Blasted Liars

Blasted Liars

Thanks to the little mouse –  Please little mouse won’t you join Jonathan Couey on his Gigaohm Biological show?   You can keep your anonymity if you wish.

Some great detective work has been done using BLAST. The narrative is under attack on all sides and the wheels are falling off.

If you BLAST that 19nt sequence you will see the list of Moderna patents that have 100% match. There are no viral sequences that have this match. Oh and BTW the most obvious match is to the patent for modified genes for cancer therapy. In this case MSH3. Moderna created a mutated version of this DNA repair gene, and a sequence from that mutated patented gene found its way into a SARS-coronavirus.

In case no one noticed, the Moderna CEO Bancel is listed as one of the authors:

GenBank: LZ959695.1

Wood, K.l•l., Whoriskey,S., 
Roy,A., Fougerolles,A.D., 
Elbashir,S.M., Ellsworth, J. L. , Guild, J. , Hatala,P., 
Chakraborty,T., Schrum,J. 
p. and Bancel,S. Ejebe,K.,
patent: JP 2017197545-A 7ege 82-Nov-2e17; 
ModernaTX Inc

In case you missed the link in the tweets, this takes you to the sub-stack article.
How to BLAST your way to the truth about the origins of COVID-19




Gigaohm Biological (20 Dec)

Gigaohm Biological (20 Dec) 1:50 min

He is back. Johnathan is back again and he is going to sharpen us so that we are the tip of the spear so to speak. We will have a firm foundation and be able to answer any questions on immunology.

Wow.  He introduces Kevin McKenan and in future episodes will talk about methylating mRNA uracil to pseudouridine.  I can’t wait.

Dr. Malone

Dr. Malone

Mark from Housatonic has shown Dr. Malone’s involvement with many of the early architects of gene therapy and the use of viruses for delivery. He has an interesting CV which links him to many of the key players and indirect military funding.   Has he had a change of mind, is he controlled opposition or is he pursuing his own agenda?   At the moment he is saying all the right things.  As Dr. McCairn says, if they are firing in the right direction then that is a bonus but you don’t want someone in your foxhole who is going to stab you in the back.   Perhaps he had a change of conscience?    I like what he is saying here (but I keep my eye on all of them) it is solid information:

Dr. Malone: “This is the Largest Experiment Performed on Human Beings in the History of the World.”(1:11)

In an exclusive and explosive one-hour interview with Veronika Kyrylenko of The New American, pioneering mRNA scientist Dr. Robert Malone explains the intensely corrupt workings of the government regulatory bodies that have mismanaged the pandemic, discusses the problems with the vaccine program and delves into potentially explosive and game-changing revelations about the shady origins of the Covid-19 pandemic in Wuhan, China.

Who is Dr. Robert Malone? While working at the Salk Institute in 1988, Dr. Malone discovered important findings about in-vivo and in-vitro RNA transfection. He continued his work on the technology a year later at the biopharma start-up Vical where he conducted additional experiments. According to his bio, “The mRNA, constructs, reagents were developed at the Salk institute and Vical by Dr. Malone.” His research has also included important work on DNA vaccines. In addition to his fundamental work developing mRNA and DNA vaccine technology, Malone is also a medical doctor. According to his bio, Dr. Malone “received his medical training at Northwestern University (MD) and Harvard University (Clinical Research Post Graduate) medical school, and in Pathology at UC Davis."

Few people are as qualified to comment on the course of the COVID pandemic and the mass vaccination campaign as Dr. Malone. In this important interview he shares his unique and deep insights on matters of critical national and international importance.

Bio source:


Most Important:

What he says at about 1:05 right at the end of the interview is the most important.  It is about establishing a platform so that they can role out genetic (mRNA) vaccines quickly. All they have to do is alter the sequence.   The delivery system etc stays the same.   So if you have Special Forces deployed to an area you can quickly protect them from enemy pathogens.  This is dual use technology.  We are now in the territory of germ warfare.  The delivery platforms are not safe.  The only way to stop this is to arrest all the scientists involved, shut down the institutes and bomb the Bio Security labs into oblivion.

The Spike enters Nucleus

The Spike enters Nucleus

This video discusses a new surprise discovery (yet to be confirmed by other scientists) that the SARS-CoV-2 full length spike protein can enter human cell nuclei and interfere with the mechanics of fixing of broken DNA damage. The authors of the study propose this might have been evolved in order to prevent the genetic recombination required to produce antibody varieties to successfully attack the virus. If true, then this could have important implications for potential negative health outcomes (another if!) and might require reconfiguration of vaccine design.

