Category: Dr. Ariyana Love

Dr. Ariyana Love First Ever Detox Protocol
Posted on by Ariyana Love

by Dr. Ariyana Love

For humanity.

I will be updating this document periodically.

Because many are unaware, I was the first person in the world to read the Covid-19 “vaccine” patents, document them and report my findings on Stew Peters Show. This was back in October 2020, in the wake of Event 201, aka “Covid-19”.

By January 2021, I had succeeded in detoxing my first client from two Pfizer jabs. Since then, I have helped hundreds of clients and thousands of people with my detox protocols.

Here is the “First Ever” protocol to emerge in the west, from Finland.

  1. ASEA Redox Molecules
  2. Stemtech
  3. Pine Needle Essential Oil
  4. Parasite Detox
  5. Microbiome Protocol
  6. Blue Green Algae

ASEA Redox Molecules

ASEA redox molecules boost glutathione levels to between 500-800% and balance all bodily functions. Read more about ASEA redox molecules and order here: ASEA Redox Molecules Anti-Aging Power.

ORDER HERE: Visit the ASEA homepage of Dr. Ariyana Love.

Stemtech

Our adult stem cell production is the second most vital function that we lose when the aging process begins, leaving every adult deficient in the ability to heal from bodily injury after the loss of adult stem cell function.

Adult stem cells are our body’s master cells. They are necessary for the self-renewal and self-repair of damaged cells, tissues and organs. Prolonged Mitochondrial Fatigue due to Reactive Oxygen Species (ROS) from GON further suppress our adult stem cell production.

After years of scientific lab research, Stemtech has isolated key super nutrients that reactivate adult stem cell production. Using all three Stemtech products gives you a 53% increase in adult stem cell production, reducing inflammation and enabling the body to heal and bounce back rapidly after cellular injury. Using Stemrelease3 alone will increase adult stem cell production by 20%.

Stemtech’s powerful antiaging meta nutrients super boost the immune system, restore Ph balance, and empower swift regeneration of cells and organs from bodily injury. The rapid rate of absorption of ASEA redox molecules effectively deposits Stemtech’s vital nutrients directly into your cells for immediate absorption and usability. Redox molecules absorb into every cell of your body in just 5 minutes, driving oxygen in and nanotech out, while repairing your DNA and supercharging your immune system. This rescues mitochondria from fatigue and pulls the body out of ROS.

ORDER HERE: Visit the Stemtech homepage of Dr. Ariyana Love.

Pine Needle Essential Oil

Pine needle oil is the most effective natural medicine that kills genetically modified mRNA parasites and all parasites. Pine needle oil surrounds all parasite varieties and suffocates them to death.

Unlike Ivermectin, Pine needle oil can be used continuously throughout your detox, as it’s classified and used by our bodies as an essential food.

Pine needle oil is a treatment against influenza A, a potent antibacterial, antifungal and a natural antibiotic. It’s an effective blood thinner, anticoagulant, antimalarial, antitumor, antimicrobial, anti-inflammatory and a powerful antioxidant with 5x the amount of vitamin C as oranges.

Pine needle oil is one of the top meta nutrients known to man, super boosting immunity. Pine oil absorbs into every cell of your body in just 20 minutes, conducting targeted cellular repair.

Pine oil super nutrients are unique because they bypass your nervous system and treat nerves directly. Pine oil remedies depression, chronic PTSD and reverses the memory of trauma in your cells. There is no replacement for pine needle oil which is essential now in every protocol, in my humble opinion. If you cannot find pine, you can also use Spruce, Douglas Fir or Ceder.

Listen to my podcast on the healing remedies of pine needle essential oil.

ORDER HERE: RED PINE NEEDLE OIL

Parasite Detox

I use Young Living Essential Oils with my clients for parasite detox. I use either Young Living Scots Pine needle essential oil or Dr. Robert Young’s Red Pine needle oil for parasite cleanse. High quality essential pine needle oil is the most effective way to thoroughly detox parasites. Turpentine 100% Pure Gum Spirits works very well also for the initial die off. The entire pine tree is edible, highly medicinal and classified as an “essential food”.

Microbiome Protocol

My Microbiome protocol blend is critical for stopping the replication of Alhydrogel, Inhalation Anthrax and Injection Anthrax and E. coli poisoning. Thus, it remedies GI and digestive issues, along with the parasite detox.

Young Living essential oils

We are all being exposed to genetically modified AI parasites. The highest quality essential oils are necessary for parasite detox because essential oils bypass the digestive process. They absorb through the tissues within minutes, traveling into your interstitial fluids (fluid between cells) making the vital nutrients accessible to the cells throughout your entire body. You cannot replace the quality of Young Living oils with any other company.

You must enroll as a “brand partner” in order to purchase products. The starter kit is optional but you must enroll to be able to order products. You will need my brand partner and sponsor number which is # 37904828.

Visit the Young Living website of Dr. Ariyana Love for additional essential oils.

ENROLL HERE: YOUNG LIVING ESSENTIAL OILS

Blue Green Algae

Blue Green Algae from Klamath Lake Oregon, is the most nutrient-dense food known to man and has miraculous healing properties. It contains all the vitamins and minerals our bodies need. It also exhibits potent antiviral activity against “HSV-1, HSV-2, human cytomegalovirus and influenza A virus”, inhibiting the initial stage of infection including the binding and internalization processes.

Blue Green Algae inhibits the initial stage of “infection” when poisoned with Covid-19, including the binding and internalization processes. It exhibits potent antiviral activity against “HSV-1, HSV-2, human cytomegalovirus and influenza A virus” (nanotech replication).

Blue Green Algae is antiparasitic, antibacterial, antifungal, and more. This single-celled miracle food works like our mitochondria to surround heavy metals and chelate them most effectively, while simultaneously repairing damaged cells. Blue Green Algae is another powerful anti-inflammatory that is rich in chlorophyll and chlorophyll prevents infection. Blue Green enables red blood cells to regenerate and this is critical because Covid-19 technology destroys red blood cells.

