Is the IMPOSTER The United States of America government aka UNITED STATES CORPORATION c. 1871 SUCCESSOR AND THE UNITED NATIONS A LAWFUL NEUTRAL WE THE PEOPLE AGENCY in the business of advancing peace, justice and truth or are they peadaphiles, rat invested zionist - jesuit criminal crime cartels engaged in foisting a One World Government over the world to enslave every man, woman and child on earth and in the process of genociding the people of the world?

YOU MAKE YOUR OWN MIND UP... 

"I care not what puppet  is placed on the throne of England to rule the Empire. The man who controls Britain's money supply controls the  British Empire and I control the British money supply." It also controls the FED and the UNITED NATIONS who's original ownership is found below (click hyper link). 

 - Nathan Mayer Rothschild

FEDERAL RESERVE Money System (same are behind the UNITED NATIONS Corporation):

Rothschild Bank of London
Rothschild Bank of Berlin
Warburg Bank of Hamburg
Warburg Bank of Amsterdam
Lazard Brothers of Paris
Israel Moses Seif Banks of Italy
Chase Manhattan Bank of New York
Goldman, Sachs of New York
Lehman Brothers of New York
Kuhn Loeb Bank of New York

and why would an American Government give $233.7Bn to Israel over six decades? Because its a ZIONIST OCCUPIED GOVERNMENT working for ZION - JESUITS One world order ... asset stripping America while enslaving Americans since the 1860's when it couped the organic American government.  

The "UN" is a corporation founded in France several years before the United Nations Charter was ever created. And here, for your edification, are the Principal Parties of Interest driving the "UN Agenda"----- Current version UN Corp dba World Bank dba FEDERAL RESERVE --- 52% owned by Rothschild Bank of London and Berlin; 8% owned by Lazard Freres Bank of Paris; 8% owned by Israel Moses Seif Bank of Italy, 8% owned by Warburg Bank of Hamburg and Amsterdam; 6% owned by Lehman Brothers of New York; 6% owned by Kuhn Loeb of New York; 6% owned by Chase Manhattan/Rockefeller Bank of New York; 6% owned by Goldman Sachs. (There may be some changes in ownership(s) since this list was compiled, but the above is accurate for the most part.)

PLEASE NOTE - EVERY ACT OF FRAUD PERPETUATED ON THE AMERICAN PEOPLE IS UNDOABLE -SO DO NOT LET ANYTHING YOU READ HERE MAKE YOU BELIEVE THE SITUATION IS UNREDEEMABLE!  IT WILL OF COURSE BE HARD TO UNDO THE TYRANNY IF NOT ENOUGH AMERICANS WAKE UP! THAT MEANS YOU HAVE TO WAKE UP OTHER AMERICANS OR ACCEPT YOUR FATE UNDER THE BOOT OF A GLOBAL ZIONIST - JESUITICAL PARASITE CLASS THAT HAS ALREADY PERPETUATED THE MASS CULLING IN RUSSIA, BALKANS, CHINA ET AL....NUMBERING 400,000,000 SINCE 1900.

THEY HAVE SAID THEY HAVE SAID THEY WANT 269,000,000 AMERICANS DEAD BY 2025 .....  IT IS UP TO YOU NOW .... 

TURN OFF THE TV - STEP AWAY FROM THE REMOTE AND UNLEARN! EVERYTHING YOU HAVE BEEN TOLD BY GOVERNMENT IS A LIE! 

 

Wake TF UP! 

 

"You are a den of vipers and thieves. I intend to rout you out, and by the Eternal God, I will rout you out."

"In A Time Of Universal Deceit, Telling The Truth Becomes A Revolutionary Act" - George Orwell, Author .....

"All Truth Passes Through Three stages. First, It Is Ridiculed, Second It Is Violently Opposed, And Third, It Is Accepted As Self-Evident" – Arthur Schopenhauer, Philosopher

 

Robin v. Hardaway 1790. Biblical Law at Common Law supersedes all laws, and Christianity is custom, custom is Law. [Remember - America operates under the American common law - not rules and statutes]

 

When you look at the UN Logo remember what that UN logo - it is not a peace keeping force - it is the NWO ORDER Genocide machine:

NOTE that the UN is not what you think it is:

 Now you have read the above have you any questions on who is running the UNITED STATES Federal Corporation [Title 28 Section 3002 (15)(A)] via the FEDERAL RESERVE Money System (same are behind the UNITED NATIONS Corporation) as shown above.

HOW MANY LIES DID THEY FORGOT TO TELL US ABOUT?

 

First some unlearning, education... please pass forward... 

 

WERE YOU AWARE THAT ZIONIST - JESUIT RAN UNITED STATES MADE EVERY AMERICAN AN ENEMY OF THE STATE IN 1933 UNDER TRADING WITH THE ENEMY ACT E.1899, Mod. 1916, Mod. 1933.  THEN RELIED ON AMERICAN LIVES TO FIGHT A ZIONIST MANUFACTURED WAR IN WHICH 250,000,000 were in effect murdered on ZIONIST - JESUITICAL LIES! 

Were you aware Two Hundred of the SO CALLED GLOBAL ELITE (BEST DESCRIBED AS FASCISTS, PSYCHOPATHS AND PARASITES) ARE CURRENTLY ENGAGED IN CARRYING OUT PLANS TO TERMINATE 90% OF THE GLOBAL POPULATION OF THE PLANET THROUGH QUIET WEAPONS / SILENT WAR PROGRAMS - YES THOSE WISPY CHEMTRAILS CLOUDS ARE POISONOUS TO ALL LIFE ON THE PLANET. See www.stopsprayingcalifornia.com www.geoengineeringwatch.org 

THE GLOBALIST TARGET FOR THE NORTH AMERICAN POPULATION (AGENDA 21, AGENDA 20230) IS 50M REMAINING BY 2030 FROM 320M TODAY: https://chemtrailsplanet.net/2017/02/22/deagel-forecast-predicts-81-us-population-reduction-by-2025/ 

THEIR BLACK NOBILITY GENOCIDE GLOBAL TARGET IS JUST 500,000,000! PLEASE NOTE THIS HAS NOTHING TO DO WITH LIES ABOUT GLOBAL WARMING OR OVERPOPULATION - IT DIRECTLY RELATES TO PARASITES CONTROLLING THE WORLD FOR THE LAST 6000 YEARS ARE LOSING CONTROL FOR TO MANY PEOPLE ARE WAKING UP! WHICH IS WHY THEY PREFER ROBOTS TO HUMANS AND ARE MAKING HUMANS OBSOLETE.

YOU KNOW ABOUT SOME OF THE PROGRAMS - GMO's, VACCINES, CHEMTRAILS, EMF, FLUORIDE, CODEX, WATER POISONING - & CONTROL, SMART METERS - ENERGY WEAPONS ET AL TO NAME BUT A FEW. WHERE DO THEY GET ALL OF THEIR IDEA FROM FOR DEPOP: https://www.youtube.com/watch?v=sWjWGVYCMvg 

PLEASE SHARE THIS SITE - RE-EDUCATING ON HOW HUMANITY HAS BEEN USED BY THE MORALLY CHALLENGED IS HOW WE END THE ZIONIST DEBT SLAVERY SYSTEM DESTROYING ALL LIFE and AN AMAZING FUTURE FOR HUMANITY.

INTRODUCTION: STARTING IN 1863, THE YOUNG AMERICAN ORGANIC REPUBLIC WAS LEFT SINIS DIS (WITHOUT DAY), - VACATED AFTER EMERGENCY WAR POWERS WAS PROCLAIMED DURING THE FOREIGN BANKSTER CONTRIVED CIVIL WAR; THE FOREIGN COUNTERFEIT UNITED STATES CORP [defacto UNITED STATES OF AMERICA, INC. Title 28 Section 3002 15a, b, and c, under U.S. Code and it's owners] WAS THEN UNLAWFULLY CREATED IN 1871 (ACT OF 1871) TO RULE OVER THE 10SQ MILES OF THE DISTRICT OF COLUMBIA [ONLY]. NOTE CREATED WITHOUT LAWFUL ORGANIC QUORUM OR AGREEMENT OF THE GOVERNMENT [WE THE PEOPLE] or the State of states! 

You are CONSIDERED an enemy of the State: http://www.apfn.org/apfn/1933.htm through your STRAWMAN Persona! 

On March 4, 1933, Franklin D. Roosevelt, a Jesuit Puppet was inaugurated as President. On March 9, 1933, Congress approved, in a special session, his Proclamation 2038 that became known as the Act of March 9, 1933:

 

"Be it enacted by the Senate and the House of

Representatives of the United States of America in

Congress assembled, That the Congress hereby

declares that a serious national emergency exists

and that itis imperatively necessary speedily to put

into effect remedies of uniform national application".

 

This is an example of the Rule of Necessity, a rule of

law where necessity knows no law. This rule was

invoked to remove the authority of the Constitution

(by traitor and seditionists that had no LAWFUL or legal authority to make any such claims for TONA proves they were engaged in a long term coup of America since 1812.)

 

Chapter 1, Title 1, Section 48, Statute 1 of this Act of March 9, 1933 is the exact same wording as Title12, USC 95(b) quoted earlier, proving that we are still under the Rule of Necessity in a declared state of national emergency.

 

12 USC 95(b) refers to the authority granted in the Act of October 6, 1917 (a/k/a The Trading with the Enemy Act or War Powers Act) which was "An Act to define, regulate, and punish trading with the enemy, and for other purposes".

 

This Act originally excluded citizens of the United States, but in the Act of March 9, 1933, Section 2 amended this to include "any person within the United States or any place subject to the jurisdiction thereof".

 

It was here that every American citizen literally became an enemy to the United States government under declaration.

 

According to the current Memorandum of American Cases and Recent English Cases on The Law of Trading With the Enemy, we have no personal Rights at law in any court, and all Rights of an enemy (all American citizens are all declared enemies) to sue in the courts are suspended, whereby the public good must prevail over private gain.

 

This also provides for the taking over of enemy private property. Now we know whywe no longer receive allodial freehold title to our land... as enemies, our property is no longer ours to have.

 ###

 UNITED STATES Inc. (Note this is the 1871 Corp created by the Act of 1871, Not the original organic Trust, The united states of America (Republic).

 

“Extra, Extra, Read all about it! United States Incorporates!”

“Congress copyrights Constitution for the thirteen united States of America and renames it the CONSTITUTION OF THE UNITED STATES OF AMERICA. New corporate government for the District of Columbia, commands all it's vessels to swear oath to new copyrighted version.” -District of Columbia Organic Act of 1871:

Forty-First Congress of the United States, Session III, Chapter 61 and 62, sec. 34 enacted February 21, 1871

UNITED STATES CODE, Title 28, 3002(15)(A) – Re-iterates

"The United States government is a foreign corporation with respect to a State" (NY re: Merriam 36 N.E. 505 1441 S. 0.1973, 14 L. Ed. 287). Volume 20: Corpus Juris Sec. 1785

The United States of America is a corporation endowed with the capacity to sue and be sued, to convey and receive property.1 Marsh. Dec. 177, 181. 

...but it is proper to observe that no suit can be brought against the United States without authority of law. Bouvier's Law , 5 definition of United States

"It is an established fact that the United States Federal Government has been dissolved by the Emergency Banking Act, March 9, 1933, 48 stat. 1, Public Law 89-719; declared by President Roosevelt, being bankrupt and insolvent, H.J.R. 192, 73rd Congress m session June 5, 1933 - Joint Resolution To Suspend The Gold Standard and Abrogate The Gold Clause dissolved the Sovereign Authority of the United States and the official capacities of all United States Governmental Offices, Officers, and Departments and is further evidence that the United States Federal Government exists today in name only.” 

United States Congressional Record, March 17, 1993 Vol. 33

The U.S. Government declared bankruptcy in 1933 in Roosevelt's executive orders 6073, 6102, 6111, AND 6260 and lost it's sovereignty. [idp note - not  true - a dc Corporation created without any we the people authority can not consume the organic enity that created the nations - wishfull thinking by the zionists)

This was confirmed in Perry v. US (1935) 294 U.S. 330-381, 79LEd 912, as well as 31 U.S.C. 5112 and 5119 and 12 U.S.C. 95a.

