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TI BOOKLET: Revised Second Edition Coming Out-Please Donate
We are happy to say that the first printing of the TI Handbook was a success. We however have run out and since we have not charged TI's for a copy and we give them free with memberships, we are now on a second printing. The printing is $700 for 100 copies. Mailing is at least $1.00. So any donations would be helpful. THANK YOU!
If you have any suggestions or have material you think should be in a book that helps TI's identify the program they have been placed in or helps describe the life that has been taken from them as a result of this horrible life destroying experience, please express your thoughts on that so it can be considered during editing.
DON'T FORGETto participate in the Global TI Survey, please send your name, address (including postal code & country) & telephone number, email to: email@example.com, attn: Kate Ryan/Karla Smith (request a link to the online survey & a code). They are the new scientific group attempt to understand victims claims of electromagnetic assaults and related covert harassment. Must submit between 6/19/2017 – 10/18/2017
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The Metallized fabrics are the latest generation of technology products at home and abroad, it is with many features, including wide frequency range, high shielding effectiveness, protective effect lasting, stable, wide field of use.
The "JUSTICE" Dept created the Electronic Harassment, Stalking and Morgellons Programs to bring "justice" to whom they consider "terrorists." This program is equal to the most hideous crimes in human history - SLAVERY AND USING UNSUSPECTING HUMANS FOR MEDICAL AND ELECTRONIC EXPERIMENTATION, COVERT IMPLANTATION, STALKING, TORTURE AND OUTRIGHT MURDER.
So, with that said, the person who wrote this article thinks that the Justice System is working for Americans. Whereas, the truth, is the "justice system" has taken every human right away from every individual. They have destroyed the Constitution, Civil Rights and the morality of all mankind. The Justice System is BROKEN when they burn, radiate, stalk and implant fungus, worms, bacteria and covert genetic changes in people to degrade their bodies and minds until death at the whim of unknown persons in a shadow government and there is no one to take responsibility for the crimes being committed. That's not justice. The Justice Department needs to be reviewed, controlled and their terrorist programs need to stop.
Protect the Justice Department From President TrumpSally Yates, The New York TimesPresident Trump’s actions appear aimed at destroying the fundamental independence of the Justice Department. All the while, he’s ripping the blindfold off Lady Justice and attempting to turn the department into a sword to seek vengeance against his perceived enemies and a shield to protect himself and his allies.
The spectacle of President Trump’s efforts to humiliate the attorney general into resigning has transfixed the country. But while we are busy staring at the wreckage of Attorney General Jeff Sessions’ relationship with the man he supported for the presidency, there is something more insidious happening.
The president is attempting to dismantle the rule of law, destroy the time-honored independence of the Justice Department, and undermine the career men and women who are devoted to seeking justice day in and day out, regardless of which political party is in power.
If we are not careful, when we wake up from the Trump presidency, our justice system may be broken beyond recognition.
The Justice Department is not just another federal agency. It is charged with fulfilling our country’s promise of equal and impartial justice for all. As an agency with the authority to deprive citizens of their liberty, its investigations and prosecutions must be conducted free from any political interference or influence, and decisions must be made based solely on the facts and the law.
WEBSITE: Smallstormblog MORGELLONS: Denial of a "Fiber" Disease is criminally deceptive when there is so much scientific evidence based on creating functional fibers using genetically altered viruses and bacteria like E. Coli and Bacillus subtillis
Insects and worms are only the vectors for transmission of Morgellons. The real damage involves genetic changes which produce continuous disease processes which lead to BRAIN death. It doesn't take much understanding to realize that Morgellons is partly bioweapon, population control, "punishment" for whistleblowers and "terrorists", and an evolutionary nightmare. A bioweapon can be distributed throughout a population many years before the full destructiveness is seen. That's why the government will not let doctors treat it or research it correctly - so it can reach its full maturation of infectious destructive power.
MORGELLONS: Purpose is to distribute Amyloid beta inclusion bodies and other misfolded proteins that degrade human brain and body.
