Holistic Health

December 26, 2022 7:42 am

HOW TO DETOXIFY THE BODY FROM THE GRAPHENE OXIDE FOUND IN THE VACCINES Here is a quick summary, along with a recommended nutrition protocol for people who received the injections and need to neutral... View MoreHOW TO DETOXIFY THE BODY FROM THE GRAPHENE OXIDE FOUND IN THE VACCINES Here is a quick summary, along with a recommended nutrition protocol for people who received the injections and need to neutralize the graphene oxide in the body. Graphene Oxide (GO) discoveries: GO fibres are in plastic masks. GO fibres are on PCR test swabs. GO is in all Covid-19 vaccines. GO creates thromboses. GO causes blood clots. GO disrupts the immune system. GO can trigger a cytokine storm. GO toxicity can instigate pneumonia. GO creates a metallic taste in the mouth. GO causes inflammation of the mucous membranes. GO produces a loss in the sense of taste and smell. GO is magnetic (especially at the injection site.) GO blocks detoxification in the body by blocking glutathione. GO may be activated by 5G frequencies. GO was already included as an adjuvant in the flu shots in 2019. GO passes thru the blood-brain barrier. So graphene oxide can act as a solo trigger for most COVID symptoms. This is not a VIRUS or spike protein, but a chemical warfare agent. Nutrition Protocol To Deactivate Graphene Oxide (Urgent for all who were injected with the â€œCovid vaccineâ€) Glutathione Suramin (which has been used to treat sleeping sickness and autism). Pine needles are loaded with suramin, vitamin C and A. Make pine needle tea. Diatomaceous earth Zeolite Quercetin or Hydroxychloroquine (HCQ): Quercetin works like HCQ. One of its mechanism of action is that it blocks the â€˜virusâ€™ (with spikes around it) from attaching. These two supplements will help with spike protein damage and apply to most organs of the body but not all. Ivermectin: Ivermectin blocks spike proteins from attaching to the cell membrane. (Alternative is Neem Oil.) Dandelion Leaf: Dandelion Leaf Extract blocks spike proteins from attaching to cell membrane. Chlorine Dioxide (CDS) or Miracle Mineral Supplement (MMS) Chlorine dioxide neutralizes and eliminates the spikes. Between a blocker (HCQ, Quercetin, IVM, Dandelion, etc), and a neutralizer (CDS/MMS, Ozone, NAC), I prefer a neutralizer because it eliminates the spikes rather than merely blocking it. (I suggest) alternating this with NAC (in case there is Graphene Oxide transmission). I worry that the blocked spikes will continue to circulate and reach the brain and cause all sorts of mental illnesses (Dr. Malone, Bahkdi, Tenpenny, Mikovits). Most people prefer Chlorine Dioxide (CDS) to de-magnetize the body and NAC along with fennel and star anise teas or white pine tea. You can buy the seeds and stock up as the FDA is trying to ban some herbs and seeds. Chlorine dioxide neutralizes the spikes. NAC or Glutathione neutralizes the GO, as well as spikes to some extent. For protection, I will alternate use of Chlorine dioxide and NAC. That is until I know more. Summary of the Spike Protein and Graphene Oxide Detoxification Protocol via David Wolfe This is the updated Nutrition protocol to protect those whoâ€™ve been injected with spike protein, graphene oxide and mRNA. The same protocol is also useful to protect those concerned with the spike protein and graphene oxide shedding coming off those whoâ€™ve been injected. We now have evidence of the latest injections containing: mRNA, spike protein, graphene oxide, SM-102, and numerous other potentially toxic substances. Also, some â€“ but not all â€“ injections appear to be higher in graphene oxide and some appear to be saline placebos. We also have evidence that this protocol works as we are compiling the testimonials of numerous people who were hospitalized or injured after injection and have recovered. If you know someone who has been injected and requires help, please provide them with this Nutrition Protocol: Colloidal Silver (1-6 drops per day, depending on degree of exposure) (Coloidial silver blocks the sulfur-bearing protein on the spikes from entering the cell. Sulfur-rich amino acids on the spike protein interact with silver causing them to fold incorrectly). NAC (N-acetyl cysteine) (accelerates detoxification and is considered a producer of the super detoxifier glutathione in the body) Dosage: 1200-2400 mg per day on an empty stomach. NAC is recommended to detoxify graphene oxide and SM-102. NAC is tough to find after