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 Hurricane Michael heated with DEW

Citizens Against Harmful Technology Newsletter
Actively Participate In Educating the Public

October 14
, 2018
 
EMAIL:  CitizensAHT@protonmail.com

NEW POST OFFICE BOX:  P.O. Box 1125, Edgewater, FL 32141
Make checks payable to CAHT.

 
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Sunday at 8:30 P.M. E. Coast, 7:30 Central, 6:30 Mountain, 5:30 W. Coast

The new call in # is (605) 475-4779, Access Code: 607080.
ID: electricrose222, Moderator: Neal
IMPORTANT ANNOUNCEMENTS
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Please print a copy of this newsletter and any newsletters you wish to maintain.  Just having them in your email won't save them. You can also copy them into a Word Document with .2 margins.  

This is an internet reference newsletter. A link to the original article is provided in the colored title line. Articles are referenced based on the subject matter that may be of interest to victims of civil rights abuses, including electronic harassment and stalking. We claim no authorship, of these references, they are presented for your education and consideration of the information. The purpose is for TI education only. The reference may contain only part of the original article due to space limitations here. CAHT neither agrees with nor disagrees with any opinions or information contained herein. Please go to the link to read the complete article. Thank you.
TI TESTIMONY

Report #85: Gretta Fahey Whistleblows on Neurotech, Nanotech, Biorobotizing

TESTIMONY 2:  Jian Liang
MK-ULTRA NEVER ENDED
 
Absolute Mind and Soul Control In Government,  Wall Street, And The Secret Space Program
 
Taken, abducted, mind controlled, sex slavery, given alternate personality
 
Proof Hurricane Michael was boosted with energy

ALERT!! Hurricane Michael Cat-5 'MAN-MADE' Storm - MUST WATCH,HERE IS PROOF!!

The bright spot in the center of Hurricane Michael is a Microwave burst. This is not normal. There was abnormally hot water in the Gulf as noted by the media weather channel. The winds had to be heated to increase the wind speed and to take up more water. Where are these directed energy hits coming from?  As you can see from the global map, there are at least 10 consecutive beams emanating from the same direction, possibly the south pole where there are under water heater arrays. They look to be an equal distance away from each other but at their origin, they may not have been. It may even be possible they came from satellites. There is an extra burst just below the hurricane. They end result was heating of the wind blowing across the Atlantic, and also the heating of the water from Columbia up towards the Gulf of Mexico.  This is global weather control.
 
Global hit at the same time as hit on Hurricane Michael:

 
 
 
This is the hurricane before being hit with microwave:

This is the hurricane after being hit with microwave:

Many have died protecting this homeland since 1776 - NOW -
The Air Force, Weather Wars are attacking us citizens w/hurricanes!

Hurricane Michael leaves more than 1 million without power

Now even the main stream media are calling it a war zone. "They" killed at least 18 and 46 persons are unaccounted for in Mexico Beach, Florida where the 155 mph winds hit a 23 mile wide swatch of land. I'd call that a massacre. This is on Trump's watch, he's the head in chief of the armed services, which includes the air force and weather services.  Who is controlling the microwave directed energy machines which heated this hurricane, pumped up the winds and sent it ashore with 165 mph winds, devastating a swath of the homeland all the way to the Atlantic? Whoever they are, they are mass murderers.

URGENT!! "Hurricane Michael" Was a TARGETED STRIKE!!!

REPORT COVERT IMPLANTED MEDICAL DEVICES

Medical Device Reporting (MDR)


MDR Overview

Each year, the FDA receives several hundred thousand medical device reports of suspected device-associated deaths, serious injuries and malfunctions. Medical Device Reporting (MDR) is one of the postmarket surveillance tools the FDA uses to monitor device performance, detect potential device-related safety issues, and contribute to benefit-risk assessments of these products.
 
Mandatory reporters (i.e., manufacturers, device user facilities, and importers) are required to submit certain types of reports for adverse events and product problems to the FDA about medical devices. In addition, the FDA also encourages health care professionals, patients, caregivers and consumers to submit voluntary reports about serious adverse events that may be associated with a medical device, as well as use errors, product quality issues, and therapeutic failures. These reports, along with data from other sources, can provide critical information that helps improve patient safety.

