The Spike Protein

[pueblo]

Posted by meat suit (here)

Posted by pueblo (here)
I post this as unverified, but if it is legit than we are up to our necks in it now.

so, I speak german and can confirm this is real... wtf... not sure what this page actually is though, not sure if its a government page. https://www.gesetze-im-internet.de/ifsg/__21.html

Yes, it appears to be real.

Did you see this link? https://germanlawarchive.iuscomp.org/?p=2487

[onawah]

THIS WEEK with Mary & Polly, Season 2, Episode 10
From RFKJr.'s Children's Health Defense
6/9/21
Must See Latest News from key experts about the dangers of the spike protein and more. tracing back how it all came about, all very updated info.
Including mistrials of Hydroxychloroquine, deadly trials of COVID shots that were covered up and much more.
(I don't know if the video can be embedded, but I've sent a request to the Mods.)
https://www.vaxxed2.com/so/aeNdnZa1V...38654c98#/main

[onawah]

Researcher: 'We Made a Big Mistake' on COVID-19 Vaccine
by Dr. Joseph Mercola
June 14, 2021
https://articles.mercola.com/sites/a...4=20110604&p5=

(Video at the link which I've asked the Mods to embed)

"STORY AT-A-GLANCE
Canadian immunologist and vaccine researcher Byram Bridle, Ph.D., has gained access to Pfizer’s biodistribution study from the Japanese regulatory agency. The research, previously unseen, demonstrates a huge problem with all COVID-19 vaccines
The assumption that vaccine developers have been working with is that the mRNA in the vaccines would primarily remain in and around the vaccination site. Pfizer’s data, however, show the mRNA and subsequent spike protein are widely distributed in the body within hours
This is a serious problem, as the spike protein is a toxin shown to cause cardiovascular and neurological damage. It also has reproductive toxicity, and Pfizer’s biodistribution data show it accumulates in women’s ovaries
Once in your blood circulation, the spike protein binds to platelet receptors and the cells that line your blood vessels. When that happens, it can cause platelets to clump together, resulting in blood clots, and/or cause abnormal bleeding
Pfizer documents submitted to the European Medicines Agency also show the company failed to follow industry-standard quality management practices during preclinical toxicology studies and that key studies did not meet good laboratory practice standards

The more we learn about the COVID-19 vaccines, the worse they look. In a recent interview1 with Alex Pierson (above), Canadian immunologist and vaccine researcher Byram Bridle, Ph.D., dropped a shocking truth bomb that immediately went viral, despite being censored by Google.

It also was featured in a “fact” check by The Poynter Institute’s Politifact,2 which pronounced Bridle’s findings as “false” after interviewing Dr. Drew Weissman,3 a UPenn scientist who is credited with helping to create the technology that enables the COVID mRNA vaccines to work. But, as you can see below, unlike Bridle, Politifact neglected to go beyond interviewing someone with such a huge stake in the vaccine’s success.

In 2020, Bridle was awarded a $230,000 government grant for research on COVID vaccine development. As part of that research, he and a team of international scientists requested a Freedom of Information Act (FOIA) access to Pfizer’s biodistribution study from the Japanese regulatory agency. The research,4,5 previously unseen, demonstrates a huge problem with all COVID-19 vaccines.

“We made a big mistake,” Bridle says. “We thought the spike protein was a great target antigen; we never knew the spike protein itself was a toxin and was a pathogenic protein. So, by vaccinating people we are inadvertently inoculating them with a toxin.”

This toxin, Bridle notes, can cause cardiovascular damage and infertility — a claim echoed by researchers such as Stephanie Seneff, Ph.D., and Judy Mikovits, Ph.D., whom I’ve interviewed about these issues.

Pfizer Omitted Industry-Standard Safety Studies
What’s more, TrialSite News reports6 that Pfizer documents submitted to the European Medicines Agency [EMA] reveal the company “did not follow industry-standard quality management practices during preclinical toxicology studies … as key studies did not meet good laboratory practice (GLP).”

Neither reproductive toxicity nor genotoxicity (DNA mutation) studies were performed, both of which are considered critical when developing a new drug or vaccine for human use. The problems now surfacing matter greatly, as they significantly alter the risk-benefit analysis underlying the vaccines’ emergency use authorization. As reported by TrialSite News:7

“Recently, there has been speculation regarding potential safety signals associated with COVID-19 mRNA vaccines. Many different unusual, prolonged, or delayed reactions have been reported, and often these are more pronounced after the second shot.

Women have reported changes in menstruation after taking mRNA vaccines. Problems with blood clotting (coagulation) — which are also common during COVID-19 disease — are also reported. In the case of the Pfizer COVID mRNA vaccine, these newly revealed documents raise additional questions about both the genotoxicity and reproductive toxicity risks of this product.

Standard studies designed to assess these risks were not performed in compliance with accepted empirical research standards. Furthermore, in key studies designed to test whether the vaccine remains near the injection site or travels throughout the body, Pfizer did not even use the commercial vaccine (BNT162b2) but instead relied on a ‘surrogate’ mRNA producing the luciferase protein.

These new disclosures seem to indicate that the U.S. and other governments are conducting a massive vaccination program with an incompletely characterized experimental vaccine.

It is certainly understandable why the vaccine was rushed into use as an experimental product under emergency use authority, but these new findings suggest that routine quality testing issues were overlooked in the rush to authorize use.

People are now receiving injections with an mRNA gene therapy-based vaccine, which produces the SARS-CoV-2 spike protein in their cells, and the vaccine may be also delivering the mRNA and producing spike protein in unintended organs and tissues (which may include ovaries).”

Toxic Spike Protein Enters Blood Circulation
The assumption that vaccine developers have been working with is that the mRNA in the vaccines (or DNA in the case of Johnson & Johnson and AstraZeneca’s vaccines) would primarily remain in and around the vaccination site, i.e., your deltoid muscle, with a small amount draining into local lymph nodes.8

Pfizer’s data, however, show this isn’t the case at all. Using mRNA programmed to produce luciferase protein, as well as mRNA tagged with a radioactive label, Pfizer showed that the majority of the mRNA initially remain near the injection site, but within hours become widely distributed within the body.9

We have known for a long time that the spike protein is a pathogenic protein. It is a toxin. It can cause damage in our body if it gets into circulation. ~ Dr. Byram Bridle
The mRNA enters your bloodstream and accumulates in a variety of organs, primarily your spleen, bone marrow, liver, adrenal glands and, in women, the ovaries. The spike protein also travel to your heart, brain and lungs, where bleeding and or blood clots can occur as a result, and is expelled in breast milk.

This is a problem, because rather than instructing your muscle cells to produce the spike protein (the antigen that triggers antibody production), spike protein is actually being produced inside your blood vessel walls and various organs, where it can do a great deal of damage.

