Category: Human Experimentation


Dees Illustration

Stephen Lendman
Activist Post

It’s no surprise. Michael Parenti calls America’s High Court its “autocratic branch.”

It’s notoriously pro-business. It’s longstanding. In Santa Clara County v. Southern Pacific Railway (1886), it granted corporations legal personhood.

More recently, in Wal-Mart Stores, Inc. v. Dukes et al (June 2011), it denied longstanding sexual discrimination class action redress. It overruled a Ninth Circuit Court of Appeals decision doing so.

In AT&T Mobility v. Concepcion (April 2011), it did so two months earlier. It blocked class action redress claiming fraud. The company’s wireless subsidiary charged sales tax on cellphones it advertised as free. Two California courts rules for plaintiffs. The High Court overruled them.

In Citizens United v. Federal Election Commission, the Supreme Court ruled for money power over democratic governance. One dollar = one vote.

Corporations and PACs can spend all they want. Doing so more than ever lets them control US elections. Voters are effectively disenfranchised. They have no say whatever.

Numerous other rulings show America’s High Court is supremely pro-business. The Roberts Court is more so than previous ones. Even The New York Times noticed.

On May 4, it headlined “Corporations Find a Friend in the Supreme Court.” It rejected an anti-trust class action suit against Comcast. Subscribers sought to prove unfair competition and overcharges. Wrongdoing was dismissed 5 – 4. It didn’t surprise. It’s consistently pro-business. Doing so facilitates corporate empowerment, discriminatory practices, willful fraud, and products harming human health.
Bowman v. Monsanto again showed where America’s High Court stands. Justice again was denied. Corporate interests alone matter. In 2007, Monsanto sued Vernon Bowman. He’s an Indiana farmer. At issue was alleged patent infringement.

He bought mixed soybean seeds. He did so from a grain elevator. He planted them a second time. He supplemented them with soybeans bought from the same source.

Monsanto’s licensing agreement forbids second plantings. It wants seeds sold used only once. It wants farmers to pay each time they plant.

Bowman claimed no patent infringement. It expired on what he first bought. He supplemented with commodity soybeans. They’re usually used for feed.

He said they naturally “self-replicate or sprout unless stored in a controlled manner.” In other words, he planted soybeans, not new seeds. He violated no law.

Justice Elena Kagan delivered the court opinion. She didn’t surprise. She and other justices spurn judicial fairness. They do so in defense of privilege. She rejected what she called “that blame-the-bean defense.”

Bowman had no chance. He was no match against Monsanto. He was ordered to pay nearly $85,000 in damages. He’s a small farmer. Doing so may bankrupt him. Longstanding agribusiness plans call for greater consolidation at the expense of small competitors.

Bowman lost at the district, appellate and High Court levels. They ruled one way. They claimed patent exhaustion doesn’t permit farmers to replant seeds and harvest them without patent holder’s permission.

Generic drug companies freely do it. The Drug Price Competition and Patent Term Restoration Act permits it. Once patents expire, holders no longer have exclusive rights.

In 2014, the last of Monsanto’s Roundup Ready US patents will expire. Monsanto’s supposed to lose exclusivity. At issue is will or won’t it happen?

Expect Monsanto to press hard to keep it. Earlier it said it wants international regulatory Roundup Ready soybeans support until 2021. It’s unclear if other companies will be able to sell generic versions. Monsanto won’t make it easy to do so.

On May 13, Food Democracy Now (FDN) denounced the Supreme Court ruling. Executive director Dave Murphy accused Washington of complicity in permitting the “corporate takeover of (America’s) food supply.”

“Today,” he said, “the Supreme Court unanimously affirmed the corporate takeover of our food supply, in a huge win for Monsanto, and a major loss for America’s farmers and consumers.”

Monsanto has long engaged in an effort to subvert family farmers that do not use their genetically-engineered seeds, and the Court has now handed corporations even more control over what our families eat.

Currently, Food Democracy Now! is a co-plaintiff in a lawsuit in the District Court of Appeals, Organic Seed Associations et Al. v Monsanto to protect America’s farmers from unwanted contamination of their crops by Monsanto’s patented genetically-engineered plants.

Our nation’s family farmers grow our food on farms where cross-pollination between organic, non-GMO crops and Monsanto’s genetically-engineered patented crops is regular and naturally-occurring process.

The Court’s decision to give Monsanto the power to control the future harvest of America’s family farmers and our county’s food supply is deeply troubling, immoral and a very bad sign for the future of our nation’s food.

In March 2013, Obama signed the Monsanto Protection Act.It’s the Farmer Assurance Provision rider in HR 933: Consolidated and Further Continuing Appropriations Act, 2013. Monsanto lawyers wrote it.

It permits circumventing judicial decisions. If courts rule GMOs unsafe, Monsanto’s free to ignore them. So can the Secretary of Agriculture.

He’s free to ignore food safety. He can let hazardous GMOs poison America’s food supply. Obama’s complicit with giant corporate interests. He’s their man in Washington. He’s beholden to monied interests. They own him.

