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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.

Dr. Ariyana Love Bio
Posted on by Ariyana Love

Dr. Ariyana Love is an official Goodwill Ambassador to Palestine. She’s a second-generation natural doctor, investigative journalist, medical and patent researcher, and founder of an international foundation revitalizing traditional Homeopathic medicines.

Dr. Love uses world renown disease reversing (anti-aging) protocols that detox and reverse vaxx and swab injuries. She is currently advocating for client retribution and compensation.

Dr. Love’s father, Dr. Eric Love, founded the first natural healing school in Northern California in 1981. Prior to training through the International Association of Homeopathy (Dad’s institute) in her early 20’s, she was certified in various healing modalities from Heartwood Institute of the Healing Arts School. With 18+ years of training and experience in the field of natural medicine and nutrition, she’s currently being mentored by scientist, Dr. Robert O. Young, and Biotech expert, Dr. Judy Mikovitz.

Dr. Love studied Motion Picture Video (film) at Montana State University and worked in Hollywood for about a year, before opting out of Hollywood and into corporate finance. Mentored in upper-level business management, she spearheaded a financial consulting company with Omega Financial and moved to Finland with her team in 1998, to acquire advanced technologies.

Dr. Love’s elder son was vaccine injured at the age of two. He was diagnosed with High Functioning Autism (Asperger) at age 7. She applied her medical knowledge and designed a dietary protocol that resulted in a total reversal of her son’s debilitating symptoms by the time he was 8. All of his allergies also disappeared.

In 2010, Dr. Love began homeschooling on a Native American reservation in the mountains of Northern California, where she lived with the indigenous Hoopa and Karook tribes. She studied traditional Native American Medicine and learned the Brickstitch weave from a generational teacher. Designing beautiful earring patterns is a favorite hobby. She and her sons also learned to track, hunt, skin, fish and forage.

Dr. Love is originally from the Emerald Triangle in Northern California, where she grew up along the Sequoia/Redwood coast. She has traveled the world learning traditional medicine from indigenous people and harvesting the purest medicines from nature reserves, such as the pine tree and chaparral.

Dr. Love pilgrimaged to the holy land of Palestine in 2012, and lived in a traditional Palestinian village in the Occupied West Bank for close to a year. She studied the root of Authentic World Judaism, Orthodox Christianity and Islam, and grew a heart felt appreciation for the Palestinian culture and their traditions. She discovered Palestine’s superior harvesting techniques and the many medicinal applications from the blessed olive tree, as well as other herbs and plants from the Middle East.

Dr. Love’s Ministry in Palestine activated her calling. Witnessing the injustice of Apartheid inspired her journalism and Human Rights Defending. In 2013, she was invited to train with Roger Landry from the The Liberty Beacon (TLB) news network. She Directed and built two successful news channels from the ground up before she was politically targeted and de-platformed across social media, beginning in 2017.

Dr. Love has been on the front lines in independent media, leading record-breaking campaigns in defense of political prisoners. She collaborated with Palestinian media professionals for 8 years, documenting and publishing Zionist occupation war crimes. Eventually the Palestinian Authorities (PA) and Gaza authorities awarded her with an official Goodwill Ambassador to Palestine role through the International Commission to Support Palestinian Rights (ICSPR).

Julian Assange invited Dr. Love to join WikiLeaks from Belmarsh Prison, in 2019.

Dr. Love was the first person in the world to read and document all the experimental modRNA “vaccine” patents and report them on Stew Peters Show. She applied her medical knowledge and research skills and designed protocols to naturally chelate heavy metals, cancel nanotech and detox the body from all poisons. Her protocols stop spike protein replication and restore the body’s original design. She’s been detoxing people successfully from jabs and swabs since October of 2020. She applies the Terrain theory to reverse cellular and DNA damage, brain injury, autoimmunity and essentially all diseases because the root cause is always the same.

Dr. Love’s detox and health protocols are highly sought after worldwide. She is mentored by scientist Dr. Robert Young and Biotech expert, Dr. Judy Mikovitz. Her work is published in Global Research and used by medical and legal teams and natural law tribunals.

Luciferase Microarray Patches Contain DARPA Hydrogel & Autonomous Insect Cyborg Sentinels
Posted on by Ariyana Love

By Dr. Ariyana Love

Queensland’s first needle-free “vaccine” facility just opened in Australia, yesterday. The microarray patch for intradermal delivery technology is also being called a Nanopatch and it’s aimed at our children.

