Covid-19 - Aw Crap….

   Covid-19 is not finished, far from it! 

  This chimera from hell (There is no doubt about this now) concocted in a Chinese lab (nor about that) is mutating as expected and becoming both more virulent and less dangerous, also as expected. 

  But the "vaccine" is another story altogether. It's long term effects are still being assessed although the suspicious surge in aggressive cancers and heart attacks in relatively young populations is becoming more and more obvious as excess deaths are being tabulated in many countries. 

  What could be the cause? Here's a possibility:

Guest Post by Karl Denninger

Well, here’s the medical facts that entirely explain why people with more shots get more covid.

I’ve been paying attention to this possibility for a while but until the study work came out that proved it all there was is speculation.  ADE (“Antibody dependent enhancement”) is a fairly poorly-understood thing; most people believe it is confined to making a particular infection more serious than it would otherwise be.  Of course having it occur when it otherwise would not fits that quite-nicely, but isn’t what people tend to think about.

Now, unfortunately, we have the evidence.  Here’s the salient graph and lots of discussion which I’ll try to recap for you here:

Let me explain this one for you because it makes very clear what’s going on.  There are multiple sub-types of IgG antibodies.  IgG are the last ones that show up; IgA typically is in the mucosa of the nose, and is a “front line” of defense if you will.  IgM shows up second; it generally is gone about two weeks or so after you recover.  IgG is the “long term” antibody recognition but it has multiple subtypes.

This is very important for human and animal life, because not all things that can elicit a serious immune response should get one.  For example: A bee sting.  A serious immune response to that could kill you and in people seriously-allergic that’s a real risk.  So why don’t most people get a serious immune response?

As it turns out they sort of do, but its focuses in one sort of IgG build, IgG4, which suppresses the cascade of events that cause the body to go after the thing in question and destroy it, along with all the side effects that produces (fever, serious inflammation, etc.)

Well, when you get Covid typically IgG3 is the one that neutralizes most of the virus.  IgG1 and 2 do some of the work, but most of it is done by IgG3.  You’re not supposed to build an IgG4 response, and with natural infection without vaccination you don’t, thus there’s no inhibition and your response is and remains effective at neutralizing whatever it is.  Typical vaccines (e.g. measles) elicit a response that looks exactly like an actual infection because that’s how they’re designed and intended; they use the whole virus and their intent is to make your body think it is being invaded by the real deal and respond as it would to the real deal.

None of the western world Covid jabs do this on purpose.  They were all crafted to use only part of the virus, and the reason for that is past experience trying to create coronavirus vaccines all ended in failure with many of them producing wild enhancement of the infection instead of protection and in animal testing reliably killed the animals.  Thus the decision was made without long-term safety and efficacy testing to use only the spike, with the idea that doing so would prevent the bad outcome.

They were wrong; it didn’t prevent the bad outcome but instead shifted it in ways that were wildly insidious and unforeseen.

As it turns out what is now in the data is that IgG3, which the component that provides most of the protection against Covid is down to a flat zero by the time you take the third shot while IgG4 which causes the body to tolerate the infection and not clear it skyrockets from nothing prior to the second shot to being extremely high for the third and subsequent.

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This was never detected in the trials because they didn’t look and it takes time to find it because the conversion only happens when you get infected after you’re jabbed. So if you only test for three months and don’t look at the IgG profile you’ll never see it happen, never mind that until you boost the data is that while its detectable after the second shot (and thus could have been detected if they bothered to look) the response curve is exponential and its the third one that basically zeros the IgG3 response if, following the first booster, you get infected again — and you will as neutralization from the booster itself wanes.

Remember, IgG4 causes the body to tolerate the infection rather than attack and clear it.

This turns you into a walking virus mutation and production factory, a source of infection to everyone around you and, to the extent that the virus does direct damage to your body systems, and we know the spike does, it also is likely to lead to very severe long-term problems that look like other conditions.  Nobody is looking for spike damage specifically in, for example, heart attacks, strokes and pulmonary embolisms, never mind the possibility of potentiating cancer by suppressing immune response if that suppression and tolerance goes beyond Covid, and it very well might.  If that’s not bad enough everyone that got jabbed has the same profile of response where the normal situation is that responses differ in different people because our body systems operate slightly differently (we’re all genetically unique.)

Now who’s most-likely to have had the most number of jabs and thus are walking around tolerating infections and giving them others?  Health care workers!  And who goes to the hospital or doctor? Compromised individuals who can least-withstand infections.  Gee, that was smart, right?

What’s worse is that we do not know if this is local to Covid or even just coronaviruses.  It might not be.  We may now have created a couple hundred million people in the US alone who have coded their immune systems to tolerate certain proteins that are common across all manner of respiratory viruses and worse, if its not local to viruses to be more-susceptible to cancer and other immune-sensitive problems with no way to reverse the effects!

If you recall I pointed out very early on in this thing that jabbing people with a non-sterilizing immune product, which these jabs all are, was wildly irresponsible because at minimum it would likely cause a decrease in symptoms and thus make it more likely rather than less that you’d go out and infect other people unknowingly.  That was and remains correct however what nobody knew because we didn’t look is that said non-sterilizing jabs had an even worse outcome in that they shift your immune response from elimination to tolerance so now, particularly after the third, you are likely to carry and not eliminate covid which makes you a literal Typhoid Mary, and if that’s not enough we have no idea if this effect is local to Covid itself (which, in the world of Omicron isn’t so awful as Omicron doesn’t seem to be killing many people) but it may extend to influenza and even RSV, and is even more-likely to extend to the other two common beta coronaviruses OC43 and HKU1.

And finally, this may be permanent in those people who took the jabs.  We don’t know.

But what we do know, factually, is that when you get infected with Covid post Jab #3 your neutralizing antibody product is a statistical zero while your “tolerance” antibody production shoots the moon.  This is exactly backward from what you want to happen and we are now left trying to figure out exactly how badly you screwed both yourself and others.