Here is another article showing more history of these self spreading vaccines:
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Exactly.You don't catch a contact buzz on people who shoot heroin. Why would a "contact vax" be any different?
Exactly.
Besides, if a drug could jump this way we'd all be on ssri's and antibiotics. Shedding is the way viruses jump hosts. Drugs aren't alive and don't need to go anywhere.Probably heroin doesn't migrate to all of your skin cells the way the vax mRNA does.
New discussion of Bat Plague vax studies has a lot of new material.
First thing we learn was there was only a 2% likelihood of the mRNA vaxxes making it through Stage 2 (efficacy) and Stage 3 (population benefit) trials.
I learned more from reading this well-written piece than anything else to date. Thank you for all you do for the RPF.Here's something troubling (p. 7). They slightly modified the spike protein to favor a stable configuration in its prefusion state. That's meant to provoke a stronger immune response.
But this might also mean the spike protein produced by the human host cell lingers in the plasma membrane bound to ACE2 receptors because of its impaired fusion capability. And we don't know what the effect of that would be.
Also, several experiments showed that producing spike protein alone failed to initiate a T cell response in animal studies. Yet the mRNA vaxxes contain only mRNA to produce the spike protein, despite its observed poor performance.
But this might also mean the spike protein produced by the human host cell lingers in the plasma membrane bound to ACE2 receptors because of its impaired fusion capability. And we don't know what the effect of that would be.
I learned more from reading this well-written piece than anything else to date. Thank you for all you do for the RPF.
Regarding the polyethylene glycol (PEG) modified lipid nanoparticles, a study showed that small doses (such as the vaccine dose) can lead to dramatic pathological immune activation. In animal studies, it was responsible for anaphylaxis and cardiovascular collapse.
ADE would mean the antibodies produced by the vaxxes were insufficient to neutralize the virus upon reexposure. (When you look at the weak antibody response to vaxxes that produced only the spike protein, like the vaxxes people are actually getting, this is a real concern.) Nevertheless, they'd bind with the virus, facilitating viral entry into cells and producing even worse illness.
This section just gets worse from there. For example, a 2019 study showed preexisting immunoglobulin antibodies, induced by prior vaccination, contributed to severe pulmonary damage by Bat Plague in macaques.
Solid find here @Nemo! Thank you. Already sent it off to some vaxxed people I know.New discussion of Bat Plague vax studies has a lot of new material.
It has a more in-depth discussion of the vax' contents than I've seen before, plus in-depth discussion of the nanolipids and PEG coating, the ADE issue, and the Mad Cow prions.
They discuss emergence of new Covid strains as a result of the vaxxes. Richard M. Fleming MD PhD JD was sounding the alarm about this back in January and he seems to have been proven right. Essentially immune-compromised people are breeding grounds for new strains resistant to the antibodies produced by the vaxxes. They predict there will be more calls for new rounds of shots every few months, and it will be "an arms race that we will probably lose."
They also discuss studies supporting environmental transmission, and a plausible process by which exosomes from dendritic cells in the spleen containing misfolded spike proteins may be transmitted via exhalation and other methods from vaxxed to unvaxxed people.
The discussion was written by Stephanie Seneff, who works at the Computer Science and Artificial Intelligence Laboratory at MIT, and Dr. Nigh, who specializes in Naturopathic Oncologogy at Immerson Health in Portland, Oregon. It was released this week in the International Journal of Vaccine Theory, Practice, and Research, and devotes a considerable space to discussing the research of Dr. J. Bart Classen, who first published a research paper on the possibility of prion-linked brain degeneration caused by the COVID-19 vaccine last month.
If you remember, Fleming discussed a study of his colleague, Kevin McCullough, with macaques, in which 100% of the monkeys got Mad Cow from the prion portion of the spike protein. Same with another study on humanized mice.
I think you'll be interested in this paper. 42 pages.
I believe this to be a part of the "Plan". We will become wholly dependent on big pharma for new cures to sustain life once we have chronic autoimmune conditions.The cherry on the ADE sundae:
Antibodies to the spike protein (the expected outcome of the Bat Plague shots) have been found to produce high levels of cross-reactive antibodies against endogenous human proteins!
This may manifest as either acute or chronic autoimmune and inflammatory conditions.
This rings true to me. Honestly this has worked brilliantly for all of the other vaccines, why wouldn’t it with these injections? The amount of allergies, chronic disease, brain and neurological illnesses, cancers and on and on can be traced back to the horrific CDC vaccine schedule in the US.I believe this to be a part of the "Plan". We will become wholly dependent on big pharma for new cures to sustain life once we have chronic autoimmune conditions.
On p. 15, you can see tissues likely to be attacked (a Peater's nightmare): tTG (associated with celiac disease), TPO (Hashimoto's), myelin basic protein (multiple sclerosis). Also liver tissue, mitochondria, nervous system, digestive system, and the pancreas.
I believe this to be a part of the "Plan". We will become wholly dependent on big pharma for new cures to sustain life once we have chronic autoimmune conditions.
On p. 17, you can see where the mRNA travels from the injection site. It goes everywhere. First to your lymph nodes, then heavily to your spleen and liver, but also to your blood, lungs, brain, etc.