Lipid Nano Particles (LNP)

Lipid Nano Particles (LNP)

Not watched this yet but as an industrial Chemist substances like the LNP substance PEG (Poly ethylene glycol) were used as surfactants/stabilisers in polymer shoots.  Something that was put in a chemical reactor not something injected into the blood stream.  When I first heard it I was flabbergasted.

 

Porky gets shredded

Porky gets shredded

Well they say all is fair in love an war and  insults and salty language are directed at Stuart Niel. I have run out of sympathy for these people and they are fair game as far as I am concerned.  They have blood on their hands. This was Stuart Niel’s  tweet:

Some responses:

Lethal Dose 50 (LD50)

We already know that the LNP distributes the spike protein everywhere and that it can cross the Blood Brain Barrier (BBB).  So the quickest way to test if inflammation and amyloidosis can be artificially  induced is to introduce it into the Brain.  They did not do LD50 testing on the vaccine.  They have tried everything to shut this experiment down including removing banking options.  Why are they so frightened?  I thought is was safe and effective?

They lied, and they coverd-up, then they lied some more.

These people cause the problem (heart attacks and strokes) then they offer their solution.  The gas-lighting is epic. This is what we are dealing with:

Dr. Peter McCullough speaks out on War Room about his Twitter lawsuit (5 min)

 

Graphenos Spectaculos Boyz R’ Back in Town (35 min)

This is a short stream (starts at 11 mins). Kevin has reached the running costs for this month ($2500). More lab work coming soon. They will do everything to stop it.

 

Lipid Nanoparticle (LNP) Harm

Lipid Nanoparticle (LNP) Harm

Told you so….

 

Here is the video in the tweet:

RTE Discussions #8 (Take Two): Evidence of Lipid Nanoparticle Harm With Marc Girardot (1:29)

 

Millions unaffected by vaccines

Millions unaffected by vaccines

This is the main argument you hear from people.  Some have had three vaccines (or more) and they are OK.  Millions of doses have been distributed and millions of vaccinated people are fine.  So what is the fuss?

This is a multi-faceted problem.  Firstly, we are all genetically different and some people can smoke and drink and abuse their bodies all their lives and live to a ripe old age. So there is a spectrum. Some people will have an immediate allergic reaction but in other people the constant doses every three months will gradually destroy the immune system.  It is not for nothing that we see huge increases in excess mortality for cardio-vascular and neurotropic diseases as well as cancers.  We now know that it is dose dependent…the more jabs the greater chance of a bad outcome.  Common sense.  You are playing Russian Roulette.  Will it be the next shot that tips your system into accelerated senescence?  Go on…just one more shot….just do it….just do it….you know its not in the chamber (lolz).  Pharma is betting on you doing it.  Please don’t deprive them of making a killing.

Degraded mRNA

We know the mRNA needs to be kept cold otherwise it degrades.  Originally they said -72°C  but that is not practicable even for hospitals (it would mean storage in liquid nitrogen). Heat and UV light will break down the mRNA and it will not  be effective.    This is why so many people still catch covid.  The body will get all sorts of degraded proteins and hopefully it will deal with the junk mRNA and clean up the mess.   So your vaccine was not effective but at least it did not make you sick.  However, if you get a purer form (lets say 80% mRNA) then you will start getting more side effects from the vaccine spike.  Northern blot has been performed on the vaccine and all sorts of protein fractions can be discerned so it is not “pure” mRNA but mRNA with junk.

Stabilized mRNA

As we pointed out in other articles they have attempted to stabilize the mRNA by methylating the uridine to pseudouridine.  This means that the body will not break down the mRNA before it can do  its job but that comes with other problems such that the RNA can possibly read through stop condons (run the red light) and encode mutant proteins forming G-quadruplexes.  When you run a red light you can cause a crash (sometimes).

Quality concerns

Not only can the mRNA be degraded  but we know that the vaccines are contaminated. Different people (including Dr Kevin McCairn) have tested them and found metals and other contaminants that come from the production process.  I used to run a lab as a Senior Chemist so I know how difficult it is to scale something up from micro-grams in a clean-lab environment using “glassware” to a major manufacturing plant (often in the third world).  What quality guarantees do we have?   We have none because it does not matter as they are not liable.   Why did our government agencies not independently test the vaccines for contamination (particulates etc)?    Back in the day I would not be allowed to send out a batch of polymer for water treatment unless it was tested and adhered to the specifications.  We even kept samples of old batches in an archive  so that we could retest them in case we got a complaint.  That was a product for waste water treatment not something injected into the blood stream.

Injecting

Which brings me to injecting and injection techniques which makes a big difference. An intramuscular injection is designed to deposit medications deep into muscle tissue and is used to prevent medication leakage, particularly for oily injections (PEG). Displace the skin and subcutaneous tissue by pulling the skin….

