XPan
The Living Force
Florian Schilling • Corona Investigative Committee, Berlin
Session No 143 "Stumbling Blocks / Stolpersteine"
English Version • 1 hour 41 minutes
Florian Schilling | Session 143: The Stolpersteine (EN)
Hier geht's zum deutschen Stream:
odysee.com
German Version • 1 hour 41 minutes
Part 6
I forgot to mention in my previous part 5 entry from the Florian Schilling interview, is that the principles of severe errors / design faults show in the Covid-19 mRNA "vaccines", are not just specific for the Covid-19 injections, but anything you would take and put into that designed genetic platform (in the future). Which means the platform itself, is prone to the same potential of countless severe illnesses, damages and deaths.
It should be the primary mission for our universities to investigative all this, in order to prevent such deeply flawed designs and products. But what have been so far been doing, with people such as professors etc, who have been critical ? We canceled them, destroyed their reputation and buried them via media.
Anti-Idiotype-Antibodies
This was both a highly interesting - but at the same time in my personal opinion, scary. It's a bit complicated, so i hope i get it right.
Imagine you encounter a virus (antigen). On it's surface there is a "epitome", which our immune system will make an anti-body for it, synchrone to that very epitome on the virus.
The anti-body will dock to the virus via its epitome - kind of like a specific serial number docking key. These are the anti-bodies we would want, e.g. after vaccination.
Now those anti-bodies also have a sort of markings (idiotopes) - which in return lead to the the creation of anti-antibodies. This is a safety feature by the body, in case something goes wrong with the production of the primary antibodies - for example when they create auto-immuniological reactions. Those anti-antibodies then will take down the primary anti-bodies.
So, those anti-antibodies are called idiotype anti-bodies. This is all normal, being part of a protection mechanism in our body.
But there is a catch.
The binding site on the anti-body, which docks to the pathogen via a "specific serial number", then the other anti-idiotype antibody can create another antibody, but this one targets the very binding site itself on the primary anti-body (which also is the same docking site or serial numbers, to the binding site to the virus). Against this, another antibody is created, too (huh ?!)
Ok... I get' it. So, the BINDING SITE of this anti-idiotype antibody, is a MIRROR IMAGE that of the epitome on the antigen (virus). You see the square block below encircled in red color - essentially being is a mirror image of the same binding-site like the original virus (enemy protein, which doesn't exist anymore)
THAT is a problem !
Think spike proteins now. When the body creates anti-bodies against the spike proteins, and on top also create anti-ideotype antibodies... from the anti-bodies - you end up with an anti-antibody, which has the same binding site (mirror image) that of the binding site from spike proteins.
You get: A type of anti-antibody, which is NOT a spike protein, but has IDENTICAL CHARACTERISTICS that of the toxic spike protein. Huston, we have a problem. Because these anti-idiotype-antibodies, you are building your entire life. As they are the creation from our own body's immune system. While the spike proteins from the jabs, via our cell production, eventually abate to be built, and the cells being destroyed by our immune system over time.
The anti-idiotype-antibodies remain lifelong.
This also means, that a patient who gets a treatments against spike proteins - those treatment fail (such as NAC, Bromelain enzyme, CDL/CLO2 etc) - because those only address spike proteins - but not anti-idiotype-antibodies and their toxic spike-protein characteristics.
Florian Schilling explains patients would need immunological treatments, such as immunosuppressive therapies, and plasma Aphaeresis - albeit the results from that have been rather mixed. You may consult a type of Apheresis to clear out the anti-idiotype-antibodies, but after some time, you're back where you started - due to the body's natural production of those (once they have been made in the past)
There are types of Aphaeresis which can filter out (free floating) amyloid blood clots, such as the H.E.L.P. Aphaeresis - then the Aphaeresis helps.
Does this H.E.L.P. Aphaeresis help against specific anti-idiotype-antibodies ? No, not at all.
There are immune absorption procedures, which can fish out those types of anti-bodies, and yes, it would help. The question is - how long ? It may only last for a certain time - until the body once again produces those anti-idiotype-antibodies anew. Schilling's experience from his own patients is, that some patients do not built those antibodies anew. It appears that when there is no trigger (reason) for them to be built... they aren't built anew. Then they don't need any immune suppressive treatments, either.
What could potentially happen is, that with renewed contact to the virus/viruses, the patients will activate and grow new anti-idiotype-antibodies, with the problem that follows in the wake of those spike protein like complications, illnesses, auto-immune reactions/related illnesses.
Schilling also says, he also knows cases which after plasma Aphaeresis, at first didn't have many anti-idiotype-antibodies - but then two weeks later, could determine that the antibodies grew anew in numbers. And after a month, they were back at square one. And you can't do plasma Aphaeresis your whole life time.