References:
COVID-19 is not a viral pneumonia — it is a viral vascular endotheliitis:
https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)30937-5/fulltext
https://academic.oup.com/eurheartj/article/41/32/3038/5901158
https://www.embopress.org/doi/full/10.15252/embr.202152744
COVID-19 is not just a respiratory disease — it can precipitate multiple organ failure, including hypoxic
and inflammatory damage to various vital organs, such as the brain, heart, liver, pancreas, kidneys, and
intestines:
https://www.nature.com/articles/d41586-021-01693-6
https://www.health.harvard.edu/blog/the-hidden-long-term-cognitive-effects-of-covid-2020100821133
https://www.nature.com/articles/s41422-020-0390-x
https://www.embopress.org/doi/full/10.15252/embj.2020106230
https://jamanetwork.com/journals/jama/fullarticle/2776538
https://pubmed.ncbi.nlm.nih.gov/32921216/
https://www.nature.com/articles/s41575-021-00426-4
https://pubmed.ncbi.nlm.nih.gov/32553666/
https://www.nature.com/articles/s41467-021-23886-3
https://pubmed.ncbi.nlm.nih.gov/34081912/
https://www.nature.com/articles/s41581-021-00452-0
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438210/
https://www.nature.com/articles/s41598-021-92740-9
Some of the most common laboratory findings in COVID-19:
https://www.uptodate.com/contents/covid-19-clinical-features
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426219/
COVID-19 can present as almost anything:
https://www.nature.com/articles/s41591-020-0968-3
https://www.frontiersin.org/articles/10.3389/fmed.2020.00526/full
COVID-19 is more severe in those with conditions that involve endothelial dysfunction, such as obesity,
hypertension, and diabetes:
https://www.dovepress.com/obesity-related-inflammation-and-endothelial-dysfunction-in-covid-19-ipeer-reviewed-fulltext-article-JIR
https://jamanetwork.com/journals/jama/fullarticle/2772071
https://mdpi-res.com/d_attachment/cells/cells-10-00933/article_deploy/cells-10-00933.pdf
The vast majority of COVID-19 cases are mild and do not cause significant disease:
https://www.webmd.com/lung/covid-recovery-overview#1
https://academic.oup.com/ofid/article/7/9/ofaa286/5875595
https://pubmed.ncbi.nlm.nih.gov/33289900/
In those who have critical COVID-19-induced sepsis, hypoxia, coagulopathy, and ARDS, the most common
treatments are intubation, injected corticosteroids, and blood thinners like heparin, which often
precipitate harmful hemorrhages:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7548860/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448713/
https://www.nejm.org/doi/full/10.1056/NEJMoa2103417
The majority of people who go on a ventilator are dying due to COVID-19 mimicking the physiology of
ischemia-reperfusion injury with prolonged transient hypoxia and ischemia, leading directly to the
formation of damaging reactive oxygen species:
https://www.journalofsurgicalresearch.com/article/S0022-4804(14)00176-0/fulltext
https://www.nature.com/articles/nature13909
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625011/
https://www.atsjournals.org/doi/full/10.1164/rccm.201401-0168CP
https://pubmed.ncbi.nlm.nih.gov/18974366/
The end-stage of COVID-19 is severe lipid peroxidation, where fats in the body start to “rust” due to
damage by oxidative stress:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768996/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357498/
https://www.liebertpub.com/doi/10.1089/ars.2021.0017
Oxidized lipids appear as foreign objects to the immune system, which recognizes and forms antibodies
against OSEs, or oxidation-specific epitopes:
https://ard.bmj.com/content/annrheumdis/early/2020/08/04/annrheumdis-2020-218145.full.pdf
https://ard.bmj.com/content/80/9/1236
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7256550/
https://www.hss.edu/conditions_top-ten-series-antiphospholipid-syndrome-coronavirus-covid-19.asp
In COVID-19, neutrophil degranulation and NETosis in the bloodstream drives severe oxidative damage;
hemoglobin becomes incapable of carrying oxygen due to heme iron being stripped out of heme by
hypochlorous acid:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757048/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7436665/
https://www.nature.com/articles/s41418-021-00805-z
https://www.sciencedirect.com/science/article/pii/S221249262030052X
SARS-CoV-2 Spike binds to ACE2. Angiotensin Converting Enzyme 2 is an enzyme that is part of the reninangiotensin-aldosterone system, or RAAS. The RAAS is a hormone control system that moderates fluid
volume and blood pressure in the body and in the bloodstream by controlling sodium/potassium
retention and excretion and vascular tone:
https://www.ncbi.nlm.nih.gov/books/NBK470410/
https://www.merckmanuals.com/home/multimedia/figure/cvs_regulating_blood_pressure_renin
This protein, ACE2, is ubiquitous in every part of the body that interfaces with the circulatory system,
particularly in vascular endothelial cells and pericytes, brain astrocytes, renal tubules and podocytes,
pancreatic islet cells, bile duct and intestinal epithelial cells, and the seminiferous ducts of the testis, all
of which SARS-CoV-2 can infect:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7167720/
https://www.frontiersin.org/articles/10.3389/fmed.2020.594495/full
https://www.frontiersin.org/articles/10.3389/fneur.2020.573095/full
SARS-CoV-2 infects a cell as follows:
https://www.nature.com/articles/s41401-020-0485-4
https://www.science.org/doi/10.1126/science.abb2507
https://www.sciencedirect.com/science/article/abs/pii/S1931312820306211
SARS-CoV-2 Spike proteins embedded in a cell can actually cause adjacent human cells to fuse together,
forming syncytia/MGCs:
https://www.nature.com/articles/s41418-021-00782-3
https://pubmed.ncbi.nlm.nih.gov/33051876/
SARS-CoV-2’s viroporins, such as its Envelope protein, act as calcium ion channels, introducing calcium
into infected cells:
https://www.nature.com/articles/s41422-021-00519-4
https://virologyj.biomedcentral.com/articles/10.1186/s12985-019-1182-0
The virus suppresses the natural interferon response, resulting in delayed inflammation:
https://www.nature.com/articles/s12276-021-00592-0
https://mdpi-res.com/d_attachment/viruses/viruses-12-01433/article_deploy/viruses-12-01433.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310780/