Title 28, 3002(15)(3): States that all departments of the UNITED STATES CORPORATION are part of the corporation.

##

THE AGENTS OF THE US CORP GUIDED BY FOREIGN MONEY INTERESTS DEBAUCHED THE MONEY IN 1913 BY SETTING UP THE FED IN A CLASSIC ROTHSCHILD MOVE (Mayer Amschel Rothschild alleged quote: "Permit me to issue and control the money of a nation, and I care not who makes its laws!"). 

THEY ORCHESTRATED THE DEPRESSION AND THE COUNTERFEIT US CORP TO BE BANKRUPTED IN 1933 ENABLING THE FOREIGN ZIONIST BANKING CARTEL TO UNLAWFULLY ASSUME TITLES TO THE LAND (FICTIONAL OVERLAY ONLY - SEE BUCK ACT AND LATER ZONE IMPROVEMENT PLAN) AND ALL THE GOLD IN AMERICA (JUNE 5TH 1933, HJR 192) IN THE NOT SO GOOD NEW DEAL.

THE NEW DEAL was alleged to TURN AMERICANS FROM SOVEREIGNS ON THE LAND IN TO INDENTURED SLAVES TO THE ZIONIST BANKSTERS. 

THE AMERICAN COURTS WERE DEBAUCHED BY 1938 TO BANKSTER OPERATED TRIBUNALS UNDER ADMIRALTY AND NOT OPERATING UNDER THE COMMON LAW WHICH IS THE STATE OF AFFAIRS TO THIS DAY. THESE COURTS AND EVERYTHING IN AMERICA (STATES, COUNTIES, CITIES, ALL PUBLIC OFFICES)WERE CONSECUTIVELY INCORPORATED. IN OUR CURRENT TIME THERE ARE VIRTUALLY NO LAWFUL GOVERNMENT OFFICE EXISTING, UNDER THE FULL FAITH AND CREDIT OF THE ORIGINAL ORGANIC GOVERNMENT.

Fraud is a wonderful thing. Anything enacted through fraud is INVALID, VOID, flushed down the toilet! All these acts were enacted on a FRAUD that the UNITED STATES was the original we the people United States / The United States of America which is of course it was no such thing!  The 1871 UNITED STATEs may have as well been called Crispy Creme for it has as much authority to proclaim itself as a we the people lawful national government as the UNITED STATES Corp of 1871! Lets also remember that the Lincoln regime that gave rise to this state of affairs was operating in violation of TONA and legitimate, therefore every act by it was illegitimate! 

We have re-posted You are an enemy of the State: http://www.apfn.org/apfn/1933.htm below for preservation:


War and the Emergency Powers 

War and The Emergency Powers and The Gold-Fringed Flag

     "The illegal we do immediately. The unconstitutional takes a little longer."--Henry Kissinger

Since March 9, 1933, the United States has been in a state of declared national emergency. In fact, there are now in effect four presidentially-proclaimed states of national emergency: In addition to the national emergency declared by President Roosevelt in 1933, there are also the national emergency proclaimed by President Truman on December 16, 1950, during the Korean conflict, and the states of national emergency declared by President Nixon on March 23, 1970, and August 15, 1971.
http://www.rallye-pointe.com/em_powers.htm

=========================================

Senate Report 93-549
War and Emergency Powers Acts,
Executive Orders and the New World Order
The Introduction to Senate Report 93-549 (93rd Congress, 1st Session, 1973) summarizes the situation that we face today - except it is far worse today than it was in 1973 !!

"A majority of the people of the United States have lived all of their lives under emergency rule. For 40 years [now 66 years], freedoms and governmental procedures guaranteed by the Constitution have, in varying degrees, been abridged by laws brought into force by states of national emergency. The problem of how a constitutional democracy reacts to great crises, however, far antedates the Great Depression. As a philosophical issue, its origins reach back to the Greek city-states and the Roman Republic. And, in the United States, actions taken by the Government in times of great crises have - from, at least, the Civil War - in important ways, shaped the present phenomenon of a permanent state of national emergency." 
http://www.barefootsworld.net/war_ep.html 
==============================================

PRESIDENTIAL POWERS IN TIMES OF EMERGENCY:
On September 14, 2001, President Bush declared that a "national emergency exists by reason of the terrorist attacks ... and the continuing and immediate threat of further attacks on the United States." When the emergency will end, no one knows.
http://writ.news.findlaw.com/dean/20020607.html

The Major Premise

(updated November 13, 2000)

The Introduction to Senate Report 93-549 (93rd Congress, 1st Session, 1973) summarizes the situation as best as possible; 

"A majority of the people of the United States have lived all of their lives under emergency rule. . . And, in the United States, actions taken by the Government in times of great crises have-from, at least, the Civil War-in important ways, shaped the present phenomenon of a permanent state of national emergency."
http://www.universalway.org/majorpremise.html   

Is the Constitution Suspended?
http://www.thenewamerican.com/tna/1996/vo12no03/vo12no03_schroder.htm

  • (a) Any authority granted to the President by section 1702 of this title may be exercised to deal with any unusual and extraordinary threat, which has its source in whole or substantial part outside the United States, to the national security, foreign policy, or economy of the United States, if the President declares a national emergency with respect to such threat. 
  • (b) The authorities granted to the President by section 1702 of this title may only be exercised to deal with an unusual and extraordinary threat with respect to which a national emergency has been declared for purposes of this chapter and may not be exercised for any other purpose. Any exercise of such authorities to deal with any new threat shall be based on a new declaration of national emergency which must be with respect to such threat. 

http://www4.law.cornell.edu/uscode/50/1701.html

Sec. 1631. Declaration of national emergency by Executive order; authority; publication in Federal Register; transmittal to Congress 


When the President declares a national emergency, no powers or authorities made available by statute for use in the event of an emergency shall be exercised unless and until the President specifies the provisions of law under which he proposes that he, or other officers will act. Such specification may be made either in the declaration of a national emergency, or by one or more contemporaneous or subsequent Executive orders published in the Federal Register and transmitted to the Congress. 

http://www4.law.cornell.edu/uscode/50/1631.html

======================================================

WE WILL NEVER COME UP WITH A SOLUTION, UNTIL WE KNOW THE PROBLEM!! WAR POWERS IS THE MAIN PROBLEM!!

Senate Report - War and Emergency Powers Acts

STUDY # 1 of 4 .... War and Emergency Powers
http://www.apfn.net/pogo/L001I060630-war-powers1.MP3

STUDY #2 of 4.... War end Emergency Powers
http://www.apfn.net/pogo/L002I060630-war-powers2.MP3

STUDY #3 OF 4 ---
http://www.apfn.net/pogo/L003I060630-war-powers3.MP3

STUDY #4 OF 4 ---
http://www.apfn.net/pogo/L004I060630-war-powers4.MP3

CONTACT SENATORS HERE
http://senate.gov/general/contact_information/senators_cfm.cfm

CONTACT HOUSE MEMBERS HERE
http://www.house.gov/writerep/

WE ARE THE ENEMY!

We the People Scoop 1/8/05 ** Special Edition **
===========================================

MEDIA RELEASE: THE PEOPLE ARE THE ENEMY

"Since March the 9th, 1933, the United States has been
in a state of declared national emergency. Under the
powers delegated by these statutes, the President may:
seize property; organize and control the means of
production; seize commodities; assign military forces
abroad; institute martial law; seize and control all
transportation and communication; regulate the
operation of private enterprise; restrict travel;
and... control the lives of all American citizens"

This situation has continued absolutely uninterrupted
since March 9, 1933. We have been in a state of
declared national emergency for nearly 63 years
without knowing it.

According to current laws, as found in 12 USC, Section
95(b), everything the President or the Secretary of
the Treasury has done since March 4, 1933 is
automatically approved:

"The actions, regulations, rules, licenses, orders and
proclamations heretofore or hereafter taken,
promulgated, made, or issued by the President of the
United States or the Secretary of the Treasury since
March the 4th, 1933, pursuant to the authority
conferred by Subsection (b) of Section 5 of the Act of
October 6th, 1917, as amended [12 USCS Sec. 95a], 
are hereby approved and confirmed. (Mar. 9, 1933, 
c. 1,Title 1, Sec. 1, 48 Stat. 1]".

On March 4, 1933, Franklin D. Roosevelt was inaugurated as President. On March 9, 1933, Congress approved, in a special session, his Proclamation 2038 that became known as the Act of March 9, 1933:

"Be it enacted by the Senate and the House of
Representatives of the United States of America in
Congress assembled, That the Congress hereby 
declaresthat a serious national emergency exists 
and that itis imperatively necessary speedily to put 
into effectremedies of uniform national application".

This is an example of the Rule of Necessity, a rule of
law where necessity knows no law. This rule was
invoked to remove the authority of the Constitution.
Chapter 1, Title 1, Section 48, Statute 1 of this Act of March 9, 1933 is the exact same wording as Title12, USC 95(b) quoted earlier, proving that we are still under the Rule of Necessity in a declared state of national emergency.

12 USC 95(b) refers to the authority granted in the Act of October 6, 1917 (a/k/a The Trading with the Enemy Act or War Powers Act) which was "An Act to define, regulate, and punish trading with the enemy, and for other purposes". 

This Act originally excluded citizens of the United States, but in the Act of March 9, 1933, Section 2 amended this to include "any person within the United States or any place subject to the jurisdiction thereof". 

It was here that every American citizen literally became an enemy to the United States government under declaration.

According to the current Memorandum of American Cases and Recent English Cases on The Law of Trading With the Enemy, we have no personal Rights at law in any court, and all Rights of an enemy (all American citizens are all declared enemies) to sue in the courts are suspended, whereby the public good must prevail over private gain. 

This also provides for the taking over of enemy private property. Now we know whywe no longer receive allodial freehold title to our land... as enemies, our property is no longer ours to have.

The only way we can do business or any type of legal
trade is to obtain permission from our government by
means of a license.

So who initiated all of these emergency powers?

(Again the abominable Federal Reserve - HR)

On March 3, 1933, the Federal Reserve Bank of New York adopted a resolution stating that the withdrawal of
currency and gold from the banks had created a national emergency, and "the Federal Reserve Board is
hereby requested to urge the President of the United
States to declare a bank holiday, Saturday March 4, and Monday, March 6".

Roosevelt was told to close down the banking system.
He did so with Proclamation 2039 under the excuse of
alleged unwarranted hoarding of gold by Americans.

Then with Proclamation 2040, he declared on March 9,
1933 the existence of a national bank emergency
whereas

"all Proclamations heretofore or hereafter issued by
the President pursuant to the authority conferred by
section 5(b) of the Act of October 6, 1917, as amended, are approved and confirmed".

Once an emergency is declared, there is no common law and the Constitution is automatically abolished. We
are no longer under law. Law has been abolished. We
are under a system of War Powers. 

Our stocks, bonds, houses, and land can be seized as Americans are considered enemies of the state. What we have is not ours under the War Powers given to the President who is the Commander-in-Chief of the military war machine.

Whenever any President proclaims that the national
emergency has ended, all War Powers shall cease to be in effect. Congress can do nothing without the
President's signature because Congress granted him
these emergency powers. 

For over 60 years, no President has been willing to give up this extraordinary power and terminate the original proclamation. 

Americans are an enemy subject to tribunal district courts under Martial Law wartime jurisdiction;

a FAUX Constitutional FOREIGN CORPORATE Dictatorship masquerading as we the people governance. 

 

Enemies?emies? That's right! It's true! You and I are the enemy of the United States government . . . defined so by law in the UNITED STATES CODE! For us to be enemies, we must be under a state of emergency. We ARE UNDER a declared state of emergency and HAVE BEEN since March 1933.

