THIS POST IS CONTINUED FROM PART 5 BELOW—
https://ajitvadakayil.blogspot.com/2020/05/covid-19-pandemic-sars-cov-2.html
VACCINES BASED ON MESSENGER RNA (MRNA) TO PRODUCE VIRAL PROTEINS IN THE BODY IS THE NEED OF THE HOUR.
MESSENGER RNA (MRNA) IS A SINGLE-STRANDED MOLECULE OF RNA THAT CORRESPONDS TO THE GENETIC SEQUENCE OF A GENE AND IS READ BY A RIBOSOME IN THE PROCESS OF SYNTHESIZING A PROTEIN.
TRADITIONAL VACCINES ARE MADE UP OF SMALL OR INACTIVATED DOSES OF THE WHOLE DISEASE-CAUSING ORGANISM, OR THE PROTEINS THAT IT PRODUCES, WHICH ARE INTRODUCED INTO THE BODY TO PROVOKE THE IMMUNE SYSTEM INTO MOUNTING A RESPONSE.
MRNA VACCINES TRICK THE BODY INTO PRODUCING SOME OF THE VIRAL PROTEINS ITSELF.
THE MRNA CONTAINS THE GENETIC CODE THAT ALLOWS OUR OWN CELLS TO MAKE PART OF THE CORONAVIRUS SPIKE PROTEIN. WHEN OUR CELLS MAKE THE PROTEIN, OUR IMMUNE CELLS CAN RECOGNISE THE PROTEIN AS FOREIGN, AND THIS LEADS TO PRODUCTION OF ANTIBODIES.
RNA MOLECULES HAVE THE TENDENCY TO SPONTANEOUSLY DEGRADE. THIS CAN BE A CRITICAL LIMITATION– A SINGLE LOWER CAN RENDER THE MRNA VACCINE INEFFECTIVE
MRNA VACCINES REQUIRES STORAGE AT -75 DEGREE C
SARS‐COV‐2 ARE ENVELOPED VIRUSES WITH A POSITIVE SINGLE‐STRANDED RNA GENOME. INSIDE THE PARTICLE, THE VIRAL RNA, WITH 29,811 NUCLEOTIDES, IS TIGHTLY COILED AND COATED BY THE NUCLEOCAPSID (N) PROTEIN. THREE GLYCOPROTEINS, CALLED SPIKE (S), MEMBRANE (M), AND ENVELOPE (E), ARE EMBEDDED IN THE LIPID OUTER MEMBRANE.
SPIKE PROTEINS FORM HOMOTRIMERS, WHICH PROTRUDE FROM THE LIPID ENVELOPE AND FORM THE CHARACTERISTIC “CORONA”. SPIKE PROTEINS MEDIATE VIRAL ENTRY INTO HOST CELLS BY BINDING TO ANGIOTENSIN‐CONVERTING ENZYME 2 (ACE2) EXPRESSED ON RESPIRATORY TRACT CELLS
MRNA, OR ‘MESSENGER RNA, IS MADE IN THE NUCLEUS USING THE NUCLEOTIDE SEQUENCE OF DNA AS A TEMPLATE. THE PROCESS INVOLVES USING NUCLEOTIDE TRIPHOSPHATES AS SUBSTRATES CATALYZED BY THE ENZYME RNA POLYMERASE II.
THE MRNA FORMED IS TRANSPORTED OUT OF THE NUCLEUS AND INTO THE CYTOPLASM WHERE IT INSTRUCTS PROTEINS TO ASSEMBLE ON THE RIBOSOMES USING THE MRNA NUCLEOTIDE SEQUENCE.
FOR SARS-COV-2 VIRUS TO ENTER HUMAN CELLS, THE SPIKE PROTEIN ON THE SURFACE OF THE VIRUS MUST BIND TO THE HOST RECEPTOR PROTEIN, ANGIOTENSIN-CONVERTING ENZYME 2 (ACE2).
GENE-BASED VACCINES CARRY THE GENETIC INSTRUCTIONS FOR THE HOST’S CELLS TO MAKE THE ANTIGEN, WHICH MORE CLOSELY MIMICS A NATURAL INFECTION. IN THE CASE OF CORONAVIRUSES, THE ANTIGEN OF INTEREST IS THE SURFACE SPIKE PROTEIN THE VIRUS USES TO BIND AND FUSE WITH HUMAN CELLS.
IN MRNA VACCINES SCIENTISTS SYNTHESIZE AND INSERT GENETIC INSTRUCTIONS FROM THE PATHOGEN OF INTEREST TO INDUCE IMMUNE RESPONSES
MRNA VACCINE DESIGNS DELIVER NAKED NUCLEIC ACIDS OR, MORE RECENTLY, ENCAPSULATE THEM IN A CARRIER NANOPARTICLE
GOLD NANO PARTICLES ARE PROMISING FOR MRNA DELIVERY BECAUSE OF THEIR SMALL SIZE AND SCALABILITY AS WELL AS NONTOXIC AND IMMUNOLOGICALLY INERT PROPERTIES.
GOLD NPS (AU-NPS) DUE TO THEIR DISTINCTIVE CATALYTIC, PHOTONIC, AND ELECTRIC CHARACTERISTICS AND CAPABILITY OF INTERACTIONS WITH A VARIETY OF BIOMOLECULES COULD BE APPLIED IN THE VIRAL DETECTION SETTINGS
THE GENE GUN METHOD, USING COMPRESSED HELIUM GAS AS AN ACCELERATION FORCE TO PUSH MRNA COATED ON THE SURFACE OF GOLD PARTICLES INTO HOST CELLS, IS AN EFFICIENT METHOD OF MRNA DELIVERY
A GENE GUN OR BIOLISTIC PARTICLE DELIVERY SYSTEM IS A DEVICE USED TO DELIVER RNA, OR PROTEIN TO CELLS.
https://ajitvadakayil.blogspot.com/2020/05/covid-19-pandemic-sars-cov-2.html
capt ajit vadakayil
..
- WE THE PEOPLE ASK MODI AND HARDHVARDHAN, WHY ARE YOU AFRAID OF BILL GATES? CHAKKAR KYA HAI?
WHY ARE YOU TREATING PUNE SERUM INSTITUTE LIKE THE CATs WHISKERS ?
BE WARNED..
WE ARE WATCHING ..
WE THE PEOPLE ASK PM MODI
FROM TODAY ONWARDS
MONITOR EVERY INCH OF WHAT PUNE SERUM INSTITUTE DOES, WITH FIELD TRAILS..
LAY OUT THE NATIONs POLICY..
ANY DEVIATION , MUST ENTAIL PUNISHMENT IN MILLIONS OF US DOLLARS FINES AND IMPRISONMENT OF ADAR POONAWALA AND HIS FATHER CYRUS..
LET THEM SPEND THEIR BILLIONS IN JAIL CANTEEN..
