That's interesting that you write this, as I've often thought that older people and the amount of medications they are on would surely have an effect when it came to the covid jab? The husband of the lady I wrote about has been ill in bed since she had her jab. The doctor can't seem to find what is wrong with him...and the flu like symptoms I had returned on the Wednesday and I didn't feel right again until the Sunday.
I think there are so many pathways for ill effects. The PEG/lipid nanoparticles can create an immediate autoimmune response (these people might never make the magic spike proteins). There is mast-cell activation autoimmune response in the healthy and athletic (hearts). There is the almost immediate weird, never-seen-before thrombosis combo with thrombocytopenia, and sometimes this hits later. A possibility of DNA integration (death sentence, and violation of law, to alter a person's dna). There is 'leakage" of the spike proteins into organs, if the vaccine took and you hijacked your cells to make them. And then contamination with rogue DNA sequences, all together a different. There is RNA-misfunction, the rogue modRNA confusing the cell's machinery. There's talk of the SV40 sequences aiding cancer, etc. So many ways for things to go wrong, so very few for them to go right.
 
It’s a good documentary imo, and here is a rough outline:
The historical background is most interesting considering that HCQ is one of the key components in the autoimmune protocol to fight latent infections and what the Cs said about the bloodlines:


A: Questions about "The Great Work" and "work on the self" and the preparations for "graduation" and so forth. Most of the clues and even direct answers have been given in the past, however we will summarize and give examples. All such aims concentrate, in essence, on or in awareness! Awareness is knowledge in action. Now, think of the concept you know as transmarginal inhibition.

Q: (L) Okay. Transmarginal inhibition is when an organism is stressed or pushed to the point where they break. It's like they become blank slates, and then they can be easily reprogrammed. Is that what we're getting at here?

A: Yes. Now think of the superimportant bit of data we sought to get through to you some years ago regarding parasitic infestations preventing a "quantum leap in awareness."

Q: (L) So you're saying that awareness is the key to the Great Work, work on the self, graduating to 4D, or whatever. Awareness involves knowledge, and quantum leaps in awareness can be prevented by parasitic infestations, which is somehow related to transmarginal inhibition.

(Pierre) How does it relate?

(Perceval) It makes people easy prey. Like toxoplasmosis in cats.

(L) So, okay... Continue.

A: The recent discoveries you have made in terms of the causation of chronic and other deadly diseases is the gathering together of the keys to the opening of a door to greater awareness!!!!

Q: (Andromeda) Huh.

(Perceval) So you don't have the key yet.

(L) When you made that remark, that was years ago... That was in 1997? That was in the context, if I remember correctly, of when I was following bloodlines. You diverted my direction by introducing this topic about quantum leaps in awareness and parasitic infestation. And then I think the topic then moved on to the discussion of an alien race wanting to take over the planet and how they would do that. Maybe we could go find that session...

[Break for finding session transcript from August 9, 1997]

(Andromeda) So we get rid of all of these bugs, all the right DNA turns on, and then we become more aware and get superpowers. That's what I'm getting from this.

(Pierre) So regarding these bloodlines, are they for example people who would graduate, but they have some weakness and they get infested by parasites that prevent them from graduation?

(L) Is it a weakness, or is it by design?

L reads from August 9, 1997 transcript:

Q: Next question: is there any relationship between the fact that Roger de Mortimer, the carrier of the last of the line of the Welsh kings, was the lover of Isabella of France, who was the daughter of Philip the Fair, the destroyer of the Templars, and the murder of Edward II, the first of the English Prince of Wales?

A: Templars are a setup, insofar as persecution is concerned. Remember your "historical records" can be distorted, in order to throw off future inquiries, such as your own.

Q: I know that. I have already figured that one out! But, it seems that no one else has made this connection. I mean, the bloodlines that converge in the Percys and the Mortimers are incredible!

A: You should know that these bloodlines become parasitically infected, harassed and tinkered with whenever a quantum leap of awareness is imminent.

Q: Whenever a quantum leap...

A: Such as "now."

Q: Did Isabella and Mortimer have a child while they were in hiding in France?

A: No. Here is something for you to digest: Why is it that your scientists have overlooked the obvious when they insist that alien beings cannot travel to earth from a distant system???

Q: And what is this obvious thing?

A: Even if speed of light travel, or "faster," were not possible, and it is, of course, there is no reason why an alien race could not construct a space "ark," living for many generations on it. They could travel great distances through time and space, looking for a suitable world for conquest. Upon finding such, they could then install this ark in a distant orbit, build bases upon various solid planes in that solar system, and proceed to patiently manipulate the chosen civilizations to develop a suitable technological infrastructure. And then, after the instituting of a long, slow, and grand mind programming project, simply step in and take it over once the situation was suitable.

