Epstein Borreliosis AIDS

Unless we start valuing the actual expertise that legitimate experts have spent lifetimes developing, “doing our own research” could lead to immeasurable, unnecessary suffering. When left to their own devices, a substantial fraction of people will choose not to fully vaccinate themselves or their children. (And we certainly can't have that now can we?) https://www.forbes.com/sites/startswithabang/2020/07/30/you-must-not-do-your-own-research-when-it-comes-to-science/#25ca90dc535e Now that Forbes convinced you to not bother your pretty little head researching science on your own but to trust the "experts", here is an article telling you Why You Should Trust The Coronavirus Vaccine https://www.forbes.com/sites/stevensalzberg/2020/07/20/why-you-should-trust-the-coronavirus-vaccine/#4367c6b23504

Re(write) gene r on - REGN-COV2 here comes the "reign" get it? Do you have eyes to see? All the whirled is a stage, Trump is an actor playing a part..all to push the vaccine or the "therapeutics" which will modify you on a genetic level and connect you with the AI in the cloud. Trump calls them a "miracle from God? Which god is that exactly? Do not be deceived. Be wise as serpents but gentle as a dove... Fox Article https://www.foxnews.com/politics/trump-coronavirus-treatment-walter-reed-regeneron-remsdesivir-dr-ronny-jackson Westchester Magazine article Biochester https://westchestermagazine.com/uncategorized/biochester/?fbclid=IwAR09EjXIeQNu0hyhMHInNXD73iyAhM5KdMx50_3MRJzfxc_Z38_StQhCEPc https://investor.regeneron.com/news-releases/news-release-details/regenerons-regn-cov2-antibody-cocktail-reduced-viral-levels-and https://www.genengnews.com/news/moderna-regeneron-covid-19-candidates-show-early-positive-data/ This Synthetic DNA Factory Is Building New Forms of Life In this DNA factory, organism engineers are using robots and automation to build completely new forms of life https://youtu.be/DxoLoOtyllU Revolutionizing Vaccine Development with Synthetic Biology https://www.biocompare.com/Editorial-Articles/174945-Revolutionizing-Vaccine-Development-with-Synthetic-Biology/?fbclid=IwAR1ijzbJn4wtHzt1NBZFAYvO3Yupwa8-1NvTMka8SqlTVFszn_jwKX3unPs ...the current repertoire of devices used in RNA synthetic biology and propose how programmable 'smart vaccines' will revolutionize the field of RNA vaccination. https://pubmed.ncbi.nlm.nih.gov/25566800/ http://webstersdictionary1828.com/Dictionary/smart The word transfection is a portmanteau of trans- and infection. Genetic material (such as supercoiled plasmid DNA or siRNA constructs), or even proteins such as antibodies, may be transfected. https://en.wikipedia.org/wiki/Transfection#Chemical-based_transfection RNAi (my brain sees rain...it stands for RNA interference) https://www.ncbi.nlm.nih.gov/probe/docs/techrnai/ https://www.thermofisher.com/us/en/home/life-science/rnai/synthetic-rnai-analysis.html https://www.genome.gov/genetics-glossary/messenger-rna Different types of RNA exist in the cell: messenger RNA (mRNA), ribosomal RNA (rRNA), and transfer RNA (tRNA). More recently, some small RNAs have been found to be involved in regulating gene expression. https://www.genome.gov/genetics-glossary/RNA-Ribonucleic-Acid The following is abstract from a 2019 thesis, which discusses successfully creating a lipid nano particle LNP delivery vehicle for the siRNA as well as Cas9 mRNA. Interesting considering they are the "new technologies" vaccines and therapeutics being rolled out at record speed with Operation Warp Speed. Trump says his Operation Warp speed is greater than the Manhattan Project. Let's not forget Operation Paperclip, where they brought over the most evil scientists to create NASA and what passes for Science today. The field of RNA therapeutics is currently undergoing both transformation and expansion. Specifically, research in lipid nanoparticle (LNP) based RNA therapeutics is gaining significant traction. Other research into mechanisms of gene regulation and manipulation, including siRNA and the CRISPR/Cas9 system have demonstrated the potential of RNA-based disease treatment. This work identifies a delivery system which can regulate expression of green fluorescent protein (GFP) in human embryonic kidney cells (HEK293) stably expressing GFP. https://opencommons.uconn.edu/cgi/viewcontent.cgi?article=1058&context=usp_projects https://www.biocentury.com/article/304691/darpa-jump-started-technologies-behind-some-of-the-leading-covid-19-vaccine-and-antibody-hopes The original Vir-Alnylam collaboration also called for developing RNAi products https://www.genengnews.com/news/coronavirus-takeda-pursues-plasma-derived-treatment-alnylam-and-vir-eye-sirna-therapy/ Derek Rossi..now-retired Harvard professor claimed in an interview with the National Post that he found a way to “reprogram” the molecules that carry the genetic instructions for cell development in the human body...called messenger RNA and the newfound ability to rewrite those instructions to produce any kind of cell within a biological organism has radically changed the course of Western medicine and science.. https://www.mintpressnews.com/darpa-covid-19-vaccine-implant-mrna/271287/ link to Human 2.0 Dr Carrie Madej discussing mRNA vaccines https://articles.mercola.com/sites/articles/archive/2020/09/12/coronavirus-vaccine-transhumanism.aspx

you can download the book from this link https://aim4truth.org/2020/09/07/eustace-mullins-and-the-one-world-order/ from the preface "I discovered that the hidden manipulators of the World Order had maintained their power by a very simple technique, which I have likened to a masked ball. The bal masque enables the Gnostics, the Knowing Ones, to identify their friends and enemies because they alone know who is wearing what costume. It is a masquerade which depends entirely upon disguise, that is, on things which are not what they seem."