Mandatory Medical Device Reporting Requirements:

The Medical Device Reporting (MDR) regulation (21 CFR 803) contains mandatory requirements for manufacturers, importers, and device user facilities to report certain device-related adverse events and product problems to the FDA.
 
Manufacturers: Manufacturers are required to report to the FDA when they learn that any of their devices may have caused or contributed to a death or serious injury. Manufacturers must also report to the FDA when they become aware that their device has malfunctioned and would be likely to cause or contribute to a death or serious injury if the malfunction were to recur.
 
Importers: Importers are required to report to the FDA and the manufacturer when they learn that one of their devices may have caused or contributed to a death or serious injury. The importer must report only to the manufacturer if their imported devices have malfunctioned and would be likely to cause or contribute to a death or serious injury if the malfunction were to recur.
 
Device User Facilities: A “device user facility” is a hospital, ambulatory surgical facility, nursing home, outpatient diagnostic facility, or outpatient treatment facility, which is not a physician’s office. User facilities must report a suspected medical device-related death to both the FDA and the manufacturer. User facilities must report a medical device-related serious injury to the manufacturer, or to the FDA if the medical device manufacturer is unknown.
 
A user facility is not required to report a device malfunction, but can voluntarily advise the FDA of such product problems using the voluntary MedWatch Form FDA 3500 under FDA’s Safety Information and Adverse Event Reporting Program. Healthcare professionals within a user facility should familiarize themselves with their institution's procedures for reporting adverse events to the FDA. See "Medical Device Reporting for User Facilities", a guidance document issued by FDA.
 
Please visit Mandatory Reporting Requirements: Manufacturers, Importers and Device User Facilities for specifics on requirements and associated processes.

Voluntary Medical Device Reporting:

The FDA encourages healthcare professionals, patients, caregivers and consumers to submit voluntary reports of significant adverse events or product problems with medical products to MedWatch, the FDA’s Safety Information and Adverse Event Reporting Program or through the MedWatcher mobile app.

How to Report a Medical Device Problem:

Medical device reports are submitted to the FDA by mandatory reporters (manufacturers, importers and device user facilities) and voluntary reporters (health care professionals, patients, caregivers and consumers).

Mandatory Reporting for Manufacturers, Importers and Device User Facilities (Form FDA 3500A):

Find information and instructions for mandatory device reporting at:
For Questions about Medical Device Reporting, including interpretation of MDR policy:
Food and Drug Administration
Center for Devices and Radiological Health
MDR Policy Branch
10903 New Hampshire Avenue
WO Bldg. 66, Room 3217
Silver Spring, MD 20993-0002

Voluntary MedWatch Reporting for Patients, Health Professionals and Consumers (Form FDA 3500):

Patients, healthcare professionals and consumers who find a problem related to a medical device are encouraged to report medical device adverse events or product problems to FDA through MedWatch, the FDA Safety Information and Adverse Event Reporting Program. Submit reports to FDA through the MedWatch program in one of the following ways:
  • Using the MedWatcher mobile app that allows individuals to submit voluntary reports of serious medical device problems to the FDA using a smart phone or tablet.
Download the MedWatcher Mobile App

To Report an Emergency

If you have identified a public health emergency, you may use the following contact information to alert the FDA:
FDA Office of Crisis Management, Emergency Operations Center
  • Voice (24hr/day) phone: 866-300-4374 or 301-796-8240
  • FAX: 301-847-8543

 

Searching Medical Device Reports

The Manufacturer and User Facility Device Experience (MAUDE) database contains mandatory reports filed by manufacturers and importers from August 1996 to present, all mandatory user facility reports from 1991 to present, and voluntary reports filed after June 1993. The MAUDE database houses MDRs submitted to the FDA by mandatory reporters (manufacturers, importers and device user facilities) and voluntary reporters such as health care professionals, patients and consumers.
 
[If you put your device problem in this database, it will be there for other researchers to show that others are being implanted, it might show just how many are being implanted against their will, if the data were left in there. Could have its pros and cons but it may be a plus to TI's. Get pictures of your implants any way you can, tell your doctor you have pain somewhere, and don't mention implants.]
 
Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use. Because of this, MDRs comprise only one of the FDA's several important postmarket surveillance data sources.
 
