mRNA Vaccine Primer: My Top 5 Concerns with the COVID jabs
There's a bunch of stuff found to be dangerous with the jabs, but these are the five that have stood out to me...
This Stack is meant to serve as a Primer - or introduction - to anybody who might finally be starting to ask questions. For most of us, this is not new news, but for someone starting from scratch I hope it can serve as a decent introduction. I put it together because, finally, I’m getting people in my circles asking questions and at least trying to listen when I respond…so keep in mind that there’s bit of fun teasing of my friends in here (they asked for the PowerPoint version because w’re corporate douchebags who PowerPoint everything…) and the language can be a bit playfully insulting as the target audience is my friends…
OK, to start with…I’m no scientist. Not in any way. No qualifications, no experience. But, I’m no slouch, either, and just like most of you I’ve spent the last 4 years reading furiously, learning what I can, and tooling myself up to serve in a war that, at present, is based on knowledge and information.
So, I’m no expert, but…
There are people out there who do have the expertise. They do have the qualifications. Or they’ve done way more than me to go from being a layperson to an informed voice. They do have the runs on the board. Most of you would already know these names but, just in case you don’t, here are (in my opinion) 5 must follows:
Jikkyleaks - The Mouse that roars
Twitter: @Jikkyleaks;
Kevin McKernan - The man who exposed the DNA contamination
Twitter: @Kevin_McKernan
Jessica Rose - The relentless surfer
Twitter: @JesslovesMJK
Walter M. Chestnut - Was calling Amyloidosis before anyone knew what it meant
Twitter: @Parsifaler
DoorlessCarp - Once a layman, but not anymore…
Twitter: @DoorlessCarp
Okie doke, let’s get going…
1) When the vaccine does what it's supposed to do, that's bad - biodistribution of the LNPs;
2) Codon Optimisation - Nice way to misfold a protein;
3) DNA Contamination - Cancer is cool, right?
4) n1-methylpseudouridine - What's wrong with a little frameshifting, amiright?
5) IgG Class Switching - Why eliminate when you can tolerate?
1) When the vaccine does what it's supposed to do, that's bad - biodistribution of the LNPs
In short - biodistribution. The vaccine does not stay in the arm, as we were told it would.
Bret Weinstein gives a nice explanation to Tucker Carlson, with some video from NZ spliced in to emphasise how we were lied to.
(NOTE: I don’t know where this video comes from so cannot give credit. If anyone could fill me in then that would be nice)
So, contrary to the lies we were told, the LNP envelopes slip out of the injection site, into the bloodstream, and distribute throughout the entire body (called Biodistribution). Tucker and Weinstein touch on the brain and the heart but there are other places that, to me, are more concerning…
https://www.tga.gov.au/sites/default/files/foi-2389-06.pdf
Therapeutic Goods Administration (Australia) - Non-Clinical Evaluation Report of Cominarty (Pfizer) Vaccine - Page 45 – Biodistribution Study.
NOTE: “FOI” in URL above stands for Freedom of Information, meaning the TGA tried to keep this document secret but were forced to release it to the public only once FOI request submitted. Basically, they were sued into releasing what they wanted to keep from the public…
TGA document is from January, 2021 and mRNA vaccines were not administered in Australia until May, 2021 – so they had this knowledge at least 4 months before a single dose administered in Down Under…
Brain and Heart mentioned in previous clip, but, worse than that…nice ovaries you have there. Would be a pity if we transfected them with LNPs that produce a protein that your body wants to kill by wiping out the cells we transfected...
Remember the menstrual issues reported during the rollout? Those would most likely have been from vaccine Spike Protein presenting in uterine tissue. The immune system would have attached the uterus once it presented Spike and so the body would have kicked in with it’s natural mechanism of shedding the uterine wall - leading to menstrual issues even among post-menopausal women.
Now, imagine the damage it has done to the ovaries. New oocytes (eggs) cannot be made. A woman has every egg she will ever have on the day she is born. Any damage is permanent and cannot be fixed with new growth or replacements.
Summary:
Vaccine is designed to have your cells produce foreign protein (the Spike Protein). Your immune system will recognise and destroy any cells that present with Spike Protein - because it sees it as a foreign invader;
Regulators assured public that mRNA vaccines stayed at the site of injection (deltoid muscle in arm), so damage would be limited to around injection area;
This was a lie. They didn’t just “get it wrong” – they knew beforehand that it distributed throughout the body and they lied about it;
Forthcoming issues (off the top of my head):
Brain – Early onset neurodegenerative diseases – Alzheimer’s, Parkinson’s etc.