the FDA recently made it illegal to purchase over the counter in the USA. Zinc (30-80mg per day depending on immunological pressure) Vitamin D3* (10,000 IUâ€™s per day) Lypospheric Vitamin C (30ml, twice daily)* Quercetin (500-1000 mg, twice daily)* Iodine* (dosage depends on brand, more is not better. Iodine is a product you have to start with small dosages and build up over time. PQQ* (20-40 mg per day) Shikimate Main Sources: Fennel and/or Star Anise Tea: These are also an excellent source of shikimate or shikimic acid (which is known to neutralize the spike protein) C60 (1-3 droppersfull per day): One of the issues we are seeing with those who have been injected is disturbances in their energetic field (magnetism) and hot spots of inflammation. C60 is a rich-source of electrons and acts like a fire extinguisher to inflammation and simultaneously (because it bio-distributes throughout the body) drives a normalization of electron flow throughout the body. In this category, we offer two products, the traditional C60 product* is made by yours truly and the C60 SuperConcentrate* is made by a carbon scientist friend of mine and contains a higher concentration of electrons. C60 is recommended to neutralize spike protein, detoxify graphene oxide and SM-102. Charcoal (2-4 capsules a day): Charcoal is the pre-eminent detoxifier and when taken on an empty stomach, works its way down into the intestines and activates a blood purification process known as â€œinterstitial dialysisâ€. Our Kohlbitr* product is the premier activated coconut charcoal in the world and we also now offer the more gentle birch charcoal.* Citrus fruit (especially blood oranges, due to their high hesperidin content â€” hesperidin is a chalcone like quercetin that deactivates spike protein) Peppermint (very high in hesperidin) Superherbs to help disable spike protein: Schizandra Berry* (high in shikimate) Triphala formulations: In Sanskrit, the word Triphala means â€œthree fruitsâ€: a combination of Indian gooseberry (Emblica officinalis), black myrobalan (Terminalia chebula) and belleric myrobalan (Terminalia belerica). The terminalia fruits are rich in shikimate. St. Johnâ€™s Wort (shikimate is found throughout the entire plant and in the flowers) Comfrey Leaf (rich in shikimate)

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sha B

You said "We also have evidence that this protocol works as we are compiling the testimonials of numerous people who were hospitalized or injured after injection and have recovered" Will these testimonies be coming out soon on this group?

March 9, 2024

Curtis McMurray

January 2, 2023 10:36 pm

Dr. Anaâ€™s Newsletter Upgrade Sign in EDTA Chelation Dissolves the Artificial Intelligence Magnetic Hydrogel Weapon Patent Review Shows Hopeful Data... View MoreDr. Anaâ€™s Newsletter Upgrade Sign in EDTA Chelation Dissolves the Artificial Intelligence Magnetic Hydrogel Weapon Patent Review Shows Hopeful Data Ana Maria Mihalcea, MD, PhD Oct 28 70 42 I have been advocating for months that EDTA Chelation as a treatment solution for the C19 injected, as it effectively removes metals, and can detoxify the body even from Graphene. As a certified Chelation practitioner, it is evident to me that EDTA is needed for the environmental bombardment of this AI parasitic life form, that we are exposed to via C19 injections, chemtrails, vax shedding, food, cosmetics, medication and many other avenues. Dr. Anaâ€™s Newsletter Is EDTA Chelation and Intravenous Vitamin C An Additional Hopeful Medical Treatment For C19 Vax Injury? How Can Toxic Metals Found in C19 Shots Synergistically Harm The Body? There has been much discussion recently regarding the toxic metal self-assembly nanoparticles in the C19 shots and their evidence in Live blood analysis of the C19 injected. The recent German Vaccine Workgroup report found extensive metals. Italian researchers found these self-assembly nanoparticles in the Live blood analysis of C19 injected peopleâ€¦ Read more 2 months ago Â· 26 likes Â· 8 comments Â· Ana Maria Mihalcea, MD, PhD We now know that the self-assembly nanotechnology that grows to micrometer size grows out of the lipid nanoparticles. Karen Kingston found the patents: Cell-friendly inverse opal hydrogels for cell encapsulation, drug and protein delivery, and functional nanoparticle encapsulation My colleague Dr. Shimon Yanowitz showed that the metal nanoparticles self assemble out of the Liposomes. Dr. Anaâ€™s Newsletter