October 02, 2007


Speedlinking on the SPP, NAU

or the militarization of medicine

(under construction)

By now you know all those alphabet soup letters and there are ever more.

Let's add to the list NAAMO
and WCO


North American Agricultural Marketing Officials

AAWCO -
NASDA



http://www.nonaiswa.org/?p=607

http://ahrp.blogspot.com/

HOW THIS WAS ACCOMPLISHED:

The New York Times reports that the US Inspector General of the Dept. of Health and Human Services has issued a new report slamming the FDA for its failure to ensure the safety of human subjects in clinical trials. The IG report shows that FDA has essentially done NOTHING to improve its oversight and enforcement of clinical trials since the IG last investigated in the year 2000.

"federal health officials did not know how many clinical trials were being conducted, audited fewer than 1 percent of the testing sites and, on the rare occasions when inspectors did appear, generally showed up long after the tests had been completed." As has been noted--"you value those whom you count."

Although human subjects are the linchpin of the multi-billion dollar clinical trial industry--without whom such trials, and the data collected from those trials, could not be conducted--no one has bothered to tally the number of human subjects. As Dr. Art Caplan, ethicist at the University of Pennsylvania concedes, "In many ways, rats and mice get greater protection as research subjects in the United States than do humans." [It is a refrain we have made since 1999.]

For a background article on nonprofits fronting for pharmaceutical companies see
http://www.motherjones.com/news/feature/1999/11/nami.html

http://tinyurl.com/3cmn7y
The Boston Globe
Drug firms' funding of advocates often escapes government scrutiny
Many patient groups depend on it, raising tricky ethical questions
By Diedtra Henderson
March 18, 2007


Just like the popular police show ‘Law & Order’ the Pandemic Flu has hit law enforcement and the justice department:

Law Enforcement Pandemic Flu Checklist

Pandemic Flu and the Justice Department

Preparing Law Enorcement for Pandemic

Fluhttp://www.nonaiswa.org/wordpress/wp-content/uploads/2007/09/geis_06_lr.pdf


The following is from
the Executive Summary, a hefty 98 page report

DoD Global Emerging Infections Surveillance and Response System
Partnering in the Fight
Against Emerging Infections
Annual Report

Partners are American Institute of Pathology
Military Infectious Disease Research Program
United States Army
United States Navy
United States Air Force
Office for the Assistant Secretary of Defense for Health Affairs
United States Regional Unified Commands
DOD Overseas Laboratories
Centers for Disease Control and Prevention
United States Department of State
Pan American Health Organization
World Health Organization
(this is 13 coordinating agencies plus the military)


Currently GEIS is the only robust, well-developed
system within the US government with a mission
of health surveillance through the monitoring of
infectious disease outbreaks using syndromic and
diagnostic methodologies. GEIS programs continue
to identify and address critical gaps in emerging
infectious disease preparedness. Through its accomplishments
and capabilities, GEIS continues to
contribute to force health protection and is a vital
partner in the global effort to identify and control
emerging infectious diseases.


www.mosquitomap.org

How to deal with the RFID chip (get organized now) at

http://www.nonaiswa.org/?p=614


Smoking Out the Avian Flu Glossary

Posted in October 2nd, 2007

The following is a glossary of terms associated with Avian Flu…discover what our UK farmers are living real time:

From: http://www.fao.org/docs/eims/upload//200354/HPAI_manual_en.pdf

ON THE ENUMERATORS

So who does the dirty work? and what happens when the populace figures it out and gets mad at the frontline worker?

NASS Confidentiality Pledge
Our Guarantee for Safeguarding Your Privacy

http://www.nonaiswa.org/wordpress/wp-content/uploads/2007/10/enumman.pdf

Every person working for or in cooperation with NASS – from the Agency Administrator to the person collecting the information – signs a confidentiality from which states that no reported survey information will be compromised. This includes sworn partners who are approved and supervised by NASS to provide statistical research.


So here next is what to do if you manage to get a "franchise operation" to collect all the data

NASS Handbook

Here is the part I looked at that caused concern (remember we are dealing with infectious diseases here) although this phrase enumerators was REALLY getting to me. It's just too Orwellian.

7.3 INSURANCE
The NASDA ENUMERATOR HANDBOOK outlines individual enumerator insurance responsibilities, coverage by NASDA, and procedures to file claims for NASDA job related injuries. NASDA does not provide health insurance coverage for enumerators or supervisory enumerators.

One can get workman's compensation, and return after a long term illness (!!) and there is a section specifically telling the Enumerator Superviser how to deal with it.

Now, about government transparency

ALLIANCE FOR HUMAN RESEARCH PROTECTION (AHRP)
Promoting Openness, Full Disclosure, and Accountability

http://www.ahrp.org and http://ahrp.blogspot.com

FYI - June 26th, 2007

Bloomberg News reports that despite a federal law requiring government
agencies to provide documents to citizens filing a request under the Freedom
of Information Act (FOIA) requests about drug and food safety hazards are
pilling up at the FDA.

Indeed, the FDA is the worst among all […]

Okay, let's get to FDA suppression of data

Without independent checks and balances--including unannounced inspections--it's anyone's guess. Worse still, the industry, with FDA support and encouragement, is outsourcing more and more clinical trials offshore to underdeveloped countries--to save money, but more importantly, to evade any oversight.

*snip*

The FDA’s 20,365 unfilled requests for information exceed the totals for the departments of Defense and Justice. One company, FOI Services Inc., accounts for 44 percent of the backlog, according to the agency. Researchers, consumer groups and individuals say the delays limit their ability to alert the public to food and drug dangers and to hold the FDA accountable.

For information on FDA coverups and threats made on drug whistleblowers revealed during Senate testimony see,
http://www.nytimes.com/2004/11/19/business/19fda.html?_r=1&oref=slogin

Historical timeline on mindcontrol/false memory syndrome in Canada

A Sad History of Abuses
Headline-making lapses in the ethical treatment of mentally ill patients include:

1950s and '60s: Dr. Ewen Cameron, Montreal psychiatrist, made extensive use of electroshock and LSD to cure relatively minor ailments. Cameron's brainwashing experiments were partially funded by the CIA. In 1992, Canada paid $100,000 to patients as compensation.

1994: The California superior court ruled that psychiatrist Dr. Richard Rose and therapist, Marche Isabella implanted false memories of child abuse in a patient and wrongly harmed her father. The case received international attention because it marked the first time a court allowed a therapist to be sued for implanting false memories.

2005: The Supreme Court of British Columbia approved a $450,000 settlement between the provincial government and nine women with mental disabilities who were sterilized while patients at Riverview Psychiatric Hospital. The women were sterilized at the hospital in nearby Coquitlam between 1940 and 1968.

Source: Star files; Compiled by Star Library staff


The activist archive


Please take a few moments to read these Cooperative Agreements. In a nutshell: NAIS is being implemented, BIG MONEY…BIG ACTION, and it is up to us to stop the firestorm!

CA 06-9153-1087 NAIS Assessment & Implementation.pdf

CA 06-9153-1087 2.pdf

CA 06-9753-1439 NAIS Implementation Kids.pdf

CA Q2 2006 Animal Tracking.pdf

CA WSDA 05-9753-1439 8-1105 2.pdf

CA WSDA 05-9753-1439 Rev 1 2 2005.pdf

CA-05-9753-1359 StartUp 1-05.pdf




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