SARS-CoV-2 N protein can also directly activate the NLRP3 inflammasome:
https://www.nature.com/articles/s41467-021-25015-6
https://www.frontiersin.org/articles/10.3389/fimmu.2020.01021/full
SARS-CoV-2 suppresses the Nrf2 antioxidant pathway, reducing the body’s own endogenous antioxidant
enzyme activity:
https://www.nature.com/articles/s41467-020-18764-3
https://ctajournal.biomedcentral.com/articles/10.1186/s13601-020-00362-7
https://mdpi-res.com/d_attachment/ijms/ijms-22-07963/article_deploy/ijms-22-07963.pdf
The suppression of ACE2 by binding with Spike causes a buildup of bradykinin that would otherwise be
broken down by ACE2:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7834250/
https://www.the-scientist.com/news-opinion/is-a-bradykinin-storm-brewing-in-covid-19–67876
This constant calcium influx into the cells results in (or is accompanied by) noticeable hypocalcemia, or
low blood calcium:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292572/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041474/
https://www.sciencedirect.com/science/article/abs/pii/S1871402121000059
Bradykinin upregulates cAMP, cGMP, COX, and Phospholipase C activity. This results in prostaglandin
release and vastly increased intracellular calcium signaling, which promotes highly aggressive ROS
release and ATP depletion:
https://www.sciencedirect.com/science/article/abs/pii/S089158490700319X?via%3Dihub
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1218972/
https://pubmed.ncbi.nlm.nih.gov/2156053/
https://www.sciencedirect.com/topics/medicine-and-dentistry/bradykinin-b2-receptor-agonist
https://www.sciencedirect.com/topics/neuroscience/bradykinin
NADPH oxidase releases superoxide into the extracellular space:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556774/
https://www.pnas.org/content/110/21/8744
Superoxide radicals react with nitric oxide to form peroxynitrite:
https://pubmed.ncbi.nlm.nih.gov/8944624/
https://www.pnas.org/content/115/23/5839
Peroxynitrite reacts with the tetrahydrobiopterin cofactor needed by endothelial nitric oxide synthase,
destroying it and “uncoupling” the eNOS enzymes, causing nitric oxide synthase to synthesize more
superoxide instead (this means that every process that upregulates NOS activity now produces
superoxide instead of nitric oxide):
https://pubmed.ncbi.nlm.nih.gov/24353182/
https://academic.oup.com/cardiovascres/article/73/1/8/316487
https://pubs.acs.org/doi/10.1021/bi9016632
This proceeds in a positive feedback loop until nitric oxide bioavailability in the circulatory system is
depleted:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276137/
Dissolved nitric oxide gas produced constantly by eNOS serves many important functions, but it is also
antiviral against SARS-like coronaviruses, preventing the palmitoylation of the viral Spike protein and
making it harder for it to bind to host receptors:
https://journal.chestnet.org/article/S0012-3692(20)34397-X/fulltext
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111989/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754882/
The loss of NO allows the virus to begin replicating with impunity in the body (clearly, the virus has an
evolutionary incentive to induce oxidative stress to destroy nitric oxide):
https://scitechdaily.com/nitric-oxide-a-possible-treatment-for-covid-19-only-substance-to-have-adirect-effect-on-sars-cov-2/
Those with endothelial dysfunction (i.e. hypertension, diabetes, obesity, old age, African-American race)
have redox equilibrium issues to begin with, giving the virus an advantage:
https://www.nature.com/articles/s41392-020-00454-7
https://www.frontiersin.org/articles/10.3389/fphys.2020.605908/full
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430889/
https://pubmed.ncbi.nlm.nih.gov/19004510/
Due to the extreme cytokine release triggered by these processes, the body summons a great deal of
neutrophils and monocyte-derived alveolar macrophages to the lungs:
https://www.frontiersin.org/articles/10.3389/fimmu.2021.652470/full
https://www.frontiersin.org/articles/10.3389/fimmu.2021.720109/full
Phagocytic cells of the innate immune system are the first-line defenders against pathogens. They work
by engulfing invaders and trying to attack them with enzymes that produce powerful oxidants, like SOD
and MPO:
https://www.frontiersin.org/articles/10.3389/fimmu.2012.00174/full
https://jlb.onlinelibrary.wiley.com/doi/full/10.1189/jlb.0809549
Superoxide dismutase takes superoxide and makes hydrogen peroxide, and myeloperoxidase takes
hydrogen peroxide and chlorine ions and makes hypochlorous acid, which is many, many times more
reactive than sodium hypochlorite bleach:
https://www.sciencedirect.com/topics/neuroscience/superoxide-dismutase
https://www.sciencedirect.com/topics/medicine-and-dentistry/myeloperoxidase
In severe and critical COVID-19, there is actually rather severe NETosis:
https://www.frontiersin.org/articles/10.3389/fphar.2021.708302/full
https://insight.jci.org/articles/view/138999
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184981/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488868/
https://ashpublications.org/blood/article/136/10/1169/461219/Neutrophil-extracellular-trapscontribute-to
https://www.sciencedirect.com/science/article/pii/S221249262030052X
Hypochlorous acid building up in the bloodstream begins to bleach the iron out of heme and compete for
O2 binding sites. Red blood cells lose the ability to transport oxygen, causing the sufferer to turn blue in
the face:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757048/
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0120737
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863623/
Unliganded iron, hydrogen peroxide, and superoxide in the bloodstream undergo the Haber-Weiss and
Fenton reactions, producing extremely reactive hydroxyl radicals that violently strip electrons from
surrounding fats and DNA, oxidizing them severely:
https://www.sciencedirect.com/science/article/pii/S0753332221000135
https://sites.kowsarpub.com/ans/articles/60038.html
https://www.sciencedirect.com/science/article/abs/pii/S0300483X00002316?via%3Dihub
https://www.sciencedirect.com/topics/chemistry/fenton-reaction
