Fu*%face Von Clownstick

This vaxx was a health disaster...
The covid vaccine is like most things in life..One size doesn't fit all. Some folks took the vaccine followed by multiple boosters and were fine. Others took one part of the two part vaccine and had very serious side effects. Unfortunately you don't know till you know, so to run around calling anyone who took the vaccine an "idiot" is pretty fucking ignorant...
 
That article was retracted nearly a year ago. A fact you would have readily realized had you taken 10 seconds to click the link to the actual journal article, which was shared in the website you posted.
THey're not hard to find...

he thrombo-inflammation and neuropathology sequence motifs of the SARS-CoV-2 spike protein appear to have been engineered into the virus​

Steven Quay, MD, PhD1

ABSTRACT
A landmark [published in Nature—Nass] paper2 entitled, “Fibrin drives thrombo-inflammation and neuropathology in COVID-19,” was published in August 2024 that concluded the mechanism of the thrombotic and neurological symptoms following a SARS-CoV-2 infection, often called “long COVID,” is attributable to the binding of fibrin to discrete portions of the spike protein, specifically three N-terminal domains. This paper is a high impact publication with >110,000 views, placing it in the 99 th percentile of articles published contemporaneously.
Here I examine the regions of the spike protein that bind to fibrin, fibrinogen, or both. The N-terminus of the spike protein contains the three strongest binding peptides and surprisingly, these regions are also the three insertions in the protein sequence that are unique to SARS-CoV-2 and not found in natural sarbecoviruses….
CONCLUSION
This paper highlights an unusual set of facts:
1. SARS-CoV-2 causes neuro-inflammation and its “long COVID” clinical findings through a mechanism whereby fibrin binds to the SARS-CoV-2 spike protein, forming proinflammatory blood clots.
2. Three of the strongest [fibrin] binding motifs identified by Ryu et. al., are in the N-terminus of the SARS-CoV-2 Spike Protein.
3. These motifs are contiguous to the three inserts identified in January 2020 that are not widely found in related-SARS viruses.
4. These inserts are shown to have primary amino acid sequence homology to portions of the HIV gp120 protein that is responsible for CD4 cell receptor binding. While the sequences are individually small, making their probabilities of being randomly significant unlikely, when they are combined as a continuous 60-amino acid sequence, the homology to HIV is highly significant. The combination is justified because the non-contiguous sequences in HIV are none-the-less brought together to form the CD4 cell receptor binding protein.
5. Antibodies from patients with HIV infections have been found which block the HIV CD4 recognition site and neutralize SARS-CoV-2. This demonstrates the three-dimensional homology of these regions in a functionally significant manner.
6. A hypothesis that both HIV and SARS-CoV-2 can infect CD4 cells via this non-ACE2 interaction is supported by abundant clinical findings.
7. HIV does not share the fibrin binding motifs seen in SARS-CoV-2 and, for the most part, evidence of direct HIV binding to fibrin has not been found.
8. RaTG13 shares 59/60 amino acid homology and, for insert 3, a nucleotide homology of 99.3%. Since there are numerous papers suggesting that RaTG13 has undergone laboratory genetic experiments, one much conclude that there is a likelihood that these unusual properties of SARS-CoV-2 did not arise naturally.
mail
Quay, Steven Pathogenesis Of Sars Cov 2 ...
3.67MB ∙ PDF file
Note that on January 23, 2020 She Zheng-Li published on RaTG13 and SARS-CoV-2, pointing out that the 3 gp120 sequences were seen in both SARS-CoV-2 and RaTG13. The origin of RaTG13 is uncertain and it certainly could have been manipulated. These sequences have not been seen in any other beta coronaviruses…

However, Jim Haslam points out that yet a third betacoronavirus, found in Laos by the US Navy (NMRC, a small unit that has long been focused on biodefense), also has the three GP120 inserts. The virus is referred to as “Laos Banal-52” on pages 175 and 415 of his book. The provenance of this virus, and identifying which labs had access to it, would be of great interest.

