«VACCINOSIS» IS THOUSANDS OF TIMES WORSE THAT COVID DISEASE — THE TERRIBLE AUTO IMMUNE EFFECTS WILL BE SEEN ONLY AFTER 20 YEARS.
PFIZER mRNA VACCINE IS ZERO PERCENT EFFECTIVE . When someone dies in covid hospitals , he is branded as “UNVACCINATED”. When someone walks after of hospital after a stay, he is branded “VACCINATED” .Actually god saved that person. In December 2020, the US FDA issued “emergency use ONLY “authorization for mRNA vaccines”.
Developed by Pfizer-BioNTech and Moderna, making them the first mRNA vaccines available to the public. HUGE BRIBES WENT AROUND. The foul propaganda was that mRNA vaccines differ from other approaches – teaching our cells to become autonomous vaccine production plants – and offering benefits of speed of production and the ability to keep up with new variants.
The propaganda was that Pfizer vaccines work by training our bodies to recognize invading viruses. Even a dimwit will say that Sars Cov-2 virus mutates, and that too in a vaccinated individual. Because the vaccinated person’s body is a devil’s workshop for mutation of this lab made virus. in the case of Moderna’s and Pfizer-biontech's mRNA vaccines, people are not injected with a whole virus or even a piece.
Instead, they are supplied mRNA that instructs their body cells to make a version of the Sars-Cov-2 spike protein. These instructions teach the cells to become their own vaccine manufacturing plants. Indeeed the “devil’s workshop”.
Israel’s stock of Pfizer vaccines are all expired/ spoint due to poor cold storage. They are desperate to sell it to other nations at half price. Side effects for mRNA vaccines kick in after several years .In the case of Mad Cow disease, i wrote eight years ago that the long incubation period for Variant Creutzfeldt Jacob Disease, is because PRIONS take that long.Today a lot of english people are silent carriers of Variant Creutzfeldt-Jakob Disease protein PRION .
Though the incubation period is long and death may occur years later , the people become dimwits. the incubation period of Variant Creutzfeldt-Jakob Disease in humans takes decades. The incubation period of PRION diseases is very long as compared with other common diseases.
mRNA VACCINES CAUSE PRION DISEASES
WHEN MARGARET THATCHER STARTED FEEDING COWS IN BRITAIN WITH WASTE MEAT WITH REAGAN’S CONNIVANCE ( BOTH WERE DEEP STATE AGENTS )
“YOU WILL HAVE TO EXTERMINATE 100% OF YOUR COWS AND THEN CREMATE THE CARCASSES. IF YOU BURY , THEN YOUR GROUND WATER WILL BE CONTAMINATED BY PRIONS“
Well, this legacy of the mad cow has now grown ugly, because the incubation periods are long.
»ΟΙ ΤΡΕΛΕΣ ΑΓΕΛΑΔΕΣ». μετά από πολύ καιρό «ωρίμανσης« στο ανθρώπινο σώμα ,παρουσιάζονται τώρα οι αρρώστιες στον άνθρωπο. ΟΙ ΑΓΕΛΑΔΕΣ ΣΤΗΝ δύση ΔΕΝ ΕΙΝΑΙ χορτοφάγα !!
Bovine spongiform encephalopathy( BSE)1988
By September 1989, Israel ( with Rothschild’s input ) and Australia had banned British beef imports; the US had done so in 1988. Up to this time, most of the British public were blissfully unaware of mad cow disease and continued to eat beef from BSE-infected cows. In November 1989, due to pressure from abroad, Britain banned the export of cattle innards.
COWS HAVE A DIGESTIVE SYSTEM WHICH CONVERTS GREEN GRASS ( ON ORGANIC SOIL ) TO COPIOUS WHITE MILK..
THE SYSTEM CANNOT HANDLE MEAT AND THAT TOO WASTE COW ENTRAILS.. IT CANT EVEN HANDLE THE OIL CAKES FED TO THEM.. COWS DON’T NEED OIL CAKE SUPPLEMENTS..
IT FORCED THE COW TO BE A CANNIBAL. GOD DOES NOT ALLOW THIS.
( Έτσι, οι επιχειρηματίες Δυτικοί αγρότες αλέθουν αυτά τα απόβλητα και τα ταΐζουν στις αγελάδες τους. Αυτές οι ανίσχυρες αγελάδες στη Δύση τρώνε όχι μόνο το δικό τους, αλλά και το φαγητό. Τρέφονται επίσης με μια συνεχή διατροφή απορριμμάτων πουλερικών.)
A “VACCINOSIS “ RELATED INCREASE IN VARIANT CREUTZFELDT-JACOB DISEASE (VCJD), A PRION DISEASE (OR PROTEIN MISFOLDING DISEASE) COMPARABLE TO MAD COW DISEASE.
PRION PROTEINS CAN SEED OTHER UNRELATED PROTEINS TO MISFOLD. THERE IS A LIST OF PROTEINS THAT WILL “CATCH THE DISEASE” WHEN THERE IS A PRION OR PRION-LIKE PROTEIN NEAR THEM, THAT MISFOLDS IN A CHARACTERISTIC WAY CALLED “BETA-SHEETS.”
PROTEIN FOLDING IS ESSENTIAL FOR LIFE, AS PROTEINS SERVE STRUCTURAL ROLES, CATALYZE ENZYMATIC REACTIONS, AND TRANSPORT MATERIALS THROUGH MEMBRANES AND CELLS, AMONG MANY OTHER FUNCTIONS..
On February 21, the BBC World Service aired an interview with a South Korean parliamentarian who expressed concerns that the Swiss and German governments are planning to export beef that could be BSE-infected to starvation stricken North Korea on "humanitarian grounds". Welcome to the brave new world of globalisation and trade without borders.
A unquantified large number of British people today carry the Variant Creutzfeldt-Jakob Disease protein Prion.
Below : Scan of original document signed by Rothschild stooge Allen Welsh Dulles longest serving Director of CIA, ( brother of John Foster Dulles, Dwight D. Eisenhower's Secretary of State). Magsaysay award is controlled by Rothschild's agent Ford.
Allen W Dulles represented I.G. Farben the German chemical manufacturer whose secretary to board of Directors was Bernhard von Lippe who founded the Bilderberg Group in 1954 with Rothschild . Allen W Dulles hooked up with George Herbert Walker, Prescott Bush’s father-in-law to finance the purchase of the Hamburg Amerika Line, a steamship company for Dulles’ client I.G. Farben.