Self-Assembly Nanostructures in C19 vials - Documented Growth and Self Assembly out of Liposomes From Thawing at Room Temperature to Incubation at Body Temperature for 7 days Please see our video link here: Self Assembly Nanostructures Dr Ana Mihalcea and Dr. Shimon Yanowitz Dr Shimon Yanowitz is an independent scientist and researcher with background in electrical engineering and computer science from Israel. Shimon analyzed Pfizer BioNTech, Moderna, J&J and Astra Zeneca vials and incubated them at body temperature finding eâ€¦ Read more 2 months ago Â· 28 likes Â· 19 comments Â· Ana Maria Mihalcea, MD, PhD The only thing that is not consistent is the scale. We see micrometer size and they speak of nanometer size. This shows that the self assembly already is active upon thawing of the C19 vials. The patent states: CELL-FRIENDLY INVERSE OPAL HYDROGELS FOR CELL ENCAPSULATION, DRUG AND PROTEIN DELIVERY, AND FUNCTIONAL NANOPARTICLE FIELD OF THE INVENTION The invention relates to polymer scaffolds for cell-based tissue engineering. BACKGROUND Tissue engineering is an approach for regeneration, replacement, and improvement of the functions of damaged tissues by manipulating materials according to the specific structure or function of the desired tissues. Porous and biodegradable polymer scaffolds, e.g., three dimensionally interconnected scaffolds, are utilized as a structural supporting matrix or as a cell adhesive substrate for cell-based tissue engineering. A highly open porous structure with interconnected pores is required to achieve sufficient cell seeding and migration within the scaffold, as well as to facilitate mass transfer of nutrients, oxygen, and metabolite waste for sequential proliferation and differentiation of large quantity of cells. Current approaches to generate porous networks in polymer scaffolds include gas foaming, salt leaching, and freeze drying; however, the limitations of those processes include irregular pore sizes, shapes, and structures, as well as limited interconnectivity. As such, there is a pressing need in the art to develop improved structured polymer scaffolds with interconnected pores. SUMMARY OF THE INVENTION The invention described herein provides the fabrication of cell- friendly inverse opal hydrogels that also allow cell-encapsulation in the hydrogel matrix. An inverse opal hydrogel scaffold device comprising a polymer matrix and a sacrificial porogen in which the porogen comprises an ionically-crosslinked polymer, a thermosensitive polymer, a thermoresponsive polymer, a pH-sensitive polymer, or a photocleavable polymer. The polymer matrix is made of a durable polymer relative to the sacrificial porogen such that the polymer matrix withstands physical or chemical changes that cause porogen sacrifice. For example, polymer matrix is covalently crosslinked, withstands a change (e.g., increase) in temperature, withstands a pH change (e.g., decrease) or change in ionic strength or composition (e.g., contact with a divalent cation chelator), or withstands exposure to light (e.g., UV light). For tissue engineering and cell scaffold applications, the polymer matrix further comprises an isolated cell, e.g., a eukaryotic cell. By "isolated cell" is meant a cell that has been separated from the other cells, components, and/or environment that naturally accompany it. Alternatively, the matrix contains prokaryotic cells such as bacteria. For example, the polymer matrix is crosslinked and comprises an isolated cell encapsulated in the crosslinked polymer matrix. An exemplary polymer matrix comprises a synthetic polymer such as one that is covalently crosslinked. Examples of polymer matrices include poly(lactide-coglycolide) (PLGA; a copoly lactic acid/glycolic acid polymer), poly(acrylic acid), polyethylene glycol (PEG), poly (vinyl alcohol), or polyphosphazene. The sacrificial porogen comprises an ionically-crosslinked polymer, a thermosensitive polymer, a thermoresponsive polymer, a pH-responsive polymer, or a photo-cleavable polymer. Exemplary polymers for a porogen include alginate, collagen, gelatin, fibrin, agarose, hyaluronic acid, or chitosan as well as thermosensitive polymer such as agarose, gelatin, or collagen, poly(N-isopropylacrylamide), poly(N-ethylacrylamide), poly(N- cyclopropymethacrylamide), poly(N-methyl-N-ethylacrylamide), poly(N- acryloylpyrrolidine) , poly(N-ethy lmethacry lamide) , poly(N-cy clopropylacry lamide) , poly(N-cyclopropylacrylamide), poly(N,N-diethylacrylamide), poly(N- isopropy