Redox signalling molecules are isolated from sea salt and stabilized with a patented technology by the company ASEA, which means to go “toward the sea”.
Redox molecules is a combination of the same reductant and oxidant molecules that are bio-identical to the ones that our mitochondria create during the production of ATP (energy). These molecules are the foundation of cellular communication and health and comprise the body’s natural operating system. Redox molecules are responsible for the protect, detect, repair and replace mechanisms of our cells. They’re also necessary for the cellular absorption of glutathione which in turn alleviates oxidative stress and inflammation.
Redox molecules open the NRF2 detox pathway, allowing the body to expel toxins more effectively. ASEA Redox works on the cellular level and on the nanoscale to replenish our bodies natural operating system, balancing all bodily functions. Using 8 ounces per daily increases endogenous glutathione tobetween 500-800%.
Healing redox molecules are cumulative, meaning the longer you consume them the greater the benefit is to your health. They have the fastest known rate of cellular absorption. In just 5 minutes, the molecules have penetrated every cell of your body, including brain cells. Vital oxygen and nutrients are driven into your cells, restoring cell signaling functions which has a canceling effect on nanotech and other toxins. These naturally occurring molecules control the cell signaling within the body of humans and animals. We all become deficient in redox molecules at about the age of 26 when a genetic switch is activated that triggers the dying process. Our cells lose the ability to absorb glutathione and the aging process begins. Glutathione is the body’s master antioxidant and without it detox is not possible.
Graphene Oxide Nanoparticles (GON), spike proteins and other toxins deplete our redox balance and induce what’s called a Reactive Oxygen Species (ROS), leading to mitochondrial fatigue. Antioxidants will not absorb properly into our cells unless activated by redox signaling molecules.
GON are designed to bypass our innate immune system and deposit poisons directly into cells. GON replicate at rapid speed inside the body so I designed my protocols to bypass the digestive system, making these vital nutrients directly accessible to cells. This method is the fastest way to rescue the immune system from ROS. Redox absorption works as a cellular driver, depositing the super nutrients from my protocols directly into your cells for rapid uptake. Redox molecules balance Ph, repair damage to DNA, turn genes back on and reverse cellular damage from radiation.
Blood sample results
Redox molecules decoagulate the blood in less than 10 minutes, as shown by the before and afters with the Dark Field Microscopy work of Dr. Peggy Marienfeld.
In the following 5 min. video you will see Dr. Peggy Marienfeld do a Live Blood Analysis and demonstrate with a Dark Field Microscope how ASEA Redox molecules reverses blood coagulation in less than 10 minutes!
Here you can listen to real life stories of people here: www.realredoxresults.com and the password is: redox. Testimonials cover everything from asthma, auto-immune, “abnormal cell formation” (cancer), head injury, neurological issues and so on.
ASEA Redox is the liquid supplement in a blue bottle and Renu28 is the topical gel that contains redox signalling molecules. This gel is also age defying when applied to the face.
How to order
On the order form you will see three ways to order.
Choose Associate if you wish to sign up as an associate and have your own webpage, and add in auto ship to the basket (click on it to be able to add it).
Choose Preferred Customer if you wish to have the monthly auto ship subscription, add the product, then go back and also add the auto ship into your basket (again – click on it to be able to add it). This gets you the discounted price. You can of course cancel at any time.
Otherwise choose Retail.
Press Enroll next to the type of ordering you wish to make.
You can reach out to me, Dr. Ariyana Love, if you need help: +1 928 892-8736.
Consultation
You can schedule a health consultation with me, Dr. Ariyana Love, for a customized detox and immune support protocol: https://calendly.com/drariyanalove
Support/Feedback group
You can join Dr. Love’s Signal support/feedback group where you can ask questions of Catherine Wells or myself, directly.
ASEA help desk
If you’re not computer savvy or without technology, you can also get the ASEA Supportto set things up for you. Give them my account number: 1800502009.
The Restore/Asea discussion: A great presentation that explains how nutrients are different to redox molecules and how they have been shown to affect genes. https://youtu.be/5zO71Pasy-I
“…they bought all the 26 patents and went to Gary Samuelson. Literally, Gary Samuelson had all the material delivered to his basement. we went through all of those pallets of science. After a year and a half, he got that stuff stable. Miracles he pulled off.”
“That’s the only thing that can proliferate mitochondria. The ageing process is really linked to how many mitochondria you have. In one week on ASEA, you can see as much as 10% to 30% increase in your total body mitochondrial population. Every eyar, in a healthy diet, when you’re really working hard, you’ll lose about 1% of your mitochondria per year. You regain 30% of your mitochondrial population in one week, reverse 30 years of ageing. That’s a profound supplement, and that’s why it’s miraculous.” – From Zach Bush and Dan Pompa in conversation.
Anti viral and antibacterial
MDI-P was the name of the company that owned the patents to make the molecules prior to their stabilisation in the form of ASEA by Dr Gary Samuelson. ASEA has anti viral and anti bacterial potential, including for HIV which has implications for vaccine induced Acquired Immune Deficiency Syndrome https://europepmc.org/article/MED/10840346
Results
The microbicidal activity of MDI-P occurred within the first minute of exposure for all the organisms tested. When 50% MDI-P was tested against cell titers of 10(5) or 10(7) colony-forming units/mL, all test organisms were killed within 1 minute; at lower MDI-P concentrations, C albicans was the most sensitive organism, and L pneumophila was the most resistant. Even with beginning cell titers of 10(9) colony-forming units/mL, killing by 50% MDI-P was >99.9% for all test strains. Furthermore, at the same beginning cell titer, killing of C albicans by MDI-P diluted to 50% with normal human serum rather than injection saline was only slightly reduced. No acute morbidity, mortality, or tissue damage was detected in mice that were intravenously given 17 mL/kg of undiluted MDI-P.
“ME/CFS is a debilitating condition, often triggered by viral and bacterial infections, leading to years-long debilitating symptoms including profound fatigue, postexertional malaise, unfreshing sleep, cognitive deficits, and orthostatic intolerance. Some are skeptical that either ME/CFS or long COVID-19 involces underlying biological abnormalities. However, in this review, we summarize the evidence that people with acute COVID-19 and with ME/CFS have biological abnormalities including redox imbalance, systemic inflammation and neuroinflammation, an impaired ability to generate adenosine triphosphate, and a general hypometabolic state.”
Here is an important conversation about ASEA and Autism Spectrum Disorders from Dr Samuelson (the physicist that stabilised the redox molecules) and his blog which describes redox science and his New Earth values for future medicine.
“The Masters of Evil Terrorize Global Citizens by Spraying Down Cities and Towns with Aerosolized Biosynthetic Ai Nanoweapons called Spike Proteins.” – Karen Kingston
by Dr. Ariyana Love
Recently I teamed up with the legendary Dr. Robert O. Young for a mega bombshell reveal about the mRNA vectors in COVID-19 vaccines.
Dr. Young is a senior scientific researcher who’s been analyzing body fluids with specialized lab equipment for over 40 years. I am a second generation Naturopathic Doctor and a 13-year veteran journalist and researcher. Like me, Dr. Young is a targeted individual.
After providing a proven curefor cancer in 1996, Dr. Young fell under attack by the Luciferian cabal who’s been hell bent on smearing his good name ever since. I have been targeted by the Izraeli state since 2017 who’ve been hell bent on smearing my good name with accusations of “racism”.
Dr. Young and I share the same views on medicine and how the body system works to heal itself from, toxic poisoning and injury. So we decided to discuss the root cause of disease and address the increase of parasitic infestation Dr. Young is seeing in clients, from all over the world. Dr. Young gives chilling evidence of unprecedented parasitic infestations in humans, of which he’s not seen in his entire career. He told that parasites are now showing up in 90% of the blood of VAXXed and non-VAXXed individuals alike.
PLEASE WATCH: Part 1 on the Root Cause Of Disease and GMO parasites:
Dr. Robert Young and Dr. Ariyana Love: “The root cause of disease & GMO parasites”
We followed up with a second broadcast for a patent review on the messenger RNA vectors being genetically modified parasites. These GMO parasites are mRNA vectors of deadly synthetic biology that’s being used by Moderna, Pfizer, Novavax, Janssen (J&J), Oxford, and more, to transform the human genome and turn humans into synthetic biology. That’s right, pharmaceutical companies are now using deadly parasites as mRNA vectors for delivering artificial genetic sequences into the human genome through the COVID “vaccination”.
PLEASE WATCH: MEGA BOMBS! Deadly GMO Parasites are the mRNA Vectors: Patent Review with Dr. Young and Dr. Love
Since our great reveal on September 28th, Pfizer whistleblower and patent expert Karen Kingston heroically delivered more bombshell information on Stew Peters Show. She eloquently tied together all aspects of this biological attack against humanity, disclosing that the GMO parasites as mRNA vectors were created with the intention of hooking humans up to AI.
Incidentally, Karen Kingston is also a targeted individual.
PART 1: PROOF COVID Is A PARASITE; Biotech Analyst Has PROOF COVID & Vaxx Are Biosynthetic Parasites
Karen Kingston on Stew Peters Show – Part 1
PART 2: PROOF COVID Is A Nano-weapon PARASITE; Biotech Analyst Has PROOF COVID & Vaxx Are Biosynthetic Parasites
There are hundreds of SEQ ID NO’s contained within the COVID serums. We are going to examine just the first two.