ARE WE THE ENEMY OF THE UNITED STATES GOVERNMENT?

http://www.barefootsworld.net/usenemy.html 

WAR POWERS TODAY IN AMERICA

 The United States is a belligerent government under international law of nations and the people therein. Yes you, dear reader, are the enemy subject and have never, ever, been a sovereign, and neither have your relatives dating back to 1787, UNLESS your relatives were one of the aristocracy having land and money and possibly a grant from the Crown. 
http://www.freedomdomain.com/sovereignty/inform10.html

Executive Orders And Laws relating to National Emergencies Laws http://www.disastercenter.com/laworder/50chap34.htm


Subject: Re: IMPORTANT: War and The Emergency Powers (Video)
Date: Fri, 15 Dec 2000 14:28:28 -0800
From: "Philip E. Jones" This email address is being protected from spambots. You need JavaScript enabled to view it.
To: This email address is being protected from spambots. You need JavaScript enabled to view it.

Dear friends, I am organizing a meeting of ALL moderate, conservative, and veterans organizations in March of next year, in San Antonio, for the purpose of consolidating our efforts by forming a coalition of organizations.  I would like to take this opportunity to invite you and any organization you are a member of to attend. Let me know if you would be interested and I will advise you of the date when we decide.  Thanks.

Philip E. Jones, Attorney at Law
126 East Main Plaza
San Antonio, Texas 78205
phone: (210) 224-1923; fax: (210) 227-4229
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.
web site:  HTTP://UNITEDVETS.TRIPOD.COM

=======================================

"War and emergency powers / Laws, regulations and rules"
http://fpc.state.gov/documents/organization/6216.pdf 

Untaught "Basics" 
(Emergency War Powers and our Constitution) 
http://home.att.net/~bellaliberty/warpwr.html

Emergency Powers Statutes
(Senate Report 93-549)
http://www.freedomsite.net/93-549.htm

==============================================

WAR AND EMERGENCY POWERS
A SPECIAL REPORT ON THE NATIONAL EMERGENCY IN 
THE UNITED STATES OF AMERICA
This page contains the complete text of the book "War and Emergency Powers" A SPECIAL REPORT ON THE NATIONAL EMERGENCY IN THE UNITED STATES OF AMERICA. Researched and written by: Gene Schroder, Alvin Jenkins, Jerry Russell, Ed Petrowsky, Russell Grieder, Darrell Schroder, Walter Marston, Lynn Bitner, Billy Schroder, Van Stafford, Fred Peters, Tinker Spain, and Paul Bailey.
Due to file size limitations we have elected not to include scanned images of the exhibits that appear in the book. 
http://usa-the-republic.com/emergency%20powers/powers_3.html

=================================================

Oklahoma City University Law Review
Volume 24, Number 3 (1999) 
THE PRESIDENT'S EMERGENCY WAR POWERS AND THE EROSION OF CIVIL LIBERTIES IN PYNCHON'S VINELAND
http://tarlton.law.utexas.edu/lpop/etext/okla/thoreen24.htm

GET THAT GOLD FRINGE OFF MY FLAG!

http://www.apfn.org/apfn/flag.htm

Senate approves police searches and seizures without warrants.

http://www.apfn.org/apfn/search&seize.htm

 CORRUPT POLICE STATE! 
http://www.apfn.org/apfn/policestate.htm 

====================================================================

U.S. PATRIOT ACT  HR 3162

http://www.apfn.org/apfn/HR3162.htm

THIS CASE IS NOT TO BE CITED OR PUBLISHED
http://www.apfn.org/apfn/secretoath.htm


The Original 13th Article of Amendment
http://www.apfn.org/apfn/13th.htm


The Law
http://www.apfn.org/apfn/thelaw.htm

The Declaration of Independence
http://www.apfn.org/apfn/declaration.htm

"PROOF" - Homeland Security was Planned Way Before 9/11
America is screwed! "Proof" - Homeland Security was planned way before 9/11! & The USA PATRIOT Act Was Planned Before 9/11 The New World Order Isn't Coming....It is Already here....
http://www.apfn.org/apfn/WTC_homeland.htm

Executive Summary of U.S. Commission on National Security Report
S. Commission on National Security Report Executive Summary of U.S. Commission on National Security Report Washington File 31 January 2001 (Group urges structural,
http://www.apfn.org/apfn/security.htm 
 
Four Washington "Wise Men" Discuss America in the Age of Terrorism
of Democratic Party nat'l security experts discussing Bush administration policy in addressing terrorism. Panel: Lee Hamilton, former Chairman, House Select Cmte on Intelligence;
http://www.apfn.org/apfn/WTC_discussion.htm 
 
9-11 Attack on America
them to happen, the national security dictatorship publicly funded, trained and shepherded the terrorists into the United States -- and went so far as to protect them from the
http://www.apfn.org/apfn/WTC.htm 
 
Sept 11th - Unanswered Questions
colossal collapse of airspace security in U.S. history? In the wake of the devastation, the answer to this last question is: obviously, yes. Somehow, the terrorists got through.
http://www.apfn.org/apfn/unanswered.htm 
 
WTC: STRANGER THAN FICTION
Over 100 megs of official records and photos detailing government lies to We The People, this website started as a subpage of a website designed to promote my film 
http://www.apfn.org/apfn/WTC_STF.htm

Shadow Government Is At Work In Secret
H. Card Jr. and national security adviser Condoleezza Rice. Many departments, including Justice and Treasury, have completed plans to delegate statutory powers to officials who
http://www.apfn.org/apfn/shadow_gov.htm

THE UNITED STATES IS STILL A BRITISH COLONY
THE UNITED STATES IS STILL A BRITISH COLONY EXTORTING TAXES FOR THE CROWN! A DOCUMENTARY REVIEW OF CHARTERS AND TREATIES August 17, 1996 An introduction by the "Informer" This is
http://www.apfn.org/apfn/bcolony.htm

The Enemy Is Very Much Within
The Enemy Is Very Much Within Subject: The Enemy Is Very Much Within Date: Sun, 30 Sep 2001 17:37:21 -0600 From: Within our own Government, that is. Specifically within certain
http://www.apfn.org/apfn/enemy_within.htm

SO WHAT DO ZIONIST AND JESUIT ENEMIES OF THE AMERICAN PEOPLE ENFORCE OVER AMERICANS TO GENOCIDE THEM:

 


IDP Admin: Vaccine_Research_Library and episode of a febrile seizure

Other topics to research:

Chemtrails, Georgia Guidestones, NWO agenda, NWO Timeline, NWO exposed 1969, NWO agenda by Jesuits - Rothschilds (see UNLEARN)

 

YT URL: https://www.youtube.com/watch?v=X4t5uzBV8So

Vimeo: https://vimeo.com/219397489 

When my children were very young my ex wife and I had already researched the vaccine issue and determined that we would avoid most vaccines and only selectively vaccinate. This was somewhere around 2003 when information was just breaking on the problems with vaccines. 

We reluctantly went ahead and gave my boy the MMR vaccine. After the vaccination one night my son started to develop a very high tempertature that I believe reached as high as 106. Prior to this he was a perfectly normal healthy baby boy. 

He eventually went limp, his eyes rolled back in to the back of his head and he started shaking and then became a rag doll. It was a nightmare experience. This was called a Febrile Seizure by the Doctor that we saw the next day. 

We tried to cool him down and we called the paramedics. We were aware the temperature causes brain swell and then the body shuts down to prevent brain damage.  The paramedics showed up in ten minutes and had my boy on a stretcher to take him to the hospital before we knew it.

I do not remember what they did but his temperature started to normalize pretty much as soon as they showed up. I believe they had him on oxygen. I can't be sure what they did at this time or if they gave him anything to cool him down. It was decided he would be better off going to bed and sleeping off what ever caused the fever.  We put him to bed and stayed with him all night and he recovered and to my knowlegde the episode never happened again! My ex wife used the STATE to abduct my boy and girl from me when the children were 7 & 5. So for 1/2 time from 2007 - 2010 I was only able to see the children for less than 50% of the time and I had no contact from 2010 - 2015 for my boy and to this day for my girl thanks to Alameda Kangaroo Court and crooked judges in bed with my ex wife parasite attorney new new husband (see Case Histories for more details on the case and criminal psychopathic STATE OF CALIFORNIA Kangaroo Court slavery system)! 

I noted the following publishing on the MMR Vaccine and febrile seizures this morning! 

I was asked by a young women yesterday if she should vaccinate here children... 

My first suggestion is DO YOUR OWN RESEARCH and come to your own conclusion. 

The above video is a good place to start. Here are hundreds of documents on the issueL Click image or URL: https://www.mediafire.com/folder/aj14280ch2qbp/Vaccine_Research_Library 

https://www.mediafire.com/folder/aj14280ch2qbp/Vaccine_Research_Library

Now - to answer the Question - would I vaccinate my children:

Absolutely not. Remember - Doctors are educated by the ones making the drugs! 

Why would you trust a CORPORATION That makes profit from death - disease - war - lies with your blessing from God. After reading through this site - you would have to be mentally challenged to trust the KHAZARIAN MAFIA UNITED STATES and the DEEP STATE crime cartel.

This site proves that we have no governments and in America we have not had a government since the 1860's. What we have are private corporations controlled by a foreign parasite class (see home page) that are farmed us. The parasites include the Khazarian Mafia - Jesuits connected to the Old World Order Vatican - Holy See system! These are the ones that have created the Open Air farms aka plantations as shown in this video: https://youtu.be/Xbp6umQT58A

 

Above Video URL: https://www.youtube.com/watch?v=Xbp6umQT58A

The farmers have exposed their methodology in a couple of publications:

Lernid Protocols of the Elders of Zion that some would say is fake. It make be fake but every strategy to enslave humanity published in it is being used to enslave the world:

Rothschilds Zionists, Protocols of the Learned Elders of Zion     

Silent Weapons for Quiet Wars: Silent Weapons for Quiet Wars     

In addition to this the FARM owners are concerned that the people are waking up and so as to save taking on 6 Billion people they have decided to reduce the global population to around 500,000,000 which they think they can manage while keeping everyone enslaved.

What is presented on this site is the proof that a global criminal cartel has already overthrown our organic sovereign governments and is now openly engaged in genociding away the global populous using Quiet Weapon - Silent War technology in what is a Mixed war on all people of the world.

The cabal has targeted  90% of the global populous for termination as they have widely publicized:

Georgia Guidestones: https://vigilantcitizen.com/sinistersites/sinister-sites-the-georgia-guidestones/ 

Deagel.com: https://chemtrailsplanet.net/2017/02/22/deagel-forecast-predicts-81-us-population-reduction-by-2025/

Now we have Kissinger Memo 200 on how the US should depopulate Africa (what they were really saying though was depopulate the world): 

Now - they would prefer the people to self elect for their own demise with energy weapons that aid sterilization and cancer (WifFi, Smart Meters et al).

More direct methods of helping us die: Poisoning our air, water, food and bodies with vaccines! 

I will end by saying - I would not trust the KHAZARIAN Mafia that is running our world to walk my dog! 

The last thing they should be trusted with is our children when they have openly admitted that they are engaged in killing us off! The most obvious evidence of this is the Chemtrails program which everyone can see in real time! If they are poisoning our air and water you can sure as hell expect that the vaccines are not created to expand your life time but to terminate it:

Hell no - I would not vaccinate children. I would get my children out of the plantation school system in to Home Schools organized by awakened parents that know what the farmers are doing and why:

My this excerpt from the document below will help you:

This is precisely why Bill Gates famously said:

The world today has 6.8 billion people... that's headed up to about 9 billion. Now if we do a really great job on new vaccines, health care, reproductive health services, we could lower that by perhaps 10 or 15 percent.

Why would Bill Gates be talking about vaccines REDUCING human population if vaccines didn't secretly contain sterilization agents? Remember, Gates is the same person who has funded all sorts of sterilization technologies including one that blasts men's scrotums with high-intensity sound waves to make them infertile.

Top tools for human depopulationGates is part of a covert medical cabal that believes aggressive human depopulation is urgently necessary to save the planet. This group, which includes many scientists and virologists, believe that the most effective tools for human depopulation are:

1) Vaccines which are covertly spiked with sterilization chemicals.
2) Genetically engineered viruses with a high mortality rate, possibly engineered to target specific races and genetic profiles.

For example, Dr. Charles Arntzen, head of The Biodesign Institute for Infectious Diseases and Vaccinology recently joked about using an engineered virus to cull the human population, saying "That's the answer! Go out and use genetic engineering to create a better virus. (laughter) Twenty-five percent of the population is supposed to go in Contagion."