The fibers found in Morgellons patients contain viral and bacterial proteins produced by genetically altered pathogens, some are the same proteins that cause Alzheimers. None of them are good.
A team of Wyss Institute researchers has revealed a novel, efficient and scalable method for building biomaterials – using E. coli bacterial colonies as biofactories – from protein structures called ‘amyloids’.
Amyloids are naturally occurring fibrous structures that have nanometer size features, and are associated with a range of biological functions. They were originally thought to be hallmarks of Alzheimer’s and Parkinson’s diseases triggered by protein misfolding, but more recently, “functional amyloids” were discovered to play beneficial roles in the protection of organisms and in their interaction with surfaces, including insects and bacteria.
A new vacuum filtration method developed by Neel Joshi’s team allows free-standing protein structures, such as the film pictured here on the left, to be produced in bacterial broth culture and then quickly and affordably separated from the broth. On the right, a scanning electron micrograph of such an amyloid film shows the imprint of pores left behind by the filtration membrane used to separate it from bacterial broth culture. At the same time, materials scientists have been interested in amyloid fibers as a powerful platform for building biomaterials due to their molecular self-assembly. Amyloid biomaterials have already been used in applications ranging from water purification to vaccines and tissue engineering.
However, despite their many useful features, there has not yet been a way to synthesize customized amyloid proteins in large enough quantities to make them practical building blocks for scalable materials. Conventional approaches to amyloid-based materials fabrication either rely on protein components isolated from natural sources, which are difficult to customize for particular applications, or they require time consuming and costly purification after recombinant production in a microbial host like E. coli.
Quick retinal scan may spot Alzheimer's years before usual diagnosis
John Murphy, MDLinx, 05/10/2016
An eye scan of the retina may indicate early signs of Alzheimer’s disease years before clinical symptoms arise, according to research presented May 5, 2016 at the annual meeting of the Association for Research in Vision and Ophthalmology (ARVO), in Seattle, WA.
Amyloid beta inclusion bodies in the retina may indicate early Alzheimer’s disease in subjects who don’t yet show cognitive symptoms. Because the retina is an extension of the central nervous system, recent research has focused on identifying neurological diseases, like Alzheimer’s, in the eye. In this small proof-of-concept study, researchers correlated amyloid beta plaques in the neocortex of the brain with amyloid beta “inclusion bodies” in the retinas of subjects with pre-clinical Alzheimer’s.
“We found fairly good correlation [r = 0.46] between the amount of these inclusion bodies in the retina and the amount of amyloid burden in the brain shown by PET imaging,” Dr. Snyder said. “Now that doesn’t prove causation, but it’s pretty suggestive.”
“There’s good animal research showing that in the very earliest stage of Alzheimer’s disease, a neuroinflammatory process occurs which involves some edema and some increase in the volume of tissue in the cortex in the brain. And we think that’s happening in the retina,” Dr. Snyder said.
Antibody reduces harmful brain amyloid plaques in Alzheimer's patients
Date:August 31, 2016
Source:University of Zurich
Aducanumab, an antibody developed by the University of Zurich, has been shown to trigger a meaningful reduction of harmful beta-amyloid plaques in patients with early-stage Alzheimer's disease. These protein deposits in the brain are a classic sign of Alzheimer's disease and contribute to the progressive degeneration of brain cells. The researchers furthermore demonstrated in an early stage clinical study that, after one year of treatment with Aducanumab, cognitive decline could be significantly slowed in antibody-treated patients as opposed to the placebo group.
Although the causes of Alzheimer's disease are still unknown, it is clear that the disease commences with progressive amyloid deposition in the brains of affected persons between ten and fifteen years before the emergence of initial clinical symptoms such as memory loss. Researchers have now been able to show that Aducanumab, a human monoclonal antibody, selectively binds brain amyloid plaques, thus enabling microglial cells to remove the plaques. A one-year treatment with the antibody, as part of a phase Ib study, resulted in almost complete clearance of the brain amyloid plaques in the study group patients. The results, which were realized by researchers at UZH together with the biotech company "Biogen" and the UZH spin-off "Neurimmune," have been published in the science journal Nature.