https://www.researchgate.net/figure/Fenton-and-Haber-Weiss-reactions-are-a-source-of-oxidativestress-The-generation-of_fig1_330729897
This condition is not unknown to medical science. The actual name for all of this is acute sepsis (but
without the traditional hallmarks of sepsis, like shock):
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056356/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886971/
https://www.futuremedicine.com/doi/10.2217/fmb-2020-0312
https://www.global-sepsis-alliance.org/news/2020/4/7/update-can-covid-19-cause-sepsis-explainingthe-relationship-between-the-coronavirus-disease-and-sepsis-cvd-novel-coronavirus
We know this is happening in COVID-19 because people who have died of the disease have noticeable
ferroptosis signatures in their tissues, as well as various other oxidative stress markers such as
nitrotyrosine, 4-HNE, and malondialdehyde:
https://onlinelibrary.wiley.com/doi/full/10.1002/ehf2.12958
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264936/
https://www.sciencedirect.com/science/article/pii/S2213231721001300
https://www.researchgate.net/publication/354129433_Preliminary_Findings_on_the_Association_of_t
he_Lipid_Peroxidation_Product_4-Hydroxynonenal_with_the_Lethal_Outcome_of_Aggressive_COVID19
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180845/
https://rupress.org/jem/article-abstract/218/6/e20210518/212093/Ferroptosis-in-infectioninflammation-and?redirectedFrom=fulltext
When you intubate someone with this condition, you are setting off a free radical bomb by supplying the
cells with O2. It’s a catch-22, because we need oxygen to make Adenosine Triphosphate (that is, to live),
but O2 is also the precursor of all these damaging radicals that lead to lipid peroxidation:
https://www.nature.com/articles/pr2009174
The correct treatment for severe COVID-19 related sepsis is non-invasive ventilation, steroids, and
antioxidant infusions:
https://covid19criticalcare.com/covid-19-protocols/math-plus-protocol/
https://journals.lww.com/ccmjournal/Abstract/2007/09001/Antioxidant_supplementation_in_sepsis_a
nd_systemic.25.aspx
https://mdpi-res.com/d_attachment/medicina/medicina-56-00619/article_deploy/medicina-56-00619-
v2.pdf
Most of the drugs repurposed for COVID-19 that show any benefit whatsoever in rescuing critically-ill
COVID-19 patients are antioxidants. N-acetylcysteine, melatonin, fluvoxamine, budesonide, famotidine,
cimetidine, and ranitidine are all antioxidants:
https://www.hindawi.com/journals/omcl/2018/6581970/
https://www.intechopen.com/chapters/62672
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708076/
https://www.karger.com/Article/Abstract/88623
https://www.sciencedirect.com/science/article/abs/pii/000629529390218L?via%3Dihub
Indomethacin prevents iron-driven oxidation of arachidonic acid to isoprostanes:
https://www.sciencedirect.com/science/article/abs/pii/0161463079900442
There are powerful antioxidants such as apocynin that have not even been tested on COVID-19 patients
yet which could defang neutrophils, prevent lipid peroxidation, restore endothelial health, and restore
oxygenation to the tissues:
https://link.springer.com/article/10.1007/s10787-020-00715-5
Scientists who know anything about pulmonary neutrophilia, ARDS, and redox biology have known or
surmised much of this since March 2020:
https://www.researchgate.net/post/NADPH_oxidase_Covid-19_Oxygen_treatment
In April 2020, Swiss scientists confirmed that COVID-19 was a systemic vascular endotheliitis:
https://www.usz.ch/en/covid-19-also-a-systemic-endotheliitis/
By late 2020, experts had already concluded that COVID-19 causes a form of viral sepsis:
https://www.healthleadersmedia.com/clinical-care/expert-severe-covid-19-illness-viral-sepsis
They also know that sepsis can be effectively treated with antioxidants:
https://jtd.amegroups.com/article/view/34870/html
https://www.evms.edu/about_evms/administrative_offices/marketing_communications/publications/is
sue_9_4/has-sepsis-met-its-match.php
None of this information is particularly new, and yet, for the most part, it has not been acted upon.
Doctors continue to use damaging intubation techniques with high PEEP settings despite high lung
compliance and poor oxygenation, killing an untold number of critically ill patients with medical
malpractice:
https://ccforum.biomedcentral.com/articles/10.1186/s13054-020-03049-4
https://jamanetwork.com/journals/jama/fullarticle/2765302
Because of the way they are constructed, Randomized Control Trials will never show any benefit for any
antiviral against COVID-19. Not Remdesivir, not Kaletra, not HCQ, and not Ivermectin. The reason for this
is simple; for the patients that they have enrolled in these studies, such as Oxford’s ludicrous RECOVERY
study, the intervention is too late to have any positive effect (i.e. these RCTs are designed in such a way
that the use of antivirals is futile, therefore, these studies are deceptive and unethical by their very
nature):
https://www.mdpi.com/1999-4915/13/6/963/htm
The clinical course of COVID-19 is such that by the time most people seek medical attention for hypoxia,
their viral load has already tapered off to almost nothing. If someone is about 10 days post-exposure and
has already been symptomatic for five days, there is hardly any virus left in their bodies, only cellular
damage and derangement that has initiated a hyperinflammatory response:
https://www.the-hospitalist.org/hospitalist/article/234869/coronavirus-updates/state-inpatient-covid19-care
https://www.sciencedirect.com/science/article/pii/S0753332220306867
It is from this group that the clinical trials for antivirals have recruited, pretty much exclusively (i.e. they
do not test prophylaxis/early treatment, only changes to the mean duration of hospitalization for those
already hospitalized):
https://www.nejm.org/doi/full/10.1056/nejmoa2023184
https://www.nejm.org/doi/full/10.1056/NEJMoa2022926
https://pubmed.ncbi.nlm.nih.gov/34318930/
India went against the instructions of the WHO and mandated the prophylactic usage of Ivermectin. They
have almost completely eradicated COVID-19:
https://ivmmeta.com
The Indian Bar Association of Mumbai has brought criminal charges against WHO Chief Scientist Dr.