3D printed microarray patches (MAP’s) are comprised of a series of micrometer-sized projections that can painlessly puncture the skin and access the epidermal/dermal layer, delivering drugs and chemicals into the interstitial fluids of the human body. It also allows for external control of delayed release of drugs and repeated dosage over time. This technology was already being developed back in the 1970’s.

In May of 2023, Micron Biomedical announced Phase 1/2 data from the first-ever clinical trial of a “vaccine” patch in children – including infants as young as nine months old. This study was tested on Gambian children.

In October of 2022, the first official Luciferase patch trial on children using a placebo, began in Brisbane, Australia. The trial was led by Vaxxas. A number of phase-one clinical trials in adults were already conducted by Vaxxas according to Project Manager, Ben Baker.

Vaxxas, founded by UQ commercialization company UniQuest in 2011, received $A30 million (US$22 million) through the Biomedical Advanced Research and Development Authority (BARDA) to support “pandemic” deployment of their high-density micro-array patch (HD-MAP). Vaxxas is partnered with the U.S. Government and funded by Bill and Melinda Gates. The microarray patch is supposedly intended to inoculate children from middle to low income countries with measles, rubella, and polio.

This microarray patch technology is scheduled to be mandated for children worldwide and it’s on the national immunization schedule for children in Australia. UNICEF is driving the research, development and scale of microarray patches for children. They’re keen on “identifying barriers for scaling and investigating the need for market pull incentives to spark interest and endorsement by vaccine manufacturers.” And of course the World Harm Organization (WHO) is involved with pushing the measles-rubella microarray patch on children.

DNA from human origin

The antibody used in the microarray (MA) patches comes from human origin, according to scientific literature (See paragraph #4 and 2.2. Antibody Stability Study). The patches use “nonspecific human Ig” and the “human hlg” which is a human leukocyte antigen, as well as other “nonspecific” amounts of human DNA plasma, including human lgG1 and human lgG2. It is well known that injecting human DNA into humans induces inflammation, autoimmunity and rapid cancer growth.

The core–shell MA patch has two delayed burst releases at days 10 and 21. Included in the patches is the use of “nondegradable poly(ethylene-co-vinyl acetate) (EVA, for the sustained release of human DNA), hyaluronic acid scaffolds, glycol chitosan, and oxidized alginate hydrogels.” (See paragraph two).

Glycol chitosan is insect DNA which is highly toxic to humans. It has never been approved by the FDA for use in humans. Hyaluronic acid based scaffolds is used for tissue engineering and so is synthetic mRNA.

Johnson and Johnson developed the Luciferase microarray patch (See paragraph entitled, 2.3. Vector) containing the Adenovirus 5 vector for targeted deletion of the E1 and E3 genes, located on the X-chromosome.

PLEASE READ: EPIGENETICS: Vaccines Are Deleting Human Genes & Transfecting Cells With Ebola/Marburg

This scientific paper reveals that Luciferase hydrogel is chimeric DNA from cross species genomic splicing. The Luciferase patches are being marketed (See bottom of page) as something that will “reduce the rate of HIV infections”. Incidentally, governments are coercing schools to mandate HIV testing of children.

DARPA hydrogel

The Defense Advanced Research Projects Agency (DARPA) is a research and development agency of the United States Department of Defense responsible for the development of emerging technologies for use by the military.

DARPA’s hydrogel replicates into rectangular crystal structures within minutes after coming into contact with body fluids. It grows a crystalline sheath above your muscle and beneath your skin which is magnetic. It acts as an antennae inside the human body that can transmit your internal data through the Internet and receive commands from towers as it replicates and expands throughout the entire body.

Whole parasite “vaccines”

Also contained within some embodiment’s of the DARPA hydrogel patches are Sentinels. Under a highly classified program DARPA has been weaponizing insects for decades such as GMO mosquitos that carry GMO parasite eggs coded with synthetic mRNA. These parasite eggs are otherwise known as “whole parasite vaccines“.

PLEASE READ: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

This peer-reviewed paper discusses “Cyropreserved Whole-Parasite Vaccines” using the deadly P. falciparum Malaria parasite to target in particular, the CD4+ T cells and destroy them by inducing cell death. Please also read here, here and here.

The Sentinels

Sentinels are also found within the DARPA hydrogel Luciferase microarray patches.

DARPA has a full Hybrid Insect MEMS program called “Sentinel”. The D.O.D. is also in on this. Much of the funding for this project comes from DARPA’s Microsystems Technology Office (MTO), which has devoted more than US$2 million to the Hybrid Insect MEMS (HI-MEMS) program.