WE THE PEOPLE WILL NOT ALLOW WANT BILL GATES TO PLAY DOCTOR TO THE PLANET.. THE WHO CHIEF IS HIS SLAVE..
HAVE WHISTLE BLOWERS LINED UP..GIVE THEM PROTECTION..
WE KNOW WHY PRINCE CHARLES AND BILL GATES TREATS PUNE SERUM INSTITUTE ( EX-STUD HORSE PARTY ) AS TAJ MAHAL..
WE THE PEOPLE WILL NOT TOLERATE INDIANS TO BE USED AS GUINEA PIGS..
COVID-19 AFFECTS THE BRAIN AND BEACHES THE BLOOD BRAIN BARRIER..
THE HUMAN BRAIN IS CONSCIOUS.. LAB RATS CANNOT SEE THEMSELVES IN MIRROR NOR CAN THEY SEE COLOUR..
https://ajitvadakayil.blogspot.com/2020/05/covid-19-pandemic-sars-cov-2.html
BEFORE CYRUS POONAWALA TOOK AN ALMIGHTY JUMP TO HUMAN VACCINES, WE KNOW WHAT THEY WERE DOING BEFORE.. I HAVE INFORMATION FROM THE INNER CIRCLE ..
MOST COVID-19 PATIENTS LOSE SENSE OF TASTE AND SMELL BEFORE THEY DIE.. THEY CANNOT EVEN TASTE SMELL STRONG VINEGAR..
ACE2, TO WHICH THE VIRUS IS BINDING TO, IS ALSO PRESENT IN THE BRAIN
THE VIRUS COULD PASSES THE BLOOD BRAIN BARRIER BY INFECTING THE ENDOTHELIAL CELLS
PATHOPHYSIOLOGY OF NEUROLOGICAL IMPLICATIONS OF COVID-19 INCLUDE: DIRECT VIRAL INVASION OF THE NERVOUS SYSTEM, AUTOIMMUNE SEQUALAE, HYPOXIA-MEDIATED INJURY, SEQUELAE OF SYSTEMIC PROINFLAMMATORY STATE, COCK SURE BRAIN BARRIER DISRUPTION SECONDARY TO SARS-COV-2 BINDING TO THE ANGIOTENSIN-CONVERTING ENZYME-2 (ACE2) RECEPTOR, AND COAGULOPATHY
INDIRECT EFFECTS OF SARS-COV-2 ON THE BRAIN INCLUDE NEURO-INFLAMMATION BY A CYTOKINE STORM, INDUCED BY THE IMMUNE SYSTEM IN REACTION TO THE VIRUS, CAN SPREAD THROUGH THE BODY, PASS THE BLOOD BRAIN BARRIER, AND CAN CAUSE BRAIN INFECTIONS OR DAMAGE NEARBY NEURONS AND GLIAL CELLS
DIRECT EFFECTS DRIVEN BY THE VIRUS, SUCH AS THE INFECTION OF BRAIN BLOOD VESSELS AND NERVE CELLS, PLAY A ROLE IN NEUROLOGIC MANIFESTATIONS OF COVID-19.
SARS-COV-2 INFECTS NEURONS AND GLIAL CELLS THROUGHOUT THE CNS
SEVERE INFLAMMATIONS, SUCH AS THOSE OBSERVED IN DEAD COVID-19 PATIENTS, MAKE THE BARRIER DISINTEGRATE,
THE IMPERMEABILITY OF THE BLOOD-BRAIN BARRIER, ALSO CAN PRESENT A PROBLEM FOR DRUG DEVELOPERS TARGETING THE BRAIN OF LIVING PATIENTS
THE VIRUS SARS COV-2 HAS BEEN FOUND IN THE CEREBROSPINAL FLUID.
DUAL-POSITIVE ACE2+TMPRSS2+ CELLS IN TISSUES BEYOND THE RESPIRATORY SYSTEM, INCLUDING OLIGODENDROCYTES IN THE BRAIN, AND INHIBITORY ENTERIC NEURONS
THERE EXISTS A HIGH EXPRESSION OF THE ACE2 RECEPTOR IN ENDOTHELIAL CELLS OF BLOOD VESSELS . THE VIRUS MAY THEREFORE INFECT ENDOTHELIAL CELLS OF THE BRAIN VASCULATURE IN THE FIRST TERM, AND IT MAY THEN SPREAD TO THE SURROUNDING ACE2+TMPRSS2+ OLIGODENDROCYTES AND, FINALLY, TO THE NEURONS
SARS SOV- 2 VIRUS CAN ENTER THE CNS THROUGH THE OLFACTORY EPITHELIUM, CROSSING THE CRIBRIFORM PLATE OF THE ETHMOID BONE AND REACHING THE OLFACTORY BULB FROM WHICH IT COULD SPREAD TO DIFFERENT AREAS OF THE BRAIN
HCOV-OC43 CORONAVIRUS WAS ISOLATED FROM THE BRAIN OF A PATIENT WHO DIED OF VIRAL ENCEPHALITIS
NECROTIZING ENCEPHALOPATHY REFLECTS THE IMPACT OF CYTOKINE STORM ON THE BREAKDOWN OF THE BLOOD BRAIN BARRIER, WITHOUT DIRECT VIRAL INVASION OF THE CNS.
ACUTE SYMPTOMATIC SEIZURES HAVE BEEN FOUND IN 32% OF COVID-19 PATIENTS WITH NO PRIOR HISTORY OF SEIZURES. MORE SEVERE TYPES OF BRAIN DISEASE (ENCEPHALOPATHY) HAVE BEEN DESCRIBED AS WELL, SUCH AS HYPOXIC ENCEPHALOPATHY, ENCEPHALITIS, AND STROKE
CONTINUED TO 2-- CONTINUED FROM 1--
MULTIPLE SCLEROSIS (MS) IS A CHRONIC AND OFTEN PROGRESSIVE INFLAMMATORY DISEASE OF THE CENTRAL NERVOUS SYSTEM (CNS) THAT RESULTS IN THE LOSS OF MYELIN SHEATH DUE TO AUTOIMMUNE REACTIONS
http://ajitvadakayil.blogspot.com/2017/02/vaccine-induced-encephalitis-mylelin.html
IMMUNE AND INFLAMMATORY REACTIONS LEAD TO DAMAGE TO THE NERVOUS SYSTEM. THE MIGRATION OF LYMPHOCYTES ACROSS THE BLOOD-BRAIN BARRIER CAUSES INFLAMMATION IN THE CNS AND LYMPHOPENIA IN THE PERIPHERAL BLOOD
ACUTE MYOCARDITIS HAS BEEN REPORTED IN PATIENTS WITH SARS-COV-2 INFECTION . THIS CARDIAC COMPLICATION COULD TRIGGER EVENTS OF BRAIN EMBOLIZATION AND STROKE, WHICH MIGHT EXPLAIN THE INCIDENCE OF CEREBRAL INFARCTIONS IN YOUNG PATIENTS WITH COVID-19 IN THE ABSENCE OF CARDIOVASCULAR RISK FACTORS.