Read Full Article Here

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Revealed Government Documents Show Vaccine Injured Children in Small African Village Used Like Lab Rats

Children vaccinated  in Africa
were severely harmed by vaccines

Christina England
Activist Post

In December 2012, vaccine tragedy hit the small village of Gouro, Chad, Africa, situated on the edge of the Sahara Desert. Five hundred children were locked into their school, threatened that if they did not agree to being force-vaccinated with a meningitis A vaccine, they would receive no further education. These children were vaccinated without their parents’ knowledge. This vaccine was an unlicensed product still going through the third and fourth phases of testing.

Within hours, one hundred six children began to suffer from headaches, vomiting, severe uncontrollable convulsions and paralysis. The children’s wait for a doctor began. They had to wait one full week for a doctor to arrive while the team of vaccinators just carried on vaccinating others from the village. More children became sick.

When the doctor finally came, he could do nothing for the children. The team of vaccinators, upon seeing what had happened, fled the village in fear.

Fifty children were finally transferred to a hospital in Faya and later taken by plane to two hospitals in N’Djamena, the capital city of Chad. After being shuttled around like cattle, these sick, weak children were dumped back in their village without a diagnosis and each family was given an unconfirmed sum of £1000 by the government. No forms were signed and no documentation was seen. They were informed that their children had not suffered a vaccine injury. However, if this were true, why would their government award each family £1000 in what has been described as hush money?

Interestingly, during the time the children spent in the hospital, two more children joined them from another village.

To read the full stories of this tragedy, please see references at the end of this article from previous Vactruth world-exclusive reports. [1,2,3,4]

Since this time, Vactruth has been passed a series of secret documents, which fill in some missing gaps in this story and expose just how corrupt the organizations behind this tragedy really are.
The Exclusive, Heartbreaking Details

On January 14, 2013, arrangements were made for seven female patients between the ages of 8-18 to be evacuated from the Hospital of Mother and Child (HME) and the General Hospital of National Referrals (HGRN) in N’Djamena and transferred by air to a clinic in Tunisia. This was scheduled to take place between January 16 and 22.

The documents in our possession state that the Chadian government arranged for the patients to be accompanied by Dr. Joseph Mad-Toingue, Chief Service of Infectious Diseases of the National General Referral Hospital; Dr. Moumar Mbaileyo, anesthesiologist employee of the National General Referral Hospital; and Mr. Dihoulne Kakiang, state-certified nurse, employee of the National General Referral Hospital.

On January 29, 2013, a letter passed between The Chief Service of Infectious Diseases of HGRN-N’Djaména and Mr. Director General of the National General Referral Hospital, stating:

Mr. Director General,

Herewith I have the honor of putting into your hands the report of the mission completed in Tunisia between 15 and 22 of January 2013 regarding the medical evacuation of 7 patients.

The Chief of Service.

Vactruth now has this report.

A Parent’s Worst Nightmare

The report states that seven female patients between the ages of 8 and 18 had suffered adverse reactions after receiving the meningitis A vaccination during a national campaign, which took place on December 11, 2012, for the prevention of this illness. These patients had originally been taken to the Regional Hospital of Faya, before being transferred on December 26, 2012, to the Hospital of Mother and Child (HME) and the General Hospital of National Referrals (HGRN) in N’Djamena.

Arrangements were later made for a medical evacuation to transfer these patients to Tunisia for further tests and treatment.

According to the report, the departure took place in N’Djaména on January 15, 2013, at 10:50 pm after a long wait at the Hassan airport in N’Djamena because of the late arrival of the plane.

The journey took place on board a Tunisian plane chartered by the International Medical Society (SMEDI). The party consisted of seven patients, three members of the medical team and seven parents (two men and five women) who accompanied the sick children.

Interestingly, the document states that the party did not fly alone.

The government report states that twenty other passengers traveling to Tunisia for the same reason (medical evacuation) also joined the party. Sadly, there were no further details on these patients in the report.

Were these patients also vaccine-damaged by the meningitis A vaccination, and where did these twenty other sick patients come from?

Just before the plane took off, an 18-year-old patient had what the report describes as a ‘shaking episode,’ and was given a 10 mg vial of diazepam before boarding the plane. Other than this incident, the flight went well.

The Specialists Say “Case Closed”

The group arrived in Tunisia on January 16, 2013, and was received by SMEDI agents who took care of the police formalities (entry visa) before dividing the group into three parties. The patients were transported by ambulance to the clinic, the medical staff was taken to a hotel, and the patients’ parents were taken to a center.

On the afternoon of January 16, the three medical staff were introduced to SMEDI’s Director General, M. Ghazi Mejbri, to get acquainted. This was followed by a work session with the medical coordinator, Dr. Folla Amara. In the course of this meeting, the condition of the patients was discussed and plans were arranged for their care.

The patients were taken to the neurological department of SMEDI’s La Sourka clinic. The clinic had received the children’s medical records in advance and was reported to have conducted their own clinical and biological tests on the patients before meeting with the medical team that had accompanied them.

On January 17, a meeting took place with Professor Rachid Namai (“chef de clinique”), Dr. Kefi and Dr. Mabet. It was concluded that the children’s ‘shaking attacks’ or convulsions were of no consequence. On the paraclinical level, the report stated that the liquor tests of five patients did not reveal any anomalies, nor did the EEG of six patients.

