Jab-Induced Immune Fatigue (ADEx): An Insidious Gateway to Transhumanism and Human Control
Is this intentional to pave the way for transhumanist implants through injecting our bodies with harmful nanoparticles and nanotechnology by weakening our immune system’s response to them?

Dr. Peter and Ginger Breggin
Twenty thousand VAERS deaths have now been reported to the FDA.1 In our book, COVID-19 and the Global Predators,2 we document why there are at least 100 unreported deaths for every one death that gets sent to the CDC’s monitoring system, called VAERS. As a result, we almost surely now have at least 2 million deaths from the mRNA “vaccines” in America.

Now we examine an overlooked method by which the COVID shots can cause physical ruination and death through exhaustion of the immune system, and how this will play into the ambitions of the global elite and especially the transhumanists.

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Both SARS-CoV-23 and the COVID jabs4 can weaken the immune system, in part by impairing the function of critical T cells. While the CDC is willing to say that the disease of COVID-19 causes impairments of the immune system, the global predatory organization, of course, does not confirm vaccine-induced immune dysfunction and weakness.

Nonetheless, as early as April 2022, four courageous researchers, Stephanie Seneff, Greg Nigh, Anthony M. Kyriakopoulos, and Peter A. McCullough, documented complex COVID “vaccine” impairments to the immune system:5

In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. … These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis [causing cancers]. We show evidence from the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA “vaccines” questions them as positive contributors to public health. [Emphases added.]

An editorial, “Repeated vaccination and ‘vaccine exhaustion’: relevance to the COVID-19 crisis,” was published online May 3, 2022 in Expert Review of Vaccines. According to the expert review, “The potential for repeated vaccination to cause vaccine exhaustion and, consequently, reduce protection against microbial infection merits further study.”6 They observe, “The European Medicines Agency has warned that repeat COVID-19 booster doses could adversely affect the immune response.”

A June 5, 2022, article in Virology Journal reported:7

Recently, The Lancet published a study on the effectiveness of COVID-19 vaccines and the waning of immunity with time. The study showed that immune function among vaccinated individuals 8 months after the administration of two doses of COVID-19 vaccine was lower than that among the unvaccinated individuals. According to European Medicines Agency recommendations, frequent COVID-19 booster shots could adversely affect the immune response and may not be feasible.

An examination of the Lancet article shows that the global predators, who have been deeply involved in pushing the worst of the narrative, manage to make lemonade out of the lemons of vaccine-induced weakening of the immune system.8 The globalist Lancet declared that the waning effectiveness of the “vaccines” indicated the need for even more booster shots!

Confirming Post COVID “Vaccine” Injuries.

On November 10, 2023, a large group of scientists and physicians from Yale and several other universities published a study of the “Post-Vaccine Syndrome,” which described the experiences of 241 individuals who joined an online project called LISTEN at Yale from May 2022 to July 2023. The median time between the jab and the onset of symptoms was a mere three days, mostly spanning 1-8 days! This strongly confirms causation.

The median age was 46, and 80% were female, which raises the threat of the affinity of jab-related spike proteins for the ovaries. In my experience, studies like this based on spontaneous reports from the victims are more likely to detect the range of adverse effects from medical treatment than any other research approach now available to us. After these adverse effects are identified, more focused studies can be used to estimate their frequency in the general population. The study summarized their findings:

The five most common symptoms were exercise intolerance (71%), excessive fatigue (69%), numbness (63%), brain fog (63%), and neuropathy (63%). In the week before survey completion, participants reported feeling unease (93%), fearfulness (82%), and overwhelmed by worries (81%), as well as feelings of helplessness (80%), anxiety (76%), depression (76%), hopelessness (72%), and worthlessness (49%) at least once.

Because these reports are coming from individuals rather than their healthcare providers or other outside observers, they are mainly psychological or emotional symptoms. As we shall see below, the CDC confirms that subjective symptoms of fatigue and brain fog are among the most common and most disabling from long COVID.

It is important to compare these symptoms related to vaccination to the symptoms of long COVID since the “vaccines” reproduce COVID by forcing the body to make the deadly spike protein found on the virus. A list of post-COVID symptoms from the CDC overlaps with many of the above post “vaccine” symptoms.9

The following chart compares three of the most common major causes of disability from Long COVID listed by the CDC, with the corresponding top 3 out of 4 symptoms from Post-Vaccine study LISTEN in brackets:

Post-COVID: Tiredness or fatigue

[Post Vaccine: excessive fatigue (69%)]

Post-COVID: Difficulty thinking or concentrating (sometimes called “brain fog”)

[Post Vaccine: brain fog 63%]

Post-COVID: Shortness of breath or difficulty breathing

[Post Vaccine: exercise intolerance (71%)]

In the general listings by the CDC of post-COVID symptoms, many are psychological, including depression and anxiety, and they too overlap with post-vaccine symptoms.

Fatigue and brain fog seem to dominate the picture of both post-COVID and post-vaccine syndromes. With the exception of very serious medical problems, these symptoms of fatigue and brain fog are the most disabling. My own experience with COVID confirms these findings. After I was hospitalized for a very serious case of COVID-like illness for five days in early April 2023, I experienced several months of Long COVID, including severe fatigue in all aspects of living as well as “brain fog” in the form of a general reduction in my speed and clarity of thinking, and a lack of engagement in life, including with my family.

Reports on post-COVID and post “vaccination” adverse effects, and my own personal experience with severe COVID, confirm my theory that all neurotoxins (poisons that affect the brain) produce a common endpoint that involves apathy, reduced engagement with life, and loss of mental acuity — and that these effects make us less sovereign and more controllable by authoritarians and totalitarians.

I have most recently described my general observation that the elite have favored brain-damaging “therapies” for humankind since the 1930s with lobotomy and electroshock (ECT), followed by the crushing antipsychotic drugs in 1954 and the subtle SSRI antidepressants in 1989. My analysis is titled, “The Elite Strategy to Physically Ruin Our Brains, Minds, and Willpower: Are they now purposely continuing to damage our brains, minds, and spirits.”10

ADE and ADEx: Their Contribution to Post-COVID and Post-Vaccine Syndromes

ADE is the acronym for “antibody-dependent enhancement.” The word “enhancement” is a bizarre euphemism for a deadly reaction in which an infection followed by a vaccine, or vice versa, a vaccine followed by an infection, combine to cause potentially deadly over-reactions of the immune system. Sometimes the deadly reaction takes the form of a cytokine storm, in which elements of the immune system called cytokines give excessive signals for more antibody responses.

In medicine, there are examples where overstimulation of a system can harm it. Cortisol suppression is an example of organ or system exhaustion and potential failure from overstimulation of the system, in this case, from almost any form of psychological or physical stress.11 In two of my earliest solo publications, I used my own hands-on animal research to draw conclusions about how excessive levels of the “fight or flight” hormone, adrenaline, produce a feedback mechanism from the hypothalamus that causes a paradoxical fatigue after the initial over-stimulation during “fight or flight.”12

ADE — the overreaction of the immune system to overstimulation — can cause immune exhaustion, which we are labeling ADEx. ADEx is one probable cause of Long COVID and post “vaccine” symptoms of frequent illnesses, fatigue and exhaustion, brain fog, and fast-growing treatment-resistant “turbo” cancers that occur when the immune system is weakened, often compounded by brain injury and mental dysfunction from the agents that compromise immunity.13 The potential adverse effects of a compromised immune system include those mentioned in the above quote by Stephanie Seneff and her coauthors: “neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, impaired DNA damage response, and tumorigenesis.”

But is ADEx purposeful? Can it accomplish something far more insidious than even cancer or death that meets the deepest needs of the elite globalists, the global predators?

A More Insidious Purposeful Result of Immune Exhaustion (ADEx)

Ginger Breggin may be the first to have recognized an even more insidious reason why the elite might want to weaken all of our immune systems. Their motivation is to enable transhumanism.

The globalists are intent on remaking human beings to perform tasks that benefit the elite. They want better warriors to impose totalitarianism on humanity. They want super-humans melded with AI computers to advance their technology and to manage their technocracies — the totalitarian institutions run by technocrats under their control. They want fewer humans, and they want them to be more docile and obedient. They want humans willing to sacrifice their well-being without reservation, and they want billions of more docile and obedient humans to serve them without rebelling. Ultimately, these elite globalists, the Apex Global Hunters, want longer, healthier lives for themselves.

What has this got to do with weakening the immune system?

Suppressing the immune system is a core strategy in transplantation medicine. The single biggest challenge when introducing a transplant into a human body is that the body’s immune system will consider the transplanted organ or other substance to be foreign and, therefore, an invader requiring attack by antibodies and specialized cells.

One of the transhumanistic goals, as being developed by Elon Musk, requires modifying the behavior of people with implantations of electronic receivers and transmitters in the brain.14 Many are concerned that the mRNA or DNA “vaccines” are also implanting metallic and other construction materials in our blood that can self-assemble nanoparticle electronic receivers and transmitters in our circulatory system that are potentially under external control. The Department of Defense is a part of the global elite, and for decades it has been experimenting with how to artificially enhance the capacity of soldiers. So has Communist China’s military. Immune responses that interfere with biomedical devices remain a challenge15 to these aspirations.

As in transplants of hearts, faces, or other body parts, the immune system often must be weakened to avoid immune rejection of them. When most of us already have immune systems weakened by genetic jabs and COVID-19, including by exhaustion of the immune system (ADEx) — transhumanists will have broken a biological barrier to making their transhumanistic fantasies come true, from building human beings more able to serve and less able to rebel against them, to preserving their own healthy lives as long as possible.

