Over on Twitter, MSNBC host Chris Hayes, who is one of the most overwrought beta males in a cable universe filled with them, writes:
So far, over 25K people have liked this Tweet, and if you make the mistake of reading through the replies, it is abundantly clear that a good 2/3 of Hayes’ followers attempting to dunk on Allen West not only don’t know that neither the vaccine nor monoclonal antibodies are actually “free” — Big Pharma is paid by US taxpayer dollars for both — but more crucially, they don’t know that the vaccinated can still acquire and pass on the virus.
I’m being quite serious. And it’s horrifying to consider.
I mean, imagine following a news personality on Twitter and watching a purported news channel like MSNBC and not knowing, 19 months in, that the vaccines you’ve taken can’t prevent you from catching or transmitting COVID; or that, as these vaccines wane, you’re actually at a higher risk of both getting and transmitting the virus than every unvaccinated person who has already had COVID-19 and carries a library of acquired immunity. This is clearly backed up by the Israeli and UK data, and now something along the lines of 29 studies from all over the world.
According to UK and Welsh data, the vaccinated are also more likely to die from a “breakthrough” case than a Covid-naive unvaccinated person, while all-cause mortality is up as well, signaling potential additional deaths from adverse events associated with universal vaccination.
But you won’t hear that from Chris Hayes or MSNBC. Which means that Chris Hayes and MSNBC will continue to crank out vocal Useful Idiots who know absolutely nothing more about SARS-CoV-2 and the investigative “vaccines” than what the official narrative allows them to know.
Then there’s the difference in mechanism of action between monoclonal antibodies and the mRNA or adenoviral “vaccines” that these cocksure morons don’t seem to understand. The MAB “target SARS-CoV-2 spike RBD and have been shown to neutralize the viral load in vivo, preventing virus-induced pathological sequelae when administered prophylactically or therapeutically […].”
The gene transfer therapeutics, conversely, don’t target the SARS-CoV-2 spike protein, but instead instruct your body how to make them, then sneak them past down-regulated toll-like receptors, resulting in a potentially permanent change to both your genes and your innate immune system.
Reading through the replies to Hayes’ Tweet, it’s impossible to believe that many — if more than a handful — of MSNBC’s audience knows any of this.
One of the major consumers of monoclonal antibody treatment are those who have been fully vaccinated but have acquired COVID-19 as a “breakthrough” case carrying an elevated viral load. MAB are an early treatment meant to stop viral replication; they use “two noncompeting IgG1 antibodies (casirivimab and imdevimab) […] in a cocktail approach…to minimize mutational viral escape.” Which is to say, they are a safer version of Merck’s anti-viral Molnupiravir pill that may soon hit the market:
Molnupiravir works by incorporating itself into the genetic material of the virus, and then causing a huge number of mutations as the virus replicates, effectively killing it. In some lab tests, the drug has also shown the ability to integrate into the genetic material of mammalian cells, causing mutations as those cells replicate.
If that were to happen in the cells of a patient being treated with molnupiravir, it could theoretically lead to cancer or birth defects.
[…]
“Proceed with caution and at your own peril,” wrote Raymond Schinazi, a professor of pediatrics and the director of the division of biochemical pharmacology at the Emory University School of Medicine, who has studied NHC for decades, in an email to Barron’s.
Scientists are split on how serious a risk this is, and in the absence of detailed data on Merck’s animal tests, and long-term human safety data, it’s difficult to know for sure.
Meanwhile, Quercetin (and over the counter drug) or HCQ, both ionophores, allow zinc into infected cells, where the zinc attacks an enzyme that prevents the spike protein from replicating. It carries no risk of mutating the virus because it doesn’t enter its genetic material; it merely disrupts replication (which we’ve known since well before the current SARS virus), while Ivermectin, used in conjunction, binds with healthy cells to prevent the virus from entering, shortening the replicating process and decreasing viral load.
Both drugs are on the WHO essential medicines list and are two of the safest medicines on the planet.
But there’s no money in generics, so, y’know…here comes Molnupiravir, likely under the next EUA.
And the ignorant arrogance of those who ingest MSNBC like they do wine spritzers will have them gobbling these pills by the fistful in their Volvos on the way to their 3rd, 4th, and 5th booster shots.