SEQ ID NO: 1 is patented and owned by the Pirbright Institute which is owned by Bill & Melinda Gates. It contains polypeptides or amino acid sequences. These are artificial proteins containing synthetic genetic sequences, in other words it’s synthetic biology. These artificial genetic sequences are messenger RNA.
SEQ ID No: 1 is “VACCINE” Patent #20130216569.
The SEQ ID NO: 1 Patent #20130216569 explicitly states that it contains the following deadly protozoan parasite pathogens; Toxoplasma Gondii, Eimeria, Plasmodium, and Theileria.
SEQ ID NO: 2 is owned by Boston Biomedical Research Institute and receives significant funding from the NIH, thus Anthony Fauci. SEQ ID NO: 2 is also synthetic mRNA proteins designed to target and prevent “embryo implantation” in mammals. FYI, humans are classified as mammals.
Embryo implantation is the moment when the fertilized egg is detached from its sheath (zona pellucida), adhered to the endometrium and anchored to it to begin its intrauterine development. Embryo implantation occurs between 5 and 6 days after fertilization. Essentially, SEQ ID NO: 1 aborts embryonic development within the first few days of conception.
SEQ ID NO: 1 can be found within the Pfizer, Moderna, Novavax, Janssen (J&J), Oxford and more, in the COVID jab patents. SEQ ID NO: 2 is found in Moderna, Pfizer and Novavax and more.
This BMC study verify’s that deadly parasites were indeed developed as messenger RNA carriers by the World Health Organization, in 2018. The most deadly of the 5 Malaria parasites, Plasmodium falciparum, the Toxoplasma gondii, the Trypanosoma cruzi and the Plasmodium spp. in particular, are all mentioned as mRNA vector exports for vaccines in mammal (human) cells.
This illustration shows the GMO parasite mRNA vectors in brown squiggly lines with a round head. You can see there are things attached to the parasites and a coil at the parasites tail to represent the genetic sequence. This graph outlines how the parasites enter the cell membrane through ruptured holes and make their way to the cell nucleus where it delivers the mRNA and genetic changes are made to the cellular DNA.
“Chagas’ disease is caused by the protozoan parasite Trypanosoma cruzi and causes potentially life-threatening disease of the heart and gastrointestinal tract.”
Is the COVID inoculation inducing a parasitic attack on the heart and other vital organs like the liver, placenta and women’s reproduction? Is the “Myocarditis” diagnosis actually CHAGAS?
Below is a recent lab photo taken by Dr. Robert Young which demonstrates a parasitic infestation in the human cell of one of his clients.
For information on how you can detox and fortify your immune system against this biological attack, you can schedule a consultation with Dr. Love, here.
Please consider donating to Dr. Love’s research, here.
In my latest interview with Stew Peters, I brought scientific studies revealing that Autism Spectrum Disorder (ASD) is caused by gene deletion in the brain, specifically in the frontal cortex.
The three regions of the brain being targeted are the temporal cortex, cerebellum, and prefrontal cortex, especially the frontal lobe. These regions were shown to have lower methylation levels of the X chromosome with ASD. The study specifies that X chromosome deletion occurs by “epigenetic dysregulation” (gene deletion) and “DNA methylation” (genetic coding).
“Although the epigenetic mechanisms involved in autism are not yet fully understood, there are findings suggestive of genome-wide dysregulation and epigenetic alterations in ASD (Autism Spectrum Disorder). These studies point to DNA methylation (gene editing) as a likely contributor in the development of the disorder.
There are certain syndromes that have been linked to ASD. DNA methylation in connection to imprinting and X-chromosome inactivation (gene deletion) could be relevant to the field of ASD research. X-chromosome inactivation is a process in which one of the copies of X chromosomes is inactivated and this is also achieved through DNA methylation. It might be associated with autism, as inactivation or removal of inactivation could lead to genetic aberrations.”
Targeted deletion of the X chromosome in other areas of the brain result in ASD conditions such as Angelman syndrome and Prader–Willi syndrome. Deletion of the X chromosome in females causes Turner syndrome which induces mental retardation, developmental delay and effects social reciprocity and communication, a condition of ASD.
Autism rates have exponentially risen over the last two decades and continues to sharply rise. Belfast, Ireland just reported that one in 14 children have ASD!
“The 1p36 gene deletion is a congenital disease — you’re born with it — and yet that was the number one serious adverse event, and if you look up the symptomology for that, it’s the elimination of your frontal cortex. Your thinking part of your brain, your decision-making part of your brain, is the number one serious adverse event listed by Pfizer.”
Previously, we were told that deletion syndromes as well as the 1p36 Deletion Syndrome, are rare phenomenons. However, now it’s “the most common human disorder” resulting from the deliberate deletion of the X chromosome in the frontal lobe. Not only does the 1p36 gene deletion cause mental retardation but it also causes genital abnormalities in males and females, affecting fertility.
Another study from 2020 reveals that 25% of people affected by “Covid-19” are loosing the electrical activity in the frontal cortex of their brain. Many of my clients, friends and associates have been reporting “brain fog.” Could this be an adverse reaction from transmission (shedding) of vaxxed persons, caused by targeted gene deletion of the frontal lobe?
In addition, the the authors suggest that the infection may have aged people cognitively by around 10 years!
In her recent report, Dr. Stephanie Seneff, a Senior Research Scientist at MIT’s Computer Science and Artificial Intelligence Laboratory in Cambridge, outlined the extensive neurological damage such as PRION, induced by the mRNA “vaccines.” In particular, she highlighted how the mRNA technology is rapidly aging people.
— To view, copy/paste this report link into your url: file:///C:/Users/metan/Desktop/20220612_MD4CE_Dr_Stephanie_Seneff%20-%20Copy.pdf
It begs the question. Have pharmaceutical companies been intentionally inducing Autism by deleting genetic codes in the human brain through their vaccination programs? The only way the deletion of the X chromosome is possible is through the use of mRNA nanotechnology.
In March, I joined Stew Peters Show for a couple of interviews, to provide insight into Putin’s purging of bioweapons labs in Ukraine. Those interviews went viral.
This article is to provide supporting evidence, links and documents for further study.
GENETIC WARFARE
Russia’s military operation in Ukraine is entirely justified and in accordance with international law. The US Government, DOD and NATO partners were funding and operating 30 Ukrainian bioweapons labs under a “Covid-19 prevention program” but in actuality, they were producing chimeric pathogens for the “vaccine” Holocaust.
The same corrupt media trickery and propaganda is being used today by the cabal, to black PR Russia/Putin and create a false narrative that spins confusion and drives division among people. It was no different during Putin’s intervention in Syria.
Moscow reports that Hunter Biden helped finance a US military ‘bioweapons’ research program in Ukraine. Hunter’s laptop emails provide the supporting evidence that he did in fact help secure millions in funding for US contractor in Ukraine, specializing in deadly pathogen research.
145 species of bioweapons have been developed in Ukraine in violation of international law and two of them were crossing into Russia. The cabal had used biological weapons in an act of war against not only Russia, but the entire world.
Routes into Europe were also being mapped. Parasites and insects that carry chimeric pathogens to infect Humans with, were being smuggled out of Ukraine and the bio-samples were being transferred abroad.
Classified documents captured by Russia reveal a paper trail between Ukrainian biolabs and the Doherty Institute in Australia. Victorian Infectious Diseases Laboratory in Melbourne was caught importing blood serum from Ukrainian biolabs. There’s 350 cryocontainers with samples of blood at the Australian Institute that are being used under the pretense of “antibody research”.
Aussie Cossak reported that Australian mercenaries have been spotted in Ukraine, in the city of Zhitomir, 150km West of Kiev.
Russia also revealed that the U.S. biolabs in Ukraine created genetic bioweapons to target certain ethnic groups for race-specific ethnic cleansing. A scientific study published in December of 2021, shows that Europeans are the most targeted ethnic group while Ashkenazi Jews (Khazars) are entirely immune to any genetic modification. Now this is some damning evidence.
Now the DNA harvesting PCR Kits under the guise of “covid testing” should make a lot more sense to you. Your DNA is so valuable to them.
BACKGROUND
George Soros has been controlling Ukraine since 2012 and stealing the regions natural resources.
Former President Barack Obama himself authorized the construction of the biolabs in Ukraine for creating dangerous pathogens, in 2005. It was the Obama/Biden deep state regime established a coup d’etat rule in Kiev, together with the Israeli state.
Former US Marine Corp Intelligence Officer Scott Ritter told George Galloway “The first troops to be trained by US and British soldiers were the neo-Nazi Azov Battalion”.
The Azov Nazi’s officially integrated into the National Guard of Ukraine in 2014. Azov violently overthrew the legitimate president of Ukraine and forced their way into the government. The newer Zelensky’s puppet regime has been using internationally banned cluster bombs and other bombs against civilians, according to a Human Rights Watch reports, while the militarized Azov Nazi’s have been committing war crimes atrocities against Russian-Christian Ukrainians, especially in Eastern Ukraine. Investigative Journalist Laura Logan confirms there are mass graves in Ukraine from Zelensky’s regime.
In October 2019, Congress wrote U.S. Secretary Mike Pompeo, asking why the State Department failed to include the Azov Battalion on the Foreign Terrorist Organization list.