A New Threat That May Depend on Our Weakened Immune Systems

Even metallic elements, which are being reported in “vaccines” and in the bloodstream, might be destroyed or rendered ineffective by the immune system.16 Reports of unidentified materials, including metals, have been increasingly reported in freshly drawn blood by Ana Maria Mihalcea17 and other experienced physicians and researchers.

David Hughes wrote a lengthy, detailed scientific review concerning findings of seemingly active objects circulating in the blood and concluded with an ominous warning:18

Between July 2021 and August 2022, evidence of undisclosed ingredients in the COVID-19 “vaccines” was published by at least 26 researchers/research teams in 16 different countries across five continents using spectroscopic and microscopic analysis. Despite operating largely independently of one another, their findings are remarkably similar and highlight the clear and present danger that the world’s population has been lied to regarding the contents of the COVID-19 “vaccines.” This raises grave questions about the true purpose of the dangerous experimental injections that have so far been shot into 5.33 billion people (over two-thirds of the human race), including children, apparently without their informed consent regarding the contents. Surprise findings include sharp-edged geometric structures, fibrous or tube-like structures, crystalline formations, “microbubbles,” and possible self-assembling nanotechnology. The blood of people who have received one or more COVID-19 “vaccines” appears, in case after case, to contain foreign bodies and to be seriously degraded, with red blood cells typically in Rouleaux formation. Taken together, these 26 studies make a powerful case for the full force of scientific investigation to be brought to bear on the COVID-19 vaccine contents. If the findings of these 26 studies are confirmed, then the political implications are nothing short of revolutionary: a global crime against humanity has been committed, in which every government, every regulator, every establishment media organization, and all the professions have been complicit.

Some of the objects found circulating in the blood are metallic.19 The immune system will sometimes attack metals, including those that rub off on the skin. A weakened or exhausted immune system would be less able to resist small metallic objects in the bloodstream if the genetic “vaccines” were also weakening the immune system.

Some of the foreign objects found in blood appear to have qualities associated with biomedical electrical devices. When larger versions of these devices are implanted for measuring or stimulating biological processes, the immune system can also fight them off if special measures are not taken.20 It seems reasonable that nanoparticle biomedical electrical devices would be much more vulnerable to attack by the immune system, again requiring measures to weaken the body’s immune response in order to protect them.

Other Potentially Lethal Effects of Weakening the Immune System

Making us unable to defend against harmful alien substances injected into our bodies along with the mRNA is not the only danger from weakened immunity or ADEx. The immune system not only fights off viruses, bacteria, and parasites, but it also fights off cancer cells and tumors.21 Some viruses have been identified as contributing to the development of cancer in immunosuppressed subjects after organ or stem cell transplantation, or with HIV infection.22

How does one explain the increase in malignant tumors, including “turbo cancers,” being seen in people who have been given the mRNA “vaccines?”

Within our own social community, we have seen too many cases of cancers that turn out to be larger, more widespread, less treatable, more rapid in development, and more fatal than expected. Doctors with great integrity are reporting the phenomena and being dismissed by establishment medicine.23

Nor are cancers the only other potential illnesses that can result from lowered immunity. Skin, intestinal, and neurological problems can occur. But most obviously, bacterial, viral, and parasitic infections can become more frequent and more deadly.

Conclusions

Have the global predators contrived their COVID genetic “vaccines” to cause deadly excessive immune overreactions, followed by vastly weakened immune responses? Have they done this purposely, along with all their other planned actions, like developing SARS-CoV in labs, spreading the virus around the world, outlawing early and effective treatments for COVID like hydroxychloroquine and ivermectin, pushing deadly treatments like Remdesivir and ventilators, enforcing injections of so-called vaccinations that have maimed and killed millions of people, and enforcing harmful and immune-compromising behaviors such as masking practices and shutdowns of schools, small businesses and churches?

Specifically, those who are imposing their will on us, the Apex Global Predators, knew the pseudo-vaccines, which many are now accurately designating as bioweapons, were unsafe for even experimenting on humans, let alone flooding most of humanity with them. They knew excessive inflammatory reactions caused by storms of antibodies would injure and kill people, and they knew that a vast array of other adverse effects would occur.

Did they also intentionally pave the way for transhumanist implants through injecting our bodies with harmful nanoparticles and nanotechnology by weakening our immune system’s response to them?24

The answer is they did this purposely, exactly as they are knowingly and for their own benefit, systematically perpetrating all their COVID assaults on us, as we demonstrate in our book, COVID-19 and the Global Predators: We Are the Prey.

References:

1 In a paragraph titled “Note of Concern to Colleagues, “Peter McCullough wrote, “As of August 25, 2023, the CDC has recorded 18,015 deaths reported to them in VAERS by healthcare professionals or pharmaceutical companies who believe the vaccine is related to the death. Approximately ~1100 deaths have occurred on the same day of vaccination.” If that were the number in August, it is probably over 20,000 now. The CDC purposely confuses the data by including reports outside the USA to their VAERS system but that is much less than half. U.S. On October 27, 2023, the VAERS system actually reported 36,501 reports of death associated with the COVID jabs, including a portion from outside America. www.openvaers.com/covid-data

2 COVID-19 and the Global Predators: We Are the Prey, Chapter 11.

3 https://covid19.nih.gov/news-and-stories/covid-19-reduces-immune-response-covid-19-vaccines and SARS-CoV-2 infection weakens immune-cell response to vaccination | National Institutes of Health (NIH) and F Gao, et al. Robust T cell responses to the Pfizer/BioNTech vaccine compared to infection and evidence of attenuated CD8+ T cell responses due to COVID-19. Immunity DOI: 10.1016/j.immuni.2023.03.005(link is external). (2023).

4 https://www.straitstimes.com/world/europe/eu-regulators-warn-frequent-covid-19-booster-shots-could-affect-immune-system and Frequent boosters spur warning on immune response – BNN Bloomberg

5 Stephanie Seneff, Greg Nigh, Anthony M. Kyriakopoulos, and Peter A. McCullough. Food Chem Toxicol. Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs. 2022 Jun; 164: 113008. Published online 2022 Apr 15. doi: 10.1016/j.fct.2022.113008 Best link: Innate immune suppression by SARS-CoV-2 mRNA vaccinations: The role of G-quadruplexes, exosomes, and MicroRNAs – PMC (nih.gov)

6 https://www.tandfonline.com/doi/full/10.1080/14760584.2022.2071705. Bold added to the quote.

7 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167431/

8 https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(22)00089-7/fulltext?s=09

9 Guidance on “Long COVID” as a Disability Under the ADA, Section | HHS.gov

10 https://gingerbreggin.substack.com/p/the-elite-strategy-to-physically

11 05 kudielka ok (researchgate.net)

12 Breggin, Peter. (1964) “The Psychophysiology of Anxiety.” Journal of Nervous Mental Diseases, 139, 558-568, 1964 thepsychophysiology.pbreggin.1964.pdf and Breggin, Peter. “The Sedative-like Effect of Epinephrine.” Archives of General Psychiatry, 12, 255-259, 1965. sedativelike.pbreggin.1965.pdf

13 The Dreadful Effects of ‘COVID Vaccines’ Are Overwhelming – America Out Loud News

14 https://www.americaoutloud.news/will-musks-neuralink-also-be-safe-and-effective-with-dr-peter-breggin/ and https://breggin.com/article-detail/post_detail/FDA-Approves-Physical-Control-of-the-Mind-by-Musks-Neuralink

15 Biomaterials: Foreign Bodies or Tuners for the Immune Response? – PMC (nih.gov)

16 https://medbroadcast.com/condition/getcondition/metal-hypersensitivity

17 My Interview With SGT Report On Darkfield Microscopy Findings Of Nanotechnology In Unvaccinated Blood And Rubbery Clot Investigation (substack.com)

18 View of What is in the so-called COVID-19 “Vaccines”? Part 1: Evidence of a Global Crime Against Humanity (ijvtpr.com)

19 (100) CV19 Bioweapon/Vax an Extinction Level Event – Dr. Ana Maria Mihalcea (substack.com)

20 https://www.nature.com/articles/natrevmats201776

21 https://ashpublications.org/hematology/article/2021/1/287/482959/How-immunodeficiency-can-lead-to-malignancy

22 Immunodeficiency-associated viral oncogenesis – ScienceDirect

23 https://sciencebasedmedicine.org/he-pushed-hydroxychloroquine-three-years-ago-harvey-risch-and-false-claim-of-turbo-cancers-caused-by-covid-19-vaccines/

24 See our book, COVID-19 and the Global Predators: We Are the Prey, with over 1,000 endnotes and many more citations within the notes.


https://substack.com/home/post/p-139021796

EDTA Snakeoil! Ana Maria Mihalcea's Medical Malfeasance Exposed
“I already have had.. uh.. patients die from shedding” - Ana Maria Mihalcea, M.D.

Dr. Ariyana Love (ND)
“My people are destroyed for lack of knowledge: because thou hast rejected knowledge, I will also reject thee, that thou shalt be no priest to me: seeing thou hast forgotten the law of thy God, I will also forget thy children.” ~ Hosea 4:6 KJV

Rockefeller Medicine

Around 1900, the science world was getting excited about new “petrochemicals” and the ability to create a variety of new compounds from oil. Some of the first products derived from petrochemicals were plastics.

In 1908, modern medicine was established by the Rockefeller’s and dubbed “Allopathy”. The Rockefeller’s created the business of modern medicine which has always been about poisoning people, Eustice Mullen explains.

This is the definition of Allopathic medicine according to the NIH:

“A system in which medical doctors and other health care professionals (such as nurses, pharmacists, and therapists) treat symptoms and diseases using drugs, radiation, or surgery.”

