April 2022: Ok, I’ll bite… I don’t normally jump on anything until it’s grown some legs, but that’s probably why it took me over a year to figure out the fact-checkers/media-lockstep, and why I wasted the first year in scientific journal publications trying to understand “SARS-CoV-2” and how the vaccines worked.
Recently, the documentary “Watch the Water” featuring Dr Bryan Ardis hypothesizes that COVID or a new bioweapon created by gain-of-function research with “snake venom” peptides tied to a virus, could be what we are dealing with.
Normally I’d wait for more evidence before something gets my precious research time (… but I didn’t jump on the Graphene train until the UK/NZ labs added their findings to the list of about 30 countries who were already blowing the whistle, and most definitely should’ve looked into that one sooner because I was wrong about that one not having legs).
Today I’m just going to take some notes to look at the evidence provided – just to see why this is a hypothesis and whether it might have legs.
This will be yet another “living document” where I just record my notes whenever I look into this hypothesis. First published: 14th April, 2022 | Last updated: 24th May, 2023
First the Patents
Venom in the Injections?
Venom in the Injections (summary of below resources) (PATENT list IS from THE SNAKE VENOM VIDEO with Dr Love (see video section) – I have not searched all the patents yet to verify / confirm what she is talking about or looking for – this whole post is just my “Notes/Draft” page, where I’m taking notes (for myself) to try and figure this out.. didn’t realize so many people would find it, my blog is usually pretty empty as Google hates me.. lol.. so just be aware, this entire page is my “notes” my … “taking notes to try and figure this theory out“)
Janssen (the manufacturer’s of J&J Covid Jabs) have 3 patents containing Snake Venom for “SARS-COV-2 vaccines”)
US Military have a patent containing Snake Venom for “Vaccines against SARS-COV-2 and other coronaviruses”.
BioNTech US Inc. (the co-manufacturers of Pfizer Covid Jabs) have a patent containing Snake Venom for “Coronavirus vaccines”
I’m not sure if we’re looking at “snake venom” or whet everyone is assuming sPLA2-IIA is strictly snake venom because the term sPLA2-IIA is also used interchangeably with “Human sPLA2-IIA“. (01)
There are also many patents containing snake venom for therapeutic uses that either “stimulate” an immune reaction, or for treating those suffering from autoimmune disorders & other conditions.
Compositions and methods for preventing and treating coronavirus infection-sars-cov-2 vaccines “A vaccine against COVID-19 to prevent COVID-19 caused by SARS-CoV-2 in individuals 18 years of age and older, comprising a recombinant human adenovirus of serotype 26 that contains nucleic acid encoding a SARS-CoV-2 S protein or fragment thereof.”
Rna replicon encoding a stabilized corona virus spike protein“RNA replicons encoding stabilized recombinant pre-fusion SARS CoV-2 S proteins are described. Also described are pharmaceutical compositions and uses of the RNA replicons.”
WO2021178971A1 (August 3rd, 2021) Henry M Jackson Foundation for the Advancement of Military Medicine, INc., The Government of the United States, as represented by The Secretary of the Army (US Military) (05)
Vaccines against sars-cov-2 and other coronaviruses“RNA replicons encoding coronavirus S proteins, in particular SARS-CoV-2 S proteins, are described. Also described are pharmaceutical compositions and uses of the RNA replicons.”
Composition and method for oral delivery of cobra venom
Publication number: 20140030354 | Filed: October 1, 2013
Abstract: A composition of sterile cobra venom and a method for its oral administration to provide significant analgesic effects to a human and/or animal are disclosed. Such cobra venom compositions comprise a sterilized solution preserved by the addition of one or more suitable food-grade preservatives. The venom composition may be conveniently administered orally by means of a metered spray device.
US8278265B2 (October 2, 2012), Fundacao de Amparo a Pesquisa do Estado de Sao Paulo FAPESP (08)
Methods, kits and compositions comprising crotamine
Patent number: 8278265
Abstract: The present invention refers to uses of crotamine and compositions containing it, based on its characteristic of interaction with genetic material. Under submicromolar quantities, the polypeptide is no longer toxic, presenting the characteristics properties of cell penetration, transport of molecules to the surface, cytoplasm or cell nucleus and particularly, selective cell penetration. The invention also refers to compositions comprising a pharmaceutically effective concentration of crotamine and its use for the treatment of diseases and dysfunctions, based on its characteristics of interaction with genetic material, such as DNA and RNA, and cell selectivity.
Date of Patent: October 2, 2012
Assignee: Fundacao de Amparo a Pesquisa do Estado de Sao Paulo—FAPESP
Modified elapid venoms as stimulators of the immune reaction was granted in July, 2010 with 14 claims. The patent describes a method of protection from infections by administering a detoxified and neurotropically active modified venom containing alpha-cobratoxin. Protection includes bacterial, viral and parasitic infections. This patent is meant to protect and support our work in our production of anti-infective treatments. Currently, this would be applied to RPI-MN and RPI-78.
Modified venom and venom components as anti-retroviral agents with 10 claims was filed in September 2005. The present invention describes a method of treatment of human subject suffering from infection with HIV, comprising administering a disease mitigating amount of a detoxified, modified cobra venom composition in an amount effective to ameliorate at least one symptom of said infection. This patent is meant to protect and support our work in the production of anti-viral treatments. Currently, this would be applied to RPI-MN and RPI-78.
Treatment of Autoimmune Disorders Using Detoxified Cobratoxin was filed in April 2007. The patent describes a method of treating patients suffering from autoimmune disorders comprising the administration of detoxified cobra venom. This patent is meant to protect and support our work in the production of drugs for the treatment of auto-immune diseases. Currently, this would be applied to RPI-78MN.
Application of cobra venom neurotoxin in drugs for treating ametropia
The invention relates to application of cobra venom neurotoxin in pharmacy, particularly in drugs for treating ametropia, belonging to technical field of biomedicine. The invention particularly relates to application of cobra venom neurotoxin or a hydrolyzed fragment of the neurotoxin. The neurotoxin or the hydrolyzed fragment of the neurotoxin can be an active ingredient used for preparing drugs for treating ametropia only or together with antibiotics. According to the invention, as an active ingredient for treating ametropia, the cobra venom neurotoxin with low dosage not only can stop signal transduction of neuromuscular junctions, but also can adjust a receptor of the cobra venom neurotoxin to balance a nerve-muscle function, thereby achieving the aim of treating ametropia.
(Ametropia refers to a group of visual disorders caused by errors in the refractive power of the eye)
US20200061185A1 Prefusion coronavirus spike proteins and their use, filed in April 2019, Inventors: Barney Graham (NIAID), Jason McLellan (Moderna) (15)
How did they file the patent for the spike protein 8 months earlier?
Why is there a patent separate than the spike protein?
Why are the spike proteins called “SARS-Cov-2 proteins” in the patent?
There’s also one called Wuhan Institute of Virology Spike Protein 2
GeoVax owned by Vanguard
My questions (to Karen, or anyone… )
Is SARS-CoV substitution “SARS-S-2P”, SARS-Cov-2? – (Because the patent doesn’t mention SARS-CoV-2, it mentions SARS-S-2P) – did you match it somehow to SARS-CoV-2? (Basically, If they are the same, how do you know?)
(I’m not doubting that evil is control of “science” right now or what is going on in the world… nor NIAID & Moderna’s involvement… trying to figure out how you know/think these are the same? A devil’s advocate would say they created spike proteins based on the known-past viruses and these are models?)
