(Natural News) Is 5G to partially blame for coronavirus deaths? Can 5G cause the blood that’s circulating in your body to be unable to carry oxygen?
What’s especially horrifying about the critical care of coronavirus patients is that they aren’t suffering from “viral pneumonia,” but rather from an inability to absorb or carry oxygen in the blood.
This has been confirmed by NYC ICU emergency physician Cameron Kyle-Sidell, who has released several videos detailing how coronavirus is not a kind of viral pneumonia. “We’re treating the wrong disease,” he says. And the ventilators are damaging the lungs of patients. He explains: COVID-19 lung disease, as far as I can see, is not a pneumonia and should not be treated as one. Rather, it appears as if some kind of viral-induced disease most resembling high altitude sickness. Is it as if tens of thousands of my fellow New Yorkers are on a plane at 30,000 feet at the cabin pressure is slowly being let out. These patients are slowly being starved of oxygen.
Watch him explain how coronavirus patients are dying from oxygen starvation, not from a viral pneumonia lung infection:
The virus, to use its full title, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), causes respiratory illness. Symptoms range from a mild cough to acute pneumonia. COVID-19 affects the lungs, like the viruses SARS and MERS, but it can also have devastating effects on the rest of the body.
The cells in your lungs, arteries, heart, kidneys, and intestines have a protein on their surface called angiotensin-converting enzyme 2 (ACE2). Once the virus binds to these proteins, it uses them as a gateway into your cells.
‘Once the virus enters the body, it enters our cells through a two-step process. In the first stage, the spike proteins on the virus bind to ACE2 receptors located on host cells,’ explains Dr Maguire.
During the second stage of the process, the virus hijacks a special enzyme called a protease that speeds up the breakdown of protein. There are lots of different proteases, but the one that SARS-CoV-2 targets is called TMPRRS2.
Dr Maguire goes on to explain that ‘the spike proteins on the virus must also bind to a protease on the host cells, thought to include the protease TMPRRS2. Once this happens, the protease cleaves the spike protein on the virus in two places, allowing the virus to fuse with the host cell and deposit its RNA into the cells.’ Once it’s inside a cell, it can cause real damage.
RNA is viral genetic material. The virus uses the mechanisms inside your cell to replicate its RNA and make copies of itself. The process destroys cells and creates thousands of new viral particles that infect other cells in the respiratory tract.
Using cryogenic electron microscopy, a team has mapped the spike protein on COVID-19, which could be used in the development of vaccines.
Scientists have announced a critical breakthrough in their research for a vaccine to comabt COVID-19 (coronavirus) by creating the first three-dimensional (3D) atomic-scale map of the section of the virus that attaches to and infects human cells.
"The coronaviruses are of four genera (equivalent to the “Homo” in “Homo sapiens”): alpha, beta, gamma, and delta. COVID-19, SARS, MERS, HCoV-OC43, and HKU1 are beta. Two other human coronaviruses, HCoV-229E and HCoV-NL63, are alpha. Many viruses that plague humans have RNA as their genetic material. It’s copied into DNA in our cells.
Anatomy of COVID-19 A virus isn’t a cell, isn’t even considered alive. It’s a nucleic acid (DNA or RNA) wrapped in a coat of proteins, some attached to sugars (glycoproteins). Many familiar viral pathogens – those that cause cold, flu, hemorrhagic fevers like Ebola, rabies, dengue, and yellow fever – are RNA viruses, notorious for mutating rapidly and unable to correct errors. The “body” of COVID-19 is basically a genome enveloped in glycoproteins, with a smear of fat and bearing the crown of spikes that inspired the name “coronavirus.” The genome is a single strand of RNA that is termed “positive-sense.” That means that the infected cell treats the viral genome as if were it’s own messenger RNA (mRNA), translating it into proteins. A “negative-sense” RNA virus requires more manipulation; a host enzyme must make a positive-sense copy. A coronavirus genome typically is 26,000-32,000 bases long. That’s hefty for a virus, but tiny compared to a human gene. Our BRCA1 gene, for example, is 125,951 bases long. Coronavirus RNAs are embellished with “caps” and “tails” like those of human mRNAs.
All coronaviruses share the “tools,” but differ in a few additional structural proteins tailored to the host species.
COVID-19’s Spikes Bind at ACE2 Receptors
Viruses have co-evolved with us, using proteins that jut from our cell surfaces. HIV and West Nile virus enter through CCR5 receptors, which dot white blood cells. Influenza viruses bind sialic acid residues. Coxsackievirus and adenovirus target part of an antibody. And herpes simplex uses 3 different doorways.