“It’s the first time ever scientists have been privy to seeing where these messenger RNA [mRNA] vaccines go after vaccination,” Bridle told Pierson.10

“Is it a safe assumption that it stays in the shoulder muscle? The short answer is: absolutely not. It’s very disconcerting … We have known for a long time that the spike protein is a pathogenic protein.

It is a toxin. It can cause damage in our body if it gets into circulation … The spike protein on its own is almost entirely responsible for the damage to the cardiovascular system, if it gets into circulation.”

The Spike Protein Is the Problem
Indeed, for many months, we’ve known that the worst symptoms of severe COVID-19, blood clotting problems in particular, are caused by the spike protein of the virus. As such, it seemed really risky to instruct the body’s cells to produce the very thing that causes severe problems.

Bridle cites research showing that laboratory animals injected with purified spike protein from SARS-CoV-2 straight into their bloodstream developed cardiovascular problems and brain damage.

Assuming that the spike protein would not enter into the circulatory system was a “grave mistake,” according to Bridle, who calls the Japanese data “clear-cut evidence” that the vaccine, and the spike protein produced by it, enters your bloodstream and accumulates in vital organs. Bridle also cites recent research showing the spike protein remained in the bloodstream of humans for 29 days.

Once in your blood circulation, the spike protein binds to platelet receptors and the cells that line your blood vessels. As explained by Bridle, when that happens, one of several things can occur:

It can cause platelets to clump together — Platelets, aka thrombocytes, are specialized cells in your blood that stop bleeding. When there’s blood vessel damage, they clump together to form a blood clot. This is why we’ve been seeing clotting disorders associated with both COVID-19 and the vaccines
It can cause abnormal bleeding
In your heart, it can cause heart problems
In your brain, it can cause neurological damage
Importantly, people who have been vaccinated against COVID-19 absolutely should not donate blood, seeing how the vaccine and the spike protein are both transferred. In fragile patients receiving the blood, the damage could be lethal.

Breastfeeding women also need to know that both the vaccine and the spike protein are being expelled in breast milk, and this could be lethal for their babies. You are not transferring antibodies. You are transferring the vaccine itself, as well as the spike protein, which could result in bleeding and/or blood clots in your child. All of this also suggests that for individuals who are at low risk for COVID-19, children and teens in particular, the risks of these vaccines far outweigh the benefits.

The Spike Protein and Blood Clotting
In related news, Dr. Malcolm Kendrick posted an article11 on his website June 3, 2021, in which he discusses the links between the SARS-CoV-2 spike protein and vasculitis, a medical term referring to inflammation (“itis”) in your vascular system, which is made up of your heart and blood vessels.

There are many different types of vasculitis, including Kawasaki’s disease, antiphospholipid syndrome, rheumatoid arthritis, scleroderma and Sjogren’s disease. According to Kendrick, all of them have two things in common:12

1.Your body for some reason starts to attack the lining of your blood vessels, thereby causing damage and inflammation — The “why” can differ from one case to another, but in all cases, your immune system identifies something foreign in the lining of the blood vessel, causing it to attack. The attack causes damage to the lining, which results in inflammation.

Blood clots are a common result, and can occur either because the platelets clump together in response to the vessel wall damage, or because your anticlotting mechanism has been compromised. Your most powerful anticlotting system is your glycocalyx, the protective layer of glycoproteins that lines your blood vessels.

Among many other things, the glycocalyx contains a wide variety of anticoagulant factors, including tissue factor inhibitor, protein C, nitric oxide and antithrombin. It also modulates the adhesion of platelets to the endothelium. When blood clots completely block a blood vessel, you end up with a stroke or a heart attack.

A reduction in platelet count, known as thrombocytopenia, is a reliable sign that blood clots are forming in your system, as the platelets are being used up in the process. Thrombocytopenia is a commonly-reported side effect of COVID-19 vaccines, as are blood clots, strokes and lethal heart attacks — all of which are pointing toward spike proteins causing vascular damage.

2.They significantly increase your risk of death, in some cases raising mortality by 50 times compared to people who do not have these conditions.

The take-home message Kendrick delivers is that “If you damage the lining of blood vessel walls, blood clots are far more likely to form. Very often, the damage is caused by the immune system going on the attack, damaging blood vessel walls, and removing several of the anti-clotting mechanisms.” The end result can be lethal, and this chain of events is exactly what these COVID-19 vaccines are setting into motion.

SARS-CoV-2 Spike Protein May Damage Mitochondrial Function
Other research suggests the SARS-CoV-2 spike protein can have a serious impact on your mitochondrial function, which is imperative for good health, innate immunity and disease prevention of all kinds.

When the spike protein interacts with the ACE2 receptor, it can disrupt mitochondrial signaling, thereby inducing the production of reactive oxygen species and oxidative stress. If the damage is serious enough, uncontrolled cell death can occur, which in turn leaks mitochondrial DNA (mtDNA) into your bloodstream.13

Aside from being detected in cases involving acute tissue injury, heart attack and sepsis, freely circulating mtDNA has also been shown to contribute to a number of chronic diseases, including systemic inflammatory response syndrome or SIRS, heart disease, liver failure, HIV infection, rheumatoid arthritis and certain cancers.14 As explained in “COVID-19: A Mitochondrial Perspective”:15

“Apart from its role in energy production, mitochondria are crucial for … innate immunity, reactive oxygen species (ROS) generation, and apoptosis; all of these are important in COVID-19 pathogenesis. Dysfunctional mitochondria predispose to oxidative stress and loss of cellular function and vitality. In addition, mitochondrial damage leads to … inappropriate and persistent inflammation.

SARS coronavirus 2 (SARS-CoV-2) … enters cell by attaching to angiotensin converting enzyme 2 (ACE2) receptors on cell surface … Following infection, there is internalization and downregulation of ACE2 receptors.

At vascular endothelium, ACE2 performs conversion of angiotensin II to angiotensin (1–7). Thus, a low ACE2 activity subsequent to SARS-CoV-2 infection leads to imbalance in renin-angiotensin system with relative excess of angiotensin II.

Angiotensin II through binding to its type 1 receptors exerts pro-inflammatory, vasoconstrictive, and prothrombotic effects, while angiotensin (1–7) has opposing effects … In addition, angiotensin II increases cytoplasmic and mitochondrial ROS generation leading to oxidative stress.