https://childrenshealthdefense.org/news/the-intertwined-history-of-myelitis-and-vaccines/?utm_source=salsa&eType=EmailBlastContent&eId=c93b0298-63e5-4177-b6cc-ccb6dd3e0f28 https://www.anti-empire.com/ex-chief-science-officer-for-pfizer-says-second-wave-conjured-up-by-flawed-test-pandemic-is-over/ https://www.bulatlat.com/2020/08/21/hazards-of-the-covid-19-vaccine/ Lies, Damned Lies and Health Statistics – the Deadly Danger of False Positives https://lockdownsceptics.org/lies-damned-lies-and-health-statistics-the-deadly-danger-of-false-positives/ https://www.bloomberg.com/features/2020-moderna-biontech-covid-shot/

in early May, the US Food and Drug Administration (FDA) granted Sherlock Biosciences an emergency use authorization (EUA) for its COVID-19 diagnostic assay, beating out other companies and academic groups trying to use the powerful gene-editing technology to figure out who is infected with the novel coronavirus. Sherlock’s test is the first FDA-authorized use of CRISPR technology for anything. https://markets.businessinsider.com/news/stocks/the-global-crispr-technology-market-size-is-seeing-exponential-growth-due-to-the-application-of-crispr-technology-in-treating-covid-19-1029619386# https://sherlock.bio/technology/ https://en.wikipedia.org/wiki/Open_Philanthropy_(organization) https://www.openphilanthropy.org/about/who-we-are SHERLOCK: A CRISPR Tool to Detect Disease This animation depicts how Cas13 -- a CRISPR-associated protein -- may be adapted to detect human disease. This new diagnostic tool, called SHERLOCK, targets RNA (rather than DNA), and has the potential to transform research and global public health. https://www.youtube.com/watch?v=ZOoUIlLmxf4 What is SHERLOCK technology? The Cas9 enzyme is also known as a programmable nuclease. This is due to the fact that one can use it to cut the targeted DNA site by providing a unique RNA. This method is harnessed further by scientist to develop SHERLOCK technology (stands for Specific High sensitive Enzymatic Reporter Unlocking). The only difference is that it uses Cas13a endonuclease enzyme rather than Cas9. The method involves the following: RNA amplification (Or DNA by enzyme reverse transcriptase). Amplified RNA is complexed with Cas13a enzyme, a guide RNA resembling target sequence, and a reporter nucleic acid sequence containing a fluorescent tag. Activation of Cas13a non-specific RNAse activity in response to the presence of the target sequence is detected in the reaction mixture As a result, the RNA reporter will be cleaved leading to activation of the fluorophore. Since the technique is based on fluorescence-based detection of the target sequence from the pool of amplified nucleotides, it is known as “Specific High sensitive Enzymatic Reporter Unlocking” i.e. SHERLOCK. Are there other similar technologies? DETECTR Technology (DNA Endonuclease Targeted CRISPR Trans Reporter): This system was first reported by scientists – Jennifer Doudna and her colleagues at the University of California. This technology is similar to SHERLOCK with a difference in the type of endonuclease used. Here the researchers used Cas12a instead of Cas13a or Cas9 which cleaves the dsDNA and leads to activation of the non-specific ssDNA breakdown. The researchers used this technique to identify carcinomas related Human Papilloma Virus (HPV). HUDSON Technology (Heating Unextracted Diagnostic Samples to Obliterate Nuclease): This method involves the release of nucleic acids directly into the solution by initiating the heat and chemical reduction based lyses of the viral envelope. The researchers have combined the HUDSON technology with SHERLOCK technology in order to detect two most fatal virus i.e. Zika and Dengue virus. How SHERLOCK Technology can be helpful? As we have looked upon the working mechanism of the technology, it is easy to guess its enormous potential in the field of biosciences. To mention the few: It can be used for detection of both viral and bacterial pathogens The evaluating viral load of HIV patients Detection of any DNA mutation and subsequent assessment of disease tendencies Rapid and precise result for TB (Tuberculosis) Instantaneous identification of pathogen-resistant genes Assessment of gene edits created by CRISPR using SHERLOCK technology https://thescientificreporters.com/crispr-based-sherlock-technology-the-detective/

