Robin Monotti
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Forwarded from Fiona Rose Diamond (Fiona CoviLeaks)
THE BIG WEEK DAY EVENT IS COMING TO LONDON!

We invite you to help make this the biggest ever weekday protest in our movement.
On the 19th of July @ 12pm we will be making a united stand as Boris delivers his 2nd speech to lift restrictions.

We stand in solidarity with all those that have suffered at the hands of the tyrannical government. We will be the voices for the voiceless. This ends when we say no!


#EndAllRestrictions
#NoMoreLockdowns
#WeStandUnited
#DividedWeFall
#DoNotComply
2001: "The illness known as Gulf war syndrome looks likely to have been caused by an illegal vaccine "booster" given by the Ministry of Defence to protect soldiers against biological weapons, according to the results of a new series of tests.
Scientists in the United States found that symptoms of the illness were the same for service personnel who received the injections whether or not they served in the Gulf."

https://theguardian.com/environment/2001/jul/30/internationalnews
The Science has spoken:

1. Covid19 severity is about your pre-existing immune system, not about "catching" SARSCoV2

2. Many are already immune to severe Covid19 simply from having fought off the flu or CMV

"The COVID-19 pandemic has revealed a range of disease phenotypes in infected patients with asymptomatic, mild, or severe clinical outcomes, but the mechanisms that determine such variable outcomes remain unresolved.

In this study, we identified immunodominant CD8 T-cell epitopes in the spike antigen using a novel TCR-binding algorithm [TCR=T-Cell Receptor]. The predicted epitopes induced robust T-cell activation in unexposed donors demonstrating pre-existing CD4 and CD8 T-cell immunity to SARS-CoV-2 antigen. The T-cell reactivity to the predicted epitopes was higher than the Spike-S1 and S2 peptide pools in the unexposed donors.

[therefore the entire thinking behind spike protein gene therapy is flawed if not irrelevant]

A key finding of our study is that pre-existing T-cell immunity to SARS-CoV-2 is contributed by TCRs that recognize common viral antigens such as Influenza and CMV, even though the viral epitopes lack sequence identity to the SARS-CoV-2 epitopes.

This finding is in contrast to multiple published studies in which pre-existing T-cell immunity is suggested to arise from shared epitopes between SARS-CoV-2 and other common cold-causing coronaviruses. However, our findings suggest that SARS-CoV-2 reactive T-cells are likely to be present in many individuals because of prior exposure to flu and CMV viruses.

In conclusion, our study demonstrates strong pre-existing CD8 T-cell immunity in many unexposed donors contributed by the engagement of cross-reactive TCRs against common CMV [Cytomegalovirus] and flu antigens. The presence of high-quality cross-reactive TCRs can protect individuals by mounting an early CD8 T-cell response and clearing the virus.

"Vaccine" trials tested entirely the wrong thing: antibodies instead of T-cells.

"Many studies have indicated that short and long-term protection against respiratory viruses requires CD8 T-cell immunity and antibody response alone is not sufficient.. Our findings along with a recent report from Peng et al. showed that a higher CD8 T-cell response correlated with a mild disease compared to patients with severe disease.. On the contrary, high levels of neutralizing antibodies were associated with severe disease and ICU visits in many COVID-19 patients suggesting an imbalanced CD4 T-cell response is not optimal for protection"

https://www.nature.com/articles/s41598-021-92521-4
You are much more likely to test Covid19 positive if you are un-"vaccinated", however you are much more likely to die from Covid19 if you have been "vaccinated" compared to un-"vaccinated".

There is a name for this: vaccine enhanced disease or VED. Some call it pathogenic priming. Antibody-dependent enhancement is one of the mechanisms of how it happens. Non neutralizing antibodies effectively act as a Trojan horse for the virus. Remember: innate immunity is from T-cells not antibodies.
Forwarded from Pebbles7799
"The virus attaches itself to the human epithelial cells through noncovalent bonding of its spike protein with the angiotensin-converting enzyme-2 (ACE2) receptor on the host cell. We hypothesized that perturbing the functionally active conformation of spike protein through reduction of its solvent accessible disulfide bond, thereby disintegrating its structural architecture, may be a feasible strategy to prevent infection. Proteomics data showed that N-acetyl cysteine (NAC), an antioxidant and mucolytic agent been widely in use in clinical medicine, forms covalent conjugates with solvent accessible cysteine residues of spike protein that were disulfide bonded in the native state. In silico analysis indicated that this covalent conjugation perturbed the stereo specific orientations of the interacting key residues of spike protein that resulted in threefold weakening in the binding affinity of spike protein with ACE2 receptor. Antiviral assay using VeroE6 cells showed that NAC caused 54.3% inhibition in SARS-CoV-2 replication. Interestingly, almost all SARS-Cov-2 variants conserved cystine residues in the spike protein."