(L) So... Are you suggesting that, for example, if there are people who get infectious diseases that cause atherosclerosis, heart disease, cancer, rheumatoid arthritis, multiple sclerosis, lupus, or any of these so-called autoimmune diseases, that these diseases are not genetically caused as they have been saying for the last 50 or 60 years, but that perhaps they were designed for people who carry certain genetic markers in their DNA, which then get labeled as the causative gene? Is that what we're getting at here?

A: Very close indeed. There is also the "tinkering" that can take place.

Q: (L) So in our particular reality and time and place, the so-called "Great Work", the alchemical self-transformation, must necessarily include work on diet and health issues and a vast increase in knowledge in those areas in order to cancel out the effects of transmarginal inhibition?

A: Yes

Q: (L) I don't know of any better way to put it. Anybody else?

(Pierre) There seems to be something else. The way they refer to parasites is that they are preventing not only the gaining of knowledge and growth of awareness, but also this quantum leap. Maybe if you have parasites, you can still increase your knowledge and awareness, but you'll reach a sort of glass ceiling that prevents you from graduating.

A: Yes

Q: (L) What's the tinkering there?

A: The parasites act as receivers.

Q: (Pierre) Yeah. The parasites act as receivers. So when you are full of parasites, you are more under the influence of bad waves, or waves sent by bad entities. You're more susceptible to those messages. There's a bad influence on you beyond the parasites.

A: Getting free of parasitic microorganisms is one of the first orders of business for transformation.
 
Biological Meltdown • (part 1)
by Florian Schilling

biological_meltdown.jpg

in English language, 3 hrs

In German language, 3 hrs

As promised
I would dive deeper into the what Florian Schilling presented in his video about the many underpinnings of the modRNA jabs. Now I also realize, that this has already been published in this thread, but I was not aware of that. I hope it doesn't make too much noise, if i bring up his video / the details again.

Before Florian Schilling talks about the severe issues in the jabs, he empathizes that the findings are hypothetical; in vitro, no data. (Which i find a bit surprising, given that several major issues revolving the modRNA jabs have been discussed and published among other medical scientists and doctors who dove into these subjects). What comes to mind are Dr Kämmerer, Dr Sabine Stebel, etc.

Notice that some themes have already been published in the Corona thread, so Schillings presentation is overlapping with what we talked / published / discussed earlier in this thread.

Schilling outlines following themes:

🔸 Promoters
🔸 Trojan Horse
🔸 Detection



🔸 Cancer rates are especially in the West, especially in young people, are on the rise (but generally are on the rise at all ages)
(people below 45, which are normally not much affected by cancer)



The differences between the Uridine component, which is part of RNA, are explained and especially focused on in the beginning of the video. Outlining, what is natural, and what is 100% artificial, e.g. the jabs containing N1-Methylpseudouridine (abbreviated m1Ψ) is 100% synthetic.

The natural pseudouridine makes up maximum 5% of all Nucleosides in RNA in nature. However, the artificial, not in nature found N1-Methylpseudouridine (or m1Ψ), makes up a whopping 20% of all nucleosides / in the genetic code. So, there is a much higher proportion for m1Ψ present


_-2024-05-12-at-12.36.59.jpg


Note / Insert :
I remember from earlier videos around 5-6 months ago - at the Corona Investigative Committee in Berlin - that N1-Methylpseudouridine had a melting point (around 69°C) which is higher compared to the other pseudouridine & uridine natural melting points (around 64°C), making the artificial m1Ψ unusual stable. At the same time m1Ψ is a very sticky substance !

With that info added, i want to remind you that this fact, makes the modRNA component well suited to glue itself to the vastly found bacterial DNA contaminants... creating hybrids (which are difficult or even impossible to filter out !!) Pfizer has in that regard used deliberately the wrong measuring methods, which are not suited for these hybrids, by making it look as if no more bacterial DNA was left. In reality, the vials where full of contaminants, e.g. the vast presence of bacterial DNA plasmids !



Frame Shifting

There is something called "frame shifting" going on in the artificial modRNA jabs, in which the code is translated in ways that created false / wrong / misaligned proteins due to the presence of the "slippery" m1Ψ (N1-Methylpseudouridine) - literally bringing disorder and misalignments in the way how translation of genetic information is done in nature. Usually when a protein is translated and created, there are so called stop points, in order to signal that at some point and information should stop, and therefore the protein is done.

The presence of artificial N1-Methyl-pseudouridine however shifts the natural translation sequence / how the code is translated / and garbles it as a result (followed by that the proteins are wrong / make no sense - in the best case).

As an example with words (to the right)

_-2024-05-12-at-12.58.16.jpg

Now the ribosomes in our cells cannot refuse to translate garbled / nonsense code and will accept it by 100% - without checking the quality of what they are producing: therefore they create even wrong proteins (due to the presence of unnatural m1Ψ; into so called "off-target protein".