https://en.wikipedia.org/wiki/Open_Philanthropy_(organization) Event 201 was supported by funding from the Open Philanthropy Project. http://www.centerforhealthsecurity.org/event201/ Open Philanthropy Project is owned by Facebook Co-founder Dustin Moskovitz, his wife and partners. NOTE-THE EXERCISE REPEATEDLY MENTIONS THE USE OF FAITH BASED ORGANIZATION PARTNERS . The videos show the 3 1/2 hour mock Pandemic Response in full . http://www.centerforhealthsecurity.org/event201/videos.html David Martin youtube channel (he was featured in Plandemic II) https://www.youtube.com/channel/UClLDXIjo_7yQPG1Uqt-n4Wg https://2020electioncenter.com/watch?id=5f610c39dc50dc07a1fe8013 BOMBSHELL: Expert Exposes Fauci’s CRIMINAL Violations (David Knight Interviews David Martin) https://www.centerforhealthsecurity.org/event201/about Abstract According to a "parasite stress" hypothesis, authoritarian governments are more likely to emerge in regions characterized by a high prevalence of disease-causing pathogens. Recent cross-national evidence is consistent with this hypothesis, but there are inferential limitations associated with that evidence. We report two studies that address some of these limitations, and provide further tests of the hypothesis. Study 1 revealed that parasite prevalence strongly predicted cross-national differences on measures assessing individuals’ authoritarian personalities, and this effect statistically mediated the relationship between parasite prevalence and authoritarian governance. The mediation result is inconsistent with an alternative explanation for previous findings. To address further limitations associated with cross-national comparisons, Study 2 tested the parasite stress hypothesis on a sample of traditional small-scale societies (the Standard Cross-Cultural Sample). Results revealed that parasite prevalence predicted measures of authoritarian governance, and did so even when statistically controlling for other threats to human welfare. (One additional threat—famine—also uniquely predicted authoritarianism.) Together, these results further substantiate the parasite stress hypothesis of authoritarianism, and suggest that societal differences in authoritarian governance result, in part, from cultural differences in individuals’ authoritarian personalities. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641067/pdf/pone.0062275.pdf?fbclid=IwAR07Z_iJzL6NhFmKnIixsInqa_IWHHR59WpwLxjxhxv-nAbV2TGW2T0t6ao https://thirtypiecesofsilver.org/2020/03/30/globalist-false-prophets-the-real-danger-ahead/

Elderberry can help you kill the infections. It attaches to stealth. https://www.facebook.com/notes/mel-thornburg/elderberry-recipes-and-such/1214881815206856/ https://pubmed.ncbi.nlm.nih.gov/27290916/ Elderberries: A Source of Ribosome-Inactivating Proteins with Lectin Activity https://www.mdpi.com/1420-3049/20/2/2364?fbclid=IwAR0HGjPnnwu4G5KWBASrZbxjY79Gevs7c8-7J8M1WvaqM98sDd5jcCeJSVI In Vivo Antitumor Effect of Supercritical CO 2 Extract of Mango Ginger ( Curcuma amada Roxb) in U-87MG Human Glioblastoma Nude Mice Xenografts https://pubmed.ncbi.nlm.nih.gov/27436761/ 6-Shogaol has anti-amyloidogenic activity and ameliorates Alzheimer's disease via CysLT1R-mediated inhibition of cathepsin B https://pubmed.ncbi.nlm.nih.gov/27286707/ Anti-Fungal Efficacy and Mechanisms of Flavonoids https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168129/?fbclid=IwAR2fxnKaAa0qoWsN2gEMzv4QSXxXS0DDWlKp4uvnNsLceT-RJVjxi06S4Mc Structure-activity relationship of immunomodulating pectins from elderberries https://pubmed.ncbi.nlm.nih.gov/25857988/ Neuroprotective Role of Natural Polyphenols https://pubmed.ncbi.nlm.nih.gov/26845551/ Root bark of Sambucus Williamsii Hance promotes rat femoral fracture healing by the BMP-2/Runx2 signaling pathway https://pubmed.ncbi.nlm.nih.gov/27178636/ Anticonvulsant activities of Sambucus nigra https://pubmed.ncbi.nlm.nih.gov/27460744/ Antiviral activity of the "Virus Blocking Factor" (VBF) derived i.a. from Pelargonium extract and Sambucus juice against different human-pathogenic cold viruses in vitro https://pubmed.ncbi.nlm.nih.gov/27717933 The Cytotoxicity of Elderberry Ribosome-Inactivating Proteins Is Not Solely Determined by Their Protein Translation Inhibition Activity https://pubmed.ncbi.nlm.nih.gov/26148207/ Anti-Toxoplasma activities of methanolic extract of Sambucus nigra (Caprifoliaceae) fruits