Every since scientists found out the Prions, a protein cause the human variant of Mad Cow disease , the CREUTZFELDT JACOB DISEASE, they have been in a quandary. For Prions cannot be destroyed by fire, freezing, strong disinfectants, sterilization procedures, incineration, intense radiation etc.
Below: Rothschild's stooges both-- refused to heed critical Risk Assessment reports.
By covering up the mad cow disease Margaret Thatcher was re-elected for a third term in 1987 and was PM till November 1990. These two criminals protected the the gigantic billion dollar meat industry of BIG BROTHER rather than their people who elected them.
Bone char—often referred to as natural carbon—is widely used by the sugar industry as a decolorizing filter, which allows the sugar cane to achieve its desirable white color.
Cow bone meal in them , ground up and added to it as a whitening agent?
The VCJD OR variant Creutzfeldt-Jakob disease related disease can incubate for probably 50 years, as per some scientists. Prions only seem to more concentrated in nervous system tissue. . In the brain, these proteins cause native cellular prion protein to deform into the infectious state, which then goes on to deform
further prion protein in an exponential cascade. This results in protein aggregates, which then form dense plaque fibers, leading to the microscopic appearance of "holes" in the brain, degeneration of physical and mental abilities, and ultimately death.
The normal form of the protein is called PrPC, while the infectious form is called PrPSc — the C refers to 'cellular' or 'common' PrP.
Just don’t expect the Evil Pharma controlled human and Big Brother controlled government to tell you any of this.
***** mRNA COVID-19 VACCINES LEAD TO PRION DISEASE vaers is criminally hiding the truth that most mRNA vaccinated people exhibit Alzheimer's type dementia, multiple sclerosis, amyotrophic lateral sclerosis (als), frontotemporal lobar degeneration (FTLD), and other types of neurodegeneration Variant Creutzfeldt-Jakob Diseases .
Read this line twice. Who/ US CDC lies that mRNA from vaccines can’t modify human DNA because it doesn’t enter the cell nucleus, where DNA is stored. These bribed/ honey trapped people tell what the Kosher vaccine Lobby tells them to. They lie that mRNA vaccines cannot cause long-term effects in humans because RNA is quickly broken down by the cell after it provides the cell with instructions to make the protein.
Tee heeeee! Can't even lie properly. PRIONS are misfolded proteins. Misfolded proteins have also been implicated in a number of other human neurological diseases, including Alzheimer’s, Parkinson’s and Huntington’s. Human PRION diseases are conceivably the most heterogeneous neurodegenerative disorders.
Two proteins central to the pathology of Alzheimer's disease act as PRIONS — misshapen proteins that spread through tissue like an infection by forcing normal proteins to adopt the same misfolded shape.You cannot do PRION experiments in non-humans ( non-conscious ) who cannot see themslves in a mirror or see colour.
Ameloid in brain is s formed from the breakdown of a larger protein, called amyloid precursor protein. One form, Beta-Amyloid 42, is thought to be especially toxic. In the Alzheimer's brain, abnormal levels of this naturally occurring protein clump together to form plaques that collect between neurons and disrupt cell function.
Magnetic Resonance Imaging (MRI) theoretically provides the spatial resolution needed to resolve amyloid-β plaques. Type I interferon (IFN-A and IFN-B) genes encode a large family of multifunctional secreted proteins involved in antiviral defence, cell growth regulation and immune activation.
IFN-A is a multifunctional immunomodulatory cytokine with profound effects on the cytokine cascade including several anti-inflammatory properties. Different RT-PCR cycles are used for vaccinated ( 25 cycles ) and unvaccinated ( 45 cycles )..People.. If you hold a mango in your hand it will test positive at 45 cycles.
VEARS IS INVOLVED IN THIS CRIME AGAINST HUMANITY . All cry—this is not peer reviewed. Who cares for per review !! WARNED MARGARET THATCHER AND RONALD REAGAN : ”DO NOT ALLOW CRIMINALS .TO EAT WASTE MEAT. BOTH REAGAN AND THATCHEFR DIED OF VARIANT CREUTZFELDT-JAKOB DISEASE—CLOAKED AS ALZHIEMERS.
THERE IS NO CURE VARIANT CREUTZFELDT-JAKOB DISEASE. PRIONS are virus-like organisms made up of a PRION protein. These elongated fibrils (green) are aggregations of the protein that makes up the infectious PRION . PRIONS attack nerve cells producing neurodegenerative brain disease. PRIONS are protein-containing biological agent that could replicate itself in living cells without nucleic acid. human PRIONS bind to neighboring normal proteins in the brain and create microscopic holes. PRIONS, therefore, turn brains into sponge-like structures and lead to dementia and death.
The folding of TDP-43 and FUS into their pathologic PRION confirmations causes als, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases. regulatory approval of the RNA based vaccines for Sars-Cov-2 ( by bribed / honey trapped scientists ) was premature and that the vaccine may cause much more harm than benefit.
PRIONS cannot be destroyed by fire, freezing, strong disinfectants, sterilization procedures, incineration, intense radiation etc. To destroy a PRION it must be denatured to the point that it can no longer cause normal proteins to misfold. sustained heat for several hours at extremely high incinerator temperatures 600 deg c may destroy a PRION. Such incinerators must have approved refractory and oxygen assisted swirling burners. people who dies of PRION diseases must be crameted—never buried.
Modern medicine treats the symptoms only. modern medicine ( allopathy ) is a disease care system and its job is to manage the disease. It is a stupid symptom suppressor. so in reality, most drugs / vaccines never really take care of the problem. Scientists think that PRION is the cause of the disease. The truth is that it is the result of the diseased tissue and not the cause.
The human body can produce friendly bacteria and viruses to combat hostile agents.. This means PRIONS are actually the "clean-up crew", formed by the body, to get rid of the toxic mess inside the body to cleanse it. We have been taught in school that germs cause disease. But germs don't cause disease anymore than flies cause garbage. Garbage causes flies , not vice versa. dead parsi bodies attract vultures to the tower of silence.
Vultures do not attract a dead parsi . I am afraid only such an example can make people think better. the body can produce its own "cleansing" agents such as a prions when the need arises. in the case of mad cow disease, humans have ingested these PRIONS by eating the flesh of the infected cow—fed with minced and putrid dead animal and parts. when these “clean up crew” start cleaning out the toxins in the body, the toxins are dumped into the blood stream to be filtered and eliminated from the body.