The EEG of the seventh patient showed minor anomalies in the immediate post-critical phase, but was reported to have stabilized. An MRI (magnetic resonance imaging) was to take place of all seven patients. After the meeting, the team visited the patients who were all reported to be well, except for one child who had developed tonsillitis and had to receive appropriate treatment.

On January 19, a second meeting took place at the La Soukra Clinic during which they examined the patients’ medical records that gave the results of all the medical tests that had taken place. Among the biological perturbations there was reported to be one case of persistent thrombopenia (a lower than normal number of blood cell fragments called platelets), two cases of of elevated immunoglobulines E (Ig E) and five cases of gram negative bacteria directly upon examination — culturing has not been contributory.

The report stated that, generally speaking, the patients showed a raised tendency for hypoalbuminemia (swelling), hypo creatininemia (renal dysfunction), and hyper glucorrhagia (no definition found).

 

Read Full Article Here

linktv linktv

Published on Apr 30, 2013

As Europe considers expanding cultivation of genetically modified crops, the European movement against GMOs heats up. A campaign film produced by Sourced TV highlights European concerns.

Watch more at http://www.linktv.org/earthfocus.

Image source

Stop the ‘Monsanto Protection Act’ Today

Activist Post

The Monsanto Protection Act is revived in the U.S. Senate and urgent help is needed to stop it in its tracks. It was late on Monday night when the biotech lobbyists slipped a biotech rider (Sec. 735) into the Senate Continuing Resolution spending bill which has nothing to do with GM crops.

If this passed, it would be the point of no return for unhindered Monsanto havoc. They would trump federal court power and courts would not be able to use authority to stop sales or planting of any illegal or hazardous genetically modified crops. Strange for biotech giants to want this rider, as the USDA already gives them unheeded approval without safety testing of their crops. Rider (Sec. 735) clinches Monsanto power – if the USDA or court system wants to halt GM crops or revoke approval, they cannot. It’s also an open backdoor to whisk in future approvals.

This action is detrimental to farmers who want to fight against Monsanto’s patent infringement lawsuits, those for the preservation of organic crops against GM contamination, and our export economy as so many other countries have adopted GM bans. This Monsanto-driven rider is simply an industry ploy to continue to plant GM crops even when a court of law has found they were approved illegally – But it’s being voted on urgently.
What can we do?

Senator Tester, joined by Senators Boxer, Gillibrand and Leahy introduced an amendment to strike the dangerous rider from the CR. You can support the Tester amendments while there is still time. Even if the Tester amendment voting is over with – make your opinion known to your Senators. It couldn’t be easier with pre-formatted letters that go directly to your Senators

Another easy-to-send letter is at Alliance for Natural Health (ANH-USA). They also have a list of phone numbers.

From Food Democracy Now!:….

Read Full Article Here

Fertility Destroying Chemical Added To Tap, Milk, Salt

Posted on:

Sunday, March 10th 2013 at 5:30 am

Written By:

Sayer Ji, Founder

Fertility Destroying Chemical Added To Tap, Milk, Salt

 

There is no question remaining that fluoride lowers IQ, at least as far as high-quality epidemiological research published in peer-reviewed journals has shown.

Take the conclusion of this systematic review of the literature published in the journal Biological and Trace Elements Research in 2008, which looked at whether fluoride exposure has increased the risk of low intelligence quotient (IQ) in China over the past 20 years:

[C]hildren who live in a fluorosis area [high fluoride exposure] have five times higher odds of developing low IQ than those who live in a nonfluorosis area or a slight fluorosis area.

[See our IQ and Fluoride research page for seven first-hand study abstracts on this connection]

Arguably, those who do question this causal connection despite the research are already under fluoride’s powerful spell, since they don’t take sufficient care to reduce their exposure to this intellectually-disabling chemical.  They’ve drank the fluoride-contaminated Kool-aid, and are unable to comprehend what is still obvious to those who have not.

But fluoride’s toxicity is not specific to only one type of tissue, i.e. neurological, but extends throughout the human body, having been linked to at least 30 distinct health problems stretching from calcification of soft tissue and endocrine glands (such as the pineal) to hypothyroidism, from hair loss to cancer. [see Fluoride Toxicity citations here]

While lawmakers, regulators and the industry using it consider the public gullible enough to believe that the IQ-lowering effects of fluoride a worthwhile price to pay for ‘healthy’ and ‘attractive’ teeth (even though fluoride exposure leads to fluorosis, an irreversible spotting, often yellowing of the enamel of the teeth), a more serious health problem lurks beneath the propaganda that has converted an industrial byproduct and pollutant into a “therapeutic” water, salt and milk additive. That problem is fluoride’s infertility and abortifacient properties.

Back in 1994, a study was published in the Journal of Toxicology and Environmental Health that found exposure to high fluoride concentrations in drinking water is associated with decreased birth rates. The researchers had reviewed the biomedical literature for fluoride toxicity and found decreased fertility in most animal species studied. This lead them to question whether fluoride would also affect human birth rates. They reported their method and results as follows:

A U.S. database of drinking water systems was used to identify index counties with water systems reporting fluoride levels of at least 3 ppm. These and adjacent counties were grouped in 30 regions spread over 9 states. For each county, two conceptionally different exposure measures were defined, and the annual total fertility rate (TFR) for women in the age range 10-49 yr was calculated for the period 1970-1988. For each region separately, the annual TFR was regressed on the fluoride measure and sociodemographic covariables. Most regions showed an association of decreasing TFR with increasing fluoride levels. Meta-analysis of the region-specific results confirmed that the combined result was a negative TFR/fluoride association with a consensus combined p value of .0002-.0004, depending on the analytical scenario.  There is no evidence that this outcome resulted from selection bias, inaccurate data, or improper analytical methods. However, the study is one that used population means rather than data on individual women. Whether or not the fluoride effect on the fertility rate found at the county level also applies to individual women remains to be investigated.