Israeli news Haaretz reported that the Jewish oligarchs will now flee to Israel where they will be given indemnity from their crimes against humanity.
H5N1 & H1N1
The US Department of State was able to control everything that happened within the Ukrainian biolabs. Tucker Carlson reported that the U.S. Government released a document in 2020 admitting that the bioweapons facilities in Ukraine are for “vaccine development”.
The Russian military discovered the plague, anthrax, tularemia, cholera, Ebola, Filoviruses’ and more, were being developed in Ukraine. Ebola is used in the J&J and Sinovax gene editing weaponry while the Filovirus is used in Moderna. Biotech companies are clearly getting their Gain-of-Function pathogens from Ukraine.
Russia also mentioned that the H5N1 and H1N1 are being produced in the U.S. biolabs. H1N1 induces Smallpox.
Israeli Mossad Microbiologist Joseph Moshe tried to warn the public in 2009 that a H5N1 biological weapons attack on humanity through “vaccination,” was imminent. He said the H5N1 is even more lethal then the H1N1.
I found an mRNA vaccine patent for cattle using the H5N1 and H1N1 and the deadly Brucella bacteria. This means the cabal has also been producing weaponry in Ukraine, to poison our food supply. The patent is owned by Khazakstanians.
Incidentally, there’s a U.S. bioweapons lab in Khazakstan that weaponized Coronavirus for aerosolized dissemination on civilian populations.
Journalist Dilyana Gaytandzheiva reports that the Pentagon has conducted biological experiments on 4,400 soldiers in Ukraine and 1,000 soldiers in Georgia, and unleashed deadly, antibiotic-resistant bacteria on the local civilian population as well as on allied troops, according to leaked documents.
The documents read that all deaths should be reported to the U.S. Government.The U.S. personnel in these biolabs were given Diplomatic Immunity, although they are not diplomats and they are indemnified from deaths and injuries to the local population.
The Pentagon project in Ukraine and Georgia was code-named GG-21 for “Arthropod-borne and zoonotic infections”.Arthropod-borne means ticks and other insects carrying deadly pathogens to infect Humans. Zoonotic infections are caused by harmful germs, bacteria, parasites, fungi and mold.
Blood samples were being obtained from 1,000 military recruits during their physical exams at a military hospital in Gori, Georgia.
The 13 deadly pathogens that were being tested on the troops are:
Bacillus anthracis
Brucella
Coxiella burnetii
Francisella tularensis
Hantavirus
Rickettsia species
Bartonella species
Borrelia species
Ehlrichia species
Leptospira species
Salmonella typhi
West Nile Virus (WNV)
The Bacillus anthracis (anthrax) bacteria can be disseminated by aerial spraying.I found a patent with a method for removing plasma (DNA) from Bacillus anthracis bacteria using CRISPR/Cas9 system and it’s owned by China. This is how they get Mycoplasmas.
Brucella is another deadly bactera. In the 1950s, the US military developed artillery shells and bombs armed with a bacterium that causes a debilitating flu-like disease in humans. In 2001, the US and DARPA artificially sequenced the Brucella suis genomeand began applying it to vaccines.Being infected with Brucellosis is like having the flu times ten, though it’s not life-threatening unless you have some other condition.The US Army likes the Brucella suis pathogen because they’re able to debilitate people without killing them, just like “COVID-19”.
Crimean-Congo hemorrhagic fever (CCHF) has been weaponized using ticks to infect Humans. It has a 40% lethality.Coxiella burnetii and Francisella tularensis are also highly infectious. You need only 10 bacteria to make you sick. The U.S. military was supposed to have destroyed the Francisella tularensis in 1973 because it has up to a 60% lethality.
TBE is tick-borne and causes encephalitis.Bartonella species cause Lyme Disease.Borrelia bacteria hides inside parasitic worms, causing chronic brain diseases.Ehlrichia is a disease from dogs. WNV (West Nile Virus) is carried by mosquitos.
CONCLUSION
Putin just cut off the head of the snake in Ukraine and exposed the whole shit-show. Now let’s make the most of it.
Dr. Li-Meng Yan claims to be a “whistleblower” who’s against the CCP. She worked as a virologist in a Hong Kong lab with her husband who is also a virologist.
On February 15th, Dr. Yan supposedly blew the whistle saying she was given inside information that the CCP was planning to disseminate biological weapons at the winter Olympics in Beijing by releasing a “virus” that will induce hemorrhagic fever. She seemed to be setting the stage for us to believe that such an attack would lead to a Marburg outbreak.
While the CCP could easily have unleashed a bioweapon on people attending the winter Olympics, would that actually be able to induce the next staged plandemic, worldwide? I think not.
More than likely this is a ruse and a diversion from the fact that Marburg has alreadybeen injected into the world’s population through the Johnson & Johnson “vaccine”. The J&J patent specifically says that it contains Ebola and Marburg, a mRNA bioweapon that induces hemorrhagic fever. In fact, Frontline doctors are already seeing Hemorrhagic Fever showing up in the vaccinated population.
Dr. Yan went on to say that the CCP has an “antidote”calledDarzalex (daratumumab). Darzalex is an experimental drug using monoclonal antibodies. Is it a coincidence that J&J also owns the Darzalex patent and is now conveniently offering the supposed “antidote”? Problem, reaction, solution?
PATENT REVIEW
The Darzalex (daratumumab) patent was filed in 2015 for the treatment of Multiple Myeloma (MM) which is cancer. It was approved in the US by the FDA, for the treatment of patients with multiple myeloma in 2018, despite that a lawsuit was filed against Janssen Biotech Inc. in 2016, for patent infringement.
It is in fact, illegal to use monoclonal antibodies for any other treatment than myeloma, like “covid” symptoms or vaccine injury, for example. Despite that, MM patients have a 4-7 year life expectancy and therefore this is an end of life treatment.
Regeneron warns that you can expect a “worsening of symptoms after treatment that may result in hospitalization”. I suppose thathow you know it’s working. Also, the side effects of monoclonal antibodies “may be life-threatening”.
Grant funding for monoclonal antibodies came from the NIH, DAPRA, the Bill and Melinda Gates Foundation, the Musk Foundation, Janssen Pharmaceuticals, Gilead Sciences Inc., Pfizer Inc, and the University of North Carolina Chapel Hill, to name a few. This so called “treatment” is also part of Operation Warp Speed.
In a 2021 video, Bill Gates was promoting monoclonal antibodies as the next singular “treatment” for Covid-19.
Monoclonal antibodies reportedly “block the SARS-COV2 spike protein RBD from binding to the human ACE2 receptor”. However, studies reveal that monoclonal antibodies lessen the likelihood of SAR-CoV-2 resistance by 100 fold.
The monoclonal antibody patent #10787501 uses “RNA and DNA vectors”, or polynucleotides. The patent also reveals this is a “vaccine“. This is experimental “Gene Therapy” using chimeric mRNA technology.
The patent mentions that “some embodiments” contains chloroquine or hydroxychloroquine while other embodiments contain only the immune suppressing agents. For example, HCDR1R is used in the “treatment” of Lupus which is a “down-regulation” of genes. HCDR2 gene clusters are also used in monoclonal antibodies for DNA binding and gene knockdowns using CRISPR.
Thermo Fischer provides monoclonal antibodies using CRISPR, for gene editing and knockdown. Labome is a key supplier of the “antibodies” used in monoclonal antibodies. Labome’s website admits it’s product is used for Human “cloning“.
The patent also says it contains LCDR2 which has Anthony Fauci’s HIV-1 patented bioweapon vector. It should be noted that the LCDR3 mentioned in the patent is the DNA of a humanized, chimeric mouse/human hybrid species. That’s definitely experimental and unsafe to inject in Humans. Any honest doctor will tell you this.
The patent says “In some embodiments, the coronavirus is selected from the group consisting of SARS-CoV-2, SARS-CoV, and MERS-CoV”. This literally means that monoclonal antibodies contain SARS and MERS. We know that SARS and MERS are bioweapons and that SARS is “aerosolized through the sweat glands”, according to Dr. Hodkinson who gave his testimony to Reiner Fuellmich.
The patent reads: “In any of the various embodiments discussed above or herein, the antibody or antigen-binding binding fragment comprises a VH3-66 or Vk1-33 variable domain sequence.” This PubMed study reveals that “theVH3-53 andVH3-66VHgenesegments encode V regions“.
This PubMed study reveals that “Nucleotide sequences of the cDNAsencoding theV-regionsof H- and L-chains of a human monoclonal antibody specific to HIV-1-gp41“. So, monoclonal antibodies contain HIV-1 which is being encoded into your cells using cDNA. This is cross-species genomics! Also, the HIV-1 bioweapon is patented and owned by Anthony Fauci.
Another PubMed study reveals that the Novel V genes quoted above, do encode cells using mRNA.
Other horrors in the monoclonal antibody patent read: “isolated antibody or antigen-binding fragment thereof that binds a SARS-CoV-2 spike protein comprising the amino acid sequence set forth in SEQ ID NO: 832″…
A company called BacDive provides the “832” gene sequence which is a mycobacterium senuense05-832. It is an “aerobe, mesophilic, rod-shaped human pathogen that was isolated from sputum (mucous)”. This means monoclonal antibodies are lab-generated, bacteria based, chimeric pathogens.