Soumya Swaminathan for recommending against the use of Ivermectin:
https://indianbarassociation.in/wp-content/uploads/2021/05/IBA-PRESS-RELEASE-MAY-26-2021.pdf
Ivermectin is not “horse dewormer”. Yes, it is sold in veterinary paste form as a dewormer for animals. It
has also been available in pill form for humans for decades, as an antiparasitic drug:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043740/
The media have disingenuously claimed that because Ivermectin is an antiparasitic drug, it has no utility
as an antivirus. This is incorrect. Ivermectin has utility as an antiviral. It blocks importin, preventing
nuclear import, effectively inhibiting viral access to cell nuclei. Many drugs currently on the market have
multiple modes of action. Ivermectin is one such drug. It is both antiparasitic and antiviral:
https://www.sciencedirect.com/science/article/abs/pii/S0166354219307211?via%3Dihub
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539925/
In Bangladesh, Ivermectin costs $1.80 for an entire 5-day course:
https://journals.lww.com/americantherapeutics/fulltext/2021/08000/ivermectin_for_prevention_and_t
reatment_of.7.aspx
Remdesivir, which is toxic to the liver, costs $3,120 for a 5-day course of the drug:
https://www.npr.org/sections/health-shots/2020/06/29/884648842/remdesivir-priced-at-more-than-3-
100-for-a-course-of-treatment
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386240/
Billions of dollars of utterly useless Remdesivir were sold to our governments on the taxpayer’s dime, and
it ended up being totally useless for treating hyperinflammatory COVID-19:
https://www.fiercepharma.com/pharma/gilead-s-1-5b-remdesivir-sales-help-buoy-greater-thanexpected-declines-for-mainstay-hiv
https://www.forbes.com/sites/jvchamary/2021/01/31/remdesivir-covidcoronavirus/?sh=7e6034e666c2
COVID-19 is airborne. The WHO carried water for China by claiming that the virus was only dropletborne. Our own CDC absurdly claimed that it was mostly transmitted by fomite-to-face contact, which,
given its rapid spread from Wuhan to the rest of the world, would have been physically impossible:
https://www.thelancet.com/article/S0140-6736(21)00869-2/fulltext
https://www.pennmedicine.org/updates/blogs/penn-physician-blog/2020/august/airborne-dropletdebate-article
The ridiculous belief in fomite-to-face being a primary mode of transmission led to the use of surface
disinfection protocols that wasted time, energy, productivity, and disinfectant:
https://www.nature.com/articles/d41586-021-00251-4
The 6-foot guidelines are absolutely useless. The minimum safe distance to protect oneself from an
aerosolized virus is to be 15+ feet away from an infected person, no closer. Realistically, no public transit
is safe:
https://www.medrxiv.org/content/10.1101/2020.08.03.20167395v1
https://khn.org/news/fact-check-airborne-transmission-coronavirus-science-behind-aerosol-spread/
Surgical masks do not protect you from aerosols. The virus is too small and the filter media has too large
of gaps to filter it out. They may catch respiratory droplets and keep the virus from being expelled by
someone who is sick, but they do not filter a cloud of infectious aerosols if someone were to walk into
said cloud:
https://ajicjournal.org/retrieve/pii/S0196655305801439
The minimum level of protection against this virus is quite literally a P100 respirator, a PAPR/CAPR, or a
40mm NATO CBRN respirator, ideally paired with a full-body tyvek or tychem suit, gloves, and booties,
with all the holes and gaps taped (in a pinch, surgical masks can be modified or worn a specific way to
increase filtration):
https://www.epa.gov/sciencematters/epa-researchers-test-effectiveness-face-masks-disinfectionmethods-against-covid-19
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409952/
Live SARS-CoV-2 may potentially be detected in sewage outflows, and there may be oral-fecal
transmission:
https://www.sciencedirect.com/science/article/pii/S0048969720325936
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0249568
https://www.nature.com/articles/s41587-020-0684-z
During the SARS outbreak in 2003, in the Amoy Gardens incident, hundreds of people were infected by
aerosolized fecal matter rising from floor drains in their apartments (there is some valid concern that
COVID-19 may also spread the same way, given its similarities to SARS):
https://pubmed.ncbi.nlm.nih.gov/16696450/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC539564/
https://www.neha.org/sites/default/files/jeh/JEH5.06-Feature-Environmental-Transmission-of-SARS.pdf
https://www.cleanlink.com/news/article/COVID-19-Could-Spread-Through-Dry-Floor-Drains–25600
The vaccines for COVID-19 are not sterilizing and do not prevent infection or transmission. They are
“leaky” vaccines. This means they remove the evolutionary pressure on the virus to become less lethal. It
also means that the vaccinated are perfect carriers. In other words, those who are vaccinated are a
threat to the unvaccinated, not the other way around:
https://www.healthline.com/health-news/leaky-vaccines-can-produce-stronger-versions-of-viruses072715
https://www.realclearscience.com/articles/2021/08/23/lets_stop_pretending_about_the_covid19_vaccines_791050.html
https://www.cdc.gov/media/releases/2021/s0730-mmwr-covid-19.html
https://www.businessinsider.com/cdc-fully-vaccinated-new-guidelines-wear-masks-indoors-delta-2021-
7?utm_source=yahoo.com&utm_medium=referral
All of the COVID-19 vaccines currently in use have undergone minimal testing, with highly accelerated
clinical trials. Though they appear to limit severe illness, the long-term safety profile of these vaccines
remains unknown:
https://www.jdsupra.com/legalnews/accelerated-covid-19-vaccine-clinical-95853/
https://www.nebraskamed.com/COVID/were-the-covid-19-vaccines-rushed
Some of these so-called “vaccines” utilize an untested new technology that has never been used in
vaccines before. Traditional vaccines use weakened or killed virus to stimulate an immune response. The
Moderna and Pfizer-BioNTech vaccines do not. They are purported to consist of an intramuscular shot
containing a suspension of lipid nanoparticles filled with messenger RNA:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439223/
https://cen.acs.org/pharmaceuticals/drug-delivery/Without-lipid-shells-mRNA-vaccines/99/i8
https://www.cdc.gov/coronavirus/2019-ncov/vaccines/different-vaccines/mrna.html
https://medlineplus.gov/genetics/understanding/therapy/mrnavaccines/
The way they generate an immune response is by fusing with cells in a vaccine recipient’s shoulder,
undergoing endocytosis, releasing their mRNA cargo into those cells, and then utilizing the ribosomes in
those cells to synthesize modified SARS-CoV-2 Spike proteins in-situ:
https://www.nature.com/articles/s41586-020-2622-0
https://coronavirus.dc.gov/sites/default/files/dc/sites/coronavirus/page_content/attachments/Cartoon
%20Explainer%20How%20the%20Moderna%20and%20Pfizer%20Vaccines%20Work.pdf
These vaccines were produced or validated with the aid of fetal cell lines HEK-293 and PER.C6, which