The trouble is that the vaccine does not stay in the muscle as pharmacokinetic studies show distribution throughout the body into all organs and persistence in the lymph system for at least sixty days.  And then there is the PEG (Poly Ethylene Glycol) which is used as an LNP (Lipid Nano Particle) like a little “fat (lipid) bubble” to “package the mRNA for delivery.  I have used PEG as a surfactant in huge reactors when shooting co-polymers but I would never put it in my blood stream.  PEG is a long chain polymer  the characteristics of which are determined in part by the length.  Once again (Knowing how polymers work) what chance is there of getting the exact molecular faction that you want?  And how pure is the PEG?   Who is doing the quality control?  Is it being made in a third world country? PEG can cause Antiphospholipid  syndrome which is a condition in which the immune system mistakenly creates antibodies that attack tissues in the body and causes clots.

Placebo

Dr Kevin McCairn has tested the vaccines live on camera and some of them contain no Phosphorus.  That means that no mRNA is present.  It seems like they deliberately left some batches as placebos.

Conclusion

If someone tells you they had three vaccines and are OK then they are very lucky.   They either got degraded batches or placebo batches…..or it could be that they will go into accelerated senescence in the next few years.

 

Gigaohm Biological (July 28)

Gigaohm Biological (July 28)

Phoshpholipid

Another excellent presentation with Walter Chestnut discussing his latest findings, also commenting on a Robert Malone video who warns about the LNP delivery mechanism causing problems such as PEG micelles stimulating production of anti-PEG IgM, which led to accelerated clearance of subsequently administered PEGylated liposomes. According to A review on phospholipids and their main applications in drug delivery systems, Phoshpholipid–PE–PEG mixtures could form micelles rather than liposomes if PE–PEG content exceeds certain critical limit.  Of course the PEG  interests me because it is used along with surfactants for micelle formation in polymerisations.  I never thought something like that would be injected into people (lolz). Below is actually a good resource on Lipids (have a look at all the pages very informative):

 

Heavy metals play a role in neurodegeneration  but lipids are important as  Anticardiolipin and other antiphospholipid antibodies (are found) in critically ill COVID-19 positive and negative patients Antiphospholipid antibodies (APLAs) are biomarkers of a spectrum of clinical features observed in antiphospholipid syndrome (APS).1 Features of APS include venous and arterial thrombosis involving multiple organs and having various presentations. Positive APLA serology was associated with more severe disease regardless of COVID-19 status.  Moreover, Persistent lgG anticardiolipin autoantibodies are associated with post-COVID syndromePersistence of various symptoms in patients who have recovered from coronavirus disease 2019 (COVID-1 9) was recently defined as ‘long COVID’ or ‘post-COVID syndrome’ (PCS). They conclude that Immunoglobulin G (lgG) anticardiolipin autoantibodies (aCL) are associated with the severity of COVID-19.  In other words an allergic or inflammatory reaction to lipid (in the heart) but also “…persistence of the virus, especially in the nervous system, could be suggested with a post-infectious inflammatory or autoimmune reaction”.  Might this have something to do with pumping the body full of phoshpholipids and mRNA spikes? What do I know? (I am just a bucket chemist who used to mix this stuff in buckets not in human bodies).

Unfortunately, many of Walter’s hypothesis are proving to be correct. He is an avid reader of the medical literature and a talented dot-connecter with a big picture overview. His sub-stack is highly recommended.  In his latest article he shows how amyloid is a double-edged sword. A large build-up will cause problems, but amyloids also serve protective functions – against autoimmune attacks.  So, they are symptomatic rather than causal factors.

Comment: Repeated infection with covids is not good even for the unjabbed and even if they got over it before. A least the omicrons have the PrP silenced. But the HIV and the other nasties and all the humanized nucleic acid etc tacked into the spike yes, will be immune insults that will catch up with us the older we are. Shortened lifetimes, yes. The younger the less shortened. Of course, the jabbed are the ones who will suffer shortest lives.

More study is needed into the mutagenic properties of the spike-protein. Perhaps this explains Nucleic Acid Acid Based Therapeutics against Respiratory Infections?

Comment: The prion promoting sequence in the spike also promotes amyloidosis. They are seeing where there won't be a positive D-dimer test but when they put blood under the scope then you see the amyloid building up. The amyloid is causing the clotting, the heart damage, etc. They look for a test for amyloid in those "rare" pre-jab liver inflammation cases and they find amyloid build up and light chains. The hepatitis victims go on to be found Dx with myloid leukemia (if I have the name correct). The Chinese are making more targeted covid viruses - but it is US research over 25 years that developed those - there is research trail from Baric, Daszak and others and a lot of patents. Baric collaborated with Shi - he trained her! That enrichment is bad news - they did that in the jab for a lot of reasons - it throws off all kinds of cascades along with the defanging IFN-1. IFN-1 has all these cascades which include regulatory ones to down regulate inflammation. But that is all gone because of the jab made to evade being recognized and take IFN-1 out. Enriching with C-G over-glycosylates it possibly more than HIV is so it sails on by more so than the virus construct.