SARS-COV WHEN INTRODUCED INTRANASALLY, ENTERS THE BRAIN AND CAN THEN BE FOUND IN SPECIFIC AREAS OF THE BRAIN RELATED TO RESPIRATION, INCLUDING THE THALAMUS AND BRAINSTEM
ACUTE NECROTIZING ENCEPHALOPATHY (ANE) IS DESCRIBED IN A CASE REPORTS OF COVID-19 PATIENTS. ANE IS A RARE DISEASE, WHICH CAN LEAD TO SEVERE BRAIN DAMAGE INCLUDING HEMORRHAGE
METABOLIC DISRUPTION, CAUSED BY LUNG DAMAGE, CAN LEAD TO AN OXYGEN DEFICIENCY ( HYPOXIA ) IN THE BRAIN
ONCE IN THE CNS, THE VIRUS ENTERS THE CEREBROSPINAL FLUID, THROUGH WHICH IT SPREADS THROUGH THE BRAIN . THE MEDULLA OBLONGATA IS THE PRIMARY RESPIRATORY CONTROL CENTER, LOCATED IN THE LOWEST PORTION OF THE BRAIN STEM. DAMAGE TO THE MEDULLA OBLONGATA, CAUSED BY DIRECT EFFECTS OF SARS-COV-2, EXPLAINS RESPIRATORY FAILURE IN COVID-19
AS A RESULT OF NEURO-INFLAMMATION THAT CAUSES OR PROGRESSES NEURODEGENERATIVE PROCESSES IN THE BRAIN, COVID-19 RESULTS IN A HIGHER INCIDENCE OF NEURODEGENERATIVE DISEASES
THE VIRUS TYPICALLY INFECTS PEOPLE THROUGH ACE-2 RECEPTORS IN THE NOSE, WHERE THEY ARE MOST COMMON. IT THEN RACES THROUGH THE BODY, INVADING CELLS IN OTHER PLACES WHERE ACE-2 IS LOCATED, INCLUDING THE INTESTINES, KIDNEYS AND HEART - EXPLAINING THE CARDIAC AND KIDNEY DAMAGE, AND ABDOMINAL PAINS, SEEN IN MANY PATIENTS.
ONCE INSIDE HUMAN CELLS, THOUGH, IT TRICKS THE BODY INTO PRODUCING MORE ACE-2 RECEPTORS WHERE THEY ARE NORMALLY ONLY PRESENT IN SMALL NUMBERS, INCLUDING IN THE LUNGS.
THIS ESSENTIALLY OPENS THE FLOODGATES AND ALLOWS COVID-19 TO RAPIDLY MULTIPLY AND SEND ARMIES OF VIRAL PARTICLES TO INFECT MORE PARTS OF THE BODY IN HUGE NUMBERS.
A BYPRODUCT OF THIS CRAFTY PROCESS IS THAT IT INTERFERES WITH THE BODY'S ABILITY TO CONTROL LEVELS OF A CHEMICAL CALLED BRADYKININ, WHICH HELPS REGULATE BLOOD PRESSURE
THE CORONAVIRUS SEEMS TO BE PUSHING BRADYKININ PRODUCTION INTO OVERDRIVE.
THIS LEADS TO A CATASTROPHIC BUILD-UP OF THE CHEMICAL, CAUSING A 'BRADYKININ STORM' WHICH MAKES BLOOD VESSELS LEAKY AND DRIVES UP THE RISK OF INFLAMMATION, BLOOD CLOTS, STROKES AND BRAIN DAMAGE - DEADLY SYMPTOMS OBSERVED IN COVID-19 SICK.
Capt ajit vadakayil
..
https://www.ndtv.com/india-news/convalescent-plasma-therapy-didnt-help-reduce-covid-19-deaths-top-medical-body-icmr-study-2292543
I ASK MY READERS
WHO WAS THE FIRST PERSON ON THE PLANET TO CATEGORICALLY SAY THAT CONVALESCENT PLASMA THERAPY WONT WORK?
https://ajitvadakayil.blogspot.com/2020/05/covid-19-pandemic-sars-cov-2.html
I DONT NEED TO BE A HEN TO JUDGE AN OMELETTE.
###################
Capt. Ajit Vadakayil July 27, 2020 at 3:50 PM
SOMEBODY ASKED ME ABOUT COVID-19 PLASMA THERAPY..
LISTEN
INDIANS ARE BEING USED A GUINEA PIGS DURING THIS COVID-19 PANDEMIC WITH SOLD OUT MEDIA PROVIDING PROPAGANDA....
DONT WORRY, CAPT AJIT VADAKAYIL KNOWS THE TRAITOR INDIAN BASTARDS WHO ARE IN KOSHER EVIL PHARMA PAYROLL..
CONVALESCENT PLASMA THERAPY REFERS TO ADMINISTERING CELLULAR PLASMA FRACTION OF BLOOD MINUS RED CELLS, WHITE CELLS, AND PLATELETS TO COVID-19 PATIENTS COLLECTED FROM THOSE WHO RECOVERED FROM THE DISEASE.
THE PLASMA THERAPY TREATMENT IS BEING TOUTED AS AN ALTERNATIVE TREATMENT TO FIGHT COVID-19 BECAUSE VACCINES OR TREATMENTS ARE STILL NOT AVAILABLE.
CONVALESCENT PLASMA THERAPY FOR COVID-19 IS BULLSHIT.. IF AT ALL SOMEBODY GOT WELL, GOD MAKE HIM RECOVER, NOT THIS BULLSHIT PLASMA THERAPY..
UNLIKE A VACCINE THAT IS PERMANENT FOR BACTERIAL DISEASES , THIS PLASMA THERAPY FOR SAR COV-2 VIRUS AFFECTED PEOPLE LASTS ONLY AS LONG AS THE ANTIBODIES ARE IN THE SICK PERSON’S BLOODSTREAM WHICH IS “LESS THAN A WEEK”..
YOU WILL NOT FIND ANY DOCTOR/ SCIENTIST ON THE INTERNET TELLING THIS NAKED TRUTH. THEY DON’T WANT TO GET ON THE WRONG SIDE OF THE EVIL PHARMA POWERS WHO CONTROL THE PLANET..
EVEN A RETARDED CHILD KNOW THAT YOUR OWN ANTI-BODIES CREATED BY GOD, IS YOUR BOUNTY MEANT FOR YOU SPECIFICALLY.. SURROGATE SYSTEMS DON’T WORK HERE..
DOCTORS JUST WANT TO REMOVE RECOVERING PATIENTS FROM THE VENTILATORS , TO HOOK IT ON TO OTHER PATIENTS. SUCH IS THE COVID-19 OVERLOAD ..