Then they’ll look down their noses at you — right up until they keel over, a smug look stretched across their faces, until the lights finally go out for good.
I have a few questions about quercetin and its use. I have some, purchased over-the-counter, including a mixture with bromelain. Any information or advice you have to offer would be gratefully appreciated.
As I mentioned in a comment a few days ago, I recovered from a mild case the alpha variant back in November of last year. The recovery was more or less completed 10 days (except for a cough that persisted for several weeks after), at least in part, I believe, due to taking an HCQ/Z-Pak/Zinc Sulfate “tri-pack”.
1) If I am unfortunate enough to be re-infected by delta or some other variant, is there any information about how much more effective ivermectin would be in treating it as opposed to quercetin? I can still get quercetin over-the-counter, but as you know, getting a supply of Ivermectin or HCQ gets increasingly more difficult as time goes by.
2) Does Bromelain really allow for better absorption, and if it does, superior ionophore activity by quercetin?
3) Is there any type of zinc supplement which is considered better at entering the cells/defeating viral reproduction? I have see claims in favor of zinc picolinate, but have no idea how to evaluate if there is any evidence to support this. How often and how much of that type of supplement is reasonable as a prophylaxis? If I am re-infected?
Quercetin IS the ionophore when used with zinc. It’s used when HCQ isn’t available, or in lower risk patients. It’s also used in prophylaxis. The zinc I use is elemental zinc. 25 mg is a safe daily dose.
The best Covid prophylaxis right now is a simple 1% iodine mixture (a few drops in a juice glass filled with water_ 2x daily; and a nasal swab of the same mixture 2x daily. Or something like Xlear spray.
It is unlikely you’ll get re-infected once you’ve cleared the virus. There are a number of data sets showing — including through the Delta waves in several countries — that the most reliable protection against Delta is prior infection and acquired immunity. In Israel, the reinfection rate was 1%; Murchu,et al put it at a similar low threshold. In the UK, the rate was .25%. In the Cleveland Clinic study of healthcare workers, there were 0 reinfections.
Keep in mind that these low percentages may be misleading on the high end: PCR tests were being run at cycles of up to 45, meaning there were likely millions of false positives worldwide. The PCR test also couldn’t distinguish between COVID-19 and flu.
I was given serology tests 9 months after clearing COVID. I showed spike protein antibodies (IgM) and the library of other immunity (IgG). It’s possible for the spike protein to remain in your body for quite some time, which might account for spike antibodies so far out from the original infection. Alternately, it could be that I had also been exposed to Delta, and my body recognized it and killed it off without my experiencing any symptoms.
Acquired immunity from clearing the virus accounts for all variants. Vaccine immunity does not, which is why we’re seeing the most vaccinated countries with the highest case rates. Delta has achieved antigenic escape. The vaccinated are becoming superspreaders.
Look up PBS Marek’s disease. Also look into vaccine-induced enhancement and pathogenic priming.
I still take Quercetin, zinc, C, D3, K2, magnesium, selenium, NAC, curcumin, and black seed oil as a daily supplement regimen, but that’s to protect against other respiratory diseases and to keep my body immune primed.
In the unlikely event of a reinfection — unless you were vaccinated on top of having cleared the virus, which has shown to deplete durable acquired immunity — elemental zinc dosage is 50 mg, 1000 for Quercetin.
Also, full dose aspirin.
If your Vitamin D levels are above 50, your chances of ending up hospitalized are very very low. I take 10,000 iu daily.
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I was already taking Vitamin c (5000 mg), Vitamin D3 (4000 mg), NAC, an elderberry gummy with Zinc everyday. I have already added K2 (because I saw you recommend it in a Tweet thread. I’ve just ordered the Xlear spray and I’m going to look at adding the others in your preventive regiment, as soon as I can find them in a relatively inexpensive way.
I’ve read most of these recommendations before, but it’s good to have them all together in one place (and there are a couple in there I don’t remember having seen from you before). I have not yet been vaccinated.
Later today, I’m going to act on another of your recommendations: I’m going to try to go to the local Labcorp and get tested for D3 levels and T-cell activation. Thanks for getting back to me on this. It’s much appreciated. I