May 17, 2021

The Dangers of Wuflu Shots

Timothy Birdnow

In a discussion about Covid and the vaccine, David Mulberry observes:

There are no animal studies or long-term effect studies. We are the guinea pigs....................https://principia-scientific.com/17-good-reasons-to-reject-the-rushed-vaccines/?fbclid=IwAR3lSgH4ROshebSZQ5FQ2mR6Uybn6EJwwgkzUMrqoTCvQv38s2A48g5m5AY

I reply:

That is exactly right
David Mulberry.

We are doing a world-girdling clinical trial with this experimental drug.

One thing I've noticed is a common theme of those promoting taking the vaccine is that we have plenty of experience with them. No we do not. This is not a vaccine at all but a gene therapy, and an experimental one at that.

We are using mRNA to reprogram cells to think they have been exposed to the virus and create the proteins needed to generate antibodies. We don't know about side effects, which could wind up being considerable and not show up for a while (like cancer in a few years).

Maybe, maybe not.

That's the whole point of clinical trials. We skipped them and have experimented on human beings.

In fact, there is a real danger of enhancing this virus with an ineffective "vaccine". https://www.bulatlat.com/2020/08/21/hazards-of-the-covid-19-vaccine/

From the article:

The fact that an entirely new RNA vaccine technology which has never been used before in humans is a danger signal that should not be ignored. Several of the US candidates (Moderna, Pfizer/BioNTech, and Arcturus Therapeutics) are using this never-before-approved technology. Exogenous mRNA is inherently immunostimulatory, and this feature of mRNA could be beneficial or detrimental. It may provide adjuvant activity and it may inhibit antigen expression and negatively affect the immune response. The paradoxical effects of innate immune sensing on different formats of mRNA vaccines are incompletely understood. Potential safety concerns include local and systemic inflammation, biodistribution and persistence of expressed immunogen, stimulation of auto-reactive antibodies, and potential toxic effects of non-native nucleotides and delivery system components. A mRNA-based vaccine could also induce potent type I interferon responses, which have been associated not only with inflammation but also potentially with autoimmunity. Another potential safety issue could derive from the extracellular RNA which has been shown to increase the permeability of tightly packed endothelial cells and may promote blood coagulation and pathological thrombus formation. (10)

Another danger of mRNA vaccines is the use of biotech "carrier systems” involving lipid nanoparticles (LNPs). LNPs "encapsulate the mRNA constructs to protect them from degradation and promote cellular uptake,” and additionally, rev up the immune system. The LNP formulations in the three mRNA Covid-19 vaccines are also "PEGylated,” meaning that the vaccine nanoparticles are
coated with a synthetic, non-biodegradable and increasingly controversial polymer called polyethylene glycol (PEG). LNPs could contribute to one or more of the following: immune reactions, infusion reactions, complement reactions, opsonation reactions, antibody reactions or reactions to the PEG from some lipids or PEG otherwise associated with the LNP, as well as adverse reactions within liver pathways or degradation of the mRNA or the LNP, any of which could lead to significant adverse events. Furthermore, PEG can also provoke severe neuropsychiatric symptoms in offsprings, including mood swings, rage, phobias and paranoia. Investigators who once assumed that the polymer was largely "inert” are now questioning its biocompatibility and warning about PEGylated particles’ promotion of tumor growth and adverse immune responses that include "probably underdiagnosed” life-threatening anaphylaxis. This is a significant concern since a 2016 US study reported detectable and sometimes high levels of anti-PEG antibodies (including first-line-of-defense IgM antibodies and later-stage IgG antibodies) in approximately 72% of contemporary human samples and about 56% of historical specimens from the 1970s through the 1990s. The manufacturers of genetically engineered adenoviral vector COVID-19 vaccines undergoing clinical trials (Johnson & Johnson, Oxford, and CanSino) also use PEG as an inexpensive additive for vaccine storage. If one of the PEGylated mRNA vaccines for Covid-19 gains approval, the increased exposure to PEG will be unprecedented and potentially disastrous. (11,12)

Like the mRNA vaccines, the adenoviral vector COVID-19 vaccines are still experimental and have not been used before in mass vaccination for infectious diseases. Given the history of poor safety record of many vaccines, the risk of unpredictable and potentially disastrous adverse effects is of utmost concern.

For example, among other dangers, the virus-vectored vaccines could undergo recombination with naturally occurring viruses and produce hybrid viruses that could have undesirable properties affecting transmission or virulence. The numerous variables affecting the probability that recombination will take place and the possible outcomes of recombination are practically impossible to quantify accurately given existing tools and knowledge. The risks, however, are real, as exemplified by the emergence of mutant types of viruses, enhanced pathogenicity and unexpected serious adverse events (including death) following haphazard mass vaccination campaigns and previous failed attempts to develop chimeric vaccines using genetic engineering technology.

This from a virus with a low mortality rate primarily confined to the sick and elderly who can be shielded. And of course the whole thing was based on bad modeling from Nial Ferguson at London's Imperial College (he predicted three million dead in Britain alone.)

So lockdowns, mask mandates, "social distancing" rules, etc. were all forced on the public, and now this risky vaccine, something we do not have reliable clinical studies to support taking.

And there has been research claiming the Wuhan virus can slip into your chromosomes and so you can show up infected after getting over it. IF the virus can get into your chromosomes, why do we not think the vaccine will not alter them likewise? https://science.sciencemag.org/content/372/6543/674.full#main-content

If people are afraid of the virus and want to take the risk of the vaccine, that's fine and their business but our authorities are pegging everything to vaccination when the damnable epidemic is already pretty much over. They won't let us live our lives unless we can prove we've taken the shot. I don't recall seeing vaccinations as part of the enumerated powers granted the Federal government by our Constitution.

I choose to be secure in my person, as is my fourth amendment right.

Posted by: Timothy Birdnow at 08:56 AM | Comments (1) | Add Comment
Post contains 984 words, total size 7 kb.

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Posted by: gclub at May 19, 2021 02:04 AM (xvrm4)

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