And playing devil’s advocate right back at Moderna.. for some reason they are able to miraculously create the SARS-CoV-2 vaccine in a couple of days and have it in bodies 66 days later and miraculously are able to manufacture & deliver millions of these vials all over the world… but they can’t make a Omicron vaccine in the same time-frame.. (I think we know already that they created these things years ago, but need relevant evidence)
Most interesting in this patent regardless if they are the same or not, is the “connection” between Moderna and the Wuhan Lab.
“Dr. Aryiana Love brings the patents and receipts proving Dr. Ardis’ claims in the Stew Peters Network exclusive documentary “Watch The Water”, exposing a long term plot to envenomate the world.”
For those who came across my post, this is the video where I got the patent ID’s from – so if Dr Love is right, the patents she lists are right, but if she’s wrong, the patents she lists are wrong. Need to investigate further to validate.
Symptoms of Snake Venom
Collation of symptoms of Snake-Bite or Spit-Venom
Symptoms of Snake-Bite or Spit-Venom (collated from below references)
Neurological (Dizziness, disturbed vision, headache, seizures. Mental status changes, delirium. Coma, faintness, collapse. Chronic neurological deficits after strokes. Drowsiness. )
Hemorrhagin directly damages the blood vessels by loosening the gaps between endothelial cells, thus injuring the basement membrane of the capillaries.
Pitting edema Edema is swelling in the body caused by excess fluid. If you press on a swollen area and an indentation or pit remains, it’s called pitting edema.
Incoagulable blood where the blood will not clot in the 20 minutes WBCT
Blisters-resulting in the accumulation of a proteinaceous fluid as a consequence of the collection of woundexudate.
Hemoglobinuria caused by intravascular hemolysis. Red colour urine
Hematuria or havingpassed dark brown/black urine.
Urticaria- Some people develop skin rashes triggered by the reaction of ASV after its administration; the skin becomes itchy, raised, red or skin-coloured.
Ptosis– is the drooping or falling of the upper eyelid.
Haematemesis is the vomiting of blood. It is caused from the internal bleeding after from the gastrointestinal tract by the effect of haemotoxic venom of Russell’s viper.
Necrosis is caused by due the effect of cytotoxic factors of snake venom which result in the unregulated digestion of cell components.
Dysphagia is the medical term for swallowing difficulties. Some people with dysphagia have problems swallowing certain foods or liquids, while others can’t swallow at all.
Pulmonary edema: Pulmonary edema is a fatal manifestation of snakebites and can occur with both viper and elapid bites.Pulmonary edema is a condition caused by excess fluid in the lungs. This fluid collects in the numerous air sacs in the lungs, making it difficult to breathe.
Cellulitis: A common and potentially serious bacterial skin infection. There is swelling of cells. Caused due to the anaerobic bacteria present in the snake’s mouth.
Oliguria is defined as a urine output that is less than 1 mL/kg/h in infants, less than 0.5 mL/kg/h in children, and less than 400 mL or 500 mL per 24h in adults – this equals 17 or 21 mL/hour.
Swelling and bruising result from increased vascular permeability attributable to venom endopeptidases, metalloproteinase hemorrhagins, membrane-damaging polypeptide toxins, phospholipases, and endogenous autacoids released by the venom, such as histamine, 5-HT, and kinins.
Local tissue necrosis results from the direct action of myotoxins and cytotoxins, and ischemia caused by thrombosis; compression of blood vessels by first-aid methods such as tight tourniquets; or by swollen muscle within a tight fascial compartment.
Myotoxins damage the muscle cell plasma membrane directly.
Most are PLA2s, either enzymatically active (aspartate-49) or enzymatically inactive (lysine-49). Cobra cardiotoxins are low-molecular weight polypeptides with cytotoxic action.
Hypotension and shock
After viper bites, leakage of plasma or blood into the bitten limb and elsewhere, or massive gastrointestinal haemorrhage, may cause hypovolaemia.
Vasodilation, especially of splanchnic vessels, and a direct effect on the myocardium may contribute to hypotension.
Profound hypotension is part of the autopharmacological syndrome that occurs within minutes of bites by D. siamensis, D. russelii, and Australasian elapids, attributable to oligopeptides (ACE inhibitors and BPPs) and vasodilating autacoids.
In some cases, direct myocardial effects of venom may be suggested by electrocardiographic (ECG) changes and autopsy findings of epicardial or endocardial haemorrhages and histopathological evidence of cardiac myonecrosis.
Elapid and some colubroid venoms activate complement via the alternative pathway (“cobra venom factor” is the snake’s C3b), whereas some viperid venoms activate the classic pathway. Complement activation affects platelets, the blood coagulation system, and other humoral mediators.
Neurotoxic polypeptides and PLA2s of snake venoms cause paralysis by blocking transmission at the neuromuscular junction.
Patients with paralysis of the bulbar muscles may die of upper airway obstruction or aspiration, but the most common mode of death after neurotoxic envenoming is respiratory paralysis.
By prolonging activity of ACh at neuromuscular junctions, anticholinesterase drugs may improve paralytic symptoms in patients bitten by snakes with neurotoxins that are predominantly postsynaptic in their action (e.g., cobras and Australasian death adders [genus Acanthophis]).
Some patients bitten by elapids or vipers are drowsy in the absence of respiratory or circulatory failure. This is unlikely to be an effect of neurotoxic polypeptides, which do not cross the blood-brain barrier.
PLA2 myotoxins and metalloproteinases are principally responsible.
They are present in venoms of most species of sea snakes, many terrestrial Australasian elapids, some species of krait (Bungarus), and Viperidae, such as the Sri Lankan Russell’s viper (D. russelii).
Release into the bloodstream of myoglobin, muscle enzymes, uric acid, potassium, and other muscle constituents is an effect in humans of presynaptic neurotoxins.
Patients may die of bulbar and respiratory muscle weakness, acute hyperkalaemia, or acute kidney injury.
Acute kidney injury
A wide range of renal histological changes has been described after snakebite.
Acute tubular necrosis is the most common, but proliferative glomerulonephritis, interstitial nephritis, toxic mesangiolysis with platelet agglutination, fibrin deposition, ischaemic changes, and distal tubular damage (“lower nephron nephrosis”), suggesting direct venom nephrotoxicity attributable to venom PLA2 and metalloproteases, and bilateral renal cortical necrosis with subsequent calcification are also reported.
Antivenom can cause immune-complexmediated kidney injury.
Acute tubular necrosis may result from prolonged hypotension and hypovolaemia, DIC, direct toxic effect of the venom on the renal tubules, haemoglobinuria, myoglobinuria, and hyperkalaemia.
Russell’s viper venom produces hypotension, DIC, direct nephrotoxicity, and, in Sri Lanka and India, intravascular haemolysis and rhabdomyolysis.
In Burmese patients envenomed by Russell’s vipers (D. siamensis), high urinary concentrations of β2-microglobulin, retinal binding protein, and N-acetyl glucosaminidase suggested failure of proximal tubular reabsorption and tubular damage.
High plasma concentrations of active renin suggested that renal ischaemia with activation of the renin-angiotensin system was involved in development of renal failure.
A massive but transient capillary and glomerular leak of albumin was an early sign of oliguric renal failure.
Snake venom–induced DIC may result in deposition of fibrin on vascular endothelium that has been activated by, for example, metalloproteinases, producing microangiopathic haemolysis.
Although the clinical picture is reminiscent of haemolytic uraemic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP), there is no evidence of depleted ADAMTS-13 levels and, therefore no justification for cryosupernatant plasmapheresis.
Generalized increase in capillary permeability
Venoms of some Viperidae, such as D. russelii and D. siamensis, can cause a generalized increase in vascular permeability, resulting in pulmonary oedema, serous effusions, conjunctival, periorbital, facial and retinal oedema, bilateral parotid enlargement, albuminuria, and haemoconcentration.
