Disease X: COVID Induced Prion Disease

This segment is part of the larger story about how Transhumanists are bringing about their Singularity utilizing 5G, Graphene Oxide, mRNA technology.. and your FEAR. I encourage you to take “GQD Particle: The Transhumanist Quantum Agenda” from the top. SPM

THE ZOMBIE CONVERSION IS STARTING: The nervous system is the main body control system of the body and regulates muscles function and glands by releasing neurotransmitters. The nervous system is intrinsically tied to the endocrine system. Collectively it is referred to as the Neuroendocrine system. The endocrine system is a network of glands and organs in the body that make hormones and release them into the bloodstream.

In theory, since artificial neurons are being grown (Neural Lace) and natural neurotransmitters are being replaced by Graphene Oxide (GO)… what would then activate muscles and glands? The answer is that they are NOT being activated. Why? In order to grow new nerve cells the GO is either destroying natural neurotransmitters or they are being replaced by reduced Graphene Oxide (rGO) which don’t function in the same way as natural neurotransmitters. This would have a profound impact on the endocrine system; the glands of the body which include the thyroid gland, pancreas, adrenal glands (and kidney), ovaries, testis, salivary glands, hypothalamus, pituitary, pineal gland, etc. ¹ ² ³

The neuroendocrine system is responsible for the control of homeostatic processes in the body, including reproduction, growth, metabolism and energy balance, and stress responsiveness So you are seeing issues such as diabetes, fertility, muscle wasting, mental health behavioural and dementia, blood pressure and cardiac issues, digestive issues etc.

And as we already know Clathrin Nanotechnology is not exclusive to only humans but can be found throughout the plant and animal community along with the “Smart Dust” the NWO has been spraying in the environment since the 90s. By now this Graphene Oxide has already permeated the entire ecosystem, the food chain, humans, and all life on the planet. ⁴

We are now witnessing chronic wasting diseases in deer populations which the media is calling “Zombie Deer Disease.” ⁵

Chronic wasting disease is a fatal infection caused by an abnormal protein called a prion. A misfolded protein that destroys brain cells in mule deer, moose, elk, sika deer and reindeer. The brain-eating disease is 100 percent fatal and highly transmissible, especially among captive populations of deer raised in confined feeding operations. It has an incubation period of 18 to 24 months. As soon as a deer is infected, it begins to shed infectious prions in semen, blood, urine, saliva and antler velvet to other deer and its surrounding habitat. Before death, an infected deer will drool, lose coordination, waste away and behave in a demented fashion. Brain-eating prions simply defy traditional biology. They are smaller than the smallest known virus and can survive in tissue long after death. They can cross the species barrier and incubate for decades. ⁶

Prion diseases are a family of rare neurodegenerative disorders that can be found in both humans and animals, impairing brain function. Perhaps the best known example is bovine spongiform encephalopathy, commonly referred to as mad cow disease.

Is this a prion disease or infection by the Graphene-based Clathrin Nanotechnology?

Reports from our medical community are indicating similar emerging pathologies in the human population with rising incidents of diabetes, dementia, metabolic disease, digestive issues etc. ⁷ ⁸ ⁹ ¹⁰ ¹¹ Even the transmission of dementia. ¹² ¹³ ¹⁴ Most of which have been linked to COVID exposure. ¹⁵ ¹⁶ ¹⁷

There is emerging evidence that COVID is also tied to prion disease. In October 2023, this condition was reported in a 62-year-old man from the United States who died from this deadly brain disease shedding light on the potential connection between the virus and neurodegenerative disorders, particularly prion diseases. And his symptoms upon hospitalization were similar to the infected deer whereby he exhibited symptoms such as diffuse bradykinesia (shuffling gait, slow muscle movement tremors, slurred speech, expressionless face), drooling, dementia, and an inability to walk and distorted memory impairment. ¹⁸ ¹⁹ ²⁰ From symptom onset to death took 3 months for the man to die.

The media is now prophesying the transmission of this fatal deer prion disease to the human population. ²¹ ²² What am I alluding to here? It appears that the “Zombie Apocalypse” is starting!

It gets worse!

Plot Twist: According to the WHO, Disease X could be due to “Prion disease”.

