According to the Wikipedia definition, the Milgram experiment on obedience to authority figures was a series of social psychology experiments conducted by Yale University psychologist Stanley Milgram. They measured the willingness of study participants, men from a diverse range of occupations with varying levels of education, to obey an authority figure who instructed them to perform acts conflicting with their personal conscience. Participants were led to believe that they were assisting an unrelated experiment, in which they had to administer electric shocks to a "learner. I am being subject to remote neural monitoring and remote neural manipulation which appears to have a built-in Milgram experiment attached to it. I am wirelessly linked to computers which are operated by neuro staff. These neuro staff were informed that they must systematically abuse a woman until she broke down and told them something. They have abused me night and day for sixteen years. I have not broken down and told me anything. I don't know what I am supposed to tell them.
experiment (4)
There is no doubt that technology is being used against victims but why? What is not being understood is that the interconnected satanic occultists across the globe are using the principles of physics to manipulate matter, space and time. They, the government scientists of the world, had at one time discovered that "electromagnetic fields, radio waves and or microwaves" are able to "open up door ways" into parallel dimensions and into other worldly space continuum's. This is why there is such a push for all the electromagnetic and microwave technologies to be built up around us..."everywhere".
In effect, they are not only creating doorways but attempting to make the entire planet one big gateway, to where the veil between the parallel worlds will no longer exist, allowing other worldly beings (the demons) to enter into our world with ease, just as the bible predicted. The electromagnetic grid that is slowly encompassing our world, I believe, in theory,is affecting our global ecosystem and disturbing our planets natural magnetic fields. Research these three subjects below and you will put the pieces of the puzzle together.
Philadelphia Experiment;
http://www.trutv.com/conspiracy/government-lies/time-travel/philadelphia-experiment.html
http://www.bibliotecapleyades.net/ciencia/time_travel/esp_ciencia_timetravel08a.htm
Montauk Project;
http://www.v-j-enterprises.com/montauk.html
Voodoo and Quantum Physics;
http://www.highbeam.com/doc/1P2-14746113.html
http://books.google.com/books/about/The_Vodou_Quantum_Leap.html?id=ptSINSgylEIC
http://www.magicalmiracles.com/indexP.htm
Paranormal, Spirits and Electromagnetic fields;
http://www.manchesterparanormal.org/Electromagnetic-Fields-and-Paranormal-Claims.php
T.S. aka egy
2010 California Code
Health and Safety Code
Chapter 1.3. Human Experimentation
Health and Safety Code
Chapter 1.3. Human Experimentation
HEALTH AND SAFETY CODE
SECTION 24170-24179.5
SECTION 24170-24179.5
24174. As used in this chapter, "medical experiment" means:
(a) The severance or penetration or damaging of tissues of a human subject or the use of a drug or device, as defined in Section 109920 or 109925, electromagnetic radiation, heat or cold, or a biological substance or organism, in or upon a human subject in the practice or research of medicine in a manner not reasonably related to maintaining or improving the health of the subject or otherwise directly benefiting the subject.
(b) The investigational use of a drug or device as provided in Sections 111590 and 111595.
(c) Withholding medical treatment from a human subject for any purpose other than maintenance or improvement of the health of the subject.
(a) The severance or penetration or damaging of tissues of a human subject or the use of a drug or device, as defined in Section 109920 or 109925, electromagnetic radiation, heat or cold, or a biological substance or organism, in or upon a human subject in the practice or research of medicine in a manner not reasonably related to maintaining or improving the health of the subject or otherwise directly benefiting the subject.
(b) The investigational use of a drug or device as provided in Sections 111590 and 111595.
(c) Withholding medical treatment from a human subject for any purpose other than maintenance or improvement of the health of the subject.
24175. (a) Except as otherwise provided in this section, no person shall be subjected to any medical experiment unless the informed consent of such person is obtained.
24176. (a) Any person who is primarily responsible for conduct of a medical experiment and who negligently allows the experiment to be conducted without a subject's informed consent, as provided in this chapter, shall be liable to the subject in an amount not to exceed ten thousand dollars ($10,000), as determined by the court. The minimum amount of damages awarded shall be five hundred dollars ($500).
(b) Any person who is primarily responsible for the conduct of a medical experiment and who willfully fails to obtain the subject's informed consent, as provided in this chapter, shall be liable to the subject in an amount not to exceed twenty-five thousand dollars ($25,000) as determined by the court. The minimum amount of damages
awarded shall be one thousand dollars ($1,000).