As I wrote on October 22, 2014, many virologists believe humans are nothing more than a "parasite" to be consumed by viruses which are the planet's "immune response" to human overpopulation. Here's a passage from the book "The Hot Zone" by Richard Preston, summarizing the way these scientists think:

...the earth is mounting an immune response against the human species. It is beginning to react to the human parasite, the flooding infection of people, the dead spots of concrete all over the planet, the cancerous rot-outs in Europe, Japan and the United States, thick with replicating primates [i.e. humans], the colonies enlarging and spreading and threatening to shock the biosphere with mass extinctions.

Perhaps the biosphere does not "like" the idea of five billion humans. Or it could also be said that the extreme amplification of the human race, which has occurred only in the past hundred years or so, has suddenly produced a very large quantity of meat, which is sitting everywhere in the biosphere and may not be able to defend itself against a life form that might want to consume it...

The earth's immune system, so to speak, has recognized the presence of the human species and is starting to kick in. The earth is attempting to rid itself of an infection by the human parasite.

What's extraordinary in all this -- both with vaccines and viruses engineered as weapons -- is how the most influential people in the scientific community have come to view humanity as an enemy to be destroyed via tools of medicine and science. Frighteningly, modern medical science has the tools to carry out its genocidal assaults on humankind through "accidental" releases of deadly viruses or "accidental" contamination of vaccines with sterilization chemicals.

The evidence of deliberate sterilization chemicals in United Nations vaccines raises the obvious question: Was the recent Ebola outbreak in West Africa also intentional? And what else might scientists, vaccine pushers, world health authorities and governments have in mind for human depopulation in the years ahead?

Is there already something in the food supply that causes sterilization? The answer is a definite YES, and just like the pandemic viruses, it too is genetically engineered.

The five vectors for destroying humanityThese are the vectors for the science-based genocidal assault on humanity:

1) Vaccines
2) Viruses
3) Food
4) Water
5) Chemtrails (i.e. atmospheric deployment of chemicals)

All five of these vectors present "opportunities" for genocidal scientists to achieve their goal of human sterilization and depopulation. That is precisely why anyone who wishes to survive the great human culling now under way must take extraordinary steps to isolate themselves from institutionally-produced food, water and medicine. The only safe food, water and medicine is that which was produced independently and far outside the control of Big Food, Big Ag and Big Pharma.

Don't drink the city water without filtering it first, and read my laboratory testing results for all popular water filters at www.WaterFilterLabs.com

Don't eat factory-produced food. Don't allow yourself to be injected with weaponized vaccines. Don't take Big Pharma's deadly medicines. Be smart by being skeptical about the claimed "safety" of all those things created by institutions and authorities that quite literally want to kill off a significant percentage of the existing world population.

If you're smart and resourceful, you might just survive this great human culling. On the other hand, those who anxiously line up to be injected with the seasonal flu shots are all admitting they are too stupid and gullible to last long in a world where "science" has declared a covert war on human life.

Learn more: http://www.naturalnews.com/047571_vaccines_sterilization_genocide.html?utm_content=buffer55aa4&utm_medium=social&utm_source=facebook.com&utm_campaign=buffer#ixzz3IoVtthYd

Some more prroof of Kissinger's plan (memo 100) put in to effect! Remember - Africa is the way it is because the controllers made it that way! It did not start out that way. The Revisionist khazarian mafia want you to think they need saving! Just more %^&*IOP lies by the parasites. The parasites did not want competition so they destroyed a continent. They wanted their resources so they killed off the majority of the people and have economically crippled the locals ever since.

 

BELOW - Chemtrails commemorative coin 1985 - Vatican Death cult! Genocide via weather wars and Aerosol poisoning: http://www.geoengineeringwatch.org 

 

 


 

 

AIDS and the DOD

AIDS virus was funded and released in vaccines by the U.S. government
Like us? www.facebook.com/Citizens.Action.Network

NOTE: The document below (designated as "Part 5") is a true copy of the transcript of the July 1, 1969 testimony of Dr. Donald MacArthur -- a high-level Defense Department biological research administrator -- before the House Committee on Appropriations, Subcommittee on Department of Defense. For those who hold the theory that AIDS is the result of a U.S. biological weapons program, this testimony is a smoking gun. MacArthur was then Deputy Director of Defense Research and Engineering. Congress approved the appropriation for the program.
Link - http://panindigan.tripod.com/aidsdodhear.html

Go to page 66 and it will contain all the info about how they spread it to 100 million people in a depopulation plan. If this is true, and I think it is, there is no limit to what these people will do.
http://webzoom.freewebs.com/tweeofmeer/PJ%2062.pdf

Video of Robert Gallo - supposed Inventor of AIDS
https://www.youtube.com/watch?v=CDxZ7PX8YGI

 

U.S. Patents for HIV AIDS and the CURE http://danieltowsey.wordpress.com/2009/02/15/us-patents-for-hiv-aids-1984-and-the-patent-for-the-cure-1997/

[Note - I will reformat the following when I get time]... 

The U.S. Cure for AIDS-Patent 5676977(Tetrasil/Imusil) By Dr.Boyd E. Graves The U.S. Cure for AIDS-Patent # 5676977 (Tetrasil/Imusil) Keywords: News, elsewhere, The U.S. Cure for AIDS-Patent # 5676977 (Tetrasil/Imusil) Date : Mon, 29 Jul 2002 21:27:06 -0700 (PDT) United States Patent 5,676,977 Antelman October 14, 1997 Method of curing AIDS with tetrasilver tetroxide molecular crystal devices Abstract The diamagnetic semiconducting molecular crystal tetrasilver tetroxide (Ag.sub.4 O.sub.4) is utilized for destroying the AIDS virus, destroying AIDS synergistic pathogens and immunity suppressing moieties (ISM) in humans. A single intravenous injection of the devices is all that is required for efficacy at levels of about 40 PPM of human blood. The device molecular crystal contains two mono and two trivalent silver ions capable of “firing” electrons capable of electrocuting the AIDS virus, pathogens and ISM. When administered into the bloodstream, the device electrons will be triggered by pathogens, a proliferating virus and ISM, and when fired will simultaneously trigger a redox chelation mechanism resulting in divalent silver moieties which chelate and bind active sites of the entities destroying them. The devices are completely non-toxic. However, they put stress on the liver causing hepatomegaly, but there is no loss of liver function. ——————————————————————————– Inventors: Antelman; Marvin S. (Rehovot, IL) Assignee: Antelman Technologies Ltd. (Providence, RI) Appl. No.: 658955 Filed: May 31, 1996 Boyd E. Graves, J.D. US Supreme Court Case No. 00-9587 http://www.supremecourtus.gov/docket/00-9587.htm Cell – 619-204-5683619-204-5683 Fax – 785-263-1568 Email – This email address is being protected from spambots. You need JavaScript enabled to view it. Web – http://www.boydgraves.com http://www.boydgraves.com