Another study published in the American Journal of Industrial Medicine in 1995 found that among fabrication workers fluoride compound exposure was associated with an increased risk of spontaneous abortion:

Read Full Article Here

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FLUORIDEGATE An American Tragedy – a David Kennedy film

Published on Jan 17, 2013

FLUORIDEGATE AN AMERICAN TRAGEDY (1:05:05)
A DOCUMENTARY FILM. By Dr. David Kennedy

WWW.FLUORIDEGATE.ORG

FLUORIDEGATE the movie is a new documentary film that reveals the tragedy of how the United States government, industry, and trade associations protect and promote a policy known to cause harm to our country and especially small children, who suffer more than any other segment of the population. While the basis of their motivation remains uncertain, the outcome is crystal clear: it is destroying our nation.


breakingtheset

Published on Feb 28, 2013

Abby Martin breaks the set on Food Safety, Hactivist Barrett Brown, and Japanese Internment Camps.

EPISODE BREAKDOWN: On this episode of Breaking the Set, Abby Martin talks to Jaydee Hanson, Policy Analyst for the Center for Food Safety, about finds of horse meat in the UK, and what this says about the potential for food fraud in the US. Abby then talks to Christian Stork of WhoWhatWhy.org about the case of online activist, Barrett Brown, and US government’s fixation on preemptive prosecution of anyone exposing government wrongdoing. BTS wraps up the show with a look the 71st anniversary of the internment of Japanese people in the US following the attack on Pearl Harbor, and how the growing surveillance state is the modern day internment camp.

 

ExperimentalVaccinesExperimentalVaccines

Published on Feb 28, 2013

http://experimentalvaccines.org/2013/…
The New World orders eugenicist program has gone into overdrive with the FDA’s approval of a new vaccine technology that uses insect cells to produce the ingredients needed for their toxic inoculations. Instead of using chicken eggs to grow the necessary viral components used in the vaccinators’ lancet the pharmacratic dictatorship have pumped massive amounts of taxpayer dollars into this exotic technology to ensure eugenicists reach their goal of population elimination on a global scale.
FluBlok is the latest concoction being created by Protein Science Corporation which was bailed out in 2009 by the United States taxpayers in order to continue the research and development of this new population reduction weapon. Pumping tens of millions of dollars into this eugenics corporation will help to further the advancements and profit margins of the pharmaceutical industries killing machines by creating more customers identified in trails as ‘severe adverse effects’. Clinical trials have shown that this insect-based influenza vaccination has caused cardiac problems respiratory disorders and in one case the death of a trial participant.
These medical Manchurian’s like to use double entendres to communicate their true objectives to the power-hungry elitists in charge. The name FluBlok would give you the impression that it blocks you from getting the flu but instead it really blocks your ability to fight the flu. Bill Gates has said on numerous occasions that if they can increase the effectiveness and efficiency of vaccinations they would be able to lower populations by 10 to 15% worldwide. The vaccines are designed to injured and damage your immune system making you more susceptible to bacteria and viruses encountered it in the wild.
We’re living on a modern-day ‘Island of Dr. Moreau’ injecting the populace with genetically modified medicines that create new allergies, diseases and illnesses while the media spin them as medical miracles. The world is being used as a giant petri dish with the goal of creating a constant state of pain and suffering which can only be alleviated through the use of their poisonous prescriptions called medications and vaccinations. The pharmaceutical corporations don’t care about people they only care about profits and the best way to ensure they make more profits is by turning people into patients and being alive into a diagnosis.

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This  does  beg  the  question…..If  this  Fall Army  worm  is one of  the  pests  that   Round Up Ready  GMO  Corn  is  manufactured  to  fight  against.  Will  it  also  become immune  to the  pesticide?  And  as  such  will the  mutation  also  cause it  to carry  different DNA structured  that  could  prove detrimental to  people when  introduced as a  vaccine? 
~Desert Rose~
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Damage

Fall armyworm generally feeds on foliage, but during heavy infestations, larvae will also feed on corn ears.  Foliar damage to corn is usually characterized by ragged feeding, and moist sawdust-like frass near the whorl and upper leaves of the plant.  Early feeding can appear to be similar to European corn borer damage; however European corn borer larvae bore into the stalk whereas fall armyworm larvae continue to feed on the foliage making larger more ragged holes.  Ear damage is similar to the damage caused by the corn earworm, chewed kernels and visible frass, except that fall armyworm tends to burrow through the husk instead of feeding down through the silks.

Fall Armyworm 44

Fall armyworm injury to corn plant. (Left) Fall armyworm larva damage on corn foliage. (Right)  Images by Eric Bohnenblust.