Increased oxidative stress may lead to endothelial dysfunction and aggravate systemic and local inflammation, thus contributing to acute lung injury, cytokine storm, and thrombosis seen in severe COVID-19 illness …

A recent algorithm showed that majority of SARS-CoV-2 genomic and structural RNAs are targeted for mitochondrial matrix. Thus it appears that SARS-CoV-2 hijacks mitochondrial machinery for its own benefit, including DMV biogenesis. Manipulation of mitochondria by virus may lead to mitochondrial dysfunction and increased oxidative stress ultimately leading to loss of mitochondrial integrity and cell death …

Mitochondrial fission enables removal of the damaged portion of a mitochondrion to be cleared by mitophagy (a special form of autophagy). Metabolomic studies suggest that SARS-CoV-2 inhibits mitophagy. Thus, there is accumulation of damaged and dysfunctional mitochondria. This not only leads to impaired MAVS [mitochondrial antiviral signaling] response but also aggravates inflammation and cell death.”

The author, Pankaj Prasun, points out that the virus’ impact on mitochondria helps explain why COVID-19 is so much deadlier for older people, the obese, and those with diabetes, high blood pressure and heart disease.

All of these risk factors have something in common: They’re all associated with mitochondrial dysfunction. If your mitochondria are already dysfunctional, the SARS-CoV-2 virus can more easily knock out more mitochondria, resulting in severe illness and death.

The Spike Protein Is a Bioweapon
In my interview with Seneff and Mikovits (see earlier hyperlink), they both stressed that the key danger — both in COVID-19 and with the vaccines — is the spike protein itself. However, while the spike protein found in the virus is bad, the spike protein your body produces in response to the vaccine is far worse. Why?

Because the synthetic mRNA in the vaccine has been programmed to instruct your cells to produce an unnatural, genetically engineered spike protein. Specific alterations make it far more toxic than that found on the virus itself. Mikovits goes so far as to call the spike protein a bioweapon, as it is a disease-causing agent that demolishes innate immunity and exhausts your natural killer (NK) cells’ ability to determine which cells are infected and which aren’t.

In short, when you get the COVID-19 vaccine, you are being injected with an agent that instructs your body to produce the bioweapon in its own cells. This is about as diabolical as it gets.

In her paper, “Worse Than The Disease: Reviewing Some Possible Unintended Consequences of mRNA Vaccines Against COVID-19,” published in the International Journal of Vaccine Theory, Practice and Research in collaboration with Dr. Greg Nigh,16 Seneff explains why the unnatural spike protein is so problematic.

In summary, normally, the spike protein on a virus will collapse on itself and fall into the cell once it attaches to the ACE2 receptor. The vaccine-induced spike protein does not do this. Instead it stays open and remains attached to the ACE2 receptor, thereby disabling it and causing a host of problems that lead to heart, lung and immune impairment.

What’s more, because the RNA code has been enriched with extra guanines (Gs) and cytosines (Cs), and configured as if it’s a human messenger RNA molecule ready to make protein by adding a polyA tail, the spike protein’s RNA sequence in the vaccine looks as if it is part bacteria,17 part human18 and part viral at the same time.

There’s also evidence suggesting the SARS-CoV-2 spike protein may be a prion, which is yet another piece of really bad news, particularly as it pertains to vaccine-induced spike protein. Prions are membrane proteins and when they misfold, they form crystals in the cytoplasm resulting in prion disease.

Since the mRNA in the vaccines has been modified to spew out very high amounts of spike protein (far greater than that of the actual virus), the risk of excessive buildup in the cytoplasm is high. And, since the spike protein doesn’t enter into the membrane of the cell, there’s a high risk that it can become problematic if indeed it works like a prion.

Remember, the research cited by Bridle at the beginning of this article found the spike protein accumulates in the spleen, among other places. Parkinson’s disease is a prion disease that has been traced back to prions originating in the spleen, that then travel up to the brain via the vagus nerve. In the same way, it’s quite possible COVID-19 vaccines may promote Parkinson’s and other human prion diseases such as Alzheimer’s.

What Are the Solutions?
While all of this is highly problematic, there is help. As noted by Mikovits, remedies to the maladies that might develop post-vaccination include:

Hydroxychloroquine and ivermectin treatments. Ivermectin appears particularly promising as it actually binds to the spike protein. Please listen to the interview that Brett Weinstein did with Dr. Pierre Kory,19 one of Dr. Paul Marik’s collaborators

Low-dose antiretroviral therapy to reeducate your immune system

Low-dose interferons such as Paximune, developed by interferon researcher Dr. Joe Cummins, to stimulate your immune system

Peptide T (an HIV entry inhibitor derived from the HIV envelope protein gp120; it blocks binding and infection of viruses that use the CCR5 receptor to infect cells)

Cannabis, to strengthen Type I interferon pathways

Dimethylglycine or betaine (trimethylglycine) to enhance methylation, thereby suppressing latent viruses

Silymarin or milk thistle to help cleanse your liver

From my perspective, I believe the best thing you can do is to build your innate immune system. To do that, you need to become metabolically flexible and optimize your diet. You’ll also want to make sure your vitamin D level is optimized to between 60 ng/mL and 80 ng/mL (100 nmol/L to 150 nmol/L), ideally through sensible sun exposure. Sunlight also has other benefits besides making vitamin D.

Use time-restricted eating and eat all your meals for the day within a six- to eight-hour window. Avoid all vegetable oils and processed foods. Focus on certified-organic foods to minimize your glyphosate exposure, and include plenty of sulfur-rich foods to keep your mitochondria and lysosomes healthy. Both are important for the clearing of cellular debris, including these spike proteins. You can also boost your sulfate by taking Epsom salt baths.

To combat the toxicity of the spike protein, you’ll want to optimize autophagy, which may help digest and remove the spike proteins. Time-restricted eating will upregulate autophagy, while sauna therapy, which upregulates heat shock proteins, will help refold misfolded proteins and also tag damaged proteins and target them for removal. It is important that your sauna is hot enough (around 170 degrees Fahrenheit) and does not have high magnetic or electric fields.
- Sources and References
1, 2, 6 International Journal of Vaccine Theory, Practice and Research May 10, 2021; 2(1): 38-79
3 Appl Environ Microbiol. 2010 May;76(9):2846-55
4 Trends Cell Biol. 2019 Mar; 29(3): 191–200
5 Cell Host & Microbe November 19, 2009; 6(5): 403-408

+ Sources and References
The Many Ways in Which COVID Vaccines May Harm Your Health
The Great Reset and Transhumanism Movement

[mountain_jim]

https://principia-scientific.com/bre...otein-binding/

(more links in text at link)

Breakthrough: Ivermectin Inhibits Covid Spike Protein Binding
Published on June 14, 2021

Written by afinalwarning.com



Ivermectin, a common anti-parasite drug, has shown great efficacy in the fight against covid-19. For the first time, medical researchers have documented how ivermectin docks to the SARS-CoV-2 spike receptor-binding domain that is attached to the ACE2 receptor.


In this way, ivermectin effectively inhibits viral attachment and replication, assisting a precise antiviral response that can target the SARS-CoV-2 spike protein at its most advantageous cleavage site. The researchers showed how ivermectin interferes with the attachment of the spike protein to the human cell membrane. Ivermectin is a simple medicine derived from the bacterium Streptomyces avermitilis.

