Jim Crenshaw – June 28th, 2022
If enough of these poor people pile up will that cause a wake up?
Source: JBossman008 on 153news.net
world orders review – June 25th, 2022
Man in America Published May 25, 2022
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Jim Crenshaw – January 1st, 2022
The poisoning of your mind will lead to the poisoning of your body.
By Dr. Ariyana Love, ND
In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased.
Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide.
You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here.
LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY
An English translation of this video can be found in the article entitled, Dr. Ariyana Discusses Nano-Biosensors/Nanorazors and Dr. Noack’s Death After He Located Graphene Hydroxide in the COVID Vaccine.
MICROSPHERES & MICROBUBBLES
Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair.
Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells.
Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this.
Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.”
Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside.
Graphene Oxide Nanotubes enable Microbubbles to self-replicate via electrical pulse. They interlink by electrodes. Microbubbles were designed to break through the blood/brain barrier and deliver their drug and chemical payload into brain cells. Ultrasound is used to help Microbubbles breach the blood/brain barrier. Here’s a video animation of how microbubbles / microspheres work to deliver drugs into the brain.
This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids.
The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies.
QUANTOM DOTS & MICROBEADS
Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents.
These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene.
Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans.They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans.
Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move.
I discussed Quantum Dots and more with Stew Peters on December 9th, 2021.
One of the Microbead patent US20110017493A1 also verifies that they’re carbon based (made from Graphene) and specifies that it’s used to create molecular barcodes in Humans.
This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dot patent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide.
Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys.
Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS!
Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect. Is that what you want to become?
BIOCHIP & HYDROGEL
Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”.
Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal.
We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc.
Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol.
There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here.
By Dr. Ariyana Love
Stockholm University just released a scientific horror. The “spike” protein in the Covid-19 “vaccines” are penetrating the cells of the vaccinated, reaching the cell nuclei, and impairing your cell’s ability to repair damaged DNA.
Pharmaceutical “vaccines” are silencing the genes responsible for DNA repair and deleting them forever in humans.
I joined Stew Peter’s Show once again, to break this shocking discovery on Red Voice Media.
Johnson & Johnson uses Adenovirus 26 (Ad26) in its “vaccine”. J&J openly admits that their Ad26 vector “codes your cells to produce a spike protein” but they don’t tell you they’re also deleting your genes.
The U.S. patent #20140017278 for Adenovirus 26 and 35 Filovirus, openly states that it codes your cells with the Ebola and Marburg chimeric proteins.
“The filovirus antigenic protein is usually a glycoprotein from an Ebola virus or a Marburg virus.”
The J&J Adenovirus 26 vector deletes your E1 gene. The patent also states that it deletes the E1 gene in humans. This is known as the X Chromosome. The E1 gene is required for accurate and instant repair of damaged DNA. Deletion of this gene is lethal.
E1 gene deletion causes embryonic lethality which means permanent sterility for men and women. It causes Lactic Acidosis in children which is the lack of oxygen in the blood. E1 gene deletion causes rapid cancer growth, Thrombosis, and the coagulation of the blood which leads to clotting. Blood clotting is the main reason people are dying from the Covid vaxxines.
E1 gene deletion causes Mitochondrial DNA-Associated Syndrome which is a process of glucose metabolism deficiency that exists in various diseases such as Alzheimer’s, epilepsy, diabetes-associated cognitive decline, and severe neurological disorders such as Leigh’s Syndrome. There’s a progressive loss of mental cognition and typically results in death within two or three years, usually due to respiratory failure.
Without your E1 gene, your cells will literally self-suicide.
U.S. patent #10695417 is the Human Adenovirus 5 vector that contains E1 and E2B gene deletions. The Adenovirus 5 vector is used in Sinovax and it encodes the cells with Ebola Glycoprotein. Glycoprotein -41 and glycoprotein -120 are HIV viral coat Proteins and Glycoprotein plays a key role in reproduction.
Sinovac is used in China, Chile, Brazil, Turkey, and the Philippines.
The Adenovirus 5 vector was developed through Gain-of-Function research.
Knocking out the E2B gene caused sterilization in male mice.
You can order the chimeric messenger RNA of the Lentivirus and the Adenovirus 5 vectors or Baculoviridae online from Thermo Fischer, for recombinant cross-species genomics (cloning).
Thermo Fischer explains how the Adenovirus 5 targets and enters the bronchial epithelial cells (lungs) and deletes the E3 and E4 genes, intentionally inducing Sjögren’s syndrome which is long-term autoimmunity (AIDS).