THE RISKS OF ADMINISTERING PLASMA . INCLUDE ALLERGY/ANAPHYLAXIS, TRANSFUSION-RELATED ACUTE LUNG INJURY (TRALI), AND TRANSFUSION-ASSOCIATED CIRCULATORY OVERLOAD (TACO) WHICH CAN CAUSE HEART FAILURE, ANAPHYLACTIC SHOCKS, ALLERGIC REACTIONS, HEMOLYSIS AND OTHER PATHOGENS BEING ACQUIRED FROM THE DONOR’S BLOOD.
MANY COVID-19 PATIENTS HAVE INCIPIENT RESPIRATORY FAILURE THAT MAY WORSEN WITH CONVALESCENT PLASMA TRANSFUSION-RELATED VOLUME LOADING
NEITHER THE METHOD TO ASSESS VIRAL NEUTRALISATION ABILITY OF CONVALESCENT PLASMA PRIOR TO ADMINISTRATION NOR THE MINIMUM TITRE OF NEUTRALISING ANTIBODY THAT IS REQUIRED FOR TREATING CRITICALLY ILL PATIENTS WITH COVID-19 IS KNOWN. ALL THIS CANNOT BE TRIED OUT ON LAB RATS.. THEY NEED HUMAN GUINEA PIGS ..
CONVALESCENT PLASMA THERAPY CARRIES THE RISK OF:--
ALLERGIC REACTIONS
LUNG DAMAGE AND DIFFICULTY BREATHING
TRANSMISSION OF INFECTIONS, INCLUDING HIV AND HEPATITIS B AND C
THE INDIAN COUNCIL OF MEDICAL RESEARCH (ICMR) HAS GIVEN PERMISSION TO STATES TO CARRY OUT EXPERIMENTAL CLINICAL TRIALS USING PLASMA THERAPY.
THESE ICMR DOCTORS ARE THE SAME DESH DROHIS WHO APPROVED FLU VACCINATIONS ON NEW BORN INDIAN BABIES.. IN USA ON AN AVERAGE 65,000 PEOPLE DIE OF COMMON SEASONAL FLU EVERY YEAR..
IN INDIA WE TREAT FLU LIKE COMMON COLD.. HARDLY ANYBODY DIES OF COMMON FLU IN INDIA.. FLU VIRUSES MUTATE AND THE VACCINE OF LAST YEAR IS NO GOOD THE NEXT YEAR.
Read all 4 parts of the post below—
http://ajitvadakayil.blogspot.com/2017/05/flu-shots-pneumococcal-vaccines-part-4.html
Capt ajit vadakayil
..
- WHEN I PUT A POST ABOUT GOLD NANO PARTICLES TO DETECT PREVENT CURE COVID-19 . GOOGLE THE AGENT OF KOSHER EVIL PHARMA DELETED IT.
https://ajitvadakayil.blogspot.com/2020/05/covid-19-pandemic-sars-cov-2.html
THE VACCINE FOR AIDS/ HIV IS STILL NOT FORTH COMING
THERE ARE MANY REASONS WHY, INCLUDING HOW HARD IT IS TO IDENTIFY THE EXACT PIECE OF AN ANTIGEN THAT WILL TRIGGER PRODUCTION OF AN EFFECTIVE ANTIBODY.
AND EVEN WHEN VACCINES EXIST, THEY FAIL WHEN B CELLS DON’T REARRANGE THEIR DNA SEGMENTS IN A WAY NECESSARY TO MANUFACTURE THE NEEDED ANTIBODIES.
http://ajitvadakayil.blogspot.com/2013/06/hiv-does-not-cause-aids-many-aids.html
JEW EDWARD JENNER LIFTED HIS WORK ( VACCINATION ) FROM A 6200 YEAR OLD AYURVEDIC TEXT CHARAKA SAMHITA..
http://ajitvadakayil.blogspot.com/2012/05/edward-jenner-leech-capt-ajit-vadakayil.html
VACCINES WORK BY COACHING THE IMMUNE SYSTEM TO FIGHT OFF A SPECIFIC PATHOGEN. WHEN YOU GET ONE, YOUR WHITE BLOOD CELLS ARE BEING INTRODUCED TO A POTENTIAL THREAT, SUCH AS A BACTERIUM. THAT GIVES THE IMMUNE SYSTEM TIME TO START MOUNTING A RESPONSE SO THAT IF THE PATHOGEN SHOWS UP ANOTHER TIME, THE BODY CAN QUICKLY NEUTRALIZE IT.
THE SARS COV-2 VIRUS IS A LAB MADE SLPICED AND GRAFTED VIRUS..
AN RNA VIRUS IS A VIRUS THAT HAS RNA (RIBONUCLEIC ACID) AS ITS GENETIC MATERIAL.
RNA VIRUSES GENERALLY HAVE VERY HIGH MUTATION RATES COMPARED TO DNA VIRUSES, BECAUSE VIRAL RNA POLYMERASES LACK THE PROOFREADING ABILITY OF DNA POLYMERASES.
THIS IS ONE REASON WHY IT IS DIFFICULT TO MAKE EFFECTIVE VACCINES TO PREVENT DISEASES CAUSED BY RNA VIRUSES—DIVERSITY IS THEIR STRENGTH…
CLASSIFICATION OF THE RNA VIRUSES IS DIFFICULT. THIS IS IN PART DUE TO THE HIGH MUTATION RATES THESE GENOMES UNDERGO.
THERE ARE THREE PROTEINS ON THE SURFACE OF THESE VIRUSES: THE ENVELOPE, MEMBRANE AND SPIKE, WHICH ENCAPSULATE A STRAND OF RNA. THIS RNA MOLECULE HOLDS THE GENETIC INSTRUCTIONS THAT MAKE UP THE VIRUS.
ONCE INSIDE, THE VIRAL RNA BECOMES PART OF THE HOST CELL’S PROTEIN PRODUCTION MACHINERY, AND PRODUCES NEW COPIES OF VIRAL PROTEINS AND RNA WHICH THEN ASSEMBLE INTO THOUSANDS OF NEW VIRUSES TO SPREAD THE DISEASE.
SO ONE WAY TO STOP A DISEASE IS TO BLOCK THE VIRUS FROM ENTERING THE CELLS. VACCINES DO THAT BY TRAINING THE BODY TO IDENTIFY AND ATTACK THE VIRUS BEFORE IT CAN INFECT HEALTHY HUMAN CELLS.
A VACCINE IS ESSENTIALLY A PURE PREPARATION OF ONE OR MORE KEY COMPONENTS OF THE VIRUS – SUCH AS THE ENVELOPE, SPIKE OR A MEMBRANE PROTEIN – THAT IS INJECTED IN THE BODY TO GIVE THE IMMUNE SYSTEM A PREVIEW OF THE VIRUS WITHOUT CAUSING DISEASE.