COVID-19 latches onto angiotensin-converting enzyme 2, aka ACE2.
To us, ACE2 is an enzyme that has an effect on blood pressure.
To COVID-19, ACE2 is a receptor, an entranceway, in the airways and alveoli (air sacs) as well as in blood vessel linings. ACE2 is also a receptor for SARS-CoV and NL63-CoV. (MERS-CoV uses a different receptor.)
Spike protein took center stage as a vaccine candidate early in the SARS outbreak, because it elicits an antibody response in mice. Various vaccine strategies – live weakened SARS, hitching spike genes to existing vaccines, circles of DNA housing spike genes and triplets of spike proteins in nanoparticles – haven’t worked well enough. But genomic technology has exploded since SARS, leading to insights with astonishing rapidity.
In an exhaustive study preprinted in bioRxiv, Arunachalam Ramaiah of the University of California, Irvine and Vaithilingaraja Arumugaswami of UCLA catalogued where key parts of the four structural proteins of COVID-19 bind to the proteins that mark immune system cell surfaces. The work implicated the spike protein, but from the perspective of the immune response rather than the receptor."
Could Covid-19 be a receptor gene therapy designed to shut down oxygen exchange? Restructure the receptor - Block oxygen supply! Could it cause changes in the brain which effect respiratory system?
Gene Therapy Leaves a Vicious Cycle
Gene therapy, colloquially called “living drug,” provides a one-time treatment option by rewriting or fixing errors in the natural genetic ciphering. Gene therapy presents itself as a breakthrough alternative with immense potential to provide a one-time treatment option for a complete cure as well as disease and disorder prevention. Gene therapy is an emerging experimental treatment that delivers functional genes into a patient's body to counter or replace malfunctioning ones, thus curing disease without pharmacological intervention, radiotherapy, or surgery. This modern approach has the potential to offer complete protection against lethal nerve gases (13, 19–22) and treat monogenic and cardiovascular diseases, immunodeficiency, cancer, and more (23–27). Apart from genetic defects, several other diseases that cannot be treated with drugs or antibodies can be cured with gene therapy.
[Comment: Covid-19 seems to have an addition of three protein in just the exact correct places to create a pathogenic protein. What are the odds of 3 different protein ending up in just the perfect place in a complicated protein to perform this novel gene therapy, never before experienced? It injects a pathogenic protein into a lung cell and uses it to produce more copies of itself. It may take up to 14 days to present symptoms of Covid-19, in which gene therapy is effective in changing the DNA as to produce an oxygen blocking effect in the cells that are used to sense or exchange oxygen in the lungs. Another possibility may even work to change the parts of the brain which control the respiratory system or makes changes in other parts of the respiratory system.]
Synthetic virology aims to reprogram naturally occurring viruses into controllable and predictable devices. The field can broadly be divided into two main endeavours: 1) engineering of the virus capsid and 2) engineering of the genetic programs encoded by the viral genome. This review will focus on virus capsid engineering as applied to gene therapy, and readers are directed elsewhere for reviews about engineering viral genomes4, 5 Viruses have evolved to deliver genetic information into host cells, which means that molecular programs that dictate how the viruses behave in vivo have already been written into their capsid structure. A goal of synthetic virology, therefore, is to rewrite the details of which biomolecular features a virus uses during its infectious process (e.g. cellular receptors).
A scientist funded by the US government has deliberately created an extremely deadly form of mousepox, a relative of the smallpox virus, through genetic engineering.
The new virus kills all mice even if they have been given antiviral drugs as well as a vaccine that would normally protect them.
The work has not stopped there. The cowpox virus, which infects a range of animals including humans, has been genetically altered in a similar way.
The new virus, which is about to be tested on animals, should be lethal only to mice, Mark Buller of the University of St Louis told New Scientist. He says his work is necessary to explore what bioterrorists might do.
But the research brings closer the prospect of pox viruses that cause only mild infections in humans being turned into diseases lethal even to people who have been vaccinated.
And vaccines are currently our main defence against smallpox and its relatives, such as the monkeypox that reached the US this year. Some researchers think the latest research is risky and unnecessary.
“I have great concern about doing this in a pox virus that can cross species,” said Ian Ramshaw of the Australian National University in Canberra on being told of Buller’s work.
