Posted on 05/22/2021 2:26:40 PM PDT by ransomnote
Here's a table for Thrombocytopenia - I've made others for cardiac, paralysis, anaphylaxis and stroke. Note that all Covid-19 shots are in the top 5 most reported for TCP.
I sorted CDC VAERS reports for all vaccines to see how the Covid vaccines compare with prior vaxs. They are at the top of the list in about 6 months of use, and that list has been built over the course of 30 years.
The data below is valid for 5/14/2021 and is strictly for the word "Thrombocytopenia" in the event description field for all vaccines in VAERS.
The CDC and pharmas knew more harm could result and never told the public. Note that thrombocytopenia is on the list.
BDParrish: VAERS data could be manipulated by a conspiracy sure but that assertion is completely beside the point. How does it kill? What hypothesis is suggested for the danger?
ransomnote: There are many ways in which the Covid-19 vaccinations kill but a commonly cited example is the production of trillions of spike proteins to produce an immune response. It works- antibodies go up. But the spike proteins, which have been found present in blood although they aren't supposed to be, attach to body cells and cross the blood-brain barrier.
The body identifies the spike proteins, AND THE CELLS TO WHICH THEY ARE ATTACHED, as pathogens and attacks, which results in a host of problems including sepsis, liver failure, heart attack, clotting, strokes etc.
ADE is a known risk of the mRNA's - all animal trials from 2005 to present for mRNA 'vaccines' failed because after 100% of the trial animals (cats) developed the desired antibodies, 100% of them died when exposed to the virus. Over reaction or Antibody Dependent Enhancement (ADE).
PEG: an allergen in Pfizer known to cause anaphylaxis
Moderna has a different toxin:
Horrifying Bombshell! Connecticut Warns Moderna VAX Contains Deadly Poison
And then the spike proteins include a component that is highly damaging and cross the blood brain barrier. The vax pushers deny that the 'vaccine' spike protein retained this component said to be found in Covid, but with so much evidence against everything else they say, I've been seeing reports that it remains an issue.
BTTT!!!
The moderna Modified RNA is coated on a lipid globule. This globule is a pass key to cross any cell membrane.
So, the spike protein, is manufactured indiscriminately, wherever it lands in your body.
The virus can only enter through the ACE2 receptor. It is limited where it can replicate. It does not infect the brain, for example.
So why do they give babies/kids 21 different 'vaccines' now?
You have absolutely no idea what that number means do you. You have absolutely no idea about how contagious this disease is. You have absolutely no idea how this disease can overwhelm a hospital system to a point where people have to make a choice about who gets treatment and you have absolutely no idea about the long haulers.
Quit misleading people.
Thank you Triple for trying to help.
I understand the lipid nanoparticle quite differently than you describe. There is some secrecy involved in the making process which they perfected quite recently, and I am at a complete loss as to how they make that. But anyway some have suggested that there is something poisonous in the lipid coat, but I cannot see how. Everything they say about it and how they must keep it so cold all makes sense to me.
The mRNA theory I knew about for a long time as there was some talk using that for many different diseases even HIV! I expect them to go forward with all that now.
https://www.contagionlive.com/view/moderna-unveils-results-of-new-mrna-vaccine-candidate-trials.
The virus enters the cell using the spike protein, yes, the cells make the spike protein as instructed by the mRNA indiscriminately, yes of course. I am not finding what the problem might be with crossing the blood/brain barrier, which is an interesting observation, but it fails me to see the mechanism of harm in that.
ransomnote gives me VAERS data etc, but my reaction to all that is that the vaccine works as advertised. I can understand idiosyncratic vaccine reactions without further instruction. Thanks ransom for trying to help. I thought you had become frustrated or angry with me. If you find a specific mechanism of harm that creates a pattern of symptoms in VAERS data please let me know. Cathi has also kindly sent me a few things.
I saw the McCollough(?) video out of Texas, and I also saw what you referenced from Vanden Bossche, which I understand you, ransom, found convincing, but I did not find there what I was looking for. I went back through your comment history and I understand your shotgun approach. Just keep throwing things at the wall until something sticks. I really have no problem with that and I do not ask you to change your approach as what you are doing will force out the truth whatever it may be!
Off to church and thanks both of you!
You have absolutely no idea what that number means do you. You have absolutely no idea about how contagious this disease is. You have absolutely no idea...
__________________________________
Projecting suits you quite well.
If you find a specific mechanism of harm that creates a pattern of symptoms in VAERS data please let me know.
~~~~~~~~~~~~~~~
Why would I waste my time? You are here to refute evidence out of hand. Yours is a different tactic. You claim you are filtering for evidence, in a sea of evidence on FR, and then, “tsk, tsk, tsk...nothing to see here.”
So you see no risk with inflammatory spike protein being manufactured in your cranium?
Nice...
You have matter of factly stated that you know “better” about the lipid coat than I do. How can you possibly be so sure of that?
Do you disagree that it (lipid coat) is a pass key through cell membranes?