HOWEVER, DEVELOPING VACCINES BASED ON VIRAL PROTEINS TAKES ANYWHERE FROM YEARS TO DECADES ,
PROTEIN-BASED VACCINES REQUIRE MASS PRODUCTION OF VIRAL PROTEINS IN FACILITIES WHICH CAN GUARANTEE THEIR PURITY. GROWING THE VIRUSES AND PURIFYING THE PROTEINS AT MEDICALLY ACCEPTABLE PHARMACEUTICAL SCALES TAKES TOO LONG.
VIRUSES DO NOT MAKE THEIR OWN COMPONENTS. INSTEAD, A CORONOVIRUS ENTERS INTO THE LUNG AND POSSIBLY OTHER RESPIRATORY TRACT CELLS BY ATTACHING THROUGH TO THEM VIA ITS SPIKE PROTEIN.
VACCINES WORK BY INDUCING THE IMMUNE SYSTEM’S B CELLS TO MANUFACTURE ANTIBODIES AGAINST SPECIFIC MOLECULES — CALLED ANTIGENS — THAT POKE OUT OF A PARTICULAR VIRUS. THE CELLS ARE ABLE TO DO THAT BECAUSE THEIR DNA CONSTANTLY AND RANDOMLY PRODUCES THE THREE BASIC COMPONENTS OF ANTIBODIES.
BUT IN NATURE’S VERSION OF JUST-IN-TIME MANUFACTURING, THE B CELL HOLDS OFF ON ASSEMBLING THE COMPONENTS UNTIL THE ARRIVAL OF VIRUSES (OR PIECES OF VIRUSES) FROM A VACCINE OR A NATURAL INFECTION.
AT THAT POINT IT SWINGS INTO ACTION, PRODUCING AND SECRETING THE PRECISE, VIRUS-MATCHING ANTIBODIES NEEDED TO DESTROY THE INVADER, OUT OF BILLIONS OF POSSIBILITIES ITS DNA IS CAPABLE OF MAKING.
MORE THAN 200 CORONAVIRUS VACCINES ARE IN DEVELOPMENT ACROSS THE WORLD.. THIS IS A VERITABLE WILD GOOSE CHASE
CONTINUED TO 2--- TO MAKE AN EFFECTIVE VACCINE MORE QUICKLY AGAINST NEVER-BEFORE-SEEN, FAST-SPREADING VIRUSES SUCH AS SARS-COV-2, WE MUST NOW EXPLORE ALTERNATE APPROACHES USING GENE BASED TECHNOLOGY ( MRNA VACCINES ) WHICH REQUIRES FREEZERS CAPABLE OF COOLING TO 80 DEG C...
IT IS TIME TO GO BACK TO THE DRAWING BOARD, ESPECIALLY WHEN COVID-19 HAS TOO MANY SYMPTOM INCLUDING LOSS OF SMELL/ TASTE EVEN WITH VINEGAR..
INSTEAD OF PROTEINS, MRNA VACCINES, WILL CARRY THE MOLECULAR INSTRUCTIONS TO MAKE THE PROTEIN.
GENETIC APPROACHES IN ADDITION TO ELICITING ANTIBODIES AND CD4+ HELPER T CELLS, THEY RECRUIT KILLER T CELLS, THROUGH THE MAJOR HISTOCOMPATIBILITY CLASS I PATHWAY.
THE PREMISE OF ANY VACCINE IS TO INDUCE A LONG-LIVED IMMUNE “MEMORY” IN THE FORM OF B AND T CELLS.
UPON ANY ENCOUNTER WITH A PATHOGEN (WHICH CAN BE BACTERIA OR VIRUSES), THESE CELLS WILL RECOGNISE THE DANGER AND FIGHT IT OFF BY DESTROYING THE PATHOGEN AND PATHOGEN-INFECTED CELLS.
THE DANGER SIGNAL TAKES THE FORM OF AN ANTIGEN, A MOLECULE THAT NOTIFIES THE IMMUNE SYSTEM OF A PATHOGEN. FOR SARS-COV-2, THE ANTIGEN TARGETED BY B AND T CELLS IS USUALLY A PROTRUDING SPIKE PROTEIN ON THE SURFACE OF THE VIRUS.
THE CHALLENGE IN VACCINATION IS INDUCING THIS RESPONSE, WHICH REQUIRES A HANDSHAKE BETWEEN AN ANTIGEN-PRESENTING CELL AND A SPECIFIC TYPE OF T CELL, WITHOUT GETTING PEOPLE SICK.
IT’S THE ANTIGEN PEPTIDE (SMALLER SECTIONS OF ANTIGEN MOLECULE) PRESENTED IN THIS INTERACTION THAT DETERMINES THE TARGET OF THE IMMUNE RESPONSE.
FOR SARS-COV-2, THE SURFACE SPIKE PROTEIN IS THE MOST COMMON TARGET TO BE TESTED FOR VACCINES.
INSERT MRNA INTO CELLS, WHICH IS TRANSLATED INTO THE EXACT PROTEIN ANTIGENS DESIGNED FOR THE IMMUNE RESPONSE. INSTEAD OF MANUFACTURING INACTIVATED VIRUS, VIRAL CARRIERS, OR PROTEINS, MANUFACTURE THESE RNA SEQUENCES.
AFTER DELIVERY, A PERSON’S CELLS ACT AS THE FACTORY, NO VIRUS NECESSARY.
BY ENABLING THE CELLS TO GENERATE THE ANTIGENS, IT AVOIDS THE COSTLY, DIFFICULT PURIFICATION OF PROTEINS AND EQUIPS THE PROTEINS WITH TYPICAL FEATURES VIRAL PROTEINS HAVE, LIKE SURFACE SUGARS AND THE CORRECT 3D SHAPE.
PROTEIN-BASED VACCINES DELIVER THE IMMUNE SYSTEM–STIMULATING ANTIGEN TO THE BODY.
BUT GENE-BASED VACCINES TAKE A DIFFERENT TACK.
THEY CARRY THE GENETIC INSTRUCTIONS FOR THE HOST’S CELLS TO MAKE THE ANTIGEN, WHICH MORE CLOSELY MIMICS A NATURAL INFECTION. IN THE CASE OF CORONAVIRUSES, THE ANTIGEN OF INTEREST IS THE SURFACE SPIKE PROTEIN THE VIRUS USES TO BIND AND FUSE WITH HUMAN CELLS.
YOU’RE NOT GIVING THEM THE PROTEIN—YOU’RE GIVING THEM THE GENETIC MATERIAL THAT THEN INSTRUCTS THEM HOW TO MAKE THAT SPIKE PROTEIN, TO WHICH THEY MAKE AN ANTIBODY RESPONSE THAT IS PROTECTIVE,
MRNA STANDS FOR MESSENGER RIBONUCLEIC ACID. IT’S A MOLECULE THAT’S COPIED FROM DNA IN A CELL’S NUCLEUS AND USED AS THE CODE FOR MAKING A SPECIFIC PROTEIN. .