The likely cause is metalloproteases that damage vascular endothelium.
Clinical syndromes of snakebite in South-East Asia - WHO
Clinical syndromes of snakebite in South-East Asia:
Local envenoming (swelling etc) with bleeding/clotting disturbances = Viperidae (all species)
Local envenoming (swelling etc) with bleeding/clotting disturbances, shock or acute kidney injury = Russell’s viper; with conjunctival oedema (chemosis) and acute pituitary insufficiency = Russell’s viper, Myanmar and South India with bilateral ptosis, external ophthalmoplegia, facial paralysis etc. and dark brown urine = Russell’s viper, Sri Lanka and South India
Local envenoming (swelling etc.) with paralysis = cobra or king cobra
Paralysis with minimal or no local envenoming: Bitten on land while sleeping on the ground with/without abdominal pain = krait Bitten in the sea, estuary and some freshwater lakes = sea snake Bitten in Indonesia Maluku or West Papua with/without bleeding/clotting disturbance = Australasian elapid
Paralysis with dark brown urine and acute kidney injury: Bitten on land (with bleeding/clotting disturbance) = Russell’s viper, Sri Lanka or South India
Long term complications:
at the bite site – tissue loss, amputation, chronic ulceration (risk of malignant change), infection, osteomyelitis, arthritis, arthrodesis, contracture and hypertrophic or keloid scars cause permanent physical disability.
Chronic kidney disease, chronic panhypopituitarism, chronic neurological deficits after strokes.
Local and/or systemic envenoming affecting organs and tissues distant from bite site that may be transient, persistent, life-threatening or permanently debilitating
Signs of extreme anxiety prompted by the frightening experience:
hyperventilation, acroparaesthesiae, tetany, dizziness/syncope, vasovagal shock with profound bradycardia, diarrhoea and vomiting, agitation, irrational behaviour, hypertension, tachycardia, sweating, trembling that may mislead medical staff and lead to persistent psychological morbidity
People with COVID-19 have had a wide range of symptoms reported – ranging from mild symptoms to severe illness. Symptoms may appear 2-14 days after exposure to the virus. Anyone can have mild to severe symptoms. People with these symptoms may have COVID-19:
Fever or chills
Shortness of breath or difficulty breathing
Muscle or body aches
New loss of taste or smell
Congestion or runny nose
Nausea or vomiting
This list does not include all possible symptoms. CDC will continue to update this list as we learn more about COVID-19. Older adults and people who have severe underlying medical conditions like heart or lung disease or diabetes seem to be at higher risk for developing more serious complications from COVID-19 illness.
Symptoms of Coronavirus - WebMD
Symptoms of Coronavirus (Accessed Apr 17, 2022) – (WebMD) (25)
(Exactly same as CDC list)
Constant pain or pressure in your chest
Bluish lips or face
Having a hard time staying awake
Coughing up blood
Liver problems or damage
Some doctors have reported rashes tied to COVID-19, including purple or blue lesions on children’s toes and feet.
Symptoms of COVID-19 (Severe) - NIH
Symptoms of COVID-19 (Severe) (NIH) (Accessed April 17, 2022) (26)
Critically ill patients may have
acute respiratory distress syndrome
septic shock that may represent virus-induced distributive shock
an exaggerated inflammatory response and/or exacerbation of underlying comorbidities
central nervous system disease
Side-effects of Remdesivir
Collation of Remdesivir side-effects
Remdesivir Side-Effects (collated from below references)
nausea and vomiting
puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue
stomach pain, continuing
unusual tiredness or weakness
yellow eyes or skin
discoloration of skin
feeling of pressure
pain, stinging, soreness, tenderness
Respiratory disorders NEC
Lower respiratory tract disorders (excluding obstruction and infection)
Coronary artery disorders
Renal and urinary disorders
Renal disorders (excluding nephropathies)
Urinary tract signs and symptoms
Infections and infestations
Viral infectious disorders
Bacterial infectious disorders
Hepatic and hepatobiliary disorders
Decreased and nonspecific blood pressure disorders and shock
Moderna COVID Vaccine and Csf white blood cell count increased (29)(Csf white blood cell count increased is found among people who get Moderna COVID Vaccine, especially for people who are male, 60+ old, and in the first week of getting the vaccine.)
Pfizer BioNTech Covid Vaccine and Csf white blood cell count increased (30)(Csf white blood cell count increased is found among people who get Pfizer BioNTech Covid Vaccine, especially for people who are male, 60+ old, and in the first week of getting the vaccine.)
Johnson and Johnson Covid Vaccine and Csf white blood cell count increased (31)(Csf white blood cell count increased is found among people who get Johnson and Johnson Covid Vaccine, especially for people who are male, 60+ old, and in the first 30 days of getting the vaccine.)
Hmm but latest Pfizer/FDA doc-dump show that the White-Blood Cell Counts DECREASE. I haven’t done a post on the latest doc drop yet because I’m working on something else just as important, if not more so, but you can download the docs from this site and then look for others who have reviewed them: https://phmpt.org/
Snake Venom - Laboratory Tests - WHO
Investigations/laboratory tests for Snakebites (WHO) (32)
20 minute whole blood clotting test (20WBCT) is a simple, informative bedside test requiring only a new, clean, dry, ordinary glass tube, bottle, vial or syringe.
Positive (non-clotting) result indicates severe consumption coagulopathy and need for immediate antivenom treatment. False positive (non-clotting) 20WBCT results from use of plastic, polystyrene or polypropylene rather than ordinary glass, or glass cleaned with detergent, soap or washing fluid that destroy surface activation of blood coagulation.
If new glass tubes not available, re-use ordinary glass vessels (e.g. antibiotic bottles), washed with “normal 0.9% saline” for intravenous infusion, without detergent or other cleaning agent, dried in hot air.
Other more sensitive laboratory tests of blood coagulation:
International Normalized Ratio (INR) based on prothrombin time (PT) (> or =1.2 is abnormal), activated partial thromboplastin time (aPPT), fibrin(ogen) related antigens (fibrin degradation products -FDP) or D-dimer.
Point-of-care (bedside) devices for measuring INR and D-dimer unreliable in snakebite victims.
“We have designed a rapid test, immunochromatographic test of cobra (ICT-Cobra), which obtained fair results in improving the diagnosis and treatment of Naja (N.) atra snakebites in Taiwan. In this study, we further investigated the feasibility of applying the kit for the detection of other cobra venoms based on the potential interspecies similarity. “
“Here, we tried to produce highly specific antibodies in goose yolks for use in a paper-based microfluidic diagnostic kit, immunochromatographic test of viper (ICT-Viper), to distinguish RVs from other vipers and even cobra snakebite in Asia. The use of the ICT-Viper in the South-East Asia region is pending additional laboratory and field investigations and regional collaboration.”
Phospholipases A2 (PLA2s) (EC 22.214.171.124) are small (about 14 kDa), stable, calcium-dependent, disulfide-rich enzymes. They degrade membrane phospholipids at the sn-2 position, releasing lysophospholipids and fatty acids. They are ubiquitously found in nature ih both intracellular and extracellular forms.
