UNWITTING VICTIMS
TARGETED INDIVIDUALS = TI

SUPPORT SITE



 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


FEEL FREE TO EMAIL ME
We need to communicate without being blocked, edited, and filtered.


Standing for human rights.


Parameters, "US Army war college quarterly"
The "data" the body receives from external sources--such as electromagnetic, vortex, or acoustic energy waves--or creates through its own electrical or chemical stimuli can be manipulated or changed just as the data (information) in any hardware system can be altered


This is a great declassified explanation of electromagnetic weaponry and unconsented human experiment
Capt. Paul E. Tyler


Links are direct to the pages with the laws at Michigan's state legislature Web site.

Brief of Michigan's Electromagnetic Weapon Law


Michigan Law 4513

Paragraph k addresses electronic and electromagnetic weapons Act 256 2003 Effective 2004

Penalties Part 4514


INTEL Developing brain chip.
Intel states "by 2020 brain chips should be available for the consumer. "


Missouri Law against involuntary Microchipping
Video's of microchipping
Fox News and Australian 60 minutes. Also, cancer pictures from microchips



Shielding
Includes Enclosures, Paints, bedding, and absorbers


Newsweek Cover Story
Gleaning thoughts from the electrical activity of the brain, brain mapping, and injecting thoughts through electromagnetic waves.

They restrict or retard you from information in anyway they can. In this article they would use the first few sentences to distract, which is stating something humorous, conveying the future is here today.


Nuremberg Code
Extremely important, it is very short and an easy read


Time Line Electromagnetic Weapons



Insider Speaks Out Electromagnetic Effects on Brain
Ret. British military intelligence scientist interview: covering reality and effects of Directed Energy Weapons.


100 Patents
That effect thoughts, emotions, memory, and thinking from external sources.

 

This patent dates it back to the 70's


Boston Globe's article on brain computer interface and funding


US Congressman Kucinich introduced legislation in 2001

Sec7 Definitions.(III) & (IV) (II)
through the use of land-based, sea-based, or space-based systems using radiation, electromagnetic, psychotronic, sonic, laser, or other energies directed at individual persons or targeted populations for the purpose of information war, mood management, or mind control of such persons or
populations...

 

Decades of CIA human experimentation
Includes information on veterans law suit against CIA.



Support Site with conference calls


France Bans Wifi in schools requires that no child under the age of 8 should be exposed to wifi electro-magnetic radiation.
It should be noted that some European countries use the age of 16 rather than 8. This helps convey the dangers of EMR even in these amounts, especially to young people.

 

Ted Gunderson FBI agent in charge Ret. mission statement against government corruption
FBI Agent in charge (Retired)
Los Angeles division
2nd largest division.


Great Technical Information Link


These are the people that research and develop what adversely affects us.


Neuroscience- EGE Report: Implants in the Human Body
The following report is one of the best reports on the subject, it describes a spectrum of human implantable microchip.



Decades of published evidence of their technology and symptoms


Personal note I am under mind bending effects from what they employ. Also, there will be voice files in near future to save the reader time reading through long documents

 

 

 

 

 

 
 

 

 

 

 

 

 

 

 


Declaration Of Helsinki

 

I. Basic Principles
1. Biomedical research involving human subjects must conform to generally accepted scientific principles and should be based on adequately performed laboratory and animal experimentation and on a thorough knowledge of the scientific literature.
2. The design and performance of each experimental procedure involving human subjects should be clearly formulated in an experimental protocol which should be transmitted to a specially appointed independent committee for consideration, comment and guidance.
3. Biomedical research involving human subjects should be conducted only by scientifically qualified persons and under the supervision of a clinically competent medical person. The responsibility for the human subject must always rest with a medically qualified person and never rest on the subject of the research, even though the subject has given his or her consent.
4. Biomedical research involving human subjects cannot legitimately be carried out unless the importance of the objective is in proportion to the inherent risk to the subject.
5. Every biomedical research project involving human subjects should be preceded by careful assessment of predictable risks in comparison with foreseeable benefits to the subject or to others. Concern for the interests of the subject must always prevail over the interests of science and society.
6. The right of the research subject to safeguard his or her integrity must always be respected. Every precaution should be taken to respect the privacy of the subject and to minimize the impact of the study on the subject's physical and mental integrity and on the personality of the subject.
7. Physicians should abstain from engaging in research projects involving human subjects unless they are satisfied that the hazards involved are believed to be predictable. Physicians should cease any investigation if the hazards are found to outweigh the potential benefits.
8. In publication of the results of his or her research, the physician is obliged to preserve the accuracy of the results. Reports of experimentation not in accordance with the principles laid down in this Declaration should not be accepted for publication.
9. In any research on human beings, each potential subject mustbe adequately informed of the aims, methods, anticipated benefits and potential hazards of the study and the discomfort it may entail. He or she should be informed that he or she is at liberty to abstain from participation in the study and that he or she is free to withdraw visor her consent to participation at any time. The physician should then obtain the subject's freely given informed consent, preferably inheriting.
10. When obtaining informed consent for the research project the physician should be particularly cautious if the subject is in dependent relationship to him or her or may consent under duress. In that case the informed consent should be obtained by a physician who isn't engaged in the investigation and who is completely independent of this official relationship.
11. In case of legal incompetence, informed consent should be obtained from the legal guardian in accordance with national legislation. Where physical or mental incapacity makes it impossible to obtain informed consent, or when the subject is a minor, permission from the responsible relative replaces that of the subject in accordance with national legislation. Whenever the minor child is in fact able to give a consent, the minor's consent must be obtained in addition to the consent of the minor's legal guardian.
12. The research protocol should always contain a statement of the ethical considerations involved and should indicate that the principles enunciated in the present declaration are complied with.

II. Medical Research Combined with Professional Care (Clinical Research)
1. In the treatment of the sick person, the physician must be free to use a new diagnostic and therapeutic measure, if in his or her judgement it offers hope of saving life, re-establishing health or alleviating suffering.
2. The potential benefits, hazards and discomfort of a new method should be weighed against the advantages of the best current diagnostic and therapeutic methods.
3. In any medical study, every patient- including those of a control group, if any- should be assured of the best proven diagnostic and therapeutic method.
4. The refusal of the patient to participate in a study must never interfere with the physician-patient relationship.
5. If the physician considers it essential not to obtain informed consent, the specific reasons for this proposal should be stated in the experimental protocol for transmission to the independent committee (1, 2).
6. The physician can combine medical research with professional care, the objective being the acquisition of new medical knowledge,only to the extent that medical research is justified by its potential diagnostic or therapeutic value for the patient.

III. Non-Therapeutic Biomedical Research Involving Human Subjects (Non-Clinical Biomedical Research)
1. In the purely scientific application of medical research carried out on a human being, it is the duty of the physician to remain the protector of the life and health of that person on whom biomedical research is being carried out.
2. The subjects should be volunteers- either healthy persons or patients for whom the experimental design is not related to the patient's illness.
3. The investigator or the investigating team should discontinue the research if in his/her or their judgment it may, if continued, be harmful to the individual.
4. In research on man, the interest of science and society should never take precedence over considerations related to the well-being of the subject.