By Boyd E. Graves This email address is being protected from spambots. You need JavaScript enabled to view it. Fax – 785-263-1568 Download Article (PDF) Add to PDF Compilation Download PDF Compilation
Email Article Add your comments (c) Independent Media Center. All content is free for reprint and rebroadcast, on the net and elsewhere, for non-commercial use, unless otherwise noted by author. IMC not for content (expand this). more… imc-nyc at lists.indymedia.org (212) 221-0521(212) 221-0521
4 W. 43rd ST, NY, NY 10036 ========================= Resources Contact Us Home Browse by: INVENTOR PATENT HOLDER PATENT NUMBER DATE Method of continuous production of retroviruses (HTLV-III) from patients with AIDS and pre-AIDS
4647773 Method of continuous production of retroviruses (HTLV-III) from patients with AIDS and pre-AIDS Inventor: Gallo, et al.
Date Issued: March 3, 1987
Application: 06/602,946
Filed: April 23, 1984
Inventors: Gallo; Robert C. (Bethesda, MD)
Popovic; Mikulas (Bethesda, MD) Assignee: The United States of America as represented by the Department of Health (Washington, DC)
Primary Examiner: Warren; Charles F.
Assistant Examiner: Tarcza; John Edward
Attorney Or Agent: Roberts, Jr.; John S.
U.S. Class: 424/208.1; 435/235.1; 435/239; 435/372.3; 435/948
Field Of Search: 435/235; 435/239; 435/240; 435/948; 435/5; 435/29; 424/89; 128/1T
International Class:
U.S Patent Documents: 4464465; 4520113
Foreign Patent Documents:
Other References: Popovic et al, Science, 224(4648):497-500, May 4, 1984..
Gallo et al, “Isolation of Human T-Cell Leukemia Virus in Acquired Immune Deficiency Syndrome (AIDS)”, Science, 220, pp. 865-867 (5-1983)..
Barre-Sinoussi et al, “Isolation of a T-Lymphotropic Retrovirus from a Patient at Risk for AIDS”, Science, 220, pp. 868-871 (5-1983)..
Marx, “Strong New Candidate for AIDS Agent”, Science, 224, pp. 475-477 (5-1984).. Abstract: A cell system is disclosed for the reproducible detection and isolation of human T-lymphotropic retroviruses (HTLV-family) with cytopathic effects (HTLV-III) from patients with the acquired immune deficiency syndrome (AIDS), pre-AIDS and in healthy carriers. One neoplastic aneuploid T-cell line derived from an adult with lymphoid leukemia, and termed HT, was susceptible to infection with the new variants of HTLV, which are transformed and providing T-cell populations which are highly susceptible and permissive from HTLV-III, and convenience for large scale production, isolation and biological detection of the virus.
Claim: We claim: 1. A method for continuous production of HTLV-III virus which comprises infecting in cell culture highly susceptible, permissive cells consisting of a neoplastic aneuploid HT-cell linewith said virus, said cells preserve the capacity for permanent growth after the infection with said virus, growing said cells under conditions suitable for cell growth and recovering said virus produced by said cells. 2. The method of claim 1, wherein said virus consists of cytopathic variants of HTLV. 3. The method of claim 1 wherein said infecting comprises cocultivating said virus with said cells to produce a cell line and recovering said cell line. 4. The method of claim 1 wherein said infecting comprises cell-free infection of said cells with said virus. 5. The method of claim 1 wherein said cells are neoplastic aneuploid T-cells derived from an adult with lymphoid leukemia. 6. A process for the continuous production of HTLV-III virus which comprises cocultivating said virus with a target HT-cell to produce an infected cell line, growing said cell line and recovering said virus from supernatants produced by saidcell line. 7. The process of claim 6 wherein said target T-cell is a neoplastic aneuploid T-cell susceptible to infection with HTLV-III. 8. A process for the continual production of HTLV-III by infecting T-cells in cultures which comprises cocultivating HTLV-III virus with an HT-clone to produce an infected cell line, said clone being an aneuploid T-cell line derived fromlymphoid leukemia, growing said cell line and recovering said virus from supernatants produced by said cell line. 9. The process in claim 8 wherein said clone is a mature T-cell phenotype of OKT3.sup.+ (62%), OKT4.sup.+ (39%) and OKT8.sup.-. 10. A method of producing a cell line containing an antigen of HTLV-III which comprises infecting an HT-cell line derived from lymphoid leukemia and susceptible to infection with HTLV-III, said cell line is capable of continuous large-scaleproduction of HTLV-III, and growing the infected cell line under conditions suitable for growth. 11. The method of claim 10 wherein said cell line is a neoplastic aneuploid T-cell line. 12. The method of claim 10 wherein said HTLV-III are variants of human T-lymphotropic retrovirus, exhibit cytopathic effects and are non-transforming. 13. A cell line containing HTLV-III designated H9/HTLV-III.sub.B, ATCC Accession CRL 8543. 14. A process for producing a cell line H9/HTLV-III.sub.B which comprises infecting a target T-cell with HTLV-III virus to produce a cell line and recovering same, said infecting process overcomes the normal cytopathic effect of HTLV-III andpreserves the immortal growth capacity of the target cell. 15. An HT cell line permanently infected with HTLV-III virus, wherein said cell line continually produces said virus.
Description: The present invention describes a cell system for the reproducibledetection and isolation of human T-lymphotropic retroviruses (HTLV-family) with cytopathic or cell killing effects (HTLV-III) from patients with the acquired immune deficiency syndrome (AIDS), pre-AIDS and in healthy carriers. One neoplastic aneuploidT-cell line derived from an adult with lymphoid leukemia, and termed HT, was susceptible to infection with the new variants of HTLV, providing T-cell populations which are highly susceptible and permissive for HTLV-III, and convenience for large scaleproduction, isolation, and biological detection of the virus. BACKGROUND OF THE INVENTION The disclosure of this invention is contained in the following journal articles: Gallo et al., “Detection, Isolation, and Continuous Production of Cytopathic Human T-Lymphotropic Retroviruses (HTLV-III) from Patients with AIDS and pre-AIDS,”Science, in press; and Gallo et al., “Human T-Lymphotropic Retrovirus, HTLV-III, Isolated from AIDS Patients and Donors at Risk for AIDS,” in press. Epidemiologic data strongly suggest that acquired immune deficiency syndrome (AIDS) is caused by an infectious agent which is apparently horizontally transmitted by intimate contact or blood products. Though the disease is manifested byopportunistic infections, predominantly Pneumocystis carcinii pneumonia and Kaposi’s sarcoma, the underlying disorder affects the patient’s cell-mediated immunity with absolute lymphopenia and reduced helper T-lymphocyte (OKT4.sup.+) subpopulation(s). Moreover, before a complete clinical manifestation of the disease occurs, its prodrome, pre-AIDS, is frequently characterized by unexplained chronical lymphadenopathy and/or leukopenia involving a helper T cell subset. This leads to the severe immunedeficiency of the patient, suggesting that a specific subset of T-cells is the primary target for an infectious agent. Although patients with AIDS or pre-AIDS are often chronically infected with cytomegalovirus or hepatitis B virus, for various reasonsthese appear to be opportunistic or coincidental infections apparently not linked to the immunological response deficiency. It is believed that the cause of AIDS may be a virus from the family of human T-cell lymphotropic retroviruses (HTLV) which,prior to the present invention, comprised two major well characterized subgroups of human retroviruses, called human T-cell leukemia/lymphoma viruses, HTLV-I and HTLV-II. The most common isolate, HTLV-I, is mainly obtained from patients with matureT-cell malignancies. Seroepidemiological studies, in vitro biological effects, and nucleic acid hybridization data indicate that HTLV-I is etiologically associated with these malignancies, affecting adults primarily in the south of Japan, the Caribbeanand Africa. HTLV of subgroup II (HTLV-II) was first isolated from a patient with a T-cell variant of hairy cell leukemia. To date, this is the only reported isolate of HTLV-II from a patient with a neoplastic disease. Virus isolation andseroepidemiological data show that HTLV of both subgroups can sometimes be found in patients with AIDS. Evidence suggests that the retrovirus(es) of the HTLV family is an etiological agent of AIDS based on the following: (1) there is precedence for an animal retrovirus cause of immune deficiency (feline leukemia virus in cats); (2) retroviruses ofthe HTLV family are T-cell tropic; (3) they preferentially infect “helper” T-cells (OKT4.sup.+); (4) they have cytopathic effects on various human and mammalian cells as demonstrated by their induction of cell syncytia formation; (5) they can alter someT-cell functions; (6) in some cases infection may result in selective T-cell killing; and (7) they are transmitted by intimate contact or through blood products. The presence of antibodies directed to cell membrane antigens of HTLV infected cells hasbeen shown in sera of more than 40% of patients with AIDS [Essex et al., Science, 220:859 (1983)]. This antigen has since been defined as part of the envelope of HTLV [Schupbach, et al., Science, in press; and Lee, et al., Proc. Nat. Acad. Sci. U.S.A., in press]. The original detection and isolation of the various HTLV isolates were made possible by two earlier developments: the discovery of T-cell growth factor (TCGF), also called Interleukin 2 (Il-2), which enabled the routine selective growth ofdifferent subsets of normal and neoplastic mature T-cells [Ruscetti, et al., J. Immunol., 119:131 (1977); and Poiesz, et al., Proc. Nat. Acad. Sci. U.S.A, 77:6134 (1980)] and the development of sensitive assays for detection of retroviruses based onreverse transcriptase assays. The methods of HTLV isolation and transmission involved a cocultivation procedure using permissive T-cells for the virus. The use of normal human T-cells in cocultivation experiments preferentially yielded HTLV of bothsubgroups with immortalizing (transforming) capability for some of the target T-cells. However, HTLV variants (now termed HTLV-III), lack immortalizing properties for normal T-cells and mainly exhibit cytopathic effects on the T-cells and is now believed to be the cause of AIDS. In fact, such variants were frequently but onlytransiently detected using these normal T-cells as targets in cocultivation or cell-free transmission experiments. The cytopathic effect was overcome by finding a highly susceptible, permissive cell for cytopathic variants of HTLV, thus preserving thecapacity for permanent growth after infection with the virus. The present invention discloses the identification and characterization of this new immortalized T-cell population and its use in the isolation and continuous high- level production of suchviruses from patients with AIDS and pre-AIDS. Early experiments identified one neoplastic aneuploid T-cell line, termed HT, derived from an adult with lymphoid leukemia, that was susceptible to infection with the new cytopathic virus isolates. This cell line is a sensitive target for transmission of these virus isolates (HTLV-III) and it allows continuous large-scale virus production and development of specific immunologic reagents and nucleic acid probes useful for comparison of thesenew isolates among themselves and with HTLV-I and HTLV-II. In addition to their differences in biological effects that distinguish them from HTLV-I and HTLV-II, HTLV-III also differs from these known HTLV subgroups in several immunological assays and inmorphology. However, these new retroviruses are T4 lymphotropic and exhibit many properties similar to HTLV-I and II, including similar properties of the reverse transcriptase, cross reactivity of structural proteins as determined by heterologouscompetition radioimmune assays with patients’ sera and with animal hyperimmune sera, and induction of syncytia. These new retrovirus isolates are collectively designated HTLV-III, together with detectable differences in some of their proteins andgenetic information, HTLV-III’s ability to kill T-cells clearly separates these variants from other members of the HTLV family. STATEMENT OF DEPOSIT A cell line corresponding to the present invention, and denoted H9/HTLV-III.sub.B, has been deposited in the ATCC (under ATCC No. CRL 8543) on April 19, 1984, prior to the filing of this patent application. This deposit assures permanence of thedeposit and ready accessibility thereto by the public. H9 is a representative and preferred cell line in accordance with the invention. UTILITY STATEMENT The cell line which is a product of the present invention (H9/HTLV-III.sub.B) is presently useful for the production of vaccines for the relief of AIDS and for the detection of antibodies to the virus in blood samples. GENERAL DESCRIPTION A susceptible cell line HT was tested for HTLV before in vitro infection and it was negative by all criteria, including lack of proviral sequences. Continuous production of HTLV-III is obtained after repeated exposure of parental HT cells(3.times.10.sup.6 cells pretreated with polybrene) to concentrated culture fluids containing HTLV-III harvested from short term cultured T-cells (grown with TCGF) which originated from patients with pre-AIDS or AIDS. The concentrated fluids were firstshown to contain particle associated reverse transcriptase (RT). When cell proliferation declined, usually 10 to 20 days after exposure to the culture fluids, the fresh (uninfected) HT parental cells are added to cultures. Culture fluids from theinfected parental cell line was positive for particulate RT activity and about 20% of the infected cell population was positive in an indirect immune fluorescent assay (IFA) using serum from a hemophilia patient with pre-AIDS (patient E.T.). Serum fromE.T. also contained antibodies to proteins of disrupted HTLV-III but did not react with proteins of HTLV-I or HTLV-II infected cells. SPECIFIC DISCLOSURE As has been mentioned above, an aneuploid HT-cell line exhibited the desired prerequisites for the continuous propagation of HTLV-III. This cell line is a neoplastic aneuploid T-cell line derived from an adult patient with lymphoid leukemia,selected for its mature T-cell phenotype [OKT3.sup.+ (62%), OKT.sup.4 + (39%) and OKT8.sup.- ], as determined by cytofluorometry using a fluorescence-activated cell sorter. Cultures of these cells are routinely maintained in RPMI/1640 with 20% fetalcalf serum and antibiotics. These cultures are shown in Example 1, Table 1. Clone H9 is preferred, with Clone H4 being secondarily preferred. HTLV-III culture fluids are isolated from cultured cells of patients with acquired immune deficiency syndrome (AIDS). Peripheral blood leukocytes from these patients are banded in Ficoll-Hypaque, incubated in growth media (RPMI 1640, 20% fetalbovine serum 0.29 mg/ml glutamine) containing 5 .mu.g/ml phytohemagglutinin (PHA-P) for 48 hours, at 37.degree. C. in a 5% CO.sub.2 atmosphere. The leukocytes are then refed with growth medium containing 10% purified T cell growth factor (TCGF);optionally, some of the cells also received rabbit antibody to alpha interferon. Cells and growth media from these lymphocytes are then assayed for the presence of HTLV subgroups I-III. Samples exhibiting more than one of the following were consideredpositive: repeated detection of a Mg.sup.++ dependent reverse transcriptase activity in supernatant fluids; virus observed by electron microscopy; intracellular expression of virus-related antigens detected with antibodies from sero-positive donors orwith hyperimmune serum; or transmission of particles, detected by reverse transcriptase assays or by electron microscopic observation, to fresh human cord blood, bone marrow, or peripheral blood T-lymphocytes. All isolates not classified as eitherHTLV-I or HTLV-II by immunological or nucleic acid analysis were classified as HTLV-III. The cells in the HTLV-III producing cell cultures, characterized using established immunological procedures, are predominantly T-lymphocytes (E rosette receptor,OKT/3 and Leu/1 positive, with a T4 phenotype (OKT4, leu 3a positive). This process is also described by Gallo, et al., in Science, 220:865-867 (1983). The infection of parental HT cells as well as other cloned cell populations occurs by exposure of these cells to concentrated or nonconcentrated culture fluids (cell-free infection) from T-cell cultures from AIDS or pre-AIDS patients, or bycocultivation; that is, HT cells are infected by exposure to HTLV-III containing cultures. The usual cell-free infection procedure is as follows: 2 to 5.times.10.sup.6 cells are treated with polybrene (2 .mu.g/ml) or DEAE dextran for 30 minutes inCO.sub.2 incubator at 37.degree. C., and then exposed to the virus inoculum (0.1 to 1 ml) for one hour in the incubator (CO.sub.2 /37.degree. C.). The cells are kept in suspension by shaking at regular intervals. After one hour of incubation aregular growth medium is added. The positivity of infected cultures for HTLV-III is assessed after one, two, and three weeks of cultivation. The infection of HT cells (clones) is also obtained by cocultivation procedure–HT cells are mixed in various proportions (usually 1:5) with short- term cultured T-cells (about 5 to 20 days) from AIDS or pre-AIDS patients. The positivity forHTLV-III was scored by the detection of viral antigens or viral nucleic acid sequences in the infected recipient cells at various intervals (7, 14, 21 days, etc.) after cocultivation. The mixed cultures are maintained in growth medium for severalmonths. EXAMPLE 1 As shown in Table 1 below, single cell HT clones were isolated as described by Popovic, et al., in Neoplasma, 18:257 (1971), and Bach, et al., Immunol. Rev., 54:5 (1981) from a long-term cultured aneuploid HT-cell line exhibiting mature T-cellphenotype (OKT3.sup.+ [62%], OKT4.sup.+ [39%] and OKT8.sup.-) as determined by cytofluorometry using a fluorescence-activated cell sorter. The cultures were routinely maintained in RPMI/1640 with 20% fetal calf serum and antibiotics. The terminal celldensity of the parental cell culture, seeded at a concentration of 2.times.10.sup.5 cells/milliliter of culture media, was in the range 10.sup.6 -1.5.times.10.sup.6 cells/ml after 5 days of culture. For detection of multinucleated cells, cell smears were prepared from cultures 6 and 14 days after infection and stained with Wright-Giemsa. Cells having more than 5 nuclei were considered as multi-nucleated cells. Cloned cells from uninfectedcultures also contained some multi-nucleated giant cells as well; however, the arrangement of multiple nuclei in a characteristic ring formation was lacking and the number of these cells was much less (0.7% to 10%). Immunofluorescence positive cells were washed with phosphate-buffered saline (PBS) and resuspended in the same buffer at concentration 10.sup.6 cells per milliliter. Approximately 50 .lambda. of cell suspension were spotted on slides, airdried, and fixed in acetone for 10 min. at room temperature. Slides were stored at -20.degree. C. until use. Twenty microliters of either hyperimmune rabbit antiserum to HTLV-III (diluted 1/2000 in PBS) or serum from the patient (E.T.) diluted 1/8 inPBS was applied to cells and incubated for 50 min. at 37.degree. C. The fluorescein-conjugated antiserum to rabbit or human immunogloblin G was diluted and applied to the fixed cells for 30 min. at room temperature. Slides then were washed extensivelybefore microscopic examinations. The uninfected parental cell line as well as the clones were consistently negative in these assays. To determine reverse transcriptase activity, virus particles were precipitated from cell-free supernatant as follows: 0.4 ml of 4M NaCl and 3.6 ml of 30% (wt/vol.) polyethylene glycol (Carbowax 6000) were added to 8 ml of harvested culture fluidsand the suspension was placed on ice overnight. The suspension was centrifuged in a Sorvall RC-3 centrifuge at 2000 rpm at 4.degree. C. for 30 min. The precipitate was resuspended in 300 .mu.l at 50% (vol/vol) glycerol (25 mM Tris-HCl, pH 7.5/5 mMdithiothreitol/150 mM KCl/0.025% Triton X-100. Particles were disrupted by addition of 100 .mu.l of 0.9% Triton X-100/1.5M KCl. Reverse transcriptase (RT) assays were performed as described by Poiesz, et al., Proc Nat. Acad. Sci. U.S.A., 77:7415(1980) and expressed in cpm per milliliter culture medium. TABLE 1 __________________________________________________________________________ Response of Cloned T-Cell Populations to HTLV-III Infection Clones Characteristics H3 H4 H6 H9 H17 H31 H35 H38 __________________________________________________________________________ Total cell number (.times. 10.sup.6) 6 days after infection 1 1.5 1.5 0.3 0.4 0.3 0.5 1.8 14 days after infection 2.2 7.3 7.5 10.0 4.7 5.0 4.5 3.2 Multinucleatedcells (%) 6 days after infection 24 42 32 7 13 14 30 45 14 days after infection 45 48 45 30 22 45 60 60 Immunofluorescence positive cells (%) 6 days after infection Rabbit antiserum to HTLV-III 55 56 32 32 39 21 10 87 Patient serum (E.T.) 56 2921 ND ND ND ND 73 14 days after infection Rabbit antiserum to HTLV-III 50 74 60 97 71 40 20 80 Patient serum 45 47 56 78 61 43 22 89 Reverse transcriptase activity (.times. 10.sup.4 cpm/ml) 6 days after infection 2.4 1.8 2.1 4.1 2.6 1.4 1.7 2.5 14 days after infection 16.2 18.1 16.1 20.2 17.1 13.4 15.1 18.2 __________________________________________________________________________ ND = not done EXAMPLE 2 As shown in Table 2 below, cocultivation with H4 recipient T-cell clone was performed with fresh mononuclear cells from peripheral blood of patients RF and SN, respectively. In the case of patients BK and LS cocultivation was performed withT-cells grown in the presence of exogenous TCGF (10% V/V) for 10 days. The ratio recipient/donor (patients’) cells was 1:5. The mixed cultures were maintained in RPMI/1640 (20% FCS and antibiotics) in the absence of exogenous TCGF. Cell-free infectionof H9 T-cell clone was performed using concentrated culture fluids harvested from T-cell cultures of the patient WT. The T-cell cultures were grown in the presence of exogenous TCGF for two weeks before the culture fluids were harvested and concentrated. Cells of H9 clones were pretreated with polybrene (2 .mu.g/ml) for 20 min. and 2.times.10.sup.6 cells were exposed for one hr. to 0.5 ml of 100-fold concentrated culture fluids positive for particulate RT activity. HTLV-III virus expression in both cocultured and cell-free infected cell cultures were assayed approximately one month after in vitro cultivation. There was considerable fluctuation in HTLV-III expression (see Table 2). For details of bothreverse transcriptase (RT) assays and indirect immunofluorescence assays (IFA) see Example 1. TABLE 2 __________________________________________________________________________ Isolation of HTLV-III from Patients with Pre-AIDS and AIDS Virus Expression IFA with RT Activity Rabbit Serum Human Serum (ET) Patient Diagnosis Origin (.times. 10 cpm) (% Positive) (% Positive) EM __________________________________________________________________________ RF AIDS Haiti 0.25 80 33 ND (heterosexual) SN Hemophiliac U.S. 6.3 10 ND + (lymphadenopathy) BK AIDS U.S. 0.24 44 5 + (homosexual) LS AIDS U.S. 0.13 64 19 + (homosexual) WT Hemophiliac U.S. 3.2 69 ND ND (lymphadenopathy) __________________________________________________________________________ RT = reverse transcriptase IFA = immunofluorescence assays EM =electron microscopy ND = not done EXAMPLE 3 To select for high permissiveness for HTLV-III and to preserve permanent growth and continuous production of virus, extensive cloning of the HT parental T-cell population was performed. A total of 51 single-cell clones was obtained by bothcapillary and limited dilution techniques using irradiated mononuclear cells from peripheral blood of a healthy donor as a feeder. The growth of these cell clones was compared after HTLV-III infection. A representative example of response to virusinfection of 8 T-cell clones which are susceptible to and permissive for HTLV-III is shown in Table 1. In parallel experiments, 2.times.10.sup.6 cells of each T-cell clone were exposed to 0.1 ml of concentrated virus. Then cell growth and morphology,expression of cellular viral antigen(s), and RT activity in culture fluids were assessed 6 and 14 days after infection. Although all 8 clones were susceptible to and permissive for the virus, there were considerable differences in their ability toproliferate after infection. The cell number decreased by 10% to 90% from the initial cell count within 6 days after infection, and a high proportion of multinucleated (giant) cells were consistently found in all 8 infected clones. The percentage ofT-cells positive for viral antigen(s) determined by immunofluorescent assays with serum from AIDS patient (E.T.) and with hyperimmune rabbit serum raised against the whole disrupted HTLV-III ranged from 10% to over 80%. Fourteen days after infection,the total cell number and the proportion of HTLV-III positive cells increased in all 8 clones. The virus positive cultures consistently showed round giant cells which contained numerous nuclei. These multinucleataed giant cells are similar to thoseinduced by HTLV-I and HTLV-II except that the nuclei exhibit a characteristic ring formation. Electron microscopic examinations showed that the cells released considerable amounts of virus. EXAMPLE 4 To determine whether HTLV-III is continuously produced by the infected T-cells in long-term cultures, both virus production and cell viability of the infected clone, H4, were followed for several months. Although the virus production fluctuated,culture fluids harvested from the H4/HTLV-III cell cultures at approximately 14-day intervals consistently exhibited particulate RT activity which has been followed for over 5 months. The viability of the cells ranged from 65% to 85% and doubling timeof the cell population, which is called H4/HTLV-III, was approximately 30-40 hours. Thus, this permanently growing T-cell population can continuously produce HTLV-III. The yield of virus produced by H4/HTLV-III cells was assessed by purification of concentrated culture fluids through a sucrose density gradient and assays of particulate RT activity in each fraction collected from the gradient. The highest RTactivity was found at density 1.16 g/ml, similar to other retroviruses. * * * * http://prod.ottawa.indymedia.org/en/2008/02/6779.shtml U.S Patent for HIV Aids.pdf