Discussed content:… __________________________________________________________________

Dr. Raszek Credentials: ____________________________________________________________________

Spike protein inside nucleus enhancing DNA damage? – COVID-19 mRNA vaccines update 18 (12 min)

Thank you for these notes made by a kind and awesome supporter:

  • 00:00 Dr Mikolaj Raszek, Phd from Merogenomics
  • 00:09 The latest widest news in Molecular Microbiology
  • 00:33 WHO? Swedish research shows spike protein enters nucleus in human cells (in vitro)
  • 00:57 this is of course, biologically verboten (*German for STRICTLY FORBIDDEN)
  • 01:04 WHAT? *Discovery* Spike protein inhibits proper fixing of broken DNA
  • 01:18 Specifics: double stranded breaks where both strands are broken
  • 01:33 HOW? *Mechanism 1* suspected interference with BRCA1 gene product’s ability to repair DNA
  • 01:48 Consequence: if BRCA1 is mutated though, then you have highest predisposition for Cancer development precisely because BRCA1 gene codes for proteins that fix DNA damage when sheared in half
  • 02:14 Significance: Consequences are so great if true that it should be double checked, verified and reinvestigated
  • 2:42 Call for a lot more studies: Revalidation
  • 2:51 HOW? *Mechanism 2* Spike also interferes with mysterious nuclear protein 53BP1 which may serve to prevent DNA breaks from re-ligating to other DNA sources ensuring 2 chromosomes don’t link together that aren’t supposed to.
  • 4:21 HOW? *Mechanism 3* Perhaps spike in Nuclei interferes with Immune cells’ mechanisms (eg.BRCA1 and 53BP1) and diversity of response to infections.
  • 4:42 *TAKEAWAY* What if Spike protein evolved as a mutagen for DNA – what would implications be for a vaccine that’s primary focus was to produce Spike?
  • 5:32 CONTEXT: Recent discovery that Spikes may circulate for months on end in Exosomes to different parts of the body and in theory enter cells well after the point of vaccination as COVID-19 mRNA vaccines update 16 discussed
  • 06:15 CONTEXT: DNA gets 70k lesions/day /cell! But only 25 are double stranded shearing damages
  • 07:25 IMPLICATIONS: So within this context, what are the chances circulating spike proteins could enter and damage DNA and predispose to cancer? In cancer, it takes months for damage to accumulate and cause symptoms. Therefore…
  • 7:45 IMPLICATION: *Vaccine Safety* Are vaccines “SAFE”? What is vaccine “Safety”? Only Time can/will tell.
  • 8:07 IMPLICATION: Yes, Vaccines don’t produce dangerous clinical symptoms in the first few months BUT we don’t know what they do in very long-term basis so can we call them safe?
  • 8:34 HOW? *Mechanism 4* Vaccines use FULL length of spike protein thus produces whole protein in body. Prior to vaccinations some scientists mentioned that FULL protein length of Spike protein was dangerous
  • 9:16 IMPLICATION: *Antibody Dependent Enhancement or ADE* could occur with use of full length of Spike protein 10:27: AUTHORS’ RECOMMENDATION: Not to use full length of spike protein but only the Receptor Binding Domain or RBD portion for vaccines 10:41 Explanation: RBD 11:29: *TAKE AWAY* *Vaccine Safety* This shows how Vaccines are still uncharacterized on what they might be doing at the molecular level once injected in us.
  • 11:52 Spike protein also uncharacterized post-infection (but learning lots now).
  • 12:00 LIKE AND SUBSCRIBE and please *SHARE*



This blog article was inspired by the work that I previously did on the Wilson Vs Couey debate and by the last Gigaohm biological stream (16 Nov) which featured this video:


Debunking the Vaccine Makers Project video (13 min)

This is a beautifully crafted video which purports to show the science behind the mRNA vaccines, and it has gone viral among the vaccinated with lots of derogatory comments about the stupidity of the anti-vaaxers who do not understand “the science”.

This is the Disney Land fantasy version of how the “vaccines” (transfections) work. It is a fictive reality because we already know that they are not effective (hence the necessity for boosters) and have many side-effects (hence they are not safe) which points to “off-site” expression.    So, the model they are proposing is wrong.  If you had robust T cell immunity etc. (as they suggest) then you would not need boosters and if the spike was formed by the process that they show, then why is the heart etc. becoming inflamed?  My intention is to explain some of the basics and then edit and retweet the video by placing inserts to scientific articles etc.

Where does the mRNA end up?