Heart – Cardiac failure, Ischemic Heart Disease, Myocarditis, Pericarditis etc. Even if no symptoms present (yet), the damage is still there and early cardiac failure is a possibility;
Bone Marrow – Cancer;
Reproductive Organs (Ovaries and Testes) – Reduced fertility. Possible infertility. Menstrual problems were known at time of vaccination campaign.
2) Codon Optimisation - Nice way to misfold a protein
OK, so the jabs have used something called Codon Optimisation to increase “fidelity” in an attempt to boost correct Spike production by your cells. Codon Optimisation is essentially:
There are 4 RNA nucleotides – A, C, G and U. These are grouped into 3s to make a Codon:
Examples: ACU, GGC, UAG etc.
64 different nucleotide combinations (or 64 Codons) – 4 x 4 x 4 = 64;
But these 64 Codons only make 20 different amino acids, so more than 1 combination can make the same amino acid;
But some combinations are more "common“ combinations (your body is used to using these) and some are "rarer“ (your body isn’t as used to making these, so higher chance of error when asked to do so);
So "rarer" combinations in SARS-CoV-2 were swapped out and replaced with more "common" combinations (that our bodies are more used to making) in the mRNA vaccines, to increase "fidelity" (how correct the translation of the code was) so the chances of properly making a Spike Protein were higher because everything was read correctly because all the things in there were the varsions that the body was used to dealing with;
Sounds good, right? Makes the vaccine more effective, right?
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594389/
Codon optimisation has additional impacts on protein production. Apart from increasing fidelity (it’s stated purpose), codon optimisation also changes the speed at which amino acids are created by the ribosome.
In essence, it makes amino acids faster because it is being given codons it is used to. “Rarer” codons would make it “pause” for a second “to think before acting”. But “common” codons are, like, “Yep, I got this! On to the next one! Let’s go!”
https://www.mpg.de/10559091/protein-folding-why-speed-matters
Unfortunately (as we will see next), translation speed impacts how a protein folds once it is made, and what 3D shape it makes...and that's important.
Real important...
https://www.nature.com/scitable/topicpage/protein-misfolding-and-degenerative-diseases-14434929/
A protein doesn’t just get it’s characteristics or abilities from the specific amino acid sequence that creates it. It is also a 3D shape and this is very important. If it is shaped incorrectly (because it did not fold correctly) then not only will it not work, but it could actually become a very bad thing…
Neurodegenerative diseases are caused by misfolded proteins…
Summary:
The mRNA vaccines underwent Codon Optimisation, which is essentially taking “rarer” codons out and swapping them with “common” codons, so your body identified them more easily and had a higher chance of correctly creating the Spike Protein;
But, the thing is…codon optimisation increases translation speed;
And translation speed it directly linked to protein folding;
So when you change translation speed you change the protein folding - you create misfolded proteins;
And misfolded proteins lead to neurodegenerative diseases like Alzheimer’s and Parkinson’s disease…or even Creutzfeldt-Jakob disease;
So, the Codon Optimisation in the mRNA vaccines has started a ticking time bomb of neurodegenerative disease that won’t manifest for decades – and by then it will be too late…
3) DNA Contamination - Cancer is cool, right?
OK, so quick summary first:
2 different processes were used for mRNA vaccine manufacture;
Process 1 - PCR amplification - used for the vaccines in the "Safety Trial" (which we know was a joke). PCR amplification is a complicated and expensive procedure, but produces a pure product at the end;
Process 2 - E. coli bacteria (and bacterial plasmids) used to mass produce vaccines for general population. This is because Process 1 was ok when only making 40,000 doses for the so-called “Safety Trial” but, when scaled up to billions and billions of doses for us schmucks…way to expensive. So, they switched to the cheaper bacterial method, which to cut a long story short is kind of like brewing beer - but bacteria in a vat, make it have the right DNA in it, keep it warm and fed and it doubles in size every 30 minutes. You weren't told that the process used was NOT the process used in the "Safety Trial", were you? You thought the vaccine you got was made using the process that had been given clearance, didn’t you?;
The manufacturer is supposed to run enzymes through bacterial batches in Process 2 that slice up and wash out bacterial DNA, leaving only mRNA for vaccines, that would then be scooped into LNP envelopes for injection;
This, well...wasn't done properly. DNA was not washed out and contaminants were left in batches. Contaminants were then scooped up into LNPs for the vaccine, along with the intended mRNA, and this was then injected into people;
In addition, Pfizer deliberately removed certain information when giving summaries to health regulators - namely that the controversial SV40 promoter/enhancer was used in the bacterial plasmids;
Health regulators have now been forced to admit the DNA is in the shots and that SV40 was used in production but Pfizer hid it from them. But they're playing the "It doesn't matter, it's still safe" card and deploying controlled assets to downplay any potential safety issues. Health regulators were lied to and now that this has been exposed they are actually helping to cover up for Pfizer and Moderna. No, seriously, this is true…
So, let's take a quick look at some docs and then I’ll include a link to a video. It's not a 5 minute video so summon up some not-short-attention-span energy.