Blue Green reverses cancer, depression and thyroid issues while activating adult stem cell production.It stimulates serotonin production significantly, reversing depression. Blue Green reverses cytotoxicity and boosts glutathione, which is our body’s master antioxidant.

Harvesting technology

There are two kinds “Blue Green Algae”, so please do not be confused. One is toxic, and the other is super healing food. Spirulina and chlorella cannot replace Blue Green. The harvesting technology used to extract Blue Green Alage determines the percentage of nutrients retained, so knowing the company you buy from is very important.

Green Earth Naturals Best Blue Green uses a superior harvesting technology that retains 95-98% of the vital nutrients in Blue Green Algae. Clause: I do not endorse their digestive enzymes. I only recommend the Blue Green Algae powder.

ORDER HERE: BLUE GREEN ALGAE (recommended source)

Vitamins

Melatonin (organic plant based)

Quercetin (Source yourself: inflammation reduction & antioxidant detox)

Vitamin D3 (10,000 IU daily as per Dr. Zev Zelenko’s recommendations)

Vitamin C Acerola

I endorse and guarantee the quality of all products from ASEA, Stemtech, Young Living, and Ph Miracle Products.

There is no need to use zinc so long as you’re using ASEA redox and/or sodium chlorite, which are both cellular drivers.

I used 1-5 natural medicines and supplements to detox people since September of 2020. I added my Microbiome Protocol after discovering that the Covid-19 “vaccine antigen” is an enhanced form of Anthrax. PLEASE READ: BREAKING: Anthrax Is The COVID-19 “Vaccine Antigen” And It’s Aerosolized!

SCHEDULE A CONSULTATION

If you would like my detox and customized protocol support, please schedule a consultation with me here: https://calendly.com/drariyanalove.

ASEA Redox Molecules Anti-Aging Power
Posted on by Ariyana Love

By Dr. Ariyana Love

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 to between 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.

Here’s an excellent Guide to your Q & A: https://www.redoxguide.com

 

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.

  1. 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).
  2. 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.
  3. Otherwise choose Retail.

Press Enroll next to the type of ordering you wish to make.

Order ASEA Redox

Dr. Ariyana Love’s ASEA website, please order here: https://drariyanalove.myasealive.com/at/index.aspx

Contact Me

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 Support to set things up for you. Give them my account number: 1800502009.

ASEA Support USA Phone
801-973-7499

ASEA Support Toll-free
888-438-5971

ASEA Science and Research

  1. Understanding Redox Signalling Molecules by Dr Lee Ostler https://redoxmatters.com
  2. The Importance of Enhancing Redox Signalling in Functional Medicine: https://healthcentersofthefuture.com/blog/the-importance-of-enhancing-redox-signaling-in-functional-medicine/
  3. 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
  4. Here is a podcast with Dr Zach Bush and Dan Pompa on the healing of the gut microbiome, Restore with ASEA: https://drpompa.com/podcasts/110-fix-leaky-gut/
  5. Redox Signalling, Vascular Function, and Hypertension: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828811/

“…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.

 

See full document here:  asea_bioactivity_us_eng_white_paper_by_dr_gary_samuelson10516

 

Redox implications for long covid, ME/CFS

“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.

Autism and Redox SignalingWebinar

Interviews

 

BREAKING: Anthrax Is The COVID-19 “Vaccine Antigen” And It’s Aerosolized!
Posted on by Ariyana Love

By Dr. Ariyana Love

Covid-19 is a biological and technological weapon system using self-replicating, programmable nanotechnology with synthetic modRNA poisons. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” because that’s medical science. But what if the Covid-19 vaccine antigen is ANTHRAX?

“…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.”

The first Anthrax was a biological weapon developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene“ into the highly toxic Bacillus Anthracis bacteria. This means that advanced technologies such as Cross-Species-Genomics capability was acquired by the government before 1950 when a lethal bacteria and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax.

Russia’s Anthrax could be treated with antibiotics even several days after exposure and thus it met the requirements under the Biological Weapons Convention. Being the bioweapon of choice, NIH funded Anthony Fauci increased Anthrax’s lethality. Russia’s Anthrax was genetically attenuated by the NIH before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more.

According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast).

Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.”

The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks but we already know that the D.O.D spearheaded this “Covid-19 vaccine” Democide.

Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides

In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Both have just been administered to the world population through inoculations, PCR swabs and aerosolization and self-replication.

Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014 creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH, also in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously in 2014, China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study admits to severe side effects.

PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses

The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in “vaccines” under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare.

In March of 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more.

Ebola is used in the J&J and Sinovax jabs while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. The H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs!

Here’s how they did it. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop it from replicating inside the human body due to it being antibiotic resistant.

The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquitoes which is part of DARPA’s weaponized insect project called The Sentinels.

Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax.

Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

SPIKE PROTEIN IS AEROSOLIZED ANTHRAX!

There’s 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.”

The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine“.

“The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.”

In layman’s terms, the poisonous Anthrax “antigen” is being used in the genetic modification of the human genome and it’s literally being encoded into the genome, after knockouts (deletions) of the genome.

The molecular basis of Anthrax “vaccines” contains “spores and DNA plasmids.“ This is a targeted weapon system. The following quote about the Anthrax “protective antigen” is particularly revealing:

“PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).”

Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want.

Luciferase is insect DNA and that’s going into the genome. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery (aerosolization), the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized.

This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic.

This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality.

ALHYDROGEL

The hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health.

According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is Alhydrogel. The Alhydrogel is infused with 750 μg of aluminum, making it magnetic. In the Alhydrogel invention, Anthrax was fused together into this nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

Again in layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death.

Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network, which is what I believe some eugenicists were trying to achieve.

Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There’s many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system.

This Alhydrogel patent demonstrates its use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability.

It begs the question, where do venereal diseases come from? But I digress.

This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades however, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

“Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA.

So, both nanoparticles and Anthrax have been used in vaccines for decades already, without Informed Consent of the public.