THIS VACCINE CANDIDATE RELIES ON INJECTING SNIPPETS OF A VIRUS’S GENETIC MATERIAL, IN THIS CASE MRNA, INTO HUMAN CELLS. THEY CREATE VIRAL PROTEINS THAT MIMIC THE CORONAVIRUS, TRAINING THE IMMUNE SYSTEM TO RECOGNIZE ITS PRESENCE.
WITH AN MRNA VACCINE, THE IDEA IS TO GET A SEGMENT OF MRNA THAT CODES FOR A SPECIFIC VIRAL PROTEIN INTO A CELL.
FOR VACCINE DEVELOPERS, THAT MEANS THAT INSTEAD OF GOING THROUGH THE TEDIOUS PROCESS OF ISOLATING AND PURIFYING SUBUNITS OF A VIRUS, THEY CAN JUST CHANGE THE CODE IN A STRAND OF MRNA.
THAT MAKES THE DEVELOPMENT PROCESS MUCH FASTER THAN CONVENTIONAL APPROACHES, WHICH CAN TAKE YEARS.
ONE OF THE CHALLENGES WITH USING MRNA IS THAT YOUR BODY CAN PERCEIVE IT AS A THREAT, AS MANY VIRUSES USE RNA TO ENCODE THEIR GENOMES. THERE ARE A LOT OF ENZYMES IN THE BODY THAT CAN READILY DIGEST RNA BEFORE IT GETS INTO A CELL. THERE ARE EVEN RNA-DIGESTING ENZYMES ON YOUR SKIN.
ONCE THE MRNA IS CODED, MODIFIED, AND ENCAPSULATED, IT CAN THEN BE INJECTED.
capt ajit vadakayil
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- https://timesofindia.indiatimes.com/world/us/us-says-it-wont-join-global-effort-to-find-covid-19-vaccine/articleshow/77881300.cms
PART OF THE KEY TO SAVING THE LIVES OF COVID-19 PATIENTS MAY NOT JUST HINGE ON ATTACKING THE VIRUS, BUT LIMITING THE BODY’S RESPONSE TO IT.
THE FIRST THING TO DO IS TO SACK THE ETHIOPIAN WHO CHIEF, A SLAVE OF BILL GATES ( THIRD WORLD DEPOPULATION KING PIN ) , THE BIGGEST DONOR TO WHO..
WHO IS BARKING UP THE WRONG TREE..
WHO MEMBERS ARE IN THE PAYROLL OF KOSHER EVIL PHARMA, WHO IS HELL BENT ON MAKING VACCINES TO HOLD THE PLANET IN THEIR KOSHER VICE GRIP..
EVEN A HALF WIT CAN FIGURE OUT THAT THAT A VARIETY OF NEUROLOGIC MANIFESTATIONS CHARACTERIZE COVID 19 PANDEMIC...
ALTHOUGH INITIALLY CONSIDERED A RESPIRATORY DISEASE, COVID-19 ACTUALLY AFFECTS A WIDE RANGE OF ORGAN SYSTEMS, INCLUDING THE CNS..
SARS COV2 IS A LAB MADE SPLICED/ GRAFTED SINGLE-STRANDED RNA-ENVELOPED VIRUS VIRUS WITHOUT A SOUL...
THE ETIOLOGICAL AGENT OF COVID-19, THE SEVERE ACUTE RESPIRATORY SYNDROME CORONAVIRUS 2 (SARS-COV-2), EXHIBITS NEUROTROPISM FOR CENTRAL AND PERIPHERAL NERVOUS SYSTEMS
THIS TERM NEUROTROPISM IS USUALLY USED TO DESCRIBE THE ABILITY OF VIRUSES TO INFECT NERVE TISSUE.
SINCE SARS-COV-2 TARGETS BLOOD VESSELS, PATIENTS WITH PRE-EXISTING DAMAGE TO THOSE VESSELS, SUCH AS FROM DIABETES AND HIGH BLOOD PRESSURE, FACE A HIGHER RISK OF SERIOUS DISEASE.
GOLD NANOPARTICLES CAN BE USED AS ADJUVANTS TO INCREASE THE EFFECTIVENESS OF VACCINES BY STIMULATING ANTIGEN-PRESENTING CELLS AND ENSURING CONTROLLED ANTIGEN RELEASE..
EVIL KOSHER PHARA DOES NOT WANT TO HEAR ABOUT GOLD NANO COLLOID USE TO DETECT/ PREVENT/ CURE COVID 19..
MY POST OF NANO GOLD COLLOID WAS DELETED BY THE AGENT OF KOSHER EVIL PHARM, GOOGLE..
GOLD NANO PARTICLES HAVE BEEN USED TO PREPARE ANTIBODIES AND VACCINES AGAINST MORE THAN 46 PATHOGENS OF VIRAL, BACTERIAL, AND PARASITIC INFECTIONS.
GNP IS PART OF 600 YEAR OLD AYURVEDIC CURE..
VARIOUSLY SHAPED GNPS HAVE BEEN USED, INCLUDING NANOSPHERES, NANORODS, NANOCAGES, NANOSTARS, NANOCUBES, NANOSHELLS, NANOPRISMS, AND NANOCLUSTERS. THE BEST EFFECT IS ACHIEVED WITH GOLD NANOSPHERES AS ANTIGEN CARRIERS.
CONJUGATION HAS BEEN CARRIED OUT BOTH BY PHYSICAL ADSORPTION AND BY CHEMISORPTION. PASSIVE ADSORPTION OF AN ANTIGEN ON THE PARTICLE SURFACE OCCURS BECAUSE OF THE ELECTROSTATIC AND HYDROPHOBIC INTERACTIONS. .
GNPS HAVE BEEN CONJUGATED TO PROTEIN OR POLYSACCHARIDE LINKERS BEFORE BEING FUNCTIONALIZED WITH AN ANTIGEN. GOLD GLYCONANOPARTICLES HAVE BEEN USED AS IMMUNOMODULATORS.
WE MUST USE GOLD NANO PARTICLES . TO BLOCK THE S SPIKE PROTEIN FROM INTERACTING WITH THE ACE2 RECEPTOR.
https://ajitvadakayil.blogspot.com/2020/05/covid-19-pandemic-sars-cov-2.html
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GOLD NANOPARTICLES DESIGNED TO MIMIC VIRUSES WITH ENGINEERED NANOSCALE MORPHOLOGY , MULTIVALENT ANTIGENS , AND COLONIZING ANTIGENS/ADJUVANTS (DANGER SIGNALS); USING A SINGLE NANOPARTICLE MAY PROMOTE IMMUNE RESPONSES VIA ANTIGEN PROCESSING AND IMMUNE SYSTEM ENGAGEMENT
NANOSCALE VLPS ( VIRUS LIKE PARTICLE ) WITH VIRAL CHARACTERISTICS ARE TRANSPORTED BETTER THROUGH THE LYMPHATICS AND CAPILLARIES IN COMPARISON WITH SMALLER SUBUNIT VACCINES .