The screenshot above is a response from the EMA (European Medicines Agency) when notified about DNA contamination in the vaccines and, more specifically, the identification of the controversial SV40 promoter/enhancer (SV40 was previously linked to cancer in the oral polio vaccine in the 50s and 60s):
In their response they admit:
SV40 elements are there (this was never disclosed to the public);
Pfizer (Cominarty) did not highlight the presence of SV40;
(Basically, what Pfizer did was give the EMA to full DNA sequence but that’s 7000 base pairs long and it’s impossible to tell what specifically is inside it when only looking at the full sequence. So, Pfizer was supposed to break that down and give a very specific list of everything in the bacterial plasmid so regulators knew what they were injecting into people. They did not list SV40, which means they deliberately hid it from EMA.)
https://www.ncbi.nlm.nih.gov/books/NBK22268/
p53 is a super important tumour suppressor gene. It is at the forefront of our immune system’s mechanisms to fight cancer. Super, super important.
We all actually get cancer pretty regularly, but as long as we’re young and our immune system is in good shape then our p53 protein (along with some other stuff) gets out there and does it’s job adn, basically, works to clear the cancerous cells from our body. It’s only when we get older, and our immune system starts slowing down, that cancer starts to get the better of our immune system and we can’t keep up, so cancer starts winning.
But our p53 production isn’t endless. You can’t just make a bazillion of them all at once. And the gene expression is not Superman. It’s limited and we need to put it to good, proper use. We need to make sure it doesn’t get wasted…
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288138/
So, here’s the bad news…
Pfizer deliberately hid the fact that they used SV40 in the mRNA vaccines.
And they never cleaned it out after production, so the vaccines are contaminated with SV40 DNA.
And, as we can see in the screenshot above, SV40 is known to inactivate our p53 expression.
Which means our cancer fighting mechanisms are shut down by the mRNA vaccines…
That’s gonna…turn out well…isn’t it? Isn’t it?
https://biosignaling.biomedcentral.com/articles/10.1186/s12964-021-00741-y
It gets worse, unfortunately - the SV40 has something called a Nuclear Localisation Signal (NLS) which, basically, drags any associated DNA through the nucleus wall and into the cell nucleus where your own DNA is. It “localises” any DNA into the nucleus of your cells, basically…
So, the SV40 that Pfizer hid from regulators (and which the regulators are now covering up) will take the contaminating bacterial DNA into your nucleus and expose your own DNA to it.
Which means that bacterial plasmid DNA risks being integrated into your own personal genome.
And, as mentioned earlier, this includes ovaries and testes…which will be used to create babies in the future…who will then have this bacterial plasmid (and SV40) DNA incorporated into their own genome from Day 1 of conception…
Summary:
Pfizer used bacteria to create the vaccines that went to market (and didn’t tell the public);
They didn’t clean out the bacterial DNA, leaving the vaccines contaminated with levels far higher than regulations allow;
They also used controversial SV40 elements and deliberately hid them from regulators. The regulators, once informed by the public, decided to run cover for Pfizer instead of holding them to account;
This contaminating DNA contains a Nuclear Localisation Signal, which drags DNA into the nucleus of your cells, where your own DNA is, and risks insertional mutagenesis (basically, integrating itself permanently into your own DNA);
Any random insertion could break functionality of any DNA sequences that your body needs to produce proteins. That’s bad. There could be proteins that your body needs to produce which it now cannot. Endless bad possibilities, there;
The SV40 promoter/enhancer could be inserted in such a fashion to act as a promoter for any oncogenic genes you may have (basically, promoting cancer). And, yes, genes that promote cancer do exist inside your DNA;
SV40 also binds to (and thus de-activates) your major tumour suppressor;
While promoting oncogenic gene expression itself;
It hijacks your DNA, makes cancer and shuts down your body's major cancer defence at the same time;
And, if it does this in your sperm or eggs, then your children will inherit these traits.