It weakens and kills parasites by interfering with their nervous system and muscle function. Ivermectin targets the glutamate-gated chloride channels in the parasite’s nerve and muscle cells, bolstering inhibitory effects in the parasite’s own neurotransmission. As the chloride ions permeate, the parasite’s cells are hyper-polarized and then paralyzed, resulting in their demise. In this study, ivermectin docked in region of leucine 91 of the spike protein and at the histidine 378 of the ACE2 receptor.

The binding energy and constancy of ivermectin was also measured and found to be sufficient at the ACE2 receptor, proving the anti-parasitic molecule a powerful force for blocking viral attachment of SARS-CoV-2.

Ivermectin Blocks SARS CoV-2 At The ACE2 Receptor In Humans

The 17 randomized controlled trials that use ivermectin for early treatment and prophylaxis report positive effects, with an estimated improvement of 73 percent and 83 percent, respectively. Out of 37 early treatment and prophylaxis studies for ivermectin, 97 percent report positive effects. One of the studies documents how ivermectin inhibits the replication of SARS-CoV-2 in vitro and displays broad-spectrum anti-viral activity against the causative virus (SARS-CoV-2).

This study showed a 5,000-fold reduction in viral RNA after just 48 hours. The study also proves that effective treatments and prophylactics can mitigate the replication and spread of a virus thousands of times faster than the paranoid, isolationist approach of social distancing and lockdowns. If antivirals were encouraged early and often, then the spread of actual infectious virus would have been mitigated at rates thousands of times faster than the insane method of treating everyone as if they are infectious.

By treating actual infections where symptoms are present, the spread is reduced at magnitudes thousands of times greater, while conveying immunity instead of terror. The SARS-CoV-2 spike protein is designed to attach to angiotensin-converting enzyme 2 (ACE2) in humans. To see whether ivermectin could dock at this receptor site and block viral attachment, the researchers used a program called AutoDock Vina Extended. This docking study showed the crystal structure of the SARS-CoV-2 spike receptor binding domain.

The researchers looked specifically at the human ACE2 receptor and calculated the root-mean-square deviation (RMSD) of its atomic positions. A lower RMSD value indicates a more accurate docking capacity. When the RMSD value is three or greater, no docking has occurred at the receptor site. Ivermectin did not dock at nine of the locations; however, it did dock at the leucine 91 region of the spike and histidine 378 at the intersection of proteins between SARS CoV-2 and the ACE2 receptor complex.

Previous studies proved ivermectin’s efficacy, but had to use high concentrations of the drug because the study relied on African green monkey kidney epithelial cells, which do not express the human ACE2 receptor. SARS-CoV-2 is specifically equipped to infect human ACE2 receptors, so this study could prove ivermectin to be effective in much smaller dosages. Clinical trials are now underway to determine if ivermectin is an effective treatment for covid-19.

The Global Conspiracy To Suppress Effective Anti-Viral Medicines

The World Health Organization, the FDA, and the NIH have repeatedly suggested that no antiviral treatments exist for covid-19, even though multiple antiviral herbs and drugs have been studied during previous SARS and MERS epidemics and found to be effective. This time around, many of these antivirals were used with great effectiveness by doctors who were willing to go out on a limb and save lives. Chinese hospitals used various antiviral herbs to treat covid-19 patients.

These hospitals studied the effects of the herbs for impeding virus-cell receptor binding, for stimulation of the host’s immunity, for blocking virus entry into host cells through action on the host’s enzymes, and for prevention of SARS-CoV-2 RNA synthesis and replication. The research found numerous phytochemicals to be effective, including: quercetin, ursolic acid, kaempferol, isorhamnetin, luteolin, glycerrhizin, and apigenin.

The top three most effective plants for treating covid-19 included licorice root, (Glycyrrhiza glabra) chicory root, (Cichorium intybus) and hibiscus flowers (Hibiscus sabdariffa). A number of antiviral plants contain compounds that target all three antiviral targets, including olive leaf (Olea europaea), white horehound (Marrubium vulgare), black cumin seed (Nigella sativa), garden cress (Lepidium sativum), Judean wormwood (Artemisia Judaica), guava (Psidium guajava), chrysanthemum (Glebionis coronaria), and Maryam’s flower (Anastatica).

Medical systems around the world are not properly equipped to strengthen the human immune response or understand what individuals need to overcome an infection. When it comes to fighting infections, the US FDA and European drug regulators parrot the same narrative of ignorance and apathy, withholding viable antivirals from the public.

By the way, this is the only legal way to bring experimental vaccines to the global marketplace, by proving that no effective treatments exist.

This suppression of science on antiviral treatments has paved the way for emergency use authorization of experimental vaccines and forced countless patients to suffer (and die) on ventilators, without treatment.

[pueblo]

I know there won't be a lot of settled science on this but does anybody have any information on Ivermectin dosage as a prophylactic against a) spike protein transmission and b) the DARPA nano hydrogel on the Covid test swabs?

Dose for parasitic infection in an adult is one dose 200mcg/kg body weight, ie 20mg if you weigh 100kg. In Goa they were talking about giving everyone Ivermectin, a 18mg dose (12mg if you weigh under 60kg) day one, three and seven and thereafter one dose weekly.

Anyone any experience with this?

*I am not seeking/offering any medical advice. Information purposes only.

[Gwin Ru]

First Autopsy of COVID Vaccinated Patient Finds Every Organ of Body Infested with Spike Proteins

Posted by EU Times on Jun 14th, 2021

The first-ever postmortem study of a patient vaccinated against COVID-19 has revealed that viral RNA was found in every organ of the patient’s body, meaning that the vaccine is either ineffective or the coronavirus actually spreads faster in vaccinated individuals.

The scientific report out of Germany published by the International Journal of Infectious Diseases in June examined the autopsy of an 86-year-old man who had received a single dose of the SARS-CoV-2 vaccine but died 4 weeks later after becoming infected with the virus by a nearby patient at a hospital.

From the “First case of postmortem study in a patient vaccinated against SARS-CoV-2“:

We report on an 86-year-old male resident of a retirement home who received vaccine against SARS-CoV-2. Past medical history included systemic arterial hypertension, chronic venous insufficiency, dementia and prostate carcinoma. On January 9, 2021, the man received lipid nanoparticle-formulated, nucleoside-modified RNA vaccine BNT162b2 in a 30 μg dose. On that day and in the following 2 weeks, he presented with no clinical symptoms.

On day 18, he was admitted to hospital for worsening diarrhea. Since he did not present with any clinical signs of COVID-19, isolation in a specific setting did not occur. Laboratory testing revealed hypochromic anemia and increased creatinine serum levels. Antigen test and polymerase chain reaction (PCR) for SARS-CoV-2 were negative.