Alhydrogel was improved and transformed into the Nanoalum adjuvant.

Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor.

The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites.

Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector!

ANTHRAX SYMPTOMS AND TREATMENT

Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and swabs which contain delayed release technology that contains a military weapon system.

Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements.

Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans it’s EXTREMELY TOXIC.

Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review

They also say the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a complete disaster. U.S. Army statistics that were never published show the Anthrax “vaccine” induces cancers.

The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis? Anthrax also coagulates the blood. Read more here and here.

“Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.”

Anthrax also causes a person to hemorrhage. So this explains all the excessive bleeding people experience after Covid-19 injections and from aerosolized exposure. In other words, shedding by transmission. Inhalation Anthrax.

Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by https://pmc.ncbi.nlm.nih.gov/articles/PMC3124019/proinflammatory cytokine signaling and histological lesions in the spleen.

Anthrax has been tested on the public already. During 9/11 Anthrax spores were intentionally released into “some environments” in NYC, according to the NIH. The FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI.

Heroine users in Europe have been tested on with Injection Anthrax.

Our skies are sprayed with smart dust and chemicals daily. Our governments have launched all out war against their constituents. We are being poisoned in a myriad of ways so please keep this in mind:

“Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by Whole Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.”

TREATMENT

If you have been inoculated with Covid-19, or PCR swabbed and you are suffering from heart pain and other severe symptoms, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated” then you may have been exposed to Inhalation Anthrax.

Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. If you have been exposed to Inhalation Anthrax, you will feel hot and very flushed, similar and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning.

Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need a good doctor with complete protocols.

I have been successfully detoxing people from the Covid-19 bioweapons for two years. I have a complete protocol for Anthrax poisoning. If you would like to schedule a consultation with me, please do so through my online booking system.

If you would like to donate to my research, please do so here.

Is C60 And EDTA Safe? Clinical Review
Posted on by Ariyana Love

by Dr. Ariyana Love

There are some pharmaceutical drugs being promoted by independent media professionals and Medical Doctors that are quite dangerous. The two drugs in question are C60 and EDTA. We are going to look at the clinical research that has been done to determine if these drugs are truly safe and effective treatments for heavy metal chelation and if there’s a better solution.

Given how Pharma and governments have lied to humanity about the safety and efficacy of Covid-19 vaxxines, I cannot comprehend why anybody would continuing trusting any pharmaceutical drug. Adding toxicity to poisoning is totally the wrong treatment! When poisoned, you must detox a person and then support their immune system with antioxidants and super nutrients so their body can recover and the cellular damage can be reversed. Pharmaceutical drugs leave a person totally exhausted and drained. Without supporting the immune system you are not giving an effective treatment protocol.

Dr. Zev Zelenko was a perfect example of medical ingenuity using the allopathic system. He knew to prescribe drugs for his patients that effectively kill parasites, like Ivermectin but he didn’t stop there. Dr. Zelenko also provided immune support and detox supplementation, like his Z-Stack and Z-Detox. This is what Pharma educated MD’s largely fail to do. You can order from Dr. Zelenko’s website, here.

C60 has been promoted by lawyer Todd Calender, as a treatment for jab injured persons and by Independent Journalist Sarah Westall, who is promoting C60 and frequency treatment for vaxxine detox. These are completely wrong treatments. I have many testimonials from jab injured clients who became severely worse just weeks after any kind of frequency treatment. This is because frequency activates the self-replication of graphene oxide nanotechnology, as explained in the toxicology report entitled, “Toxicology of chemically modified graphene-based materials for medical application”.

C60

EDTA and C60 are cytotoxic and neurotoxic acidic forming poisons. They are being falsely marketed as antioxidants when in fact they are oxidants. An oxidant has a low Ph and a high Oxidative Reduction Potential. They are acid chemicals that burn right through everything an destroy your body’s cells.

C60 is a CHEMO drug and a Pharma “treatment” for HIV. C60 and EDTA contain metallic nanoparticles that can cross the Blood Brain Barrier (BBB). Metallic nanoparticles are toxic to living cells. Studies show that C60 also induces cancer growth. Isn’t it diabolical how Pharma always uses drugs that induce cancer when “treating” cancer?

Fullerene C60 is also being marketed as a nutritional supplement when in fact C60 is an industrial lubricant. This study shows that C60 induces chronic nephrotoxicity. Mice who were injected with C60 had macroscopic lesions of the kidney(s) and this study showed that C60 failed to prolong the life span of mice. So why the hell are people using it?

C60 damages your DNA and proliferates cancer growth, another study shows.

“A large-scale association study for nanoparticle C60 uncovers mechanisms of nanotoxicity disrupting the native conformations of DNA/RNA C60 enables to disrupt the structure of G-quadruplex DNA, and thereby provides a possibility to activate the telomerase by facilitating its access to telomeres and in this way promotes the proliferation of tumor cells.”

Another study alarmingly reveals that fullerene C60 accumulates in the body following repeated exposure and therefore increases the concern for a potential to induce detrimental health effects in the long-term. If your immune system cannot process the metallic nanoparticles and eliminate them then you are essentially poisoning yourself.

What’s most disturbing is that C60 has a resonant mode shape in the Terra Hz band. This would make it an ideal body control medium through phase array that can be focused in on an individual or group for targeted activation. Terahertz antennas can excite the C60 nano molecules at their resonant frequency and cause the cell they are near or in, to burst.

EDTA

EDTA is another dangerous pharmacopeia drug that Ana Maria Mihalcea (MD) is promoting as a heavy metal chelator and antioxidant. Again, EDTA is an oxidant.

EDTA was found to be genotoxic in laboratory animals. Itinduces cell death and damages the human genome. EDTA inhibits DNA synthesis by disrupting the natural process of DNA replication. EDTA causes morphological changes of chromatin, interfering in cell replication. EDTA induces gene mutations and chromosomal breakage, meaning that it will have a damaging effect on your offspring, effecting generations to come, according to this Genetic Toxicicology of EDTA study.

Another study reveals that EDTA improves transfection of embryonic stem cells lines (hESC) in humans.