(c) Any person who is primarily responsible for the conduct of a medical experiment and who willfully fails to obtain the subject's informed consent, as provided in this chapter, and thereby exposes a subject to a known substantial risk of serious injury, either bodily harm or psychological harm, shall be guilty of a misdemeanor
punishable by imprisonment in the county jail for a period not to exceed one year or a fine of fifty thousand dollars ($50,000), or both.
(d) Any representative or employee of a pharmaceutical company, who is directly responsible for contracting with another person for the conduct of a medical experiment, and who has knowledge of risks or hazards with respect to the experiment, and who willfully withholds information of the risks and hazards from the person contracting for the conduct of the medical experiment, and thereby exposes a subject to substantial risk of serious injury, either bodily harm or psychological harm, shall be guilty of a misdemeanor punishable by imprisonment in the county jail for a period not to exceed one year or a fine of fifty thousand dollars ($50,000), or both.
(e) Each and every medical experiment performed in violation of any provision of this chapter is a separate and actionable offense.
(f) Any attempted or purported waiver of the rights guaranteed, or requirements prescribed by this chapter, whether by a subject or by a subject's conservator or guardian, or other representative, as specified in Section 24175, is void.
(g) Nothing in this section shall be construed to limit or expand the right of an injured subject to recover damages under any other applicable law.
(b) Any person who is primarily responsible for the conduct of a medical experiment and who willfully fails to obtain the subject's informed consent, as provided in this chapter, shall be liable to the subject in an amount not to exceed twenty-five thousand dollars ($25,000) as determined by the court. The minimum amount of damages
awarded shall be one thousand dollars ($1,000).
(c) Any person who is primarily responsible for the conduct of a medical experiment and who willfully fails to obtain the subject's informed consent, as provided in this chapter, and thereby exposes a subject to a known substantial risk of serious injury, either bodily harm or psychological harm, shall be guilty of a misdemeanor
punishable by imprisonment in the county jail for a period not to exceed one year or a fine of fifty thousand dollars ($50,000), or both.
(d) Any representative or employee of a pharmaceutical company, who is directly responsible for contracting with another person for the conduct of a medical experiment, and who has knowledge of risks or hazards with respect to the experiment, and who willfully withholds information of the risks and hazards from the person contracting for the conduct of the medical experiment, and thereby exposes a subject to substantial risk of serious injury, either bodily harm or psychological harm, shall be guilty of a misdemeanor punishable by imprisonment in the county jail for a period not to exceed one year or a fine of fifty thousand dollars ($50,000), or both.
(e) Each and every medical experiment performed in violation of any provision of this chapter is a separate and actionable offense.
(f) Any attempted or purported waiver of the rights guaranteed, or requirements prescribed by this chapter, whether by a subject or by a subject's conservator or guardian, or other representative, as specified in Section 24175, is void.
(g) Nothing in this section shall be construed to limit or expand the right of an injured subject to recover damages under any other applicable law.
24177.5. (a) This chapter shall not apply to any medical experimental treatment that benefits a patient subject to a life-threatening emergency if all of the following conditions are met:
(1) Care is provided in accordance with the procedures and the additional protections of the rights and welfare of the patient set forth in Part 50 of Title 21 of, and Part 46 of Title 45 of, the Code of Federal Regulations, in effect on December 31, 2010.
(2) The patient is in a life-threatening situation necessitating urgent intervention and available treatments are unproven or unsatisfactory.
(3) The patient is unable to give informed consent as a result of the patient's medical condition.
(4) Obtaining informed consent from the patient's legally authorized representatives is not feasible before the treatment must be administered. The proposed investigational plan shall define the length of time of the potential therapeutic window based on scientific evidence, and the investigator shall commit to attempting to contact a legally authorized representative for each subject within that length of time and, if feasible, to asking the legally authorized representative contacted for consent within that length of time rather than proceeding without consent.
(5) There is no reasonable way to identify prospectively the individuals likely to become eligible for participation in the clinical investigation.
(6) Valid scientific studies have been conducted that support the potential for the intervention to provide a direct benefit to the patient. Risks associated with the investigation shall be reasonable in relation to what is known about the medical condition of the potential class of subjects, the risks and benefits of standard
therapy, if any, and what is known about the risks and benefits of the proposed intervention or activity.