The Rockefeller Institute for Medicine, founded in 1908, marked the advent of the re-creation of synthetic versions of natural cures. Prior to 1908, every place of healing in America, Europe and the world, used only ancient traditional natural medicinal cures. Every hospital was a “Homeopathic Hospital”. Most of these magnificent buildings were converted into mental health asylums where a system of torture and electric shock was established to “cure” mental illness.


John D. Rockefeller created the oil industry and used it to crush traditional medicine in order to enslave people. They also financed the Eugenics movement. One of the perks of modern medicine is depopulation.

“Everyone knows that the infamous Roe v. Wade opinion legalized abortion, but almost no one knows that legal abortion was a strategy by eugenicists, as early as 1939, to “genetically improve” the population by “reducing” it.”

In the book, “Rockefeller Medicine Men: Medicine and Capitalism in America”, authored by E. Richard Brown, he tells the hidden story of the financial, political, and institutional manipulations whereby a diverse and eclectic range of traditional healing modalities available to the North American public was summarily canceled and pared down to a singular style of medicine that would become the predominant medicine of the Western world and a major force in global medical culture during the 20th century. This was brought about largely by the collaboration of the American Medical Association, the philanthropies of Andrew Carnegie and John D. Rockefeller, and the development of a revolutionary curriculum by the Johns Hopkins School of Medicine. Brown documents the story of how a powerful professional elite gained virtual hegemony in the Western theatre of healing by effectively taking control of the ethos and practice of Western medicine. E. Richard Brown describes how, in 1905, the American Medical Association’s new Council on Medical Education funded by Carnegie and Rockefeller commenced serious activity. They employed the services of Abraham Flexner who proceeded to visit and “assess” every single medical school in the US and Canada. Within a short time of this development, medical schools all around the US began to collapse or consolidate. By 1910, 30 schools had merged, and 21 had closed their doors. Of the 166 medical schools operating in 1904, 133 had survived by 1910, and 104 by 1915. Fifteen years later, only 76 schools of medicine existed in the US and they all followed the same curriculum.

The 1910 Flexner Report laid the foundations of the modern medical system, dubbed “Rockefeller medicine” (Allopathy). Since 1910, corporate interests have established near total control of the medical field, both though pharmacology and through their impact on medical education.

In 1935, vitamin C became the first vitamin to be artificially synthesized in Switzerland. Rockefeller saw a big opportunity with the possibility that vitamins and medications could be developed from petroleum. He saw the chance to control and monopolize multiple industries at once: petroleum, chemical and medical. Petrochemicals were ideal from a business perspective because they could be patented, owned and sold for high profits.

Today, the petrochemicals in plastics are causing a slew of illnesses including neurodevelopmental disorders, diabetes, chronic respiratory disease, and cancer, which have increased between 28% and 150% between 1990 and 2019. Petrochemicals in microplastics are also rapidly reducing fertility in males in particular, and polluting our environment. Please also read more here, here, and here.

The first pharmaceutical drug was an arsenic named Salvarsan. That’s right, an ARSENIC!

DEATH is an all-to-common side effect of pharmaceutical drugs which is only logical when you administer poisons internally. The following pages demonstrate the many deaths of people around the world, most of them children, who were fatally poisoned during the first mass medication experiments with Rockefeller’s Allopathic health. The paper is entitled, Toward Responsibility in International Health: Death following Treatment in Rockefeller Hookworm Campaigns, 1914–1934.

What is EDTA?

EDTA is synthesized on an industrial scale using 1, 2-diaminoethane (ethylene diamine), formaldehyde, water and sodium cyanide.

Ethylene diamine induced acute and subchronic toxicity in lab animals, also allergic hypersensitivity. The liver and kidneys are target organs of ethylenediamine, where they simply stop working.


Read more: Is C60 And EDTA Safe? Clinical Review


Absorption of large amounts of formaldehyde via any route can cause severe systemic toxicity, leading to metabolic acidosis, tissue and organ damage, and coma, according to the CDC.

Exposure to sodium cyanide can be rapidly fatal. It has whole-body (systemic) effects, particularly affecting those organ systems most sensitive to low oxygen levels: the central nervous system (brain), the cardiovascular system (heart and blood vessels), and the pulmonary system (lungs), according to the CDC.

EDTA is an industrial poison. The textile industry required a chelating agent to remove calcium during textile processing and this led to the synthesis of polyamino-carboxylic acids, one of which was EDTA. A patent was filed for EDTA in Germany in 1935, for industrial chemical use. EDTA is a synthetic acid effectively used to clean boiler rooms in nuclear power plants. In 1945, Franz Munz obtained a US EDTA patent in 1945. In 1947, EDTA was approved by the US Food and Drug Administration (FDA) as a food additive in “low doses” because it’s a forever chemical and a preservative.

There are two different types of EDTA approved by the U.S. FDA. In 1953, Edetate calcium disodium also known as Calcium EDTA (marketed under the trade name Calcium Disodium Versenate registered ) was approved for the treatment of lead poisoning. Three years later, in 1956, a related EDTA compound, Edetate disodium, was also approved for clinical use. This compound, also known as Disodium EDTA, has been marketed under the trade names Disotate (registered) and Endrate (registered). The essential difference between these two compounds is that Calcium EDTA's structure has an incorporated Ca super(2+) moiety while Disodium EDTA does not. The use of the latter compound, Disodium EDTA, has been associated with life-threatening and fatal hypocalcemia.

EDTA trial DEATHS

An EDTA trial (Sloth-Nielsen et al., 1981) on the possible antiatherogenic effect of EDTA with 6 patients, showed clinical signs of potentially lethal hypocalcemia from abnormally low calcium levels caused by EDTA.

Another EDTA chelation human trial in 2003-2005 resulted in DEATHS due to hypocalcemia.

A 2006 EDTA chelation trial also resulted in DEATHS due to hypocalcemia.

There were several DEATHS reported from cardiac arrest due to lethal hypocalcemia in EDTA trials in 2006 and 2008 and (Brown, Willis, Omalu, & Leiker, 2006; Baxter & Krenzelok, 2008), from calcium deficiency inducing alterations in the brain, and osteoporosis, which causes the bones to become brittle.

In 2008, a clinical trial with EDTA chelation on autistic children also proved fatal, resulting in DEATHS of children.

A 2007 EDTA chelation study proved KIDNEY FAILURE in humans.

Decades of clinical studies demonstrate that EDTA treatment is associated with severe, life-threatening adverse effects, as Science Direct explained in 2016.

“It should be emphasized that EDTA treatment is associated with severe, life-threatening adverse effects.

EDTA for cardiovascular disease DEBUNKED

Many Allopathic specialists tried to popularize the use of EDTA for chelation, to no avail. In the 1980s, Richard Casdorph, a practicing cardiologist, claimed improvements in ejection fractions of the heart and in cerebral blood flow with EDTA chelation therapy in several articles. McDonagh, Rudolph, and Cheraskin published about 30 articles documenting various positive effects of EDTA chelation. This group wrote articles showing no problems with kidney function in patients treated with EDTA according to the published protocol. At the same time, conventional cardiologists wrote several editorials against EDTA chelation. So the American Medical Association called for studies to see if chelation worked. The American Board of Chelation Therapy in 1983 was formed to certify doctors who give the therapy. It was later called the American Board of Clinical Metal Toxicology. ACAM also certified doctors who took its workshop on chelation therapy and passed its written and oral examinations. The Great Lakes College of Clinical Medicine, later called the International College of Integrative Medicine (ICIM), was formed in 1983 to teach and do research on chelation and other integrative therapies. After complex negotiations, in the late 1980's Walter Reed Army Hospital agreed to do a randomized clinical trial on EDTA chelation therapy, but part way through the study it was suddenly discontinued for unknown reasons.

However, in a paper by Seely, Wu, and Mills, (2005), a systematic review of published articles in this field was undertaken. The authors concluded that the best current available evidence did not support the therapeutic use of EDTA chelation therapy in the treatment of cardiovascular disease. Similar results have been reported in review papers by Shrihari, Roy, Prabhakaran, and Reddy (2006) and Crisponi et al. (2015).

While a 2002 EDTA large randomized clinical trial “showed benefit”, smaller studies were inconsistent.

In the 1990s, the Federal Trade Commission filed a complaint against ACAM for making a claim in a brochure that chelation was effective for vascular disease. ACAM submitted almost 100 articles in support of the claim, but the FTC insisted that a large randomized trial was required to make that claim. ACAM finally gave up after spending a million dollars in legal fees and signed a consent order saying they would not make such a claim anymore, based on the evidence at that time.

In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up.

A slew of other adverse events such as lacrimation, nasal congestion, mucocutaneous lesions, glycosuria, hypotension, and ECG abnormalities (DISEASE OF THE HEART AND LUNGS) have also been reported as well as allergic reactions (Wax, 2013) to EDTA. Prolonged treatment with calcium EDTA gives rise to depletion of magnesium and trace-metal depletion, the most marked being due to the excretion of zinc. Zinc depletion destroys your cells’ ability to absorb nutrients and leads to diabetes.

A 2015 study entitled, Quality of Life Outcomes with a Disodium EDTA Chelation Regimen for Coronary Disease: Results from the TACT Randomized Trial concluded with this statement:

“In conclusion, our study shows that in a population of stable, largely asymptomatic coronary artery disease patients with prior myocardial infarction, use of EDTA chelation therapy did not produce a measurable change in health-related quality of life over 2 years of follow-up.”

Severe kidney damage from EDTA chelation therapy was reported in a (Nissel 1986) trial. In a very short period of time, EDTA causes kidneys to shut down in complete failure.

A study from 2015 suggests EDTA chelation for myocardial infarction with “modest” benefits to cardio health. However, I would suggest that the moderate benefits of this study were due to the high doses of vitamin C administered.

