I don't know how effective this is, but after doing some research using duckduckgo.com I stumbled upon these articles that provide some ideas on how someone can neturalize the effects of vaccinations such as the COVID vaccine
Some background info on Vaccines
Many vaccine ingredients linger in the body, especially the viruses. Vaccines are cocktails of preservatives, pathogens, and adjuvants. Adjuvants are intended to stimulate your immune response to the vaccine-introduced pathogens, and they do stimulate your immune system successfully, but they destroy tissues in the process. Mercury and aluminum are used as adjuvants and preservatives, so this is a case where the treatment for the disease (the vaccine) can be worse than the disease.
It should be easy to understand now why the majority of vaccine toxins will have to be expelled from the body before the body can quit reacting to the disease the vaccine was intended to protect against.
Vaccine ingredients can also cause severe allergic reactions to certain proteins that have been injected into the body, creating an immediate allergic reaction (anaphylaxis) or a food sensitivity like a peanut or egg allergy. The body will not stop reacting to the allergens until the body has expelled the vaccine ingredients and has been returned to full health.
Vaccines severely distort the balance of minerals in the body, which causes vitamin and other nutrient imbalances as well. This leads to a weakened endocrine system, which causes hormonal imbalances and poor brain function, along with fatigue. Eventually, if the gut is not healed, the body will deteriorate into an autoimmune state. (Sometimes this happens very quickly and other times very slowly.) Almost all disease is based on inflammation. Vaccines are designed to cause an immune response, which causes inflammation. Until the vaccine ingredients are expelled from the body, the body is in a constant inflammatory state. It’s no wonder multiple sclerosis, cancer, fibromyalgia, lupus, diabetes, and so many other autoimmune diseases can be tied back to vaccinations.
https://www.organiclifestylemagazine.co ... d-children
How to Neutralize Potential Damage from mRNA Vaccines
Therapeutic Agents and Their Mechanisms
A substantial number of agents have already been found to be highly effective in resolving COVID infections, and even more are continuing to be discovered as worldwide research efforts have so intensely focused on curing this infection (Levy, 2020). Some of the most effective agents and their mechanisms of actions include the following:
Hydrogen peroxide (HP) nebulization. Correctly applied, this treatment eliminates acute COVID pathogen presence and any other chronic pathogen colonizations persisting in the aerodigestive tract. Also, a positive healing effect on the lower digestive tract is typically seen, as less pathogens and their associated pro-oxidant toxins are chronically swallowed. Stunning anecdotal evidence has already been seen documenting the ability of HP nebulization to cure even advanced COVID infections (20 of 20 cases) as a monotherapy. (Levy, 2021). All of the supporting research, scientific analysis, and practical suggestions on this therapy is available as a free eBook download [Rapid Virus Recovery] (Levy, 2021).
Vitamin C. Vitamin C works synergistically with HP in eradicating pathogens. It gives strong general immune support, while working to support the optimal healing of damaged cells and tissues. Clinically, it is the most potent antitoxin ever described in the literature, and no reports of it failing to neutralize any acute intoxication when administered appropriately have been published. Continuing persistent and highly-dosed vitamin C in all its forms will prove to be the most useful intervention when there is a large amount of circulating toxic spike protein present. Intravenous, regular oral forms, and liposome-encapsulated oral forms are all very useful in resolving any infection and neutralizing any toxin (Levy, 2002). There is also a polyphenol-based supplement that appears to allow some humans to synthesize their own vitamin C, which could prove to be of enormous protective and healing capacity with COVID patients and vaccine recipients. (
https://formula216.com/).
Ivermectin. This agent has powerful antiparasitic and antiviral properties. Evidence indicates that ivermectin binds the ACE2 receptor site that the spike protein needs to bind to proceed with entry into the cell and the replication of viral protein (Lehrer and Rheinstein, 2020; Eweas et al., 2021). Also, under some circumstances, the binding of the spike protein to the ACE2 receptor does not activate the enzymes needed to enter the cell. Possibly, ivermectin might also competitively displace such bound spike protein from the cell walls as well when a sufficient dose is taken. It also appears that circulating spike protein can be bound up directly by ivermectin, rendering it inactive and making it accessible for metabolic processing and excretion (Saha and Raihan, 2021). Where there has been mass administration of ivermectin for parasitic diseases in Africa there has also been noted a significantly lower incidence of COVID-19 infection (Hellwig and Maia, 2021). Ivermectin is also very safe when administered appropriately (Munoz et al., 2018).
Hydroxychloroquine (HCQ) and Chloroquine (CQ). Both HCQ and CQ have been shown to be very effective agents in resolving acute COVID-19 infections. They have also both been shown to be zinc ionophores that can increase intracellular zinc levels which can then inhibit the enzyme activity needed for viral replication. However, both HCQ and CQ have also been found to block the binding of COVID virus spike proteins to the ACE2 receptors needed to initiate viral entry into the cells, giving scientific support for their utility as more directly interfering with spike protein activity before the virus ever breaches the cell (Fantini et al., 2020; Sehailia and Chemat, 2020; Wang et al., 2020).
