VMAT2 “God Gene” Has Been Studied Extensively Throughout the Years – And is Being Used in CRISPR Studies/Vaccines

According to studies, scientists can manipulate and “tightly experimentally tune” our level of spirituality.

As word of the vaccines affecting our spirituality and “God gene” spreads, it’s prudent to investigate these claims even deeper, as it involves our own human mind, body and soul . While some theories have been speculated upon, the studies and research that have been published throughout the years bears an extremely uncanny (if not direct) resemblance into the events that are going on around us, and have been for decades.

With that being said, here are some interesting correlations of the VMAT2 gene specifically, for further consideration. I will be selecting some excerpts from published medical reports, studies, documents and citing their sources to show an eerie connection to what may be going on today.

Quarterly FunVax Review

These documents were found from the following website: FunVax: Fundamentalist Vaccine
Pentagon Video, Document Reveal Aerial Vaccination Plan
as a pdf format, that can be found here (unless removed…): [ https://www.wanttoknow.info/health/funvax070601.pdf ]

The article that these documents were made available questions the authenticity and proposes that there is the possibility that it could be a fake/hoax. However, they also suggest that it is likely that it isn’t, citing numerous sources on the validity of such a project. It’s also interesting to consider that the linked article was allegedly originally created 10 years ago, in September of 2011. And as we’ll see throughout further sections of this post, as well as additional notes giving credence to these concepts, there are NUMEROUS studies involving the VMAT2 gene, proving that this has been worked on extensively throughout the years.

Here are some screenshots and excerpts of the documents in question. Some embellishment has been added for emphasis:

Screenshot taken from [ https://www.wanttoknow.info/health/funvax070601.pdf / page 1]

The objective of this phase of project ID 149AZ2 is to prepare a viral vector that will inhibit/decrease the expression of VMAT2 within a human population. Currently, tests are only scheduled for animal models. Infection of Rhesus Monkey, according to the timeline set out in Appendix 1, will begin as early as 07/02/07. A clinical team coordinated by [redacted] of [redacted] will be brought in to supervise the experiments once Rhesus Monkeys are being exposed to virus. The timeline for human trials and field tests will be determined by [redacted], and the role of the research group will be as support only. Upscale of the virus will be handled by [redacted]. The coordination between the research, clinical and manufacturing groups is outline in a report due on 06/15/07 and is in the process of being prepared by [redacted].”

Screenshot taken from [ https://www.wanttoknow.info/health/funvax070601.pdf / page 3]

“Airborne VSV Containing VMAT2 Disruption Gene

Abstract – Because of the vesicular stomatitis virus’ ability to infect brain cells and its two step life cycle, cytolytic infections in mammals and transmission by insects, it provided a starting point to design an airborne virus that has the ability to infect the respiratory system as well as brain cells. The newly designed virus contains the typical VSV genome, a homologous region to VMAT2 and a gene from adenovirus that allows attachment to the coxsackie-adenovirus receptor (CAR) on host cells. This design allows the virus to infect the respiratory track where cytolytic infection occurs and then subsequent diffusion across the blood brain barrier to infect brain cells. 600 strains of the virus were tested in duplicate on 1,200 mice. Mice were inoculated via needle and brains tissue examined three weeks after inoculation. VSV287 had the least amount of endogenous VMAT2 protein and will be further tested to verify that it is the most efficient of the 600 strains.”

Noteworthy mentions of some of the terminology:

“Vesicular stomatitis virus”[ https://pubmed.ncbi.nlm.nih.gov/26605499/ ] “Characterization of the glycoproteins of bat-derived influenza viruses” (2016)

Recently found bat-derived influenza viruses (BatIVs) have hemagglutinin (HA) and neuraminidase (NA) gene segments distinct from those of previously known influenza A viruses. However, pathogenicities of these BatIVs remain unknown since infectious virus strains have not been isolated yet. To gain insight into the biological properties of BatIVs, we generated vesicular stomatitis viruses (VSVs) pseudotyped with the BatIV HA and NA. We found that VSVs pseudotyped with BatIV HAs and NAs efficiently infected particular bat cell lines but not those derived from primates, and that proteolytic cleavage with a trypsin-like protease was necessary for HA-mediated virus entry.”