Curcumin Hidden deep in the plant's bright yellow roots is an extraordinarily powerful compound called curcumin that has the unique ability to block an enzyme that causes inflammation, while combatting free radical damage to highly sensitive vital organs like your brain and heart.
Fortunately, curcumin can help to neutralize the harmful effects of the free radicals that can cause inflammation. But that's not all it can do!
Gold-standard clinical studies have shown that curcumin is perhaps the most effective natural substance on earth at inhibiting COX-2, an enzyme that is responsible for sparking your body's inflammatory response.
4 Signs of Systemic Inflammation As scientists begin to understand the body's complex systems better, a clearer picture of how silent inflammation can impact your health is emerging.
Here are four of the most common symptoms:*
Brain Fog: Unfortunately, many people start to believe that scattered thoughts and poor concentration are an inevitable part of aging—but they're not! Silent inflammation is likely the culprit.
Memory Impairment: When the brain is inflamed, memory formation and recall both suffer. Research has shown a link between memory impairment and the presence of neurological inflammation.
Aches and Pains: Silent inflammation creates heightened pain sensitivity in the body, as well as common everyday aches and pains in joints and muscles. If your body feels sore and stiff, systemic inflammation is likely to blame.
Mood Issues: While neurotransmitter imbalances may be the primary cause of mood issues, recent research suggests that these imbalances may be related to inflammation in the brain.
Here's a quick "cheat sheet" so you know what to look for when shopping:
Potency: Look for a turmeric extract standardized to 95% curcuminoids. Some formulas are standardized only to 50%, which is a watered-down level that cheats you of the key curcuminoids shown to have the most effects.
Dosage: You need a serving size of at least 1,000 mg daily. Some brands think a mere 50 mg is enough, but you're throwing your money away for such pixie-dust levels. That's only 5% of the levels you need for the optimal brain, cardiovascular and joint benefits you want.
Absorption: The best supplements include 20 mg of black pepper extract, which has been shown to increase absorption by up to 2,000%!This is an excellent solution to the absorption problems that curcumin is widely known to have.
CoQ10: Very few curcumin supplements contain CoQ10, and this is a critical miss. Without CoQ10, you can take curcumin yet still not feel your best. Insist that the curcumin supplement you take have at least 100 mg of pure CoQ10.
Programmable biofilm-based materials from engineered curli nanofibres
The significant role of biofilms in pathogenicity has spurred research into preventing their formation and promoting their disruption, resulting in overlooked opportunities to develop biofilms as a synthetic biological platform for self-assembling functional materials. Here we present Biofilm-Integrated Nanofiber Display (BIND) as a strategy for the molecular programming of the bacterial extracellular matrix material by genetically appending peptide domains to the amyloid protein CsgA, the dominant proteinaceous component in Escherichia coli biofilms. These engineered CsgA fusion proteins are successfully secreted and extracellularly self-assemble into amyloid nanofibre networks that retain the functions of the displayed peptide domains. We show the use of BIND to confer diverse artificial functions to the biofilm matrix, such as nanoparticle biotemplating, substrate adhesion, covalent immobilization of proteins or a combination thereof. BIND is a versatile nanobiotechnological platform for developing robust materials with programmable functions, demonstrating the potential of utilizing biofilms as large-scale designable biomaterials.
Advances in our understanding of bacterial systems in the past century have expanded the role of the microbe from being regarded solely as a health threat to being exploited as a genetically programmable factory for the production of biomolecules and chemicals. We view bacterial biofilms as embarking on a similar trajectory vis-à-vis functional advanced materials. The majority of bacteria in the natural world exist as biofilms: organized communities of cells ensconced in a network of extracellular matrix (ECM) composed of polysaccharides, proteins, nucleic acids and other biomolecular components1. This self-generated ECM protects bacteria from environmental rigours and mediates substrate adhesion, thus promoting microbial persistence and pathogenicity. Hence, the majority of biofilm research has focused on their eradication because of the negative roles biofilms play in clinical infection2.