Quercetin. Similar to HCQ and CQ, quercetin also serves as a zinc ionophore. And like HCQ and CQ, quercetin appears to also work to block the binding of COVID virus spike proteins to the ACE2 receptors, impairing spike protein-virus entry into the cell, or impairing spike protein alonef from entering the cells (Pan et al., 2020; Derosa et al., 2021). Many other phytochemicals and bioflavonoids are demonstrating this ACE2 binding capacity as well (Pandey et al., 2020; Maiti and Banerjee, 2021).
Other Bio-Oxidative Therapies. These include ozone, ultraviolet blood irradiation, and hyperbaric oxygen therapy (in addition to hydrogen peroxide and vitamin C). These three therapies are highly effective in patients with acute COVID infections. It is less clear how effective they would be for long-haul COVID syndrome and patients suffering from ongoing vaccine-generated spike protein syndromes. That is not to say, however, that all three would not prove to be just as excellent for dealing with the spike
https://vitalitymagazine.com/article/re ... e-protein/
In this second article. It would be great if those from the medical community can comment. I did not like the introduction as it sounded a bit on the conspiracy side. However, a quick cursory check supported some of the author's claims.
This antidote to the contagion, is called Suramin, an isolated compound originally derived from an extract of pine needle oil.
Yet anyone can now take advantage of this solution by tapping its root origin, pine needle tea, an antidote that is freely available today in evergreen forests and in many people’s backyards. (Sources for buying it are also listed below.)
How can this simple remedy work so well in the face of such a seemingly insurmountable condition?
There is a direct relationship between Suramin (the isolated extract), pine needle tea (a hot water extract of the pine, fir, cedar, and spruce needles), and pine oil (which is derived from the needles though an essential oil steam distillation process).
The Trail from Suramin to Pine Needle Tea
Here is the trail of science and data that shows the derivative relationship between pine needles and Suramin (“the elist’s antidote” to microbial illnesses) – and which also provides a potential antidote for those affected by the spike protein contagion (for reasons explained within the following data):
https://en.wikipedia.org/wiki/Suramin
Suramin is used for treatment of human sleeping sickness caused by trypanosomes.[1] [a parasite] Specifically, it is used for treatment of first-stage African trypanosomiasis caused by Trypanosoma brucei rhodesiense and Trypanosoma brucei gambiense without involvement of central nervous system.[9][10] It is considered first-line treatment for Trypanosoma brucei rhodesiense, and second-line treatment for early-stage Trypanosoma brucei gambiense, where pentamidine is recommended as first line.[10]
It has been used in the treatment of river blindness (onchocerciasis).[2]
Suramin has been available to the medical profession for almost 100 years. A summary of its antioxidant benefits are outlined in this report – 100 Years of Suramin (attached as a PDF).
The most relevant parts of the summary are outlined below with supportive evidence:
SURAMIN, THE FRUIT OF EARLY MEDICINAL CHEMISTRY
When suramin was introduced for the treatment of African sleeping sickness in 1922, it was one of the first anti-infective agents that had been developed in a medicinal chemistry program. Starting from the antitrypanosomal activity of the dye trypan blue, synthesized in 1904 by Paul Ehrlich, Bayer made a series of colorless and more potent derivatives. Molecule 205 was suramin (Fig. 1), synthesized by Oskar Dressel, Richard Kothe, and Bernhard Heymann in 1916. Sleeping sickness (also known as human African trypanosomiasis [HAT]) was at the forefront of research at that time, not a neglected disease as it is today, and the development of suramin was a breakthrough for the emerging field of chemotherapy.
Suramin further decreases the activities of a large number of enzymes involved in DNA and RNA synthesis and modification: DNA polymerases (103, 104), RNA polymerases (103, 105, 106), reverse transcriptase (18, 103), telomerase (67), and enzymes involved in winding/ unwinding of DNA (107, 108) are inhibited by suramin, as well as histone- and chromatin-modifying enzymes like chromobox proteins (109), methyltransferases (110), and sirtuin histone deacetylases (111)
Suramin also showed inhibitory effects against components of the coagulation cascade (71, 130)
A 2011 Korean study demonstrated using pine needles in tea was the best way to access the antioxidant benefits from pine needles.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180677/
The study demonstrated that the hot water extract of pine needle proanthocyanidins and catechins offer the highest levels of antioxidant benefits compared with chemical extract processes.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180677/
https://rightsfreedoms.wordpress.com/20 ... accinated/
Link to the PDF file 100 Years of Suramin
https://discovery.dundee.ac.uk/ws/porta ... 9.full.pdf