“(HA) Hemagglutinin”What is Hemagglutination?

Hemagglutination is a reaction that causes clumping of red blood cells in presence of some enveloped viruses, such as the influenza virus. A glycoprotein on the viral surface, namely hemagglutinin, interacts with red blood cells, leading to the clumping of red blood cells and the formation of a lattice.”

“(NA) Neuraminidase” – [ https://pubmed.ncbi.nlm.nih.gov/28356530/ ] “Role of Neuraminidase in Influenza A(H7N9) Virus Receptor Binding” (2017)

“Typically, the HA is responsible for binding to the sialic acid to allow virus internalization and the NA is a sialidase responsible for cleaving sialic acid to aid virus spread and release.”

The interaction of influenza A virus glycoproteins with cell surface receptors is a major determinant of infectivity and therefore transmissibility. Understanding these interactions is important for understanding which factors are necessary to determine pandemic potential.

“Coxsackie-adenovirus receptor (CAR)” – [ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926969/ ] “Coxsackie and adenovirus receptor (CAR) is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemia” (2013)

“A heritable component in risk for ventricular fibrillation (VF) during myocardial infarction (MI) has been well established. A recent genome-wide association study (GWAS) for VF during acute MI has led to the identification of a locus on chromosome 21q21 (rs2824292) in the vicinity of the CXADR gene. CXADR encodes the coxsackie and adenovirus receptor (CAR), a cell adhesion molecule predominantly located at intercalated discs of the cardiomyocyte.

Ventricular fibrillation (VF) is a frequent and potentially lethal complication of acute myocardial infarction (MI). In this setting, VF is the consequence of disturbed electrical properties of the ischemic myocardium, which includes a decrease in cardiomyocyte excitability and cell-to-cell coupling. These factors result in conduction slowing of the cardiac electrical impulse, which is a prerequisite for the occurrence of life-threatening arrhythmias such as VF in MI.

CAR has been recognized primarily for its involvement in virus-mediated myocarditis”

Continuing on with the Quarterly FunVax Review documents:

Screenshot taken from [ https://www.wanttoknow.info/health/funvax070601.pdf / page 3]

“Dispersal Options of Vesicular Stomatitis Virus

“Six methods of vesicular stomatitis virus dispersal were tested – high altitude release, water supply release, insect transmission, diffusion by a ground level object such as a car, diffusion from a stationary object such as a bottle and infection of food supply such as cattle or produce.”

Some possible connections to the above proposed “dispersal methods” of the Vesicular Stomatitis Virus:

High altitude release: chemtrails/contrails – with the pretense of protecting the world from climate change/global warming

Chemtrails Real Purpose And There’s Nothing You Can Do
Rosalind Peterson Talks Chemtrails & Geoengineering

Water supply release:

FARM FATALE | Shocking cover-up behind Dark Waters chemical leaks which left cows with GREEN organs and 99% of Americans infected
There’s Poison in the Tap Water. The Government Must Act.

Insect transmission: under the pretense of reducing insect species/population (allegedly to lower the chances of infectious disease spread…)

[ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269423/ ] “Science, Regulation, and Precedent for Genetically Modified Insects”
Why Are Gates and Pentagon Releasing GMO Mosquitoes in Florida Keys?

Infection of food supply such as cattle or produce:

Why Is Bill Gates (And China) Buying America’s Farmland?
GMO Dangers: Facts You Need to Know

While the Quarterly FunVax Review document was allegedly created in 2007, stating that the proposed dispersal methods above were already tested, we would be remiss if we didn’t realize that these studies would be ongoing and have been conducted in subsequent years to the present.

Screenshot taken from [ https://www.wanttoknow.info/health/funvax070601.pdf / page 4]

“VMAT2 Rhesus Monkey KO

“Abstract – VMAT2 homozygous knockout monkeys die within three days while the heterozygous monkey lives what appears to be a normal life span. VMAT2 is responsible for packaging dopamine and other monoamines into vesicles that will be released at the synapse. Dopamine disruption has been shown to damage dopamine neurons. While the KO monkeys were alive, they did not feed and upon the autopsy it was concluded that they died of starvation. It appears that they had no will to live.”