lacry lamide) , poly(N- inylcaprolactam) , poly(N-n-propy lmethacry lamide) , poly(N-methyl-N-isopropylacrylamide), poly (N-n-propy lacry lamide), poly(N-methyl-N-n- propy lacry lamide), and poly(N-acryloylpiperidine). Hydrogel (also called aquagel) is a network of polymer chains that are hydrophilic, and are sometimes found as a colloidal gel in which water is the dispersion medium. Hydrogels are highly absorbent (they can contain over 99% water) natural or synthetic polymers. Hydrogels also possess a degree of flexibility very similar to natural tissue, due to their significant water content. Hydrogel shaped as an inverted opal exhibits much higher swelling ratios, and its swelling kinetics is an order of magnitude faster as well. The engineered scaffolds (i.e., inverse opal hydrogels) described herein possess desirable mechanical and optical properties that can facilitate tissue regeneration while allowing for continuous high-resolution optical monitoring of cell proliferation and cell-cell interaction within the scaffold. Methods of producing an inverse opal hydrogel with open, interconnected pores are carried out by compressing a plurality of template porogen particles into a mold, and subsequently adding a composition comprising a polymer solution and a plurality of cells to the interstitial space between template porogen particles in the mold to polymerize the template porogen particles. The template porogen particles are removed from the mold, thereby producing an inverse opal hydrogel with open, interconnected pores, wherein the cells are encapsulated in the inverse opal hydrogel. The template porogen particles are removed without using toxic organic solvents or lyophilization. For example, thermosensitive hydrogel beads are removed by controlling the temperature to change the solid phase of the beads. The template porogen particle is an ionically crosslinked polymer, a thermosensitive polymer, a thermoresponsive polymer, a pH-responsive polymer, or a photo- cleavable polymer. For example, the ionically crosslinked polymer is alginate. The ionically crosslinked polymer is removed by adding a metal-chelating agent selected from the group consisting of citric acid, ethylenediamine, ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTP A), and N,N-bis(carboxymethyl)glycine (NTA). Suitable thermosensitive polymers include agarose, gelatin, and collagen. The thermosensitive polymer is removed by increasing the temperature of the polymer, thereby altering the phase of the polymer to liquid phase. Examples of photocleavable polymers include chromophore-based crosslinkers for photodegradable hydrogels, (4-vinylpyridine) (P4VP) and poly (methylmethacrylate). Methods of producing an inverse opal hydrogel with open, interconnected pores are carried out by compressing a plurality of template porogen particles into a mold, adding a composition comprising a polymer solution and an agent to the interstitial space between template porogen particles in the mold to polymerize the template porogen particles, and removing the template porogen particles, thereby producing an inverse opal hydrogel with open, interconnected pores. The agent is selected from the group consisting of a drug, a nanoparticle (e.g., magnetic nanoparticles or gold nanoparticles), a growth factor (e.g., vascular endothelial growth factor (VEGF), platelet derived growth factor (PDGF), brain derived neurotrophic factor (BDNF), epidermal growth factor (EGF), or fibroblast growth factor (FGF)), a cytokine (e.g., interferon gamma (IFN-Î³), erythropoietin (EPO), thrombopoietin (TPO), interleukin-1 (IL-1), IL-4), a chemokine (e.g., a CC chemokine, a CXC chemokine, a C chemokine, or a CX3C chemokine), a hormone (e.g., insulin, growth hormone, vasopressin, testosterone, or Cortisol), a protein, a nucleic acid, or a small molecule. In one example, nanoparticles are encapsulated within the hydrogel matrix, and cells are dispersed within the open-interconnected pores. Example 1 : Alginate Beads as a Sacrificial Template Described herein is an example of the fabrication of a cell- friendly inverse opal hydrogel. Alginate beads, formed using Ca2+-crosslinking were used as the porogen, and 50 mM EDTA solution, a metal chelating agent, was used as the template removal solution. To evaluate if EDTA can dissolve the alginate beads efficiently, three different sized alginate beads were prepared using 2% alginate solution in 100 mM Ca2+ solution (Figure 3, upper row). Rhodamine-labeled bovine serum albumin (BSA) was encapsulated in alginate beads to visualize the beads and their dissolution. The resulting alginate beads were incubated in 50 mM EDTA solution under shaking. After 20 min, all alginate beads dissolved in EDTA solution and lost their spherical morphology, and this resulted in a pink solution due to released rhodamine-labeled BSA from alginate beads (Figure 3, lower row). This demonstrates that the alginate beads were used as sacrificial template by using EDTA as leaching solution. Figure 3 is a series of photomicrographs demonstrating that ethylenediaminetetraacetic acid (EDTA) efficiently dissolves alginate beads in IOHs. Figure 5 a is a series of photomicrographs showing cell viability after treatment with EDTA for up to 3 hours. Figure 5b is a bar chart showing about 98% viability of cells after 3 hour incubation in EDTA. Figure 6a is a series of photomicrographs showing cell viability after treatment with EDTA for up to 7 days. Figure 6b is a bar chart demonstrating the proliferation of cells encapsulated in IOHs. Example 3: EDTA is Non-Toxic to Cells Encapsulated in IOHs To evaluate if incubation in EDTA solution is toxic to cells, cell viability was checked after incubation in 50 mM EDTA solution. Mouse mesenchymal stem cells (MSCs) were cultured in a flask, and incubated in a 50 mM EDTA solution for 10, 30, 60, 120, or 180 min. Subsequently, the viability of cells was measured with a live/dead cell assay by using calcein AM and ethidium homodimer-1. Although the cell morphology changed to a round shape, the representative fluorescent images of the live/dead assay showed that there was no significant toxicity of the EDTA solution to the cells for up to 3 h incubation (Figure 5a). Quantitative analysis also showed -98% viability even after 3h incubation in EDTA solution (Figure 5b). Based on these observations, incubation of the gels in 50 mM EDTA solution for up to 3 h to remove alginate beads was determined as a nontoxic process to cells encapsulated in IOHs. Ionically crosslinked hydrogel beads (e.g., alginate) are removed by using various metal-chelating agents including citric acid, ethylenediamine, ethylenediammetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTP A), N,N- bis(carboxymethyl)glycine (NTA), etc. The chelating agents bind with metal ions used as the crosslinker of templating beads, which results in the generation of pores via the dissociation of metal ions and polymers forming beads. For example, various chemical drugs including small molecules and functional proteins (growth factors, cytokines, chemokines, hormones, etc) are mixed with the polymer precursor solution to be added into the template beads in the mold. After polymerization of the polymer precursors and removal of the template beads, the encapsulated molecules are released slowly. The release profiles depend on crosslinking density, the affinity of molecules to the polymer chain, the size of molecules, etc. In this context, the inverse opal hydrogels are used as delivery systems for the cells encapsulated in the hydrogel or the cells outside the hydrogel. The methods described herein also encapsulate functional nanoparticles to actuate the porous hydrogel systems to release cells, drugs, proteins, and growth factors on demand. The nanoparticles are encapsulated in the hydrogel in a similar manner in which cells and drugs are encapsulated. Specifically, the functional nanoparticles are mixed with polymer precursors and added into the template beads in the mold. For example, magnetic nanoparticles or gold nanoparticles are encapsulated in the polymer matrix and the resulting porous hydrogels are responsive to an external magnetic field or light, respectively. The guest molecules are released upon detection of the external stimulus. In the case of magnetic nanoparticles, the external magnetic force modulates the volume of pores in the inverse opal hydrogel due to its high porosity. The guest molecules encapsulated or seeded in the inverse opal hydrogels are released by the mechanical forces via convection. In addition, both magnetic nanoparticles and gold nanoparticles are used as hyperthermic moieties. Magnetic nanoparticles and gold nanoparticles generate heat by alternating magnetic fields and irradiation with lasers, respectively. Thus, both magnetic and gold nanoparticles allow thermal motion of the polymer matrix and the encapsulated guest