Also mentioned in the monoclonal antibody patent is SEQ ID NO: 202. The “202” sequence patent says this is a “dystrophin gene” which is a nucleic acid being used for “gene silencing“ with “RNA interference”.
There is in fact so many genetic sequences mentioned in the monoclonal antibody patent that it would take days to break it down.
MARKER GENES & mRNA
The second monoclonal antibody patent #US10954289B1 states that marker/reporter genes are implemented using an artificial “Jurkat T cell line” and use Luciferase. This is an immortalized Human cell line that also contains insect DNA (Luciferase). That right there is cross-species genomics, aka cloning.
There are many patents listed within the monoclonal antibody patents. One patent in particular contains chimeric proteins that come from experimental humanized animal hybrid DNA. The patents specify that the chimeric proteins “can enter the cells and deliver the replacement enzyme activity lysosome”. The only way cell penetration is possible is if lipid-nanoparticles are used.
Another patent goes on to say that “recombinant RNA molecules comprising a sequence of a gene-editing molecule mRNA” is being used.
Monoclonal antibodies is a mRNA nanotechnology vaccine.
IMMUNE SYSTEMDESTRUCTION
Monoclonal antibodies target and destroy your body’s T-cells or killer cells while cloning a new hybrid cell line. Your T-cells are a vitally important part of your immune system and without them your body is left without any defense against disease. This will serve as the final nail in the coffin for vaccinated persons, or the “final solution” as Bill Gates calls it. Since the “vaccinated” are loosing 5% of their immune system every week, according to a UK Government study, they can’t afford to loose anymore.
The theory is that monoclonal antibodies suppress your natural immune system, enabling your B-cells to generate an antibody response to chimeric proteins. Do I need to explain how wrong this is? Doctors don’t believe it’s possible to detoxify “vaccinated” persons so instead they use their patients as lab rats for Big Pharma in unethical medical interventions.
Some Naturopathic Doctors like myself are succeeding to detoxify vaccinated persons. You can schedule a consultation with Dr. Ariyana Love (ND) or contact me for more information: metanutrients@protonmail.com.
The U.S. Army just announced their new creation of a Spike Ferritin Nanoparticle (SpFN) “vaccine”, claiming that it works “against all existing COVID & SARS variants”. Without animal testing or safety studies, Human trials are already underway.
The U.S. Army published a series of preclinical studies claiming the Spike Ferritin Nanoparticle serum “protects against heterologous challenge with B.1.1.7 and B.1.351 virus variants” during an animal trial. This is key to understanding what they’re really doing with these death jabs.
“B.1.1.7” and “B.1.351” are literal genetic lineages that contain your God-given genetic information. Heterologous challenges result from cross-species genomics. When you delete genes and code Human cells with insect DNA (Luciferase) and monkey DNA, bad things happen. It’s called genetic mutation.
The official narrative explains that the B.1.1.7 Alpha variant of SARS-CoV-2, the supposed “virus” that causes COVID-19, has turned up in the UK and the B.1.351 Beta variant in South Africa. Then there’s the B.1.1.529 Omicron variant which is new on the scene. Now I’m going to explain to you how you’re being fooled because first they fool you then they rule you.
The CDC website mentions the “variant of concern (VOC), lineage B.1.1.7 is also referred to as VOC 202012/01 or 20I/501Y.V1”. Another page of the CDC website says about the B.1.1.7 variant, “This variant has a mutation in the receptor binding domain (RBD) of the spike protein at position 501, where the amino acid asparagine (N) has been replacedwith tyrosine (Y). The shorthand for this mutation is N501Y”.
The key word in that quotation is REPLACED.
TheBullfrog
Look up N501Y and you find that it’s a genetic mutation resulting from reverse genetics (cloning). Reverse genetics involves directed gene deletions and point mutations (site-directed mutagenesis) to create null alleles (non-functional); which is gene knockouts. These gene deletions lead to permanent loss-of-function.
CRISPR-Cas9 – technology is raping your cells’ genome and cutting it at a specific location to allow genes to be removed and new engineered sequences to be inserted using RNA interferenceto permanently silence genes. Genetic knockdowns are typically temporary whereas genetic knockouts are permanent.
Moderna and other pharmaceutical bioterrorists researched extensively the knockout of genes in regards to “curing cancer” and what the reduction of amino acid asparagine (N) causes. The CDC says the amino acid asparagine (N) has been replaced with tyrosine (Y). When you knockout genes, the protein associated with that gene stops being produced by your cells. In this case it’s the amino acid asparagine (N) that has been replaced with tyrosine (Y) which causes rapid cancer growth. They want you sick and dying.
The N501Ymutationis being induced by gene deletion, to cross the species barrier so that animal diseases (monkey disease) can create infection in Human cells that would not naturally occur. Since animal diseases do not infect Humans, cloning is necessary.
The UK Government says the “VOC-202012/01 variant includes 23 changes in the “virus” with eight mutations (changes) in the outer “spike” protein; nine changes that alter the amino acid sequence of proteins elsewhere in the virus genome, and six changes that do not alter the amino acid sequence of proteins elsewhere in the virus genome”.
What they are really talking about is YOU. Since viruses are still a theory and have never been proven to exist, governments and the pharmaceutical cartel are using the word “virus” to deceive the medical community and divert our attention away from their Bioterrorism. They want us to believe that a boogey virus mysteriously jumped from bats to Humans when actually they’re making changes to the Human genome.
This study confirms that SARS-CoV is nothing but “S glycoproteins” made using an unnatural genetic sequences that fools your cells into thinking it’s natural so your body will not reject the biohacking technology.
The Spike Ferritin Nanoparticle SpFN WO2021178971A1 patent, also confirms that the SARS-CoV is an “glycoprotein S” which is the “spike protein”.
So there you go, mystery solved. The infamous “spike protein” is not a “spike” protein from a “virus” after all. The glycoprotein S is a chimeric Bioweapon.
The SpFN patent also contains the transfection agent HEK293T/17 which is Human embryonic kidney DNA. It’s a chimeric “pcDNA” for cloning.
Thermo Fischer is using a “pcDNA cloning kit” which also does gene deletion.
The SpFN patent also contains HIV-1 which is patented and owned by the treasonous, mass murdering, Genocidal Anthony Fauci. It also has Luciferase (insect DNA) for tracking your every move. Oh yeah… and the patent confirms it came from Wuhan, China!
Aluminum Hydroxide is also listed in the SpFN patent and Aluminum Hydroxideis made from Graphene Oxide. They call it “Alhydrogel”. So… Graphene Oxide is irrefutably in the SpFN Bioweapon shots!
It gets even more disgusting. They’re using bullfrog DNA to create their chimeric glycoprotein “S”.
Who wouldn’t want to be transfected and cloned with bullfrog? Because if you don’t accept their Franken-vaxx, then you’re a racist… against the bullfrog species!
GENE DELETION
Studies show that the B.1.1.7 “variant” is directly caused by gene 69-70 deletion in Humans. The B.1.351 “variant” is directly caused by gene241–243 deletion.
The CDC openly admits that the Omicron variant is the result of an “S gene drop out” caused by “gene 69-70 deletion”.
The World Health Organization says that the S gene is not present in the Omicron variant. In its report titled “Classification of Omicron (B.1.1.529): SARS-CoV-2 Variant of Concern“, the WHO’s Technical Advisory Group on SARS-CoV-2 Virus Evolution (TAG-VE) confirmed that the RT-PCR kits which are designed to target the S gene, detect a complete dropout of the S gene.
Thermo Fisher’s Genetic Sciences Division revealed that the B.1.1.7 variant is the result of gene mutation caused by the gene deletion of the “S gene”. Thermo Fisher explains that the “S gene” is a 69-70 deletion. Thermo Fisher admits that gene deletion mutations is the cause of all SARS-CoV-2 variants, Lambda, Alpha, Beta, Gamma, Delta, etc.
Are you catching on? The “S” gene is the glycoprotein S Bioweapon, an artificial genetic sequence that’s being coded into Human cells (transfection/cloning) after gene knockout.
“The Omicron variant has been found to include the 69-70del mutation of the S gene, first identified as a mutation in the Alpha variant. This mutation causes a dropout of the S-gene target in results from widely used TaqPath COVID-19 Detection Kits. An S-gene failure does not mean a result is negative, only that the S gene was not detected. Multiple public health organizations have noted that this pattern of detection (i.e. S-gene dropout) can be used as a marker for this variant, pending sequencing confirmation.”
So there you have it. The PCR kits target genes for gene deletions and monitor the cloning progress.
All Covid vaxx patents mention gene deletion. Both Pfizer and Moderna claim their serums “protect against” the variants. The Moderna patent states it’s death jab is “folding proteins”. The folding of proteins induces genetic mutations.
The Pfizer patent directly states that it’s serum is deleting genes 69-70 and 242-244. So these lying bastards are not “protecting” against anything. They are inducing the scary variants through gene deletion.
Do not drink their poison.
The Pfizer vaxx patent also mentions the N501Y mutation due to but not limited to 69-70 gene deletions. Remember, 144 gene deletion causes rapid cancer growth.
Pfizer patentWO2021213945A1
Thermo Fisher owns the patent to a PCR kit that “targets genes”. The PCR kit is also a marker to “test” for gene deletions to determine if the jabbed are patent eligible.
