We also have solid evidence wrt why all mRNA causes harm. “Yet, nobody wants to talk about it.” These first-order negative effects, which are based on Nobel-Prize-Winning discoveries that have been taught in med-schools for decades, are explained by experts in the refs below, using understandable layperson terms.
Basically, when a cell is infected by mRNA, it is tricked into making foreign, non-self-proteins, which essentially marks this mRNA-infected cell for violent death by “complement” (killer system #2 in body), if antibodies are present (as they would be after 1st shot). Thus, mRNA causes the body to attack itself, making all things with mRNA unsafe:
* Blood vessels damaged first, causing blood clots and leaks, which then enable damage to surrounding organs
* Above mechanisms explain sudden death and most other mRNA injuries
This item is for those that think the covid debacle was due to accident and/or incompetence. This Yeadon video supports Bhakdi video and also provides solid evidence that the covid crimes against humanity were intentional.
Not a transcript, but hope below will help to get most of the key points across.
.
Summary:
* Antibodies generated by covid.shots are both useless and dangerous (even if spike protein was not dangerous in its own right); that is, they:
___* Never leave bloodstream in order to reach cells lining airways, where they would need to be in order to capture/neutralize viruses that are breathed in
___* Automatically activate "complement" (killer system #2) to kill cells that produce spike protein (a non-self, foreign protein)
* Basis for above can be found in attached briefing by Dr Bhakdi MD, and in annotated slides below
.
Note = Similar issues exist for non-mRNA covid.shots because these also use spike protein, which is not only a non-self, foreign protein, but also a human developed bioweapon (patented by Pfizer in 1990)
.
=====
.
Slide-A
* T-cells (killer system #1) recognize:
___* Self proteins from birth (using random sequenced receptors generated in womb)
______* Nobel prize awarded for this discovery
______* Killer functions against self proteins are kept in-check throughout life
___* Non-self proteins from birth
* Such friend/foe detections appear to be based on presence/absence of known "pilot" nucleic acid sequences in protein
.
Slide-B
* Depicts T-cell detection/activation mechanisms for self-proteins and non-self-proteins
* Cross indicates that, although T-cells detect self-proteins, they are not activated by them (to destroy cell)
.
Slide-C
* Antibodies:
___* Are made by B-cells activated as a result of T-cell activation by fragments of non-self proteins
___* Capture/neutralize foreign proteins identified by T-cells
___* Play a very subordinate role relative to T-cells immunity, which all humans have from birth
* Cells making foreign proteins are targeted for destruction by:
___* Killer System #1 = T-cells
______* Activated by detection of foreign protein fragments on surface of cells replicating viruses
______* Death is "silent" (w/o severe inflammation)
___* Killer System #2 = "Complement"
______* Activated by antibody interactions with foreign protein emerging from an infected cell
_____* Death is "violent" (w/ severe inflammation, which can kill if not suppressed)
* Virus mutations affect at most two protein fragments at a time, so:
___* Human immune system is robust to virus variants (and this is strongly supported by studies using animal models)
___* New vaccines are not needed for immunity to virus variants (if safe/effective vaccines of this type are ever developed)
.
Slide-D
* Process by which observed mRNA vaccine injuries are likely to occur:
___* #1 = mRNA gene (to cause cells to make spike protein) in blood stream is packaged inside of a lipid nano-particle (LNP) in order to:
______* Hide it from immune system (which would destroy it otherwise)
______* Enable easy penetration of cell membranes (via its electric charge, which also enables more severe effects on ovaries, where charges also matter a lot)
___* #2 = lipid nano-particle enters a cell (lining inside of blood vessel)
___* #3 = mRNA gene, exists LNP, and causes cell to make spike protein (a non-self, foreign protein)
___* #4 = spike protein (a non-self, foreign protein) emerges from cell (lining inside of blood vessel) and interacts with antibody (in blood stream) which activates "complement" (killer system #2)
___* #5 = "Complement" (killer system #2) attacks and fatally injures infected cell (in inside lining of blood vessel)
___* #6 = Injured cell sloughs off into blood stream
___* #7 = Missing cell in blood vessel lining allows mRNA gene (inside LNP) to infect other cells in surrounding organ, causing them to make foreign protein (spike protein), which in-turn causes cell to be attacked by "complement" (killer system #2), resulting in organ damage and even more severe inflammation
___* #8 = Damage to blood vessel lining automatically triggers clotting to stop leaks (such clots can cause strokes in brain, plug capillaries in lungs, etc)
* Lipid nano-particles (LNP) in covid.shots are:
___* Very tiny and designed to penetrate cell membranes, and are thus not constrained to muscle injection site as claimed (even blood-brain barrier is penetrated)
___* Able to damage any organs they reach (with brain/heart organs being unable to heal normally from such damage, like other organs are able to do)
___* Much longer-lasting than claimed, weeks to months vice days, so time window for damage is significantly expanded over what was expected.
We also have solid evidence wrt why all mRNA causes harm. “Yet, nobody wants to talk about it.” These first-order negative effects, which are based on Nobel-Prize-Winning discoveries that have been taught in med-schools for decades, are explained by experts in the refs below, using understandable layperson terms.
Two items that refute ongoing narratives are that all mRNA is unsafe due to its fundamental flaws and antibodies play only a minor role in human immune responses. Understandable explanations are given by an expert in 00:45-22:00+ of https://rumble.com/v1p3855-friday-roundtable-worrying-developments-with-michael-palmer-m.d.-sucharit-b.html.