I refer to myself as a “bucket chemist” who has done some biology (worked in plant pathology as a junior scientist) and worked for many years in the chemical industry as a Senior Chemist running a quality control lab for polymer production. The field of genetics and virology etc. is very specialized so I will break down some of these concepts for my own benefit as much as for yours.   The first point that I want to stress is that this is an experiment.   Even though they have hypotheses and are building on years of previous research there is still a lot unknown.  We are dealing with complex systems. Here follow some recent quotes in scientific papers that immediately put the video in context:

“Hence, delivery of exogeneous mRNA to the cytoplasm is essential for antigen expression, but whether this is mediated through endosomal uptake and/or direct entry through the plasma membrane is not entirely clear”. Clinical and immunological effects of mRNA vaccines in malignant diseases Heine, A., Juranek, S. & Brossart, P. Clinical and immunological effects of mRNA vaccines in malignant diseases. Mol Cancer 20, 52 (2021).

Now the following article is not about mRNA but about exosomes which can act like a pseudo-virus.  The mRNA is encapsulated in a Lipid Nano Particle and as such acts like a pseudo-virus. Who is to say that the mRNA in the cell is not also absorbed by exosomes?  Exosomes have a bi-layered lipid structure (a bit like the mRNA adjuvant) and….

“Exosomes are also able to use pathways similar to viruses to avoid lysosomal degradation. In dendritic cells internalised exosomes can bypass lysosomal degradation by being routed to a specialised, surface-accessible CD81 positive LAMP-1 negative intracellular compartment contiguous with the plasma membrane, in a manner similar to HIV-1 particles …“Another concern is the presence of naturally incorporated cellular genetic impurities with potential immunogenicity….” The exosome journey: from biogenesis to uptake and intracellular signalling Gurung, S., Perocheau, D., Touramanidou, L. et al. The exosome journey: from biogenesis to uptake and intracellular signalling. Cell Commun Signal 19, 47 (2021).

If you remember, when I quoted the paper below, it got me banned off twitter for a week:

So, according to the above paper it is entirely plausible that the exosome can absorb the S-protein…..but…but…hey….I thought it was the dendritic cell?

Off-site expression

We were told that the mRNA is injected into your arm muscle and stays there.  We know this is false form studies that showed the bio-distribution and Pharmacokinetic properties.   Japanese data shows that the spike protein of the Pfizer ‘vaccine’ gets into the blood where it circulates for several days post-vaccination and then accumulated in organs and tissues including the spleen, bone marrow, the liver, adrenal glands, and in the ovaries.

“The primary activity of a coronavirus particle is to safely deliver its genetic information (RNA) to the appropriate host cell and initiate a new infection……In addition to the viral genome and four structural proteins, it is likely that the SARS-CoV-2 particle contains host cell proteins picked up by the virus as it escapes an infected cell, but what might be included has not yet been established”. Getting to know the new coronavirus

The Moderna literature explains how it gets into the bone marrow.

Have a look at Moderna’ s promo.  It makes for an informative read but understand that mRNA is a gene therapy with potentially huge benefits for curing genetic diseases.  And that is how they sell it.   However, it also has potential for great evil.  It could be used to control populations. It could be used to engineer a sub-human servant class and a super healthy long-lived transhuman elite class (gods).  I am sure they will choose well (lolz).  Or it could (the most likely outcome in my humble opinion) go disastrously wrong and cause a mass extinction.  This technology changes the stem cells.  Despite what they say this has the chance of integrating into human DNA.  Instead of creating a super race it is more likely that we create X-men (Jewish comic book) mutants.  Generations of retards.

So, are we surprised that we get off-site expression?  That we have inflamed hearts and that it can cross the Blood Brain Barrier (BBB) potentially leading to neurodegenerative diseases?   The injection technique has a lot to do with where (and how fast) the S-protein expresses itself.  The mRNA is delivered intramuscularly but what if it is injected Intravenously? In mice it causes myopericarditis. In some people we see an almost immediate response.  Is that because it is mainlined?  Straight to the heart and boom.

Lipid nanoparticles (LNP)

A large portion of the debate between Wilson and Couey was around the adjuvant characteristic of mRNA.  Is mRNA a self-adjuvant?  Is mRNA immunogenic?  According to a Nature article “the mRNA can serve as both immunogen (encoding the viral protein) and adjuvant, owing to intrinsic immunostimulatory properties of RNA”.Wilson claimed that they solved the problem of immunogenicity by stabilising the mRNA (as pseudouridine) but as we have seen this can lead to other problems.   This is from [page 38] of the highly recommended article in IJVTPR (I have downloaded the PDF version):