“Research Group Meeting 03/21/07
Topics that were discussed

– Current update on experiments in progress, round table
– VSV287, [redacted]
– Review of timeline, [redacted]
Proposal for a suicide gene, [redacted]
– Dispersal Methods, [redacted]
– Testing efficiency in the field, [redacted]
Inhibitors that may target a specific population, [redacted]
– Monkey knockout/knockdown progess, [redacted]
Future experiments, [redacted]

Screenshot taken from [ https://www.wanttoknow.info/health/funvax070601.pdf / page 5]

“Summary of Recommendation

1. Quantitative PCR of all 600 animal subjects should be done to ensure that the data from the ELISA experiments, which showed a decrease in endogenous VMAT2 is occurring because of viral insertion and not natural variation.

2. Of the 600 variants of Vesicular Stomatitis Virus tested, VSV287 had the greatest decrease of endogenous VMAT2 within mice. However, this may not be the case for human subjects. All 600 strains of VSV should be retested on human subjects by the clinical group. The clinical group should be involved with this ASAP.

3. Bradford assays should be done on infected subjects to determine endogenous VMAT2 concentrations before and after infection, not just after infection.

4. Mice or other subjects should not be injected with virus since this does not test the actual dispersal method. Future experiments of VSV287 or similar strains should allow the subject to breath in the virus rather than being injected with it.

5. The use of FunVax could see an immediate effect within the target zones and a way to measure the rate of infection should be examined and tested before the virus is released. Two or three of the following methods should be used to approximate efficiency. The results of the mass inoculation should be proportionate to the rate of infection and could be quantitated by either behavior or biological tests.

Behavior Indicators

a. Significant decrease in suicide bombings.

b. Decrease in armed resistance in conflict zones.

c. In non-conflict zones effectiveness could be measured by a decrease in people attending religious activities such as khutbahs or noon prayer.

d. Measureable increase in communications, telephone, email, and other forms of communication that express discontent with religion or God.

Screenshot taken from [ https://www.wanttoknow.info/health/funvax070601.pdf / pages 8&9]

“3. Based on the findings by [redacted] VSV287 has been shown to be safe with minimal serious side effects and has accomplished 8 of the 9 bench marks laid out in the “Summary of FunVax Objectives” including the two most important objectives at this stage –

a. An airborne virus that can insert a modified VMAT2 gene into brain cells.
b. a significant decrease of expression of endogenous VMAT2.

Only human trails [trials] can determine VSV287’s effect on religiosity and spirituality.

4. Dispersal methods are still being tested. High atmospheric dispersal or dispersal by ground level moving objects appear to be the most practical. Test will be conducted using VSV287. Once initial dispersal is accomplished infection will be transmitted person to person. The clinical group will examine the rates of person to person transmission.

Brief timeline (those within the same year may not be in ascending order) of some suspicious events that may have led to these studies:

1917Rudolf Steiner predicts vaccines that will remove spirituality from individuals

2004 – Dean Hamer proposes the God Gene theory in his book: “The God Gene: How Faith is Hardwired Into Our Genes”

2005FunVax Pentagon footage (allegedly created in 2005) at a Pentagon/DOD conference

2007 – Quarterly FunVax Review Documents were allegedly created

2007 – CRISPR technology became more well-known: “CRISPR (Clustered Regularly Interspaced Short Palindromic Repeat) sequences were initially discovered in the E. coli genome in 1987, but their function as a safeguard against bacteriophages was not elucidated until 2007”
[ https://www.addgene.org/crispr/history/ ]

2011 – Joey Lombardi purportedly leaked the Pentagon video discussing reducing “religious fanaticism” in the Middle East using a respiratory illness.