These toxins then cause symptoms which the doctor diagnoses as "disease" and the doctor then names the disease according to the symptoms it produces. have you seen the way the modern doctors call every disease genetic for which they do not know the cause.
The human body cures itself , not the pharma medicines/ vaccines pumped in. good doctors will not prescribe antibiotics for viral diseases.
Lichens were used to embalm the pharaoh’s body along with cinnamon. probably lichens can downgrade PRIONS . A lot of white men who died of so called "alzhiemers " in their death certificates-have died to absorbing deadly indestructible PRIONS from soft gels which they use in capsules like for Ωmega 3 fatty acids and surgical sutures.
PRIONS only seem to more concentrated in nervous system tissue. . in the brain, these proteins cause native cellular PRION protein to deform into the infectious state, which then goes on to deform further PRION protein in an exponential cascade.This results in protein aggregates, which then form dense plaque fibers, leading to the microscopic appearance of "holes" in the brain, degeneration of physical and mental abilities, and ultimately death.
The abnormal PRION touches a normal PRION and changes the normal PRIO'S shape into an abnormal one, thereby destroying the normal PRION'S original function. the nerve cell tries to get rid of the abnormal PRIONS by clumping them together in small sacs that merge with its "stomach" (lysosome).
Because the nerve cells cannot digest the abnormal PRIONS , they accumulate in the lysosomes. The PRION mode of action is very different to bacteria and viruses as they are simply proteins, devoid of any genetic material. once a misfolded PRION enters a healthy person it converts correctly-folded proteins into the disease-associated form.
A PRION is neither a virus nor a bacteria. PRIONS are proteins that contain no DNA or ,RNA two substances previously felt to be essential for reproduction of a living tissue. the lysosomes grow and engorge the nerve cell, which eventually dies. when the cell dies, the abnormal PRIONS are released to infect other cells. large, sponge-like holes are left where many cells die. numerous nerve cell deaths lead to loss of brain function, and the person eventually dies.
None of the hospitals have adopted effective method of sterilizing surgical instruments contaminated with the human form of “mad cow” disease ,VCJD , just because it did not fit in with its established washing procedures. A lot of people have had their lives blighted by surgery performed with instruments contaminated the PRION protein responsible for VCJD — they did not eat the «mad cow» or have blood transfusions or whatever.
The lethal PRION protein, which sticks to the stainless steel of surgical instruments like superglue and can survive the high temperatures and sterilization procedures of hospital autoclaves. A lot of people in UK are silent carriers of the infectious long incubation PRION protein that causes Variant Creutzfeldt–Jakob Disease (VCJD).
Due to the long incubation period, the full extent of the human VCJD outbreak is still not known. the incubation period of the killer PRION will be as much as 50 years. Shocked? Yes, mRNA vaccine side efects take that long. It causes auto immune diseasse, down syndrome babies, homosexuality etc. Ozone sterilization must be studied as a potential method for PRION denaturation and deactivation.
Evil pharma will not like it though. Today people in USA and the west consume large amounts of pure virgin coconut oil daily to help combat alzheimer’s—all their false and immoral campaign against coconut oil has now officially ended. Cannabis can prevent PRIONS for incubating to dangerous levels. Cannabis can disrupt the progression of PRION disease Variant Creutzfeld-Jakob Disease as they can protects neurons against PRION toxicity.
DNA contains instructions which get re-written in RNA , and then the instructions in RNA get translated into protein. so changes in a person’s DNA can cause changes in the proteins their cells produce. Everyone has a gene called PrNP which codes for the protein called PrP , and most of the time this protein is perfectly healthy and fine.
Some people have mutations in the DNA of their PrNP gene, which cause it to produce mutant forms of PrP. These mutant forms don’t form PRIONS instantly, and most people with PrNP mutations live perfectly healthy for decades. PRIONS ,like viruses, are not actually alive, although both can reproduce by hijacking the functions of living cells. : the normal form of the protein is called PrPC , while the infectious form is called PrPSC — the C refers to 'cellular' or 'common' PrP.
But as people get older, the mutant forms of PrP are more and more likely to fold up the wrong way and form PRIONS . Once they do, the person has a rapid neurodegenerative disease like VCJD . Just don’t expect the evil pharma controlled and big brother controlled government to tell you any of this. they will sell expensive vaccines to you.
As early as 4200 bc, Charaka, the father of medicine , used cannabis leaves for osmosis hot water immersion baths for dementia he knew the anti-oxidative , neuro-protective and anti-inflammatory properties of cannabis. Thec is more effective at blocking clumps of protein that can inhibit memory and cognition in alzheimer’s patients.
TDP-43 OR FUS-INDUCED MISFOLDED HUMAN WILD-TYPE SOD1 CAN PROPAGATE INTERCELLULARLY IN A PRION-LIKE FASHION..
MISFOLDED HUMAN WILD-TYPE (HUWT) SOD1 HAS BEEN DETECTED IN BOTH FAMILIAL AND SPORADIC ALS PATIENTS.
PRIONS ARE INFECTIOUS PROTEINS THAT CAN CONVERT TO AN ALTERNATIVE CONFORMATION . THIS ALTERNATIVE CONFORMATION TYPICALLY HARBORS A REGION THAT ADOPTS THE AMYLOID FOLD. AMYLOID IS COMPRISED OF STACKED BETA SHEETS WHICH CAN TEMPLATE THE CONVERSION OF NATIVE PROTEIN TO THE AMYLOID FOLD..
TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES (TSES OR PRION DISEASES) OF INVARIABLY FATAL NEURODEGENERATIVE DISORDERS AFFECT HUMANS AND OTHER MAMMALS. TSES ARE PROTEIN MISFOLDING DISEASES THAT INVOLVE THE ACCUMULATION OF AN ABNORMALLY AGGREGATED FORM OF THE NORMAL HOST PRION PROTEIN (PrP).
IT CAUSES OTHER PROTEINS IN THAT SAME CELL TO MISFOLD IN THAT SAME WAY AND TO BIND TOGETHER IN FIBRILS THAT EVENTUALLY PRECIPITATE OUT. ALZHEIMER’S IS A CLASSIC PRION-LIKE DISEASE. THE AMYLOID BETA PLAQUE IS LINKED TO ALZHEIMER’S.
AMYLOID BETA PLAQUES NORMALLY FOLD AS ALPHA HELICES, THEY ARE LIKE SCREWS THAT GO INTO THE MEMBRANE. ALL PRION PROTEINS HAVE THAT CHARACTERISTIC. THEY NORMALLY GO INTO A MEMBRANE AND FORM AN ALPHA HELIX.