Individuals are also able to request information related to Medical Device Reports by submitting a Freedom of Information Act (FOIA) request either in writing or online.

Contact

For general questions, please contact the Division of Industry and Consumer Education (DICE) by telephone at (301) 796-7100, or by email at DICE@fda.hhs.gov.

Additional Resources

War on Truth - Dollar Vigilante Newsletter
The War Has Begun on 10/10... FBIBook Purges Hundreds of Alternative Media Pages
 
Activist sites are being taken off Facebook!
5G Network Uses Same EMF Wave as Pentagon Crowd Control System
 
Written By: Terrence Newton October 8, 2018
 
The Technocrat leaders of the 5G revolution go way beyond just cell-phone carriers and include any all proponents of Smart Cities, Internet of Things, autonomous vehicles, ubiquitous surveillance and law enforcement. In the rush to ‘light up IoT”, safety testing has been scrapped and/or ignored.  ⁃ TN Editor
 
The global rollout of 5G is well underway, and we soon may see new small cell towers near all schools, on every residential street, dispersed throughout the natural environment, and pretty much everywhere. But the safety of this technology is in serious question, and there is a raging battle to stop the taxpayer funded implementation of 5G.
 
The new cell network uses high band radio frequency millimeter waves to deliver high bandwidth data to any device within line of sight.
 
“Today’s cellular and Wi-Fi networks rely on microwaves – a type of electromagnetic radiation utilizing frequencies up to 6 gigahertz (GHz) in order to wirelessly transmit voice or data. However, 5G applications will require unlocking of new spectrum bands in higher frequency ranges above 6 GHz to 100 GHz and beyond, utilizing submillimeter and millimeter waves – to allow ultra-high rates of data to be transmitted in the same amount of time as compared with previous deployments of microwave radiation.” [Source]
“One of the ways 5G will enable this is by tapping into new, unused bands at the top of the radio spectrum. These high bands are known as millimeter waves (mmwaves), and have been recently been opened up by regulators for licensing. They’ve largely been untouched by the public, since the equipment required to use them effectively has typically been expensive and inaccessible.” [Source]
 
Among the many potential problems with exposure to 5G radio waves are issues with the skin, which is interesting when you consider that this technology is already being used in the military for crowd control purposes.
 
“This kind of technology, which is in many of our homes, actually interacts with human skin and eyes. The shocking finding was made public via Israeli research studies that were presented at an international conference on the subject last year. Below you can find a lecture from Dr. Ben-Ishai of the Department of Physics at Hebrew University. He goes through how human sweat ducts act like a number of helical antennas when exposed to these wavelengths that are put out by the devices that employ 5G technology.” [Source]
 
The U.S. military developed a non-lethal crowd control weapon system called the Active Denial System (ADS). It uses radio frequency millimeter waves in the 95GHz range to penetrate the top 1/64 of an inch layer of skin on the targeted individual, instantly producing an intolerable heating sensation that causes them to flee.
 
This technology is becoming ubiquitous in top world militaries, demonstrating how genuinely effective this radio frequency energy can be at causing harm to humans and anything else.
 
“U.S., Russian, and Chinese defense agencieshave been active in developing weapons that rely on the capability of this electromagnetic technology to create burning sensations on the skin, for crowd control. The waves are Millimetre waves, also used by the U.S. Army in crowd dispersal guns called Active Denial Systems.” [Source]

Final Thoughts

The fight over 5G is heating up at the community level, and awareness of this important issue is spreading fast. For more background on 5G, watch this video from Take Back Your Power, featuring Tom Wheeler, Former FCC Chairman and corporate lobbyist, who delivers a rather intimidating and presumptuous speech praising this new technology. The fight over 5G is heating up at the community level, though, and now is the time to speak out against it.