So, the mRNA needs to be encased in a nanoparticle that will keep it hidden from the immune system. The second issue is getting the cells to take up the nanoparticles. This can be solved in part by incorporating phospholipids into the nanoparticle to take advantage of natural pathways of lipid particle endocytosis. The third problem is to activate the machinery that is involved in translating RNA into protein. In the case of SARS-CoV-2, the protein that is produced is the spike protein. Following spike protein synthesis, antigen-presenting cells need to present the spike protein to T cells, which will ultimately produce protective memory antibodies (Moderna, 2020). This step is not particularly straightforward, because the nanoparticles are mostly taken up by muscle cells, which, being immobile, are not necessarily equipped to launch an immune response. As we will see, the likely scenario is that the spike protein is synthesized by muscle cells and then handed over to macrophages acting as antigen-presenting cells, which then launch the standard B-cell-based antibody-generating cascade response. Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19 (May 10 2021). The International Journal of Vaccine Theory, Practice, and Research (IJVTPR)Stephanie Seneff and Greg Nigh (MIT)

Now, Lipid nanoparticles (LNP) are of interest to me because we used similar products (PEG, Span, Tween) in polymerizations for creating micelles. This is because we made emulsions using oil and water phases and oil and water do not mix so you need to use surfactants (soaps) to create micelles:

The surfactant is depicted looking like a tadpole with a long tail and a functional “head”.  It all depends what charge (polarity) the head and the tail have as to whether it attracts or repels the water (hydrophobic or hydrophilic).  The polymerization happened inside the micelle.  This is what I found immensely interesting (recommended if interested in chemistry):

“As mentioned above, cationic lipids are used to formulate LNPs containing nucleic acids [17]. Cationic amino groups within these lipids interact with nucleic acids' negatively charged phosphate groups, resulting in engraftment in an LNP. In 1989, a lipoplex
structure containing synthetic cationic lipid DOTMA (N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride) and helper lipid DOPE (dioleoylphosphatidylethanolamine)was used to generate Luc mRNA LNPs that successfully transfected several cell types [41].
Further, in vitro transfections have long used cationic lipids including commercially available Lipofectamine, which is widely used for RNA and DNA in vitro transfections despite its known cytotoxicity [42]. While separated, both cationic and anionic lipids in cell membranes display a cylindrical shape, which supports bilayer structure formation. However,when these lipids interact together via negatively and positively charged headgroups, they
form cone-shaped structures that promote hexagonal 1--111 phase formation. This hexagonal phase disorganizes bilayer structures and correlates with membrane fusion as well as the disruption that is partially responsible for cationic lipid toxicity [43]. When systemically delivered, LNPs with permanent surface charge interact with serum proteins, and this inter- action causes rapid clearance from the circulation [44,45]. Indeed, cationic LNPs have been shown to generate toxicity towards phagocytic cells in vitro. [46]. Additionally, systemically delivering cationic LNPs induces a strong immune response by activating the interferon type I response and instigating expression of INFY, and the pro-inflammatory cytokine IL-2. [47]. Excessive immune reaction to LNPs is not desirable because uncontrolled cytokine release can lead to life-threating conditions……” Lipid Nanoparticles for Organ-Specific mRNA Therapeutic Deliverẏ Zak, M.M.; Zangi, L. Lipid Pharmaceutics 2021, 13, 1675.

The bold emphasis is mine.  You get the picture…. a lot can go wrong.  When it happens in a reactor and the reactor goes solid you just dig it out and clean it.  Not so easy in a human brain (lolz).  All joking aside these molecules have different characteristics at different molecular weights and disassociate differently depending on pH.  Apparently, they can be made to target different organs depending on those characteristics.  It all works well in theory.  In practice when we did stuff on the plant, and it went horribly wrong and blew a reactor up the research department said…. well, that never happened in the lab (or worse still) …it only happened once, we thought it wouldn’t be a problem (lolz).  We cleaned the glasswork, and it was all Hunky Dory. A lot can go wrong (and that is leaving aside the anaphylactic shock that is often triggered by these compounds).

So much of the biochemistry is modelled by computers based on mathematics and chemical properties of proteins etc.  One such open-source model is Martini 3 (which sounds like a bunch of drunk scientists to me).  While it is true that electron microscopy and tomography etc. is used, there is still much that is speculative.

“The viral envelope is flexible and lacks symmetry. The structures of E, M and S proteins have not been resolved experimentally. There are some structural insights available on S trimers and E pentamers, but there is no accurate model of the M dimer…..Moreover, the nature of the interactions between these three proteins is believed to be more complex than originally expected. The complexity and plasticity of the virus make it challenging to study the structure of the viral envelope”.                                          

The furin cleavage site

The virus was man made and originated in a lab. It was deliberately released to provide cover for collapsing the system and bringing in the NWO. I know who did it and why. Suffice to say it was not just China. There were global institutes involved and this is driven by the bankers. This article is not going to go into that, but I did want to provide a few pointers for those (like me) who are completely lost in all the technical jargon etc. So, some simple basics.