Micro-Electro-Mechanical Systems (MEMS), otherwise known as micromachined devices uses organic insects that have been morphed into externally controllable electromechanical devices and ‘living’ biosensors, using genetically modified microorganisms. Micro-mechanical systems are placed inside the insects during the early stages of metamorphosis, allowing for tissue-machine interface and control over insect locomotion. Insect cyborgs have most of the machine component inside the insect body providing stealthy robots that use muscle actuators. Motion trajectories are obtained either from GPS coordinates, or using RF, optical, ultrasonic signals based remote control. The Sentinels work as microsensors and they also can modulate light beams. Through heterogeneous integration, they have merged the Sentinels into a circuitry nanotech system.

While this is a highly classified and secretive project, there’s a paper trail. In 2018, the U.S. Government awarded DARPA a research and development contract funding DARPA’s SENTINEL # HR001118S0005 project to the tune of 10 million dollars. The first Sentinel patent was registered by GeneNews, in 2010. The second Sentinel patent # 7,662,558, entitled “Method of profiling gene expression in a human subject” was registered in 2018.

But who could anticipate that Sentinels would be used inside the human body? Since 2009, Sentinels have been used internally for a breast cancer excision. They can slice right through tumors which explains why my clients are being internally lacerated by these Sentinels, inflicting terrible pain and causing red skin lesions to appear. Also according to client testimonials and peer-reviewed literature, Sentinels shoot out electromagnetic beams and attempt to influence your nervous system using electricity. They borrow into the nervous system and can “read thoughts,” anticipate your movements and attempt to control their host.

The hydrogel-based encapsulation (nanotech) system for genetically modified organisms (GMMs) incorporates a biocompatible multilayer tough shell and an alginate-based core. Sentinels are the core controller of the Operating System. They regulate cell to cell communication between the AI parasites, organoids, hydras, worms and poisonous anaerobic bacteria in vivo, as the linked document shows.

“Microelectronic integrated circuits can be thought of as the “brains” of a system and MEMS augments this decision-making capability with “eyes” and “arms”, to allow microsystems to sense and control the environment. Sensors gather information from the environment through measuring mechanical, thermal, biological, chemical, optical, and magnetic phenomena. The electronics then process the information derived from the sensors and through some decision making capability direct the actuators to respond by moving, positioning, regulating, pumping, and filtering, thereby controlling the environment for some desired outcome or purpose. Furthermore, because MEMS devices are manufactured using batch fabrication techniques, similar to ICs, unprecedented levels of functionality, reliability, and sophistication can be placed on a small silicon chip at a relatively low cost.”

DARPA openly admits to using AI for brain computer interface with humans through it’s Explainable Artificial Intelligence (XAI) program. Sentinels are contained within a small silicon chip that looks very similar to the chips Dr. Pablo Campra found in the Covid-19 vials.

In 2017, Finland developed nanocellulose-alginate hydrogel suitable for 3D printing.

Implantable hydrogel biosensors are scheduled to be used in Covid-19 inoculations and microarray patches. Hillman Laboratories partnered with John Hopkins University, admit that they want to “take the microarray patches door to door“.

One of my clients was a victim of a U.S. government pilot project in Seattle Washington. GMO mosquitos are being unleashed in Florida and other states as well. My client, her daughter and best friend were congregated at a church function outdoors when they were “beaten by mosquito’s,” as she put it. These mosquito’s were smaller than the typical mosquitos they have in Washington state and they had unusual markings. They could not feel the bites but saw the mosquito’s biting. Later, people from the congregation broke out in welts where they were bitten and had terrible pains all over their bodies. Now my client and her daughter are riddled with Sentinels which crawl everywhere in their bodies and torture them. These Sentinels belong to DARPA’s weaponized insects project. My clients best friend could not endure and she died before they discovered my protocols. I have several other clients whom are being tortured by Sentinels and my protocols are helping them. Other clients have already detoxed the Sentinel and DARPA hydrogel out of their bodies.

ALSO READ: “YIKES! Hydrogel Nano-biotechnology in Vaccines and Nasal Swab Tests Capable of Electronically Linking Human Brains to Cloud Wirelessly” by State of The Nation.

Please consider donating to Dr. Ariyana Love’s investigative research and ministry, here.

If you require a health consultation please schedule with Dr. Love, here.

Contact Dr. Love at metanutrients@mailfence.com or call her cell at +1 928-892-8736.

Follow Dr. Love on Telegram @DrAriyanaLove and on Twitter @drloveariyana.

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.

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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!

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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