Since dissociation factors such as EDTA act via loosening the tight junctions between hESC cell surfaces, we proposed that treatment with a dissociation factor would improve hESC transfection efficiency.

In other words, EDTA is used as a precursor to break down DNA in order to make the reverse transcription of the human genome with modified RNA (modRNA) more effective.

“We found that chemically abrading the differentiated CACO-2 human intestinal epithelial cell layer by a trypsin and EDTA pretreatment (before the use of detergent-like transfection reagents) dramatically improved transfection efficiency in this polar, differentiated model. Although this treatment did improve the transfection efficiency, it also induced leakiness in the epithelial barrier by both opening tight junctional complexes and by creating holes in the cell layer because of low-level cell death and detachment. Thus, this approach to enhance the transfection efficiency of polar, differentiated cells will be useful for assessment of the effect of the transfected/expressed protein on (re)formation of an epithelial barrier…”

Here’s Thermo Fischers formula for human cellular transfection using EDTA.

“Formaldehyde solution, Thermo Scientific Shandon Immu-Mount, Hoechst 33 342 (1.0 mg mL−1 in water) and propidium iodide (PI, 1.0 mg mL−1 in water) were purchased from Thermo Fisher Scientific Inc. (MA, USA). ScreenFectA transfection reagent was obtained from ScreenFect (Eggenstein-Leopoldshafen, Germany). Fetal calf serum (FCS), RPMI-1640 cell culture medium, 0.25% trypsin/EDTA, Dulbecco’s Modified Eagle’s Medium (DMEM), 1% penicillin/streptomycin solution were purchased from Gibco, Life Technologies GmbH (Darmstadt, Germany). Ham’s F12 medium was purchased from Biowest (Nuaillé, France).”

In addition, EDTA causes mineral and zinc deficiency. Zinc is important for the immune function and wound healing while minerals are critical to hydration.

“The binding of divalent and trivalent cations by EDTA can cause mineral deficiencies, which seem to be responsible for all of the known pharmacological and toxicological effects. Sensitivity to the toxic effects of EDTA is, at least in part, related to the deficiency of zinc.”

EDTA was also determined to be an environmental hazard. It inhibits chlorophyll synthesis which is critical for our bodies to generate red blood cells. It also inhibits cellular division.

According to another study, EDTA induces human cell death and cancer in response to an acidified extracellular environment. EDTA induces human T-cell death-associated with gene 8 (TDAG8) by over expressed HEK293T cells. T-cells are the critical part of our immune system that stops foreign invaders from entering our cells. EDTA is essentially assisting the Covid-19 jabs to take out your immune system. EDTA also induces ovarian cancer from the G-protein-coupled receptor 1 in human leukemia cell line HL-60.

Lastly I wish to point out how animals were severely harmed in the testing of EDTA and C60.

NATURAL DETOX SOLUTIONS

There are plenty of natural medicines that will effectively detox your body of heavy metals. Nature is always more superior to synthetic, chemical drugs because they work with our body and empower our bodies to heal and restore to balance. Sea salt is the greatest chelator of all and it’s all natural without any toxic side effects.

For example, redox molecules are isolated from sea salt and redox molecules repair damaged DNA. They chelate or remove toxic metals, increasing natural endogenous production of antioxidants, enhancing protection from free radicals and promote apoptosis (death of cancerous or mutated cells). There’s plenty of research demonstrating how redox molecules effectively chelate metals so there’s never a need to use dangerous, toxic drugs such as EDTA. Redox molecules also increase endogenous glutathione by 800%.

You can read more about redox molecules here and you can order redox molecules here.

Ph Miracle Products Prime Ph supplement is a natural sodium chlorite solution that’s also derived from sea salt. It is a powerful oxidant that’s activated by our stomach acids. It chelates the body of toxic metals and binds to the bad acids through our stomach, easily expelling them from the body. Order Prime Ph here.

Blue Green Algae from Klamath Lake, Orgeon, is another natural heavy metal chelator. Blue Green Algae is the most nutrient dense food known to man, far superior to Spirulina. Blue Green Algae increases adult stem cell production and does targeted cellular repair. Read more and order here.

Boron is another effective heavy metal chelator. This natural salt derivative is a powerful treatment for autoimmune disease, reduces inflammation and treats chronic pain. Make sure you use a natural source.

Red Pine needle oil is the superior treatment for destroying parasites, especially when you combine it with geranium and/or sage. Order Red Pine needle oil here.

MEGA BOMBS! GMO Parasites Are The mRNA Vectors!
Posted on by Ariyana Love

“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 cure for 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

Please also review Karen Kingston’s accompanying article to see additional shocking evidence of this biological assault: Part 1: Dismantling the the Deceptions of the COVID-19 Story.

SEQ ID NO: 1 and SEQ ID NO: 2

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.

PFIZER

Pfizer Coronavirus Vaccine Patent #WO2021213945A1 contains both SEQ ID NO: 1 and SEQ ID NO: 2, deadly protozoan parasites and birth control without Informed Consent.

Pfizer vaxx patent

MODERNA

Moderna Sars-cov-2 mRNA Domain Vaccines Patent #WO2021159040A2 contains SEQ ID NO: 2 birth control without Informed Consent.

Moderna vaxx patent #1

Moderna Delivery and Formulation of Engineered Nuclei Acids Vaccine Patent #US10898574B2 contains SEQ ID NO: 1, with deadly protozoan parasites without Informed Consent.

Moderna vaxx patent #2

NOVAVAX

Novavax Coronavirus Vaccine Formulations Patent #US20210228709A1 contains both SEQ ID NO: 1 and SEQ ID NO: 2 thus it contains both birth control and deadly protozoan parasites without Informed Consent.

Novavax vaxx patent
Novavax vaxx patent

JANSSEN (J&J)

Janssen (J&J) Compositions and Methods for Preventing and Treating Coronavirus Infection-SARS-Cov-2 Vaccines Patent #WO2021155323A1 contains SEQ ID NO: 1 with deadly protozoan parasites.