The WHO says, “Disease X represents the knowledge that a serious international epidemic could be caused by a pathogen currently unknown to cause human disease.” Various pathogens, including viruses, bacteria, fungi, parasites, and prions, can potentially be pathogen X. ²³ The average survival time from prion disease onset to death is 4 to 10 months and 2 to 3 months post diagnosis using Lumbar puncture. ²⁴

‘Disease X’. According to experts, the new virus may be deadlier than Covid-19 and may have a similar impact as the Spanish Flu. The World Health Organisation (WHO) has dubbed the anticipated next pandemic as ‘Disease X’, stating that it might already be “on its way”. ²⁵ They are calling it the new “Disease X” but it all arises from the exact same COVID bioweapon! And their “cure” is more vaccinations. Are they “rebranding” the exact same COVID vaccines?

And look who was at the center of prion research; a perfect marriage between Nazi Whitecoat Robert Gallo at Fort Detrick and the NWOs Luciferian Rosslyn Institute in Edinburgh:

“Robert Gallo, co-discoverer of HIV and director of the Institute of Human Virology in Baltimore, has become involved in research to develop a cheap and reliable blood test for vCJD. He has taken on the role of the principle investigator and head of the scientific advisory board of Prion Developmental Laboratories (PDL), a private Maryland-based company.” ²⁶

“Mad cow disease, CJD, and a sheep disease called scrapie are all transmissible spongiform encephalopathies (TSEs), which turn brain tissue into something resembling a sponge. Most researchers believe the culprits are prions, normal cellular proteins that turn deadly when they undergo a shape change. Because prions have no DNA or RNA, they can’t be detected with sensitive genetic assays like those used to detect HIV. To sidestep the obstacles, prion researcher Gino Miele and colleagues at the Roslin Institute in Midlothian, Scotland, took an indirect approach. Taking a cue from recent research suggesting that prions multiply in the spleen before invading the brain, the team members focused their attention on that organ.” ²⁷

Plot Twist: The idea that the COVID spike protein might be neurotoxic through prion-like capabilities is not new. In 2020 researchers proposed that peptides derived from the spike protein might cross-seed with existing amyloidogenic human proteins to accelerate prion formation and cause neurodegeneration of brain cells leading to prion disease. ²⁸ ²⁹

Plot Twist: In 2020, our researchers at CIN theorized that under high Electromagnetic Frequencies “spike proteins” could undergo conformational changes (folding) that could activate their release into general circulation. ³⁰ At that time we did not make the connection with prion proteins however, current research using yeast prions show that activation, propagation of release of prions occurs under high electromagnetic fields in the 5G range of 2.0 Giga Hz and under a 50Hz Extremely Low Frequency (ELF) range. ³¹

Plot Twist: A human prion protein found in HIV infection is implicated in HIV-associated neurocognitive impairment and mediates inflammation of the nervous system and neurodegeneration. ³² Furthermore, direct binding of the HIV glycoprotein GP120 with the immune system modulating CCR5 receptor requires a prion protein. ³³ This mechanism is similar to the binding of the COVID “spike protein” which mediates viral entry into cells. ³⁴ It is not surprising that the CCR5 receptor is implicated in a host of diseases from HIV to COVID to Cancer and in theory all of which may be regulated by what their scientists are referring to as “spike proteins” or “prions”. ³⁵

Plot Twist: This madness just won’t stop! Prion uptake into cells is via endocytosis… yes… we are back to the evil Vitaliano geniuses. ³⁶ Prion uptake is mediated via Clathrin endocytosis. ³⁷ Their research was centered around the treatment of neurodegenerative diseases such as Alzheimer’s using Clathrin nanotechnology that would deliver Brain derived neurotrophic factor (BDNF) promotes the growth, differentiation, maintenance and survival of neurons. ³⁸ We told you they were building brains at Harvard’s MacLean Hospital. Medicine is a double-edged sword; those that build also know the mechanism to destroy. ³⁹

Final Plot Twist: Guess what the early symptoms of Prion Disease are? Apathy, detachment, impaired thinking, anxiety and depression. You see, the sheeple were always meant to be an oppressed species, to accept their culling with indifference and fear… and to go quietly into the good night.

For our protocols on deactivating the nano technology, see; “Deactivating the Graphene Quantum Dots & Decoupling your Brain from the Clathrin mRNA Neural Interface”, and remember, NO FEAR.