WHEN PRION PROTEINS MISFOLD, AND THEY CAN MISFOLD WHEN YOU GET TOO MANY OF THEM IN THE CYTOPLASM, FOR EXAMPLE IF THERE IS TOO MUCH ALPHA-SYNUCLEIN AMYLOID-BETA, THOSE ALPHA-SYNUCLEIN AMYLOID-BETA MOLECULES START GLOMMING TOGETHER IN THESE BETA SHEETS THAT ARE QUITE SOLUBLE, SO THEY END UP WITH SOLUBLE COMPLEXES OF BETA SHEETS THAT ARE MANY AMYLOID BETAS.
### ALPHA-SYNUCLEIN MISFOLDING GOES WITH PARKINSON’S DISEASE..
### AMYLOID-BETA GOES WITH ALZHEIMER’S..
### TDP43 GOES WITH ALS..
AMYLOID BETA, ALPHA-SYNUCLEIN AND THE SPIKE PROTEIN ARE ALL PRION-LIKE PROTEINS BECAUSE THEY HAVE SIMILAR CHARACTERISTICS. THE CHARACTERISTICS ARE WELL-DEFINED IN TERMS OF THE PROTEIN ITSELF BECAUSE THERE IS A SPECIFIC PATTERN, CALLED A GLYCINE ZIPPER. THE GLYCINE ZIPPER HAS A SIGNIFICANT STRUCTURAL IMPACT, ENGENDERING A STRONG DRIVING FORCE FOR RIGHT-HANDED PACKING AGAINST A NEIGHBORING HELIX.
IT’S A PATTERN OF GXXXG, TWO GLYCINES (AMINO ACID), SEPARATED BY THREE WILD CARDS, IT COULD BE ANY AMINO ACIDS. PROTEINS ARE BUILT FROM AMINO ACIDS LIKE BEADS ON A STRING.
YOU HAVE 20 AMINO ACIDS THAT MAKE UP THE CORE OF ALL THE PROTEINS. YOU HAVE THE DNA CODE THAT INSTRUCTS HOW THE PROTEIN IS MADE. THIS GXXXG PATTERN IS A CHARACTERISTIC PRION PATTERN CALLED A GLYCINE ZIPPER.
AMYLOID BETA HAS FOUR GLYCINE ZIPPERS. AND THE SPIKE PROTEIN HAS FIVE. SO IT’S IN SOME
PRION-LIKE PROTEINS CAUSE DISEASES BY INDUCING CERTAIN NORMAL PROTEINS TO FOLD INCORRECTLY. THERE IS A LIST OF PROTEINS NORMALLY FOUND IN THE BODY THAT ARE SUSCEPTIBLE TO MISFOLDING IN THE PRESENCE OF THESE PRION-LIKE PROTEINS.
CREUTZFELDT-JACOB DISEASE (CJD), THE HUMAN EQUIVALENT OF MAD COW DISEASE, IS ALSO A PRION DISEASE. WHEN MISFOLDED PROTEINS BECOME TOO ABUNDANT IN THE CELL’S CYTOPLASM, THEY CAN START PACKING TOGETHER IN SOLUBLE FIBRILS OR PLAQUES, SUCH AS THE AMYLOID BETA SHEETS IN ALZHEIMER’S, AND CREATE TISSUE DAMAGE.
IN PARKINSON’S DISEASE, AN AMYLOID PROTEIN (CALLED CURLI) PRODUCED BY E. COLI IN THE GUT, IS TRANSPORTED BY IMMUNE CELLS TO THE SPLEEN.
IN THE SPLEEN’S GERMINAL CENTRES (GERMINAL CENTRES ARE AREAS IN LYMPHOID TISSUE WHERE MATURE B CELLS, WHICH PRODUCE ANTIBODIES, PROLIFERATE, DIFFERENTIATE, AND MUTATE), THE IMMUNE CELLS PACK UP THE PRION PROTEIN INTO LITTLE PARTICLES THAT THEY RELEASE AS EXOSOMES, WHICH ARE MEMBRANE-BOUND EXTRACELLULAR VESICLES.
THE CELL IS TRYING TO GET RID OF THESE DANGEROUS, MISFOLDED PROTEINS BY EXPORTING THEM IN EXOSOMES. THESE EXOSOMES GET TRANSPORTED BY THE VAGUS NERVE TO THE BRAIN STEM AND CAN ALSO END UP BEING COUGHED OUT, OR SHED IN THE SWEAT, AND EVEN POSSIBLY GET INTO BREAST MILK.
THERE IS A SPECIFIC PATTERN, CALLED THE GLYCINE ZIPPER, THAT IS CHARACTERISTIC OF PRION-LIKE PROTEINS. IT CONSISTS OF TWO GLYCINES (GLYCINE IS AN AMINO ACID) SEPARATED BY ANY OTHER THREE OTHER AMINO ACIDS (GXXXG). AGAIN, AMYLOID BETA, WHICH CAUSES ALZHEIMER’S, HAS FOUR GLYCINE ZIPPERS. THE SPIKE PROTEIN HAS FIVE.
PARKINSON’S IS AN EXAMPLE. YOU CAN START WITH A PROTEIN PRODUCED BY E. COLI THAT IS A PRION-LIKE PROTEIN. IF IT GETS TOO MUCH, IT STARTS TO MISFOLD, IT STARTS TO BUILD THE PRION C IN THE GUT. AND THEN THE IMMUNE CELLS PICK UP THAT PROTEIN, TRANSPORT IT INTO THE SPLEEN.
THERE ARE GERMINAL CENTRES IN THE SPLEEN WHERE THE PRION PROTEINS REALLY GET GOING. SPLEEN IS A KIND OF A SPECIAL FACTORY FOR TRYING TO DEAL WITH PRION PROTEINS TO GET RID OF THEM. IN THE GERMINAL CENTRES IN THE SPLEEN, THE IMMUNE CELLS PACK UP PRION PROTEINS INTO LITTLE PARTICLES THAT THEY RELEASE AS EXOSOMES.
SPLEEN FIGHTS INVADING GERMS IN THE BLOOD (THE SPLEEN CONTAINS INFECTION-FIGHTING WHITE BLOOD CELLS) IT CONTROLS THE LEVEL OF BLOOD CELLS (WHITE BLOOD CELLS, RED BLOOD CELLS AND PLATELETS) IT FILTERS THE BLOOD AND REMOVES ANY OLD OR DAMAGED RED BLOOD CELLS.