and leaves https://pubmed.ncbi.nlm.nih.gov/26299111/ In it's molecular forms called Prion Proteins In it's most basic forms it is called Myco PLASMA, Ana PLASMOSIS, Toxo PLASMOSIS or Spiro PLASMA--Exosomes, Blebs, Gemma, TAU. And your baaad cholesterol. In it's viral forms it is host gene dependent LEGIONS. In its bacterial forms it is MANY esp. Ehrlichia and H.pylori, TB, According to where it resides . It's infectious organisms protected in fungus. You can kill the infections but the immune suppression they cause isn't easily fixed. All of your so called viruses are simply morphological forms of infinite host gene variations.....Their cystic viral morphologies and secreted blebs containing seed formerly known as Prion and flagellum that recombines and grows with infectious DNA. https://pubmed.ncbi.nlm.nih.gov/?term=elderberry%20sambucus&fbclid=IwAR2uu2h1Qw1V4lht_LdBAWTfhRz85Ptw3hHL-p7NtnjgVD3w0mAOTODquh0 Anticancer Potential of Ginger: Mechanistic and Pharmaceutical Aspects https://pubmed.ncbi.nlm.nih.gov/27290916/ In vitro bactericidal activity of promising nutraceuticals for targeting multidrug resistant Pseudomonas aeruginosa Conclusion: G. glabra (licorice), a flavoring agent; Z. officinale (ginger), a condiment; and Mentha piperita (mint), a fragrance component, showed significant therapeutic potential against multidrug resistant strains of P. aeruginosa. https://pubmed.ncbi.nlm.nih.gov/27083519/ Zerumbone, a Phytochemical of Subtropical Ginger, Protects against Hyperglycemia-Induced Retinal Damage in Experimental Diabetic Rats https://pubmed.ncbi.nlm.nih.gov/27463726/ Revealing the effect of 6-gingerol, 6-shogaol and curcumin on mPGES-1, GSK-3β and β-catenin pathway in A549 cell line https://pubmed.ncbi.nlm.nih.gov/27645308/ The results showed that the high molecular RG-I containing polymers exhibit the highest dose-dependent complement fixing and macrophage stimulating activities. http://www.ncbi.nlm.nih.gov/pubmed/27475233 https://pubmed.ncbi.nlm.nih.gov/27484408/ The beneficial effects on blood pressure, dyslipidemia and oxidative stress of Sambucus nigra extract associated with renin inhibitors https://www.tandfonline.com/doi/full/10.1080/13880209.2016.1207088?fbclid=IwAR2KoNafsHPAyLnjK8WUaOSLLhoGw9FpPJaYXqmu59cy8k_bQPqa9sVHboE Diabetes the same as BP....funny how that works! https://www.ncbi.nlm.nih.gov/pubmed/28025494 https://pubmed.ncbi.nlm.nih.gov/28303711/ Parkinson's Epsteins Borreliosis AIDS... https://www.ncbi.nlm.nih.gov/pubmed/28214539 Interfering With Lipid Raft Association: A Mechanism to Control Influenza Virus Infection By Sambucus Nigra https://pubmed.ncbi.nlm.nih.gov/29201101/ Iran can treat intracellular parasites with elderberry. https://www.ncbi.nlm.nih.gov/pubmed/31858914 https://pubmed.ncbi.nlm.nih.gov/28783175/

Though it took three decades for the Geys to succeed with their efforts to create a human cell line, after their success with HeLa, culturing cells became suspiciously easy. Researchers cultivated tissue samples from their own bodies and the bodies of their families and patients. Most grew successfully. Sure, the samples struggled during the first few weeks, or even months, in culture, but then, suddenly, they flourished. Samples blossomed into full-blown healthy cell lines with the strength of, well, the HeLa cell. In 1974, a researcher by the name of Walter Nelson-Rees started what everyone called a nasty rumor: HeLa cells, he claimed, had infiltrated the world's stock of cell cultures. No one wanted to believe him. For almost three decades researchers had done complex experiments on what they thought were breast cells, prostate cells, or placental cells, and suddenly, rumor had it they'd been working with HeLa cells all along. To believe this would be to believe that years of work and millions of dollars had, in essence, been wasted. http://berkeleysciencereview.com/article/good-bad-hela/?fbclid=IwAR2uy6aL_zN5s23QhE9-WkQq9ZhRINrCaLtmpJyg70J5i60ZlVBRgQfefwo After sterilising everything and donning a surgical cap and mask, she cut the sample into one-millimetre dice, dropped each tiny square onto a chicken blood clot in a test tube, and covered it with a few drops of the mixture of broths, salts and umbilical cord blood that was the cells’ experimental plat du jour. She then plugged each test tube with a rubber stopper, labelled it ‘HeLa’ for the patient’s