time of high contamination delivers best results. Everything and everyone is so contaminated, that the best strategy is to detox with EDTA and Vitamin C while using all the other supplements to enhance immune function. I still use Nattokinase, but you have seen in my article above, that does not prevent the hydrogel rubbery clots. The two individuals who’s blood I tested here were both on 20.000 Units of Nattokinase daily. I use Methylene Blue at a dose of 50mg to 100mg daily depending on the person - from compounding pharmacies if no contraindications exist. You can see from the blood results, that Methylene Blue is a significant contender in helping us against these rubbery clots.

    I wanted to mention that persistence, determination and a fighting spirit is absolutely necessary to maintain your health. Many people do not even fight for their life, they just ignore the threat. Some people give up at first defeat, because it is too hard and inconvenient. What is still coming in illness in death will be unfathomable for most people’s comprehension. People do not want to hear that because it is too uncomfortable. I suggest you start fighting for your life and rearranging priorities. I have seen many people crushed who just wanted to keep ignoring shedding and partying on - until they got their very advanced cancer diagnosis or their blood clotting event. Its everywhere, in all age groups. And those cancers grow fast and furious. I have already had many unvaccinated patients die from shedding. I know because their cancer came after excessive exposure to vaccinated people. Open your eyes and see it. And then do what you can to save your own life and clean your own blood.

    In our meeting with the attorney today we were discussing the timeline of getting a verdict for the main trial. It was estimated at a year.

    I tell you, many people may not have a year with this in their blood and without mitigation strategies. That is not science fiction or fear mongering on my part, as much as my colleagues deny my findings. Look at the rubber clots and contemplate the potential outcome on a human of any age with this in their body. Despite the C19 bioweapon uptake going down, the blood contamination of people is going up, indicating persistent replication of synthetic biology and nanotechnology. I find this CATASTROPHIC in what it suggests for the future of humanity.

    Decontaminating The Blood From Synthetic Biology Hydrogel With EDTA Chelation - Live Blood Documentation

    THERE IS HOPE - EDTA CHELATION WORKS and What Really IS COVID???

    Hope Wins: Before And After Intravenous EDTA Chelation + Vitamin C - Dark Field Live Blood Analysis - A Case Report