Bottom line:

  • IMHO, the GP120 segments were clearly added to a coronavirus spike backbone.
  • So were adjacent regions that strongly bind fibrin or related molecules, inducing blood clots and inflammation.
  • Ralph Baric’s repeat protestations against these regions being engineered (see Chapter 16 of Haslam’s book), combined with Baric’s reputation as the most accomplished coronavirus engineer, suggest he had something to do with the engineering, or at least knows more than he has said about it.
  • It is likely, but uncertain, that the fibrin-binding domains were added to enhance pathogenicity.
  • The Navy’s Laos-Banal-52 sample requires further investigation. Was it natural, or might it turn out to be an early iteration of SARS-CoV-2?
 
folks took the vaccine followed by multiple boosters and were fine. Others took one part of the two part vaccine and had very serious side effects. Unfortunately you don't know till you know
They were fine???? really... are you sure... maybe they were but aren't going to be for much longer.. Maybe all the side effects presented as so many different diseases that they never put it together that their new health problems might be related to the vaxx... Like people with compromised immune systems. Turbo cancer, blood clots, neurological issues like dimentia and neuropathy, myocarditis and heart attacks, heart arrythmia. The list goes on.

Anyone that has even a basic undersanding of the history of vaxxines would not touch that covid vaxx...

Anyone that has even a basic understanding of how big Pharma operates would not touch that vaxx...

Anyone that's old enough to remember how the MSM bombarded the airwaves with WMD propaganda, from Fox to NPR, should have had the sense to recognize the gaslighting when they heard it repeated at that level, all over the news again... safe and effective, safe and efective, safe and effective... x 1 million...

Anyone with a bit of common sense should have realized that you can't skip the animal studies, then test a brand new medical technology for 2 months before putting it on the market, without the drug still being experimental. You can't do long term safety studies in 2 years, much less two months... There was zero way to call that vaxx safe, no matter if you were a PhD, or in 5th grade.

Anyone with a bit of common sense should have looked up the ingredients before taking this novel treatment. And if they had, they would have realized that the list of ingredients was never available. And without the list of ingredients, you can't have informed consent. And that should have made you pretty suspiscious about why they were hiding the ingredients.

ANyone with a bit of common sense who missed all that and took the vaxx anyhow, should now realize that they were duped. And they should apologize to the people that tried to warn them not to take that vaxx... They didn't listen... and now they're paying the price.. and what good did it do? It was all for naught.
 
@Daniel are you still falsely advertising as a certified arborist? With all the time and effort you put into this shit, clean up your own house.
You’re meshing apples and oranges.
Lyme? Bioengineered?
Vaccine bad..
Covid bioengineered ?
Hell no don’t take any of the vaccines!

So are the vaccine companies bioengineering epidemics/pandemics for the deep dark?

If for a second these bugs are bioengineered why would there be a global effort to make a cure to fix the oopsies?
 
Ask polio survivors how they feel about vaxines
The polio vaxxine is causing polio Tom...


NEW DELHI: At least 400 children in India would have developed polio after receiving the oral polio vaccine (OPV) over the past five years, a top Indian paediatrician has revealed in a just published scientific paper that questions the ethics of the continued use of OPV.
T Jacob John, who has earlier advised the World Health Organisation and the Indian government on polio eradication policies, has described the continued use of OPV as an “ethical anomaly” that is causing avoidable polio to children.
India has been free from wild polio virus since 2011, but the Ministry of Health and Family Welfare has never released data on vaccine associated polio paralysis (VAPP), a rare adverse effect of OPV that causes infantile paralysis.
All children under 6 in the country have been receiving multiple doses of OPV — that contain live polio viruses — since 1994, through pulse polio programme while the government also launched injectible polio virus schedule for children in 2015.
John challenged the current policy saying the government has continued with OPV because “it’s easy and commercially more viable”. “For the sake of convenience, ethical issues have been ignored by several poor countries like India; the existing programme needs to be reviewed,” added John, an emeritus professor at Christian Medical College, Vellore.
He has published the analysis jointly with Mumbai-based paediatrician Dhanya Dharmpalan in the Indian Journal of Ethical Issues. John has pointed out that in nearly 40 countries, governments had long stopped OPV due to risk of polio associated with it.
In the OPV given to children worldwide, Type 2 vaccine viruses was withdrawn from use in 2016; it continues to contain Type 1 and 3 strains of viruses that can cause VAPP. Children in India are given two intradermal fractional doses of IPV at 14 weeks and 6 years in lieu of the recommended one full dose intramuscular IPV at 14 weeks.
The paper has highlighted that in last five years, globally, cases of polio caused by vaccine viruses have outnumbered those of polio caused by wild polio viruses.
 