Hard to believe that the m1Ψ actually got the Nobel 👿 Prize 🤡


A magicians trick.

The modRNA injections do not only create nonsense off-target proteins (Pfizer, Moderna), but as well massive immune reactions leading to ongoing inflammations. [leading to auto immune diseases, where the body attacks itself - so called "Molecular Mimicry"] This happens when the off-target proteins happens to look similarly to body cells - than the immune system will kill not only the off-taget invaded cell, but also the own body's cells that resemble the off-target protein.

Isn't it "funny" that AstraZeneca's jab was taken off the market world wide, which lets face it, favors the permanent push of Pfizer injections. Like a limited hangout, sacrificing the little lamb in the spotlight in everyones eyes... so that the real big Elefant in the room, can continue to stay "invisible" and create enormous damages with the Pfizer jabs.

A classic magicians trick in other words.

We also have the problem with that off-taget proteins, can fold wrongly, so called prions, creating amyloids. (Alzheimers, Creutzfeldt-Jakobs disease / Mad Cow disease, the which apparently is highly contagious (?). We all have seen the images of monster clots that have been pulled out of diseased body's.

Another severe side effect is that these off-target proteins, e.g. those that are creating mis-folded proteins, can then change healthy proteins into prions ! And so can the spike-proteins do the same thing. One or the other way... same result. :scared:

Yum. Sorry for the irony here.

_-2024-05-12-at-13.22.01.jpg
 
Biological Meltdown • (part 2)
by Florian Schilling

biological_meltdown.jpg

Zeta Potential / Lipid Nanoparticles (LNP)

This is a subject that is largely unknown and not much reported about at all. Schilling recommends to dig deeper into the subject molecular biologi, via a specialist Christie Laura Grace, which writes in her substack about Zeta Potential (the charge that a partial has, vs the overall charge potential, and what that does with our cells in the body).




So, we are talking about a lipid nanoparticles. They contains different ingredients as follow:

_-2024-05-12-at-13.29.43.jpg

From what I remember - out of memory - none of the (stand alone) components such as (cationic or "positive" charged lipids) ALC-0315 and ALC-0159 were never approved to be used on humans - due to the highly carcinogen nature, neither allowed in humans nor animals. Extreme small portions have a highly negative impact on biological beings. But overall, they have been put into the modRNA jabs... Just. Like. That. The the classic style like "Move along. Nothing to see here". (the forbidden components got a silent "backdoor license" )

Well, things are to get really nasty:

It is about the electric charge of particles.

Cationic = positive charge
Anionic = negative charge
Total outward charge = ZETA Potential

The issue is that a particle has one charge, but the overall assembly in a mixture can have a DIFFERENT OUTWARD charge. The latter is called the ZETA Potential. In this case, we are talking about a negative charge ! Which is a key factor in the interaction with human cells, cell core, DNA etc.

There have been numerous investigations, on the biodistribution of lipid-nanoparticles in animal bodies.

++ (highly positive charged) Nanoparticle structures -> primarily go to the Lungs
--
(highly negative charged) Nanoparticle structures -> primarily go to the Spleen
- near neutral/slightly negative Nanoparticles go to the Liver


according to a paper, by Cheng et al, Nature Nanotech, 2020


What does that mean ?

The more negative the ZETA POTENTIAL of Lipid-Nanoparticles are, the more prone are those end up in:

HEART
BLOOD VESSELS
SPLEEN

Sounds familiar, doesn't it ? Endotheliitis, Clotting, Myocarditis...

In tests with monkeys who got injected (containing ALC-0315 and ALC-0159) - they found that after 48 hours, only 25% of the injection content was left at the injection site. So, where did the rest of the 75% go ?!

When it was said, that the "vaccine" stayed at the injections site - it was a blund lie. It is that simple.

The official Pfizer data, claims that the Lipid Nanoparticles have a Zeta Potential charge of -3mV (negative 3 millivolt). IN other words, that would be almost a neutral charge. It also means if true, those lipids nanolipids would end up in the liver.

Did they ? NO.


So, how did this all unfold ?

In the Trial and eyes of the official authorities, Pfizer used the PCR process, in order to multiply the modRNA - which is extreme expensive, yet also a sterile process. (it would probably have eaten up all the "lovely" Green God [read profit money], in order to make so much modRNA for 12+ billion jabs. Now the first PCR process, Pfizer measured the ZETA potential charge of the lipid-nanoparticels according to -3 millivolt / -3mV

In the real world later, the final industrial process of making those jabs - they used a different process; one that was never approved, by using bacterial (genetically modified, fast growing E. coli bacteria plasmids, in order to create and multiply the final modRNA). Now in this process, the ZETA potential charge of those lipid nanoparticles are much, much more negativ charged due to the vast presence of double stranded bacterial DNA (contaminations) This concerns for both Pfizer as well Moderna jabs.