Tetanus vaccines found spiked with sterilization chemical to carry out genocide

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Kairi:
Tetanus vaccines found spiked with sterilization chemical to carry out race-based genocide against Africans

Saturday, November 08, 2014

by Mike Adams, the Health Ranger

NaturalNews) Tetanus vaccines given to millions of young women in Kenya have been confirmed by laboratories to contain a sterilization chemical that causes miscarriages, reports the Kenya Catholic Doctors Association, a pro-vaccine organization.

A whopping 2.3 million young girls and women are in the process of being given the vaccine, pushed by UNICEF and the World Health Organization.

"We sent six samples from around Kenya to laboratories in South Africa. They tested positive for the HCG antigen," Dr. Muhame Ngare of the Mercy Medical Centre in Nairobi told LifeSiteNews. "They were all laced with HCG."

Chemical causes a woman's body to destroy its own fetus with vaccine-induced antibodiesHCG is a chemical developed by the World Health Organization for sterilization purposes. When injected into the body of a young woman, it causes a pregnancy to be destroyed by the body's own antibody response to the HCG, resulting in a spontaneous abortion. Its effectiveness lasts for years, causing abortions in women up to three years after the injections.

Dr. Ngare explained "...this WHO campaign is not about eradicating neonatal tetanus but a well-coordinated forceful population control mass sterilization exercise using a proven fertility regulating vaccine."

The Kenyan government, of course, insists the vaccine is perfectly safe. Dr. Tabu of Kenya's Health Ministry even told the media that because some young women are still having babies, the vaccine therefore must not contain any sterilization agent. However, this claim belies the fact that HCG doesn't work 100% of the time. It only sterilizes the majority of those injected with it, not all of them.

More importantly, the Kenyan Catholic Church is a pro-vaccine organization. "What reason do the Catholic doctors have for lying?" asked Dr. Ngare as reported in the LifeSiteNews article linked above. "The Catholic Church has been here in Kenya providing health care and vaccinating for 100 years for longer than Kenya has existed as a country."

In other words, the very group exposing the sterilization agenda of the tetanus vaccines is in fact a pro-vaccination group. Yet even they have now come to realize the horrifying truth: vaccines are the perfect vector for governments to deviously insert covert chemical or viral agents which are never revealed to the public.

The smoking gun: a five-shot course over two yearsWhat really raised red flags about this so-called tetanus vaccine was the highly unusual inoculation schedule. This vaccine demanded five shots over two years -- a schedule that isn't used for tetanus.

"The only time tetanus vaccine has been given in five doses is when it is used as a carrier in fertility regulating vaccines laced with the pregnancy hormone, Human Chorionic Gonadotropin (HCG) developed by WHO in 1992." explained Dr. Ngare.

Furthermore, the vaccine was only being given to women of child-bearing years, not men or women beyond the age of fertility.

As Dr. Ngare explains, the same vaccine sterilization campaign was used in 1993 in Mexico and both Nicaragua and the Philippines in 1994. WHO attempted to bring it to Kenya in the 1990's, Ngare says, but the effort was stopped by the Catholic Church.

According to Brian Clowes of Human Life International, the United Nations is not refuting the laboratory testing and confirmation of HCG in the vaccines. Instead, it claims some vaccines were "contaminated" in the manufacturing process -- an absurd claim that no reasonable person would believe because HCG should never even be anywhere near a vaccine manufacturing operation unless someone put it there deliberately.

LifeSiteNews reports that it:

has obtained a UN report on an August 1992 meeting at its world headquarters in Geneva of 10 scientists from "Australia, Europe, India and the U.S.A" and 10 "women's health advocates" from around the world, to discuss the use of "fertility regulating vaccines." It describes the "anti-Human Chorionic Gonadotropin vaccine" as the most advanced.


United Nations, WHO and UNICEF all engaged in vaccination genocideYou will not see this news reported by any mainstream media outlet in the United States. All truth about vaccines is censored, even if the truth is that the United Nations is deliberately engaged in a campaign of vaccine genocide against people of Africa.

What is happening in Kenya is a crime against humanity, and it is a crime committed with deliberate racial discrimination. Normally, the liberal media in the United States would be all over a story involving racial discrimination and genocide -- or even a single police shooting of a black teenager -- but because this genocide is being committed with vaccines, the entire mainstream media excuses it. Apparently, medical crimes against black people are perfectly acceptable to the liberal media as long as vaccines are used as the weapon.