2012 – MERS Outbreak (“Middle East Respiratory Syndrome (MERS) is an illness caused by a virus (more specifically, a coronavirus) called Middle East Respiratory Syndrome Coronavirus (MERS-CoV). Most MERS patients developed severe respiratory illness with symptoms of fever, cough and shortness of breath. About 3 or 4 out of every 10 patients reported with MERS have died.”
[ https://www.cdc.gov/coronavirus/mers/about/index.html ]

2012 – “George Church, Jennifer Doudna, Emmanuelle Charpentier, and Feng Zhang discovered that by designing guide RNA to target a specific region in the genome, “the CRISPR-Cas9 system can be used as a “cut-and-paste” tool to modify genomes. As a DNA-editing tool, CRISPR-Cas9 can remove or introduce new genes as well as silence or activate genes.”
[ https://bitesizebio.com/47927/history-crispr/ ]

2012 – clip from the FunVax Documentary was released on youtube with Dean Hamer (of the National Institutes of Health) and the FunVax scientist speaking on the validity of removing “spirituality/religiosity” in individuals through the VMAT2 gene.
[ https://www.youtube.com/watch?v=vPyWZ4dbVQc ]

2019-ongoing – “COVID”, a coronavirus/respiratory illness, hits at the tail-end of 2019 and has upended the way of life we once knew. Perhaps setting the stage for…

2020 – Study of a “Double-Barreled CRISPR Technology as a Novel Treatment Strategy For COVID-19”: “over 200 vaccines are being tested in preclinical stage or in different stages of clinical trials worldwide.” / “In addition to DNA-targeting Cas9, the RNA-targeting CRISPR-Cas13 has also been successfully demonstrated as an antiviral strategy against single-strand RNA viruses such as lymphocytic choriomeningitis virus (LCMV), influenza A virus (IAV), and vesicular stomatitis virus (VSV) in human cells.”
[ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469881/ ]

2021 – Worldwide efforts to vaccinate everyone on the planet with the use of mRNA/DNA vaccines, even though there are already effective treatments, and the fact that natural immunity is far-superior than vaccines.

Some key takeaways from the contents of this post:

Is CRISPR being used/studied to create vaccines? | YES
[ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102830/ ] “CRISPR/Cas System: A Potential Technology for the Prevention and Control of COVID-19 and Emerging Infectious Diseases” (2021)

Biological tools based on CRISPR/Cas systems have been widely used in biomedicine. In particular, they are advantageous in pathogen detection, clinical antiviral therapy, drug, and vaccine development.”

Are VSV vectors being used/studied to create vaccines? | YES
[ https://pubmed.ncbi.nlm.nih.gov/31368826/ ] ” Recombinant vesicular stomatitis virus vector vaccines for WHO blueprint priority pathogens” (2019)

“The vesicular stomatitis virus (VSV) has been established as a robust vaccine vector backbone for infectious diseases for well over a decade.”

Are VSV vectors being used/studied with the use of the CRISPR/Cas9 technology? | YES
[ https://pubmed.ncbi.nlm.nih.gov/30195783/ ] “VSV-G-Enveloped Vesicles for Traceless Delivery of CRISPR-Cas9 ” (2018)

“The method of delivery of CRISPR-Cas9 into target cells is a strong determinant of efficacy and specificity in genome editing. Even though high efficiency of Cas9 delivery is necessary for optimal editing, its long-term and high levels of expression correlate with increased off-target activity. We developed vesicles (VEsiCas) carrying CRISPR-SpCas9 ribonucleoprotein complexes (RNPs) that are efficiently delivered into target cells through the fusogenic glycoprotein of the vesicular stomatitis virus (VSV-G).

Has the VMAT2 gene been studied specifically to measure spiritual/religious inclinations? | YES

[ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2262126/ ] “Experimenting with Spirituality: Analyzing The God Gene in a Nonmajors Laboratory Course” (2008)

“In his book, Hamer contends that one’s predisposition toward spirituality is influenced by genetic factors. More controversially, he proposes that the VMAT2 gene is one of many potential genes that impinge on spirituality.

