Defeat And Excrete The Toxic Graphene

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Reversing the known damage from graphene oxide.

A share of the formula I finally hit upon to defeat the graphene.

Yes, glutathione I shared was helpful, one of the most helpful glutathione supplements I’ve ever used. Most other things did little to nothing, that is Sodium Ascorbate (Vitamin C), zinc, and just about everything else I tried except time. I haven’t seen any evidence that anything aside from glutathione works specifically for graphene detox. Quite the opposite, they can’t wait to combine graphene with everything and place it in every delivery system to get it in you (including e-cigarettes) to bio ‘sensor’. I did also add Dandelion Tea but before trying this. Experience tells me to look to nature to see how nature is degrading this toxic chemical so that is usually how I proceed.

As shown in this post one of the things that must be done is to get the immune system to ‘see’ again as graphene is a TLR4 pathway intoxicant that induces necrosis in macrophages.

Upon uptake into macrophages, GO accumulated primarily in cytoplasm causing dramatic morphologic alterations and a significant reduction of the macrophagic ability in phagocytosis.

Macrophagic uptake of GO may not be required for induction of necrosis. GO exposure also caused a large increase of intracellular reactive oxygen species (ROS), which contributed to the cause of cell death.

After five weeks in I was healing but the thought of spending three months as they claim to rid my body of this toxicity I decided that was not good enough for me so…

I knew it was back to making maf for me but I had to be sure it worked fast and it did. Since I have extensive knowledge on all things milk I created this new formula for myself.

I was pleasantly surprised that newer glutathione supplements actually seemed to work; above is a reduced form.

Graphene Excretion & Detoxification

Graphene is excreted via the lungs and kidneys and eventually via the lymphatic system provided the immune system is capable of doing this; which it has a great deal of trouble doing as graphene accumulates deep in the lungs and disables and suppresses the immune system. It appears a compensatory mechanism (the body always has compensatory mechanisms) for dispersing graphene is to draw fluid from other tissues. Graphene disperses in water and it appears it has a tendency to aggregate, especially in lungs. This is the reported cause of the unique bilateral pneumonia. Graphene appears to also deplete hemoglobin, non oxygen restorative; as well as having magnetic capabilities along with being a conductor, amplifier and appears to have a polarizing effect that could have a devastating effect on cell signaling. White blood cells are inactivated and in the injected are almost non existent as shown by microscopy. It appears as though the immune defense system is completely disabled. It takes up to 8 weeks for complete replacement of red blood cells and according to some research up to three months to excrete graphene.

In essence; imperative to activate all systems capable of detoxification before too much damage (necrosis) and apoptosis occurs.

I’ve done enough learning to know I do not want this damage to accrue with the time it naturally takes to excrete. No way.

Maf video. Sorry, early morning dentist appt. today. Not my usual self. Edited to adjust audio and then realized it wasn’t the audio, it was my earphones not working properly so choose whichever sounds best to you.

So here is this formula I created to ensure all forms of macrophage activation and works super fast.

1. Lactase

One scoop.

Why lactase?

This ensures that with the proper enzymatic catalyst I will be reducing to galactose without having to reduce from milk which is fine and it will do that eventually but this is faster. Lactase is important for organisms as a key provider in the production of energy and a source of carbons through the break down of lactose to galactose and glucose.

2. Acid Whey

At least 1/4 cup. Must be acid whey from kefir or yogurt, not cheese whey.

Why acid whey?

Super fast absorption. You can find more benefits of acid whey here in my book, Chapter 4. In my humble observation, helps to activate a different macrophage pool in the innate immune system. I used the whey from my home made kefir because I know it separates, I keep it in a glass bottle and I can just pour the acid whey off the top. Lifeway Kefir does separate but I did not use this, you can try it, keep in a glass container for a day or so, that way you can be sure it separates. You can separate whey from yogurt but I did not do this either, you can also try this. I would be adding a Raw Probiotic to ensure plenty of organisms similar to home made kefir. A pic can be found in the link.