Control

Fall armyworm larvae can be difficult to control due to the timing of infestation in Pennsylvania.  Corn plants often are too tall to spray with conventional ground rigs when populations are detected in Pennsylvania.  However, because populations are usually low applying insecticides is rarely profitable.  Therefore, insecticide control options should be attempted only in extreme situations (e.g., 100 percent of the plants are infested and they are less than 30 inches high).

Transgenic corn varieties are a more viable option for preventing/controlling fall armyworm.  There are several varieties on the market that suppress/control of fall armyworm and many other lepidopteran pests.  Be sure to follow refuge requirements associated with the use of Bt corn as different varieties have different requirements.  Also, adding to the importance of following refuge requirements, a field population of fall armyworm in Puerto Rico has been found to be resistant to the Cry 1F toxin in many Bt lines.  With proper management, resistance development is highly unlikely, but if refuge requirements are not followed serious consequences could occur.

Radioactive Waste

By Dr. Mercola

If you had a choice to purchase eyeglasses or a stainless steel water bottle that was either radioactive, albeit only slightly, or not, which would you choose? You would almost certainly choose the non-radioactive product, as it is well- known that no amount of radiation exposure is “safe.”

Yet the U.S. government – specifically the Department of Energy (DOE) – has released a proposal1 that would allow nearly 14,000 tons of radioactive metals to be recycled for use in consumer goods…

Department of Energy Wants to Recycle Their Radioactive Waste Metal Into Common Products

There is currently a suspension in place that restricts the release of scrap metal originating from radiological areas at U.S. DOE facilities (such as research laboratories or nuclear weapons facilities) for the purpose of recycling.

This suspension, which has been in place since 2000, is there for obvious reasons – it was imposed because of public concerns about the potential health and environmental effects of radioactive metals coming from these sites.

Now the DOE has issued a proposal to modify the suspension to allow scrap metals to be released to private industry to be used for any purpose, including recycling.

The draft proposal notes that only metal with the potential for surface, not volume, radioactivity, would be included in this plan, and they are touting it as benefit to the environment “from a decrease in the need for the mining and refining of metals due to the recycling of these materials.” The draft noted:

“Mining and smelting activities are large users of water and power, both of which would be reduced by the recycling of these materials.

In addition, there would be benefits to the environment resulting from reduced land use, reduced disturbance of geology and soils, reduced GHG [greenhouse gas] and other emissions, and reduced occupational injuries associated with the reduced need for mining and refining of metal ores attributable to the recycling of these materials.”

It is unclear just how significant these purported environmental “benefits” could truly be, considering the draft also notes that the radioactive metal in question represents only an “extremely small fraction (of the order of 0.004 percent) of the total metal recycled” in the United States. Of course, it also doesn’t hurt that sales of the metals could bring in up to $40 million a year for the DOE …2

Radioactive Metals Could Increase Cancer Risks and be Used by Pregnant Women and Children

According to the DOE, only a “negligible individual dose” of radiation would be gleaned from exposure to their contaminated metals. They likened the annual exposure amount to half the amount of radiation you’d get from flying across country.

This is an inappropriate comparison, as the internalization of low-dose radioisotopes can have decades-long, severe toxicological consequences due to their bioaccumulation and persistence within the body, whereas external natural radiation exposure only lasts as long as the body is exposed, e.g. the several hour duration of a flight.

Also, the DOE’s minimization of the risks involved do not take into account mistakes that have already happened in the past when the government recycled metal from nuclear sites in the 1990s to 2000s. During that time inadequate testing of the materials was noted, and one test in particular showed metals with radioactivity levels several times higher than were supposed to be allowed.3

Other unanswered questions include the risks that could be posed to workers who must handle the radioactive metals on a daily basis, or to those who end up with a “slightly” radioactive surgical implant or set of braces. The Wall Street Journal reported on just a peppering of the backlash that has already surfaced:4

Some critics argue the DOE’s proposed exposure standards are too high and that information provided in its 50-page document explaining the proposal is even more worrisome.

Higher exposures could occur if contaminated metal is made into items such as belt buckles or hip-replacement joints, said Daniel Hirsch, a lecturer on nuclear policy at the University of California, Santa Cruz, and critic of the government’s proposal. Such exposures would further increase a person’s cancer risk, he said.

…Rep. Ed Markey wrote to Energy Secretary Steven Chu, calling the recycling proposal ‘unwise’ and stating the proposal ‘should be immediately abandoned.’ The Massachusetts Democrat added that contaminated products could ‘ultimately be utilized by pregnant women, children and other vulnerable populations.’”

Radioactive Scrap Metal is Already a Problem

The DOE’s proposal would only add to the growing amount of radioactive scrap metal circulating globally. You may remember headlines from last year when radioactive metal tissue boxes were found at Bed, Bath and Beyond stores in the United States. In this case the products were tainted with cobalt-60, a radioactive compound used in the medical industry to diagnose and treat cancer.5 The radiation-safety chief for one of the world’s biggest stainless-steel scrap yards actually told the Seattle Times last year that:6

“The major risk we face in our industry is radiation… You can talk about security all you want, but I’ve found weapons-grade uranium in scrap. Where was the security?”