The guy who found this contamination – Kevin McKernan (linked at thebeginning of this Stack, so make sure you’re subscribed and following him) – has given many talks on the issue and a quick search should bring up plenty of interviews and presentations.
But here’s a 25 min presentation given to the Croatian Parliament on the issue as one example:
(Click the screenshot above to be taken to the video)
4) n1-methylpseudouridine - What's wrong with a little frameshifting, amiright?
https://www.nature.com/collections/bieheeeddf
Remember, hilariously, when the 2023 Nobel Prize was given for the technology that allowed the mRNA vaccines?
Basically, it was given for taking Uridine (the U in the 4 nucleotides mentioned earlier – A, C, G and U) and replacing it with synthetic n1-methylpsuedouridine (Ψ);
This made the mRNA non-immunogenic, meaning less reaction from your immune system when encountering Ψ, and thus paved the way for use of mRNA tech in medicine, and thus the mRNA vaccines.
https://www.nature.com/articles/s41586-023-06800-3
Well, turns out that this same "Nobel Prize winning technology" actually causes a phenomenon called “frameshifting” when the ribosome is reading the mRNA to produce the desired protein...
So, what the Hell does that mean...?
Summary:
RNA is made up of 4 nucleotides - A, C, G and U. The U = Uridine, as previously mentioned;
mRNA jab tech swaps out U for the “Nobel Prize winning” n1-methylpseudouridine – which is symbolised as Ψ;
The ribosome reads these 4 letters and groups them into 3s to make codons;
Example - CGUAAGUCAUCG gets split into codons CGU / AAG / UCA / UCG;
But the jabs swap out the Us with Ψs - so now we have CGΨ / AAG / ΨCA / ΨCG;
But the ribosome isn't used to reading Ψ, so it pauses (basically to think and figure it out). Then, it basically says "Fuck this!" and skips onto the next nucleotide - so Ψ is at risk of being ignored;
So, now we have (taking out all the Ψs because the ribosome went “Fuck this!” and skipped them) CGA / AGC / ACG;
So the ribosome is coding completely different codons and producing a completely different protein once there is a SINGLE SKIP (frameshift);
What protein is produced? I don't fucking know. No one does. Depends where the skip is and how many skips there are;
Frankenstein proteins, baby!
https://anandamide.substack.com/.../frameshiting-slippery...
There are 801 substitutions of U for Ψ in each mRNA strand. There are 300 billion (Pfizer) to 500 billion (Moderna) mRNA strands in EACH SHOT. So, 240 TRILLION substitutions in each Pfizer shot and 400 TRILLION substitutions in each Moderna shot.
Frankenstein proteins, baby!
Oh, and STOP CODONS (that tell the ribosome to stop making protein and finish the job…you know, so you can actually have the correct protein…)...have n1-methylpseudouridine in them...
So if the frame skips there...at the Stop Codon…the ribosome keeps reading past the Stop Codon (which it is not meant to do) and it reads into what’s called the into the Poly-A tail...which is NOT meant to be read...and the ribosome uses code it is not meant to read to keep making the protein…
Frankenstein proteins, baby!
Frankly (no pun intended), I don’t think Frankenstein proteins are things I want in my body. Nor in my kids’ bodies. How will our immune system react? Will those proteins be able to do anything…? Personally, I don’t want to find out…
5) IgG Class Switching - Why eliminate when you can tolerate?
Our immune systems produces different antibodies for different reasons, and antibodies come in different types and different classes – IgA, IgM, IgG etc.
Relevant here are:
IgG3 - Which aims to eliminate;
IgG4 - Which aims to tolerate.
Think of the difference as something roughly like this:
IgG3 = "Oh, shit! That's something foreign and it's REPLICATING!!! Eliminate it before it makes too much of itself and we get overrun!!!"