Ramshaw was a member of the team that accidentally discovered how to make mousepox more deadly (New Scientist, 13 January 2001). But the modified mousepox his team created was not as deadly as Buller’s.
Henry Kissinger & Bill Gates Call For Mass Vaccination & Global Governance
April 6, 2020
By Spiro Skouras
We are in the middle of the worst global health pandemic of our lives according to the Media, the Government and the United Nations. We are witnessing an unprecedented global lockdown in response to the Coronavirus outbreak known as COVID19.
The global population living in Western countries have been taught for more than a generation to live in a constant state of fear ever since 9/11. We have been encouraged to sacrifice our liberty for a false sense of security, being conditioned more and more each day to rely on the state for protection, and now many of us find ourselves relying on the state to pay our bills.
Despite the government’s budget and deficit continuing to grow exponentially every day… some are beginning to see that there may be more to the official story than what we are led to believe. The very few may have seen this coming and are waiting for the next phase of what very well could be another step closer to global governance. The very men and women, the exact same individuals and government agencies, in addition to global institutions who stand to benefit the most, are the ones calling the shots…
Welcome to COVID-1984 and the official rollout of the New World Order…
The first draft of the civil rights-eroding USA PATRIOT Act was magically introduced one week after the 9/11 attacks. Legislators later admitted that they hadn't even had time to read through the hundreds of pages of the history-shaping bill before passing it the next month, yet somehow its authors were able to gather all the necessary information and write the whole entire thing in a week.
This was because most of the work had already been done. CNET reported the following back in 2008:
"Months before the Oklahoma City bombing took place, [then-Senator Joe] Biden introduced another bill called the Omnibus Counterterrorism Act of 1995. It previewed the 2001 Patriot Act by allowing secret evidence to be used in prosecutions, expanding the Foreign Intelligence Surveillance Act and wiretap laws, creating a new federal crime of 'terrorism' that could be invoked based on political beliefs, permitting the U.S. military to be used in civilian law enforcement, and allowing permanent detention of non-U.S. citizens without judicial review. The Center for National Security Studies said the bill would erode 'constitutional and statutory due process protections' and would 'authorize the Justice Department to pick and choose crimes to investigate and prosecute based on political beliefs and associations.'
Biden's bill was never put to a vote, but after 9/11 then-Attorney General John Ashcroft reportedly credited his bill with the foundations of the USA PATRIOT Act.
"Civil libertarians were opposed to it," Biden said in 2002 of his bill. "Right after 1994, and you can ask the attorney general this, because I got a call when he introduced the Patriot Act. He said, 'Joe, I'm introducing the act basically as you wrote it in 1994.'"
I point this out because it is now more important than ever to be aware that power structures (and their goons like Biden) can and will seize on opportunities to roll out pre-existing authoritarian agendas. We know it happened after 9/11, and we may be absolutely certain that it is happening now.
Good thread compiling the many, many authoritarian measures which governments around the world have implemented and are preparing to implement to deal with the virus. https://t.co/cZ3KnMzdPp
CoronaVirus Predictive Programming by Dr Leonard Horowitz
Coronavirus Predictive Programming is a 52-minute docu-commentary freely and exclusively viewable online at RevolutionTelevision.net. This public education production is presented courtesy of award-winning filmmaker Dr. Leonard G. Horowitz in association with Medical Veritas International Inc.
Leading lab virus expert Horowitz slams international “crisis capitalists” in this video production, claiming coronavirus “predictive programmers” are accountable for neglecting, downplaying, and misdirecting the media and governments’ responses to the coronavirus pandemic expanding and risking millions of lives.
Shocking revelations in this video includes the solid science proving the 2019 coronavirus outbreaking in China includes the AIDS-virus envelop gene weaponizing the mutant bioweapon against the human immune system.
In addition, detailed analysis of the “Event 201” coronavirus preparedness conference sponsored by the Bill & Melinda Gates Foundation, Johns Hopkins University, and the World Economic Forum, provides ‘probable cause’ for officials to investigate ‘industrial espionage’ and ‘commercial bioterrorism’ as motive for the intentional release of the mutant virus. Dr. Horowitz evidences here, better than anyone, the purposeful release of the ‘corona/SARS/HIV lab virus’ by ‘Deep State‘ special interests leveraging both governments–U.S. and China.
TI's have been enduring this already, losing jobs, staying at home, being surveilled, attacked with biological weapons and now this
The State of Western Australia has given itself the power to install surveillance devices in homes, or compel people to wear them, to ensure that those required to isolate during the coronavirus crisis don’t interact with the community.