Loss of your E4 gene deletes your cognitive function. Deletion of your E3 gene degenerates your brain, causes dementia, gradual loss of memory, judgment, and the overall ability to function.
Here’s a study describing how you knockout the E3 gene.
The knockout of these genes affects the moisture-producing glands of your body. It’s not the “spike protein” that’s causing the blood of the vaxxed to coagulate, it’s the gene silencing (deletion). Without moisture, your blood coagulates and clots.
Adenovirus 5 also alters the cell signaling pathways and leads to Lymphoma due to destruction to the immune system. This causes cancers to grow and the blood to coagulate.
This is proof positive they’re creating the next “pandemic” with lethal injections that will gradually induce AIDS in the inoculated masses through gene deletion. The pharmaceutical cartel has not only injected Ebola and Marburg into people but they’re also transfecting people’s cells with these catastrophic chimeric pathogens. The vaxxed will battle chronic infections and lifelong disabilities while the cells of the vaxxed continuously replicate with the synthetic genetic sequences of Ebola and Marburg until it kills them unless they detoxify continuously.
The immune system of the vaxxed is depreciating 5% each week according to a recent UK Government study. Everyone who vaxxed age 30 and above, will have no immunity left by Christmas.
But that’s not all. As the cells of the vaxxed replicate Ebola and Marburg “spike proteins” and their cells decay and die, they will shed the chimeric disease throughout the population via transmission. Therefore it’s crucial for the unvaxxed to continuously detoxify as well.
According to a UK government declaration from the NIH, we are presently in a Phase III clinical trial on Humans using the Adenovirus 5 vector to “fight Covid-19” which began in January 22, 2021.
“This is a global phase III clinical trial to evaluate efficacy, safety, immuogenicity of Ad5-nCoV manufactured by Cansino and Beijing Institute of Biotechnology in health adults aged 18 years old and above.”
So the UK Government is partners with the Chinese Communist Party (CCP) to exterminate Humans.
The World Health Organization (WHO) also published to their website that we are in an Ebola Vaccine Stage III Clinical Trial but later they scrubbed it.
Viruses are still an unproven theory. Given the advances in scientific lab equipment and considering that we’re able to observe nanotechnology under microscopy and spectroscopy, would somebody please explain to me why we still can’t identify a virus? Could Germ Theory be the big pharmacopeia lie in modern medicine and Terrain Theory be the more relevant truth?
Governments enhanced the airborne transmissibility in mammals (humans) of highly virulent avian influenza strains. The history of making pathogens transmissible goes back at least to the synthesis of viable influenza A H1N1 from 1918. Incidentally, the 2009 swine flu Pandemic was also induced by inoculation using the H1N1 “vaccine”. So this is nothing new under the sun.
Sinister shadow governments have been weaponizing nature, producing diseases through vaxxine injection and genetically manipulating Humans for at least the past 100 years. But where did they get this technology from?
The U.S. National Library of Medicine revealed something rather interesting. The USSR’s ‘invisible anthrax’ is a Gain-of-Function bioweapon created by introducing an “alien gene“ into Bacillus anthracis (bacteria). That’s how they made Anthrax. They used an alien gene and genetically altered bacterial immunological properties to produce a deadly pathogen to Humans. Where did they get an alien gene from? Your guess is as good as mine. A UFO crash perhaps.
The U.S. Government has been testing this germ warfare technology on its own military troops since the 1950s, using Adenovirus 4, Ad5, and Ad7 vectors with HIV encoding Envelope (clade C.1086). The Ad7 vector delivered in enteric capsules has been used to “vaccinate” U.S. military personnel “against respiratory and gastrointestinal illness”, since the 1970s.
Monkeypox is also made from the same chimeric pathogens like Ebola and Marburg. Ebola and Marburg can kill nine out of ten people it infects. Although this is not really an infection, it’s transfection (human cloning).
Ebola and Marburg cause hemorrhagic fevers (VHF). They simultaneously affect multiple organ systems in the body and may be accompanied by hemorrhage, or bleeding. These pathogens cause high fever, chills, muscle aches, and vomiting. The patients worsen rapidly until they bleed from every orifice in their body, including needle puncture wounds. They usually die within 1-3 days.
Bill and Melinda Gates say on their Gavi website to expect the next pandemic to be a Marburg outbreak. These two psychics or psychos also claim that Ebola and Marburg are carried by African Green Monkeys.
The lying CDC claims that people can get “Ebola Virus disease” through direct contact with an infected animal (bat or nonhuman primate). They’re taking the absolute piss out of us! Never in the history of medicine has an animal disease infected humans! The only way this is possible is through cross-species genomics with Adenvirus or mRNA and Nanotechnology.