@Daniel are you still falsely advertising as a certified arborist? With all the time and effort you put into this shit, clean up your own house.
You’re meshing apples and oranges.
Lyme? Bioengineered?
Vaccine bad..
Covid bioengineered ?
Hell no don’t take any of the vaccines!

So are the vaccine companies bioengineering epidemics/pandemics for the deep dark?

If for a second these bugs are bioengineered why would there be a global effort to make a cure to fix the oopsies?
You see, it's not enough to just engineer a bug to kill some people, you wanna use the fear of the bug to force everyone to take a shot that will kill basically everyone that takes it. This way, it outs the disobedient ones so that they can be rounded up and shot. Jokes on them though because only a relatively small fraction of the people that were supposed to die actually did, because of course, the people in charge are also wildy incompetent. Am I getting this right according to @Daniel ? I gotta say, it is pretty nice to not see his bullshit here anymore.
 
  • Haha
Reactions: evo
How does the ISA feel about him doing that? If there are no consequences for lying about it, what is the point of the cert?
It's not exactly lying. I was certified when the website was built. CA PD-1649. Should still have the card around here somewhere. I haven't made any changes to the website since before the cert lapsed... Last time I took the test, I studied for 3 hours and got a 94... Re-certing wouldn't be hard... I just don't see the point...

ps.. I love that you guys are doing homework on me.
 
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It has everything to do with a persons character and credibility. Lying about being a CA and copping a dismissive attitude about whether the test is easy or not puts the bright shining light of truth on the stage of life

What else is being lied about if ghe truth can’t be told about the easy stuff
 
The polio vaxxine is causing polio Tom...


NEW DELHI: At least 400 children in India would have developed polio after receiving the oral polio vaccine (OPV) over the past five years, a top Indian paediatrician has revealed in a just published scientific paper that questions the ethics of the continued use of OPV.
T Jacob John, who has earlier advised the World Health Organisation and the Indian government on polio eradication policies, has described the continued use of OPV as an “ethical anomaly” that is causing avoidable polio to children.
India has been free from wild polio virus since 2011, but the Ministry of Health and Family Welfare has never released data on vaccine associated polio paralysis (VAPP), a rare adverse effect of OPV that causes infantile paralysis.
All children under 6 in the country have been receiving multiple doses of OPV — that contain live polio viruses — since 1994, through pulse polio programme while the government also launched injectible polio virus schedule for children in 2015.
John challenged the current policy saying the government has continued with OPV because “it’s easy and commercially more viable”. “For the sake of convenience, ethical issues have been ignored by several poor countries like India; the existing programme needs to be reviewed,” added John, an emeritus professor at Christian Medical College, Vellore.
He has published the analysis jointly with Mumbai-based paediatrician Dhanya Dharmpalan in the Indian Journal of Ethical Issues. John has pointed out that in nearly 40 countries, governments had long stopped OPV due to risk of polio associated with it.
In the OPV given to children worldwide, Type 2 vaccine viruses was withdrawn from use in 2016; it continues to contain Type 1 and 3 strains of viruses that can cause VAPP. Children in India are given two intradermal fractional doses of IPV at 14 weeks and 6 years in lieu of the recommended one full dose intramuscular IPV at 14 weeks.
The paper has highlighted that in last five years, globally, cases of polio caused by vaccine viruses have outnumbered those of polio caused by wild polio viruses.
@Daniel And…without the vax what would things look like
 

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