Basically, when a cell is infected by mRNA, it is tricked into making foreign, non-self-proteins, which essentially marks this mRNA-infected cell for violent death by “complement” (killer system #2 in body), if antibodies are present (as they would be after 1st shot). Thus, mRNA causes the body to attack itself, making all things with mRNA unsafe:
* Blood vessels damaged first, causing blood clots and leaks, which then enable damage to surrounding organs
* Above mechanisms explain sudden death and most other mRNA injuries
(good ref = “Roitt's Essential Immunology” Chapter-1)
This item is for those that think the covid debacle was due to accident and/or incompetence. This Yeadon video supports Bhakdi video and also provides solid evidence that the covid crimes against humanity were intentional.
* Link = https://sp.rmbl.ws/s8/2/o/3/7/w/o37wi.caa.mp4?u=8msc5&b=0
* Time Marks:
___11:00 drug design
___11:30 3 clues jabs designed to injure/maim/kill
___12:08 #1 = toxicity of antigen
___13:03 #2 = protection for payload
___15:00 #3 = why all mRNA jabs are harmful
___16:06 tptb are moving all jabs to mRNA = disaster for humanity
Too bad. Rumble is inaccessible to me and millions of other people with hearing issues.
It's been the law to provide captioning on prime time TV since 1993.
In the era of auto captioning there is no excuse for cheapskates with their own private YouTube to not provide captions.
In a word, Rumble Sucks.
You can download a free new book on this topic here (https://doctors4covidethics.org/)
Not a transcript, but hope below will help to get most of the key points across.
.
Summary:
* Antibodies generated by covid.shots are both useless and dangerous (even if spike protein was not dangerous in its own right); that is, they:
___* Never leave bloodstream in order to reach cells lining airways, where they would need to be in order to capture/neutralize viruses that are breathed in
___* Automatically activate "complement" (killer system #2) to kill cells that produce spike protein (a non-self, foreign protein)
* Basis for above can be found in attached briefing by Dr Bhakdi MD, and in annotated slides below
.
Note = Similar issues exist for non-mRNA covid.shots because these also use spike protein, which is not only a non-self, foreign protein, but also a human developed bioweapon (patented by Pfizer in 1990)
.
=====
.
Slide-A
* T-cells (killer system #1) recognize:
___* Self proteins from birth (using random sequenced receptors generated in womb)
______* Nobel prize awarded for this discovery
______* Killer functions against self proteins are kept in-check throughout life
___* Non-self proteins from birth
* Such friend/foe detections appear to be based on presence/absence of known "pilot" nucleic acid sequences in protein
.
Slide-B
* Depicts T-cell detection/activation mechanisms for self-proteins and non-self-proteins
* Cross indicates that, although T-cells detect self-proteins, they are not activated by them (to destroy cell)
.
Slide-C
* Antibodies:
___* Are made by B-cells activated as a result of T-cell activation by fragments of non-self proteins
___* Capture/neutralize foreign proteins identified by T-cells
___* Play a very subordinate role relative to T-cells immunity, which all humans have from birth
* Cells making foreign proteins are targeted for destruction by:
___* Killer System #1 = T-cells
______* Activated by detection of foreign protein fragments on surface of cells replicating viruses
______* Death is "silent" (w/o severe inflammation)
___* Killer System #2 = "Complement"
______* Activated by antibody interactions with foreign protein emerging from an infected cell
_____* Death is "violent" (w/ severe inflammation, which can kill if not suppressed)
* Virus mutations affect at most two protein fragments at a time, so:
___* Human immune system is robust to virus variants (and this is strongly supported by studies using animal models)
___* New vaccines are not needed for immunity to virus variants (if safe/effective vaccines of this type are ever developed)
.
Slide-D
* Process by which observed mRNA vaccine injuries are likely to occur:
___* #1 = mRNA gene (to cause cells to make spike protein) in blood stream is packaged inside of a lipid nano-particle (LNP) in order to:
______* Hide it from immune system (which would destroy it otherwise)
______* Enable easy penetration of cell membranes (via its electric charge, which also enables more severe effects on ovaries, where charges also matter a lot)
___* #2 = lipid nano-particle enters a cell (lining inside of blood vessel)
___* #3 = mRNA gene, exists LNP, and causes cell to make spike protein (a non-self, foreign protein)
___* #4 = spike protein (a non-self, foreign protein) emerges from cell (lining inside of blood vessel) and interacts with antibody (in blood stream) which activates "complement" (killer system #2)
___* #5 = "Complement" (killer system #2) attacks and fatally injures infected cell (in inside lining of blood vessel)
___* #6 = Injured cell sloughs off into blood stream
___* #7 = Missing cell in blood vessel lining allows mRNA gene (inside LNP) to infect other cells in surrounding organ, causing them to make foreign protein (spike protein), which in-turn causes cell to be attacked by "complement" (killer system #2), resulting in organ damage and even more severe inflammation
___* #8 = Damage to blood vessel lining automatically triggers clotting to stop leaks (such clots can cause strokes in brain, plug capillaries in lungs, etc)
* Lipid nano-particles (LNP) in covid.shots are:
___* Very tiny and designed to penetrate cell membranes, and are thus not constrained to muscle injection site as claimed (even blood-brain barrier is penetrated)
___* Able to damage any organs they reach (with brain/heart organs being unable to heal normally from such damage, like other organs are able to do)
___* Much longer-lasting than claimed, weeks to months vice days, so time window for damage is significantly expanded over what was expected.
.