But the study notes that by day 25, that vaccinated patient had tested positive for COVID-19, presumably from a nearby COVID-infected patient in his hospital room, and died of kidney and respiratory failure the following day.

SARS-CoV-2 spike proteins were present in nearly all the vaccinated patient’s organs.

“In summary, the results of our autopsy case study in a patient with mRNA vaccine confirm the view that by first dose of vaccination against SARS-CoV-2 immunogenicity can already be induced, while sterile immunity is not adequately developed,” the study concluded.

In other words, although the COVID-19 vaccine triggered an immune response within the body, it didn’t appear to stop the spread of the virus, and therefore the spread of harmful viral spike proteins, throughout the body.

This is just more bombshell scientific evidence that the COVID-19 vaccine likely does more harm than good, and may actually even accelerate the spread of the coronavirus.

The vaccine used is BNT162b2. This is the Pfizer BioNTech vaccine.

Source

[Richter]

First case of postmortem study in a patient vaccinated against SARS-CoV-2

Abstract
A previously symptomless 86-year-old man received the first dose of the BNT162b2 mRNA COVID-19 vaccine. He died 4 weeks later from acute renal and respiratory failure. Although he did not present with any COVID-19-specific symptoms, he tested positive for SARS-CoV-2 before he died. Spike protein (S1) antigen-binding showed significant levels for immunoglobulin (Ig) G, while nucleocapsid IgG/IgM was not elicited. Acute bronchopneumonia and tubular failure were assigned as the cause of death at autopsy; however, we did not observe any characteristic morphological features of COVID-19. Postmortem molecular mapping by real-time polymerase chain reaction revealed relevant SARS-CoV-2 cycle threshold values in all organs examined (oropharynx, olfactory mucosa, trachea, lungs, heart, kidney and cerebrum) except for the liver and olfactory bulb. These results might suggest that the first vaccination induces immunogenicity but not sterile immunity.

CONTINUE: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051011/

NB: One of the conclusions is that the spike protein was found in almost every organ.

[ThePythonicCow]

Posted by Gwin Ru (here)
SARS-CoV-2 spike proteins were present in nearly all the vaccinated patient’s organs.
“In summary, the results of our autopsy case study in a patient with mRNA vaccine confirm the view that by first dose of vaccination against SARS-CoV-2 immunogenicity can already be induced, while sterile immunity is not adequately developed,” the study concluded.
In other words, although the COVID-19 vaccine triggered an immune response within the body, it didn’t appear to stop the spread of the virus, and therefore the spread of harmful viral spike proteins, throughout the body.]

I can see two ways to read this:

1. More vaccines, given earlier, would have enabled the vaccine to prompt the body to develop sufficient immunity to the COVID-19 virus spike protein.
   
2. The vaccine, itself, is deliberately instructing many cells of the body to construct that toxic spike protein.

My money (were I a wagering man, which I'm not usually) would be on (2).

Moreover, as I've posted elsewhere, here, I suspect that that the "vaccines" are up to more nasty effects than just teaching our body's cells to make toxic spike proteins, with the inherent risk of major organ collapse when our body's immune system attacks our own cells that are making that toxic spike protein.

The "vaccines" may also be teaching our cells to make proteins that bind with ferritin (iron) and then attach to targeted tissues, making us magnetic and also making these targeted tissues vulnerable to, reactive to, magnetic fields.

[Journeyman]

Well worth a read:

https://raypeatforum.com/community/t...protein.40924/

Please understand the major finding. All of this is due to the SPIKE PROTEIN's interactions. COVID-19 produces a severe systemic inflammatory reaction likely the result of increased free heme levels and decreased levels of HO-1 activity and functional hemoprotein. The spike protein of COVID-19 binds ACE-2 receptors and porphyrin molecules with weak and strong affinity, respectively. Porphyrins are the building blocks of heme and allow COVID-19 access to invade cells along with ACE-2 receptors and bind functional hemoprotein within the cell.

[ThePythonicCow]

Posted by ThePythonicCow (here)
I can see two ways to read this:

1. More vaccines, given earlier, would have enabled the vaccine to prompt the body to develop sufficient immunity to the COVID-19 virus spike protein.
   
2. ...

This first way, that vaccines administered during the height of a pandemic would result in stronger viral variants, due to the virus encountering an incomplete and not yet adequate immune response that is just in the process of being formed as a result of a recent vaccination, is, I believe, the main point of Dr G.V.Bossche, as discussed in this thread: Dr Geert Vanden Bossche, top vaccine developer, warns against vaccine rollout.

In private discussions elsewhere, I have vigorously disagreed with this position of Dr G.V.Bossche, since I first learned of it in the middle of March of 2021.

The problem will not be additional, more virulent, variations of the Wuhan virus, due to some oopsie of administering the vaccines at the wrong time. That is just a limited hangout intended to provide cover for the rapidly rising rates of death and disease that arise in the weeks and months following mass vaccination.

The problem not the virus. It is the vaccine itself, and the evil bastards pushing it. This is genocide by evil bastards, not genocide by toxic bat soup.

The Elite Evil Bastards have been pushing vaccines hard, for at least the last half century, millions of weakened children, tens of thousands of dead children, and hundreds of uppity doctors who got "suicided" for getting in the way, all be damned.

[Gwin Ru]

Pardon my Woo - Explorers' Guide to SciFi World

• Watch

First published at 20:36 UTC on June 19th, 2021.

clif_high
clif_high

vaxxx War Elites Spikes Reaction

Source: https://www.bitchute.com/video/04yI8MuKjfVL

... the virus wasn't virulently lethal enough to start with... hence the vaccines...

[avid]

Oh dear.. my son just sent me this..
https://blogs.sciencemag.org/pipelin...otein-behavior

Negating Byram Bridle’s compelling evidence,
Plus
https://byrambridle.com
This trashes Byram Bridle

Also more negative commentary
https://healthfeedback.org/claimrevi...sents-studies/


And
https://www.politifact.com/factcheck...ccines-spike-/

All trashing Byram Bridle’s viewpoints…
This is very important, as are the above links deliberately trashing, or is there any truth in their presentation?

I need to respond to my son’s obviously furious response begging him to stop my grandson’s 2nd jab. I believe Byram’s honest presentation, but my son wants to justify his choice to get my grandson, an ex-prem baby who is now very athletic, a second jab.
Quandary, heart issues or just bury my head and let them get on with it? Very very afraid.

Now what ?

[avid]

This is extremely serious, the obvious dismantling of a vaccine specialist who spoke out.
What are concerned family to do against this barrage of negativity that actually imitates the real person to trash them?
The twisting of data so that a lay-person cannot decipher the truth?
However, it would appear my son’s utter determination to trash both myself and any opposition to having his vulnerable son double jabbed is paramount. Of course they want to go abroad soonest. i am horrified at the gullibility of folk swallowing all these ‘fact checking’ sites.