Thermo Fisher sells the Microbeads used in the death jabs and markets them as Dynabeads and SPIONs. Then they have a PCR kit to “test” how their cloning project is going.
Cloning any species results in mutations that are unpredictable, as I previously documented in my articles here, here and here.
CONCLUSION
Variants are caused by gene deletion from fake vaccines and fake tests. Stop complying to your Democide and Mark of The Beast enslavement.
Serve the war criminals (anyone pushing the death jab) with Notices of Liability.
Contact me or book a free consultation and I will help you design a detox protocol that fits your needs and your budget, to remove the biological poisons we are being bombarded with. Do not loose hope because there are solutions to save and protect your health.
NOTE: Sometimes the patents read ambiguously and in code language. They refer to the “Spike Protein” which is synonymous with the “Glycoprotein S”. Other times the descriptions could be referring to RNA and DNA changes, like coding new genetic sequences using “cDNA”. They sometimes read with words “in some embodiment’s” which likely means in some vials.
TABLE OF CONTENTS:
Moderna
Pfizer
Janssen (J & J)
Oxford University
AstraZeneca
GlaxoSmithKline (GSK)
Novavax
Gilead
MODERNA
“Lentivirus shows up in a couple of patents:Modernatx, Inc., Sars-Cov-2 mRNA domain vaccines November 4th, 2021.
The “Lentivirus” or “Lentiviral vector” is messenger RNA (mRNA) which contains the SARS, MERS, HIV 1-3 and SRV-1 Gain-and-Loss-of-Function bioweapons.
ASTRAZENECA AstraZeneca: Dapagliflozin and Ambrisentan for the prevention and treatment of covid-19 https://patents.google.com/patent/WO2021219691A1/en Lentivirus Not mentioned in the patent cDNA Not mentioned in the patent Deletion Not mentioned in the patent ORF Not mentioned in the patent
LentivirusNot mentioned in the patent cDNA Mentioned but seems only to refer to the formula. DeletionMentioned for mice. Probably just for preparation purposes. ORFNot mentioned in the patent
I compiled all the evidence we have into this article that prove Graphene Oxide, Graphene Hydroxide and other Graphene variants are in fact being injected into people by governments and Big Pharma, with intent to kill.
This evidence was discovered and proven numerous times already by independent research teams, scientists, Biotech whistleblowers and the few ethical Journalists remaining.
There’s a concerted effort by the pharmaceutical cartel funded “fact checkers,” Big Tech platforms and mainstream media, to hide the evidence and slander the people bringing this to light.
Once you go over the evidence provided here, you must take action for the safety of you and your families. Serve all war criminals participating in this COVID death jab program with a Notice of Liability for the murders they are committing. This is definitive action that any person can take, worldwide. The notices are already drafted by legal teams so why not use them and let our enemies be on the defensive. The criminals will be reminded of the Nuremberg trials, and informed that they will be brought to justice. They need to cease and desist from acting knowingly and willfully in mandating “vaccine” death jabs and enforcing them. The evidence to the danger is clear and deaths have been proven. Anyone administering or mandating these “vaccine” kill shots are doing so without Informed Consent.
COMPILATION OF EVIDENCE
On November 2nd, a prominent Professor at the University of Almeria, Dr. Pablo Campra, revealed his detection of Graphene in multiple Covid-19 “vaccine” vials, using Micro-Raman Spectroscopy. The Dr. Campra’s University of Almeria report demonstrated the detection of Graphene and Graphene Oxide in 8 samples from various “vaccine” manufacturers.
In response, Dr. Andreas Noack released a scathing video commenting on Dr. Campra’s report. Dr. Noack is a chemist and the world’s leading expert in activated carbon engineering and GRAPHENE. Dr. Noack did his PhD doctoral thesis on how to turn Graphene Oxide into Graphene Hydroxide.
The video is of crucial importance. Dr. Noack said that two of the frequency bands that Dr. Campra detected were of Graphene Hydroxide. Graphene Hydroxide (GHO) is a mono-layer activated carbon, 50nm long and 0.1nm thick (an atom layer thick). Thus, the injections contain nano-razorblades of exceptional stability, which are non-biodegrable (a fact that every chemist knows).
In effect, these nano-razorblades cut up and destroy the heart, brain and cardiovascular system. The epithelial cells become rough so things stick to them. He says that toxicologists cannot find them in a petri dish by normal methods as they do not move and they don’t expect to discover nano-sized razor blades. Moreover, any doctor who injects them with knowledge of this issue, is a murderer.
Graphene Hydroxide is a new material and toxicologists aren’t aware of it yet. This is why people are dropping dead from these lethal shots, especially athletes, Dr. Noack explains. This is a “highly intelligent poison”.
What’s even more horrifying is that if you perform an autopsy you will not find anything. This stealthweapon is even untraceable after death. The Graphene Hydroxide nano-razerblades cause people to bleed to death internally.
“Even if people don’t drop dead immediately, it cuts up the blood vessels little by little… I can say as a chemist that we are absolutely certain that the Graphene Hydroxide is in there… as a chemist, if you inject this into the blood, you know you are a murderer.”
Dr. Noack died the next day, after blowing the whistle on Graphene Hydroxide in the COVID kill shots. His wife made an announcement that it was a “brutal sneak attack”. She pleaded with us to have the courage to BELIEVE in Dr. Noack’s message about nanoscale razorblades and to ACT NOW! She said her husband is a kind soul and he did this for us, he died for all of us.
That same evening Dr. Noack released his dire warning, there was strange electrical activity at his house and an electrical outage at the same time he developed “stroke-like” symptoms. These are both indicative of Directed Energy Weapon (DEW) radiation which is what his wife thought had killed Dr. Noack. Also see link here.
Dr. Noack’s widow believes he may have been attacked by a radiation beam because he has said in the past that radiation weaponry exists and this technology can be used by “them” to take people out. She mentions the radiation in her full interview in German.
The mainstream media is ever silent about Dr. Noack’s death and his grave warning that Graphene Hydroxide is in the COVID shots. There were a few independent media publications about his untimely death and there are others who expressed belief that he was murdered, possibly by rays from afar.
Here’s Dr. Noack’s widow’s latest update in English subtitles. Some say he died of a stroke. We may never know. But what we do know is that Graphene Oxide, Graphene Hydroxide nanoscale razorblades and other Graphene variants are indeed in these shots and the pharmaceutical cartel and world governments want to inject them into every man, woman and child!
Send out this video and my article to all doctors, experts and world leaders now. Governments are already injecting 5-year-olds with Pharma’s kill shots containing Graphene Hydroxide razors. This technology will cut up their insides and delivery a gruesome, painful death to our kids!
Last year the Austrian police busted down Dr. Noack’s door and arrested him in an attempt to stop him from speaking out. The incident was recorded on camera. He was clearly a target.
Dr Pablo Campra was the first to deduce that the Pfizer serum contains Graphene Oxide flakes using Transmission Electron Microscopy in July, 2021. His techniques of detection also included infrared spectroscopy combined with optical microscopy.
Prior to Dr. Campra’s discovery, another Spanish research team named La Quinta Columna, released their discovery in June, that the COVID serums in all their variants, AstraZeneca, Pfizer, Moderna, Sinovac, Janssen, Johnson & Johnson, etc., contain a considerable dose of Graphene Oxide Nanoparticles, reported by Global Research.
Dr. Ricardo Delgado a biostatistician and founder of La Quinta Columna, discovered that 99% of the Pfizer contents are Graphene Oxide. His team was smeared by fact checkers who provided no evidence of their libelous claims.
In my article entitled, “Graphene Oxide The Vector For Covid-19 Democide,” I explain the chemical process involved in reducing Graphene Oxide to a clear liquid serum by reducing its oxygen content. By doing so, Reduced Graphene Oxide (RGO) is more lethal. So yes, it’s scientifically possible that COVID serums can be 99% Graphene Oxide.
“The problem is that this is not a vaccine, this is a dose of graphene to a person.” – Dr. Ricardo Delgado
Whitney Webb attempted a smear piece on La Quinta Columna and the University of Almeria’s discovery, where she directly attacked Dr. Ricardo Delgado’s credibility without anything substantial. Investigative Journalist Ramola D. and myself debunked Whitney’s Webb of lies.
On August 19, another research team going by the name “The Scientist Club” found Graphene in 7 prominent Biotech serums using Optical Microscope, Dark-Field Microscope, UV absorbance and fluorescence spectroscope, Scanning Electron Microscopes, Transmission Electron Microscope, Energy Dispersive Spectroscope, X-ray Diffractometer, and Nuclear Magnetic Resonance instruments to verify the serums morphologies and contents. For the high-technology measurements and the care of the investigation, all the controls were activated and reference measurements adopted in order to obtain validated results.
For obvious reasons, The Scientist Club kept their identity secret. They analyzed Pfizer, Moderna, Janssen and AstraZeneca and found a Carbon-based substrate with nanoparticles embedded, Graphene sheets and Graphene Oxide.
Undeclared metal-containing components were found by scientists in Japan, which caused the Japanese Government to halt the use of Moderna’s serums. The Japanese Ministry reported that the particles found reacted to magnets and was therefore suspected to be a metal contaminant. Graphene, Graphene Oxide (GO) and Reduced Graphene Oxide (RDO) all have paramagnetic properties.