The advantage of my home made kefir whey is that I know it contains many more organisms than Lifeway kefir, the same as found in the kefir itself as it is much more potent than store bought.

Does Lifeway kefir work? Yes, it does so in no way do I want to imply that it doesn’t, some things are just a matter of degree as to how much effort or time you have to accomplish a result.

Graphene Is Being Cross Transmitted From The Injected – Must See Blood Cells

Acid whey activates CNS macrophages

Microglial cells are the resident macrophages of the central nervous system (CNS), including the retina, and play a pivotal role in innate immune responses.

Despite being cells of the mononuclear phagocyte lineage, their CNS-specific location and morphology clearly distinguishes them from other macrophage populations.

Acid whey reverses neurodegenerative and retina inflammation by activating CNS macrophages.

Milk whey protein combats iron overload oxidative stress and DNA damage. Whey protein combats ROS.

High phagocytic clearance of apoptotic debris by microglia is regarded as an important anti-inflammatory feature. Whey acidic protein inhibits pro-inflammatory gene expression and increases phagocytic uptake of apoptotic debris.

3. Yogurt – Whole Milk

I used a few tablespoons in a glass.

4. Colostrum

Tsp. to a tbsp. is fine.

5. Raw Honey

This is optional but it provides more enzymes.

6. Digestive Enzymes

Also optional but digesting colostrum completely provides many benefits. Since this brand has lactase and I had it on hand I used it before I bought lactase as a stand alone. Digestive enzymes are not suitable for long term use.

7. Kefir

I used a few tablespoons of my raw kefir.

8. Milk

Whole fat regular pasteurized milk. If you can tolerate raw milk, fine but since graphene is an immune blinding/suppressing intoxicant as seen here in ‘vaccinated’ polluted blood (numerous bacteria and parasites), I wouldn’t be taking any chances, however transmitted injection blood is definitely not in the same state aside from the macrophages being inactive.

By the time all ingredients were added I probably had an 8-12 oz. quantity of ingredients. I didn’t do much measuring.

9. Cod Liver Oil

Last optional. If you feel you do not have enough vitamin D. A staple in my house. Never use either form of synthetic D.

About the formula:

Will this work for you? I won’t make any promises but I don’t see why it wouldn’t regardless of what immune dysfunction one is trying to recover from, it is simply a faster way to make an maf with basic chemistry to ensure a more rapid catalytic enzymatic conversion. I had all things on hand; my usual daily drink and the only new purchase was lactase. I purchased the glutathione almost immediately. I’ll add a video update at some point.

By day two I noticed much greater improvement especially lymphatic drainage and detox but as stated I was already well on my way just not fast enough for me and I did not want this in my system any longer. I also avoid crowds and will until all injections stop, they will however be finding new ways to ‘intoxicate’ with these chemicals, I have no doubt about that. Chemicals do not change inherent properties and no one will be developing immunity to this any more than they will to DDT or Agent Orange.

The hype about C60 (carbon nano supplement) is hype, zero safety evidence and ample evidence of cytotoxicity dependent upon cell type, exposure and concentration.

Graphene is excreted via lungs and kidneys and eventually makes its way through the lymphatic system provided the immune system is capable of doing this. Detoxification is part of a healthy immune system.

Most elderly are clearly not capable.

In fact, graphene alone negatively impacts 4 out of 10 according to studies and the same studies show that chloroquine helps attenuate the negative impact. Myeloperoxidase (MPO), is a peroxide enzyme released by neutrophils and is of little to no help if your neutrophils are being destroyed by graphene chemical intoxicants, which they are; making this a CYA statement to detract from a multiple pathway immune attack; as shown in this post and true population impact.