VMAT2 encodes a transporter protein that imports several monoamine neurotransmitters into vesicles in the brain (reviewed in Zheng et al., 2006 blue right-pointing triangle). Thus, an alteration in the transporter could potentially affect the levels of multiple types of neurotransmitters, resulting in altered brain function. Changes in this monoamine transporter’s sequence or expression have been associated with substance abuse and Parkinson’s disease.

[ https://symbiosisonlinepublishing.com/genetic-science/genetic-science12.php ] “VMAT2 Gene Molecular study of 2,000 peoples in the Religious Behavior and Belief in God of the citizens of the city of Tabriz in IRAN” (2016)

“VMAT2 codes for a vesicular monoamine transporter that plays a key role in regulating the levels of the brain chemicals serotonin, dopamine and norepinephrine. These monoamine transmitters are in turn postulated to play an important role in regulating the brain activities associated with mystic beliefs.”

Is the VMAT2 gene being used/studied in CRISPR technology? | YES
[ https://www.biorxiv.org/content/10.1101/2021.09.10.459766v1 ] “Combining CRISPR/Cas9 and brain imaging: from genes to proteins to networks” (2021)

“Here, we combine CRISPR/Cas9 gene-editing with in vivo positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) to investigate the direct link between genes, proteins, and the brain connectome. The extensive knowledge of the Slc18a2 gene encoding the vesicular monoamine transporter (VMAT2), involved in the storage and release of dopamine, makes it an excellent basis for studying the gene networks relationships.

[ https://onlinelibrary.wiley.com/doi/full/10.1111/apha.13725 ] “Vesicular monoamine transporter 2 (SLC18A2) regulates monoamine turnover and brain development in zebrafish” (2021)

A zebrafish strain lacking functional Vmat2 was generated with the CRISPR/Cas9 system.

Amine synthesising and degrading enzymes, and genes essential for brain development, were analysed with quantitative PCR, in situ hybridisation and immunocytochemistry.

VMAT2 blockers reserpine and tetrabenazine induce depressive symptoms in both humans and animals, and altered pharmacodynamics of VMAT2 binding in platelets of children with depression have been reported.

CRISPR/Cas9 technology has been recently applied to modify the vmat2 gene in zebrafish. The zebrafish (Danio rerio) has become a popular model organism in neuroscience because it shares genetic homology with humans and possesses the main neurotransmitters present in humans.

Is the VMAT2 gene being used/studied and used for the development of vaccines/drugs? | YES

[ https://pubmed.ncbi.nlm.nih.gov/17985233/ ] “Inhibition of vesicular monoamine transporter-2 activity in alpha-synuclein stably transfected SH-SY5Y cells” (2008)

“alpha-Synuclein plays a key role in the pathological neurodegeneration in Parkinson’s disease.

“These data suggest that Up-regulated alpha-synuclein expression inhibits the activity of vesicular monoamine transporter-2, thereby interrupting dopamine homeostasis and resulting in dopaminergic neuron injury in Parkinson’s disease.”

[ https://pubmed.ncbi.nlm.nih.gov/23390095/ ] “Parkinson’s disease and alpha synuclein: is Parkinson’s disease a prion-like disorder?” (2013)

“Importantly, duplication/triplication of the wild type α-synuclein gene also cause a form of PD, indicating that increased levels of the normal α-synuclein protein is sufficient to cause the disease.

Recent evidence now suggests the possibility that α-synuclein is a prion-like protein and that PD is a prion-like disease.

– these findings support the hypothesis that α-synuclein is a prion-like protein that can adopt a self-propagating conformation that causes neurodegeneration.”

[ https://pubmed.ncbi.nlm.nih.gov/23771222/ ] “α-Synuclein vaccination prevents the accumulation of parkinson disease-like pathologic inclusions in striatum in association with regulatory T cell recruitment in a rat model” (2013)

– brains of patients with Parkinson disease (PD) and the presence in serum of α-synuclein (α-syn)-specific antibodies suggest that the peripheral immune system may have an active role in the progression of PD. We designed a vaccination strategy to attempt to control these processes and mediate protection against disease progression – “

[ https://pubmed.ncbi.nlm.nih.gov/25220836/ ] “VMAT2 and Parkinson’s disease: harnessing the dopamine vesicle” (2014)

Human studies demonstrate that the vesicular monoamine transporter 2 (VMAT2; SLC18A2) is dysfunctional in PD brain.