first and last names, and inserted it into a crazy rig that George Gey had fashioned out of junkyard scraps to keep the cells warm and in constant motion. A couple of days later, the little clots at the bottom of the test tubes had sprouted a whitish ring of new cells. Mary Kubicek didn’t think much of it. Many of the samples she had cultured over the years had survived and reproduced initially, only to die off after a few days. The next time she looked, however, she noticed that these cells weren’t just growing, they were proliferating. She split them up into new test tubes. They kept on multiplying, doubling approximately every 24 hours, ‘spreading like crabgrass’, as she later recalled. As long as they were kept warm and fed, HeLa cells seemed indestructible, unstoppable, potentially immortal. The Geys were ecstatic, and started to send out samples to colleagues. They sent HeLa cells to Texas, New York, Amsterdam, India and Chile, in cardboard boxes packed with sawdust, in the shirt-pockets of pilots and air stewards, and on one occasion, in the saddlebag of a mule. On 10 April 1951, George Gey appeared on local television waving a pint bottle full of HeLa, and predicting the medical marvels that it would make possible. Lacks had been combined with tobacco DNA to produce the first human/plant hybrid. In time, however, this mid-century idealism metamorphosed into hubris. In 1954, Chester Southam, the chief of virology at the Sloan-Kettering Institute for Cancer Research, began to inject HeLa cells into the arms of cancer patients to see if he could induce tumours. He failed to inform his research subjects that the cells were cancerous, on the grounds that it might upset them, and went on to do the same experiment on healthy volunteers from a state penitentiary, and on hundreds of gynaecological surgery patients. In 1963, he made the mistake of trying to involve three doctors at the Jewish Chronic Disease Hospital in Brooklyn, whose memories of the Nuremberg Doctors’ Trial were vivid enough for them to make the connection between his research and Nazi medical atrocities. Their protest led to others, culminating in the revelation of the Tuskegee syphilis study https://www.lrb.co.uk/the-paper/v32/n11/cathy-gere/dying-and-not-dying Stealth secretions: https://pubmed.ncbi.nlm.nih.gov/26812803/ https://www.biocompare.com/Editorial-Articles/348977-Authenticate-Combating-Misidentified-and-Contaminated-Cell-Lines/?fbclid=IwAR0Jg86kxD0MSsjfkwStpd5sMvl-T1OLP1rhEJGMxkqXSnPBQ2kOxiUp0-I https://www.legacy.com/amp/obituaries/sfgate/123425949?fbclid=IwAR3vCPZjcnSmfKkOBrXGdlxfNcvasj4dWQh43E2WENgFjB6JsVCKVQbeUII https://vimeo.com/9581140?fbclid=IwAR15tirLYwRHClMIK0djV4MXDz3TjP3N1VKcT9eBSIJ0zg7M10e69aVpZ2g https://spirochetesunwound.blogspot.com/2009/01/watch-videos-of-lyme-disease-spirochete.html?m=1&fbclid=IwAR0Jg86kxD0MSsjfkwStpd5sMvl-T1OLP1rhEJGMxkqXSnPBQ2kOxiUp0-I https://www.sciencedirect.com/science/article/pii/S0378113503003687?fbclid=IwAR0pTGnu1KYVHADQCWpZTV28q9Zg4J5QniwLgsw737ushNSopQYaoj0F084 https://cmr.asm.org/content/16/1/65.full?fbclid=IwAR1XKwlg7vbyCDMTn17ct_Rv24-tXAk0fr5NcdiAVNKMTplfmEPEJtrHP9A https://www.dailymail.co.uk/health/article-4986000/Results-30-000-published-studies-wrong.html?fbclid=IwAR2-quDIX4w-Jcv5IPWJzTvAHrs9Ddx_lbZS31D622P5fYq7_Fma0C0Wzzg

Gammaherpesvirus Infection of Human Neuronal Cells Importance: To date, no in vitro study has demonstrated gammaherpesvirus infection of neuronal cells. Moreover, worldwide clinical findings have linked EBV to neuronal pathologies, including multiple sclerosis, primary central nervous system lymphoma, and Alzheimer's disease. In this study, for the first time, we have successfully demonstrated the in vitro infection of Sh-Sy5y and Ntera2 cells, as well as human primary neurons. We have also determined that the infection is predominately LYTIC. Additionally, we also report infection of neuronal cells by KSHV in vitro similar to that by EBV. These findings may open new avenues of consideration related to neuronal pathologies and infection with these viruses. Furthermore, their contribution to chronic infection linked to neuronal disease will provide new clues to potential new therapies. https://pubmed.ncbi.nlm.nih.gov/26628726/ There's no such things as viruses. They are "lytic" ~bacterial associated, stress induced morphological forms of infinite antigenic