people with certain religious convictions may object strongly to:
https://www.health.nd.gov/sites/www/files/documents/COVID%20Vaccine%20Page/COVID19_Vaccine_Fetal_Cell_Handout.pdf
SARS-CoV-2 Spike is a highly pathogenic protein on its own. It is impossible to overstate the danger
presented by introducing this protein into the human body:
https://mcusercontent.com/22e41db63deaf4a84be439c0f/files/6a33980b-683f-4ee4-67d4-
cc98dc7fcd37/20210601_Guide_to_COVID_19_vaccines_for_parents.pdf
https://rightsfreedoms.wordpress.com/2021/06/16/researcher-we-made-a-big-mistake-on-covid-19-
vaccine/
It is claimed by vaccine manufacturers that the vaccine remains in cells in the shoulder, and that SARSCoV-2 Spike produced and expressed by these cells from the vaccine’s genetic material is harmless and
inert, thanks to the insertion of prolines in the Spike sequence to stabilize it in the prefusion
conformation, preventing the Spike from becoming active and fusing with other cells:
https://www.nature.com/articles/s41467-020-20321-x
https://cen.acs.org/pharmaceuticals/vaccines/tiny-tweak-behind-COVID-19/98/i38
However, a pharmacokinetic study from Japan showed that the lipid nanoparticles and mRNA from the
Pfizer vaccine did not stay in the shoulder, and in fact bioaccumulated in many different organs,
including the reproductive organs and adrenal glands, meaning that modified Spike is being expressed
quite literally all over the place:
https://files.catbox.moe/0vwcmj.pdf
These lipid nanoparticles may trigger anaphylaxis in an unlucky few:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8441754/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862013/
Messenger RNA is normally consumed right after it is produced in the body, being translated into a
protein by a ribosome. COVID-19 vaccine mRNA is produced outside the body, long before a ribosome
translates it. In the meantime, it could accumulate damage if inadequately preserved. When a ribosome
attempts to translate a damaged strand of mRNA, it can become stalled:
https://elifesciences.org/articles/61984
https://www.frontiersin.org/articles/10.3389/fgene.2018.00431/full
Certain proteins, including SARS-CoV-2 Spike, have proteolytic cleavage sites that are basically like little
dotted lines that say “cut here”, which attract a living organism’s own proteases (essentially, molecular
scissors) to cut them. There is a possibility that S1 may be proteolytically cleaved from S2, causing active
S1 to float away into the bloodstream while leaving the S2 “stalk” embedded in the membrane of the cell
that expressed the protein:
https://academic.oup.com/cid/advance-article/doi/10.1093/cid/ciab465/6279075
https://www.nature.com/articles/s41564-021-00908-w
https://www.life-science-alliance.org/content/3/9/e202000786
SARS-CoV-2 Spike has a Superantigenic region (SAg), which may promote extreme inflammation:
https://www.pnas.org/content/117/41/25254
https://www.nature.com/articles/s41577-021-00502-5
Anti-Spike antibodies were found in one study to function as autoantibodies and attack the body’s own
cells:
https://www.researchsquare.com/article/rs-612103/v2
Those who have been immunized with COVID-19 vaccines have developed blood clots, myocarditis,
Guillain-Barre Syndrome, Bell’s Palsy, and multiple sclerosis flares, indicating that the vaccine promotes
autoimmune reactions against healthy tissue:
https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-july-13-2021
https://www.medpagetoday.com/infectiousdisease/covid19vaccine/94061?xid=nl_mpt_DHE_2021-08-
17
SARS-CoV-2 Spike does not only bind to ACE2. It was suspected to have regions that bind to basigin,
integrins, neuropilin-1, and bacterial lipopolysaccharides as well:
https://www.nature.com/articles/s41564-021-00958-0
https://www.mdpi.com/1422-0067/22/3/992/pdf
https://pubs.acs.org/doi/10.1021/acschemneuro.0c00619
https://www.science.org/doi/full/10.1126/science.abd3072
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0253347
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7799037/
SARS-CoV-2 Spike, on its own, can potentially bind any of these things and act as a ligand for them,
triggering unspecified and likely highly inflammatory cellular activity:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827936/
SARS-CoV-2 Spike contains an unusual PRRA insert that forms a furin cleavage site. Furin is a ubiquitous
human protease, making this an ideal property for the Spike to have, giving it a high degree of cell
tropism. No wild-type SARS-like coronaviruses related to SARS-CoV-2 possess this feature, making it
highly suspicious, and perhaps a sign of human tampering:
https://journals.asm.org/doi/full/10.1128/JVI.01751-20
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457603/
https://yurideigin.medium.com/lab-made-cov2-genealogy-through-the-lens-of-gain-of-functionresearch-f96dd7413748
SARS-CoV-2 Spike has a prion-like domain that enhances its infectiousness:
https://www.preprints.org/manuscript/202003.0422/v1
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0023664
The Spike S1 RBD may bind to heparin-binding proteins and promote amyloid aggregation. In humans,
this could lead to Parkinson’s, Lewy Body Dementia, premature Alzheimer’s, or various other
neurodegenerative diseases:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988450/
This is very concerning because SARS-CoV-2 S1 is capable of penetrating the blood-brain barrier and
entering the brain. It is capable of increasing the permeability of the blood-brain barrier to itself and
other molecules by injuring and disrupting it directly:
https://www.nature.com/articles/s41593-020-00771-8
https://www.nature.com/articles/s41392-021-00719-9
https://pubmed.ncbi.nlm.nih.gov/33053430/
SARS-CoV-2, like other betacoronaviruses, may have Dengue-like ADE, or antibody-dependent
enhancement of disease:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943455/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7454712/
https://www.journalofinfection.com/article/S0163-4453(21)00392-3/fulltext
https://sharylattkisson.com/2021/08/study-why-so-many-vaccinated-people-are-getting-sick/
https://www.nature.com/articles/s41564-020-00789-5
https://www.sciencedirect.com/science/article/pii/S1201971220307311
https://pubmed.ncbi.nlm.nih.gov/31826992/
https://www.biorxiv.org/content/10.1101/2021.08.22.457114v1
There is something called Original Antigenic Sin, which is the observation that the body prefers to
produce antibodies based on previously-encountered strains of a virus over newly-encountered ones:
https://www.jimmunol.org/content/202/2/335
https://en.wikipedia.org/wiki/Original_antigenic_sin
In ADE, antibodies from a previous infection become non-neutralizing due to mutations in the virus’s
proteins. These non-neutralizing antibodies then act as trojan horses, allowing live, active virus to be
pulled into macrophages through their Fc receptor pathways:
https://en.wikipedia.org/wiki/Antibody-dependent_enhancement
https://www.cdc.gov/dengue/training/cme/ccm/page57857.html
It is possible for vaccines to sensitize someone to disease. There is a precedent for this in recent history.