THIS IMPROVES CELLULAR UPTAKE AND REDUCES THE SYSTEMIC INFLAMMATORY RESPONSE BESIDES, THE ABILITY TO DELIVER MULTIPLE ANTIGENS PROMOTES ANTIGEN-PRESENTING CELL OR ACCESSORY CELLS TO FUNCTION MORE EFFECTIVELY,
T CELL RECEPTORS CAN RECOGNIZE THE SYNTHESIZED COMPLEXES THAT INCREASE IMMUNOGENICITY AND POTENCY OF THE VACCINE, WHICH COULD PROTECT THE SAFETY AND WELFARE OF THE PATIENTS
INNATE IMMUNE SYSTEM ACTIVATION AND BETTER CELLULAR UPTAKE OF VLPS, CONSISTING OF RECOMBINANT VIRAL ANTIGENS AND ADJUVANTS, CAN ENHANCE THE EFFECTS OF THE COMPLEMENT CASCADE TO ATTACK PATHOGENS AND THE PRESENTATION TO FOLLICULAR DENDRITIC CELLS, WHICH LEAD TO B CELL ACTIVATION AND POTENTIATION OF THE IMMUNE SYSTEM BY INDUCING PROACTIVE IMMUNE RESPONSES AGAINST VIRAL INFECTIONS.
CONTINUED TO 2 --
- https://www.hindustantimes.com/india-news/serum-institute-denies-reports-indians-to-get-free-shots-of-covid-19-vaccine-in-73-days/story-i5loiapg3c4kb5j9tfxuun.html
WE THE PEOPLE WARN THE BILLIONAIRE POONAWALAS ( EX RACING STUD HORSE SERUM MANUFACTURERS ) WHO DID A CLANDESTINE POLE VAULT FROM HORSES TO HUMANS.. ..
DO NOT USE INDIANS AS GUINEA PIGS FOR UNTESTED DANGEROUS VACCINES..
WE KNOW WHY BILL GATES AND PRINCE CHARLES TREAT PUNE SERUM INSTITUTE AS THE TAJ MAHAL..
COVID-19 AFFECTS THE BRAIN VIA BREACH OF BLOOD BRAIN BARRIER.. A BIG PERCENTAGE OF RECOVERED PATIENTS HAVE LOSS OF SMELL AND TASTE..
EXPERIMENTS CANNOT BE DONE ON LAB RATS.. YOU SEE CONSCIOUS HUMAN BRAINS ..
MODIFYING MICE TO CARRY HUMANISED ACE2 GENES IS PURE BULLSHIT
WE KNOW HOW HPV VACCINES WERE USED ON INDIAN SCHOOL GIRLS WITHOUT PARENTAL PERMISSION..
WE KNOW WHO ALL WERE BRIBED AND WHO ALL WENT FOR PEDOPHILE SEXUAL JAUNTS TO BANGKOK AND AMSTERDAM..
http://ajitvadakayil.blogspot.com/2016/03/say-no-to-hpv-vaccination-for-indian.html
AFTER CLANDESTINE TRIALS ON INDIAN SCHOOL GIRLS GARDASIL WAS FAST-TRACKED TO THE MARKET, ACHIEVING FDA APPROVAL IN SIX MONTHS, WHICH USUALLY TAKES FOUR YEARS..
THE CLINICAL TRIALS MERCK CONDUCTED FOR THE GARDASIL HPV VACCINE WERE FLAGRANTLY DECEPTIVE AND UNSCIENTIFIC.
CLINICAL TRIALS (HUMAN TESTING) THAT VICTIMS ALLEGE WERE FRAUDULENTLY CONDUCTED AND REPORTED. AND THEN INDIAN CHOOL GIRL ERE UED AS LAB RATS
THE RATE OF GARDASIL DEATHS IN THE CLINICAL TRIALS WAS 9 PER 10,000, NEARLY DOUBLE THE BACKGROUND U.S. DEATH RATE FOR YOUNG WOMEN AGES 15 TO 20.
CLINICAL TRIAL SUBJECTS RECEIVED ALUMINUM-CONTAINING ADJUVANTS, CHEMICAL MIXTURES, AND OTHER VACCINES, WHICH MASKED ADVERSE EVENTS AND MADE GARDASIL SEEM SAFER THAN IT WOULD HAVE OTHERWISE.
GARDASIL INGREDIENTS INCLUDED VIRUS LIKE PARTICLES (VLPS) WHICH ARE GENETICALLY ENGINEERED FROM A PROTEIN OF HPV TYPES 6, 11, 16, 18 (AND GARDASIL 9 INCLUDES ADDITIONAL TYPES: 31, 33, 45, 52, AND 58); AMORPHOUS ALUMINUM HYDROXYPHOSPHATE SULFATE (AKA, AAHS); YEAST PROTEIN; SODIUM CHLORIDE; L-HISTIDINE; POLYSORBATE 80; SODIUM BORATE; AND WATER FOR INJECTION. AS YOU CAN SEE, EACH GARDASIL SHOT CONTAINS INGREDIENTS IN ADDITION TO THE GENETICALLY MODIFIED VIRUS LIKE PARTICLES. THESE INGREDIENTS ARE CAPABLE OF CAUSING ADVERSE REACTIONS IN THEIR OWN RIGHT WHICH INCLUDES LOSS OF FERTILITY
NEW BORN INDIAN BABIES WERE INJECTED WITH FLU SHOTS HAVING DANGEROUS ALUMINIUM ADJUVANTS REDUCING THEIR BRAIN POWER.. IN INDIA WE TREAT FLU LIKE COMMON COLD..
READ ALL 4 PARTS OF THE POST BELOW--
http://ajitvadakayil.blogspot.com/2017/05/flue-shots-pneumococcal-vaccines-capt.html
THE VACCINE ADVERSE EVENTS REPORTING SYSTEM (VAERS) WAS ESTABLISHED IN 1990 AS A MEANS OF DETECTING PROBLEMS IN VACCINES. THE KOSHER SYSTEM IS MANAGED BY THE FDA AND THE CENTERS FOR DISEASE CONTROL AND PREVENTION (CDC) ALL BRIBED BY THE DEEP STATE...
THE VAERS DATABASE CONTAINS OVER 53,000 CASE REPORTS OF ADVERSE REACTIONS TIED TO HPV VACCINES IN USA ALONE.
ONLY 0.07 % OF SERIOUS ADVERSE EVENTS ARE ACTUALLY REPORTED TO VAERS.