A September, a German team revealed damning evidence of “vaccine” contaminants and autopsies linking “vaccines” to deaths.
Dr. T. made a call out to all medical professionals in this urgent announcement asking medical professionals to report magnetic phenomenon because she believes that Graphene Oxide flakes are responsible for the “vaccine”-induced magnetism that we have witnessed internationally. Dr. Andrew Goldsworthy (retired) of Imperial College London has explained the possible mechanism here.
Pfizer Whistleblower Karen Kingston revealed in August, how Graphene Oxide was hidden under a trade secret and that’s why it wasn’t listed in the patents. However Kingston explains, it is in fact the key ingredient in the Covid-19 serums.
Another Chief Scientist for Pfizer blew the whistle in November, leaking internal emails on Stew Peter’s Show from top Pfizer executives and scientists discussing how they were going to hide from the public that Graphene Oxide is in their serums.
In April 2021,Health Canada recalleda million and a half KN95 face masks containing Graphene. Children had been forced to wear these masks in Canadian schools. Health Canada compared wearing them to breathing in asbestos all day long. These poisonous masks came from China’s Shandong Shengquan New Materials Co. Ltd.
Dr. Robert Young used Scanning & Transmission Electron Microscopy which revealed Graphene Oxide in four Covid-19 trade marked serums, September 11, 2021.
Dr. Antonietta Gatti did a recent video interview on the toxicity of Graphene Oxide Nanometallic particulates to cells. She has found them in the “vaccines”, PCR kits and face masks.
In her groundbreaking 2017 report with Dr. Stefano Montanari, Dr. Antoinetta Gatti explains Nanoparticles inside cells destroy the innate defense mechanism of cells and cause blood clots, deadly inflammation, thrombi, and multi-organ failure posed by nanometallic particulates, which are non-biodegradable and indeedbiopersistent. They can both enter cells, harm DNA, and be carried by the blood to bind with organic matter and coagulate in organs.
A Slovakian team analyzed PCR kit nasal swabs using SD Biosensor, Abbott and Nadal in a hospital laboratory from Bratislava. The team found that when DARPA’s Graphene Oxide Hydrogels come in contact with organic fluid (e.g., saliva) within a few minutes they begin to form rectangular crystal structures. These gradually grow in a fractal manner. A German research team also filmed the crystalline growth of the GO Hydrogels.
SCIENCE PAPERS & PATENTS
Several scientific papers show that Graphene Oxide is being used in gene therapy as a scaffold or platform for the delivery of mRNA into cells by way of its high electrical conductivity and ability to permeate cell membranes. The crystalline networks form in bodily fluid and replicate after injection and in the serum itself, as shown in this video of the Pfizer serum. It sure does look like nano high frequency antennas.
Graphene Oxide sheets
Scientists have developed a novel way of making carbon nanotubes at the NanoScience Center of the University of Jyväskylä, Finland, and atHarvard University, in the US.
Graphene was part of the first human genome project initiated in 2001. mRNA gene therapy Nanotech using Graphene Oxide as a vector, runs on CRISPR technology and it was developed by Pfizer,Moderna, and BioNTech, as a treatment for sick cancer patients. Due to its cytotoxicity (cell death) in healthy cells and the fact that all the animals died in the animal trials, Graphene Oxide Nanotechnology was never approved for use on Humans! Why is this technology now being used on healthy people and on children, who are at no risk of COVID?
It should be quite clear to everyone by now that the pharmaceutical cartel is using this technology worldwide, in illegal Human trials and trying to mandate their poisonous “vaccines” on everyone, with impunity.
Nanografiis manufacturing Graphene OxideNanotubes and intranasal vaccinesforCovid-19 drug delivery.
Scientists have already studied the Nose-to-Brain Translocation and Cerebral Biodegradation by intra-nasal spray, using thin Graphene Oxide Nanosheets. Make no mistake about it, nasal spray “vaccines” contain Graphene Oxide Nanoparticles.
If you’re still not convinced, here’s a main stream media article trying to pitch Graphene Oxide “flu vaccine” nasal spray as some kind of protective intervention.
Dr. Chunhong Dong is lead author of a study from the Institute for Biomedical Sciences in China where he boasts,
“This study gives new insights into developing high performance intranasal vaccine systems with two-dimensional sheet-like nanoparticles.”
Graphene Oxide has been carefully engineered as a “vaccine adjuvant for immunotherapy” and Polyethylene glycol (PEG), another highly toxic poison,is used as coating polymers. PEGs are widely used as additives in pharmaceuticals, cosmetics, and food. But PEGs come with potential life-threatening hypersensitivity reactions including anaphylaxis.
This is not a big name brand but they do mention “Carbon graphene loaded nano particles and micro-particles” in their Sars-Cov2 patent invention.
Here’s a list of peer reviewed medical studies on Graphene Oxide Toxicity and how itcoagulates the blood. How much more evidence do you need to BELIEVE?
Dr. Armin Koroknay, Research director of Private Consultants and Research Institute of Zürich, analyzed the effects of COVID “Vaccination” on Blood.
Dr. Bärbel Ghitalla and her team put different brands under a microscope and found things they could not explain, but are explained in the “Covid-19 vaccine” patents.
ARE YOU A BELIEVER NOW?
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“That Thing” was discovered in the Covid Vaxx under microscopy by Dr. Carrie Madej and released on Stew Peter’s Show, on September 29th. It turned out to be a transgenic Hydra Vulgaris.
Because Pharma savages purposefully hide their injurious vaxxine ingredientsunder a trade secret, I knew the only way to get to the bottom of the mystery of why Hydras and parasites are in the Covid Vaxx, is to read through the peer-reviewed literature. A tedious job that even evades experts.
I appeared on the Stew Peter’s Show on October 27, to break my findings.
DOCTOR: HYDRAS AND PARASITES IN VAXX,TRANSFECTING HUMANS INTO NEW SPECIES
Transgenic Hydra lines were developed for GAIN-and Loss-of-Functionuse in humans at the Wuhan Institute in China and funded by Anthony Fauci, the NIH, and partly by DARPA. Karen Kingston revealed on Stew Peter’s Show that the patents holders are Israeli Zionists.
Hydras and parasites are being first transfected with chimeric pathogens using Plasmid DNA (E. coli bacteria and fungus) to produce a new genetically modified line of Hydras. They are coded with the synthetic genetic sequences of the Lentivirus and Luciferase. These are the infamous “spike proteins” that are being coded into human cells using the Covid-19 “vaccination” program.
Lentivirus is a combination of SARS, MERS, HIV 1-3, and SRV-1 (AIDS). Luciferase is a luminescent Green Flourescent Protein reporter system that allows for the 24/7 tracking of hybrid humans (the vaxxed) through an externalcomputer interface. These are GAIN-and-Loss-of-Function bioweapons.
Transgenic Hydra lines work as vectors, carrying the messenger RNA (mRNA) of the Lentivirus and Luciferase. The GMO Hydras polyps and parasite eggs are carried on the lipid coating of programmable nanoparticles which are delivered on Graphene Oxide sheets.
The coding of human cells with chimeric “spike proteins” through Reverse Genetics, is done by electroporation using programmable Gold Nanobots and CRISPR-Cas9. This technology is all part of an operating system that’s being shot into the veins of our children for the purpose of transfecting them with the most deadly pathogens ever created by governments.
Transgenic Hydra and parasites are assimilated into the human host through Homoplastic transplantation. Once human cells are coded with the artificial reporter genes, the cell signaling of the human alters permanently and synthesizes with the transgenic Hydras cell signaling, called Cantenin Signaling. The entire process of cloning ultimately constructs a new neural network and an artificial brainin humans, as well as a third strand to the DNA.
BLAST technology is being used to create new DNA sequences for cross-species genomics, and yes, this is cloning. The Covid Vaxx inserts an operating system enabling a computer interface that stores your internal data on an external database, for totalitarian control of transgenic humans (the vaxxed) using the Internet.
The operating system is gene silencing and knocking out the genetic sequences your patent holders don’t want you to have, while coding your cells with new, artificial genetic sequences through external interfaces. Essentially, they’re playing god’s. Your patent holders will be able to upregulate and downregulate your genetic sequences through external controls. This is called the “Hybrid Genome Assembly”.
The intended result of this genetic experiment is a mass die-off and rapid cloning of the human race to create an artificial hybridized species. Most people will become sterilized after Covid-19 inoculation and their lineage terminated, many will die and be exterminated because the human body cannot withstand this toxic experiment.
A small percentage of genetically cloned humans will be able to procreate but I strongly advise the vaxxed DO NOT PRODUCE OFFSPRING because they will not contain our God-given human genetic codes! Your offspring will not be human. If you want to have children for God’s sake, do not take the Mark Of The Beast. The operating system targets embryonic cells also cloning your offspring and thus hybridizing future generations. Cloned genetic mutations are always unpredictable so there is a great risk to your hybrid children.
A breaking news report from Mike Adams, The Health Ranger of Natural News, revealed a new scientific discovery that is indeed a “true horror”. Catch the Brighteon podcast here.