https://chemrxiv.org/engage/chemrxiv/article-details/60c753ec4c89190f3bad43ca
Forwarded from B
All warfare is based on deception.

The supreme art of war is to subdue the enemy without fighting.

Hence to fight and conquer in all your battles is not supreme excellence; supreme excellence consists in breaking the enemy's resistance without fighting.

-Sun Tsu
Media is too big
VIEW IN TELEGRAM
Dr. David Bauer from the Francis Crick Institute: the jabs don't work: let's have more of them!
Media is too big
VIEW IN TELEGRAM
Robin Monotti with Uwe Alschner on Klartext: DEFENDING SOCIETY.

English / German Version of an Interview with Robin Monotti on Democracy, Responsibility and Freedom. 

FULL VIDEO:
https://odysee.com/@klartext:d/defending-society:c

More shorter excerpts coming soon..
Forwarded from Mike Yeadon
https://aapsonline.org/majority-of-physicians-decline-covid-shots-according-to-survey/

Though propagandists smear this medical association it’s statements, as far as I can tell, are at least as balanced (if not more so) than are governments’ statements.

For example, the Federal Government claims that 96% of practising physicians are fully vaccinated against covid19, based on a survey of 300 American physicians.

AAPS conducted a similar survey (small at 700 practising physicians) which found that a far lower 40% had been vaccinated. The association does not claim that the findings are definitive. They did their survey because they suspected the government was lying and it appears they were right to be suspicious.

Thanks,
Mike
Via Dr Mike Yeadon:

"The Treatment of Viral Diseases: Has the
Truth Been Suppressed for Decades?

Lee D. Merritt , M.D.

Since I started medical school in 1976, until 2020, I have
heard the dogma that viral diseases are not treatable (with
some exceptions such as antivirals for HIV/AIDS), certainly
not with antimicrobials. My older son, a newly minted general
surgeon, was educated much more recently, but with the same
misunderstanding. Since viral diseases are not treatable, our
only weapon is vaccination. A friend who spent his life as an
academic university physician retiring in 2016 had never heard
this fact either.
As the “pandemic” broke out, I constantly watched and read
online publications. After reading about the Chinese, Indian,
and Korean use of hydroxychloroquine (HCQ), an antimalarial
agent, against coronavirus, within an hour I found more than
20 scientific papers, written in the last 40 years on the use of
lysosomotropic agents—specifically chloroquine—to treat
viruses. Like Rip Van Winkle, I suddenly awoke, after decades, to
a completely new medical reality.
For example, “numerous investigations have reported
in vitro antiviral activity of AZ [azithromycin] against viral
pathogens with 50% inhibitory concentrations ranging from ~
1–6 μM, with the exception of H1N1 influenza,” write Damle et al.1
They state that in vitro evidence suggests that AZ has antiviral
properties at concentrations that are physiologically achievable
with doses used to treat bacterial infections in the lung.
Intracellular sequestration of AZ may prevent viral replication.
AZ is being used against COVID-19, with the generally stated
rationale being its antibacterial or antiinflammatory activity.
Antibiotics used in Lyme disease, including tetracyclines,
macrolides, metronidazole, and ciprofloxacin, may have activity
against a number of viruses.2
How could all our medical education “overlook” this basic
science?
It may be difficult for non-physicians to appreciate the
magnitude of this world-shaking scientific omission—and
probable cover-up. It is the pharmaceutical equivalent of being
told for 40 years the world is flat—only to have it conclusively
exposed overnight to be round. This idea that viruses—like
the current pandemic SARS-CoV-2 virus—can be killed by
commonly used drugs—antibiotics, antimalarial, or antiparasitic
agents—profoundly changes the practice of medicine."

https://www.jpands.org/vol25no3/merritt.pdf