This is very complex and there is so much that we do not know. As someone commented.

Code that codes for multiple things depending happening on how it’s parsed with the folds everybody producing the spikes internally become a mini gain of function study. multiply by a billion consecutive studies running concurrently.

It is not just the structure of the protein but how it folds and polarity as in hydrophilic or hydrophobic nature and charge.  Who is to say that the same protein might not fold differently under other circumstances thereby acquiring different properties?  Repeat expansions have been proposed to cause disease by both the repeat RNA forming foci that sequester RNA-binding proteins and through toxic dipeptide repeat proteins generated by repeat-associated non-ATG translation discussed in the article  G-quadruplex-binding small molecules ameliorate C9orf72 FTD/ALS pathology in vitro and in vivo.  

C9orf72 (chromosome 9 open reading frame 72) is a protein which in humans is encoded by the gene C9orf72. The protein is found in many regions of the brain, in the cytoplasm of neurons as well as in presynaptic terminals. The mutations in C9orf72 are significant because it is the first pathogenic mechanism identified to be a genetic link between familial frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). The mutation of C9ORF72 is a hexanucleotide repeat expansion of the six-letter string of nucleotides GGGGCC.

I wonder, I wonder if pumping the body full of mRNA instructions to make spike proteins will deliver the spike proteins that they want?  We know already that the mRNA vaccines are not pure but contain fragments.   The start codon of a gene is always “ATG” so repeat associated non-ATG translation means that it does not read the correct starting point, or you could say that it reads through the stop condon (runs the red light).  It looks like read-through can cause disease. Is that why the above experiment attempted to improve dementia using small peptides that stick to the G-quadruplex?

Walter Chesnut LIVE: Gigaohm Biological High Resistance Low Noise Information Brief (2:50)

Globo-homo

Globo-homo

A three hour stream in which  WEF’s Juval Harari Globo-homo Wet Dream For Ukraine is contrasted with the Actual Facts On The Ground.

Dojo Time Stamps:

Virus evolution and LNP

Virus evolution and LNP

The Explosion of Cancer and Latent Disease: The Lipid Nanoparticle Platform Is Asking for Trouble (5 min)

Virus evolution by antibodies + BA 2 Omicron – COVID-19 vaccines update 40 (17 min)

How does the virus evolve inside an infected person – we commence this story with a new demonstration in a vaccinated patient, and relapse to a well-documented history in COVID-19 patients, and how antibodies can be contributing to such viral evolution. This also leads us to a hypothesis as to why evolving variants might show up in wastewater prior to taking over a population. We conclude with how the BA2 variant of the Omicron is different from the BA1 variant, demonstrating continuous uninterrupted evolution of the virus.

Described content: Vaccine patient variants: https://www.sciencedirect.com/science… Variants database: https://cov-lineages.org/lineage_list… Innunocompromised host: https://www.nejm.org/doi/10.1056/NEJM… Cancer host: https://linkinghub.elsevier.com/retri… HIV host: https://www.medrxiv.org/content/10.11… Prolonged infection variants: https://academic.oup.com/ve/article/7… Evolution speed: https://www.clinicalmicrobiologyandin… Immune escape co-evolution: https://www.science.org/doi/10.1126/s… Convalescent plasma host: https://www.nature.com/articles/s4158… GIT variant evolution: https://genomemedicine.biomedcentral…. GIT viral load: https://www.gastrojournal.org/article… Viral load impact: https://academic.oup.com/ve/article/7… BA2 Omicron: https://arxiv.org/abs/2202.05031

Gigaohm Biological Breakthrough(20 April)

Gigaohm Biological Breakthrough(20 April)

Highly Recommended

This stream by Jonathan Couey is highly recommend and so is the previous stream by Dr Kevin  McCairn under the Lab Chronicles tab.

Jonathan is on fire and on the verge of a big break-through.  He was contacted by someone important whose, “voice we would recognize”.   I wonder who that could be?  Perhaps the person he tweeted about recently?

Senator Robert F. Kennedy Jr. from Children’s Health Defense. Kennedy is a son of U.S. senator Robert F. Kennedy and a nephew of President John F. Kennedy. He saw them both slaughtered by the Deep State and is called an anti-vaxxer and conspiracy theorist by Wikipedia. No higher recommendation is possible (lolz).