Janssen (J&J) patent

OXFORD

Oxford Compositions and Methods For Inducing An Immune Response Vaccine Patent #WO2021181100A1 contains SEQ ID NO: 1 with deadly protozoan parasites.

Oxford vaxx patent

PARASITES AS mRNA VECTORS

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.

mRNA parasites – BMC

According to the NIH website:

“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.

Dr. Robert Young image

Follow Dr. Robert Young’s work here.

Follow Dr. Ariyana Love’s Telegram channel here.

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.

Transhumanist Nightmare: Nanowires Torture the Vaxxed and Scaffold New Tissue!
Posted on by Ariyana Love

by Dr. Ariyana Love, ND

The samples pulled out of the veins and arteries of COVID vaxxed corpses shocked the world and exposed that something more than just “vaccination” is taking place.

In my latest interview with Stew Peters entitled, Human Umbilical Cord Being Injected In Kids: Tissue Scaffolding Technology In Covid Jab, I revealed in detail what the strange “blood clot” samples found by embalmer Richard Herschman, actually are. The story was first aired by Dr. Jane Ruby on Stew Peters Show in January and was recently examined LIVE on air by scientist Mike Adams in the InfoWars studio, in a worldwide medical bombshell.

The samples pulled out of the veins and arteries of COVID vaccinated corpses shocked the world and exposed that something more than just “vaccination” is happening with the COVID vaxx. The fact that mainstream media did not pick up on this story is more proof we’re in dystopian times.

Embalmer Richard Heirschman’s samples published by Dr. Jane Ruby
Embalmer Richard Herischman’s sample published by Mike Adams of Natural News

These images show synthetic tissue is being grown inside humans from the COVID vaxx. This is most likely the cause of “Sudden Adult Death Syndrome.”

Please see the following studies:

Tissue-Engineered Blood Vessels (2005)
Researchers Grow New Blood Vessels In Just Seven Days (2014)
Arterial reconstruction with human bioengineered acellular blood vessels in patients with peripheral arterial disease
From Autologous Flaps to Engineered Vascularized Grafts for Bone Regeneration

China constructing blood vessels (2020)

Bioactive polymeric scaffolds for tissue engineering

Below are images of artificially grown blood vessels by lab scientists.

Artificial blood vessels
Artificial blood vessels

There are synthetic and natural polymers. They are elastic and made from these five different materials:

  1. Polyester polymers PLLA and PGA are among the most commonly used biodegradable synthetic polymers.
  1. Silk fibroin protein is extruded from insects and worms. It has biocompatible properties with the human body and ossess relatively high tensile strength.
  1. Collagenis used for bone construction.
  1. Hyaluronic acid (HA) is a form of hydrogel material for both hard and soft tissue construction.
  1. Chitosan is biodegradable polysaccharide that comes from chitin via chemical hydrolysis. It’s used in a gel, sponge, or fiber form.

I believe the below image from the embalmer and published by InfoWars, is a Silk fibroin tissue construct.

Certified embalmer Richard Hirschman’s sample – infoWars

NANOWIRES

Nanowires are being used for the hybridization of humans. Pharmaceutical companies and world governments are attempting to grow artificial tissue inside humans, using organic matter from cross-species genomics. They appear to be trying to merge humans with electronic devices for internal tracking and remote control.

Nanowires are superconducter batteries used for tissue scaffolding inside the human body. I wrote about tissue scaffolding technology in December of 2021, in my article entitled, Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State.

See studies and patent examples:

Nanowires

Nanowire arrays for neurotechnology and other applications

Internalization of ferromagnetic nanowires by different living cells (2010)

Hydrophobic copper nanowires for enhancing condensation heat transfer

Rotational Maneuver of Ferromagnetic Nanowires for Cell Manipulation

Internalization of ferromagnetic nanowires by different living cells

Ultrathin gold nanowires to enhance radiation therapy

The presence of gold nanowires cause elevated lipid peroxidation and intracellular oxidative stress under radiation. This can literally fry people from the inside using microwave frequency. This could explain why vaxxed persons are reporting torture by electrical activity in their head and their body.

I believe the image below that was shared by Mike Adams on InfoWars, shows a gold Nanowire.

Gold Nanowire – InfoWars

This study entitled, Macroporous nanowire nanoelectronic scaffolds for synthetic tissues, reveals electrical sensors made from silicon which are lab-on-a-chip pharmacological platforms and hybrid 3D electronics-tissue materials for synthetic biology and tissue construction for inside the human body. These are planar devices used to probe electrical activity near the surface of the heart, brain and skin, acting as transmitters, transistor and receivers.

“This is nanoelectronics throughout biomaterials and synthetic tissues in 3D using macroporous nanoelectronic scaffolds. They are using silicon nanowire field effect transistor (FET)-based nanoelectronic biomaterials, given their capability for recording both extracellular and intracellular signals with subcellular resolution.”

Nanowires are also called detectors, metal electrode or carbon nanotube/nanofiber or NanoES. They are implantable microelectrodes, nanoscale semiconductors and flexible/stretchable electrodes. The sensor network is flecible, macroporous and 3D. They are used to construct artificial tissue with embedded nanoelectric sensory capabilities.

Below is an image of Nanowires.

Nanowires

ORGANOIDS

Organoids are used to construct a new brain inside humans, for mind control. Organoids and transgenic hydras are being used to build a new neural network inside the body. The studies showing this can be found in my article entitled, Pharma Exposed! Autism Spectrum Disorder (ASD) Is Targeted Gene Deletion!

Also see: Transgenic Hydras & Parasites A Biological Weapons System For Rapid HumanCloning.

MICROSPHERES

I wrote about Microspheres, Microbubbles and Microbeads delayed release technology in my article entitled, Quantum Dots, DNA Barcoding, Nano-Razors & The IsraeliState.

Microspheres are in the COVID shots. They are also used for tissue engineering and scaffolding, simultaneous drug delivery and for growing cells inside the human body. The technology is externally controlled by EMF transmission. Microspheres can release their payload, weeks, months and even years later.