Lives are in the balance.

[pueblo]

Posted by avid (here)
Oh dear.. my son just sent me this..
https://blogs.sciencemag.org/pipelin...otein-behavior

Negating Byram Bridle’s compelling evidence,
Plus
https://byrambridle.com
This trashes Byram Bridle

Also more negative commentary
https://healthfeedback.org/claimrevi...sents-studies/


And
https://www.politifact.com/factcheck...ccines-spike-/

All trashing Byram Bridle’s viewpoints…
This is very important, as are the above links deliberately trashing, or is there any truth in their presentation?

I need to respond to my son’s obviously furious response begging him to stop my grandson’s 2nd jab. I believe Byram’s honest presentation, but my son wants to justify his choice to get my grandson, an ex-prem baby who is now very athletic, a second jab.
Quandary, heart issues or just bury my head and let them get on with it? Very very afraid.

Now what ?

There is so much conflicting info out there at the moment, it is very difficult to know what is true and what isn't.

The only advice I would give you is to really try and put away the fear. There is ultimately nothing to fear, we are SPIRIT and all will be well in the end. We will look back on our experiences here in this messed up 3D projection and laugh!!

It is, imo, important to remember that we can not take on responsibility for other people or their beliefs/actions. What will be will be, it's not your responsibility. Love wins in the end no matter what happens in between! You have made your views known, now you have to let go.

TC

[avid]

Thank you Pueblo, but this is life and death information, the disinfo stuff should be trashed. However, the disinfo stuff seems to be winning in its overwhelming platitudinal patronising sycophantic tripe everywhere. It absolutes infuriates me that so many lies can be proliferated without question, yet when real evidence is presented, the whitewash brigade emerge en masse.

[Bill Ryan]

Posted by avid (here)
Oh dear.. my son just sent me this..
https://blogs.sciencemag.org/pipelin...otein-behavior

Negating Byram Bridle’s compelling evidence

Here's Dr Bridle's detailed rebuttal. It's two hours long, with quite a lot of conversation, but ask (or tell!) your son to watch this to the end.

If he wants science, give him science.

Source: https://youtube.com/watch?v=3S6hMhCohAQ

[Sue (Ayt)]

This article may be reprinted free of charge provided 1) that there is clear attribution to the Orthomolecular Medicine News Service, and 2) that both the OMNS free subscription link http://orthomolecular.org/subscribe.html and also the OMNS archive link http://orthomolecular.org/resources/omns/index.shtml are included.

FOR IMMEDIATE RELEASE
Orthomolecular Medicine News Service, June 21, 2021

Resolving "Long-Haul COVID" and Vaccine Toxicity: Neutralizing the Spike Protein

Commentary by Thomas E. Levy, MD, JD

(OMNS June 21, 2021) Although the mainstream media outlets might have you believe otherwise, the vaccines that continue to be administered for the COVID pandemic are emerging as very substantial sources of morbidity and mortality themselves. While the degree to which these negative outcomes of the COVID vaccines can be debated, there is no question that enough disease and death have already occurred to warrant cessation of the administration of these vaccines until additional, completely scientifically-based research can examine the balance between its now clear-cut side effects versus its potential (and still not yet clearly proven) ability to prevent new COVID infections.

Nevertheless, enough vaccinations have already been administered to warrant concern that a new "pandemic" of illness and death may well be emerging from the side effects that continue to be documented in steadily increasing numbers. The vaccine-induced "culprit" that is now receiving most of the attention and is the focus of much new research is the COVID virus fragment known as the spike protein. Its physiological impact appears to be doing far more harm than good (COVID antibody induction), and its manner of introduction appears to be fueling its ongoing replication with a continuing presence inside the body for an indefinite length of time.

The physical appearance of the COVID virus can been depicted as a central sphere of viral protein surrounded completely by spear-like appendages. Known as spike proteins, they are very analogous to the quills surrounding a porcupine. And just as the porcupine stabs its victim, these spike proteins penetrate into cell membranes throughout the body. After this penetration, protein-dissolving enzymes are activated, the cell membrane breaks down, the viral sphere enters the cytoplasm through this membrane breach, and the metabolism of the cell is subsequently "hijacked" to manufacture more viral particles. These spike proteins are the focus of a great deal of ongoing research examining vaccine side effects (Belouzard et al., 2012; Shang et al., 2020).

The spike protein first attaches to ACE2 (angiotensin converting enzyme 2) receptors in the cell membranes (Pillay, 2020). This initial binding step is vital to triggering the subsequent sequence of events that brings the virus inside the cell. When this binding is blocked by competition or prompt enough displacement with an appropriate therapeutic agent, the virus cannot enter the cell, the infectious process is effectively stopped, and the immune defenses of the body are freed to mop up, metabolize, and eliminate the viral pathogens, or just the spike protein alone if free and no longer attached to a viral particle.

Although ACE2 is found in many different cells throughout the body, it is especially noteworthy to realize that it is the initial target bound by coronavirus on the epithelial cells lining the airways after pathogen inhalation (Hoffmann et al., 2020). ACE2 expression (concentration) is also especially high on lung alveolar epithelial cells (Alifano et al., 2020). This cell membrane-bound virus can then begin the process that eventually results in the severe acute respiratory syndrome (SARS) seen in clinically-advanced COVID infections (Perrotta et al., 2020; Saponaro et al., 2020). The SARS presentation manifests most clearly when the degree of oxidative stress in the lungs is very elevated. This stage of COVID infection-related extreme oxidative stress is often referred to in the literature as a cytokine storm, and left unchecked this invariably leads to death (Hu et al., 2021).

Increasing concern has focused on the continued presence of the spike protein in the blood by itself, unattached to a virion, following COVID vaccination. Supposedly intended to initiate an immune response to the entire virus particle, the spike protein injections are disseminating throughout the body rather than staying put in the upper arm at the vaccine site while the immune response to it evolves. Furthermore, it also appears that these circulating spike proteins can enter cells on their own and replicate themselves without attached virus particles. This not only wreaks havoc inside those cells, it helps to assure the indefinite presence of the spike protein throughout the body.

It has also been suggested that large amounts of spike protein are just binding ACE2 receptors and not proceeding any further into the cell, effectively blocking or disabling normal ACE2 function in a given tissue. Additionally, when the spike protein binds a cell wall and "stops" there, the spike protein serves as a hapten (antigen) which can then initiate an autoimmune (antibody or antibody-like) response to the cell itself, rather than to the virus particle to which it is usually attached. Depending on the cell types to which such spike proteins bind, a wide variety of diseases with autoimmune qualities can result.