Polio vaccines used in the late 1950s and early 1960s were intentionally contaminated with a bacterial pathogen called the “Simian Virus” 40 (SV40) present in monkey kidney cells. The Simian Virus is used for infecting humans. It was “accidentally administered to humans” through Polio “vaccines”.
The “Vaccinia virus” is similar to the “smallpox virus” but it’s not naturally occurring after all. Scientific Direct reported that “vaccinee-to-cattle and cattle-to-human Transmissions occurred on Farms”, proving the transmission of pathogens between animal to human species is being done by genetic engineering and administered through vaxxines.
Knocking out the E1 and E3 genes is necessary when transfecting cross-species in order to make the pathogen replicate. The Vaccinia pathogen has been used on a wide scale to produce many different kinds of chimeric proteins, including HIV-1 and it encodes approximately 250 genes.
Ebola and Marburg are Gain-of-Function bioweapons and both are created using the “Green Monkey disease“, a chimeric pathogen that you can purchase online!
Adenovirus’ are from human/monkey clone origin and are used with chimeric Lentiviruses, as well as the Filoviruses. Of course, none of these are actual viruses! All the Adenoviruses are chimeric weapons. All the messenger RNA (mRNA) were developed as Gain-of-Function and Loss-of-Function Bioweapons. All vaxxines now code your cells to reproduce deadly chimeric proteins used to both silence genes and program artificial genetic sequences. They are inducing diseases and making up disease names and syndromes to hide the fact that it’s coming from vaxxines!
Ebola, Marburg, and Monkeypox are Gain-of-Function bioweapons created using the “Green Monkey disease”. It’s an Adenovirus made from E. coli bacteria from the decaying flesh of a human/monkey hybrid’s kidney tissue culture. Adenovirus vectors transfect humans with monkey DNA, Ebola, and HIV. Adenovirus vectors are transfecting humans with monkey DNA and Human DNA from a Chimpanzee/Human clone to be exact.
There are 49 immunologically distinct types of adenovirus that can cause infection for long-term gene expression. They’re made with Sialic Acid which is a group of derivatives of neuraminic acid found in animal tissues. Adenovirus 5 is of “Chimpanzee origin”. There’s that Green Monkey clone again!
Polio vaxxines used in the late 1950s and early 1960s were “contaminated with a virus” or rather a bacterial pathogen called the Simian Virus 40 (SV40) which is present in monkey kidney cells used to grow the vaxxine.
Sialic Acid is the primary entry receptor used in Adenovirus. Sialic Acid is an animal DNA from “Species D” Adenovirus which is used in both Adenovirus 5 and Adenovirus 26 (Sinovac and J&J) to transfect Ebola and HIV into human cells using Sialic Acid-bearing glycans (animal DNA) as a primary cell entry receptor. Sialic acid proliferates tumor growth and metastases. N-acetylneuraminic acid (Neu5Ac) is made from E. coli bacteria. See the study’s here and here.
The Pharma death cult is inducing diseases with their “vaccination” racket and making up names and syndromes that they can then profit from by “treating” later when people become diseased. What would life be like without Big Pharma disabling our children and killing healthy people in the name of science and medicine?
There are no viruses involved in the making of any of the mRNA or Adenovirus vaxxines, only GAIN-and Loss-of-Function chimeric pathogens which they keep naming “viruses”. Pharma is using E. coli bacteria as the base for these chimeric diseases because bacteria DNA replicates. They’re also using other plasmids and mixing fungus and yeasts and “several mammal-based systems” (Human/Chimpanzee clone), then genetically enhancing them to increase lethality.
They’re also using baculovirus-mediated insect cell expression. This means Pharma is transfecting human cells with insect DNA. This could explain the strange mutations and Morgellons.
Marburg is simply Ebola with Ricin added to make it more lethal. Both cause hemorrhagic fevers (VHF) and attack multiple organ systems in the body, accompanied by bleeding. Pharma and the Eugenicists already have a PCR kit for “testing” for Marburg disease and a vaxxine to immunize against, called RiVax. The main component of RiVax is “a genetically altered version of a Ricin Toxin.” Ricin is more toxic than Graphene Oxide, by the way.
I think it’s high time people stop trusting our governments and take our children out of public schools like Dr. Zev Zelenko suggested.
PLEASE SEE: Dr. Love’s Detox Protocol
For additional information please don’t hesitate to reach out to me: firstname.lastname@example.org