In mammals, PLA2s play important roles in fertilization, cell proliferation, smooth muscle contraction, hypersensitization and chronic inflammatory diseases. They are also important in cellular functions such as signal transduction via biosynthesis of prostaglandins and leukotrienes, and membrane homeostasis including the maintenance of cellular phospholipid pools and membrane repair through deacylation/reacylation (Kini, 2003).(38)
Venom PLA2s are produced by almost all venomous animals, with snake venom PLA2s (svPLA2s) being the most studied. svPLA2s, in addition to their possible role in the digestion of the prey, show a wide variety of pharmacological effects. They exhibit pre-/post-synaptic neurotoxicity, myonecrosis, cardiotoxicity, anticoagulant property, inhibition/activation of platelet aggregation, hemorrhage, hemolysis, hypotensive and edema-inducing activities. Natural catalytically inactive (Lys49-PLA2s or PLA2 homologs) and the chemically inactivated svPLA2 enzymes conserve some of their biological activities.
Activity: myotoxin – local and systemic skeletal muscle degeneration.
Activity: presynaptic neurotoxin – PLA2 neurotoxins interfere specifically with the release of acetylcholine from motor neurons, and their PLA2 activity is essential for the irreversible blockade of neuromuscular transmission.
Activity: hemolysis – disruption of the cell membrane.
Activity: platelet aggregation activating toxin – PLA2s can induce platelet aggregation by release of arachidonic acid.
Activity: platelet aggregation inhibiting toxin – PLA2s can inhibit platelet aggregation by physical destruction of the integrity of the platelet membrane via hydrolysis of the membrane phospholipids, which could affect the functions of receptors that play important roles in platelet aggregation.
More than 90% of snake venom (dry weight) is protein.
Each venom contains more than a hundred different proteins: enzymes (constituting 80-90 % of viperid and 25- 70 % of elapid venoms), non-enzymatic polypeptide toxins, and non-toxic proteins such as nerve growth factor.
Nonprotein ingredients include carbohydrates and metals (often part of glycoprotein metalloprotein enzymes), lipids, free amino acids, nucleosides, and biogenic amines such as serotonin and acetylcholine.
These include digestive hydrolases (proteinases, exopeptidase, endopeptidases, phosphodiesterases, metalloproteinases, and phospholipases), hyaluronidase (spreading fator), and activators or inactivators of physiological processes, such as kininogenases.
Most venoms contain l-amino acid oxidase (containing a riboflavin 5’-phosphate prosthetic group that confers the yellow colour of many venoms), phospho monoand di- esterases, 5′-nucleotidase, DNAase, NAD-nucleosidase, phospholipase A2, and peptidases.
degrade basement membrane components, leading to endothelial cell damage and contributing to spontaneous systemic bleeding.
venoms of Viperidae and some Elapidae and Colubridae contain serine proteases and other procoagulant enzymes that are thrombin-like or activate factors V, X, prothrombin and other clotting factors.
These enzymes stimulate blood clotting with formation of fibrin in the blood stream.
Paradoxically, this process results in incoagulable blood because most of the fibrin clot is broken down immediately by the body’s own plasmin fibrinolytic system.
Sometimes within 30 minutes of the bite, the levels of clotting factors have been so depleted that the blood will not clot (“consumption coagulopathy”).
Some venoms contain multiple antihaemostatic factors. For example, Russell’s viper venom contains toxins that activate factors II (prothrombin), V, X, IX and XIII, fibrinolysis and protein C, and cause platelet aggregation, anticoagulation and haemorrhage.
Phospholipases A2 (lecithinase):
are most widespread and extensively studied of all venom enzymes.
They damage mitochondria, red blood cells, leucocytes, platelets, peripheral nerve endings, skeletal muscle, vascular endothelium, and other membranes
producing presynaptic neurotoxic activity, cardiotoxicity, myotoxicity, necrosis, hypotension, haemolysis, haemorrhage, plasma leakage (oedemainduction), opiate-like sedative effects and autopharmacological release of histamine and other autacoids.
They are anticoagulant, either by hydrolysing plasma or platelet membrane phospholipids, or by interacting with different coagulation factors.
although found in most elapid venoms, may cause fasciculation.
promotes the spread of venom through tissues by increasing permeability but can also contribute to tissue damage.
Proteolytic enzymes (metalloproteinases, endopeptidases or hydrolases) and polypetide cytotoxins (“cardiotoxins”):
increase vascular permeability causing oedema, blistering, bruising and necrosis at the site of the bite.
Venom polypeptide toxins (“neurotoxins”) :
Postsynaptic (α) neurotoxins such as α-bungarotoxin and cobrotoxin, consist of 60-62 or 66- 74 amino acids.
They bind to acetylcholine receptors at the motor endplate.
Presynaptic (β) neurotoxins such as β-bungarotoxin,, and taipoxin, contain 120-140 amino-acids and a phospholipase A subunit.
These release acetylcholine at the nerve endings at neuromuscular junctions and then damage the endings, preventing further release of transmitter.
(have barely even started this search, need to work now so will come back to this..)
Snake venom is being recently touted as an “anti-HIV” drug, since January 2022. There’s six PLA2s from Snake Venoms patents “against HIV”. These synthetically derived snake venoms are marketed under the guise of being “antiviral” and as a preventive treatment for HIV infection.
“Earlier, it was shown that phospholipases A2 (PLA2s) from bee and snake venoms block HIV replication, the effect being independent on catalytic PLA2 activity. However, the antiviral activity of human PLA2s against Lentiviruses depended on catalytic function and was mediated through the destruction of the viral membrane. To clarify the role of phospholipolytic activity in antiviral effects, we analyzed the anti-HIV activity of several snake PLA2s and found that the mechanisms of their antiviral activity were similar to that of mammalian PLA2. Our results indicate that snake PLA2s are capable of inhibiting syncytium formation between chronically HIV-infected cells and healthy CD4-positive cells and block HIV binding to cells.“
The study claims snake venom works to “protect against Lentiviruses” through the “destruction of the viral membrane.” However, this is a lie because we know the Lentiviruses are a lab generated, chimeric mRNA bioweapon containing SARS, MERS, HIV 1-3 and SRV-1 (AIDS). (42)
In actuality, snake venom is being used to destroy the human cell membrane not the “viral membrane”, so that nanoparticles can enter the cell and code your genome. This PubMed study proves that HIV is being encoded into people’s cells to produce a new cell line persistently. So snake venom assists mRNA to clone your cells. The J&J patent also mentions “RNA Replicons” which are forever replicating proteins. (43)
Journal Publications - Cobra Venom
Journal Publications on the Therapeutic uses of Cobra Venom
“The findings from the current study revealed that, cobra venom at lethal dose causes multiple organ failure in experimental animal which could be considered among the factors that lead to death.
“Results from the histopathological examination showed mainly inflammatory cellular infiltration, vacuolation in renal tubules, shrinking of glomeruli, raising space between the walls of Bowman’s capsule in renal tissue and alveolar haemorrhage, inflammatory cellular infiltration and edema in pulmonary tissue.”