That company alone found 145 nuclear items in their scrap metal in 2011 and another 200 in 2010. It’s unclear how much of this radioactive metal slips through the cracks and ends up getting processed into metal goods that are then sold to unassuming consumers…

And this isn’t only a matter of cancer. Radiation exposure of the developing embryo or fetus during pregnancy can also contribute to the development of diseases other than cancer in children. There is evidence of radiation exposure leading to increased incidence of cataracts, and there is also a phenomenon known as the “bystander effect,” which multiplies the dose and harm from radiation exposures. According to Dr. Mae-Wan Ho, cells that have not been exposed to radiation can be harmed by nearby cells that have. Writing for ISIS, Dr. Ho explains:7

“…low dose radiation is all the more dangerous because it does not kill the targeted cell, but allows its influence to spread widely to adjacent cells, thus multiplying the radiation effect (about 100 fold) …a wide range of bystander effects in cells not directly exposed to ionizing radiation have been found, which are the same as or similar to those in the cells that were exposed, including cell death and chromosomal instability.”

Share Your Concerns About the Release of Radioactive Scrap Metal

Although the 30-day comment period for the DOE draft proposal to release radioactive scrap metal for recycling has ended, late comments may still be considered. You can share your comments with the Department of Energy by emailing:

Scrap_PEA_Comments@hq.doe.gov

Written comments can be mailed to:

Dr. Jane Summerson, DOE NNSA
P.O. Box 5400
Bldg 401
KAFB East
Albuquerque, NM 87185

Protecting Yourself in Our “Radioactive World”

“The general public basically isn’t aware that they’re living in a radioactive world,” said Ross Bartley, technical director for the Bureau of International Recycling.8 Indeed, today’s “background” levels of radiation have been greatly increased by discharges from nuclear activities including tests of nuclear weapons, use of depleted uranium, and uranium mining, not to mention environmental catastrophes like the Fukushima nuclear plant. If you’re looking for strategies to help prevent damage caused by radiation exposure, there are several I recommend, including:

  • Vitamin D3 (also known as calcitriol) may offer protection against a variety of radiation-induced damages, including even those caused by background radiation or a low-level nuclear incident.
  • Spirulina – a blue-green algae – might be another useful alternative to protect against the effects of radiation. Spirulina was actually used to treat children exposed to chronic low levels of radiation after the Chernobyl nuclear disaster.
  • Turmeric contains a broad spectrum of water, fat and alcohol-soluble components, all of which may contribute to reducing damage associated with both external radiation and internalized radioisotope exposures.
  • Whey: the use of a high-quality whey protein concentrate may help protect against absorbing radioactive minerals.

The following foods, herbs and supplements may also help support your overall health in the event of radiation exposure:

Ginseng Kelp and other seaweeds (high in natural iodine) Zeolites (to neutralize radiation) or bentonite clays
Ashwaganda (an adaptogenic herb) Fulvic Acid Reishi mushrooms (strong immune support)
High-dose vitamin C Magnesium Selenium
Coconut oil, which supports optimal thyroid health Astaxanthin (has some protective function against ionizing radiation) Chlorella (contains chlorophyll, which will increase your resistance to radiation)

Mercola.com

Call Toll Free: 877-985-2695

Inside LSD Full Length Documentary

Uploaded on Oct 19, 2011

Lysergic acid diethylamide, abbreviated LSD or LSD-25, also known as lysergide and colloquially as acid, is a semisynthetic psychedelic drug of the ergoline family, well known for its psychological effects which can include altered thinking processes, closed and open eye visuals, synaesthesia, an altered sense of time and spiritual experiences, as well as for its key role in 1960s counterculture. It is used mainly as an entheogen, recreational drug, and as an agent in psychedelic therapy. LSD is non-addictive, is not known to cause brain damage, and has extremely low toxicity relative to dose, although in rare cases adverse psychiatric reactions such as anxiety or delusions are possible.[3]

LSD was first synthesized by Albert Hofmann in 1938 from ergotamine, a chemical derived by Arthur Stoll from ergot, a grain fungus that typically grows on rye. The short form “LSD” comes from its early code name LSD-25, which is an abbreviation for the German “Lysergsäure-diethylamid” followed by a sequential number.[4][5] LSD is sensitive to oxygen, ultraviolet light, and chlorine, especially in solution, though its potency may last for years if it is stored away from light and moisture at low temperature. In pure form it is a colorless, odorless, and mildly bitter solid.[6] LSD is typically delivered orally, usually on a substrate such as absorbent blotter paper, a sugar cube, or gelatin. In its liquid form, it can also be administered by intramuscular or intravenous injection. LSD is very potent, with 20–30 µg (micrograms) being the threshold dose.[7]

Introduced by Sandoz Laboratories, with trade-name Delysid, as a drug with various psychiatric uses in 1947, LSD quickly became a therapeutic agent that appeared to show great promise.[8] In the 1950s the CIA thought it might be applicable to mind control and chemical warfare; the agency’s MKULTRA research program propagated the drug among young servicemen and students. The subsequent recreational use of the drug by youth culture in the Western world during the 1960s led to a political firestorm that resulted in its prohibition.[9] Currently, a number of organizations—including the Beckley Foundation, MAPS, Heffter Research Institute and the Albert Hofmann Foundation—exist to fund, encourage and coordinate research into the medicinal and spiritual uses of LSD and related psychedelics.[10]

BBC Horizon: Psychedelic Science – (DMT, LSD, Ibogaine)

Uploaded on May 7, 2011

A documentary about the psychedelic drugs: DMT, LSD and the newly rediscovered Ibogaine.