This tech was developed with the purpose of destroying cancerous tumor cells and now it’s being misused for the Democide of humanity.

The study entitled, Nanostructured injectable cell microcarriers for tissue regeneration, demonstrates that nanostructured microspheres include nanocomposite and nanofibrous microspheres which have been employed as cell carriers for tissue construction. They produce cell attachment and growth, promote cell-carrier interactions and facilitate stem cell differentiation for target tissue construction inside the human body.

A study entitled, PHBV Microspheres as Tissue Engineering Scaffold for Neurons, demonstrates that Polymeric microspheres are being used to grow artificial neurons inside humans.

A study entitled, Breathing life into engineered tissues using oxygen-releasing biomaterials reveals that the artificial cells feeds on your blood to grow and survive! This may explain the strange blood clots we’re seeing in vaxxed injured persons. Human umbilical vein endothelial cells are used to grow the artificial cells.

This study entitled, Generation and differentiation of microtissues from multipotent precurser cells for use in tissue engineering, reveals that Microspheres use unrestricted somatic stem cells from human umbilical cord blood.

This technology is truly vampiric and relies on human baby tissue in order to be grown inside humans. This should not be injected into anyone, especially not children!

——————————————————————————————————

Daniel 2:43 (KJV)

(43) And whereas thou sawest iron mixed with miry clay, they shall mingle themselves with the seed of men: but they shall not cleave one to another, even as iron is not mixed with clay.

Pharma Exposed! Autism Spectrum Disorder (ASD) Is Targeted Gene Deletion!
Posted on by Ariyana Love

By Dr. Ariyana Love, ND

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 article I referenced from Nature entitled, Epigenetics and cerebral organoids: promising directions in autism spectrum disorders, explains that the inactivation of the X chromosome in the brain is what causes Autism Spectrum Disorder (ASD).

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.

Another study entitled, DIA1R Is an X-Linked Gene Related to Deleted In Autism-1 confirms X chromosome deletion explaining, “A DIA1 deletion coincided with a classical autism diagnosis.”

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!

DELETION SYNDROMES

In an interview with Maria Zeee, Attorney Todd Callender stated:

“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

By the way, the E1 gene is on the X chromosome genetic lineage. I previously documented how pharmaceutical “vaccines” are deleting the E1 gene in my article entitled, EPIGENETICS: Vaccines Are Deleting Human Genes & Transfecting Cells WithEbola/Marburg.

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.

Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero
Posted on by Ariyana Love

By Dr. Ariyana Love, N.D.

In a recent interview with Maria Zeee on Zeee Media, I discussed another very troubling discovery about the mRNA bioweapons technology. Maria Zeee asked me to shed more light on the Doherty Institutes involvement with the US biolabs in Ukraine.

Russian reports revealed that 350 cryocontainers with blood serum samples were transferred from the Public Health Centre of the Ministry of Health of Ukraine to a reference laboratory for infectious diseases at the Doherty Institute in Australia.

Under the guise of tackling Placental Malaria, the Doherty Institute has been directly involved in research using insects such as mosquitos and tics as bioweapons carriers. The Doherty Institute also developed a “vaccine” that uses a parasite to target the placenta of pregnant women to abort their babies in utero, under the pretext of “antibody research”.

During the testing of this novel technology, mosquitos were developed as carriers of a genetically attenuated parasite called the P. falciparum which is the most deadly of the 5 Malaria causing parasites. The World Health Organization (WHO) and the U.S. Government were also directly involved in this research to “immunize” via mosquito bite using radiation-attenuated Sporozoites.

In May of 2021, a Bill Gates-funded firm began releasing genetically modified mosquitoes in the wild.

Clinical trials conducted by the WHO in 2020, used 11 human volunteers who were “immunized” with more than 1000 bites by irradiated mosquitos infected by Sporozoites (Spz) from the P. falciparum NF54 strain or 3D7/NF54 clone.

The female Anopheles mosquito inject a minimum of Sporozoites (Spz) (~ 100) during its bite. It was tested on adolescents, children and infants aged 6 months old. 1 out of the 6 volunteers developed parasitaemia 12 days after exposure. Parasitaemia means parasites in the blood.

The parasite “vaccines” use radiation-attenuated Sporozoite, administered under drug coverage. Genetically-attenuated Sporozoite “vaccines” and recombinant protein “vaccines” (RTS,S and R21) and recombinant viral vectors “vaccines” (Chad63 MVA ME-TRAP, CSVAC, ChAd63 METRAP and MVA METRAP with the matrix-M adjuvant) are all used.

Sporozoite recombinant proteins, DNA or viral vectored protein fragments (mRNA) and attenuated Sporozoite “vaccines” induce malaria reactive CD4+ and CD8+ T-lymphocyte counts. Radiation-attenuated Sporozoite (RAS), genetically-attenuated parasite (GAP) and Sporozoite are administered under drug coverage, according to the WHO study. Here’s another WHO study from 2021.

By 2021, they had a P. falciparum Sporozoite (PfSPZ) “vaccine” as the main candidate containing live, radiation-attenuated, whole, aseptic and metabolically active Sporozoite which have been isolated from the salivary glands of mosquitos infected by P. falciparum. They tested their novel “vaccine” on infants in Kenya.

Another study conducted by the NIAID in 2022, used Malian children 6-10 years old and injected them with three doses of the PfSpz “vaccine” to induce an “infection” by “parasitic disease” of a “vector borne disease” using the P. falciparum.

Another study in 2021 carried out by the U.S. Government, experimented on 336 infants aged 5-12 months, in Kenya, inoculating them with the P. falciparum “vaccine”. This is not in fact a “vaccine” but a weapons system for the murder of babies in utero and this is a bioweapon which is transmissible to others, according to the WHO research.

In addition, the WHO’s P. falciparum research helped in the development of monoclonal antibodies. In fact, the P. falciparum parasite is a critical component in the monoclonal antibodies bioweapon system.