Therapeutic manipulation of VMAT2 level or function has the potential to improve efficacy of dopamine derived from administered levodopa, increase dopamine neurotransmission from remaining midbrain dopamine neurons and protect against neurotoxic insults. Thus, the development of drugs to enhance the storage of release of dopamine may be a fruitful avenue of research for PD.”

[ https://pubmed.ncbi.nlm.nih.gov/29669468/ ] “Inducible Alpha-Synuclein Expression Affects Human Neural Stem Cells’ Behavior” (2018)

“In this study, we present a novel human Tet-on human neural stem cell (hNSC) line, in which aSyn timing and level of expression can be tightly experimentally tuned.”

[ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990466/ ] “Treating Parkinson’s Disease with Antibodies: Previous Studies and Future Directions” (2021)

“aSyn was also found to modulate dopamine homeostasis through the inhibition of tyrosine hydroxylase (TH) expression, interaction with the dopamine transporter (DAT), and vesicular transporter VMAT2 which stores dopamine in synaptic vesicles.”

“In clinical trials, the company Affiris is assessing the efficacy of two next generation AFFITOPE® vaccines (PD01A and PD03A) which are peptides that mimic the C-terminus of aSyn.”

Just as a reminder to everyone, what is the leading adverse event that is being reported due to the “COVID vaccine“?

Aside from “general disorders and administration site conditions”:

“nervous system disorders” is the leading side effect of all 4 (Pfizer/Comirnaty, Moderna, J&J, AstraZeneca) COVID vaccines with a combined total of ~443,000 incidences as of September 11, 2021. And that’s just the number of people who have reported, with an estimated 1-10% (generous estimate) of cases being reported; many cases go un-reported.

Parkinson’s disease (PD) is a progressive disorder, which targets the nervous system that is responsible for body movement in the brain. This disorder causes many symptoms such as slowness, tremors, balance problems, as well as body stiffness. All of that happens because of the death of dopamine-producing neurons.” – How Does Parkinson Affect The Nervous System?

All of these correlations seems to suggest that the “COVID vaccine” may be nothing more than a giant experiment on the human race in order to manipulate our immune system, moods and behavior, and our spirituality and will to live.

And with companies like AC Immune, who are and have been working on vaccines to treat Parkinson’s, one has to wonder if they are a part of this whole big pharma conglomerate as well; just waiting in the wings to present their miracle cure (at the right cost, of course – which may also keep people numbed down and apathetic, depending on the severity of their vaccines’ effects) while the rest of us succumb to the harmful effects of the “COVID vaccines” and/or viral shedding of the spike proteins and toxins in our water, air, foods, etc. – which are damaging us not only physically, but emotionally and spiritually as well.

“FunVax a hoax?”

No. This is exactly what they were aiming for all these years. And with the the advent of CRISPR and a worldwide goal to vaccinate the whole population, they now know exactly what to target.

FunVax scientist: “On the left over here, we have individuals who are religious fundamentalists, religious fanatics. And this is the expression of rt-pcr, real-time pcr expression of the VMAT2 gene.

Over here we have individuals, so – so let me complete –  so over here we have individuals who are not particularly fundamentalists, not particularly religious, and you can see there’s a much reduced expression of this particular gene – that the VMAT2 gene.

Another evidence that, that supports our hypothesis for the development of this approach. -“

Audience attendee: “What you’re suggesting here is by, by spreading this virus we’re going to eliminate individuals from donning on a bomb vest and going into a market, blowing up the market.”

FunVax scientist: “So our hypothesis is that these are fanatical people, that they have over expression of the VMAT2 gene and that by vaccinating them against this, will eliminate this behavior.

So we have some, some very, very remarkable data in this next slide. Here we have two brain scans, these are fMRIs – these are two different individuals with different levels of expression of the VMAT2.