Graphene

Their new golden goose

In the event you think I am off track in the industrial and commercial plans they have for graphene/s and graphene derived novel chemical intoxicants; just visit this page that I found as I was looking for a cover image. It alone contains hundreds of graphene applications and feature articles.

graphene applications

Graphene Imprinting

Now everything can be ‘tagged’.

GRAPHENE CAN BE WRITTEN ON ANYTHING FORMING CIRCUITS

Synthesis and Toxicity of Graphene Oxide Nanoparticles: A Literature Review of In Vitro and In Vivo Studies

2021

Graphene oxide (GO), an oxidized derivative of graphene, is currently used in biotechnology and medicine for cancer treatment, drug delivery, and cellular imaging. Also, GO is characterized by various physicochemical properties, including nanoscale size, high surface area, and electrical charge. However, the toxic effect of GO on living cells and organs is a limiting factor that limits its use in the medical field. Recently, numerous studies have evaluated the biocompatibility and toxicity of GO in vivo and in vitro. In general, the severity of this nanomaterial’s toxic effects varies according to the administration route, the dose to be administered, the method of GO synthesis, and its physicochemical properties.

Whitewashing Liability – Sue Them

One reminder could’ve all been prevented with one sentence.

the whole scamdemic (no EUA) could’ve been stopped with one phrase (safe and effective treatment)….

Why it wasn’t. One word. Liability. Protecting criminal racketeering. They might think they have immunity (no immunity for felonies or fraud). Other GO medical products are not covered under this shield that doesn’t exist; especially one in which they broke their own contract.

If you prefer:

The bio-medical pioneers in GcMaf treatments and products, now available in the US.

Sasei Mirai Clinic, Japan. Now triple strength formula GcMaf. Post clinical trial info for the toxicity syndrome known as CV19.

Sasei Mirai

Bravo™ yogurt.

Bravo®

Alternavita: All you need to know (critical info in a nutshell)..... by focusing exclusively on these foundational health and immune development issues up to 90% of chronic conditions can be eliminated.

WHO STATEMENTS: 2017 Millennium Goal

Breastfeeding,
food (security)
and water security (sanitation)

are major protective factors against malnutrition and critical factors in the maturation of healthy gut microbiota, characterized by a transient bifidobacterial bloom before a global rise in anaerobes. Early depletion in gut Bifidobacterium longum, a typical maternal probiotic, known to inhibit pathogens, represents the first step in gut microbiota alteration associated with severe acute malnutrition (SAM). Later, the absence of the Healthy Mature Anaerobic Gut Microbiota (HMAGM) leads to deficient energy harvest, vitamin biosynthesis and immune protection, and is associated with diarrhea, malabsorption and systemic invasion by microbial pathogens. A therapeutic diet and infection treatment may be unable to restore bifidobacteria and HMAGM.

Researchers found that malnourished children’s microbiota failed to follow the healthy pattern they identified in healthy children. The microbiota of malnourished children is immature, lagging in development behind that of their healthy peers. Supplementing these children’s meals with widely used therapeutic foods that increase calories and nutrient density reduces deaths from malnutrition, but it does not fix their persistent microbiota immaturity.

“Perhaps more insidious than slowing growth is malnutrition’s effect on less visible aspects of health, including impaired brain development and dysfunctional immunity, which follow these children throughout their lives”.

The Father of The Microbiome

Dr. Jeffrey Gordon

SIBO

SIBO can cause severe malabsorption, serious malnutrition and immune deficiency syndromes in children (non breastfed) and adults.

Prognosis is usually serious, determined mostly by the underlying disease that led to SIBO.

Immunizations

The WHO recommends that immunization or treatment be orally administered due to economic, logistical and security reasons. Furthermore, this route offers important advantages over systemic administration, such as reducing side effects, as the molecules are administered locally and have the ability to stimulate the GALT immune responses (Levine and Dougan, 1998; Neutra and Kozlowski, 2006; Bermúdez-Humarán et al., 2011).