Do you agree that sars-cov-2 binds / accesses cells only through the ACE -2 protein in the cell membrane?
And yet it (modified RNA coated in a pass-key lipid) still leaves you with no cause for cornerman.
—-GMAB
You wrote:
...the US has recorded the lowest Covid numbers since last June and the reason for that is the vaccines ...
Or else the reason is this usually mild, sometimes almost asymptomatic, cold/flu virus, like its predecessors, has run its course and we have reached herd immunity.
You quote me that I know “better” than you. Please note the actual words I used. There is no implied insult. Here I will offer you an implied insult: You are angry and frustrated at the perceived failure of your argument, so you took umbrage at my comment. This concerns me not in the least.
OK so, at your prodding, I am looking at stuff now about Sars-Cov-2 s1 protein crossing the blood/brain barrier. Here is the best I found:
https://www.nature.com/articles/s41593-020-00771-8.pdf
You need not read it, I just show you what would be the limit of my awareness of this. I know that antibodies cannot protect the brain from a direct attack by SARS2 on the brain as they do not pass.
If you demonstrate that the S1 produced by the mRNA vaccine is as dangerous as the SARS-Cov-2 spike protein, would you point me to it?
Here is what I know about the lipid bilayer:
https://blogs.sciencemag.org/pipeline/archives/2021/01/11/rna-vaccines-and-their-lipids
You may wish to skip to the Jan 11 comments by Dr. Ulm.
Correct me in any way you may, I am happy to listen to you.
I believe I paraphrased, not quoted. Here is what you wrote exactly.
“I understand the lipid nanoparticle quite differently than you describe. There is some secrecy involved in the making process which they perfected quite recently, and I am at a complete loss as to how they make that. But anyway some have suggested that there is something poisonous in the lipid coat, but I cannot see how. Everything they say about it and how they must keep it so cold all makes sense to me.” BDP
I still read that as you think your different understanding is more complete and correct, therefore better.
https://www.biorxiv.org/content/10.1101/2021.03.16.435700v1
Title of above linked scientific article: “SARS-CoV-2 spike protein induces inflammation via TLR2-dependent activation of the NF-κB pathway”
———//—-
The spike protein, is inflammatory.
The mRNA vaccines can cause its manufacture in any cell, because unlike the virus, it uses a pass-key like lipid layer to enter cells.
The virus can only enter through the ACE2 protein on the cell membrane. Not all cells have this viral entry point.
I will let you do the math with the above facts.
OK I’ll check that out.
The s1 that Moderna describes which I can allow might be a complete fiction, is so simple in structure, that it oughta work as described/intended. As data comes in, which is a nice way of saying that the bodies of the dead will continue to pile up, then we can look at patterns which will suggest a back door into how the vaccine causes the harm. This is in God’s hands and much as I hate it, this is the sin-cursed world we live in.
“Work as intended” to my mind means that the mechanism of danger, assuming there is one, will be found in the effect of the vaccine spike itself. This is what is currently being explored in the literature around brain clots, crashing platelet count, and myocarditis, especially in teens. There is a big clue in that last one. I’m watching for what they may find.
I started reading virology back in the late eighties. I was trying to understand why the Spanish flu was so deadly. Because I knew Latin, I found I could understand the literature. When COVID-19 hit, because of open access I got from Elsevier free login credentials which also included science direct, and for over a year I can read anything I want.
What you may interpret as arrogance on my part, and I am as prideful as the next guy, may come from my hurrying past things that I believe would not be productive. My faith and my family teaches me NOT to be disrespectful, but I know that my attitude and approach serves my own curiosity first, and devalues you as a person and your opinions.
Regards and thanks!
FYI There are two other entry pathways I know about, TMPRSS2 and neuropilin-1 for SARS-Cov-2. Even so I do not follow your argument, as I am missing something which you leave unstated. I enjoyed the BioRx14 article! Thanks. It does not show a pathogenicity for the mRNA-created spike protein, but I'll read it again tomorrow.
You are arguing that the actual spike protein and the synthetic genetically engineered protein from the Pfizer modified RNA are significantly different, but close enough for immunity. That is a pretty narrow slot.
You do agree that the native spike protein is inflammatory, right?
Also, I don’t think you are stating that the native virus has a pass-key like entry into any cell, as the modified RNA with the lipid coat in the Pfizer injection has.
Are you? (That would be really silly.)
Later...
Please don't misunderstand me. I am NOT trying to convince you of anything. I will try to get things out of you by trying to poke holes in your arguments, nothing personal with you or anybody else. Usually something will surface sometimes unintended. From you I got another good read, Khan et al., on the inflammatory effect of the spike protein, (Thanks!) and an interesting thought on the immune response to the vaxx s1 in the brain. There is a line of inquiry there that will apply to the risk of post vaxx ITP in all the vaccines. (Interesting)
If there is anything else you would like to help me with then please state it directly. I am on to other things for now.
bttt
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