(b) Nothing in this section is intended to relieve any party of any other legal duty, including, but not limited to, the duty to act in a nonnegligent manner.
(c) This section shall remain in effect only until January 1, 2014, and as of that date is repealed, unless a later enacted statute, that is enacted before January 1, 2014, deletes or extends that date.
(1) Care is provided in accordance with the procedures and the additional protections of the rights and welfare of the patient set forth in Part 50 of Title 21 of, and Part 46 of Title 45 of, the Code of Federal Regulations, in effect on December 31, 2010.
(2) The patient is in a life-threatening situation necessitating urgent intervention and available treatments are unproven or unsatisfactory.
(3) The patient is unable to give informed consent as a result of the patient's medical condition.
(4) Obtaining informed consent from the patient's legally authorized representatives is not feasible before the treatment must be administered. The proposed investigational plan shall define the length of time of the potential therapeutic window based on scientific evidence, and the investigator shall commit to attempting to contact a legally authorized representative for each subject within that length of time and, if feasible, to asking the legally authorized representative contacted for consent within that length of time rather than proceeding without consent.
(5) There is no reasonable way to identify prospectively the individuals likely to become eligible for participation in the clinical investigation.
(6) Valid scientific studies have been conducted that support the potential for the intervention to provide a direct benefit to the patient. Risks associated with the investigation shall be reasonable in relation to what is known about the medical condition of the potential class of subjects, the risks and benefits of standard
therapy, if any, and what is known about the risks and benefits of the proposed intervention or activity.
(b) Nothing in this section is intended to relieve any party of any other legal duty, including, but not limited to, the duty to act in a nonnegligent manner.
(c) This section shall remain in effect only until January 1, 2014, and as of that date is repealed, unless a later enacted statute, that is enacted before January 1, 2014, deletes or extends that date.
Read more about Laws Against Criminal Uses of Electromagnetic Energy Weapons https://peacepink.ning.com/profiles/blogs/laws-against-criminal-uses-of