Infections

For ANY infectious or parasitic disease to start, it is ALWAYS a requisite that the host suffer IMMUNODEFICIENCY. At the same time, infectious and parasitic diseases themselves cause additional IMMUNE SUPPRESSION and more MALNUTRITION. This immune suppression is SECONDARY to the accumulation of free radicals, especially oxidizing species, that occurs during and after infectious and parasitic diseases.

Clinical Aspects of Immunology and Biochem J.

Current IBD Research 2016

Currently available treatments for IBD, which target the systemic immune system, induce immunosuppression, thereby exposing the patient to the risk of infections and malignancy. The interplay between the gut and the systemic immune system determines the final effect on target organs, including the bowel mucosa. Inflammatory bowel diseases (IBD) are associated with an altered systemic immune response leading to inflammation-mediated damage to the gut and other organs.

Clinical & Translational Immunology (2016)
Gastroenterology and Liver Units, Department of Medicine, Hebrew University-Hadassah Medical Center, Jerusalem, Israel

Most importantly, the immune modulatory agents used today for IBD do not achieve remission in many patients.

Not all IBD patients benefit from currently available drugs. Young people with IBD do not want to be on long-term drug therapy. Oral immune therapy, while not yet studied in large cohorts of patients, may provide an answer to this unmet need.

Clinical & Translational Immunology (2016)
Gastroenterology and Liver Units, Department of Medicine, Hebrew University-Hadassah Medical Center, Jerusalem, Israel

Tolerance

Tolerance is the ability of the immune system to ‘see’ and respond appropriately. Without galactose (a necessary sugar) the immune system can not 'see'. Your immune system would not be able to function without galactose Your body wouldn’t know which cells are “good” and what cells are “bad.” Your body wouldn’t know who the invaders were and which ones should be attacked by antibodies. As you will learn the importance of these ‘sugars’ in gut microbiota health is a rapidly expanding field of research, only recently discovered, including HMO's (human milk oligosaccharides).

Why galactose? Milk sugar aka lactose has been shown to be very beneficial for the human body though unlike sucrose, lactose is made up of glucose and galactose. There is no fructose in lactose. It is a healthy disaccharide sugar. Galactose is known as the “brain sugar” and supports brain development of babies and children. Galactose helps triggers long-term memory formation. Galactose has been shown to inhibit tumor growth and stop its spread, particularly to the liver. This beneficial sugar can also enhance wound healing, decrease inflammation, enhances cellular communication, and increases calcium absorption.
What does immune ‘tolerance’ mean in simple language?
Immune tolerance, or immunological tolerance, or immunotolerance, is a state of unresponsiveness of the immune system to substances or tissue that have the capacity to elicit an immune response in a given organism. The Th1 cytokine profile is vital for clearance of certain organisms and ancillary immune activity, and a limiting effect on this cytokine profile may result in reduced chances for overcoming infections especially intra-cellular organisms residing within macrophages. Effective clearance will depend on appropriate macrophage activation (which occurs through IFN≥ release by Th1 and NK cells) and production of nitric oxide. If this pathway is disrupted IFN≥ secretion is blocked, impairing macrophage activation. Persistent blockade of these inhibitory receptors has lead to the breakdown in immune self tolerance, thereby increasing susceptibility to autoimmune or auto-inflammatory side effects, including rash, colitis, hepatitis and endocrinopathies. Many drugs may cause checkpoint blockade toxicity including pharmaceutical drugs termed ‘immuno therapy’ by pharmaceutical companies, these include Mab drugs and cancer treatments. Checkpoint Inhibitor–Induced Colitis: A New Type of Inflammatory Bowel Disease? Madeline Bertha, MD MS, corresponding author1 Emanuelle Bellaguara, MD, Timothy Kuzel, MD, and Stephen Hanauer, MD ACG Case Rep J. 2017; 4: e112. Published online 2017 Oct 11. doi: 10.14309/crj.2017.112 PMCID: PMC5636906 PMID: 29043290

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