All the fuss is around the furin cleavage site which so far is different from any animal version. It is a combination of different animal cleavage sites (bat and pangolin). Furin should be understood as the scissors that cuts the cleavage site near the Receptor Binding Domain (RBD). SARS-CoV-2 entry requires sequential cleavage of the spike glycoprotein at the S1/S2 and the S2ʹ cleavage sites to mediate membrane fusion. SARS-CoV-2 has a polybasic insertion (PRRAR) at the S1/S2 cleavage site that can be cleaved by furin.

Furin is a protease enzyme that in humans and other animals is encoded by the FURIN gene. Some proteins are inactive when they are first synthesized, and must have sections removed in order to become active. Furin cleaves these sections and activates the proteins. Furin is enriched in the Golgi apparatus, where it functions to cleave other proteins into their mature/active forms. Furin cleaves proteins just downstream of a basic amino acid target sequence (canonically, Arg-X-(Arg/Lys) -Arg'). In addition to processing cellular precursor proteins, furin is also utilized by a number of pathogens. For example, the envelope proteins of viruses such as HIV, influenza, dengue fever, several filoviruses including ebola and marburg virus, and the spike protein of SARS-CoV-2, must be cleaved by furin or furin-like proteases to become fully functional.

PRRA and ccu cgg cgg gca

The furin cleavage site consists of four amino acids PRRA, which are encoded by 12 inserted nucleotides in the S gene. A characteristic feature of this site is an arginine doublet. This insertion could have occurred by random insertion mutation, recombination or by laboratory insertion. The researchers say the possibility of random insertion is too low to explain the origin of this motif.
Surprisingly, the CGGCGG codons encoding the two arginines of the doublet in SARS-CoV-2 are not found in any of the furin sites in other viral proteins expressed by a wide range of viruses.
Even within the SARS-CoV-2, where arginine is encoded by six codons, only a minority of arginine residues are encoded by the CGG codon. Again, only two of the 42 arginines in the SARS-CoV-2 spike are encoded by this codon – and these are in the PRRA motif.
For recombination to occur, there must be a donor, from another furin site and probably from another virus. In the absence of a known virus containing this arginine doublet encoded by the CGGCGG codons, the researchers discount the recombination theory as the mechanism underlying the emergence of PRRA in SARS-CoV-2.
This genetic material, called RNA, and which some viruses inherit from others, works like an instruction manual for manufacturing the proteins that form SARS-CoV-2. The genome of the new coronavirus has around 30,000 letters with enough instructions to penetrate a cell, hijack its machinery and make thousands of copies of itself. The instructions for the human cell to manufacture the virus’s main weapon – its spike protein used as a key by new viruses to gain access to more and more cells – is contained in around 4,000 letters. The coronavirus spike protein is like a double-faceted key. It first latches onto the lock – the human cell’s ACE2 receptor. Its next step is to control the binding of the virus’s membrane to the cell’s membrane. The main difference between SARS-CoV-2 and other coronaviruses is the appearance of 12 extra letters in its genome. The experts flag up this extremely short sequence as the main culprit regarding its virulence.

With some exceptions, a three-nucleotide codon in a nucleic acid sequence specifies a single amino acid. In other words, the mRNA inside the corona virus codes for the amino acids in the DNA.  There are four nitrogenous bases that occur in DNA molecules: cytosine, guanine, adenine, and thymine (abbreviated as C, G, A, and T). RNA molecules contain cytosine, guanine, and adenine, but they have a different nitrogenous base, uracil (U) instead of thymine. The building blocks of DNA are nucleotides, which are made up of three parts: a deoxyribose (5-carbon sugar), a phosphate group, and a nitrogenous base. It provides the instructions. These are the twelve letters (four sets of three condons) that changed the world ccu cgg cgg gca ……….. c=cytosine, u=uracil, g=guanine, a=adenine and this is what they code for:

  • ccu > ENCODES > P (Proline)
  • cgg > ENCODES > R (Arginine)
  • cgg > ENCODES > R (Arginine)
  • gca > ENCODES > A (Alanine)


mRNA stability

mRNA stability

This post was inspired by the Couey vs Wilson debate which I am still transcribing and which can be found here:

Couey vs Wilson debate

The debate got rather heated and complex on the question of whether or not mRNA is an adjuvant or a self-adjuvant as their are studies that indicate that it could be used as an adjuvant.  Now, an adjuvant is a compound or chemical that irritates or triggers the immune system.