Potential Risks to Human Health from Future Sub-MM Communication Systems: Paul Ben-Ishai, PhD
https://www.youtube.com/watch?time_continue=2&v=VuVtGldYXK4

Military Ray Gun • ADS Electromagnetic Radiation Weapon

https://www.youtube.com/watch?time_continue=25&v=KEhmFp-Gvyc
Your children belong to the New World Order

Kids are being Indoctrinated into the New World Order

 
Geoengineering:  NEXRAD Sequential Heterodyne Wave Generation
Herodyning is used very widely in communications engineering to generate new frequencies and move information from one frequency channel to another. Besides its use in the superheterodyne circuit which is found in almost every radio and television receivers, it is used in radio transmitters, modems, radar, satellite communications and set-top boxes, radio telescopes, telemetry systems, cell phones, cable television boxes and head-ends, microwave relays, etc.
How NEXRAD works

How Nexrad HAARP Works: Turning Natural Storms into Biblical Floods

 
Metal electromagnetic conductors burn up-not twigs

California Fires & Electromagnetic Conductors

The extreme heat caused the guard rails to burn because of the metal screws and bolts, but did not consume the twigs in front of sign.
 

Guard Rails On Fire at Keswick Dam + Utility Poles Strange Effects

https://www.youtube.com/watch?v=SF5a5xmuLm4
 
 
SPIRITUAL ENCOURAGEMENT
 
PSALM 118:13-17 (NIV)

I was pushed back and about
to fall, but the Lord helped me.
The Lord is my strength and my
defense; He has become my
salvation. Shouts of joy and
victory resound in the tents of
the righteous: "The Lord’s right
hand has done mighty things!
The Lord’s right hand is lifted
high; the Lord’s right hand has
done mighty things!” I will not
die but live, and will proclaim
what the Lord has done.
 
COMMENT: With God there
is always hope.
MileHiTI.com
Monday:  11:55 pm
Wednesday:
Time: 7:00 pm Mountain time
Call Number: 641-715-0872
Code: 198158
Playback number is 641-715-3579
Code: 198158
Moderator: Linda Goldthorpe
Phone: 720-645-450
ELLA FREE ACTIVISM
"Please join us every Tuesday & Thursday on Free Conference Call
 
Call-in  515.739.1285
enter PIN 400014#
Online Meeting ID: Tiangel2016
 
You can also find support information on our website:
under the support tab
 
You can listen to our recorded shows on our YouTube channel:
 
For further information you can email Ella at Tiangel2016@gmail.com"

Ella Free
Coordinator, Media Outreach & Podcast Host
Board Member & Director of Promotions
NEW SUPPORT GROUP-British Columbia, Canada
Vancouver, BC meetings¨will be held at:Location: Vancouver Public Library
Meeting Room
350 West Georgia Street
Vancouver, BC V6B 6B1
Contact:  Genet - absinya@yahoo.com
CONFERENCE CALL:  Oregon TI's
OREGON CONFERENCE CALL Saturday 12:30 PM Pacific Dial-in number: 515-739-6045 Access code number 874647 On Free Conference Call. This conference call is for all those targeted in Oregon. Please participate. Amy 971-207-3401
ACTIVIST:  Dr. Millicent Black

TARGETED INDIVIDUAL COMMUNITY CONFERENCE CALLS
Your new dial-in number for Talkshoe is 605-562-0444
Sunday
 
Moderator:  Neal
Citizens Against Harmful Technology
(605) 475-4779, Access Code: 607080
 
 
Moderator:  Renata
Time:  3 p.m. Eastern
Talkshoe:  605-562-0444, Pin #114616
 
 
 

 
 
 
 
 
Thursday
 
Moderator:  Mike Mason
Time:  6:00 pm Eastern
641-715-0632

ID 116202#
 
Moderator:  Ella
Time:  9:00 p.m. Eastern
Talkshoe:  605-562-0444, Pin# 141476
 
After Ella's Podcast:
Vulcan Wolverine
Talkshoe:  605-562-0444, 142394#
 
Moderator:  Kyle
Time:  After Ella’s call
Talkshoe:  605-562-0444, Pin #142394
 
Monday
 
Moderator:  Derrick
Time:  9:00 p.m. Eastern
Free Conference:
319-527-2701, Code 248671
 
Moderator:  Mike Mason
Time:  6:00 p.m. Eastern
Free Conference:  641-715-0632,
Code 116202
  
Friday
 
Moderator:  Frank Allen
Time:  6:00 pm. Eastern
646-749-3112
450-414-3112#
 
Moderator:  Loren W.
Time:  9:00 p.m.
Talkshoe:  605-562-0444, 798056#
712-432 3900
 