On top is an individual who’s a religious fanatic, and individual, and we’ve repeated this numerous times that, that has high levels of VMAT2. Now, um, this individual down here who had low levels of the VMAT2 gene, this individual would self-describe as, as not particularly religious. In each case, these individuals were read a religious text – this individual light – lit up the right middle frontal gyrus, shown here, and that’s a part of the brain that’s associated with theory of mind. It’s a part of the brain that has to do with intense and in beliefs and desires.

In contrast, in mark contrast, here’s an individual who would not particularly self-describe as, as religious, and when they’re read a religious text, what you see is that this part of the brain called the anterior insula lights up. This is a part of the brain that’s associated with disgust or displeasure on hearing something.”

Audience attendee: “Do you suggesting, like, take a CT scan with me when I’m evaluating people to determine whether I put a bullet in their head?”

FunVax scientist: “So, so um the data that I’m presenting here, uh, supports the concept that we’re proposing, uh, and I think that we would not propose to do CT scans or fMRIs on individuals out in the hinterlands of Afghanistan.

The virus would immunize against this VMAT2 gene and that would have the effect that you see here which is, it’s essentially to turn a fanatic into a, a normal person. And we think that will have major effects in the Middle East.”

Audience attendee: “How would you suggest that this is going to be dispersed? Aerosol? Or…?”

FunVax scientist: “Well, so, so the present plan, and the test that we’ve done so far have used respiratory viruses such as flu, or rhinoviruses, and we believe that that’s a satisfactory way to get the exposure of the largest part of the population. Most of us, of course, have been exposed to both of those viruses and we’re, we’re quite confident that this will be a very successful approach.”

Audience attendee: “This is fascinating. What’s the name of this proposal?”

FunVax scientiest: “Yes, so, so the name of this project is FunVax, which is the vaccine for religious fundamentalism.

Audience attendee: “And you have a proposal already?”

FunVax Scientist: “The proposal has just been submitted and I think that the data that I have shown you today would, would support the, the development of this project and we think it has great promise.”

From the FUNVAX Documentary footage:

Narrator @ 03:57: “So let’s get back to reality for a minute. Is a vaccine against religious fundamentalism even possible?”

Same FunVax scientist from leaked 2005 footage: “So somebody asked me to design a vaccine for religious fundamentalism or fanaticism, uh, basically what I would do is to try to better understand why people are fanatical. Why do they have extreme behavior? Uh, it’s pretty clear these days that, that all behavior results from, uh, activity of our own brains. And so there must be pathways that are important in generating this kind of behavior.”

Dean Hamer (worked as director of the Gene Structure and Regulation Unit and as an independent research at the NIH): “So if indeed spirituality is this series of chemical reactions in the brain, and if it can be enhanced by certain types of drug, then, naturally it follows that it can be inhibited as well. ‘Cause for every activator there must be an inhibitor. And so I can easily imagine under the right circumstances, the right stimuli, or the right drugs, and the right inhibitors, might have some effect on a person’s spirituality.

At least in the short run. Whether or not that would have a long term effect, or people would undergo homeostasis and alter, uh, is an open question. We really don’t know the answer to that.”

FunVax scientist: “It would be quite useful to eliminate some of the fanatical, um… religious nuts in the world. And I think that, that, um, maybe a vaccine would be the way to do that. It’s difficult to know how successful it would be, but it’s certainly an interesting idea. From the point of view of a, uh, medical professional, um, the question of spreading a virus that is – has not been approved by regulatory agencies, such as the FDA, is a major issue.

One last mention, if one is to look at the top left side of the leaked Pentagon footage, we can see the following identifier: “DOD ID 149AZ2

Does that sound familiar? It should. It’s the same project ID that is listed on the Quarterly FunVax Review documents from above.

Fact checking is extremely important. I want to reiterate not to take everything at face value; no matter what you read, where you read it from, or who you hear it from. And to be clear, do not rely on “fact checking” websites to give you accurate information either. These are just as likely, (if not even more likely…), to feed false information and false debunking accounts to manipulate the reader. Please take everything into consideration before adhering to a certain narrative – and always keep your mind open to other possibilities.

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