All vaccines have adjuvants and Dr Wilson (citing a scientific study) showed that mRNA could act as a self-adjuvant.    In other words there would be no need for the addition of an adjuvant.    The objection voiced by Jonathan was that mRNA is highly immunogenic. In other words it could trigger all sorts of autoimmune diseases and inflamation, especially if it was free floating in the blood.

In order to prevent this they need to do two things 1. encapsulate the mRNA in a Lipid Nano Particle (LNP)  and 2. stabilize the mRNA.  It turns out they do use PEG and polysorbate 80 as adjuvants.


PEG is a long chain polymer and its characteristics are different depending on the length of the polymer chain.  Polysorbate 80 is similar to PEG.   I have useed these substances as surfactants etc when making polymers. They have certain hydrophobic and hydrophilic qualities which can be used when mixing aqueous and oil phases and in micelle formation. The above paper lists MF59 adjuvant as an emulsion adjuvant composed of an oil phase (squalene 4.3%): and an aqueous phase (polysorbate 80:0.5%, sorbitan trioleate 0.5%). These vaccines do use an adjuvant, therefore Dr Wilson was incorrect.

Polyethylene glycol

A PEGylated lipid is used as an excipient in both the Moderna and Pfizer–BioNTech vaccines for SARS-CoV-2. Both RNA vaccines consist of messenger RNA, or mRNA, encased in a bubble of oily molecules called lipids. Proprietary lipid technology is used for each. In both vaccines, the bubbles are coated with a stabilizing molecule of polyethylene glycol.[medical citation needed] As of December 2020 there is some concern that PEG could trigger allergic reaction, and in fact allergic reactions are the driver for both the United Kingdom and Canadian regulators to issue an advisory, noting that: two “individuals in the U.K… were treated and have recovered” from anaphylactic shock. As of 18 December, the US CDC stated that in their jurisdiction six cases of “severe allergic reaction” had been recorded from more than 250,000 vaccinations, and of those six only one person had a “history of vaccination reactions”

Two things to mention here, firstly, many of the anaphylactic reactions are cause by the adjuvants like PEG and secondly, PEG and other polymers are being examined as delivery mechanisms for drugs because they cross the Blood Brain Barrier (BBB). If that is the case then they should also be able to deliver the spike protein across the BBB and evidence is emerging that happens.  That is not a good thing. There is a reason the brain is protected and segregated from the circulatory system and while it might be desirable to cross the BBB to treat diseases like dementia and Parkinson’s it comes with a risk.

So, as far as the debate is concerned Jonathan is correct. The vaccines do have an adjuvant and it is a LNP.  Note that the Wikipedia quote above uses the word excipient rather than adjuvant. An excipient is an inactive substance ….but is it really inactive? How can it be “inactive” when PEG antibodies are found and when some people suffer anaphylactic shock?

Polyethylene Glycol Immunogenicity: Theoretical, Clinical, and Practical Aspects of Anti-Polyethylene Glycol Antibodies


Wilson claimed that the self-adjuvant effect of mRNA was due to the pseudourodilatation of the mRNA. Pseudouridine is supposed to be more stable.

Ψ (pseudouridine) is also found in mRNAs which are the template for protein synthesis. Ψ residues in mRNA can affect the coding specificity of stop codons UAA, UGA, and UAG. In these stop codons both a U→Ψ modification and a U→C mutation both promote nonsense suppression.[6] In the SARS-CoV2 vaccine from BioNTech/Pfizer, also known as BNT162b2, Tozinameran or Comirnaty, all U's have been substituted with N1-methylpseudouridine,[7] a nucleoside related to Ψ that contains a methyl group added to N1 atom.

This is the tweet (second one Tishbite) that I sent out (well worth reading):


They’ve fiddled around with codon optimization to increase stability, but that translates into (1) enormous quantities produced of spike and (2) a different spike protein which could be even more pathogenic.


In case the above tweet disappears the link takes you here:

They are making people disappear off twitter (and FB)….this guy is good:


None of that fills me with confidence especially the fact that it can misfold.  That can lead to prions and neurodegeneration. Expect to see more diseases of the Central Nervous System,  dementia, Parkinson and CJD as well as more strokes, cancers and heart attacks. Don’t let them go anywhere near the kids with this.  We have been warning for more than a year and a half.  Is anyone listening?

Come out of her

Come out of her

In the Apocalypse the angel sent by Jesus appeals for the people of God to come out of Babylon.

"And I heard another voice from heaven, saying, Come out of her, my people, that ye be not partakers of her sins, and that ye receive not of her plagues" (Rev 18:4).

Of course many Christians will say that is not literal…it is metaphorical. It is a state of mind, a refusal to participate in the things of the world and that is all true but soon many Christians will be forced to chose between a vaccine and living a normal life.  They will be treated as second class citizens, discriminated against and an apartheid system of passports and access will be implemented.  Even essential health services and medicines will be off limits.  Those who refuse will find their lives shrinking.