Diaphragmatic breathing is a type of a breathing exercise that helps strengthen your diaphragm, an important muscle that helps you breathe. This breathing exercise is also sometimes called belly breathing or abdominal breathing.
It has a number of benefits that affect your entire body. It’s the basis for almost all meditation or relaxation techniquesTrusted Source, which can lower your stress levels, reduce your blood pressure, and regulate other important bodily processes.
Let’s learn more about how diaphragmatic breathing benefits you, how to get started, and what the research says about it.
The new device integrates two sets of photovoltaic cells onto semiconductor chips.
Japanese researchers describe a new implantable device no bigger than the width of a coin that can be used to control brain patterns. The device, which can be read about in AIP Advances, converts infrared light into blue light to control neural activity and is both the smallest and lightest wireless optical biodevice to be reported.
For centuries, it has been known that chemicals can change neural behavior. The field of optogenetics proved that neural behavior can also be changed with mere light. It is now known that light can activate certain proteins in the brain to change brain patterns. Accordingly, scientists have implanted optical devices to successfully control the behavior of rodents using nothing more than light of specific wavelengths as the stimulus. However, the devices are often bulky, akin to wearing a football helmet or something heavier, and cause discomfort and distress to the animals.
Takashi Tokuda, an associate professor at the Nara Institute of Science and Technology (NAIST), has been investigating ways to miniaturize implantable optical devices.
“Size is always the challenge. No one likes having large implants,” he says.
The miniaturization of implantable devices has been hindered by a dependency on electromagnetics. In such devices, both the voltage and the current decrease with a reduction in size, thus limiting the power. On the other hand, in devices that depend on photovoltaics, voltage remains unchanged as size is reduced.
The new device uses a complementary metal-oxide semiconductor that controls photovoltaic power. “We integrated two sets of photovoltaic cells onto semiconductor chips. Ten cells were integrated for powering, and seven cells for biasing,” he says.
The device includes an InGan LED chip, which causes the device to emit blue light. A more distinguishing feature of the device, however, is that it can be activated with infrared light. Infrared is used in many light therapies, because it can penetrate deep in the body, whereas blue light cannot go much deeper than the surface. Therefore, the device can be implanted several centimeters into the body.
At just 1 mm3 and 2.3 mg, the volume and weight of the device are almost one order of magnitude than any other reported device, leading Tokuda to call it “the world's smallest wireless optical neural stimulator.”
At the same time, Tokuda acknowledges that the device needs modifications before reaching its fullest potential.
“The device can be applied only for pulse stimulations and requires a charge time for each stimulation. Most optogenetics use multiple pulses. We need to improve the power receiving and conversion efficiency,” he says.
This research has been supported by PRESTO (Precursory Research for Embryonic Science and Technology), one of the strategic basic research programs under Japan Science and Technology Agency. .
Removing nanoparticles from the blood
Electric fields remove nanoparticles from blood with ease
Engineers at the University of California, San Diego developed a new technology that uses an oscillating electric field to easily and quickly isolate drug-delivery nanoparticles from blood. The technology could serve as a general tool to separate and recover nanoparticles from other complex fluids for medical, environmental, and industrial applications.
Nanoparticles, which are generally one thousand times smaller than the width of a human hair, are difficult to separate from plasma, the liquid component of blood, due to their small size and low density. Traditional methods to remove nanoparticles from plasma samples typically involve diluting the plasma, adding a high concentration sugar solution to the plasma and spinning it in a centrifuge, or attaching a targeting agent to the surface of the nanoparticles. These methods either alter the normal behavior of the nanoparticles or cannot be applied to some of the most common nanoparticle types.
"This is the first example of isolating a wide range of nanoparticles out of plasma with a minimum amount of manipulation," said Stuart Ibsen, a postdoctoral fellow in the Department of NanoEngineering at UC San Diego and first author of the study published October in the journal Small. "We've designed a very versatile technique that can be used to recover nanoparticles in a lot of different processes."
This new nanoparticle separation technology will enable researchers—particularly those who design and study drug-delivery nanoparticles for disease therapies—to better monitor what happens to nanoparticles circulating in a patient's bloodstream. One of the questions that researchers face is how blood proteins bind to the surfaces of drug-delivery nanoparticles and make them less effective. Researchers could also use this technology in the clinic to determine if the blood chemistry of a particular patient is compatible with the surfaces of certain drug-delivery nanoparticles.