A 2017 study on EDTA chelation for atherosclerosis and Miocardial Infraction concluded:

“Unsubstantiated claims of chelation therapy as an effective treatment of atherosclerosis should be avoided and patients made aware of the inadequate evidence for efficacy and potential adverse effects, especially the harm that can occur if used as a substitute for proven therapies.”

In a 2018 EDTA trial it was concluded:

“These results… are not sufficient to support the routine use of chelation therapy for treatment of patients who have had an MI (Miocardial Infraction)”.

A study from 2023 entitled, Chelation Therapy Associated with Antioxidant Supplementation Can Decrease Oxidative Stress and Inflammation in Multiple Sclerosis: Preliminary Results proved a flop with two participants discontinuing their trial participation.

EDTA for lead poisoning DEBUNKED

EDTA has also been touted as a treatment for lead poisoning. Because of its adverse effects, calcium EDTA was replaced by DMSA in the treatment of lead poisoning (Aposhian et al., 1995) in 1995. CaEDTA has also been used for the treatment of cases with manganese toxicity, but the result was neurotoxic symptoms resembling PARKINSONISM (Andersen, 1999).

A 2004 trial showed that EDTA actually REDISTRIBUTES LEAD TO THE BRAIN after acute or chronic lead exposure (Andersen, 2004).

Another trial proved adverse effects in 5 patients receiving EDTA at an outpatient chelation clinic in 2002, and all patients experienced gastrointestinal and musculoskeletal symptoms.

Oral exposure to EDTA (2002) had produced adverse reproductive and developmental effects in animals. EDTA did not make it past the animal or human trials, so why are medical doctors using it in humans?

A 2002 EDTA trial was performed on humans as a test for “chelation” therapy by a chelation clinic, demonstrating adverse events in 5 out of 5 patients.

Additionally, EDTA is a persistent organic pollutant (POP). In that case, each intake would only be partially excreted, while the remaining chemicals build up in the body and produce cell death. And long-term exposure to calcium disodium EDTA creates toxicity and kidney damage.

EDTA Snakeoil Salesmen

In March 2023, Ana Maria Mihalcea interviewed Dr. Michael Roth who claims that EDTA is a “synthetic amino acid related to vinegar.” Together they make a slew of medical claims that are not scientifically proven, such as that EDTA “detoxifies covid vaccine, heavy metals, graphene oxide, parasites, hydrogels, and nanoparticles”.

The only scientific tool Ana Maria uses to back her claims is dark field microscopy. You cannot see nanoparticles with a dark field microscope. It takes a spectroscopy microscope to identify nanoparticles. Her medical claims are simply fabricated and unscientific lies.

Ana Maria and Dr. Ross made additional unproven medical statements that “EDTA removes the effects of a heart attack, can bring back the elderly from senility and Alzheimer’s, reduces blood pressure, detoxifies several snake and spider venoms, lowers insulin, smooths skin and wrinkles, ” and a host of other laughable health claims that aren’t backed by anything.

Incidentally, Dr. Ross is now dead.

“Dr. Roth sadly passed away on March 11/2023”


My sources informed me that Dr. Rashid Buttar was using EDTA. Given that he was already severely poisoned as Stew Peter’s reported, using EDTA Acid would have been enough to tip him over the edge and kill him.

EDTA is not an approved pharmaceutical drug. It was Covid Emergency approved by the FDA under an Emergency Use Authorization (EUA), just like the modified RNA (modRNA) Covid-19 vaccine nanotechnology.

The National Center for Complementary and Integrative Health (.gov) makes it clear that the use of EDTA chelation for heart disease has not been approved by the FDA.

Ana Maria has been touting EDTA as an “antioxidant” when it is not. She even published to her Substack that EDTA is an “Antioxidant” when in fact it’s an acid poison and an oxidant. Many people saw it on her Substack before she removed it.

I’ve had over a dozen clients come to me extremely sick from EDTA pills and EDTA IV infusion. Some told me they thought it was a natural substance due to Ana Maria’s false advertising and medical malfeasance. A Medical Doctor is licensed to know wether EDTA Acid is an oxidant poison or an antioxidant. Not knowing this and inducing the death of a patient is not an acceptable excuse. Ana Maria is criminally liable.


EDTA is an oxidant when used internally. The studies that refer to EDTA as an “antioxidant” are in vitro lab studies, not in vivo (inside the body).

EDTA is used to preserve cell specimens for chemistry lab work because it prevents blood coagulation and oxidation of cells in a petri dish where it’s used for diagnostic purposes. This is the kind of “antioxidant” the studies are referring to. But when you infuse EDTA Acid into the human body, it acts as an oxidant poison.

EDTA also will not decoagulate the blood in vivo (inside the body). But I can see how people who cannot read peer-reviewed literature could be deceived and manipulated by snake oil salesmen.

For example, a study entitled, “Comparative study of the antioxidant capability of EDTA and Irganox”. EDTA is a preservative used in laboratories to preserve cells for scientific lab research. EDTA prevents the oxidation of cells in a petri dish. Oxygen causes cells to deteriorate, but labs need them to last longer for research purposes. When used inside the human body (in vivo), it’s a different story. Then EDTA acts as an oxidant poison, not an antioxidant. So this has a very different meaning.

One of the well documented and widely known adverse events from EDTA “chelation” is DEATH, according to Mount Sinai.

Other serious side effects that have been reported include low blood sugar, diminished calcium levels, headache, nausea, dangerously low blood pressure, kidney failure, organ damage, irregular heartbeat, seizures, or even death.

I have to wonder if Ana Maria Mihalcea is informing her patients that death is a potential adverse event to EDTA chelation? In a March 24, 2024, broadcast that Ana Maria released, at the 53:24 minute mark, she makes a chilling confession:

“I already have had… uh… patients die from the shedding”

How many of Ana Maria Mihalcea’s patients have been killed by her EDTA infusion protocol? I was horrified when I heard Ana Maria’s confession because I haven’t had any clients die from shedding! I’ve treated many people who were extremely sick from shedding, and I helped them all to detox effectively. Some clients came to me after several hospitalizations from extreme shedding but none of them died in my care! Nobody needs to die from shedding if they use an effective detox protocol.

Between 1-2 years, Ana Maria has been claiming that EDTA detoxes graphene, dissolves graphene and chelates heavy metals, but experts such as Dr. Robert Young and Dr. Judy Mikovitz told me this is impossible.

Ana Maria has gone so far as to produce a medical study with unscientific claims right in the title, “EDTA Chelation Dissolves the Artificial Intelligence Magnetic Hydrogel Weapon”. The study was also promoted by Health Canada. In her study, Ana Maria claims that EDTA can “detoxify the body even from Graphene”.

EDTA is not a detox agent! Again, it’s an oxidant that degrades cells whereas genuine antioxidants repair cells.

Ana Maria does in fact know about oxidant poisons. In an interview from December 2022, she referred to graphene as an oxidant. At least she’s correct about something.

Saul Green, Ph.D., and Wallace I. Sampson, M.D. wrote in great detail about the Implausibility of EDTA Chelation Therapy, stating:

“EDTA chelation effectiveness is implausible; (2) the preponderance of evidence shows ineffectiveness; and (3) EDTA augments oxidative reactions involving iron instead of inhibiting them, resulting in increased likelihood of production of oxygen free radicals rather than neutralization of them, as claimed.”

EDTA a precurser to cellular transfection

The Rockefeller Institue of Medicine has done clinical research on EDTA. One particular study entitled, Studies of Cell Deformity from 1967, shows that cells will degrade from EDTA exposure, which also induces “deformation” on their surfaces. The trial demonstrated that EDTA stops cellular synthesis of calcium. They learned that calcium is bound to anionic sites at the cell periphery, some of which are located at the cellular electrokinetic surface.

Due to Rockefeller’s research, EDTA is now used in electrophoresis which is a laboratory technique used to separate DNA, RNA or protein molecules based on their size and electrical charge. An electric current is used to move the molecules through a gel or other matrix, according to the National Human Genome Research Institute.

In agarose gel electrophoresis, EDTA is added for chelating the magnesium ions which are cofactors for DNA nucleases. Hence, activity of DNA nucleases that may be present is inhibited, and “DNA is protected from degrading”. This is why EDTA is an effective transfection agent because it dissolves parts of your DNA, preserving cells for lab research in vitro.

Gel electrophoresis using EDTA is routinely used for detection and size analysis of proteins and nucleic acid. DMSO is used with EDTA in this process. This destruction of cells makes transfection (gene editing) of cells easier using CRISPR-Cas9 which splices and dices the genome in vivo, as this study explains entitled, “Inhibition of CRISPR-Cas9 ribonucleoprotein complex assembly by anti-CRISPR AcrIIC2”.


EDTA was found to be genotoxic in laboratory animals. A study from 1983 demonstrates that EDTA induces gene mutations and chromosomal breakage, meaning that genetic mutations will be passed on your offspring, affecting generations to come, according to this Genetic Toxicology of EDTA study from 1983.

Calcium chelate of EDTA (CaEDTA) “chelation” has shown teratogenic effects (Catsch & Harmuth-Hoene, 1976), which are central nervous system depression and peripheral neuropathy. EDTA produced abnormalities in pups of rats removed by cesarian section on day 21 of the study. Increases in several abnormalities (cleft palate, adactyly or syndactyly, abnormal rib or abnormal vertebrae) were observed with increased doses of CaEDTA.

EDTA improves transfection of embryonic stem cells lines (hESC) in cells, according to the NIH.

According to a peer reviewed paper from the NIH, EDTA is a precursor to cellular transfection.

“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..."

Thermo Fisher Scientific Inc. Fetal Bovine Serum for human transfection also uses EDTA.


An NIH study entitled, “Kinetic Basis for DNA Target Specificity of CRISPR-Cas12a” reveals that EDTA enables rapid binding to DNA during gene editing (transfection).

Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” explains:

“CAS12a is an RNA-guided, programmable genome editing enzyme found within bacterial adaptive immune pathways. Unlike CRISPR-Cas9, Cas12a uses only a single catalytic site to both cleave target double-stranded DNA (dsDNA) (cis-activity) and indiscriminately degrade single-stranded DNA (ssDNA) (trans-activity).”

According to the study, “A DNA loading buffer of 45% formamide and 15 mM EDTA, with a trace amount of xylene cyanol and bromophenol blue…” is used to transfect the human genome.

So, EDTA is a transfection agent used with CRISPR-Cas9 to edit the human genome. Does EDTA actually dissolve graphene, as Ana Maria claims? The answer is NO! EDTA oxidant is used to reduce graphene to Reduced Graphene Oxide (RGO) form. Graphene is reduced by oxidation. Rather than dissolving graphene, EDTA reduces it to Graphene Oxide Nanoparticles otherwise known as Quantum Dots.

Graphene oxide is more toxic than graphene, as I documented in my article entitled, “Graphene Oxide The Vector For Covid-19 Democide”.

I will emphasize again that Graphene Oxide Quantum Dots cannot be seen with a dark field microscope. So Ana Maria’s claims that EDTA is detoxing graphene from the human body is unscientific.

EDTA chelation for graphene nanocomposites

EDTA chelation is NOT effective in removing metals from the human body. It's actually a different kind of chelation that’s used to create electrochemical sensors (biosensors) when combined with GRAPHENE!

EDTA serves as a connecting mediator between NiHCF (Graphene Oxide Nanoparticles and Nickle) and graphene nanosheets. EDTA is used with metal nanoparticles, metal oxides, graphene, carbon nanotubes, and quantum dots to stabilize the technology for a more uniform distribution throughout the body.

A Science Direct paper entitled, “Highly sensitive ascorbid acid sensors from EDTA chelation derived nickel hexacyanoferrate/graphene nanocomposites” reveals that EDTA is used to create Graphene/Nickel, AA sensor nanocomposites.

“EDTA chelation stragey” is used for the “homogeneously distrubuted" NiHCF” (Nickel hexacyanoferrate composite) on graphene sheets. EDTA residue-supported pyramidal and spherical nanoparticles of NiHCF deposited on graphene sheets is used to create biosensors for the formation of Graphene/Nickel hydrogels.


The graphene hydrogel nanocomposite sensors (Gr/NiHCF) are used as externally controlled biosensing tools. They tell us it’s used to test for ascorbic acid, but the application of this technology is for “human life” as well as for industrial use. See link here.


Graphene oxide/Lauric acid nanoparticles are modified using EDTA. Lauric acid nanoparticles is suggested as a “prospective drug carrier” for oral nanoparticle-mediated sustained drug delivery (timed release technology) used for the removal of Pb(II) ions (lead). However, studies show there are cytotoxic results.

Another study entitled, “Improved genome editing by an engineered CRISPR-Cas12a” demonstrates how EDTA improves transfection and modification of the human genome.

Once Graphene is reduced to Graphene Oxide, due to its small particulate size, you can no longer identify it using a Dark Field Microscope. Ana Maria is using a dark field scope, not a spectroscopy microscope, which is the only instrument that can measure GON and Quantum Dots.

So what is Ana Maria doing with EDTA infusions? She’s creating a metal-EDTA complex that stabilizes and strengthens the graphene-based nanotech weapon system and enables it to spread more readily throughout the body, for human transfection. She uses “light and sound healing techniques” to activate the delayed release technology before administering EDTA infusion, as she reveals in an interview here.

EDTA is a poison acid that dissolves DNA. It's used to prime the cells’ DNA for transfection. EDTA disrupts the surface of skin cells so that other chemicals can penetrate more easily and CRISPR-Cas9 gene editing technology can work more efficiently.

The NIH describes EDTA’s enhanced cellular transfection:

“Flow cytometric analysis using an enhanced green fluorescent protein vector showed a significantly increased transfection efficiency of EDTA method compared to standard enzyme method. In addition, the EDTA approach maintained stable cell viability and recovery rate of hESCs after transfection.”

Another study published in Research Gate, confirms that EDTA increases cellular transfection, along with using chloroquine.

Graphene Oxide Quantum Dots (GOQD-HA) nanocomposite use EDTA for tissue-specific delivery of Metformin, an anti-diabetic drug otherwise known as insulin.


Conclusion

Beware of snakeoil salesmen! Never trust pharmaceuticals! Superior heavy metal chelation supplements exist such as ASEA redox molecules and Master Peace, sign up and order here. Medicines made from nature are always superior to pharmaceutical drugs. Finally, be sure your Naturopathic Doctor is competent!

Schedule a health consultation with me for a customized detox protocol and complete cellular health restoration.

https://substack.com/home/post/p-144979143

Ana Maria Mihalcea's Defamation Against ASEA Redox Molecules
Dr. Ariyana Love (ND)
I met Ana Maria Mihalcea while I was working in Spain, in July 2022. I was meeting weekly with the Medical Doctors For Covid Ethics (MD4CE) group since October 2021. Ana Maria was invited into MD4CE group in the summer of 2022.

Ana Maria learned from others in the MD4CE group that I was successfully detoxing people from the Covid-19 vaccines. She approached me early in July and asked me to do a Skype call with her. During the video call she told me that she’s a “Medical Doctor who now uses only Naturopathic Medicines”. She did this in order to get me to trust her but it’s obviously a lie because now she’s promoting unapproved industrial poisons such as EDTA and Methylene Blue.

Ana Maria showed me two images that were supposedly of her own blood, and said that she had been “poisoned”. The blood image was clearly contaminated with Covid-19 tech. Ana Maria claimed that the tech induced brain injury and caused her to lose some of her cognitive ability. I could see the brain damage from the way she slurred her words and struggled to find words.

Ana Maria told me she’d “tried everything to get the tech out” of her body but nothing worked, and she asked me if I could help her. I gave her a free consultation and instructed her to use 16 ounces of ASEA Redox daily, along with other supplements in my protocol. She further asked me if there was anything else that could be used to detox besides the Redox supplement. I told her that Humic Acid might work or at least it would help, along with other natural medicines in my protocol. I also told her that Humic Acid is natural nano-minerals so it’s aborption rate into cells is rapid, and it works as a cellular driver of nutrients.

After the free consultation, Ana Maria began buying about 4 cases of the ASEA Redox supplement from me each month. Her first purchase was on July 10th 2022. She continued to buy 4 cases of the Redox supplement for 5 consecutive months.

In September 2022, Ana Maria began telling people in the MD4CE group that redox molecules do not work. Despite this, she continued buying 4 cases per month from me.

In October 2022, Ana Maria publicly addressed the MD4CE group on a weekly call with about 100 of the world’s leading experts in attendance, exclaiming that “ASEA Redox doesn’t work Ariyana”. I was stunned. That was a bald-faced lie!

Ana Maria continued to purchase 4 cases of ASEA Redox in November 2022. Her last purchase was on December 27th, 2022. So, while Ana Maria was defaming me and ASEA to my colleagues and peers, she was simultaneously using my protocol to detox herself. Then she turned around and gave credit to EDTA. How bloody devious!

The MD4CE group includes some of the world’s leading experts in the fields of medicine, science, biology, chemistry, and more. Ana Maria’s defamation resulted in members of the group lashing out at me, abusing me and putting me down. Despite the fact that the group is led by medical experts, they failed to do any due diligence and failed to read from the hundreds of thousands of peer-reviewed papers on the healing power of redox molecules, before inflicting damaging to my career.

Ana Maria further stole my research and began using Humic Acid in her protocols with her patients! She did this without crediting me because she obviously felt entitled to do so.

After Ana Maria lied about me and the efficacy of redox molecules to the medical doctors, the founder of the group, Dr. Stephen Frost, began censoring and defaming me as well. He and the moderator, Charles (CK), decided that I would no longer be allowed to speak in the group, despite that I’d been speaking freely in the group for an entire year, without any problems.

I captured this screenshot on October 13, 2022, while I was in a MD4CE call when residing in Hollola, Finland.


Dr. Stephen Frost contacted me in October 2021, asking me to join and give a presentation to the MD4CE group. I was in the group for several months before Charles joined and began moderating. Prior to Charles joining, the group operated democratically, and each member could raise their hand and have a turn at speaking and asking questions of other presenters.

Treating me in this way and censoring my ability to interact in the group was degrading and hurtful. I took a screenshot of their undemocratic abuse and posted it onto the group chat for everyone to see. I wanted the others to know that I was being targeted. Immediately, Charles and Stephen removed me from the group and stopped sending me invites.

Right before I was removed from MD4CE, I invited Dr. Robert Young into the group in October 2022. Despite that Dr. Young had analyzed ASEA’s redox molecules in a science lab and knew their efficacy, the medical doctors took Ana Maria’s word without question. Dr. Frost did not bother to consult with Dr. Young. He failed to read the research papers such as “ASEA And The Big Three” which demonstrates how redox molecules boost glutathione levels up to between 500-800%.


Dr. Frost proceeded to defame me. I had a couple members of MD4CE reach out to tell me that Dr. Frost refused to give them my contact information when they asked him for it and told me he was attacking my good character.

The Israeli-Zionists in MD4CE had also been pressuring Dr. Frost to remove me from the group ever since I joined. They attacked everyone who was exposing Graphene Oxide Nanoparticles in the Covid-19 jabs, including Karen Kingston and La Quinta Columna.

MD4CE knowledge of redox molecules and our body’s natural operating system is close to non-existent. A few members were complaining that the Redox supplement was “too expensive”. They didn’t want ASEA to get the credit they deserve, possibly because it’s from nature and not a pharmaceutical. Instead of researching redox molecules, they chose to cancel me and inflict harm on my career. Dr. Frost has made no effort to apologize to me. He too feels entitled to discriminate against me.