Tuesday
 
Moderator:  Terry
Time:  3:00 pm PST/6 pm EST to
6:00 pm PST/9:00 EST
Bring Awareness about Gangstalking
Talkshoe: 605-562-0444 Call ID: 143944
 
Moderator:  Ella
Time:  9:00 Eastern
Talkshoe: 605-562-0444, 141476
 
Moderator:  Kyle (Vulcan Wolverine)
Time:  After Ella’s call
Talkshoe:  605-562-0444, 142394
 
 
 Wednesday
 
Moderator: Frank Allen

Targeted Individual Massachusetts
Time: 9:00 pm Eastern
Call-in Number: 646-749-3112
Access Code: 450-414-301
Join by Computer:

https://global.gotomeeting.com/join/450414301
 
Moderator:  Julia
Engage in Prayer
Time:  9 pm Eastern/ 8 pm Central/
7 pm Mountain/ 6 pm Pacific
Call-in number: (515) 739-1405

International Dial-in Numbers: https://www.freeconferencecall.com/                   

wall/julia1113#international
Call ID: 141476
Access Code: 381878
Saturday
 
Moderator:  Terry
Time:  12:00 am Eastern
Talkshoe:  605-562-0444, 143944
 
Moderator:  Dr. Millicent Black
Church Conference Call
Time:  6:00 pm Eastern
Talkshoe:  140567
 
Moderator:  Frank Allen
Phone:  646-749-3112
450-414 3112#
 
Moderator:  Ella
Freedom for Targeted Individuals
International Activism
Time:  7:00 pm Eastern
Free Conference:  541-275-1131
 
Moderator:  Lauron
8:00 pm. Eastern
Talkshoe:  605-562-0444, 142124
 
Moderator:  Scott Snitzer
Time:  5:00 pm Eastern
Snitzer's TI Contact Call
Talkshoe:  605-562-0444, 138602
 
Moderator:  Derrick
Time:  9:00 pm Eastern
Phone:  319-527-2701
ID:  248671#
 
 
 
Activism/Support Groups
Denver, Colorado
Area Support Group
Contact:  Xontu Garcia
Email:  xontu44@icloud.com
 
Atlanta, Georgia
Support Group Meeting

Contact:  Carol Dimas
Phone:  470-312-6578
Email:  jamesdimas45@gmail.com
 
New York City Support Group
Contact:  Angel Acevedo
Email:  sorasuarez6@gmail.com
Phone: 646-806-8654
 
Houston, Texas
  For more information, you may contact
  Tereza Dutta - terezaxdutta@gmail.com

  
Seattle, Washington
Location: Broadview Branch Library at:

12755 Greenwood Ave. N.
Seattle, Washington 98133-7901

For more information, you may contact
Laura Solway - 206-365-6139
Curtis Kimble – 817-901-8720
 

Portland,Oregon

Hollywood District Public Library
Please attend the next Portland, Oregon Targeted Individual
 
I hope everyone is coping well. A thank-you to those who came to the October 13 Targeted PDX Meeting. For those who weren't able to attend, there is still support for you in other ways. You can always call. We're all in this gargantuan mess of a matrix together. I'm so grateful for the library and how it has worked for our community for three years. It's been a safe haven to spill out the unspeakable stories that we harbor. Please plan on attending the next valued scheduled Portland meeting.
 
Next Meeting Saturday November 17, 2018
4040 Northeast Tillamook
Portland, Oregon
Contact person;  Amy – 971-207-3401
 

 
Vancouver, BC V6B 6B1, Canada
Location: Vancouver Public Library
  1428 Cedar Cottage Mews, V5N 5Z1
       Meeting Room
Time: 3.00PM - 5.00PM
350 West Georgia Street
Contact- Genet at email -absinya@yahoo.com.
 
Canada
The West Coast Society For All Victims Of Organized Stalking And Electronic Harassment
PO Box 534
Heriot Bay, British Columbia V0P 1H0
westcoast.oseh@gmail.com
 
South Carolina
  For more information, you may contact
  Gail - mhisinhim4evr@gmail.com

 
TI'S IN CHINA
An Announcement To The Whole World By Chinese Victims
Of Electronic And Psychotronic Weapons

Disclaimer
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