variations in less than 2 seconds under antibiotic stress! https://www.youtube.com/watch?v=lVmCa70bAxE&fbclid=IwAR11L3tmFlz8sIHO60hYned80en5X7BmQAQWwN7S4qOI3VTRWWpIdeuK2UE&app=desktop https://pubmed.ncbi.nlm.nih.gov/27813134/ https://www.facebook.com/melthornburg0007/posts/10212167064805988 https://pubmed.ncbi.nlm.nih.gov/28935930/ https://www.lymeneteurope.org/forum/viewtopic.php?f=13&t=5147&start=20&fbclid=IwAR05zZwg9VrN0tHHrUL7xA7LurlO-S_zMnWZwDiDOu6HNx1EVQaQGBbxC3c https://en.m.wikipedia.org/wiki/List_of_contaminated_cell_lines?fbclid=IwAR1yblVy9Wr7_SJlfVM0aTdhgo7vDN8edGq5BorYVzTVMqw98U9nQEJrjdI Establishment and characterization of a novel Hodgkin lymphoma cell line, AM-HLH, carrying the Epstein-Barr virus genome integrated into the host chromosome https://pubmed.ncbi.nlm.nih.gov/27813134/ EBV infection is prevalent in the adenoid and palatine tonsils in adults https://pubmed.ncbi.nlm.nih.gov/27864888/ Novel Spiroplasma Spp. Cultured From Brains and Lymph Nodes From Ruminants Affected With Transmissible Spongiform Encephalopathy https://pubmed.ncbi.nlm.nih.gov/29155968/ https://www.asianscientist.com/2014/05/in-the-lab/scientists-uncover-ebv-hides-2014/?fbclid=IwAR1du45KlN4kRvOPpN9bqnyxGptpsZQcP5peLDv6Hxt8hZHuyGNAvAeWGgU Schizophrenia is Associated With an Aberrant Immune Response to Epstein-Barr Virus https://pubmed.ncbi.nlm.nih.gov/30462333/ Morphological investigation of neurofibrillary tangles in Alzheimer's disease https://pubmed.ncbi.nlm.nih.gov/7933715/ In it's molecular forms called Prion Proteins In it's most basic forms it is called Myco PLASMA, Ana PLASMOSIS, Toxo PLASMOSIS or Spiro PLASMA--Exosomes, Blebs, Gemma, TAU. And your baaad cholesterol. In it's viral forms it is host gene dependent LEGIONS. In its bacterial forms it is MANY esp. Ehrlichia and H.pylori, TB, According to where it resides . It's infectious organisms protected in fungus. You can kill the infections but the immune suppression they cause isn't easily fixed. All of your so called viruses are simply morphological forms of infinite host gene variations.....Their cystic viral morphologies and secreted blebs containing seed formerly known as Prion and flagellum that recombines and grows with infectious DNA. Discussion The results reported here point to a possible primary target for the cytotoxicity expressed by the RepA-WH1 prionoid in E. coli: the bacterial internal cell membrane. Three distinct mechanisms have been proposed for membrane disruption by amyloidogenic proteins8, including: i) the formation of pores by the assembly of protein monomers into ring-shaped oligomers; ii) membrane thinning and iii) lipid (detergent-like) extraction. Since the last mechanism should imply the lysis of a significant fraction of the vesicles, which was not the case under our experimental conditions, and the second one seems incompatible with the observed persistence of aggregates bound to the membranes (Figs 3–5), the formation of pores by protein insertion into the lipid bilayer, as first proposed for Aβ and α-synuclein39, was the most likely mechanism for vesicle leakage induced by RepA-WH1. ....leading to the characterization of RepA-WH1 as the first synthetic bacterial prionoid! https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794723/pdf/srep23144.pdf

In it's molecular forms called Prion Proteins In it's most basic forms it is called Myco PLASMA, Ana PLASMOSIS, Toxo PLASMOSIS or Spiro PLASMA--Exosomes, Blebs, Gemma, TAU. And your baaad cholesterol. In it's viral forms it is host gene dependent LEGIONS. In its bacterial forms it is MANY esp. Ehrlichia and H.pylori, TB, According to where it resides . It's infectious organisms protected in fungus. You can kill the infections but the immune suppression they cause isn't easily fixed. All of your so called viruses are simply morphological forms of infinite host gene variations.....Their cystic viral morphologies and secreted blebs containing seed formerly known as Prion and flagellum that recombines and grows with infectious DNA. I go through this all pretty quickly and I realize it is alot of information Mel's links are public. You should go to her page and check out her stuff. https://m.facebook.com/story.php?story_fbid=10209868849152033&id=1657389649&ref=m_notif&notif_t=comment_mention&refid=52&__tn__=R https://m.facebook.com/story.php?story_fbid=10212310154383138&id=1657389649&ref=m_notif&notif_t=comment_mention