I have posted numerous articles and scientific papers on the medical dangers associated with these experimental “vaccines” (transfections) which have already killed and injured thousands of people and will injure more people in the future but my argument here is not about the medical dangers (see the PDF below if you want information on immunology)  but about the spiritual dangers.  The apostle Paul says the following:

"Know ye not that your bodies are the members of Christ? shall I then take the members of Christ, and make them the members of an harlot? God forbid.  What? know ye not that he which is joined to an harlot is one body? for two, saith he, shall be one flesh.  But he that is joined unto the Lord is one spirit" (1 Cor 6:15-17).

We are instructed not to join the body of Christ to a Whore.  The great Harlot has deceived all nations with her sorceries (pharmakeia).    The wretched whore has seduced the great men and the merchants of the earth to commit fornication (porneia) with her.   Who is behind the pharma, the porn and mammon?   Who?

Fourth Industrial Revolution

The idea of the “fourth Industrial Revolution” was sold by the harlot to the “great men of the earth” .  It allows them to completely dominate human behavior and link medical status with ID and mammon. That combination is spiritual death and it is all linked to vaccines.   These are not ordinary sterilizing LAV vaccines but mRNA transfections which form part of a vast experiment to transform human genetics in a project which encompasses Artificial Intelligence , human augmentation and  gene therapy. The project is called transhumanism and the goal is to transcend what it is to be human (made in the image of God) to aspire to become  god-like.  It is the original sin of Eden where the serpent seduced humanity with a lie.


In order to achieve this goal they released a bio-weapon and an unprecedented propaganda campaign to nudge human behavior.  If you need to lie and murder to build your lovely new world order then I want no part in it.

Those who doubt human intervention or posit a natural origin are deluding themselves.  The Chinese data base and the American data base (Ft Detrick) were both taken down and are no longer available. We have the emails showing collusion. We have the grant applications. We have patents.  We have scientific research papers. We know race targeting was involved. We have videos where they were boasting.  We have conflict of interest. We have a cabal of scientists involved with Epstein and his “philanthropy” and Lolita trips. It is no longer deniable especially because we are digging up evidence of medical malfeasance that goes back decades.  This was not just a singular incident but a slow, deliberate relentless program.  They have already killed millions (AIDS).  They have blood on their hands.  They have perfected their craft (sorcery =pharma).

This is all about code… code and genetic code.  It is not a coincidence that the Special Virus Cancer Program was launched in the same decade that saw the incorporation of Microsoft and renewed interest in Artificial Intelligence.   A virus can be used to hack a computer and it can be used to hack humans.  The virus is a tool to change human or computer software. They want to install a new operating system in your body – one that they can control.

Hackers always sign their malware.  It shows how clever they are and allows them to claim credit when flaunting their superior intellect to fellow hackers. I earnestly believe that the Spirit guided me to this revelation (at least  15 months ago) showing me who was behind this terrible viral attack and deception:


Obey the Government

It is sickening to hear Christians quote Romans 13 out of context to justify their behavior.  In the time of Paul  non-Roman religions were divided into religiones licitae (“licensed worships”) and religiones illicitae (“unlicensed”).  Judaism already had recognition and Paul was seeking to set a legal precedent by demonstrating that Christians were not revolutionaries seeking to destabilize the Roman Empire. The Jews accused Christians of setting up their own king (Jesus Christ) in competition to Caesar. Of course, they were twisting words and lying – Paul sought to rectify this by pointing out that Christians were good citizens as Jesus had instructed them to render unto Caesar what is his (tax money) but unto God what is his.   This is why Jesus asked what image was on the coin.

"And when they were come, they say unto him, Master, we know that thou art true, and carest for no man: for thou regardest not the person of men, but teachest the way of God in truth: Is it lawful to give tribute to Caesar, or not?  Shall we give, or shall we not give? But he, knowing their hypocrisy, said unto them, Why tempt ye me? bring me a penny, that I may see it.  And they brought it. And he saith unto them, Whose is this image and superscription? And they said unto him, Caesar's.  And Jesus answering said unto them, Render to Caesar the things that are Caesar's, and to God the things that are God's. And they marvelled at him".