Ana Maria’s defamation was successful, but it didn’t stop there. She went straight to Stew Peters and got me canceled from his show with her viscous lies. My last interview with Stew Peters was a year ago, where I revealed that the patent for the PCR “test” is linked to human cloning. The interview was in September 2022.

Dr. Judy Mikovitz went on the Thrivetime Show on InfoWars, and backed my research. Clay Clark played a clip of that interview with Stew Peters and asked Dr. Judy Mikovitz to comment on the PCR swabs being cloning devices. She not only backed my research, but she also revealed that SARS-Cov-2 is a “synthetic retrovirus" which is part of HIV and XRV (snake venom syncytin). It was a great interview that was unfortuneately censored!

While many have heralded Ana Maria Mihalcea as a hero for mainstreaming a deadly industrial poison as a “detox” for Covid-19 vaccine injuries, and touting it as a miracle treatment for everybody else, it’s important to take a closer look at her shady character.

Ana Maria is deeply involved in Ramtha’s teachings. Ramtha is a male entity channeled by a woman. Ana Maria’s testimonial was featured on Ramtha’s RSE Newsletter in 2014, where she boasts about Ramtha’s spiritual guidance enabling her to win more money by gambling on slot machines in a casino.

In Ana Maria’s own words:

“This past week, after a days work, and maintaining my Peace, I won:

9/2/14 $1,300 Net on Rainbow Riches
9//3/14 $1,715.75 Jackpot on Cheetah (Net $1,520)
9/4/14 $700 Net on Cheetah
9/5/14 $750 Net on Rainbow Riches
9/7/14 $1,973 Jackpot on Count Vampire (Net $1,898)

I went to the Casino on 9/6. I for the first time in days got angry about something at work and did not immediately self correct. I won that evening, but did not walk out with a net Win. That was a great lesson that Nothing and Nobody is worth loosing my Peace for and interrupting my future Consciousness Stream.”



Now, are these spiritual values? I hope this sheds more light into Ana Maria’s ambitions.

The MD4CE complained many times to me that ASEA Redox is “too expensive” but the EDTA chelation is about $2,000 per visit, not including travel! Whereas a case of ASEA Redox is $160 at retail price, and $130 wholesale, with a monthly subscription.

ASEA Redox is perhaps the world’s most effective heavy metal chelator and this is why Ana Maria defamed me after using my protocol to detox herself while giving credit to EDTA “chelation”. She knows redox molecules are effective, but she had an agenda to get rich and sell EDTA snakeoil poison to people.

Now Ana Maria is attacking Master Peace through a nurse practitioner. They’re falsely claiming that Master Peace includes self-assembling nanotechnology in an insidious attempt to defame the company and prevent people from achieving true detox. Ana Maria is defaming all the best supplements that are in competition with her EDTA snakeoil.

Master Peace is another critical breakthrough in medicine. It’s affordable for all and is one of the best heavy metal chelators to exist. It works synergistically with redox molecules, increasing their efficacy.

Please review the detailed peer reviewed literature on redox molecules and review the Dark Field Microscopy images of blood before and after using ASEA Redox, through the work of a colleague, Dr. Peggy Marienfeld.


PLEASE READ: EDTA Snakeoil! Ana Maria Mihalcea’s Medical Malfeasance Exposed



https://substack.com/home/post/p-144981224

C19 Uninjected Individuals Expelling Fluorescent Filaments Through Skin - Similar To C19 Injected - Darkfield Microscopy Of Filaments And Correlation To Live Blood
Ana Maria Mihalcea, MD, PhD

https://donshafi911.blogspot.com/2024/05/c19-uninjected-individuals-expelling.html

C19 Unvaccinated Turned Magnetic From Shedding – Correlation With Darkfield Microscopy Live Blood Analysis
Image: C19 unvaccinated blood with many construction sites and clot formation seen This is an interesting case report of a C19 unvaccinated …
http://donshafi911.business.blog/2024/04/09/c19-unvaccinated-turned-magnetic-from-shedding-correlation-with-darkfield-microscopy-live-blood-analysis/

There's also a ton of information from the IEC regarding international Standards surrounding Biodigital convergence.

Quantum Dots are programmable graphene oxide nanoparticles which serve many functions, including biometric data harvesting (spying).

The demons want to build their Smart Cities from this material!

https://ambassadorlove.blog/2021/12/17/quantum-dots-dna-barcoding-nano-razors-the-israeli-state/


Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State
December 17, 2021 by Dr. Ariyana Love
December 2, 2021
By Dr. Ariyana Love, ND

In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased.

Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide.

You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here.

LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY

An English translation of this video can be found in the article entitled, Dr. Ariyana Discusses Nano-Biosensors/Nanorazors and Dr. Noack’s Death After He Located Graphene Hydroxide in the COVID Vaccine.

MICROSPHERES & MICROBUBBLES

Microbeads and Microspheres are listed as an active ingredient in the Pfizer death jab patent. Microspheres and Microbubbles are listed in the Moderna death jab patent.

Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair.


Microbubbles and Microspheres (bottom right)
Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells.

Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this.

Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.”

This technology is being used for DNA-based tissue engineering and “scaffolding” of Humans, without their Informed Consent. See more scaffolding images from a Slovakian study of the death jab, here.

Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside.

Graphene Oxide Nanotubes enable Microbubbles to self-replicate via electrical pulse. They interlink by electrodes. Microbubbles were designed to break through the blood/brain barrier and deliver their drug and chemical payload into brain cells. Ultrasound is used to help Microbubbles breach the blood/brain barrier. Here’s a video animation of how microbubbles / microspheres work to deliver drugs into the brain.

This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids.

The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies.


Moderna patent US10703789B2 delayed drug release
QUANTOM DOTS & MICROBEADS

Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents.

These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene.

Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans. They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans.

Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move.

I discussed Quantum Dots and more with Stew Peters on December 9th, 2021.

Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021
Microbead patent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and Microbead patent ES2784361T3/en specifies that it’s used to create molecular barcodes in Humans.

Thermo Ficher sells Microbeads and markets them as Dynabeads and SPIONs. See SPIONS here.

THE ISRAELI STATE

This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dot patent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide.

Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys.

Moderna’s patents are owned by Israel. Pfizer patents are owned by Israel. Pfizer CEO is in bed with Israel. Moderna is partnered with Israel in medical maleficence.

Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS!


Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect. Is that what you want to become?


BIOCHIP & HYDROGEL

Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”.


Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal.

We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc.

Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol.

PROTOCOL

There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here.

https://donshafi911.blogspot.com/2024/02/quantum-dots-dna-barcoding-nano-razors.html

Environmental Filaments UV Light Fluorescence Darkfield Microscopy
Ana Maria Mihalcea, MD, PhD

Image: Environmental filaments collected in regular light and under UV light

I was visited by Dr. Justin Coy, a former Defense Department Contractor who has been following and validating my research. He brought me an environmental filament sample and a UV flashlight - 365nm. In this post, I am documenting the darkfield microscopy of these filaments and experiments with UV light. He was suspecting Luciferase to be present in the filaments and asked me to take a look. From my research there are metal nanoparticles in the filaments and they can cause fluorescence. Luciferase is used in in molecular biology that uses the luciferase enzyme and a substrate (such as luciferin) to study gene regulation at the level of transcription. I do not think that is the mechanism of the fluorescence of the polymers as other mechanisms using metals have been described in the literature and since Clifford Carnicoms analysis showed huge amounts of metals in the filaments that could be plausible.

There have been developments of bright orange proteins fused with Luciferase in biological systems - this remains a question for further research and discovery.

Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals

We know that embedded Quantum Dot technology can make filaments emit different light and filaments found in the blood have been shown to have bifringence. We also know that UV light can be used as an energy source by nano sensors which can embed themselves in the self assembly polymers. Karl C has done some remarkable microscopy research showing this unusual light emission which I posted here: Extraordinary Microscopy Of Self Assembly Nanotechnology - A Request For Funding Help For Karl C


Here are different images of the filaments analyzed by me observing how they change with normal light and then UV light:


Image: Darkfield Microscopy: UV light off left, UV light on right


Image above: normal light


Image: UV light

I then wanted to see if different aspects of the filament react differently to UV light, and they appear to. Some areas are more luminescent then others.


Image: UV light on, both pictures.

Below you can see a closer view of the filament under UV light, and there being very specific region that react to the UV light more:


Off the orange appearing filament a white one came forth. Magnification of 2000x on the right shows a central cavitation of the filament


Below you can see the orange environmental filament compared to a "self assembly nanotechnology hydrogel” filament from shedding in C19 unvaccinated blood with many visible Quantum Dot like structures seen embedded. The filament composition look the same except the colors differ.


Here are different areas of the filament that have enormous glow under UV light, magnification 2000x:


Here is an area of the filament with UV light:


Same without UV light:


Here are some research articles on fluorescent polymers:

New 'smart' polymer glows brighter when stretched

Spider fossils glow under UV light, a clue to their remarkable preservation

Plastics shine bright to warn of invisible cracks Damage to polymers ruptures microcapsules, releasing fluorescent molecules

I have been speaking about spider silk which is a polyamide protein and recently did microscopy on an environmental filament found:

Spider Silk Polymer Sprayed Via Geoengineering Operations From California - Darkfield Microscopy Analysis

This article explains that if metals are introduced the the nanofibers, florescence can be achieved:

Optical fluorescent spider silk electrospun nanofibers with embedded cerium oxide nanoparticles

The work demonstrates an electrospun nanocomposite of recombinant spider silk protein (rSSp) nanofibers with embedded cerium oxide (ceria) nanoparticles. RSSP (MaSp1) has been produced, extracted from goat milk, and fabricated into nanofibers using an electrospinning process. The resulting electrospun nanofibers have a mean diameter of ∼50 nm. Furthermore, ceria nanoparticles of mean diameter 10 nm were added in the spinning dope to be embedded within the generated nanofibers. These nanoparticles show certain optical activity due to optical trivaliant cerium ions, associated with formed oxygen vacancies. The formed nanocomposite shows promising mechanical properties such as the Young's modulus, elasticity (or elongation at break), and toughness. In addition, the electrospun mat becomes fluorescent with 520-nm emission upon exposure to UV light, due to excitation of the optically active ceria nanoparticles. Also, the formed nanocomposite shows a decay of its electric resistance over time upon exposure to cyclic loads at different humidity conditions. The synthesized nanocomposite can be utilized in different biomedical, textile, and sensing applications.