THE SPLEEN IS THE LARGEST LYMPHATIC ORGAN IN THE BODY. THE SPLEEN PLAYS AN IMPORTANT ROLE IN THE IMMUNE SYSTEM.
mRNA VACCINES RE-ENGINEER THE PROTEIN TO MAKE IT MORE PRION-LIKE THAN IT NORMALLY IS. BECAUSE THEY HAVE MUCKED WITH THE PROTEIN STRUCTURE TO GIVE IT A PAIR OF PROLINES THAT ARE NEXT DOOR TO EACH OTHER.
THEY’VE MODIFIED THE SPIKE PROTEIN DESIGN FOR THE VACCINE SUCH THAT IT COULDN’T GO INTO THE MEMBRANE THE PROTEIN IS MADE BY THESE CELLS UNDER INSTRUCTION FROM THE VACCINE, AND THEN IT’S RELEASED AND EXPOSED ON THEIR MEMBRANE.
THE IMMUNE CELLS PICK UP THE VACCINES, THEY OPEN UP THAT DON’T UNDERSTAND WHAT’S GOING ON HERE. THEY’VE NEVER SEEN ANYTHING LIKE THIS BEFORE EVERYTHING IS NOT NATURAL IN THESE VACCINES. SO THE IMMUNE CELLS GET REALLY WORRIED AND THEY GO INTO THE LYMPH SYSTEM.
LOTS OF WOMEN ARE GETTING SWOLLEN LYMPH NODES UNDER THEIR ARM WHICH IS A CHARACTERISTIC FEATURE OF BREAST CANCER. FROM THE LYMPH NODES, IT GETS INTO THE LYMPH SYSTEM AND IT WORKS ITS WAY TO THE SPLEEN.
INTRAMUSCULAR CORONAVIRUS 2019 (COVID-19) VACCINATIONS COULD INDUCE IPSILATERAL AXILLARY LYMPH NODE REACTIVITY
IPSILATERAL AXILLARY NODAL REACTIVITY IS COMMONLY SEEN AFTER THE INTRAMUSCULAR ADMINISTRATION OF THE COVID-19 mRNA VACCINES,
THE ENLARGED LYMPH NODES ARE BIG ENOUGH TO BE VISIBLE ON IMAGING SCANS, SUCH AS MAMMOGRAMS, CT SCANS, MRIS, AND ULTRASOUNDS.
AND WHEN YOU GET TOO MUCH OF A PRION PROTEIN IN THE CYTOPLASM, THAT’S WHEN YOU GET IN TROUBLE WITH OTHER PROTEINS MISFOLDING. AND THESE IMMUNE CELLS ACTUALLY UPREGULATE ALPHA-SYNUCLEIN IN RESPONSE TO STRESS. SO THEY’VE GOT TREMENDOUS STRESS IN THOSE DENDRITIC CELLS IN THOSE GERMINAL CENTRES IN THE SPLEEN.
SPIKE PROTEIN IS A PRION-LIKE PROTEIN.
THERE IS AN OLD SAYING IN MEDICINE THAT “THE CURE MAY BE WORSE THAN THE DISEASE.” THE PHRASE CAN BE APPLIED TO mRNA VACCINES.
VACCINE CREATED PRIONS ARE BEING USED AS BIOWEAPONS..
TDP-43 AND FUS ARE NUCLEAR PROTEINS WITH MULTIPLE FUNCTIONS IN mRNA PROCESSING. THEY PLAY KEY ROLES IN ALS (AMYOTROPHIC LATERAL SCLEROSIS) AND FTD (FRONTOTEMPORAL DEMENTIA), WHERE THEY ARE PARTIALLY LOST FROM THE NUCLEUS AND AGGREGATE IN THE CYTOPLASM OF NEURONS AND GLIAL CELLS.
FUNCTIONS OF TDP-43.
TDP-43 PERFORMS SEVERAL mRNA-RELATED PROCESSES IN THE NUCLEUS, SUCH AS TRANSCRIPTION, SPLICING, MAINTAINING RNA STABILITY AS WELL AS MIRNA AND LNCRNA PROCESSING. IT IS PREDOMINANTLY A NUCLEAR PROTEIN BUT ALSO SHUTTLES BETWEEN THE NUCLEUS AND THE CYTOPLASM
THE STRIKING FUNCTIONAL AND STRUCTURAL SIMILARITIES OF TDP-43 AND FUS, WHICH ARE BOTH DNA/RNA BINDING PROTEINS, IMPLY THAT ABNORMAL RNA METABOLISM IS A PIVOTAL EVENT,
FUS (FUS RNA BINDING PROTEIN) IS A PROTEIN CODING GENE. DISEASES ASSOCIATED WITH FUS INCLUDE AMYOTROPHIC LATERAL SCLEROSIS.. FUS IS UBIQUITOUSLY EXPRESSED IN ALL CELLS.
THE FUS PROTEIN ATTACHES (BINDS) TO DNA AND REGULATES AN ACTIVITY CALLED TRANSCRIPTION, WHICH IS THE FIRST STEP IN THE PRODUCTION OF PROTEINS FROM GENES. THE FUS PROTEIN IS ALSO INVOLVED IN PROCESSING MOLECULES CALLED MESSENGER RNA (mRNA), WHICH SERVE AS THE GENETIC BLUEPRINTS FOR MAKING PROTEINS.
THESE BINDING PROTEINS HAVE AMINO ACID REGIONS, BINDING MOTIFS THAT BIND SPECIFIC RNA SEQUENCES. BINDING TO CERTAIN RNA SEQUENCES WHEN THE PROTEINS ARE IN THE CYTOPLASM IS THE REASON WHY MOLECULES TO FOLD IN CERTAIN WAYS LEADING TO PATHOLOGIC AGGREGATION AND PRION FORMATION IN THE CYTOPLASM
COVID-19 VACCINE CONTAINS RNA SEQUENCES THAT HAVE BEEN SHOWN TO HAVE HIGH AFFINITY FOR TDP-43 OR FUS THAT INDUCE CHRONIC DEGENERATIVE NEUROLOGICAL DISEASES.
More inter-governmental cooperation is needed using Artificial Intelligence to fight Covid-19 Coronavirus.