Please also see: Monoclonal Antibodies Is Experimental Gene Therapy – PatentReview

PATENT

The PRIMVAC “vaccine” candidate was in government trials in 2016. By 2020, the PRIMVAC “vaccine” adjuvanted with Alhydrogel was in clinical trials. The Alhydrogel patent shows unsafe levels of aluminum and other heavy metals.

A VAR2CSA plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) patent for a synthetic protein was registered in December, 2014. The VAR2CSA “vaccine” is owned by the U.S. Government.

The CDC is also involved in this VAR2CSA bioweapons development.

STERILIZATION OF THE NATIONS

Children’s Health Defence reported in August that the Covid-19 injections are dangerous for mothers and babies. According to former Chief Scientist of Pfizer, Dr. Mike Yeadon, the injected ingredients is building up in the ovaries and attacking the placenta of pregnant women.

A preliminary findings of mRNA Covid-19 vaccine safety in pregnant persons found that 4 out of 5 pregnant women are loosing their unborn baby to spontaneous abortions.

A recent report released in March of this year, shows that fetal deaths due to “covid vaccines” are almost 2,000% greater than deaths associated with other vaccines.

Below are a few highlights from the WHO study Plasmodium falciparum pre-erythrocytic stage vaccine development that I want to draw your attention to.

RECOMBINANT VIRAL VECTOR “VACCINES”

“Viral vectors represent promising tools for vaccine development, because they enable intracellular antigens to be expressed by increasing the ability to generate robust cytotoxic T-lymphocyte responses and proinflammatory interferon and cytokine production without the need for an adjuvant. However, there is great concern regarding their genotoxicity due to possible viral genome integration; this has led to many efforts aimed at finding a high level of safety and efficacy.”

“Several viral, bacterial, and parasite vectors have been used in anti-malarial vaccine candidates; currently, many clinical trials are exploring their advantages to increase their potential and accelerate their use in vaccines.”

CHAD63 MVA ME-TRAP

“This anti-malarial vaccine was developed using chimpanzee adenovirus 63 (Chad63) and modified Vaccinia virus Ankara (MVA) into which were inserted genes encoding the thrombospondin-related adhesion protein (TRAP) multiple epitope (ME) chain.”

“The ME-TRAP hybrid is thus a 2398 base pair (bp) insert encoding a single 789 aa-long peptide, covering the complete P. falciparum TRAP sequence, fused to a chain of 20 malaria T- and B-cell epitopes (14 targeting MHC class I, 3 MHC class II and 1 murine).”

PCR

“A trial involving adults in Senegal to assess vaccine efficacy using a polymerase chain reaction (PCR) assay was able to detect > 10 parasites/μl blood. PCR was positive for 12 out of 57 participants vaccinated with ChAd63 ME-TRAP with a booster dose of MVA ME-TRAP and 13 out of 58 control patients who received an anti-rabies vaccine were positive by PCR, giving 8% efficacy (which was not statistically significant). They thus grouped the results with the 67% efficacy obtained in a study in Kenya and, using Cox regression, showed 50% overall vaccine efficacy in both populations.”

CSVAC

“CSVAC, a vaccine from Chad63 and MVA to encode the P. falciparum CS protein, continued such line of research into plasmid DNA anti-malarial vaccines; the CS insert was a codon-optimized cDNA encoding the CS protein truncated at the C-terminal extreme thereby lacking 14 C-terminal aa and thus omitting the GPI anchor.”

FUTURE DIRECTIONS

“Nanovaccinology” with Self-Assembling Protein Nanoparticles (SAPNs)… The next major challenge concerns the host’s genetic variability and parasite proteins’ interaction with the human immune system.”

“The choice of antigen to be used is quite complicated due to factors such as the parasite’s complex life-cycle involving two reproduction cycles (sexual and asexual), different development stages and two hosts (the Anopheles mosquito and human beings). All this can be added to the multiple invasion routes described so far for each of its target cells (hepatocytes and/or erythrocytes), the parasite’s ability to modify its gene expression and the genetic variability between P. falciparum circulating strains.”

“The next major challenge concerns the host’s genetic variability, particularly major histocompatibility class II (MHCII) complex molecules exerting their mechanism by synthesizing proteins encoded by the HLA-DR regions β1*, β3*, β4* and β5* where the HLA-DR β1* region encodes more than 1500 genetic variants grouped into 16 allele families called HLA-DRβ1*01, *03, *04, *07, etc. Parasite proteins’ interaction with the human immune system should be analysed by predicting B and T epitopes (using NetMHCIIpan 3.2 or other predictors).”

UPDATE: 6/6/2022

Please see: Pfizer’s mRNA Vaccine Goes Into Liver Cells and Is Converted to DNA: Study

Snake Venom Key Ingredient In “Covid-19 Vaccine” Patents
Posted on by Ariyana Love

By Dr. Ariyana Love, ND

The world premier documentary Watch The Water aired on Red Voice Media this week. Dr. Bryan Ardis dropped a bombshell during his interview with Stew Peters about one of the greatest conspiracy truths of all time. The intentional poisoning of the world’s population through our municipal water supply using snake venom.

Please see: VenomTech company announces massive library of SNAKE VENOM peptides for pharmaceutical development; “nanocarriers” stabilize snake venom in WATER (PubMed)

SNAKE VENOM PATENTS

Most snake venoms contain proteolytic enzymes. I found Snake venom in ten Covid-19 vaccine patents listed as “venom” and “proteolytic” (enzyme).

Snake venom is being recently touted as an “anti-HIV” drug, since January 2022. There’s six PLA2s from Snake Venoms patents “against HIV”. These synthetically derived snake venoms are marketed under the guise of being “antiviral” and as a preventive treatment for HIV infection.

The study claims snake venom works to “protect against Lentiviruses” through the “destruction of the viral membrane.” However, this is a lie because we know the Lentiviruses are a lab generated, chimeric mRNA bioweapon containing SARS, MERS, HIV 1-3 and SRV-1 (AIDS), as I documented in my article entitled, Transgenic Hydras & Parasites A Biological Weapons System For Rapid HumanCloning.