We envision instead the domestication of biofilms as a platform for programmable and modular self-assembling extracellular nanomaterials, with the bacterium serving as a living foundry for the synthesis of raw building blocks, their assembly into higher order structures upon secretion and the maintenance of the material as a whole over time. Although there has been some investigation into the use of biofilms for beneficial purposes such as energy generation3, wastewater treatment4 and biotransformations5,6, these studies have primarily focused on altering the population of the biofilm microbial consortia rather than the ECM material itself. Another example is recent exciting work from the Wood group, in which they describe the design of synthetic genetic circuits that modulate the population balance in a dual-species biofilm to control biofilm formation and dispersal based on quorum-sensing7.
Our approach to engineering the biofilm ECM material for practical applications focuses on the curli system–the primary proteinaceous structural component of E. coli biofilms. Curli are highly robust functional amyloid nanofibres with a diameter of approximately 4–7 nm that exist as extended tangled networks encapsulating the cells. Curli are formed from the extracellular self-assembly of CsgA, a small secreted 13-kDa protein. A homologous outer-membrane protein, CsgB, nucleates CsgA assembly and also anchors the nanofibres to the bacterial surface. Detached curli fibres can also exist as non-cell-associated structural components of the ECM. The curli genes exist as two divergently transcribed operons (csgBAC and csgDEFG)8, whose seven products mediate the structure (CsgA), nucleation (CsgB), processing (CsgE, F), secretion (CsgC, G) and direct transcriptional regulation (CsgD) of curli nanofibres.
The curli system exhibits numerous features that make it an ideal platform for the type of materials engineering by way of synthetic biology that we envision. First, as the curli nanofibre is composed primarily from the self-assembly of one small protein, it presents a tractable entry point towards creating a large diversity of biofilm extracellular matrices with conventional genetic engineering methods. In contrast, it would be more difficult to engineer the exopolysaccharide component of biofilms, as polysaccharide synthesis is often tied to multi-step pathways with a limited tolerance for chemically diverse monomers compared with the protein synthetic machinery. Second, the functional amyloid fibres formed by CsgA are extremely robust, being able to withstand boiling in detergents9 and extended incubation in solvents, increasing their potential utility in harsh environments. Similar amyloid nanofibres have been shown to have a strength comparable to steel and a mechanical stiffness comparable to silk10, suggesting that biofilms with high amyloid content would be able to withstand mechanically demanding environments. Third, functional amyloid fibrils are abundant in many naturally occurring bacterial biofilms and can constitute up to 10–40% of the total biovolume of a biofilm11, indicating that curli can be artificially engineered to comprise a significant portion of the biofilm. In addition, although analogous extracellular functional amyloids are produced by many bacteria, the curli system is currently the best studied and is native to the canonical model bacterium E. coli, making it an attractive starting platform for the development of engineered materials. Finally, recent findings have shown that the curli system can be used to efficiently export natively unfolded polypeptides and was capable of producing a functional camelid antibody fragment, suggesting that the curli system can be used in a broad and modular way for the display of various functional peptides throughout the E. coli biofilm ECM12,13.
Here we show a Biofilm-Integrated Nanofiber Display (BIND) system to enable precise genetic programming of the E. coli biofilm ECM material by fusing functional peptide domains onto the CsgA protein. We demonstrate that the chimeric CsgA variants are secreted by the native cellular export machinery and assemble into networks of curli fibres resembling the wild-type system. We also show that this technique is compatible with a wide range of peptide domains of various lengths and secondary structures. Last, we demonstrate that the peptide domains maintain their function after secretion and assembly and confer artificial functions to the biofilm as a whole. Very recently, Chen et al.14 have demonstrated a parallel curli-based system similar to our BIND concept, and show controlled multiscale patterning of single amyloid fibres and the use of engineered curli for the organization of gold nanoparticles and quantum dots for nanoelectronics applications. Herein, we expand on the functions that can be engineered into curli nanofibres by demonstrating three broad functions that we artificially introduce into the E. coli biofilm ECM: inorganic nanoparticle templating, specific abiotic substrate adhesion and the site-specific covalent immobilization of an arbitrary functionalized recombinant protein.
