What we need to do is to distill everything down to simple words that the mass population can understand and then maybe they’ll recognize that they are being subject to be in lab rats for RNA injections!
Concurrent infections of cells by two pathogens can enable a reactivation of the first pathogen and the second pathogen's accelerated T-cell exhaustion
IgG4, on the other hand, responds to allergens. If you get stung by a bee for example, your body might react with IgG3 or other antibodies and cause you to have an allergic reaction. To avoid this, your body learns how to recognise relatively insignificant foreign objects by switching to IgG4. Instead of increased inflammation to fight the foreign object, your immune system recognises that this is nothing major. Long term exposure, for example in bee keepers, produces this response. Immunotherapy also works this way by training your body with the foreign object you are allergic to until it is trained to produce an IgG4 response.
So what would happen to the Vaxxers if a lab-made pathogen was released that was designed to exploit the above situation as well as what you have discussed in the presentation?
Would it be possible to spread such a pathogen and severely sicken/kill most if not all Vaxxers due to their damaged immunity?
author
Dr. Kevin Stillwagon
58 mins ago
Author
Yes it is possible. There are elites among us that think the world is overpopulated. The easiest way to reduce that population is to convince people to willingly inject something that they think will protect them, but it does the opposite. And the elites get richer doing it.
'Knowing what we already know, it is a travesty that such large swathes of the public still have confidence in covid-19 vaccines, the vehemence of this position in the public’s mind reflecting the power of the machine driving the agenda.'
Why after getting jabbed 4 times or more and then still getting infected 4-5 times does anyone still believe that the jabs are what is going to end the pandemic? If they haven’t ended it after 3 years and another round is coming then why in the blue blazes aren’t people waking up to the scam?
Most of the information in the article was what Geert was warning about before the jabs came out. You do not vaccinate during a hot epidemic! And what’s even more damning about the jabs is that the number of infections were going down just before everyone started getting jabbed. You can see that on the graphs. Good chance that this epidemic would have ended years ago if the jabs hadn’t been given.
I used claude.ai to automatically summarize Geert's “Immunological correlates of vaccine breakthrough infections caused by SARS-CoV-2 variants in highly C-19 vaccinated populations”
I don't know if it is accurate.
Here is a summary of the key points from the article:
1.Steric immune refocusing (SIR) is a major game changer in the COVID-19 pandemic. SIR enables the host immune system to redirect its response to more conserved, less immunogenic spike protein epitopes after vaccine-induced antibodies lose neutralizing capacity against immune escape variants like Omicron. This results in delayed maturation of low affinity, broadly neutralizing antibodies into IgG4 antibodies, promoting further immune escape.
2. SIR-enabling vaccine breakthrough infections (VBTIs) drive viral immune escape while enabling cross-reactivity with unrelated antigens. Prolonged immune refocusing can lead to antibodies that recognize 'self' antigens, causing autoimmunity, or 'altered self' antigens on cancer cells, enabling immune evasion by tumors.
3. Elevated IgG4 antibody levels link enhanced viral immune escape to increased rates of cancer and autoimmune disease in highly vaccinated populations via SIR. SIR-disabling VBTIs with highly infectious variants cause generalized immune suppression, leading to cancer reactivation and flare-ups of chronic infections.
4.The likelihood of vaccinees developing immune pathology after VBTIs is primarily determined by time elapsed since initial SIR events, not individual risk factors. More SIR events over time raise probability of pathogenic antibodies.
5. Viral immune escape is driven by evolutionary pressure to establish herd immunity and protect the human species, not viral survival strategy. Frequent SIR-enabling VBTIs slow viral evolution until innate immunity can control variants.
6. mRNA vaccines raise IgG4 levels when given before natural infection, promoting SIR and immune escape. Immune protection from natural infection is superior to current COVID vaccines.
7. In conclusion, increasing IgG4 antibody levels link enhanced viral immune escape to non-COVID morbidity/mortality. This signals impending risk of healthcare crisis in highly vaccinated populations as virus evolves resistance to population immunity.
Connecting the dots between vaccine breakthrough infections, immune escape, high IgG4 antibody levels and.....excess deaths!
What we need to do is to distill everything down to simple words that the mass population can understand and then maybe they’ll recognize that they are being subject to be in lab rats for RNA injections!
autoimmune flare ups can cause neurological symptoms. lots of people going cuckoo for cocoa puffs lately.
It gets more ominous now...
https://drkevinstillwagon.substack.com/p/the-mechanisms-of-two-types-of-antibody
Fast Eddy
2 hrs ago
This is the smoking gun that confirms that mass murder was carried out for the purpose of frightening people into injecting the covid 'vaccines'... as we can see - the deaths were caused by Midazolam -- https://theviraldelusion.substack.com/p/the-great-lie-and-the-data-that-shows/
This establishes malicious intent.