In other words, the contamination via bacterial plasmids, lead to much more negatively charged lipid nanoparticles. And with that, the lipid nano particles didn't end up in the liver, but in the heart, blood vessles and spleen instead. With all the tremendous complications and illnesses that followed/follows from it. And we are only talking about the lipid nanoparticles here....

BAM !


_-2024-05-12-at-14.05.14.jpg
 
Biological Meltdown • (part 3)
by Florian Schilling

biological_meltdown.jpg

Inside a human cell, we have the nucleus - we find our human DNA. Usually the nucleus is strong protected capsule protecing our genetic DNA material. It too has a metabolism, in order to exchange and get rid of waste products - therefore there are pores in both cell, as well surrounding the nucleus or cell core membrane. Those are called "nucleopores", like little portals allowing substance to be exchanged. While those nucleopores offer a high level of protection for our genome, this protection isn't 100%.



_-2024-05-12-at-14.13.52.jpg

If molecules are very small - and on top also are negativ charged - than that promotes translocation into the nucleus / cell core. Meaning that such small as well negative charged particles can pass the nucleopores, and dive right into the cell core where our DNA is stored.

The artificial lipid nanoparticles (LNP's) are small enough, as well have a Zeta potential that is highly negative... and therefore go - together with the cargo, right into the CELL CORE ! Schiller says, in his eyes, there is a significant risk that our DNA is compromised.

I would say, the conditions for corrupting human DNA is pretty clear, and all that what can follow in terms of illnesses when DNA is compromised: promoting all types and forms of cancer. Especially given that we also have other factors playing in, such as sequences of the SV40 promoter/enhancer in the modRNA, due to the presence of bacterial, double stranded DNA for sure / to a high degree is translated into the cell core DNA, corrupting it.

Aren't the jabs equivalent to an intricate Trojan horse at many levels ?

In my personal opinion, from everything i have read and listened to over the course of several years - yes they are Trojan Horses. Or to say it bluntly; isn't that what we see, when we observe of what is going on with people in our surrounding, as well in the world ?



The proof is in the pudding
anno year 2000

_-2024-05-12-at-14.25.18.jpg

When dsDNA (double stranded DNA) is present together with NEGATIVE charged lipidnanoparticles, e.g. the electric outward CHARGE is the key factor which leads to that the lipid-nanoparticles end up IN THE CELL CORE, not just in the cell. It means, that bacterial double stranded DNA is getting transported into the cell core, where our human genome resides. That is also what the Moderna and Pfizer commercial injections "happen" to be made of.

BAM !

I repeat; these findings have been harvested in year 2000. Anyone still claiming; "they didn't know what they were doing ?" 🤡

None of the aforementioned aspects, at no step of the registration process, has been investigated by neither Pfizer, Moderna or any other regulatory body.



All proteins in our body
too, have an electrical charge. For example Albumin or the haemoglobin in our red blood cells, responsible for the transport of oxygen in our body.

Dependent on the charge, it is potentially possible that the lipid-nanoparticles can bind to proteins in our body. The consequneces of such binding, has influence on the red blood cells; it's shape and deformability (for example its ability to push itself though tiny, tiny bloodvessles barely larger than one red blood cell. In order to do so, it needs flexibility to squeeze though) But this ability can be influenced by the blinding via the highly negative charged lipid-nanoparticles to the haemoglobin of the red blood cells.

Tissue with tiny blood vessels, may suffer from hypoxia, due to the lack of oxygen, due to the binding (charge) of the lipid-nanoparticles.

Our regulatory bodies and instances, totally neglect these issues, because they insist on "trusting" the offical data from Pfizer, that the ZETA potential is -3mV (negative 3 millivolt). Which isn't true what so ever, due to the bacterial contaminations, also altering the true electrical charge of the lipid-nanoparticles into highly negative charged ones.



A third consequence of the highly negative Zeta potential: ApoE
Lipid-nanoparticles can, based on their electrical charge, recruit something called ApoE proteins. ApoE are proteins that allow our cells to take up lipoproteins; such as LDL, especially cholesterol.

The nanoparticles however have the ability to bind the ApoE on their surface, and is being taking into the cell, together with the cargo inside the lipid-nanoparticles, and there the bacterial double stranded DNA that bind to the modRNA, is getting released, creating garbage proteins / degraded target mRNA

Florian Schiller empathizes following; because all human cells with high amounts of ApoE receptors are especially prone to take up the lipid nanoparticles to a high degree ! It means that those cell get highly contaminated as well (with bacterial plasmids + modRNA)

Schiller says, given to where we have cells with many / high density ApoE receptors, in many of our organs, is highly concerning. (Especially in our BRAINS, and REPRODUCTIVE ORGANS) Ovaries are highly sensitive organs, that normally are highly protected !

Many nanoparticles will go in those organs...

_-2024-05-12-at-15.03.06.jpg

BAM ! - I would say.