Artificial Intelligence (AI) has greatly facilitated exchanges of views and information between the scientific community. What we have not seen so much is the use of AI for inter-governmental cooperation on all these issues. Jan Kleijssen, Director of Information Society Action against Crime looks at the Council of Europe’s contribution to looking at Artificial Intelligence and its role in tackling Covid-19. https://www.coe.int/en/web/portal/covid-19-artificial-intelligence
Artificial Intelligence (AI) applications for COVID-19 pandemic
THE VIRAL SPIKE PROTEIN, CODED BY THE VACCINE RNA SEQUENCE, BINDS ACE2 AN ENZYME CONTAINING ZINC MOLECULES THIS INTERACTION INCREASES INTRACELLULAR ZINC LEVELS LEADING TO PRION DISEASE
THE INITIAL BINDING IS BETWEEN SPIKE PROTEINS ON THE SURFACE OF THE CELL TRANSFECTED BY THE MRNA VACCINE AND ACE2 ON THE SURFACE OF AN ADJACENT CELL.
THE INTERACTION COULD INITIALLY TAKE PLACE IN THE CYTOPLASM OF A CELL THAT MAKES ACE2 AND HAS BEEN TRANSFECTED WITH THE VACCINE RNA CODING FOR THE SPIKE PROTEIN.
THE INTERACTION IS QUITE CONCERNING GIVEN THE SUSPICION THAT THE WUHAN VIRUS CAUSING COVID-19, SARS-COV-2, IS A BIOWEAPON AND IT IS POSSIBLE THAT THE VIRAL SPIKE PROTEIN MAY HAVE BEEN DESIGNED TO CAUSE PRION DISEASE
AI AND COVID-19 | DISCOVER ARTIFICIAL INTELLIGENCE WITH ANGELIKI DEDOPOULOU
PFIZER VACCINE USES A UNIQUE RNA NUCLEOSIDE 1-METHYL-3′-PSEUDOURIDYLYL -- THIS NUCLEOSIDE WAS CHOSEN TO REDUCE ACTIVATION OF THE INNATE IMMUNE SYSTEM
RNA MOLECULES CONTAINING THIS NUCLEOSIDE WILL UNDOUBTEDLY HAVE ALTERED BINDING
THE USE OF THIS NUCLEOSIDE IN A VACCINE CAN POTENTIALLY ENHANCE THE BINDING AFFINITY OF RNA SEQUENCES CAPABLE OF CAUSING TDP-43 AND FUS TO ASSUME TOXIC CONFIGURATIONS. THE VACCINE PLACES A NOVEL MOLECULE, SPIKE PROTEIN, IN/ON THE SURFACE OF HOST CELLS.
THE NORMAL PROGRESSION OF PARKINSON’S DISEASE SHOW HOW HOW THE SPIKE PROTEIN ACTS AS A DISEASE-PRODUCING PRION.
PD IS A PRION DISORDER RESULTING FROM INCREASED PRODUCTION AND/OR IMPAIRED CLEARANCE OF PROTEINS SUCH AS Α-SYNUCLEIN, LEADING TO MISFOLDING AND THE FORMATION OF TOXIC OLIGOMERS, AGGREGATES, AND CELL DEATH.
MODERNA AND PFIZER-BIONTECH’S “PSEUDO-VACCINES” FOR COVID-19 CONTAIN MRNA
ENVELOPED BY LIPID NANOPARTICLES (LNP) AND POLYETHYLENE GLYCOL (PEG). NONE OF THESE 3 COMPONENTS HAVE BEEN APPROVED FOR VACCINES MODERNA AND PFIZERBIONTECH USE LNPS THAT ARE “PEGYLATED”, THAT IS, CHEMICALLY BOUND TO PEG MOLECULES TO INCREASE STABILITY AND PREVENT THEIR METABOLISM
THIS EXPERIMENTAL IGT THERAPY AND ITS LNP + PEG-BASED DELIVERY SYSTEM HAVE NEVER BEEN APPROVED FOR USE IN A VACCINE OR DRUG4. EVEN THESE 2 VACCINES WERE ONLY “AUTHORIZED FOR EMERGENCY
USE” BY THE FDA OF THE UNITED STATES, BUT “IT HAS NOT BEEN APPROVED FOR ROUTINE CLINICAL USE”.. “GENE THERAPIES AND DRUGS BASED ON MRNA CAN ACTIVATE ONE OR MORE IMMUNE RESPONSES AGAINST EACH AND EVERY ONE OF THE DRUG’S COMPONENTS ... LEADING TO TERRIBLE ADVERSE EVENTS RELATED TO THE IMMUNE REACTION
THE IMMUNE CELLS KEEP MAKING THE SPIKE PROTEIN BECAUSE THE RNA IN THE VACCINE HAS BEEN ENGINEERED TO BE VERY STURDY. NORMAL RNA WOULD JUST DISINTEGRATE IF YOU INJECTED IT INTO THE BODY. BUT THEY HAVE ADDED POLYETHYLENE GLYCOL AND CHANGED ONE OF THE NUCLEOTIDES IN THE VACCINE RNA, AMONG OTHER THINGS, TO KEEP IT FROM BREAKING DOWN.
THIS MEANS THAT CELLS CAN’T STOP THEMSELVES FROM MAKING THE SPIKE PROTEIN. IT IS WHEN YOU HAVE TOO MUCH OF A PRION PROTEIN IN THE CYTOPLASM THAT YOU ARE IN DANGER OF HAVING MISFOLDING.
T RETROVIRUSES INTRODUCE THEIR GENETIC MATERIAL PERMANENTLY INTO OUR DNA. IN FACT, 8% OF OUR GENETIC CODE IS OF VIRAL ORIGIN, KNOWN AS “RETROVIRAL GENES”
UNTIL NOW, MRNA VACCINES HAD NEVER BEEN USED CLINICALLY WE DON’T KNOW – THOUGH PFIZER / MODERNA COMPANIES THAT MANUFACTURE MRNA VACCINES, FIRMLY ASSURE THAT SAID GENETIC MATERIAL CANNOT BE INTRODUCED INTO OUR GENOME.
I WILL DWELL BRIEFLY FOR THE LCD..