“The body apparently does not produce an antitoxin to combat the deadly venom of the cobra in the same way that it fights the poison of the diphtheria germ. Evidence of the persistence of the poison in the tissues could be obtained in some cases a month after the injection. This gives rise to no symptoms, but the animal succumbs to a subminimal additional dose. He also believes that it is probably held in the nerve ends since he could not find any trace of the toxin in the blood.”(45)
“This work aimed to investigate the effects of the Crotalus durissus terrificus(Cdt) venom in the liver. Plasma activities of alanine aminotransferase and aspartate aminotransferase and hepatic glutathione S-transferase and catalase presented significant elevation in rats inoculated with 300 μg ⋅ kg(-1) Cdt venom. Liver lipoperoxidation was enormously increased by venom doses of 100, 200, and 300 μg ⋅kg(-1) , whereas glutathione S-transferase was not changed. Perfused livers from rats inoculated with 1500 μg ⋅kg(-1) venom showed increased production of lactate, pyruvate, and ammonia when alanine was the metabolic substrate.”(47)
Ifit’s snake venom, and ifwe’re going off “What we know has worked for millions so far”, then the protocols we’ve already researched doesn’t need to be adjusted (we still need a constant reminder to get fresh, quality, un-poisoned food & water). We’ve all recovered from whatever they’ve thrown at us so far using the same things that have helped people with:
“Spike-Protein” poisoning (which include COVID symptoms, Long-Haul symptoms, Vax-Illness symptoms)
“Graphene-Oxide” poisoning / “Magnetic Phenomenon” / Loss of or Metallic Smell/Taste
“Vax-Reactions relating to the Spike Protein” (flu-symptoms & loss of smell/taste)
The standard lot:
Glutathione, NAC, Melatonin, Zinc, Vitamin D, Vitamin C, Antihistamines, Heavy Metal Detox, Parasite Cleanse, Greens, Aspirin, Turmeric, Ivermectin, HCQ, Borax, Milk Thistle, COQ10, CDS, among others.
Melatonin is a snake-bite inhibitor/reduces inflammation.
Milk Thistle for the liver.
COQ10 for the heart.
Asprin for the clots.
Supps because those who have severe covid symptoms have lower levels of those.
NAC because it increases our glutithione levels.
*IF* it’s venom, don’t imagine that they are gathering all these serpents to “milk them”. That’s old school. These days, everything is grown in a lab. These days everything is biowarfare & genetic manipulation. These days, they can recreate “extinct” animals in a lab, so creating a venom en masse is a walk in the park. And they’ve been able to do it for decades.
( Not the only one who thinks this, just came across another researcher who’s gone a step further and found evidence of this, she says “Organoids are being grown a lab to mass produce snake venom. Organoids of snake glands can produce snake venom artificially, without the entire snake.”) (54)(55)
I haven’t looked up antidotes yet and I need to do some work now so I’ll come back to this post later.
“Snake venom” antidotes thus far:
Local Plants as antidote to snake venom
Local plants as antidote to snake venom
Scientists have recently validated some local plant as herbal medicines for snakebite management.(56)
Commonly called English wild custard apple, Annona senegalensis belongs to the plant family Annonaceae. The researchers from Department of Biochemistry, Faculty of Science, University of Maiduguri, Borno State, found that the root extract of Annona senegalensis possesses potent snake venom neutralising capacity and may provide protection against the toxicity posed by the Bitisarietans venom and could be used for therapeutic purposes in case of snakebite.
“Beyond melatonin’s well-known antioxidant and anti-inflammatory actions which have proven the efficacy of this molecule in the treatment of diseases/ conditions where excessive free radical-mediated oxidative damage and hyperinflammation are causative factors, the studies summarized herein also support its use as a possible treatment for COVID-19 disease. Melatonin has been proposed as a potential effective inhibitor of the destructive inflammatory consequences of a SARS-CoV-2 infection, an idea supported by observed and predicted improvements in the outcome of patients with this disease.”
“The results demonstrated that melatonin efficiently alleviated EC venom-induced hemorrhage and myonecrosis. It also mitigated the altered levels of inflammatory mediators and oxidative stress markers of blood components in liver and kidney homogenates, and documented renal and hepatoprotective action of melatonin. The histopathology of skin, muscle, liver, and kidney tissues further substantiated the overall protection offered by melatonin against viper bite toxicities.“
Aqueous extracts of this plant have been reported to neutralize venom of the Indian speckled cobra
Ethanolic seed (extract of Acacia catechu)
Has been studied for its hepatoprotective, antipyretic, antidiarrheal, hypoglycemic, anti-inflammatory, immunomodulatory, antinociceptive, antimicrobial, free radical scavenging, and antioxidant activities. (63)
Ayurvedic Use: The Acacia catechu is known as Cutch tree, Terra Japonica as well as Black Catechu. In Hindi it is called Khair and Khadira in Sanskrit. This herb was previously known as Kat or Cacho.
Used as anti-fungal, natural birth control, swelling in liver / liver sluggishness, blood clotting, gingivitis, management of Leukaemia, Asthma, Bronchitis, relieves diarrhoea, sores, skin afflictions, anti-inflammatory, psoriasis, anaemia, ulcers, leprosy, swelling in spleen, skin disorders, constipation, and pain in the chest. (64)
Confirmed protective activity against the lethal action of snake venom with whatever the hell these plants are: Aristolochia indica, Hemidesmus indicus, Gloriosa superba, Strychnos nux-vomica, Eclipta prostrata, and Andrographis paniculata
Information on medicinal plants was collected from the traditional healers called “Vaidyars”. This survey covers 72 medicinal plants belonging to 53 families that are used for the treatment of snakebite in a traditional way.
Potent neutralizing effect against the venom.
Publication contains a whole heap of plants like the above-mentioned that I don’t recognize – probably all natural to India. I’m trying to find publications with stuff we already have access to without having to take a course just to figure out what it is! (Although it did mention Doxycycline, in combination with Tetracyclines)
Doxycycline is a known COVID-19 treatment (from doctors who read the science, not the pharma-funded fact-checkers and who are not brainwashed or under-duress by corrupt health authorities). (65)(66)
Pretty sure you’ll never see a journal publication on this or favourable agreement in the mainstream… but here goes:
“Hear me out. I’ve got all the evidence that you have something for free inside of you right now that will take care of anything, any health problem that you might be suffering from and neutralize any damage you may have already received for almost the entire course of the 20th century,” ~ Dr Group (Global Healing Institute)
“I can honestly say right now that I think urotherapy is the most overlooked and suppressed medical secret in the history of the world. It is urine therapy. Doctors and researchers have proven that human urine is an enormous source of over 2,500 vital nutrients, vitamins, hormones, enzymes and critical antibodies that cannot be duplicated or derived from any other source as well as up to six unidentified compounds not yet known to man.Urine has also been used to treat cancer, heart disease, allergies, autoimmune diseases, diabetes, asthma, infertility, infections, poisoning and wounds, among others.
“It can also serve as poison antidote” “In nature, there are snakes, spiders, bees or anything that punctures the skin and injects poison and that this creates a reaction called a cytokine storm.” “Let your body produce an anti-venom.” “It’s been known in India and other parts of the world for thousands of years [that] to survive a poisonous snake bite, you drink your own urine. You put urine under your tongue for 15 seconds and your body produces the anti-venom and it produces the antibodies and you don’t die from the poisonous snake bite,”
Snake Charmers & Snake Bite using Uropathy stories:
Snake Bite, Cobras“… he had a local doctor inject the region of the bite along with drinking his urine and applying it topically.”
Snake charmers“Lord Sushrut has mentioned autourine as an antipoisonous substance and a good tonic. Snakecharmers keep a bowlful of urine handy while catching a snake so that he may be able to drink and apply it without loss of time in case of a snake bite. Jain monks say that one who drinks urine regularly for six months becomes immune to snake poison. The same is the opinion of many other sadhus.”Manav Mootra by R. M. Patel
 Science: An antidote for all snake bites (67)
“Antibodies for antivenins are extracted from the blood of horses after their immune systems have been exposed to harmless doses of a snake venom.”
“…a substance in the blood of a poisonous snake which neutralises its own venom. Scientists isolated the substance/protein, called Notechis scutatus inhibitor (NSI), and an Australian laboratory tested the protein against the venom of six other snakes and NSI inhibited the venom of all of them.” “another Team found NSI protected all but rattlesnake venom”
“NSI acts against many venoms because all snakes mix their toxic cocktails from phospholipase A2, an enzyme found in cells. NSI inhibits this enzyme. The toxins usually kill by blocking the nerve cells which control the breathing or heartbeat.”