As this story clearly demonstrates, "vaccine violence" is very real in our world. Vaccines are the perfect weapon for population control for several reasons:

1) Nobody really knows what's in them.
2) They can be easily spiked with hidden chemicals.
3) They can be administered under the cover of "public health."
4) All governments and establishment media will deliberately collaborate with the genocide in order to protect vaccines from being recognized as medical weapons against women.

Thus, vaccines can be routinely used to inject populations with birth control chemicals or even stealth cancer viruses. In fact, this is exactly what happened to as many as 98 million Americans during the mass polio vaccinations of the 1960's and 70's. The CDC even documented the "accidental" injection of millions of Americans with the cancer-causing SV40 simian virus, but the agency scrubbed all that history from its website in 2013.

In Kenya today, government authorities also claim the sterilization chemical was an "accidental" contamination. That's the excuse that can always be used as a cover story in weaponized vaccination schemes, where governments deliberately taint vaccines with known chemicals that end life, promote cancer or cause spontaneous abortions.

Vaccines as weapons = Medical crimes against humanityThe deliberate adding of HCG to vaccines without full disclosure to the population is a heinous violation of human rights and human dignity. Here are just a few of the crimes now being committed against humanity under the guise of vaccinations:

CRIME #1) No informed consent. None of these women in Kenya were told the truth that they were being injected with a sterilization chemical designed to cause infertility.

CRIME #2) Race-based genocide. The targeting of Kenyan women with this vaccine is a deliberate selection based on their race. By any reasonable standard, this would be called a racially-motivated hate crime resulting in genocide.

CRIME #3) The deliberate killing of a human being. The spontaneous abortions caused by these HCG-spiked vaccines results in the ending of a human life inside the mother's body. These killings take place without the consent or permission of the mother, nor any opportunity for defense of the life of the unborn child.

CRIME #4) Violation of Geneva Convention limitations on medical experimentation. All these Kenyan women injected with this vaccine are being used as human guinea pigs in a covert, criminal medical experiment. None of these women voluntarily signed up for this medical experiment, nor were they even informed. This is a medical crime against human beings.

CRIME #5) Crimes against women. Only women were selected for this targeted sterilization vaccine effort, proving that this is not only a race-based crime but also a gender-based crime against women.

If you add all this up, you've got weaponized vaccines being intentionally spiked with a known sterilization chemical developed by the WHO, then deployed in a racially-motivated genocidal manner that targets women to be used in an illegal medical experiment administered via vaccine inoculations.

When administered via vaccines, genocide and murder are apparently not newsYet, despite all this, the mainstream media is perfectly okay with this activity. The World Health Organizations endorses it. The United Nations organizes it. Governments help fund it. Vaccine-pushing scientists excuse it. Media outlets cover it up and censor the story, hoping you don't read Natural News or Life Site News to learn the truth.

When pharmacies in your neighborhood push flu shots and other vaccines, they don't tell you they are part of a branch of medicine steeped in genocide, racially-motivated hate crimes and a medical war on women. They don't tell you that flu shots still contain toxic mercury at concentrations 100 times the mercury found in ocean fish. They don't tell you anything about what's in those vaccines for the same reason that women in Kenya are never told what's in them, either.

Vaccines are the perfect weapons against women and childrenThe truth is that vaccines are easily deployed as weapons against humanity under the false cover story that they are saving humanity. What better way to pursue deliberate chemically-induced population control than to convince people they are being injected "for their own good?"

This is precisely why Bill Gates famously said:

The world today has 6.8 billion people... that's headed up to about 9 billion. Now if we do a really great job on new vaccines, health care, reproductive health services, we could lower that by perhaps 10 or 15 percent.

Why would Bill Gates be talking about vaccines REDUCING human population if vaccines didn't secretly contain sterilization agents? Remember, Gates is the same person who has funded all sorts of sterilization technologies including one that blasts men's scrotums with high-intensity sound waves to make them infertile.

Top tools for human depopulationGates is part of a covert medical cabal that believes aggressive human depopulation is urgently necessary to save the planet. This group, which includes many scientists and virologists, believe that the most effective tools for human depopulation are:

1) Vaccines which are covertly spiked with sterilization chemicals.
2) Genetically engineered viruses with a high mortality rate, possibly engineered to target specific races and genetic profiles.

For example, Dr. Charles Arntzen, head of The Biodesign Institute for Infectious Diseases and Vaccinology recently joked about using an engineered virus to cull the human population, saying "That's the answer! Go out and use genetic engineering to create a better virus. (laughter) Twenty-five percent of the population is supposed to go in Contagion."

As I wrote on October 22, 2014, many virologists believe humans are nothing more than a "parasite" to be consumed by viruses which are the planet's "immune response" to human overpopulation. Here's a passage from the book "The Hot Zone" by Richard Preston, summarizing the way these scientists think:

...the earth is mounting an immune response against the human species. It is beginning to react to the human parasite, the flooding infection of people, the dead spots of concrete all over the planet, the cancerous rot-outs in Europe, Japan and the United States, thick with replicating primates [i.e. humans], the colonies enlarging and spreading and threatening to shock the biosphere with mass extinctions.

Perhaps the biosphere does not "like" the idea of five billion humans. Or it could also be said that the extreme amplification of the human race, which has occurred only in the past hundred years or so, has suddenly produced a very large quantity of meat, which is sitting everywhere in the biosphere and may not be able to defend itself against a life form that might want to consume it...

The earth's immune system, so to speak, has recognized the presence of the human species and is starting to kick in. The earth is attempting to rid itself of an infection by the human parasite.

What's extraordinary in all this -- both with vaccines and viruses engineered as weapons -- is how the most influential people in the scientific community have come to view humanity as an enemy to be destroyed via tools of medicine and science. Frighteningly, modern medical science has the tools to carry out its genocidal assaults on humankind through "accidental" releases of deadly viruses or "accidental" contamination of vaccines with sterilization chemicals.

The evidence of deliberate sterilization chemicals in United Nations vaccines raises the obvious question: Was the recent Ebola outbreak in West Africa also intentional? And what else might scientists, vaccine pushers, world health authorities and governments have in mind for human depopulation in the years ahead?

Is there already something in the food supply that causes sterilization? The answer is a definite YES, and just like the pandemic viruses, it too is genetically engineered.

The five vectors for destroying humanityThese are the vectors for the science-based genocidal assault on humanity:

1) Vaccines
2) Viruses
3) Food
4) Water
5) Chemtrails (i.e. atmospheric deployment of chemicals)

All five of these vectors present "opportunities" for genocidal scientists to achieve their goal of human sterilization and depopulation. That is precisely why anyone who wishes to survive the great human culling now under way must take extraordinary steps to isolate themselves from institutionally-produced food, water and medicine. The only safe food, water and medicine is that which was produced independently and far outside the control of Big Food, Big Ag and Big Pharma.

Don't drink the city water without filtering it first, and read my laboratory testing results for all popular water filters at www.WaterFilterLabs.com

Don't eat factory-produced food. Don't allow yourself to be injected with weaponized vaccines. Don't take Big Pharma's deadly medicines. Be smart by being skeptical about the claimed "safety" of all those things created by institutions and authorities that quite literally want to kill off a significant percentage of the existing world population.

If you're smart and resourceful, you might just survive this great human culling. On the other hand, those who anxiously line up to be injected with the seasonal flu shots are all admitting they are too stupid and gullible to last long in a world where "science" has declared a covert war on human life.

Learn more: http://www.naturalnews.com/047571_vaccines_sterilization_genocide.html?utm_content=buffer55aa4&utm_medium=social&utm_source=facebook.com&utm_campaign=buffer#ixzz3IoVtthYd




Learn more: http://www.naturalnews.com/047571_vaccines_sterilization_genocide.html?utm_content=buffer55aa4&utm_medium=social&utm_source=facebook.com&utm_campaign=buffer#ixzz3IoVM1T8F

Kairi:
Are New Vaccines Laced with Birth-Control Drugs?

      During the early 1990s, the World Health Organization (WHO) had been overseeing massive vaccination campaigns against tetanus in a number of countries, among them Nicaragua, Mexico, and the Philippines. In October 1994, HLI received a communication from its Mexican affiliate, the Comite' Pro Vida de Mexico, regarding that country's anti-tetanus campaign. Suspicious of the campaign protocols, the Comite' obtained several vials of the vaccine and had them analyzed by chemists. Some of the vials were found to contain human chorionic gonadotrophin (hCG), a naturally occurring hormone essential for maintaining a pregnancy.

hCG and Anti-hCG Antibodies

In nature the hCG hormone alerts the woman's body that she is pregnant and causes the release of other hormones to prepare the uterine lining for the implantation of the fertilized egg. The rapid rise in hCG levels after conception makes it an excellent marker for confirmation of pregnancy: when a woman takes a pregnancy test she is not tested for the pregnancy itself, but for the elevated presence of hCG.

However, when introduced into the body coupled with a tetanus toxoid carrier, antibodies will be formed not only against tetanus but also against hCG. In this case the body fails to recognize hCG as a friend and will produce anti-hCG antibodies. The antibodies will attack subsequent pregnancies by killing the hCG which naturally sustains a pregnancy; when a woman has sufficient anti-hCG antibodies in her system, she is rendered incapable of maintaining a pregnancy.(1)

HLI reported the sketchy facts regarding the Mexican tetanus vaccines to its World Council members and affiliates in more than 60 countries.(2) Soon additional reports of vaccines laced with hCG hormones began to drift in from the Philippines, where more than 3.4 million women were recently vaccinated. Similar reports came from Nicaragua, which had conducted its own vaccination campaign in 1993.

The Known Facts

Here are the known facts concerning the tetanus vaccination campaigns in Mexico and the Philippines:

* Only women are vaccinated, and only the women between the ages of 15 and 45. (In Nicaragua the age range was 12-49.) But aren't men at least as likely as young women to come into contact with tetanus? And what of the children? Why are they excluded?

* Human chorionic gonadotrophin (hCG) hormone has been found in the vaccines. It does not belong there -- in the parlance of the O.J. Simpson murder trial, the vaccine has been "contaminated."

* The vaccination protocols call for multiple injections -- three within three months and a total of five altogether. But, since tetanus vaccinations provide protection for ten years or more, why are multiple inoculations called for?(3)

* WHO has been actively involved for more than 20 years in the development of an anti-fertility vaccine utilizing hCG tied to tetanus toxoid as a carrier -- the exact same coupling as has been found in the Mexican-Philippine-Nicaragua vaccines.(4)

The Anti-Fertility Gang

Allied with the WHO in the development of an anti-fertility vaccine (AFV) using hCG with tetanus and other carriers have been UNFPA, the UN Development Programme (UNDP), the World Bank, the Population Council, the Rockefeller Foundation, the All India Institute of Medical Sciences, and a number of universities, including Uppsala, Helsinki, and Ohio State.(5) The U.S. National Institute of Child Health and Human Development (part of NIH) was the supplier of the hCG hormone in some of the AFV experiments.(6)

The WHO begain its "Special Programme" in human reproduction in 1972, and by 1993 had spent more than $356 million on "reproductive health" research.(7) It is this "Programme" which has pioneered the development of the abortificant vaccine. Over $90 million of this Programme's funds were contributed by Sweden; Great Britain donated more than $52 million, while Norway, Denmark and Germany kicked in for $41 million , $27 million, and $12 million, respectively. The U.S., thanks to the cut-off of such funding during the Reagan-Bush administrations, has contributed "only" $5.7 million, including a new payment in 1993 by the Clinton administration of $2.5 million. Other major contibutors to the WHO Programme include UNFPA, $61 million; the World Bank, $15.5 million; the Rockefeller Foundation, $2.5 million; the Ford Foundation, over $1 million; and the IDRC (International Research and Development Centre of Canada), $716.5 thousand.

WHO and Philippine Health Department Excuses

When the first reports surfaced in the Philippines of tetanus toxoid vaccine being laced with hCG hormones, the WHO and the Philippine Department of Health (DOH) immediately denied that the vaccine contained hCG. Confronted with the results of laboratory tests which detected its presence in three of the four vials of tetanus toxoid examined, the WHO and DOH scoffed at the evidence coming from "right-to-life and Catholic" sources. Four new vials of the tetanus vaccine were submitted by DOH to St. Luke's (Lutheran) Medical Center in Manila -- and all four vials tested positive for hCG!