molecules, which accelerates the release rate of guest molecules. Summary and next steps: This patent shows that the Hydrogel can be dissolved with EDTA Chelation. The metal nanoparticles that are in the Hydrogel to change its magnetic properties and regulate the release of guest molecules, for example toxins or other substances, can also be removed from the body by EDTA. It is my suspicion that the ribbons we see in live blood analysis of C19 injected people as well as in the un injected via shedding and environmental exposure are made of this hydrogel that also can have carbon nanotubes in various forms associated with it as well as metallic nanoparticles. WE MUST TEST THE LARGE CLOTS FOUND IN THE DECEASED INJECTED TO SEE IF THIS IS AI HYDROGEL AS KAREN KINGSTON SUGGESTS. My suspicion is that she is absolutely right. Fibrin can be one of the guest molecules and the metal particles of Aluminum and Tin that Mike Adams found in his analysis, also suggest what is found in this patent - a hydrogel polymer with metal nanoparticle enclosures. EDTA Chelation should be utilized in all vax injury treatment protocols and prophylactically for the injected and un injected alike - to treat this unprecedented attack of diabolical Artificial Intelligence parasitic life form weapon upon humanity. All of us medical practitioners who do Live blood analysis need to look at before and after samples to see if dissolution of ribbons occurs and how many treatment it takes to clear the blood. Routine repetition of EDTA Chelation IV Therapy should be done to prevent re accumulation of this artificial life form in the body, in particular since the exposure now is coming from literally everywhere. If you have not yet seen this brilliant interview of Karen Kinston with Maria Zeee, please do so right now : Uncensored: Karen Kingston â€“ People Now Connected to the Demonic Realm Through COVID-19 Injections, Nanotech STOP THE SHOTS. STOP GEOENGINEERING. STOP 5G. STOP POISENING OUR FOOD AND WATER SUPPLY. STOP POISENING THE BODY WITH BIG PHARMA TOXINS. Special Thanks to Karen Kingston for her brilliant work in finding these patents. Dr. Anaâ€™s Newsletter is a reader-supported publication. To receive new posts and support my work, consider becoming a free or paid subscriber. Upgrade to paid Like Comment Share 70 likes 42 Comments Write a commentâ€¦ Sandy K Oct 28 Thank you, Dr. Ana! Please keep your readers informed regarding EDTA chelation. So many people have been injected with this bioweapon, and they are scared. Anyone who is practicing any kind of healing work is looking for ways to help them. So many are unable to accept the truth, but those who are willing to do so should have an option to reverse as much as possible the damages. I worked in veterinary medicine for many years and am now an ecologist, but I would still want to lead people to potential help. 8 Reply Gift a subscription Collapse 2 replies mejbcart Writes mejbcartâ€™s Newsletter Nov 6 Liked by Ana Maria Mihalcea, MD, PhD mejbcart, who 'Writes mejbcartâ€™s Newsletter' wrote on Oct 11 athttps://anamihalceamdphd.substack.com/p/conversations-with-pharma-insider/comment/9667888 : "EDTA in addition to metal chelation, dissolves 'the hydrogels', it can FUNCTIONALIZE graphene. What really decomposes grahene lattice, drills HOLES IN IT, is HYDROGEN PEROXIDE. " That was more than week ago, but I was writing about that essential EDTA hydrogels degrading property for the last 2 YEARs... Seems like nobody read that or listened, now comes the patent from the same 2011 book about synthetic biology, I was citing all these years.... 1 Reply Gift a subscription Collapse 1 reply 40 more commentsâ€¦ Alarming New Report from Working Group of Vaccine Analysis in Germany and Other Countries Vaccines Must Be Stopped Immediately! ANA MARIA MIHALCEA, MD, PHD AUG 8 146 67 Computerized Thermographic Imaging and Live Blood Analysis Post C19 Injection Shocking New Images - Stop The Shots Now! ANA MARIA MIHALCEA, MD, PHD AUG 22 184 186 Thoughts and Comments about "Died Suddenly" Documentary Please click on this link to see this brilliant documentary: Died suddenly full documentary I hope people have watched Stew Peters new excellentâ€¦ ANA MARIA MIHALCEA, MD, PHD NOV 25 147 113 See all Ready for more? Subscribe Â© 2022 Ana Mihalcea, MD, PhD Privacy âˆ™ Terms âˆ™ Collection notice Publish on Substack Get the app Substack is the home for great writing

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