Concurrent infections of cells by two pathogens can enable a reactivation of the first pathogen and the second pathogen's accelerated T-cell exhaustion
https://hiddencomplexity.substack.com/p/the-intricacies-of-t-cell-exhaustion
IgG4, on the other hand, responds to allergens. If you get stung by a bee for example, your body might react with IgG3 or other antibodies and cause you to have an allergic reaction. To avoid this, your body learns how to recognise relatively insignificant foreign objects by switching to IgG4. Instead of increased inflammation to fight the foreign object, your immune system recognises that this is nothing major. Long term exposure, for example in bee keepers, produces this response. Immunotherapy also works this way by training your body with the foreign object you are allergic to until it is trained to produce an IgG4 response.
https://nakedemperor.substack.com/p/igg4-antibody-class-switch-good-news
So what would happen to the Vaxxers if a lab-made pathogen was released that was designed to exploit the above situation as well as what you have discussed in the presentation?
Would it be possible to spread such a pathogen and severely sicken/kill most if not all Vaxxers due to their damaged immunity?
author
Dr. Kevin Stillwagon
58 mins ago
Author
Yes it is possible. There are elites among us that think the world is overpopulated. The easiest way to reduce that population is to convince people to willingly inject something that they think will protect them, but it does the opposite. And the elites get richer doing it.
From the article:
'Knowing what we already know, it is a travesty that such large swathes of the public still have confidence in covid-19 vaccines, the vehemence of this position in the public’s mind reflecting the power of the machine driving the agenda.'
Why after getting jabbed 4 times or more and then still getting infected 4-5 times does anyone still believe that the jabs are what is going to end the pandemic? If they haven’t ended it after 3 years and another round is coming then why in the blue blazes aren’t people waking up to the scam?
Most of the information in the article was what Geert was warning about before the jabs came out. You do not vaccinate during a hot epidemic! And what’s even more damning about the jabs is that the number of infections were going down just before everyone started getting jabbed. You can see that on the graphs. Good chance that this epidemic would have ended years ago if the jabs hadn’t been given.
Thank u GVB.... The government still approves the jabs , they are not stupid or misinformed, this only means one thing ... purposeful depopulation.
The Good News Is:
We Are Not Fighting To Save Anyone - Any More.
We Were Fighting To Save People From The Shots.
We Don't Have To Do That Any More.
We Saved More Than We Needed To. We Saved Plenty.
Now We Are All Fighting Against Those Dumb Enough
To Have Believed The Lie:
The Dead - The Dumb- And The Suffering -
Are Now The Enemies Of The Majority.
So - Keep Beating The Living Shit Out Of Them.
'Like Your Intuition Tells You To.
I used claude.ai to automatically summarize Geert's “Immunological correlates of vaccine breakthrough infections caused by SARS-CoV-2 variants in highly C-19 vaccinated populations”
I don't know if it is accurate.
Here is a summary of the key points from the article:
1.Steric immune refocusing (SIR) is a major game changer in the COVID-19 pandemic. SIR enables the host immune system to redirect its response to more conserved, less immunogenic spike protein epitopes after vaccine-induced antibodies lose neutralizing capacity against immune escape variants like Omicron. This results in delayed maturation of low affinity, broadly neutralizing antibodies into IgG4 antibodies, promoting further immune escape.
2. SIR-enabling vaccine breakthrough infections (VBTIs) drive viral immune escape while enabling cross-reactivity with unrelated antigens. Prolonged immune refocusing can lead to antibodies that recognize 'self' antigens, causing autoimmunity, or 'altered self' antigens on cancer cells, enabling immune evasion by tumors.
3. Elevated IgG4 antibody levels link enhanced viral immune escape to increased rates of cancer and autoimmune disease in highly vaccinated populations via SIR. SIR-disabling VBTIs with highly infectious variants cause generalized immune suppression, leading to cancer reactivation and flare-ups of chronic infections.
4.The likelihood of vaccinees developing immune pathology after VBTIs is primarily determined by time elapsed since initial SIR events, not individual risk factors. More SIR events over time raise probability of pathogenic antibodies.
5. Viral immune escape is driven by evolutionary pressure to establish herd immunity and protect the human species, not viral survival strategy. Frequent SIR-enabling VBTIs slow viral evolution until innate immunity can control variants.
6. mRNA vaccines raise IgG4 levels when given before natural infection, promoting SIR and immune escape. Immune protection from natural infection is superior to current COVID vaccines.
7. In conclusion, increasing IgG4 antibody levels link enhanced viral immune escape to non-COVID morbidity/mortality. This signals impending risk of healthcare crisis in highly vaccinated populations as virus evolves resistance to population immunity.
Dr. Vanden Bossche and fellow subscribers — this is a little off topic and quite long and detailed but urge you to have a look.
https://open.substack.com/pub/georgewebb/p/george-webbs-schwab-me-no-more?r=lm4tj&utm_campaign=post&utm_medium=web
My SIL's mom was just diagnosed with an immunological disease. Of course, her mom is quadruple jabbed.
Keep banging the drum!