In actuality, snake venom is being used to destroy the human cell membrane not the “viral membrane”, so that nanoparticles can enter the cell and code your genome.This PubMed study proves that HIV is being encoded into people’s cells to produce a new cell line persistently. So snake venom assists mRNA to clone your cells. The J&J patent also mentions “RNA Replicons” which are forever replicating proteins.

Our Satanic “elites” have programmed the AI to create bioweapons far more complex than humans could ever come up with and the AI came up with 40,000 of the most deadly bioweapons to date.

THE SPIKE PROTEIN

The ACE2 protein acts as an anti-inflammatory, keeping immune cells from inflicting damage on the body’s own cells. The ACE2 receptor helps muscles contract and acts as a messenger between nerves, muscles and cells. It’s crucial in your cell signaling processes.

The ACE2 molecule acts as a gateway, preventing toxins from entering your cells. The mainstream narrative says that SARS-CoV-2 or the “spike protein”, attaches to human cells and blocks the ACE2 receptors. Snake venoms are postsynaptic neurotoxins, meaning they block the Ace2 receptors. So, I think we’ve identified the “spike protein”.

Snake venom latches onto ACE2 proteins and they get knocked out of commission. This destroys the body’s cell signaling function and enables the nanotech weapons system to enter the cells and reach the nucleus, where the mRNA is reverse-transcribed and integrated into the human genome.

Snake venom causes paralysis, the loss of muscle function and respiratory failure. It also causes inflammation, cytokine storms and induces auto-immune illness. Studies say snake venom triggers irreversible intracellular alterations, organ failure and continued cell death.

Heart and lung cells are covered with these ACE2 surface proteins which could explain why there’s so many reports of acute Myocardial injury following “Covid-19 vaccination”. I am receiving a lot of reports from my clients of prolonged stomach pain from these lethal jabs, another causation of snake venom which affects your digestion.

Speaking of digestion, the Food and Agriculture Organization of the US approved the use of snake venom in food last year (2021). According to the FAO/WHO the PLA2 enzyme (snake venom) complies with the General Specifications and Considerations for Enzyme Preparations Used in Food Processing. They’re using a combination of snake venom and a genetically modified Streptomyces violaceoruber bacteria (strain pChi).In other words, it will alter your genome.

Notice the conflict of interest in this safety study that declares the pChi strain is not harmful for consumption. The study does admit that this bacterial strain modifies your genome. I don’t believe that any level of genetic modification of humans is at all safe.

CROTOXIN

60% of snake venom consists of a neurotoxic substance called Crotoxin. It was the first proteinic toxin to be crystallized into protein crystallization.Once crystallized it can be used in structural biology. You can even buy Crotoxin online.

ORGANOIDS

Organoids are being grown a lab to mass produce snake venom. Organoids of snake glands can produce snake venom artificially, without the entire snake.

MONOCLONAL ANTIBODIES

Monoclonal antibodies were funded and developed by DARPA and Bill Gates. All monoclonal antibody patents reveal this is a mRNA “vaccine” that codes your cells with HIV-1. Just like the “Covid-19 vaccines”, monoclonal antibodies never underwent clinical safety trials. They’ve never been approved for use on humans and were passed under the Emergency Use Authorization.

In his interview with Mike Adams, Dr. Bryan Ardis mentioned a study funded by Fauci and the NIH that proved monoclonal antibodies are in fact, unsafe. They specifically target and destroy your T-cells (killer cells) through cytotoxicity. Thermo Fisher’s monoclonal antibodies actually contain snake venom (PLA2)!

Please read: Monoclonal Antibodies Is Experimental Gene Therapy – PatentReview

All monoclonal antibodies contain Hydroxychloroquine or chloroquine in “some embodiments”. This explains why some people report feeling better after using monoclonal antibodies at first and that’s enough to fool doctors but later they become extremely fatigued. The long-term effects are still unknown but they cannot be good. When your immune system is destroyed, your body cannot fight off disease.

NANOBODIES

The Oxford patent mentions “Nanobodies” and says that “antibodies have been replaced with Nanobodies”. The whole purpose of the “Covid-19 vaccines” was to invoke an “antibody response”. Now that lie too is exposed. The nanotechnology is being programmed to kill.

ANTIDOTE

There are breakthrough medicines and supplements that work antidotally against all poisons, including snake venom. In the Dr. Bryan Ardis interview with Dr. Braun, he mentioned the power of redox molecules against snake poison.

A peer-reviewed study from 2018, shows that Melatonin inhibits snake venom and antivenom induced oxidative stress:

“Besides antibodies, molecules like melatonin are reported to underlie the antivenom effect. The study of such was established in Egyptian cobra (Naja haje) venom using a rat model; the vital organs, like kidney, liver and heart, of the rat were protected from the venomous effect.”

Contact me on Telegram for information on where you can obtain the redox molecule supplement that enables your body to remove all poisons and restores all of your body system functions.

Also, follow my Telegram channel here.

Watch my latest interview with Stew Peters at Red Voice Media, here.

Posted on by Ariyana Love

By Dr. Ariyana Love, N.D.

Intro:

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.

First interview: Putin’s Secret War: Ukrainian Bioweapon Labs Exposed

Second interview: Horrifying Russian Report: Ukrainian Biolabs Creating Special Bioweapons For Ethnic Cleansing

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 US has admitted to the bioweapons labs but is desperately trying to destroy and hide the evidence that they violated Article 1 of the Biological and Toxic Weapons Convention of 1973. The UN is participating in the cover-up by rebranding the bioweapons facilities as “Public Health laboratories”.

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.

Jewish oligarch billionaires in Ukraine with dual nationality to Israel, such as Igor Kolomoisky, funded the neo-Nazi Azov Battalion while the Israeli state armed them.

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.

I also found an mRNA vaxxine patent for animals that uses the Brucella melitensis for US and UK cattle.

WEAPONS TESTING

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 genome and 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.