My brief synopsis:The jabbed are going to become legally patentable and patented by genetic editing through transfection and reverse transcriptase facilitated through the cationic nano lipids in these inoculations also by mechanism of gene cleavage/deletion. They are also going to become remotely controlled by designer drugs and DREADDS also through RF/ EMF/ optogenetics facilitated by a nano ferritin and graphene induced cellular and protoplasmic dendritical response and subcutaneous/hematologic/interstitial/optical; galvanic/Faradic/photoactivated vestibular, synapse, neuron, basal ganglia and dendrite stimulation and axon excitation. Thus effecting one’s efferent motor skills, afferent sensory perception and totally hijacking their cognitive function. Of which they will not be cognizant. The target of these jabs are the limbic system, central nervous system as well as peripheral nervous system which is divided by the autonomic and somatic nervous systems. The lymphatic system is targeted by nano swimmers designed for remote drug delivery. While theragripper based biosensors will be distributed throughout the body. The jabs also contain self assembling nano technology that is driven by mechanism of teslaphoresis which facilitates self assembly of nano routers as part of both a intermural and intramural biometric bilateral wireless human interphase device. This is accomplished through a chronological administration of a predisposed number of injections. One of the major complications of this is what I believe is the mechanism of action causing kreutzfelt jakobs disease in which gliosis causes a deficit in myelin. This is likely a product of graphene oxide and the toxicological damage to the CNS and being a highly conductive material present in the capillaries of the brain which is compounded by the deficiency in myelin to maintain sheaths. Myelin is a lipid rich material that insulates axons and separates action potentials in excitable nerves. Due to the nature of the piezoelectric effect I believe graphene also serves as a power source to drive, power and charge the nano scale components derived from the jabs.They also contain a hydrogel polymer which I suspect it’s composition is that of Na2Sio3 or an analogous compound with a substitution K2Sio3 which are silicate based binders.I suspect that any small amount of cesium was incorporated to be used in nanobots that contain biometric sensors especially anything related to quantitative volumetric analyses.It is also used in video camera tubes, night vision goggles and some lenses, it can convert electricity or heat into light and or light or heat into electricity. Cesium emits most of it's light in the near infrared spectrum. Cesium is also used in magnetometers. It could also be exploited and or employed for these properties in optic sensing/recording, nanobot navigation/propulsion, electromagnetic sensing, optogenetic applications, photo/thermo/electro activation, and or power generation applications. (photoemissive) (photoelectric) (electroluminescent) (thermoluminescent) (photosensitive) (thermionic) (paramagnetic) (electrohydrodynamic)The luminopsins (luciferase) are for optogenetics used for excitation and mitigation of action potentials in excitable nerves. This mechanism of action can also be complimented or interchanged with external LED/LCD light.
How do we get these contaminations out? It's like this!
What we need is a re-engineered and or retrofitted dialysis machine that incorporates one or more of these components which will facilitate removal of graphene oxide. A powerfully induced electromagnetic field and or a graphene based slouch box. It may also be highly effective to have a multi gradient perforated graphene mesh as graphene is known to pick up other graphene atoms to complete or repair its lattice structure. This method will also remove the dynabeads produced by thermofisher scientific I am certain, they are the small spherical structures observed in microscopic analysis which are magnetic. Zeolite may also be incorporated due to its inherent filtration qualities and its ability to capture atomic sized particulate. This application could cause iron deficient anemia and or metabolic acidosis. We can resolve this with a buffer. I suspect that the clots are a product of hydrogel which I suspect it’s composition is that of Na2Sio3 or an analogous compound with a substitution K2Sio3. Which I again suspect why the supposedly vaccinated were still required to wear masks due to the alveolar gas equation and the hypoxic effects from wearing masks. You see, C02 accelerates and facilitates polymerization of this substance. We can incorporate a chamber with an atmosphere rich in C02 which will polymerize the substance outside of the body where it can then be captured. The DREADDS however will not be removed with these applications. Obviously it goes without saying that this would be a very massively intense, monotonous and difficult feat but I believe it’s possible while it may take subsequent cyclical visits. I cannot fathom any other means.
Temperatures were to keep the venom peptides and proteins cold as venom must be cryogenically preserved to remain viable within an hour of extraction or synthesis. It was included to reduce the effect of clotting as an anticoagulant to try to reduce the impact of the polymerization of the Na2Sio3 hydrogel. The graphene itself is cardiotoxic, cytotoxic, hepatotoxic, genotoxic, neurotoxic, nephrotoxic. It also causes the protein corona effect! Polysorbate80 was included to help perforate blood tissue barriers and mitigate the performance of exclusion of macromolecules from the organs. While the PEG was included to prevent solidification and reduce thawing times for administration! No organic nor biological material was found in a number of mass spectrometric assays.
The theragrippers, nano swimmers and routers are I suspect powered by rechargeable cobalt potassium ion batteries that are recharged by the piezoelectric effect with graphene! While the carcinogenic effect, cardiovascular and reproductive damage and harms should be by now pretty common knowledge! It goes without saying we aren't going to see a general consensus on the constituents of the jabs due to the fact that there are a series of jabs with different compositions which are intended to be chronologically administered. It's also plausible that limited dose finding trials were being done at the onset and some jabs may have intentionally contained an LD50 of toxic constituents. Another reason also why some jabbed are not showing any adverse or common reactions that were intentional is because they are intended to be diluted with a saline solution and many administrators of the jabs have been working from the inside and have been purposely giving just the saline in order to save lives. These people are heroes!`
It goes without saying that any deletions or alterations to the genome will not be repaired or circumvented by these methods and are likely to be permanent and irreversible.