Finally, another very worrisome property of the spike protein which alone would be of great concern is that the spike protein itself appears to be highly toxic. This intrinsic toxicity, along with the apparent ability of the spike protein to replicate itself indefinitely within the cells it enters, probably represents the way in which the vaccine can inflict its worst long-term damage, as the production of this toxin can continue indefinitely without other external factors at play.

In fact, the long-haul COVID syndrome likely represents a low-grade unresolved smoldering COVID infection with the same kind of spike protein persistence and clinical impact as is seen in many individuals after their COVID vaccinations (Mendelson et al., 2020; Aucott and Rebman, 2021; Raveendran, 2021).

While the totality of the mechanisms involved are far from being completely understood and worked out, the increasing occurrence of post-vaccine clinical complications is nevertheless very clear-cut and must be addressed as rapidly and effectively as possible. By itself, the disruption of ACE2 receptor function in so many areas of the body has resulted in an array of different side effects (Ashraf et al., 2021). Such clinical complications being seen in different organ systems and areas of the body, can all occur in the following three clinical situations. All three are "spike protein syndromes," although the acute infection always includes the entirety of the virus particles along with the spike protein during the initial phases of the infection.

in an active COVID-19 infection,
during the long-haul COVID syndrome, or
in response to a spike protein-laden vaccine, include the following:
Heart failure, heart injury, heart attack, myocarditis (Chen et al., 2020; Sawalha et al., 2021)
Pulmonary hypertension, pulmonary thromboembolism and thrombosis, lung tissue damage, possible pulmonary fibrosis (McDonald, 2020; Mishra et al., 2020; Pasqualetto et al., 2020; Potus et al., 2020; Dhawan et al., 2021)
Increased venous and arterial thromboembolic events (Ali and Spinler, 2021)
Diabetes (Yang et al., 2010; Lima-Martinez et al., 2021)
Neurological complications, including encephalopathy, seizures, headaches, and neuromuscular diseases. Also, hypercoagulability and stroke (AboTaleb, 2020; Bobker and Robbins, 2020; Hassett et al., 2020; Hess et al., 2020)
Gut dysbiosis, inflammatory bowel disease, and leaky gut (Perisetti et al., 2020; Zeppa et al., 2020; Hunt et al., 2021)
Kidney damage (Han and Ye, 2021)
Impaired male reproductive capacity (Seymen, 2021)
Skin lesions and other cutaneous manifestations (Galli et al., 2020)
General autoimmune diseases, autoimmune hemolytic anemia (Jacobs and Eichbaum, 2021; Liu et al., 2021)
Liver injury (Roth et al., 2021)
In structuring a clinical protocol to stop the ravages of persistent spike protein presence throughout the body, it is first important to realize that the protocol should be able to effectively treat any aspect of COVID infection, including those periods during active infection, after "active" infection (long-haul COVID), and during ongoing spike protein presence secondary to either "chronic" COVID infection or resulting from COVID vaccine administration.

As is the case with any treatment for any condition, factors of expense, availability, and patient compliance always play a role in determining what treatment a given patient will actually undergo for a given period of time. As such, no one specific protocol will be appropriate for all patients, even if the same pathology is present. Ideally, of course, the best protocol is to use all of the options discussed below. When the entirety of the protocol is not possible or feasible, which is most often the case, the combination of HP nebulization, high-dose vitamin C, and appropriately-dosed ivermectin is an excellent way to effectively address long-haul COVID and persistent spike protein syndromes.

Much of the rationale of the protocols is based on what is known about the spike protein and how it appears to inflict its harm. The following aspects of spike protein pathophysiology need to all be considered in crafting an optimal treatment protocol:

The ongoing production of spike protein by the vaccine-supplied mRNA into the cells for the purpose of stimulating the production of neutralizing antibodies (Khehra et al., 2021)
The binding of the spike protein, with or without an attached virion, to an ACE2 binding site on the cell wall, as an initial step to dissolving that portion of the cell wall, permitting the spike protein (and attached virus particle if present) into the cell
The binding of the spike protein to an ACE2 binding site, but just remaining bound to that site and not initiating enzymatic degradation of the cell wall, with or without an attached virion
The degree to which circulating spike protein is present in the blood and actively disseminating throughout the body
The fact that the spike protein by itself is toxic (pro-oxidant in nature) and capable of generating disease-generating oxidative stress throughout the body. This is addressed most directly by persistent and highly-dosed vitamin C.

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 protein as with the intact virus. It just remains to be determined.

Baseline Vital Immune Support Supplementation. There are definitely hundreds, and perhaps thousands, of quality vitamin, mineral, and nutrient supplements that are all capable of making some contribution to reaching and maintaining optimal health, while minimizing the chances of contracting any kind of infectious disease. A baseline regimen of supplementation that factors in expense, overall health impact, and convenience should include vitamin C, vitamin D3, magnesium chloride (other forms good, but chloride form optimal for antiviral impact), vitamin K2, zinc, and an iodine supplement, such as Lugol's solution or iodoral. More specific guidance in dosing can be found in Appendix A of Hidden Epidemic, also available as a free eBook download (Levy, 2017). Specifics on mixing up a solution of magnesium chloride for regular supplementation are also available (Levy, 2020).
[More detail on the therapeutic agents above is available in Chapter 10 of Rapid Virus Recovery]

The suggested optimal way to deal with acute COVID that has evolved into long-haul COVID, or with symptoms consistent with the toxic effects of circulating spike protein post-vaccination, is to always eliminate any active or chronic areas of pathogen proliferation with HP nebulization. Vitamin C supplementation should be optimized at the same time. 50-gram infusions of sodium ascorbate should be administered at least several times weekly as long as there is symptomatology attributable to long-haul COVID and circulating spike protein. Initially, a 25-gram infusion of sodium ascorbate given three times a day should prove to be even more effective as circulating vitamin C is rapidly excreted. Oral vitamin C supplementation should be taken as well, either as several grams of liposome-encapsulated vitamin C daily, or as a teaspoon of sodium ascorbate powder several times daily. One capsule daily of Formula 216 can be added to this as well.

With the "foundation" of HP nebulization and vitamin C supplementation in place, the best prescription medicines to counter long-haul COVID and circulating spike protein would be with ivermectin first, and then HCQ or HQ if the clinical response is not acceptable. Dosages would need to be determined by the prescribing physician.

Along with the baseline immune support supplements noted above, quercetin, 500 to 1,000 mg daily, should be added as well.

Any and all of the above recommendations should be undertaken with the guidance of a trusted physician or other appropriately-trained health care professional.

Recap

Even as the COVID pandemic appears to be slowly subsiding, many individuals are now chronically ill with long-haul COVID and/or with the side effects of a COVID vaccination. It would appear that both clinical situations are primarily characterized by persistent presence of the spike protein and its negative impact on different tissues and organs.

