at 9:39 is that diagram which shows excess deaths between Feb 2020 and Dec 2023. Everything related to covid19 HAS TO BE OBVIOUSLY analyzed in 2 periods:
A. Jan2020-Dec2020 = ONLY NATURAL covid19
B. Dec2020 until this day with = Effects of ALL covid injections + covid19 + shedding
A had ZERO excess deaths, B starts with the injections AND immediate excessive deaths
=> the INJECTIONS and possibly shedding are responsible for the deaths.
There are 2 TYPES of Spikes, the 'natural one' (engineered in biolabs and coming with the ENTIRE VIRUS) and the SINGLE ISOLATED SPike from injections, carrying the -PP- mutation, which forces all the SINGLE Spike proteins, produced INSIDE OF EVERY accessible cell, to reside in its cellular membrane. The only 'natural Spike' is always embeded in the entire virus, which only 'opens' when fusing with the native membranes, and even then Spike stays in the viral membranes, except for the few responsible for the fusion process. The extremely excessive SPIKE production by the covid injections, apparently in trillions(!!!!) exceeds the number of infecting virusesx100 by many orders of magnitude (wiki:Examination of virions using cryo-electron microscopy suggests that there are approximately 25[26] to 100 spike trimers per virion.[21][25]).
That -PP- mutation causes that the 'vaccinated' and expressed Spikes are NOT easy digestible, or at least more difficult than the native, PLUS the INJECTED SINGLE spikes accumulate in the membranes, including the vascular membranes, THEN leading to a narrower inner volume of the entire vessel, leading to the topic of this presentation!!!
For anything Spike related: DIGESTIVE ENZYMES, molecules that bind it, like IVERMECTIN, and subsequent elimination.
For anything modmRNA of the SPike related='vaccines'=> PROHIBIT THEM ALL NOW and lock up all MD's who are administering them!!!!
how does a virus get into the blood stream??? A normal cold does not come with bleedings. Imagining only open wounds, looking at all the layers of every single blood vessel...
I posted the following on youtube with intentional misspellings:
In the case of someone that has never been exposed to the spike protein before, what is the first thing that starts / triggers the damage process? Is it the B cell recognizing / detecting something? An antibody detecting something? A natural killer cell (i.e. specialized T-cell, a specialized lymphocyte) that recognizes the foreign protein exposed on the infected cell?
I think it is the natural killer cell (the T-Cell). If so, could any mess. ganatic ribonucleic acid therapy work? ever?
The damage is done by the immune system attacking cells that are infected.
The steps are:
1. The infected cells present fragments of the spike in on the surface.
2. Natural killer cells, T-cells, detect this foreign protein fragment and kill the cell.
All the clots and the myocarditis and endothelium damage is due to the person's own immune system! There is no weird reaction between the foreign spike protein and heart cells or lung cells or endothelium cells or some blood component that is causing the damage. It is the persons own immune system doing the damage. This will happen with *ALL* MRNA vaccines thus there is *NO* way to make a safe MRNA vaccine. The person's own immune cells (natural killer T-cells) will always create damage that HURTS the person far more often than any benefit from the MRNA vaccine. If I don't have this opinion or the terminology correct, please correct me - I am only a mechanical engineer that has studied the immune system.
Cron and Behrens' textbook on cytokine storm syndrome says "HLH [hemophagocytic lymphohistiocytosis] may be associated with severe bacterial infections such as in sepsis... the eight diagnostic criteria of HLH are commonly found in varying extent in patients with sepsis, systemic inflammatory response syndrome (SIRS) and MODS [multiple organ dysfunction syndrome] where HLH is at the extreme end of this ladder of (hyper)inflammation before death. Notably, patients treated in the ICU with a clinical presentation of sepsis/septic shock but with no identified infectious pathogen, and who are unresponsive to sepsis-directed therapy, may have an undiagnosed HLH". HLH is recognised as being a severe cytokine storm syndrome. I have personally treated several multiple sclerosis patients with coma from sepsis (usually secondary to a urinary tract infection) with high-dose steroids with good results. The bottom line is that the cytokine storm is the end result of numerous triggers, including various pathogens, some medications and other things... such as spike protein. It is not surprising that if a virus with the right spike protein configuration sets off a storm then the spike protein itself may do the same. Of course, with M-RNA "vaccines" the body is induced to produce an unknown quantity of spike for an unknown time, running the risk of developing a prolonged hyperimmune state.
The World Council for Health is running an interesting study on detoxification, including from spike, at the moment. Worth checking out.
You might check:
https://inmodia.de/en/
or
https://mmd-labor.de/de/ (no real website in English language; you have to use a translator)
Both in Germany.