Or should I say; again, again, and again.



PS: (I will take a break from this, and write later)
 
As a follow up, Slovakia is also rejecting the WHO treaty


Hmm it seems UK does refuse to sign the WHO pandemic treaty? Would be interesting to see if other countries do as well, and which ones.


However as noted in one of the comment, might have to take into account it is an election year


Finally found the following source:

Might be good to check if there are further sources.
 
Biological Meltdown • (part 4)
by Florian Schilling

I continue here with the video by Florian Schilling called "Biological Meltdown".

biological_meltdown.jpg


From the biodistribution study
conducted in Japan, we know that the lipid nanoparticles go to the bone marrow and brain, as well ovaries in particularly. But officially "we do not know". (Talk about scientism). No wait - I should say something along "science-sham-ism", because the whole thing isn't funny anymore, because it has gone so far and so wrong.

Summarization:
The Zeta potential offers the risk of 🔸 poor oxygen supply, 🔸 enhanced clotting, 🔸 transportation of exogenous modRNA and dsDNA (double stranded DNA) into the nucleus of our cells with unknown consequences to/of our genome, 🔸 preferred distribution of the lipid nanoparticles in highly sensitive organs such as brain, bone marrow and reproductive tissues (male & female)




MANUFACTURING PROCESS
(plasmid contaminations)

I have written about plasmids before. This subject it is also part of Florian Schillings presentation, therefore I will go into what he talks about in terms of Plasmids (bacterial DNA contamination in the Pfizer vials)

The production process of the jabs, require huge amounts of RNA. You can't produce (copy) RNA directly, and you need huge amounts of template DNA, in order to get then a transformed opposite; which is the single stranded RNA - and then putting those into the injections or "vaccine" (embedded into lipid nanoparticles surrounding the modRNA).

The modRNA / mRNA is basically the code instruction, that when read off in the cell, making proteins.

_-2024-05-13-at-12.14.01.jpg


Process 1

The original process that Pfizer used in order to get "certified", was to multiply the DNA template in a PCR process. Each circle doubles the amount of DNA. This process is very expensive, especially if you aim at injecting billion of people, with ten of billions of modRNA particles in every injection. Also; Process 1 would take far too long time. Which explains that the manufacturer didn't rely on the PCR process version, but used a different process in the commercial rollout of the modRNA injections.

_-2024-05-13-at-12.21.17.jpg


Process 2

_-2024-05-13-at-12.27.16.jpg

The illustrations shows the final, commercial process that has been used, to create modRNA via bacterial DNA + plasmids (by using a genetically manipulated version of E.coli bacterium) for multiplication of the desired DNA producing modRNA.

Many bacteria contain two different forms of DNA:

The main portion is the Bacterial DNA, which are freely floating forms of DNA inside the bacteria - They don't have a nucleus like human cells. The second one, comes in a circular form, so called plasmids. Those are double stranded DNA forming a closed ring. The bacteria uses these to exchange genetic information; for example - if one bacteria has discovered a new approach to develop resistance against antibiotica - it can put that genetic information into a plasmid, and exchange that with its neighbour, so the information can spread.

Let's keep in mind: plasmids are double stranded, circular DNA in bacteria, that specifically designed to exchange genetic information between different cells between different organisms

So, in the process, they then extract plasmids from the bacteria, and cut out a piece of it. Then you insert a DNA template snippet which altogether becomes a genetically engineered plasmid - in order to have it replicated. (From what I understand is, that the snippet code they insert, is made up ENTIRELY artificial code !) It has nothing to do with a snippet from a natural virus... 🤔

The inserted snippet in the plasmid is then transfered into a bacteria and out into a cell culture (if there is sufficient with nutrients for them) - multiplying into millions of new bacterias. With each replication cycle they will also replicate the genetically altered plasmid (recombinant DNA plasmid)

Then you kill the bacteria, and set free the plasmids. The last step after that is purification: DNAse and Endo / Endotoxins (e.g. LPS or Lipopolysaccharides) LPS causes inflammation in humans. It means to get rid of unwanted bacterial components. You also have to use specific enzymes (DNAse) in order to cut down those (ring) plasmids, in order to extract the snippet DNA template you wanted in the first place, and getting rid of the rest of bacterial DNA.

After you cut the snippet out of the plasmids, got rid of the rest of bacterial DNA - you have left a linear double stranded DNA, from which you can make RNA.

_-2024-05-13-at-13.04.00.jpg

Well, that's the theory on paper...



Reality Check

The purification process is in real life is complete mess / disaster
- revealing nanogram to microgram quantities of bacterial dsDNA per "vaccine" dose. In other words, huge masses of bacterial DNA, up to 30% from the totals (modRNA) in the vials.

Our body is equipped with sensing bacterial DNA, and certain, highly inflammatory processes are then activated in order, or with the attempt, to get rid / trying to fight back the bacterial genetic material. Florian Schiller outlines one particular pathway (from many that get activated).