Stunning new research published in Viruses, part of the SARS-CoV-2 Host Cell Interactions edition of MDPI (Open Access Journals) reveals that vaccine spike proteins enter cell nuclei and wreak havoc on cells’ DNA repair mechanism, suppressing DNA repair by as much as 90%.”
Make no mistake about it humanity is facing a totalitarian biological attack using a very advanced weapons system that contains programmable nanobots and GMO’d microscopic organisms. Everything I’m reporting here is open-source, viewable online, and linked into my article on Red Voice Media entitled, What’s In the Vaxx? Transgenic Hydra And Parasite Implants Used As Rapid Human Cloning weapon system.
Dr. Christiane Northrop appeared on Gene Decode with Nicholas Veniamin to discuss detox protocols. Nicholas revealed that organic/synthetic insect DNA is also being used in the vaxx and this is what’s causing Morgellons.
The transhumanist dystopian nightmare we find ourselves in is taking a new turn with the shocking discovery of Hydra Vulgaris and PARASITES in the so-called Covid-19 “vaccines”.
Dr. Carrie Madej revealed her Hydra findings on the Stew Peter’s Show on September 29th, 2021, followed by Dr. Zandre Botha’s stunning discovery of microscopic, self-assembling medical devices in the blood of her vaxxed patients. The red blood cells are dangerously deformed and coagulated, things she says she’s never seen before in her 15 years as a blood doctor.
Hydra Vulgaris identified in Pfizer & Moderna Covid-19 serums
About 10 days later, “That Thing” (Hydra Vulgaris) was also identified in Pfizer vials by Dr. Franc Zalewski. He took the science to a new level and did a chemical analysis of the Hydra, exposing that the chemical compound of the creature contains Aluminum, Carbon, and Bromium. This means the Hydra’s are being genetically modified before they’re injected into humans. The good doctor also identified parasites in the vials.
Dr. Jane Ruby, a pharmaceutical researcher, gave vital commentary on Stew Peter’s Show about Dr. Zalewski’s findings, emphasizing that the dormant Hydra “eggs” become active, grow and multiply when exposed to Graphite tape and heat.
Earlier in August, parasites and other horrors were identified by Dr. Robert Young in four Covid-19 vials. Dr. Jane Ruby again joined Stew Peters to give crucial commentary on Dr. Young’s findings.
Investigative Journalist Ramola D. provided us with further information about the parasites discovered by Dr. Young and did an expose in October.
Back in July, La Quinta Columna studied four “vaccines”; Pfizer, Moderna, AstraZeneca, and Johnson & Johnson, and found toxic nano metallic particulates, particularly nanographene oxide, in significant amounts, as well as lipid nanoparticles and the parasite Trypanosoma cruzii, in the Pfizer-BioNTech serum.
Pfizer whistleblower Karen Kingston appeared on Stew Peter’s Show in July and walked us through a presentation on how Graphene Oxide is in all Covid-19 serums. Graphene Oxide was not listed in the patent filings and was deliberately concealed under a trade secrete because it’s known to be poisonous to humans.
As a result of these horrifying discoveries, I did my own research on Graphene Oxide Nanoparticles and Toxicity and wrote an article entitled “Graphene Oxide The Vector For Covid-19 Democide“. I reveal how humanity is being saturated with Graphene Oxide Nanoparticles in a myriad of ways.
I also wrote an article on protocols for detoxifying Graphene Oxide from your body, here.
The openly declared ingredients in Covid-19 serums should be enough to dissuade anybody from taking them. Now it’s clear there are additional poisonous and other horrors not being disclosed to the public by the Biotech pharma industry.
Karen Kingston has backed up all these terrifying discoveries with the patent filings and receipts, on Stew Peter’s Show. Kingston explains that the vaxxines are a “gateway to an obedience platform and potentially an execution platform if you are not obedient to your score”.
Informed Consent has been waived and therefore people didn’t know they’re being injected with smart devices and bioweapons. The patents also reveal that it was alreadyknown by Pfizer that the vaxxed would become “super spreaders” and transmit deadly pathogens to healthy individuals.
There’s an AI component to these vaxxines Kingston explains, “they’re committed to replacing the American people with Artificial Intelligence”. She continues disclosing that “Hong Kong is ready to replace the American people with robots right now”.
Due to the fact that patent filings do not reveal the components to Biotech’s vaxxine ingredients, I began researching scientific peer-reviewed studies involving Hydra Vulgaris and parasites to see if I could identify why they’re being injected into humans.
GAIN-OF-FUNCTION
Everything I’m writing here is based on evidence from open-source, peer-reviewed literature of scientific breakthroughs and technological developments that extend through the past decades and are linked in this article. As sci-fi thrilling as this information may sound, the technology has already been deployed and is being injected into the veins of our children as we speak. You can read the studies for yourself, as I have done.
DNA hybridization began in 1980 with Nadrian C. Seeman who started constructing self-assembled nanostructures. Hydra Vulgaris transgenesis technology was developed over the last 30 years. This is the process of transferring genes and organisms from one species to another which creates a new cloned species.
The Human Genome Project began in the year 2,000. Hydra’s are used in the human genome assembly for gene silencing of humans. Messenger RNA (mRNA), SPIONS (Super Paramagnetic Iron Oxide Nanoparticles), DNA coated lipid-nanoparticles containing drugs and chemicals, transgenic Hydra’s and parasites are all part of an “operating system” which is bypassing the human immune system. You can read more about Moderna’s “operating system”from their own website,here.
Graphene Oxide sheets are used to slice open the membrane of your cells so that programmable Nanorobots can reach the cell nuclei to turn off undesired genes (gene silencing) and code artificial gene sequences. This process is called biohacking.
Graphene Oxide sheets are able to slice open every cell membrane of the human body within 15 minutes after inoculation, according to Dr. Robert Martin.
The Sixth International Workshop on DNA Nanotechnology was held August 26–28, in 2017, in Beijing, China where the forum showcased the applications of self-assembled DNA nanostructures.
CHIMERIC SPIKE PROTEIN
The “spike protein” in the Covid-19 vaxxines that everyone is talking about is called a Lentivirus. The Lentivirus contains a combination of HIV types 1-3, SRV-1/AIDS, MERS,andSARS. These are the most deadly Gain-Of-Function bioweapons ever developed, thanks to mass-murdering Fauci.
A Stanford study reveals that the Lentivirus is a “genus of retroviruses that cause chronic and deadly diseases characterized by long incubation periods, in humans”. It enables long-term transgene expression. The best-known Lentivirus is the human immunodeficiency pathogen, which causes AIDS. This is why we’re seeing an autoimmune and neurodegenerative decline after Covid-19 inoculation. This is an induced condition known as PRION.
The mRNA from the Lentivirus chimeric cocktail is inserted into the DNA of human cells through an invasive procedure that permanently changes the genome of that cell. Once inside the host cell’s cytoplasm, lipid-coated nanobots take the reverse transcriptase enzyme in the Lentivirus to produce DNA from the mRNA genome, the reverse of the usual pattern, thus retro.
Morphogenesis and stem-cell control using the Hydras were developed to learn the neurobiological functions of humans and for in vivo tracing of cells. Transgenic Hydraallows in vivotracking of individual stem cells during morphogenesis (tissue and cell growth).
Transgenic Hydra lines are generated by embryo microinjection with plasmid DNA from self-replicating DNA found in bacteria. This is a permanent transmissible change of genetic material (DNA) resulting in the decreased production of a protein. The merging of the two species is a“cloning”processcalled transfection. A new generation of transgenic Hydra polyps continues reproducing the chimeric genetic expression in their offspring.
These GMO Hydra polyps are now genetically codedvectors, carrying a variety of programmed synthetic genomic sequences and mRNA (messenger RNA) for the purpose of transfecting humans. Once inside the human body, these transgenic Hydra polyps serve to rewire and control the ancestral circuitry of human beings.
BLAST Sequence technology is being used to create new DNA sequences and find similar genetic sequences between species, performing alignment functions for same-species and cross-species genetic splicing for the purpose of transcription.
Proteins regulate gene expression. This technology targets the cell organelles of the nuclei which store genetic information; mitochondria, which produce chemical energy; and ribosomes, which assemble proteins, using mRNA to make mitochondrial sequences.
A 2017 Gain-Of-Function research project from Germany, demonstrates how RNA extraction and quantitative reverse transcription-polymerase chain reaction or reverse genetics is used to knockout and knockdown genes using Hydra’s and CRISPR/Cas9.
The genetically modified Hydra lines in the Covid-19 operating system is first coded with chimeric gene sequences (Lentivirus) which is then being coded into human cells using CRISPR-Cas9 technology and electroporation.
Electrodes attached to gold programmable nanorobots transfect human cells, silencing your innate God-given genetic sequences and coding your cells to reproduce the synthetic genetic sequence of the chimeric spike protein (Lentivirus), indefinitely. More simply stated, your cells will continue to replicate themselves over and over again with the new genetic sequence of the chimeric pathogen you were injected with. The same chimeric pathogen was funded by bioterrorist Anthony Fauci and developed in Wuhan, China.
Parasites are also transfected with bacteria and used as transfection vectors for DNA binding and genetic sequencing in humans. Parasites can evade drugs, escape the immune system and regulate genes.