GARDASIL SIDE EFFECTS:--
ACUTE DISSEMINATED ENCEPHALOMYELITIS
ARTHRITIS
AUTO-IMMUNE DISORDERS
BIRTH DEFECTS
CERVICAL INTRAEPITHELIAL NEOPLASIA – CIN 2/3
CHRONIC FATIGUE SYNDROMES
CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY (CIDP)
CHRONIC PAIN SYNDROMES
COMA
DEATHS
EPILEPSY (SEIZURE DISORDER)
FIBROMYALGIA
GUILLAIN-BARRE SYNDROME
HEART PROBLEMS, INCLUDING SEVERE ARRHYTHMIA AND HEART ATTACKS
INFLAMMATORY DISORDERS
INTERCONNECTIVE TISSUE DISORDER
LUPUS
MISCARRIAGE
MOVEMENT DISORDERS
MULTIPLE SCLEROSIS
NEUROLOGICAL DISORDERS
PARALYSIS
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME (POTS)
PULMONARY EMBOLISM
REPRODUCTIVE DISORDERS, INCLUDING PREMATURE OVARIAN FAILURE
RHEUMATOLOGICAL DISORDERS
SMALL FIBER NEUROPATHY
STROKE
Capt ajit vadakayil
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TO BE CONTINUED --
CAPT AJIT VADAKAYIL
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CAPT AJIT VADAKAYIL DECLARES
SOME TOP SHOTS OF NCB NARCOTICS CONTROL BUREAU ARE IN THE PAYROLL OF THE JEWISH DEEP STATE WHO SPONSORS KOSHER EVIL PHARMA
IF NON ADDICTIVE MEDICAL CANNABIS/ MAJIJUANA IS DECRIMINALIZED EVIL PHARMA WILL SHUT DOWN.
WHY IS NCW AFTER CANNABIS? WHY HAVE THEY GONE OFF TANGENT SUDDENLY ?
CANNABIS IS BAD ONLY IF IT HAS BEEN SOAKED IN ADDICTIVE SYNTHETIC DRUGS.. FOR EXAMPLE DOOB….
BHANG WE CONSUME ON HOLI IS NOT SOME INJECTABLE ADDICTIVE DRUG LIKE HEROIN.
COFFEE AND NICOTINE IS MORE ADDICTIVE THAN MARIJUANA.
http://ajitvadakayil.blogspot.com/2012/10/say-no-to-plastics-human-suffering-and.html
NATURAL NON ADDICTIVE CANNABIS IS SHIVAs BOUNTY FOR INDIA..
ORDINARY CANNABIS GROWN IN SUNLIGHT IS NOT ADDICTIVE..
INDICA STRAINS ARE RELAXING, SLOW DOWN HEART BEAT, THEY KILL THE EGO AND REDUCE FIGHT AND FLIGHT REFLEX -- PERFECT FOR PTSD SUFFERING US WAR VETERANS..
WE USE INDICA CANNABIS BHANG MIXED WITH MILK ON FESTIVAL HOLI.. IT CAUSES ENEMIES TO BECOME FRIENDS.. HOLI FESTIVAL IS A GREAT LEVELER..
http://ajitvadakayil.blogspot.com/2013/03/holi-celebrations-immoral-attack-on.html
WE DONT USE SATIVA STRAIN IN INDIA, WHICH IS AN UPPER-- IT INCREASES HEART BEAT ..
CBD (CANNABIDIOL) AND THC (TETRAHYDROCANNABINOL) ARE THE MOST COMMON CANNABINOIDS FOUND IN CANNABIS PRODUCTS.
ALTHOUGH BOTH CBD AND THC SHARE A SIMILAR MOLECULAR FORMULA, CBD DOES NOT INDUCE ANY SORT OF PSYCHOACTIVE EFFECTS ON THE USER.
CANNABIDIOL CAN BE EXTRACTED FROM BOTH INDUSTRIAL HEMP AS WELL AS MARIJUANA; HOWEVER, THE MAJORITY OF CBD MADE FOR PURCHASE IN THE US TODAY IS EXTRACTED FROM INDUSTRIAL HEMP.
THIS IS BECAUSE THE FEDERAL RULING STATES THAT ALL HEMP PLANTS THAT ARE USED FOR CBD EXTRACTION MUST MEET THE CRITERIA OF CONTAINING LESS THAN 0.3 PERCENT THC IN THE ENTIRETY OF THE PLANT..
MARIJUANA PLANTS WILL CONTAIN HIGHER CONCENTRATIONS OF THC, MAKING EXTRACTION AND SALE OF CBD FROM THESE PLANTS ILLEGAL IN MOST STATES AS WELL AS ILLEGAL ON A FEDERAL LEVEL.
EVIL KOSHER PHARMA WANTS TO MONOPOLIZE THC AND MINT MONEY..
THC AND CBD ARE IN BOTH MARIJUANA AND HEMP. MARIJUANA CONTAINS MUCH MORE THC THAN HEMP, WHILE HEMP HAS A LOT OF CBD.
CBD AND THC HAVE THE SAME CHEMICAL FORMULA -- 21 CARBON ATOMS, 30 HYDROGEN ATOMS, AND TWO OXYGEN ATOMS. THE DIFFERENCE LIES IN THE WAY THE ATOMS ARE ARRANGED.
THAT GIVES CBD AND THC DIFFERENT CHEMICAL PROPERTIES, AND THEY AFFECT YOUR BODY DIFFERENTLY.
EVEN TODAY NOBODY KNOWS ABOUT THE JEWISH SACKLER FAMILY ( PURDUE EVIL PHARMA ) TO ADDICTED AMERICA WITH OPIOD DRUGS..
https://en.wikipedia.org/wiki/Sackler_family
AS YOU GET TOLERANT TO OXYCONTIN ( HIGHLY ADDICTIVE OPIUM BASED DRUG ) TABLETS, PEOPLE GRADUATED TO CHEAPER HEROIN INJECTIONS..
THERE WAS A NEXUS BETWEEN KOSHER EVIL PHARMA AND THE AMERICAN DRUG RUNNERS..
NOW EVIL PHARMA IS TAKING OVER MEDICAL MARIJUANA IS AMERICA.. POP AND MOM STORES IN CALIFORNIA HAVE CLOSED DOWN..
CONGRESSMEN AND SENATORS IN EVIL PHARMA PAYROLL KEEP THE LICENCING FEES TOO HIGH , SO THAT BIG KOSHER FISH CAN DRIVE AWAY SMALL CHRISTIAN POP AND MOM FISH AWAY FROM THE CANNABIS MARKET..
CANNABIS IS NOW BEING GENETICALLY MODIFIED TO SUIT THE EVIL INTERESTS OF BIG PHARMA ...
THESE STRAINS ARE GROWN INDOORS IN HUGE WAREHOUSE BUILDINGS WITH ARTIFICIAL LIGHTS TO CONTROL GROWTH AND HAVE MORE HARVESTS IN A YEAR..
https://www.youtube.com/watch?v=TtJ0yoiJWfs
ADDICTIVE VOLATILE CANNABIS OILS ARE CREATED ..
https://www.youtube.com/watch?v=urBi1xewboE
NCB BE WARNED.. WE KNOW THE TRAITORS IN FOREIGN PAYROLL.. JAIL AWAITS YOU..
YOU MUST STRICTLY STICK TO ADDICTIVE DRUGS ..
Capt ajit vadakayil
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