Sanofi’s Dengvaxia vaccine for Dengue failed because it caused immune sensitization in people whose
immune systems were Dengue-naïve:
https://www.frontiersin.org/articles/10.3389/fcimb.2020.572681/full
https://news.unchealthcare.org/2021/06/scientists-discover-how-dengue-vaccine-fails-to-protectagainst-disease/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739535/
https://www.scientificamerican.com/article/how-the-worlds-first-dengue-vaccination-drive-ended-indisaster/
In mice immunized against SARS-CoV and challenged with the virus, a close relative of SARS-CoV-2, they
developed immune sensitization, Th2 immunopathology, and eosinophil infiltration in their lungs:
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0035421
We have been told that SARS-CoV-2 mRNA vaccines cannot be integrated into the human genome,
because messenger RNA cannot be turned back into DNA. This is false. There are elements in human cells
called LINE-1 retrotransposons, which can indeed integrate mRNA into a human genome by endogenous
reverse transcription:
https://pubmed.ncbi.nlm.nih.gov/33330870/
https://rightsfreedoms.wordpress.com/2021/08/13/mit-harvard-study-suggests-mrna-vaccine-mightpermanently-alter-dna-after-all/
The vaccine and the virus were made by the same people. In 2014, there was a moratorium on SARS
gain-of-function research that lasted until 2017:
https://www.phe.gov/s3/dualuse/documents/gain-of-function.pdf
https://www.scientificamerican.com/article/u-s-lifts-moratorium-on-funding-controversial-high-riskvirus-research/
https://www.nih.gov/about-nih/who-we-are/nih-director/statements/nih-lifts-funding-pause-gainfunction-research
Ralph Baric is a virologist and SARS expert at UNC Chapel Hill in North Carolina. This is who Anthony
Fauci was referring to when he insisted, before Congress, that if any gain-of-function research was being
conducted, it was being conducted in North Carolina:
Ralph Baric: On the Front Lines of Coronavirus for Three Decades
Ralph Baric and Shi Zhengli are colleagues and have co-written papers together:
https://www.nature.com/articles/nm.3985/
Ralph Baric mentored Shi Zhengli in his gain-of-function manipulation techniques, particularly serial
passage, which results in a virus that appears as if it originated naturally. In other words, deniable
bioweapons. Serial passage in humanized hACE2 mice may have produced something like SARS-CoV-2:
https://www.technologyreview.com/2021/06/29/1027290/gain-of-function-risky-bat-virus-engineeringlinks-america-to-wuhan/
https://usrtk.org/biohazards-blog/ralph-baric-emails/
https://www.paul.senate.gov/newsweek-op-ed-congress-must-pursue-answers-about-origin-covid-19
https://nymag.com/intelligencer/article/coronavirus-lab-escape-theory.html
The funding for the gain-of-function research being conducted at the Wuhan Institute of Virology came
from Peter Daszak. Peter Daszak runs an NGO called EcoHealth Alliance:
https://peterdaszak.com/
https://peterdaszak.com/interceptdocs.pdf
NIH Documents Provide New Evidence U.S. Funded Gain-of-Function Research in Wuhan
https://nationalfile.com/bombshell-fauci-kept-funding-peter-daszaks-wuhan-gain-of-functionexperiments-with-7-5-million-after-trump-canceled-grant/
EcoHealth Alliance received millions of dollars in grant money from the National Institutes of
Health/National Institute of Allergy and Infectious Diseases (that is, Anthony Fauci), the Defense Threat
Reduction Agency (part of the US Department of Defense), and the United States Agency for
International Development. NIH/NIAID contributed a few million dollars, and DTRA and USAID each
contributed tens of millions of dollars towards this research. Altogether, it was over a hundred million
dollars:
https://www.independentsciencenews.org/wp-content/uploads/2020/12/EcoHealth-Funding-as-of01_10_2020-Fed.-Grants-Contracts.pdf
EcoHealth Alliance subcontracted these grants to the Wuhan Institute of Virology, a lab in China with a
very questionable safety record and poorly-trained staff, so that they could conduct gain-of-function
research:
https://www.algora.com/Algora_blog/2021/09/22/ecohealth-alliance-darpa-toyed-with-infecting-wildchinese-bats-with-covid-leaked-docs-allege
https://nypost.com/2021/07/01/pentagon-gave-millions-to-ecohealth-alliance-for-wuhan-lab/
https://www.judicialwatch.org/press-releases/wuhan-lab-fauci-grants/
https://scholar.harvard.edu/files/kleelerner/files/20200414_wapo_-
_state_department_cables_warned_of_safety_issues_at_wuhan_lab_studying_bat_coronaviruses_-
_the_washington_post.pdf
https://www.businessinsider.com/us-officials-raised-alarms-about-safety-issues-in-wuhan-lab-report2020-4?op=1
Chinese scientists in Wuhan reported being routinely bitten and urinated on by laboratory animals:
https://img-prod.tgcom24.mediaset.it/images/2020/02/16/114720192-5eb8307f-017c-4075-a697-
348628da0204.pdf
https://web.archive.org/web/20200214144447/https:/www.researchgate.net/publication/339070128_
The_possible_origins_of_2019-nCoV_coronavirus
In November of 2019, three technicians at the Wuhan Institute of Virology developed symptoms
consistent with a flu-like illness:
https://www.webmd.com/lung/news/20210524/wuhan-lab-researchers-illness
https://thehill.com/policy/healthcare/556815-fauci-calls-on-china-to-release-medical-records-ofwuhan-researchers
December 12th, 2019, Ralph Baric signed a Material Transfer Agreement (essentially, an NDA) to receive
Coronavirus mRNA vaccine-related materials co-owned by Moderna and NIH:
https://rightsfreedoms.wordpress.com/2021/06/26/confidential-documents-reveal-moderna-sentmrna-coronavirus-vaccine-candidate-to-university-researchers-weeks-before-emergence-of-covid-19/
https://s3.documentcloud.org/documents/6935295/NIH-Moderna-Confidential-Agreements.pdf
It wasn’t until a whole month later, on January 11th, 2020, that China allegedly sent us the sequence to
what would become known as SARS-CoV-2:
https://www.cidrap.umn.edu/news-perspective/2020/01/china-releases-genetic-data-new-coronavirusnow-deadly
https://www.sciencedaily.com/releases/2020/01/200131114748.htm
Moderna claims, rather absurdly, that they developed a working vaccine from this sequence in under 48
hours:
https://www.businessinsider.com/moderna-designed-coronavirus-vaccine-in-2-days-2020-11
https://globalnews.ca/news/7492076/moderna-coronavirus-vaccine-technology-how-it-works/
https://nymag.com/intelligencer/2020/12/moderna-covid-19-vaccine-design.html
Stéphane Bancel, the current CEO of Moderna, was formerly the CEO of bioMérieux, a French
multinational corporation specializing in medical diagnostic tech, founded by one Alain Mérieux:
https://www.biomerieux.com/en/board-directors-biomerieux-chaired-alain-merieux-has-appointedstephane-bancel-directeur-general
https://en.wikipedia.org/wiki/St%C3%A9phane_Bancel
https://www.himss.org/global-conference/speaker-stephane-bancel
Alain Mérieux was one of the individuals who was instrumental in the construction of the Wuhan
Institute of Virology’s P4 lab:
https://www.fondation-merieux.org/en/news/alain-merieux-receives-the-prestigious-chinese-reformfriendship-award/
https://medicalxpress.com/news/2020-04-wuhan-lab-core-virus-controversy.html
http://english.whiov.cas.cn/ne/201712/t20171212_187624.html
https://web.archive.org/web/20210921133410/http://english.whiov.cas.cn/ne/201712/t20171212_187
624.html
The sequence given as the closest relative to SARS-CoV-2, RaTG13, is not a real virus. It is a forgery:
https://nerdhaspower.weebly.com/ratg13-is-fake.html
https://gnews.org/192144/
https://www.peakprosperity.com/forum-topic/scientific-history-of-ratg13/
The animal reservoir of SARS-CoV-2 has never been found:
https://www.technologyreview.com/2021/03/26/1021263/bat-covid-coronavirus-cause-origin-wuhan/
https://www.who.int/news-room/feature-stories/detail/how-who-is-working-to-track-down-theanimal-reservoir-of-the-sars-cov-2-virus
The FBI raided Allure Medical in Shelby Township north of Detroit for billing insurance for “fraudulent
COVID-19 cures”. The treatment they were using? Intravenous Vitamin C. An antioxidant. Which, as
described above, is an entirely valid treatment for COVID-19-induced sepsis, and indeed, is now part of
the MATH+ protocol advanced by Dr. Paul E. Marik:
https://www.freep.com/story/news/local/michigan/macomb/2020/04/28/allure-medical-spa-shelbycovid-vitamin-c/3038801001/
https://www.detroitnews.com/story/news/local/macomb-county/2020/05/15/doctor-got-loan-whilepeddling-phony-covid-19-cure-feds-say/5197315002/
https://covid19criticalcare.com/covid-19-protocols/math-plus-protocol/
https://covid19criticalcare.com/wp-content/uploads/2021/01/FLCCC-Alliance-MATHplus-ProtocolENGLISH.pdf
https://pubmed.ncbi.nlm.nih.gov/31978969/
https://www.sciencedirect.com/science/article/abs/pii/S0883944119316107?via%3Dihub
https://www.npr.org/sections/health-shots/2019/10/01/766029397/mixed-results-for-a-test-ofvitamin-c-for-sepsis
https://www.nutraingredients.com/Article/2020/01/28/Ethically-and-morally-unacceptable-Reactionto-vitamin-C-for-sepsis-trial
The FDA banned ranitidine (Zantac) due to supposed NDMA (N-nitrosodimethylamine) contamination:
https://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-ndmazantac-ranitidine
https://www.raps.org/news-and-articles/news-articles/2021/6/fda-studies-no-post-ingestion-ndmafrom-ranitidine
Ranitidine is not only an H2 blocker used as antacid, but also has a powerful antioxidant effect,
scavenging hydroxyl radicals. This gives it utility in treating COVID-19:
https://onlinelibrary.wiley.com/doi/10.1111/j.1472-8206.2009.00810.x
https://www.sciencedirect.com/science/article/pii/S1347861319342203
The FDA also attempted to take N-acetylcysteine, a harmless amino acid supplement and antioxidant, off
the shelves, compelling Amazon to remove it from their online storefront:
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warningletters/les-labs-593764-07232020
https://www.naturalproductsinsider.com/regulatory/us-senator-npa-press-fda-nac-supplements
https://www.nutraingredients-usa.com/Article/2021/05/11/CRN-This-is-not-the-final-word-on-NAC
https://www.naturalproductsinsider.com/regulatory/amazon-confirms-plans-removing-nacsupplements
On June 9th, 2020, Charles Lieber, a Harvard nanotechnology researcher with decades of experience, was
indicted by the DOJ for fraud:
https://www.justice.gov/opa/pr/harvard-university-professor-and-two-chinese-nationals-chargedthree-separate-china-related
Charles Lieber received millions of dollars in grant money from the US Department of Defense,
specifically the military think tanks DARPA, AFOSR, and ONR, as well as NIH and MITRE:
http://cml.harvard.edu/resources/research-sponsors
His specialty is the use of silicon nanowires in lieu of patch clamp electrodes to monitor and modulate
intracellular activity, something he has been working on at Harvard for the past twenty years:
https://www.harvardmagazine.com/2011/01/virus-sized-transistors
He was claimed to have been working on silicon nanowire batteries in China, but none of his colleagues
can recall him ever having worked on battery technology in his life; all of his research deals with
bionanotechnology, or the blending of nanotech with living cells:
https://www.science.org/news/2020/02/why-did-chinese-university-hire-charles-lieber-do-batteryresearch
https://news.harvard.edu/gazette/story/2019/07/harvard-researchers-present-nanowire-devicesupdate/
The indictment was over his collaboration with the Wuhan University of Technology. He had doubledipped, against the terms of his DOD grants, and taken money from the PRC’s Thousand Talents plan, a
program which the Chinese government uses to bribe Western scientists into sharing proprietary R&D
information that can be exploited by the PLA for strategic advantage (this risk has been known for a very
long time):
https://www.justice.gov/usao-ma/pr/harvard-university-professor-indicted-false-statement-charges
https://www.nytimes.com/2020/02/06/us/chinas-lavish-funds-lured-us-scientists-what-did-it-get-inreturn.html
https://www.nature.com/articles/d41586-020-00291-2
https://www.hsgac.senate.gov/imo/media/doc/2019-11-18%20PSI%20Staff%20Report%20-
%20China’s%20Talent%20Recruitment%20Plans.pdf
https://www.research.psu.edu/sites/default/files/FBI_Risks_To_Academia.pdf
https://www.chinacenter.net/2020/china_currents/19-3/scholars-or-spies-u-s-china-tension-inacademic-collaboration/
https://www.drdavidzweig.com/wp-content/uploads/2020/05/Zweig-Kang-TTP.pdf
Charles Lieber’s own papers describe the use of silicon nanowires for brain-computer interfaces, or
“neural lace” technology. His papers describe how neurons can endocytose whole silicon nanowires or
parts of them, monitoring and even modulating neuronal activity:
http://cml.harvard.edu/assets/Nanowire-probes-could-drive-high-resolution-brain-machineinterfaces.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531316/
https://spectrum.ieee.org/human-cells-eat-nanowires
Charles Lieber was a colleague of Robert Langer. Together, along with Daniel S. Kohane, they worked on
a paper describing artificial tissue scaffolds that could be implanted in a human heart to monitor its
activity remotely:
https://cml.harvard.edu/assets/Cyborg-tissues_-Merging-engineered-human-tissues-with-biocompatible-nanoscale-wires.pdf