THEY ARE BASED ON THE CONCEPT OF UNIDIRECTIONALITY OF THE FLOW OF CELLULAR GENETIC INFORMATION TO AFFIRM THAT THERE IS NO POSSIBILITY OF MUTAGENESIS OF OUR DNA BY INSERTION OF MRNA SINCE IT IS LITERALLY IMPOSSIBLE FOR IT TO ENTER THE CELL NUCLEUS. WITH PFIZER HAVING JAWS 1/ JAWS 2 / JAWS 3 BOOSTER JAWS THERE IS 99.9%
LIKEHOOD THAT SAID GENETIC MATERIAL WILL END UP FORMING PART OF OUR CHROMOSOMES. DURING CELL DIVISION (MITOSIS AND MEIOSIS), THERE ARE PHASES IN WHICH THE NUCLEAR MEMBRANE DISAPPEARS, AND THE CHROMOSOMES MIX WITH THE CYTOPLASM. AFTER THESE PHASES, THE NUCLEAR MEMBRANE IS REBUILT,
AND IT IS EMINENTLY POSSIBLE FOR MRNA FROM VACCINES TO BE INCLUDED INSIDE THE NEW NUCLEUS . AFTER CELL DIVISIONS, A NEW NUCLEAR MEMBRANE IS RECREATED, AND THE CHROMOSOMES REVERT TO A NONCOMPACTED CONFORMATIONAL SITUATION.
THIS DECONDENSATION OF THE CHROMOSOMES GIVES RISE TO CHROMATIN, WHICH REPRESENTS A FULLY FUNCTIONAL STATE OF OUR DNA. UNDER THESE CONDITIONS, THE INTRODUCTION OF THE VACCINE MRNA INTO OUR GENETIC MATERIAL IS ONLY A MATTER OF TIME MITOSIS: IT IS THE PROCESS OF CELL DIVISION WHOSE RESULT IS THE FORMATION OF TWO DAUGHTER CELLS WITH THE SAME NUMBER OF CHROMOSOMES.
IT DEVELOPS OVER FIVE PHASES: PROPHASE, PROMETAPHASE, METAPHASE, ANAPHASE, AND TELOPHASE. DURING PROMETAPHASE, THERE IS A FRAGMENTATION OF THE NUCLEAR MEMBRANE IN MULTIPLE VESICLES. NEXT, THE MITOTIC SPINDLE IS FORMED.
IT IS A SET OF MICROTUBULES THAT ARISE FROM THE CENTRIOLES DURING THE PROCESSES OF CELL DIVISION (WHETHER MITOSIS OR MEIOSIS) AND THAT GO FROM THE CENTROMERES OF THE CHROMOSOMES TO THE CENTRIOLES LOCATED AT THE POLES.
IT IS IMPORTANT TO UNDERSTAND THAT SINCE THE CENTRIOLES ARE LOCATED OUTSIDE THE NUCLEUS, THE MICROTUBULES OF THE SPINDLE CANNOT ATTACH TO THE CENTROMERES OF THE CHROMOSOMES UNTIL THE NUCLEAR MEMBRANE IS BROKEN. ONCE THE MITOTIC SPINDLE IS CREATED, THE SISTER CHROMATIDS ARE PULLED IN OPPOSITE DIRECTIONS TOWARDS BOTH POLES OF THE SAME AND WILL GIVE RISE TO THE FUTURE DAUGHTER CHROMOSOMES.
DURING TELOPHASE, THE DAUGHTER CHROMOSOMES ELONGATE, LOSE CONDENSATION AND THE NUCLEAR MEMBRANE IS RECOVERED, WHICH IS FORMED AGAIN FROM THE ROUGH ENDOPLASMIC RETICULUM
DURING MITOSIS THERE IS A TOTAL REORGANIZATION OF THE CELLULAR MATERIAL DURING WHICH, THE MOLECULES PRESENTED IN THE CELL CYTOPLASM (PROTEINS, LIPIDS, MRNA) CAN END UP BEING INCLUDED DURING TELOPHASE WITHIN THE NEW CELL NUCLEUS AND LATER JOIN OUR DNA THROUGH AN RT.
MITOSIS INVOLVES THE DIVISION OF BODY CELLS, WHILE MEIOSIS INVOLVES THE DIVISION OF SEX CELLS. THE DIVISION OF A CELL OCCURS ONCE IN MITOSIS BUT TWICE IN MEIOSIS.
MEIOSIS IS THE PROCESS OF CELL DIVISION, TYPICAL OF EUKARYOTIC REPRODUCTIVE CELLS, IN WHICH THE NUMBER OF CHROMOSOMES IS REDUCED BY HALF TO CREATE HAPLOID SEX CELLS OR GAMETES (EGGS AND SPERM) THAT CONTAIN A SINGLE COPY OF EACH CHROMOSOME WHICH, WHEN THEY UNITE, WILL FORM A ZYGOTE WITH THE COMPLETE NUMBER OF CHROMOSOMES.
THE MEIOSIS PROCESS TAKES THE FORM OF DNA REPLICATION FOLLOWED BY TWO SUCCESSIVE NUCLEAR AND CELLULAR DIVISIONS. THESE DIVISIONS OR PHASES ARE CALLED MEIOSIS I AND MEIOSIS II . AS IN MITOSIS,
MEIOSIS I IS PRECEDED BY INTERPHASE, A PROCESS OF DNA REPLICATION THAT TURNS EACH CHROMOSOME INTO TWO SISTER CHROMATIDS. MEIOSIS I IS A SPECIAL CELL DIVISION IN WHICH HOMOLOGOUS PAIRS OF CHROMOSOMES ARE SEPARATED AND THEIR GENETIC MATERIAL IS REDUCED FROM A DIPLOID CELL TO A HAPLOID CELL.
A SECOND PHASE OF GROWTH CALLED INTERKINESIS CAN OCCUR BETWEEN MEIOSIS I AND II, HOWEVER, DNA REPLICATION DOES NOT OCCUR AT THIS STAGE .
THE EVENTS OF MEIOSIS II ARE ANALOGOUS TO THOSE OF A MITOTIC DIVISION, ALTHOUGH THE NUMBER OF CHROMOSOMES INVOLVED HAS BEEN REDUCED BY HALF. MEIOSIS IS A BASIC PROCESS TO GENERATE A GREATER GENETIC DIVERSITY IN OFFSPRING SINCE THE GAMETES OF BOTH PARENTS WILL CONTRIBUTE HALF OF THE GENETIC LOAD TO THE CREATED ZYGOTE ..