STING pathway

When this pathway is getting activated, it starts a pro inflammatory processes; in this example two such as the transcription process called NF-KappaB and the other is Interferon. Now when NF-kappaB gets activated, then genes are being turned on, with the production of highly inflammatory molecules, so called cytokines (IL-1, IL-6, TNF-α or written (Interleukin-1, Interleukin-6, TNF-alpha)

If there is an incision of those molecules, the consequences of the local cell-tissue can be quite dire:

🔸 Tissue damage
🔸 Silent inflammation
🔸 Neuroinflammation
🔸 Autoimmunity


🔸 MAPK proliferation;
the promotion of stimulating cells to increase cell division / growth. Uncontrolled proliferation leads to the formation of tumors and cancer.

🔸 Metabolic changes in the affected cells, so called Warburg mode,
or the decease of the mitochondrial energy production as well the increase of sugar fermentation.
This is a typical metabolic mode we find in cancer cells.


All the factors aforementioned, act synergistically together ! In the end, you get a very impressive cascade of detrimental affects. (think of the classic domino effect).

That is the summarization of what happens with cells, that take up dsDNA (double stranded bacterial DNA)

_-2024-05-13-at-13.32.14.jpg
 
Biological Meltdown • (part 5)
by Florian Schilling

biological_meltdown.jpg

In a cancer research paper from 2023
it is an already known phenomena (described in my previous entry), that when RNA and DNA are packaged into lipid nanoparticles for the delivery to cancer cells in the body, the aforementioned negative effects occur; gene alterations, mutations !

Researchers makes it very clear
in this paper, that if you put plasmid DNA into lipid nano particles - and if that is taken up by a human cell - then the plasmid DNA is set free - and will observe gene alterations (the genome of the cells gets compromised), leading to the occurrence of mutations, leading to oncogenic / cancerous processes.

(Kind of "funny" when you think about this vs. Pfizer announcement of having mRNA "vaccines" against cancer. What is it we see here? The technology literally stimulates highly detrimental, negative effects that you can think of, plus the rapid growth of cancer, and god knows what else.

Or like the C:s once mildly expressed it ... "tinkering with DNA is at best iffy". )

It is total hubris, to say the least

_-2024-05-13-at-13.42.36.jpg




Exogenous DNA vs sperm cells

This is something that has been known for quite a long time... namely a paper published in year 1992 !

_-2024-05-13-at-13.56.39.jpg

The experiment that was performed here, was quite simple. The researcher did incubate sperm cells with exogenous DNA in form of plasmid DNA in order to observe what would happen. The result is pretty clear: Within a short period the sperm cells took up dsDNA. We are talking here about a time span within 15-30 minutes in which massive amounts of DNA was taken up by the sperm cells !

The DNA that was discovered in the "C-19 vaccines", covers almost the whole range in the experiment that was conducted in 1992 (yellow color), revolving the basepair (bs) sizes of dsDNA.

• The bigger the size of the dsDNA was, the easier it was to uptake them in the sperm cells.
• There also was a positive correlation with a highly NEGATIVE ZETA charge of the dsDNA !
• All this occurred within a very short time frame, less than 1 hour.

How long where the coponents of the C-19 injections residing in our bodies ?! endlessly longer than just 1 hour.

Make the math, what effect that has on fertility in men and women over time.



Researchers even went a step further
following a publication is from year 1989 (!) Sperm cells as vectors for introducing foreign DNA into eggs: Genetic transformation of mice.

Here they didn't only observe the uptake of exogenous DNA by the sperm cells up to 15 minutes, but went one step further with the subsequent fertilization of ovocytes / eggs. After that they performed sequencing of the vector-DNA (dsDNA from the foreign plasmids) in order if they could detect any of that DNA in the offspring.

They discovered that 30% of the offspring contained foreign DNA - meaning that the offspring integrated foreign DNA in the native genome. The researchers at the time, where quite happy and stated "Suitable method for the production of transgenic organisms".

Known since year 1989.

Is that, what the transhumanism actually is all about ? Humanity as a giant lab-rat experimentation for transgenic humans with the wet dream to create some frikkin "super soldiers" or other types in order to see "what perhaps sticks - and what not" ? Well, that is what comes to my personal mind. If part of the dark elite / the hidden hands know that earth is going though cyclical cataclysms, well then the cynic would say "what the heck - anything goes, right" ?

Male fertility / sperm cells
Same dangers loom also for the male sperm cells / fertility, when a man get's vaccinated with the modRNA injections contaminated with foreign, bacterial dsDNA, given how fast those get penetrated within a short timespan.