    Med Five Patented EDTA
    Rubbery Clot Development Observations In C19 Unvaccinated Blood With Different Anti Oxidant Compounds - Comparison with Clifford Carnicoms CDB/Morgellons Historical Culture Work Ana Maria Mihalcea, MD, PhD Image: C19 unvaccinated blood from 2 different individuals. First 4 syringes contain Alpha lipoic Acid, Glutathione, Plaquex and Control sample. Second Set contain Methylene Blue and Glutathione and a Control Sample. I had previously posted experiments with C19 unvaccinated blood and different compounds that could inhibit the production of the rubbery clot material that Clifford Carnicom and I have shown to be Cross Domain Bacteria ( CDB) or Morgellon’s like - a polymerized protein that creates the rubbery clots. My most successful clot inhibition was with EDTA and Vitamin C. I have written multiple substacks regarding this research of the rubbery clot formation: Rubbery Clot Development In C19 Unvaccinated Individual With Previous Deep Vein Thrombosis and Massive Pulmonary Emboli - While On Eliquis, Nattokinase, Lumbrokinase and Serreptase Correlation Of Severity Of Live Blood Contamination Seen On Darkfield Microscopy With Visible Clotting In C19 Unvaccinated Individual C19 Unvaccinated Have Same Blood Clotting Problem As C19 Vaccinated - EDTA And Vitamin C Prevents Blood Clotting In C19 Unvaccinated What Happens To A Human When There Is More Hydrogel, Nanotechnology And Synthetic Biology Then Blood? And A HAARP Warning BY Cathy O'Brien From 1990's - Is 4Hz Accelerating This Process? Blood Clot Analysis From Living & Deceased Individuals Shows Consistent Findings: A Rubber Like Polymerized Protein - Microscopy Shows Filaments. Part 1 of 3 - Dr. Ana Mihalcea With Clifford Carnicom Blood Clot Analysis From Living And Deceased Individuals Near Infrared Spectroscopy Shows Multiple Hydrogel Polymer Components - Part 2 of 3 - Dr. Ana Mihalcea With Clifford Carnicom Blood Clot Analysis From Living And Deceased Individuals - Preliminary Chemical Solubility Testing - Part 3 of 3 - Dr. Ana Mihalcea With Clifford Carnicom The original research by Clifford Carnicom has similar results. Vitamin C had a very strong inhibition of replication of the CDB/ Morgellons which we have correlated to the rubbery clot development in the studies outlined above. NAC was also effective with Glutathione having some effects compared to no treatment but being less effective than the other two. Here are Cliffords historical articles: Growth Inhibition Achieved - Original article on Vitamin C, NAC, Glutathione testing Morgellons : A Working Hypothesis – PART III POTENTIAL MITIGATING STRATEGIES (RESEARCH BASED) Image: CDB cultures and inhibitory effects of Vitamin C, NAC, Glutathione by Carnicom Institute In the first image above, I show blood drawn from two C19 unvaccinated individuals mixed with different compounds - ages 40’s and 50’s. The blood was left to sit overnight before the syringes were examined. Both patients have been on detoxification strategies. This is the first set of C19 unvaccinated control blood, a rubbery clot clearly developed. I want to reiterate how abnormal this is and absolutely catastrophic for the human species. If you count medical school, I have been in the medical field now for 30 years. I have never ever seen blood turn into rubber until this past year, when I started looking at this nanotechnology and synthetic biology phenomenon - after the C19 bioweapon roll out. I was just part of a court hearing and will be part of the upcoming trial as a witness. Is there someone that comprehends the catastrophic nature of this single finding in clinical practice? Someone who can look at this and via sheer logic understand the ramifications of what this means - that unvaccinated people are developing the same rubbery clots as the C19 injected due to shedding? Image - courtesy Karen Kingston, FDA guidance on shedding Still, most people ignore these findings and think they are safe, even though more and more people, including the unvaccinated are developing turbo cancers and are dying suddenly. I believe the reason for this development can be found in the blood, and if not mitigated or ignored, can have detrimental health effects. Image: C19 Unvaccinated blood control shows yellow rubbery hydrogel development In the video below you see the sample of 30 ml of C19 unvaccinated blood mixed with 1 cc Glutathione 200mg/ml concentration: Here is Methylene Blue, a molecule used for anti aging purposes, a precursor for Hydroxychloroquine. I use Methylene Blue a lot due to its ability as a direct electron donor bypassing mitochondrial dysfunction and its capacity to increase oxygen delivery between 30-70 %. You can see that the hydrogel development was inhibited, while the blood clot part was still rubbery. Normally you should be able to break apart a clot with your hands and I am not able to do anything to this rubber. This is C19 unvaccinated blood from a second person - this time mixed with Alpha Lipoic Acid 1 ml - Concentration 200mg/ ml. No inhibition of hydrogel seen. Here is it mixed with Plaquex, a patented form of Phosphatidylcholine that reverses Atherosclerosis. While these molecules do not inhibit growth after blood is drawn, I still highly recommend them for other functions. Plaquex has been shown to work amazing in reversing oxidative stress affecting the cell membranes of red blood cells and appears to make them more resistant to the assault of the CBD/ microbots. I have shown this in previous live blood analysis. This is the control sample without anything in it except C19 unvaccinated blood. Huge hydrogel rubbery clot developed that sticks to the syringe. I tested Glutathione again, this is actually my third time and it does not inhibit the hydrogel/ CDB growth. Summary: I am still exploring mitigation strategies and test molecules that I have been using already for my detoxification protocol to help support the body. In my clinic, I have seen that oral supplements must be supported with iv therapy - if you take supplements my mouth only, even EDTA - it is simply not enough anymore. A maintenance with oral EDTA/ Minerals and regular IV therapy at this time of high contamination delivers best results. Everything and everyone is so contaminated, that the best strategy is to detox with EDTA and Vitamin C while using all the other supplements to enhance immune function. I still use Nattokinase, but you have seen in my article above, that does not prevent the hydrogel rubbery clots. The two individuals who’s blood I tested here were both on 20.000 Units of Nattokinase daily. I use Methylene Blue at a dose of 50mg to 100mg daily depending on the person - from compounding pharmacies if no contraindications exist. You can see from the blood results, that Methylene Blue is a significant contender in helping us against these rubbery clots. I wanted to mention that persistence, determination and a fighting spirit is absolutely necessary to maintain your health. Many people do not even fight for their life, they just ignore the threat. Some people give up at first defeat, because it is too hard and inconvenient. What is still coming in illness in death will be unfathomable for most people’s comprehension. People do not want to hear that because it is too uncomfortable. I suggest you start fighting for your life and rearranging priorities. I have seen many people crushed who just wanted to keep ignoring shedding and partying on - until they got their very advanced cancer diagnosis or their blood clotting event. Its everywhere, in all age groups. And those cancers grow fast and furious. I have already had many unvaccinated patients die from shedding. I know because their cancer came after excessive exposure to vaccinated people. Open your eyes and see it. And then do what you can to save your own life and clean your own blood. In our meeting with the attorney today we were discussing the timeline of getting a verdict for the main trial. It was estimated at a year. I tell you, many people may not have a year with this in their blood and without mitigation strategies. That is not science fiction or fear mongering on my part, as much as my colleagues deny my findings. Look at the rubber clots and contemplate the potential outcome on a human of any age with this in their body. Despite the C19 bioweapon uptake going down, the blood contamination of people is going up, indicating persistent replication of synthetic biology and nanotechnology. I find this CATASTROPHIC in what it suggests for the future of humanity. Decontaminating The Blood From Synthetic Biology Hydrogel With EDTA Chelation - Live Blood Documentation THERE IS HOPE - EDTA CHELATION WORKS and What Really IS COVID??? Hope Wins: Before And After Intravenous EDTA Chelation + Vitamin C - Dark Field Live Blood Analysis - A Case Report Med Five Patented EDTA
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  • This clip shows a kinesin, a motor protein that moves molecules around the cell. It's powered by ATP and transport molecules along microtube filaments at a rate of 2000 nm/s
    This clip shows a kinesin, a motor protein that moves molecules around the cell. It's powered by ATP and transport molecules along microtube filaments at a rate of 2000 nm/s
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  • Bob Yirka - Rethinking the incandescent lightbulb:

    https://phys.org/news/2023-04-rethinking-incandescent-lightbulb.html

    #IncandescentBulb #Lightbulb #Filament #CarbonNanotube #Boron #Nitrogen #PhotonRecycling #EnergyEfficiency #Physics
    Bob Yirka - Rethinking the incandescent lightbulb: https://phys.org/news/2023-04-rethinking-incandescent-lightbulb.html #IncandescentBulb #Lightbulb #Filament #CarbonNanotube #Boron #Nitrogen #PhotonRecycling #EnergyEfficiency #Physics
    PHYS.ORG
    Rethinking the incandescent lightbulb
    A team of material scientists and engineers affiliated with a host of institutions in China took a new look at the incandescent light bulb and found a way to improve its efficiency. In their paper published in the journal Science Advances, the group describes the changes they made to their test bulbs and how much improvement they saw.
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  • The white bat flower

    It is a very beautiful unusual plant with deep purple flowers reminiscent of a flying bat, as well as bristly wings and long dangling filaments. The flowers can bloom indoors and outdoors in semitropical areas in spring and last until early autumn.
    Excelente toma del fotógrafo ''David Clode''
    The white bat flower It is a very beautiful unusual plant with deep purple flowers reminiscent of a flying bat, as well as bristly wings and long dangling filaments. The flowers can bloom indoors and outdoors in semitropical areas in spring and last until early autumn. Excelente toma del fotógrafo ''David Clode''
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