IgG4 = "Oh, shit! That's something foreign but...HOLD ON!!! It's not replicating, so our filters (liver etc.) will eliminate it. So, chill out!"
https://pubmed.ncbi.nlm.nih.gov/36548397/
So, what do we find after mRNA vaccination?
Well, IgG4 starts increasing...so the body begins to dampen inflammation (which we use to flush stuff out and protect us) and instead it begins to engage tolerance...it allows the virus to stay…
This only happens, though, with the mRNA vaccines (Pfizer and Moderna). It doesn't happen with adeno-virus vaccines (AstraZeneca)...
Nice, right? Right?
You know the thing you jabbed yourself with to stop the virus?
Well, yeah, now it's telling your body to tolerate the virus...
Nice, right? Right?
https://www.medrxiv.org/content/10.1101/2022.12.17.22283625v1.full
The unfortunate result of the vaccines is that – exactly opposite to what you were promised would happen – once you’re into multiple jabs your body starts to tell itself to tolerate the virus, rather than eliminate it.
Once again unfortunately, this is why (and you have never been told this, I’d bet) the vaccinated have become more likely to get infected with SARS-CoV-2 than the unvaccinated.
Cleveland Clinic (the Gold Standard) data (amongst others) shown above clearly demonstrates that the more vaccines you have, the more infections your vaccinated group has.
Summary:
Each time you take a COVID-19 mRNA vaccine you force your body to start pumping out anti-bodies.
This, in the end, if you take enough (which is 2 or more), wears your body down.
So, it instructs itself to stop pumping out those IgG3s (which eliminate) and, instead, start producing IgG4 responses (which tolerate).
IgG4 will not eliminate a threat. Instead, it will tolerate it.
So, in the end, your body stops defending against the Spike when it sees it and, so, if you get infected, you put up reduced resistance.
The end result is that the more vaccines you take, the higher chance there is that an encounter with SARS-CoV-2 will lead to an infection.
The jabs make you more likely to get infected.
No, I’m being serious…
END SUMMARY
So, that's my Top 5:
Early Cancer;
Early Neurodegenerative Diseases;
Early Cardiac Failure
Decreased Immune System;
Increased chance of catching COVID-19;
Altering of your DNA;
Including your Ovaries and Sperm;
So your unborn children now have early cancer and neurodegenerative disease, a reduced immune system and their own fertility problems;
Autoimmune disease right across your body that you may not even know you have but which will get you later in life (subclinical heart damage, for example, leading to early cardiac failure).
And that's just my Top 5. All sourced. No conspiracy theories.
There's more…
But, you know...for now...I'm cool with the Top 5...to help people with an introduction.
END COMMENT
Look, I know this is not good. And if you’re just starting to ask questions and you read all that stuff above then that’s kinda…fucked, to be honest.
And you might be scared. And so you might wanna just go put your head in the sand, ignore it, pretend it’s not true and hope it all goes away if you never think of it again.
But here’s the blunt truth, friends - it’s done. And no sticking your head in the sand is going to make it go away.
And they did it to kids. And this is the worst part. Your kids, my kids, our neighbours…
So we can’t hide. We must speak up about this. We must push back against the people that lied to you.
They told you it stopped infection. It didn’t. They told you it stopped transmission. It didn’t. They told you it stayed in the arm. It didn’t. They told you it wasn’t contaminated. It is. They told you it can’t alter your DNA. It can.
All confirmed lies. And now they’re lying to cover their tracks.
And here’s the rub - if anything can be done to help people (that’s possibly you, and possibly your kids, and possibly your family, and possibly your beighbours) then the only way this can occur, and people can be helped, is if we raise fucking Hell about this.
If we don’t - if we stay silent because we’re scared, if we stick our heads in the sand because we want it to just go away and not be true - then the problem won’t be exposed. And if it’s not exposed then there can be no admission that something needs to be done to help people. And if no one admits this then we can’t turn our resources to investigating it and finding solutions. And if we never expose and investigate, then…we’ll never find ways to help people.
So, it’s impossible to help you (and your family, and your neighbours) unless we speak.
Raise Hell » Force them to acknowledge what they have done » Take our resources and put them towards a solution.
Be brave. Ask questions. Subscribe and follow the people at the beginning of this Stack. Don’t be silent.
Everyone is counting on you. And you can do it.
Be brave. God bless.
I liked the way you added in some of your slang and humour into a rather scary summary.
So much harm done by these jabs.
Great summary