Normally the sperm cells are protected by the Blood-Testis-Barrier (relying on tight junctions to protect the sperm cells from harmful exogenous factors, maybe such as microbes, toxins, etc) Unfortunately that barrier has pores with a size of less than 200 nanometers, while the lipid nanoparticles are between 50-100 mn in size, easily traversing the Blood-Testis-Barrier. Also remember that the nanoparticles are highly negative charged (Zeta potential), which is what creates an enhanced uptake into the sperm cells ! And the next issue that the testis is an area with large, dense packed ApoE receptors to which the highly negative charged lipid nanoparticles are drawn to particularly, after they pass the Blood-Testis-Barrier, easily docking to the ApoE recepters, where the dsDNA is released and surely being taken up into the sperm cells.

The genomic information can then be passed on to the offsprings...

_-2024-05-13-at-14.33.10.jpg


Confirmation of that integration process indeed is happening;
foreign DNA integrated into the human nucleus and expressed in the offspring
from 2022.

_-2024-05-13-at-14.34.41.jpg

It is simply... mind boggling - all what is coming to the fore.

Note:
Unfortunately I am only though HALF of the 3 hours video yet. So, there will be more a lot more important info.
 
Rather concerning information...

Via Dr. Shankara Chetty, the South Afrikan doctor's Telegram channel - the guy who during the Plandemic cured thousands people using off label medicine, and discovered that the Covid-19 illness had a two-stage character to it; first seven days more like an influenza, but then very rapidly on day no 8, it would turn into an allergic reaction illness instead (He spoke about it a couple times at the Corona Investigative Committee, Berlin).

Anyway, he referred to a 4.5 minute video with Sasha Latypova - which frankly spoken chocked me.


HUMAN GUINEA PIGS; PFIZER VIALS CONTAIN VARYING LEVELS OF TOXICITY AND INGREDIENTS WHICH WERE TESTED ON THE PEOPLE Pfizer deliberately have been using the people as human guinea pigs, testing the levels of toxicity and formulations

Sasha Latypova

The FDA allowed Pfizer to trial different versions of the drug, different categories entirely; Modified RNA, unmodified RNA and self amplifying RNA . They also used the spike protein as a product by itself. This is why we’re seeing some batches much more toxic than others leading to greater number of deaths and adverse events

So, from what I understood it as, Pfizer used another sleeve of evil tricks during their trial, in order to become certified / approved for their Covid-19 "vaccine" - but in reality used a whole bunch of different types of "vaccines" under the same application for one Covid-19 "vaccine" product. Which clearly is forbidden to experiment and test various versions, or even worse, totally different types of "vaccines".

What chocked me the most was, not only did they use modRNA, RNA as well testing stand-alone spike proteins as a product - but tested on human beings (if i understood that correctly) with self amplifying modRNA or saRNA. So, not just theory then...

I remember vaguely writing about self-amplifying RNA in early 2021, (7 Feb 2021) which appeared at the 38th Corona Investigative Committee in Berlin, via a guy (Markus Fiedler) who explained that abhorrent technology.


4 July 2022 I wrote the second entry about saRNA

I have recently made an entry about that the saRNA self-amplifying "vaccine" (BNT162c2), which is already in the 'clinical trial II/III', explained deeper in the substack blog by "Unacceptable Jessica", who wrote deeper about these types of vaccines... So, here below you can find the pdf attached, showing the Pfizer/BioNTech document - albeit with the critical parts redacted.


"Unacceptable Jessica" explains here the saRNA tech more in detail at her substack.

The rabbit hole seemingly never ends, does it ?
 
I searched to see if this had been discussed previously / if any members had connected that info together, but I did not find any post about it. Since this thread is so huge, I might have missed it. Here is it:

1- Dr. Ardis claims that his research into Covid shows a link between snake venom peptides and that using nicotine may sometimes help to relieve Long Covid symptoms.

Link: Dr. Bryan Ardis releases huge allegations: The covid-19 virus, vaccines and some treatments are all derived from SNAKE VENOM – NaturalNews.com

Quote: "A 2021 study also connected the Chinese Krait and King Cobra to the Covid-19 spike protein, explaining, “the discovery of a superantigen-like motif in the S1 Spike protein, as well as two other neurotoxin-like motifs that have peptide similarities to neurotoxins from Ophiophagus (cobra) and Bungarus genera.“
Later during the interview, Dr. Ardis touched on the fact that hydroxychloroquine, defamed by the media, has been known to block nicotine receptors in the brainstem from being injured by cobra and viper venom."


The study: Toxin-like peptides in plasma, urine and faecal samples from COVID-19 patients
Results: Toxin-like peptides, almost identical to toxic components of venoms from animals, like conotoxins, phospholipases, phosphodiesterases, zinc metal proteinases, and bradykinins, were identified in samples from COVID-19 patients, but not in control samples.