“An extract of human urine has shown great promise for the treatment of pulmonary and cardiovascular diseases, as well as certain deadly diseases caused by the formation of blood clots. He said the extract in urine called urokinase activates substances in the bloodstream that dissolve clots.”
 UROKINASE “breaks-up blood clots. It is used to treat large blood clots formed in the lungs”. (68)
 Urokinase (Abbokinase) “a thrombolytic drug, sometimes called a “clot-busting” drug. It helps your body produce a substance that dissolves unwanted blood clots. Urokinase is used to treat blood clots in the lungs”.(69)
 Urokinase clears blot clots in stroke patients “Swiss surgeons have significantly improved mechanical removal of blood clots in stroke patients by intra-arterial administration of the thromolytic urokinase”(70)
Documents / Downloads
Antisnake Venom Properties of Medicinal Plants (PDF) (71)
“Traditional herbal medicine and plants are used either single or in combination, as antidotes for snake envenomation by about 54 million indigenous people in rural populations in many parts of the world. Plants are reputed to neutralize the action of snake venom, with a plethora of plants claimed to be antidotes for snakebites in folk medicine.
Topical application of plant extracts on bitten area, chewing leaves or barks, drinking or injecting extracts, can counteract snake venom activity.“
(I didn’t recognize the names of any of the plant extracts listed in the table – may have to look up each individually to find out what their “friendly-name” is.)
Therapeutic application of natural inhibitors against snake venom phospholipase A2 (PDF) (72)
“Naturally available inhibitors occupy an important place in the potential to neutralize the toxic effects caused by snake venom proteins. It has been well recognized for several years that animal sera, some plant and marine extracts, antibiotics from synthetic chemicals are the most potent in neutralizing snake venoms.”
Uropathy is a Divine Therapy, Urine is a Universal Medicine (PDF)
“In case of Snake bite, Scorpion bite, rabid dog bite, rat bite and poisoning from opium or any other substance, Urine is to be given immediately. If the patient cannot pass urine, urine of a healthy person may be given along with putting urine packs on the wound”
Uropathy – Shivambu – Urine Therapy – The Golden Secret for Health and Longevity (PDF)
What is this Snake-Venom Theory Anyway?
What is this snake-venom theory...
The documentary “Watch the Water” featuring Dr Bryan Ardis hypothesizes that COVID is not a respiratory virus of any kind, but ‘venom-poisoning’ – a bioweapon created by gain-of-function research with synthesized peptides & proteins from “snake venom”.
“Did you know you can safely drink venom? Venom is actually not poison. Venom injected into the bloodstream via needle or bite can kill but not in water. Research before reacting and sharing false information. There is no covid, there was no spike in deaths, this was a PLANdemic and a testing pandemic, made up, statistics based on a false test. No one has covid, no one can catch covid, there is no drug for covid, there is no such thing. Let me help you through this sensationalist piece called Watch the Water and break things down for you. Did you know that antibodies are produced to help the body get rid of wastes? So when you are toxic, you make them, to cleanse! So that is all their therapies are doing, grabbing all sorts of wastes. Yes, they are trying to kill a lot of people, but we already know this. We don’t need more muddy waters, we need to focus on the facts: there is no new disease and never was, it is a scam from tip to tail and they are still playing us with it!”
“The false “Watch the Water” video is spreading like wildfire because they are trying to push a new clinical trial for another inoculation/drug and some how trying to prove it is from nature. If it went against their agenda people would have a hard time trying to find this video/documentary but nope you can literally find that BS video anywhere. They had a study in Arizona over a year ago talking about rattle snake venom and how it can be a life saving treatment for convid. It’s planned to the finest details.”
Videos - Dr Bryan Ardis - Interviews & Documentary
“Dr. Braun is a U.S. National Counterterrorism & EMS Advisor and Trainer, Chief Scientist, CounterBioterrorism Division, BioChem Engineering, Executive Director of the Violence Prevention Agency, and Clinical Psychologist. He researched and discovered the origin of Covid 19 was snake venom, before Dr. Ardis. “
“Dr. Tau Braun, US Counterterrorism Expert featured in COVENOM, joins DeAnna Lorraine to delve deeper into proof that Snake Venom is in the Covid bioweapon, how it effects the human body, heart and mind, and more. Mass push by deep-state companies like 23AndMe to steal our DNA and use it to tailor the Vaccine based on individual genetic makeup.”
This video looks at the paper cited by Dr Bryan Ardis as the main evidence that snake venom plays a role in the current plandemic. The paper purports to have found a potential association between venom-like peptides found from various animals and Covid-19. Dr. Kaufman gives an overview of the relevant issues related to the snake venom controversy and gives a critical appraisal of the experiment and conclusions.
Pittsburgh & Wuhan are sister cities, the Chinese scientists at the Univ. of Pittsburgh had been studying viruses and determined this virus was similar to SARS/MERS, Bing Liu was mysteriously gunned-down May 2nd 2020, he was looking at the cellular basis for the infection of COVID, how & where it attaches, etc. He & his colleagues were making pretty-good progress because 2 days before he was murdered, Univ. of Pittsburgh scientists announced they believe they had found a potential vaccine (bandaid/patch with microneedles, not mRNA, where you actually take the spike from the virus), so they made this big announcement on the last day of April 2020. May 1st they published their study of their findings, and then May 2nd Bing Liu is riddled with bullets. He was at the fore-front of looking at the cellular mechanisms. His name isn’t published on the new study, but it’s interesting. Then, we never hear of the bandaid-associated vaccine ever again.
“Brazilian researchers have found that a molecule in the venom of a type of snake inhibited coronavirus reproduction in monkey cells, a possible first step toward a drug to combat the virus causing Covid-19.”(84)(85)
April 16, 2022 – Snake Venom and COVID-19 – In some circles an insane amount of attention was paid this week to the theories of a chiropractor previously celebrated for speaking out on the fraudulent Remdesivir saga in the US. Here is my take. – Pierre Kory MD
Disagrees with diaphragmatic paralysis as the cause of respiratory failure in COVID as he has known of not one reported or published instance of it in COVID death, and he has cared for hundreds of COVID patients.
Disagrees that the most common day of death in the hospital is day 9.
Agrees that remdesivir is a fraud with known toxic side effects.
Disagrees that “They were banning doctors for using monoclonal antibodies.” – he knows of not one instance of “banning or punished doctors” for using monoclonal antibodies.
Says doctors were fired and investigated… for “off-label” prescribing of highly effective repurposed drugs (Ivermectin & HCQ) – not NIH and FDA approved or EUA approved drugs.
(Ummm actually they did revoke authorization for two popular Monoclonal Antibody treatments – see this video news press conference – ProjectVeritas – timestamp 1:08 – Penny)
Agrees there may be some truth in the main theory, “that SARS-CoV2 largely acts as a snake venom and that remdesivir is also made from snake venom”.
There is indeed a short sequence of RNA coding for amino acids that make up a part of the receptor binding domain (RBD) portion of the spike protein that is identical to snake venom.
Problem with calling COVID-19 snake venom: this protein sequence is just a small part of one protein of the 29 made made by SARS-CoV2 when it replicates.
This does NOT mean the virus came from a snake but it does have a little snake venom protein in it. Why it is in there who knows, I suppose I can ask Fauci or Baric or Dazak or the Chinese Military the next time I run into one of them.
Disagrees with the Multi-Organ Failure in COVID – Says very few patients die of multi-organ failure in COVID and that the vast majority actually die of single organ failure (respiratory failure), and occasional kidney failure, but admits late stage sepsis (a complication of progressive severe COVID) sometimes causes multi-organ failure but for many/most, they die simply of lung failure.