We do know that these polymers are used for transhumanist surveillance and synthetic biology. Here they used spider silk as an inspiration. Note how they describe that these polymers can wrap around nerves, muscles and hearts and be the next generation tissue electronic interface:

Polymer films inspired by spider silk connect biological tissues and electronic devices

Linking biological tissues with electronic devices is challenging owing to the softness of tissues and their arbitrary shapes and sizes. An innovative water-responsive, supercontractile polymer film, inspired by spider silk, allows the construction of soft, stretchable and shape-adaptive tissue–electronic interfaces.

We designed water-responsive supercontractile polymer films composed of poly(ethylene oxide) and poly(ethylene glycol)-α-cyclodextrin inclusion complex, which are initially dry, flexible and stable under ambient conditions, contract by more than 50% of their original length within seconds (about 30% per second) after wetting and become soft (about 100 kPa) and stretchable (around 600%) hydrogel thin films thereafter. This supercontraction is attributed to the aligned microporous hierarchical structures of the films, which also facilitate electronic integration. We used this film to fabricate shape-adaptive electrode arrays that simplify the implantation procedure through supercontraction and conformally wrap around nerves, muscles and hearts of different sizes when wetted for in vivo nerve stimulation and electrophysiological signal recording. This study demonstrates that this water-responsive material can play an important part in shaping the next-generation tissue–electronics interfaces as well as broadening the biomedical application of shape-adaptive materials.

Here is video of the microscopy UV light on in both videos:

UV light on playing with the focus:

I took a blood sample and applied the UV light to see what happens to the micro robots. As in my experiments with the 450nm cold laser, the robots are quite happy and seem to absorb the extra energy - if you look at the robot its light emission intensifies, and that is consistent with the WBAN article I just posted that light is an energy source for the biosensors. Energy Harvesting From The Human Body By Wireless Body Area Network - A Cause For The Electrical Conductivity Loss in Human Blood?

https://anamihalceamdphd.substack.com/p/environmental-filaments-uv-light?utm_medium=ios

Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State
December 17, 2021 by Dr. Ariyana Love
December 2, 2021
By Dr. Ariyana Love, ND

In my latest interview with Stew Peter’s, I brought evidence confirming that Dr. Andreas Noack, the good doctor who risked his life to warn humanity of the extreme dangers of the death jab, is in fact deceased.

Days after Dr. Noack’s mysterious death, a video was leaked revealing Graphene Hydroxide nano-razors inside the Pfizer death jab, under Dark Field Microscopy. The sample is loaded with Graphene Hydroxide.

You will see an individual Microsphere releasing it’s payload of nanoscale Graphene Hydroxide which looks exactly like razorblades when zoomed in on the individual shiny specs. See more images here.

LEAKED FOOTAGE: GRAPHENE HYDROXIDE NANO-RAZORBLADES – DARK FIELD MICROSCOPY

An English translation of this video can be found in the article entitled, Dr. Ariyana Discusses Nano-Biosensors/Nanorazors and Dr. Noack’s Death After He Located Graphene Hydroxide in the COVID Vaccine.

MICROSPHERES & MICROBUBBLES

Microbeads and Microspheres are listed as an active ingredient in the Pfizer death jab patent. Microspheres and Microbubbles are listed in the Moderna death jab patent.

Microspheres and Microbubbles are micrometer size devices approximately equal in size to a red blood cell, according to the NIH. That’s about the width of a Human hair.


Microbubbles and Microspheres (bottom right)
Microspheres and Microbubbles are made from Poly(lactic-co-glycolic) acid (PLGA). PLGA is a copolymer made from Graphene Oxide (GO). Graphene Oxide-PLGA nanofibers are used in a host of Food and Drug Administration (FDA) approved “therapeutic” devices. However, the ingredients of these devices are cytotoxic, meaning they destroy cells.

Graphene Oxide PLGA Toxicity induces an inflammatory response and deadly cytokine storm reaction, according to animal studies. The FDA should be investigated for this.

Microspheres are coated with gold nanoparticles. Microspheres are used for scaffolding, which is artificial tissue engineering inside the Human body. PubMed writes, “Scaffolds are materials that have been engineered to cause desirable cellular interactions to contribute to the formation of new functional tissues for medical purposes. Cells are often ‘seeded’ into these structures capable of supporting three-dimensional tissue formation.”

This technology is being used for DNA-based tissue engineering and “scaffolding” of Humans, without their Informed Consent. See more scaffolding images from a Slovakian study of the death jab, here.

Microbubbles contain one or more “viral vectors coding CRISPR-Cas-9 system“. It’s a “state-of-the-art” drug and chemical delivery method. They contain lab enhanced chimeric proteins of the messenger RNA/DNA. Microbubbles have a lipid and nickel-coated quartz substrate. They contain a drug and chemical payload in the outer, lipid-coating and another payload on the inside.

Graphene Oxide Nanotubes enable Microbubbles to self-replicate via electrical pulse. They interlink by electrodes. Microbubbles were designed to break through the blood/brain barrier and deliver their drug and chemical payload into brain cells. Ultrasound is used to help Microbubbles breach the blood/brain barrier. Here’s a video animation of how microbubbles / microspheres work to deliver drugs into the brain.

This gene delivery technology was funded and developed for the purpose of treating sick people, not healthy people. It was intended to be used as a treatment for cancer, not as a medical intervention for our healthy kids.

The Microbubble and Microsphere devices carry drug and chemical payloads for controlled release of encapsulated DNA. It’s targeted drug delivery can be unloaded over an extended period of time. This is very important to understand. They can be formulated for “sustained release” and programmed to release it’s payload at a later date, over a period of days, weeks, months or years, as the Moderna patent specifies.


Moderna patent US10703789B2 delayed drug release
QUANTOM DOTS & MICROBEADS

Atomic scale nanometer devices called Quantum Dots and Microbeads, are also components of the death jab weapons system. They are found in the Pfizer and Moderna patents.

These nanoscale technological devices are 1000 times smaller than a micrometer. Quantum Dots have nothing to do with plastic particles, these are carbon based nanocrystals, 10-50 atoms thick, and made from Graphene.

Quantom Dots are used for DNA barcoding of Humans using CRISPR-Cas-9 technology. They are super conductors made for bio-imaging and bio-tracking of Humans. They too were developed for “therapeutic” use, to eradicate cancers, not to enslave Humans.

Quantum Dots are artificial, color based, bioluminescent marker genes. They use three colors taken from the enzymatic proteins of insects (Luciferase), glow worms and jellyfish. The chimeric proteins are being barcoded onto Human genes to make them trackable, programmable and encoded, so Human cells will light up, enabling the NWO oligarchs to monitor your every move.

I discussed Quantum Dots and more with Stew Peters on December 9th, 2021.

Dr. Ariyana Love on Stew Peters Show, Dec. 9, 2021
Microbead patent US20110017493A1, verifies that Microbeads “carbon based” (made from Graphene) and Microbead patent ES2784361T3/en specifies that it’s used to create molecular barcodes in Humans.

Thermo Ficher sells Microbeads and markets them as Dynabeads and SPIONs. See SPIONS here.

THE ISRAELI STATE

This technology was developed at the Hebrew University in occupied Jerusalem. The Quantum Dot patent WO201413562A1 is owned by Yissum, a Hebrew University company owned by the Israeli state and co-owned by Nanosys, a Silicon Valley based company. These two companies are sublicensing the technology, worldwide.

Yissum business partners include Google, Intel, Johnson & Johnson, Merck, Microsoft, and many more, while Samsung has a partnership with Nanosys.

Moderna’s patents are owned by Israel. Pfizer patents are owned by Israel. Pfizer CEO is in bed with Israel. Moderna is partnered with Israel in medical maleficence.

Moderna’s CEO Stephane Bancel, wants every man, women and child injected with Moderna’s poison #DeathJab, including INFANTS!


Is it clear to you now who it is that has the greatest vested interest in branding and enslaving Humans like cattle? The cloning of insect DNA (Luciferase) into Humans is called cross-species genomics. This is the process of manually adding DNA from insects into Humans by transfection, a process also known as cloning, in order to change the genetic makeup of cells. It works by deleting one or more gene from the Human host and encodes Human cells to express the new genetic trait of an insect. Is that what you want to become?


BIOCHIP & HYDROGEL

Dr. Pablo Campra mentioned that nano-biosensors are in the death jabs. They can be found in the DARPA patent US7427497B2/en which lists “T-shaped micro-fluidic Biochips”.


Hydrogels contain the entire mRNA weapons system. They need us saturated with their cloning technology in order to succeed in genetically modifying Humans to the point of patent eligibility. They will do so by injections, masks, nasal swabs, hand sanitizer, aerial spraying, and any other means necessary to achieve their end goal.

We are in fact being saturated with Graphene Oxide Hydrogels. They’re being inserted into our food, clothing, hair and make-up products, household cleaners, alcohol, pharmaceutical drugs, sanitary items, water supply, etc.