Conclusions: The presence of toxin-like peptides could potentially be connected to SARS-CoV-2 infection. Their presence suggests a possible association between COVID-19 disease and the release in the body of (oligo-)peptides almost identical to toxic components of venoms from animals. Their involvement in a large set of heterogeneous extra-pulmonary COVID-19 clinical manifestations, like neurological ones, cannot be excluded. Although the presence of each individual symptom is not selective of the disease, their combination might be related to COVID-19 by the coexistence of the panel of the here detected toxin-like peptides. The presence of these peptides opens new scenarios on the aetiology of the COVID-19 clinical symptoms observed up to now, including neurological manifestations.



2- Laura's research led her to find that nicotine is beneficial for certain genetic profiles to enhance psychic abilities.

And also: "Paradoxically, nicotinic receptors are the ones best known to neurologists, who have been studying them for decades, given that there are both substances that stimulate these receptors, like acetylcholine and nicotine, and others that block them, like curare and the venom of certain snakes. Indeed, by one of those curious conincidences, tobacco, curare, and snake venom all fit into exactly the same locks inside our brains. [Dr. Narby, 1998]"

Link: Diet and Health Questions and Can Smoking be Good for You?


3- And this Session confirms a link between the intent behind Covid (which was to control people), and most likely the neuroreceptors of nicotine that enhance psychic abilities, thus why the spike protein would have venom peptides in it:
A: The virus did not appear first in China. There were experiments at Fort Detrick regarding the creation of a vaccine that would make humans more controllable. This vaccine had unexpected effects and in some cases did the opposite of what was intended.

Here's a video where Dr. Ardis explains his theory
Episode - NICOTINE! UNDERSTANDING THE WEAPON AND THE TARGET!!!

In this episode, Dr. Ardis reveals important and very relevant information on the real dangers of Covid-19 and the shots. He explains what nicotine receptors are and how venoms shut off nerve function like taste, smell, diaphragm contraction, hearing and brain function.
There is a false belief that ACE2 receptors are the target. The target is actually nicotine receptors and the antidote is nicotine! You will learn how nicotine impacts specific cognitive impairments like dementia, alzheimer's disease and even psychosis.
Why did smokers benefit from nicotine for Covid -19, Long Haul Covid and the Covid-19 Vaccine Injuries?!!! Please watch and share this episode! Support The Dr. Ardis Show and get up to date information, protocols and supplements.
 
A predicted here on the forum, they openly started to blame Fauci for all the COVID scam.
Prosecute/Fauci

New York Post goes after Fauci for his lies about dangerous virus research at the Wuhan institute of Virology.

Not saying he shouldn´t be prosecuted, he should, but what will happen even if they will - nothing.
The laws and regulations are already written that will allow them to implement any emergency they invent, digital IDs are already on the way, etc etc....

The deed is done, it only needs implementation on pertinence of disease X or some created Black Swan event or what not, unless this opens more eyes to the situation and more people wake up.
I´m not holding my breath...

Edited: I´ve put the Tweet in quotes so it doesn´t load.
 

US cow-derived H5N1 virus flown to Porton Down under strict security for UK testing
UK officials confirm they have taken delivery of the virus in order to understand if it poses a risk to UK livestock
A new unit set up to tackle H5N1 is testing imported samples of the virus at the high-security laboratories at Porton Down, in a race to understand if it poses a substantial risk to British livestock
In a race to set out the potential risks to world's livestock, it seems.
Virus extracted from sick cattle in the US has been shipped to three secure UK laboratories in Porton Down, London and Weybridge, Prof Ashley Banyard of the Animal Plant and Health Agency (APHA) told The Telegraph.
The task force is trying to determine whether the outbreak of H5N1 in America, which has so far been linked to outbreaks in 49 dairy herds across nine states, is a one-off spillover event, or if the virus has adapted to replicate in cattle – which means it could impact UK livestock.
Oh... They are going to make sure it replicates
An outbreak in the UK could have a significant impact on the dairy industry as it already has in the US. It would also increase the risk of the virus ‘ jumping’ to humans, either through contact with agricultural workers or via food products like meat and dairy. In the US at least one farm worker has been infected and several species of mammals including farm cats, wild possums and foxes.
What a great opportunity to the psycos!
“The occurrence of events in America has led to us taking preparatory measures and a more watchful eye,” said Prof Banyard.

“Samples have been shared with our very high containment secure labs, and we’re having a look to understand if there is genuinely something different about this clade of virus.”
Riight! A "very secure lab", I guess time is running out and they need to cook something soon.
 
Yes they don't want to give us too much breathing space, sans virus, so I agree. The next one seems to be on the agenda and heading our way. I am sure they will definitely target animals to reduce the amount of decent food people could be eating. The chickens will be implicated probably as eggs are a good source of cheap protein for poor people, as mentioned by the C's. Far more of the public are wary of the vaccinations now so it will take a severe event for them to get the public on board with mandated vaccinations again. I think covid was the taster with the main course yet to be presented at the table.
 
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