From outright denial the stories now shifted to the allegedly "insignificant" quantity of the hCG present; the volume of hCG present is insufficient to produce anti-hCG antibodies.

But new tests designed to detect the presence of hCG antibodies in the blood sera of women vaccinated with the tetauns toxoid vaccine were undertaken by Philippine pro-life and Catholic groups. Of thirty women tested subsequent to receiving tetanus toxoid vaccine, twenty-six tested positive for high levels of anti-hCG! If there were no hCG in the vaccine, or if it were present in only "insignificant" quantities, why were the vaccinated women found to be harboring anti-hCG antibodies? The WHO and the DOH had no answers.

New arguments surfaced: hCG's apparent presence in the vaccine was due to "false positives" resulting from the particular substances mixed in the vaccine or in the chemicals testing for hCG. And even if hCG was really there, its presence derived from the manufacturing process.

But the finding of hCG antibodies in the blood sera of vaccinated women obviated the need to get bogged down in such debates. It was no longer necessary to argue about what may or may not have been the cause of the hCG presence, when one now had the effect of the hCG. There is no known way for the vaccinated women to have hCG antibodies in their blood unless hCG had been artificially introduced into their bodies!

Why A Tetanus Toxoid "Carrier"?

Because the human body does not attack its own naturally occurring hormone hCG, the body has to be fooled into treating hCG as an invading enemy in order to develop a successful anti-fertility vaccine utilizing hCG antibodies. A paper delivered at the 4th International Congress of Reproductive Immunology (Kiel, West Germany, 26-29 July 1989) spelled it out: "Linkage to a carrier was done to overcome the immunological tolerance to hCG."( 8  )

Vaccine Untested by Drug Bureau

After the vaccine controversy had reached a fever pitch, a new bombshell exploded; none of the three different brands of tetanus vaccine being used had ever been licensed for sale and distribution or registered with the Philippine Bureau of Food and Drugs (BFAD), as required by law. The head of the BFAD lamely explained that the companies distributing these brands "did not apply for registration."(9) The companies in question are Connaught Laboratories Ltd. and Intervex, both from Canada, and CSL Laboratories from Australia.

It seemed that the BFAD might belatedly require re-testing, but the idea was quickly rejected when the Secretary of Health declared that, since the vaccines had been certified by the WHO -- there they are again! -- there was assurance enough that the "vaccines come from reputable manufacturers."(10)

Just how "reputable" one of the manufacturers might be is open to some question. In the mid-`80s Connaught Laboratories was found to be knowingly distributing vials of AIDS-contaminated blood products.(11)

Epilogue

At this juncture, evidence is beginning to appear from Africa.(12) HLI has called for a Congressional investigation of the situation, inasmuch as nearly every agency involved in the development of an anti-fertility vaccine is funded, at least in part, with U.S. monies.

Link -  http://thinktwice.com/birthcon.htm

Kairi:


‘A mass sterilization exercise’: Kenyan doctors find anti-fertility agent in UN tetanus vaccine

Steve Weatherbe

POPULATION CONTROLThu Nov 6, 2014 - 2:29 pm EST

Kenya’s Catholic bishops are charging two United Nations organizations with sterilizing millions of girls and women under cover of an anti-tetanus inoculation program sponsored by the Kenyan government.

According to a statement released Tuesday by the Kenya Catholic Doctors Association, the organization has found an antigen that causes miscarriages in a vaccine being administered to 2.3 million girls and women by the World Health Organization and UNICEF. Priests throughout Kenya reportedly are advising their congregations to refuse the vaccine.

“We sent six samples from around Kenya to laboratories in South Africa. They tested positive for the HCG antigen,” Dr. Muhame Ngare of the Mercy Medical Centre in Nairobi told LifeSiteNews. “They were all laced with HCG.”

Dr. Ngare, spokesman for the Kenya Catholic Doctors Association, stated in a bulletin released November 4, “This proved right our worst fears; that this WHO campaign is not about eradicating neonatal tetanus but a well-coordinated forceful population control mass sterilization exercise using a proven fertility regulating vaccine. This evidence was presented to the Ministry of Health before the third round of immunization but was ignored.”

But the government says the vaccine is safe. Health Minister James Macharia even told the BBC, “I would recommend my own daughter and wife to take it because I entirely 100% agree with it and have confidence it has no adverse health effects.” 

And Dr. Collins Tabu, head of the Health Ministry’s immunization branch, told the Kenyan Nation, that “there is no other additive in the vaccine other than the tetanus antigen.”

Tabu said the same vaccine has been used for 30 years in Kenya. Moreover, “there are women who were vaccinated in October 2013 and March this year who are expectant. Therefore we deny that the vaccines are laced with contraceptives.”

Newspaper stories also report women getting pregnant after being vaccinated.

Responds Dr. Ngare: “Either we are lying or the government is lying. But ask yourself, ‘What reason do the Catholic doctors have for lying?’” Dr. Ngare added: “The Catholic Church has been here in Kenya providing health care and vaccinating for 100 years for longer than Kenya has existed as a country.”

Dr. Ngare told LifeSiteNews that several things alerted doctors in the Church’s far-flung medical system of 54 hospitals, 83 health centres, and 17 medical and nursing schools to the possibility the anti-tetanus campaign was secretly an anti-fertility campaign.

Why, they ask does it involve an unprecedented five shots (or “jabs” as they are known, in Kenya) over more than two years and why is it applied only to women of child-bearing years, and why is it not being conducted without the usual fanfare of government publicity?


“Usually we give a series three shots over two to three years, we give it anyone who comes into the clinic with an open wound, men, women or children.” said Dr. Ngare. “If this is intended to inoculate children in the womb, why give it to girls starting at 15 years? You cannot get married till you are 18.” The usual way to vaccinate children is to wait till they are six weeks old.”

But it is the five-vaccination regime that is most alarming. “The only time tetanus vaccine has been given in five doses is when it is used as a carrier in fertility regulating vaccines laced with the pregnancy hormone, Human Chorionic Gonadotropin (HCG) developed by WHO in 1992.”

It is HCG that has been found in all six samples sent to the University of Nairobi medical laboratory and another in South Africa. The bishops and doctors warn that injecting women with HCG , which mimics a natural hormone produced by pregnant women, causes them to develop antibodies against it. When they do get pregnant, and produce their own version of HCG, it triggers the production of antibodies that cause a miscarriage.

“We knew that the last time this vaccination with five injections has been used was in Mexico in 1993 and Nicaragua and the Philippines in 1994,” said Dr. Ngare. “It didn’t cause miscarriages till three years later,” which is why, he added, the counterclaims that women who got the vaccination recently and then got pregnant are meaningless.

Ngare said WHO tried to bring the same anti-fertility program into Kenya in the 1990s. “We alerted the government and it stopped the vaccination. But this time they haven’t done so.”

Ngare also contrasted the secrecy of this campaign with the usual fanfare accompanying national vaccination efforts. “They usually bring all the stakeholders together three months before the campaign, like they did with polio a little while ago. And they use staff in all the centres to give out the vaccine.” But with this anti-tetanus campaign, “only a few operatives from the government are allowed to give it out. They come with a police escort. They take it away with them when they are finished. Why not leave it with the local medical staff to administer?”

Brian Clowes of Human Life International in Virginia told LifeSite News that WHO was not involved in the Nicaragua, Mexican and Philippines campaigns. “They try to maintain a spotless record. They let organizations like United Nations Population Fund and USAID do the dirty work.”

In the previous cases, said Clowes, the vaccinators insisted their product was pure until it was shown not to be. Then they claimed the positive tests for HCG were isolated, accidental contaminations in the manufacturing process.

LifeSiteNews has obtained a UN report on an August 1992 meeting at its world headquarters in Geneva of 10 scientists from “Australia, Europe, India and the U.S.A” and 10 “women’s health advocates” from around the world, to discuss the use of “fertility regulating vaccines.” It describes the “anti-Human Chorionic Gonadotropin vaccine” as the most advanced.  

One million Kenyan women and girls have been vaccinated so far with another 1.3 million to go. The vaccination is targeting women, according to the government, in order to inoculate their children in the womb against tetanus as well. The government says 550 children die of tetanus yearly.


In covering the contest of words the pro-government Nation found plenty of women who had been vaccinated and were now pregnant, even one who was the wife of a former Catholic priest who left the Church to marry. The paper ignored Kenya’s reliance on the Catholic medical system, while setting the bishops’ stand in a questionable historical context of irrational responses “largely based on religious beliefs,” the more recent murder of vaccination teams in Nigeria, and even of CIA conspiracy theories.

Why would the UN want to suppress the population in developing countries? “Racism,” is Brian Clowes’ first explanation.  “Also, the developed countries want to get hold of their natural resources. And lately, there is the whole bogus global warming thing.”

Dr. Ngare said it was the Catholic Church’s hope that the government could have resolved the matter quietly by testing the vaccine. “But the government has chosen to be combative,” forcing Kenya’s bishops and Catholic doctors to go public.

WHO’s Kenyan office and several WHO media contacts in Washington, D.C. failed to respond to LifeSiteNews enquiries over a 24-hour period.  




Source - https://www.lifesitenews.com/news/a-mass-sterilization-exercise-kenyan-doctors-find-anti-fertility-agent-in-u

Kairi:
Thu Mar 11, 2004 - 12:15 pm EST

NICEF Nigerian Polio Vaccine Contaminated with Sterilizing Agents Scientist Finds

LifeSiteNews.com



KADUNA, Nigeria, March 11, 2004 (LifeSiteNews.com) - A UNICEF campaign to vaccinate Nigeria’s youth against polio may have been a front for sterilizing the nation. Dr. Haruna Kaita, a pharmaceutical scientist and Dean of the Faculty of Pharmaceutical Sciences of Ahmadu Bello University in Zaria, took samples of the vaccine to labs in India for analysis.

Using WHO-recommended technologies like Gas Chromatography (GC) and Radio-Immuno assay, Dr. Kaita, upon analysis, found evidence of serious contamination. “Some of the things we discovered in the vaccines are harmful, toxic; some have direct effects on the human reproductive system,” he said in an interview with Kaduna’s Weekly Trust. “I and some other professional colleagues who are Indians who were in the Lab could not believe the discovery,” he said.  A Nigerian government doctor tried to persuade Dr. Kaita that the contaminants would have no bearing on human reproduction. “…I was surprised when one of the federal government doctors was telling me something contrary to what I have learned, studied, taught and is the common knowledge of all pharmaceutical scientists—that estrogen cannot induce an anti-fertility response in humans,” he said. “I found that argument very disturbing and ridiculous.”  When asked by the Trust why Dr. Kaita felt the drug manufacturers would have contaminated the Oral Polio Vaccine, he gave three reasons: “These manufacturers or promoters of these harmful things have a secret agenda which only further research can reveal. Secondly they have always taken us in the third world for granted, thinking we don’t have the capacity, knowledge and equipment to conduct tests that would reveal such contaminants. And very unfortunately they also have people to defend their atrocities within our midst, and worst still some of these are supposed to be our own professionals who we rely on to protect our interests.”  Dr. Kaita is demanding that “those who imported this fake drug in the name of Polio Vaccines…be prosecuted like any other criminal.”  The campaign to rid Nigeria of polio is in its fourth year. Officials there claim that all contaminated vaccines have been exhausted and replaced by uncontaminated batches.

In a rhetorical conclusion to the interview, Dr. Kaita asked “What plans has the government put in place to help children who have been given these toxic and contaminated vaccines in case they start reacting to them?”  This is not the first time UNICEF has been embroiled in a controversy over sterilizing agents in vaccines.  LifeSiteNews.com reported that in 1995, the Catholic Women’s League of the Philippines won a court order halting a UNICEF anti-tetanus program because the vaccine had been laced with B-hCG, which when given in a vaccine permanently causes women to be unable to sustain a pregnancy. The Supreme Court of the Philippines found the surreptitious sterilization program had already vaccinated three million women, aged 12 to 45. B-hCG-laced vaccine was also found in at least four other developing countries.

Source - https://www.lifesitenews.com/news/unicef-nigerian-polio-vaccine-contaminated-with-sterilizing-agents-scientis