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.

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.

TRANSCRIPT

“I am a natural doctor. I have about 1,600 patients, many are vaccinated, just to give you a little backstory about my credibility.

“What I’ve seen so far is all information from physicians, medical physicians, natural physicians and also immunization and virology doctors, things like that and then, also nurses.

“So, what I’m about to share with you is the first vaxxine, the second vaxxine and then the boosters and what it does to you.

“The first vaxxine, as it goes into your body has a small amount of saline and a bunch of ingredients that are very catastrophic to your cellular system.

“What that does to your immune system, which is your deep bone marrow, your thymus gland, your spleen and all other systems associated with your immune system, it decreases your ability to produce white blood cells by 50% from your first vaxxine.

“Then, 8 weeks later, which is white blood cell reproductive system, so your ability to make another generation of white blood cells is 8 weeks, that’s why they set it up 8 weeks later, to hit it again. So, you hit the white blood cell ability while it’s down.

“So now what they do is they decrease the saline in the second one and they increase the harmful ingredients, so now you have a shift in the ingredients…

“And then, what they do is there is a second dose attacks your ability to make white blood cells by an additional 25%.

“So now, you only have the ability to make white blood cells functioning at 25%. So you just wiped out 75% of your military and the ability to make that military.

“Then what they do is they set in the booster. The booster has 81 strands of foreign bacteria that your cells have never come across. You don’t have the antibodies to fight it. You only have 25% of your white blood cell production to be able to fight it, so it’s a losing battle.

“So then what starts to happen is you start to get chronic inflammation that goes to the areas that you had predisposition. So if you are someone with gut health issues, that’s your area that this is going to focus on and you’re going to have inflammation in the gut health.

“If you have tumors or a cancer or if you have, say endometriosis or you have a skin condition, whatever that is, it’s going to inflame that area, because now the body has hit the parasympathetic nervous system, which is the fight or flight and your body is in a chronic inflammatory state with a low immunity and a low immune response.

“Then, you get your second booster. What the second booster has is it has 8 strands of HIV and now, what that does is it completely shuts off your ability to make white blood cells and if you Google what disease it is, it is HIV.

“So now, we have people walking around with no immune system, no ability to make an immune system, 81 strands of foreign bacteria and then, 8 strands of foreign HIV, along with all the other harmful ingredients, and then they remove all the saline from the first and second booster.

“Now, to make matters worse, during this process, 20-30% of the population is going to die, every single series of this process. There’s four series.

“They have 3 more boosters that are coming out and the reason why is because once they’ve made you so that your immune system can’t make white blood cells anymore, you become dependent on the boosters to survive, just like how someone’s life becomes dependent on insulin.

“Big Pharma is looking for people that either die off…for population control and then, those that don’t die off, they will have recurring customers for life, with the boosters so that they have to maintain income and collect the money back from all the funding that they put in to make these vaxxines in the first place.

“So, I hope that was helpful, I hope that you listened to this properly and I hope that you take the time to do your own critical thinking and just give it two to three years.

“Every single animal that participated in this study for any of these vaxxines had a 100% death rate and I encourage you all to just take a moment and look around you and just wait it out.

“And let’s just see, let Nature take it course and let’s just see what happens. Thank you.”

Source: Forbidden Knowledge

Former Pfizer employee Karen Kingston blew the whistle on Stew Peters Show last month, revealing that the Covid vaxxines are intentionally inducing AIDS and Anthony Facui is profiting from this Democide.