Possible roles of amyloids in malaria pathophysiology https://pubmed.ncbi.nlm.nih.gov/28031872/ RepA-WH1, the agent of an amyloid proteinopathy in bacteria, builds oligomeric pores through lipid vesicles https://pubmed.ncbi.nlm.nih.gov/26984374/ Influenza virus exploits tunneling nanotubes for cell-to-cell spread https://pubmed.ncbi.nlm.nih.gov/28059146 Hepatitis C virus-induced prion protein expression facilitates hepatitis C virus replication https://pubmed.ncbi.nlm.nih.gov/29076011/ https://newspunch.com/cdc-morgellons-disease/ Evidence that DNA is present in abnormal tubulofilamentous structures found in scrapie. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC280256/?fbclid=IwAR0UcBqDfu8ox_0aOS_6C2b2KyeOQLvzN3Rx-SP8vw8lUC_fHs-IwapDqMc https://www.niaid.nih.gov/diseases-conditions/prion-diseases?fbclid=IwAR32irgoLtC0R5Ss3USS6Y-N1oZIb2LsgkMfqzh4yOGajTswTDZJZNEO1jM HeLa Cells https://vimeo.com/9581140?fbclid=IwAR2DDNDtC1syWYdGmVEuiWPvKV0AH1FMSmrW328BjlvGXpt4yxz8bqnxpxk https://www.lymeneteurope.org/forum/viewtopic.php?f=13&t=5147&sid=de93486fc7230ab25920cdc670dd61cd&fbclid=IwAR2VjjqtOKqvkQfwwkh1NcLmu-iGl7AsN_C3DI_xqwmQc-2PydrM31Avr9g https://m.facebook.com/story.php?story_fbid=10209868849152033&id=1657389649&ref=m_notif&notif_t=comment_mention&refid=52&__tn__=R MicroRNAs of Epstein-Barr Virus Control Innate and Adaptive Antiviral Immunity Abstract Epstein-Barr virus (EBV) has established lifelong infection in more than 90% of humanity. While infection is usually controlled by the immune system, the human host fails to completely eliminate the pathogen. Several herpesviral proteins are known to act as immunoevasins, preventing or reducing recognition of EBV-infected cells. Only recently were microRNAs of EBV identified to reduce immune recognition further. This Gem summarizes what we know about immunomodulatory microRNAs of herpesviruses. Keywords: cancer; human herpesviruses; immune evasion; immune surveillance; microRNA. https://pubmed.ncbi.nlm.nih.gov/28592533/ "Epstein Borrielosis Aids is like the serpent constantly shedding it's skin. I have often wondered if that is where they got the serpents on the staff of medi sin" Epstein-Barr virus: a master epigenetic manipulator Abstract Like all herpesviruses, the ability of Epstein-Barr virus (EBV) to establish life-long persistent infections is related to a biphasic viral lifecycle that involves latency and reactivation/lytic replication. Memory B cells serve as the EBV latency compartment where silencing of viral gene expression allows maintenance of the viral genome, avoidance of immune surveillance, and life-long carriage. Upon viral reactivation, viral gene expression is induced for replication, progeny virion production, and viral spread. EBV uses the host epigenetic machinery to regulate its distinct viral gene expression states. However, epigenetic manipulation by EBV affects the host epigenome by reprogramming cells in ways that leave long-lasting, oncogenic phenotypes. Such virally-induced epigenetic alterations are evident in EBV-associated cancers. https://pubmed.ncbi.nlm.nih.gov/28780440/ https://www.truthcures.org/ https://www.lymeneteurope.org/ How the Internet of cells has biologists buzzing Networks of nanotubes may allow cells to share everything from infections and cancer to dementia-linked proteins. https://www.nature.com/news/how-the-internet-of-cells-has-biologists-buzzing-1.22645 https://phys.org/news/2019-02-tunneling-nanotubes-tnts-concept-cell.html https://sites.google.com/view/doxy-cancer/home?fbclid=IwAR1wovyL3Y7g7UAjvyr1gO7ul10ohQRMnsdtsWtzz7faksu_A0B0ZRqsNO4

ALL disease is Epstein Borreliosis AIDS infinite antigen variation adapts to host DNA, activated by any immune response...all the purdy ribbons of the rainbow: AIDS, Cancer, ALS, MS, Autism, Diabetes, Alzheimers, Morgellons etc . In it's molecular forms called Prion Proteins In it's most basic forms it is called Myco PLASMA, Ana PLASMOSIS, Toxo PLASMOSIS or Spiro PLASMA--Exosomes, Blebs, Gemma, TAU. And your baaad cholesterol. In it's viral forms it is host gene dependent LEGIONS. In its bacterial forms it is MANY esp. Ehrlichia and H.pylori, TB, According to where it resides . It's infectious organisms protected in fungus. You can kill the infections but the immune suppression they cause isn't easily fixed. All of your so