The human Malaria Genome Projectdeveloped at Stanford University, used CRISPR technology and bacterial plasmids which can replicate rapidly inside parasites. They transfected bacterial plasmids into parasites, disrupting a series of gene encoding molecules. In that study, scientists transfected Malaria parasites with Luciferase to use it for gene targeting and transgene expression in humans.
T. gondiiandP. falciparum and other parasites were also used in transfection studies. It’s important to be aware that from the P. falciparum they designed a Chloroquine-resistant transgenic parasite strain called Dd2.
LUCIFERASE
Hydra polyps are also being coded with the overexpressed chimeric proteincalled Luciferase, which is a Green Florescent Protein derived from the firefly. Transgenic Hydra also carries the Luciferase RNA trigger to code your cells with and silence genesin human cells.
Holstein lab investigated the repressing activity of HySp5 on the HyWnt3 promoter, performing Luciferase reporter assays in human HEK293T cells for DNA-binding and transplanting Hydra into humans by invading human tissues.
The transgenic Hydra and parasites replicate andmerge with humans during transfection. They are integrated with the transgenes (Luciferase and Lentivirus) into one of the epithelial cell lineages and assimilated into the human host. Thetransplanting of Hydra’s into humans is called Homoplastic transplantation using induced Hydranth as “implants”.
Epithelial cells are stem cell lineages responsible for cell signaling. Transgenic Hydra’s reporter genes are cell-signaling with each other inside humans, much like neurons in a neural network. Transgenic Hydra’s cell signaling becomes synthesized with human cell signaling in a process called catenin signaling, which is induced by mutations of genes in humans through upregulation (cell response) to the plasmids expressing activators in the Hydra (HySp5–2992:Luc); aka transfection.
Transgenic Hydra and parasites induce humans to generate a new electrochemical signal by organizing enzymes spatially to create a programmable redox enzymatic cascade pathway, changing the predictable generation of electrochemical signals in humans. The newly established synthetic gene sequences are now shared between the transgenic Hydra’s, parasites, and newly hybridized humans.
A team of scientists from UC Davis and Rice University was boasting back in July about manipulating the nervous system of Hydra Vulgaris and humans to “build a new brain from the bottom up”, in order to control neural pathways and human behavior. This technology was developed over the last decade through the Human Brain Project.
Graphene implants can record electrical activity in the brain at extremely low frequencies and over large areas, “unlocking the wealth of information found below 0.1 Hz”.
A Russian initiative called 2045 wants to use neural interfaces for an “improvement of man himself” because mankind is “standing at the edge of a total loss of the conceptual guidelines necessary for further evolution”. This demonstrates the anti-human mindset of eugenicists who want to clone the entire human race.
The fluorescent (Luciferase) Hydra’s were also tested with externally applied electrical fields to see how much voltage they could endure, to “facilitate the future use of electric fields as an experimental means to redistribute intracellular constituents in developing tissues”. I presume this was to test Hydra’s ability to survive 5G frequency?
THE OPERATING SYSTEM
Hydra’s and parasites also serve as a reporter system. Luciferase exhibits bright green fluorescence when exposed to light in the blue to the ultraviolet range, enabling the vaxxed to be traced externally. Genes of interest can be turned off occasionally or turned on at will by your patent holders through what’s called transregulation.
This means you’re not only externally traced 24/7but you’ll also be externally controlled. Your patent holders will be able to upregulate and downregulate your genetic codes through an external database, through the Eukaryotic Genome Annotation Pipeline for transgenic humans.
Did you think the Starlink satellite network’s “Precision Tracking Space System” had something to do with defense? Don’t worry, you’ll be “happy” owning nothing so long as they get your dopamine levels worked out.
ADDGene is selling a variety of CRISPR parasites to be used as gene vectors for human transfection. These are not “vaccines” at all but a WEAPONS SYSTEM (my words) for the RAPID CLONING (their words) of humans, through gene knockout (silencing), artificial gene sequencing (coding) and to monitor transfectants inside of humans (tracing).
ProSplign is a worldwide protein-to-genome alignment tool enabling Human DNA to be easily synthesized from a single-stranded RNA template and catalyzed by an enzyme for reverse transcriptase.
ADDGene also offers a Lentiviral Envelope and Packaging Plasmids for transfecting humans using transgenic Hydra. They offer“Non-overlapping NEURAL NETWORKS” (their words) using Hydra Vulgaris for building anew neural networkin Hydra’s. This technology is being deployed in humans through the Coivd-19 Quackccine program now.
Dr. Carrie Madej also disclosed in her latest interview on Stew Peter’s Show that the vaxxine operating system is building an artificial neural network in humans.
ADDGene offers a Tetracycline off system for on/off gene expression, “fusing tetR with the C-terminal domain of VP16 (virion protein 16), an essential transcriptional activation domain fromHSV (herpes simplex virus) which is being used for “reduced gene expression” in humans. This uses the chimeric E. coli bacteria and Lentivirus.
After Luciferase is infused and coded for targeted genes via a computer, it’s then mapped onto the Human through the public Galaxy server to perform “differential expression analysis”. Proteins can be targeted, upregulated, and downregulated.
Then there’s Vector Biolabs whose selling Adenovirus’ for human sp5 shRNA silencing. A Knockout vector system (adenovirus) for knocking down the expression of particular genes (gene silencing), is being marketed online and sold by Vector Builder. You can create artificial genome sequences and merge genomes of different species.
The Genome Data Viewer (GDV) will help you select genome assemblies (DNA sequences) for humans from primarily finished human clones, that were sequenced as part of the Human Genome Project.
VIGENE offers multiple shRNA cloning options for your gene silencing experiments. They’re packaging transfer Plasmids, Adenovirus’ (AAV) and Lentivirus’ and they guarantee at least a 70% knockdown of your gene of interest. They have a catalog of over 27,000 shRNA plasmid sets targeting the human genome.
This table lists common Lentiviral envelope and packaging plasmids that can be used with 2nd and 3rd generation lentivirus technologies.
ADDGene’s lentiviral genome is delivered to a target cell upon infection using CRISPR gRNA. They explain how the Lentiviral genome encodes genetic material that the “researcher” (or patent holders and Big Pharma) wants to be delivered to specific target cells. The genome is encoded by plasmids called “transfer plasmids,” which can be modified to encode a wide range of gene products.
ADDGene admits their DNA-targeting enzymes very often will delete, insert or otherwise alter the targeted RNA or DNA, so don’t let the fake media fool you.
Lentiviral Plasmids can be ordered through ADDGene here.
BEHAVIOR CONTROL
Vector Biolabs offers an Adenovirus (AAV) expressing shRNA for the knockout (gene silencing) of Human SP5. When developing this technology during the animal trials, social recognition, spatial learning, and memory were impaired after 4 weeks.
In an animal study using reverse transcriptase-polymerase chain reaction (RT-PCR) with an Adenovirus vector and drugs, scientists were able to induce Huntington’s Disease by targeting the Corpus striatum of the brain which resulted in 100 fold neurodegeneration and motor behavioral impairment.
REPRODUCTION & FERTILITY
The transgenic Hydra’s are used to induce gene silencing predominantly targeting embryonic cellsin the testes of men and the ovaries of women and also nerve cells. This is why we’re seeing neurological degeneration (PRION) after inoculation. It also explains why 82% of expectant mothers who take the “jab” are having spontaneous abortions.
Microinjection of foreign DNA into the pro-nucleus of single-cell embryos of fertilized mice to control the genetic expression of future generations has been perfected, since 2008.
Proteins control gene expression. Transgenic Hydra is instrumental in encoding the human SP5 (shRNAsilencing AAV) which is a gene on chromosome 2q31.1 that encodes a protein that binds to the GC-box promoter elements, thought to play a role in coordinating the intricate changes in transcription which occur in the developing embryo.
Wnt-3 is a protein that in humansis encoded by the WNT3gene. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis.
The point I’m making here is that the operating system is DNA-binding, downregulation, and upregulating genes using the transgenic Hydra’s, targeting human embryosand embryonic cells, leading to developmental alterations from binding genes to the Wnt/β-catenin signaling pathway.
Do you understand what this means? It’s not only the vaxxed who are being genetically modified, cloned, and hybridized, but SO ARE THEIR OFFSPRING! That is of course if you’re still able to reproduce at all after the jab! Most people will just be sterilized and their babies aborted. This is a human cloning experiment as well as extermination.
Microinjection of Retrovirus transgenes (Lentivirus & Luciferase) integrates randomly into the genome which poses enormous risks for the vaxxed as well as their hybrid offspring. This can create strange and unpredictable mutations of DNA by the addition of one or more base pairs. This is precisely why we’re seeing freaky mutations and why doctors are removing blood clots with Hydra-like tentacles from teenagers!
Dr. Carrie Madej shares an image of a blood clot with Hydra-like mutational growth that was removed from the heart of an early teen who received a Covid vaxx.
“It is a deadly protein” explains Dr. McCullough. “It is the first time in medicine that we are injecting vaccines and asking the human body to make a potentially lethal protein” .
While the Covid-19 serums appear on the surface to be only a clear liquid, under microscopy you can visibly see all the many components of the computer-interface operating system, which is a sophisticated biological weapons system for the cloning and extermination of the human race.
If you would like more information on detox protocols and disrupting the blood coagulation cascade which leads to blood clots from the jab or for protocols that will protect you from the adverse effects of transmission, please contact me directly at: metanutrients@mailfence.com