Disagrees with his claims that the virus/venom and/or remdesivir/venom causes ARDS initially.
On “Elevated phospholipase A2 enzymes were found in COVID patients”, he said it’s true the enzyme has properties similar to snake venom, but doesn’t agree that all the hospitalized patients who died with remdesivir is equivalent to “remdesivir is snake venom enzyme”
Disagrees with the symptoms of snake venom being the same symptoms as COVID – the 19 snake venom symptoms listed in the study mentioned, said they cause cardiovascular dysfunction, muscular paralysis, nausea, blurred vision, and systemic effects such as hemorrhage, and in the diagram from the paper showing damage to the body (coagulation, anticoagulation, tissue damage, sudden shock, muscle damage, dizziness/headache, neuromuscular paralysis and systemic hemorrhage). Pierre said that most of these injurious pathways.. do not happen routinely (or at all) in COVID, and said out of the listed symptoms, he can only endorse hyper coagulation and headache and… nothing else.
April 15, 2022 – About Those Venom Proteins… At least 10 people asked me, too, about the venom proteins. I offer a plausible explanation, what do you think? – James Lyons-Weiler
“Dr. Nass says the snake venom stuff is “hooey”. My analysis says yes, let’s move on to more productive pathways. I share two possible explanations for their presences in COVID-19 patients, one of which I favor over the other.”
April 14, 2022 – Snakes Poisoning the Well. The rattlesnake enzyme in question is different from a similar-but-not-the-same human enzyme that is a possible culprit in COVID-19 deaths. – Stephanie Brail
“Snake venom can have as much as 50-100 different proteins/enzymes. ONE enzyme does not equal full-blown snake venom. An enzyme, by the way, is typically made of protein (sometimes enzymes are also made from RNA). Enzymes are simply catalysts that spur chemical reactions in the body. The “rattlesnake enzyme” in question is NOT the same exact enzyme found in humans causing COVID-19 deaths. They are very SIMILAR but not the SAME. The human enzyme is found naturally in the body and normally protects us from bacterial infections. When it is produced too much, it gets out of control and attacks our organ tissue instead of just pathogens.“
“Our findings suggest that 2019-nCoV has most similar genetic information with bat coronavirus and most similar codon usage bias with snake.”
“The presence of toxin-like peptides…suggests a possible association between COVID-19 disease and the release in the body of (oligo-)peptides almost identical to toxic components of venoms from animals….The presence of these peptides opens new scenarios on the aetiology of the COVID-19 clinical symptoms observed up to now, including neurological manifestations.”
“Coronaviruses have genetic material that is highly recombinant, meaning different regions of the virus’s genome can be derived from multiple sources,”
“The Spike Protein has numerous “fingerprints” pointing to a manufactured biological weapon, it can be aerosolised and can easily be deployed as a chemical weapon with devastating short term and long-term impacts.”
“SARS2 was rapidly labelled a respiratory disease. However, my research has revealed that the primary destructive mechanism of SARS2 and the S-Protein is an envenomation.“
In a 1977 paper, a lectin – a form of venom, a plant-based venom – was attached to, or combined with, a coronavirus. “You really need to think about glycoproteins, venom and plant-based venom, which are called lectins – you need to think of them like two sides of Velcro and there’s interplay between the two of them. Ultimately, they act as switches and so when your body needs to understand what it’s dealing with it will have places in the body where lectins and venoms combine. And that sets off all kinds of chain reactions,”
There are two homologues, synthetic versions of the venom, in the spike protein. “You can call it a cobra venom but it may not actually be from the cobra snake. It is from a lab and even then, more importantly, it doesn’t have to actually come from the cobra snake. That venom could be a perfect match, evolutionary, to a cone snail … it could also come from parasites … There are two venoms that are in the S protein of SARS-CoV-2 and they are cobra and krait, a coagulant and an anti-coagulant. And you have all kinds of disruptive mechanisms of those two weapons … the venom aspect is just one aspect of this multipurpose tool that makes up the spike,”
“There is already loads of data, there is already loads of science, around the fact that the viral component is only one part of this problem. The bigger problem is the spike protein … They took that highly lethal pathogenic short-term and long-term poison, a venom – a venom-based poison – I cannot be any more clear, they took that and they gave you, if you took the vaccine, a code. And that code is a trick – a cell that would not normally accept that code was told ‘hey suck this code in and start printing more of this poison.”
“While it’s true there is some overlap between the effects of poisonous peptides present in some snake venom and those of SARS-COV2 spike protein, claiming COVID is ultimately derived from snake venom is a poorly substantiated hypothesis.“
Things I found along the way that I found intriguing.
Summary of below intriguing things
A company named “Cobra Therapeutics” manufacturers AstraZeneca
A company named “VenomTech” just announced (April 12, 2022) a collaboration with Charles River Laboratories (who specialize in gene therapy & cell therapy for the Pharmaceutical, Medical device and Biotechnology industries).
The WEF publishes an article about synthetic snake venom peptides being synthetically created with RNA/DNA advancements.
Cobra Therapeutics (AstraZeneca)
Interesting name of a DNA/Gene-therapy Vaccine Manufacturer
AstraZeneca vaccine in the UK is manufactured on Oxford Universities behalf by two biotech companies, Oxford BioMedica and Cobra Therapeutics, and filled and finished by Wockhart in Wrexham. (126)
Coulter Pharmaceutical, Inc. and Cobra Therapeutics Ltd, the gene therapy subsidiary of ML Laboratories, have entered into a collaboration to jointly develop and commercialise Cobra’s platform gene expression technology.
The technology, known as Ubiquitous Chromatin Opening Elements (UCOEs), is a new class of gene expression elements which induce efficient productivity from genes introduced into target cells.
UCOE transfected cells yield more predictable, high-level expression of gene products in a sustained fashion.
UCOEs have a wide range of potential applications including gene therapy, functional genomics and the manufacture of therapeutic proteins including recombinant antibodies.
Cobra Therapeutics is one of Europe’s leading research groups developing novel DNA technologies for applications in human gene therapy, the genomics revolution and manufacturing of biological products.
In addition Cobra manufacturers DNA and viral products on a contract basis for several pharmaceutical and biotechnology companies including Glaxo Welcome at its GMP manufacturing facility in Keele, Staffs, which is one of only a small number of such facilities in Europe.
A company actually named “VenomTech” just did a press-release on April 12, 2022 on medical.net announcing a collaboration with Charles River Laboratories (an American pharmaceutical company specializing in a variety of preclinical and clinical laboratory, gene therapy and cell therapy services for the Pharmaceutical, Medical device and Biotechnology industries):
Venomtech is collaborating with Charles River Laboratories, International Inc. to help drug developers explore venom-derived compounds for a wide range of therapeutic targets.
This newly formed collaboration will bring together Venomtech’s biology expertise and vast venom-derived peptide library, with Charles River’s drug development and screening knowhow, providing pharmaceutical manufacturers with a one-stop service to explore this unique natural resource.
Millions of years of evolution have made venom-derived peptides highly specific, even for many of the hardest-to-hit drug targets.
Venomtech’s Targeted-Venom Discovery Array™ (T-VDA™) libraries provide researchers with a straightforward solution to rapidly screen thousands of individual venom fragments, with each array specifically designed to maximise hits for a specific target.
Through the new collaboration, Charles River will be able to use this innovative resource – closely supported by Venomtech – to accelerate its clients’ pipelines, addressing difficult therapeutic targets, uncovering new mechanisms of action and minimising off-target effects.