Treatment is aimed at neutralizing the direct toxic impact of spike protein, while working to block its ability to bind the receptors needed to hijack the metabolism of the cell into making new viruses and/or more spike protein. At the same time, treatment measures are taken to assure that there is as complete an elimination of active or smoldering COVID infection remaining in the patient.

The views expressed in this article are the author's and not necessarily those of the Orthomolecular Medicine News Service or all members of its Editorial Board. OMNS invites alternative viewpoints. Submissions may be sent directly to Andrew W. Saul, Editor, at the email contact address further below.

[jaybee]

Posted by avid (here)
Oh dear.. my son just sent me this..
https://blogs.sciencemag.org/pipelin...otein-behavior

Negating Byram Bridle’s compelling evidence,
Plus
https://byrambridle.com
This trashes Byram Bridle

Also more negative commentary
https://healthfeedback.org/claimrevi...sents-studies/


And
https://www.politifact.com/factcheck...ccines-spike-/

All trashing Byram Bridle’s viewpoints…
This is very important, as are the above links deliberately trashing, or is there any truth in their presentation?

I need to respond to my son’s obviously furious response begging him to stop my grandson’s 2nd jab. I believe Byram’s honest presentation, but my son wants to justify his choice to get my grandson, an ex-prem baby who is now very athletic, a second jab.
Quandary, heart issues or just bury my head and let them get on with it? Very very afraid.

Now what ?

I've had a look at a couple of these links (the top two)... and can see that a (desperate?) coordinated attack is being launched on Byram Bridle...

When ever the subject comes up about the lipid nano particles / spike protein code carriers - the general assertion is that MOST of them stay in the upper arm area and lymph cells... and do not go into the blood stream - (and if they do nothing to worry about because they are designed to stick to the outer areas of the cells and do not enter the nucleus...)

Often it is what is NOT said and what is avoided that gives big clues to what's going on and as far as I can see no one on the Official Narrative side of things EVER talks about how many lipid nano particles are in each injection - this surely is key and yet it is never mentioned....?

Dr Sherri Tenpenny said a while back that it was around 50 BILLION.... and she had got this from one of the 'vaccine' patents that she read....

So when those supporting the Official Narrative say that most of the nano particles (with the spike protein creating message in)... say that most of them stay in the upper arm and lymph nodes how many are they talking about - 40 billion... 30 billion...?

How many 'escape' into the bloodstream..? .... 20 billion... 10 billion - 1 billion - a few million..?

They never talk in specific terms about how many lipid nano particles (which are I presume are recognized as foreign bodies by our immune system,) are injected into the body..

There are thousands and thousands of professional reputations on the line - so no wonder they are adamant that everything is ok with the 'vaccine'...

And more than this... politicians and government health advisors could in the future be charged with some kind of gross negligence / manslaughter / crimes against humanity.... as the numbers of deaths climb and the injuries grow... caused by the jab - no wonder they are going to stick together no matter what - self preservation will be a big motivation for them now...

Just having a think aloud about all this.... and the attacks that Bridle is being subjected to - and he said in the long video posted by Bill that they are even going for his parents... this shows they want him gone and silenced no matter what and is a warning to others what they can expect if they open up the Can of Worms regarding the experimental 'vaccine'...

~~~~~~~~~~~~~~~

edit to add.... what a horrible and frightening situation you are in with your son and grandson and your attempts to alert them to the dangers... my sympathies go out to you -

[Gwin Ru]

Posted by avid (here)
[...]
Lives are in the balance.

40 Links Why Big Pharma’s Covid 19 Gene Therapy “Vaccine” Is Bad, Harmful, Deadly & To Be Avoided At All Costs!

by pensiamentopeligroso
June 22, 2021 ·

Vaccine Manufacturers Are Pirates & Merchants Of Death!

Covid 19 Vaccine – deadliest vaccine in U.S. history HERE, HERE and HERE .

Nobel Prize Laureate virologist says no hope for vaccinated HERE get out the body bags and the incinerators!

Big pharma doesn’t want you to know any of this.

You see, they are relying upon billions in revenue. Meanwhile, the eugenicists such as Bill Gates and others want you dead anyway, because you are “SURPLUS POPULATION”!

CDC now acknowledges Covid vaccine deaths reach record high HERE.

VAERS reporting HERE.

International lawyer says “pandemic is a crime” HERE

Kids harmed by vaccine – who cares say U.S. leaders.

Former Pfizer V.P. and medical doctor speaks HERE.

British Rocker Eric Clapton speaks out HERE & HERE.

Developer of mRNA technology speaks out HERE.

Updated stats and info HERE.

Doctor talks HERE and HERE and there’s a series of stories you can follow, just stay on the Bitchute site.

Canadian doctors speak out HERE.

New York University Professor of Propaganda gets cancelled HERE.

The New Covid Order HERE.

Tucker Carlson points out health threats to the young from vaccine HERE.

Ignoramus Federal judge dismisses valid law suit HERE.

Anthony Fauci in 2012 spills the beans HERE.

Bill Gates on Video wants to use vaccines for population control HERE and HERE.

Sweden reports adverse reactions HERE.

The vaccine is the disease HERE.

Pfizer study in their own words HERE.

Tucker Carlson comments HERE.

Totally absurd video hypocrisy by media HERE.

Covid need to know HERE.

What does MIT have to say HERE?

Surgeon discusses with Tucker Carlson what to do if you’ve already had Covid HERE.

Children’s Health Defense statistics HERE.

Dangerous stuff HERE.

Unvaccinated suffering because of the vaccinated HERE.

Forced mandatory vaccinations HERE.

Lots of tid bits HERE.

17 reasons masks are harmful HERE.

Lumber prices up because of Covid and a corrupt government and greedy business people HERE.

Say it with a T-Shirt HERE & HERE. Be a walking billboard!


DID YOU KNOW that all of those desperately needed ventilators are now going into landfills because they are no longer desperately needed?

Do you think Bill Gates could afford to pay 50 different lobbyists $1million a year to lobby for mandated vaccines? Bill Gates probably earns conservatively $250 a second, $15,000 a minute, $900,000 an hour, $21.6million a day net of taxes. He can afford it – it would be one week’s worth of pay to gain a few extra billion dollars.

[Bill Ryan]

Last night Joe Rogan broadcast what he uniquely called "an emergency podcast", the only one he's ever done, with Bret Weinstein and Dr Pierre Kory. It's quite long and is ALL about Ivermectin, from start to finish.

At 2:11:45, Dr Pierre Kory starts talking about the post-'vaccine' spike protein problems, which he's very aware of. He states that Ivermectin will handle the spike proteins too, as it binds to the spike proteins and neutralizes them. So the remedy for post-'vaccine' side-effects, mild or serious, may well simply be Ivermectin — if you can get it.

• https://projectavalon.net/Joe_Rogan_..._June_2021.mp3