called viruses are simply morphological forms of infinite host gene variations.....Their cystic viral morphologies and secreted blebs containing seed formerly known as Prion and flagellum that recombines and grows with infectious DNA. RepA-WH1, the agent of an amyloid proteinopathy in bacteria, builds oligomeric pores through lipid vesicles https://pubmed.ncbi.nlm.nih.gov/26984374/ Possible roles of amyloids in malaria pathophysiology https://pubmed.ncbi.nlm.nih.gov/28031872/ Spiroplasma spp. biofilm formation is instrumental for their role in the pathogenesis of plant, insect and animal diseases https://pubmed.ncbi.nlm.nih.gov/22552100/ (RepA-WH1 -first synthetic bacterial prionoid) Discussion The results reported here point to a possible primary target for the cytotoxicity expressed by the RepA-WH1 prionoid in E. coli: the bacterial internal cell membrane. Three distinct mechanisms have been proposed for membrane disruption by amyloidogenic proteins8, including: i) the formation of pores by the assembly of protein monomers into ring-shaped oligomers; ii) membrane thinning and iii) lipid (detergent-like) extraction. Since the last mechanism should imply the lysis of a significant fraction of the vesicles, which was not the case under our experimental conditions, and the second one seems incompatible with the observed persistence of aggregates bound to the membranes (Figs 3–5), the formation of pores by protein insertion into the lipid bilayer, as first proposed for Aβ and α-synuclein39, was the most likely mechanism for vesicle leakage induced by RepA-WH1. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794723/pdf/srep23144.pdf https://www.lymeneteurope.org/forum/viewtopic.php?f=13&t=5399&hilit=anthrax&sid=34adf8c1b8ca65ea2c267f521d9994f1&start=10&fbclid=IwAR3EAz8iRggx4cM2Na4-tFppLL_Mpt6IUnjhhV5YrMD27BhG9m9bSIp15lE https://www.lymeneteurope.org/forum/viewtopic.php?f=13&t=5147&start=30&fbclid=IwAR287sNwR32lfh8yXyEet7v-QtwDhwhK8BgXrNVaLCigh3_72fVn1Ylg95w https://www.lymeneteurope.org/forum/viewtopic.php?f=6&t=4840&p=36246&fbclid=IwAR2y0lar0Z7OelH2bx99gVXNHABKbpFGWAjJaY9fso0IgTXy_qsXSaVo-8k#p36246 https://www.chicagotribune.com/news/breaking/chi-great-lakes-plastic-fibers-scientists-20150109-story.html malaria epidemic 406,000 in 2018 http://hisz.rsoe.hu/alertmap/database/?pageid=event_summary&edis_id=EH-20180424-62784-VEN&fbclid=IwAR0SYJ-kxq44vPHLRmURj6b_iTy23q2DOqyPYXJPO0IgzZLCAVnr6yMrEYA Treating Autism With Antibiotics (France 3 19/20, Feb 17, 2012) https://www.youtube.com/watch?v=yOno_2m_8LY&fbclid=IwAR3KBiW_h8C2okAY7U-PQNO2T4f4bTc1ROLvSzKjdA5l3KmGBbDVmj8XFok&app=desktop Artemisinin and its derivatives in treating protozoan infections beyond malaria https://pubmed.ncbi.nlm.nih.gov/27867026/ Good pics of Spirochetal AIDS. Notice the round bodies still there. https://pdfs.semanticscholar.org/017c/f5dacaf19d207de7f5e51eb75dd847e20446.pdf https://sites.google.com/view/doxy-cancer/home?fbclid=IwAR1wovyL3Y7g7UAjvyr1gO7ul10ohQRMnsdtsWtzz7faksu_A0B0ZRqsNO4

https://summit.news/2020/09/11/author-of-dystopian-classics-predicted-face-masks-to-enforce-conformity-70-years-ago/?fbclid=IwAR2Z4Cey-p4HpG8-8dXGOFsd-ewCUPuxU03V91Am66DJgGLYALhOHz4ycEI https://nikiraapana.blogspot.com/ I mentioned Niki and Nordica's book in the video but did not know there is a free pdf online so please check it out! http://nord.twu.net/acl/ebookdownload/2020_ebook.pdf https://en.wikipedia.org/wiki/Amitai_Etzioni

So I had this thought pop into my head to lookup quantum computers and demons. I came up with this blog about Gordie Rose and his company Kindred. You could say, both Kindred and D-Wave are basically in the same business: building Artificial Intelligence or AI https://endofwesternciv.blogspot.com/2018/08/ai-computers-will-contain-demon.html?fbclid=IwAR2e9bXnJKxcMrYdNfVhDF8q4SkSqq5EQ_XNKfBa7N95Dx6uvEBvh2OS50s https://fanon.fandom.com/wiki/Kindred?fbclid=IwAR0agX2sHKAmYG2meqsWfjFBQagpEzcOkNAVH9spgvMfUTko9qtbumXAe4s Originally when I made the video I was under the impression that Rose's Kindred was the same company making a deal with Vaxart for a vaccine. I was wrong. Rose's Kindred is Kindred Systems Inc, and the company partnering with Vaxart is Kindred Biosciences. My bad. Still Geordie Rose's choice for the name of his company with a mission is to build machines with human-like intelligence Kindred is still creepy if you ask me.