Robert Langer, an MIT alumnus and expert in nanotech drug delivery, is one of the co-founders of
Moderna:
https://www.modernatx.com/modernas-board-directors
His net worth is now $5.1 billion USD thanks to Moderna’s mRNA-1273 vaccine sales:
https://www.forbes.com/sites/giacomotognini/2020/11/12/mit-scientist-bob-langer-becomes-abillionaire-thanks-to-moderna-stock-rally/?sh=41c3819a3a90
Both Charles Lieber and Robert Langer’s bibliographies describe, essentially, techniques for human
enhancement, i.e. transhumanism:
http://cml.harvard.edu/
Klaus Schwab, the founder of the World Economic Forum and the architect behind the so-called “Great
Reset”, has long spoken of the “blending of biology and machinery” in his books:
https://invesbrain.com/klaus-schwab-great-reset-will-lead-to-fusion-of-our-physical-digital-biologicalidentity/
https://www.penguinrandomhouse.com/books/598250/shaping-the-future-of-the-fourth-industrialrevolution-by-klaus-schwab-founder-and-executive-chairman-world-economic-forum-with-nicholasdavis/
Since these revelations, it has come to the attention of independent researchers that the COVID-19
vaccines (and even some surgical masks) may contain reduced graphene oxide nanoparticles:
https://ambassadorlove.wordpress.com/2021/08/09/confirmed-graphene-oxide-main-ingredient-incovid-shots/
https://www.orwell.city/2021/06/vaccination-vial-analysis-explained.html
https://www.nature.com/articles/s41428-020-0350-9
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141029/
https://www.cbc.ca/news/canada/montreal/masks-early-pulmonary-toxicity-quebec-schools-daycares1.5966387
https://humansarefree.com/2021/04/bombshell-disposable-blue-face-masks-found-to-contain-toxicasbestos-like-substance-that-destroys-lungs.html
Japanese researchers have also found unexplained contaminants in COVID-19 vaccines:
https://www.nbcnews.com/news/world/japan-suspends-1-6m-doses-moderna-shot-aftercontamination-reports-n1277669
https://www.fiercepharma.com/pharma/contaminant-moderna-covid-19-vaccine-vials-found-japanwas-metallic-particles-report
https://www.theburningplatform.com/2021/08/27/japan-suspects-contaminant-in-moderna-vaccinesis-metallic-reacts-to-magnets/
Graphene oxide is an anxiolytic. It has been shown to reduce the anxiety of laboratory mice when
injected into their brains:
https://www.sciencedirect.com/science/article/pii/S0142961221001058
https://graphene-flagship.eu/graphene/news/soothing-the-symptoms-of-anxiety-with-graphene-oxide/
Indeed, given SARS-CoV-2 Spike’s propensity to compromise the blood-brain barrier and increase its
permeability, it is the perfect protein for preparing brain tissue for extravasation of nanoparticles from
the bloodstream and into the brain:
https://www.templehealth.org/about/news/sars-cov-2-spike-proteins-disrupt-the-blood-brain-barrierpotentially-raising-risk-of-neurological-damage-in-covid-19-patients
https://www.croiconference.org/abstract/neuromodulatory-effects-of-sars-cov-2-on-the-blood-brainbarrier/
https://www.nature.com/articles/s41598-020-75253-
9?utm_source=xmol&utm_medium=affiliate&utm_content=meta&utm_campaign=DDCN_1_GL01_met
adata_scirep
https://pubs.acs.org/doi/10.1021/acsanm.8b02056
https://www.sciencedirect.com/science/article/pii/S0168365916303236
Graphene is also highly conductive and, in some circumstances, paramagnetic:
https://www.livescience.com/graphene-hides-rare-magnetism.html
https://www.sciencedirect.com/science/article/pii/S0008622319305809
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474003/
https://www.naturalnews.com/2021-07-19-graphene-based-neuromodulation-technology-is-realinbrain-neuroelectronics.html
BRAIN is an acronym for Brain Research Through Advancing Innovative Neurotechnologies®. This
program involves the development of brain-computer interface technologies for the military, particularly
non-invasive, injectable systems that cause minimal damage to brain tissue when removed:
https://www.darpa.mil/program/our-research/darpa-and-the-brain-initiative
Various methods have been proposed for achieving this, including optogenetics, magnetogenetics,
ultrasound, implanted electrodes, and transcranial electromagnetic stimulation. In all instances, the goal
is to obtain read or read-write capability over neurons:
https://www.darpa.mil/news-events/2019-05-20
Wireless brain-computer interfaces may interact with current or future wireless GSM infrastructure,
creating neurological data security concerns:
https://neuralink.com/
https://www.frontiersin.org/articles/10.3389/fnins.2019.00112/full
https://www.intechopen.com/chapters/44252
https://www.brown.edu/news/2021-03-31/braingate-wireless
https://www.psychologytoday.com/us/blog/the-future-brain/202107/ai-and-vr-transform-thoughtsaction-wireless-bci
A BCI that is capable of altering the contents of one’s mind would theoretically be capable of altering
mood and personality, or perhaps even subjugating someone’s very will, rendering them utterly obedient
to authority:
https://link.springer.com/article/10.1007/s11023-012-9298-7
Mind reading and brain computer interface technology: the future is coming, fast
BCIs could be used to unscrupulously alter perceptions of basic things such as emotions and values,
changing people’s thresholds of satiety, happiness, anger, disgust, and so forth:
http://www.buffalo.edu/news/releases/2010/07/11518.html
Brain-machine interfaces may be used to study and regulate mood
https://www.nature.com/articles/s41593-019-0488-y
For the wealthy, neural laces would be an unequaled boon, giving them the opportunity to enhance their
intelligence with neuroprosthetics (i.e. an “exocortex”):
https://www.adforum.com/agency/6664937/press-releases/70226/opinion-the-last-humans-and-thenext-brands
https://ieeexplore.ieee.org/document/6893912
The people who rule over us are Dark Triad types who cannot be trusted with such power:
https://www.egonzehnder.com/de/insight/can-dark-triad-leaders-be-a-good-choice-for-a-leadershipposition
https://www.sakkyndig.com/psykologi/artvit/babiak2010.pdf
https://www.theatlantic.com/health/archive/2012/07/the-startling-accuracy-of-referring-to-politiciansas-psychopaths/260517/
https://medium.com/world-issues-politics-economics-and-more/the-rise-of-the-psychopath-andsociopath-to-political-power-b67ef9073477
https://fortune.com/2021/06/06/corporate-psychopaths-business-leadership-csr/
https://www.washingtonpost.com/news/on-small-business/wp/2016/09/16/gene-marks-21-percent-ofceos-are-psychopaths-only-21-percent/
https://www.forbes.com/sites/jackmccullough/2019/12/09/the-psychopathic-ceo/
https://en.wikipedia.org/wiki/Psychopathy_in_the_workplace