The list of human experiment in Japan after the WWII, and the list of 731 and Japanese Army related people who got job in the university hospitals, etc after the war. 731 mad scientists have been working in the famous hospitals and medical manufacturers. And the human experiments often held in university hospitals toward the mental patients. My guess is that the gang stalking victims are often claimed as mentally ill to be become the new pray for the secret human experiments in the hospitals.
人体実験には精神病患者やマイノリティが世界的にも選ばれていたようですが、意外と精神病でっち上げを行う理由には人体実験用の対象者が必要なのか もしれません。孤独な人や精神病だと見なされて周囲に無視されているような人の場合は、精神科医が何をやっても告発の可能性は低いでしょうからね。日本でも、精神病患者に対しての人体実験は多数報告されています。集団ストーカーが勧める精神病院や精神科医について調べれば、最新の実験を行っているのが何処かとか誰が関わっているのかわかるかもしれません。あるサイトでは、精神病患者だけでなく、自衛官にも行っていることが書かれていますが、同じレベルで知恵遅れなどとみなされてるんでしょうか。アメリカでも軍人が人体実験に使われていた過去があります。それから、日本での人体実験は７３１部隊と比較されてもいいと思います。年表を見ると、大学病院は気をつけたほうがいいみたいですね。７３１部隊関係の人たちも一部は大学病院に転職してるみたいですし、結局彼らが現在でも実験を行っているとしても、おかしくないでしょうね。
戦後日本の人体実験年表
1951 年
国立第1病院等で乳児に致死性大腸菌 を感染させる人体実験が行われた。感染性ありと報告。
1952年
名古屋市立乳児院 で乳児に大腸菌を感染させる人体実験。
1952-56 年
米軍援助金による新潟精神病院でのツツガムシ人体実験。精神病患者にツツ ガムシを接種した。8名死亡､1名自殺。
1965年3月 24日
名古屋市の興和製薬で、昭和38年10月に同社のかぜ薬新薬キセナラミンを社員ら187人に投与し、人体実験していたと被害者らが人権侵害 と東京法務局に告発。
1966年4月7日
千葉大医学部の 鈴木充医師が同大学内や川崎製鉄などの64人にチフス、赤痢を接種する人体実験をした容疑で逮捕。1審無罪、1976年4月東京高裁で有罪、1982年5月最高裁で懲役6年確定。
1967年
自衛隊員に赤痢 菌と赤痢予防薬（未承認薬）の人体実験、隊員1089人のうち577人に急性食中毒発生。
1969年9月
香港インフルエンザワク チ ンを少年自衛官335人に人体実験と『防衛衛生』が発表。
1969年10月14日
広島大学の岩森茂助教授らが悪性貧血患者3人 にガ ン細胞を移植して免疫抗体をつくる人体実験を行い、学会で発表。
1971年3月27日
東大医学部台弘教授が20年前にやった 精神病患者へのロボトミー手術は人体実験だったと告発される。
1984年5月23日
岐阜大学医学部精神科の難波益之教授グループの 助手竹内巧治助手が、岐阜県内の私立病院に通院していた妊娠中の女性分裂症患者を大学病院に転院させ、本人の同意を得ずに中絶手術をした上、胎児の脳を解剖した と、学会で内部告発。竹内助手は、妊娠中の分裂病患者が服用した向精神薬（ハロペリドール）の胎児の脳への分布を調べた。
1993 年
新潟市内の大学病院で不整脈のため診察を受けた主婦に検査と偽って新薬の臨床試験。他の検査結果も隠匿。
1989年
オウ ム真理教、 ヘッドギアPSI開発のために幹部信者で人体実験。
1990年
オウム真理教、反抗的信者でボツリヌスやコレラ使用の細 菌兵器の人体実験。
(http://homepage.mac.com/ehara_gen/jealous_gay/medical_experiments.html)
七 三一部隊関係
石井四郎 （第一・三代部隊長）
北野政次 （第二代部隊長） ミドリ十字共同設立者・取締役／日本学術会議南極特別委員／文部省百日咳研究会
吉村寿人 （凍傷研究班） 京都府立医科大学学長／日本学術会議南極特別委員／生気象学会会長
笠原四郎 （ウイルス研究班） 北里研究所
田中英雄 （ペストノミ研究班） 大阪市立大 学医学部長
湊政雄 （コレラ研究班） 京都大学教授
田部井和 （チフス研究班） 京都大学細菌学 教授／兵庫県立医科大学教授
所安夫 （流行性出血熱研究班） 東京大学教授／帝京大学教授
江島真平 （赤痢研究班） 国立予防衛生研究所
二木秀雄 （結核研究班） ミドリ十字共同設立者
岡本耕造 （病理研究班） 京都大学医学部長／近畿大学医学部長
石川太刀雄丸（病理研究班） 金沢大学医学部長／金沢大学癌研究所所長 ／日本学術会議会員
草味政夫 （薬理研究班） 昭和薬科大学教授
八木沢行正 （植物学研究班） 国 立予防衛生研究所／日本抗生物質学術協議会理事
朝比奈正二郎（発疹チフス・ワクチン製造班） 国立予防衛生研究所
園口忠男 （細菌戦 研究班） 陸上自衛隊衛生学校副校長
増田美保 （細菌戦研究班） 防衛大学校教授
安東洪次 （大連 支部長） 東京大学伝染病研究所教授／実験動物中央研究所所長
春日忠善 （大連支部長） 北里研究所／文 部省百日咳研究会
村田良介 （南京一六四四部隊） 国立予防衛生研究所所長（第七代）
小川透 （南京一六四四部 隊） 名古屋市立大学医学部教授
陸軍軍医学校防疫研究室関係
内藤良一 （陸軍軍医学校防疫研 究室） ミドリ十 字共同設立者・社長・会長
宮川米次 （東京帝国大学伝染病研究所長） 東芝生物物理化学研究所所長
緒方富雄 （東京帝国大学伝染病 研究所助教授）東京大学医学部教授
細谷省吾 （東京帝国大学伝染病研究所教授） 東京大学伝染病研究所教授
柳沢謙 （結核研究） 国立予防衛生研究所所長（第五代）
小島三郎 （東京帝国大学伝染病研究所教授） 国立予防衛生研究所所長（第二代）
小 林六造 （京都帝国大学教授） 国立予防衛生研究所所長（初代）
戸田正三 （京都帝国大学教授） 南極特別委員／金 沢大学学長
木村廉 （京都帝国大学教授） 日本医学会副会頭／名古屋市立大学学長
正路倫之助 （京都帝国大学教授） 第一期学術会議会員
(http://homepage.mac.com/ehara_gen/jealous_gay/unit731.html)