Skyline productions

CIA LSD Experiment – Schizophrenic Model Psychosis Induced by LSD-25 – Art Drawing (1955)

Published on Jul 10, 2012

Artists and scientists have been interested in the effect of LSD on drawing and painting since it first became available for legal use and general consumption. Dr. Oscar Janiger was one of the pioneers in the field studying the relationship between LSD and creativity. What fascinated Janiger was that “paintings, under the influence of LSD, had some of the attributes of what looked like the work done by schizophrenics”. Janiger maintained that trained artists could “maintain a certain balance, riding the edge” of the LSD induced psychosis, “ride his creative Pegasus”. Janiger coined the term ‘”dry schizophrenia,” where a person was able to control the surroundings and yet be “crazy” at the same time’.

Many artists and their surviving relatives have kept LSD artwork from this period. One patient of Dr. Janiger, bipolar and alcoholic artist Frank Murdoch, was given a controlled, experimental dose of LSD for several months as an attempt to cure his late stage alcoholism. Janiger had Murdoch paint still-lives both on and off LSD, including a Kachina doll (that he reportedly had 70 other patients also paint). Murdoch also continued to paint as an artist while on LSD, including most of his underwater paintings.

In the Netherlands, Dr. Stanislav Grof practiced “LSD Psychotherapy” in the 1980s, which included having his patients paint on LSD. Some of his artist patients painted numerous paintings while on LSD.

http://en.wikipedia.org/wiki/LSD_art

LSD was first synthesized on November 16, 1938 by Swiss chemist Albert Hofmann at the Sandoz Laboratories in Basel, Switzerland as part of a large research program searching for medically useful ergot alkaloid derivatives. LSD’s psychedelic properties were discovered 5 years later when Hofmann himself accidentally ingested an unknown quantity of the chemical. The first intentional ingestion of LSD occurred on April 19, 1943, when Hofmann ingested 250 µg of LSD. He said, this would be a threshold dose based on the dosages of other ergot alkaloids. Hofmann found the effects to be much stronger than he anticipated. Sandoz Laboratories introduced LSD as a psychiatric drug in 1947.

Beginning in the 1950s the US Central Intelligence Agency began a research program code named Project MKULTRA. Experiments included administering LSD to CIA employees, military personnel, doctors, other government agents, prostitutes, mentally ill patients, and members of the general public in order to study their reactions, usually without the subject’s knowledge. The project was revealed in the US congressional Rockefeller Commission report in 1975.

In 1963 the Sandoz patents expired on LSD. Also in 1963, the US Food and Drug Administration classified LSD as an Investigational New Drug, which meant new restrictions on medical and scientific use. Several figures, including Aldous Huxley, Timothy Leary, and Al Hubbard, began to advocate the consumption of LSD. LSD became central to the counterculture of the 1960s. On October 24, 1968, possession of LSD was made illegal in the United States. The last FDA approved study of LSD in patients ended in 1980, while a study in healthy volunteers was made in the late 1980s. Legally approved and regulated psychiatric use of LSD continued in Switzerland until 1993. Today, medical research is resuming around the world.

http://en.wikipedia.org/wiki/Lysergic_acid_diethylamide

MKULTRA Compendium: http://www.amazon.com/gp/product/1441499733/ref=as_li_tf_tl?ie=UTF8&camp=…

‘CIA – LSD experiment’ sends French village mad.

Uploaded on Mar 11, 2010

* Residents suddenly go psychotic
* Local baker cops the blame
* Turns out CIA may have spiked bread

A US writer has uncovered evidence suggesting the CIA spiked a French village’s food with the hallucinogenic drug LSD

Journalist H P Albarelli Jr came across CIA documents while investigating the suspicious suicide of a biochemist who fell from a 13th floor window two years after a mystery illness that caused an entire French village to go temporarily mad 50 years ago.

Hundreds of residents in picturesque Pont-Saint-Esprit were suddenly struck down with mass insanity and hallucinations on August 16, 1951.

At least five people in the southern French village died and dozens were locked up in asylums after witnessing terrifying hallucinations of dragons and fire.

In the horror scenes an 11-year-old tried to strangle his grandmother. Another man shouted: “I am a plane”, before jumping out of a second-floor window, breaking his legs.

For decades the bizarre “Cursed Bread” incident was blamed on a local baker whose baguettes had been poisoned with either a psychedelic mould or mercury.

But new evidence points the finger at the CIA who are accused of spiking bread with LSD in a mind control experiment.

The incident – which took place at the height of the Cold War – was investigated by a Swiss pharmaceutical company Sandoz. The company has been revealed as the same organisation that secretly supplied the CIA with LSD.

One note transcribes a conversation between a CIA agent and a Sandoz official who mentions the “secret of Pont-Saint-Esprit” and explains that it was not “at all” caused by mould but by diethylamide – the D in LSD.