Venomtech announces new drug development collaboration with Charles River(128)
VenomTech company announces massive library of SNAKE VENOM peptides for pharmaceutical development; “nanocarriers” stabilize snake venom in WATER (131)
World Economic Forum 'DNA/RNA Synthetic Snake Venom Peptides'
In November 2018, the World Economic Forum (WEF) published an article announcing that scientists had come up with a way to artificially synthesize snake venom peptides for drug development purposes.(132)
“Advancements in DNA and RNA technology, make it possible to synthesize snake venom as opposed to extracting it from the animal as was previously required”
“Traditionally, live venom would be extracted from the animal, then injected into an unsuspecting live rodent or fish to study its impact”
“Nowadays, the DNA and RNA of the venom have already been identified, which allows researchers to synthesize its components and test out their theories.”
“I like to describe venom as a cluster bomb, its job is to shut down the normal function of the prey and in doing so, it fans out (and) hits several targets, which is a great thing for pharmaceutical development because you have several avenues to explore.”
“Because it’s so fast acting, so potent and highly specific to its target, venom has all of the ingredients necessary for making a drug.”
~ Mandë Holford, World Economic Forum’s Young Scientists
PhD from Rockefeller University (relevant, extremely relevant, wait for upcoming post)(133)
Co-Founder, Killer Snails (Killer Snails creates immersive games that inspire a love of science.) (134)
Killer Snails is developing a new immersive experience called WaterWays. The augmented reality (AR) experience is funded by the National Institute of Health (NIH) and aligned to the Next Generation Science Standards. Students in grades 3-5 will work in augmented reality (via iPads, Chromebooks, or other tablets) and personalized online science journals to gather data, answer questions, construct models and develop and test hypotheses. In WaterWays, students will get to study organisms like mako sharks and learn more about human impacts on water, and water’s impact on humans. While developing knowledge of the connections between ecology and human health, students will also apply that understanding to come up with solutions to problems like plastic pollution.
Professor Mandë Holford Named A World Economic Forum Sustainability Pioneer “Holford is the only U.S. public university researcher among the Sustainibility Pioneers, a group of entrepreneurs, innovators, and scientists who are tackling challenges to achieving the U.N. Sustainable Development Goals by 2030.” “She also plans to work on a new initiative, 2030STEM, that is focused on addressing the systemic and institutionalized racism that hinders Black and Latinx individuals from entering and excelling in STEM.”(136)
She has received several awards including being named a 2020 Sustainability Pioneer and 2015 New Champion Young Scientist by the World Economic Forum. (137)
4 ways science should transform after COVID-19. World Economic Forum Agenda, 17 June 2020.(138)
World Economic Forum Videos & Articles (Mande Holford)
The therapeutic power of snail venom | Mande Holford – 2015 WEF Video featuring snake, snail, and centipede venom (139)(140)
5 tips for working from home as a woman in STEM. World Economic Forum Agenda, 1 May 2020. (141)
Children should be playing more games in the classroom. Here’s why (142)
Too hot, too cold. What porridge can tell us about women in science(143)
2020 TedTalk The power of venom — and how it could one day save your life | Mandë Holford “Venom can kill… or it can cure. Marine chemical biologist Mandë Holford shares her research into animal venom, from killer sea snails to platypuses and slow lorises, and explores its potential to one day treat human diseases like cancer. Someday, snail venom might just save your life.”(144)(145)
On her holfordlab.com website “Injecting flies with snail venom could help us discover molecules for developing new drugs” – 2019 (146)
—^^^ now I expect to find “Funded by Bill & Melinda Gates foundation or Rockefeller Foundation” somewhere lol ^^^ — I bet I find a connection now…
WHOOMP there it is …(dance break) 𝅘𝅥𝅮𝅘𝅥𝅮𝅘𝅥𝅮 𝅘𝅥𝅱 ♭♭ ♯𝄞 𝄢𝆔𝆕𝅘𝅥𝅘𝅥
“Holford and her research partner, Li Zhao of The Rockefeller University, received $1.5 million to study immunity and its evolution.“ – Feb 2022 (147)
“Holford and Zhao are leading a project to better understand how immune genes that code for tiny proteins called micropeptides evolve. The team will characterize several poorly understood immune-related micropeptides in humans and fruit flies and will zero in on newly evolved micropeptides to better understand their evolution and their role in the immune system.”
My “thoughts” in April 2022 after going through the above was that there was no snake venom to worry about pertaining to how it was explained in the documentary (yes, snake venom & synthetic venom(s) of all kinds of poisons are in a lot of things, and Evil-only knows what’s really in those jabs), but the snake-symbolism can be used as a metaphor-warning for the NWO takeover, this insidious, evil war we’re in-full of globalist snakes and their shills with disinformation & propaganda everywhere. I’m more concerned with the ‘snakes’ orchestrating and carrying out this war on humanity and the other weapons being thrown at us (geo-engineering, radiation, graphene, nanotech, transhumanism, GMOs, the social-credit system, etc.) than the snake ‘venom’ in the water-but check out the ‘antidotes’ section if you’re worried about venom to dissipate any fears you have about it. There’s also the fact that this is a global experiment, and all sorts of shit could be being used, and they definitely do experiment with poisons such as snake and snail venom. Our health agencies are captured, our governments are captured, there is no honest oversight to what they are doing to our world.
My thoughts in May 2023 , a year later – maybe there is more to it than I first realized… I’m still confused, but there’s a lot more information out there now that suggests that it’s possible that it’s part of the bioweapon being used against us, and I hadn’t kept up-to-date about this new information since I last updated this post in April 2022, but with the sudden death of Dr Rashid Buttar (who believed in the venom theory), I found a lot more videos when looking him up. So – don’t rely on my post for the latest information about snake venom, but I need to kick my own butt for not keeping up-to-date with the findings of other people since.
Unfortunately the PDF option doesn't print citations or any text that needs expanding. Will find another PDF solution another day - I've already lost half the day trying to get it to work. ~ May 9th, 2023
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Sept 1, 2021 – Snake venom may be tool to fight Covid-19: Study – Reuters “Brazilian researchers have found that a molecule in the venom of a type of snake inhibited coronavirus reproduction in monkey cells, a possible first step toward a drug to combat the virus causing Covid-19.”
TedX Speaker Page “Mandë Holford investigates the power of venom to transform organisms (and lives) when it is adapted to create new therapeutics that treat human diseases and disorders.” https://www.ted.com/speakers/mande_holford
Leffler, A. E., Kuryatov, A., Zebroski, H. A., Powell, S. R., Filipenko, P., Hussein, A. K., . . . Holford, M. (2017). Discovery of peptide ligands through docking and virtual screening at nicotinic acetylcholine receptor homology models. Proc Natl Acad Sci U S A, 114(38), E8100-E8109. doi: 10.1073/pnas.1703952114
Achrak E, Ferd J, Schulman J, Dang T, Krampis K, Holford M. VenomFlow: An automated bioinformatic pipeline for identification of disulfide-rich peptides from venom arsenals.Edited series Marine Genomics in Methods in Molecular Biology, published by Springer Nature, in press, 2021.
Truth-seeker, ever-questioning, ever-learning, ever-researching, ever delving further and deeper, ever trying to 'figure it out'. This site is a legacy of sorts, a place to collect thoughts, notes, book summaries, & random points of interests.
DISCLAIMER: The information on this website is not medical science or medical advice. I do not have any medical training aside from my own research and interest in this area. The information I publish is not intended to diagnose, treat, cure or prevent any disease, disorder, pain, injury, deformity, or physical or mental condition. I just report my own results, understanding & research.