AS IN THE PROMETAPHASE OF MITOSIS, DURING THE PROMETAPHASE OF MEIOSIS I AND II, A FRAGMENTATION OF THE NUCLEAR MEMBRANE OCCURS IN MULTIPLE VESICLES. IN THE SAME WAY, DURING BOTH PHASES OF MEIOSIS, A TOTAL REORGANIZATION OF THE CELLULAR MATERIAL OCCURS DURING WHICH,
THE MOLECULES PRESENT IN THE CELL CYTOPLASM (PROTEINS, LIPIDS, MRNA) CAN END UP WRAPPED WITHIN THE NEW CELL NUCLEUS AND THEREFORE JOIN TO OUR DNA IN THE SAME WAY AS IN MITOSIS . HOWEVER, IN THIS CASE, THE CONSEQUENCES MAY BE MORE SERIOUS BECAUSE SAID GENETIC MUTATION WOULD BE TRANSMITTED TO OUR OFFSPRING
THE BINDING OF GENETIC MATERIAL TO LIPID COATINGS SIGNIFICANTLY IMPROVES PENETRATION INTO THE NUCLEUS.
THESE COATINGS PROMOTE NUCLEAR ENTRY THROUGH FUSION WITH THE NUCLEAR ENVELOPE (LIPOPLEXES) OR PERMEATION OF THE NUCLEAR MEMBRANE (POLYPLEXES)., BY MEANS OF POLYMERASE CHAIN REACTION AND ELECTRON MICROSCOPY ANALYSIS, IT WAS DISCOVERED THAT WHEN WE INTRODUCE PLASMIDS, PROTECTED BY LIPOPLEXES AND POLLEXES, INTO THE CYTOPLASM, BETWEEN 1 AND 10% MANAGE TO PENETRATE THE NUCLEO
THE ELECTRICAL CHARGES OF THESE MOLECULES AND THE MEMBRANE COULD BE AN EXPLANATION FOR THIS PROCESS THE BINDING OF THE IMPORTIN COMPLEX TO AN NLS INCREASES ITS BINDING TO DNA, DILATES THE NUCLEAR PORES AND INCREASES THE TRANSLOCATION OF GENETIC MATERIAL FROM THE CYTOPLASM TO THE NUCLEUS..
BELOW: AT 1.53-- DR ANTHONY FAUCI
PHARMACEUTICAL RESEARCH AND MANUFACTURERS OF AMERICA IS JUST A PIMP OF THE JWISH VACCINE LOBBY WHO BRIBES / HONEY TRAPS US CONGRESSMEN/ SENATORS/ JUDGES/ FBI/ CIA/ POLICE/ MEDIA/ FAKE OPINION POLL CONDUCTORS/ HASBARAS/ HEALTH CARE MOVERS AND SHAKERS/ STATISTICS HOUSES...
THE PHARMACEUTICAL RESEARCH AND MANUFACTURERS OF AMERICA (PHRMA), PUBLICLY ENDORSED PORTIONS OF THE PATIENT PROTECTION AND AFFORDABLE CARE ACT, AS DID SEVERAL OTHER MAJOR PHARMACEUTICAL MANUFACTURERS. THIS ORG IS A DEMOCRAT PARTY WING.
WHEN MAIN STREAM MEDIA REPORTS LOBBYING EXPENSE – MULTIPLY BY FOUR AS A THUMBRULE.
HUNDREDS OF MILLIONS OF US DOLLARS ARE SPENT IN LOBBYING ( PIMPING )..MORE MONEY IS SPENT IN BRIBING THAN FOR ACTUAL MEDICAL RESEARCH SOMETIMES.
IN 2020 MORE THAN 600 MILLION USD FOR SPENT BY KOSHER BIG PHARMA FOR LOBBYING.
NOMENT FOR REDRESS — IS PROTECTED BY THE FIRST AMENDMENT OF THE CONSTITUTION. LOBBYISTS DONATE MONEY TO CANDIDATES. THIS IS PERFECTLY LEGAL!!!
SOME INTEREST GROUPS WILL SEND MEMBERS OF CONGRESS AND THEIR STAFFS ON TRIPS, SOMETIMES TO PEDOPHILE ISLAND OF JEW JEFFREY EPSTEIN.
MILLIONS OF COVID PATIENTS HAVE DIED DUE TO LIVER DAMAGE BY PARACETAMOL..
KILLER PARACETAMOL VS LIFE SAVER IVERMECTIN, POLL
PFIZER INC IS BULLYING LATIN AMERICAN NATIONS TO CHANGE THEIR LAWS TO PROVIDE PROTECTION FOR ITS HIGH-PRICED VACCINE. REMEMBER THAT PFIZER’S PARTNER BIONTECH GOT $445 MILLION FROM JEWESS ANGELA MERKEL ( WITH HILTER’S EYES AND CHIN WHO CAN NEVER WIN AN ELECTION UNLESS IT IS RIGGED ) THE GERMAN GOVERNMENT TO DEVELOP THIS VACCINE..
JEW BARACK OBAMA ( HIS MOTHER IS A WHITE JEWESS ) WAS A PENNILESS BUM DURING AFTER HIS COLLEGE DAYS..
JEWISH PFIZER IS A CRIMINAL COMPANY.. WORSE THAN PURDUE
Video: Pfizer’s Criminal Record. Largest Medical “Fraudulent Marketing” Case in US History
The 2020-2021 mRNA vaccine violations far surpass the health care fraud committed by Pfizer Inc in 2009.
“Fraudulent marketing” is an understatement: The mRNA vaccine announced by Pfizer – BioNTech is based on an experimental gene editing mRNA technology which has a bearing on the human genome. The standard animal lab tests using mice or ferrets were not conducted. Pfizer “went straight to human “guinea pigs.”
M. Ch, Global Research Editor, May 15, 2021
VIDEO. US Department of Justice (DOJ) Statement
$2.3 Billion Medical Fraud settlement with Pfizer
PFIZER PAID KICKBACKS TO HEALTH CARE PROVIDERS TO INDUCE THEM TO PRESCRIBE THESE, AS WELL AS OTHER, DRUGS.
SIX WHISTLE BLOWERS RECEIVED PAYMENTS TOTALING MORE THAN $102 MILLION FROM THE FEDERAL SHARE OF THE CIVIL RECOVERY.
5G TOWERS COV 19 COMPUTER MOTHERBOARD INTERFACE - SHOW THIS TO EVERYONE....
5G TOWERS AT THE SAFE FREQUENCY CAN BE BENEFICIAL AT TO HIGH A FREQUENCY CAN BE DEADLY..
COMBINE THIS HIGH FREQUENCY 5G WITH 5G CELL PHONES AND ACTIVATED IT WILL KILL.
AGENDA 2020 21
GET THE WORD OUT TO ALL
WE HAVE TO STOP THIS.
IT'S NOT CONSPIRACY SEE THE VIDEO.
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