We propose an acoustic and visual signal based person-to-person violence detection system for indoor security application. A final decision is determined by fusing those detection results from each visual and acoustic detector. Information fusion is made with a Bayesian framework.
On July 14, Google’s bio-lab began releasing the first batches of the 20 million bacteria-filled mosquitoes they plan to set free in the heart of California in an effort to shrink the population of mosquitoes that can carry life-threatening diseases. The project, called Debug Fresno, is an initiative led by Verily Life Sciences, an offshoot of Google’s parent company Alphabet, in collaboration with MosquitoMate and Fresno County’s Consolidated Mosquito Abatement District.
According to the scientists, the goal of the project is to cut the population of Aedes aegypti mosquitoes — which are known for spreading Zika, dengue, and chikungunya. Over the course of 20 weeks, the company will release 1 million sterile, non-biting male mosquitoes in two 300-acre neighborhoods in Fresno County every week.
Releasing lab-bred mosquitoes into the wild The mosquitoes being released are not genetically modified, though they are made in a lab. The male mosquitoes are bred by a robot and infected with Wolbachia, a bacterium that makes male mosquitoes sterile to any female that doesn’t have a Wolbachia infection herself. This makes it unable to successfully breed and will reduce the mosquito populations with every new generation.
According to The Daily Mail Online, Verily isn’t the only company hoping to use robotics and artificial intelligence to help stop the spread of deadly diseases. In Texas, for instance, Microsoft is experimenting with a “smart trap” that can isolate and capture Aedes aegypti mosquitoes. What could possibly go wrong?
The Daily Coin, however, isn’t so sure about the company’s intention to release infected mosquitoes into the wild. Are these mosquitoes sorted correctly by gender and what if the Wolbachia mutates? If that happens we could have released something far worse than Zika into the world. Furthermore, giving scientists the permission to conduct field studies without the permission of citizens is just criminal. Though this might be a rather harmless experiment, what will stop these researchers from turning our neighborhoods into test facilities for less innocent experiments that could feed the depopulation agenda of the elite?
This righteousness is given through faith in Jesus Christ to all who believe. There is no difference between Jew and Gentile, for all have sinned and fall short of the glory of God, and all are justified freely by His grace through the redemption that came by Christ Jesus. God presented Christ as a sacrifice of atonement through the shedding of His blood---to be received by faith. He did this to demonstrate His righteousness, because in His forbearance He had left the sins committed beforehand unpunished---He did it to demonstrate His righteousness at the present time, so as to be just and the one who justifies those who have faith in Jesus.
COMMENT: Ephesians 2:8-9 For it is by grace you have been saved, through faith---and this is not from yourselves, it is the gift of God---not by works, so that no one can boast.
ACTIVIST: Mike Mason
Freedom for Targeted Individuals International Call: Every Saturday we invite you to join us for Freedom for Targeted Individuals International Podcast * To call in Internationally, use your country's international call in number first (link), after the automated prompt, you enter 541.275.1131# www.freedomfortargetedindividuals.org Starting at 3 pm EST/ 12 pm PST 1.541.275.1131 (no pins required) International Dial -in Numbers To join online https://www.uberconference.com/tiangel201
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If you have a tent, you can just tape some pieces of Linqstat together and drape them over the tent. You could make it the exact shape as the rain cover. You can ground it to an outlet, to a ground with a banana clip or attach a TENS electrode to it to create an energy field through the material. Using a tent structure that's already got places to attach the Linqstat make it a lot easier. You can even get a simple one and put it on your bed to drape the Linqstat over. Completely covering an already-made tent like this one with Linqstat is pretty easy and you can just put the TENS pad on the outside of it and "light it up", keeping the frequencies on the outside.
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