J.C.  was also contacted by Senator Ronald Harold Johnson is an American accountant, businessman, and politician serving as the senior United States senator from Wisconsin. A Republican, Johnson was first elected to the U.S. Senate in 2010. Johnson chaired the Covid Opinion panel with a number of top doctors and scientists.

These are two of the subjects touched upon by Jonathan…..(shocking….shocking….)

Immunomythology Update: Gigaohm Biological High Resistance Low Noise Information Brief  (2:08)

TGA Judicial Review

TGA Judicial Review

I have come across Julian Gillespie before and knew he was perusing a judicial review in Australia and have just been reminded (by my sister) of the progress  he is making.

The TGA is similar to the FDA in the USA. The Therapeutic Goods Administration (TGA) is the medicine and therapeutic regulatory agency of the Australian Government. As part of the Department of Health, the TGA regulates the quality, supply and advertising of medicines, pathology devices, medical devices, blood products and most other therapeutics.

Mr Julian Gillespie is a retired lawyer and former barrister who has come out of retirement to fight the legal battle against the COVID vaccination. He believes that the Australian people have not been given accurate information around COVID deaths, and deaths from the COVID vaccinations.

He is currently managing proceedings in the Federal Court of Australia related to “Australian Vaccination-Risks Network Incorporated v. Secretary, Department of Health.”

COVID UNDER QUESTION is a cross-party inquiry into the Government’s response to COVID held on 23rd March 2022. COVID Under Question was hosted by Senator Malcolm Roberts (One Nation Federal Senator for Queensland) and attended by Stephen Andrew (One Nation Queensland State MP for Mirani), George Christensen (Federal Nationals MP for Dawson), Gerard Rennick (Federal Liberal Senator for Queensland), Alex Antic (Federal Liberal Senator for South Australia) and Craig Kelly (Federal Palmer United Australia MP for Hughes).

Parliamentarians heard from a range of Doctors, experts, economists and everyday people about how the Government’s response to COVID has affected them and at times defied belief. The absurdity of Chief Health Officer dictates and power hungry politicians is all laid bare.

The full day’s proceedings were recorded and are available here: https://www.malcolmrobertsqld.com.au/covid-under-question-a-cross-party-inquiry/

COVID Under Question: Mr Julian Gillespie on March 24  (34 min)

TGA Judicial Review update #4 with Julian Gillespie March 8 (1:01)

Walter M Chestnut

Walter M Chestnut

This video features an interview with the Independent researcher and twitter phenomenon that is Walter Chestnut who is a composer by trade and who has a prodigious capacity to consume research articles and find links thus enabling him to suggest different hypotheses which are documented on his website https://wmcresearch.org/  and tweeted out. His work has already borne fruit as he made Kevin aware of the prion domain and prion genesis. He has however been dismissed by the likes of Kristian Andersen who wrote to Anthony Fauci about the possibility of an engineered coronavirus and then later back-tracked and participated in the cover-up.  As far as these people are concerned if you are not credentialed you should just shut-up and listen to your betters (while they screw you over). However, many of Walter’s theories have proven correct and it is refreshing to have someone with a sharp mind and unhindered by bias and preconception proposing hypotheses.  In case anyone has forgotten that is how science progresses.  It never progresses through consensus.

Kevin and Walter discuss a leaked report by  Acuitas Therapeutics on how testing LNP (Lipid nano-particles) caused damage to rats. Report: “[A Tissue Distribution Study of a [³H]-Labelled Lipid Nanoparticle-mRNA Formulation Containing ALC-0315 and ALC-0159 Following Intramuscular Administration in Wistar Han Rats]

The story of the therapeutics company Acuitas is interesting because the accusation went out on twitter that the Trudeau Foundation owned 40% of Acuitas.  That was quickly debunked as false and had the fact checkers crawling all over it.  However, is it false?

Is their evidence of malfeasance? I think their is and Trudeau has “form” with other scandals. This was the main chance to get in on the ground floor and make a killing on new technology. Acuitas Therapeutics is a private company and you will never prove it as their are multiple shell companies and no transparency.  Basically they are crooks. Malone certainly thinks it is true and he is (was) an insider:

Here then is the four hour stream with the Dojo links underneath.

Dojo links with timestamps:

  • 00:00:27 Start
  • 00:17:38 Report: “[A Tissue Distribution Study of a [³H]-Labelled Lipid Nanoparticle-mRNA Formulation Containing ALC-0315 and ALC-0159 Following Intramuscular Administration in Wistar Han Rats](https://phmpt.org/wp-content/uploads/2022/03/125742_S1_M4_4223_185350.pdf)”, “SPONSOR: Acuitas Therapeutics Inc. 6190 Agronomy Road, Suite 402, Vancouver, British Columbia, V6T 1Z3 Canada”
  • 00:21:50 Neurotoxins, MPTP, Parkinson’s