Ethylene Oxide in masks and on PCR swabs, is in fact Graphene Oxide, Poly(ethylene oxide) Graphene Nanoribbons. The bad news is that Fauci and the NIH funded mRNA nanotechnology which is skin-penetrating and can be dispensed via aerial spraying, as reported by InfoWars. The good news is this weapons system can also be expelled through the skin, if you know how to properly detox. The key to protecting yourself from this biological attack is to boost your immune system and remain on a continued Protocol.

PROTOCOL

There is a special natural supplement that disables the operating system, kills the parasites, and removes Graphene and other metals, effectively expelling them from your body. This supplement increases endogenous glutathione by 800%, repairs damage to your cells and to your DNA, and turns genes on, according to scientific research. This medical breakthrough is being used now by doctors who are able to reverse the coagulation cascade in just minutes. You will find this supplement in my Protocol here.

https://ambassadorlove.blog/2021/12/17/quantum-dots-dna-barcoding-nano-razors-the-israeli-state/

Rubbery Clot Development Observations In C19 Unvaccinated Blood With Different Anti Oxidant Compounds - Comparison with Clifford Carnicoms CDB/Morgellons Historical Culture Work
Ana Maria Mihalcea, MD, PhD

Image: C19 unvaccinated blood from 2 different individuals. First 4 syringes contain Alpha lipoic Acid, Glutathione, Plaquex and Control sample. Second Set contain Methylene Blue and Glutathione and a Control Sample.

I had previously posted experiments with C19 unvaccinated blood and different compounds that could inhibit the production of the rubbery clot material that Clifford Carnicom and I have shown to be Cross Domain Bacteria ( CDB) or Morgellon’s like - a polymerized protein that creates the rubbery clots. My most successful clot inhibition was with EDTA and Vitamin C. I have written multiple substacks regarding this research of the rubbery clot formation:

Rubbery Clot Development In C19 Unvaccinated Individual With Previous Deep Vein Thrombosis and Massive Pulmonary Emboli - While On Eliquis, Nattokinase, Lumbrokinase and Serreptase

Correlation Of Severity Of Live Blood Contamination Seen On Darkfield Microscopy With Visible Clotting In C19 Unvaccinated Individual

C19 Unvaccinated Have Same Blood Clotting Problem As C19 Vaccinated - EDTA And Vitamin C Prevents Blood Clotting In C19 Unvaccinated

What Happens To A Human When There Is More Hydrogel, Nanotechnology And Synthetic Biology Then Blood? And A HAARP Warning BY Cathy O'Brien From 1990's - Is 4Hz Accelerating This Process?

Blood Clot Analysis From Living & Deceased Individuals Shows Consistent Findings: A Rubber Like Polymerized Protein - Microscopy Shows Filaments. Part 1 of 3 - Dr. Ana Mihalcea With Clifford Carnicom

Blood Clot Analysis From Living And Deceased Individuals Near Infrared Spectroscopy Shows Multiple Hydrogel Polymer Components - Part 2 of 3 - Dr. Ana Mihalcea With Clifford Carnicom

Blood Clot Analysis From Living And Deceased Individuals - Preliminary Chemical Solubility Testing - Part 3 of 3 - Dr. Ana Mihalcea With Clifford Carnicom

The original research by Clifford Carnicom has similar results. Vitamin C had a very strong inhibition of replication of the CDB/ Morgellons which we have correlated to the rubbery clot development in the studies outlined above. NAC was also effective with Glutathione having some effects compared to no treatment but being less effective than the other two. Here are Cliffords historical articles:

Growth Inhibition Achieved - Original article on Vitamin C, NAC, Glutathione testing

Morgellons : A Working Hypothesis – PART III POTENTIAL MITIGATING STRATEGIES (RESEARCH BASED)


Image: CDB cultures and inhibitory effects of Vitamin C, NAC, Glutathione by Carnicom Institute

In the first image above, I show blood drawn from two C19 unvaccinated individuals mixed with different compounds - ages 40’s and 50’s. The blood was left to sit overnight before the syringes were examined. Both patients have been on detoxification strategies. This is the first set of C19 unvaccinated control blood, a rubbery clot clearly developed. I want to reiterate how abnormal this is and absolutely catastrophic for the human species. If you count medical school, I have been in the medical field now for 30 years. I have never ever seen blood turn into rubber until this past year, when I started looking at this nanotechnology and synthetic biology phenomenon - after the C19 bioweapon roll out. I was just part of a court hearing and will be part of the upcoming trial as a witness. Is there someone that comprehends the catastrophic nature of this single finding in clinical practice? Someone who can look at this and via sheer logic understand the ramifications of what this means - that unvaccinated people are developing the same rubbery clots as the C19 injected due to shedding?


Image - courtesy Karen Kingston, FDA guidance on shedding

Still, most people ignore these findings and think they are safe, even though more and more people, including the unvaccinated are developing turbo cancers and are dying suddenly. I believe the reason for this development can be found in the blood, and if not mitigated or ignored, can have detrimental health effects.


Image: C19 Unvaccinated blood control shows yellow rubbery hydrogel development

In the video below you see the sample of 30 ml of C19 unvaccinated blood mixed with 1 cc Glutathione 200mg/ml concentration:

Here is Methylene Blue, a molecule used for anti aging purposes, a precursor for Hydroxychloroquine. I use Methylene Blue a lot due to its ability as a direct electron donor bypassing mitochondrial dysfunction and its capacity to increase oxygen delivery between 30-70 %. You can see that the hydrogel development was inhibited, while the blood clot part was still rubbery. Normally you should be able to break apart a clot with your hands and I am not able to do anything to this rubber.

This is C19 unvaccinated blood from a second person - this time mixed with Alpha Lipoic Acid 1 ml - Concentration 200mg/ ml. No inhibition of hydrogel seen.

Here is it mixed with Plaquex, a patented form of Phosphatidylcholine that reverses Atherosclerosis. While these molecules do not inhibit growth after blood is drawn, I still highly recommend them for other functions. Plaquex has been shown to work amazing in reversing oxidative stress affecting the cell membranes of red blood cells and appears to make them more resistant to the assault of the CBD/ microbots. I have shown this in previous live blood analysis.

This is the control sample without anything in it except C19 unvaccinated blood. Huge hydrogel rubbery clot developed that sticks to the syringe.

I tested Glutathione again, this is actually my third time and it does not inhibit the hydrogel/ CDB growth.

Summary:

I am still exploring mitigation strategies and test molecules that I have been using already for my detoxification protocol to help support the body. In my clinic, I have seen that oral supplements must be supported with iv therapy - if you take supplements my mouth only, even EDTA - it is simply not enough anymore. A maintenance with oral EDTA/ Minerals and regular IV therapy at this time of high contamination delivers best results. Everything and everyone is so contaminated, that the best strategy is to detox with EDTA and Vitamin C while using all the other supplements to enhance immune function. I still use Nattokinase, but you have seen in my article above, that does not prevent the hydrogel rubbery clots. The two individuals who’s blood I tested here were both on 20.000 Units of Nattokinase daily. I use Methylene Blue at a dose of 50mg to 100mg daily depending on the person - from compounding pharmacies if no contraindications exist. You can see from the blood results, that Methylene Blue is a significant contender in helping us against these rubbery clots.

I wanted to mention that persistence, determination and a fighting spirit is absolutely necessary to maintain your health. Many people do not even fight for their life, they just ignore the threat. Some people give up at first defeat, because it is too hard and inconvenient. What is still coming in illness in death will be unfathomable for most people’s comprehension. People do not want to hear that because it is too uncomfortable. I suggest you start fighting for your life and rearranging priorities. I have seen many people crushed who just wanted to keep ignoring shedding and partying on - until they got their very advanced cancer diagnosis or their blood clotting event. Its everywhere, in all age groups. And those cancers grow fast and furious. I have already had many unvaccinated patients die from shedding. I know because their cancer came after excessive exposure to vaccinated people. Open your eyes and see it. And then do what you can to save your own life and clean your own blood.

In our meeting with the attorney today we were discussing the timeline of getting a verdict for the main trial. It was estimated at a year.

I tell you, many people may not have a year with this in their blood and without mitigation strategies. That is not science fiction or fear mongering on my part, as much as my colleagues deny my findings. Look at the rubber clots and contemplate the potential outcome on a human of any age with this in their body. Despite the C19 bioweapon uptake going down, the blood contamination of people is going up, indicating persistent replication of synthetic biology and nanotechnology. I find this CATASTROPHIC in what it suggests for the future of humanity.

Decontaminating The Blood From Synthetic Biology Hydrogel With EDTA Chelation - Live Blood Documentation

THERE IS HOPE - EDTA CHELATION WORKS and What Really IS COVID???

Hope Wins: Before And After Intravenous EDTA Chelation + Vitamin C - Dark Field Live Blood Analysis - A Case Report


Med Five Patented EDTA

Kelly Oakes - Solving a long-standing problem in transmission electron microscopy:

https://phys.org/news/2023-11-long-standing-problem-transmission-electron-microscopy.html

#ScanningPrecession #ElectronDiffraction #SPED #DifferentialPhaseContrast #DPC #STEMDPC #STEM #TEM #ProbeWandering #ElectronMicroscopy #Microscopy #Physics

California Institute of Technology - Quantum entanglement of photons doubles microscope resolution:

https://phys.org/news/2023-05-quantum-entanglement-photons-microscope-resolution.html

#QuantumEntanglement #Entanglement #Biphoton #Photons #DawesLimit #HeisenbergLimit #OpticalResolution #Optics #QuantumMechanics #QuantumMicroscopyByCoincidence #QMC #LASER #Microscopy #QuantumPhysics #Physics