MEGA
🇩🇪 MMD some PDF’S translated
https://mega.nz/folder/Jusj2Bja#xcqQmuKflO5zmGn7h98QMg
…❌…
⬇️
PDF TRANSLATOR WEBSITE
https://www.onlinedoctranslator.com/en/translationform
at 9:39 is that diagram which shows excess deaths between Feb 2020 and Dec 2023. Everything related to covid19 HAS TO BE OBVIOUSLY analyzed in 2 periods:
A. Jan2020-Dec2020 = ONLY NATURAL covid19
B. Dec2020 until this day with = Effects of ALL covid injections + covid19 + shedding
A had ZERO excess deaths, B starts with the injections AND immediate excessive deaths
=> the INJECTIONS and possibly shedding are responsible for the deaths.
There are 2 TYPES of Spikes, the 'natural one' (engineered in biolabs and coming with the ENTIRE VIRUS) and the SINGLE ISOLATED SPike from injections, carrying the -PP- mutation, which forces all the SINGLE Spike proteins, produced INSIDE OF EVERY accessible cell, to reside in its cellular membrane. The only 'natural Spike' is always embeded in the entire virus, which only 'opens' when fusing with the native membranes, and even then Spike stays in the viral membranes, except for the few responsible for the fusion process. The extremely excessive SPIKE production by the covid injections, apparently in trillions(!!!!) exceeds the number of infecting virusesx100 by many orders of magnitude (wiki:Examination of virions using cryo-electron microscopy suggests that there are approximately 25[26] to 100 spike trimers per virion.[21][25]).
That -PP- mutation causes that the 'vaccinated' and expressed Spikes are NOT easy digestible, or at least more difficult than the native, PLUS the INJECTED SINGLE spikes accumulate in the membranes, including the vascular membranes, THEN leading to a narrower inner volume of the entire vessel, leading to the topic of this presentation!!!
For anything Spike related: DIGESTIVE ENZYMES, molecules that bind it, like IVERMECTIN, and subsequent elimination.
For anything modmRNA of the SPike related='vaccines'=> PROHIBIT THEM ALL NOW and lock up all MD's who are administering them!!!!
how does a virus get into the blood stream??? A normal cold does not come with bleedings. Imagining only open wounds, looking at all the layers of every single blood vessel...
I posted the following on youtube with intentional misspellings:
In the case of someone that has never been exposed to the spike protein before, what is the first thing that starts / triggers the damage process? Is it the B cell recognizing / detecting something? An antibody detecting something? A natural killer cell (i.e. specialized T-cell, a specialized lymphocyte) that recognizes the foreign protein exposed on the infected cell?
I think it is the natural killer cell (the T-Cell). If so, could any mess. ganatic ribonucleic acid therapy work? ever?
The damage is done by the immune system attacking cells that are infected.
The steps are:
1. The infected cells present fragments of the spike in on the surface.
2. Natural killer cells, T-cells, detect this foreign protein fragment and kill the cell.
All the clots and the myocarditis and endothelium damage is due to the person's own immune system! There is no weird reaction between the foreign spike protein and heart cells or lung cells or endothelium cells or some blood component that is causing the damage. It is the persons own immune system doing the damage. This will happen with *ALL* MRNA vaccines thus there is *NO* way to make a safe MRNA vaccine. The person's own immune cells (natural killer T-cells) will always create damage that HURTS the person far more often than any benefit from the MRNA vaccine. If I don't have this opinion or the terminology correct, please correct me - I am only a mechanical engineer that has studied the immune system.
No damage by immune cells (that‘s right!) without a source.
Am I the only one who keeps hearing about people getting and/or dying from sepsis, and is this related in any way to the STORM?
Cron and Behrens' textbook on cytokine storm syndrome says "HLH [hemophagocytic lymphohistiocytosis] may be associated with severe bacterial infections such as in sepsis... the eight diagnostic criteria of HLH are commonly found in varying extent in patients with sepsis, systemic inflammatory response syndrome (SIRS) and MODS [multiple organ dysfunction syndrome] where HLH is at the extreme end of this ladder of (hyper)inflammation before death. Notably, patients treated in the ICU with a clinical presentation of sepsis/septic shock but with no identified infectious pathogen, and who are unresponsive to sepsis-directed therapy, may have an undiagnosed HLH". HLH is recognised as being a severe cytokine storm syndrome. I have personally treated several multiple sclerosis patients with coma from sepsis (usually secondary to a urinary tract infection) with high-dose steroids with good results. The bottom line is that the cytokine storm is the end result of numerous triggers, including various pathogens, some medications and other things... such as spike protein. It is not surprising that if a virus with the right spike protein configuration sets off a storm then the spike protein itself may do the same. Of course, with M-RNA "vaccines" the body is induced to produce an unknown quantity of spike for an unknown time, running the risk of developing a prolonged hyperimmune state.
No. I, as an intensive care doctor, am seeing the same.
Has the human genome ever contained spike proteins? I only see it in reference to C19.