"We were interested in a fast and easy way to take these nanoparticles out of plasma so we could find out what's going on at their surfaces and redesign them to work more effectively in blood," said Michael Heller, a nanoengineering professor at the UC San Diego Jacobs School of Engineering and senior author of the study.
The device used to isolate the drug-delivery nanoparticles was a dime-sized electric chip manufactured by La Jolla-based Biological Dynamics, which licensed the original technology from UC San Diego. The chip contains hundreds of tiny electrodes that generate a rapidly oscillating electric field that selectively pulls the nanoparticles out of a plasma sample. Researchers inserted a drop of plasma spiked with nanoparticles into the electric chip and demonstrated nanoparticle recovery within 7 minutes. The technology worked on different types of drug-delivery nanoparticles that are typically studied in various labs.
The breakthrough in the technology relies on designing a chip that can work in the high salt concentration of blood plasma. The chip's ability to pull the nanoparticles out of plasma is based on differences in the material properties between the nanoparticles and plasma components. When the chip's electrodes apply an oscillating electric field, the positive and negative charges inside the nanoparticles reorient themselves at a different speed than the charges in the surrounding plasma. This momentary imbalance in the charges creates an attractive force between the nanoparticles and the electrodes. As the electric field oscillates, the nanoparticles are continually pulled towards the electrodes, leaving the rest of the plasma behind. Also, the electric field is designed to oscillate at just the right frequency: 15,000 times per second.
"It's amazing that this method works without any modifications to the plasma samples or to the nanoparticles," said Ibsen.
Manuka honey, a special type of honey produced in New Zealand by bees that pollinate the native manuka bush, has a broad spectrum of action, unlike any other known natural antimicrobial. It inhibits pathogenic bacteria that colonize the skin and wounds, including MRSA and Pseudomonas aeruginosa. (10) The powerful antimicrobial effects of manuka honey are due primarily to the presence of methylglyoxal (MGO), a naturally occurring phytochemical found in the nectar of Leptospermum flowers that damages bacterial DNA, RNA, and proteins. When selecting manuka honey for medicinal uses, you need to consider the UMF, a quality trademark and grading system that rates the strength of the honey. (UMF stands for “unique manuka factor” and is an official designation granted only to authentic manuka honey produced and jarred in New Zealand.) (11) UMF 10+ is the minimum strength honey recommended for medicinal use; it is best for less serious infections such as acne. For more stubborn infections, I recommend UMF 15+ or 20+.
That’s right. Congress could reauthorize the draconian surveillance powers embedded in the Patriot Act for the Trump administration. Worse still, some Democrats have joined Republicans in this effort. They want to give invasive spying powers that endanger vulnerable communities — like people of color, trans folks, activists and journalists — to a president they just impeached for abuse of power.
“I’m a constituent, and I’m calling to say that reauthorizing the Patriot Act, and the invasive spying powers within it, is unacceptable. I need my elected officials to stand up for my privacy rights. Congress should not give President Trump even more power to spy on people like me.”
Targeted Individual Needs Help - Please donate
The court case didnt go well. I tried to get adjournment but judge defaulted with a warrant of eviction. I'm very stressed out over this. I started calling tv news stations and newspapers about the landlord, who is a corporation, and breached my lease allowing neighbors to make noise daily night causing more health, pain problems and sleep loss.
I will use the go fund me money also for movers (and storage unit if needed) and shielding material, microwave scanning being done on victims in USA, and food, travel costs. I don't eat 3 meals a day, due to trauma, sometimes I don't eat for days because they try to take over me and they also drug my delivered food. I don't want to eat and they choke me to try and force me too.
Treasonous policies have been put in place by the DOJ, FBI, law enforcement, Fusion Centers to legally permit covert use of radiation weapons and neuroweapons in Vendetta, Surveillance, non-consensual experimentation, electronic warfare field weapons testing on citizens. Are we in the middle of a cold civil war? Do we still have a Fourth Amendment and is the United States being run by an unconstitutional secret government? https://drive.google.com/file/d/1rhLI89vXu4s9Hg0MYFvIhib0OwtPCrrw/view
INTERNATIONAL APPEAL Stop 5G on Earth and in Space
There are 182,894 signatories from 207 nations and territories as of December 1st, 2019
To the UN, WHO, EU, Council of Europe and governments of all nations
We the undersigned scientists, doctors, environmental organizations and citizens from (__) countries, urgently call for a halt to the deployment of the 5G (fifth generation) wireless network, including 5G from space satellites. 5G will massively increase exposure to radio frequency (RF) radiation on top of the 2G, 3G and 4G networks for telecommunications already in place. RF radiation has been proven harmful for humans and the environment. The deployment of 5G constitutes an experiment on humanity and the environment that is defined as a crime under international law.