The French Government has officially denied any involvement in the case. According to US reports, French intelligence chief have demanded the CIA explain itself. The CIA is yet to come forward.

Cat on LSD

Uploaded on Apr 22, 2007

Government experiments on cats using drugs.

For those of you too stupid to figure it out: I did not create this video. Our government did.

To make it even clearer: this cat was long dead by the time I was even born.

Government Mind Control: MKULTRA & LSD | Brainwash Update

Published on Dec 20, 2012

Abby Martin takes a look at the US government’s morbid history of mind-control, MKULTRA, and the testing of deadly chemicals on US citizens.

1960′s Chidlren on LSD

Uploaded on Sep 26, 2006

This is not a joke. This is merely to show that the drug lsd was administered to children, like lab rats. kinda scary.

The Net: The Unabomber, LSD and the Internet [HQ FULL]

Published on Mar 16, 2012

Full version of Lutz Dammbecks 2003 documentary.
Highest quality on YouTube.

The Net explores the complex back-story of Ted Kaczynski, the infamous Unabomber. An inquiry into the rationale of this notable figure situates him within a late 20th Century web of technology – a system that he grew to oppose. Incorporating a subversive approach to the history of the Internet, the documentary combines speculative travelogue and investigative journalism to trace contrasting counter cultural responses to the cybernetic revolution.

For those who resist these intrusive systems of technological control, the Unabomber has come to symbolize an ultimate figure of refusal. For those that embrace it, as did the early champions of media art like Marshall McLuhan, Nam June Paik, and Stewart Brand, the promises of worldwide networking and instantaneous communication outweighed the perils.

Working through themes of utopianism, anarchism, terrorism, and providing insights on the CIA, LSD, Project MK-ULTRA, Timothy Leary, Ken Kesey and the Merry Pranksters, Dammbeck provides a fascinating view of the wider picture of the most famous neo-luddite.

- shortened and altered summary originally from Amazon.com

 

GMO Hemp

Barbara H. Peterson

Farm Wars

Let’s get this straight. There is cannabis, and there is CANNABIS. One has relatively no THC levels, and the other does. It’s like two dogs – one a Chihuahua, the other a Great Dane. Same species, different breeds. The one with higher levels of THC is normally referred to as marijuana. That is the one that gets you high if heated. The other one, without high THC levels, is hemp. Smoke a pound of it and you’ll only get a headache… maybe. Yet, these are both illegal according to the U.S. government. Why? That’s a very good question.

Federal Hypocrisy in Action

One of the arguments against cannabis legalization in the U.S. is that “getting high” via THC is evidently unacceptable. Go drink a fifth of whiskey or down some barbiturates courtesy of your local licensed Big Pharma drug pusher instead. But don’t do both together, or you might die. In fact, you could die from either one, but that’s evidently irrelevant, as long as it is approved by our corporate government. In other words, don’t use your own drugs, use ours. Yeah, that’s safer. Take for example, Intermezzo, just in case you have that occasional sleepless night.

 Intermezzo

http://www.myintermezzo.com/portal/f?p=800:SAFETY:0::NO:::

“…the FDA is fully aware that the drugs it certifies as safe have been killing Americans at the rate of 100,000 per year.” (Jon Rappoport)

Here’s a novel idea – Before selling pain killers or sleeping pills, why not force Big Pharma to take the “high” out of them? Why not hold Big Pharma meds to the same standards? After all, that is the objectionable part to marijuana, isn’t it? Or so we’ve been told.

The only thing that anyone can complain about regarding the weed is that you are liable to get a little goofy if you take it. No side effects. None. Use enough and you go to sleep. Period. No depression, no vomiting or death by asphyxiation.

But that’s different, you say?

Why?

Well, what about the “gateway” theory that smoking marijuana will lead to stronger drugs?

The real gateway is the medicine cabinet in our own homes. Just count the prescriptions in there, then try and tell your child that drugs are bad. Yes, you can get high smoking marijuana, big deal. You can also get high doing any number of dangerous things, smoking marijuana NOT being one of them. Industrial hemp, however, will not get anyone high!

liarLies, Lies, and more Lies

Since the U.S. government does not differentiate between high THC content marijuana and its low content relation, industrial hemp, both are banned. Not because the government somehow missed the class on the difference between the two, that’s just plain silly.

So, why the ban?

It only makes sense if you understand that our government doesn’t care one lick about our health, or the health of the planet. The people in our government just want to keep their corporate donors flush in profits, power, and control. So, what to do? Simple. Conduct a war on the one plant that could quite possibly, if it was legal, put those donors out of business. At least for the time being…

So, here’s the spin – Have the government declare that cannabis, all cannabis, has no medicinal value and is illegal to grow, or even possess if it is the wrong breed. In fact, as recently as 2011, “the federal government ruled that it has no accepted medical use and should remain classified as a highly dangerous drug like heroin.

Really???? Well, that says it all, eh? But wait! There is a government study from 1999 that says just the opposite!

And here is a patent for medical marijuana assigned to the US government:

http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=6630507.PN.&OS=PN/6630507&RS=PN/6630507

Another patent:

http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=8337908.PN.&OS=PN/8337908&RS=PN/8337908

Hmmmm…  Methinks the lies are starting to unravel before our very eyes.

 

Read Full Article Here

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