It was a reminder that they were made in the mage of God and therefore had to render to God what was his.   They were not transhuman.  He did not instruct them to volunteer for genetic experimentation that would change their fundamental nature.   You think I am exaggerating?  This is the beginning of a program that will be rolled out to everyone.  Surely you are not foolish enough to think they are going to stop?  They have 240 mRNA vaccines in the pipeline and this is just the start of their new program.  All the data is being fed into Artificial Intelligence.  We are talking billions of people and billions of bits of information. That represents thousands of hours of human experimentation that will enable them to adjust and fine tune their platform.  This is not over by a long shot.  You will never be returning to the old normal. Even if you vaccinate.   In Israel you no longer count as vaccinated if you only have two shots (lolz).

The biggest lie of all is that we have no treatment protocols. We have multiple ways of treating covid with drugs and supplements but they are not being used. They would rather let people die than give them non-vaccine treatments.  So this is not about your health.  This is about implementing the Beast system.

So, I will not obey people who release diseases and who lie.  People who gas-light, manipulate and are prepared to injure and murder to achieve their Babylon government.   However, this is not even about obeying because you have volunteered.    Vaccines are not mandated by lawyou were given a choice.  Granted that it is a difficult choice (an extreme choice)  but it is a choice none the less.  If you choose not to vaccinate your existence becomes very limited and you may loose everything including your life….but it is still a voluntary choice.    You are not “disobeying” the Government (that is nonsense) you are simply resisting being bullied and manipulated (what they call psychological nudging).  They are lying to you about everything…..even about the (Australian) law:


WAKE UP – this is a mind game. They want you to volunteer.

It is not the unvaccinated who are being selfish it is the vaccinated.   They are putting pressure on everyone else to comply with an evil agenda so that they can keep their privileges.   They have submitted to bullying and been manipulated into compliance. Once you take the first step the second step is easier….by the third step you won’t even bat an eyelid.  You have been psychologically re-framed by means of fear and lies.   If you have vaccinated you just made life incredibly difficult for everyone else.  Once enough people volunteer they can imprison (quarantine) the remainder and you must bear responsibility for what comes next.

 My position

I pray that I might have the strength not to comply or to consent to this abomination. The Beast system wants to possess the bodies and souls of men (Rev 18: 13). I understand why some have given into pressure.  It is difficult if you have jobs or businesses or need medical attention. I empathize and feel for what they have done to people…putting them into an intolerable position.  However, at the very least do not justify yourself and recognize that it is human weakness. Pray to God because he is forgiving and merciful.  I pray for everyone…both for the vaccinated and the unvaccinated. I will never let them sow division but neither will I hold my peace and excuse weakness…not my own weakness or anyone else. Selah.

"I keep asking that the God of our Lord Jesus Christ, the glorious Father, may give you the Spirit of wisdom and revelation, so that you may know him better" (Ephesians 1:17 NIV).

The Beast is slowly being revealed but my body and soul belong to God. I will not be joined to a Harlot through vaccines or any other way.  I take my example from the Lord who urged us to take up his cross and follow him (Matthew 10: 34-42).  What comes next is going to be very hard and very difficult and although the war has already been won we must demonstrate a good confession in this last battle and overcome. I am free and will never be a slave to their system.  They have no authority over me.

If the Son therefore shall make you free, ye shall be free indeed.



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Giants or pygmies?

Giants or pygmies?

We saw that Vejon Health lauded Geert Vanden Bossche  (Expert vaccine developer from Belgium) and Robert Malone MD (Inventor of mRNA vaccines from the USA) as Covid Giants.

Are they really Covid Giants?  We know that they were both deeply involved with the vaccine industry.  One way to control the opposition is to lead it.  Perhaps they really are white hats. They are certainly making all the correct noises but I am suspicious.   They are articulating genuine concerns and gaining trust but will their criticism be used to capture and direct the opposition.  All roads will eventually lead to vaccines and digital ID. My advice is be careful and filter your information. 

Here are a number of one minute shorts by Mark from Housatonic.

Robert Malone, Epivax, USAMRIID, DoD, Qiagen, Sina Bavari

Solvay Pharmaceuticals, likely direct cell-based influenza vax handoff Malone to Vanden Bossche 2007




Robert Malone the “inventor of mRNA vaccines” has emerged out of nowhere saying all the right things.  He has warned about vaccines etc but what do we really know about his past?

But first watch this one minute short about the origin of West Nile Virus (WNV). West Nile virus  is a single-stranded RNA virus that causes West Nile fever.The virus is primarily transmitted by mosquitoes effects humans and horses. First identified in 1937 in Uganda and somehow (???) endemic in the USA. Sounds a bit like a bat virus becoming endemic.

Ep 108.2: OneHealth Bushmeat! We are alone in fact-checking Malone (1 hour 50 min)



Everything is not always what it seems and many of these “natural” pandemics including “Spanish Flu” are because  these nutters have been messing with genetics and viruses for decades.   Malone is saying all the right things….but he is suspect… wary.