Just letting you know I have a monthly public outreach and awareness campaign going. It's every monday starting in Oct - Aug in Nj. Please let people know if they are interested. Best Regards, Krissy
Targeted Individual NJ Activism Schedule
Starting in October the first Monday of every month we will be spreading awareness in the most populated cities in NJ. This is an eleven month campaign leading to next years annual Targeted Individual day. On August 28, 2020 we will hold a protest/ rally in Trenton, NJ at the capitol and attend the NYC rally the next day.
April. 6 - 11am - 7pm - Trenton City Offices, 319 E State St, Trenton, NJ 08608
May. 4 - 11am - 7pm - City Hall - Train Station, Camden, NJ 08102
Jun. 1 - 11am - 7pm - Passaic City Hall - 330 Passaic St, Passaic, NJ 07055
Jul. 6 - 11am - 7pm - City Hall Union City - 3715 Palisade Ave # 2, Union City, NJ 07087, NJ
Aug. 3 - 11am - 7pm - Cherry Hill Mall - 2000 NJ-38, Cherry Hill, NJ 08002
*** Aug. 28 - Capital Building - Trenton, NJ Targeted Individual Rally *** *** Aug. 29 - Targeted Individual Day - NYC ***
$75 with shipping. Protect your brain! Cap with 4 layers of metal and one layer of blackout rubber fabric, two magnets and grounding strap and rubber mouse pad comes with hat.
The new cap has a tab connected to the metal fabric for grounding. You can put a grounding clip on this and the other end on a magnet or a piece of carbon and it is grounded. You can use it without a grounding strap. You can put more magnets on it and move them around to where your implants are or over your ears. If you get hot, you can put an ice pack inside. The head is the best place to cool the body. It comes with a large round rubber mouse pad you can take out if you want. The shielding works best if it blocks EMF and sound, so you need metal and rubber.
This is not guaranteed to stop V2K. If you hear voices, you may have a radio connection, a real radio connected to your brain and it is always connected. A hat will probably not stop that, but it may reduce the feedback they get.
Email: CitizensAHT@protonmail to order if overseas because extra shipping is incurred for tracking overseas and going through customs. Overseaes tracked and insured through customs is about $35-54. Uninsured is $24-27.
M size best fit for 58-59cm 22.8-23.2in 7 1/4-7 3/8; L size best fit for 60-61cm 23.6-24in 7 1/2-7 5/8
This hat has been chosen for shielding because it is large enough to come down over your ears to cover ear implants.
Protect your brain, wear shielding on your head and cover your cochlear implants. Metal fabrics block tuning of implants and return signals. Has been noted to stop subliminal intrusion and electronic dreams.
Removable insert is 4 layers metallic fabric, one layer light-blocking rubber and a layer of broadcloth to protect the metal. 2 removable magnets, grounding strap, tracked shipping included, $110, except overseas (calculated by post office $17-$50).
INSERT ONLY: $95, shipping included, except overseas has an added fee. 4 layers of metal and light and sound blocker + protective cover
Order on CAHT website or by emailing CitizensAHT@protonmail.com. We will send you an invoice.
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NEW BOOKLET: "How Are You Being Targeted?" (on hand 200) Comes with free copy of WBAN press release
Booklet is $8.00 + $2.00 shipping. Overseas is $7.00 for shipping total $15.00. You will also receive a copy of the Press Release on the Body Area Network. You can support our organization's activities by ordering by email. We will send you an invoice. Pay by Paypal or debit/credit card at CitizensAHT@protonmail.com.
We focus on education/raisingpublic awarenessabout the RICO crimes of organized stalking, directed energy torture and other violations of physical/mental sovereignty andactionsyou can take to help win this war.
Hope Franklin, Research and Communications Director
SoundEnemy via ActionNetwork.org<email@example.com>
Come out to the second Targeted Activism NJ meeting at Barnes & Nobles in Paramus, NJ on Feb. 18. Please come out meet others and join in the the discussion. We can only make a difference with numbers and actions.
Below is a link to the details - Please RSVP -
If you can't make it, but still would like to contribute make a donation using links at the bottom. ** Please Join Us **
[ soundenemy ] @soundenemyx
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